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Propensity-Score Matched Comparison of Midterm Angiographic Outcomes of Sirolimus- Versus Everolimus- and Biolimus-Eluting Stents for De Novo Coronary Stenosis.
Suzuki, Kenichiro; Ishikawa, Tetsuya; Mutoh, Makoto; Sakamoto, Hiroshi; Mori, Chikara; Ogawa, Takayuki; Hashimoto, Koichi; Kubota, Takeyuki; Komukai, Kimiaki; Yoshimura, Michihiro.
Afiliação
  • Suzuki K; Division of Cardiology, Department of Internal Medicine, The Jikei University Kashiwa Hospital.
  • Ishikawa T; Division of Cardiology, Department of Internal Medicine, The Jikei University Kashiwa Hospital.
  • Mutoh M; Division of Cardiology, Saitama Cardiovascular Respiratory Center.
  • Sakamoto H; Division of Cardiology, Saitama Cardiovascular Respiratory Center.
  • Mori C; Division of Cardiology, Fuji City General Hospital.
  • Ogawa T; Division of Cardiology, Department of Internal Medicine, The Jikei University School of Medicine, Daisan Hospital.
  • Hashimoto K; Division of Cardiology, Department of Internal Medicine, The Jikei University School of Medicine.
  • Kubota T; Division of Cardiology, Nishisaitama-chuo National Hospital.
  • Komukai K; Division of Cardiology, Department of Internal Medicine, The Jikei University Kashiwa Hospital.
  • Yoshimura M; Division of Cardiology, Department of Internal Medicine, The Jikei University Kashiwa Hospital.
Int Heart J ; 58(3): 320-327, 2017 May 31.
Article em En | MEDLINE | ID: mdl-28484124
ABSTRACT
We conducted propensity-score matched comparisons of midterm angiographic outcomes of sirolimus (SES) versus either everolimus- (EES) or biolimus- (BES) eluting stents after placements for coronary stenosis in a daily practice environment since previous randomized trials did not demonstrate the superiority of EES and BES over SES in terms of midterm angiographic outcomes.The present study was a non-randomized, retrospective, and lesion-based study, recruiting angiographically followed-up lesions within 550 days after successful and elective SES (n = 1793), EES (n = 1303), or BES (n = 324) placement for de novo native coronary stenosis during the period from August 2004 to January 2014 at 6 institutes. The endpoint, as an angiographic surrogate marker of clinical efficacy, was the distribution of in-stent follow-up percent diameter stenosis (%DS) which comprised the percentages of 1) follow-up %DS < 20 and 2) follow-up %DS > 50. Propensityscore matched analyses were conducted to adjust 21 baselines.In 1215 baseline adjusted lesions, the endpoints in the EES group [1) 74.1%, and 2) 4.6%] were significantly different from those in the SES group [57.9%; P < 0.001, 7.2%; P = 0.006, respectively). In 307 baseline adjusted lesions, the endpoints in the BES group [1) 80.5%, 2) 2.0%] were significantly different from those in the SES group [59.3%; P < 0.001, 2) 8.1%; P = 0.001, respectively].The present study is the first to confirm the superiority of midterm angiographic outcomes after the placement of EES and BES over SES for de novo coronary stenosis in a clinical setting.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Angiografia Coronária / Vasos Coronários / Sirolimo / Estenose Coronária / Stents Farmacológicos / Intervenção Coronária Percutânea / Everolimo Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Angiografia Coronária / Vasos Coronários / Sirolimo / Estenose Coronária / Stents Farmacológicos / Intervenção Coronária Percutânea / Everolimo Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article