The efficacy of adductor canal blockade after minor arthroscopic knee surgery - a randomised controlled trial

Background Adductor canal blockade (ACB) has been demonstrated to be effective in the treatment of post‐operative pain after major knee surgery. We hypothesised that the ACB would reduce pain and analgesic requirements after minor arthroscopic knee surgery. Methods Seventy‐two patients scheduled for...

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Published inActa anaesthesiologica Scandinavica Vol. 58; no. 3; pp. 273 - 280
Main Authors ESPELUND, M., FOMSGAARD, J. S., HARASZUK, J., DAHL, J. B., MATHIESEN, O.
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.03.2014
Wiley Subscription Services, Inc
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Summary:Background Adductor canal blockade (ACB) has been demonstrated to be effective in the treatment of post‐operative pain after major knee surgery. We hypothesised that the ACB would reduce pain and analgesic requirements after minor arthroscopic knee surgery. Methods Seventy‐two patients scheduled for minor knee surgery were enrolled in this placebo‐controlled, blinded trial. The patients were randomised to receive an ACB with either 30 ml ropivacaine 7.5 mg/ml (n = 36) or saline (n = 35) in addition to a basic analgesic regimen with paracetamol and ibuprofen. Primary outcome measure was pain during standing at 2 h after surgery. Secondary outcomes were pain at rest, while standing and after a 5‐m walk; opioid consumption and opioid‐related side effects 0–24 h after surgery. Results Pain scores {median [interquartile range (IQR)]}, regarding primary outcome were 15 (0–26) mm in the ropivacaine vs. 17 (5–28) mm in the control group, 95% confidence interval (CI) (−10 to 4) mm, P = 0.41. Ketobemidone consumption 0–2 h post‐operatively [median (IQR)] was lower in the ropivacaine vs. the control group: 0.0 (0.0–2.5) mg vs. 2.5 (0.0–5.0) mg, 95% CI: −2.5 to 0 mg, P = 0.01. No differences were observed for any other outcome. Conclusion No significant analgesic effect of the ACB could be detected after minor arthroscopic knee surgery with a basic analgesic regimen with acetaminophen and ibuprofen, except from a minor reduction in immediate requirements for supplemental opioids. Clinicaltrials.gov Identifier: NCT01254825.
Bibliography:istex:439DFB047D0647DF0936F3FC355EB4B383C7B57B
ArticleID:AAS12224
Department of Anaesthesiology, University of Copenhagen, Glostrup Hospital, Capital Region of Denmark
ark:/67375/WNG-DDL2GX4G-4
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-News-1
ObjectType-Feature-3
content type line 23
ISSN:0001-5172
1399-6576
DOI:10.1111/aas.12224