Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, BC, Canada.
Lancet. 2011 Jan 15;377(9761):219-27. doi: 10.1016/S0140-6736(10)61351-7. Epub 2010 Dec 23.
Pre-eclampsia is a leading cause of maternal deaths. These deaths mainly result from eclampsia, uncontrolled hypertension, or systemic inflammation. We developed and validated the fullPIERS model with the aim of identifying the risk of fatal or life-threatening complications in women with pre-eclampsia within 48 h of hospital admission for the disorder.
We developed and internally validated the fullPIERS model in a prospective, multicentre study in women who were admitted to tertiary obstetric centres with pre-eclampsia or who developed pre-eclampsia after admission. The outcome of interest was maternal mortality or other serious complications of pre-eclampsia. Routinely reported and informative variables were included in a stepwise backward elimination regression model to predict the adverse maternal outcome. We assessed performance using the area under the curve (AUC) of the receiver operating characteristic (ROC). Standard bootstrapping techniques were used to assess potential overfitting.
261 of 2023 women with pre-eclampsia had adverse outcomes at any time after hospital admission (106 [5%] within 48 h of admission). Predictors of adverse maternal outcome included gestational age, chest pain or dyspnoea, oxygen saturation, platelet count, and creatinine and aspartate transaminase concentrations. The fullPIERS model predicted adverse maternal outcomes within 48 h of study eligibility (AUC ROC 0·88, 95% CI 0·84-0·92). There was no significant overfitting. fullPIERS performed well (AUC ROC >0·7) up to 7 days after eligibility.
The fullPIERS model identifies women at increased risk of adverse outcomes up to 7 days before complications arise and can thereby modify direct patient care (eg, timing of delivery, place of care), improve the design of clinical trials, and inform biomedical investigations related to pre-eclampsia.
Canadian Institutes of Health Research; UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development, and Research Training in Human Reproduction; Preeclampsia Foundation; International Federation of Obstetricians and Gynecologists; Michael Smith Foundation for Health Research; and Child and Family Research Institute.
子痫前期是导致产妇死亡的主要原因。这些死亡主要是由于子痫、未控制的高血压或全身炎症引起的。我们开发并验证了完整的 PIERS 模型,旨在识别在因该疾病住院 48 小时内患有子痫前期的女性发生致命或危及生命的并发症的风险。
我们在一项前瞻性、多中心研究中开发并内部验证了完整的 PIERS 模型,该研究纳入了因子痫前期或入院后发生子痫前期而入住三级产科中心的女性。感兴趣的结局是产妇死亡或子痫前期的其他严重并发症。将常规报告且有信息价值的变量纳入逐步向后消除回归模型,以预测不良的产妇结局。我们使用接收者操作特征(ROC)曲线下面积(AUC)评估性能。使用标准的自举技术来评估潜在的过度拟合。
2023 例子痫前期女性中有 261 例在入院后任何时间发生不良结局(入院后 48 小时内 106 例[5%])。不良产妇结局的预测因素包括胎龄、胸痛或呼吸困难、血氧饱和度、血小板计数以及肌酐和天冬氨酸转氨酶浓度。完整的 PIERS 模型在研究入选后 48 小时内预测不良产妇结局(AUC-ROC 0.88,95%CI 0.84-0.92)。没有明显的过度拟合。完整的 PIERS 在入选后 7 天内表现良好(AUC-ROC>0.7)。
完整的 PIERS 模型可识别出在出现并发症前长达 7 天风险增加的女性,并由此改变直接的患者护理(例如,分娩时机、护理地点),改进临床试验设计,并为与子痫前期相关的生物医学研究提供信息。
加拿大卫生研究院;联合国开发计划署/联合国人口基金/世界卫生组织/世界银行人类生殖研究、发展和研究培训特别方案;子痫前期基金会;国际妇产科医师学会;迈克尔·史密斯基金会;儿童和家庭研究所。