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Combination therapy with nifedipine GITS 60 mg: subanalysis of a prospective, 12-week observational study (AdADOSE).
Motaweih, Ahmed K; Usova, Elena; Hussain, Wajid; Dello, Ziad; Petri, Thomas.
Afiliação
  • Motaweih AK; a Cardiovascular Medicine Department, Faculty of Medicine, Azhar University , Giza , Egypt .
  • Usova E; b Outpatient Department , Clinical Hospital 122 , Saint Petersburg , Russia .
  • Hussain W; c Department of Cardiology , Baqai Institute of Cardiovascular Diseases , Karachi , Pakistan .
  • Dello Z; d Department of Cardiology , Dallah Hospital , Riyadh , Saudi Arabia , and.
  • Petri T; e Global Medical Affairs Primary Care, Bayer Pharma AG , Berlin , Germany.
Clin Exp Hypertens ; 38(1): 71-80, 2016.
Article em En | MEDLINE | ID: mdl-26331311
BACKGROUND: AdADOSE was a 12-week, international, observational study conducted in the Middle East and Russia where patients received nifedipine gastrointestinal therapeutic system (GITS) at a daily dose of 30, 60, or 90 mg as part of an antihypertensive combination therapy. This subgroup analysis of the AdADOSE study assesses the efficacy and tolerability of nifedipine GITS combination therapy when used specifically at the 60-mg strength. METHODS: Patients with hypertension who received a daily nifedipine GITS dose of 60 mg, either at constant dose (n = 686) or up-titrated from 30 mg (n = 392), were analyzed. Target blood pressure (BP) was <140/90 mmHg (or <130/80 mmHg for those at high/very high cardiovascular risk). RESULTS: Following nifedipine GITS combination therapy, target BP was achieved by 33.7% patients in the 60 mg group (previously untreated, 42.5%; previously treated, 32.0%) and 32.4% patients in the 30-60 mg group (previously untreated, 45.2%; previously treated, 30.7%). Mean systolic BP/diastolic BP changes were -40.3/-20.7 mmHg and -35.6/-18.5 mmHg, respectively, and were similar regardless of previous antihypertensive treatment or the number of concomitant diseases. Incidences of drug-related adverse events (AEs) were low (3.2%, 60 mg; 2.0%, 30-60 mg group), few patients discontinued because of AEs (0.6% and 1.0%, respectively), and there were no serious AEs. CONCLUSION: Combination therapy with nifedipine GITS 60 mg in a real-life observational setting was effective and well tolerated in hypertensive patients, with low rates of treatment-related AEs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pressão Sanguínea / Nifedipino / Hipertensão Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia / Europa Idioma: En Revista: Clin Exp Hypertens Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pressão Sanguínea / Nifedipino / Hipertensão Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia / Europa Idioma: En Revista: Clin Exp Hypertens Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Egito