AIRR - ANZCA Institutional Research Repository
Skip navigation
Please use this identifier to cite or link to this item: https://hdl.handle.net/11055/198
Full metadata record
DC FieldValueLanguage
dc.contributor.authorLaw, CJ-
dc.contributor.authorJacobson, G M-
dc.contributor.authorKluger, M-
dc.contributor.authorChaddock, M-
dc.contributor.authorScott, M-
dc.contributor.authorSleigh, JW-
dc.date2013-
dc.date.accessioned2018-03-08T00:21:01Z-
dc.date.available2018-03-08T00:21:01Z-
dc.date.issued2014-04-
dc.identifier.citationBritish journal of anaesthesia 2014-04; 112(4): 675-80-
dc.identifier.urihttp://hdl.handle.net/11055/198-
dc.description.abstractOur hypothesis was that deep anaesthesia, as estimated by a low target bispectral index (BIS) of 30-40, would result in less postoperative pain than that achieved at a conventional depth of anaesthesia. We undertook a randomized double-blind controlled study at two tertiary teaching hospitals in New Zealand (2010-1) recruiting 135 adult patients ASA I-II presenting for non-emergent surgery under general anaesthesia requiring tracheal intubation. Anaesthesia was maintained with desflurane and a multimodal analgesia regimen comprising fentanyl infusion, i.v. paracetamol, and parecoxib. Patients were randomly assigned to either a low BIS (30-40) group or a high BIS (45-60) group. Desflurane concentrations were titrated to achieve these targets. Postoperative pain was assessed by: the pain on awakening (0-10, verbal rating scale, VRS(awake)) in the post-anaesthetic care unit; pain on activity at 20-24 h after operation (VRS(d1A)); and the rate of morphine patient-controlled analgesia (PCA) usage over the first 24 h. There was no statistically significant difference between the two groups for any of the pain scores. The median [inter-quartile range (IQR)] VRS(awake) was 4.0 (0-8) for the low and 4.0 (0-8) for the high BIS groups (P=0.56). The median (IQR) VRS(d1A) was 3.0 (1-5) for the low and 3.0 (1.5-4.5) for the high BIS groups (P=0.83). The median PCA morphine consumption in the low BIS group was 0.61 mg h(-1) (0.04-1.5) vs 0.43 mg h(-1) (0-1.59) in the high BIS group (P=0.98). We conclude that there is no clinically useful analgesic effect of a deep anaesthesia regimen.-
dc.language.isoeng-
dc.subject.meshAdolescent-
dc.subject.meshAged-
dc.subject.meshAnalgesia, Patient-Controlled-
dc.subject.meshAnalgesics, Opioid-
dc.subject.meshAnesthesia, General-
dc.subject.meshAnesthetics, Inhalation-
dc.subject.meshDouble-Blind Method-
dc.subject.meshDrug Administration Schedule-
dc.subject.meshElectroencephalography-
dc.subject.meshFentanyl-
dc.subject.meshIsoflurane-
dc.subject.meshMonitoring, Intraoperative-
dc.subject.meshMorphine-
dc.subject.meshPain Measurement-
dc.subject.meshPain, Postoperative-
dc.subject.meshYoung Adult-
dc.titleRandomized controlled trial of the effect of depth of anaesthesia on postoperative pain.-
dc.typeJournal Article-
dc.typeMulticenter Study-
dc.typeRandomized Controlled Trial-
dc.typeResearch Support, Non-U.S. Gov't-
dc.identifier.journaltitleBritish journal of anaesthesia-
dc.identifier.doi10.1093/bja/aet419-
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/24322572-
dc.identifier.pubmedid24322572-
dc.ispartof.anzcaresearchfoundationYes-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.cerifentitytypePublications-
item.cerifentitytypePublications-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.openairetypeMulticenter Study-
item.openairetypeRandomized Controlled Trial-
item.openairetypeResearch Support, Non-U.S. Gov't-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
Appears in Collections:Scholarly and Clinical
Show simple item record

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.