Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial

Detalhes bibliográficos
Autor(a) principal: Menezes,Daniel C.
Data de Publicação: 2019
Outros Autores: Vidal,Edison I.O., Costa,Cesar M., Mizubuti,Glenio B., Ho,Anthony M.H., Barros,Guilherme A.M., Fukushima,Fernanda B.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Brasileira de Anestesiologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0034-70942019000400001
Resumo: Abstract Background Postoperative pain represents an important concern when remifentanil is used for total intravenous anesthesia because of its ultrashort half-life. Longer acting opioids, such as sufentanil, have been used during induction of remifentanil-based total intravenous anesthesia as a means to overcome this shortcoming. However, the effectiveness and safety of such strategy still lacks evidence from randomized clinical trials. Hence, we aimed to assess the postoperative analgesic efficacy and safety of a single dose of sufentanil administered during the induction of remifentanil-based total intravenous anesthesia. Methods Forty patients, scheduled for elective open abdominal surgery, were randomized to receive remifentanil-based total intravenous anesthesia with or without a single dose of sufentanil upon induction. We assessed the postoperative morphine consumption administered through a patient-controlled analgesia pump. Self-reported pain scores and the occurrence of nausea, vomiting, pruritus, agitation, somnolence and respiratory depression were also assessed up to 2 days after surgery. Results The mean difference between the sufentanil and control groups regarding morphine consumption in the post-anesthetic care unit and at 12, 24 and 48 h after surgery were -7.2 mg (95%CI: -12.5 to -2.1, p < 0.001), -3.9 mg (95%CI: -11.9 to 4.7, p = 0.26), -0.6 mg (95%CI: (-12.7 to 12.7, p = 0.80), and -1.8 mg (95%CI: (-11.6 to 15.6, p = 0.94), respectively. Neither self-reported pain nor the incidence of adverse events were significantly different between groups at any time point. Conclusion Our findings suggest that the administration of sufentanil during induction of remifentanil-based total intravenous anesthesia is associated with decreased early postoperative opioid consumption.
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spelling Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trialAcute painPainOpioidTotal intravenous anesthesiaAbstract Background Postoperative pain represents an important concern when remifentanil is used for total intravenous anesthesia because of its ultrashort half-life. Longer acting opioids, such as sufentanil, have been used during induction of remifentanil-based total intravenous anesthesia as a means to overcome this shortcoming. However, the effectiveness and safety of such strategy still lacks evidence from randomized clinical trials. Hence, we aimed to assess the postoperative analgesic efficacy and safety of a single dose of sufentanil administered during the induction of remifentanil-based total intravenous anesthesia. Methods Forty patients, scheduled for elective open abdominal surgery, were randomized to receive remifentanil-based total intravenous anesthesia with or without a single dose of sufentanil upon induction. We assessed the postoperative morphine consumption administered through a patient-controlled analgesia pump. Self-reported pain scores and the occurrence of nausea, vomiting, pruritus, agitation, somnolence and respiratory depression were also assessed up to 2 days after surgery. Results The mean difference between the sufentanil and control groups regarding morphine consumption in the post-anesthetic care unit and at 12, 24 and 48 h after surgery were -7.2 mg (95%CI: -12.5 to -2.1, p < 0.001), -3.9 mg (95%CI: -11.9 to 4.7, p = 0.26), -0.6 mg (95%CI: (-12.7 to 12.7, p = 0.80), and -1.8 mg (95%CI: (-11.6 to 15.6, p = 0.94), respectively. Neither self-reported pain nor the incidence of adverse events were significantly different between groups at any time point. Conclusion Our findings suggest that the administration of sufentanil during induction of remifentanil-based total intravenous anesthesia is associated with decreased early postoperative opioid consumption.Sociedade Brasileira de Anestesiologia2019-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0034-70942019000400001Revista Brasileira de Anestesiologia v.69 n.4 2019reponame:Revista Brasileira de Anestesiologia (Online)instname:Sociedade Brasileira de Anestesiologia (SBA)instacron:SBA10.1016/j.bjane.2019.04.001info:eu-repo/semantics/openAccessMenezes,Daniel C.Vidal,Edison I.O.Costa,Cesar M.Mizubuti,Glenio B.Ho,Anthony M.H.Barros,Guilherme A.M.Fukushima,Fernanda B.eng2019-10-08T00:00:00Zoai:scielo:S0034-70942019000400001Revistahttps://www.sbahq.org/revista/https://old.scielo.br/oai/scielo-oai.php||sba2000@openlink.com.br1806-907X0034-7094opendoar:2019-10-08T00:00Revista Brasileira de Anestesiologia (Online) - Sociedade Brasileira de Anestesiologia (SBA)false
dc.title.none.fl_str_mv Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
title Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
spellingShingle Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
Menezes,Daniel C.
