Oral analgesia in fixed-time interval administration versus spinal morphine for post-Cesarean pain: a randomised controlled trial.


Journal

Archives of gynecology and obstetrics
ISSN: 1432-0711
Titre abrégé: Arch Gynecol Obstet
Pays: Germany
ID NLM: 8710213

Informations de publication

Date de publication:
04 2022
Historique:
received: 09 01 2021
accepted: 17 08 2021
pubmed: 1 9 2021
medline: 2 4 2022
entrez: 31 8 2021
Statut: ppublish

Résumé

To compare the efficacy of fixed-time-interval oral analgesia and spinal-morphine for management of post-Cesarean pain. In this open-label, parallel-group, randomized, controlled trial, 200 women due to undergo elective Caesarean section with spinal anaesthesia were enrolled between July 2015 and April 2016. Patients were randomly assigned to receive either spinal fentanyl followed by oral doses of tramadol, paracetamol, and diclofenac at predetermined regular intervals of 6 h for the first 48 h, and rescue treatment with percocet (oxycodone and paracetamol; oral analgesia group), or spinal morphine and rescue treatment with oral tramadol, paracetamol, and diclofenac (spinal-morphine group). The primary outcomes were pain intensity during the postoperative 48 h, measured on a 10-point numeric rating scale (NRS) and expressed as area under the curve (AUC), and the number of breakthrough events of moderate to severe pain (defined as NRS score ≥ 4). The oral analgesia group compared to the spinal-morphine group had similar mean pain intensity (AUC (120 ± 35 versus 121 ± 31, respectively; p = 0.8) but more events of moderate-to-severe breakthrough pain (4.8 ± 2 versus 3.8 ± 1.7, respectively; p = 0.0002). Higher rates and longer durations of pruritus, nausea, and vomiting were reported among patients receiving spinal morphine, as compared with oral analgesia. Satisfaction scores were high in both groups (8.2 ± 2.4 versus 8.7 ± 1.8 in the oral analgesia and spinal morphine, respectively; p = 0.23). Both oral analgesia at fixed time intervals and spinal morphine are satisfactory methods for treating post-Caesarean pain. ClinicalTrials.gov Identifier: NCT02440399, date of registration: 07/05/ 2015. URL: https://clinicaltrials.gov/ct2/show/NCT02440399?term=enav+yefet&rank=7 .

Identifiants

pubmed: 34463805
doi: 10.1007/s00404-021-06196-3
pii: 10.1007/s00404-021-06196-3
pmc: PMC8406016
doi:

Substances chimiques

Analgesics, Opioid 0
Morphine 76I7G6D29C

Banques de données

ClinicalTrials.gov
['NCT02440399']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

893-901

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Enav Yefet (E)

Department of Obstetrics and Gynecology, Emek Medical Center, Afula, Israel. enavy1@gmail.com.
Department of Obstetrics and Gynecology, Baruch Padeh Medical Center Poriya, Tiberias, Israel. enavy1@gmail.com.
Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel. enavy1@gmail.com.

Salih Nassar (S)

Department of Obstetrics and Gynecology, Emek Medical Center, Afula, Israel.

Julia Carmeli (J)

Department of Anesthesiology, Emek Medical Center, Afula, Israel.

Manal Massalha (M)

Department of Obstetrics and Gynecology, Emek Medical Center, Afula, Israel.
Rappaport Faculty of Medicine, Technion, Haifa, Israel.

Jamal Hasanein (J)

Department of Neonatology, Emek Medical Center, Afula, Israel.

Noah Zafran (N)

Department of Obstetrics and Gynecology, Emek Medical Center, Afula, Israel.
Rappaport Faculty of Medicine, Technion, Haifa, Israel.

Michael Rudin (M)

Department of Anesthesiology, Emek Medical Center, Afula, Israel.

Zohar Nachum (Z)

Department of Obstetrics and Gynecology, Emek Medical Center, Afula, Israel.
Rappaport Faculty of Medicine, Technion, Haifa, Israel.

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