Michael Dinsmore, Kristof Nijs, Eric Plitman, Emad Al Azazi, Lashmi Venkatraghavan, Karim Ladha, Hance Clarke
{"title":"口服氯胺酮用于急性术后镇痛(OKAPA)试验:随机对照单中心试点研究。","authors":"Michael Dinsmore, Kristof Nijs, Eric Plitman, Emad Al Azazi, Lashmi Venkatraghavan, Karim Ladha, Hance Clarke","doi":"10.1016/j.jclinane.2024.111690","DOIUrl":null,"url":null,"abstract":"<p><strong>Study objective: </strong>Although opioids represent the mainstay of treating surgical pain, their use is associated with significant side effects. There is an urgent need to find new pain relievers with safer side effect profiles. One drug that has been receiving increasing attention is ketamine. By using the oral route of administration, ketamine could potentially be used by patients in a less resource-intensive manner with similar efficacy. This study aims to examine the role of oral ketamine in improving recovery after major spine surgery.</p><p><strong>Design: </strong>A prospective, single-center, double blinded parallel arm, placebo controlled randomized feasibility trial.</p><p><strong>Setting: </strong>Toronto Western Hospital (TWH), UHN, Toronto, Canada.</p><p><strong>Patients: </strong>Adult patients (aged 18-75) undergoing multi-level lumbar spine decompression and fusion with planned overnight admission in hospital.</p><p><strong>Interventions: </strong>Study treatment (oral ketamine 30 mg) or matching placebo for three days (nine doses total) or until hospital discharge.</p><p><strong>Measurements: </strong>The primary outcome was the patient-reported Quality of Recovery-15 score (QoR-15). Secondary outcomes were opioid use, pain intensity, pain interference (PROMIS-pain interference questionnaire), mood (PHQ-9) and, side-effects (Generic Assessment of Side Effects Scale).</p><p><strong>Main results: </strong>Data from 35 patients were analyzed, of which 18 patients in the ketamine group and 17 patients in the placebo group. There were no significant differences identified in QoR-15 scores at postoperative days 1,3,7, and 30. There were also no significant differences found in pain intensity scale scores at postoperative days 1, 3, 7, and 30, and PROMIS and PHQ-9 scores at postoperative days 7 and 30. Significantly less oral opioids were used in the ketamine group compared to the placebo group on postoperative day 3 and by postoperative day 7. In addition, patients in the ketamine group spent significantly less days on oral opioids and trended to be discharged from hospital earlier.</p><p><strong>Conclusion: </strong>This pilot study demonstrated that low dose oral ketamine can be safely used as an adjunct in postoperative pain treatment to help reduce opioid consumption after major spine surgery.</p>","PeriodicalId":15506,"journal":{"name":"Journal of Clinical Anesthesia","volume":"100 ","pages":"111690"},"PeriodicalIF":5.0000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oral ketamine for acute postoperative analgesia (OKAPA) trial: A randomized controlled, single center pilot study.\",\"authors\":\"Michael Dinsmore, Kristof Nijs, Eric Plitman, Emad Al Azazi, Lashmi Venkatraghavan, Karim Ladha, Hance Clarke\",\"doi\":\"10.1016/j.jclinane.2024.111690\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Study objective: </strong>Although opioids represent the mainstay of treating surgical pain, their use is associated with significant side effects. There is an urgent need to find new pain relievers with safer side effect profiles. One drug that has been receiving increasing attention is ketamine. By using the oral route of administration, ketamine could potentially be used by patients in a less resource-intensive manner with similar efficacy. This study aims to examine the role of oral ketamine in improving recovery after major spine surgery.</p><p><strong>Design: </strong>A prospective, single-center, double blinded parallel arm, placebo controlled randomized feasibility trial.</p><p><strong>Setting: </strong>Toronto Western Hospital (TWH), UHN, Toronto, Canada.</p><p><strong>Patients: </strong>Adult patients (aged 18-75) undergoing multi-level lumbar spine decompression and fusion with planned overnight admission in hospital.</p><p><strong>Interventions: </strong>Study treatment (oral ketamine 30 mg) or matching placebo for three days (nine doses total) or until hospital discharge.</p><p><strong>Measurements: </strong>The primary outcome was the patient-reported Quality of Recovery-15 score (QoR-15). Secondary outcomes were opioid use, pain intensity, pain interference (PROMIS-pain interference questionnaire), mood (PHQ-9) and, side-effects (Generic Assessment of Side Effects Scale).</p><p><strong>Main results: </strong>Data from 35 patients were analyzed, of which 18 patients in the ketamine group and 17 patients in the placebo group. There were no significant differences identified in QoR-15 scores at postoperative days 1,3,7, and 30. There were also no significant differences found in pain intensity scale scores at postoperative days 1, 3, 7, and 30, and PROMIS and PHQ-9 scores at postoperative days 7 and 30. Significantly less oral opioids were used in the ketamine group compared to the placebo group on postoperative day 3 and by postoperative day 7. 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Oral ketamine for acute postoperative analgesia (OKAPA) trial: A randomized controlled, single center pilot study.
Study objective: Although opioids represent the mainstay of treating surgical pain, their use is associated with significant side effects. There is an urgent need to find new pain relievers with safer side effect profiles. One drug that has been receiving increasing attention is ketamine. By using the oral route of administration, ketamine could potentially be used by patients in a less resource-intensive manner with similar efficacy. This study aims to examine the role of oral ketamine in improving recovery after major spine surgery.
Setting: Toronto Western Hospital (TWH), UHN, Toronto, Canada.
Patients: Adult patients (aged 18-75) undergoing multi-level lumbar spine decompression and fusion with planned overnight admission in hospital.
Interventions: Study treatment (oral ketamine 30 mg) or matching placebo for three days (nine doses total) or until hospital discharge.
Measurements: The primary outcome was the patient-reported Quality of Recovery-15 score (QoR-15). Secondary outcomes were opioid use, pain intensity, pain interference (PROMIS-pain interference questionnaire), mood (PHQ-9) and, side-effects (Generic Assessment of Side Effects Scale).
Main results: Data from 35 patients were analyzed, of which 18 patients in the ketamine group and 17 patients in the placebo group. There were no significant differences identified in QoR-15 scores at postoperative days 1,3,7, and 30. There were also no significant differences found in pain intensity scale scores at postoperative days 1, 3, 7, and 30, and PROMIS and PHQ-9 scores at postoperative days 7 and 30. Significantly less oral opioids were used in the ketamine group compared to the placebo group on postoperative day 3 and by postoperative day 7. In addition, patients in the ketamine group spent significantly less days on oral opioids and trended to be discharged from hospital earlier.
Conclusion: This pilot study demonstrated that low dose oral ketamine can be safely used as an adjunct in postoperative pain treatment to help reduce opioid consumption after major spine surgery.
期刊介绍:
The Journal of Clinical Anesthesia (JCA) addresses all aspects of anesthesia practice, including anesthetic administration, pharmacokinetics, preoperative and postoperative considerations, coexisting disease and other complicating factors, cost issues, and similar concerns anesthesiologists contend with daily. Exceptionally high standards of presentation and accuracy are maintained.
The core of the journal is original contributions on subjects relevant to clinical practice, and rigorously peer-reviewed. Highly respected international experts have joined together to form the Editorial Board, sharing their years of experience and clinical expertise. Specialized section editors cover the various subspecialties within the field. To keep your practical clinical skills current, the journal bridges the gap between the laboratory and the clinical practice of anesthesiology and critical care to clarify how new insights can improve daily practice.