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Treatment of coronary in-stent restenosis: a systematic review

机译:冠状动脉支架内再狭窄的治疗:系统评价

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摘要

Coronary stent implantation has significantly improved percutaneous coronary intervention and enabled the management of early complications of plain balloon angioplasty. However, a new complication has accompanied these improvements: in-stent restenosis (ISR) arising from neointimal hyperplasia. ISR after coronary angioplasty is currently one of the main limitations of this method, leading to the recurrence of exertional angina pectoris or acute coronary syndromes. The clinical incidence of ISR after bare-metal stent (BMS) implantation is approximately 20%–35%. The use of drug-eluting stents (DES) has led to a further decrease in the occurrence of ISR to 5%–10%. Evidence resulting from controlled clinical studies suggests that DES and drug-eluting balloon catheters (DEB) provide the best clinical and angiographic results in the treatment of ISR. We undertook a systematic review of the pathophysiology, diagnostics and treatment options for BMS- and DES-ISR. We discuss recent randomised studies, comparing different DES or DEB used for BMS or DES-ISR treatment, as well as the use of new biovascular scafolds and the topic of scafold restenosis.
机译:冠状动脉支架植入术显着改善了经皮冠状动脉介入治疗,并能处理平原气囊血管成形术的早期并发症。但是,新的并发症伴随着这些改善:新内膜增生引起的支架内再狭窄(ISR)。目前,冠状动脉成形术后的ISR是该方法的主要局限性之一,导致运动性心绞痛或急性冠状动脉综合征的复发。植入金属裸支架(BMS)后ISR的临床发生率约为20%–35%。使用药物洗脱支架(DES)使ISR的发生率进一步降低至5%–10%。受控临床研究的证据表明,DES和药物洗脱球囊导管(DEB)在ISR的治疗中提供了最佳的临床和血管造影结果。我们对BMS-和DES-ISR的病理生理,诊断和治疗选择进行了系统的审查。我们讨论了最近的随机研究,比较了用于BMS或DES-ISR治疗的不同DES或DEB,以及使用新的生物血管支架和支架再狭窄的话题。

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