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室间隔完整型肺动脉闭锁成年幸存者的临床结局。

Clinical outcomes of adult survivors of pulmonary atresia with intact ventricular septum.

机构信息

Division of Cardiovascular Diseases, Internal Medicine, and Pediatric Cardiology, Mayo Clinic, Rochester, MN, United States.

出版信息

Int J Cardiol. 2012 Nov 1;161(1):13-7. doi: 10.1016/j.ijcard.2011.04.026. Epub 2011 May 18.

DOI:10.1016/j.ijcard.2011.04.026
PMID:21596450
Abstract

BACKGROUND

There are no studies on the long term clinical outcomes and complications in the adult patient with pulmonary atresia with intact ventricular septum (PA/IVS). This study reviews our experience with a limited group of adult survivors of PA/IVS seen in our adult congenital clinics.

METHODS

Twenty adult patients with PA/IVS (1998 to 2009) were identified from Mayo Clinic adult congenital heart disease databases. Surgical history and clinical outcomes were reviewed.

RESULTS

Mean age at last evaluation was 29 years (19-39 years). There were five deaths within the study period (1998-2009). Median age at death was 32 years (30-37 years). Seven patients underwent the Fontan operation, eight patients had a biventricular repair, and five patients remained with palliative shunts. All patients required re-interventions in adulthood. Tricuspid valve (TV) (n=5), pulmonary valve (PV)/conduit (n=6), and mitral valve (n=2) replacements were the most frequent re-intervention in the biventricular repair subset. Atrial arrhythmias were present in 80% of the total cohort, the highest rate among Fontan repairs (n=7) and biventricular repairs (n=7). Ventricular arrhythmias occurred in 15% of the cohort.

CONCLUSIONS

Although limited in number, the adult PA/IVS patients in this series continue to have high rates of morbidity and mortality, with arrhythmias and need for re-operations as the major causes. Patients with biventricular repairs had the highest re-intervention rate in adulthood. While this subset of patients might not be representative of all adult PA/IVS survivors, continued follow-up at centers with expertise in adult congenital cardiology is recommended for all patients.

摘要

背景

目前尚无关于肺动脉闭锁伴完整室间隔(PA/IVS)成年患者的长期临床结局和并发症的研究。本研究回顾了我们在成人先天性心脏病门诊中所见的有限数量的 PA/IVS 成年幸存者的经验。

方法

从梅奥诊所成人先天性心脏病数据库中确定了 20 例 PA/IVS 成年患者(1998 年至 2009 年)。回顾了手术史和临床结局。

结果

最后一次评估的平均年龄为 29 岁(19-39 岁)。研究期间有 5 例死亡(1998-2009 年)。死亡的中位年龄为 32 岁(30-37 岁)。7 例患者接受了 Fontan 手术,8 例患者接受了双心室修复,5 例患者仍有姑息性分流。所有患者在成年后都需要再次干预。三尖瓣(TV)(n=5)、肺动脉瓣(PV)/导管(n=6)和二尖瓣(n=2)置换是双心室修复亚组中最常见的再次干预。总队列中 80%存在房性心律失常,Fontan 修复组(n=7)和双心室修复组(n=7)的发生率最高。该队列中有 15%发生了室性心律失常。

结论

尽管数量有限,但本系列中的成年 PA/IVS 患者仍有很高的发病率和死亡率,心律失常和需要再次手术是主要原因。双心室修复患者在成年后的再次干预率最高。虽然这组患者可能不能代表所有成年 PA/IVS 幸存者,但建议所有患者在具有成人先天性心脏病专业知识的中心继续随访。

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