妊娠期肺动脉高压和艾森曼格综合征的管理和结果:前瞻性观察队列研究

N. Jha, M. B. Divya, A.K. Jha
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引用次数: 1

摘要

(BJOG.2023;130(10):1258–1268)妊娠并发肺动脉高压(PAH)和艾森曼格综合征通常会导致严重的母体和胎儿发病率和死亡率。临床医生通常会建议患有这些疾病的妇女避免怀孕或终止妊娠。然而,多学科专科中心却为这些高危妇女及其胎儿带来了良好的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management and Outcomes of Pulmonary Artery Hypertension and Eisenmenger Syndrome During Pregnancy: A Prospective Observational Cohort Study
(BJOG. 2023;130(10):1258–1268) Pregnancies complicated by pulmonary arterial hypertension (PAH) and Eisenmenger syndrome often result in severe maternal and fetal morbidity and mortality. Clinicians often counsel women with these conditions to avoid pregnancy or terminate a pregnancy. Multidisciplinary specialty centers, however, have seen good outcomes in these high-risk women and their babies.
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