Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trial

Abstract Objective Assess patients submitted to elective cesarean section under spinal anesthesia, and the efficacy of different doses of fentanyl associated with bupivacaine. Methods The study included 124 pregnant women randomly distributed into 4 groups (n = 31) according to different doses of fentanyl (15 µg, 10 µg, 7.5 µg), Groups I, II, and III, respectively, and control group IV, associated with 0.5% hyperbaric bupivacaine (10 mg). An epidural catheter was inserted in case epidural top-up was required. We assessed the anesthetic blockage characteristics, negative maternal and neonatal outcomes, and maternal side effects. Statistical analysis was performed using Kruskal-Wallis, Fisher’s exact and chi-square tests. The level of significance was 5% (p< 0.05). Results The quality of analgesia, time for the first complaint of pain and motor block recovery time were significantly better for groups that received fentanyl in comparison to controls (p< 0.001). None of the groups had negative maternal-fetal outcomes. Nausea was significantly more frequent in patients in Groups II (10 µg) and III (7.5 µg) when compared to Groups I (15 µg) and IV (no fentanyl). Vomiting was more frequent in Group III than in Group I (p= 0.006). The incidence of pruritus was significantly higher in the groups receiving fentanyl (p= 0.012). Conclusions Among the solutions studied, the spinal anesthesia technique using 15 µg of fentanyl associated with 10 mg of hyperbaric bupivacaine provided satisfactory analgesia and very low incidence of adverse effects for patients submitted to cesarean section. Trial Registration Number UTN U1111-1199-0285. REBEC RBR-5XWT6T.

Saved in:
Bibliographic Details
Main Authors: Ferrarezi,Wesla Packer Pfeifer, Braga,Angélica de Fátima de Assunção, Ferreira,Valdir Batista, Mendes,Sara Quinta, Brandão,Maria José Nascimento, Braga,Franklin Sarmento da Silva, Carvalho,Vanessa Henriques
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Anestesiologia (SBA) 2021
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2352-22912021000600642
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S2352-22912021000600642
record_format ojs
spelling oai:scielo:S2352-229120210006006422021-11-18Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trialFerrarezi,Wesla Packer PfeiferBraga,Angélica de Fátima de AssunçãoFerreira,Valdir BatistaMendes,Sara QuintaBrandão,Maria José NascimentoBraga,Franklin Sarmento da SilvaCarvalho,Vanessa Henriques Cesarean Spinal anesthesia Bupivacaine Fentanyl Abstract Objective Assess patients submitted to elective cesarean section under spinal anesthesia, and the efficacy of different doses of fentanyl associated with bupivacaine. Methods The study included 124 pregnant women randomly distributed into 4 groups (n = 31) according to different doses of fentanyl (15 µg, 10 µg, 7.5 µg), Groups I, II, and III, respectively, and control group IV, associated with 0.5% hyperbaric bupivacaine (10 mg). An epidural catheter was inserted in case epidural top-up was required. We assessed the anesthetic blockage characteristics, negative maternal and neonatal outcomes, and maternal side effects. Statistical analysis was performed using Kruskal-Wallis, Fisher’s exact and chi-square tests. The level of significance was 5% (p< 0.05). Results The quality of analgesia, time for the first complaint of pain and motor block recovery time were significantly better for groups that received fentanyl in comparison to controls (p< 0.001). None of the groups had negative maternal-fetal outcomes. Nausea was significantly more frequent in patients in Groups II (10 µg) and III (7.5 µg) when compared to Groups I (15 µg) and IV (no fentanyl). Vomiting was more frequent in Group III than in Group I (p= 0.006). The incidence of pruritus was significantly higher in the groups receiving fentanyl (p= 0.012). Conclusions Among the solutions studied, the spinal anesthesia technique using 15 µg of fentanyl associated with 10 mg of hyperbaric bupivacaine provided satisfactory analgesia and very low incidence of adverse effects for patients submitted to cesarean section. Trial Registration Number UTN U1111-1199-0285. REBEC RBR-5XWT6T.info:eu-repo/semantics/openAccessSociedade Brasileira de Anestesiologia (SBA)Brazilian Journal of Anesthesiology v.71 n.6 20212021-12-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2352-22912021000600642en10.1016/j.bjane.2021.03.030
