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Prediction of Adverse Maternal Outcomes in Preeclampsia Using a Risk Prediction Model

机译:使用风险预测模型预测先兆子痫的不良孕妇结果

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Background This study was conducted to evaluate how the preeclampsia integrated estimate of risk (fullPIERS) model performs in the prediction of adverse maternal outcomes when the predictor variables are all obtained within 24-h of admission for preeclampsia. Methods A prospective cohort study on 323 women who fulfilled definite inclusion and exclusion criteria was conducted. Subjects were monitored for clinical symptoms of preeclampsia, biochemical parameters, and adverse maternal and neonatal outcomes. A risk prediction score was calculated using the fullPIERS calculator. Statistical analysis of rates and ratios was carried out by assessing χ 2 test and odds ratio. Results 18.3?% ( n =?60) had adverse maternal outcome and 42.8?% ( n =?138) had adverse fetal outcome, and 43 (13.35?%) had combined adverse maternal and perinatal outcome. Dyspnea, visual disturbances, epigastric pain, and SpO2 appeared to be highly significant risk factors. In the biochemical variables studied, serum creatinine and serum uric acid were found to have a significant association. The association between adverse perinatal outcome and vaginal delivery was highly significant (OR 0.35, 95?% CI 0.19, 0.63), and the P value was 0.0005. The likelihood ratio associated with the highest risk group (predicted probability of the outcome ≥30?%) showed excellent performance (i.e., 17.5) of fullPIERS model as a rule in test. Conclusion The fullPIERS model performed well in the prediction of adverse maternal outcomes in women with preeclampsia. It is easy to use. The model is based on the use of few important clinical and biochemical parameters and does not require extensive laboratory testing. Although it might be of limited use in a well-equipped tertiary care facility, this model can be utilized in the setting of district or sub-district level hospitals to identify patients who are at risk of complications due to preeclampsia. Timely referral to a higher center will help in reducing the morbidity and mortality associated with this condition. Electronic supplementary material The online version of this article (
机译:背景本研究旨在评估先兆子痫风险综合评估(fullPIERS)模型在先兆子痫患者入院后24小时内均获得预测变量时,在预测孕妇不良预后方面的表现。方法对323名符合明确纳入和排除标准的女性进行前瞻性队列研究。监测受试者的先兆子痫的临床症状,生化参数以及不良的母婴结果。使用fullPIERS计算器计算了风险预测分数。通过评估χ 2 检验和比值比对比率和比率进行统计分析。结果孕妇不良结局为18.3%(n = 60),胎儿不良结局为42.8%(n = 138),孕产妇和围产期不良结局为43(13.35%)。呼吸困难,视觉障碍,上腹痛和Sp O 2 似乎是高度重要的危险因素。在所研究的生化变量中,发现血清肌酐和血清尿酸有显着相关性。围产期不良结局与阴道分娩之间的相关性非常显着(OR 0.35,95%CI 0.19,0.63),P值为0.0005。通常,与最高风险组相关的似然比(预测结果的可能性≥30%)显示出fullPIERS模型的出色性能(即17.5)。结论fullPIERS模型在先兆子痫妇女的不良产妇预后中表现良好。这个用起来很简单。该模型基于使用一些重要的临床和生化参数,不需要大量的实验室测试。尽管在设备完善的三级医疗机构中可能使用有限,但该模型可用于地区或县级医院,以识别因先兆子痫而有并发症风险的患者。及时转诊至更高的中心将有助于减少与此疾病相关的发病率和死亡率。电子补充材料本文的在线版本(

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