Intravenous S-ketamine’s analgesic efficacy in third molar surgery. A randomized placebo-controlled double-blind clinical trial

Author:

Eriksson Lars B12ORCID,Gordh Torsten13,Karlsten Rolf13,LoMartire Riccardo2,Thor Andreas14,Tegelberg Åke56

Affiliation:

1. Department of Surgical Sciences, Uppsala University, Uppsala, Sweden

2. Centre for Clinical Research, Uppsala University, Falun, Sweden

3. Multidisciplinary Pain Centre, Uppsala University, Uppsala, Sweden

4. Plastic & Oral and Maxillofacial Surgery, Uppsala University, Uppsala, Sweden

5. Centre for Clinical Research, Uppsala University, Västerås, Sweden

6. Department of Orofacial pain and jaw function, Faculty of Odontology, Malmö University, Malmö, Sweden

Abstract

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.

Funder

Regionala Forskningsrådet Uppsala/Örebro

Public Dental Care Dalarna, Sweden

Centre for Clinical Research, Dalarna

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine

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