Publicação

Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre

Ver documento

Detalhes bibliográficos
Resumo:Introduction: Calcineurin inhibitors are currently considered the cornerstone of maintenance immunosuppression in renal transplantation. The extended release formulation of tacrolimus (ER-TAC) was developed to improve drug adherence in these patients. The long-term safety and efficacy of the conversion from the twice-daily tacrolimus to the ER-TAC is still undetermined. Subjects and Methods: Retrospective registry-based single centre study including all renal transplant recipients converted from TAC twice-daily to the ER-TAC on a 1: 1 mg basis. We collected biometric data, induction regimens, acute rejection episodes and death. Variables of interest [serum creatinine, blood urea nitrogen, fasting glucose, urinalysis, haemoglobin, TAC dose (mg/kg) and TAC trough levels (ng/ml)] were registered at conversion and 1, 6, 12 months and at last follow-up post-conversion. Results: We analysed 127 patients, 71.9 % male, mean age at conversion (± SD) was 49.8 ± 13.6 years. Conversion occurred at 4.10 ± 3.83 years after transplant and our mean follow-up time was 2.56 ± 0.55 years. TAC trough levels (ng/ml) progressively decreased from pre-conversion to the following stages (pre-conversion: 7.41 ± 2.61 vs. last followup: 5.04 ± 1.86, p < 0.001) but no significant dose adjustments were necessary for attaining predetermined target levels. Renal function remained stable and there were no significant differences in glucose metabolism pre and post conversion. No significant adverse effects were verified. There were no episodes of acute rejection throughout the follow-up. Conclusions: The conversion to ER-TAC ensured effective immunosuppression over a follow-up of 2 years suggesting that this formulation is an excellent alternative to the conventional one
Autores principais:Rodrigues,Luís
Outros Autores:Macário,Fernando; Pego,Cátia; Neves,Marta; Romaozinho,Catarina; Santos,Lidia; Alves,Rui; Sa,Helena; Mota,Alfredo; Campos,Mário
Assunto:Conversion extended release immunosuppression renal transplantation tacrolimus
Ano:2015
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Fundação para a Ciência e Tecnologia
Idioma:inglês
Origem:SciELO Portugal
_version_ 1868441695327092736
author Rodrigues,Luís
author2 Macário,Fernando
Pego,Cátia
Neves,Marta
Romaozinho,Catarina
Santos,Lidia
Alves,Rui
Sa,Helena
Mota,Alfredo
Campos,Mário
author2_role author
author
author
author
author
author
author
author
author
author_facet Rodrigues,Luís
Macário,Fernando
Pego,Cátia
Neves,Marta
Romaozinho,Catarina
Santos,Lidia
Alves,Rui
Sa,Helena
Mota,Alfredo
Campos,Mário
author_role author
country_str PT
creators_json_txt [{\"Person.name\":\"Rodrigues,Luís\"},{\"Person.name\":\"Macário,Fernando\"},{\"Person.name\":\"Pego,Cátia\"},{\"Person.name\":\"Neves,Marta\"},{\"Person.name\":\"Romaozinho,Catarina\"},{\"Person.name\":\"Santos,Lidia\"},{\"Person.name\":\"Alves,Rui\"},{\"Person.name\":\"Sa,Helena\"},{\"Person.name\":\"Mota,Alfredo\"},{\"Person.name\":\"Campos,Mário\"}]
datacite.creators.creator.creatorName.fl_str_mv Rodrigues,Luís
Macário,Fernando
Pego,Cátia
Neves,Marta
Romaozinho,Catarina
Santos,Lidia
Alves,Rui
Sa,Helena
Mota,Alfredo
Campos,Mário
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Conversion
extended release
immunosuppression
renal transplantation
tacrolimus
datacite.titles.title.fl_str_mv Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
dc.creator.none.fl_str_mv Rodrigues,Luís
Macário,Fernando
Pego,Cátia
Neves,Marta
Romaozinho,Catarina
Santos,Lidia
Alves,Rui
Sa,Helena
Mota,Alfredo
Campos,Mário
dc.format.none.fl_str_mv text/html
dc.identifier.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000100007
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.source.none.fl_str_mv Portuguese Journal of Nephrology &amp; Hypertension v.29 n.1 2015
dc.subject.none.fl_str_mv Conversion
extended release
immunosuppression
renal transplantation
tacrolimus
dc.title.fl_str_mv Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description Introduction: Calcineurin inhibitors are currently considered the cornerstone of maintenance immunosuppression in renal transplantation. The extended release formulation of tacrolimus (ER-TAC) was developed to improve drug adherence in these patients. The long-term safety and efficacy of the conversion from the twice-daily tacrolimus to the ER-TAC is still undetermined. Subjects and Methods: Retrospective registry-based single centre study including all renal transplant recipients converted from TAC twice-daily to the ER-TAC on a 1: 1 mg basis. We collected biometric data, induction regimens, acute rejection episodes and death. Variables of interest [serum creatinine, blood urea nitrogen, fasting glucose, urinalysis, haemoglobin, TAC dose (mg/kg) and TAC trough levels (ng/ml)] were registered at conversion and 1, 6, 12 months and at last follow-up post-conversion. Results: We analysed 127 patients, 71.9 % male, mean age at conversion (± SD) was 49.8 ± 