Department of Obstetrics, Gynecology and Reproductive Medicine, North Lisbon Hospital Centre, Santa Maria University Hospital, Lisbon, Portugal.
Int J Gynaecol Obstet. 2018 Sep;142(3):277-282. doi: 10.1002/ijgo.12536. Epub 2018 Jun 13.
To evaluate the accuracy of a 12-hour urine collection to diagnose pre-eclampsia and to determine whether time of collection influences the performance of this test.
A prospective observational study was conducted in a tertiary obstetric center in Portugal between November 1, 2015, and November 30, 2016. Pregnant women (≥20 weeks) admitted for observation with suspected pre-eclampsia were eligible for inclusion. Two consecutive 12-hour urine samples were collected (07:00-19:00 hours vs 19:00-07:00 hours). Protein levels were measured in each 12-hour sample, as well as in a pooled sample (07:00-07:00 hours). The diagnostic cut-off values for pre-eclampsia were 150 mg (12-hour samples) and 300 mg (24-hour sample).
The study included 99 patients and diagnoses of pre-eclampsia were confirmed among 42 (42%) patients. In all, 456 12-hour urine samples were analyzed (equivalent to 228 24-hour samples). Qualitative analysis (pre-eclampsia vs no pre-eclampsia) indicated substantial agreement between the 12- and 24-hour samples (Cohen κ 0.779). The sensitivity was 85.9% (95% confidence interval [CI] 81%-90%) and the specificity was 91.7% (95% CI 88%-95%). No statistically significant difference was found between the two 12-hour collections.
The 12-hour test showed acceptable accuracy for detecting pre-eclampsia, regardless of the time of collection.
评估 12 小时尿液收集诊断子痫前期的准确性,并确定收集时间是否会影响该检测的性能。
2015 年 11 月 1 日至 2016 年 11 月 30 日,在葡萄牙的一家三级产科中心进行了一项前瞻性观察性研究。纳入因疑似子痫前期而入院观察的孕妇(≥20 周)。连续采集两次 12 小时尿液样本(07:00-19:00 小时比 19:00-07:00 小时)。测量每份 12 小时样本以及混合样本(07:00-07:00 小时)中的蛋白水平。子痫前期的诊断截断值为 150mg(12 小时样本)和 300mg(24 小时样本)。
该研究纳入了 99 例患者,其中 42 例(42%)患者被确诊为子痫前期。共分析了 456 份 12 小时尿液样本(相当于 228 份 24 小时样本)。定性分析(子痫前期与无子痫前期)表明 12 小时和 24 小时样本之间具有高度一致性(Cohen κ 0.779)。敏感性为 85.9%(95%可信区间 81%-90%),特异性为 91.7%(95%可信区间 88%-95%)。两次 12 小时采集之间未发现统计学差异。
无论采集时间如何,12 小时检测对检测子痫前期均具有可接受的准确性。