Can risk prediction models help us individualise stillbirth prevention? A systematic review and critical appraisal of published risk models

批判性评价 医学 病理 替代医学
作者
Rosemary Townsend,Arif Manji,John Allotey,Alexander Heazell,Lise Nistrup Jørgensen,Laura A. Magee,Ben W. Mol,Kym I E Snell,Richard D Riley,Jane Sandall,Gordon C. S. Smith,Mulchand S. Patel,B. Thilaganathan,Peter von Dadelszen,Shakila Thangaratinam,Asma Khalil
出处
期刊:Bjog: An International Journal Of Obstetrics And Gynaecology [Wiley]
卷期号:128 (2): 214-224 被引量:16
标识
DOI:10.1111/1471-0528.16487
摘要

Stillbirth prevention is an international priority - risk prediction models could individualise care and reduce unnecessary intervention, but their use requires evaluation.To identify risk prediction models for stillbirth, and assess their potential accuracy and clinical benefit in practice.MEDLINE, Embase, DH-DATA and AMED databases were searched from inception to June 2019 using terms relevant to stillbirth, perinatal mortality and prediction models. The search was compliant with Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines.Studies developing and/or validating prediction models for risk of stillbirth developed for application during pregnancy.Study screening and data extraction were conducted in duplicate, using the CHARMS checklist. Risk of bias was appraised using the PROBAST tool.The search identified 2751 citations. Fourteen studies reporting development of 69 models were included. Variables consistently included were: ethnicity, body mass index, uterine artery Doppler, pregnancy-associated plasma protein and placental growth factor. For almost all models there were significant concerns about risk of bias. Apparent model performance (i.e. in the development dataset) was highest in models developed for use later in pregnancy and including maternal characteristics, and ultrasound and biochemical variables, but few were internally validated and none were externally validated.Almost all models identified were at high risk of bias. There are first-trimester models of possible clinical benefit in early risk stratification; these require validation and clinical evaluation. There were few later pregnancy models but, if validated, these could be most relevant to individualised discussions around timing of birth.Prediction models using maternal factors, blood tests and ultrasound could individualise stillbirth prevention, but existing models are at high risk of bias.
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