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Ferrarezi,Wesla Packer Pfeifer
Braga,Angélica de Fátima de Assunção
Ferreira,Valdir Batista
Mendes,Sara Quinta
Brandão,Maria José Nascimento
Braga,Franklin Sarmento da Silva
Carvalho,Vanessa Henriques
spellingShingle Ferrarezi,Wesla Packer Pfeifer
Braga,Angélica de Fátima de Assunção
Ferreira,Valdir Batista
Mendes,Sara Quinta
Brandão,Maria José Nascimento
Braga,Franklin Sarmento da Silva
Carvalho,Vanessa Henriques
Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trial
author_facet Ferrarezi,Wesla Packer Pfeifer
Braga,Angélica de Fátima de Assunção
Ferreira,Valdir Batista
Mendes,Sara Quinta
Brandão,Maria José Nascimento
Braga,Franklin Sarmento da Silva
Carvalho,Vanessa Henriques
author_sort Ferrarezi,Wesla Packer Pfeifer
title Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trial
title_short Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trial
title_full Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trial
title_fullStr Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trial
title_full_unstemmed Spinal anesthesia for elective cesarean section. Bupivacaine associated with different doses of fentanyl: randomized clinical trial
title_sort spinal anesthesia for elective cesarean section. bupivacaine associated with different doses of fentanyl: randomized clinical trial
description Abstract Objective Assess patients submitted to elective cesarean section under spinal anesthesia, and the efficacy of different doses of fentanyl associated with bupivacaine. Methods The study included 124 pregnant women randomly distributed into 4 groups (n = 31) according to different doses of fentanyl (15 µg, 10 µg, 7.5 µg), Groups I, II, and III, respectively, and control group IV, associated with 0.5% hyperbaric bupivacaine (10 mg). An epidural catheter was inserted in case epidural top-up was required. We assessed the anesthetic blockage characteristics, negative maternal and neonatal outcomes, and maternal side effects. Statistical analysis was performed using Kruskal-Wallis, Fisher’s exact and chi-square tests. The level of significance was 5% (p< 0.05). Results The quality of analgesia, time for the first complaint of pain and motor block recovery time were significantly better for groups that received fentanyl in comparison to controls (p< 0.001). None of the groups had negative maternal-fetal outcomes. Nausea was significantly more frequent in patients in Groups II (10 µg) and III (7.5 µg) when compared to Groups I (15 µg) and IV (no fentanyl). Vomiting was more frequent in Group III than in Group I (p= 0.006). The incidence of pruritus was significantly higher in the groups receiving fentanyl (p= 0.012). Conclusions Among the solutions studied, the spinal anesthesia technique using 15 µg of fentanyl associated with 10 mg of hyperbaric bupivacaine provided satisfactory analgesia and very low incidence of adverse effects for patients submitted to cesarean section. Trial Registration Number UTN U1111-1199-0285. REBEC RBR-5XWT6T.
publisher Sociedade Brasileira de Anestesiologia (SBA)
publishDate 2021
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2352-22912021000600642
work_keys_str_mv AT ferrareziweslapackerpfeifer spinalanesthesiaforelectivecesareansectionbupivacaineassociatedwithdifferentdosesoffentanylrandomizedclinicaltrial
AT bragaangelicadefatimadeassuncao spinalanesthesiaforelectivecesareansectionbupivacaineassociatedwithdifferentdosesoffentanylrandomizedclinicaltrial
AT ferreiravaldirbatista spinalanesthesiaforelectivecesareansectionbupivacaineassociatedwithdifferentdosesoffentanylrandomizedclinicaltrial
AT mendessaraquinta spinalanesthesiaforelectivecesareansectionbupivacaineassociatedwithdifferentdosesoffentanylrandomizedclinicaltrial
AT brandaomariajosenascimento spinalanesthesiaforelectivecesareansectionbupivacaineassociatedwithdifferentdosesoffentanylrandomizedclinicaltrial
AT bragafranklinsarmentodasilva spinalanesthesiaforelectivecesareansectionbupivacaineassociatedwithdifferentdosesoffentanylrandomizedclinicaltrial
AT carvalhovanessahenriques spinalanesthesiaforelectivecesareansectionbupivacaineassociatedwithdifferentdosesoffentanylrandomizedclinicaltrial
_version_ 1756441227185618944