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儿童移植后冠状动脉疾病。一项全国多中心调查。

Posttransplant coronary artery disease in children. A multicenter national survey.

作者信息

Pahl E, Zales V R, Fricker F J, Addonizio L J

机构信息

Department of Pediatrics, University of Pittsburgh.

出版信息

Circulation. 1994 Nov;90(5 Pt 2):II56-60.

PMID:7955283
Abstract

BACKGROUND

Accelerated coronary atherosclerosis after heart transplantation (TCAD) is a major cause of late death. It is progressive and eventually fatal, and currently no therapy exists. The purpose of this study was to determine the incidence as well as the clinical and age-dependent characteristics of pediatric patients with TCAD.

METHODS AND RESULTS

Pediatric heart transplantation centers were surveyed on patient outcome and incidence of TCAD from August 1974 to March 1993. A follow-up questionnaire was sent to examine patient-specific details, including age at transplantation and at death, time to diagnosis, and rejection history. Data on coronary angiography and autopsy findings were requested. Replies were received from 17 US centers that performed 815 pediatric heart transplantations (including 188 neonates), with 560 survivors (69%). TCAD was identified in 58 patients (7.3%) by either coronary angiography, autopsy, or both. Detailed data were available for 45 patients. The mean age at diagnosis of TCAD was 9.9 years (0.2 to 26 years), and mean posttransplantation time was 2.2 years (0.1 to 7.7 years). TCAD occurred in 16 patients who received transplants before age 2 years. Many deaths were sudden and unexpected. Only 9 of 58 patients are alive, including 5 who had a second transplant. Four or more treated cellular rejection episodes and one or more courses of monoclonal antibody were used in 60% of patients with TCAD. Angiography was performed in 45 and was normal in 15 patients who later died of TCAD. An autopsy, performed in 36 of the 49 who died, showed severe coronary stenosis in 28 (78%) and concurrent cellular rejection in 26 (72%).

CONCLUSIONS

TCAD is a serious problem in transplant recipients and may affect patients of any age, even neonates. Diagnosis is difficult, and incidence of TCAD may be under-estimated. TCAD appears to be associated with cellular rejection; thus, higher surveillance in patients with frequent rejection episodes is indicated. Better surveillance methods, such as intravascular ultrasound and quantitative analysis of angiographic data, are needed to improve detection and assess new treatment strategies.

摘要

背景

心脏移植术后加速性冠状动脉粥样硬化(TCAD)是晚期死亡的主要原因。它呈进行性发展,最终可导致死亡,目前尚无有效的治疗方法。本研究旨在确定小儿TCAD患者的发病率以及临床和年龄相关特征。

方法与结果

对1974年8月至1993年3月期间小儿心脏移植中心的患者结局和TCAD发病率进行了调查。发放了一份随访问卷,以了解患者的具体细节,包括移植时和死亡时的年龄、诊断时间以及排斥反应史。要求提供冠状动脉造影和尸检结果的数据。收到了来自美国17个中心的回复,这些中心共进行了815例小儿心脏移植(包括188例新生儿),其中560例存活(69%)。通过冠状动脉造影、尸检或两者兼用,在58例患者(7.3%)中发现了TCAD。45例患者有详细数据。TCAD诊断时的平均年龄为9.9岁(0.2至26岁),移植后的平均时间为2.2年(0.1至7.7年)。16例在2岁前接受移植的患者发生了TCAD。许多死亡是突然且意外的。58例患者中仅9例存活,其中5例接受了二次移植。60%的TCAD患者发生过4次或更多次经治疗的细胞排斥反应且使用过一个或多个疗程的单克隆抗体。45例患者进行了血管造影,其中15例后来死于TCAD的患者血管造影结果正常。49例死亡患者中的36例进行了尸检,28例(78%)显示严重冠状动脉狭窄,26例(72%)同时存在细胞排斥反应。

结论

TCAD是移植受者中的一个严重问题,可能影响任何年龄的患者,甚至新生儿。诊断困难,TCAD的发病率可能被低估。TCAD似乎与细胞排斥反应有关;因此,对于频繁发生排斥反应的患者应加强监测。需要更好的监测方法,如血管内超声和血管造影数据的定量分析,以提高检测率并评估新的治疗策略。

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