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1.
Artigo em Inglês | LILACS | ID: biblio-1538343

RESUMO

Introduction: primary care action strategies are relevant for disease prevention and health promotion, as well as for the initial management of suspected cases and the individual monitoring of patients with confirmed diagnoses of COVID-19. This study aimed to evaluate the outcome of clinical worsening and demographic, occupational, and clinical variables of workers with COVID-19 in a community health center at a public university in southeastern Brazil. Methods: a retrospective cohort study was conducted with 1,459 symptomatic workers with COVID-19. Data were extracted from the database of the unit's epidemiological surveillance center between March 2020 and March 2021. Results: The average age of participants was 41.1 (SD 10.8) years, most women (71.1%), who had obesity (19.9%) and hypertension (17.0%). Among the symptoms, headache (75.3%) and cough (74.9%) stood out. The worsening of clinical outcome during follow-up occurred in 3.4% of cases. The demographic, occupational and clinical factors associated with clinical worsening were gender, professional category, hypertension, diabetes mellitus, obesity, dyslipidemia, olfactory disorders, cough, fever, and dyspnea. The Poisson regression showed that the prevalence of clinical worsening was greater with age, obesity, fever, and dyspnea. Conclusion: Clinical wors-ening occurred in 3.4% of the cases and was more prevalent according to age, obesity, fever, and dyspnea. The follow-up has shown promise in the early detection and treatment of COVID-19 (AU).


Introdução: as estratégias de ação da atenção primária são relevantes para a prevenção de doenças e promoção da saúde, bem como para o manejo inicial de casos suspeitos e acompanhamento individual de pacientes com diagnóstico confirmado de COVID-19. Este estudo teve como objetivo avaliar o desfecho da piora clínica e variáveis demográficas, ocupacionais e clínicas de trabalhadores com COVID-19 em um centro comunitário de saúde de uma universidade pública do sudeste do Brasil. Métodos: estudo de coorte retrospectivo com 1.459 trabalhadores sin-tomáticos com COVID-19. Os dados foram extraídos do banco de dados do núcleo de vigilância epidemiológica da unidade entre março de 2020 e março de 2021. Resultados: A média de idade dos participantes foi de 41,1 (DP 10,8) anos, sendo a maioria mulheres (71,1%), com obesidade (19,9%) e hipertensão (17,0%). Dentre os sintomas, destacaram-se a cefaleia (75,3%) e a tosse (74,9%). A piora do quadro clínico durante o seguimento ocorreu em 3,4% dos casos. Os fatores demográficos, ocupacionais e clínicos associados à piora clínica foram sexo, categoria profissional, hipertensão arterial, diabetes mellitus, obesidade, dislipidemia, distúrbios do olfato, tosse, febre e dispneia. A regressão de Poisson mostrou que a prevalência de piora clínica foi maior com a idade, obesidade, febre e dispneia. Conclusão: A piora clínica ocorreu em 3,4% dos casos e foi mais prevalente conforme idade, obesidade, febre e dispneia. O acompanhamento mostrou-se promissor na detecção precoce e no tratamento da COVID-19 (AU).


Assuntos
Humanos , Atenção Primária à Saúde , SARS-CoV-2 , COVID-19/epidemiologia
2.
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1360789

RESUMO

ABSTRACT As leprosy and leprosy reactions are the most prevalent infectious cause of physical disability, it is important to commit efforts to better understand these chronic reactions. Infections, even when asymptomatic, can trigger leprosy reactions and Bartonella spp. in turn, can cause chronic infections. We presented a case of a 51-year-old man who was admitted presenting with chronic type 2 leprosy reactions. He had a lepromatous form of leprosy that was histologically diagnosed six months after the onset of signs and symptoms compatible with a chronic type 2 reaction. He reported a history of a previous hepatitis B diagnosis. During a 24-month multidrug therapy (MDT), chronic reactions were partially controlled with prednisone and thalidomide. Thirty-three months following the leprosy treatment, he still experienced chronic reactions, and whole bacilli as well as globi were found on a new skin biopsy. Since coinfections can trigger type 2 reactions and the patient had close contact with animals and ticks, we investigated the presence of a Bartonella sp. infection. Bartonella henselae DNA was detected in a skin fragment obtained before the beginning of the leprosy retreatment. However, even after six months of a second leprosy MDT, he continued to experience type 2 chronic reactions. He was admitted to the hospital to undergo an intravenous antibiotic therapy for 14 days and then complete the treatment per os for ten more weeks. Leprosy reactions improved following the treatment for B. henselae. After completing the MDT treatment, he has been accompanied for sixty months with no signs of leprosy or leprosy reactions. The asymptomatic infection by B. henselaein this patient was considered the putative trigger of chronic leprosy reactions and leprosy relapse.

