Intravenous Patient-controlled Analgesia Versus Thoracic Epidural Analgesia After Open Liver Surgery: A Prospective, Randomized, Controlled, Noninferiority Trial.


Journal

Annals of surgery
ISSN: 1528-1140
Titre abrégé: Ann Surg
Pays: United States
ID NLM: 0372354

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 25 1 2019
medline: 24 1 2020
entrez: 25 1 2019
Statut: ppublish

Résumé

We conducted a randomized, controlled, noninferiority trial to investigate if intravenous, multimodal, patient-controlled analgesia (IV-PCA) could be noninferior to multimodal thoracic epidural analgesia (TEA) in patients undergoing open liver surgery. The increasing use of minimally invasive techniques and fast track protocols have questioned the position of epidural analgesia as the optimal method of pain management after abdominal surgery. Patients operated with open liver resection between February 2012 and February 2016 were randomly assigned to receive either IV-PCA enhanced with ketorolac/diclofenac (IV-PCA, n = 66) or TEA (n = 77) within an enhanced recovery after surgery protocol. Noninferiority would be declared if the mean pain score on the numeric rating scale (NRS) for postoperative days (PODs) 0 to 5 in the IV-PCA group was no worse than the mean pain score in the TEA group by a margin of <1 point on an 11-point scale (0-10). The primary endpoint, mean NRS pain score was 1.7 in the IV-PCA group and 1.6 in the TEA group, establishing noninferiority. Pain scores were lower in the TEA group on PODs 0 and 1, but higher or equal on PODs 2 and 5. Postoperative hospital stay was significantly shorter for patients in the IV-PCA group (74 vs 104 h, P < 0.001). The total opioid consumption during the first 3 days was significantly lower in the IV-PCA group. IV-PCA was noninferior to TEA for the treatment of postoperative pain in patients undergoing open liver resection.

Sections du résumé

OBJECTIVE
We conducted a randomized, controlled, noninferiority trial to investigate if intravenous, multimodal, patient-controlled analgesia (IV-PCA) could be noninferior to multimodal thoracic epidural analgesia (TEA) in patients undergoing open liver surgery.
SUMMARY BACKGROUND DATA
The increasing use of minimally invasive techniques and fast track protocols have questioned the position of epidural analgesia as the optimal method of pain management after abdominal surgery.
METHODS
Patients operated with open liver resection between February 2012 and February 2016 were randomly assigned to receive either IV-PCA enhanced with ketorolac/diclofenac (IV-PCA, n = 66) or TEA (n = 77) within an enhanced recovery after surgery protocol. Noninferiority would be declared if the mean pain score on the numeric rating scale (NRS) for postoperative days (PODs) 0 to 5 in the IV-PCA group was no worse than the mean pain score in the TEA group by a margin of <1 point on an 11-point scale (0-10).
RESULTS
The primary endpoint, mean NRS pain score was 1.7 in the IV-PCA group and 1.6 in the TEA group, establishing noninferiority. Pain scores were lower in the TEA group on PODs 0 and 1, but higher or equal on PODs 2 and 5. Postoperative hospital stay was significantly shorter for patients in the IV-PCA group (74 vs 104 h, P < 0.001). The total opioid consumption during the first 3 days was significantly lower in the IV-PCA group.
CONCLUSIONS
IV-PCA was noninferior to TEA for the treatment of postoperative pain in patients undergoing open liver resection.

Identifiants

pubmed: 30676382
doi: 10.1097/SLA.0000000000003209
doi:

Substances chimiques

Analgesics, Opioid 0
Anti-Inflammatory Agents, Non-Steroidal 0
Diclofenac 144O8QL0L1
Ketorolac YZI5105V0L

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

193-199

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

John Hausken (J)

Department of Anesthesiology, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.

Åsmund Avdem Fretland (ÅA)

The Intervention Centre, Oslo University Hospital, Oslo, Norway.
Department of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Oslo, Norway.
Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Bjørn Edwin (B)

The Intervention Centre, Oslo University Hospital, Oslo, Norway.
Department of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Oslo, Norway.
Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Marit Helen Andersen (MH)

Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
Department of Health Science, University of Oslo, Oslo, Norway.

Vegar Johansen Dagenborg (VJ)

Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Department of Gastroenterological Surgery, Oslo University Hospital, Oslo, Norway.
Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Gudrun Maria Waaler Bjørnelv (GMW)

The Intervention Centre, Oslo University Hospital, Oslo, Norway.
Institute of Health and Society, University of Oslo, Oslo, Norway.

Ronny Kristiansen (R)

The Intervention Centre, Oslo University Hospital, Oslo, Norway.
Department of Information Technology, Oslo University Hospital, Oslo, Norway.

Kjetil Røysland (K)

Department of Biostatistics, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.

Gunnvald Kvarstein (G)

Department of Clinical Medicine, UiT, The Arctic University of Norway, Tromsø, Norway.

Tor Inge Tønnessen (TI)

Department of Anesthesiology, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

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