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The Operating Theatre Journal Digital Edition September 2018

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Register reinforces standards<br />

for patient safety through<br />

qualifications and training<br />

THE need for greater safeguards for patients in hospitals through the<br />

introduction of a recognised national standard of competence for<br />

health care professionals working in the life sciences industry has been<br />

pressed by HC Skills CEO Diane Irvine.<br />

In an article written for MDET, the official quarterly journal of the<br />

National Association of Medical Device Educators, she highlights the<br />

fact that the Professional Standards Authority for Health and Social<br />

Care had recently introduced a credentialing register.<br />

Under the scheme, practitioners who are required to be present in<br />

patient-facing areas will have to verify that they belong to a register<br />

that meets the PSA’s benchmarks.<br />

This will help safeguard patients and staff, by risk-managing access,<br />

improving infection control, ensuring that the right people have the<br />

right qualification and standard of training to be in a hospital setting.<br />

<strong>The</strong> article explains that commercial visitors such as medical device<br />

experts or administrative teams on hospital premises effectively<br />

become members of staff in the eyes of the law.<br />

As a result, the hospital is potentially liable for their behaviour and<br />

actions, and the impact of these on the safety of staff and patients.<br />

In admitting a patient, hospitals immediately take on a duty of care for<br />

that individual.<br />

Medical negligence claims are valid when both of the following<br />

parameters are established:<br />

• A breach in that duty of care is established<br />

• <strong>The</strong> breach is proven to have caused harm to the patient<br />

When it comes to operating theatre protocols, for example, if a<br />

patient is harmed and it is established that the hospital failed to check<br />

whether the company representative who was present – effectively an<br />

employee – had undergone the appropriate training, then it is deemed<br />

a foreseeable risk that could have been avoided.<br />

Sterile and single-use Anetic Aid<br />

Toe-niquetsTM - with built-in safety features<br />

Like any quality clinical equipment provider, Anetic Aid always makes<br />

patient safety its highest priority. It’s built into the design of every<br />

item in the company’s product range - from sophisticated QA4 Day<br />

Surgery Systems, to the small, single-use ‘Toe-niquetsTM’ used for<br />

surgery on fingers and toes.<br />

Anetic Aid’s Toe-niquets were specially redesigned following a report<br />

by the UK NHS National Patient Safety Agency (now NHS Improvement),<br />

which highlighted risks to patients caused by some digital tourniquets<br />

being left on too long after surgery.<br />

A summary of the report (reference NPSA/2007/RRR007), published by<br />

the British Medical <strong>Journal</strong> explained:’Tourniquets are used in hand<br />

and foot surgery because of the need for a bloodless field to allow for<br />

careful dissection. <strong>The</strong>y are used in a range of settings, such as operating<br />

theatres, emergency departments, community sites (for example, for<br />

minor surgery in podiatry clinics). Although rare, complications can<br />

lead to serious harm, including, at worst, irreversible ischaemia.<br />

‘Between August 2005 and November 2009, healthcare staff in England<br />

and Wales reported 15 serious incidents in which tourniquets had been<br />

left on fingers<br />

Tourniquet<br />

or toes by mistake. Ten patients<br />

System<br />

needed further surgery<br />

and Ideal two for incidents single or bi-lateral resulted orthopaedic in amputation. surgery At least six of the incidents<br />

and pain management<br />

related to surgical gloves being used Premier as tourniquets.’<br />

• OLED (Organic Light Emitting Diode)<br />

technology for a brighter display<br />

re-usable<br />

Anetic • Dual, colour-coded Aid’s sterile, channels single-use Toe-niquetsTM and robust for were already specifically<br />

long term use<br />

designed-for-purpose<br />

• Automatic self-diagnostic checks<br />

devices, and in light of the findings in this report,<br />

• Superbly manoeuvrable and stable with<br />

another<br />

integral stand<br />

feature<br />

and built-in accessory<br />

was<br />

storage<br />

added. It’s a simple Six-use Day tag attached by a nylon tie<br />

• Self-compensating<br />

Tourniquet<br />

which makes Toe-niquetsTM even easier Cuffs for practitioners to remove<br />

• Visual and audible warnings<br />

limited life,<br />

easy to clean<br />

from • IVRA a (Bier’s patient, block) guidance post feature procedure.<br />

Innovative technology – practically applied<br />

For more information about Anetic Aid Toe-niquetsTM - or other items<br />

Single-use,<br />

in the AT4 Tourniquet and accessories Sterile range - see aneticaid.com or ring<br />

Tourniquet<br />

01943 878647<br />

Cuffs<br />

Suggested illustration combination of:<br />

T 01943 878647 sales@aneticaid.com<br />

Sapper Jordan Rossi Business Park,<br />

Otley Road, Baildon BD17 7AX<br />

aneticaid.com<br />

Tourniquet<br />

Cuffs<br />

and cost<br />

effective<br />

providing<br />

sterility when<br />

the risk of<br />

infection is key<br />

<strong>The</strong>refore, the hospital is deemed liable.<br />

And that liability can be running up colossal costs. <strong>The</strong> annual amount<br />

set aside for NHS negligence claims is now standing at £65 billion.<br />

Negligence and liability are words that can sometimes lose their<br />

meaning – until a theoretical case becomes reality.<br />

Effective risk management is essential to protect patients and<br />

healthcare providers. <strong>The</strong>refore, policy compliance and national<br />

standards are important considerations that everyone should address.<br />

To discuss our training programmes, qualifications and professional<br />

standards in further detail, please contact us.<br />

Jane Bruce, Tel: +44(0) 141 946 6482<br />

E-mail: jane@healthcareskills.com<br />

Availability of diamorphine<br />

(5mg and 10mg)<br />

In the last edition of its newsletter CQC informed readers of a<br />

manufacturing issue with one of the suppliers of diamorphine 5mg<br />

and 10mg injection.<br />

Department of Health and Social Care (DHSC) and NHS England<br />

(NHSE) have continued to work with Accord and their supplier<br />

in Germany and the manufacture of diamorphine 5mg and 10mg<br />

injection will soon resume with an anticipated resupply date<br />

of beginning of <strong>September</strong> <strong>2018</strong>. DHSC and NHSE have also been<br />

working with the remaining supplier, Wockhardt, to support the<br />

supply issue. Wockhardt have been able to increase their production<br />

of diamorphine 5mg and 10mg but were unable to support the<br />

entire market in July and August.<br />

When responding to articles please quote ‘OTJ’<br />

Did YOU know you can read and download the<br />

larger, digital version of <strong>The</strong> <strong>Operating</strong> <strong>The</strong>atre<br />

<strong>Journal</strong> for FREE every month?<br />

Simply register at the top right hand corner of<br />

otjonline.com and you’ll receive a notification<br />

every time the next issue is available.<br />

<strong>The</strong> simple way to stay up to date!<br />

Find out more 02921 680068 • e-mail admin@lawrand.com Issue 336 <strong>September</strong> <strong>2018</strong> 5

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