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Diabetes<br />

& Primary Care Australia<br />

Vol 2 No 2 2017<br />

The primary care diabetes journal for healthcare professionals in Australia<br />

Pre-gestational diabetes in pregnancy<br />

This <strong>issue</strong> includes guidance on how<br />

to optimise pregnancy outcomes<br />

through pre-conception care and the<br />

resources available for mothers with<br />

pre-gestational diabetes and healthcare<br />

professionals who care for them.<br />

E-learning on pre-conception care for<br />

women with pre-gestational diabetes is<br />

available at www.pcdsa.au.org/cpd.<br />

Page 54<br />

IN THIS ISSUE<br />

Bone health<br />

The relationship between<br />

diabetes and bone health,<br />

and the impact of poor bone<br />

health on patients. Page 61<br />

Preventing falls<br />

A clinical review of the<br />

screening, assessment and<br />

management of older people<br />

at risk of falls. Page 69<br />

Diabetes and skin<br />

Considering the skin of<br />

people with diabetes and the<br />

importance of skin care before<br />

and after ulceration. Page 75<br />

WEBSITE<br />

Journal content online at<br />

www.pcdsa.com.au/journal


The PCDSA is a multidisciplinary society with the aim<br />

of supporting primary health care professionals to deliver<br />

high quality, clinically effective care in order to improve<br />

the lives of people with diabetes.<br />

The PCDSA will<br />

Share best practice in delivering quality diabetes care.<br />

Provide high-quality education tailored to health professional needs.<br />

Promote and participate in high quality research in diabetes.<br />

Disseminate up-to-date, evidence-based information to health<br />

professionals.<br />

Form partnerships and collaborate with other diabetes related,<br />

high level professional organisations committed to the care of<br />

people with diabetes.<br />

Promote co-ordinated and timely interdisciplinary care.<br />

Membership of the PCDSA is free and members get access to a quarterly<br />

online journal and continuing professional development activities. Our first<br />

annual conference will feature internationally and nationally regarded experts<br />

in the field of diabetes.<br />

To register, visit our website:<br />

www.pcdsa.com.au


Contents<br />

Diabetes<br />

& Primary Care Australia<br />

Volume 2 No 2 2017<br />

Website: www.pcdsa.com.au/journal<br />

Editorial<br />

Diabetes and pregnancy 45<br />

Rajna Ogrin introduces this <strong>issue</strong>, which has a focus on pregnancy and pre-conception care for women with pre-gestational diabetes.<br />

From the other side of the desktop<br />

Through diagnosis to pregnancy: My journey with diabetes 47<br />

Karen Barrett gives a first-hand perspective on her journey with diabetes and how it affected her pregnancies.<br />

CPD module<br />

Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care 54<br />

Glynis Ross provides guidance to support early detection of peripheral arterial disease using evidence-based clinical tests.<br />

Articles<br />

Resources to support preconception care for women with diabetes 50<br />

Melinda Morrison, Ralph Audehm, Alison Barry and colleagues describe the resources available for health professionals and women with<br />

diabetes and provide up-to-date, evidence-based information on pregnancy and diabetes.<br />

Diabetes and bone health 61<br />

Vidhya Jahagirdar and Neil J Gittoes explore the current literature on diabetes and bone health, its impact on patients and the management<br />

strategies that may be considered in primary care to minimise risk of diabetes-related bone disease and to improve outcomes.<br />

Falls prevention in older adults with diabetes: A clinical review of screening, assessment and management recommendations 69<br />

Anna Chapman and Claudia Meyer review the screening, assessment and management recommendations for fall prevention in older people.<br />

The effect of diabetes on the skin before and after ulceration 75<br />

Roy Rasalam and Lesley Weaving look at the changes that occur in the skin of people with diabetes and the importance of skin care in<br />

relation to ulceration.<br />

Editor-in-Chief<br />

Rajna Ogrin<br />

Senior Research Fellow, RDNS<br />

Institute, St Kilda, Vic<br />

Associate Editor<br />

Gary Kilov<br />

Practice Principal, The Seaport<br />

Practice, and Senior Lecturer,<br />

University of Tasmania,<br />

Launceston, Tas<br />

Editorial Board<br />

Ralph Audehm<br />

GP Director, Dianella Community<br />

Health, and Associate Professor,<br />

University of Melbourne,<br />

Melbourne, Vic<br />

Werner Bischof<br />

Periodontist, and Associate<br />

Professor, LaTrobe University,<br />

Bendigo, Vic<br />

Jessica Browne<br />

Senior Research Fellow, School of<br />

Psychology, Deakin University,<br />

Melbourne, Vic<br />

Anna Chapman<br />

Research Fellow, School of<br />

Primary Health Care, Monash<br />

University, Melbourne, Vic<br />

Laura Dean<br />

Course Director of the Graduate<br />

Certificate in Pharmacy<br />

Practice, Monash University, Vic<br />

Nicholas Forgione<br />

Principal, Trigg Health Care<br />

Centre, Perth, WA<br />

John Furler<br />

Principal Research Fellow and<br />

Associate Professor,<br />

University of Melbourne, Vic<br />

Mark Kennedy<br />

Medical Director, Northern Bay<br />

Health, Geelong, and Honorary<br />

Clinical Associate Professor,<br />

University of Melbourne,<br />

Melbourne, Vic<br />

Peter Lazzarini<br />

Senior Research Fellow,<br />

Queensland University of<br />

Technology, Brisbane, Qld<br />

Roy Rasalam<br />

Head of Clinical Skills and<br />

Medical Director,<br />

James Cook University, and<br />

Clinical Researcher, Townsville<br />

Hospital, Townsville, Qld<br />

Suzane Ryan<br />

Practice Principal, Newcastle<br />

Family Practice, Newcastle, NSW<br />

Editor<br />

Olivia Tamburello<br />

Editorial Manager<br />

Richard Owen<br />

Publisher<br />

Simon Breed<br />

© OmniaMed SB and the Primary Care<br />

Diabetes Society of Australia<br />

Published by OmniaMed SB,<br />

1–2 Hatfields, London<br />

SE1 9PG, UK<br />

All rights reserved. No part of this<br />

journal may be reproduced or transmitted<br />

in any form, by any means, electronic<br />

or mechanic, including photocopying,<br />

recording or any information retrieval<br />

system, without the publisher’s<br />

permission.<br />

ISSN 2397-2254<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 43


Call for papers<br />

Would you like to write an article<br />

for Diabetes & Primary Care Australia?<br />

The new journal from the Primary Care Diabetes Society of Australia<br />

To submit an article or if you have any queries, please contact: gary.kilov@pcdsa.com.au.<br />

Title page<br />

Please include the article title, the full names of the authors<br />

and their institutional affiliations, as well as full details of<br />

each author’s current appointment. This page should also have<br />

the name, address and contact telephone number(s) of the<br />

corresponding author.<br />

Article points and key words<br />

Four or five sentences of 15–20 words that summarise the major<br />

themes of the article. Please also provide four or five key words<br />

that highlight the content of the article.<br />

Abstract<br />

Approximately 150 words briefly introducing your article,<br />

outlining the discussion points and main conclusions.<br />

Introduction<br />

In 60–120 words, this should aim to draw the reader into the<br />

article as well as broadly stating what the article is about.<br />

Main body<br />

Use sub-headings liberally and apply formatting to differentiate<br />

between heading levels (you may have up to three heading levels).<br />

The article must have a conclusion, which should be succinct and<br />

logically ordered, ideally identifying gaps in present knowledge and<br />

implications for practice, as well as suggesting future initiatives.<br />

Tables and illustrations<br />

Tables and figures – particularly photographs – are encouraged<br />

wherever appropriate. Figures and tables should be numbered<br />

consecutively in the order of their first citation in the text. Present<br />

tables at the end of the articles; supply figures as logically labelled<br />

separate files. If a figure or table has been published previously,<br />

acknowledge the original source and submit written permission<br />

from the copyright holder to reproduce the material.<br />

References<br />

In the text<br />

Use the name and year (Harvard) system for references in the<br />

text, as exemplified by the following:<br />

● As Smith and Jones (2013) have shown …<br />

● As already reported (Smith and Jones, 2013) …<br />

For three or more authors, give the first author’s surname<br />

followed by et al:<br />

● As Robson et al (2015) have shown …<br />

Simultaneous references should be ordered chronologically first,<br />

and then alphabetically:<br />

● (Smith and Jones, 2013; Young, 2013; Black, 2014).<br />

Statements based on a personal communication should be<br />

indicated as such, with the name of the person and the year.<br />

In the reference list<br />

The total number of references should not exceed 30 without prior<br />

discussion with the Editor. Arrange references alphabetically first,<br />

and then chronologically. Give the surnames and initials of all<br />

authors for references with four or fewer authors; for five or more,<br />

give the first three and add “et al”. Papers accepted but not yet<br />

published may be included in the reference list as being “[In press]”.<br />

Journal article example: Robson R, Seed J, Khan E et al (2015)<br />

Diabetes in childhood. Diabetes Journal 9: 119–23<br />

Whole book example: White F, Moore B (2014) Childhood<br />

Diabetes. Academic Press, Melbourne<br />

Book chapter example: Fisher M (2012) The role of age. In: Merson<br />

A, Kriek U (eds). Diabetes in Children. 2nd edn. Academic Press,<br />

Melbourne: 15–32<br />

Document on website example: Department of Health (2009)<br />

Australian type 2 diabetes risk assessment tool (AUSDRISK).<br />

Australian Government, Canberra. Available at: http://www.<br />

health.gov.au/preventionoftype2diabetes (accessed 22.07.15)<br />

Article types<br />

Articles may fall into the categories below. All articles should be<br />

1700–2300 words in length and written with consideration of<br />

the journal’s readership (general practitioners, practice nurses,<br />

prescribing advisers and other healthcare professionals with an<br />

interest in primary care diabetes).<br />

Clinical reviews should present a balanced consideration of a<br />

particular clinical area, covering the evidence that exists. The<br />

relevance to practice should be highlighted where appropriate.<br />

Original research articles should be presented with sections<br />

for the background, aims, methods, results, discussion and<br />

conclusion. The discussion should consider the implications<br />

for practice.<br />

Clinical guideline articles should appraise newly published<br />

clinical guidelines and assess how they will sit alongside<br />

existing guidelines and impact on the management of diabetes.<br />

Organisational articles could provide information on newly<br />

published organisational guidelines or explain how a particular<br />

local service has been organised to benefit people with diabetes.<br />

— Diabetes & Primary Care Australia —


Editorial<br />

Diabetes and pregnancy<br />

It is well known that diabetes is a systemic<br />

condition and, if not managed efficiently,<br />

can have a life-changing impact on the eyes,<br />

feet and kidneys. In this <strong>issue</strong>, we consider<br />

the impact of uncontrolled hyperglycaemia on<br />

other body systems and functions – from skin<br />

to bone, and from pregnancy to older age. On<br />

page 75, Roy Rasalam and Lesley Weaving<br />

discuss the practical aspects of maintaining<br />

healthy skin in people with diabetes, and<br />

Neil Gittoes and Vidhya Jahagirdar provide a<br />

clinical review of the potential complications<br />

to bone health as a result of diabetes (page 61).<br />

There is a special section on diabetes and<br />

pregnancy covering preconception care in<br />

primary care and the resources available<br />

for women with diabetes and health care<br />

professionals (starting from page 47). Finally,<br />

there is a paper by Anna Chapman and<br />

Claudia Meyer on the increased risk of falls<br />

in older people with diabetes and what can be<br />

done to lower the risk (page 69). This topic is<br />

especially pertinent with the growing ageing<br />

population seen in Australia and globally.<br />

Diabetes and pregnancy<br />

One relatively new area of research in<br />

diabetes and pregnancy that has caught my<br />

eye is epigenetics – the effect of environment<br />

on genetics. Questions are being raised<br />

as to whether the maternal environment<br />

(e.g. maternal obesity, poor nutrition and<br />

hyperglycaemia) may “program” type 2<br />

diabetes in offspring. There is some evidence<br />

that suggests that shared genetic and<br />

environmental risk, as well as developmental<br />

programming, may lead to children born to<br />

women with diabetes during pregnancy at<br />

greater risk of developing type 2 diabetes in<br />

later life (Berends and Ozanne, 2012). If the<br />

female offspring then have their own children,<br />

it is thought that an intergenerational<br />

cycle of diabetes risk could be established<br />

(Dabelea and Crume, 2011). The intricacies<br />

of this are important to understand, as many<br />

women with pre-existing type 2 diabetes<br />

are often overweight or obese. They often<br />

continue to gain weight with each additional<br />

pregnancy and are sometimes reluctant to<br />

engage with health services (Bandyopadhyay<br />

et al, 2011). Women of South East Asian<br />

origin are at particularly high risk of diabetes<br />

during pregnancy, so by developing effective<br />

strategies to specifically address these factors,<br />

the risk of future diabetes to offspring may be<br />

reduced (Greenhalgh et al, 2015).<br />

What other considerations need to be<br />

made to avoid the increased risk of adverse<br />

pregnancy outcomes as a result of diabetes?<br />

Pre-gestational diabetes (type 1 and<br />

type 2 diabetes) is present in approximately<br />

1% of pregnant women in Australia and the<br />

prevalence is increasing not only here, but<br />

around the world. Women with pre-existing<br />

diabetes are at high risk of complications<br />

during pregnancy, with up to four times<br />

the rate of congenital malformations, and<br />

up to a five-fold increased risk of stillbirth<br />

and perinatal mortality compared to women<br />

without diabetes. By safely optimising blood<br />

glucose management, women can significantly<br />

reduce their risk of complications, and<br />

preconception care has been shown to reduce<br />

these risks (Inkster et al, 2006).<br />

Women of child-bearing age with diabetes<br />

need to be informed of the availability and<br />

importance of preconception care, which<br />

can be provided by both primary and<br />

specialised diabetes services; many women<br />

with type 1 diabetes access diabetes specialist<br />

services, while the majority of women with<br />

type 2 diabetes are managed in primary care.<br />

Included in preconception care is appropriate<br />

contraception advice. Here, primary care<br />

providers can make a real difference in<br />

promoting and providing appropriate<br />

contraception to women with diabetes to<br />

prevent unplanned pregnancies.<br />

In this pregnancy special, there are three<br />

pieces related to pregnancy and diabetes. There<br />

is a CPD module outlining the requirements<br />

of preconception care for women with<br />

Rajna Ogrin<br />

Editor of Diabetes & Primary Care<br />

Australia, and Senior Research<br />

Fellow, RDNS Institute,<br />

St Kilda, Vic.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 45


Editorial<br />

“By considering the<br />

health and wellbeing of<br />

women with diabetes<br />

prior to pregnancy,<br />

we anticipate<br />

that meaningful<br />

improvements in<br />

pregnancy outcomes<br />

are possible.”<br />

diabetes, including practical information for<br />

health care providers, as well as case studies to<br />

highlight the application of this information<br />

in clinical practice (page 54). There is also<br />

a wealth of resources for the clinician and<br />

woman with diabetes to optimise healthy<br />

pregnancy outcomes. Melinda Morrison from<br />

the National Diabetes Services Scheme and<br />

colleagues outline the resources available,<br />

such as apps, booklets and online resources<br />

(page 50). We also have the first “From<br />

the other side of the desk” feature – a<br />

new series to inform clinical care from the<br />

perspectives of people with diabetes. In the<br />

first of the series, Karen Barrett discusses her<br />

journey with diabetes and how it affected her<br />

pregnancies (page 47).<br />

By considering the health and wellbeing<br />

of women with diabetes prior to pregnancy,<br />

and utilising the resources that have been<br />

developed specifically to support this group<br />

before, during and after pregnancy, we<br />

anticipate that meaningful improvements in<br />

pregnancy outcomes are possible. n<br />

2017 NATIONAL CONFERENCE<br />

Saturday 6th May 2017 – Melbourne Convention and Exhibition Centre, Victoria, Australia<br />

The conference has been specifically designed for all primary care health<br />

professionals working in diabetes care to:<br />

Advance their education and learning in the field of diabetes health care<br />

Promote best practice standards and clinically effective care in the management of diabetes<br />

Facilitate collaboration between health professionals to improve the quality of diabetes<br />

primary care across Australia<br />

6TH MAY 2017 CONFERENCE PROGRAM<br />

The 2017 PCDSA national conference program will combine cutting edge scientific content with<br />

practical clinical sessions, basing the education on much more than just knowing the guidelines.<br />

The distinguished panel of speakers will share their specialised experience in an environment<br />

conducive to optimal learning. The Speaking faculty include, amongst others:<br />

Associate Professor<br />

Neale Cohen<br />

Director Clinical Diabetes<br />

Baker Heart and<br />

Diabetes Institute<br />

“Diabetes management<br />

and research in primary<br />

care – key components<br />

to improving outcomes”<br />

Doctor Christel<br />

Hendrieckx<br />

Senior Research Fellow<br />

The Australian Centre<br />

for Behavioural Research<br />

in Diabetes<br />

“The emotional health of<br />

people living with diabetes”<br />

For further information including the full 2017 program<br />

and to register for the conference please visit:<br />

www.eventful.com.au/pcdsa2017<br />

If you have any questions regarding the conference,<br />

please contact the Conference Secretariat;<br />

Toll free telephone: 1800 898 499<br />

Email: pcdsa@eventful.com.au<br />

Ms Renza Scibilia<br />

Manager - Type 1 Diabetes<br />

and Consumer Voice<br />

Diabetes Australia<br />

“Engaging people with<br />

diabetes, the diabetes<br />

online community and<br />

apps for diabetes”<br />

Doctor Gautam<br />

Vaddadi<br />

Consultant Cardiologist<br />

Alfred Health, Northern Health,<br />

University of Melbourne<br />

“The emerging importance<br />

of cardiac failure diagnosis<br />

and management in people<br />

with type 2 diabetes”<br />

pcdsa.com.au<br />

Bandyopadhyay M, Small R, Davey MA et al (2011) Lived<br />

experience of gestational diabetes mellitus among immigrant<br />

South Asian women in Australia. Aust N Z J Obstet Gynaecol<br />

51: 360–4<br />

Berends LM, Ozanne SE (2012) Early determinants of type 2<br />

diabetes. Best Pract Res Clin Endocrinol Metab 26: 569–80<br />

Dabelea D, Crume T (2011) Maternal environment and the<br />

transgenerational cycle of obesity and diabetes. Diabetes 60:<br />

1849–55<br />

Greenhalgh T, Clinch M, Afsar N et al (2015) Socio-cultural<br />

influences on the behaviour of South Asian women with<br />

diabetes in pregnancy: qualitative study using a multi-level<br />

theoretical approach. BMC Med 13: 120<br />

Inkster ME, Fahey TP, Donnan PT et al (2006) Poor glycated<br />

haemoglobin control and adverse pregnancy outcomes in<br />

type 1 and type 2 diabetes mellitus: Systematic review of<br />

observational studies BMC Pregnancy Childbirth 6: 30<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017


