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Effect of patient-controlled epidural analgesia with and without automatic intermittent bolus on levobupivacaine consumption during labour: A single-centre prospective double-blinded randomised controlled study.
Bourgès, Jennifer; Gakuba, Clément; Plass, Felipe; Gérard, Jean-Louis; Simonet, Thérèse; Hanouz, Jean-Luc.
Afiliación
  • Bourgès J; Department of Anaesthesia and Intensive Care Medicine, Caen University Hospital, Avenue de la Côte de Nacre, CS 30001, F-14000 Caen, France; Normandie University, UNICAEN, INSERM UMR-S U1237, 14000 Caen, France.
  • Gakuba C; Department of Anaesthesia and Intensive Care Medicine, Caen University Hospital, Avenue de la Côte de Nacre, CS 30001, F-14000 Caen, France; Normandie University, UNICAEN, INSERM UMR-S U1237, 14000 Caen, France.
  • Plass F; Department of Anaesthesia and Intensive Care Medicine, Caen University Hospital, Avenue de la Côte de Nacre, CS 30001, F-14000 Caen, France.
  • Gérard JL; Department of Anaesthesia and Intensive Care Medicine, Caen University Hospital, Avenue de la Côte de Nacre, CS 30001, F-14000 Caen, France.
  • Simonet T; Department of Anaesthesia and Intensive Care Medicine, Caen University Hospital, Avenue de la Côte de Nacre, CS 30001, F-14000 Caen, France.
  • Hanouz JL; Department of Anaesthesia and Intensive Care Medicine, Caen University Hospital, Avenue de la Côte de Nacre, CS 30001, F-14000 Caen, France. Electronic address: hanouz-jl@chu-caen.fr.
Anaesth Crit Care Pain Med ; 40(5): 100936, 2021 10.
Article en En | MEDLINE | ID: mdl-34391982
ABSTRACT

BACKGROUND:

During labour, the effects of adding a programmed intermittent epidural bolus (PIEB) baseline analgesic regimen to patient-controlled epidural analgesia (PCEA) remain uncertain.

METHODS:

This single centre prospective double-blinded controlled study randomised nulliparous women over 35 weeks of gestational age in a PCEA + PIEB or PCEA only group. After an epidural analgesia catheter was inserted, a specific pump administered a solution of levobupivacaine 0.625 mg mL-1, sufentanil 0.25 µg mL-1, and clonidine 0.375 µg mL-1. In both groups the PCEA mode delivered an 8 mL bolus with a lockout period of 8 min. In the PCEA + PIEB group, women also received a programmed 8 mL bolus every 60 min. Additional bolus were allowed if required. The primary outcome was the hourly consumption of levobupivacaine from epidural catheter placement to new-born delivery. Secondary outcome were motor block, oxytocin use, sufentanil consumption, additional bolus required, instrumental vaginal delivery, unplanned caesarean section, pain during labour and women's satisfaction.

RESULTS:

Analysis included 162 and 155 women in the PCEA and PCEA + PIEB groups, respectively. The median [IQR] hourly consumption of levobupivacaine was significantly lower in the PCEA group (9.9 (7.8-12.4] mg h-1) as compared to the PCEA + PIEB group (11.2 [7.9-14.3] mg h-1; p = 0.046). The difference between medians was 1.3 mg h-1 95 % CI (0.1-2.9). There was no difference between groups for secondary outcomes.

CONCLUSIONS:

PCEA only modestly decreased the hourly consumption of local anaesthetic as compared to PCEA + PIEB but the difference was not clinically relevant.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Analgesia Epidural / Analgesia Obstétrica Tipo de estudio: Clinical_trials / Observational_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Anaesth Crit Care Pain Med Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Analgesia Epidural / Analgesia Obstétrica Tipo de estudio: Clinical_trials / Observational_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Anaesth Crit Care Pain Med Año: 2021 Tipo del documento: Article País de afiliación: Francia
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