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Intravenous S-ketamine’s analgesic efficacy in third molar surgery: A randomized placebo-controlled double-blind clinical trial
Department of Surgical Sciences, Uppsala University, Uppsala, Sweden;Centre for Clinical Research, Uppsala University, Falun, Sweden.ORCID iD: 0009-0002-1818-7347
Department of Surgical Sciences, Uppsala University, Uppsala, Sweden;Multidisciplinary Pain Centre, Uppsala University, Uppsala, Sweden.
Department of Surgical Sciences, Uppsala University, Uppsala, Sweden;Multidisciplinary Pain Centre, Uppsala University, Uppsala, Sweden.
Centre for Clinical Research, Uppsala University, Falun, Sweden.
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2024 (English)In: British Journal of Pain, ISSN 2049-4637, Vol. 18, no 2, p. 197-208Article in journal (Refereed) Published
Abstract [en]

Background: In most cases, a combination of paracetamol and ibuprofen are the optimal treatment for postoperative pain in third molar surgery. If stronger analgesia is required, opioids are traditionally administered. In day-case, surgery; however, opioids should be avoided. Thus, the anaesthetic agent S-ketamine in analgesic doses might be preferred.

Methods: The study was designed as a randomized placebo-controlled double-blind clinical trial. The study enrolled healthy subjects according to the American Society of Anaesthesiologists classification; I or II (ASA), aged 18 to 44 years, with a body weight between 50 and 100 kg. The patients were randomized into three groups where two doses of S-ketamine were compared (high: 0.25 mg/kg or low: 0.125 mg/kg) with placebo (saline).

Results: A primary outcome of the study was that VAS at 4 h postoperatively, showed no significant difference between the placebo and high-dose S-ketamine group or in the low-dose group. We found a significant difference between the groups for the first 24 h, with a lower VAS-score in the high-dose S-ketamine group. The time to when 50% had taken their first rescue medication was 12 min later in the high-dose ketamine group.

Conclusions: Pre-emptive S-ketamine 0.25 mg/kg gave a global significant reduction of pain by VAS during the first 24 h postoperatively. The time from end of surgery to first rescue medication were longer in the high-dose ketamine group compared to both low-dose ketamine and placebo groups.

Place, publisher, year, edition, pages
Sage Publications, 2024. Vol. 18, no 2, p. 197-208
National Category
Anesthesiology and Intensive Care
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URN: urn:nbn:se:mau:diva-64755DOI: 10.1177/20494637231222327ISI: 001125533900001PubMedID: 38545499Scopus ID: 2-s2.0-85179947499OAI: oai:DiVA.org:mau-64755DiVA, id: diva2:1822709
Available from: 2023-12-27 Created: 2023-12-27 Last updated: 2024-04-26Bibliographically approved

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Tegelberg, Åke

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CiteExportLink to record
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