From the other side of the desk<br />

From the other side of the desk:<br />

Patient perspective<br />

Through diagnosis to pregnancy:<br />

My journey with diabetes<br />

Karen Barrett<br />

I<br />

was diagnosed with type 1 diabetes on Valentine’s<br />

Day, 1983, a day meant for chocolates, roses<br />

and sweets. What an irony it turned out to be.<br />

Dressed in my school uniform and ready for school,<br />

my Mum, being a nurse, had known for some time<br />

that something wasn’t right. I had lost a substantial<br />

amount of weight and the bathroom seemed to<br />

be my best friend, as did my unquenchable thirst.<br />

“Oh what a bombshell!” my Mum’s colleague said<br />

that day after hearing my diagnosis. I never really<br />

comprehended the significance of the diagnosis at<br />

the time. I had felt fine.<br />

In the early days after my diagnosis, to see my<br />

diabetes specialist meant a day off school and a trip<br />

to Canberra – that was the good part. The not-sogood<br />

part became the endless questions from the<br />

doctor – what was I putting in my mouth and at<br />

exactly what time of the day – measurements on the<br />

scales, numbers in books, pathology results and eye<br />

tests. On and on it went. Would I pass or fail? Had<br />

I been good or bad? I hated it.<br />

There was never a time that I let my diabetes<br />

stand in the way. I was quite sporty growing up<br />

in a small country town, later trying triathlons<br />

and endurance sports. But in my school life, I was<br />

sometimes left out, missing the first school camp<br />

because everyone was so very nervous to have a<br />

person with diabetes at camp and friends’ parents<br />

being reluctant to have me over, afraid of what or<br />

what not to feed me.<br />

As an adolescent, I was studious and quite fit and<br />

healthy, with an obsessive personality. That was<br />

until my late teens, when I seemed to burn out with<br />

school, with life and with diabetes. Life became<br />

tricky. I found solace in food and subsequently paid<br />

the price, gaining weight.<br />

My family, of course, was concerned, but the<br />

constant questions about how many blood sugar<br />

tests I was doing and whether I was looking after<br />

myself was a continuous reminder of my diabetes,<br />

something I wanted to forget. I ate in secret and lied<br />

to keep them satisfied while continuing to silently<br />

struggle. I was tired of all the rules, tired of all the<br />

questions and tired of being different and feeling<br />

restricted. As I entered adulthood, I thought I kept<br />

my struggles well hidden from others for many<br />

years. I went on to study nursing at university and<br />

the big wide world gave me even more freedom<br />

to hide from the reality of diabetes. Somehow,<br />

I stayed on the tightrope of avoiding routine<br />

doctor’s appointments while also avoiding more<br />

serious hospital admissions. A visit to the doctor<br />

would mean tests, which I knew I would fail, and<br />

questions that I would be ashamed to answer – I<br />

wasn’t up for the interrogations and judgements.<br />

But, I didn’t feel like I was failing! I was eating what<br />

I wanted, when I wanted, and being like the rest of<br />

my friends and peers.<br />

Time to get real<br />

Then I found out I was pregnant…unplanned.<br />

For me, I realised it was not fair to have a child,<br />

with the high risk of complications to me and my<br />

baby as a result of me not looking after myself.<br />

A decision, that I feel to this day, even though I<br />

agreed, had already been made for me. Time to get<br />

real. If I was to ever create a family of my own, it<br />

meant facing the <strong>issue</strong>s I had so long avoided – the<br />

medical world testing me on passing or failing at<br />

diabetes.<br />

Unable, and not allowing myself, to be anything<br />

other than perfectly controlled, I became a<br />

Citation: Barrett K (2017) Through<br />

diagnosis to pregnancy: My journey<br />

with diabetes. Diabetes & Primary<br />

Care Australia 1: 47–8<br />

About this series<br />

The aim of the “From the other<br />

side of the desk” series is to<br />

provide a patient perspective on<br />

a topic within diabetes, to reflect<br />

on the doctor–patient relationship<br />

and to inform clinical care.<br />

Author<br />

Karen Barrett, Registered Nurse<br />

and Coordinator, Central Coast,<br />

NSW.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 47


From the other side of the desk<br />

“As a person with<br />

diabetes, my advice<br />

to the medical world<br />

would be to consider<br />

the person in front<br />

of you without their<br />

diabetes diagnosis.”<br />

champion of the tests. It was an intense time but<br />

my motivation to have healthy babies drove me<br />

to that perfection, and I went on to have three<br />

babies in 3 years. I told the medical team what they<br />

wanted to hear, but this time I wasn’t lying.<br />

It became my obsession to get the numbers<br />

right. Averaging about 12–14 blood sugars daily<br />

and the never-ending specialist appointments were<br />

vital to achieving the desired outcome. I was lucky<br />

that the care I received from my diabetes team<br />

during my pregnancies was excellent and well<br />

planned. I feel that it is vital to have a trusting<br />

relationship with an endocrinologist before, during<br />

and after pregnancies, and I was very fortunate<br />

to have that. But pregnancy with diabetes is not<br />

without its difficulties; the severe hypos during the<br />

first trimesters became frequent and increasingly<br />

exhausting, and with every pregnancy, I had<br />

another toddler to care for. My first-born was<br />

diagnosed with cerebral palsy (totally unrelated<br />

to my diabetes), and as if that was not sufficiently<br />

challenging, I became a single Mum when my<br />

youngest was 11 months old. Juggling three<br />

toddlers, a part-time job to survive financially and<br />

my diabetes became routine. The all-or-nothing<br />

personality has some advantages and in those<br />

3 years, I was switched to “all”, determined to be<br />

a good Mum.<br />

However, as the years went by, I let those<br />

numbers slip again. My three gorgeous children,<br />

my world, were growing up fast, and at aged 6, 7<br />

and 8 years, they kept me busy. I kept the medical<br />

team at length – I knew I wasn’t going to “pass the<br />

test”. My 7-year-old daughter, Presley, had spirit<br />

(sometimes too much!) and when she came down<br />

with a viral illness, as a mum with diabetes would,<br />

I checked her blood sugar. My Mum had suggested<br />

the “D” word as Presley kept sleeping through the<br />

day, which was very much unlike her. I still recall<br />

that moment, and I think I too knew something<br />

wasn’t right. Weeks later, Presley mentioned to me<br />

that she was waking through the night to go to the<br />

bathroom. I knew. I waited.<br />

My beautiful girl was dressed in her swimmers<br />

ready to go swimming. I did her blood sugar and<br />

there I was – the mother of a child with diabetes.<br />

Now it was me answering the questions not as a<br />

person with diabetes, but as a Mum. It was more<br />

than my own tests – I had to pass all of Presley’s<br />

tests as well.<br />

I felt my skills as a parent were put under the<br />

microscope. I believed it was all my fault if her<br />

numbers weren’t right. What was she eating when<br />

I wasn’t there? Was she exerting too much energy<br />

during lunchtime at school? Could she recognise<br />

a hypo? I felt like I had to live in her head, and<br />

I became the “helicopter” Mum. Presley too<br />

hated the medical world, clamming up at all the<br />

questions and hating the scales and numbers. At<br />

home, she dealt with the never-ending motherly<br />

concerns and requests to check her blood sugar,<br />

blaming every ailment or headache on diabetes,<br />

whether or not it was.<br />

Where I am now<br />

Despite some complications of my own, at 44 years<br />

of age, I now take care of myself and feel as well as<br />

I can feel, given my past “bad behaviour”. I have<br />

a good relationship with my team and appreciate<br />

the rapport I have with them, which has taken<br />

many years to establish and develop. I now take<br />

charge of my appointments and we talk about the<br />

concerns I have. The first questions asked are not<br />

“shall we look at the numbers?” or “how many<br />

highs/lows are you having?”; rather, “how are you,<br />

and what’s going on in your world?”<br />

I have had a lovely relationship with my<br />

psychologist who somehow allows me to be proud<br />

of who I am and what I have achieved. I am now<br />

free of the judgement calls that I thought were<br />

placed on me as a person with diabetes and then<br />

as the mother of a child with diabetes. Mistakes<br />

are human. Rough patches enable us all to make<br />

better choices, and experience allows us to call the<br />

shots. It’s OK not to be perfect. I truly hope that<br />

if anything, I can pass this on to my children and<br />

that they reach this point a whole lot sooner than<br />

I did.<br />

As a person with diabetes, my advice to the<br />

medical world would be to consider the person<br />

in front of you without their diabetes diagnosis.<br />

Diabetes management is far more than looking<br />

at the numbers. Consider their state of mind<br />

and the unsaid pressures they may have put on<br />

themselves. The bravest thing one can do is to ask<br />

for help and say that we’re not OK, and creating<br />

an environment where people with diabetes feel<br />

comfortable and safe to do so is vital. n<br />

48 Diabetes & Primary Care Australia Vol 2 No 2 2017


2017 NATIONAL CONFERENCE<br />

Saturday 6th May 2017 – Melbourne Convention and Exhibition Centre, Victoria, Australia<br />

The conference has been specifically designed for all primary care health<br />

professionals working in diabetes care to:<br />

<br />

<br />

<br />

Advance their education and learning in the field of diabetes health care<br />

Promote best practice standards and clinically effective care in the management of diabetes<br />

Facilitate collaboration between health professionals to improve the quality of diabetes<br />

primary care across Australia<br />

6TH MAY 2017 CONFERENCE PROGRAM<br />

The 2017 PCDSA national conference program will combine cutting edge scientific content with<br />

practical clinical sessions, basing the education on much more than just knowing the guidelines.<br />

The distinguished panel of speakers will share their specialised experience in an environment<br />

conducive to optimal learning. The Speaking faculty include, amongst others:<br />

Associate Professor<br />

Neale Cohen<br />

Director Clinical Diabetes<br />

Baker Heart and<br />

Diabetes Institute<br />

“Diabetes management<br />

and research in primary<br />

care – key components<br />

to improving outcomes”<br />

Doctor Christel<br />

Hendrieckx<br />

Senior Research Fellow<br />

The Australian Centre<br />

for Behavioural Research<br />

in Diabetes<br />

“The emotional health of<br />

people living with diabetes”<br />

Ms Renza Scibilia<br />

Manager - Type 1 Diabetes<br />

and Consumer Voice<br />

Diabetes Australia<br />

“Engaging people with<br />

diabetes, the diabetes<br />

online community and<br />

apps for diabetes”<br />

Doctor Gautam<br />

Vaddadi<br />

Consultant Cardiologist<br />

Alfred Health, Northern Health,<br />

University of Melbourne<br />

“The emerging importance<br />

of cardiac failure diagnosis<br />

and management in people<br />

with type 2 diabetes”<br />

For further information including the full 2017 program<br />

and to register for the conference please visit:<br />

www.eventful.com.au/pcdsa2017<br />

If you have any questions regarding the conference,<br />

please contact the Conference Secretariat;<br />

Toll free telephone: 1800 898 499<br />

Email: pcdsa@eventful.com.au<br />

pcdsa.com.au


Article<br />

Resources to support preconception care<br />

for women with diabetes<br />

Citation: Morrison M, Audehm R,<br />

Barry A et al (2017) Resources to<br />

support preconception care for<br />

women with diabetes. Diabetes &<br />

Primary Care Australia 2: 50–3<br />

Article points<br />

1. Women with diabetes are<br />

at increased risk of adverse<br />

pregnancy outcomes. Early<br />

intervention and planning<br />

can reduce the risks.<br />

2. Primary health care<br />

professionals have a key role<br />

in providing appropriate<br />

contraception to women with<br />

diabetes to prevent unplanned<br />

pregnancies, as well as<br />

encouraging optimal pregnancy<br />

planning and preparation.<br />

3. To address the gap in<br />

information for women with<br />

diabetes who are seeking<br />

or already accessing prepregnancy<br />

advice and<br />

care, Diabetes Australia<br />

has developed a suite of<br />

resources with funding<br />

through the National<br />

Diabetes Services Scheme.<br />

Key words<br />

– Diabetes in pregnancy<br />

– Education<br />

– Preconception care<br />

– Pregnancy<br />

– Resources<br />

– Type 1 diabetes<br />

– Type 2 diabetes<br />

Authors<br />

See page 53 for details.<br />

Melinda Morrison, Ralph Audehm, Alison Barry, Christel Hendrieckx,<br />

Alison Nankervis, Cynthia Porter, Renza Scibilia, Glynis P Ross<br />

Preconception care has been shown to reduce the rates of adverse pregnancy outcomes<br />

in women with pre-existing type 1 or type 2 diabetes. With an increasing prevalence of<br />

diabetes among women of child-bearing age, health professionals working in primary<br />

care have an important role in encouraging women with diabetes to plan and prepare<br />

for pregnancy. New resources, described here, are available for health professionals and<br />

women with diabetes and provide up to date, evidence-based information on pregnancy<br />

and diabetes.<br />

Pre-existing diabetes (type 1 or<br />

type 2 diabetes) is estimated to affect<br />

approximately 1% of pregnant women<br />

in Australia (Australian Institute of Health and<br />

Welfare, 2016), and evidence suggests that the<br />

prevalence is increasing (Abouzeid et al, 2014).<br />

In particular, the prevalence of type 2 diabetes in<br />

pregnant women is expected to increase as a result<br />

of older maternal age, high rates of obesity and an<br />

ethnically diverse population (Cheung et al, 2005;<br />

Temple and Murphy, 2010).<br />

Diabetes in pregnancy has many welldocumented<br />

risks to both mother and baby<br />

(Macintosh et al, 2006; Dunne et al, 2009;<br />

Kitzmiller et al, 2010); however, these risks can<br />

be mitigated by effective preconception and<br />

pregnancy care, and most women with diabetes<br />

will go on to have a healthy pregnancy and a<br />

healthy baby (Ray et al, 2001; Wahabi et al, 2010;<br />

Holmes et al, 2017).<br />

While most women with type 1 diabetes access<br />

specialist services, the majority of women with<br />

type 2 diabetes are managed in primary care.<br />

Health professionals in primary care are often the<br />

first point of contact for women seeking pregnancy<br />

information, and have a key role in promoting and<br />

providing appropriate contraception to women<br />

with pre-existing diabetes to prevent unplanned<br />

pregnancies, and in specialist referral. They are<br />

also critically important in encouraging diabetesspecific<br />

preconception care in all women with<br />

pre-existing diabetes to optimise maternal and<br />

fetal outcomes (Temple and Murphy, 2010). In<br />

the National Diabetes Services Scheme (NDSS)*<br />

Contraception, Pregnancy & Women’s Health<br />

Survey (2015) women with type 1 or type 2<br />

diabetes (n=967) indicated that diabetes specialists<br />

(endocrinologists and diabetes educators) and<br />

general practitioners were the health professionals<br />

with whom pregnancy and diabetes was most<br />

frequently discussed. Interestingly, the majority<br />

of women reported that they, rather than health<br />

professionals, initiated the conversation about<br />

pregnancy and diabetes.<br />

Preconception care in the primary<br />

health setting<br />

Despite the documented benefits of preconception<br />

care for women with pre-existing diabetes (Ray<br />

et al, 2001; Wahabi et al, 2010), many women<br />

with diabetes do not plan their pregnancies. Zhu<br />

et al (2012) reported that 45% of pregnancies in<br />

women with diabetes attending a tertiary obstetric<br />

hospital in Western Australia during 2009–2010<br />

*The National Diabetes Services Scheme (NDSS) is an<br />

initiative of the Australian Government administered<br />

with the assistance of Diabetes Australia.<br />

50 Diabetes & Primary Care Australia Vol 2 No 2 2017


Resources to support preconception care for women with diabetes<br />

were unplanned. While in an earlier Australian<br />

multicentre study of pregnancies complicated<br />

by diabetes, pre-pregnancy counselling was<br />

documented in only 20% of women – 28% of<br />

those with type 1 diabetes and 12% of those with<br />

type 2 diabetes (McElduff et al, 2005).<br />

Planning for pregnancy<br />

The primary health care setting is where many<br />

women with diabetes seek advice on reproductive<br />

<strong>issue</strong>s and access contraception. However, in the<br />

NDSS Contraception, Pregnancy & Women’s<br />

Health Survey (2015) only 49% of Australian<br />

women with type 1 or type 2 diabetes could<br />

recall being advised by a health professional to<br />

use some form of contraception to prevent an<br />

unplanned pregnancy, and 55% could recall being<br />

advised by a health professional that they should<br />

access diabetes-specific pre-pregnancy care before<br />

becoming pregnant or planning a pregnancy.<br />

These results differed by type of diabetes, with<br />

those with type 2 diabetes being less likely to recall<br />

receiving advice. These findings are consistent<br />

with those reported in the TRIAD (Translating<br />

Research into Action for Diabetes) preconception<br />

study of US women aged 18–45 years enrolled<br />

in managed care (Kim et al, 2005). Of these<br />

women, 52% recalled discussions with a health<br />

professional regarding glucose control before<br />

conception, and 37% could recall receiving family<br />

planning advice.<br />

Due to the impact of an unplanned pregnancy<br />

on both the developing fetus and mother, adequate<br />

contraception should be maintained until<br />

glycaemia and all aspects of care are optimised.<br />

The longer-acting reversible contraceptives are an<br />

excellent choice (e.g. intrauterine contraceptive<br />

devices or implant) and are safe for women with<br />

diabetes to use. When reviewing contraception in<br />

women with diabetes, timing of pregnancy should<br />

be discussed. Preconception planning for women<br />

with diabetes should occur well before conception.<br />

If available, involvement of a specialist diabetes in<br />

pregnancy service is recommended.<br />

New NDSS resources to support<br />

preconception care<br />

To address the gap in information for<br />

women with diabetes who are seeking or<br />

already accessing pre-pregnancy advice<br />

and care, Diabetes Australia has developed<br />

a suite of resources with funding through<br />

the NDSS. These resources were developed<br />

following extensive consumer and stakeholder<br />

consultation, and provide up-to-date, evidencebased<br />

pregnancy information for women living<br />

with type 1 or type 2 diabetes. The NDSS<br />

resources available include the following:<br />

l www.pregnancyanddiabetes.com.au: A<br />

website dedicated to pregnancy and diabetes<br />

information.<br />

l Pregnancy planning checklist: A checklist<br />

to help women with diabetes prepare for a<br />

healthy pregnancy. The checklist can be<br />

completed as an online tool or downloaded<br />

as a printable checklist (Figure 1).<br />

l Having a Healthy Baby booklets: Booklets<br />

providing comprehensive information on<br />

planning and managing pregnancy. Separate<br />

booklets are available for women with<br />

type 1 or type 2 diabetes (Figure 2).<br />

l NDSS pregnancy and diabetes factsheet:<br />

Available for download in English, Arabic,<br />

Chinese, Vietnamese, Korean, Turkish,<br />

Urdu, Greek, Italian and Spanish.<br />

l Plan for the best start e-newsletter: A<br />

quarterly e-newsletter for women with<br />

diabetes and health professionals. It<br />

provides information on planning and<br />

preparing for pregnancy, and there is access<br />

to the latest NDSS resources and research<br />

updates.<br />

l Health professional continuing professional<br />

development learning: E-learning modules<br />

for primary health care providers on the<br />

topic of preconception care for women<br />

with type 1 or type 2 diabetes. The course<br />

includes three modules with two nonassessed<br />

case studies and can be accessed<br />

from the NDSS pregnancy and diabetes<br />

website. CPD points are available for<br />

eligible health professionals.<br />

These resources for patients and health<br />

care professionals can be accessed at<br />

www.pregnancyanddiabetes.com.au. Hard<br />

copies of the booklets can be ordered online or<br />

by phoning the NDSS Helpline (1300 136 588).<br />

Page points<br />

1. Due to the impact of an<br />

unplanned pregnancy on<br />

both the developing fetus and<br />

mother, adequate contraception<br />

should be maintained until<br />

glycaemia and all aspects of<br />

care are optimised.<br />

2. Preconception planning for<br />

women with diabetes should<br />

occur well before conception.<br />

3. Resources for patients and<br />

health care professionals<br />

can be accessed at www.<br />

pregnancyanddiabetes.com.au.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 51


Resources to support preconception care for women with diabetes<br />

Pregnancy Planning Checklist<br />

Plan and prepare at least 3-6 months before you start<br />

trying for a baby<br />

What you need to do BEFORE you fall pregnant<br />

Use contraception until you are ready to start trying for<br />

a baby (ask your doctor if this is the most reliable<br />

contraception suitable for you)<br />

Talk to your doctor for general pregnancy planning advice<br />

Make an appointment with health professionals who<br />

specialise in pregnancy and diabetes<br />

Aim for an HbA1c of less than 53mmol/mol (7%) if you<br />

have type 1 diabetes or 42mmol/mol (6%) or less if<br />

you have type 2 diabetes<br />

Review your diabetes management with your diabetes<br />

health professionals<br />

Have all your medications checked to see if they are<br />

safe to take during pregnancy<br />

Start taking a high-dose (2.5mg-5mg) folic acid<br />

supplement each day<br />

Have a full diabetes complications screening and<br />

your blood pressure checked<br />

Aim for a healthy weight before you fall pregnant<br />

For women<br />

with type 1<br />

or type 2<br />

diabetes<br />

Use this checklist as a guide to discuss with your health professionals<br />

www.pregnancyanddiabetes.com.au<br />

This checklist is intended as a guide only. It should not replace individual medical advice and if you have any<br />

concerns about your health or further questions, you should contact your health professional.<br />

