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Effect of evidence-based therapy for secondary prevention of cardiovascular disease: Systematic review and meta-analysis.
Ma, Tian-Tian; Wong, Ian C K; Man, Kenneth K C; Chen, Yang; Crake, Thomas; Ozkor, Muhiddin A; Ding, Ling-Qing; Wang, Zi-Xuan; Zhang, Lin; Wei, Li.
Afiliación
  • Ma TT; Research Department of Practice and Policy, UCL School of Pharmacy, London, United Kingdom.
  • Wong ICK; Research Department of Practice and Policy, UCL School of Pharmacy, London, United Kingdom.
  • Man KKC; Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Chen Y; Research Department of Practice and Policy, UCL School of Pharmacy, London, United Kingdom.
  • Crake T; Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Ozkor MA; UCL Institute of Cardiovascular Science, Univeristy College London, London, United Kingdom.
  • Ding LQ; Barts Heart Centre, St. Bartholomew's Hospital, West Smithfield, London, United Kingdom.
  • Wang ZX; Barts Heart Centre, St. Bartholomew's Hospital, West Smithfield, London, United Kingdom.
  • Zhang L; Department of Pharmacy, The Affiliated Cardiovascular Hospital of Xiamen University, Xiamen, China.
  • Wei L; Research Department of Practice and Policy, UCL School of Pharmacy, London, United Kingdom.
PLoS One ; 14(1): e0210988, 2019.
Article en En | MEDLINE | ID: mdl-30657781
BACKGROUND: The combination pharmacotherapy of antiplatelet agents, lipid-modifiers, ACE inhibitors/ARBs and beta-blockers are recommended by international guidelines. However, data on effectiveness of the evidence-based combination pharmacotherapy (EBCP) is limited. OBJECTIVES: To determine the effect of EBCP on mortality and Cardiovascular events in patients with Coronary Heart Disease (CHD) or cerebrovascular disease. METHODS: Publications in EMBASE and Medline up to October 2018 were searched for cohort and case-control studies on EBCP for the secondary prevention of cardiovascular disease. The main outcomes were all-cause mortality and major cardiovascular events. Meta-analyses were performed based on random effects models. RESULTS: 21 studies were included. Comparing EBCP to either monotherapy or no therapy, the pooled risk ratios were 0.60 (95% confidence interval 0.55 to 0.66) for all-cause mortality, 0.70 (0.62 to 0.79) for vascular mortality, 0.73 (0.64 to 0.83) for myocardial infarction and 0.79 (0.68 to 0.91) for cerebrovascular events. Optimal EBCP (all 4 classes of drug prescribed) had a risk ratio for all-cause mortality of 0.50 (0.40 to 0.64). This benefit became more dilute as the number of different classes of drug comprising EBCP was decreased-for 3 classes of drug prescribed the risk ratio was 0.58 (0.49 to 0.69) and for 2 classes, the risk ratio was 0.67 (0.60 to 0.76). CONCLUSIONS: EBCP reduces the risk of all-cause mortality and cardiovascular events in patients with CHD or cerebrovascular disease. The different classes of drugs comprising EBCP work in an additive manner, with optimal EBCP conferring the greatest benefit.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares Tipo de estudio: Guideline / Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares Tipo de estudio: Guideline / Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido