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Randomized Pilot Study to Compare DCB-Based versus DST-Based Strategies for the Treatment of True or Complex Coronary Bifurcation Lesions.
Ke, Dan; He, Xi; Chen, Canqiang; Lin, Chaogui; Luo, Yukun; Fan, Lin; Li, Sumei; Zheng, Xingchun; Chen, Lianglong.
  • Ke D; Department of Cardiology, Fujian Medical University Union Hospital, 350001 Fuzhou, Fujian, China.
  • He X; Fujian Institute of Coronary Artery Disease, 350001 Fuzhou, Fujian, China.
  • Chen C; Department of Cardiology, Fujian Medical University Union Hospital, 350001 Fuzhou, Fujian, China.
  • Lin C; Fujian Institute of Coronary Artery Disease, 350001 Fuzhou, Fujian, China.
  • Luo Y; Department of Cardiology, Fujian Medical University Union Hospital, 350001 Fuzhou, Fujian, China.
  • Fan L; Fujian Institute of Coronary Artery Disease, 350001 Fuzhou, Fujian, China.
  • Li S; Department of Cardiology, Fujian Medical University Union Hospital, 350001 Fuzhou, Fujian, China.
  • Zheng X; Fujian Institute of Coronary Artery Disease, 350001 Fuzhou, Fujian, China.
  • Chen L; Department of Cardiology, Fujian Medical University Union Hospital, 350001 Fuzhou, Fujian, China.
Rev Cardiovasc Med ; 24(4): 99, 2023 Apr.
Article en En | MEDLINE | ID: mdl-39076266
ABSTRACT

Background:

Dual stenting technique (DST) is still mandatory for some true bifurcation lesions (BLs), but drug-coated balloon (DCB) alone may offer a new optional treatment with the potential benefits of fewer implants. However, procedural safety presents a concern when using DCB-only to treat true BLs. This study sought to explore the safety and efficacy of the DCB-only strategy for the treatment of true BLs.

Methods:

Sixty patients with TBLs were randomly assigned to be treated by a DCB-based strategy or DST-based strategy. All patients received angiographic follow-up scheduled after one-year and staged clinical follow-up. The primary endpoint was the one-year late lumen loss (LLL) and cumulative major cardiac adverse events (MACEs) composed of cardiac death (CD), target vessel myocardial infarction (TVMI), target lesion thrombosis (TVT), or target vessel/lesion revascularization (TLR/TVR). The secondary endpoint was the one-year minimal lumen diameter (MLD), diameter stenosis percentage (DSP) or binary restenosis (BRS), and each MACE component.

Results:

The baseline clinical and lesioncharacteristics were comparable with similar proportions (20.0% vs. 23.3%, p = 1.000) of the complex BLs between the two groups. At the one-year follow-up, LLL was significantly lower in the DCB-based group (main-vessel 0.05 ± 0.24 mm vs. 0.25 ± 0.35 mm, p = 0.013; side-branch -0.02 ± 0.19 mm vs. 0.11 ± 0.15 mm, p = 0.005). MLD, DSP and TLR/TVR were comparable between the groups. The one-year cumulative MACE, all driven by TLR/TVR (6.7% vs. 13.3%, p = 0.667), was low and similar without CD, TVMI or TVT in both groups.

Conclusions:

Compared to the DST strategy, the DCB- based strategy may be safe and effective in treatment of the selected true BLs. Clinical Trial Registration Clinical registration number is ChiCTR1900024914.
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