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Prevention of hypertension in patients with pre-hypertension: Protocol for the PREVER-prevention trial

dc.contributor.authorFuchs, Flávio D.
dc.contributor.authorFuchs, Sandra C.
dc.contributor.authorMoreira, Leila B.
dc.contributor.authorGus, Miguel
dc.contributor.authorNóbrega, Antônio C.
dc.contributor.authorPoli-de-Figueiredo, Carlos E.
dc.contributor.authorMion, Décio
dc.contributor.authorBortoloto, Luiz
dc.contributor.authorConsolim-Colombo, Fernanda
dc.contributor.authorNobre, Fernando
dc.contributor.authorCoelho, Eduardo B.
dc.contributor.authorVilela-Martin, José F.
dc.contributor.authorMoreno Jr, Heitor
dc.contributor.authorCesarino, Evandro J.
dc.contributor.authorFranco, Roberto [UNESP]
dc.contributor.authorBrandão, Andréa A.
dc.contributor.authorde Sousa, Marcos R.
dc.contributor.authorRibeiro, Antônio L.P.
dc.contributor.authorJardim, Paulo C.
dc.contributor.authorNeto, Abrahão A.
dc.contributor.authorScala, Luiz C.N.
dc.contributor.authorMota, Marco
dc.contributor.authorChaves, Hilton
dc.contributor.authorAlves, João G.
dc.contributor.authorFilho, Dario C.S.
dc.contributor.authorPereira e Silva, Ricardo
dc.contributor.authorNeto, José A.F.
dc.contributor.authorIrigoyen, Maria C.
dc.contributor.authorCastro, Iran
dc.contributor.authorSteffens, André A.
dc.contributor.authorSchlatter, Rosane
dc.contributor.authorde Mello, Renato B.
dc.contributor.authorMosele, Francisca
dc.contributor.authorGhizzoni, Flávia
dc.contributor.authorBerwanger, Otávio
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)
dc.contributor.institutionUniversidade Federal Fluminense (UFF)
dc.contributor.institutionPontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionFaculdade de Medicina São José do Rio Preto
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade do Estado do Rio de Janeiro (UERJ)
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionUniversidade Federal de Goiás (UFG)
dc.contributor.institutionAnis Rassi Hospital
dc.contributor.institutionUniversidade Federal de Mato Grosso
dc.contributor.institutionUniversidade de Ciências da Saúde Alagoas
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)
dc.contributor.institutionInstituto de Medicina Integral Prof Fernando Figueira
dc.contributor.institutionUniversidade de Pernambuco
dc.contributor.institutionUniversidade Federal do Ceará (UFC)
dc.contributor.institutionUniversidade Federal Maranhão
dc.contributor.institutionFundação Universitária de Cardiologia
dc.contributor.institutionUniversidade Federal de Pelotas (UFPEL)
dc.contributor.institutionHospital do Coração
dc.date.accessioned2014-05-27T11:25:30Z
dc.date.available2014-05-27T11:25:30Z
dc.date.issued2011-03-05
dc.description.abstractBackground: Blood pressure (BP) within pre-hypertensive levels confers higher cardiovascular risk and is an intermediate stage for full hypertension, which develops in an annual rate of 7 out of 100 individuals with 40 to 50 years of age. Non-drug interventions to prevent hypertension have had low effectiveness. In individuals with previous cardiovascular disease or diabetes, the use of BP-lowering agents reduces the incidence of major cardiovascular events. In the absence of higher baseline risk, the use of BP agents reduces the incidence of hypertension. The PREVER-prevention trial aims to investigate the efficacy, safety and feasibility of a population-based intervention to prevent the incidence of hypertension and the development of target-organ damage.Methods: This is a randomized, double-blind, placebo-controlled clinical trial, with participants aged 30 to 70 years, with pre-hypertension. The trial arms will be chlorthalidone 12.5 mg plus amiloride 2.5 mg or identical placebo. The primary outcomes will be the incidence of hypertension, adverse events and development or worsening of microalbuminuria and of left ventricular hypertrophy in the EKG. The secondary outcomes will be fatal or non-fatal cardiovascular events: myocardial infarction, stroke, heart failure, evidence of new sub-clinical atherosclerosis, and sudden death. The study will last 18 months. The sample size was calculated on the basis of an incidence of hypertension of 14% in the control group, a size effect of 40%, power of 85% and P alpha of 5%, resulting in 625 participants per group. The project was approved by the Ethics committee of each participating institution.Discussion: The early use of blood pressure-lowering drugs, particularly diuretics, which act on the main mechanism of blood pressure rising with age, may prevent cardiovascular events and the incidence of hypertension in individuals with hypertension. If this intervention shows to be effective and safe in a population-based perspective, it could be the basis for an innovative public health program to prevent hypertension in Brazil.Trial Registration: Clinical Trials NCT00970931. © 2011 Fuchs et al; licensee BioMed Central Ltd.en
