Volume 58, Issue 3 pp. 322-329
Coronary Artery Disease

Intracoronary beta-brachytherapy in chronic total occlusions: A subgroup analysis from the RENO registry

Deepak Jain MD

Corresponding Author

Deepak Jain MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

Medizinische Klinik II, Universitätsklinikum Lübeck, Ratzeburger Allee 160, D-23538 Lübeck, GermanySearch for more papers by this author
Volker Geist MD

Volker Geist MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

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Hans-Peter Lorenzen MD

Hans-Peter Lorenzen MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

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Franz Hartmann MD

Franz Hartmann MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

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Karl Wegscheider MD

Karl Wegscheider MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

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Raoul Bonan MD

Raoul Bonan MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

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Philip Urban MD

Philip Urban MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

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Gert Richardt MD

Gert Richardt MD

Medizinische Klinik II, Universitätsklinikum Lübeck, Lübeck, Germany

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First published: 19 February 2003
Citations: 5

Abstract

Conventional interventional therapy has been less rewarding in chronic total occlusion (CTO). Brachytherapy by its antiproliferative and positive remodeling effect may be more efficacious. Forty-six centers registered 1,098 consecutive patients undergoing brachytherapy with the BetaCath system. Of these, 78 patients had 82 lesions (CTO) at presentation—the study population. With 67% in-stent CTO, 8% graft CTO, 4% recurrent CTO, long lesions (27.6 ± 20.9 mm), and 31% diabetes, the cohort had high risk for recurrence. The in-hospital event rate was 1.3%. Six-month follow-up revealed 1.3% death, 5.1% myocardial infarction, 21.8% target vessel revascularization, 77.8% improved angina, 34.5% binary restenosis, 12.7% reocclusion, and 10.3% late thrombosis. The results were comparable to all other patients in the registry, although late thrombosis rate was higher in the CTO group (10.3% vs. 5.0%; P = 0.047). In the in-stent CTO subgroup (n = 52; 66.7%), there was no in-hospital event, no follow-up death or myocardial infarction, restenosis in 35.1%, and reocclusion in 10.8% of patients. In comparison, death or myocardial infarction was significantly higher in de novo CTO subgroup (P = 0.005). Compared to all other in-stent restenosis patients in the registry, the patients with in-stent CTO had similar clinical and angiographic event rate. Thus, beta-brachytherapy was safe, feasible, and effective in this broad population of high-risk patients with CTO presenting in day-to-day practice. It was particularly effective in in-stent CTO, where conventional interventional strategies are disappointing. Cathet Cardiovasc Intervent 2003;58:322–329. © 2003 Wiley-Liss, Inc.

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