The National Diabetes Services Scheme (NDSS) is an initiative of the Australian Government administered with the assistance of Diabetes Australia.<br />

Figure 1. Pregnancy planning checklist, to help women with diabetes<br />

prepare for a healthy pregnancy. Produced by the National Diabetes<br />

Service Scheme.<br />

Other resources<br />

The Australasian Diabetes in Pregnancy<br />

Society (ADIPS)-endorsed Pregnant<br />

with Diabetes app has been developed<br />

for pregnant women with diabetes, and<br />

women with diabetes who intend to<br />

become pregnant (Figure 3). It is written by<br />

Prof. Elisabeth R Mathiesen and Prof. Peter<br />

Damm and is based on the recommendations<br />

of the Centre for Pregnant Women with<br />

Diabetes at Rigshospitalet in Copenhagen,<br />

Denmark. The Australian version has been<br />

adapted by an Australian working party<br />

to reflect the ADIPS guidelines. The app<br />

can be downloaded from app stores free<br />

of charge. The information covered in the<br />

app is suitable for women with gestational,<br />

type 1 and type 2 diabetes and covers<br />

topics such as: how to plan for pregnancy,<br />

Figure 2. Booklets for women with type 1 and type 2<br />

diabetes. Produced by the National Diabetes Services<br />

Scheme.<br />

goal blood glucose levels, gestational weight<br />

gain, diet and carbohydrate intake, physical<br />

activity and insulin dosing.<br />

52 Diabetes & Primary Care Australia Vol 2 No 2 2017


Resources to support preconception care for women with diabetes<br />

National Development Program Expert<br />

Reference Group (2013–16). We acknowledge<br />

D. Charron-Prochownik for permission<br />

to reproduce questions from the RHAB<br />

questionnaire and V. Holmes for permission to<br />

use reproductive health knowledge questions<br />

in the NDSS Contraception, Pregnancy &<br />

Women’s Health Survey.<br />

Abouzeid M, Versace VL, Janus ED et al (2014) A population-based<br />

observational study of diabetes during pregnancy in Victoria,<br />

Australia, 1999–2008. BMJ Open 4: e005394<br />

Australian Institute of Health and Welfare (2016) Australia’s<br />

mothers and babies 2014-in brief. Perinatal statistics. AIHW,<br />

Canberra, ACT. Available at: http://www.aihw.gov.au/<br />

publication-detail/?id=60129557656 (accessed 14.03.17)<br />

“Primary care health<br />

professionals are<br />

also ideally placed to<br />

increase the awareness<br />

of women with<br />

diabetes about the<br />

available resources<br />

which are being<br />

actively reviewed and<br />

developed to meet<br />

their needs.”<br />

Cheung N, McElduff A, Ross G (2005) Type 2 diabetes in<br />

pregnancy: a wolf in sheep’s clothing. Aust N Z J Obstet<br />

Gynaecol 45: 479–83<br />

Figure 3. The Australasian Diabetes in Pregnancy<br />

Society (ADIPS)-endorsed Pregnant with Diabetes app.<br />

Conclusion<br />

Primary health care providers play an important<br />

role in promoting effective contraception use<br />

and encouraging women with pre-existing<br />

type 1 or type 2 diabetes to plan and prepare<br />

for pregnancy. They are also ideally placed to<br />

increase the awareness of women with diabetes<br />

about the available resources which are being<br />

actively reviewed and developed to meet their<br />

needs.<br />

n<br />

Acknowledgements<br />

The authors are grateful to the women who took<br />

part in the NDSS Contraception, Pregnancy<br />

& Women’s Health Survey, to the Australasian<br />

Diabetes in Pregnancy Society for approving the<br />

use of the image of the Pregnant with Diabetes<br />

app and to Effie Houvardas and Kaye Farrell,<br />

for their contribution to Diabetes in Pregnancy<br />

Dunne FP, Avalos G, Durkan M et al (2009) ATLANTIC DIP:<br />

pregnancy outcome for women with pregestational diabetes<br />

along the Irish Atlantic seaboard. Diabetes Care 32: 1205–6<br />

Holmes VA, Hamill, LL, Alderdice FA et al (2017) Effect of<br />

implementation of a preconception counselling resource for<br />

women with diabetes: A population based study. Primary Care<br />

Diabetes 11: 37–45<br />

Kim C, Ferrara A, McEwan LN et al (2005) Preconception care in<br />

managed care: the translating research into action for diabetes<br />

study. Am J Obstet Gynecol 192: 227–32<br />

Kitzmiller JL, Wallerstein R, Correa A, Kwan S (2010)<br />

Preconception care for women with diabetes and prevention of<br />

major congenital malformations. Birth Defects Res A Clin Mol<br />

Teratol 88: 791–803<br />

Macintosh MC, Fleming KM, Bailey JA et al (2006) Perinatal<br />

mortality and congenital anomalies in babies of women with<br />

type 1 or type 2 diabetes in England, Wales, and Northern<br />

Ireland: population based study. BMJ 333: 177<br />

McElduff A, Ross GP, Lagstrom JA et al (2005) Pregestational<br />

diabetes and pregnancy: an Australian experience. Diabetes<br />

Care 28: 1260–1<br />

National Diabetes Services Scheme (2015) NDSS Diabetes<br />

in Pregnancy National Development Program, Registrant<br />

Consultation and Needs Assessment Report. NDSS, Canberra,<br />

ACT<br />

Ray JG, O’Brien TE, Chan WS (2001) Preconception care and the<br />

risk of congenital anomalies in the offspring of women with<br />

diabetes mellitus: a meta-analysis. QJM 94: 435–44<br />

Temple RC, Murphy H (2010) Type 2 diabetes in pregnancy - an<br />

increasing problem. Best Pract Res Clin Endocrinol Metab 24:<br />

591–603<br />

Wahabi HA, Alzeidan RA, Bawazeer GA et al (2010)<br />

Preconception care for diabetic women for improving maternal<br />

and fetal outcomes: a systematic review and meta-analysis.<br />

BMC Pregnancy Childbirth 10: 63<br />

Zhu H, Graham D, Teh RW, Hornbuckle J (2012) Utilisation of<br />

preconception care in women with pregestational diabetes in<br />

Western Australia. Aust N Z J Obstet Gynaecol 52: 593–6<br />

Authors<br />

Melinda Morrison, NDSS<br />

Diabetes in Pregnancy Priority<br />

Area Leader*, Diabetes, NSW,<br />

Glebe, NSW; Ralph Audehm,<br />

General Practitioner, Carlton<br />

Family Medical and Department<br />

of General Practice, University<br />

of Melbourne, Vic; Alison Barry,<br />

Credentialled Diabetes Educator<br />

and Midwife, Mater Mothers’<br />

Hospital, South Brisbane, Qld;<br />

Christel Hendrieckx, Senior<br />

Research Fellow, The Australian<br />

Centre for Behavioural Research<br />

in Diabetes, Deakin University,<br />

Geelong, Vic; Alison Nankervis,<br />

Senior Physician to the Diabetes<br />

Service, The Royal Women’s<br />

Hospital and Clinical Head,<br />

Diabetes, Royal Melbourne<br />

Hospital, Parkville, Vic; Cynthia<br />

Porter, Advanced Accredited<br />

Practising Dietitian/Credentialled<br />

Diabetes Educator, Geraldton<br />

Diabetes Clinic, Geraldton, WA;<br />

Renza Scibilia, Manager Type 1<br />

Diabetes and Consumer Voice,<br />

Diabetes Australia, Melbourne,<br />

Vic; Glynis P Ross, Visiting<br />

Endocrinologist, Royal Prince<br />

Alfred Hospital, Camperdown,<br />

NSW, and Senior Endocrinologist,<br />

Bankstown-Lidcombe Hospital,<br />

Bankstown, NSW.<br />

*Melinda Morrison is representing<br />

Diabetes Australia/National<br />

Diabetes Service Scheme.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 53


CPD module<br />

Optimising pregnancy outcomes for<br />

women with pre-gestational diabetes in<br />

primary health care<br />

Glynis P Ross<br />

Citation: Ross GP (2017) Optimising<br />

pregnancy outcomes for women<br />

with pre-gestational diabetes in<br />

primary health care. Diabetes &<br />

Primary Care Australia 2: 54–9<br />

Learning objectives<br />

After reading this article, the<br />

participant should be able to:<br />

1. Identify the increased<br />

risks of adverse pregnancy<br />

outcomes to mother and<br />

baby that are associated with<br />

pre-gestational diabetes.<br />

2. Describe the ideal<br />

preconception care<br />

consultation and the key<br />

elements of care that a pregnant<br />

woman with pre-existing<br />

diabetes should receive.<br />

3. Implement a checklist for<br />

preconception care for<br />

women with diabetes.<br />

Key words<br />

– Preconception care<br />

– Pre-gestational diabetes<br />

– Pregnancy<br />

– Type 1 diabetes<br />

– Type 2 diabetes<br />

Author<br />

Glynis P Ross, Visiting<br />

Endocrinologist, Royal Prince<br />

Alfred Hospital, Camperdown<br />

NSW, and Senior Endocrinologist,<br />

Bankstown-Lidcombe Hospital,<br />

Bankstown, NSW.<br />

Preconception care for women with pre-existing diabetes (type 1 or type 2) is critical to<br />

optimise pregnancy outcomes and reduce the risk of adverse outcomes, including miscarriage,<br />

congenital anomalies, hypertension, caesarean deliveries and perinatal mortality. Pregestational<br />

diabetes is present in approximately 1% of pregnant women in Australia, and the<br />

prevalence is increasing. Women with pre-gestational diabetes need to be informed on the<br />

availability and importance of preconception care, which can be provided by both primary<br />

care and specialised diabetes services. The key elements of preconception care for women<br />

with diabetes are outlined in this article with two case examples to illustrate.<br />

