Department of Obstetrics and Gynecology, Warren Alpert Medical School of Brown University, Providence, RI.
Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
Am J Obstet Gynecol. 2021 Dec;225(6):634-644. doi: 10.1016/j.ajog.2021.05.009. Epub 2021 May 21.
In the United States, the common approach to detecting gestational diabetes mellitus is the 2-step protocol recommended by the American College of Obstetricians and Gynecologists. A 50 g, 1-hour glucose challenge at 24 to 28 weeks' gestation is followed by a 100 g, 3-hour oral glucose tolerance test when a screening test threshold is exceeded. Notably, 2 or more elevated values diagnose gestational diabetes mellitus. The 2-step screening test is administered without regard to the time of the last meal, providing convenience by eliminating the requirement for fasting. However, depending upon the cutoff used and population risk factors, approximately 15% to 20% of screened women require the 100 g, 3-hour oral glucose tolerance test. The International Association of Diabetes and Pregnancy Study Groups recommends a protocol of no screening test but rather a diagnostic 75 g, 2-hour oral glucose tolerance test. One or more values above threshold diagnose gestational diabetes mellitus. The 1-step approach requires that women be fasting for the test but does not require a second visit and lasts 2 hours rather than 3. Primarily because of needing only a single elevated value, the 1-step approach identifies 18% to 20% of pregnant women as having gestational diabetes mellitus, 2 to 3 times the rate with the 2-step procedure, but lower than the current United States prediabetes rate of 24% in reproductive aged women. The resources needed for the increase in gestational diabetes mellitus are parallel to the resources needed for the increased prediabetes and diabetes in the nonpregnant population. A recent randomized controlled trial sought to assess the relative population benefits of the above 2 approaches to gestational diabetes mellitus screening and diagnosis. The investigators concluded that there was no significant difference between the 2-step screening protocol and 1-step diagnostic testing protocol in their impact on population adverse short-term pregnancy outcomes. An accompanying editorial concluded that perinatal benefits of the 1-step approach to diagnosing gestational diabetes mellitus "appear to be insufficient to justify the associated patient and healthcare costs of broadening the diagnosis." We raise several concerns about this conclusion. The investigators posited that a 20% improvement in adverse outcomes among the entire pregnancy cohort would be necessary to demonstrate an advantage to the 1-step approach and estimated the sample size based on that presumption, which we believe to be unlikely given the number of cases that would be identified. In addition, 27% of the women randomized to the 1-step protocol underwent 2-step testing; 6% of the study cohort had no testing at all. A subset of women assigned to 2-step testing did not meet the criteria for gestational diabetes mellitus but were treated as such because of elevated fasting plasma glucose levels, presumably contributing to the reduction in adverse outcomes but not to the number of gestational diabetes mellitus identified, increasing the apparent efficacy of the 2-step approach. No consideration was given to long-term benefits for mothers and offspring. All these factors may have contributed to obscuring the benefits of 1-step testing; most importantly, the study was not powered to identify what we understand to be the likely impact of 1-step testing on population health.
在美国,检测妊娠期糖尿病的常用方法是美国妇产科医师学会推荐的两步法方案。在 24 至 28 周妊娠时,先进行 50g、1 小时葡萄糖挑战,当筛查试验阈值超过时,再进行 100g、3 小时口服葡萄糖耐量试验。值得注意的是,2 次或以上升高值可诊断为妊娠期糖尿病。两步筛查试验在不考虑最后一餐时间的情况下进行,通过消除禁食要求提供了便利。然而,根据使用的截止值和人群危险因素,大约 15%至 20%的筛查女性需要进行 100g、3 小时口服葡萄糖耐量试验。国际糖尿病与妊娠研究组建议采用无筛查试验的方案,而是采用诊断性 75g、2 小时口服葡萄糖耐量试验。一个或多个值超过阈值可诊断为妊娠期糖尿病。一步法要求女性在试验前禁食,但不需要第二次就诊,且持续时间为 2 小时而不是 3 小时。主要由于只需要单次升高值,一步法检测出 18%至 20%的孕妇患有妊娠期糖尿病,是两步法的 2 至 3 倍,但低于美国当前育龄女性的 24%的糖尿病前期率。增加妊娠期糖尿病所需的资源与非妊娠人群中增加糖尿病前期和糖尿病所需的资源相当。最近一项随机对照试验旨在评估上述两种妊娠期糖尿病筛查和诊断方法对人群的相对益处。研究人员得出结论,两步筛查方案与一步诊断检测方案在对人群短期妊娠结局的影响方面没有显著差异。一篇随附的社论得出结论,一步法诊断妊娠期糖尿病的围产期益处“似乎不足以证明扩大诊断相关的患者和医疗保健成本是合理的”。我们对这一结论提出了几点担忧。研究人员假设,整个妊娠队列中不良结局改善 20%将有助于证明一步法的优势,并根据这一假设估计样本量,我们认为这不太可能,因为要确定的病例数量很少。此外,随机分配到一步法方案的 27%的女性接受了两步法检测;研究队列中有 6%的女性根本没有接受检测。被分配到两步法检测的女性中有一部分不符合妊娠期糖尿病的标准,但由于空腹血糖水平升高而被视为妊娠期糖尿病,这可能导致不良结局减少,但不增加妊娠期糖尿病的检出数量,从而增加两步法方案的疗效。没有考虑到对母亲和后代的长期益处。所有这些因素都可能导致一步法检测的益处被掩盖;最重要的是,该研究没有足够的能力来确定我们所理解的一步法检测对人群健康的可能影响。