Comparative Efficacy of Endovascular Revascularization Modalities for Symptomatic Infrapopliteal Peripheral Artery Disease: A Network Meta-Analysis
Recommended Citation
Mufarrih SH, Qureshi NQ, Secemsky E, Kazimuddin M, Onofrey K, Giri J, Shishehbor M, Banerjee S, Aronow HD. Comparative Efficacy of Endovascular Revascularization Modalities for Symptomatic Infrapopliteal Peripheral Artery Disease: A Network Meta-Analysis. JACC Cardiovasc Interv. 2026;19(13):1780-1792.
Document Type
Article
Publication Date
7-13-2026
Publication Title
JACC Cardiovasc Interv
Keywords
Aged, Female, Humans, Male, Middle Aged, Angioplasty, Balloon, Chi-Square Distribution, Coated Materials, Biocompatible, Drug-Eluting Stents, Limb Salvage, Metals, Odds Ratio, Peripheral Arterial Disease, Popliteal Artery, Prosthesis Design, Randomized Controlled Trials as Topic, Recurrence, Risk Factors, Stents, Time Factors, Treatment Outcome, Vascular Access Devices, Vascular Patency
Abstract
BACKGROUND: Patients with infrapopliteal peripheral artery disease (PAD) are at elevated risk for amputation and mortality. The comparative efficacy of available endovascular devices for treating infrapopliteal PAD is unknown.
OBJECTIVES: The aim of this study was to compare the efficacy of percutaneous transluminal angioplasty (PTA), bare-metal stents (BMS), drug-coated balloons (DCBs), and drug-eluting stents (DES), including bioresorbable DES, in patients with symptomatic infrapopliteal PAD.
METHODS: Online databases were searched for published randomized controlled trials comparing PTA, BMS, DCB, and DES in patients with infrapopliteal PAD. Random-effects models were used to estimate ORs for binary variables and mean differences (MDs) for continuous variables.
RESULTS: Twenty-one randomized controlled trials comprising 2,958 patients were included (PTA, n = 1,102; BMS, n = 284; DCBs, n = 903; DES, n = 695). Compared with PTA, both DCBs and DES had higher primary patency (DCB OR: 2.66 [95% CI: 1.52-4.64; P = 0.001]; DES OR: 2.41 [95% CI: 1.23-4.73; P = 0.01]) and lower target lesion binary (>50%) restenosis (DCB OR: 0.40 [95% CI: 0.21-0.77; P = 0.006]; DES OR: 0.28 [95% CI: 0.13-0.62; P = 0.002]). DCBs also lowered late lumen loss (MD: 0.34; 95% CI: -0.63 to -0.05; P = 0.02), in-lesion diameter stenosis (MD: -10.04; 95% CI: -19.20 to -0.88; P = 0.03), and clinically driven target lesion revascularization (OR: 0.47; 95% CI: 0.29-0.76; P = 0.002). Conversely, BMS decreased the odds of complete wound healing (OR: 0.41; 95% CI: 0.20-0.85; P = 0.02). No significant differences in amputation or mortality were observed across the 4 comparator groups.
CONCLUSIONS: Compared with PTA, DCBs and DES demonstrated higher primary patency and lower binary restenosis, and DCBs reduced late lumen loss, percentage in-lesion diameter stenosis, and clinically driven target lesion revascularization.
Medical Subject Headings
Aged; Female; Humans; Male; Middle Aged; Angioplasty, Balloon; Chi-Square Distribution; Coated Materials, Biocompatible; Drug-Eluting Stents; Limb Salvage; Metals; Odds Ratio; Peripheral Arterial Disease; Popliteal Artery; Prosthesis Design; Randomized Controlled Trials as Topic; Recurrence; Risk Factors; Stents; Time Factors; Treatment Outcome; Vascular Access Devices; Vascular Patency
PubMed ID
42442894
Volume
19
Issue
13
First Page
1780
Last Page
1792
