Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome

Detalhes bibliográficos
Autor(a) principal: Nie, Xiangbi
Data de Publicação: 2023
Outros Autores: Lou, Liqiong, Xu, Hui, Xiong, Wei, Wang, Zenggeng
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/211871
Resumo: The innate immune response plays an important role in the pathophysiology of acute respiratory distress syndrome (ARDS); however, no drug has been proven to be beneficial in the management of ARDS. Therefore, the aim of this study was to investigate the effects of using combined sedatives on systemic inflammatory responses in patients with ARDS. A total of 90 patients with ARDS and an intubation time of > 120 h were randomly divided into the propofol group (group P), midazolam group (group M), and combined sedation group (group U). Patients in groups P and M were sedated with propofol and midazolam, respectively, whereas patients in group U were sedated with a combination of propofol, midazolam, and dexmedetomidine. The dosage of sedatives and vasoactive drugs, duration of mechanical ventilation, and incidence of sedative adverse reactions were documented. The dosage of sedatives and vasoactive drugs, as well as the incidence of sedative adverse reactions in group U, was significantly lower than those in groups P and M. Similarly, the duration of mechanical ventilation in group U was significantly shorter than that in groups P and M. Hence, inducing sedation through a combination of multiple drugs can significantly reduce their adverse effects, improve their sedative effect, inhibit systemic inflammatory responses, and improve oxygenation in patients with ARDS.
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spelling Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndromeAcute respiratory distress syndrome; Combined sedation; Propofol; Midazolam; Dexmedetomidine; CytokinesThe innate immune response plays an important role in the pathophysiology of acute respiratory distress syndrome (ARDS); however, no drug has been proven to be beneficial in the management of ARDS. Therefore, the aim of this study was to investigate the effects of using combined sedatives on systemic inflammatory responses in patients with ARDS. A total of 90 patients with ARDS and an intubation time of > 120 h were randomly divided into the propofol group (group P), midazolam group (group M), and combined sedation group (group U). Patients in groups P and M were sedated with propofol and midazolam, respectively, whereas patients in group U were sedated with a combination of propofol, midazolam, and dexmedetomidine. The dosage of sedatives and vasoactive drugs, duration of mechanical ventilation, and incidence of sedative adverse reactions were documented. The dosage of sedatives and vasoactive drugs, as well as the incidence of sedative adverse reactions in group U, was significantly lower than those in groups P and M. Similarly, the duration of mechanical ventilation in group U was significantly shorter than that in groups P and M. Hence, inducing sedation through a combination of multiple drugs can significantly reduce their adverse effects, improve their sedative effect, inhibit systemic inflammatory responses, and improve oxygenation in patients with ARDS.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2023-04-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/21187110.1590/s2175-97902023e21461Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21461Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e21461Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e214612175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/211871/194615https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessNie, XiangbiLou, LiqiongXu, HuiXiong, WeiWang, Zenggeng2023-05-31T19:15:09Zoai:revistas.usp.br:article/211871Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-05-31T19:15:09Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
title Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
spellingShingle Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
Nie, Xiangbi
Acute respiratory distress syndrome; Combined sedation; Propofol; Midazolam; Dexmedetomidine; Cytokines
title_short Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
title_full Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
title_fullStr Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
title_full_unstemmed Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
title_sort Effect of combined sedation using multiple drugs on inflammatory cytokines in patients with acute respiratory distress syndrome
author Nie, Xiangbi
author_facet Nie, Xiangbi
Lou, Liqiong
Xu, Hui
Xiong, Wei
Wang, Zenggeng
author_role author
author2 Lou, Liqiong
Xu, Hui
Xiong, Wei
Wang, Zenggeng
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Nie, Xiangbi
Lou, Liqiong
Xu, Hui
Xiong, Wei
Wang, Zenggeng
dc.subject.por.fl_str_mv Acute respiratory distress syndrome; Combined sedation; Propofol; Midazolam; Dexmedetomidine; Cytokines
topic Acute respiratory distress syndrome; Combined sedation; Propofol; Midazolam; Dexmedetomidine; Cytokines
description The innate immune response plays an important role in the pathophysiology of acute respiratory distress syndrome (ARDS); however, no drug has been proven to be beneficial in the management of ARDS. Therefore, the aim of this study was to investigate the effects of using combined sedatives on systemic inflammatory responses in patients with ARDS. A total of 90 patients with ARDS and an intubation time of > 120 h were randomly divided into the propofol group (group P), midazolam group (group M), and combined sedation group (group U). Patients in groups P and M were sedated with propofol and midazolam, respectively, whereas patients in group U were sedated with a combination of propofol, midazolam, and dexmedetomidine. The dosage of sedatives and vasoactive drugs, duration of mechanical ventilation, and incidence of sedative adverse reactions were documented. The dosage of sedatives and vasoactive drugs, as well as the incidence of sedative adverse reactions in group U, was significantly lower than those in groups P and M. Similarly, the duration of mechanical ventilation in group U was significantly shorter than that in groups P and M. Hence, inducing sedation through a combination of multiple drugs can significantly reduce their adverse effects, improve their sedative effect, inhibit systemic inflammatory responses, and improve oxygenation in patients with ARDS.
publishDate 2023
dc.date.none.fl_str_mv 2023-04-28
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/bjps/article/view/211871
10.1590/s2175-97902023e21461
url https://www.revistas.usp.br/bjps/article/view/211871
identifier_str_mv 10.1590/s2175-97902023e21461
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/211871/194615
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21461
Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e21461
Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21461
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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