Fetal Medicine Research Institute, King's College Hospital, London, United Kingdom.
Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom; Institute of Women and Children's Health, King's Health Partners, London, United Kingdom.
Am J Obstet Gynecol. 2021 May;224(5):518.e1-518.e11. doi: 10.1016/j.ajog.2020.11.004. Epub 2020 Nov 6.
Any definition of preeclampsia should identify women and babies at greatest risk of adverse outcomes.
This study aimed to investigate the ability of the American College of Obstetricians and Gynecologists and International Society for the Study of Hypertension in Pregnancy definitions of preeclampsia at term gestational age (≥37 0/7 weeks) to identify adverse maternal and perinatal outcomes.
In this prospective cohort study at 2 maternity hospitals in England, women attending a routine hospital visit at 35 0/7 to 36 6/7 weeks' gestation underwent assessment that included history; ultrasonographic estimated fetal weight; Doppler measurements of the pulsatility index in the uterine, umbilical, and fetal middle cerebral arteries; and serum placental growth factor-to-soluble fms-like tyrosine kinase-1 ratio. Obstetrical records were examined for all women with chronic hypertension and those who developed new-onset hypertension, with preeclampsia (de novo or superimposed on chronic hypertension) defined in 5 ways: traditional, based on new-onset proteinuria; American College of Obstetricians and Gynecologists 2013 definition; International Society for the Study of Hypertension in Pregnancy maternal factors definition; International Society for the Study of Hypertension in Pregnancy maternal factors plus fetal death or fetal growth restriction definition, defined according to the 35 0/7 to 36 6/7 weeks' gestation scan as either estimated fetal weight <3rd percentile or estimated fetal weight at the 3rd to 10th percentile with any of uterine artery pulsatility index >95th percentile, umbilical artery pulsatility index >95th percentile, or middle cerebral artery pulsatility index <5th percentile; and International Society for the Study of Hypertension in Pregnancy maternal-fetal factors plus angiogenic imbalance definition, defined as placental growth factor <5th percentile or soluble fms-like tyrosine kinase-1-to-serum placental growth factor >95th percentile. Detection rates for outcomes of interest (ie, severe maternal hypertension, major maternal morbidity, perinatal mortality or major neonatal morbidity, neonatal unit admission ≥48 hours, and birthweight <10th percentile) were compared using the chi-square test, and P<.05 was considered significant.
Among 15,248 singleton pregnancies, the identification of women with preeclampsia varied by definition: traditional, 15 of 281 (1.8%; 248); American College of Obstetricians and Gynecologists, 15 of 326 (2.1%; 248); International Society for the Study of Hypertension in Pregnancy maternal factors, 15 of 400 (2.6%; 248); International Society for the Study of Hypertension in Pregnancy maternal-fetal factors, 15 of 434 (2.8%; 248); and International Society for the Study of Hypertension in Pregnancy maternal-fetal factors plus angiogenic imbalance, 15 of 500 (3.3%; 248). Compared with the traditional definition of preeclampsia, the International Society for the Study of Hypertension in Pregnancy maternal-fetal factors plus angiogenic imbalance best identified the adverse outcomes: severe hypertension (40.6% [traditional] vs 66.9% [International Society for the Study of Hypertension in Pregnancy maternal-fetal factors plus angiogenic imbalance, P<.0001], 59.2% [International Society for the Study of Hypertension in Pregnancy maternal-fetal factors, P=.004], 56.2% [International Society for the Study of Hypertension in Pregnancy maternal factors, P=.013], 46.1% [American College of Obstetricians and Gynecologists, P=.449]); P<.0001); composite maternal severe adverse event (72.2% [traditional] vs 100% for all others; P=.046); composite of perinatal mortality and morbidity (46.9% [traditional] vs 71.1% [International Society for the Study of Hypertension in Pregnancy maternal-fetal factors plus angiogenic imbalance, P=.002], 62.2% [International Society for the Study of Hypertension in Pregnancy maternal-fetal factors, P=.06], 59.8% [International Society for the Study of Hypertension in Pregnancy maternal factors, P=.117], 49.4% [American College of Obstetricians and Gynecologists, P=.875]); neonatal unit admission for ≥48 hours (51.4% [traditional] vs 73.4% [International Society for the Study of Hypertension in Pregnancy maternal-fetal factors plus angiogenic imbalance, P=.001], 64.5% [International Society for the Study of Hypertension in Pregnancy maternal-fetal factors, P=.070], 60.7% [International Society for the Study of Hypertension in Pregnancy maternal factors, P=.213], 53.3% [American College of Obstetricians and Gynecologists, P=.890]); birthweight <10th percentile (40.5% [traditional] vs 78.7% [International Society for the Study of Hypertension in Pregnancy maternal-fetal factors plus angiogenic imbalance, P<.0001], 70.1% [International Society for the Study of Hypertension in Pregnancy maternal-fetal, P<.0001], 51.3% [International Society for the Study of Hypertension in Pregnancy maternal factors, P=.064], 46.3% [American College of Obstetricians and Gynecologists, P=.349]).
