Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2022 |
| Tipo de documento: | Artigo |
| Idioma: | por |
| Título da fonte: | BEPA. Boletim epidemiológico paulista (Online) |
| Texto Completo: | https://periodicos.saude.sp.gov.br/BEPA182/article/view/37659 |
Resumo: | Cerebral toxoplasmosis (CT) continues to cause high morbimortality in developingcountries. The association of sulfadiazine and pyrimetamine (PS) is considered themainstay therapy, however, it has several disadvantages: toxicity, cost, burden of pills,low availability and the lack of a parenteral formulation. Prospective, open, single-armclinical trial to evaluate the efficacy and safety of trimethoprim- sulfamethoxazole (TMPSMX) in the treatment of CT in AIDS patients. Eligible AIDS patients had presumptiveCT, were more than 18 years old, no known allergy to the study drugs, and had noconcomitant infection of the central nervous system. Patients received TMP 10 mg/kg/day plus SMX 50 mg/kg/day BID, given orally or intravenously. Clinical and laboratoryevaluation were performed at study entry and weekly thereafter. Computed tomographyscans were performed at study entry and after 2 weeks of treatment. Clinical response wasdefined as resolution of at least 50% of neurological symptoms similarly; radiologicalresponse consisted in more than 50% decrease in number and size of initial lesions. Fortysix patients were included (23 males, median age 35) Median of CD4 cell count was 74cells/mm³. The main symptoms were headache, hemiparesis and altered mental status.First time of presumptive CT was reported in 33 (72%) patients and for 21% CT was thedefining aids condition. After two weeks of treatment, clinical and radiological responseoccurred in 39 (85%) patients. Overall, TMP-SMX was safe, 5 (11%) patients had adverseevents; 3 (6%) patients presented a Grade 1-2 skin rash, 1(2%) patient a clinical adverseevent grade 2 and 1 (2%) patient a laboratory abnormality grade 3. During a twelve-weekfollow up, a high relapse rate (22%) was observed and was associated to non-adherence,TMP-SMX was used to treat all relapses and was effective in 90% of patients. Mortalitywas 2% at 4 weeks and 9% at 12 weeks and overall mortality was 11%. In this study,TMP-SMX was effective and well tolerated in AIDS patients with CT |
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Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patientsEficácia da associação trimetoprim-sulfametoxazol no tratamento da toxoplasmose cerebral em pacientes com AidsCerebral toxoplasmosis (CT) continues to cause high morbimortality in developingcountries. The association of sulfadiazine and pyrimetamine (PS) is considered themainstay therapy, however, it has several disadvantages: toxicity, cost, burden of pills,low availability and the lack of a parenteral formulation. Prospective, open, single-armclinical trial to evaluate the efficacy and safety of trimethoprim- sulfamethoxazole (TMPSMX) in the treatment of CT in AIDS patients. Eligible AIDS patients had presumptiveCT, were more than 18 years old, no known allergy to the study drugs, and had noconcomitant infection of the central nervous system. Patients received TMP 10 mg/kg/day plus SMX 50 mg/kg/day BID, given orally or intravenously. Clinical and laboratoryevaluation were performed at study entry and weekly thereafter. Computed tomographyscans were performed at study entry and after 2 weeks of treatment. Clinical response wasdefined as resolution of at least 50% of neurological symptoms similarly; radiologicalresponse consisted in more than 50% decrease in number and size of initial lesions. Fortysix patients were included (23 males, median age 35) Median of CD4 cell count was 74cells/mm³. The main symptoms were headache, hemiparesis and altered mental status.First time of presumptive CT was reported in 33 (72%) patients and for 21% CT was thedefining aids condition. After two weeks of treatment, clinical and radiological responseoccurred in 39 (85%) patients. Overall, TMP-SMX was safe, 5 (11%) patients had adverseevents; 3 (6%) patients presented a Grade 1-2 skin rash, 1(2%) patient a clinical adverseevent grade 2 and 1 (2%) patient a laboratory abnormality grade 3. During a twelve-weekfollow up, a high relapse rate (22%) was observed and was associated to non-adherence,TMP-SMX was used to treat all relapses and was effective in 90% of patients. Mortalitywas 2% at 4 weeks and 9% at 12 weeks and overall mortality was 11%. In this study,TMP-SMX was effective and well tolerated in AIDS patients with CTA toxoplasmose cerebral (TC) continua causando alta morbimortalidade em países emdesenvolvimento. A associação sulfadiazina e pirimetamina é considerada o tratamentopadrão, entretanto, o uso de trimetroprim-sulfametoxazol (TMP-SMX) oferece diversasvantagens potenciais: menor toxicidade, menor custo, facilidade posológica, maioracessibilidade e disponibilidade de formulação parenteral. Estudo piloto, aberto,prospectivo, para avaliar a eficácia e segurança do TMP-SMX no tratamento da TC empacientes com aids. Foram incluídos pacientes adultos, infectados pelo HIV, com TCpresuntiva, sem alergia às drogas do estudo e sem infecção concomitante do sistemanervoso central. Os pacientes receberam TMP 10 mg/kg/dia e SMX 50 mg/kg/dia12/12h (por via oral ou parenteral) por 6 semanas e em seguida, metade da dose inicial.Avaliações clínicas e laboratoriais foram realizadas na entrada do estudo e semanalmente.As tomografias computadorizadas de crânio foram realizadas na entrada do estudo e apósduas semanas. As respostas clínica e radiológica foram definidas como 50% ou maisde melhora nos sintomas neurológicos e 50% ou mais de decréscimo no número e/outamanho das lesões iniciais, respectivamente. Quarenta e seis pacientes foram incluídos(23 do sexo masculino, a média de idade foi de 35 anos). A contagem média de CD4 foide 74 células/mm3. Para 34 (72%) pacientes este era o primeiro episódio de TC, e em21% a TC foi doença definidora de aids. Os sintomas mais frequentes foram cefaleia,déficit focal e confusão mental. Os achados radiológicos mais frequentes foram lesõesfocais expansivas (supratentoriais) com realce anelar ou nodular pós-contraste, 39 (85%)pacientes apresentaram melhora clínico radiológica. O TMP-SMX foi bem tolerado, 5pacientes (11%) apresentaram reações adversas, sendo 3 (6%) erupções cutâneas grau1-2, uma reação adversa clínica grau 2 (2%) e uma alteração laboratorial grau 3 (2%)resultaram na descontinuação do TMP-SMX. Durante o seguimento de 12 semanas,10 (22%) pacientes apresentaram recidivas por não adesão ao TMP-SMX, todos foramretratados com TMP-SMX e 90% evoluíram com resposta clínico radiológica após 2semanas. A letalidade na 2ª semana foi de 0%, na 4ª semana de 2%, na 12ª semana de9% e a letalidade global do estudo foi de 11%. Neste estudo, TMP-SMX foi eficaz e bemtolerado em pacientes com aids e TC.Coordenadoria de Controle de Doenças - Secretaria de Estado da Saúde de São Paulo2022-06-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionNão avaliado pelos paresapplication/pdfhttps://periodicos.saude.sp.gov.br/BEPA182/article/view/37659BEPA. Boletim Epidemiológico Paulista; Vol. 16 No. 188 (2019)BEPA. Boletim Epidemiológico Paulista; Vol. 16 Núm. 188 (2019)BEPA. Boletim Epidemiológico Paulista ; v. 16 n. 188 (2019)1806-42721806-423Xreponame:BEPA. Boletim epidemiológico paulista (Online)instname:Secretaria de Estado da Saúde de São Paulo (SES-SP)instacron:SESSPporhttps://periodicos.saude.sp.gov.br/BEPA182/article/view/37659/35675Copyright (c) 2022 Daniela Otilia Rabenschlag Pellegrinoinfo:eu-repo/semantics/openAccessOtilia Rabenschlag Pellegrino, Daniela 2023-11-08T14:21:35Zoai:ojs.periodicos.saude.sp.gov.br:article/37659Revistahttps://periodicos.saude.sp.gov.br/BEPA182/indexPUBhttps://periodicos.saude.sp.gov.br/BEPA182/oaibepa@saude.sp.gov.br | periodicossp@saude.sp.gov.brhttps://doi.org/10.57148/bepa1806-42721806-423Xopendoar:2023-11-08T14:21:35BEPA. Boletim epidemiológico paulista (Online) - Secretaria de Estado da Saúde de São Paulo (SES-SP)false |
| dc.title.none.fl_str_mv |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients Eficácia da associação trimetoprim-sulfametoxazol no tratamento da toxoplasmose cerebral em pacientes com Aids |
| title |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients |
| spellingShingle |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients Otilia Rabenschlag Pellegrino, Daniela |
| title_short |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients |
| title_full |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients |
| title_fullStr |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients |
| title_full_unstemmed |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients |
| title_sort |
Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients |
| author |
Otilia Rabenschlag Pellegrino, Daniela |
| author_facet |
Otilia Rabenschlag Pellegrino, Daniela |
| author_role |
author |
| dc.contributor.author.fl_str_mv |
Otilia Rabenschlag Pellegrino, Daniela |
| description |
