Mathai M, Thomas T J, Kuruvila S, Jairaj P
Christian Medical College and Hospital, Tamil Nadu, India.
Natl Med J India. 1994 Jul-Aug;7(4):160-2.
The oral glucose tolerance test for detecting women with gestational diabetes is too complicated and prolonged for routine use. Similar and less time consuming screening tests have been proposed including random plasma glucose estimation and the glucose challenge test (blood glucose estimation one hour after a 50 g glucose load). However, in practice, correct timing of the blood sample, which is of critical importance in the interpretation of the results of these tests, is difficult to ensure. This study was designed to evaluate these two screening tests in identifying women with abnormal glucose tolerance in pregnancy.
One hundred and eleven consecutive pregnant women at risk for gestational diabetes and 121 consecutive pregnant women with no risk factors had random plasma glucose estimation followed by the 50 g glucose challenge test at 26 to 30 weeks of gestation. A 100 g 3 hour oral glucose tolerance test was done within two weeks of the screening tests. The sensitivity and specificity of screening tests in predicting abnormal glucose tolerance were calculated.
Seven (6.3%) women in the high risk group and four (3.3%) in the low risk group had gestational diabetes, while 11 (9.9%) and 8 (6.6%) had impaired glucose tolerance. Random plasma glucose level of 90 mg/dl or greater had a sensitivity of 63% and specificity of 66% in predicting abnormal glucose tolerance, while a threshold level of 115 mg/dl for the glucose challenge test yielded a sensitivity of 63% and a specificity of 55%.
Neither random plasma glucose estimation nor the glucose challenge test is a useful screening procedure for abnormal glucose tolerance in pregnancy.
用于检测妊娠期糖尿病女性的口服葡萄糖耐量试验过于复杂且耗时,不适合常规使用。已提出了类似且耗时较短的筛查试验,包括随机血浆葡萄糖测定和葡萄糖耐量试验(口服50克葡萄糖后1小时测定血糖)。然而,在实际操作中,血样采集的正确时间对于这些试验结果的解读至关重要,但很难确保。本研究旨在评估这两种筛查试验在识别妊娠期间糖耐量异常女性方面的效果。
111例连续的有妊娠期糖尿病风险的孕妇和121例连续的无风险因素的孕妇在妊娠26至30周时进行了随机血浆葡萄糖测定,随后进行了50克葡萄糖耐量试验。在筛查试验后的两周内进行了100克3小时口服葡萄糖耐量试验。计算了筛查试验预测糖耐量异常的敏感性和特异性。
高危组中有7例(6.3%)女性患有妊娠期糖尿病,低危组中有4例(3.3%);而糖耐量受损的分别有11例(9.9%)和8例(6.6%)。随机血浆葡萄糖水平≥90毫克/分升预测糖耐量异常的敏感性为63%,特异性为66%;葡萄糖耐量试验的阈值水平为115毫克/分升时,敏感性为63%,特异性为55%。
随机血浆葡萄糖测定和葡萄糖耐量试验都不是用于筛查妊娠期间糖耐量异常的有效方法。