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Optimal Medical Therapy in Patients with Malignancy Undergoing Percutaneous Coronary Intervention for Acute Coronary Syndrome: a BleeMACS Sub-Study.
Iannaccone, Mario; D Ascenzo, Fabrizio; De Filippo, Ovidio; Gagliardi, Marco; Southern, Danielle A; Raposeiras-Roubín, Sergio; Abu-Assi, Emad; Henriques, Jose Paulo Simao; Saucedo, Jorge; González-Juanatey, José Ramón; Wilton, Stephen B; Kikkert, Wouter J; Nuñez-Gil, Iván; Ariza-Sole, Albert; Song, Xiantao; Alexopoulos, Dimitrios; Liebetrau, Christoph; Kawaji, Tetsuma; Huczek, Zenon; Nie, Shao-Ping; Fujii, Toshiharu; Correia, Luis; Kawashiri, Masa-Aki; García-Acuña, José María; Alfonso, Emilio; Terol, Belén; Garay, Alberto; Zhang, Dongfeng; Chen, Yalei; Xanthopoulou, Ioanna; Osman, Neriman; Möllmann, Helge; Shiomi, Hiroki; Kowara, Michal; Filipiak, Krzysztof; Wang, Xiao; Yan, Yan; Fan, Jing-Yao; Ikari, Yuji; Nakahashi, Takuya; Sakata, Kenji; Yamagishi, Masakazu; Moretti, Claudio; Gaita, Fiorenzo; Kalpak, Oliver; Kedev, Sasko.
Afiliación
  • Iannaccone M; Divisione di Cardiologia, Dipartimento di Scienze Mediche, Città della Salute e della Scienza, Turin, Italy. mario.iannaccone@hotmail.it.
  • D Ascenzo F; Divisione di Cardiologia, Dipartimento di Scienze Mediche, Città della Salute e della Scienza, Turin, Italy.
  • De Filippo O; Divisione di Cardiologia, Dipartimento di Scienze Mediche, Città della Salute e della Scienza, Turin, Italy.
  • Gagliardi M; Divisione di Cardiologia, Dipartimento di Scienze Mediche, Città della Salute e della Scienza, Turin, Italy.
  • Southern DA; Libin Cardiovascular Institute of Alberta and Institute for Public Health, Calgary, AB, Canada.
  • Raposeiras-Roubín S; University Clinical Hospital, Santiago de Compostela, Spain.
  • Abu-Assi E; University Clinical Hospital, Santiago de Compostela, Spain.
  • Henriques JPS; University Academic Medical Center, Amsterdam, The Netherlands.
  • Saucedo J; NorthShore University Hospital, Chicago, IL, USA.
  • González-Juanatey JR; University Clinical Hospital, Santiago de Compostela, Spain.
  • Wilton SB; Libin Cardiovascular Institute of Alberta and Institute for Public Health, Calgary, AB, Canada.
  • Kikkert WJ; University Academic Medical Center, Amsterdam, The Netherlands.
  • Nuñez-Gil I; San Carlos Hospital, Madrid, Spain.
  • Ariza-Sole A; Bellvitge Hospital, Barcelona, Spain.
  • Song X; Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
  • Alexopoulos D; University Patras Hospital, Athens, Greece.
  • Liebetrau C; Kerckhoff Heart and Thorax Center, Frankfurt, Germany.
  • Kawaji T; University Clinical Hospital, Kyoto, Japan.
  • Huczek Z; University Clinical Hospital, Warsaw, Poland.
  • Nie SP; Institute of Heart, Lung and Blood Vessel Disease, Beijing, China.
  • Fujii T; Tokai University School of Medicine, Tokyo, Japan.
  • Correia L; Hospital Sao Rafael, Salvador, Brazil.
  • Kawashiri MA; Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
  • García-Acuña JM; Divisione di Cardiologia, Dipartimento di Scienze Mediche, Città della Salute e della Scienza, Turin, Italy.
  • Alfonso E; San Carlos Hospital, Madrid, Spain.
  • Terol B; San Carlos Hospital, Madrid, Spain.
  • Garay A; Bellvitge Hospital, Barcelona, Spain.
  • Zhang D; Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
  • Chen Y; Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
  • Xanthopoulou I; University Patras Hospital, Athens, Greece.
  • Osman N; Kerckhoff Heart and Thorax Center, Frankfurt, Germany.
  • Möllmann H; Kerckhoff Heart and Thorax Center, Frankfurt, Germany.
  • Shiomi H; University Clinical Hospital, Kyoto, Japan.
  • Kowara M; University Clinical Hospital, Warsaw, Poland.
  • Filipiak K; University Clinical Hospital, Warsaw, Poland.
  • Wang X; Institute of Heart, Lung and Blood Vessel Disease, Beijing, China.
  • Yan Y; Institute of Heart, Lung and Blood Vessel Disease, Beijing, China.
  • Fan JY; Institute of Heart, Lung and Blood Vessel Disease, Beijing, China.
  • Ikari Y; Tokai University School of Medicine, Tokyo, Japan.
  • Nakahashi T; Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
  • Sakata K; Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
  • Yamagishi M; Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
  • Moretti C; Divisione di Cardiologia, Dipartimento di Scienze Mediche, Città della Salute e della Scienza, Turin, Italy.
  • Gaita F; Divisione di Cardiologia, Dipartimento di Scienze Mediche, Città della Salute e della Scienza, Turin, Italy.
  • Kalpak O; University Clinic of Cardiology, Skopje, Macedonia.
  • Kedev S; University Clinic of Cardiology, Skopje, Macedonia.
Am J Cardiovasc Drugs ; 17(1): 61-71, 2017 Feb.
Article en En | MEDLINE | ID: mdl-27738920
ABSTRACT

