Clinical research: interventional cardiology
Cutting balloon versus conventional balloon angioplasty for the treatment of in-stent restenosis: Results of the restenosis cutting balloon evaluation trial (RESCUT)

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Abstract

Objectives

The aim of this trial was to compare cutting balloon angioplasty (CBA) with conventional balloon angioplasty (i.e., percutaneous transluminal coronary angioplasty [PTCA]) for the treatment of patients with coronary in-stent restenosis (ISR).

Background

Retrospective studies suggest CBA might be superior to conventional PTCA in the treatment of ISR.

Methods

The Restenosis Cutting Balloon Evaluation Trial (RESCUT) is a multicenter, randomized, prospective European trial including 428 patients with all types of ISR (e.g., focal, multifocal, diffuse, proliferative).

Results

In both groups, the majority of ISR lesions were shorter than 20 mm. The length of restenotic stents was similar (CBA: 18.6 ± 9.7 mm; PTCA: 18.3 ± 8.7 mm). The number of balloons used to treat ISR was lower in the CBA group: only one balloon was used in 82.3% of CBA cases, compared with 75% of PTCA procedures (p = 0.03). Balloon slippage was less frequent in the CBA group (CBA 6.5%, PTCA 25%; p < 0.01). There was a trend toward a lower need for additional stenting in the CBA group (CBA 3.9%, PTCA 8.0%; p = 0.07). At seven-month angiographic follow-up, the binary restenosis rate was not different between the groups (CBA 29.8%, PTCA 31.4%; p = 0.82), with a similar pattern of recurrent restenosis. Clinical events at seven months were also similar.

Conclusions

Cutting balloon angioplasty did not reduce recurrent ISR and major adverse cardiac events, as compared with conventional PTCA. However, CBA was associated with some procedural advantages, such as use of fewer balloons, less requirement for additional stenting, and a lower incidence of balloon slippage.

Abbreviations

CABG
coronary artery bypass graft surgery
CBA
cutting balloon angioplasty
CK
creatine kinase
%DS
percent diameter stenosis
ISR
in-stent restenosis
IVUS
intravascular ultrasound
MACE
major adverse cardiac events
MLD
minimum lumen diameter
PTCA
percutaneous transluminal coronary angioplasty
QCA
quantitative coronary angiography
RESCUT
Restenosis Cutting Balloon Evaluation Trial

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This study was supported by Boston Scientific Europe Corporation, Paris, France.