13.6 years. Conversion occurred at 4.10 ± 3.83 years after transplant and our mean follow-up time was 2.56 ± 0.55 years. TAC trough levels (ng/ml) progressively decreased from pre-conversion to the following stages (pre-conversion: 7.41 ± 2.61 vs. last followup: 5.04 ± 1.86, p < 0.001) but no significant dose adjustments were necessary for attaining predetermined target levels. Renal function remained stable and there were no significant differences in glucose metabolism pre and post conversion. No significant adverse effects were verified. There were no episodes of acute rejection throughout the follow-up. Conclusions: The conversion to ER-TAC ensured effective immunosuppression over a follow-up of 2 years suggesting that this formulation is an excellent alternative to the conventional one
dirty 0
eu_rights_str_mv openAccess
format article
id scielopt_4e7e3971d38f8b29a1b3c2aa4653d6aa
identifier.url.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000100007
instacron_str SciELO
institution Fundação para a Ciência e Tecnologia
instname_str Fundação para a Ciência e Tecnologia
language eng
network_acronym_str scielopt
network_name_str SciELO Portugal
oai_identifier_str oai:scielo:S0872-01692015000100007
organization_str_mv urn:organizationAcronym:scielo
person_str_mv Rodrigues,Luís
Macário,Fernando
Pego,Cátia
Neves,Marta
Romaozinho,Catarina
Santos,Lidia
Alves,Rui
Sa,Helena
Mota,Alfredo
Campos,Mário
publishDate 2015
publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
reponame_str SciELO Portugal
repository_id_str urn:repositoryAcronym:scielopt
service_str_mv urn:repositoryAcronym:scielopt
spelling Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centreRodrigues,LuísMacário,FernandoPego,CátiaNeves,MartaRomaozinho,CatarinaSantos,LidiaAlves,RuiSa,HelenaMota,AlfredoCampos,MárioConversionextended releaseimmunosuppressionrenal transplantationtacrolimusopen accesshttp://purl.org/coar/access_right/c_abf2http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000100007URLhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000100007URLHasVersion2015-03-01Introduction: Calcineurin inhibitors are currently considered the cornerstone of maintenance immunosuppression in renal transplantation. The extended release formulation of tacrolimus (ER-TAC) was developed to improve drug adherence in these patients. The long-term safety and efficacy of the conversion from the twice-daily tacrolimus to the ER-TAC is still undetermined. Subjects and Methods: Retrospective registry-based single centre study including all renal transplant recipients converted from TAC twice-daily to the ER-TAC on a 1: 1 mg basis. We collected biometric data, induction regimens, acute rejection episodes and death. Variables of interest [serum creatinine, blood urea nitrogen, fasting glucose, urinalysis, haemoglobin, TAC dose (mg/kg) and TAC trough levels (ng/ml)] were registered at conversion and 1, 6, 12 months and at last follow-up post-conversion. Results: We analysed 127 patients, 71.9 % male, mean age at conversion (± SD) was 49.8 ± 13.6 years. Conversion occurred at 4.10 ± 3.83 years after transplant and our mean follow-up time was 2.56 ± 0.55 years. TAC trough levels (ng/ml) progressively decreased from pre-conversion to the following stages (pre-conversion: 7.41 ± 2.61 vs. last followup: 5.04 ± 1.86, p < 0.001) but no significant dose adjustments were necessary for attaining predetermined target levels. Renal function remained stable and there were no significant differences in glucose metabolism pre and post conversion. No significant adverse effects were verified. There were no episodes of acute rejection throughout the follow-up. Conclusions: The conversion to ER-TAC ensured effective immunosuppression over a follow-up of 2 years suggesting that this formulation is an excellent alternative to the conventional oneSociedade Portuguesa de NefrologiaPortuguese Journal of Nephrology &amp; Hypertension v.29 n.1 2015text/htmlengjournal articlehttp://purl.org/coar/resource_type/c_6501literature
spellingShingle Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
Rodrigues,Luís
Conversion
extended release
immunosuppression
renal transplantation
tacrolimus
status SINGLETON
subject.fl_str_mv Conversion
extended release
immunosuppression
renal transplantation
tacrolimus
title Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
title_full Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
title_fullStr Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
title_full_unstemmed Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
title_short Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
title_sort Conversion from twice-daily tacrolimus to an extended release formulation in stable kidney transplant recipients: 2-year follow-up results of a single centre
topic Conversion
extended release
immunosuppression
renal transplantation
tacrolimus
topic_facet Conversion
extended release
immunosuppression
renal transplantation
tacrolimus
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000100007
visible 1