...
首页> 外文期刊>BJOG: an international journal of obstetrics and gynaecology >Implementation of routine first trimester combined screening for pre-eclampsia: a clinical effectiveness study
【24h】

Implementation of routine first trimester combined screening for pre-eclampsia: a clinical effectiveness study

机译:常规妊娠期妊娠期综合筛查的实施:临床有效性研究

获取原文
获取原文并翻译 | 示例

摘要

Objective Evaluate clinical effectiveness of the first trimester combined (FMF) pre-eclampsia screening programme when implemented in a public healthcare setting. Design Retrospective cohort study. Setting London tertiary hospital from January 2017 to March 2019. Methods 7720 women screened for pre-eclampsia according to National Institute for Health and Care Excellence (NICE) risk-based guidance and 4841 by the Fetal Medical Foundation (FMF) algorithm which combined maternal risk factors, blood pressure, PAPP-A and uterine artery Doppler indices in the first trimester. High risk was defined by standard NICE criteria in the pre-intervention cohort (prescribed 75 mg aspirin) or a risk of >= 1:50 for preterm pre-eclampsia from the FMF algorithm in the post-intervention cohort (prescribed 150 mg aspirin). Main outcome measures Screening effectiveness, rates of pre-eclampsia. Results The FMF screening programme resulted in a significant reduction in the screen-positive rate (16.1 versus 8.2%, odds ratio [OR] 0.50, 95% confidence interval [CI] 0.41-0.53) with a concurrent increase in targeted aspirin use in women classified as high risk for pre-eclampsia (28.9 versus 99.0%, OR 241.6, 95% CI 89.6-652.0). Screening indices were uniformly improved for the FMF algorithm with receiver operating characteristic (ROC) analysis demonstrating excellent discrimination for preterm pre-eclampsia (area under the curve [AUC] = 0.846, 95% CI 0.778-0.915,Pvalue <.001). Interrupted time series analysis showed that the FMF screening programme resulted in a significant 21-month relative effect reduction of 80% (P = .025) and 89% (P = .017), for preterm and early pre-eclampsia, respectively. Conclusions First trimester combined screening for pre-eclampsia is both feasible and effective in a public healthcare setting. Such an approach results in a two-fold de-escalation of risk, doubling of pre-eclampsia detection, near total physician compliance of aspirin use and a significant reduction in the prevalence of preterm pre-eclampsia. Tweetable abstract Implementation of 1st trimester combined pre-eclampsia screening effectively reduces prevalence of the disorder.
机译:客观评价在公共医疗环境中实施第一个妊娠期(FMF)前普利坦斯筛查计划的临床效果。设计回顾性队列研究。从2017年1月到2019年3月设定伦敦大学医院。方法根据国家健康和护理卓越卓越(尼斯)风险的指导研究所(FMF)遗传学(FMF)算法,7720名妇女根据国家健康和护理卓越卓越指导和4841举行筛选第一个三个月的因素,血压,PAPP-A和子宫动脉多普勒指数。在干预队队列(规定的75毫克Aspirin)中标准漂亮标准或用于从干预后队列的FMF算法(规定的150mgAspirin)的FMF算法(规定的150mgAspirin)的预防措施(规定的75mgAspirin)或= 1:50的风险(规定的75mg Aspirin)或> = 1:50的风险定义。主要结果测量筛查有效性,预先印痫前的率。结果FMF筛选程序导致筛选率显着降低(16.1与8.2%,差距[或] 0.50,95%置信区间[CI] 0.41-0.53),其在女性中的靶向阿司匹林使用同时增加归类为预普利坦斯预混物的高风险(28.9与99.0%,或241.6,95%CI 89.6-652.0)。对接收器操作特性(ROC)分析的FMF算法均匀地改善了筛选指数,证明了对早产预痫的良好辨别(曲线下的面积= 0.846,95%CI 0.778-0.915,Pvalue <.001)。中断的时间序列分析表明,FMF筛查程序导致80%(p = .025)和89%(p = .017)的显着21个月相对效果降低,分别为早产和早期预先预先预痫。结论前妊娠期前妊娠期筛查综合筛查在公共医疗保健环境中是可行的和有效的。这种方法导致脱升升级的风险,预先升级,预先升级的检测,接近阿司匹林使用的总体医师依从性和早产预痫的普遍性的显着降低。 Tweetable Abstract实施第1孕孕孕前预普利坦斯筛查有效减少了疾病的患病率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号