Women with pre-gestational type 1<br />

or type 2 diabetes are at high risk<br />

of complications during pregnancy<br />

and of adverse outcomes including miscarriage,<br />

congenital anomalies and perinatal mortality.<br />

Despite advances in diabetes management, rates<br />

of congenital anomalies are 2–4 times higher<br />

than that of the background population and<br />

there is a 3–5 fold increased risk of stillbirth<br />

and perinatal mortality for births to women<br />

with diabetes (Macintosh et al, 2006; Dunne et<br />

al, 2009; Kitzmiller et al, 2010). Data from the<br />

Australian Institute of Health and Welfare (2010)<br />

show that in 2005–2007, more than half of all<br />

Australian women with pre-gestational diabetes<br />

underwent caesarean delivery (59%; 71% type 1<br />

and 56% type 2 diabetes), compared to a third of<br />

women without diabetes. Following birth, 58%<br />

of infants born to women with diabetes were<br />

admitted to a special care nursery or neonatal<br />

intensive care unit, compared to 14% of babies<br />

born to mothers without diabetes.<br />

Glycaemic control in early pregnancy is strongly<br />

associated with the risk of adverse pregnancy<br />

outcomes (Nielsen et al, 2004; Guerin et al, 2007,<br />

Jensen et al, 2009). Research shows that for every<br />

10.93 mmol/mol (1%) increase in HbA 1c<br />

above<br />

53 mmol/mol (7%), there is a 5.5% increase in<br />

risk of adverse outcomes (Nielsen et al, 2004). The<br />

American Diabetes Association (2017) states that<br />

the lowest rates of adverse pregnancy outcomes<br />

are seen in association with an early gestation<br />

HbA 1c<br />

of 42–48 mmol/mol (6.0–6.5%).<br />

Preconception care for women with existing<br />

diabetes provides an opportunity to optimise<br />

glycaemic control, as well as other aspects of<br />

maternal health such as folic acid supplementation,<br />

diabetes complications screening and<br />

discontinuation of teratogenic medications prior<br />

to conception (McElduff et al, 2005; Mahmud<br />

and Mazza, 2010; Egan et al, 2015). Attendance<br />

at diabetes-specific preconception care has<br />

been associated with a reduction in congenital<br />

anomalies (relative risk [RR], 0.25), perinatal<br />

mortality (RR, 0.35) and reduced first trimester<br />

HbA 1c<br />

by an average of 26 mmol/mol (2.4%;<br />

Wahabi et al, 2010).<br />

Advice<br />

Preconception planning and assessment is<br />

recommended for all women considering<br />

pregnancy, but it is particularly important for<br />

women with diabetes or other medical disorders.<br />

Primary health care providers are well placed to<br />

complete most of the preconception screening<br />

and risk assessment, and can facilitate many of<br />

54 Diabetes & Primary Care Australia Vol 2 No 2 2017


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

the interventions and appropriate referrals that<br />

may be required. A checklist, such as below,<br />

may be useful when undertaking pre-pregnancy<br />

counselling.<br />

ADVICE AND CONSIDERATIONS<br />

FOR ALL WOMEN CONSIDERING<br />

PREGNANCY<br />

o Appropriate contraception until<br />

optimal situation for pregnancy.<br />

o Review ALL current medications<br />

and ensure they are safe and<br />

appropriate for pregnancy.<br />

o Check blood pressure.<br />

o (For women not known to<br />

have diabetes, assess risk,<br />

and test appropriately for<br />

abnormal glucose tolerance.)<br />

o Promote a healthy lifestyle<br />

with regard to diet, exercise<br />

and optimal weight – this is<br />

also advisable for partners!<br />

o Encourage smoking cessation.<br />

o Advise to cease alcohol intake.<br />

o Advise to stop any<br />

recreational drug use.<br />

o Reduce caffeine intake.<br />

o Dental check.<br />

o Complete breast check<br />

and pap smear.<br />

o Assess immunity to rubella<br />

and varicella zoster, and, if<br />

necessary, organise vaccinations<br />

with appropriate waiting<br />

periods before conception.<br />

o Consider vaccinations for<br />

influenza and whooping cough.<br />

o Commence folic acid 3 months<br />

prior to pregnancy at 0.5 mg daily<br />

(see below for dose adjustments<br />

for women with known diabetes).<br />

o Commence an iodine-containing<br />

supplement (unless active<br />

thyrotoxicosis is present).<br />

o Consider checking thyroid<br />

function, iron, B12 (especially if<br />

vegetarian or taking metformin)<br />

and vitamin D status (if at risk).<br />

ADDITIONAL ADVICE AND<br />

CONSIDERATIONS FOR WOMEN<br />

WITH PRE-GESTATIONAL DIABETES<br />

CONSIDERING PREGNANCY<br />

o Refer to a diabetes specialist<br />

or team if not already under<br />

their care for assessment.<br />

o Optimise glycaemic control<br />

o In type 1 diabetes, pre-pregnancy<br />

HbA 1c<br />

should ideally be<br />


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

Page points<br />

1. Preconception care should be<br />

individualised.<br />

2. Women should be advised<br />

to continue to use effective<br />

contraception until the best<br />

possible conditions for a<br />

safe pregnancy and birth are<br />

achieved.<br />

3. Regular monitoring and<br />

recording of blood glucose<br />

levels during the preconception<br />

stage and pregnancy can be<br />

helpful in optimising pregnancy<br />

outcomes.<br />

Case studies<br />

Outlined on the following two pages are two case<br />

studies illustrating some of the considerations to<br />

address during the preconception period. Given<br />

the range of situations that may be encountered,<br />

all care needs to be individualised. Ideally, most<br />

women with diabetes should be assessed before<br />

conception by a diabetes specialist or team with<br />

expertise in diabetes and pregnancy. This is<br />

particularly important when there are diabetes<br />

complications or additional medical disorders.<br />

For women in rural and remote areas, review<br />

in a regional centre or via telehealth with a<br />

specialist centre may be an appropriate option.<br />

This is especially important for women with more<br />

complex situations such as type 1 diabetes, type 2<br />

diabetes requiring multiple medications, diabetes<br />

vascular complications and/or other vascular risk<br />

factors.<br />

Case 1<br />

Maria is a 41-year old woman and has come<br />

to see you for a pap smear. You last saw her<br />

4 months ago when she wanted a script for<br />

the oral contraceptive pill (OCP). On routine<br />

questioning when you are completing the<br />

pathology request for cervical cytology she says<br />

that she is considering having a break from the<br />

pill as she and her husband are thinking about<br />

having another baby.<br />

History<br />

Maria has two children aged 9 and 12 years.<br />

The first pregnancy was uncomplicated and she<br />

had spontaneous vaginal delivery at term. Her<br />

daughter weighed 3450 g and was breastfed<br />

for 12 months. Before her second pregnancy,<br />

Maria had gained 8 kg in weight and her BMI<br />

was 28 kg/m 2 . At 28 weeks during her second<br />

pregnancy, Maria was diagnosed with gestational<br />

diabetes. She was able to manage this with diet<br />

modification alone and had spontaneous vaginal<br />

delivery at 39 +3 weeks of a 3720 g son. He was<br />

also breastfed for 12 months.<br />

Three years ago (age 38 years), Maria’s<br />

weight had risen and her BMI was 31 kg/m 2<br />

(class 1 obesity range). Her fasting glucose was<br />

7.2 mmol/L and her HbA 1c<br />

was 49 mmol/mol<br />

(6.6%) and a diagnosis of type 2 diabetes was<br />

made. Initially she was treated with metformin<br />

XR 2 g daily. Despite the metformin and Maria<br />

trying to follow dietary guidelines, 4 months<br />

ago her HbA 1c<br />

was 62 mmol/mol (7.8%) and so<br />

empagliflozin was added to her regimen. She<br />

continued to struggle to find time to exercise.<br />

Maria has a strong family history of<br />

type 2 diabetes (both parents, her older brother<br />

and all grandparents) and hypertension (father<br />

and paternal grandmother). Her father had a<br />

myocardial infarct at the age of 39 years with<br />

subsequent stenting. For 7 years, Maria has also<br />

been treated for hypertension with telmisartan,<br />

and dyslipidaemia for which she is taking<br />

atorvastatin and fenofibrate. She and her husband<br />

smoke, but Maria has said she is trying to stop<br />

so is only smoking in the evenings after dinner.<br />

Discussion<br />

Maria has several factors that increase her<br />

risk of adverse pregnancy outcomes. She is of<br />

advanced maternal age, is obese, a smoker, and<br />

has type 2 diabetes, hypertension, dyslipidaemia<br />

and a family history of early-onset ischaemic<br />

heart disease.<br />

Her glycaemic control is not satisfactory for<br />

pregnancy, and although metformin can be<br />

continued during pregnancy, empagliflozin<br />

will need to be stopped and insulin therapy<br />

commenced and titrated. She will need to increase<br />

her blood glucose monitoring and recording of<br />

results, preferably including dietary information.<br />

Review with a dietitian, diabetes educator and<br />

preferably an exercise physiologist is advisable.<br />

She should be seen by a diabetes physician with<br />

expertise in diabetes and pregnancy.<br />

She has multiple vascular risk factors and a<br />

high risk of developing a hypertensive disorder of<br />

pregnancy. She should be appropriately counselled<br />

regarding smoking cessation. The medication she<br />

is on for hypertension needs to be changed and<br />

the lipid management will need to be stopped<br />

for pregnancy. As she has hypertension it would<br />

be preferable that she is also seen by a renal or<br />

obstetric medicine physician, especially if she<br />

fails to achieve blood pressure targets or if she<br />

has overt proteinuria. Given the multiple vascular<br />

risk factors, she should have a pre-pregnancy<br />

cardiac assessment.<br />

56 Diabetes & Primary Care Australia Vol 2 No 2 2017


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

Advice<br />

You advise Maria that she should stay on the<br />

OCP for the time being and that preconception<br />

planning is needed in view of her multiple medical<br />

conditions and medications. If she still wishes to<br />

become pregnant, she should commence highdose<br />

folic acid and have routine pre-pregnancy<br />

checks. If she conceives, her contraception choice<br />

should be reviewed following the pregnancy as it<br />

is not advisable for her to continue on the OCP<br />

given her age and vascular risk status.<br />

Case 2<br />

Jennifer has come to see you for a referral letter to<br />

her gynaecologist. She wants to have her intrauterine<br />

contraceptive device (IUCD) removed as she is<br />

keen to start a family. Jennifer is a 30-year-old<br />

woman who has had type 1 diabetes for 21 years.<br />

For the last 3 years, she has been using insulin<br />

pump therapy. Jennifer’s most recent HbA 1c<br />

of<br />

70 mmol/mol (8.6%) was higher than usual after a<br />

recent overseas holiday with her husband.<br />

History<br />

In her teens, Jennifer struggled with her diabetes<br />

control but in the past 5 years has been managing<br />

quite well. Her last episode of diabetic ketoacidosis<br />

was 18 months ago when there was a problem with<br />

insulin delivery through her pump. She has not<br />

had severe hypoglycaemia (requiring the assistance<br />

of another person) for 5 years and is using a<br />

continuous glucose monitoring system (CGMS)<br />

with predictive low-glucose suspend, as she knows<br />

that she does not reliably sense hypoglycaemia.<br />

Jennifer has diabetic retinopathy that has<br />

previously required laser photocoagulation.<br />

However, she has not had her eyes checked for<br />

about 2 years as she missed an appointment and<br />

did not find time to reschedule. She has overt<br />

proteinuria (0.5 g per day) and is on ramipril for<br />

nephroprotection. Her eGFR is 62 mL/min/1.73 m 2<br />

and she has previously been assessed for other<br />

causes of renal disease by a nephrologist. Her<br />

blood pressure and lipids are normal. She has<br />

a moderate degree of asymptomatic peripheral<br />

neuropathy with loss of distal sensation to light<br />

touch and vibration, as well as loss of ankle<br />

reflexes. She senses a monofilament and has had<br />

no diabetes-related foot complications.<br />

Discussion<br />

If conception is successful, this will be Jennifer’s<br />

first pregnancy. As she is on insulin pump therapy<br />

and uses a CGM device, she will already be under<br />

a specialist diabetes team. Her glycaemic control<br />

is sub-optimal and significantly increases her<br />

risk of adverse pregnancy outcomes, including<br />

miscarriage and congenital anomalies. Even<br />

though the recommended HbA 1c<br />

target for women<br />

with type 1 diabetes in the preconception stage is<br />

≤53 mmol/mol (7%), given her long duration<br />

of type 1 diabetes and poor hypoglycaemic<br />

awareness, it may not be safe to reduce her HbA 1c<br />

below 58 mmol/mol (7.5%) due to the increasing<br />

risk of severe hypoglycaemia at lower levels. She<br />

needs specific specialist assessment and advice<br />

regarding her HbA 1c<br />

as well as review of all<br />

aspects of her diabetes self-management (e.g. diet,<br />

exercise, BGL testing and recording, insulin pump<br />

settings review, pump management skills, driving<br />

considerations, and hypoglycaemia and diabetic<br />

ketoacidosis prevention and management).<br />

Jennifer also needs an urgent diabetes eye<br />

review. If there is active proliferative retinopathy or<br />

macular oedema she will need to delay pregnancy<br />

plans until the retinopathy has been treated and<br />

is stable. As she has overt proteinuria, she should<br />

be assessed pre-pregnancy by a renal or obstetric<br />

medicine physician who will be able to continue<br />

to manage her in pregnancy. Her risk of preeclampsia<br />

and poor fetal outcomes, including<br />

intrauterine growth restriction (IUGR), will be<br />

increased. Although she is not known to have<br />

autonomic neuropathy, she should be assessed for<br />

this by her diabetes specialist.<br />

Advice<br />

You advise Jennifer to not have the IUCD<br />

removed yet and that preconception planning is<br />

needed in view of her complex diabetes situation<br />

– especially her overall glycaemic control,<br />

nephropathy and retinopathy. You also ask her<br />

whether she has discussed pregnancy with her<br />

endocrinologist and check the date of her next<br />

scheduled appointment. Following diabetes<br />

complications assessment and optimising<br />

glycaemic management, Jennifer should<br />

commence high-dose folic acid and have routine<br />

pre-pregnancy checks.<br />

”If a woman has<br />

been diagnosed with<br />

retinopathy, it is<br />

important to ensure<br />

it has been treated<br />

and is stable prior to<br />

pregnancy.”<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 57


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

“Primary health<br />

care providers have<br />

critical roles to play<br />

in the assessment<br />

and management of<br />

contraception,<br />

pre-pregnancy<br />

assessment<br />

and care.”<br />

Conclusion<br />

Women of child-bearing age with pre-gestational<br />

type 1 or type 2 diabetes need to be counselled<br />

on the need for appropriate contraception at all<br />

times unless trying for pregnancy in the best<br />

possible circumstances to avoid adverse pregnancy<br />

outcomes. Most women with pre-gestational<br />

diabetes are able to have successful pregnancies.<br />

However, they are at much higher risk of having<br />

adverse pregnancy outcomes than women without<br />

diabetes (Macintosh et al, 2006; Dunne et al,<br />

2009). It has been shown that women who have<br />

had optimal pre-pregnancy care and best practice<br />

management of their diabetes, both before and<br />

throughout pregnancy, will have a substantially<br />

lower rate of adverse outcomes (Ray et al, 2001;<br />

Wahabi et al, 2010).<br />

Ideally, care should involve services that are<br />

specialised in diabetes in pregnancy. However,<br />

primary health care providers also have critical<br />

roles to play in the assessment and management of<br />

contraception, pre-pregnancy assessment and care,<br />

coordination of specialist services and ongoing<br />

support prior to, as well as throughout and<br />

following, the pregnancy. <br />

n<br />

Acknowledgement<br />

The author would like to acknowledge Melinda<br />

Morrison for assistance with article editing and<br />

referencing.<br />

American Diabetes Association (2017) Standards of Medical Care in<br />

Diabetes—2017. Diabetes Care 40(Suppl 1): S4–S5<br />

Australian Institute of Health and Welfare (2010) Diabetes in<br />

pregnancy: its impact on Australian women and their babies.<br />

AIHW, Canberra, ACT<br />

Dunne FP, Avalos G, Durkan M et al (2009) ATLANTIC DIP:<br />

pregnancy outcome for women with pregestational diabetes<br />

along the Irish Atlantic seaboard. Diabetes Care 32: 1205–6<br />

Egan, AM, Murphy HR, Dunne FP (2015) The management of type 1<br />

and type 2 diabetes in pregnancy. QJM: An International Journal<br />

of Medicine 108: 923–7<br />

Guerin A, Nisenbaum R, Ray JG (2007) Use of maternal GHb<br />

concentration to estimate the risk of congenital anomalies in the<br />

offspring of women with prepregnancy diabetes. Diabetes Care<br />

30: 1920–5<br />

Inkster ME, Fahey TP, Donnan PT et al (2006) Poor glycated<br />

haemoglobin control and adverse pregnancy outcomes in type 1<br />

and type 2 diabetes mellitus: Systematic review of observational<br />

studies. BMC Pregnancy Childbirth 6: 30<br />

Jensen DM, KorsholmL, Ovesen P et al (2009) Periconceptional A1C<br />

and risk of serious adverse pregnancy outcome in 933 women<br />

with type 1 diabetes. Diabetes Care 32: 1046–8<br />

Kitzmiller JL, Wallerstein R, Correa A, Kwan S (2010) Preconception<br />

care for women with diabetes and prevention of major congenital<br />

malformations. Birth Defects Res A Clin Mol Teratol 88: 791–803<br />

Macintosh MC, Fleming KM, Bailey JA et al (2006) Perinatal<br />

mortality and congenital anomalies in babies of women with<br />

type 1 or type 2 diabetes in England, Wales, and Northern<br />

Ireland: population based study. BMJ 333: 177<br />

Mahmud M, Mazza D (2010) Preconception care of women with<br />

diabetes: a review of current guideline recommendations. BMC<br />

Womens Health 10: 5<br />

McElduff A, Cheung NW, McIntyre HD et al (2005) The Australasian<br />

Diabetes in Pregnancy Society consensus guidelines for the<br />

management of type 1 and type 2 diabetes in relation to<br />

pregnancy. Med J Aust 183: 373–7<br />

Nielsen LR, Ekbom P, Damm P et al (2004) HbA1c levels are<br />

significantly lower in early and late pregnancy. Diabetes Care 27:<br />

1200–1<br />

Ray JG, O’Brien TE, Chan WS (2001) Preconception care and the risk<br />

of congenital anomalies in the offspring of women with diabetes<br />

mellitus: a meta-analysis. QJM 94: 435–44<br />

Wahabi HA, Alzeidan RA, Bawazeer GA et al (2010), Preconception<br />

care for diabetic women for improving maternal and fetal<br />

outcomes: a systematic review and meta-analysis. BMC<br />

Pregnancy Childbirth 10: 63<br />

58 Diabetes & Primary Care Australia Vol 2 No 2 2017


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

Online CPD activity<br />

Visit www.pcdsa.com.au/cpd to record your answers and gain a certificate of participation<br />

Participants should read the preceding article before answering the multiple choice questions below. There is ONE correct answer to each question.<br />

After submitting your answers online, you will be immediately notified of your score. A pass mark of 70% is required to obtain a certificate of<br />

successful participation; however, it is possible to take the test a maximum of three times. A short explanation of the correct answer is provided.<br />

Before accessing your certificate, you will be given the opportunity to evaluate the activity and reflect on the module, stating how you will use what<br />

you have learnt in practice. The CPD centre keeps a record of your CPD activities and provides the option to add items to an action plan, which will<br />

help you to collate evidence for your annual appraisal.<br />

1. What percentage of pregnant women are<br />

affected by pre-gestational diabetes?<br />

Select ONE option only.<br />

A. 0.1%<br />

B. 1%<br />

C. 2.5%<br />

D. 5%<br />

E. 10%<br />

2. A woman with type 2 diabetes has an<br />

HbA 1c<br />

of 69 mmol/mol (8.5%) in early<br />

pregnancy. Which ONE of the following<br />

statements is NOT true?<br />

A. She is at increased risk of miscarriage.<br />

B. She is at increased risk of hypertension<br />

in late pregnancy.<br />

C. She is at increased risk of developing<br />

retinopathy in pregnancy.<br />

D. She will not have an increased risk of<br />

pregnancy complications unless she is<br />

obese.<br />

E. It is safe for her to continue taking<br />

metformin.<br />

3. A 31-year-old woman with type 2 diabetes<br />

has just found she is pregnant. She is<br />

currently being treated with gliclazide and<br />

metformin. Which of the following options<br />

is most appropriate? Choose ONE option<br />

only.<br />

A. Stop gliclazide immediately<br />

B. Continue gliclazide and metformin<br />

initially<br />

C. Check HbA 1c<br />

D. Start self-monitoring of blood glucose<br />

(finger-prick testing)<br />

E. B, C and D<br />

4. Attendance at diabetes-specific<br />

preconception care has been associated<br />

with which one of the following? Choose<br />

ONE option only.<br />

A. A reduction in congenital anomalies<br />

B. A reduction in perinatal mortality<br />

C. A reduction in first trimester HbA 1c<br />

D. A, B and C<br />

E. None of the above<br />

5. Rachel has long-standing type 1<br />

diabetes. Her most recent HbA 1c<br />

is<br />

70 mmol/mol (8.6%). She is keen to<br />

conceive soon. Which of the following<br />

statements is INCORRECT? Select ONE<br />

option only.<br />

A. She should avoid pregnancy until her<br />

HbA 1c<br />

is close to 53 mmol/mol (7%)<br />

while still minimising hypoglycaemia<br />

risk.<br />

B. She should start taking folic acid 5 mg<br />

daily at least 3 months before she starts<br />

trying to conceive.<br />

C. She should be referred to a specialist<br />

diabetes and pregnancy unit to<br />

optimise her diabetes management<br />

prior to conceiving.<br />

D. She should be advised to terminate the<br />

pregnancy if she falls pregnant before<br />

her HbA 1c<br />

has improved as risk to her<br />

and the fetus would be unacceptable.<br />

E. She should delay pregnancy plans if<br />

she has active retinopathy until it has<br />

been treated.<br />

6. A 43-year-old woman with type 2 diabetes<br />

is currently 6 weeks pregnant. She has<br />

a past medical history that includes<br />

pernicious anaemia, hypertension<br />

and hyperlipidaemia. Which of her<br />

medications, if any, should she now STOP?<br />

Choose ONE option only.<br />

A. Metformin<br />

B. Hydroxocobalamin 1 mg 3-monthly<br />

C. Labetalol 200 mg twice daily<br />

D. Simvastatin 20 mg daily<br />

E. None of the above<br />

7. Which of the following antidiabetes<br />

agents, if any, are SAFE to prescribe for<br />

a woman with type 2 diabetes planning<br />

pregnancy? Choose ONE option only.<br />

A. A sodium–glucose co-transporter 2<br />

(SGLT2) inhibitor<br />

B. A dipeptidyl peptidase-4 (DPP-4)<br />

inhibitor<br />

C. A glucagon-like peptide-1(GLP-1)<br />

receptor agonist<br />

D. Thiazolidinedione<br />

E. Insulin<br />

8. A 37-year-old woman with pre-gestational<br />

type 2 diabetes is advised to monitor<br />

her blood glucose levels as she has<br />

recently commenced insulin to control<br />

her diabetes. Which of the following<br />

is the most appropriate to monitor her<br />

glycaemia? Choose ONE option only.<br />

A. HbA 1c<br />

B. Self-monitoring of blood glucose<br />

(finger-prick testing)<br />

C. Fructosamine<br />

D. Continuous blood glucose monitoring<br />

E. A and B<br />

9. Which of the following insulins does not<br />

have regulatory approval for use during<br />

pregnancy? Select ONE option only.<br />

A. Insulin glulisine (Apidra ® )<br />

B. Protaphane/Humulin NPH<br />

C. Insulin detemir (Levemir ® )<br />

D. Insulin aspart (Novorapid ® )<br />

E. None of the above; they are all<br />

approved for use in pregnancy<br />

10. Ideally, what should the pre-pregnancy<br />

HbA 1c<br />

target for women with type 2<br />

diabetes be? Choose ONE option only.<br />

A.


2017 NATIONAL CONFERENCE<br />

Saturday 6th May 2017 – Melbourne Convention and Exhibition Centre, Victoria, Australia<br />

The conference has been specifically designed for all primary care health<br />

professionals working in diabetes care to:<br />

<br />

<br />

<br />

Advance their education and learning in the field of diabetes health care<br />

Promote best practice standards and clinically effective care in the management of diabetes<br />

Facilitate collaboration between health professionals to improve the quality of diabetes<br />

primary care across Australia<br />

6TH MAY 2017 CONFERENCE PROGRAM<br />

The 2017 PCDSA national conference program will combine cutting edge scientific content with<br />

practical clinical sessions, basing the education on much more than just knowing the guidelines.<br />

The distinguished panel of speakers will share their specialised experience in an environment<br />

conducive to optimal learning. The Speaking faculty include, amongst others:<br />

Associate Professor<br />

Neale Cohen<br />

Director Clinical Diabetes<br />

Baker Heart and<br />

Diabetes Institute<br />

“Diabetes management<br />

and research in primary<br />

care – key components<br />

to improving outcomes”<br />

Doctor Christel<br />

Hendrieckx<br />

Senior Research Fellow<br />

The Australian Centre<br />

for Behavioural Research<br />

in Diabetes<br />

“The emotional health of<br />

people living with diabetes”<br />

Ms Renza Scibilia<br />

Manager - Type 1 Diabetes<br />

and Consumer Voice<br />

Diabetes Australia<br />

“Engaging people with<br />

diabetes, the diabetes<br />

online community and<br />

apps for diabetes”<br />

Doctor Gautam<br />

Vaddadi<br />

Consultant Cardiologist<br />

Alfred Health, Northern Health,<br />

University of Melbourne<br />

“The emerging importance<br />

of cardiac failure diagnosis<br />

and management in people<br />

with type 2 diabetes”<br />

For further information including the full 2017 program<br />

and to register for the conference please visit:<br />

www.eventful.com.au/pcdsa2017<br />

If you have any questions regarding the conference,<br />

please contact the Conference Secretariat;<br />

Toll free telephone: 1800 898 499<br />

Email: pcdsa@eventful.com.au<br />

pcdsa.com.au


Article<br />

Diabetes and bone health<br />

Vidhya Jahagirdar, Neil J Gittoes<br />

Diabetes and osteoporosis represent two major public health challenges. Osteoporosis<br />

is characterised by decreased bone mineral density and micro-architectural changes of<br />

the bone leading to increased risk of low trauma (fragility) fractures. Both diabetes and<br />

osteoporosis are associated with significant morbidity, decreased quality of life and reduced<br />

life expectancy. This article will explore the current literature on the inter-relationships<br />

between diabetes and bone health, the impact on patients and the management strategies<br />

that may be considered in primary care to minimise risk of diabetes-related bone disease<br />

