Urine Congo red test for the detection of preeclampsia in pregnant women presenting with suspected preeclampsia.

IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Journal of Maternal-Fetal & Neonatal Medicine Pub Date : 2024-12-01 Epub Date: 2024-03-27 DOI:10.1080/14767058.2024.2332787
Phusit Tuntivararut, Kasem Raungrongmorakot, Noppadol Chaiyasit, Nutnaree Yuenyongdechawat, Piya Chaemsaithong
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Abstract

Objectives: 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.

Methods: A prospective multi-center cohort study was conducted to include women with suspected preeclampsia (n = 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.

Results: 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, p-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; p < .01).

Conclusion: 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.

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用于检测疑似子痫前期孕妇尿液刚果红试验。
目的确定尿液刚果红床旁检验对识别疑似子痫前期妇女的预测性能:一项前瞻性多中心队列研究纳入了疑似子痫前期的妇女(n = 244)。测定尿液刚果红试验(评分范围 1-8)。子痫前期的诊断基于美国妇产科医师学会提出的标准。主要结果是刚果红试剂盒检测对子痫前期诊断的预测性能(灵敏度、特异性、阴性和阳性预测值以及似然比):结果:54%(131/244)的疑似子痫前期妇女随后出现了子痫前期。尿液刚果红检验的灵敏度和特异性分别为49.6%和94.7%(以刚果红≥4为临界值)。检测结果与尿蛋白水平呈明显的正相关(Pearson 相关性为 0.61,P 值为 p):尿液刚果红试剂盒检测对子痫前期的鉴定具有较高的阳性预测性能,且重现性高。对于疑似子痫前期的妇女,该检验可作为排除子痫前期诊断的床边检验。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
217
审稿时长
2-3 weeks
期刊介绍: The official journal of The European Association of Perinatal Medicine, The Federation of Asia and Oceania Perinatal Societies and The International Society of Perinatal Obstetricians. The journal publishes a wide range of peer-reviewed research on the obstetric, medical, genetic, mental health and surgical complications of pregnancy and their effects on the mother, fetus and neonate. Research on audit, evaluation and clinical care in maternal-fetal and perinatal medicine is also featured.
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