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1.
Int J STD AIDS ; 24(4): 263-8, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23635810

RESUMO

Management of tuberculosis (TB)-HIV co-infection is complicated by interactions between the diseases and their therapies. We developed and evaluated a strategy to (i) treat co-infected patients in a single co-infection clinic, (ii) maximize use of first-line drugs, (iii) delay antiretroviral therapy (ART) until two months post-TB treatment except in severe immunosuppression, (iv) commence efavirenz at 600 mg daily with therapeutic drug monitoring (TDM) and (v) target treatment completion. We conducted a prospective cohort review over 5.5 years in a UK tertiary referral center where 56 HIV-positive patients treated for TB were followed-up for a median 30 months. Main outcome measures were treatment completion, adverse events, immune reconstitution inflammatory syndrome, immunological and virological parameters, and TDM for efavirenz. Treatment completion rates were 88% (49/56); four patients were lost to local follow-up and three (5.4%) died during treatment; no deaths were TB-related. Adverse events were common (55%), but caused no treatment interruptions. Standard doses (600 mg daily) of efavirenz with rifampicin achieved or exceeded therapeutic levels in 25/28 (89%). This study supports combined management for TB-HIV co-infected patients. Delaying ART to two months post-TB treatment did not seem to result in poor clinical outcomes in this well-resourced context. Although efavirenz 600 mg daily usually achieved satisfactory levels, TDM is recommended.


Assuntos
Antibióticos Antituberculose/uso terapêutico , Monitoramento de Medicamentos/métodos , Infecções por HIV/complicações , Tuberculose/tratamento farmacológico , Adulto , Alcinos , Fármacos Anti-HIV/uso terapêutico , Antibióticos Antituberculose/efeitos adversos , Benzoxazinas/uso terapêutico , Coinfecção/complicações , Coinfecção/tratamento farmacológico , Ciclopropanos , Infecções por HIV/tratamento farmacológico , Humanos , Pessoa de Meia-Idade , Mycobacterium/isolamento & purificação , Estudos Prospectivos , Rifampina/uso terapêutico , Fatores de Tempo , Resultado do Tratamento , Tuberculose/complicações , Reino Unido , Carga Viral
2.
J Obstet Gynaecol ; 29(1): 44-8, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19280495

RESUMO

This study aims to ascertain the perception of cervical screening practices among HIV-positive women attending an ART clinic in urban South Africa. It is a prospective cross-sectional study of 100 randomly selected patients using semi-structured interviews. Answers to fixed-response questions were recorded for statistical analysis and themes were identified from responses to open-ended questions. The study found that 59% of women surveyed reported ever having had a Papanicolau (Pap) smear and that 41% of these women had never been notified of the result. Many women surveyed lacked understanding of cervical screening; 78% had never heard of cervical cancer and around 40% had no correct knowledge about Pap smears. The findings suggest that cervical screening practices among HIV-positive women living in urban South Africa do not comply with the recommendations that are based on evidence of increased risk for this population. Systematic cervical screening programmes should be offered to HIV-positive women attending ART clinics in South Africa.


Assuntos
Infecções por HIV , Conhecimentos, Atitudes e Prática em Saúde , Teste de Papanicolaou , Displasia do Colo do Útero/prevenção & controle , Neoplasias do Colo do Útero/prevenção & controle , Esfregaço Vaginal/psicologia , Adulto , Instituições de Assistência Ambulatorial , Estudos Transversais , Feminino , Infecções por HIV/complicações , Humanos , Fatores de Risco , África do Sul , Displasia do Colo do Útero/complicações , Neoplasias do Colo do Útero/complicações
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