and improve outcomes.<br />

Preface<br />

Nick Forgione, General Practitioner, Trigg Health<br />

Care Centre, Perth, WA<br />

The connection between diabetes and<br />

osteoporosis is often overlooked in the<br />

busy management schedule of people<br />

with diabetes. However, there is an accumulation<br />

of evidence suggesting that type 2 diabetes may<br />

be an independent risk factor for osteoporosis.<br />

Despite the fact that bone mineral density<br />

(BMD) is often higher in people with<br />

type 2 diabetes compared to those without, it<br />

is paradoxical that people with type 2 diabetes<br />

have a higher risk of fracture. It is likely that the<br />

explanation for this paradox is multifactorial,<br />

including changes in trabecular bone,<br />

microarchitectural changes in bone leading<br />

to reduced bone strength and changes in the<br />

material property of bone due to accumulation<br />

of advanced glycation end products (AGEs).<br />

Medications used in the management of diabetes<br />

may also play a part.<br />

Diabetes and osteoporosis represent<br />

two major public health challenges.<br />

Osteoporosis is characterised by<br />

decreased bone mineral density (BMD) and<br />

micro-architectural changes of the bone leading<br />

to increased risk of low trauma or fragility<br />

fractures that are sustained as a result of a fall<br />

from standing height or less (Figure 1). Both<br />

There is much that remains unclear about<br />

people with diabetes-related osteoporosis.<br />

Assessment of fracture risk must be approached<br />

with caution as people with diabetes tend to<br />

have a higher fracture risk for a given BMD<br />

t-score compared to those without diabetes.<br />

Also it is unclear whether antiresorptive agents<br />

reduce fracture risk in type 2 diabetes to the<br />

same extent as those without diabetes (Rubin et<br />

al, 2013).<br />

As the number of people with type 2 diabetes<br />

increases and their life is extended through<br />

improvements in management, ensuring early<br />

detection and appropriate management of<br />

osteoporosis in this population becomes another<br />

priority for primary care management. Until<br />

there is further clarification of whether or not<br />

individuals with type 2 diabetes should be<br />

screened and managed differently to the rest<br />

of the population, it is important to at least<br />

ensure that the current RACGP guidelines for<br />

the detection and treatment of osteoporosis are<br />

followed.<br />

diabetes and osteoporosis are associated with<br />

significant morbidity, decreased quality of life<br />

and reduced life expectancy. In Australia, the<br />

total number of adults with diabetes is projected<br />

to rise to between 2 and 3 million by 2025<br />

(Magliano et al, 2009). Osteoporosis is also<br />

a condition that increases in prevalence with<br />

ageing (Figure 2). Age-related bone loss and<br />

Citation: Jahagirdar V, Gittoes NJ<br />

(2016) Diabetes and bone health.<br />

Diabetes & Primary Care Australia<br />

2: 61–8<br />

Article points<br />

1. Diabetes and osteoporosis are<br />

increasingly prevalent diseases.<br />

2. Diabetes and its complications<br />

influence important<br />

determinants of bone strength<br />

such as the material properties<br />

of bone, bone density and<br />

mineral content as well as<br />

bone micro-architecture<br />

and bone turnover.<br />

3. Diabetes is an important<br />

clinical risk factor for<br />

osteoporosis and fracture,<br />

and as clinicians it is<br />

important to remember this<br />

association when managing<br />

people with diabetes.<br />

Key words<br />

– Bone<br />

– Metabolic disorder<br />

– Osteoporosis<br />

Authors<br />

Vidhya Jahagirdar is Specialty<br />

Trainee Registrar in Diabetes,<br />

Endocrinology and General<br />

Internal Medicine; Neil Gittoes is<br />

Consultant & Honorary Professor<br />

of Endocrinology, Head, Centre<br />

for Endocrinology, Diabetes and<br />

Metabolism. Both are at the<br />

Department of Endocrinology,<br />

University Hospitals Birmingham<br />

NHS Foundation Trust,<br />

Birmingham, UK.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 61


Diabetes and bone health<br />

Page points<br />

1. The prevalence of osteoporosis<br />

based on bone mass density<br />

(BMD) is significantly lower in<br />

type 2 diabetes compared to<br />

age-matched controls.<br />

2. Age, female gender,<br />

glucocorticoid use and family<br />

history are well-recognised risk<br />

factors for osteoporosis and<br />

osteoporotic fractures, but the<br />

association between diabetes<br />

and osteoporosis is tantalising,<br />

but poorly understood.<br />

3. As type 1 diabetes is usually<br />

diagnosed in children, the early<br />

and chronic alterations in bone<br />

metabolism may result in lower<br />

peak bone mass.<br />

Figure 1. Osteoporosis is characterised by decreased<br />

bone mineral density and micro-architectural changes<br />

of the bone leading to increased risk of low trauma<br />

fractures (Blausen Medical Communications, 2016).<br />

post-menopausal physiological changes result in<br />

an increased prevalence of osteoporosis from 2%<br />

at 50 years to 25% at 80 years of age (NICE,<br />

2012). One in two women and one in five men<br />

sustain one or more osteoporotic fractures in their<br />

lifetime. In 2012, there were 140 822 fractures<br />

as a result of osteoporosis or osteopaenia in<br />

Australians over the age of 55 years, with a total<br />

cost of $2.75 billion. This is expected to increase to<br />

around $3.84 billion by 2022 (Watts et al, 2013).<br />

While age, female gender, glucocorticoid use<br />

and family history are well-recognised risk factors<br />

for osteoporosis and osteoporotic fractures, the<br />

association between diabetes and osteoporosis<br />

is tantalising, but poorly understood. Other<br />

disease conditions associated with diabetes, such<br />

as diabetic nephropathy, retinopathy, neuropathy<br />

and obesity, as well as medication used in<br />

the management of diabetes, may affect bone<br />

health, increase risk of falls and predispose<br />

patients to osteoporotic fractures. These factors<br />

are confounders in attempting to delineate causal<br />

links between diabetes and osteoporosis.<br />

The aim of this article is to explore the current<br />

literature on the inter-relationships between<br />

diabetes and bone health, the impact on patients<br />

and the management strategies that may be<br />

considered in primary care to minimise risk<br />

of diabetes-related bone disease and improve<br />

outcomes.<br />

Epidemiology of fractures in diabetes<br />

The interaction between diabetes and osteoporosis<br />

is poorly understood. Both type 1 and type 2<br />

diabetes are associated with increased risk of<br />

osteoporosis and fracture, and this risk is greater<br />

in type 1 than type 2 (Vestergaard, 2007).<br />

Various factors, such as type of diabetes, onset<br />

and duration, metabolic control, BMI, BMD,<br />

falls risk, diabetic complications and treatment,<br />

may influence bone health in diabetes. There are<br />

no well-designed randomised controlled trials<br />

(RCTs) or carefully evaluated epidemiological<br />

studies that have looked into all the above<br />

factors as potential attributors to fracture risk in<br />

diabetes.<br />

Figure 2. Peak bone mass is reached at 30 years of age. Bone mass then decreases with age, more<br />

so in women (Anatomy & Physiology, 2013).<br />

Type 1 diabetes<br />

BMD is lower in children and adolescents with<br />

type 1 diabetes than children without diabetes.<br />

As type 1 diabetes is usually diagnosed in<br />

children, the early and chronic alterations in<br />

bone metabolism may result in lower peak<br />

bone mass. This may contribute to osteoporosis<br />

and an increased risk of fracture in later life<br />

(Bonjour and Chevalley, 2014).<br />

According to a recent meta-analysis, type 1<br />

diabetes is associated with three times increased<br />

background risk of any fracture and the risk is<br />

elevated in both men and women. In individuals<br />

62 Diabetes & Primary Care Australia Vol 2 No 2 2017


Diabetes and bone health<br />

Secondary causes<br />

associated with diabetes<br />

l Coeliac disease<br />

l Graves thyrotoxicosis<br />

l Hypothyroidism<br />

l Hypogonadism<br />

l Vitamin D deficiency<br />

Anti-diabetes medication<br />

l TZDs<br />

l GLP-1 receptor agonists<br />

l DPP-4 inhibitors<br />

l SGLT2 inhibitors<br />

Falls risk<br />

l Diabetic retinopathy<br />

l Diabetic neuropathy<br />

l Obesity<br />

l Hypoglycaemia<br />

Decreased bone<br />

turnover<br />

CKD–MBD secondary to<br />

diabetic nephropathy<br />

Fracture risk<br />

Abnormal bone architecture<br />

Decreased bone mineral density<br />

via collagen cross links<br />

Decreased osteoblast differentiation<br />

Osteoblast dysfunction<br />

Increased osteoclast activity<br />

Increased adipogenesis<br />

Increased AGE<br />

Increased PPAR-gamma<br />

Decreased insulin/<br />

IGF-1 secretion<br />

Oxidative stress<br />

Figure 3. The factors influencing bone health and fracture risk in diabetes. AGE=advanced glycation end-products; CKD–MBD=chronic kidney<br />

disease–mineral and bone disorder; DPP-4=dipeptidyl peptidase-4; GLP-1=glucagon-like peptide-1; IGF-1=insulin-like growth factor-1; PPAR-gamma=<br />

peroxisome proliferator-activated receptor-gamma; SGLT2=sodium–glucose cotransporter 2; TZD=thiazolidinedione.<br />

with type 1 diabetes compared to people<br />

without the condition, the relative risk (RR) for<br />

hip fracture was 3.78 (95% confidence interval<br />

[CI], 2.05–6.98; P


Diabetes and bone health<br />

Page points<br />

1. Insulin deficiency and reduced<br />

insulin-like growth factor-1 have<br />

been linked to the inhibition of<br />

osteoblast differentiation and<br />

osteopaenia in type 1 diabetes.<br />

2. People with diabetes are at<br />

increased risk of falls and this is<br />

multifactorial due to advancing<br />

age, diabetes complications,<br />

hypoglycaemia and high BMI.<br />

3. Cortical bone mass is reduced<br />

in the feet and hands in severe<br />

diabetic peripheral neuropathy<br />

and may predispose to<br />

metatarsal fracture and diabetic<br />

Charcot’s osteoarthropathy.<br />

Fracture risk has also been reported to be<br />

independent of other usually reliable predictors<br />

of fracture risk in type 2 diabetes, including age,<br />

physical activity and BMI (RR 2.6 [95% CI],<br />

1.5–4.5; Janghorbani et al, 2007).<br />

How does diabetes affect bone?<br />

Diabetes and its complications influence<br />

important determinants of bone strength such<br />

as the material properties of bone, bone density<br />

and mineral content as well as bone microarchitecture<br />

and bone turnover (Figure 3).<br />

Oxidative stress<br />

Diabetes is reported to affect bone metabolism<br />

adversely through several mechanisms. Advanced<br />

glycation end-products (AGE) are produced as<br />

a result of oxidative stress in diabetes and are<br />

important mediators of diabetic complications<br />

such as diabetic retinopathy, nephropathy,<br />

neuropathy and atherosclerosis (Goh and<br />

Cooper, 2008). AGE accumulation in bones is<br />

also detrimental and leads to abnormal structure<br />

and alignment of collagen, contributing to bone<br />

fragility (Katayama et al, 1996).<br />

Insulin deficiency<br />

Insulin has an anabolic effect on bone. Insulin<br />

deficiency and reduced insulin-like growth<br />

factor-1 (IGF-1) have been linked to inhibition<br />

of osteoblast differentiation and osteopaenia<br />

in type 1 diabetes (Kanazawa et al, 2011).<br />

Treatment with insulin has been reported to<br />

stabilise BMD (Hofbauer et al, 2007). Hence,<br />

adequate optimisation of glycaemic control<br />

with insulin in type 1 diabetes may prevent<br />

osteopaenia and osteoporosis later in life.<br />

Diabetic nephropathy and chronic kidney<br />

disease (CKD)<br />

Diabetic nephropathy often leads to CKD and<br />

is the most common cause of end-stage renal<br />

disease in Australia (Kidney Health Australia,<br />

2015). The risk of developing moderate to severe<br />

CKD (stages 3b, 4 and 5) is eight times greater<br />

in women and twelve times greater in men with<br />

type 1 diabetes than in people without diabetes<br />

(Hippisley-Cox and Coupland, 2010). Similar to<br />

diabetes and osteoporosis, the risk of developing<br />

CKD increases with age.<br />

Clinical expression of mineral and bone disorders<br />

in CKD (CKD–MBD) is often asymptomatic<br />

until late in its course. Abnormalities in<br />

bone turnover and mineralisation can result<br />

in osteitis fibrosa cystica (brown tumours;<br />

Figure 4), adynamic bone disease, osteomalacia<br />

and secondary hyperparathyroidism caused by<br />

phosphate retention, decreased calcium and<br />

1,25-dihydroxy(OH) vitamin D (calcitriol)<br />

concentration, and uraemic osteodystrophy.<br />

These conditions increase the risk of fractures due<br />

to changes in bone quality. While abnormalities<br />

in calcium and phosphate levels are detected<br />

even at CKD stages 1 and 2, the clinical<br />

significance of these abnormalities is unclear.<br />

Hence, management is focussed on optimising<br />

calcium and phosphate levels in CKD stages 3,<br />

4 and 5.<br />

Factors affecting falls risk<br />

People with diabetes are at increased risk of falls<br />

and this is multifactorial due to advancing age,<br />

diabetes complications, hypoglycaemia and high<br />

BMI (Figure 3).<br />

Peripheral neuropathy<br />

The ABC health study showed that individuals<br />

with type 2 diabetes who develop fractures<br />

are more likely to have peripheral neuropathy,<br />

cerebrovascular disease and falls compared<br />

with people with diabetes without fractures<br />

(Strotmeyer et al, 2005). Cortical bone mass is<br />

reduced in the feet and hands in severe diabetic<br />

peripheral neuropathy and may predispose<br />

to metatarsal fracture and diabetic Charcot’s<br />

osteoarthropathy (Cundy et al, 1985), which can<br />

cause foot deformity and gait disturbance, further<br />

increasing fracture risk by increasing falls. People<br />

with diabetic peripheral neuropathy are more<br />

likely to fall when compared to age-matched<br />

controls. While the underlying causative factors<br />

are not entirely understood, reduced muscle<br />

strength and stability (Handsaker et al, 2014)<br />

and foot deformity are likely to be contributing<br />

factors.<br />

Retinopathy<br />

The Blue Mountain Eye study showed that, in<br />

64 Diabetes & Primary Care Australia Vol 2 No 2 2017


Diabetes and bone health<br />

Page points<br />

1. Individuals with diabetic<br />

retinopathy or cataracts, or<br />

both, with reduced visual acuity<br />

are prone to falls.<br />

2. Obesity is also associated with<br />

decreased bioavailability of<br />

vitamin D due to distribution in<br />

the subcutaneous t<strong>issue</strong> leading<br />

to vitamin D deficiency, another<br />

risk factor for osteoporosis.<br />

3. There is a high incidence of<br />

fragility fracture in people who<br />

experience hypoglycaemic<br />

events.<br />

Figure 4. Brown tumours of the hands in an individual with hyperparathyroidism (Gaillard, 2008).<br />

