Cytomegalovirus infection in transplant recipients
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/101088 |
Resumo: | Cytomegalovirus infection is a frequent complication after transplantation. This infection occurs due to transmission from the transplanted organ, due to reactivation of latent infection, or after a primary infection in seronegative patients and can be defined as follows: latent infection, active infection, viral syndrome or invasive disease. This condition occurs mainly between 30 and 90 days after transplantation. In hematopoietic stem cell transplantation in particular, infection usually occurs within the first 30 days after transplantation and in the presence of graft-versus-host disease. The major risk factors are when the recipient is cytomegalovirus seronegative and the donor is seropositive as well as when lymphocyte-depleting antibodies are used. There are two methods for the diagnosis of cytomegalovirus infection: the pp65 antigenemia assay and polymerase chain reaction. Serology has no value for the diagnosis of active disease, whereas histology of the affected tissue and bronchoalveolar lavage analysis are useful in the diagnosis of invasive disease. Cytomegalovirus disease can be prevented by prophylaxis (the administration of antiviral drugs to all or to a subgroup of patients who are at higher risk of viral replication) or by preemptive therapy (the early diagnosis of viral replication before development of the disease and prescription of antiviral treatment to prevent the appearance of clinical disease). The drug used is intravenous or oral ganciclovir; oral valganciclovir; or, less frequently, valacyclovir. Prophylaxis should continue for 90 to 180 days. Treatment is always indicated in cytomegalovirus disease, and the gold-standard drug is intravenous ganciclovir. Treatment should be given for 2 to 3 weeks and should be continued for an additional 7 days after the first negative result for viremia. |
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Clinics |
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Cytomegalovirus infection in transplant recipients Cytomegalovirus infection is a frequent complication after transplantation. This infection occurs due to transmission from the transplanted organ, due to reactivation of latent infection, or after a primary infection in seronegative patients and can be defined as follows: latent infection, active infection, viral syndrome or invasive disease. This condition occurs mainly between 30 and 90 days after transplantation. In hematopoietic stem cell transplantation in particular, infection usually occurs within the first 30 days after transplantation and in the presence of graft-versus-host disease. The major risk factors are when the recipient is cytomegalovirus seronegative and the donor is seropositive as well as when lymphocyte-depleting antibodies are used. There are two methods for the diagnosis of cytomegalovirus infection: the pp65 antigenemia assay and polymerase chain reaction. Serology has no value for the diagnosis of active disease, whereas histology of the affected tissue and bronchoalveolar lavage analysis are useful in the diagnosis of invasive disease. Cytomegalovirus disease can be prevented by prophylaxis (the administration of antiviral drugs to all or to a subgroup of patients who are at higher risk of viral replication) or by preemptive therapy (the early diagnosis of viral replication before development of the disease and prescription of antiviral treatment to prevent the appearance of clinical disease). The drug used is intravenous or oral ganciclovir; oral valganciclovir; or, less frequently, valacyclovir. Prophylaxis should continue for 90 to 180 days. Treatment is always indicated in cytomegalovirus disease, and the gold-standard drug is intravenous ganciclovir. Treatment should be given for 2 to 3 weeks and should be continued for an additional 7 days after the first negative result for viremia. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2015-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/10108810.6061/clinics/2015(07)09Clinics; Vol. 70 No. 7 (2015); 515-523Clinics; v. 70 n. 7 (2015); 515-523Clinics; Vol. 70 Núm. 7 (2015); 515-5231980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/101088/99747Copyright (c) 2015 Clinicsinfo:eu-repo/semantics/openAccessAzevedo, Luiz Sergio Pierrotti, Lígia Camera Abdala, Edson Costa, Silvia Figueiredo Strabelli, Tânia Mara Varejão Campos, Silvia Vidal Ramos, Jéssica Fernandes Latif, Acram Zahredine Abdul Litvinov, Nadia Maluf, Natalya Zaidan Filho, Helio Hehl Caiaffa Pannuti, Claudio Sergio Lopes, Marta Heloisa Santos, Vera Aparecida dos Linardi, Camila da Cruz Gouveia Yasuda, Maria Aparecida Shikanai Marques, Heloisa Helena de Sousa 2015-07-28T16:48:23Zoai:revistas.usp.br:article/101088Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2015-07-28T16:48:23Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Cytomegalovirus infection in transplant recipients |
