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Rationale, design, methods and baseline demography of participants of the Anglo-Scandinavian Cardiac Outcomes Trial. ASCOT investigators.
Sever, P S; Dahlöf, B; Poulter, N R; Wedel, H; Beevers, G; Caulfield, M; Collins, R; Kjeldsen, S E; McInnes, G T; Mehlsen, J; Nieminen, M; O'Brien, E; Ostergren, J.
Afiliação
  • Sever PS; Imperial College School of Medicine, London, UK. p.sever@ic.ac.uk
J Hypertens ; 19(6): 1139-47, 2001 Jun.
Article em En | MEDLINE | ID: mdl-11403364
ABSTRACT

OBJECTIVE:

To test the primary hypothesis that a newer antihypertensive treatment regimen (calcium channel blocker +/- an angiotensin converting enzyme inhibitor) is more effective than an older regimen (beta-blocker +/- a diuretic) in the primary prevention of coronary heart disease (CHD). To test a second primary hypothesis that a statin compared with placebo will further protect against CHD endpoints in hypertensive subjects with a total cholesterol < or = 6.5 mmol/l.

DESIGN:

Prospective, randomized, open, blinded endpoint trial with a double-blinded 2 x 2 factorial component.

SETTING:

Patients were recruited mainly from general practices. PATIENTS Men and women aged 40-79 were eligible if their blood pressure was > or = 160 mmHg systolic or > or = 100 mmHg diastolic (untreated) or > or = 140 mmHg systolic or > or = 90 mmHg diastolic (treated) at randomization.

INTERVENTIONS:

Patients received either amlodipine (5/ 10 mg) +/- perindopril (4/8 mg) or atenolol (50/ 100 mg) +/- bendroflumethiazide (1.25/2.5 mg) +K+ with further therapy as required to reach a blood pressure of < or = 140 mmHg systolic and 90 mmHg diastolic. Patients with a total cholesterol of < or = 6.5 mmol/l were further randomized to receive either atorvastatin 10 mg or placebo daily. MAIN OUTCOME

MEASURE:

Non-fatal myocardial infarction (MI) and fatal coronary heart disease (CHD).

RESULTS:

19 342 men and women were initially randomized, of these 10297 were also randomized into the lipid-lowering limb. All patients had three or more additional cardiovascular risk factors.

CONCLUSIONS:

The study has 80% power (at the 5% level) to detect a relative difference of 20% in CHD endpoints between the calcium channel blocker-based regimen and the beta-blocker-based regimen. The lipid-lowering limb of the study has 90% power at the 1% level to detect a relative difference of 30% in CHD endpoints between groups.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença das Coronárias / Hipertensão Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: J Hypertens Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Reino Unido
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença das Coronárias / Hipertensão Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: J Hypertens Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Reino Unido