Cerebral toxoplasmosis (CT) continues to cause high morbimortality in developingcountries. The association of sulfadiazine and pyrimetamine (PS) is considered themainstay therapy, however, it has several disadvantages: toxicity, cost, burden of pills,low availability and the lack of a parenteral formulation. Prospective, open, single-armclinical trial to evaluate the efficacy and safety of trimethoprim- sulfamethoxazole (TMPSMX) in the treatment of CT in AIDS patients. Eligible AIDS patients had presumptiveCT, were more than 18 years old, no known allergy to the study drugs, and had noconcomitant infection of the central nervous system. Patients received TMP 10 mg/kg/day plus SMX 50 mg/kg/day BID, given orally or intravenously. Clinical and laboratoryevaluation were performed at study entry and weekly thereafter. Computed tomographyscans were performed at study entry and after 2 weeks of treatment. Clinical response wasdefined as resolution of at least 50% of neurological symptoms similarly; radiologicalresponse consisted in more than 50% decrease in number and size of initial lesions. Fortysix patients were included (23 males, median age 35) Median of CD4 cell count was 74cells/mm³. The main symptoms were headache, hemiparesis and altered mental status.First time of presumptive CT was reported in 33 (72%) patients and for 21% CT was thedefining aids condition. After two weeks of treatment, clinical and radiological responseoccurred in 39 (85%) patients. Overall, TMP-SMX was safe, 5 (11%) patients had adverseevents; 3 (6%) patients presented a Grade 1-2 skin rash, 1(2%) patient a clinical adverseevent grade 2 and 1 (2%) patient a laboratory abnormality grade 3. During a twelve-weekfollow up, a high relapse rate (22%) was observed and was associated to non-adherence,TMP-SMX was used to treat all relapses and was effective in 90% of patients. Mortalitywas 2% at 4 weeks and 9% at 12 weeks and overall mortality was 11%. In this study,TMP-SMX was effective and well tolerated in AIDS patients with CT |
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2022 |
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2022-06-11 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Não avaliado pelos pares |
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article |
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publishedVersion |
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https://periodicos.saude.sp.gov.br/BEPA182/article/view/37659 |
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https://periodicos.saude.sp.gov.br/BEPA182/article/view/37659 |
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por |
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por |
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https://periodicos.saude.sp.gov.br/BEPA182/article/view/37659/35675 |
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Copyright (c) 2022 Daniela Otilia Rabenschlag Pellegrino info:eu-repo/semantics/openAccess |
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Copyright (c) 2022 Daniela Otilia Rabenschlag Pellegrino |
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openAccess |
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application/pdf |
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Coordenadoria de Controle de Doenças - Secretaria de Estado da Saúde de São Paulo |
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Coordenadoria de Controle de Doenças - Secretaria de Estado da Saúde de São Paulo |
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BEPA. Boletim Epidemiológico Paulista; Vol. 16 No. 188 (2019) BEPA. Boletim Epidemiológico Paulista; Vol. 16 Núm. 188 (2019) BEPA. Boletim Epidemiológico Paulista ; v. 16 n. 188 (2019) 1806-4272 1806-423X reponame:BEPA. Boletim epidemiológico paulista (Online) instname:Secretaria de Estado da Saúde de São Paulo (SES-SP) instacron:SESSP |
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Secretaria de Estado da Saúde de São Paulo (SES-SP) |
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SESSP |
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SESSP |
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BEPA. Boletim epidemiológico paulista (Online) |
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BEPA. Boletim epidemiológico paulista (Online) |
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BEPA. Boletim epidemiológico paulista (Online) - Secretaria de Estado da Saúde de São Paulo (SES-SP) |
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bepa@saude.sp.gov.br | periodicossp@saude.sp.gov.br |
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1838465356810682368 |