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[严重下肢缺血的医学治疗:基因与细胞治疗的现状与未来展望]

[Medical treatment of critical leg ischemia: current status and future perspectives of gene and cell therapy].

作者信息

Emmerich Joseph, Fiessinger Jean-Noël

机构信息

Université Paris-Descartes, INSERM U765, Service de Médecine Vasculaire - HTA, Hôpital Européen Georges Pompidou, 20 rue Leblanc, 75908 Paris 15.

出版信息

Bull Acad Natl Med. 2006 Mar;190(3):667-80; discussion 680-1, 683-4.

PMID:17140102
Abstract

Critical limb ischemia (CLI) is associated with a high risk of amputation and death. For patients who cannot be surgically revascularized, medical options include prostanoids, spinal cord stimulation and lumbar sympathectomy, but none of these treatments has a demonstrated impact on the amputation rate at six months. Gene and cell therapy, aimed at stimulating angiogenesis, have mainly been tested in phase I and II clinical trials. These approaches appear to be feasible and safe in the short-term, but large randomized studies are necessary to demonstrate their clinical benefits and long-term safety.

摘要

严重肢体缺血(CLI)与截肢和死亡的高风险相关。对于无法通过手术实现血管再通的患者,药物治疗选择包括前列腺素、脊髓刺激和腰交感神经切除术,但这些治疗方法均未显示对六个月时的截肢率有影响。旨在刺激血管生成的基因和细胞疗法主要在I期和II期临床试验中进行了测试。这些方法在短期内似乎是可行且安全的,但需要大型随机研究来证明其临床益处和长期安全性。

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