Siegel Leslie, Quirk Kyle, Houchard Gary, Ehrman Sarah, McLaughlin Eric, Hajmousa Omar, Saphire Maureen
Department of Pharmacy, The Ohio State University James Comprehensive Cancer Center, Columbus, Ohio, USA.
Department of Internal Medicine, Division of Palliative Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
J Pain Palliat Care Pharmacother. 2024 Dec;38(4):414-422. doi: 10.1080/15360288.2024.2374297. Epub 2024 Jul 11.
Although weak evidence exists to support subanesthetic ketamine for cancer pain treatment, successful use may be hindered in the absence of standardized dosing guidance. We aimed to compare the success rates of intravenous ketamine fixed-rate versus weight-based dosing strategies for cancer pain treatment, and to assess patient characteristics that correlate with treatment success. We conducted a single-center retrospective review including non-critically ill adults with cancer pain who received subanesthetic ketamine for at least 24-h. All patients received fixed-rate ketamine; weight-based doses were retrospectively determined using total body weight. Treatment was considered successful if after reaching the maximum prescribed ketamine dose the patient had a 30% reduction in: baseline pain score, as-needed opioid use, or total morphine equivalent daily dose over a standardized 24-h. Of 105 included patients, 51 (48.6%) successfully responded to ketamine. Responders had lower fixed-rate ketamine doses compared to non-responders (median[IQR] 15 mg/hr[10-15] vs. 15 mg/hr[15-20], = 0.043), but no difference in retrospectively calculated weight-based doses (0.201 ± 0.09 mg/kg/hr vs. 0.209 ± 0.08 mg/kg/hr, = 0.59). Responders had higher daily opioid requirements at baseline compared to non-responders ( = 0.04). Though underpowered, our findings suggest that weight-based ketamine dosing may not convey additional benefit over fixed-rate dosing.
尽管支持亚麻醉剂量氯胺酮用于癌症疼痛治疗的证据不足,但在缺乏标准化给药指导的情况下,其成功应用可能会受到阻碍。我们旨在比较静脉注射氯胺酮固定剂量与基于体重的给药策略用于癌症疼痛治疗的成功率,并评估与治疗成功相关的患者特征。我们进行了一项单中心回顾性研究,纳入了患有癌症疼痛的非危重症成人患者,这些患者接受亚麻醉剂量氯胺酮治疗至少24小时。所有患者均接受固定剂量的氯胺酮治疗;基于体重的剂量通过回顾性计算总体重来确定。如果在达到规定的氯胺酮最大剂量后,患者在标准化的24小时内基线疼痛评分、按需使用阿片类药物量或总吗啡当量日剂量降低30%,则认为治疗成功。在纳入的105例患者中,51例(48.6%)对氯胺酮治疗有成功反应。与无反应者相比,有反应者的固定剂量氯胺酮较低(中位数[四分位间距]15毫克/小时[10 - 15] vs. 15毫克/小时[15 - 20],P = 0.043),但回顾性计算的基于体重的剂量无差异(0.201±0.09毫克/千克/小时 vs. 0.209±0.08毫克/千克/小时,P = 0.59)。与无反应者相比,有反应者在基线时每日阿片类药物需求量更高(P = 0.04)。尽管样本量不足,但我们的研究结果表明,基于体重的氯胺酮给药可能不会比固定剂量给药带来额外益处。