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严重肢体缺血中的干细胞治疗:现状与未来趋势

Stem cell therapy in critical limb ischemia: Current scenario and future trends.

作者信息

Sharma Arun, Sinha Mumun, Pandey Niraj Nirmal, Chandrashekhara S H

机构信息

Department of Cardiovascular Radiology and Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India.

Department of Radiodiagnosis, BRAIRCH, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Indian J Radiol Imaging. 2019 Oct-Dec;29(4):397-403. doi: 10.4103/ijri.IJRI_385_19. Epub 2019 Dec 31.

DOI:10.4103/ijri.IJRI_385_19
PMID:31949342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6958876/
Abstract

Critical limb ischemia (CLI) represents the most severe manifestation of peripheral arterial disease (PAD). It imposes a huge economic burden and is associated with high short-term mortality and adverse cardiovascular outcomes. Prompt recognition and early revascularization, surgical or endovascular, with the aim of improving the inline bloodflow to the ischemic limb, are currently the standard of care. However, this strategy may not always be feasible or effective; hence, evaluation of newer pharmacological or angiogenic therapies for alleviating the symptoms of this alarming condition is of utmost importance. Cell-based therapies have shown promise in smaller studies; however, large-scale studies, demonstrating definite survival benefits, are entailed to ascertain their role in the management of CLI.

摘要

严重肢体缺血(CLI)是外周动脉疾病(PAD)最严重的表现形式。它带来了巨大的经济负担,且与高短期死亡率及不良心血管结局相关。目前,以改善缺血肢体的顺行血流为目标,迅速识别并尽早进行外科或血管内血运重建是标准治疗方法。然而,这一策略并非总是可行或有效的;因此,评估用于缓解这种严重疾病症状的新型药物或血管生成疗法至关重要。在规模较小的研究中,基于细胞的疗法已显示出前景;然而,需要大规模研究来证实其在CLI治疗中的作用,以明确其对生存的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/664f/6958876/0aede6d36954/IJRI-29-397-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/664f/6958876/0aede6d36954/IJRI-29-397-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/664f/6958876/0aede6d36954/IJRI-29-397-g001.jpg

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Cochrane Database Syst Rev. 2018 Aug 29;8(8):CD010747. doi: 10.1002/14651858.CD010747.pub2.
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Med Sci Monit. 2020 Aug 29;26:e923287. doi: 10.12659/MSM.923287.
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