OBJECTIVE:

Our objective was to define the most appropriate treatment for acute coronary syndrome (ACS) in patients with malignancy. METHODS AND

RESULTS:

The BleeMACS project is a worldwide multicenter observational prospective registry in 16 hospitals enrolling patients with ACS undergoing percutaneous coronary intervention. Primary endpoints were death, re-infarction, and major adverse cardiac events (MACE; composite of death and re-infarction) after 1 year of follow-up. The secondary endpoint was bleeding events during follow-up. We performed sub-study analyses according to whether ß-blockers (BBs), angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs), statins, or proton pump inhibitors (PPIs) were prescribed at discharge. We also calculated the propensity score for optimal medical therapy (OMT; combination of BB, ACEI/ARB, and statins). The study included 926 patients. According to the multivariate analysis, ACEIs/ARBs (hazard ratio [HR] 0.58, 95 % confidence interval [CI] 0.36-1.94; p = 0.03) and statins (HR 0.37, 95 % CI 0.23-0.61; p < 0.01) reduced the risk of MACE, while the effects of BBs (HR 0.85, 95 % CI 0.55-1.32; p = 0.48) and PPIs (HR 1.33, 95 % CI 0.83-2.12; p = 0.23) were not significant. OMT was prescribed at discharge in 300 (32.4 %) patients; after propensity score analysis, OMT showed a significant reduction in death (3 % vs. 12.5 %, HR 0.21, 95 % CI 0.1-0.4; log-rank p < 0.001) and MACE (6.7 vs. 15.2 %, log-rank p = 0.01).

CONCLUSION:

In patients with ACS and malignancy, OMT reduces the risk of adverse events at 1 year; in particular, ACEIs/ARBs and statins were the most protective drugs. (Clinical trials identifier NCT02466854).
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Sistema de Registros / Síndrome Coronario Agudo / Intervención Coronaria Percutánea / Neoplasias Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Cardiovasc Drugs Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2017 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Asunto principal: Sistema de Registros / Síndrome Coronario Agudo / Intervención Coronaria Percutánea / Neoplasias Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Cardiovasc Drugs Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2017 Tipo del documento: Article País de afiliación: Italia