000 03385nam a22004577a 4500
008 240807s20242024 xxu||||| |||| 00| 0 eng d
022 _a1878-0938
024 _aS1553-8389(24)00496-2 [pii]
040 _aOvid MEDLINE(R)
099 _a38845281
245 _aDrug-coated balloons for coronary artery disease: An updated review with future perspectives. [Review]
251 _aCardiovascular Revascularization Medicine. 2024 May 23
252 _aCardiovasc Revasc Med. 2024 May 23
253 _aCardiovascular revascularization medicine : including molecular interventions
260 _c2024
260 _fFY2024
260 _p2024 May 23
265 _saheadofprint
265 _tPublisher
266 _d2024-08-07
266 _z2024/06/07 02:06
501 _aAvailable in print through MWHC library: 2002 - present
520 _aSince the advent of coronary stents, two of the most common long-term complications after percutaneous coronary intervention (PCI) are in-stent restenosis (ISR) and stent thrombosis (ST). Although the rates of ST have been nearly abolished and ISR rates have declined with the current gold-standard second-generation drug-eluting stents (DES), late ISR of DES remains a valid concern in the field of interventional cardiology. The drug-coated balloon (DCB) is a non-stent technology that relies on the concept of targeted homogeneous drug delivery from an inflated balloon to restore luminal vascularity, treat atherosclerosis, and overcome some limitations of PCI, including ISR and prolonged dual antiplatelet therapy to prevent ST by leaving nothing behind. Most clinical evidence on coronary DCBs predominantly comes from small, randomized data and registries using paclitaxel DCBs for ISR and de novo lesions in the coronary space. Since 2014, outside the United States, DCBs have been approved for the treatment of ISR, with a class I recommendation by the European Society of Cardiology. The Food and Drug Administration very recently approved the Agent DCB to treat ISR in patients with coronary artery disease in the US. Additionally, recent randomized clinical data also showed DCB's safety and efficacy for the treatment of de novo small-vessel disease and high-bleeding-risk patients, while their role for other clinical situations including acute coronary syndrome, large-vessel disease, bifurcation lesions, and long-diffuse distal lesions is currently under investigation. Herein, we review the evidence-based role of DCBs in the treatment of coronary lesions and offer future perspectives. Copyright © 2024. Published by Elsevier Inc.
546 _aEnglish
650 _aIN PROCESS -- NOT YET INDEXED
650 _zAutomated
651 _aMedStar Heart & Vascular Institute
651 _aMedStar Washington Hospital Center
656 _aCardiovascular Disease Fellowship
657 _aJournal Article
657 _aReview
700 _aBen-Dor, Itsik
_bMHVI
700 _aBhogal, Sukhdeep
_bMHVI
700 _aHill, Andrew
_bMWHC
_cCardiovascular Disease Fellowship
_dMD
700 _aMerdler, Ilan
_bMHVI
700 _aWaksman, Ron
_bMHVI
700 _aWermers, Jason P
_bMHVI
790 _aBhogal S, Hill AP, Merdler I, Wermers JP, Ben-Dor I, Waksman R
856 _uhttps://dx.doi.org/10.1016/j.carrev.2024.05.027
_zhttps://dx.doi.org/10.1016/j.carrev.2024.05.027
942 _cART
_dArticle
999 _c14400
_d14400