Efficacy of trimethoprim-sulfamethoxazole in the treatment of cerebral toxoplasmosis in Aids patients

Detalhes bibliográficos
Autor(a) principal: Otilia Rabenschlag Pellegrino, Daniela
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
id SESSP_e1e98aa8db18117724c7f73695281f93
oai_identifier_str oai:ojs.periodicos.saude.sp.gov.br:article/37659
network_acronym_str SESSP
network_name_str BEPA. Boletim epidemiológico paulista (Online)
repository_id_str
spelling 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
publishDate 2022
dc.date.none.fl_str_mv 2022-06-11
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Não avaliado pelos pares
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://periodicos.saude.sp.gov.br/BEPA182/article/view/37659
url https://periodicos.saude.sp.gov.br/BEPA182/article/view/37659
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://periodicos.saude.sp.gov.br/BEPA182/article/view/37659/35675
dc.rights.driver.fl_str_mv Copyright (c) 2022 Daniela Otilia Rabenschlag Pellegrino
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Daniela Otilia Rabenschlag Pellegrino
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Coordenadoria de Controle de Doenças - Secretaria de Estado da Saúde de São Paulo
publisher.none.fl_str_mv Coordenadoria de Controle de Doenças - Secretaria de Estado da Saúde de São Paulo
dc.source.none.fl_str_mv 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
instname_str Secretaria de Estado da Saúde de São Paulo (SES-SP)
instacron_str SESSP
institution SESSP
reponame_str BEPA. Boletim epidemiológico paulista (Online)
collection BEPA. Boletim epidemiológico paulista (Online)
repository.name.fl_str_mv BEPA. Boletim epidemiológico paulista (Online) - Secretaria de Estado da Saúde de São Paulo (SES-SP)
repository.mail.fl_str_mv bepa@saude.sp.gov.br | periodicossp@saude.sp.gov.br
_version_ 1838465356810682368