{"title":"Ketamine for acute and chronic pain: beyond anaesthesia.","authors":"Hao G Duong, Tariq G Pulskamp, Daniel J Berlau","doi":"10.1080/17581869.2026.2627884","DOIUrl":null,"url":null,"abstract":"<p><p>Ketamine's clinical role has expanded beyond anesthesia into a mechanism-based, non-opioid analgesic used across acute, perioperative, and chronic pain settings. As a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist, ketamine attenuates central sensitization, modulates opioid tolerance, and enhances descending inhibitory control. At subanaesthetic doses (0.1-0.5 mg/kg), it consistently reduces pain scores and postoperative opioid consumption while maintaining hemodynamic and respiratory stability. In acute and perioperative care, analgesic efficacy is comparable to opioids, though clear superiority has not been demonstrated. In chronic pain, particularly complex regional pain syndrome (CRPS), multi-day infusions provide temporary relief, but durability remains limited. In cancer-related pain, ketamine offers adjuvant benefits for opioid-refractory syndromes with variable outcomes. Short-term adverse effects such as dizziness and mild dysphoria are common, whereas psychomimetic symptoms, hepatobiliary injury, and cystitis restrict prolonged use. Overall, ketamine provides context-dependent, opioid-sparing analgesia with defined but specific clinical utility. Its evolving role in pain management will likely remain targeted, emphasizing patient selection, standardized dosing, and realistic expectations for benefit.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":" ","pages":"523-533"},"PeriodicalIF":1.5000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pain management","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/17581869.2026.2627884","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/9 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Ketamine's clinical role has expanded beyond anesthesia into a mechanism-based, non-opioid analgesic used across acute, perioperative, and chronic pain settings. As a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist, ketamine attenuates central sensitization, modulates opioid tolerance, and enhances descending inhibitory control. At subanaesthetic doses (0.1-0.5 mg/kg), it consistently reduces pain scores and postoperative opioid consumption while maintaining hemodynamic and respiratory stability. In acute and perioperative care, analgesic efficacy is comparable to opioids, though clear superiority has not been demonstrated. In chronic pain, particularly complex regional pain syndrome (CRPS), multi-day infusions provide temporary relief, but durability remains limited. In cancer-related pain, ketamine offers adjuvant benefits for opioid-refractory syndromes with variable outcomes. Short-term adverse effects such as dizziness and mild dysphoria are common, whereas psychomimetic symptoms, hepatobiliary injury, and cystitis restrict prolonged use. Overall, ketamine provides context-dependent, opioid-sparing analgesia with defined but specific clinical utility. Its evolving role in pain management will likely remain targeted, emphasizing patient selection, standardized dosing, and realistic expectations for benefit.
氯胺酮的临床作用已经超越了麻醉,成为一种基于机制的非阿片类镇痛药,用于急性、围手术期和慢性疼痛。作为一种非竞争性n -甲基- d -天冬氨酸(NMDA)受体拮抗剂,氯胺酮可减轻中枢致敏,调节阿片耐受性,并增强下行抑制控制。在亚麻醉剂量(0.1-0.5 mg/kg)下,它持续降低疼痛评分和术后阿片类药物消耗,同时保持血液动力学和呼吸稳定。在急性期和围手术期护理中,镇痛效果与阿片类药物相当,尽管没有明确的优势。对于慢性疼痛,特别是复杂的局部疼痛综合征(CRPS),多日的输液可以暂时缓解,但持久性仍然有限。在癌症相关疼痛中,氯胺酮为阿片类药物难治综合征提供了不同结果的辅助益处。短期不良反应如头晕和轻度烦躁是常见的,而拟精神病症状、肝胆损伤和膀胱炎限制了长期使用。总的来说,氯胺酮提供情境依赖,阿片类镇痛具有明确但具体的临床用途。它在疼痛管理中不断发展的作用可能仍然是有针对性的,强调病人的选择,标准化的剂量,以及对利益的现实期望。