DO WE KNOW-HOW TO SCREEN FOR GESTATIONAL DIABETES - CURRENT PRACTICE IN ONE REGIONAL HEALTH AUTHORITY

Citation
C. Nelsonpiercy et Eam. Gale, DO WE KNOW-HOW TO SCREEN FOR GESTATIONAL DIABETES - CURRENT PRACTICE IN ONE REGIONAL HEALTH AUTHORITY, Diabetic medicine, 11(5), 1994, pp. 493-498
Citations number
NO
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
Journal title
ISSN journal
07423071
Volume
11
Issue
5
Year of publication
1994
Pages
493 - 498
Database
ISI
SICI code
0742-3071(1994)11:5<493:DWKTSF>2.0.ZU;2-T
Abstract
To review current practice for screening and diagnosis of gestational diabetes (GDM) in the North East Thames health region, clinical direct ors and other relevant individuals in all 17 obstetric units within NE Thames were interviewed personally. Additional information was obtain ed from local midwives, diabetologists, and chemical pathologists. Thi rteen centres had a formal policy for screening and diagnosis of GDM. One centre ran two policies. Six of 18 centres performed a routine blo od glucose (BG) screen on all pregnant women, proceeding to OGTT eithe r on the basis of raised BG alone (3 centres), or on the basis of rais ed BG and/or clinical risk factors (3 centres). Of the remainder, 10 p erformed a diagnostic test (OGTT or equivalent) in all those with risk factors, and 2 via an intermediate screening BG. The choice and inter pretation of screening and diagnostic tests varied considerably. Six c entres used random BG, with cut-off ranging from > 5.8 mmol l-1 to > 9 .0 mmol l-1, one used a single fasting BG > 5.0 mmol l-1, and another a 50 g oral glucose challenge (1 h level > 8.0 mmol l-1). Diagnosis of GDM was based on a 75 g (13 centres) or a 50 g OGTT (2 centres), whil e 1 used a standard mixed meal, and another a timed post-prandial gluc ose sample. Timing of tests ranged from booking to 36 weeks gestation and the diagnostic cut-off levels for GDM varied (fasting: 5.0-8.0 mmo l l-1; 2 h: 6.0-1 0.1 mmol l-1). There is no consensus concerning scre ening and diagnosis of GDM in the NE Thames region. This may reflect u ncertainty about the value of screening for this condition.