title |
Cytomegalovirus infection in transplant recipients |
spellingShingle |
Cytomegalovirus infection in transplant recipients Azevedo, Luiz Sergio |
title_short |
Cytomegalovirus infection in transplant recipients |
title_full |
Cytomegalovirus infection in transplant recipients |
title_fullStr |
Cytomegalovirus infection in transplant recipients |
title_full_unstemmed |
Cytomegalovirus infection in transplant recipients |
title_sort |
Cytomegalovirus infection in transplant recipients |
author |
Azevedo, Luiz Sergio |
author_facet |
Azevedo, Luiz Sergio Pierrotti, Lígia Camera Abdala, Edson Costa, Silvia Figueiredo Strabelli, Tânia Mara Varejão Campos, Silvia Vidal Ramos, Jéssica Fernandes Latif, Acram Zahredine Abdul Litvinov, Nadia Maluf, Natalya Zaidan Filho, Helio Hehl Caiaffa Pannuti, Claudio Sergio Lopes, Marta Heloisa Santos, Vera Aparecida dos Linardi, Camila da Cruz Gouveia Yasuda, Maria Aparecida Shikanai Marques, Heloisa Helena de Sousa |
author_role |
author |
author2 |
Pierrotti, Lígia Camera Abdala, Edson Costa, Silvia Figueiredo Strabelli, Tânia Mara Varejão Campos, Silvia Vidal Ramos, Jéssica Fernandes Latif, Acram Zahredine Abdul Litvinov, Nadia Maluf, Natalya Zaidan Filho, Helio Hehl Caiaffa Pannuti, Claudio Sergio Lopes, Marta Heloisa Santos, Vera Aparecida dos Linardi, Camila da Cruz Gouveia Yasuda, Maria Aparecida Shikanai Marques, Heloisa Helena de Sousa |
author2_role |
author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Azevedo, Luiz Sergio Pierrotti, Lígia Camera Abdala, Edson Costa, Silvia Figueiredo Strabelli, Tânia Mara Varejão Campos, Silvia Vidal Ramos, Jéssica Fernandes Latif, Acram Zahredine Abdul Litvinov, Nadia Maluf, Natalya Zaidan Filho, Helio Hehl Caiaffa Pannuti, Claudio Sergio Lopes, Marta Heloisa Santos, Vera Aparecida dos Linardi, Camila da Cruz Gouveia Yasuda, Maria Aparecida Shikanai Marques, Heloisa Helena de Sousa |
description |
Cytomegalovirus infection is a frequent complication after transplantation. This infection occurs due to transmission from the transplanted organ, due to reactivation of latent infection, or after a primary infection in seronegative patients and can be defined as follows: latent infection, active infection, viral syndrome or invasive disease. This condition occurs mainly between 30 and 90 days after transplantation. In hematopoietic stem cell transplantation in particular, infection usually occurs within the first 30 days after transplantation and in the presence of graft-versus-host disease. The major risk factors are when the recipient is cytomegalovirus seronegative and the donor is seropositive as well as when lymphocyte-depleting antibodies are used. There are two methods for the diagnosis of cytomegalovirus infection: the pp65 antigenemia assay and polymerase chain reaction. Serology has no value for the diagnosis of active disease, whereas histology of the affected tissue and bronchoalveolar lavage analysis are useful in the diagnosis of invasive disease. Cytomegalovirus disease can be prevented by prophylaxis (the administration of antiviral drugs to all or to a subgroup of patients who are at higher risk of viral replication) or by preemptive therapy (the early diagnosis of viral replication before development of the disease and prescription of antiviral treatment to prevent the appearance of clinical disease). The drug used is intravenous or oral ganciclovir; oral valganciclovir; or, less frequently, valacyclovir. Prophylaxis should continue for 90 to 180 days. Treatment is always indicated in cytomegalovirus disease, and the gold-standard drug is intravenous ganciclovir. Treatment should be given for 2 to 3 weeks and should be continued for an additional 7 days after the first negative result for viremia. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-07-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/101088 10.6061/clinics/2015(07)09 |
url |
https://www.revistas.usp.br/clinics/article/view/101088 |
identifier_str_mv |
10.6061/clinics/2015(07)09 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/101088/99747 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2015 Clinics info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2015 Clinics |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 70 No. 7 (2015); 515-523 Clinics; v. 70 n. 7 (2015); 515-523 Clinics; Vol. 70 Núm. 7 (2015); 515-523 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222762176872448 |