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Severe pulmonary hypertension and reduced right ventricle systolic function associated with maternal mortality in pregnant uncorrected congenital heart diseases

机译:严重的肺动脉高压和孕妇死亡率患有孕妇未校正先天性心脏病的孕产性肺动脉血清功能

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Background: Pregnant uncorrected congenital heart disease patients, especially those who already developed pulmonary hypertension, have increased risk for maternal mortality. The pulmonary hypertension severity and right ventricle function may be associated with higher maternal mortality. The study aimed to investigate the mortality rate of pregnant uncorrected congenital heart disease and the impact of pulmonary hypertension severity on mortality. Methods: This is the sub study of COngenital HeARt Disease in adult and Pulmonary Hypertension Registry. The data of pregnant uncorrected congenital heart disease patients were analyzed from registry database. The maternal mortality was recorded. The data of demography, clinics, obstetrics, and transthoracic echocardiography were collected. The factors that influenced maternal mortality were analyzed. A statistical significance was determined when p value 0.05. Results: From 2012 until 2017, there were 78 pregnant congenital heart disease patients. Of them, 56 patients were eligible for analyses. The majority of congenital heart disease was atrial septal defect (91.1%). The maternal mortality rate was 10.7% (6 of 56). Pulmonary hypertension occurred in 48 patients, therefore the maternal mortality rate among congenital heart diseasepulmonary hypertension with majority of atrial septal defect was 12.5% (6 of 48). Among nonsurvivors, 100% suffered from severe pulmonary hypertension as compared to survivors (56.0%), p ? 0.041. Most nonsurvivors were Eisenmenger syndrome (83.3%), significantly higher compared to survivors (22.0%), p ? 0.006. Nonsurvivors had significantly worsened WHO functional class, reduced right ventricle systolic function, and right heart failure. The modes of maternal death were severe oxygen desaturation (66.7%) and respiratory failure and sepsis (33.3%). Most of the maternal deaths occurred within 24 h postpartum period. Conclusion: Maternal mortality rate among pregnant uncorrected congenital heart disease with majority of atrial septal defect was 10.7% and among congenital heart disease-pulmonary hypertension with majority of atrial septal defect was 12.5%. Factors related with maternal mortality were severe pulmonary hypertension, Eisenmenger syndrome, and reduced right ventricle systolic function.
机译:背景:怀孕未经校正的先天性心脏病患者,尤其是那些已经发展肺动脉高压的人,具有增加的孕产妇死亡风险。肺动脉高压严重程度和右心室功能可能与较高的孕产妇死亡率相关。该研究旨在探讨怀孕未校正先天性心脏病的死亡率及肺动脉高压严重程度对死亡率的影响。方法:这是成人和肺动脉高压登记处先天性心脏病的亚研究。从注册表数据库分析怀孕未校正先天性心脏病患者的数据。记录孕产妇死亡率。收集了人口统计学,诊所,产科和经线超声心动图的数据。分析了影响母体死亡率的因素。当P值&时测定统计学意义。 0.05。结果:从2012年到2017年,有78例怀孕的先天性心脏病患者。其中,56名患者有资格分析。大多数先天性心脏病是心房隔膜缺陷(91.1%)。母体死亡率为10.7%(56共分)。 48例患者发生肺动脉高压,因此先天性心肺血症高血压的孕产妇死亡率为12.5%(68条)。与幸存者相比0.041。大多数非尿道综合征(83.3%),与幸存者(22.0%)相比显着高,P? 0.006。 Nonsurvivers显着恶化了Who函数类,右心室收缩功能和右心力衰竭。母体死亡的模式严重氧气去饱和度(66.7%)和呼吸衰竭和败血症(33.3%)。大多数产妇死亡发生在产后24小时内。结论:孕妇未校正先天性心脏病患有大多数心房隔膜缺陷的孕产妇死亡率为10.7%,并且先天性心脏病 - 肺动脉高压,大多数间隔缺损为12.5%。与孕产妇死亡率有关的因素是严重的肺动脉高压,艾森梅格综合征,减少右心室收缩功能。

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