Poon Leona C Y, Kametas Nikos A, Pandeva Ivilina, Valencia Catalina, Nicolaides Kypros H
Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, Denmark Hill, London SE5 9RS, United Kingdom.
Hypertension. 2008 Apr;51(4):1027-33. doi: 10.1161/HYPERTENSIONAHA.107.104646. Epub 2008 Feb 7.
This study aimed to determine the performance of screening for preeclampsia (PE) by maternal medical history and mean arterial pressure (MAP) at 11(+0) to 13(+6) weeks. In 5590 women with singleton pregnancies attending for routine care at 11(+0) to 13(+6) week's gestation we recorded maternal variables and measured the MAP. We excluded 397 because they had missing outcome data or the pregnancies resulted in miscarriage or termination. In 104 patients there was subsequent development of PE, 97 developed gestational hypertension, 574 delivered small-for-gestational-age newborns, and 4418 were unaffected by PE, gestational hypertension, or small for gestational age. A multivariate Gaussian model was fitted to the distribution of log multiple of the median MAP in the PE and unaffected groups. Likelihood ratios for log multiple of the median MAP were computed and used together with maternal variables to produce patient-specific risks for each case. Detection rates and false-positive rates were calculated by taking the proportions with risks above a given risk threshold. In the unaffected group, log MAP was influenced by maternal age, ethnic origin, smoking, family and personal history of PE, and fetal crown-rump length. In the prediction of PE, significant contributions were provided by log multiple of the median MAP, ethnic origin, body mass index, and personal history of PE. The detection rate of PE by log multiple of the median MAP and maternal variables was 62.5% for a false-positive rate of 10%. Maternal variables, together with MAP, at 11(+0) to 13(+6) weeks identify a group at high risk for development of PE.
本研究旨在确定在孕11(+0)至13(+6)周时,通过产妇病史和平均动脉压(MAP)筛查子痫前期(PE)的效果。在5590例孕11(+0)至13(+6)周接受常规产检的单胎妊娠妇女中,我们记录了产妇的各项变量并测量了MAP。我们排除了397例,因为她们有缺失的结局数据,或者妊娠以流产或终止妊娠告终。104例患者随后发生了PE,97例发生了妊娠高血压,574例分娩了小于胎龄儿,4418例未受PE、妊娠高血压或小于胎龄的影响。对PE组和未受影响组中MAP中位数对数倍数的分布拟合了多元高斯模型。计算了MAP中位数对数倍数的似然比,并将其与产妇变量一起用于得出每个病例的个体特异性风险。通过计算风险高于给定风险阈值的比例来计算检测率和假阳性率。在未受影响组中,MAP对数受产妇年龄、种族、吸烟、PE家族史和个人史以及胎儿顶臀长的影响。在PE的预测中,MAP中位数对数倍数、种族、体重指数和PE个人史有显著贡献。对于10%的假阳性率,MAP中位数对数倍数和产妇变量对PE的检测率为62.5%。在孕11(+0)至13(+6)周时,产妇变量与MAP一起可识别出发生PE风险较高的一组人群。