TY - JOUR
T1 - Sub-analysis of perfusion balloon predilatation with intracoronary nicorandil vs. distal protection for acute coronary syndrome
T2 - A comparative evaluation
AU - Yoshinaga, Masataka
AU - Muramatsu, Takashi
AU - Uwatoko, Takashi
AU - Miyazaki, Akane
AU - Toriya, Takuo
AU - Matsuwaki, Yuji
AU - Ishikawa, Masato
AU - Ukai, Yuko
AU - Kobayashi, Yohei
AU - Ito, Katsuyoshi
AU - Ota, Hideaki
AU - Sobue, Yoshihiro
AU - Watanabe, Eiichi
AU - Izawa, Hideo
N1 - Publisher Copyright:
© 2026 Masataka Yoshinaga, MD, PhD et al.
PY - 2026
Y1 - 2026
N2 - Objectives: Slow-flow or no-reflow events occur as a complication during percutaneous coronary intervention for acute coronary syndrome (ACS). A previous study demonstrated that prolonged perfusion balloon (PB) predilatation combined with intracoronary administration of nicorandil attenuates this phenomenon. This subanalysis compared the efficacy of the PB approach with that of conventional distal protection (DP). Methods: The study had a retrospective, single-center, observational design and included patients who underwent percutaneous coronary intervention for ACS between April 2020 and April 2022. The patients were divided into a PB group and a DP group. The PB group underwent thrombus aspiration, followed by 3 minutes of predilatation using the Ryusei® PB, with simultaneous intracoronary administration of nicorandil 2 mg without a DP device and subsequent placement of a drug-eluting stent. The DP group underwent direct stenting or predilatation with a standard balloon combined with a DP device without a PB. Primary endpoints included the incidence of slow-flow or no-reflow events. Results: Sixty-four patients with ACS were enrolled (PB group, n=32; DP group, n=32). The incidence of slow-flow or no-reflow events was significantly lower in the PB group (3.1% vs. 46.8%, p<0.01), as was procedure time (87.1±26.4 minutes vs. 108.6±42.3 minutes, p=0.02) and volume of contrast used (186.0±65.0 mL vs. 228±75.8 mL, p=0.02). Conclusions: PB predilatation with intracoronary nicorandil significantly reduced the number of slow-flow or no-reflow events, shortened procedure time, and reduced the volume of contrast used. This method could be at least as effective as DP.
AB - Objectives: Slow-flow or no-reflow events occur as a complication during percutaneous coronary intervention for acute coronary syndrome (ACS). A previous study demonstrated that prolonged perfusion balloon (PB) predilatation combined with intracoronary administration of nicorandil attenuates this phenomenon. This subanalysis compared the efficacy of the PB approach with that of conventional distal protection (DP). Methods: The study had a retrospective, single-center, observational design and included patients who underwent percutaneous coronary intervention for ACS between April 2020 and April 2022. The patients were divided into a PB group and a DP group. The PB group underwent thrombus aspiration, followed by 3 minutes of predilatation using the Ryusei® PB, with simultaneous intracoronary administration of nicorandil 2 mg without a DP device and subsequent placement of a drug-eluting stent. The DP group underwent direct stenting or predilatation with a standard balloon combined with a DP device without a PB. Primary endpoints included the incidence of slow-flow or no-reflow events. Results: Sixty-four patients with ACS were enrolled (PB group, n=32; DP group, n=32). The incidence of slow-flow or no-reflow events was significantly lower in the PB group (3.1% vs. 46.8%, p<0.01), as was procedure time (87.1±26.4 minutes vs. 108.6±42.3 minutes, p=0.02) and volume of contrast used (186.0±65.0 mL vs. 228±75.8 mL, p=0.02). Conclusions: PB predilatation with intracoronary nicorandil significantly reduced the number of slow-flow or no-reflow events, shortened procedure time, and reduced the volume of contrast used. This method could be at least as effective as DP.
KW - Acute coronary syndrome
KW - Complication
KW - Percutaneous coronary intervention
KW - Perfusion balloon
KW - Slow-flow
UR - https://www.scopus.com/pages/publications/105029733595
UR - https://www.scopus.com/pages/publications/105029733595#tab=citedBy
U2 - 10.20407/fmj.2025-009
DO - 10.20407/fmj.2025-009
M3 - Article
AN - SCOPUS:105029733595
SN - 2189-7247
VL - 12
SP - 50
EP - 59
JO - Fujita Medical Journal
JF - Fujita Medical Journal
IS - 1
ER -