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[1990年小儿心脏移植]

[Pediatric heart transplantation 1990].

作者信息

Chartrand C

机构信息

Département de chirurgie cardio-vasculaire, Hôpital Sainte-Justine, Montréal, Qué.

出版信息

Can J Surg. 1991 Dec;34(6):573-7.

PMID:1747835
Abstract

In this presentation the author updates the progress made in pediatric cardiac transplantation through a review of the results obtained at Ste-Justine Hospital (SJH) and of the recent literature. Of 56 children referred to SJH for cardiac transplantation, 27 met the selection criteria; 10 died before receiving a new heart and 2 are still awaiting transplantation. Fifteen children, aged 3 to 16 years, have received a transplant. Ten of them had 32 birth defects, all of which were repaired at the time of transplantation thanks to improved graft removal methods and innovative surgical techniques. This study demonstrates that birth defects are not a contraindication to cardiac transplantation in children. Triple-drug immunosuppression was used, and the cyclosporine blood levels were maintained in the range of 100 to 200 ng/mL. Survival at 2 years was 78%. Episodes of acute rejection occurred at a rate of 0.5 per patient, 85% of them within the first 3 months after transplantation. Adequate renal function was preserved (creatinine clearance between 89 and 102 mL/min.m-2). The use of low-dose cyclosporine might explain in part the lack of significant nephrotoxicity. Reversible high blood pressure was observed in 5 of 13 patients during the first 6 months postoperatively. Multifactorial analysis identified, as a likely cause, a higher dose of steroids and cyclosporine during this period. Annual coronary angiography did not reveal any lesion, and apart from the acute rejection episodes, cardiac function was normal at rest, and the transplanted children have maintained an excellent level of activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本报告中,作者通过回顾圣贾斯汀医院(SJH)取得的成果以及近期文献,介绍了小儿心脏移植的进展情况。在转至SJH接受心脏移植的56名儿童中,27名符合选择标准;10名在接受新心脏前死亡,2名仍在等待移植。15名年龄在3至16岁的儿童接受了移植。其中10名有32种先天性缺陷,由于改进了移植物移除方法和创新手术技术,所有这些缺陷在移植时均得到修复。这项研究表明,先天性缺陷并非儿童心脏移植的禁忌证。采用三联药物免疫抑制,环孢素血药浓度维持在100至200 ng/mL范围内。2年生存率为78%。急性排斥反应发生率为每位患者0.5次,其中85%发生在移植后的前3个月内。肾功能得到充分保留(肌酐清除率在89至102 mL/min·m²之间)。低剂量环孢素的使用可能部分解释了为何没有明显的肾毒性。13名患者中有5名在术后前6个月出现可逆性高血压。多因素分析确定,在此期间较高剂量的类固醇和环孢素可能是原因。年度冠状动脉造影未发现任何病变,除急性排斥反应外,静息时心脏功能正常,接受移植的儿童保持了良好的活动水平。(摘要截选至250字)

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