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室间隔完整的肺动脉闭锁:210例连续患者的治疗及预后

Pulmonary atresia with intact ventricular septum: management of, and outcomes for, a cohort of 210 consecutive patients.

作者信息

Dyamenahalli Umesh, McCrindle Brian W, McDonald Cathy, Trivedi Kalyani R, Smallhorn Jeffrey F, Benson Lee N, Coles John, Williams William G, Freedom Robert M

机构信息

Department of Pediatrics, Division of Cardiology, The Hospital for Sick Children, University of Toronto, Toronto, Canada.

出版信息

Cardiol Young. 2004 Jun;14(3):299-308. doi: 10.1017/S1047951104003087.

Abstract

OBJECTIVES

We sought to determine trends, and outcomes, for a cohort of patients with pulmonary atresia with intact ventricular septum born between 1965 and 1998.

BACKGROUND

Pulmonary atresia with intact ventricular septum is a complex lesion that remains a therapeutic challenge, particularly regarding the suitability for biventricular repair.

METHODS

We identified 210 consecutive patients, and reviewed their medical records, initial angiograms, and echocardiograms, along with the relevant surgical and pathology reports.

RESULTS

The mean initial Z-score for the diameter of the tricuspid valve was -0.99 +/- 1.95, with Ebstein's malformation in 8%. A right ventricular dependent coronary arterial circulation was found in 23%. The proportion of patients who received treatment increased over time, although placement of an arterial shunt was the predominant initial procedure throughout the experience. At the last follow-up, 107 patients had not reached the planned final stage of their repair, and 79% of these had died. Of the 103 reaching the final stage of planned repair, 58 had undergone attempted biventricular repair, with 34% dying; 14 had undergone attempted one and a half ventricular repair, with 7% dying, and 31 had undergone attempted functionally univentricular repair, with 10% dying. Overall, survival was 57% at the age of 1 year, 48% at 5 years, and 43% at 10 years. Survival improved over time, with survival of 75% at 1 year, and 67% at 5 years, for patients born between 1992 and 1998. An earlier date of birth, the presence of Ebstein's malformation, and prematurity were all significant independent factors associated with decreased survival. A greater severity of coronary arterial abnormalities was significantly associated with a greater likelihood of left ventricular dysfunction during follow-up.

CONCLUSIONS

The outcomes for patients born with pulmonary atresia with intact ventricular septum have improved over time, albeit that careful initial management, and better selection, is still indicated for those planned to undergo biventricular repair.

摘要

目的

我们试图确定1965年至1998年出生的一组室间隔完整的肺动脉闭锁患者的治疗趋势和治疗结果。

背景

室间隔完整的肺动脉闭锁是一种复杂病变,仍然是治疗上的挑战,尤其是在双心室修复的适用性方面。

方法

我们确定了210例连续患者,并查阅了他们的病历、初始血管造影和超声心动图,以及相关的手术和病理报告。

结果

三尖瓣直径的平均初始Z值为-0.99±1.95,8%的患者有埃布斯坦畸形。23%的患者发现有右心室依赖型冠状动脉循环。接受治疗的患者比例随时间增加,尽管在整个治疗过程中,动脉分流术是主要的初始治疗方法。在最后一次随访时,107例患者尚未达到计划的最终修复阶段,其中79%已经死亡。在103例达到计划修复最终阶段的患者中,58例尝试进行双心室修复,34%死亡;14例尝试进行1.5心室修复,7%死亡;31例尝试进行功能性单心室修复,10%死亡。总体而言,1岁时生存率为57%,5岁时为48%,10岁时为43%。随着时间推移生存率有所提高,1992年至1998年出生的患者1岁时生存率为75%,5岁时为67%。较早的出生日期、埃布斯坦畸形的存在和早产都是与生存率降低相关的显著独立因素。冠状动脉异常的严重程度越高,随访期间左心室功能障碍的可能性就越大。

结论

室间隔完整的肺动脉闭锁患者的治疗结果随时间有所改善,尽管对于计划进行双心室修复的患者仍需要谨慎的初始管理和更好的选择。

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