评估中低收入国家产后临床评分方法和足长测量在估计新生儿胎龄和出生体重方面的诊断准确性:系统综述和荟萃分析。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-08-30 DOI:10.1136/bmjpo-2024-002717
Shiyam Sunder Tikmani, Thomas Mårtensson, Sumaira Khalid, Muhammad Uzair, Qammerulanissa Ali, Anum Rahim, Andreas Mårtensson, Sarah Saleem, Nick Brown
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引用次数: 0

摘要

背景:本研究旨在更新有关中低收入国家(LMICs)产后临床评分(PCS)方法和足长(FL)测量用于评估胎龄(GA)和出生体重的诊断准确性的系统综述和荟萃分析。此外,还评估了参考标准的质量,包括产前超声(A-US)、末次月经(LMP)、PCS 和新生儿体重秤:方法:使用 PubMed、Web of Science、Cochrane Library、CINAHL 和 Scopus 等数据库检索了 2000 年 1 月至 2024 年 2 月间发表的来自低收入和中等收入国家的研究。纳入了将 PCS 和/或 FL 与 LMP 和/或 A-US 进行比较以估计 GA 或使用校准过的新生儿体重秤估计出生体重的研究。使用诊断准确性研究质量评估工具(Quality Assessment of Diagnostic Accuracy Studies-II)对偏倚风险进行评估,并对参考标准的质量进行评价。在数据充足的情况下,采用随机效应模型计算汇总估计值:结果:共纳入 50 项研究。如果由医生使用胎儿生物测量法和哈德洛克法进行GA评估,A-US是一种合理的GA评估工具。如果妇女有规律的月经周期、知道自己的 LMP、未使用避孕药且 LMP 数据由医疗服务提供者收集,则 LMP 是合理的。当使用 A-US 作为参考标准时,PCS 方法估计 GA 的精确度为 ±2.8 至 ±3.2 周。FL测量 结论:本系统综述和荟萃分析凸显了在低收入国家使用 PCS 方法和 FL 测量方法估算 GA 和 LBW 时存在的显著差异和方法上的不一致。观察到的各研究间的高度异质性表明,对结果的解释应谨慎:CRD42020209455。
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Assessing the diagnostic accuracy of postnatal clinical scoring methods and foot length measurement for estimating gestational age and birthweight of newborns in low- and middle-income countries: a systematic review and meta-analysis.

Background: This study aimed to update systematic reviews and meta-analyses on the diagnostic accuracy of postnatal clinical scoring (PCS) methods and foot length (FL) measurement for assessing gestational age (GA) and birth weight in low-income and middle-income countries (LMICs). In addition, the quality of reference standards, including antenatal ultrasound (A-US), last menstrual period (LMP), PCS and newborn weighing scales, was also evaluated.

Methods: Studies from LMICs published between January 2000 and February 2024 were searched, using databases such as PubMed, Web of Science, Cochrane Library, CINAHL and Scopus. Studies that compared PCS and/or FL with LMP and/or A-US to estimate GA or used calibrated newborn weighing scales for birthweight estimation were included. The risk of bias was assessed using the Quality Assessment of Diagnostic Accuracy Studies-II tool and evaluated the quality of the reference standards. When sufficient data were available, pooled estimates were calculated using random-effects models.

Results: A total of 50 studies were included. A-US was a reasonable tool for GA assessment if conducted by physicians using fetal biometry and the Hadlock method for GA estimation. LMP was reasonable when women had regular cycles, knew their LMP, were not using contraceptives and LMP data were collected by healthcare providers. When A-US was used as the reference standard, PCS methods estimated GA with a precision of ±2.8 to ±3.2 weeks. FL measurement <7.5 cm showed a pooled sensitivity of 76.2% and specificity of 36.6% for identifying preterm birth. FL measurement ≤7.6 cm had a pooled sensitivity of 78.6% and specificity of 65.7% for identifying low birth weight (LBW). High heterogeneity across studies was observed.

Conclusion: This systematic review and meta-analysis highlights significant variability and methodological inconsistencies in using PCS methods and FL measurement for estimating GA and LBW in LMICs. The observed high heterogeneity across studies suggests a cautious interpretation of the results.

Prospero registration number: CRD42020209455.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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