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Performance of drug-coated balloons in coronary and below-the-knee arteries: Anatomical, physiological and
Rafic Ramses1, Simon Kennedy2, Richard Good3
1Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Institute of Cardiology, Catholic University of the Sacred Heart, Rome, Italy; Division of Biomedical Engineering, University of Glasgow, United Kingdom.
Drug-coated balloons (DCBs) show no advantage over plain balloon angioplasty for below-the-knee atherosclerotic disease. This review explores reasons for differing outcomes between infrapopliteal and coronary artery interventions.
Area of Science:
- Vascular Surgery
- Interventional Cardiology
- Peripheral Artery Disease
Background:
- Below-the-knee atherosclerotic disease, or chronic limb-threatening ischemia (CLTI), poses significant challenges for endovascular treatment.
- CLTI leads to pain, tissue atrophy, high amputation rates (30%), and 25% 1-year mortality.
Purpose of the Study:
- To review the efficacy of drug-coated balloons (DCBs) in infrapopliteal arteries compared to plain balloon angioplasty.
- To explore anatomical, physiological, and pathological differences influencing DCB outcomes in infrapopliteal versus coronary arteries.
Main Methods:
- Review of randomized multicentre trials comparing endovascular interventions for infrapopliteal arterial disease.
- Analysis of existing literature on drug-eluting stents (DES) and DCBs in femoropopliteal, coronary, and infrapopliteal arteries.
Main Results:
- Drug-eluting stents (DES) improve patency and reduce revascularization compared to plain balloon angioplasty and bare-metal stents in focal infrapopliteal lesions.
- Multicentre trials found no advantage of DCBs over plain balloon angioplasty for infrapopliteal arteries, contrary to findings in coronary and femoropopliteal arteries.
Conclusions:
- The effectiveness of DCBs in infrapopliteal arteries is limited, potentially due to lesion complexity and arterial characteristics.
- Understanding anatomical and pathological differences is crucial for optimizing endovascular treatment strategies for CLTI.
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