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A comparison between diuretics and angiotensin-receptor blocker agents in patients with stage I hypertension (PREVER-treatment trial): Study protocol for a randomized double-blind controlled 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.authorBortolotto, 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.authorPinho Ribeiro, Antônio L.
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.authorSobral Filho, Dario C.
dc.contributor.authore Silva, Ricardo P.
dc.contributor.authorFigueiredo Neto, José A.
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.institutionSão 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.accessioned2014-05-27T11:25:28Z
dc.date.available2014-05-27T11:25:28Z
dc.date.issued2011-02-24
dc.description.abstractBackground: Cardiovascular disease is the leading cause of death in Brazil, and hypertension is its major risk factor. The benefit of its drug treatment to prevent major cardiovascular events was consistently demonstrated. Angiotensin-receptor blockers (ARB) have been the preferential drugs in the management of hypertension worldwide, despite the absence of any consistent evidence of advantage over older agents, and the concern that they may be associated with lower renal protection and risk for cancer. Diuretics are as efficacious as other agents, are well tolerated, have longer duration of action and low cost, but have been scarcely compared with ARBs. A study comparing diuretic and ARB is therefore warranted.Methods/design: This is a randomized, double-blind, clinical trial, comparing the association of chlorthalidone and amiloride with losartan as first drug option in patients aged 30 to 70 years, with stage I hypertension. The primary outcomes will be variation of blood pressure by time, 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 subclinical atherosclerosis and sudden death. The study will last 18 months. The sample size will be of 1200 participants for group in order to confer enough power to test for all primary outcomes. The project was approved by the Ethics committee of each participating institution.Discussion: The putative pleiotropic effects of ARB agents, particularly renal protection, have been disputed, and they have been scarcely compared with diuretics in large clinical trials, despite that they have been at least as efficacious as newer agents in managing hypertension. Even if the null hypothesis is not rejected, the information will be useful for health care policy to treat hypertension in Brazil. Clinical trials registration number: ClinicalTrials.gov: NCT00971165. © 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/10.1186/1745-6215-12-53
dc.identifier.citationTrials, v. 12.
dc.identifier.doi10.1186/1745-6215-12-53
dc.identifier.file2-s2.0-79951956492.pdf
dc.identifier.issn1745-6215
dc.identifier.scopus2-s2.0-79951956492
dc.identifier.urihttp://hdl.handle.net/11449/72312
dc.language.isoeng
dc.relation.ispartofTrials
dc.relation.ispartofjcr2.067
dc.relation.ispartofsjr1,291
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectamiloride
dc.subjectamlodipine
dc.subjectchlortalidone
dc.subjectdipeptidyl carboxypeptidase inhibitor
dc.subjectlosartan
dc.subjectpotassium sparing diuretic agent
dc.subjectpropranolol
dc.subjectangiotensin 1 receptor antagonist
dc.subjectantihypertensive agent
dc.subjectdiuretic agent
dc.subjectatherosclerosis
dc.subjectblood pressure
dc.subjectblood pressure measurement
dc.subjectdisease severity
dc.subjectdouble blind procedure
dc.subjectelectrocardiogram
dc.subjectethics
dc.subjectfollow up
dc.subjectheart arrhythmia
dc.subjectheart failure
dc.subjectheart infarction
dc.subjectheart left ventricle hypertrophy
dc.subjecthuman
dc.subjecthyperglycemia
dc.subjecthypertension
dc.subjecthypokalemia
dc.subjectlifestyle modification
dc.subjectmedical research
dc.subjectmicroalbuminuria
dc.subjectoutcome assessment
dc.subjectoutpatient
dc.subjectrandomized controlled trial
dc.subjectrenal protection
dc.subjectstroke
dc.subjectsudden death
dc.subjectadult
dc.subjectaged
dc.subjectBrazil
dc.subjectclinical trial
dc.subjectcomparative study
dc.subjectcontrolled clinical trial
dc.subjectcontrolled study
dc.subjectdrug combination
dc.subjectdrug effect
dc.subjectfemale
dc.subjecthospitalization
dc.subjectmale
dc.subjectmethodology
dc.subjectmiddle aged
dc.subjectmulticenter study
dc.subjectpathophysiology
dc.subjecttime
dc.subjecttreatment outcome
dc.subjectAdult
dc.subjectAged
dc.subjectAmiloride
dc.subjectAngiotensin II Type 1 Receptor Blockers
dc.subjectAntihypertensive Agents
dc.subjectBlood Pressure
dc.subjectChlorthalidone
dc.subjectDiuretics
dc.subjectDouble-Blind Method
dc.subjectDrug Therapy, Combination
dc.subjectFemale
dc.subjectHumans
dc.subjectHypertension
dc.subjectLosartan
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectResearch Design
dc.subjectSeverity of Illness Index
dc.subjectTime Factors
dc.subjectTreatment Outcome
dc.titleA comparison between diuretics and angiotensin-receptor blocker agents in patients with stage I hypertension (PREVER-treatment trial): Study protocol for a randomized double-blind controlled 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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