Desai Kinjal, Di Lorenzo Michael, Zuckerman Warren A, Emeruwa Ezinne, Krishnan Usha S
Division of Pediatric Cardiology, New York Presbyterian Morgan Stanley Children's Hospital, New York, NY 10032, USA.
Columbia University Vagelos College of Physicians and Surgeons, New York, NY 10032, USA.
Children (Basel). 2023 Jan 31;10(2):270. doi: 10.3390/children10020270.
Pulmonary hypertension (PH) is a multifactorial, progressive disease with poor outcomes. Group 2 PH is defined by pulmonary vascular disease with elevated pulmonary capillary wedge pressure including both left-sided obstructive lesions and diastolic heart failure (HF). Sildenafil was historically discouraged in this population as pulmonary vasodilation can lead to pulmonary edema. However, evidence suggests that sildenafil can help to treat the precapillary component of PH. This is a single center, retrospective pilot study of pediatric PH patients with left-sided HF who were treated with sildenafil for ≥ 4 weeks. HF patients without mechanical support (HF group) and HF patients with a left ventricular assist device (HF-VAD) were analyzed. The exploratory analysis described the safety and side effects of the drug. Echocardiographic parameters were compared before and after sildenafil treatment in a paired analysis. The changes in medical therapy during treatment, mechanical support, and mortality was reported; 19/22 patients tolerated sildenafil. Pulmonary edema in two patients resolved upon discontinuation of sildenafil. In the HF group, both the right atrial volume and right ventricular diastolic area decreased, and the tricuspid regurgitation (TR) S/D ratio decreased after therapy ( = 0.02). Across both the groups, four patients weaned off milrinone and seven weaned off inhaled nitric oxide. Of the thirteen HF patients, four received a transplant, and all of the nine HF-VAD patients received a transplant. Sildenafil can be safely used in carefully selected patients with HF and mixed pre/postcapillary PH with judicious titration and inpatient surveillance, with patients showing improvements in echocardiographic parameters.
肺动脉高压(PH)是一种多因素的进行性疾病,预后较差。2类PH由肺血管疾病定义,伴有肺毛细血管楔压升高,包括左侧阻塞性病变和舒张性心力衰竭(HF)。由于肺血管扩张可导致肺水肿,历史上西地那非在该人群中不被推荐使用。然而,有证据表明西地那非有助于治疗PH的毛细血管前成分。这是一项单中心回顾性试点研究,纳入了接受西地那非治疗≥4周的左侧HF的儿科PH患者。分析了无机械支持的HF患者(HF组)和植入左心室辅助装置的HF患者(HF-VAD)。探索性分析描述了该药物的安全性和副作用。在配对分析中比较了西地那非治疗前后的超声心动图参数。报告了治疗期间药物治疗、机械支持和死亡率的变化;22例患者中有19例耐受西地那非。两名患者停用西地那非后肺水肿消退。在HF组中,治疗后右心房容积和右心室舒张面积均减小,三尖瓣反流(TR)S/D比值降低(P=0.02)。在两组中,4例患者停用米力农,7例患者停用吸入一氧化氮。13例HF患者中有4例接受了移植手术,9例HF-VAD患者全部接受了移植手术。西地那非可在经过仔细挑选的HF以及毛细血管前/后混合型PH患者中安全使用,需谨慎滴定并进行住院监测,患者的超声心动图参数会有所改善。