people with diabetes, there was a significantly<br />

increased risk of proximal humerus fracture<br />

associated with diabetic retinopathy, cortical<br />

cataract, longer diabetes duration (>10 years) and<br />

insulin treatment (Ivers et al, 2001). Individuals<br />

with diabetic retinopathy or cataracts, or both,<br />

with reduced visual acuity are prone to falls. Thus,<br />

the attendant increased risk of falls contributes to<br />

greater risk of fracture.<br />

Obesity<br />

In total, 90% of people with type 2 diabetes are<br />

overweight or obese. Obesity is commonly thought<br />

to have a protective effect on bone as BMD tends<br />

to increase with load bearing associated with<br />

being overweight. In post-menopausal women,<br />

obesity increased the risk of fractures at the<br />

humerus and ankle while decreased the risk at<br />

the hip, pelvis and wrist (Gonnelli et al, 2014).<br />

Fewer data are available for men. The reasons for<br />

site-specific fractures in obesity could be related<br />

to fat padding protecting the hip and pelvis and<br />

a tendency to fall backwards or sideways rather<br />

than fall forward on outstretched arm leading<br />

to wrist fracture. Obesity is also associated with<br />

decreased bioavailability of vitamin D due to<br />

distribution in the subcutaneous t<strong>issue</strong> leading<br />

to vitamin D deficiency, another risk factor<br />

for osteoporosis. Hence, in spite of increased<br />

BMD, obesity is associated with increased risk<br />

of fracture at particular sites, which is likely<br />

to be due to the pattern of fall and vitamin D<br />

deficiency.<br />

Hypoglycaemia<br />

There is a higher incidence of fragility fracture<br />

in people who experience hypoglycaemic events<br />

(Signorovitch et al, 2013). Intensive glycaemic<br />

control (HbA 1c<br />


Diabetes and bone health<br />

Page points<br />

1. Type 1 diabetes can be<br />

associated with other<br />

autoimmune conditions such as<br />

coeliac disease, hypothyroidism<br />

and Graves’ thyrotoxicosis,<br />

which also increase this risk of<br />

fracture and osteoporosis.<br />

2. Hyperthyroidism and overtreated<br />

hypothyroidism are<br />

associated with lower bone<br />

mineral density and increased<br />

risk of fracture.<br />

3. It is important to be aware<br />

of the effect different antidiabetes<br />

medication can have<br />

on bone mineral density and<br />

osteoporosis.<br />

relationship between hypoglycaemia and<br />

falls risk. It is intuitive, however, to speculate<br />

that with frequent hypoglycaemic episodes<br />

contributing to loss of consciousness, falls risk<br />

would increase. Thus, hypoglycaemia-induced<br />

falls with underlying low bone density in diabetes<br />

would increase risk of fragility fracture.<br />

Secondary causes for osteoporosis associated<br />

with diabetes<br />

Type 1 diabetes can be associated with other<br />

autoimmune conditions such as coeliac disease,<br />

hypothyroidism and Graves’ thyrotoxicosis.<br />

About one-third of people with coeliac disease<br />

have osteoporosis and may be at a higher risk of<br />

fractures. Both hyperthyroidism and over-treated<br />

hypothyroidism are associated with lower BMD<br />

and increased risk of fracture (Mirza and Canalis,<br />

2015). Hypogonadotrophic hypogonadism (low<br />

gonadotropins and low testosterone) is found<br />

in 25% of people with type 2 diabetes. Low<br />

testosterone levels in men are associated with<br />

low BMD and hypogonadism is a recognised<br />

cause of osteoporosis, but there are no reliable<br />

data available on fracture rates in people with<br />

type 2 diabetes and hypogonadism (Dandona<br />

and Dhindsa, 2011). Though epidemiological<br />

observational studies have shown associations<br />

between vitamin D deficiency and type 1 and<br />

type 2 diabetes, the evidence is inconclusive<br />

(Suzuki et al, 2006; Tahrani et al, 2010), as it<br />

is for many associations between suboptimal<br />

vitamin D and major health outcomes.<br />

Anti-diabetes medication<br />

Thiazolidinediones<br />

Expression of peroxisome proliferator-activated<br />

receptor-gamma (PPAR-gamma) is increased<br />

in diabetes. This induces adipogenesis and<br />

inhibits osteogenesis (Botolin and McCabe,<br />

2006; Montagnani and Gonnelli, 2013).<br />

Thiazolidinediones (pioglitazone and rosiglitazone)<br />

are PPAR-gamma agonists. They improve insulin<br />

sensitivity through their action on adipose t<strong>issue</strong><br />

and liver by increasing glucose utilisation and<br />

decreasing glucose production. Thiazolidinediones,<br />

through their action on PPAR-gamma, enhance<br />

the effect of inhibiting osteoblast formation and<br />

increase risk of fracture in type 2 diabetes.<br />

Both pioglitazone and rosiglitazone are<br />

associated with increased fractures in women<br />

but not in men. A meta-analysis by Zhu et al<br />

(2014) reported this risk as independent of age<br />

and with no clear association with duration of<br />

treatment. Thiazolidinedione use was associated<br />

with significant changes in BMD and increased<br />

fractures not only in the upper and lower limbs<br />

but also at the lumbar spine and femoral neck<br />

(Zhu et al, 2014). The benefit of improving<br />

glycaemic control versus the risk of fracture<br />

should be assessed carefully on an individual<br />

case basis, especially in post-menopausal women,<br />

before commencing treatment with pioglitazone<br />

in type 2 diabetes.<br />

Incretin-based medicines<br />

Glucagon-like peptide 1 (GLP-1) agonists are<br />

recommended in the management of obese people<br />

with type 2 diabetes and their effect on the risk<br />

of bone fractures is beginning to be established.<br />

In a meta-analysis of RCTs, liraglutide was<br />

associated with significantly reduced risk of<br />

fracture and exenatide was associated with an<br />

elevated risk of incident bone fractures (Su<br />

et al, 2015). Protective effects of dipeptidyl<br />

peptidase-4 (DPP-4) inhibitors on bone have<br />

also been reported in a recent meta-analysis.<br />

These data should be interpreted with caution as<br />

the trials included in the meta-analysis were not<br />

sufficiently long to assess fracture risk and the<br />

effect on bone was not assessed as a primary endpoint<br />

(Monami et al, 2011). The effects of DPP-4<br />

inhibitors and GLP-1 agonists on bone health<br />

need to be confirmed with well-designed RCTs.<br />

Sodium–glucose cotransporter 2 (SGLT2)<br />

inhibitors<br />

In October 2015, the US Food and Drug<br />

Administration (FDA; 2015) <strong>issue</strong>d a warning<br />

for the SGLT2 inhibitor canagliflozin relating to<br />

increased risk of hip fractures and fractures of the<br />

lower spine. More evidence is needed to ascertain<br />

if this is a drug class effect.<br />

Insulin<br />

One large longitudinal study, using a German<br />

database of over 100 000 people with type 2<br />

diabetes in general practice found non-significant<br />

66 Diabetes & Primary Care Australia Vol 2 No 2 2017


Diabetes and bone health<br />

increase in risk of fracture in people on basal<br />

insulin (glargine, insulin detemir and NPH<br />

insulin) compared to oral hypoglycaemia agents<br />

(Pscherer et al, 2016). This could possibly be<br />

due to increased insulin-induced hypoglycaemiarelated<br />

falls as discussed above, rather than direct<br />

effect of insulin on the bone. In the absence of<br />

RCT data at present, there is no clear evidence<br />

to suggest that insulin increases the risk of<br />

osteoporosis or fracture.<br />

Management<br />

There is no specific guideline for the management<br />

of bone disorders in diabetes. Investigations and<br />

treatment of osteoporosis should be based on<br />

patients’ absolute risk of fracture taking into<br />

consideration age, gender, menopausal status,<br />

personal and family history of fractures, body<br />

weight, falls risk, thiazolinediones use and<br />

associated secondary causes of osteoporosis.<br />

Fracture risk assessment based on FRAX,<br />

Garvan or QFracture assessment tools can help<br />

predict the risk of fracture. However, these may<br />

under-estimate fracture risk in type 2 diabetes,<br />

as paradoxically, BMD is often higher than in<br />

those without diabetes, despite the increased risk<br />

of fracture (Schwartz et al, 2011). Type 2 diabetes<br />

is not an explicitly recognised risk factor included<br />

in the risk assessment tool and BMD in type 2<br />

diabetes can be normal or elevated in spite of<br />

increased fracture risk. As BMD does not predict<br />

fracture risk in renal osteodystrophy, it need not<br />

be performed routinely in CKD stages 3–5 in<br />

the presence of CKD-MBD (Kidney Disease:<br />

Improving Global Outcomes [KDIGO] CKD-<br />

MBD Work Group, 2009).<br />

Bone mineral disorders in CKD can be identified<br />

early by detecting decreasing serum calcium,<br />

phosphate and vitamin D concentrations, and<br />

increasing serum parathyroid hormone (PTH)<br />

concentrations. The KDIGO clinical practice<br />

guideline suggests monitoring for serum calcium,<br />

phosphorus, 25-hydroxy vitamin D deficiency<br />

and PTH routinely for CKD stages 3–5 with the<br />

frequency of monitoring based on stage, rate of<br />

progression and whether specific therapies have<br />

been initiated (KDIGO CKD-MBD Work Group,<br />

2009). PTH and bone alkaline phosphatase can<br />

be used to evaluate CKD–MBD.<br />

Anti-resorptive agents such as bisphosphonates<br />

can be used as first-line agents to treat osteoporosis<br />

and high fracture risk in diabetes and in CKD<br />

stages 1, 2 and 3 (estimated glomerular filtration<br />

rate [GFR] >30 mL/min/1.73 m 2 ) in the absence<br />

of abnormal bone mineral markers. The effect of<br />

drug treatment should be reviewed after 5 years<br />

for alendronate and after 3 years for intravenous<br />

zolendronic acid with a view to making a decision<br />

regarding a drug holiday or continuing or switching<br />

treatment. No studies have specifically looked at<br />

optimal treatment for people with fractures where<br />

thiazolidinediones have been implicated.<br />

Screening for coeliac disease with t<strong>issue</strong><br />

transglutaminase antibodies (TTG) is<br />

recommended at the time of diagnosis of type 1<br />

diabetes and if a young adult with type 1 develops<br />

intestinal or extra-intestinal symptoms consistent<br />

with coeliac disease (NICE, 2009). Annual<br />

screening for thyroid status is also recommended.<br />

Screening for hypogonadism in people with type 2<br />

diabetes and replacing with testosterone if found<br />

deficient is also recommended (Dandona and<br />

Dhindsa, 2011).<br />

Good glycaemic control and blood pressure<br />

control delays the progression of microvascular<br />

complications, which are associated with increased<br />

risk of falls and fracture. HbA 1c<br />

targets should be<br />

individualised and less stringent control (HbA 1c<br />


Diabetes and bone health<br />

“It is important,<br />

where possible, to<br />

ensure that messages<br />

from different<br />

clinicians pertaining<br />

to lifestyle factors are<br />

aligned and overlap as<br />

much as possible.”<br />

Conclusion<br />

Diabetes and osteoporosis are increasingly<br />

prevalent diseases. Diabetes is an important<br />

clinical risk factor for osteoporosis and fracture,<br />

and as clinicians it is important to remember this<br />

association when managing people with diabetes.<br />

Diabetes-related complications, hypoglycaemia<br />

and obesity could increase the risk of falls<br />

and fragility fracture. HbA 1c<br />

targets should be<br />

individualised taking into consideration age,<br />

frailty, diabetes complications and falls risk.<br />

While there is much to learn regarding the<br />

associations between diabetes, osteoporosis<br />

and fractures, it is important to recognise the<br />

value of performing a multifactorial fracture<br />

risk assessment, including falls risk. Tools are<br />

available to conveniently assess this risk and<br />

measurement of BMD by performing a DXA<br />

scan may provide additional useful information<br />

to help target those patients who are most<br />

at risk of fracture with appropriate fracture<br />

prevention drug therapies. The value of lifestyle<br />

modification to address fracture and falls risk<br />

cannot be underestimated. It is also convenient<br />

that the lifestyle modifications required to<br />

optimise bone health very much overlap with<br />

the lifestyle guidance that is offered to optimise<br />

the management of the underlying diabetes and<br />

obesity. It is important, where possible, to ensure<br />

that our messages to patients pertaining to<br />

lifestyle factors are aligned and overlap as much<br />

as possible, rather than conveying different sets<br />

of instructions for different disease areas. This<br />

is where diabetes and osteoporosis management<br />

from a self-help perspective very much align. n<br />

Acknowledgement<br />

This article has been modified from one<br />

previously published in Diabetes & Primary Care<br />

(2016, 2: 68–74).<br />

Anatomy & Physiology (2013) Age and Bone Mass. Wikimedia<br />

Commons. Available at: https://commons.wikimedia.org/wiki/<br />

File:615_Age_and_Bone_Mass.jpg (accessed 22.03.16)<br />

Blausen Medical Communications (2016) Osteoporosis locations.<br />

Wikimedia Commons. Available at: https://commons.wikimedia.org/<br />

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68 Diabetes & Primary Care Australia Vol 2 No 2 2017


Article<br />

Falls prevention in older adults<br />

with diabetes: A clinical review of<br />

screening, assessment and management<br />

recommendations<br />

Anna Chapman, Claudia Meyer<br />

Older adults with diabetes have an increased rate of falls, recurrent falls and rate of<br />

fracture following a fall. Falls can contribute to a heightened fear of further falling, social<br />

isolation, avoidance of daily activities, and can increase the likelihood of premature<br />

admission to residential aged-care facilities. The most common risk factors for falls within<br />

this population group include peripheral neuropathy, foot complications, impaired postural<br />

control, polypharmacy and insulin use, sub-optimal glycaemic control and hypoglycaemia,<br />

as well as vision and cognitive impairment. Falls risk screening should be undertaken every<br />

12 months for all older people with diabetes, followed by a more detailed falls assessment<br />

for those deemed high risk to identify the contributory risk factors and management<br />

strategies. Individualised strategies should be co-designed with individuals and where<br />

appropriate, their carer(s), may involve referral to other health professionals, and should<br />

be monitored and reviewed at regular intervals.<br />

Falls are a complication of diabetes and<br />

are being increasingly acknowledged<br />

as impacting the overall health and<br />

wellbeing of older adults (International Diabetes<br />

Federation [IDF], 2013). Within the general<br />

community-dwelling population of older adults,<br />

approximately one in three people fall per<br />

year (Moyer, 2012). The combination of age<br />

(≥65 years) and diabetes increases the risk of<br />

recurrent falls by 67% (Pijpers et al, 2012); and<br />

older adults with diabetes are twice as likely to<br />

have injurious falls (Roman de Mettelinge et al,<br />

2013). At the individual level, falls can contribute<br />

to a loss of confidence and reduced activity levels,<br />

loss of lower-limb muscle and bone strength<br />

(Karinkanta et al, 2010), and a heightened<br />

fear of further falling (Zijlstra et al, 2007). For<br />

the public health system, there are expanding<br />

costs associated with falls-related hospitalisations<br />

(Bradley, 2012).<br />

Key to the prevention of falls is the identification<br />

of at-risk individuals and the implementation of<br />

appropriate interventions. Given the increased<br />

prevalence and negative consequences associated<br />

with falls among older adults with diabetes, falls<br />

prevention should be considered an integral<br />

component of diabetes care, and primary care<br />

practitioners are well-placed to offer proactive,<br />

comprehensive and individualised falls prevention<br />

strategies. This article will assist primary care<br />

practitioners in this role, providing an overview<br />

of potential screening tools and outlining fallsrelated<br />

risk factors pertinent to an older person<br />

with diabetes. In addition, this paper will<br />

consider the evidence and recommend actions<br />

for older adults with diabetes, specifically for the<br />

community-dwelling population (rather than the<br />

hospital or residential aged-care setting).<br />

Falls risk screening<br />

Falls risk screening refers to the process of<br />

identifying individuals who are at-risk of a fall,<br />

to determine if a detailed falls assessment is<br />

appropriate. To be effective, screening tools need<br />

Citation: Chapman A, Meyer C<br />

(2017) Falls prevention in older<br />

adults with diabetes: A clinical<br />

review of screening, assessment and<br />

management recommendations.<br />

Diabetes & Primary Care Australia<br />

2: 69–74<br />

Article points<br />

1. Falls-related risk factors<br />

for older people with<br />

diabetes include peripheral<br />

neuropathy, impaired postural<br />

control, polypharmacy,<br />

visual impairment,<br />

cognitive impairment, foot<br />

complications, and suboptimal<br />

glycaemic control.<br />

3. Valid and reliable risk screens<br />

exist to identify individuals<br />

at-risk of falls. As with all<br />

older adults, individuals with<br />

diabetes should be screened for<br />

falls at least once every year.<br />

4. Individuals at increased risk<br />

of falls require a multifactorial<br />

assessment that examines<br />

the wide range of fallsrelated<br />

risk factors.<br />

5. Falls prevention interventions<br />

should systematically address<br />

the risk factors identified and<br />

should be developed with the<br />

older person with diabetes, and<br />

where applicable their carer(s).<br />

Key words<br />

– Falls<br />

– Older people<br />

Authors<br />

Author details are on page 74.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 69


Falls prevention in older adults with diabetes<br />

Page points<br />

1. Falls risk screening tools need<br />

to be validated, quick and easy<br />

to administer, cost-effective and<br />

clinically relevant.<br />

2. Falls risk screening should<br />

be incorporated into routine<br />

consultations, involving<br />

assessment of an individual’s<br />

falls history over the last<br />

12 months together with<br />

examination of balance and<br />

mobility.<br />

3. When classified as high risk,<br />

individuals should undergo a<br />

comprehensive falls assessment<br />

in a timely manner to guide<br />

appropriate and individualised<br />

falls prevention strategies.<br />

to be validated, quick and easy to administer,<br />

cost-effective and clinically relevant. The<br />

selection of a screening tool should complement<br />

the setting (community, hospital or residential<br />

aged-care) and the older adult being screened,<br />

particularly with regard to age, ethnicity, as<br />

well as cognitive and functional status.<br />

The Global Guideline for Managing Older<br />

People with Type 2 Diabetes recommends that<br />

falls risk screening be performed during an<br />

initial visit to a health care provider, reviewed<br />

annually at a minimum and additionally<br />

following a fall event (IDF, 2013). Falls<br />

risk screening should be incorporated into<br />

routine consultations, involving assessment<br />

of an individual’s falls history over the last<br />

12 months (frequency of falls, circumstances<br />

surrounding each fall, and number of injurious<br />

falls), together with examination of balance<br />

and mobility. Table 1 provides a summary<br />

of available tools and tests for use in the<br />

primary care setting. As with any screening<br />

procedure, all falls risk screening outcomes<br />

should be documented and discussed with the<br />

older person and their carer(s), and information<br />

provided to individuals.<br />

Falls risk assessment to identify fallsrisk<br />

factors<br />

Falls risk screening identifies individuals at<br />

high risk of falls. When classified as such,<br />

individuals should undergo a comprehensive<br />

falls assessment in a timely manner to guide<br />

appropriate and individualised falls prevention<br />

strategies.<br />

A recommended falls assessment tool can<br />

be used to assess the overall risk of falls (as<br />

summarised in Table 2). In addition, specific<br />

assessment of individual factors known to<br />

contribute to falls risk among older adults with<br />

diabetes can be undertaken. It is important to<br />

acknowledge, that although falls-related risk<br />

factors are often referred to independently,<br />

most falls occur as a result of the interaction<br />

between intrinsic and extrinsic risk factors<br />

(Tinetti et al, 1986). A description of the<br />

specific risk factors that are primarily targeted<br />

for further assessment with older adults with<br />

diabetes are discussed below with assessment<br />

and management recommendations provided<br />

(Australian Commission on Safety and Quality<br />

in Healthcare, 2009; American Geriatrics<br />

Society and British Geriatrics Society, 2010).<br />

Table 1. Summary of validated tools and tests recommended for screening of falls risk.<br />

Falls risk screen Description Time to implement Scoring interpretation*<br />

Balance and mobility tests<br />

Timed Up and Go (TUG) test<br />

(Podsiadlo and Richardson, 1991)<br />

A measure of dynamic balance that assesses the time taken for an individual<br />

to rise from a chair, walk 3 metres, turn around, walk back to the chair, and<br />

sit down. Requires a stop-watch and a 43 cm-high straight-backed chair<br />

with solid seat.<br />

1–2 minutes<br />

≥12 seconds is indicative of<br />

an increased risk of falling.<br />

Five Times Sit To Stand<br />

(FTSTS) test<br />

(Tiedemann et al, 2008)<br />

A measure of lower-limb strength that assesses the time taken for an<br />

individual to stand up and sit down as quickly as possible five times, with<br />

their arms folded across their chest. Requires a stop-watch and a 43 cm-high<br />

straight-backed chair with solid seat.<br />

1–2 minutes<br />

≥12 seconds is indicative of<br />

an increased risk of falling.<br />

Alternate Step Test (AST)<br />

(Tiedemann et al, 2008)<br />

A measure of lateral stability that involves weight shifting. An individual<br />

is required to alternately place the right and left feet (no shoes) as fast as<br />

possible on a step that is 18 cm high and 40 cm deep, for a total of eight<br />

steps. A stop-watch is required.<br />

1–2 minutes<br />

≥10 seconds is indicative of<br />

an increased risk of falling.<br />

Multi-item screening tool<br />

Falls Risk for Older People in the<br />

Community (FROP-Com) Screen<br />

(Russell et al, 2009)<br />

A 3-item screening tool that addresses 12-month falls history, self-perceived<br />

need for assistance to perform activities of daily living, and the objective<br />

assessment of steadiness through the observation of an individual standing,<br />

walking a few metres, turning and sitting.<br />

Available at: http://bit.ly/2m6PXZX<br />

1–2 minutes<br />

Responses for each item are<br />

scored from 0–3. A total<br />

score between 0–3 indicates<br />

low-risk. Scores between<br />

4–9 indicate high-risk.<br />

*Scoring criterion based on cut-off scores specified within best practice guidelines for falls prevention (Australian Commission on Safety and Quality in Healthcare, 2009).<br />

Note: Above mentioned tools not specifically validated for older adults with diabetes.<br />

70 Diabetes & Primary Care Australia Vol 2 No 2 2017


Falls prevention in older adults with diabetes<br />

Table 2. Summary of recommended falls assessment tools.<br />

Falls assessment tool Description Time to implement Scoring interpretation*<br />

FallScreen © : Physiological<br />

Profile Assessment<br />

(Lord et al, 2003)<br />

The short form is a validated five-item instrument that includes a single<br />

assessment of vision, peripheral sensation, lower-limb strength, reaction<br />

time and body sway. There is an associated cost for the purchase of the<br />

tool.<br />

Available at: http://bit.ly/2lYqPU7<br />

15–20 minutes<br />

≥1 is indicative of an<br />

increased risk of falling.<br />

FROP-Com<br />

(Russell et al, 2008)<br />

A detailed falls risk factor assessment tool that includes 26 items that<br />

address 13 falls-related risk factors. The tool includes guidelines for<br />

scoring, and evidence-based referrals and interventions. No equipment is<br />

required and the tool is available at no cost.<br />

Available at: http://bit.ly/2mFR8mD<br />

10–15 minutes<br />

Total score range is 0–60.<br />

Scores >18 is indicative of<br />

high risk.<br />

QuickScreen ©<br />

(Tiedemann et al, 2008)<br />

A multifactorial falls assessment tool comprised of the following items:<br />

previous falls, medication usage, vision, peripheral sensation, lower-limb<br />

strength, balance and co-ordination. Minimal equipment is required. There<br />

is an associated cost for the purchase of the tool.<br />

Available at: http://bit.ly/2mlM7P5<br />

10 minutes<br />

≥4 is indicative of an<br />

increased risk of falling.<br />

*Scoring criterion based on cut-off scores specified within best practice guidelines for falls prevention (Australian Commission on Safety and Quality in Healthcare, 2009).<br />

The above scores should be used for the purpose of assessment and re-assessment over time.<br />

Note: Above mentioned tools not specifically validated for older adults with diabetes.<br />

Peripheral neuropathy<br />

The most common falls-related risk factor related<br />

to diabetes is peripheral neuropathy, present<br />

in approximately 50–70% of older adults with<br />

diabetes (Kirkman et al, 2012). Peripheral<br />

neuropathy results in changes to the motor<br />

and/or sensory components of the foot and<br />

ankle, potentially leading to postural instability,<br />

foot complications, altered walking function<br />

and muscle atrophy (Boulton, 2004; Palma et al,<br />

2013; Brown et al, 2015). Clinical emphasis is<br />

placed on the prevention of peripheral neuropathy<br />

by means of optimal glycaemic control, as well as<br />

the early recognition of the condition (Royal<br />

Australian College of General Practitioners<br />

[RACGP], 2016). Peripheral neuropathy should<br />

be assessed annually using either the Diabetic<br />

Neuropathy Symptom (DNS) score (Meijer<br />

et al, 2002) and/or routine sensory tests (i.e.<br />

a 10-g monofilament and palpating foot).<br />

Postural instability<br />

An increase in postural instability is a risk factor<br />

for falls (Ganz et al, 2007; Drootin, 2011), which<br />

is particularly important for people with diabetes<br />

who experience a decrease in the functioning of<br />

the neuromuscular and sensorimotor systems<br />

(Crews et al, 2013). Control of balance to<br />

maintain postural stability involves a complex<br />

interplay of the sensory and motor systems and<br />

integration of, and reaction to, this information<br />

by the central nervous system.<br />

In the primary care setting, the assessment<br />

of postural stability can be easily performed<br />

by balance and mobility tests (e.g. Table 1).<br />

To address postural instability, falls prevention<br />

exercise programs are encouraged (Australian<br />

Commission on Safety and Quality in Healthcare,<br />

2009; Gillespie et al, 2012). Exercise interventions<br />

have recently been found to be effective for older<br />

adults with diabetes with regard to lower-limb<br />

strength, static balance and gait measures<br />

(outcomes vital in the maintenance of postural<br />

stability; Chapman et al, 2016). In particular,<br />

individuals are likely to benefit from exercise<br />

programs that incorporate a challenge to balance,<br />

when delivered with sufficient frequency (e.g. total<br />

of 50 hours, preferably at least 2 hours per week).<br />

It should also be noted that walking programs,<br />

although beneficial for metabolic control and<br />

improvement of cardiovascular disease risk, have<br />

been associated with an increased risk of falls<br />

(Sherrington et al, 2011). Exercise programs<br />

should be tailored to existing levels of fitness<br />

and should consider an individual’s lifestyle<br />

and any medical contraindications. Referral<br />

to an appropriate health professional (e.g. a<br />

physiotherapist or exercise physiologist) may be<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 71


