Outcome of 30 Pregnant Women with Pulmonary Hypertension at Bangladesh Medical University, Dhaka, Bangladesh.

Mymensingh medical journal : MMJ Pub Date : 2026-10-01
N Sheikh, C M Ahmed, J Arzu, Z Jamali, S S Shakil, M Al-Amin
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Abstract

In the recent years, pregnancy outcomes in the patient with pulmonary hypertension (PH) improved with the development of health monitoring system and applications of pulmonary vascular-targeted drugs. But the maternal mortality is still high. So, the purpose of this study was to describe the maternal and foetal outcomes in pregnant women with PH. The clinical data of 30 pregnant women with PH who were admitted to the department of cardiology, Bangladesh Medical University, Dhaka, Bangladesh from January 2020 to December 2022 were collected and descriptively analyzed. Among the 30 pregnant women with pulmonary hypertension, 5(16.6%) had idiopathic pulmonary hypertension (iPAH), 17(56.6%) had pulmonary arterial hypertension (PAH) associated with congenital heart disease (CHD-PAH), 2(6.66%) had PH related to left heart disease (LHD-PH) and 6(20.0%) had PAH due to other diseases (oPAH). The mean systolic pulmonary artery pressure was <30 mmHg in 8(26.6%) patients, 30-40 mmHg was in 8(26.6%) patients and >40 mmHg in 15(50.0%) patients. Four (13.33%) patients were died within 7 days after delivery and CHD-PAH patients had the highest mortality rate (3/17, 17.64%). Three patients (10.0%) were admitted to the intensive care unit (ICU) and the incidence of heart failure during pregnancy was 20.0%. A total of 63.33% of the patients underwent caesarean section; 63.33% had premature infants; 40.0% had low-birth-weight (LBW) infants; 13.33% had very-low-birth-weight (VLBW) infants; 6.66% had extremely-low-birth-weight (ELBW) infants; 56.66% had small for gestational age (SGA) infants and 3.0% experienced neonatal mortality. Though there was difference in the maternal and foetal outcomes I iPAH, CHD-PAH, LHD-PH and oPAH, it was not statistically significant. Maternal mortality was highest in the CHD-PAH. Therefore, CHD-PAH patients should be advised to avoid pregnancy. Standardized and multidiscipline-assisted maternal management is the key to improve maternal and foetal outcome.

孟加拉国达卡医科大学30名肺动脉高压孕妇的结局
近年来,随着健康监测系统的发展和肺血管靶向药物的应用,肺动脉高压(PH)患者的妊娠结局有所改善。但产妇死亡率仍然很高。因此,本研究的目的是描述PH孕妇的母胎结局。收集2020年1月至2022年12月在孟加拉国达卡孟加拉国医科大学心内科收治的30例PH孕妇的临床资料并进行描述性分析。30例肺动脉高压孕妇中,5例(16.6%)为特发性肺动脉高压(iPAH), 17例(56.6%)为肺动脉高压(PAH)合并先天性心脏病(CHD-PAH), 2例(6.66%)为左心相关肺动脉高压(LHD-PH), 6例(20.0%)为其他疾病(oPAH)所致肺动脉高压。15例(50.0%)患者平均肺动脉收缩压为40 mmHg。产后7 d内死亡4例(13.33%),其中冠心病- pah患者死亡率最高(3/17,17.64%)。3例(10.0%)入住重症监护病房(ICU),妊娠期心力衰竭发生率为20.0%。63.33%的患者行剖宫产;早产儿63.33%;40.0%为低出生体重儿(LBW);13.33%为极低出生体重儿(VLBW);6.66%为极低出生体重儿(ELBW);56.66%为小胎龄儿(SGA), 3.0%为新生儿死亡。虽然iPAH、CHD-PAH、LHD-PH和oPAH的母婴结局存在差异,但差异无统计学意义。CHD-PAH患者的产妇死亡率最高。因此,建议冠心病- pah患者避免妊娠。规范化、多学科辅助的孕产妇管理是改善母婴结局的关键。
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