Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model

Detalhes bibliográficos
Autor(a) principal: Medeiros, Israel L.
Data de Publicação: 2012
Outros Autores: Pêgo-Fernandes, Paulo M., Mariani, Alessandro W., Fernandes, Flávio G., Unterpertinger, Fernando V., Canzian, Mauro, Jatene, Fabio B.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/45878
Resumo: OBJECTIVE: Experimental studies on lung preservation have always been performed using animal models. We present ex vivo lung perfusion as a new model for the study of lung preservation. Using human lungs instead of animal models may bring the results of experimental studies closer to what could be expected in clinical practice. METHOD: Brain-dead donors whose lungs had been declined by transplantation teams were used. The cases were randomized into two groups. In Group 1, Perfadex®was used for pulmonary preservation, and in Group 2, LPDnac, a solution manufactured in Brazil, was used. An ex vivo lung perfusion system was used, and the lungs were ventilated and perfused after 10 hours of cold ischemia. The extent of ischemic-reperfusion injury was measured using functional and histological parameters. RESULTS: After reperfusion, the mean oxygenation capacity was 405.3 mmHg in Group 1 and 406.0 mmHg in Group 2 (p = 0.98). The mean pulmonary vascular resistance values were 697.6 and 378.3 dyn·s·cm-5, respectively (p =0.035). The mean pulmonary compliance was 46.8 cm H20 in Group 1 and 49.3 ml/cm H20 in Group 2 (p =0.816). The mean wet/dry weight ratios were 2.06 and 2.02, respectively (p=0.87). The mean Lung Injury Scores for the biopsy performed after reperfusion were 4.37 and 4.37 in Groups 1 and 2, respectively (p = 1.0), and the apoptotic cell counts were 118.75/mm² and 137.50/mm², respectively (p=0.71). CONCLUSION: The locally produced preservation solution proved to be as good as Perfadex®. The clinical use of LPDnac may reduce costs in our centers. Therefore, it is important to develop new models to study lung preservation.
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spelling Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental modelLung TransplantationOrgan PreservationIschemia-Reperfusion InjuryOBJECTIVE: Experimental studies on lung preservation have always been performed using animal models. We present ex vivo lung perfusion as a new model for the study of lung preservation. Using human lungs instead of animal models may bring the results of experimental studies closer to what could be expected in clinical practice. METHOD: Brain-dead donors whose lungs had been declined by transplantation teams were used. The cases were randomized into two groups. In Group 1, Perfadex®was used for pulmonary preservation, and in Group 2, LPDnac, a solution manufactured in Brazil, was used. An ex vivo lung perfusion system was used, and the lungs were ventilated and perfused after 10 hours of cold ischemia. The extent of ischemic-reperfusion injury was measured using functional and histological parameters. RESULTS: After reperfusion, the mean oxygenation capacity was 405.3 mmHg in Group 1 and 406.0 mmHg in Group 2 (p = 0.98). The mean pulmonary vascular resistance values were 697.6 and 378.3 dyn·s·cm-5, respectively (p =0.035). The mean pulmonary compliance was 46.8 cm H20 in Group 1 and 49.3 ml/cm H20 in Group 2 (p =0.816). The mean wet/dry weight ratios were 2.06 and 2.02, respectively (p=0.87). The mean Lung Injury Scores for the biopsy performed after reperfusion were 4.37 and 4.37 in Groups 1 and 2, respectively (p = 1.0), and the apoptotic cell counts were 118.75/mm² and 137.50/mm², respectively (p=0.71). CONCLUSION: The locally produced preservation solution proved to be as good as Perfadex®. The clinical use of LPDnac may reduce costs in our centers. Therefore, it is important to develop new models to study lung preservation.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2012-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/4587810.6061/clinics/2012(09)19Clinics; v. 67 n. 9 (2012); 1101-1106Clinics; Vol. 67 Núm. 9 (2012); 1101-1106Clinics; Vol. 67 No. 9 (2012); 1101-11061980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/45878/49481Medeiros, Israel L.Pêgo-Fernandes, Paulo M.Mariani, Alessandro W.Fernandes, Flávio G.Unterpertinger, Fernando V.Canzian, MauroJatene, Fabio B.info:eu-repo/semantics/openAccess2012-10-10T20:42:48Zoai:revistas.usp.br:article/45878Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-10-10T20:42:48Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
title Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
spellingShingle Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
Medeiros, Israel L.
