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Conference Proceedings - School of Nursing & Midwifery - Trinity ...

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<strong>School</strong> <strong>of</strong> <strong>Nursing</strong> & <strong>Midwifery</strong>, <strong>Trinity</strong> College Dublin: 8 th Annual Interdisciplinary Research <strong>Conference</strong><br />

Transforming Healthcare Through Research, Education & Technology: 7 th – 9 th November 2007<br />

<strong>Conference</strong> <strong>Proceedings</strong><br />

Back to contents page<br />

Insulin Glargine versus NPH Insulin for the Management <strong>of</strong><br />

Pre-existing Diabetes in Pregnancy<br />

Loretta Hothersall Ph.D., FNPC. Maine Centers for Endocrinology<br />

and Diabetes 175 Route One, Scarborough, Maine, 04074 USA. (1-<br />

207) 885-7710. hothel@mmc.org<br />

Elaine Caron MS, RN,CDE. Maine Centers for Endocrinology and<br />

Diabetes 175 Route One, Scarborough, Maine 04074,USA<br />

Insulin therapy becomes an integral part <strong>of</strong> management for women<br />

with pre-existing diabetes and pregnancy. Tight glycemic control<br />

can be attained with multiple daily injections <strong>of</strong> human insulin.<br />

Conventional therapy (NPH) may result in frequent hypoglycemic<br />

events with rebounding hyperglycemia. Serum ketosis may develop<br />

having a deleterious impact upon both mother and fetus. This study<br />

addressed the use <strong>of</strong> Glargine insulin (a recombinant human insulin<br />

analog) in pregnancy.<br />

To date there is limited research and no well controlled clinical<br />

studies in the use <strong>of</strong> Glargine insulin in pregnancy as well as the<br />

lack <strong>of</strong> FDA approval. Therefore many practices are hesitant to have<br />

patients continue on the analog. Usually women are converted back<br />

to conventional therapy (NPH) which leads to a period <strong>of</strong> suboptimal<br />

control. During this period <strong>of</strong> hyperglycemia there is increased risk<br />

for perinatal complications. The lack <strong>of</strong> safety data (in the continued<br />

use <strong>of</strong> Glargine) usually becomes a clinical decision by the provider.<br />

This study assessed a matched cohort <strong>of</strong> pregnant women with<br />

either type 1 diabetes or type 2 diabetes who chose to remain on<br />

Glargine insulin versus those women with either type 1 diabetes or<br />

type 2 diabetes who chose to remain or opted to switch to NPH<br />

insulin during their pregnancies. The purpose <strong>of</strong> the study was to<br />

evaluate the frequency <strong>of</strong> hypoglycemic events, the over all<br />

glycemic control <strong>of</strong> women in both groups, the incidence <strong>of</strong> perinatal<br />

complications as well as the incidence <strong>of</strong> neonatal complications.<br />

It was proposed that glycemic control would be as good in those<br />

women who chose to remain on Glargine insulin versus the glycemic<br />

control <strong>of</strong> those women who chose conventional therapy (NPH). The<br />

rate <strong>of</strong> fetal /neonatal complications such as neural tube defects,<br />

cardiac anomalies, macrosomia, respiratory distress syndrome,<br />

neonatal hypoglycemia, and hyperbilirubinemia would be no greater<br />

in the <strong>of</strong>fspring <strong>of</strong> those women who chose to remain on Glargine<br />

insulin<br />

Versus the <strong>of</strong>fspring <strong>of</strong> those women on conventional therapy<br />

(NPH).<br />

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