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A multicenter randomized comparison of paclitaxel-coated balloon catheter with conventional balloon angioplasty in patients with bare-metal stent restenosis and drug-eluting stent restenosis - 07/09/13

Doi : 10.1016/j.ahj.2013.07.002 
Seiji Habara, MD a, , Masashi Iwabuchi, MD b, Naoto Inoue, MD c, Shigeru Nakamura, MD d, Ryuta Asano, MD e, Shinsuke Nanto, MD f, Yasuhiko Hayashi, MD g, Nobuo Shiode, MD g, Shigeru Saito, MD h, Yuji Ikari, MD i, Takeshi Kimura, MD j, Joji Hosokawa, MD k, Masato Nakamura, MD l, Jun-ichi Kotani, MD m, Ken Kozuma, MD n, Kazuaki Mitsudo, MD a
a Department of Cardiology, Kurashiki Central Hospital, Kurashiki, Japan 
b Kokura Memorial Hospital,Kitakyushu, Japan 
c Sendai Kousei Hospital, Sendai, Japan 
d Kyoto-Katsura Hospital, Kyoto, Japan 
e Sakakibara Heart Institute, Tokyo, Japan 
f Osaka University Graduate School of Medicine, Osaka, Japan 
g Tsuchiya General Hospital, Hiroshima, Japan 
h Shonan Kamakura General Hospital, Kamakura, Japan 
i Tokai University Hospital, Isehara, Japan 
j Kyoto University, Kyoto, Japan 
k Tokyo Heart Center, Tokyo, Japan 
l Toho University Ohashi Medical Center, Tokyo, Japan 
m National Cardiovascular Center, Suita, Japan 
n Teikyo University Hospital, Tokyo, Japan 

Reprint requests: Seiji Habara, MD, Department of Cardiology, Kurashiki Central Hospital, 1-1-1 Miwa, Kurashiki-shi, Okayama 710-8602, Japan.

Riassunto

Background

The aim of this study was to investigate the efficacy and safety of paclitaxel-coated balloon (PCB) for the treatment of the bare-metal stent restenosis (BMS-ISR) and drug-eluting stent restenosis (DES-ISR).

Methods

This study was a prospective, multicenter, randomized (2:1) trial conducted in 208 patients with 213 in-stent restenosis lesions (BMS-ISR: 123 lesions, DES-ISR: 90 lesions) at 13 centers in Japan. Patients were randomly assigned to a PCB group (137 patients with 142 lesions) or a conventional balloon angioplasty (BA) group (71 patients with 71 lesions). The primary end point was target vessel failure at 6-month follow-up.

Results

Clinical and angiographic follow-up 6 months after intervention was performed in 207 patients (99.5%) with 208 lesions (97.7%). Target vessel failure was noted in 6.6% of the PCB group and 31.0% of the BA group (P < .001). Recurrent restenosis occurred in 4.3% of the PCB group and 31.9% of the BA group (P < .001). Late lumen loss was lower in the PCB group than in the BA group (0.11 ± 0.33 mm vs 0.49 ± 0.50 mm, P < .001). In PCB-treated lesions, recurrent restenosis occurred in 1.1% of patients with BMS-ISR and in 9.1% of patients with DES-ISR (P = .04). Late lumen loss was lower in patients with BMS-ISR than in patients with DES-ISR (0.05 ± 0.28 mm vs 0.18 ± 0.38 mm, P = .03).

Conclusions

This randomized clinical study suggested that PCB provided much better clinical and angiographic outcomes than did conventional BA in patients with BMS-ISR and DES-ISR. Drug-eluting stent restenosis was associated with poorer outcomes compared with BMS-ISR after treatment with PCB.

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 Randomized controlled trial registration no. UMIN000008681.


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P. 527 - settembre 2013 Ritorno al numero
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