Reinaldo José Gianini
University of São Paulo
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Cadernos De Saude Publica | 2006
Luciana Maragno; Moisés Goldbaum; Reinaldo José Gianini; Hillegonda Maria Dutilh Novaes; Chester Luiz Galvão Cesar
The prevalence of common mental disorders has increased in many countries. Cases are often not identified and adequately treated because traditional health care services are rarely prepared to deal with this problem. The Family Health Program (FHP) has been implemented in Brazil since 1995-1996 and provides a new primary health care model with the potential for better care for these patients. This study investigates common mental disorders prevalence according to FHP coverage and associated socio-demographic factors. A large health and health care survey was conducted from January to March 2001 in areas partly covered by the FHP in a peripheral area of the city of Sao Paulo and included common mental disorders screening in 2,337 individuals > 15 years of age. There was no significant difference in common mental disorders prevalence according to FHP. Common mental disorders prevalence was significantly higher among females (PR = 1.34), elderly (PR = 1.56), and individuals with lower income (PR = 2.64) or less schooling (PR = 2.83). Common mental disorders was associated with indicators of social disadvantage, implying the need to focus on specific health problems and risk groups to improve the impact of care.
Revista De Saude Publica | 2005
Moisés Goldbaum; Reinaldo José Gianini; Hillegonda Maria Dutilh Novaes; Chester Luiz Galvão Cesar
OBJETIVO: O Programa de Saude da Familia se constitui em estrategia de reorganizacao do sistema de atencao a saude para o Sistema Unico de Saude. O objetivo do estudo foi verificar mudancas no perfil de utilizacao de servicos de saude apos implantacao do Programa, identificando fatores associados as mudancas observadas. METODOS: Foram analisados dados de utilizacao de servicos e procura por assistencia em duas amostras definidas por conglomerados e representativas da populacao coberta (n=1.865) e nao coberta pelo Programa de Saude da Familia (n=2.036) de dois distritos do Municipio de Sao Paulo. Os dados fazem parte de inquerito populacional realizado em 2001. Foi empregada a analise estatistica propria para conglomerados. RESULTADOS: Na utilizacao de servicos, nas areas cobertas pelo Programa de Saude da Familia, nao foram observadas razoes de prevalencia significantemente diferentes segundo escolaridade e renda, e nas areas nao cobertas as razoes de prevalencia foram mais elevadas para maior escolaridade e renda. Na procura por assistencia em pessoas com episodios de morbidade, nas areas cobertas pelo Programa a razao de prevalencia foi maior em pessoas com grau de limitacao intenso, e nas areas nao cobertas a razao de prevalencia foi mais elevada para maior escolaridade e menor para os inativos. CONCLUSOES: Nas areas estudadas, na populacao coberta pelo Programa de Saude da Familia a renda e escolaridade nao se constituem em fatores que diferenciam de forma significativa o perfil de utilizacao de servicos de saude e de procura por assistencia, indicando que o programa pode estar contribuindo para maior equidade nessas condicoes.
Journal of Epidemiology and Community Health | 2011
José Ricardo Mello Brandão; Reinaldo José Gianini; Hilegonda Maria Dutilh Novaes; Moisés Goldbaum
Background The Family Health Strategy (FHS) has been implemented as a strategy for primary care improvement in Brazil. Working with teams that include one doctor, one nurse, auxiliary nurses and community health workers in predefined areas, the FHS began in 1994 (known then as the Family Health Program) and has since grown considerably. The programme has only recently undergone assessment of outcomes, in contrast to more routine evaluations of infrastructure and process. Methods In 2001, a health survey was carried out in two administrative districts (with 190 000 inhabitants) on the outskirts of the city of São Paulo, both partially served by the FHS. Chronic morbidity (hypertension, diabetes and ischaemic heart disease) of individuals aged 15 or older was studied in areas covered and not covered by the programme. Stratified univariate analysis was applied for sex, age, education, income, working status and social insurance of these populations. Multivariate analysis was applied where applicable. Results There was a distinct pattern in the morbidity profile of these populations, suggesting differentiated self-knowledge on chronic disease status in the areas served by the FHS. Conclusion The FHS can increase population awareness of chronic diseases, possibly through increasing access to primary care.
