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Review
. 2024 May;17(5):e013302.
doi: 10.1161/CIRCINTERVENTIONS.123.013302. Epub 2024 May 21.

Drug-Coated Balloons in the Management of Coronary Artery Disease

Affiliations
Review

Drug-Coated Balloons in the Management of Coronary Artery Disease

Serge Korjian et al. Circ Cardiovasc Interv. 2024 May.

Abstract

Drug-coated balloons (DCBs) are specialized coronary devices comprised of a semicompliant balloon catheter with an engineered coating that allows the delivery of antiproliferative agents locally to the vessel wall during percutaneous coronary intervention. Although DCBs were initially developed more than a decade ago, their potential in coronary interventions has recently sparked renewed interest, especially in the United States. Originally designed to overcome the limitations of conventional balloon angioplasty and stenting, they aim to match or even improve upon the outcomes of drug-eluting stents without leaving a permanent implant. Presently, in-stent restenosis is the condition with the most robust evidence supporting the use of DCBs. DCBs provide improved long-term vessel patency compared with conventional balloon angioplasty and may be comparable to drug-eluting stents without the need for an additional stent layer, supporting their use as a first-line therapy for in-stent restenosis. Beyond the treatment of in-stent restenosis, DCBs provide an additional tool for de novo lesions for a strategy that avoids a permanent metal scaffold, which may be especially useful for the management of technically challenging anatomies such as small vessels and bifurcations. DCBs might also be advantageous for patients with high bleeding risk due to the decreased necessity for extended antiplatelet therapy, and in patients with diabetes and patients with diffuse disease to minimize long-stented segments. Further studies are crucial to confirm these broader applications for DCBs and to further validate safety and efficacy.

Keywords: antiplatelet therapy; antiproliferative; drug-coated balloons; in-stent restenosis; paclitaxel.

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Conflict of interest statement

Disclosures Dr Yeh has investigator-initiated research grants and is a consultant for Abbott Vascular, Boston Scientific and Medtronic, is a consultant for CathWorks, Elixir Medical, InfraRedx, Shockwave Medical, and Zoll Medical, and has investigator-initiated research grants with BD Bard, Cook and Philips Medical. Dr Cutlip has received research funding paid to institution from MedAlliance/Cordis. Dr Kirtane reports institutional funding to Columbia University and Cardiovascular Research Foundation from Medtronic, Boston Scientific, Abbott Vascular, Amgen, CathWorks, CSI, Philips, ReCor Medical, Neurotronic, Biotronik, Chiesi, Bolt Medical, Magenta Medical, Canon, SoniVie, and Shockwave Medical. In addition to research grants, institutional funding includes fees paid to Columbia University and Cardiovascular Research Foundation for consulting and speaking engagements in which Dr Kirtane controlled the content. Personal: travel expenses/meals from Amgen, Medtronic, Biotronik, Boston Scientific, Abbott Vascular, CathWorks, Concept Medical, Edwards, CSI, Novartis, Philips, Abiomed, ReCor Medical, Chiesi, Zoll, Shockwave, and Regeneron. Dr McEntegart reports research support paid to the institution from Boston Scientific and is a consultant for Shockwave, and part of the speakers bureau for Teleflex, Asahi, and Medtronic. The other authors report no conflicts.

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