Our findings present an evidence base for the broad definition of preeclampsia. Our data suggest that compared with a traditional definition, a broad definition of preeclampsia can better identify women and babies at risk of adverse outcomes. Compared with the American College of Obstetricians and Gynecologists definition, the more inclusive International Society for the Study of Hypertension in Pregnancy definition of maternal end-organ dysfunction seems to be more sensitive. The addition of uteroplacental dysfunction to the broad definition optimizes the identification of women and babies at risk, particularly when angiogenic factors are included.
任何子痫前期的定义都应确定具有最大不良结局风险的妇女和婴儿。
本研究旨在探讨美国妇产科医师学会和国际妊娠高血压学会在足月妊娠(≥37 0/7 周)定义子痫前期的能力,以确定不良的母婴围生期结局。
在英格兰的 2 家产科医院进行这项前瞻性队列研究,在 35 0/7 至 36 6/7 周妊娠时接受常规医院就诊的女性接受了病史评估;超声估计胎儿体重;子宫、脐动脉和胎儿大脑中动脉的搏动指数多普勒测量;以及胎盘生长因子-可溶性 fms 样酪氨酸激酶-1 比值。检查所有患有慢性高血压的女性和新出现高血压的女性的产科记录,定义子痫前期(新发或叠加在慢性高血压上)有 5 种方式:传统的基于新出现的蛋白尿;美国妇产科医师学会 2013 年定义;国际妊娠高血压学会母体因素定义;国际妊娠高血压学会母体因素加上胎儿死亡或胎儿生长受限定义,根据 35 0/7 至 36 6/7 周的扫描定义为估计胎儿体重<第 3 百分位数或第 3 至第 10 百分位数,同时任何子宫动脉搏动指数>第 95 百分位数、脐动脉搏动指数>第 95 百分位数或大脑中动脉搏动指数<第 5 百分位数;以及国际妊娠高血压学会母体-胎儿因素加上血管生成失衡定义,定义为胎盘生长因子<第 5 百分位数或可溶性 fms 样酪氨酸激酶-1-胎盘生长因子>第 95 百分位数。使用卡方检验比较感兴趣结局(即严重高血压、主要母体发病率、围产儿死亡率或主要新生儿发病率、新生儿病房入住≥48 小时和出生体重<第 10 百分位数)的检出率,P<.05 为差异有统计学意义。
在 15248 例单胎妊娠中,子痫前期的女性识别因定义而异:传统定义为 15/281(1.8%;248);美国妇产科医师学会为 15/326(2.1%;248);国际妊娠高血压学会母体因素为 15/400(2.6%;248);国际妊娠高血压学会母体-胎儿因素为 15/434(2.8%;248);国际妊娠高血压学会母体-胎儿因素加上血管生成失衡为 15/500(3.3%;248)。与传统的子痫前期定义相比,国际妊娠高血压学会母体-胎儿因素加上血管生成失衡最佳识别不良结局:严重高血压(40.6%[传统]与 66.9%[国际妊娠高血压学会母体-胎儿因素加上血管生成失衡,P<.0001]、59.2%[国际妊娠高血压学会母体-胎儿因素,P=.004]、56.2%[国际妊娠高血压学会母体-胎儿因素,P=.013]、46.1%[美国妇产科医师学会,P=.449]);P<.0001);复合母体严重不良事件(72.2%[传统]与所有其他情况的 100%;P=.046);围产儿死亡率和发病率的复合(46.9%[传统]与 71.1%[国际妊娠高血压学会母体-胎儿因素加上血管生成失衡,P=.002]、62.2%[国际妊娠高血压学会母体-胎儿因素,P=.06]、59.8%[国际妊娠高血压学会母体-胎儿因素,P=.117]、49.4%[美国妇产科医师学会,P=.875]);新生儿病房入住≥48 小时(51.4%[传统]与 73.4%[国际妊娠高血压学会母体-胎儿因素加上血管生成失衡,P=.001]、64.5%[国际妊娠高血压学会母体-胎儿因素,P=.070]、60.7%[国际妊娠高血压学会母体-胎儿因素,P=.213]、53.3%[美国妇产科医师学会,P=.890);出生体重<第 10 百分位数(40.5%[传统]与 78.7%[国际妊娠高血压学会母体-胎儿因素加上血管生成失衡,P<.0001]、70.1%[国际妊娠高血压学会母体-胎儿,P<.0001]、51.3%[国际妊娠高血压学会母体-胎儿因素,P=.064]、46.3%[美国妇产科医师学会,P=.349])。
我们的研究结果为子痫前期的广泛定义提供了证据基础。我们的数据表明,与传统定义相比,广泛的子痫前期定义可以更好地识别具有不良结局风险的妇女和婴儿。与美国妇产科医师学会的定义相比,国际妊娠高血压学会的母体终末器官功能障碍的更广泛定义似乎更敏感。广泛定义中加入胎盘功能障碍可以更好地识别具有风险的妇女和婴儿,尤其是当包括血管生成因素时。