Aids Patient Care and Stds | 2008
Maria Cássia Mendes-Correa; Azzo Widman; Maria Luiza Paes Brussi; Cristina Fátima Guastini; Reinaldo José Gianini
The aim of this study was to examine the incidence and factors associated with the severity of liver fibrosis in 234 coinfected patients in Brazil. Patients were cared for in our clinic, from 1996 to 2004. Eligible patients were defined as patients with documented HIV and hepatitis C virus (HCV) infections and had previously undergone a liver biopsy. Patients with persistently normal alanine aminotransferase (ALT) were also included. The variables selected for study were age, gender, risk category, history of high alcohol consumption, CD4(+) T cell count, antiretroviral therapy usage, HCV genotype and duration of HCV infection. Stage of fibrosis was scored as follows: F0, no fibrosis; F1, portal fibrosis with no septa; F2, portal fibrosis with few septa; F3, bridging fibrosis with many septa; and F4, cirrhosis. The liver fibrosis stage was F3 in 39 (16.6%) and F4 in 20(8.5%) patients. Among patients with normal ALT, the liver fibrosis stage was F3-F4 in three patients (5.6%). Predictors of severe liver fibrosis (F3-F4) by multivariate analysis were age (older patients) and genotype 3 (genotype 1 = odds ratio [OR], 0.28; 95% confidence interval [CI], 0.12 0.65). In summary, in the present study severe liver fibrosis was found in 25% of our patients and was associated with an age of more than 38 years at the time of liver biopsy as well as, HCV genotype 3. No differences were found with respect to CD4(+) T cell counts although patients with a CD4(+) T cell count greater than 50 were excluded.
PLOS ONE | 2012
Olinda do Carmo Luiz; Reinaldo José Gianini; Fernanda de Toledo Gonçalves; Guilherme Francisco; Cyro Festa-Neto; José A. Sanches; Gilka Jorge Figaro Gattás; Roger Chammas; José Eluf-Neto
Background Over the last century the incidence of cutaneous melanoma has increased worldwide, a trend that has also been observed in Brazil. The identified risk factors for melanoma include the pattern of sun exposure, family history, and certain phenotypic features. In addition, the incidence of melanoma might be influenced by ethnicity. Like many countries, Brazil has high immigration rates and consequently a heterogenous population. However, Brazil is unique among such countries in that the ethnic heterogeneity of its population is primarily attributable to admixture. This study aimed to evaluate the contribution of European ethnicity to the risk of cutaneous melanoma in Brazil. Methodology/Principal Findings We carried out a hospital-based case-control study in the metropolitan area of Sao Paulo, Brazil. We evaluated 424 hospitalized patients (202 melanoma patients and 222 control patients) regarding phenotypic features, sun exposure, and number of grandparents born in Europe. Through multivariate logistic regression analysis, we found the following variables to be independently associated with melanoma: grandparents born in Europe—Spain (OR = 3.01, 95% CI: 1.03–8.77), Italy (OR = 3.47, 95% CI: 1.41–8.57), a Germanic/Slavic country (OR = 3.06, 95% CI: 1.05–8.93), or ≥2 European countries (OR = 2.82, 95% CI: 1.06–7.47); eye color—light brown (OR = 1.99, 95% CI: 1.14–3.84) and green/blue (OR = 4.62; 95% CI 2.22–9.58); pigmented lesion removal (OR = 3.78; 95% CI: 2.21–6.49); no lifetime sunscreen use (OR = 3.08; 95% CI: 1.03–9.22); and lifetime severe sunburn (OR = 1.81; 95% CI: 1.03–3.19). Conclusions Our results indicate that European ancestry is a risk factor for cutaneous melanoma. Such risk appears to be related not only to skin type, eye color, and tanning capacity but also to others specific characteristics of European populations introduced in the New World by European immigrants.
