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Profilaxis de enfermedad de Chagas en niños y adultos sometidos a trasplante de órganos sólidos y de precursores hematopoyéticos / Prophylaxis against Chagas disease in pediatric and adult patients undergoing solid organ and hematopoietic stem cells transplantation
Benítez, Rosana; Noemí, Isabel; Tassara, Renzo; Catalán, Paula; Aviles, Carmen L.
  • Benítez, Rosana; Hospital DIPRECA. Servicio de Medicina. Santiago. CL
  • Noemí, Isabel; Hospital Dr. Luis Calvo Mackenna. Departamento de Pediatría. Santiago. CL
  • Tassara, Renzo; Universidad de Chile. Facultad de Medicina. CL
  • Catalán, Paula; Hospital Dr. Luis Calvo Mackenna. Unidad de Trasplante de Precursores Hematopoyéticos. Santiago. CL
  • Aviles, Carmen L; Universidad de Chile. Facultad de Medicina. CL
Rev. chil. infectol ; 29(supl.1): 41-44, set. 2012. tab
Article in Spanish | LILACS | ID: lil-656326
ABSTRACT
Chagas disease is a zoonosis caused by T. cruzi. The estimated prevalence in endemic areas is 0.6-0.9 / 100,000. In immunocompromised behaves as an opportunistic pathogen highly aggressive and can evolve with meningoencephalitis, myocarditis or systemic disease. We recommend obtaining serology for all donor and recipient of SOT and HSCT. An infected donor should be discarded as such. In the case of D (-) R (+) exists controversy between prophylaxis and pre emptive therapy. The chosen drug for prophylaxis is nifurtimox for 3 months, effective but with relevant adverse effects. Monitoring should be done with RPC and MicroStrout weekly until six months post-transplant, then on a monthly basis for the duration of immunosuppression and continued for life clinical monitoring (C3).
RESUMEN
La enfermedad de Chagas es una zoonosis producida por T. cruzi. La prevalencia estimada en áreas endémicas es de 0,6-0,9/100.000 habitantes . En inmunocomprome-tidos se comporta como un patógeno oportunista de alta agresividad, pudiendo evolucionar con cuadros meningo-encefálicos, miocárdicos o sistémicos. Se recomienda obtener serología para todo donante y receptor de TOS y TPH. Un donante infectado se descarta como tal. En caso de D (-) R (+) existe controversia entre realizar proilaxis o vigilancia más terapia anticipada. La proilaxis aceptada es con nifurtimox por tres meses, efectiva pero con efectos adversos importantes. El seguimiento debe realizarse con RPC y MicroStrout semanal hasta los seis meses post-trasplante; luego, en forma mensual mientras dure la inmunosupresión y continuar de por vida la vigilancia clínica (C3).
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Trypanocidal Agents / Organ Transplantation / Chagas Disease / Stem Cell Transplantation / Nifurtimox Type of study: Practice guideline / Observational study / Prognostic study / Risk factors Limits: Adult / Child / Humans Language: Spanish Journal: Rev. chil. infectol Journal subject: Communicable Diseases Year: 2012 Type: Article Affiliation country: Chile Institution/Affiliation country: Hospital DIPRECA/CL / Hospital Dr. Luis Calvo Mackenna/CL / Universidad de Chile/CL

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Full text: Available Index: LILACS (Americas) Main subject: Trypanocidal Agents / Organ Transplantation / Chagas Disease / Stem Cell Transplantation / Nifurtimox Type of study: Practice guideline / Observational study / Prognostic study / Risk factors Limits: Adult / Child / Humans Language: Spanish Journal: Rev. chil. infectol Journal subject: Communicable Diseases Year: 2012 Type: Article Affiliation country: Chile Institution/Affiliation country: Hospital DIPRECA/CL / Hospital Dr. Luis Calvo Mackenna/CL / Universidad de Chile/CL