Your browser doesn't support javascript.
loading
Rivaroxaban Plus Aspirin in Obese and Overweight Patients With Vascular Disease in the COMPASS Trial.
Guzik, Tomasz J; Ramasundarahettige, Chinthanie; Pogosova, Nana; Lopez-Jaramillo, Patricio; Dyal, Leanne; Berkowitz, Scott D; Muehlhofer, Eva; Bhatt, Deepak L; Fox, Keith A A; Yusuf, Salim; Eikelboom, John W.
Afiliação
  • Guzik TJ; British Heart Foundation Centre for Cardiovascular Research, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom; Department of Internal and Agricultural Medicine, Jagiellonian University, Collegium Medicum, Krakow, Poland. Electronic address: tomasz.guzi
  • Ramasundarahettige C; Population Health Research Institute, McMaster University, Hamilton Health Sciences, Hamilton, Ontario, Canada; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Pogosova N; National Medical Research Center of Cardiology, Moscow, Russia.
  • Lopez-Jaramillo P; Masira Research Institute, Universidad de Santander (UDES), Bucaramanga, Colombia.
  • Dyal L; Population Health Research Institute, McMaster University, Hamilton Health Sciences, Hamilton, Ontario, Canada; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Berkowitz SD; Clinical Development, Group Head Thrombosis, Bayer U.S. LLC, Research & Development, Pharmaceuticals, Thrombosis & Hematology Therapeutic Area, Whippany, New Jersey, USA.
  • Muehlhofer E; Bayer AG, Research & Development, Pharmaceuticals, Therapeutic Area Thrombosis & Vascular Medicine, Wuppertal, Germany.
  • Bhatt DL; Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Fox KAA; Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
  • Yusuf S; Population Health Research Institute, McMaster University, Hamilton Health Sciences, Hamilton, Ontario, Canada; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Eikelboom JW; Population Health Research Institute, McMaster University, Hamilton Health Sciences, Hamilton, Ontario, Canada; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
J Am Coll Cardiol ; 77(5): 511-525, 2021 02 09.
Article em En | MEDLINE | ID: mdl-33538248
ABSTRACT

BACKGROUND:

Direct oral anticoagulants are administered in fixed doses irrespective of body weight, but guidelines recommend against their use in patients with extremes of body weight.

OBJECTIVES:

This study determined the effects of dual-pathway inhibition antithrombotic regimen (rivaroxaban 2.5 mg twice daily plus aspirin 100 mg/day) compared with aspirin Halone across a range of patient body mass indexes (BMIs) and body weights.

METHODS:

This was a secondary analysis of the COMPASS (Cardiovascular OutcoMes for People using Anticoagulation StrategieS) trial, which included patients with chronic coronary artery disease or peripheral artery disease. Efficacy and safety outcomes were studied in relation to BMI (normal 18.5 ≤BMI <25 kg/m2, overweight 25 ≤BMI <30 kg/m2, obese ≥30 kg/m2) and body weight (≤70 kg, 70 < weight ≤90 kg, and >90 kg; as well as ≤120 kg vs. >120 kg).

RESULTS:

Among 27,395 randomized patients, 6,459 (24%) had normal BMI, 12,047 (44%) were overweight, and 8,701 (32%) were obese. The combination of rivaroxaban and aspirin compared with aspirin produced a consistent reduction in the primary outcome of cardiovascular death, stroke, or myocardial infarction, irrespective of BMI or body weight. For 18.5 ≤BMI <25 kg/m2 3.5% vs. 5.0%; hazard ratio (HR) 0.73 (95% credible interval [CrI] 0.58 to 0.90); 25 ≤ BMI <30 kg/m2 4.3% vs. 5.1%; HR 0.80 (95% CrI 0.66 to 0.96); BMI ≥30 kg/m2 4.2% vs. 6.1%; HR 0.71 (95% CrI 0.57 to 0.86). For body weight ≤70 kg 4.1% vs. 5.3%; HR 0.75 (95% CrI 0.62 to 0.91); 70 < weight ≤90 kg 4.1% vs. 5.3%; HR 0.76 (95% CrI 0.65 to 0.89); >90 kg 4.2% vs. 5.7%; HR 0.74 (95% CrI 0.61 to 0.90). Effects on bleeding, mortality, and net clinical benefit were consistent irrespective of BMI or bodyweight.

CONCLUSIONS:

The effects of dual-pathway antithrombotic therapy are consistent irrespective of BMI or body weight, suggesting no need for dose adjustments in the ranges of weights and BMI of patients enrolled in the COMPASS trial. Further studies need to address this problem in relation to greater extremes of body weight. (Rivaroxaban for the Prevention of Major Cardiovascular Events in Coronary or Peripheral Artery Disease [COMPASS]; NCT01776424).
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Índice de Massa Corporal / Aspirina / Sobrepeso / Rivaroxabana / Obesidade Tipo de estudo: Clinical_trials / Etiology_studies / Guideline Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Índice de Massa Corporal / Aspirina / Sobrepeso / Rivaroxabana / Obesidade Tipo de estudo: Clinical_trials / Etiology_studies / Guideline Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article