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先天性心脏病的部分心脏移植

Partial Heart Transplant for Congenital Heart Disease.

作者信息

Overbey Douglas M, Aykut Berk, Kucera John A, Medina Cathlyn K, Sethi Neeta J, Barker Piers C A, Shea Erin V, Turek Joseph W

机构信息

Congenital Heart Surgery Research and Training Laboratory, Duke University, Durham, North Carolina.

Duke Children's Pediatric and Congenital Heart Center, Duke University, Durham, North Carolina.

出版信息

JAMA. 2025 Sep 23;334(12):1077-1083. doi: 10.1001/jama.2025.13580.

Abstract

IMPORTANCE

Partial heart transplant, or living valve replacement, has the potential to advance surgical management of irreparable valvular disease by providing a viable option with capacity for growth.

OBJECTIVES

To describe the early experience and assess the feasibility, safety, and efficacy of partial heart transplant in patients with congenital heart valve disease.

DESIGN, SETTING, AND PARTICIPANTS: Case series of the first 19 patients to undergo partial heart transplant at a single high-volume pediatric cardiac surgery and transplant center in the US between April 2022 and December 2024. No patients were excluded or lost to follow-up.

EXPOSURES

Partial heart transplant using semilunar valves from donor hearts. Maintenance immunosuppression consisted of tacrolimus monotherapy with a trough level goal of 4 to 8 ng/mL.

MAIN OUTCOMES AND MEASURES

Efficacy was defined as growth of the transplanted valve annulus and leaflets over time. Secondary outcomes included valve dysfunction and complications related to immunosuppression.

RESULTS

Among the 19 participants with irreparable congenital heart valve dysfunction, 53% were male and 47% female. The median age at the time of transplant was 97 days. The median follow-up was 26 weeks. Three patients received partial heart transplant of both semilunar valves, 7 underwent living pulmonary valve replacement in the pulmonary position, 2 had a living aortic valve allograft in the aortic position, and 7 had a living aortic valve allograft in the pulmonary position. Nine patients constituting the initial cohort of partial heart transplant recipients had their annular diameter and valve leaflet length longitudinally analyzed for growth. All valves functioned well and demonstrated growth along appropriate z scores. Annular diameter increased from medians of 7 mm (aortic valve) and 9 mm (pulmonary valve) to 14 mm (aortic valve) and 17 mm (pulmonary valve), respectively. Leaflet length similarly increased from medians of 0.5 mm (aortic valve) and 0.49 mm (pulmonary valve) to 1 mm (aortic valve) and 0.675 mm (pulmonary valve), respectively. One patient required reoperation unrelated to the implanted valve. No significant complications related to immunosuppression were observed.

CONCLUSIONS AND RELEVANCE

Partial heart transplant appears feasible, safe, and efficacious. All transplanted valves demonstrated growth based on annular and leaflet length measurements. Careful follow-up and monitoring are crucial to support the continued expansion of this novel technique.

摘要

重要性

部分心脏移植,即活体瓣膜置换,有可能通过提供一种具有生长能力的可行选择来推进对无法修复的瓣膜疾病的手术治疗。

目的

描述早期经验,并评估先天性心脏瓣膜病患者进行部分心脏移植的可行性、安全性和有效性。

设计、地点和参与者:对2022年4月至2024年12月期间在美国一家大型儿科心脏手术和移植中心接受部分心脏移植的首批19例患者进行病例系列研究。没有患者被排除或失访。

暴露因素

使用供体心脏的半月瓣进行部分心脏移植。维持性免疫抑制采用他克莫司单药治疗,谷浓度目标为4至8 ng/mL。

主要结局和测量指标

有效性定义为移植瓣膜环和瓣叶随时间的生长。次要结局包括瓣膜功能障碍和与免疫抑制相关的并发症。

结果

在19例患有无法修复的先天性心脏瓣膜功能障碍的参与者中,53%为男性,47%为女性。移植时的中位年龄为97天。中位随访时间为26周。3例患者接受了两个半月瓣的部分心脏移植,7例在肺动脉位置进行了活体肺动脉瓣置换,2例在主动脉位置进行了活体主动脉瓣同种异体移植,7例在肺动脉位置进行了活体主动脉瓣同种异体移植。对构成部分心脏移植受者初始队列的9例患者的瓣环直径和瓣叶长度进行了纵向生长分析。所有瓣膜功能良好,并显示出沿适当z值的生长。瓣环直径分别从主动脉瓣的中位数7 mm和肺动脉瓣的中位数9 mm增加到14 mm(主动脉瓣)和17 mm(肺动脉瓣)。瓣叶长度同样分别从主动脉瓣的中位数0.5 mm和肺动脉瓣的中位数0.49 mm增加到1 mm(主动脉瓣)和0.675 mm(肺动脉瓣)。1例患者需要进行与植入瓣膜无关的再次手术。未观察到与免疫抑制相关的重大并发症。

结论和意义

部分心脏移植似乎可行、安全且有效。根据瓣环和瓣叶长度测量,所有移植瓣膜均显示出生长。仔细的随访和监测对于支持这项新技术的持续推广至关重要。

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本文引用的文献

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Partial Heart Transplantation: Early Experience With Pediatric Heart Valve Replacements That Grow.
Circulation. 2025 May 20;151(20):1477-1490. doi: 10.1161/CIRCULATIONAHA.124.072626. Epub 2025 May 19.
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