Specific risk factors for heart-lung transplantation

Justin Issard , Jérôme Le Pavec , Gaelle Dauriat , Estibaliz Valdeolmillos , Sébastien Hascoet , Jean Noel Andarelli , Sylvain Diop , Thibaut Genty , Laurent Savale , Olaf Mercier , Elie Fadel
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Abstract

Background

Heart-lung transplantation (HLTx) has become increasingly rare, with fewer than 50 procedures performed annually worldwide. This decline reflects evolving indications, notably the predominance of Eisenmenger syndrome (ES) complicating congenital heart disease (CHD). HLTx remains a complex procedure associated with significant perioperative and long-term risks, particularly in this patient population.

Methods

This review synthesizes current literature and registry data to identify specific risk factors associated with HLTx in its modern indications. It examines changes in patient selection, timing of listing, perioperative challenges, and postoperative outcomes, with a focus on ES and CHD-related cases.

Results

HLTx candidates often present with prior thoracic surgeries, polycythemia, systemic arterial collaterals, and multi-organ dysfunction, all contributing to increased surgical complexity and bleeding risk. Long waitlist times and donor shortages further complicate management. Despite these challenges, recent data from expert centers show improved early survival, with 1-year survival rates exceeding 85%. HLTx may offer protective effects against chronic graft dysfunctions such as bronchiolitis obliterans syndrome and coronary artery vasculopathy compared to isolated organ transplants.

Conclusions

HLTx remains the treatment of choice for select patients with complex cardiopulmonary disease, particularly ES with CHD. Optimizing outcomes requires early referral, careful risk stratification, and management in high-volume expert centers. Advances in surgical techniques and perioperative care have improved survival, but HLTx continues to demand multidisciplinary expertise and individualized patient assessment.
心肺移植的特殊危险因素
背景:心肺移植(HLTx)已经变得越来越罕见,全世界每年进行的手术不到50例。这种下降反映了适应症的演变,特别是艾森门格综合征(ES)合并先天性心脏病(CHD)的优势。HLTx仍然是一个复杂的手术,具有显著的围手术期和长期风险,特别是在该患者群体中。方法本综述综合了现有文献和注册数据,以确定与HLTx现代适应症相关的特定危险因素。它研究了患者选择、名单时间、围手术期挑战和术后结果的变化,重点是ES和冠心病相关病例。结果shltx患者通常有胸外科手术史、红细胞增多症、全身动脉侧支和多器官功能障碍,这些都增加了手术复杂性和出血风险。漫长的等待时间和捐赠者短缺进一步使管理复杂化。尽管存在这些挑战,但来自专家中心的最新数据显示,早期生存率有所提高,1年生存率超过85%。与分离器官移植相比,HLTx可能对慢性移植物功能障碍如闭塞性细支气管炎综合征和冠状动脉血管病变具有保护作用。结论shltx仍然是复杂心肺疾病患者的治疗选择,特别是ES合并CHD。优化结果需要早期转诊,仔细的风险分层,并在大容量专家中心进行管理。手术技术和围手术期护理的进步提高了生存率,但HLTx仍然需要多学科的专业知识和个性化的患者评估。
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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