Lung Transplantation
Organ Preservation
Ischemia-Reperfusion Injury
title_short Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
title_full Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
title_fullStr Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
title_full_unstemmed Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
title_sort Comparison of lung preservation solutions in human lungs using an ex vivo lung perfusion experimental model
author Medeiros, Israel L.
author_facet Medeiros, Israel L.
Pêgo-Fernandes, Paulo M.
Mariani, Alessandro W.
Fernandes, Flávio G.
Unterpertinger, Fernando V.
Canzian, Mauro
Jatene, Fabio B.
author_role author
author2 Pêgo-Fernandes, Paulo M.
Mariani, Alessandro W.
Fernandes, Flávio G.
Unterpertinger, Fernando V.
Canzian, Mauro
Jatene, Fabio B.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Medeiros, Israel L.
Pêgo-Fernandes, Paulo M.
Mariani, Alessandro W.
Fernandes, Flávio G.
Unterpertinger, Fernando V.
Canzian, Mauro
Jatene, Fabio B.
dc.subject.por.fl_str_mv Lung Transplantation
Organ Preservation
Ischemia-Reperfusion Injury
topic Lung Transplantation
Organ Preservation
Ischemia-Reperfusion Injury
description OBJECTIVE: Experimental studies on lung preservation have always been performed using animal models. We present ex vivo lung perfusion as a new model for the study of lung preservation. Using human lungs instead of animal models may bring the results of experimental studies closer to what could be expected in clinical practice. METHOD: Brain-dead donors whose lungs had been declined by transplantation teams were used. The cases were randomized into two groups. In Group 1, Perfadex®was used for pulmonary preservation, and in Group 2, LPDnac, a solution manufactured in Brazil, was used. An ex vivo lung perfusion system was used, and the lungs were ventilated and perfused after 10 hours of cold ischemia. The extent of ischemic-reperfusion injury was measured using functional and histological parameters. RESULTS: After reperfusion, the mean oxygenation capacity was 405.3 mmHg in Group 1 and 406.0 mmHg in Group 2 (p = 0.98). The mean pulmonary vascular resistance values were 697.6 and 378.3 dyn·s·cm-5, respectively (p =0.035). The mean pulmonary compliance was 46.8 cm H20 in Group 1 and 49.3 ml/cm H20 in Group 2 (p =0.816). The mean wet/dry weight ratios were 2.06 and 2.02, respectively (p=0.87). The mean Lung Injury Scores for the biopsy performed after reperfusion were 4.37 and 4.37 in Groups 1 and 2, respectively (p = 1.0), and the apoptotic cell counts were 118.75/mm² and 137.50/mm², respectively (p=0.71). CONCLUSION: The locally produced preservation solution proved to be as good as Perfadex®. The clinical use of LPDnac may reduce costs in our centers. Therefore, it is important to develop new models to study lung preservation.
publishDate 2012
dc.date.none.fl_str_mv 2012-09-01
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/45878
10.6061/clinics/2012(09)19
url https://www.revistas.usp.br/clinics/article/view/45878
identifier_str_mv 10.6061/clinics/2012(09)19
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/45878/49481
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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; v. 67 n. 9 (2012); 1101-1106
Clinics; Vol. 67 Núm. 9 (2012); 1101-1106
Clinics; Vol. 67 No. 9 (2012); 1101-1106
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
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