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Drug-Coated Balloons for Coronary Artery Disease: Third Report of the International DCB Consensus Group
Raban V Jeger1, Simon Eccleshall2, Wan Azman Wan Ahmad3
1University Hospital Basel, University of Basel, Basel, Switzerland.
Insights
Drug-coated balloons (DCBs) offer a novel alternative to stenting for coronary artery disease, particularly in specific situations like small vessels. DCBs provide drug delivery without permanent implants, showing promise in various patient groups.
Area of Science:
- Interventional Cardiology
- Vascular Medicine
- Biomaterials Science
Background:
- Drug-eluting stents are standard for coronary artery disease.
- Drug-coated balloons (DCBs) offer an implant-free therapeutic option.
- DCBs utilize antiproliferative drugs delivered via a lipophilic matrix.
Purpose of the Study:
- To provide an updated consensus on drug-coated balloons (DCBs).
- To summarize the historical background, technical aspects, and indications for DCBs.
- To discuss future perspectives for DCB technology in interventional cardiology.
Main Methods:
- Review of recent randomized clinical data.
- Analysis of technical considerations for DCB device selection and implantation.
- Consensus-based recommendations from the International DCB Consensus Group.
Main Results:
- DCBs demonstrate efficacy and safety in de novo small-vessel disease and high bleeding risk patients.
- Established use for in-stent restenosis of both bare-metal and drug-eluting stents.
- Emerging indications include bifurcation lesions, large vessels, diabetes, and acute coronary syndromes.
Conclusions:
- DCBs are a viable alternative to stenting in select coronary artery disease scenarios.
- The efficacy of DCBs is device- and formulation-dependent, lacking a "class effect".
- Ongoing research and evolving indications highlight the expanding role of DCBs.
Abstract:
Although drug-eluting stents are still the default interventional treatment of coronary artery disease, drug-coated balloons (DCBs) represent a novel alternative therapeutic strategy in certain anatomic conditions. The effect of DCBs is based on the fast and homogenous transfer of antiproliferative drugs into the vessel wall during single balloon inflation by means of a lipophilic matrix without the use of permanent implants. Although their use is established for in-stent restenosis of both bare-metal and drug-eluting stents, recent randomized clinical data demonstrate a good efficacy and safety profile in de novo small-vessel disease and high bleeding risk. In addition, there are other emerging indications (e.g., bifurcation lesions, large-vessel disease, diabetes mellitus, acute coronary syndromes). Because the interaction among the different delivery balloon designs, doses, formulations, and release kinetics of the drugs used is important, there seems to be no "class effect" of DCBs. On the basis of the amount of recently published data, the International DCB Consensus Group provides this update of previous recommendations summarizing the historical background, technical considerations such as choice of device and implantation technique, possible indications, and future perspectives.
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