Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis

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Background & Aims: Vasoactive agents with endoscopic therapy are used to treat acute variceal bleeding (AVB). There are two main groups of vasoactive agents: terlipressin and vasopressin (T-V), and octreotide and somatostatin (O-S). However, the benefit/harm balance is unclear. Our aim was to as...

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Detalles Bibliográficos
Autores: Huaringa-Marcelo, Jorge, Huaman, Mariella R., Brañez-Condorena, Ana, Villacorta-Landeo, Pamela, Pinto-Ruiz, Diego F., Urday-Ipanaqué, Diana, García-Gomero, David, Montes-Teves, Pedro, Miranda, Adelina Lozano
Formato: artículo
Fecha de Publicación:2021
Institución:Universidad Peruana de Ciencias Aplicadas
Repositorio:UPC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorioacademico.upc.edu.pe:10757/655881
Enlace del recurso:http://hdl.handle.net/10757/655881
Nivel de acceso:acceso abierto
Materia:Liver cirrhosis
Octreotide
Somatostatin
Terlipressin
Vasopressin
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dc.title.en_US.fl_str_mv Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
title Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
spellingShingle Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
Huaringa-Marcelo, Jorge
Liver cirrhosis
Octreotide
Somatostatin
Terlipressin
Vasopressin
title_short Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
title_full Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
title_fullStr Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
title_full_unstemmed Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
title_sort Vasoactive agents for the management of acute variceal bleeding: A systematic review and meta-analysis
author Huaringa-Marcelo, Jorge
author_facet Huaringa-Marcelo, Jorge
Huaman, Mariella R.
Brañez-Condorena, Ana
Villacorta-Landeo, Pamela
Pinto-Ruiz, Diego F.
Urday-Ipanaqué, Diana
García-Gomero, David
Montes-Teves, Pedro
Miranda, Adelina Lozano
author_role author
author2 Huaman, Mariella R.
Brañez-Condorena, Ana
Villacorta-Landeo, Pamela
Pinto-Ruiz, Diego F.
Urday-Ipanaqué, Diana
García-Gomero, David
Montes-Teves, Pedro
Miranda, Adelina Lozano
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Huaringa-Marcelo, Jorge
Huaman, Mariella R.
Brañez-Condorena, Ana
Villacorta-Landeo, Pamela
Pinto-Ruiz, Diego F.
Urday-Ipanaqué, Diana
García-Gomero, David
Montes-Teves, Pedro
Miranda, Adelina Lozano
dc.subject.en_US.fl_str_mv Liver cirrhosis
Octreotide
Somatostatin
Terlipressin
Vasopressin
topic Liver cirrhosis
Octreotide
Somatostatin
Terlipressin
Vasopressin
description Background & Aims: Vasoactive agents with endoscopic therapy are used to treat acute variceal bleeding (AVB). There are two main groups of vasoactive agents: terlipressin and vasopressin (T-V), and octreotide and somatostatin (O-S). However, the benefit/harm balance is unclear. Our aim was to assess the efficacy and safety of T-V versus O-S for the management of AVB. Methods: We performed a systematic search for randomized controlled trials (RCTs) in PubMed, Scopus, and CENTRAL. Our main outcomes were mortality and adverse events. Secondary outcomes were bleeding control, rebleeding, blood transfusion, hospital stay. We evaluated the certainty of evidence using GRADE methodology. Results: We included 21 RCTs. The risk of mortality (RR: 1.01; 95%CI: 0.83-1.22), bleeding control (RR: 0.96; 95%CI: 0.91-1.02; I2=53%), early rebleeding (RR: 0.91; 95%CI: 0.66-1.24: I2=0%), late rebleeding (RR: 0.94; 95 CI: 0.56-1.60; I2=0%), blood transfusion (MD: 0.04; 95%CI:-0.31-0.39; I2=68%) and hospital stay (MD:-1.06; 95%CI:-2.80-0.69; I2=0%) were similar between T-V and O-S groups. Only 15 studies reported adverse events, which were significantly higher in the T-V compared to the O-S group (RR 2.39; 95%CI: 1.58-3.63; I2=57%). The certainty of evidence was moderate for the main outcomes, and low or very low for others. Conclusions: In cirrhotic patients with AVB, those treated with T-V had similar mortality risk compared to O-S. However, the use of T-V showed an increased risk of adverse events compared to O-S.
publishDate 2021
dc.date.accessioned.none.fl_str_mv 2021-05-07T14:40:20Z
dc.date.available.none.fl_str_mv 2021-05-07T14:40:20Z
dc.date.issued.fl_str_mv 2021-01-01
dc.type.en_US.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.issn.none.fl_str_mv 18418724
dc.identifier.doi.none.fl_str_mv 10.15403/jgld-3191
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10757/655881
dc.identifier.journal.en_US.fl_str_mv Journal of Gastrointestinal and Liver Diseases
dc.identifier.eid.none.fl_str_mv 2-s2.0-85103062404
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Journal of Gastrointestinal and Liver Diseases
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url http://hdl.handle.net/10757/655881
dc.language.iso.en_US.fl_str_mv eng
language eng
dc.relation.url.en_US.fl_str_mv https://www.jgld.ro/jgld/index.php/jgld/article/view/3191/1692
dc.rights.en_US.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.*.fl_str_mv Attribution-NonCommercial-ShareAlike 4.0 International
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
eu_rights_str_mv openAccess
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dc.format.en_US.fl_str_mv application/pdf
dc.publisher.en_US.fl_str_mv Romanian Society of Gastroenterology
dc.source.es_PE.fl_str_mv Universidad Peruana de Ciencias Aplicadas (UPC)
Repositorio Academico - UPC
dc.source.none.fl_str_mv reponame:UPC-Institucional
instname:Universidad Peruana de Ciencias Aplicadas
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instname_str Universidad Peruana de Ciencias Aplicadas
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dc.source.journaltitle.none.fl_str_mv Journal of Gastrointestinal and Liver Diseases
dc.source.volume.none.fl_str_mv 30
dc.source.issue.none.fl_str_mv 1
dc.source.beginpage.none.fl_str_mv 110
dc.source.endpage.none.fl_str_mv 121
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However, the benefit/harm balance is unclear. Our aim was to assess the efficacy and safety of T-V versus O-S for the management of AVB. Methods: We performed a systematic search for randomized controlled trials (RCTs) in PubMed, Scopus, and CENTRAL. Our main outcomes were mortality and adverse events. Secondary outcomes were bleeding control, rebleeding, blood transfusion, hospital stay. We evaluated the certainty of evidence using GRADE methodology. Results: We included 21 RCTs. The risk of mortality (RR: 1.01; 95%CI: 0.83-1.22), bleeding control (RR: 0.96; 95%CI: 0.91-1.02; I2=53%), early rebleeding (RR: 0.91; 95%CI: 0.66-1.24: I2=0%), late rebleeding (RR: 0.94; 95 CI: 0.56-1.60; I2=0%), blood transfusion (MD: 0.04; 95%CI:-0.31-0.39; I2=68%) and hospital stay (MD:-1.06; 95%CI:-2.80-0.69; I2=0%) were similar between T-V and O-S groups. Only 15 studies reported adverse events, which were significantly higher in the T-V compared to the O-S group (RR 2.39; 95%CI: 1.58-3.63; I2=57%). The certainty of evidence was moderate for the main outcomes, and low or very low for others. Conclusions: In cirrhotic patients with AVB, those treated with T-V had similar mortality risk compared to O-S. 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