Falls prevention in older adults with diabetes<br />

Page points<br />

1. Foot complications, including<br />

foot pain, foot ulceration and<br />

consequent amputations, are<br />

common among older adults<br />

with diabetes and are significant<br />

contributors to increased falls<br />

risk.<br />

2. Falls risk among adults with<br />

diabetes has been found to<br />

increase steadily at four or more<br />

prescription medications.<br />

3. It is important that primary care<br />

practitioners comprehend the<br />

overall medication burden as<br />

it has the potential to lead to<br />

medication-related problems<br />

including non-adherence,<br />

hypoglycaemia and increased<br />

risk of falls.<br />

warranted for a detailed assessment of balance,<br />

and the design of challenging, yet safe exercise<br />

programs (Australian Commission on Safety<br />

and Quality in Healthcare, 2009).<br />

Foot complications<br />

Foot complications, including foot pain, foot<br />

ulceration and consequent amputations, are<br />

common among older adults with diabetes and<br />

are significant contributors to increased falls<br />

risk (Al-Rubeaan et al, 2015). In brief, foot-care<br />

education should be provided to all people<br />

with diabetes to assist in the prevention of foot<br />

complications. Education should consist of basic<br />

foot-care recommendations and, of particular<br />

relevance to falls, advice regarding appropriate<br />

footwear. Screening and risk stratification for<br />

potential foot complications should also be<br />

performed for all adults with diabetes, with the<br />

intensity of monitoring and review dependent<br />

on the associated level of risk. For individuals<br />

classified as being at intermediate or high risk,<br />

a podiatry assessment is an integral component<br />

of a foot protection program (Menz et al, 2006;<br />

R ACGP, 2016).<br />

Diabetes-related foot ulcers deserve specific<br />

mention when considering falls risk. Offloading<br />

footwear is a common recommendation for<br />

foot ulcers, yet it has a negative effect on<br />

postural stability (van Deursen, 2008). In<br />

particular, total contact casts and removable<br />

or non-removable cast-walkers are problematic<br />

for falls. Given their rigid nature, they do not<br />

allow the foot to make its usual adjustments on<br />

uneven terrain.<br />

Sub-optimal glycaemic control<br />

and hypoglycaemia<br />

Hypoglycaemia, hypoglycaemic unawareness<br />

and severe hyperglycaemia are well-established<br />

risk factors for falls among older adults with<br />

diabetes (Jafari and Britton, 2015; Sinclair et<br />

al, 2015). Optimising an individual’s glycaemic<br />

control can reduce short- and long-term<br />

complications of diabetes, and can improve<br />

quality of life, and functional and cognitive<br />

ability. However, the potential harmful effects<br />

of hypoglycaemia should be considered when<br />

setting individual glycaemic targets. Targets<br />

need be personalised and balanced against<br />

factors such as an individual’s capabilities,<br />

life expectancy, medical comorbidities, and<br />

the potential risk of severe hypoglycaemia,<br />

especially among frail, older adults with an<br />

increased risk of falls (RACGP, 2016). For older<br />

adults with diabetes who have a life expectancy<br />

>10 years and are functionally independent and<br />

fit, an HbA 1c<br />

target of 53 mmol/mol (7.0%) is<br />

often appropriate. However, less stringent HbA 1c<br />

targets (i.e. 64 mmol/mol [8%]) are appropriate<br />

for those with long-standing diabetes, a<br />

history of severe hypoglycaemia, limited life<br />

expectancy, advanced complications, and/or<br />

extensive comorbid conditions (RACGP, 2016).<br />

Medication and polypharmacy<br />

Older adults with diabetes are often required<br />

to take multiple medications in an effort to<br />

control diabetes-related outcomes and other<br />

comorbidities, and a significant proportion of<br />

individuals take upwards of eight medications<br />

(RACGP, 2016). Falls risk among adults with<br />

diabetes has been found to increase steadily at<br />

four or more prescription medications (Huang<br />

et al, 2010). Falls risk can be heightened as a<br />

result of medication interaction, medication<br />

side effects (e.g. dizziness) and even the intended<br />

effects of medications (e.g. glucose-lowering<br />

leading to hypoglycaemia). Certain classes of<br />

medication are more likely to increase the risk<br />

of falls, and those commonly implicated in falls<br />

related to older people with diabetes include<br />

insulin, psychoactive medications (in particular<br />

benzodiazepines), diuretics, antiarrhythmics<br />

(class 1a), digoxin, and antidepressants (Berlie<br />

and Garwood, 2010; Huang et al, 2010).<br />

It is important that primary care practitioners<br />

comprehend the overall medication burden<br />

as it has the potential to lead to medicationrelated<br />

problems including non-adherence,<br />

hypoglycaemia and increased risk of falls.<br />

Medication use (both conventional and<br />

complementary), should be reviewed at least<br />

once per year as part of the annual cycle of<br />

care (RACGP, 2016). Referral for a Home<br />

Medicines Review has the potential to identify<br />

medications implicated in falls and consider the<br />

ongoing need for these medications.<br />

72 Diabetes & Primary Care Australia Vol 2 No 2 2017


Falls prevention in older adults with diabetes<br />

Vision impairment<br />

Vision impairment is an important risk factor<br />

for falls in community-dwelling older adults,<br />

with vision being a key sensory input for the<br />

maintenance of balance and the avoidance of<br />

obstacles. Diabetic retinopathy, occurring as<br />

a result of microvascular disease of the retina,<br />

causes visual impairment and blindness, and<br />

affects more than 30% of adults with diabetes<br />

(Dirani, 2013).<br />

All older adults with diabetes should have a<br />

visual acuity assessment at diagnosis, and at least<br />

every 2 years (more frequently if vision noted to<br />

have concerns). Primary care practitioners can<br />

monitor individuals for retinopathy via retinal<br />

photography or by examining the eyes through<br />

dilated pupils. If practitioners are not confident<br />

with fundoscopy and assessment of the retina,<br />

referral to an eye specialist is recommended.<br />

Older people may additionally benefit from an<br />

assessment by an eye specialist for the provision<br />

of appropriate spectacle correction (RACGP,<br />

2016). The use of bifocal or multifocal lenses<br />

by older people in the community is associated<br />

with a doubled risk of falls as a result of<br />

tripping. Individuals with an increased risk of<br />

falls or established falls history are, therefore,<br />

recommended to wear single-vision distance<br />

spectacles when walking and negotiating steps<br />

(Australian Commission on Safety and Quality<br />

in Healthcare, 2009; Haran et al, 2010). Other<br />

effective fall prevention strategies for vision<br />

include maximising vision through cataract<br />

surgery on the first eye (Lord et al, 2010).<br />

Cognition<br />

Cognitive impairment is a risk factor for falls,<br />

with 50–80% of people with dementia falling<br />

in a given year (Allan et al, 2009), and mild<br />

cognitive impairment linked to greater risk of<br />

injurious and multiple falls (Delbaere et al, 2012).<br />

There appears to be a crucial link between the<br />

decline of cognition and the use of executive<br />

functioning for the purposes of balance, with this<br />

decline evident in decreasing ability to control and<br />

integrate cognitive abilities related to attention<br />

and perception (Liu-Ambrose et al, 2008). People<br />

with cognitive impairment may have difficulty<br />

with planning and executing movements related<br />

to balance and mobility, and may have difficulty<br />

limiting sensory input which affects attention to a<br />

task (e.g. walking while talking; Liu-Ambrose et<br />

al, 2008). Medication use in people with cognitive<br />

impairment also impacts falls risk, particularly<br />

psychotropic medications that may magnify side<br />

effects of other medications (Hill and Wee, 2012).<br />

There is no specific literature relating falls,<br />

diabetes and cognitive impairment. There<br />

is, however, an emerging body of evidence for<br />

effective falls prevention strategies for people with<br />

dementia (Drootin, 2011), with studies showing<br />

“traditional” falls prevention programs to be<br />

unsuccessful with people with dementia (Shaw<br />

et al, 2003). However, a different approach to<br />

adoption of falls prevention strategies may be<br />

beneficial with elements of health professional<br />

involvement, inclusion of the caregiving dyad<br />

and accommodation of individual needs and<br />

preferences likely to be important (Meyer et al,<br />

2013).<br />

Built environment<br />

Environmental hazards are considered a risk for<br />

falls: clutter can be a tripping hazard; lighting<br />

should be sufficient in order to prevent shadows;<br />

flooring should be clear of rugs and provide a<br />

contrast to furniture; and bathroom setup needs<br />

to prevent slippage on wet surfaces, with grab<br />

rails provided as needed. Home safety assessment<br />

and modification interventions are effective in<br />

decreasing falls risk and rates, especially for<br />

people with severe visual impairment, which is of<br />

relevance to the person with diabetes (Gillespie et<br />

al, 2012).<br />

Adaptation and modification of the environment<br />

with an occupational therapist who is trained<br />

to identify and maximise the benefits of the<br />

person–environment fit is the crucial factor in<br />

reducing risk (Clemson et al, 2014). Shared<br />

decision-making processes with the person with<br />

diabetes, and with their carer(s) if appropriate, will<br />

most likely enhance the uptake of environmental<br />

modifications.<br />

Conclusion<br />

Reducing the number of falls among older adults<br />

with diabetes is dependent upon the identification<br />

of at-risk individuals and the coordination of<br />

Page points<br />

1. Vision impairment is an<br />

important risk factor for falls<br />

in community-dwelling older<br />

adults, with vision being a<br />

key sensory input for the<br />

maintenance of balance and the<br />

avoidance of obstacles.<br />

2. There appears to be a crucial<br />

link between the decline<br />

of cognition and the use of<br />

executive functioning for the<br />

purposes of balance.<br />

3. Environmental hazards are<br />

considered a risk for falls, and<br />

efforts should be made to avoid<br />

them where possible.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 73


Falls prevention in older adults with diabetes<br />

“All primary care<br />

practitioners should<br />

have access to<br />

education about<br />

falls prevention, and<br />

every attempt should<br />

be made to provide<br />

comprehensive<br />

and individualised<br />

education about falls<br />

to older adults with<br />

diabetes and where<br />

appropriate, their<br />

caregivers and family.”<br />

Authors<br />

Anna Chapman, Research Fellow,<br />

School of Primary Health Care,<br />

Monash University, Melbourne, Vic;<br />

Claudia Meyer, Research Fellow,<br />

Centre for Health Communication,<br />

School of Public Health and Human<br />

Biosciences, La Trobe University,<br />

Melbourne, Vic. Both are at the<br />

RDNS Institute, St Kilda, Vic.<br />

appropriate preventive strategies. A diagnosis<br />

of diabetes in an older adult should trigger to<br />

primary care practitioners the potential for<br />

increased falls risk. Systems need to be established<br />

in the diabetes care pathway to enable falls<br />

risk screening to be performed annually. All<br />

primary care practitioners should have access<br />

to education about falls prevention, and every<br />

attempt should be made to provide comprehensive<br />

and individualised education about falls to older<br />

adults with diabetes and where appropriate, their<br />

caregivers and family. <br />

n<br />

Al-Rubeaan K, Al Derwish M, Ouizi S et al (2015) Diabetic foot<br />

complications and their risk factors from a large retrospective<br />

cohort study. PLoS ONE 10: e0124446<br />

Allan L, Ballard C, Rowan E, Kenny R (2009) Incidence and prediction<br />

of falls in dementia: A prospective study in older people. PLoS ONE<br />

4: e5521<br />

American Geriatrics Society & British Geriatrics Society (2010)<br />

Prevention of Falls in Older Persons: AGS/BGS Clinical Practice<br />

Guideline. AGS/BGS<br />

Australian Commission On Safety And Quality In Healthcare (2009)<br />

Preventing falls and harm from falls in older people: Best practice<br />

guidelines for Australian community care. ACSQHC, Canberra,<br />

ACT<br />

Berlie HD, Garwood CL (2010) Diabetes medications related to an<br />

increased risk of falls and fall-related morbidity in the elderly. Ann<br />

Pharmacother 44: 712–7<br />

Boulton AJ (2004) The diabetic foot: from art to science. The 18th<br />

Camillo Golgi lecture. Diabetologia 47: 1343–53<br />

Bradley C (2012) Hospitalisations due to falls in older people, Australia<br />

2008-09. Australian Institute for Health and Welfare, Canberra,<br />

ACT. Available at: http://bit.ly/2mlESXq (accessed 08.03.17)<br />

Brown SJ, Handsaker JC, Bowling FL et al (2015) Diabetic peripheral<br />

neuropathy compromises balance during daily activities.<br />

Diabetes Care 38: 1116–22<br />

Chapman A, Meyer C, Renehan E et al (2016) Exercise interventions<br />

for the improvement of falls-related outcomes among older adults<br />

with diabetes mellitus: A systematic review and meta-analyses.<br />

J Diabetes Complications 31: 631–45<br />

Clemson L, Donaldson A, Hill K, Day L (2014) Implementing personenvironment<br />

approaches to prevent falls: a qualitative inquiry in<br />

applying the Westmead approach to occupational therapy home<br />

visits. Aust Occup Ther J 61: 325–34<br />

Crews R, Yalla S, Fleischer A, Wu S (2013) A growing troubling triad:<br />

diabetes, aging, and falls. J Aging Res 2013: 342650<br />

Delbaere K, Kochan NA, Close JC et al (2012) Mild cognitive<br />

impairment as a predictor of falls in community-dwelling older<br />

people. Am J Geriatr Psychiatry 20: 845–53<br />

Dirani M (2013) Out of sight: A report into diabetic eye disease in<br />

Australia. Baker IDI Heart and Diabetes Institute and Centre for Eye<br />

Research Australia, Australia<br />

Drootin M (2011) Summary of the updated American Geriatrics<br />

Society/British Geriatrics Society clinical practice guideline for<br />

prevention of falls in older persons. J Am Geriatr Soc 59: 148–57<br />

Ganz D, Bao Y, Shekelle P, Rubenstein L (2007) Will my patient fall?<br />

JAMA 297: 77–86<br />

Gillespie L, Robertson M, Gillespie W et al (2012) Interventions for<br />

preventing falls in older people living in the community. Cochrane<br />

Database Syst Rev 12: CD007146<br />

Haran MJ, Cameron ID, Ivers RQ et al (2010) Effect on falls of<br />

providing single lens distance vision glasses to multifocal glasses<br />

wearers: VISIBLE randomised controlled trial. BMJ 340: c2265<br />

Hill K, Wee R (2012) Psychotropic drug-induced falls in older people:<br />

A review of interventions aimed at reducing the problem. Drugs<br />

Aging 29: 15–30<br />

Huang ES, Karter AJ, Danielson KK et al (2010) the association<br />

between the number of prescription medications and incident falls<br />

in a multi-ethnic population of adult type-2 diabetes patients: The<br />

Diabetes and Aging Study. J Gen Intern Med 25: 141–6<br />

International Diabetes Federation (2013) IDF Global Guideline for<br />

Managing Older People with Type 2 Diabetes. International<br />

Diabetes Federation, Brussels, Belgium<br />

Jafari B, Britton ME (2015) Hypoglycaemia in elderly patients with<br />

type 2 diabetes mellitus: a review of risk factors, consequences and<br />

prevention. J Pharmacy Practice Research 45: 459–69<br />

Karinkanta S, Piirtola M, Sievanen H et al (2010) Physical therapy<br />

approaches to reduce fall and fracture risk among older adults.<br />

Nature Reviews Endocrinology 6: 396–407<br />

Kirkman MS, Briscoe VJ, Clark N et al (2012) Diabetes in older adults.<br />

Diabetes Care 35: 2650–64<br />

Liu-Ambrose T, Ahamed Y, Graf P et al (2008) Older fallers with poor<br />

working memory overestimate their postural limits. Arch Phys Med<br />

Rehabil 89: 1335–40<br />

Lord SR, Menz HB, Tiedemann A (2003) A physiological profile<br />

approach to falls risk assessment and prevention. Phys Ther 83:<br />

237–52<br />

Lord SR, Smith ST, Menant JC (2010) Vision and falls in older people:<br />

Risk factors and intervention strategies. Clinics Geriatr Med 26:<br />

569–81<br />

Meijer JW, Smit AJ, Sonderen EV et al (2002) Symptom scoring<br />

systems to diagnose distal polyneuropathy in diabetes: the Diabetic<br />

Neuropathy Symptom score. Diabet Med 19: 962–5<br />

Menz G, Morris M, Lord S (2006) Foot and ankle risk factors for falls<br />

in older people: a prospective study. J Gerontol A Biol Sci Med Sci<br />

61: 866–70<br />

Meyer C, Hill S, Dow B et al (2013) Translating falls prevention<br />

knowledge to community-dwelling older PLWD: A mixed-method<br />

systematic review. Gerontologist 55: 560–74<br />

Moyer VA (2012) Prevention of falls in community-dwelling older<br />

adults: U.S. Preventive Services Task Force recommendation<br />

statement. Ann Intern Med 157: 197–204<br />

Palma F, Antigual D, Martinez S et al (2013) Static balance in patients<br />

presenting diabetes mellitus type 2 with and without diabetic<br />

polyneuropathy. Arch Endocrinol Metab 57: 722–6<br />

Pijpers E, Ferreira I, De Jongh R et al (2012) Older individuals<br />

with diabetes have an increased risk of recurrent falls: analysis<br />

of potential mediating factors: the Longitudinal Ageing Study<br />

Amsterdam. Age Ageing 41: 358–65<br />

Podsiadlo D, Richardson S (1991) The Timed “Up & Go”: A test of<br />

basic functional mobility for frail elderly persons. J Amer Geriatr<br />

Soc 39: 142–8<br />

Roman De Mettelinge T, Cambier D, Calders P et al (2013)<br />

Understanding the relationship between type 2 diabetes mellitus<br />

and falls in older adults: A Prospective Cohort Study. PLoS ONE 8:<br />

e67055<br />

Royal Australian College Of General Practitioners (2016) General<br />

practice management of type 2 diabetes: 2016-18. RACGP, East<br />

Melbourne, Vic<br />

Russell MA, Hill KD, Blackberry I et al (2008) The reliability and<br />

predictive accuracy of the falls risk for older people in the<br />

community assessment (FROP-Com) tool. Age Ageing 37: 634–9<br />

Russell MA, Hill KD, Day L et al (2009) Development of the Falls Risk<br />

for Older People in the Community (FROP-Com) screening tool.<br />

Age Ageing 38: 40–6<br />

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after a fall in older people with cognitive impairment and<br />

dementia presenting to the accident and emergency department:<br />

Randomised controlled trial. BMJ 326:<br />

Sherrington C, Tiedemann A, Fairhall N et al (2011) Exercise to prevent<br />

falls in older adults: An updated meta-analysis and best practice<br />

recommendations. N S W Public Health Bull 22: 78–83<br />

Sinclair A, Dunning T, Rodriguez-Mañas L (2015) Diabetes in older<br />

people: new insights and remaining challenges. Lancet Diabetes<br />

Endocrinol 3: 275–85<br />

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ability of eight functional mobility tests for predicting falls in<br />

community-dwelling older people. Age Ageing 37: 430–5<br />

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elderly patients based on number of chronic disabilities. Am J Med<br />

80: 429–34<br />

van Deursen, R (2008) Footwear for the neuropathic patient:<br />

offloading and stability. Diabetes Metab Res Rev 24: S96–S100<br />

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Interventions to reduce fear of falling in community-living older<br />

people: A systematic review. J Am Geriatr Soc 55: 603–15<br />

74 Diabetes & Primary Care Australia Vol 2 No 2 2017


Article<br />

The effect of diabetes on the skin<br />

before and after ulceration<br />

Lesley Weaving, Roy Rasalam<br />

Diabetes affects the skin in many different ways at a microcirculatory level, making it<br />

more prone to injury and ulceration. These changes not only have an impact on healing<br />

but also on the resulting scar t<strong>issue</strong>, which is not as strong as the skin was prior to injury.<br />

