27 research outputs found

    Estudo de seguimento por dois anos de idosos residentes em SĂŁo Paulo, Brasil: metodologia e resultados preliminares

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    INTRODUCTION: Previous cross-sectional studies have shown a high prevalence of chronic disease and disability among the elderly. Given Brazil s rapid aging process and the obvious consequences of the growing number of old people with chronic diseases and associated disabilities for the provision of health services, a need was felt for a study that would overcome the limitations of cross-sectional data and shed some light on the main factors determining whether a person will live longer and free of disabling diseases, the so-called successful aging. The methodology of the first follow-up study of elderly residents in Brazil is presented. METHOD: The profile of the initial cohort is compared with previous cross-sectional data and an in-depth analysis of nonresponse is carried out in order to assess the validity of future longitudinal analysis. The EPIDOSO ( Epidemiologia do Idoso ) Study conducted a two-year follow-up of 1,667 elderly people (65+), living in S. Paulo. The study consisted of two waves, each consisting of household, clinical, and biochemical surveys. RESULTS AND CONCLUSIONS: In general, the initial cohort showed a similar profile to previous cross-sectional samples in S. Paulo. There was a majority of women, mostly widows, living in multigenerational households, and a high prevalence of chronic illnesses, psychiatric disturbances, and physical disabilities. Despite all the difficulties inherent in follow-up studies, there was a fairly low rate of nonresponse to the household survey after two years, which did not actually affect the representation of the cohort at the final household assessment, making unbiased longitudinal analysis possible. Concerning the clinical and blood sampling surveys, the respondents tended to be younger and less disabled than the nonrespondents, limiting the use of the clinical and laboratory data to longitudinal analysis aimed at a healthier cohort. It is worth mentioning that gender, education, family support, and socioeconomic status were not important determinants of nonresponse, as is often the case.INTRODUÇÃO: Estudos transversais recentes mostraram alta prevalĂȘncia de doenças crĂŽnicas e incapacidades fĂ­sicas entre idosos. Considerando o rĂĄpido processo de envelhecimento do Brasil e as conseqĂŒĂȘncias que esse aumento de idosos com doenças crĂŽnicas e incapacidades associadas acarretarĂĄ para o sistema de saĂșde, fazia-se necessĂĄrio estudo que pudesse superar as limitaçÔes dos dados transversais, permitindo determinar quais os fatores determinantes de uma vida longa e livre de doenças incapacitantes, o chamado envelhecimento bem sucedido. É apresentada a metodologia do primeiro estudo epidemiolĂłgico longitudinal com idosos residentes na comunidade, no Brasil. MÉTODO: O perfil do cohorte inicial Ă© comparado com dados de estudos anteriores a com o perfil dos nĂŁo respondentes para avaliar a validade de anĂĄlises longitudinais futuras.O projeto EPIDOSO (Epidemiologia do Idoso) seguiu por dois anos 1.667 idosos (65+), residentes em SĂŁo Paulo. Consistiu de duas ondas, cada qual com trĂȘs inquĂ©ritos: domiciliar, clĂ­nico e laboratorial. RESULTADOS E CONCLUSÕES: O perfil da população nĂŁo diferiu de estudos anteriores, mostrando maioria de mulheres, viĂșvas, vivendo em domicĂ­lios multigeracionais, com uma alta prevalĂȘncia de doenças crĂŽnicas, distĂșrbios psiquiĂĄtricos e incapacidades fĂ­sicas. A despeito de todas as dificuldades inerentes a um estudo longitudinal, o grupo de nĂŁo-respondentes ao segundo inquĂ©rito domiciliar nĂŁo diferiu significativamente dos respondentes, assegurando anĂĄlises longitudinais livres desse tipo de viĂ©s. Em relação aos inquĂ©ritos clĂ­nico e laboratorial, os nĂŁo-respondentes mostraram-se mais velhos e mais incapacitados que os respondentes, limitando o uso dos dados clĂ­nicos e laboratoriais a anĂĄlises pertinentes a uma cohorte mais jovem e saudĂĄvel. Sexo, educação, apoio familiar e nĂ­vel socioeconĂŽmico nĂŁo influenciaram de forma significativa a taxa de nĂŁo - resposta, ao contrĂĄrio do que se costuma verificar.Universidade Federal de SĂŁo Paulo (UNIFESP)UNIFESPSciEL

    The cost-effectiveness of influenza vaccination for people aged 50 to 64 years: an international model.

