New therapy of pleural empyema by deoxyribonuclease

Detalhes bibliográficos
Autor(a) principal: Kacprzak,Grzegorz
Data de Publicação: 2013
Outros Autores: Majewski,Andrzej, Kolodziej,Jerzy, Rzechonek,Adam, Gürlich,Robert, Bobek,Vladimir
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Brazilian Journal of Infectious Diseases
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702013000100015
Resumo: Empyema is a severe complication of different diseases and traumas. Management of this complication is difficult and should comprise general and local procedures. The general procedure is mainly based on administering wide-spectrum antibiotics. Local management depends on patient general condition, but in all cases the essential procedure is to insert a drain into the pleural cavity and to evacuate the pus. Sometimes pus is very thick and its evacuation and following re-expansion of the lung is rather impossible. In these patients surgical intervention is needed. The use of intrapleural enzymes to support the drainage was first described in 1949 by Tillett and Sherry using a mixture of streptokinase and streptococcal deoxyribonuclease. Nowadays, purified streptokinase has come into widespread use, but recent studies reported no streptokinase effect on pus viscosity. On the other side, deoxyribonuclease reduces pus viscosity and may be more useful in treatment. We report two cases of intrapleural administration of Pulmozyme (alfa dornase - deoxyribonuclease (HOFFMANN-LA ROCHE AG) in dosage 2 × 2.5 mg with a significant improvement caused by changes in pus viscosity.
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spelling New therapy of pleural empyema by deoxyribonucleaseEmpyemaLungViscosityDeoxyribonucleaseEmpyema is a severe complication of different diseases and traumas. Management of this complication is difficult and should comprise general and local procedures. The general procedure is mainly based on administering wide-spectrum antibiotics. Local management depends on patient general condition, but in all cases the essential procedure is to insert a drain into the pleural cavity and to evacuate the pus. Sometimes pus is very thick and its evacuation and following re-expansion of the lung is rather impossible. In these patients surgical intervention is needed. The use of intrapleural enzymes to support the drainage was first described in 1949 by Tillett and Sherry using a mixture of streptokinase and streptococcal deoxyribonuclease. Nowadays, purified streptokinase has come into widespread use, but recent studies reported no streptokinase effect on pus viscosity. On the other side, deoxyribonuclease reduces pus viscosity and may be more useful in treatment. We report two cases of intrapleural administration of Pulmozyme (alfa dornase - deoxyribonuclease (HOFFMANN-LA ROCHE AG) in dosage 2 × 2.5 mg with a significant improvement caused by changes in pus viscosity.Brazilian Society of Infectious Diseases2013-02-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702013000100015Brazilian Journal of Infectious Diseases v.17 n.1 2013reponame:Brazilian Journal of Infectious Diseasesinstname:Brazilian Society of Infectious Diseases (BSID)instacron:BSID10.1016/j.bjid.2012.08.019info:eu-repo/semantics/openAccessKacprzak,GrzegorzMajewski,AndrzejKolodziej,JerzyRzechonek,AdamGürlich,RobertBobek,Vladimireng2013-02-20T00:00:00Zoai:scielo:S1413-86702013000100015Revistahttps://www.bjid.org.br/https://old.scielo.br/oai/scielo-oai.phpbjid@bjid.org.br||lgoldani@ufrgs.br1678-43911413-8670opendoar:2013-02-20T00:00Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)false
dc.title.none.fl_str_mv New therapy of pleural empyema by deoxyribonuclease
title New therapy of pleural empyema by deoxyribonuclease
spellingShingle New therapy of pleural empyema by deoxyribonuclease
Kacprzak,Grzegorz
Empyema
Lung
Viscosity
Deoxyribonuclease
title_short New therapy of pleural empyema by deoxyribonuclease
title_full New therapy of pleural empyema by deoxyribonuclease
title_fullStr New therapy of pleural empyema by deoxyribonuclease
title_full_unstemmed New therapy of pleural empyema by deoxyribonuclease
title_sort New therapy of pleural empyema by deoxyribonuclease
author Kacprzak,Grzegorz
author_facet Kacprzak,Grzegorz
Majewski,Andrzej
Kolodziej,Jerzy
Rzechonek,Adam
Gürlich,Robert
Bobek,Vladimir
author_role author
author2 Majewski,Andrzej
Kolodziej,Jerzy
Rzechonek,Adam
Gürlich,Robert
Bobek,Vladimir
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Kacprzak,Grzegorz
Majewski,Andrzej
Kolodziej,Jerzy
Rzechonek,Adam
Gürlich,Robert
Bobek,Vladimir
dc.subject.por.fl_str_mv Empyema
Lung
Viscosity
Deoxyribonuclease
topic Empyema
Lung
Viscosity
Deoxyribonuclease
description Empyema is a severe complication of different diseases and traumas. Management of this complication is difficult and should comprise general and local procedures. The general procedure is mainly based on administering wide-spectrum antibiotics. Local management depends on patient general condition, but in all cases the essential procedure is to insert a drain into the pleural cavity and to evacuate the pus. Sometimes pus is very thick and its evacuation and following re-expansion of the lung is rather impossible. In these patients surgical intervention is needed. The use of intrapleural enzymes to support the drainage was first described in 1949 by Tillett and Sherry using a mixture of streptokinase and streptococcal deoxyribonuclease. Nowadays, purified streptokinase has come into widespread use, but recent studies reported no streptokinase effect on pus viscosity. On the other side, deoxyribonuclease reduces pus viscosity and may be more useful in treatment. We report two cases of intrapleural administration of Pulmozyme (alfa dornase - deoxyribonuclease (HOFFMANN-LA ROCHE AG) in dosage 2 × 2.5 mg with a significant improvement caused by changes in pus viscosity.
publishDate 2013
dc.date.none.fl_str_mv 2013-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702013000100015
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702013000100015
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.bjid.2012.08.019
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
dc.source.none.fl_str_mv Brazilian Journal of Infectious Diseases v.17 n.1 2013
reponame:Brazilian Journal of Infectious Diseases
instname:Brazilian Society of Infectious Diseases (BSID)
instacron:BSID
instname_str Brazilian Society of Infectious Diseases (BSID)
instacron_str BSID
institution BSID
reponame_str Brazilian Journal of Infectious Diseases
collection Brazilian Journal of Infectious Diseases
repository.name.fl_str_mv Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)
repository.mail.fl_str_mv bjid@bjid.org.br||lgoldani@ufrgs.br
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