Division of Pediatric Anesthesiology, Department of Anesthesiology, The University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
Department of Pediatrics, The University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
Pain Med. 2022 Dec 1;23(12):2042-2049. doi: 10.1093/pm/pnac094.
Recurrent, severely painful episodes, known as vaso-occlusive crises (VOCs) are the hallmark of sickle cell disease (SCD) and the primary reason for hospitalization. Opioids have been the gold standard for VOC treatment without significant improvement pain outcomes. To aid analgesia and combat opioid related adverse effects (ORAEs), some SCD clinicians have trialed infusions of sub-anesthetic ketamine along with opioids to treat VOCs. In this retrospective analysis, we compared adult SCD patients who received early vs late adjunctive sub-anesthetic ketamine infusions for VOCs.
We identified adult SCD patients (age 18-50 years) who presented to Duke University with a VOC and received sub-anesthetic ketamine infusions from July 2015 to June 2019. We assessed both daily opioid consumption (measured as oral morphine milligram equivalents (MME)) and self-reported 0-10 numeric pain ratings (NPR) at 1, 2, and 3 days after infusion initiation, as well as 1 day after discontinuation.
A total of 56 patients were identified with a median age of 30 years. Compared to late administration, early infusion of sub-anesthetic ketamine was associated with a 24.5% (P = .0003) and 25.9% (P = .0006) reduction, respectively, in median NPR at 1 day and 2 days after infusion initiation but did not persist at 3 days following initiation of the infusion. A statistically significant reduction in MME was not observed.
In a nonrandomized study of sickle cell patients with VOCs, early sub-anesthetic ketamine infusion led to greater reduction in subjective pain intensity than late initiation of the infusion. Randomized studies should further explore whether early vs late ketamine infusion improves management of acute SCD pain.
反复发作的剧烈疼痛发作,称为血管阻塞危象(VOC),是镰状细胞病(SCD)的标志,也是住院的主要原因。阿片类药物一直是治疗 VOC 的金标准,但并没有显著改善疼痛结局。为了辅助镇痛和对抗阿片类药物相关不良反应(ORAEs),一些 SCD 临床医生尝试在使用阿片类药物的同时输注亚麻醉剂量的氯胺酮来治疗 VOC。在这项回顾性分析中,我们比较了接受早期与晚期辅助亚麻醉剂量氯胺酮输注治疗 VOC 的成年 SCD 患者。
我们确定了 2015 年 7 月至 2019 年 6 月期间因 VOC 就诊于杜克大学的成年 SCD 患者,并接受了亚麻醉剂量的氯胺酮输注。我们评估了输注开始后 1、2 和 3 天以及输注停止后 1 天的每日阿片类药物消耗量(以口服吗啡毫克当量(MME)表示)和自我报告的 0-10 数字疼痛评分(NPR)。
共确定了 56 例患者,中位年龄为 30 岁。与晚期给药相比,早期输注亚麻醉剂量的氯胺酮分别使输注开始后 1 天和 2 天的 NPR 中位数降低了 24.5%(P=0.0003)和 25.9%(P=0.0006),但在输注开始后 3 天并未持续。未观察到 MME 的统计学显著降低。
在一项非随机的 SCD 患者 VOC 研究中,早期亚麻醉剂量氯胺酮输注可使主观疼痛强度较晚开始输注时显著降低。应进一步开展随机研究,以探讨早期与晚期氯胺酮输注是否能改善急性 SCD 疼痛的管理。