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1.
An Bras Dermatol ; 99(5): 670-679, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38851892

RESUMO

BACKGROUND: Hidradenitis suppurativa (HS) is a chronic inflammatory disease that leads to the formation of nodules, abscesses and fistulas, with the formation of scars and fibrosis, causing significant impairment in patient quality of life. The diagnosis is clinical, using scores to classify the severity of the condition; currently the most recommended classification is the International Hidradenitis Suppurativa Severity Scoring System (IHS4). Doppler ultrasound has been used to complement the clinical evaluation of patients with HS. It is possible to observe subclinical lesions that change the staging, the severity of the case, and its treatment, either clinical or surgical. Correct treatment is essential to minimize the consequences of this disease for the patient. OBJECTIVE: To establish an outpatient protocol for the use of Doppler ultrasound in the care of patients with HS. METHODS: A narrative review of the literature was carried out on the use of Doppler ultrasound in patients with hidradenitis suppurativa; a referring protocol and technique orientations for imaging assessment in HS were created. RESULTS: Recommendation to perform ultrasound evaluation of symptomatic areas eight weeks after using antibiotics and four, 12, and 24 weeks after starting immunobiologicals; apply SOS-HS ultrasound severity classification. STUDY LIMITATIONS: The review did not cover all literature on ultrasound and HS; no systematic review was carried out, but rather a narrative one. CONCLUSIONS: The correct assessment of patients staging must be carried out using dermatological ultrasound to avoid progression to scars and fibrosis, which compromise patients quality of life.


Assuntos
Hidradenite Supurativa , Índice de Gravidade de Doença , Ultrassonografia Doppler , Hidradenite Supurativa/diagnóstico por imagem , Humanos , Ultrassonografia Doppler/métodos , Protocolos Clínicos , Qualidade de Vida
2.
Braz J Infect Dis ; 21(6): 606-612, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28759746

RESUMO

INTRODUCTION: The etiology of pulmonary infections in HIV patients is determined by several variables including geographic region and availability of antiretroviral therapy. MATERIALS AND METHODS: A cross-sectional prospective study was conducted from 2012 to 2016 to evaluate the occurrence of pulmonary fungal infection in HIV-patients hospitalized due to pulmonary infections. Patients' serums were tested for (1-3)-ß-D-Glugan, galactomannan, and lactate dehydrogenase. The association among the variables was analyzed by univariate and multivariate regression analysis. RESULTS: 60 patients were included in the study. The patients were classified in three groups: Pneumocystis jirovecii pneumonia (19 patients), community-acquired pneumonia (18 patients), and other infections (23 patients). The overall mortality was 13.3%. The time since diagnosis of HIV infection was shorter in the pneumocystosis group (4.94 years; p=0.001) than for the other two groups of patients. The multivariate analysis showed that higher (1-3)-ß-D-Glucan level (mean: 241pg/mL) and lactate dehydrogenase (mean: 762U/L) were associated with the diagnosis of pneumocystosis. Pneumocystosis was the aids-defining illness in 11 out of 16 newly diagnosed HIV-infected patients. CONCLUSION: In the era of antiretroviral therapy, PJP was still the most prevalent pulmonary infection and (1-3)-ß-D-Glucan and lactate dehydrogenase may be suitable markers to help diagnosing pneumocystosis in our HIV population.


Assuntos
Infecções Oportunistas Relacionadas com a AIDS/diagnóstico , L-Lactato Desidrogenase/sangue , Pneumopatias Fúngicas/diagnóstico , Mananas/sangue , beta-Glucanas/sangue , Infecções Oportunistas Relacionadas com a AIDS/sangue , Biomarcadores/sangue , Estudos Transversais , Feminino , Galactose/análogos & derivados , Humanos , Pneumopatias Fúngicas/sangue , Masculino , Valor Preditivo dos Testes , Estudos Prospectivos , Proteoglicanas , Análise de Regressão , Sensibilidade e Especificidade
3.
Braz. j. infect. dis ; Braz. j. infect. dis;21(6): 606-612, Nov.-Dec. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-888923

RESUMO

ABSTRACT Introduction: The etiology of pulmonary infections in HIV patients is determined by several variables including geographic region and availability of antiretroviral therapy. Materials and methods: A cross-sectional prospective study was conducted from 2012 to 2016 to evaluate the occurrence of pulmonary fungal infection in HIV-patients hospitalized due to pulmonary infections. Patients' serums were tested for (1-3)-β-D-Glugan, galactomannan, and lactate dehydrogenase. The association among the variables was analyzed by univariate and multivariate regression analysis. Results: 60 patients were included in the study. The patients were classified in three groups: Pneumocystis jirovecii pneumonia (19 patients), community-acquired pneumonia (18 patients), and other infections (23 patients). The overall mortality was 13.3%. The time since diagnosis of HIV infection was shorter in the pneumocystosis group (4.94 years; p = 0.001) than for the other two groups of patients. The multivariate analysis showed that higher (1-3)-β-D-Glucan level (mean: 241 pg/mL) and lactate dehydrogenase (mean: 762 U/L) were associated with the diagnosis of pneumocystosis. Pneumocystosis was the aids-defining illness in 11 out of 16 newly diagnosed HIV-infected patients. Conclusion: In the era of antiretroviral therapy, PJP was still the most prevalent pulmonary infection and (1-3)-β-D-Glucan and lactate dehydrogenase may be suitable markers to help diagnosing pneumocystosis in our HIV population.


Assuntos
Humanos , Masculino , Feminino , Infecções Oportunistas Relacionadas com a AIDS/diagnóstico , beta-Glucanas/sangue , L-Lactato Desidrogenase/sangue , Pneumopatias Fúngicas/diagnóstico , Mananas/sangue , Biomarcadores/sangue , Estudos Transversais , Valor Preditivo dos Testes , Estudos Prospectivos , Análise de Regressão , Sensibilidade e Especificidade , Infecções Oportunistas Relacionadas com a AIDS/sangue , Pneumopatias Fúngicas/sangue
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