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Systematic review on the effects of drug-coated balloon therapy on plaque morphology in patients with acute coronary
Kavithra Harihararajah1, Zaynah Nawaz1, Laiba Qadir1
1Aston Medical School, College of Health and Life Sciences, Aston University, Birmingham, B47ET, UK.
Insights
Drug-coated balloons (DCBs) may improve coronary plaque morphology in Acute Coronary Syndromes (ACS). This review found DCBs reduced plaque size and lipid burden, suggesting potential benefits beyond stenting.
Area of Science:
- Cardiology
- Interventional Cardiology
- Vascular Biology
Background:
- Drug-coated balloons (DCBs) offer a "leave nothing behind" alternative to drug-eluting stents for coronary artery disease.
- The impact of DCBs on coronary plaque morphology in Acute Coronary Syndromes (ACS) requires further characterization.
Purpose of the Study:
- To systematically review the effects of DCB therapy on coronary plaque morphology in patients presenting with ACS.
- To evaluate imaging-based changes in plaque characteristics following DCB treatment in ACS patients.
Main Methods:
- Systematic literature search of major databases (PubMed, Cochrane, Scopus, ScienceDirect).
- Inclusion of six studies assessing plaque morphology using intravascular ultrasound (IVUS), optical coherence tomography (OCT), near-infrared spectroscopy (NIRS), or angiography.
- Analysis of plaque burden, volume, area, lipid burden, and calcification.
Main Results:
- DCB therapy was associated with favorable imaging changes, including reduced plaque area, burden, and atheroma volume, and increased lumen dimensions.
- Studies indicated DCB treatment led to reduced lipid core burden and lower calcification scores compared to stent strategies.
- Heterogeneity in study design and methods limits direct comparisons and causal inference.
Conclusions:
- Current evidence suggests DCB therapy can favorably modify plaque morphology in ACS patients.
- DCBs show potential for plaque regression, lipid reduction, and positive vascular remodeling in ACS.
- Further research in dedicated ACS cohorts with advanced imaging is needed to confirm benefits and identify optimal patient selection.
Background:
In the treatment of diseased coronary arteries, drug-coated balloons (DCBs) have emerged as a "leave nothing behind" alternative to drug-eluting stents, yet their effects on coronary plaque morphology in Acute Coronary Syndromes (ACS) are not well characterised. This systematic review evaluates the impact of DCB therapy on plaque morphology in patients presenting with ACS.
Method:
A systematic search of PubMed, Cochrane Library, Scopus, and ScienceDirect identified studies reporting plaque-related outcomes following DCB treatment in adult patients with ACS. Six studies met the inclusion criteria, incorporating intravascular ultrasound (IVUS), optical coherence tomography (OCT), near-infrared spectroscopy (NIRS) or angiographic assessments of plaque burden, plaque volume, plaque area, lipid burden, or calcification.
Results:
Across comparative and non-comparative studies, DCB therapy was consistently associated with favourable imaging changes, including reductions in plaque area, plaque burden, or plaque atheroma volume, and increased lumen dimensions. In studies assessing compositional characteristics, DCB therapy was linked with reductions in lipid core burden and lower calcification scores compared with stent-based strategies. However, heterogeneity in study design, imaging methods, and outcome reporting limits direct comparison between studies, and causality cannot be conclusively inferred.
Conclusion:
Available evidence suggests that DCB therapy may favourably modify plaque morphology in ACS, influencing plaque size and composition. The potential for DCBs to promote plaque regression, reduce lipid burden, and facilitate positive vascular remodelling warrants further investigation in larger, dedicated ACS cohorts. Future studies integrating advanced imaging and molecular profiling may clarify mechanistic pathways and identify patient groups most likely to benefit from DCB-based strategies.
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