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在 COVID-19 环境下,基于空腹血糖的策略对不良结局风险增加的妊娠期糖尿病女性进行诊断。

Development of a fasting blood glucose-based strategy to diagnose women with gestational diabetes mellitus at increased risk of adverse outcomes in a COVID-19 environment.

机构信息

Royal Brisbane and Women's Hospital, Herston, Queensland, Australia.

University of Queensland, Brisbane, Australia.

出版信息

PLoS One. 2020 Dec 3;15(12):e0243192. doi: 10.1371/journal.pone.0243192. eCollection 2020.

DOI:10.1371/journal.pone.0243192
PMID:33270719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7714128/
Abstract

OBJECTIVE

To evaluate the role of fasting blood glucose (FBG) to minimise the use of the oral glucose tolerance test in pregnancy (POGTT) for the diagnosis of gestational diabetes mellitus (GDM).

RESEARCH DESIGN AND METHODS

We analysed the POGTTs of 26,242 pregnant women in Queensland, Australia, performed between 1 January 2015 and 30 June 2015. A receiver operator characteristics (ROC) assessment was undertaken to indicate the FBG level that most effectively identified women at low risk of an abnormal result.

RESULTS

There were 3,946 (15.0%) patients having GDM with 2,262 (8.6%) having FBG ≥ 5.1mmol/l. The ROC identified FBG levels >4.6mmol/l having the best specificity (77%) and sensitivity (54%) for elevated 1 and/or 2hr BGLs. There were 19,321 (73.7%) women having FBG < 4.7mmol/l with a prevalence of GDM of 4.0%, less than 1/3rd the overall rate. Only 4,638 (17.7%) women having FBGs from 4.7-5.0mmol/l would require further evaluation to confirm or exclude the diagnosis.

CONCLUSION

This contemporary study of women across the state of Queensland, Australia suggests the FBG can be used effectively to define glucose tolerance in pregnancy, minimising their contact with pathology laboratories and potential exposure to the corona virus. This analysis, used in conjunction with outcome data from the HAPO study, provides reassurance to women and their health professionals that FBG < 4.7mmol/l has both a low rate of abnormal glucose tolerance and minimal adverse pregnancy-associated complications.

摘要

目的

评估空腹血糖(FBG)在减少妊娠口服葡萄糖耐量试验(POGTT)用于诊断妊娠糖尿病(GDM)中的作用。

研究设计和方法

我们分析了 2015 年 1 月 1 日至 2015 年 6 月 30 日期间在澳大利亚昆士兰州进行的 26242 例孕妇的 POGTT。进行了受试者工作特征(ROC)评估,以确定最有效地识别低风险异常结果的女性的 FBG 水平。

结果

有 3946 例(15.0%)患者患有 GDM,其中 2262 例(8.6%)的 FBG≥5.1mmol/L。ROC 确定 FBG 水平>4.6mmol/L 具有最佳的特异性(77%)和敏感性(54%),可用于升高 1 小时和/或 2 小时 BGL。有 19321 例(73.7%)女性的 FBG<4.7mmol/L,GDM 的患病率为 4.0%,不到总患病率的三分之一。只有 4638 例(17.7%)FBG 为 4.7-5.0mmol/L 的女性需要进一步评估以确认或排除诊断。

结论

这项针对澳大利亚昆士兰州妇女的当代研究表明,FBG 可有效用于定义妊娠期间的葡萄糖耐量,减少其与病理实验室的接触和潜在的冠状病毒暴露。这项分析与 HAPO 研究的结果数据结合使用,向妇女及其卫生专业人员保证,FBG<4.7mmol/L 具有较低的异常葡萄糖耐量发生率和最小的不良妊娠相关并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b8/7714128/f34f0a50159e/pone.0243192.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b8/7714128/a4623ceb4af3/pone.0243192.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b8/7714128/f34f0a50159e/pone.0243192.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b8/7714128/a4623ceb4af3/pone.0243192.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b8/7714128/f34f0a50159e/pone.0243192.g002.jpg

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