Fisk N M, Fysh J, Child A G, Gatenby P A, Jeffery H, Bradfield A H
Department of Obstetrics and Gynaecology, King George V Hospital, Royal Prince Alfred Hospital, Sydney, Australia.
Br J Obstet Gynaecol. 1987 Dec;94(12):1159-64. doi: 10.1111/j.1471-0528.1987.tb02316.x.
In a prospective blind study 380 daily serum samples from 55 women with preterm premature rupture of the membranes were analysed for C-reactive protein (CRP). Although the last CRP before delivery was higher in patients with histological chorioamnionitis (P = 0.007), considerable overlap between infected and non-infected pregnancies occurred, precluding the use of CRP as a diagnostic test if published normal levels were used. When upper limits were set at 30, 35, or 40 mg/l, the last CRP before delivery proved 90, 95 and 100% specific and 88, 92 and 100% positively predictive of infection in singleton pregnancies. Such high specificities are needed to prevent inappropriate intervention based on false positive results. We therefore propose upper limits for single estimations of 30, 35, or 40 mg/l depending on the relative risks of preterm delivery versus infection at various gestational ages. In addition, consecutive values greater than 20 mg/l appeared highly predictive of infection.
在一项前瞻性盲法研究中,对55例胎膜早破孕妇的380份每日血清样本进行了C反应蛋白(CRP)分析。虽然组织学绒毛膜羊膜炎患者分娩前的最后一次CRP水平较高(P = 0.007),但感染与未感染妊娠之间存在相当大的重叠,如果采用已公布的正常水平,就无法将CRP用作诊断检测。当上限设定为30、35或40mg/L时,分娩前的最后一次CRP在单胎妊娠中对感染的特异性分别为90%、95%和100%,阳性预测值分别为88%、92%和100%。需要如此高的特异性来防止基于假阳性结果的不适当干预。因此,我们建议根据不同孕周早产与感染的相对风险,将单次检测的上限设定为30、35或40mg/L。此外,连续值大于20mg/L似乎对感染具有高度预测性。