3.
Braz. j. infect. dis ; 16(3): 232-236, May-June 2012. ilus, tab
Artigo em Inglês | LILACS | ID: lil-638555

RESUMO

BACKGROUND: Pegylated interferon (Peg-IFN) and standard interferon (IFN) play a significant role in the treatment of hepatitis C virus (HCV) infection. Biosimilar standard IFN is widely available in Brazil for the treatment of HCV infection genotypes 2 or 3, but its efficacy compared to Peg-IFN is unknown. OBJECTIVE: To compare the sustained virological response (SVR) rates following treatment with biosimilar standard IFN plus ribavirin (RBV) versus Peg-IFN plus RBV in patients with HCV genotypes 2 or 3 infection. METHODS: A retrospective cohort study was conducted in patients with HCV genotypes 2 or 3 infection treated with biosimilar standard IFN plus RBV or with Peg-IFN plus RBV. SVR rates of the two treatments were compared. RESULTS: From January 2005 to December 2010, 172 patients with a mean age of 44 +/- 9.3 years were included. There were eight (4.7%) patients with HCV genotype 2 infections. One hundred fourteen (66.3%) were treated with biosimilar standard IFN plus RBV, whist 58 (33.7%) patients were treated with Peg-IFN plus RBV. Between the two groups, there were no significant differences regarding age, gender, glucose level, platelet count, hepatic necroinflammatory grade, and hepatic fibrosis stage. Overall, 59.3% (102/172) patients had SVR. In patients treated with Peg-IFN plus RBV, 79.3% (46/58) had SVR compared to 49.1% (56/114) among those treated with biosimilar standard IFN plus RBV (p = 0.0001). CONCLUSION: In patients with HCV genotypes 2 or 3 infection, a higher SVR was observed in patients receiving Peg-IFN plus RBV related to patients treated with biosimilar standard IFN plus RBV.


Assuntos
Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Antivirais/administração & dosagem , Hepacivirus/genética , Hepatite C Crônica/tratamento farmacológico , Interferon-alfa/administração & dosagem , Interferons/administração & dosagem , Polietilenoglicóis/administração & dosagem , Ribavirina/administração & dosagem , Estudos de Coortes , Quimioterapia Combinada , Genótipo , Estudos Retrospectivos , RNA Viral/análise , Proteínas Recombinantes/administração & dosagem , Resultado do Tratamento , Carga Viral
4.
Braz. j. infect. dis ; 15(5): 449-456, Sept.-Oct. 2011. tab
Artigo em Inglês | LILACS | ID: lil-612703

RESUMO

OBJECTIVE: The treatment of the chronic hepatitis C (HCV) with α-interferon is associated with thyroid dysfunction (TD). The aim of this study was to evaluate thyroid function outcome among patients with chronic HCV under treatment with conventional interferon (IFN) or peguilated interferon (PEG-IFN) in association with ribavirin. PATIENTS AND METHODS: We studied 293 patients with chronic HCV, submitted to drug therapy for 24 or 48 weeks. Initially, we evaluated FT4, TSH, TPOAb, TgAb, and continued to monitor FT4 and TSH every three months during therapy and six months thereafter. RESULTS: At baseline, TD prevalence was 6.82 percent (n = 20); 6.14 percent hypothyroidism; 0.68 percent hyperthyroidism. TPOAb was present in 5.46 percent of euthyroid patients. Out of 273 euthyroid patients at baseline, 19 percent developed TD: 17.2 percent hypothyroidism; 1.8 percent hyperthyroidism; 5.1 percent destructive thyroiditis (DT). 90 percent of TPOAb-positive patients at baseline developed hypothyroidism vs 14.5 percent of TPOAb-negative patients (p < 0.001). On average, TD occurred after 25.8 ± 15.5 weeks of treatment. 87.2 percent of patients who developed hypothyroidism did so during the first therapeutic cycle (p = 0.004; OR = 3.52; 95 percent CI = 1.36-9.65). Patients infected with genotype 1 virus were 2.13 times more likely to develop hypothyroidism (p = 0.036; 95 percent CI = 1.04-4.38). Hypothyroid and DT patients presented higher TSH levels before-treatment than patients who had remained euthyroid (p < 0.001; p = 0.002, respectively). DT patients presented lower qALT (p = 0.012) than euthyroid patients. CONCLUSION: Hypothyroidism was the most frequent TD, especially during the first cycle of α-interferon. Genotype 1 virus was associated with a risk two times higher for developing the illness. There was no need to interrupt or to change HCV treatment. Therefore, approximately 34 percent of TD was transient.