dc.description.affiliationHospital de Clínicas de Porto Alegre Universidade Federal do Rio Grande do Sul, Porto Alegre
dc.description.affiliationHospital Universitário Antônio Pedro Universidade Federal Fluminense, Niterói
dc.description.affiliationHospital São Lucas Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre
dc.description.affiliationHospital das Clinicas Universidade de São Paulo, São Paulo
dc.description.affiliationInstituto do Coração Universidade de São Paulo, São Paulo
dc.description.affiliationFaculdade de Medicina de Ribeirão Preto Universidade de São Paulo, Ribeirão Preto
dc.description.affiliationFaculdade de Medicina São José do Rio Preto, São José do Rio Preto
dc.description.affiliationFaculdade de Ciências Médicas Universidade de Campinas, Campinas
dc.description.affiliationFaculdade de Ciências Farmacêuticas Universidade de São Paulo, Ribeirão Preto
dc.description.affiliationFaculdade de Medicina de Botucatu Universidade Estadual de São Paulo, Botucatu
dc.description.affiliationUniversidade do Estado do Rio de Janeiro, Rio de Janeiro
dc.description.affiliationHospital das Clínicas Universidade Federal de Minas Gerais, Belo Horizonte
dc.description.affiliationHospital das Clínicas de Goiânia Universidade Federal de Goiás, Goiânia
dc.description.affiliationAnis Rassi Hospital, Goiânia
dc.description.affiliationHospital Universitário Júlio Muller Universidade Federal de Mato Grosso, Cuiabá
dc.description.affiliationFaculdade de Medicina Universidade de Ciências da Saúde Alagoas, Maceió
dc.description.affiliationFaculdade de Medicina Universidade Federal de Pernambuco, Recife
dc.description.affiliationInstituto de Medicina Integral Prof Fernando Figueira, Recife
dc.description.affiliationHospital Universitário Oswaldo Cruz/PROCAPE Universidade de Pernambuco, Recife
dc.description.affiliationHospital Universitário Valter Cantídio Universidade Federal do Ceará, Fortaleza
dc.description.affiliationHospital Universitário Universidade Federal Maranhão, São Luiz
dc.description.affiliationInstituto de Cardiologia Fundação Universitária de Cardiologia, Porto Alegre
dc.description.affiliationFaculdade de Medicina Universidade Federal de Pelotas, Pelotas
dc.description.affiliationHospital do Coração, São Paulo
dc.description.affiliationUnespFaculdade de Medicina de Botucatu Universidade Estadual de São Paulo, Botucatu
dc.identifierhttp://dx.doi.org/10.1186/1745-6215-12-65
dc.identifier.citationTrials, v. 12, n. 65.
dc.identifier.doi10.1186/1745-6215-12-65
dc.identifier.file2-s2.0-79952197520.pdf
dc.identifier.issn1745-6215
dc.identifier.scopus2-s2.0-79952197520
dc.identifier.urihttp://hdl.handle.net/11449/72338
dc.language.isoeng
dc.relation.ispartofTrials
dc.relation.ispartofjcr2.067
dc.relation.ispartofsjr1,291
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectamiloride
dc.subjectbeta adrenergic receptor blocking agent
dc.subjectchlortalidone
dc.subjectdipeptidyl carboxypeptidase inhibitor
dc.subjectdiuretic agent
dc.subjecthydrochlorothiazide
dc.subjectatherosclerosis
dc.subjectblood pressure measurement
dc.subjectcardiovascular risk
dc.subjectclinical protocol
dc.subjectcost effectiveness analysis
dc.subjectdiabetes mellitus
dc.subjectdouble blind procedure
dc.subjectdrug efficacy
dc.subjectdrug safety
dc.subjectheart infarction
dc.subjectheart left ventricle hypertrophy
dc.subjecthypertension
dc.subjecthypokalemia
dc.subjectinsulin resistance
dc.subjectischemic heart disease
dc.subjectlow drug dose
dc.subjectmicroalbuminuria
dc.subjectobesity
dc.subjectoutcome assessment
dc.subjectprehypertension
dc.subjectrandomized controlled trial
dc.subjectsodium restriction
dc.subjectsudden death
dc.subjectvascular disease
dc.titlePrevention of hypertension in patients with pre-hypertension: Protocol for the PREVER-prevention trialen
dc.typeArtigopt
dcterms.licensehttp://www.biomedcentral.com/about/license
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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