Key result
Treatment of in-stent restenosis with BTHC-PCB resulted in comparable 1-year rates of major adverse cardiac events compared to iopromide-based PCB (15.0% vs 15.8%, P=0.879).
Why the study?
Does butyryl-tri-hexyl citrate (BTHC) paclitaxel-coated balloon reduce major adverse cardiac events compared to iopromide-based paclitaxel-coated balloon in patients with in-stent restenosis?
Cohort (n=194)
No
Does butyryl-tri-hexyl citrate (BTHC) paclitaxel-coated balloon reduce major adverse cardiac events compared to iopromide-based paclitaxel-coated balloon in patients with in-stent restenosis?
Absolute Event Rate: 15% vs 15.8%
p-value: p=0.879
BTHC-based and iopromide-based paclitaxel-coated balloons show comparable 1-year and long-term clinical outcomes for the treatment of in-stent restenosis.
Comparable MACE rates with BTHC-PCB in ISR cohort; leaves open need for randomized confirmation before practice change.
BACKGROUND: Treatment of in-stent restenosis (ISR) is still a clinical challenge in interventional cardiology. Paclitaxel-coated balloons (PCBs) are an attractive therapeutic option for ISR. There are several different types of PCBs available for percutaneous coronary intervention, but to date, comparative data between different types of PCBs for the treatment of ISR are scarce. PATIENTS AND METHODS: This single centre, nonrandomized, retrospective study under real-world condition included 194 patients with 194 ISR treated by repeat percutaneous coronary intervention with PCBs. The primary end point was major adverse cardiac events (MACEs), defined as cardiac death, myocardial infarction and need for target lesion revascularization (TLR) at 1 year. Secondary end points were MACE and TLR at long-term follow-up. RESULTS: Baseline clinical and angiographic parameters were comparable between the two groups. Patients in the iopromide-based PCB and butyryl-tri-hexyl citrate (BTHC)-PCB groups were followed up for 32.2±20.5 and 24.2±13.3 months, respectively (P=0.001). MACEs at 1-year follow-up were 15.0 and 15.8% (P=0.879) for the BTHC-PCB and iopromide-based PCB groups, respectively. TLR, myocardial infarction and cardiac death for BTHC-PCB versus iopromide-based PCB at 1-year follow-up were 9.6 versus 11.8%, P=0.622; 5.3 versus 3.9%, P=0.640; and 5.3 versus 3.9%, P=0.640, respectively. If complete follow-up periods were included in the analysis, BTHC-PCB and iopromide-based PCB had comparable rates of MACE (P=0.835) and TLR (P=0.792). CONCLUSION: BTHC-PCB and iopromide-based PCB had comparable rates of MACE and TLR for the treatment of ISR at 1-year and long-term follow-up.
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Schröder et al. (2018) conducted a cohort in in-stent restenosis (ISR) (n=194). butyryl-tri-hexyl citrate (BTHC)-PCB vs. iopromide-based PCB was evaluated on major adverse cardiac events (MACEs), defined as cardiac death, myocardial infarction and need for target lesion revascularization (TLR) at 1 year (p=0.879). Treatment of in-stent restenosis with BTHC-PCB resulted in comparable 1-year rates of major adverse cardiac events compared to iopromide-based PCB (15.0% vs 15.8%, P=0.879).
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