Eight-five percent of amputations are preceded by ulceration, with re-ulceration rates<br />

reported to be as high as 70% after 5 years. This article looks at the changes that occur<br />

in the skin of people with diabetes and the importance of skin care before and after<br />

ulceration.<br />

A<br />

history of ulceration is considered<br />

to be a significant risk factor for<br />

re-ulceration, and as such, people<br />

with diabetes are classed as high risk if they<br />

have a history of foot ulceration (National<br />

Institute for Health and Care Excellence,<br />

2015). Australia’s amputation rate as a result<br />

of diabetes appears to have increased in the<br />

last decade and is a major contributor to the<br />

national burden of condition (Lazzarini et al,<br />

2012). Eighty-five per cent of amputations are<br />

preceded by ulcers (International Diabetes<br />

Federation, 2016); therefore, the prevention of<br />

re-ulceration is an important consideration in<br />

reducing amputation rates. Varying rates of reulceration<br />

have been reported in the literature,<br />

but the rate of re-ulceration is known to<br />

increase over time from initial ulceration;<br />

Miller et al (2014) reported 34% re-ulceration<br />

at 1 year, 61% at 3 years and 70% at 5 years.<br />

A critical triad of neuropathy, minor foot<br />

trauma and foot deformity is present in >63%<br />

of patients’ causal pathways to foot ulceration<br />

(Reiber et al, 1999). There are many reasons<br />

that determine whether people with diabetes<br />

develop ulcers, including their vascular<br />

status, nutritional status and compliance with<br />

preventative therapies, such as custom-made<br />

shoes or insoles (Miller et al, 2014). Despite<br />

these interventions, one study has reported a<br />

30% re-ulceration rate over a 2-year period,<br />

during which individuals received regular<br />

podiatric review (Westphal et al, 2011). With<br />

this in mind, do we need to consider other<br />

factors, such as the health of the skin? What is<br />

the effect of ulceration on the skin during and<br />

after healing, and does it play a role in the risk<br />

of re-ulceration?<br />

The skin<br />

The skin is the largest organ of the body.<br />

Its main functions are to act as a barrier<br />

to substances entering the body and in the<br />

prevention of moisture loss. It helps to regulate<br />

temperature and provides sensory information<br />

(e.g. pain, touch and temperature). It has<br />

three layers: the epidermis, the dermis and a<br />

fat (subcutaneous) layer (see Figure 1). The<br />

epidermis is the thin outer layer, made of five<br />

layers. The outermost layer is the stratum<br />

corneum, which consists of dead cells and is the<br />

major barrier to chemical and bacterial transfer<br />

through the skin. The epidermis is thicker on<br />

the plantar aspect of the foot and is relatively<br />

waterproof. The second layer of the skin is the<br />

dermis, which contains nerve endings, sweat<br />

glands, oil (sebaceous) glands, hair follicles<br />

and blood vessels. It consists of a thick layer<br />

of fibrous and elastic t<strong>issue</strong>, giving the skin its<br />

flexibility and strength. Below the dermis is a<br />

Citation: Weaving L,<br />

Rasalam R (2017) The effect<br />

of diabetes on the skin before<br />

and after ulceration. Diabetes &<br />

Primary Care Australia 2: 75–9<br />

Article points<br />

1. People with diabetes<br />

are more prone to skin<br />

injury and ulceration.<br />

2. Diabetes impairs the<br />

skin’s ability to heal.<br />

3. Scar t<strong>issue</strong> is not as strong as<br />

the t<strong>issue</strong> was before injury.<br />

4. Skin should be kept in the<br />

best condition possible to<br />

prevent re-ulceration.<br />

Key words<br />

– Healing<br />

– Re-ulceration<br />

– Scar t<strong>issue</strong><br />

– Skin<br />

Authors<br />

Lesley Weaving is diabetes<br />

specialist podiatrist, Leicestershire<br />

Partnership Trust, Coalville<br />

Community Hospital, Coalville,<br />

Leicestershire, UK; Roy Rasalam<br />

is Director of Clinical Studies,<br />

College of Medicine, James Cook<br />

University, Qld, Australia.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 75


The effect of diabetes on the skin before and after ulceration<br />

80% of the tensile strength of normal skin<br />

(Ousey, 2009). Many factors play a role in<br />

how closely the healed skin resembles the<br />

original uninjured t<strong>issue</strong>, including the size,<br />

depth and location of the wound, as well as<br />

the nutritional status and overall health of the<br />

individual (Teller and White, 2009).<br />

Figure 1. Cross-section through the skin.<br />

Page points<br />

1. Skin conditions, such as<br />

infection, xerosis and<br />

psoriasis, are common in<br />

people with diabetes.<br />

2. Regular moisturising of dry skin<br />

is recommended as part of a<br />

routine foot care regimen.<br />

3. Scar t<strong>issue</strong> is not as strong<br />

as the original uninjured<br />

t<strong>issue</strong> and so is at increased<br />

risk of damage.<br />

subcutaneous layer of fat that helps insulate the<br />

body from heat and cold, provides protective<br />

padding and serves as an energy store (Health<br />

and Safety Executive, 2016).<br />

The healing process<br />

When the skin is damaged, a complex healing<br />

process takes place that can be divided<br />

into four phases (Box 1). The final stage<br />

of healing, maturation, lasts from 21 days<br />

to 2 years. During this process, epithelial<br />

cells reduce the size of the wound. This is<br />

followed by re-organisation of the collagen<br />

by macrophages to form a scar (Brown, 2015).<br />

In healthy individuals, the resulting scar<br />

t<strong>issue</strong> formed after injury has approximately<br />

Box 1. The wound healing process.<br />

l Vascular response (haemostasis): injured<br />

vessels constrict, a clot forms consisting<br />

of a fibrin mesh that forms a scab, and<br />

vasodilation of the vessels commences.<br />

l Inflammation: occurs in acute wounds<br />

3–5 days after injury and is prolonged in<br />

chronic wounds.<br />

l Proliferation: collagen fibres form to<br />

replace lost t<strong>issue</strong>.<br />

l Maturation: in healthy individuals, this<br />

stage commences 21 days after injury.<br />

Scarring develops, and the new t<strong>issue</strong> is<br />

avascular and contains no hair, sebaceous<br />

or sweat glands.<br />

The effect of diabetes on skin healing<br />

Diabetes can affect the skin in different<br />

ways. Autonomic neuropathy is a common<br />

complication of diabetes leading to dry<br />

skin, loss of sweating and the subsequent<br />

development of fissures and cracks that break<br />

the skin barrier, allowing microorganisms to<br />

enter (Vinik et al, 2003).<br />

It is now understood that a complex<br />

relationship exists between sensory<br />

nerve function and vascular response in<br />

type 2 diabetes. Dermal neurovascular<br />

function is regulated by peripheral<br />

C fibre neurons, which are damaged in<br />

diabetic neuropathy. This results in an<br />

imbalance between vasodilators (nitric<br />

oxide, substance P, and calcitonin generelated<br />

peptide) and vasoconstrictors<br />

(angiotensin II and endothelin). This<br />

dysregulation leads to decreased pain and<br />

warm thermal perception, leaving skin<br />

vulnerable to heat and t<strong>issue</strong> injury (Vinik et<br />

al, 2001).<br />

It has also been demonstrated that there is<br />

a reduced oxygen supply within the t<strong>issue</strong> of<br />

people with diabetes, which is accentuated<br />

in the presence of neuropathy (Greenman<br />

et al, 2005). Other skin conditions are also<br />

commonly seen in people with diabetes,<br />

the prevalences of which are reported to be<br />

between 30% and 91.2% (Demirseren et al,<br />

2014). The most frequently reported skin<br />

condition in people with diabetes is cutaneous<br />

infection (mainly fungal), followed by xerosis<br />

(dry skin) and inflammatory skin diseases<br />

such as psoriasis (Figure 2). These conditions<br />

are more common in people with diabetes<br />

who have nephropathy than in those without<br />

nephropathy, and those who have an HbA 1c<br />

of >64 mmol/mol (8%) are at the greatest risk<br />

(Demirseren et al, 2014).<br />

76 Diabetes & Primary Care Australia Vol 2 No 2 2017


The effect of diabetes on the skin before and after ulceration<br />

Figure 2. Psoriasis is one of the most common skin<br />

conditions experienced by people with diabetes.<br />

Vascular endothelial cells line the entire<br />

circulatory system, from the heart to<br />

capillaries. These cells are important for<br />

vascular biology and become impaired not only<br />

with age but also as a result of hyperglycaemia,<br />

which results in the impairment of blood flow<br />

to the t<strong>issue</strong>s (Petrofsky, 2011). When pressure<br />

is applied to healthy skin, the affected t<strong>issue</strong><br />

can become hypoxic; once the pressure is<br />

released there is reactive hyperaemia (increase<br />

in blood flow) to oxygenate the t<strong>issue</strong>. Vascular<br />

endothelial dysfunction can diminish this<br />

response. It has also been demonstrated that<br />

in a standing position, the average person still<br />

has circulation in the skin but in people with<br />

diabetes (even those with normal weight) there<br />

is occlusion to the skin (McLellan et al, 2009).<br />

This occlusion, together with reduced or no<br />

post-occlusive hyperaemia, may be the reason<br />

that feet are so susceptible to wounds and<br />

skin injury, particularly in people with type 2<br />

diabetes (Petrofsky, 2011).<br />

Emollients<br />

Regular moisturising of dry skin is<br />

recommended as part of a routine foot care<br />

regimen to reduce the risk of cracking and<br />

ulceration. What is not always clear is which<br />

emollient to use. There is little evidence<br />

available as to the most effective emollient,<br />

not only for the general population, but also<br />

for people with diabetes. A moisturiser that<br />

the patient is willing or happy to use that<br />

is supported by the available evidence is<br />

preferable. The clinician should also check<br />

that the patient likes the smell, texture and<br />

absorption of the cream before recommending<br />

or prescribing one. There is some evidence<br />

that high-concentration, urea-based emollients<br />

are beneficial, and these have been shown to<br />

improve dryness on the feet of people with<br />

diabetes (Bristow, 2013).<br />

For twice-a-day application, it is<br />

recommended that an emollient is applied just<br />

before getting into bed. Covering the foot with<br />

a damp undersock and then a dry oversock may<br />

enhance the effect of the emollient (Bristow,<br />

2013). For once-a-day application, the cream<br />

should form part of a patient’s daily regimen<br />

of washing, drying and checking their feet<br />

thoroughly. It is recommended that emollients<br />

be used to lubricate the skin, but not between<br />

the toes (International Working Group on<br />

the Diabetic Foot, 2015). A pump dispenser<br />

is considered by some clinicians a more userfriendly<br />

way of delivering the right amount of<br />

emollient than a tub and also decreases the risk<br />

of contamination (Carr et al, 2008), although<br />

tubes are also commonly used.<br />

Silicones<br />

Once skin has healed, silicone gel has been<br />

proven to be effective in scar-t<strong>issue</strong> management<br />

on non-weight-bearing areas; however there<br />

is little evidence to support its use on weightbearing<br />

areas (Westphal et al, 2011). Figure 3<br />

and Figure 4 demonstrate that silicone gel may<br />

be useful in protecting newly healed skin<br />

during the maturation process. A person with<br />

type 2 diabetes who suffered from psoriasis<br />

had developed ulceration and subsequent<br />

osteomyelitis at the base of the fifth metatarsal<br />

Page points<br />

1. Regular moisturising of dry<br />

skin is recommended as<br />

part of a routine foot-care<br />

regimen to reduce the risk<br />

of cracking and ulceration.<br />

2. Once skin has healed,<br />

silicone gel has been proven<br />

to be effective in scar-t<strong>issue</strong><br />

management on non-weightbearing<br />

areas; however there<br />

is little evidence to support its<br />

use on weight-bearing areas.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 77


The effect of diabetes on the skin before and after ulceration<br />

Page points<br />

1. There are many factors<br />

affecting a person’s skin<br />

when they have diabetes.<br />

2. From available evidence, the<br />

healing of a diabetic foot ulcer<br />

should not be considered<br />

the end result of a patient’s<br />

journey, but the beginning of<br />

a process to remain healed.<br />

3. Further research is required<br />

on the most-effective<br />

way to care for the skin of<br />

people with diabetes.<br />

head, which had healed well with the use of<br />

a removable cast device. However, once they<br />

returned to wearing their bespoke shoes with<br />

total contact insole, the skin re-ulcerated<br />

(Figure 3). Silicone sheeting was used to protect<br />

the area once epithelisation was achieved and for<br />

8 weeks afterwards, and no further ulceration<br />

occurred during this time (Figure 4). This<br />

suggests that the silicone sheeting provided<br />

some protection to the newly healed skin during<br />

the early stages of the maturation process<br />

(Weaving, 2014). However, a pilot study of<br />

30 people with diabetes found that silicone gel<br />

sheeting did not reduce the risk of ulceration<br />

(Westphal, 2011).<br />

Why it’s important to keep the<br />

skin healthy<br />

There are many factors affecting a person’s skin<br />

when they have diabetes. These factors can lead<br />

to ulceration and contribute to delayed healing.<br />

Poor glycaemic control of diabetes has been<br />

shown to affect the microcirculation, along<br />

with poor oxygen supply, occlusion in the skin<br />

during weight bearing, changes to the vascular<br />

endothelial cells, dry skin and reduction in<br />

elasticity all putting the skin at greater risk<br />

of injury. This is further complicated by the<br />

reduced strength of the scar t<strong>issue</strong> that forms<br />

after the ulcer has healed.<br />

Eighty per cent of ulcers are caused by some<br />

form of trauma and are, therefore, considered<br />

to be preventable (Healy et al, 2013). While<br />

custom-made footwear is used to prevent<br />

re-ulceration, it appears to be most effective for<br />

those with foot deformity (Reiber et al, 2002).<br />

Not every insole or shoe is a perfect fit to each<br />

patient’s foot (Miller et al, 2014). It is therefore<br />

important that the skin on the foot is kept in the<br />

best condition it can be to cope with the stresses<br />

placed upon it, whether it is from shoe wear or<br />

simple day-to-day weight-bearing activities.<br />

Conclusion<br />

There is little evidence on how best to look<br />

after the skin of people with diabetes. From<br />

the available evidence, the healing of a diabetic<br />

foot ulcer should not be considered the end<br />

result of a patient’s journey, but the beginning<br />

Figure 3. A patient with type 2 diabetes and psoriasis<br />

experienced re-ulceration after changing from a<br />

removable cast device back to their bespoke shoes.<br />

Figure 4. The patient continued to use silicone sheeting<br />

for 8 weeks after the ulcer had healed, which prevented<br />

re-ulceration.<br />

of a process to remain “healed”. We want<br />

patients to be active and keep mobile to<br />

help with their overall health and wellbeing;<br />

however, the impact of diabetes on their skin<br />

makes them vulnerable to skin breakdown,<br />

particularly where there is scar t<strong>issue</strong> from<br />

previous ulceration. Further research is<br />

required on the most-effective way to care<br />

for the skin of people with diabetes not just<br />

when dry, but also post-healing during the<br />

maturation process when the stresses and<br />

strains of simple weight bearing could lead<br />

to re-ulceration and, subsequently, potential<br />

78 Diabetes & Primary Care Australia Vol 2 No 2 2017


The effect of diabetes on the skin before and after ulceration<br />

loss of a limb. This is a worthwhile endeavour<br />

when we consider that every 30 seconds a<br />

lower limb is lost somewhere in the world as a<br />

consequence of diabetes (Boulton et al, 2005).<br />

<br />

n<br />

Acknowledgement<br />

This article has been modified from one<br />

previously published in The Diabetic Foot Journal<br />

(2016, 3: 142–8).<br />

Lazzarini PA, Gurr JM, Rogers JR et al (2012) Diabetes foot<br />

disease: the Cinderella of Australian diabetes management?<br />

J Foot Ankle Res 5: 24<br />

McLellan K, Petrofsky JS, Zimmerman G et al (2009) The<br />

influence of environmental temperature on the response<br />

of the skin to local pressure: the impact of aging and<br />

diabetes. Diabetes Technol Ther 11: 791–8<br />

Miller JD, Salloum M, Button A et al (2014) How can I<br />

maintain my patient with diabetes and history of foot ulcer<br />

in remission? Int J Low Extrem Wounds 13: 371–7<br />

“This is a worthwhile<br />

endeavour when we<br />

consider that every<br />

30 seconds a lower<br />

limb is lost somewhere<br />

in the world as a<br />

consequence of<br />

diabetes.”<br />

Boulton AJ, Vilikyte L, Ragnarson-Tennvall G et al (2005)<br />

The global burden of diabetic foot disease. Lancet 366:<br />

1719–24<br />

National Institute for Health and Care Excellence (2015)<br />

NICE guideline 19. Diabetic foot problems: prevention<br />

and management. NICE, London, UK. Available at: www.<br />

nice.org.uk/guidance/ng19 (accessed 02.09.2016)<br />

Bristow I (2013) Emollients in the care of the diabetic foot.<br />

The Diabetic Foot Journal 16: 61–6<br />

Ousey K (2009) Chronic wounds – an overview. J Commun<br />

Nursing 21: 4–9<br />

Brown A (2015) Wound management 1: Phases of the wound<br />

healing process. Nursing Times 111: 12–3<br />

Carr J, Akram M, Sultan A et al (2008) Contamination of<br />

emollient creams and ointments with Staphylococcus<br />

aureus in children with atopic dermatitis. Dermatitis 19:<br />

282<br />

Demirseren DD, Emre S, Akoglu G et al (2014) Relationship<br />

between skin diseases and extracutaneous complications<br />

of diabetes mellitus: clinical analysis of 750 patients.<br />

Am J Dermatol 15: 65–70<br />

Greenman RL, Panasyuk S, Wang X et al (2005) Early<br />

changes in the microcirculation and muscle metabolism<br />

of the diabetic foot. Lancet 366: 1711–5<br />

Healy A, Naemi R, Chockalingam N (2013) The effectiveness<br />

of footwear as an intervention to prevent or to reduce<br />

biomechanical risk factors associated with diabetic foot<br />

ulceration: a systematic review. J Diabetes Complications<br />

27: 391–400<br />

Petrofsky JS (2011) The effect of type-2-diabetes-related<br />

vascular endothelial dysfunction on skin physiology and<br />

activities of daily living. J Diabetes Sci Technol 5: 657–67<br />

Reiber GE, Vileikyte L, Boyko EJ et al (1999) Causal pathways<br />

for incident lower-extremity ulcers in patients with diabetes<br />

from two settings. Diabetes Care 22: 157–62<br />

Reiber GE, Smith DG, Wallace C et al (2002) Effect of<br />

therapeutic footwear on foot reulceration in patients<br />

with diabetes. A randomised controlled trial. JAMA 287:<br />

2552–8<br />

Teller P, White TK (2009) The physiology of wound healing:<br />

injury through maturation. Surg Clin North Am 89: 599–<br />

610<br />

Vinik AI, Erbas T, Park TS (2001) Dermal neurovascular<br />

dysfunction in type 2 diabetes. Diabetes Care 24: 1468–75<br />

Health and Safety Executive (2016) Structure and<br />

functions of the skin. HSE, London, UK. Available at:<br />

http://bit.ly/ZIW36y (accessed 02.09.16)<br />

Vinik AI, Maser RE, Mitchell BD, Freeman R (2003) Diabetic<br />

autonomic neuropathy. Diabetes Care 26: 1553–66<br />

International Diabetes Federation (2016) Diabetes<br />

and the Foot. IDF, Brussels, Belgium. Available at:<br />

http://bit.ly/2cUTPJB (accessed 13.09.16)<br />

Weaving L (2014) KerraPro pressure reducing pads<br />

in preventing pressure ulceration. Harrogate 2014<br />

Conference Posters. Harrogate, Wounds UK, UK. Available<br />

at: http://bit.ly/2m75Rab (accessed 02.09.16)<br />

International Working Group on the Diabetic Foot (2015)<br />

Prevention and management of foot problems in diabetes:<br />

a Summary Guidance for daily practice 2015. IWGDF<br />

Guidance documents. IDF, Brussels, Belgium. Available at:<br />

http://bit.ly/2kLpS69 (accessed 22.02.16)<br />

Westphal C, Neame IM, Harrison JC, et al (2011) A diabetic<br />

foot ulcer pilot study: does silicone gel shee ting reduce<br />

the incidence of reulceration? J Am Podiatr Med Assoc<br />

101: 116–23<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 79


The PCDSA is a multidisciplinary society with the aim<br />

of supporting primary health care professionals to deliver<br />

high quality, clinically effective care in order to improve<br />

the lives of people with diabetes.<br />

The PCDSA will<br />

Share best practice in delivering quality diabetes care.<br />

Provide high-quality education tailored to health professional needs.<br />

Promote and participate in high quality research in diabetes.<br />

Disseminate up-to-date, evidence-based information to health<br />

professionals.<br />

Form partnerships and collaborate with other diabetes related,<br />

high level professional organisations committed to the care of<br />

people with diabetes.<br />

Promote co-ordinated and timely interdisciplinary care.<br />

Membership of the PCDSA is free and members get access to a quarterly<br />

online journal and continuing professional development activities. Our first<br />

annual conference will feature internationally and nationally regarded experts<br />

in the field of diabetes.<br />

To register, visit our website:<br />

www.pcdsa.com.au

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