Sirimarco Mariana Pinto, Guerra Helena Maciel, Lisboa Eduardo Guimarães, Vernini Joice Monalisa, Cassetari Bianca Nicolosi, de Araujo Costa Roberto Antonio, Rudge Marilza Vieira Cunha, de Mattos Paranhos Calderon Iracema
GP Program in Gynecology, Obstetrics and Mastology (PGGOM), Botucatu Medical School/Unesp (FMB/Unesp), Botucatu, Brazil.
Department of Gynecology and Obstetrics, FMB/Unesp, Botucatu, Brazil.
Diabetol Metab Syndr. 2017 Jan 3;9:2. doi: 10.1186/s13098-016-0200-2. eCollection 2017.
In August 2011, the Specialized Center for Diabetes and Pregnancy of the Botucatu Medical School/Unesp adopted a new diagnostic protocol for gestational diabetes mellitus, recommended by the American Diabetes Association and the International Association of the Diabetes and Pregnancy Study Group. The glycemic profile was evaluated using the 75-g oral glucose tolerance test (OGTT) used to diagnose mild gestational hyperglycemia, recognized and treated in our department as gestational diabetes mellitus. The cost-effectiveness of the new guidelines and the continued need for the evaluation of the glycemic profile, as part of our Service protocol, are controversial and require further investigation. We aimed to assess the impact of the new guidelines on the evaluation of mild gestational hyperglycemia and gestational diabetes mellitus, the incidence of adverse perinatal outcomes, and the association between the 75-g OGTT and the glycemic profile for the diagnosis of mild gestational hyperglycemia.
This cross-sectional study was performed identifying a convenience sample of pregnant women and their newborns. The women used our Service for diagnostic procedures, prenatal care and delivery, both before (January 2008 to August 14, 2011) and after (August 15, 2011 to December 2014) the protocol modification. The following variables were compared, following stratification according to diagnostic protocol: prevalence of gestational diabetes mellitus and mild gestational hyperglycemia, newborns large for gestational age, macrosomia, first cesarean delivery, and newborn hospital stay. Statistical analysis was performed using Poisson regression, the Student's t test, the Chi square or Fisher's exact test and risk estimate. The statistical significance threshold was set at 95% (p < 0.05).
The new protocol resulted in an 85% increase in the number of women with GDM, but failed to identify 17.3% of pregnant women classified as having mild gestational hyperglycemia, despite a normal 75-g OGTT. The new guidelines did not affect perinatal outcome.
These results support the validity of maintaining the glycemic profile as part of the diagnostic protocol at our hospital. Large multicenter studies with an adequate sample size are required for conclusive evidence on the cost-effectiveness of the new protocol.
2011年8月,博图卡图医学院/圣保罗州立大学糖尿病与妊娠专科中心采用了由美国糖尿病协会和国际糖尿病与妊娠研究组协会推荐的妊娠期糖尿病新诊断方案。使用75克口服葡萄糖耐量试验(OGTT)评估血糖情况,该试验用于诊断轻度妊娠期高血糖,在我们科室被认定并作为妊娠期糖尿病进行治疗。新指南的成本效益以及作为我们服务方案一部分的血糖情况评估的持续必要性存在争议,需要进一步调查。我们旨在评估新指南对轻度妊娠期高血糖和妊娠期糖尿病评估的影响、围产期不良结局的发生率,以及75克OGTT与诊断轻度妊娠期高血糖的血糖情况之间的关联。
本横断面研究通过确定孕妇及其新生儿的便利样本进行。这些女性在方案修改之前(2008年1月至2011年8月14日)和之后(2011年8月15日至2014年12月)都使用我们的服务进行诊断程序、产前护理和分娩。根据诊断方案分层后,比较以下变量:妊娠期糖尿病和轻度妊娠期高血糖的患病率、大于胎龄儿、巨大儿、首次剖宫产以及新生儿住院时间。使用泊松回归、学生t检验、卡方检验或费舍尔精确检验以及风险估计进行统计分析。统计学显著性阈值设定为95%(p < 0.05)。
新方案使妊娠期糖尿病女性人数增加了85%,但未能识别出17.3%被归类为轻度妊娠期高血糖的孕妇,尽管其75克OGTT结果正常。新指南未影响围产期结局。
这些结果支持了在我们医院将血糖情况作为诊断方案一部分的有效性。需要进行样本量充足的大型多中心研究,以获取关于新方案成本效益的确凿证据。