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血管内近距离放射治疗:关于其在降低外周动脉疾病血管内治疗后再狭窄中的作用的系统评价

Intravascular brachytherapy: a systematic review of its role in reducing restenosis after endovascular treatment in peripheral arterial disease.

作者信息

Hansrani M, Overbeck K, Smout J, Stansby G

机构信息

Department of Surgery, University of Newcastle Upon Tyne, UK.

出版信息

Eur J Vasc Endovasc Surg. 2002 Nov;24(5):377-82. doi: 10.1053/ejvs.2002.1742.

Abstract

INTRODUCTION

Intravascular brachytherapy (IVBT) utilises the percutaneous insertion of a radioactive source to inhibit myointimal hyperplasia in arteries treated by balloon angioplasty or stenting. A systematic review was performed of trials of IVBT in patients with Peripheral Arterial Disease (PAD).

METHODS

Search strategy - the reviewers searched Medline, Embase, the Cochrane Peripheral Vascular Diseases Group trials register, DARE, CCT and NHS EED for clinical studies and trials of adjuvant IVBT in PAD. Two reviewers assessed trial quality independently.

RESULTS

Fourteen clinical trials were identified by the search, representing five clinical studies (all allocated D for not randomised) and one randomised controlled trial (allocated A). The randomised trial showed a benefit for IVBT compared with placebo (OR 0.35, 95% CI 0.24-0.53). In the non-randomised studies, 12 month cumulative patency rates ranged from 60-87%. There were few technical complications. In the only report involving IVBT and routine concurrent stent insertion acute thrombosis occurred in 7 (21%) of patients.

CONCLUSION

Early reports have confirmed the safety and technical feasibility of IVBT. However, follow-up is too short at present to assess the durability and long-term complications of this new therapeutic option.

摘要

引言

血管内近距离放射治疗(IVBT)通过经皮插入放射源,以抑制经球囊血管成形术或支架置入术治疗的动脉中的肌内膜增生。对周围动脉疾病(PAD)患者进行IVBT试验的系统评价。

方法

检索策略——综述作者检索了Medline、Embase、Cochrane外周血管疾病组试验注册库、DARE、CCT和NHS EED,以查找PAD辅助IVBT的临床研究和试验。两名综述作者独立评估试验质量。

结果

检索共识别出14项临床试验,代表5项临床研究(均因未随机分配而评为D级)和1项随机对照试验(评为A级)。随机试验显示,与安慰剂相比,IVBT有益(OR 0.35,95%CI 0.24-0.53)。在非随机研究中,12个月的累积通畅率为60%-87%。技术并发症很少。在唯一一篇涉及IVBT和常规同期支架置入的报告中,7例(21%)患者发生急性血栓形成。

结论

早期报告证实了IVBT的安全性和技术可行性。然而,目前随访时间过短,无法评估这种新治疗选择的持久性和长期并发症。

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