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先天性心脏病变修复联合肺移植治疗重度肺动脉高压:13年经验

Repair of congenital heart lesions combined with lung transplantation for the treatment of severe pulmonary hypertension: a 13-year experience.

作者信息

Choong Cliff K, Sweet Stuart C, Guthrie Tracey J, Mendeloff Eric N, Haddad Fabio J, Schuler Pam, De La Morena Maite, Huddleston Charles B

机构信息

Division of Cardiothoracic Surgery, Department of Surgery, Washington University School of Medicine, St. Louis Children's Hospital, MO, USA.

出版信息

J Thorac Cardiovasc Surg. 2005 Mar;129(3):661-9. doi: 10.1016/j.jtcvs.2004.07.058.

Abstract

OBJECTIVE

In patients with severe pulmonary hypertension associated with congenital heart disease, we prefer to perform repair of the congenital heart disease and lung transplantation whenever feasible so as to augment the donor pool and avoid the cardiac complications associated with heart transplantation. We report our experience with repair of congenital heart disease and lung transplantation and compare the results with those of patients who underwent heart-lung transplantation during the same period.

METHODS

The records of patients who had repair of congenital heart disease and lung transplantation (n = 35) and heart-lung transplantation (n = 16) between 1990 and 2003 were reviewed.

RESULTS

The underlying congenital heart disease in the repair of congenital heart disease and lung transplantation group included transposition of great vessels (n = 2), atrioventricular canal defect (n = 2), ventricular septal defect (n = 9), pulmonary venous obstruction (n = 7), scimitar syndrome (n = 2), pulmonary arterial atresia or stenosis (n = 5), and others (n = 8). Thirteen of the patients undergoing repair of congenital heart disease and lung transplantation (37.1%) had the congenital heart disease repaired before lung transplantation; the remaining congenital heart disease repairs were performed concurrently with transplantation. Sixteen patients underwent heart-lung transplantation because of poor left ventricular function or single-ventricle anatomy. Freedoms from bronchiolitis obliterans at 1, 3, and 5 years were 72.9%, 54.7%, and 54.7% for the repair of congenital heart disease and lung transplantation group and 77.8%, 51.9%, and 38.9% for the heart-lung transplantation group, respectively. Survivals at 1, 3, and 5 years were 62.9%, 51.4%, and 51.4% for the repair of congenital heart disease and lung transplantation group and 66.5%, 66.5%, and 60% for the heart-lung transplantation group, respectively.

CONCLUSION

Repair of congenital heart disease and lung transplantation is a feasible treatment option. Long-term outcome is determined by associated complications related to lung transplantation. Despite the complexity of combined congenital heart disease repair with lung transplantation and the resulting perioperative morbidity, the patients had similar outcomes to those of patients who underwent heart-lung transplantation.

摘要

目的

对于患有与先天性心脏病相关的严重肺动脉高压的患者,只要可行,我们更倾向于进行先天性心脏病修复和肺移植,以扩大供体库并避免与心脏移植相关的心脏并发症。我们报告我们在先天性心脏病修复和肺移植方面的经验,并将结果与同期接受心肺移植的患者进行比较。

方法

回顾了1990年至2003年间接受先天性心脏病修复和肺移植(n = 35)以及心肺移植(n = 16)的患者的记录。

结果

先天性心脏病修复和肺移植组的潜在先天性心脏病包括大血管转位(n = 2)、房室管缺损(n = 2)、室间隔缺损(n = 9)、肺静脉阻塞(n = 7)、弯刀综合征(n = 2)、肺动脉闭锁或狭窄(n = 5)以及其他(n = 8)。接受先天性心脏病修复和肺移植的患者中有13例(占37.1%)在肺移植前进行了先天性心脏病修复;其余的先天性心脏病修复与移植同时进行。16例患者因左心室功能差或单心室解剖结构而接受了心肺移植。先天性心脏病修复和肺移植组1年、3年和5年时无闭塞性细支气管炎的生存率分别为72.9%、54.7%和54.7%,心肺移植组分别为77.8%、51.9%和38.9%。先天性心脏病修复和肺移植组1年、3年和5年时的生存率分别为62.9%、51.4%和51.4%,心肺移植组分别为66.5%、66.5%和60%。

结论

先天性心脏病修复和肺移植是一种可行的治疗选择。长期结果取决于与肺移植相关的并发症。尽管先天性心脏病修复与肺移植联合手术复杂且围手术期发病率高,但患者的结局与接受心肺移植的患者相似。

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