Sildenafil in Pulmonary Hypertension Associated with Bronchopulmonary Dysplasia: Friend or Foe?

Current health sciences journal Pub Date : 2023-07-01 Epub Date: 2023-09-30 DOI:10.12865/CHSJ.49.03.03
Irina Branescu, Simona Vladareanu, Sandeep Shetty, Dragos Ovidiu Alexandru, Anay Kulkarni
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Abstract

Introduction: Sildenafil is a phosphodiesterase-5 inhibitor used to treat pulmonary hypertension, although its efficiency remains disputed in the neonatal population. We aimed to assess the clinical use of this drug in extremely premature infants diagnosed with pulmonary hypertension associated to bronchopulmonary dysplasia.

Study design: This is a retrospective study of 18 patients born at ≤ 32 weeks gestational age with pulmonary hypertension complicating moderate to severe bronchopulmonary dysplasia, which was diagnosed on echocardiography at 36 weeks corrected gestational age. Median corrected gestational age at starting sildenafil was 48 weeks (range 32-60). In 4 cases there was a period of > 2 weeks between the evidence of moderate-severe pulmonary hypertension and starting sildenafil. In all other cases it was started as soon as the diagnosis was suspected or confirmed.

Results: All infants tolerated the use of sildenafil. However, 5 babies (26.31%) died despite ongoing intensive care, and 5 babies (26.31%) died after having care redirected due to severe chronic lung disease (1 due to co-existing neurological abnormality), with on overall mortality of this study of 52.62%. Eight babies (42.1%) survived: 5 continued on sildenafil until hospital discharge, 1 continued on transfer to the paediatric intensive care unit and 2 stopped while inpatients. Upon follow up to 2 years of age, out of the 5 patients who continued upon hospital discharge, 4 stopped at 6, 7, 12 and 18 months respectively, with 1 child being lost to follow up. Two patients (10.52%) restarted sildenafil use later in childhood. Echocardiographic evidence of improvement was noted in 58% (11 cases), with no improvement in 6 cases (32%) and incorrect original diagnosis in 1 case (5%). One infant died less than a week from the initiation of treatment.

Conclusion: sildenafil use showed no clinical improvement of pulmonary hypertension complicating moderate to severe bronchopulmonary dysplasia in extremely premature infants.

西地那非治疗与支气管肺发育不良相关的肺动脉高压:是敌是友?
简介西地那非是一种磷酸二酯酶-5抑制剂,用于治疗肺动脉高压,但其在新生儿中的疗效仍存在争议。我们的目的是评估这种药物在确诊为肺动脉高压伴支气管肺发育不良的极早产儿中的临床应用情况:这是一项回顾性研究,研究对象是 18 名胎龄小于 32 周出生的肺动脉高压并发中重度支气管肺发育不良的患者。开始服用西地那非时的中位校正胎龄为 48 周(32-60 周不等)。有 4 例患者从出现中度-重度肺动脉高压到开始服用西地那非之间的间隔时间超过 2 周。其他所有病例都是在怀疑或确诊后立即开始使用西地那非:所有婴儿都能耐受西地那非。然而,5名婴儿(26.31%)在接受重症监护后死亡,5名婴儿(26.31%)因严重的慢性肺部疾病(1名婴儿因同时存在神经系统异常)而在重新调整监护后死亡,本研究的总死亡率为52.62%。8名婴儿(42.1%)存活下来:5名婴儿继续服用西地那非直到出院,1名婴儿在转入儿科重症监护室后继续服用,2名婴儿在住院期间停止服用。随访至 2 岁时,在出院时继续服用的 5 名患者中,有 4 名分别在 6、7、12 和 18 个月时停止服用,1 名儿童失去了随访机会。两名患者(10.52%)在儿童期后期重新开始使用西地那非。58%的患者(11例)超声心动图显示病情有所好转,6例(32%)无好转,1例(5%)原始诊断不正确。结论:使用西地那非后,极早产儿中重度支气管肺发育不良并发肺动脉高压的临床症状没有改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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