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Bilateral lung transplantation after caesarean section in pregnancy with severe pulmonary arterial hypertension: A case report

机译:双侧肺移植在妊娠期患者患者中,具有严重的肺动脉高压:案例报告

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Rationale: Pulmonary arterial hypertension (PAH) can lead to an increase in right ventricular load and subsequently heart failure, making severe PAH a contraindication for pregnancy. In addition, PAH may worsen during pregnancy and puerperium, which requires high-quality critical care. This report is the first instance in which a patient with severe PAH, survived a successful atrial septal defect (ASD) repair and bilateral lung transplantation during puerperium. Patient concerns: A 42-year-old pregnant woman with congenital heart disease (CHD) and severe PAH was admitted to our hospital for the management of pregnancy and delivery. The patient was diagnosed with severe PAH in 2013, and no significant improvements or deteriorations were found until this pregnancy-related hospital admission. Diagnosis: The patient was diagnosed with CHD and severe PAH in 2013 with color Doppler echocardiography, right cardiac catheterization, and pulmonary perfusion imaging. The patient's mean pulmonary arterial pressure increased to 140 mm Hg during pregnancy, suggesting an exacerbated PAH with high risks to both her and the unborn child. Interventions: The patient was treated with PAH-targeting treprostinil injection to reduce pulmonary artery pressure. Caesarean section was performed at 27 weeks and 5 days of gestation. The patient was put under extracorporeal membrane oxygenation (ECMO) with the help of local anesthesia before the operation. The investigators finally conducted a bilateral lung transplantation with a shell incision of the sternum under cardiopulmonary bypass. Outcomes: The mother and the neonate survived and recovered well after the operation, and were discharged from the hospital on the fourth month post-hospitalization. Lessons: Severe PAH is an absolute contraindication for pregnancy. However, for patients who insist on a pregnancy, it could be plausible to proceed with a targeted drug therapy and ECMO after conducting a cesarean section, and finally, a lung transplantation . Multidisciplinary diagnosis and treatment is the key to the successful treatment of a PAH-complicated pregnancy.
机译:理由:肺动脉高压(PAH)可以导致右心室载荷的增加和随后的心力衰竭,使严重的PAH对妊娠的禁忌症。此外,PAH可能在怀孕和产褥期下恶化,这需要高质量的批判性护理。本报告是第一个患有严重PAH的患者的实例,在蒲特期间存活了一个成功的心房隔膜缺陷(ASD)修复和双侧肺移植。患者担忧:一名42岁的孕妇,具有先天性心脏病(CHD)和严重PAH的患者被录取为我们的医院进行怀孕和交付管理。患者于2013年诊断患有严重的PAH,并且在这种与妊娠相关的医院入院之前没有发现显着的改善或劣化。诊断:2013年患者诊断患有CHD和严重PAH,彩色多普勒超声心动图,右心导管和肺灌注成像。患者的平均肺动脉压在怀孕期间增加到140毫米HG,表明她和未出生的孩子的风险高的恶化的PAH。干预措施:用PAH靶向Treprostinil注射治疗患者以减少肺动脉压。剖腹产在27周和5天的妊娠期进行。在手术前的局部麻醉的帮助下,患者在体外膜氧合(ECMO)下。研究人员最终用胸骨旁路下的胸骨切口进行双侧肺移植。结果:母亲和新生儿在手术后幸存并恢复了良好,并在住院后第四个月从医院出院。课程:严重PAH是怀孕的绝对禁忌症。然而,对于坚持怀孕的患者,在进行剖宫产后,它可能具有靶向药物治疗和ECMO可能是合理的,最后是一种肺移植。多学科诊断和治疗是成功治疗PAH-复杂的妊娠的关键。

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