Revista De Saude Publica | 2004
Reinaldo José Gianini; Eduardo de Masi; Eliane Cleto Coelho; Franck Ricardo Oréfice; Renato Augusto de Moraes
OBJETIVO: A baixa acuidade visual tem elevada prevalencia e o diagnostico precoce e necessario pelos danos que pode causar ao desenvolvimento e aprendizado infantis. O estudo realizado objetivou descrever e analisar a prevalencia de baixa acuidade visual em escolares da rede de ensino fundamental. METODOS: A partir do diagnostico da acuidade visual, 9.640 escolares de primeira e quarta series da rede publica de ensino fundamental de Sorocaba, Estado de Sao Paulo, no ano 2000, foram analisados e classificados seus registros segundo sexo, serie, uso de oculos, area de residencia e grau de acesso a assistencia medica supletiva. Foram realizados testes de correlacao de Pearson e analise de regressao linear. RESULTADOS: A populacao estudada apresentou prevalencia de baixa acuidade visual de 13,1% (IC 95%=12,5-13,8%), sendo significantemente menor no sexo masculino (11,5%) quando comparado ao feminino (14,9%) - (RP=0,77); significantemente maior nos escolares de primeira serie (14,1%) quando comparados aos de quarta serie (11,5%) - (RP=1,22); e significantemente menor em nao-usuarios de oculos (12,1%) quando comparados aos usuarios (42,0%) - (RP=0,29). Dentre os locais estudados, o bairro de Cajuru apresentou a menor prevalencia de baixa acuidade visual (1,8%) e o bairro de Vila Sabia a maior prevalencia (32,4%). Foi encontrada correlacao positiva, segundo a area de residencia entre a proporcao de individuos que tem acesso a assistencia medica supletiva e a proporcao de usuarios de oculos (r=0,64, p<0,001). CONCLUSOES: A prevalencia de baixa acuidade visual aponta falhas no diagnostico precoce e na continuidade da assistencia, indicando urgente necessidade de implementacao de um programa publico de saude.
Journal of Medical Virology | 2010
Maria Cássia Mendes-Correa; João Renato Rebelo Pinho; Stephen Locarnini; Lilly Yuen; R. Sitnik; R.A.F. Santana; Michele Soares Gomes-Gouvêa; O.M. Leite; L.G. Martins; Mariliza Henrique da Silva; Reinaldo José Gianini; D.E. Uip
This study analyzed the genotype distribution and frequency of lamivudine (LAM) and tenofovir (TDF) resistance mutations in a group of patients co‐infected with HIV and hepatitis B virus (HBV). A cross‐sectional study of 847 patients with HIV was conducted. Patients provided blood samples for HBsAg detection. The load of HBV was determined using an “in‐house” real‐time polymerase chain reaction. HBV genotypes/subgenotypes, antiviral resistance, basal core promoter (BCP), and precore mutations were detected by DNA sequencing. Twenty‐eight patients with co‐infection were identified. The distribution of HBV genotypes among these patients was A (n = 9; 50%), D (n = 4; 22.2%), G (n = 3; 16.7%), and F (n = 2; 11.1%). Eighteen patients were treated with LAM and six patients were treated with LAM plus TDF. The length of exposure to LAM and TDF varied from 4 to 216 months. LAM resistance substitutions (rtL180M + rtM204V) were detected in 10 (50%) of the 20 patients with viremia. This pattern and an accompanying rtV173L mutation was found in four patients. Three patients with the triple polymerase substitution pattern (rtV173L + rtL180M + rtM204V) had associated changes in the envelope gene (sE164D + sI195M). Mutations in the BCP region (A1762T, G1764A) and in the precore region (G1896A, G1899A) were also found. No putative TDF resistance substitution was detected. The data suggest that prolonged LAM use is associated with the emergence of particular changes in the HBV genome, including substitutions that may elicit a vaccine escape phenotype. No putative TDF resistance change was detected after prolonged use of TDF. J. Med. Virol. 82:1481–1488, 2010.
