Department of Obstetrics and Gynecology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Department of Obstetrics and Gynaecology, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
J Matern Fetal Neonatal Med. 2024 Dec;37(1):2332787. doi: 10.1080/14767058.2024.2332787. Epub 2024 Mar 27.
To determine the predictive performance of the urine Congo red point-of-care test for the identification of preeclampsia in women presenting with suspected preeclampsia.
A prospective multi-center cohort study was conducted to include women with suspected preeclampsia ( = 244). The urine Congo red test was determined (score range 1-8). The diagnosis of preeclampsia was based on criteria proposed by The American College of Obstetricians and Gynecologists. The primary outcome was the predictive performance (sensitivity, specificity, negative and positive predictive values, as well as likelihood ratios) of the Congo red kit test for the diagnosis of preeclampsia.
Fifty-four percent (131/244) of women with suspected preeclampsia subsequently developed preeclampsia. The sensitivity and specificity of the urine Congo red test were 49.6% and 94.7%, respectively, when using a cutoff for Congo red ≥4. The test had a significant positive correlation with the level of urine protein (Pearson correlation 0.61, -value <.01). Intra- and inter-observer reliabilities were good (intra-class correlation coefficient and Cohen's kappa coefficient of 0.88 and 0.75, respectively; < .01).
The urine Congo red kit test has a high positive predictive performance for the identification of preeclampsia with high reproducibility. This test may be used as a bed side test to rule-in the diagnosis of preeclampsia in women presenting with suspected preeclampsia.
确定尿液刚果红即时检测用于识别疑似子痫前期妇女子痫前期的预测性能。
进行了一项前瞻性多中心队列研究,纳入了 244 名疑似子痫前期的女性。测定尿液刚果红试验(评分范围 1-8)。子痫前期的诊断依据美国妇产科医师学会提出的标准。主要结局是刚果红试剂盒检测对子痫前期的诊断的预测性能(灵敏度、特异性、阴性和阳性预测值以及似然比)。
244 名疑似子痫前期的女性中,54%(131/244)随后发生子痫前期。当使用刚果红≥4 的截断值时,尿液刚果红试验的灵敏度和特异性分别为 49.6%和 94.7%。该试验与尿液蛋白水平呈显著正相关(Pearson 相关系数 0.61,-值 <.01)。观察者内和观察者间的可靠性均良好(组内相关系数和 Cohen's kappa 系数分别为 0.88 和 0.75;均 <.01)。
尿液刚果红试剂盒试验对识别子痫前期具有较高的阳性预测性能,且重复性较高。该试验可作为床边试验,用于疑似子痫前期妇女子痫前期的诊断。