Lanzarone Valeria, Polkinghorne Adam, Eslick Guy, Branley James
Christopher Kohlenberg Department of Perinatal Ultrasound, Nepean Hospital, Penrith, New South Wales, Australia.
Department of Microbiology and Infectious Diseases, New South Wales Health Pathology, Nepean Blue Mountains Pathology Service, Penrith, New South Wales, Australia.
Aust N Z J Obstet Gynaecol. 2025 Feb;65(1):13-24. doi: 10.1111/ajo.13864. Epub 2024 Aug 12.
Infection of the amniotic cavity is an important driver and/or consequence of preterm prelabour rupture of membranes (PPROM). Prediction of infection is challenging, limiting guidance for interventions during the antenatal period. Infection typically triggers a host inflammatory response, and non-invasive indirect markers of the maternal or fetal inflammatory response have been reported in the context of PPROM and intra-amniotic infection. Some of these markers have also been tested in amniotic fluid (AF) samples.
This study compared markers of the inflammatory response in women with PPROM against the outcome standard of histological chorioamnionitis (HCA) or funisitis (FUS).
Searches were conducted for studies reporting diagnostic test sensitivity and specificity for proven HCA or FUS in pregnant women with PPROM after 20 weeks' gestation. Weighted mean pooled sensitivity (Se), specificity (Sp), positive predictive value, negative predictive value, diagnostic odds ratio and 95% confidence intervals were calculated for each of the selected diagnostic tests.
Except ultrasonographic detection of fetal thymic involution, almost all index tests analysed showed relatively low sensitivity. Maternal white cell count, interleukin-6 (IL-6) and AF IL-6 had credible specificity. Testing of AF markers, while more consistent than serum markers, showed no clear diagnostic accuracy improvement.
There is a clear lack of evidence for the reliability of any individual diagnostic test to assist in the detection of HCA or FUS in women with PPROM. Combining several markers into a predictive model for improved diagnosis may be worth investigating.
羊膜腔感染是胎膜早破(PPROM)的一个重要驱动因素和/或后果。感染的预测具有挑战性,限制了产前干预的指导。感染通常会引发宿主炎症反应,并且在PPROM和羊膜腔内感染的背景下,已经报道了母体或胎儿炎症反应的非侵入性间接标志物。其中一些标志物也已在羊水(AF)样本中进行了检测。
本研究比较了PPROM女性炎症反应标志物与组织学绒毛膜羊膜炎(HCA)或脐带炎(FUS)的结局标准。
检索了关于妊娠20周后PPROM孕妇中已证实的HCA或FUS的诊断试验敏感性和特异性的研究。为每个选定的诊断试验计算加权平均合并敏感性(Se)、特异性(Sp)、阳性预测值、阴性预测值、诊断比值比和95%置信区间。
除了超声检测胎儿胸腺退化外,几乎所有分析的指标试验都显示出相对较低的敏感性。母体白细胞计数、白细胞介素-6(IL-6)和羊水IL-6具有可靠的特异性。羊水标志物的检测虽然比血清标志物更一致,但并没有显示出明显的诊断准确性提高。
明显缺乏证据表明任何单一诊断试验在检测PPROM女性的HCA或FUS方面的可靠性。将几种标志物组合成一个预测模型以改善诊断可能值得研究。