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    OBJECTIVES: Routine influenza vaccination is currently recommended in several countries for people aged more than 60 or 65 years or with high risk of complications. A lower age threshold of 50 years has been recommended in the United States since 1999. To help policymakers consider whether such a policy should be adopted more widely, we conducted an economic evaluation of lowering the age limit for routine influenza vaccination to 50 years in Brazil, France, Germany, and Italy. METHODS: The probabilistic model was designed to compare in a single season the costs and clinical outcomes associated with two alternative vaccination policies for persons aged 50 to 64 years: reimbursement only for people at high risk of complications (current policy), and reimbursement for all individuals in this age group (proposed policy). Two perspectives were considered: third-party payer (TPP) and societal. Model inputs were obtained primarily from the published literature and validated through expert opinion. The historical distribution of annual influenza-like illness (ILI) incidence was used to simulate the uncertain incidence in any given season. We estimated gains in unadjusted and quality-adjusted life expectancy, and the cost per quality-adjusted life-year (QALY) gained. Deterministic and probabilistic sensitivity analyses were conducted. RESULTS: Comparing the proposed to the current policy, the estimated mean costs per QALY gained were R4,100,EURO13,200,EURO31,400andEURO15,700forBrazil,France,Germany,andItaly,respectively,fromaTPPperspective.Fromthesocietalperspective,theage−basedpolicyispredictedtoyieldnetcostsavingsinGermanyandItaly,whereasthecostperQALYdecreasedtoR4,100, EURO 13,200, EURO 31,400 and EURO 15,700 for Brazil, France, Germany, and Italy, respectively, from a TPP perspective. From the societal perspective, the age-based policy is predicted to yield net cost savings in Germany and Italy, whereas the cost per QALY decreased to R2800 for Brazil and EURO 8000 for France. The results were particularly sensitive to the ILI incidence rate, vaccine uptake, influenza fatality rate, and the costs of administering vaccination. Assuming a cost-effectiveness threshold ratio of EURO 50,000 per QALY gained, the probabilities of the new policy being cost-effective were 94% and 95% for France, 72% and near 100% for Germany, and 89% and 99% for Italy, from the TPP and societal perspectives, respectively. CONCLUSIONS: Extending routine influenza vaccination to people more than 50 years of age is likely to be cost-effective in all four countries studied

    Two Distinct Compound Heterozygous Constellations (R277X/IVS34-1G〉C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred with Congenital Goiter and Defective TG Synthesis

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    In this study, we have extended our initial molecular studies of a nonconsanguineous family with two affected siblings and one of their nephews with congenital goiter, hypothyroidism, and marked impairment of thyroglobulin synthesis. Genomic DNA sequencing revealed that the index patient (affected nephew) was heterozygous for a single base change of a cytosine to a thymine at nucleotide 886 in exon 7 (886C〉T, mother's mutation) in one allele and for a novel guanine to cytosine transversion at position-1 of the splice acceptor site in intron 34 (IVS34-1G〉C, father's mutation) in the other allele. The two affected siblings inherited the 886C〉T mutation from their mother and a previously reported cytosine to thymine transition at nucleotide 4588 in exon 22 from their father (4588C〉T). The 886C〉T and 4588C〉T substitutions resulted in premature stop codons at amino acids 277 (R277X) and 1511 (R1511X), respectively. In vitro transcription analysis showed that the exon 35 is skipped entirely when the IVS34-1G〉C mutation is present, whereas the wild-type allele is correctly spliced. SSCP (exon 7 and 35) and restriction analysis (exon 22) using Taq I indicated that the two affected siblings, the affected nephew, his mother, and his unaffected brother were all heterozygous for the R277X mutation. The two affected siblings, their father, and three unaffected siblings were all heterozygous for the R1511X mutation, whereas the affected nephew and his father were heterozygous for the IVS34-1G〉C mutation. Moreover, in this kindred, we have characterized polymorphisms (insertion/deletion, microsatellite, and single nucleotide polymorphism) located within introns 18 and 29 and exon 44 that are associated with the described mutations. Haplotype analysis with these polymorphic markers in two unrelated Brazilian families (present family studied and previously reported family) harboring the R277X mutation suggests a founder effect for the R277X mutation. In conclusion, the affected individuals of this family are either compound heterozygous for R277X/IVS34-1G〉C or R277X/R1511X. This observation further supports that thyroglobulin gene mutations display significant intraallelic heterogeneity.Fil: Gutnisky, Viviana J.. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂ­mica; ArgentinaFil: Moya, Christian M.. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂ­mica; ArgentinaFil: Rivolta, Carina Marcela. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂ­mica; ArgentinaFil: Domene, Sabina. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂ­mica; ArgentinaFil: Varela, Viviana. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂ­mica; ArgentinaFil: Toniolo, Jussara V.. Sao Paulo University School of Medicine; BrasilFil: Medeiros Neto, Geraldo. Sao Paulo University School of Medicine; BrasilFil: Targovnik, Hector Manuel. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂ­mica; Argentin
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