Outcomes With Limus- vs PaclitaxelCoated Balloons for Percutaneous Coronary Intervention Meta-Analysis of Randomized Controlled Trials

被引:10
作者
Sedhom, Ramy [1 ]
Hamed, Mohamed [2 ]
Elbadawi, Ayman [3 ,4 ]
Mohsen, Amr [1 ]
Swamy, Pooja [1 ]
Athar, Ahmed [5 ]
Bharadwaj, Aditya S. [1 ]
Prasad, Vinoy [1 ]
Elgendy, Islam Y. [6 ]
Alfonso, Fernando [7 ]
机构
[1] Loma Linda Univ, Med Ctr, Div Cardiol, Loma Linda, CA USA
[2] Florida Atlantic Univ, Div Cardiol, Boca Raton, FL USA
[3] Christus Good Shepherd Med Ctr, Div Cardiol, Longview, TX USA
[4] Texas A&M Sch Med, Bryan, TX USA
[5] Jerry L Pettis Mem Vet Adm Med Ctr, Cardiol Sect, Loma Linda, CA USA
[6] Univ Kentucky, Gill Heart Inst, Div Cardiovasc Med, Lexington, KY USA
[7] Hosp Univ La Princesa, Univ Autonoma Madrid, Cardiol Dept, IIS IP,CIBER CV, Madrid, Spain
关键词
biolimus; drug-coated balloon; paclitaxel; sirolimus; ELUTING STENT RESTENOSIS; DRUG-COATED BALLOONS; SIROLIMUS; RELEASE;
D O I
10.1016/j.jcin.2024.04.042
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Randomized controlled trials (RCTs) examining the outcomes with limus drug-coated balloons (DCBs) vs paclitaxel DCBs were small and underpowered for clinical endpoints. OBJECTIVES This study sought to compare the angiographic and clinical outcomes with limus DCBs vs paclitaxel DCBs for percutaneous coronary intervention (PCI). METHODS An electronic search of Medline, EMBASE, and Cochrane databases was performed through January 2024 for RCTs comparing limus DCBs vs paclitaxel DCBs for PCI. The primary endpoint was clinically driven target lesion revascularization (TLR). The secondary endpoints were late angiographic findings. Summary estimates were constructed using a random effects model. RESULTS Six RCTs with 821 patients were included; 446 patients received a limus DCB, and 375 patients received a paclitaxel DCB. There was no difference between limus DCBs and paclitaxel DCBs in the incidence of TLR at a mean of 13.4 months (10.3% vs 7.8%; risk ratio [RR]: 1.32; 95% CI: 0.84-2.08). Subgroup analysis suggested no signi ficant interaction among studies for de novo coronary lesions vs in-stent restenosis (P interaction = 0.58). There were no differences in the risk of major adverse cardiovascular events, cardiac mortality, or target vessel myocardial infarction between groups. However, limus DCBs were associated with a higher risk of binary restenosis (RR: 1.89; 95% CI: 1.143.12), late lumen loss (mean difference = 0.16; 95% CI: 0.03-0.28), and a smaller minimum lumen diameter (mean difference =-0.12; 95% CI:-0.22 to-0.02) at late follow-up. In addition, late lumen enlargement occurred more frequently (50% vs 27.5%; RR: 0.59; 95% CI: 0.45-0.77) with paclitaxel DCBs. CONCLUSIONS Among patients undergoing DCB-only PCI, there were no differences in the risk of clinically driven TLR and other clinical outcomes between limus DCBs and paclitaxel DCBs. However, paclitaxel DCBs were associated with better late angiographic outcomes. These findings support the need for future trials to establish the role of newgeneration limus DCBs for PCI. (JACC Cardiovasc Interv 2024;17:1533 -1543) Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:1533 / 1543
页数:11
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