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Review
. 2018 Feb 12;20(2):7.
doi: 10.1007/s11886-018-0952-4.

Therapeutic Options for In-Stent Restenosis

Affiliations
Review

Therapeutic Options for In-Stent Restenosis

Charles Nicolais et al. Curr Cardiol Rep. .

Abstract

Purpose of review: In-stent restenosis (ISR) is a complex disease process that became apparent shortly after the introduction of stents into clinical practice. This review seeks to define in-stent restenosis (ISR) as well as to summarize the major treatment options that have been developed and studied over the past two decades.

Recent findings: Recent developments in drug-coated balloons and bioresorbable vascular scaffolds have added new potential treatments for ISR. Two recent network meta-analyses performed a head-to-head comparison of all the various treatment modalities in order to identify the best approach to management of ISR. Current data suggests that repeat stenting with second-generation drug-eluting stents is most likely to lead to the best angiographic and clinical outcomes. In situations where repeat stenting is not preferable, drug-coated balloon therapy seems to be a reasonably effective alternative.

Keywords: Balloon angioplasty; Bare metal stent; Drug-eluting stent; In-stent restenosis; Neo atherosclerosis; Rotational atherectomy.

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References

    1. Eur Heart J. 2004 Nov;25(22):2040-7 - PubMed
    1. JAMA. 2006 Mar 15;295(11):1264-73 - PubMed
    1. Am J Cardiol. 1999 Apr 15;83(8):1268-70, A9 - PubMed
    1. JACC Cardiovasc Interv. 2010 Apr;3(4):403-11 - PubMed
    1. Minerva Cardioangiol. 2012 Oct;60(5):473-89 - PubMed

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