Assuntos
Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Antivirais/efeitos adversos , Hepacivirus/genética , Hepatite C Crônica/tratamento farmacológico , Hipotireoidismo/induzido quimicamente , Interferon-alfa/efeitos adversos , Polietilenoglicóis/efeitos adversos , Ribavirina/efeitos adversos , Antivirais/uso terapêutico , Autoanticorpos/sangue , Quimioterapia Combinada , Genótipo , Hipertireoidismo/induzido quimicamente , Interferon-alfa/uso terapêutico , Estudos Prospectivos , Polietilenoglicóis/uso terapêutico , Proteínas Recombinantes/efeitos adversos , Proteínas Recombinantes/uso terapêutico , Ribavirina/uso terapêutico
5.
Braz. j. infect. dis ; 8(6): 431-439, Dec. 2004. tab
Artigo em Inglês | LILACS | ID: lil-401717

RESUMO

Occult hepatitis B virus (HBV) infections have been identified in patients with chronic hepatitis C virus (HCV) infection, although the clinical relevance of occult HBV infection remains controversial. We searched for serum HBV DNA in 106 HBsAg negative/anti-HBc positive patients with chronic HCV infection and in 150 blood donors HBsAg negative/anti-HBc positive/anti-HCV negative (control group) by nested-PCR. HCV genotyping was done in 98 patients and percutaneous needle liver biopsies were performed in 59 patients. Fifty-two patients were treated for HCV infection with interferon alone (n=4) or combined with ribavirin (n=48) during one year. At the end and 24 weeks after stopping therapy, they were tested for HCV-RNA to evaluate the sustained virological response (SVR). Among the 106 HCV-positive patients, 15 (14 percent) were HBV-DNA positive and among the 150 HCV-negative blood donors, 6 (4 percent) were HBV-DNA positive. Liver biopsy gave a diagnosis of liver cirrhosis in 2/10 (20 percent) of the HBV-DNA positive patients and in 6/49 (12 percent) of the HBV-DNA negative patients. The degree of liver fibrosis and portal inflammation was similar in HCV-infected patients HBV-DNA, irrespective of HBV-DNA status. SVR was obtained in 37.5 percent of the HBV-DNA positive patients and in 20.5 percent of the HBV-DNA negative patients; this difference was not significant. In conclusion, these data suggested that occult HBV infection, which occurs at a relatively high frequency among Brazilian HCV-infected patients, was not associated with more severe grades of inflammation, liver fibrosis or cirrhosis development and did not affect the SVR rates when the patients were treated with interferon or with interferon plus ribavirin.


Assuntos
Humanos , Masculino , Feminino , Antivirais/uso terapêutico , Hepatite B/tratamento farmacológico , Hepatite C Crônica/tratamento farmacológico , Interferons/uso terapêutico , Fígado/virologia , Ribavirina/uso terapêutico , Biópsia por Agulha , Estudos de Casos e Controles , DNA Viral/análise , Quimioterapia Combinada , Genótipo , Vírus da Hepatite B/genética , Hepatite B/complicações , Hepatite B/patologia , Hepatite C Crônica/complicações , Hepatite C Crônica/patologia , Fígado/patologia , Reação em Cadeia da Polimerase , Fatores de Risco
6.
In. Cimerman, Sérgio; Cimerman, Benjamin. Medicina tropical. São Paulo, Atheneu, 2003. p.397-423, ilus, tab, graf.
Monografia em Português | LILACS, SES-SP | ID: lil-344618
7.
Rev. Inst. Med. Trop. Säo Paulo ; 40(4): 219-24, July-Aug. 1998. tab
Artigo em Inglês | LILACS | ID: lil-225879

RESUMO

A determinacao dos niveis de alanina aminotransferase (ALT) tem sido util para o diagnostico de hepatopatias. Ultimamente, a elevacao dos niveis sericos de ALT em doadores de sangue, tem sido associada a um maior risco de hepatites pos-tranfusionais. Este estudo busca identificar os fatores associados com elevados niveis de ALT entre doadores voluntarios de sangue e avaliar as relacoes entre estes aumentos de ALT e o desenvolvimento de infeccao pelo virus da hepatite C. Assim, 116 doadores voluntarios de sangue com niveis de ALT elevados, quando da primeira doacao, foram estudados. Todos foram questionados sobre hepatopatias previas, exposicao a hepatites, exposicao a produtos quimicos, uso de drogas ou medicamentos, comportamento sexual, contacto com sangue ou secrecoes e consumo de alcool...


Assuntos
Alanina Transaminase/análise , Doadores de Sangue , Hepatite C/prevenção & controle , Abdome , Seguimentos , Anticorpos Anti-Hepatite C/imunologia , Hepatite C/diagnóstico , Hepatopatias/diagnóstico , Fatores de Risco , Transfusão de Sangue/efeitos adversos
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