Revista Brasileira De Reumatologia | 2011
Gilberto Santos Novaes; Mariana Ortega Perez; Maria Beatriz Bray Beraldo; Camila Rodrigues Costa Pinto; Reinaldo José Gianini
OBJECTIVE: To investigate the correlation of fatigue with pain in rheumatoid arthritis patients and with disability in osteoarthritis patients. METHODS: Twenty patients with rheumatoid arthritis and 20 patients with osteoarthritis were evaluated. The degree of fatigue was evaluated with a visual analogue scale and the Multidimensional Assessment of Fatigue. Pain was evaluated with a visual analogue scale as well as Patient Global Assessment. For disability evaluation, the Health Assessment Questionnaire was performed. Age, gender, disease duration, education, income, antirheumatic drugs used and comorbidity were also obtained. Statistical analysis included Fisher exact, Shapiro-Wilk, Kruskal-Wallis and Spearman tests. The significance level was 0.05. RESULTS: Fatigue was more significantly increased in patients with osteoarthritis than in patients with rheumatoid arthritis when evaluated with Multidimensional Assessment of Fatigue (P < 0.05). Pain was found to correlate with fatigue evaluated with visual analogue scale or Multidimensional Assessment of Fatigue in patients with rheumatoid arthritis (r = 0.46; P < 0.05). Health Assessment Questionnaire was associated with fatigue visual analogue scale in patients with osteoarthritis (r = 0.54; P < 0.05). Patient Global Assessment correlates with fatigue visual analogue scale (r = 0.44; P < 0.003). Patients were similar in both groups: all females, similar mean age, with long disease duration and low income. CONCLUSION: Our results corroborate that fatigue in rheumatoid arthritis patients correlates with the degree of pain, while in osteoarthritis patients it is associated with disability. Therefore, we found that fatigue has different correlates in osteoarthritis and rheumatoid arthritis, and we suggest that disability, not pain, is a correlate of fatigue in osteoarthritis patients.
International Journal of Std & Aids | 2008
M C Mendes-Correa; N P Cavalheiro; C Mello; A A Barone; Reinaldo José Gianini
Summary: Information on hepatitis C virus (HCV) genotypic distribution among HIV-HCV co-infected patients is lacking in Brazil as well as other Latin American countries. The objective of this study was to evaluate the level of exposure to different risk factors associated with HCV transmission among a group of co-infected patients and to characterize the genotypic distribution of HCV in this cluster. A series of 100 HIV-HCV co-infected patients was analysed. The data to be analysed were collected from specific laboratory tests. Information was collected through a questionnaire. HCV genotyping was carried out by sequencing the 5′ non-coding region of HCV. Chi-square and Fischer association tests or Kruskal-Wallis test were used to study the association between HCV transmission-related variables and the established genotypes. In conclusion, exposure to multiple risk factors associated with HCV transmission was common among HIV co-infected patients and an association between HCV genotype 3 and intravenous drug user was observed.
BMC Infectious Diseases | 2011
Maria Cássia Jacintho Mendes-Correa; João Renato Rebello Pinho; Michele Soares Gomes-Gouvêa; Adriana Cristina da Silva; Cristina Fátima Guastini; Luiz G. A. Martins; A.G. Leite; Mariliza Henrique da Silva; Reinaldo José Gianini; David Everson Uip
BackgroundHBV-HIV co-infection is associated with an increased liver-related morbidity and mortality. However, little is known about the natural history of chronic hepatitis B in HIV-infected individuals under highly active antiretroviral therapy (HAART) receiving at least one of the two drugs that also affect HBV (TDF and LAM). Information about HBeAg status and HBV viremia in HIV/HBV co-infected patients is scarce. The objective of this study was to search for clinical and virological variables associated with HBeAg status and HBV viremia in patients of an HIV/HBV co-infected cohort.MethodsA retrospective cross-sectional study was performed, of HBsAg-positive HIV-infected patients in treatment between 1994 and 2007 in two AIDS outpatient clinics located in the São Paulo metropolitan area, Brazil. The baseline data were age, sex, CD4 T+ cell count, ALT level, HIV and HBV viral load, HBV genotype, and duration of antiretroviral use. The variables associated to HBeAg status and HBV viremia were assessed using logistic regression.ResultsA total of 86 HBsAg patients were included in the study. Of these, 48 (56%) were using combination therapy that included lamivudine (LAM) and tenofovir (TDF), 31 (36%) were using LAM monotherapy, and 7 patients had no previous use of either one. Duration of use of TDF and LAM varied from 4 to 21 and 7 to 144 months, respectively. A total of 42 (48. 9%) patients were HBeAg positive and 44 (51. 1%) were HBeAg negative. The multivariate analysis revealed that the use of TDF for longer than 12 months was associated with undetectable HBV DNA viral load (serum HBV DNA level < 60 UI/ml) (p = 0. 047). HBeAg positivity was associated with HBV DNA > 60 UI/ml (p = 0. 001) and ALT levels above normality (p = 0. 038).ConclusionProlonged use of TDF containing HAART is associated with undetectable HBV DNA viral load. HBeAg positivity is associated with HBV viremia and increased ALT levels.