Extracorporeal membrane oxygenation (ECMO) support for children with pulmonary hypertension: A single-institutional experience of outcomes.

IF 2.2 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pulmonary Circulation Pub Date : 2024-10-25 eCollection Date: 2024-10-01 DOI:10.1002/pul2.12442
Christopher Nemeh, Nicholas Schmoke, William Patten, Eunice Clark, Yeu S Wu, Pengchen Wang, Paul Kurlansky, William Middlesworth, Eva W Cheung, Erika B Rosenzweig
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Abstract

Pediatric pulmonary arterial hypertension (PAH) can present with a wide spectrum of disease severity. Pulmonary hypertension (PH) crises can lead to acute decompensation requiring extracorporeal membrane oxygenation (ECMO) support, including extracorporeal cardiopulmonary resuscitation (eCPR). We evaluated outcomes for pediatric PH patients requiring ECMO. A single-institution retrospective review of pediatric PAH patients with World Symposium on PH (WSPH) groups 1 and 3 requiring ECMO cannulation from 2010 through 2022 (n = 20) was performed. Primary outcome was survival to hospital discharge. Secondary outcomes were survival to decannulation and 1-year survival. Of 20 ECMO patients, 16 (80%) survived to decannulation and 8 (40%) survived to discharge and 1 year follow up. Of three patients who had two ECMO runs; none survived. There were five patients who had eCPR for the first run; one survived to discharge. The univariate logistic regression model showed that venovenous ECMO was associated with better survival to hospital discharge than venoarterial ECMO, (OR: 0.12, 95% CI: 0.01-0.86, p = 0.046). PH medications (administered before, during, or after ECMO) were not associated with survival to discharge. For children with decompensated PAH requiring ECMO, mortality rate is high, and management is challenging. While VA ECMO is the main configuration for decompensated PH, VV ECMO could be considered if there is adequate ventricular function, presence of a systemic to pulmonary shunt, or an intercurrent treatable illness to improve survival to discharge. A multidisciplinary approach with requisite expertise should be utilized on a case-by-case basis until more reliable data is available to predict outcomes.

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为肺动脉高压患儿提供体外膜肺氧合(ECMO)支持:单一机构的成果经验。
小儿肺动脉高压(PAH)的病情严重程度不一。肺动脉高压(PH)危象可导致急性失代偿,需要体外膜肺氧合(ECMO)支持,包括体外心肺复苏(eCPR)。我们评估了需要 ECMO 的小儿 PH 患者的治疗效果。我们对 2010 年至 2022 年期间需要 ECMO 插管的世界 PH(WSPH)研讨会 1 组和 3 组小儿 PAH 患者(n = 20)进行了单机构回顾性研究。主要结果是出院后的存活率。次要结果是撤除插管后的存活率和 1 年存活率。在 20 名 ECMO 患者中,16 人(80%)存活至拔管,8 人(40%)存活至出院和 1 年随访。有 3 名患者进行了两次 ECMO,但无一存活。有五名患者第一次进行了 eCPR,其中一人存活到出院。单变量逻辑回归模型显示,静脉 ECMO 比静脉动脉 ECMO 的出院存活率更高(OR: 0.12,95% CI: 0.01-0.86,P = 0.046)。PH 药物(在 ECMO 之前、期间或之后使用)与出院存活率无关。对于需要进行 ECMO 的失代偿 PAH 患儿来说,死亡率很高,管理也极具挑战性。虽然 VA ECMO 是失代偿性 PH 的主要配置,但如果有足够的心室功能、存在系统性肺分流或并发可治疗疾病,则可考虑 VV ECMO,以提高出院存活率。在获得更可靠的数据预测预后之前,应根据具体情况采用具有必要专业知识的多学科方法。
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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来源期刊
Pulmonary Circulation
Pulmonary Circulation Medicine-Pulmonary and Respiratory Medicine
CiteScore
4.20
自引率
11.50%
发文量
153
审稿时长
15 weeks
期刊介绍: Pulmonary Circulation''s main goal is to encourage basic, translational, and clinical research by investigators, physician-scientists, and clinicans, in the hope of increasing survival rates for pulmonary hypertension and other pulmonary vascular diseases worldwide, and developing new therapeutic approaches for the diseases. Freely available online, Pulmonary Circulation allows diverse knowledge of research, techniques, and case studies to reach a wide readership of specialists in order to improve patient care and treatment outcomes.
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