Acute pain
Pain
Opioid
Total intravenous anesthesia
title_short Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
title_full Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
title_fullStr Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
title_full_unstemmed Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
title_sort Sufentanil during anesthetic induction of remifentanil-based total intravenous anesthesia: a randomized controlled trial
author Menezes,Daniel C.
author_facet Menezes,Daniel C.
Vidal,Edison I.O.
Costa,Cesar M.
Mizubuti,Glenio B.
Ho,Anthony M.H.
Barros,Guilherme A.M.
Fukushima,Fernanda B.
author_role author
author2 Vidal,Edison I.O.
Costa,Cesar M.
Mizubuti,Glenio B.
Ho,Anthony M.H.
Barros,Guilherme A.M.
Fukushima,Fernanda B.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Menezes,Daniel C.
Vidal,Edison I.O.
Costa,Cesar M.
Mizubuti,Glenio B.
Ho,Anthony M.H.
Barros,Guilherme A.M.
Fukushima,Fernanda B.
dc.subject.por.fl_str_mv Acute pain
Pain
Opioid
Total intravenous anesthesia
topic Acute pain
Pain
Opioid
Total intravenous anesthesia
description Abstract Background Postoperative pain represents an important concern when remifentanil is used for total intravenous anesthesia because of its ultrashort half-life. Longer acting opioids, such as sufentanil, have been used during induction of remifentanil-based total intravenous anesthesia as a means to overcome this shortcoming. However, the effectiveness and safety of such strategy still lacks evidence from randomized clinical trials. Hence, we aimed to assess the postoperative analgesic efficacy and safety of a single dose of sufentanil administered during the induction of remifentanil-based total intravenous anesthesia. Methods Forty patients, scheduled for elective open abdominal surgery, were randomized to receive remifentanil-based total intravenous anesthesia with or without a single dose of sufentanil upon induction. We assessed the postoperative morphine consumption administered through a patient-controlled analgesia pump. Self-reported pain scores and the occurrence of nausea, vomiting, pruritus, agitation, somnolence and respiratory depression were also assessed up to 2 days after surgery. Results The mean difference between the sufentanil and control groups regarding morphine consumption in the post-anesthetic care unit and at 12, 24 and 48 h after surgery were -7.2 mg (95%CI: -12.5 to -2.1, p < 0.001), -3.9 mg (95%CI: -11.9 to 4.7, p = 0.26), -0.6 mg (95%CI: (-12.7 to 12.7, p = 0.80), and -1.8 mg (95%CI: (-11.6 to 15.6, p = 0.94), respectively. Neither self-reported pain nor the incidence of adverse events were significantly different between groups at any time point. Conclusion Our findings suggest that the administration of sufentanil during induction of remifentanil-based total intravenous anesthesia is associated with decreased early postoperative opioid consumption.
publishDate 2019
dc.date.none.fl_str_mv 2019-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.relation.none.fl_str_mv 10.1016/j.bjane.2019.04.001
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Anestesiologia
publisher.none.fl_str_mv Sociedade Brasileira de Anestesiologia
dc.source.none.fl_str_mv Revista Brasileira de Anestesiologia v.69 n.4 2019
reponame:Revista Brasileira de Anestesiologia (Online)
instname:Sociedade Brasileira de Anestesiologia (SBA)
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reponame_str Revista Brasileira de Anestesiologia (Online)
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