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Letter to the Editor: Low-dose ketamine for pain control in patients with multiple rib fractures

机译:致编辑的信:多重肋骨骨折患者疼痛控制的低剂量氯胺酮

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To the Editor In a randomized control trial by Carver and colleagues1 assessing ketamine infusion for pain control in adult patients with multiple rib fractures, they showed that low-dose ketamine failed to decrease numeric pain score (NPS) or oral morphine equivalent (OME) within the overall cohort, but a decrease in OME was noted in patients with an Injury Severity Score greater than 15. Many things of this study were correctly done. The authors used a prospective, randomized, double-blind placebo-controlled trial with a consistent study subjects (multiple rib fractures). Furthermore, they attempted to control most factors affecting the pain control, such as age, gender, Injury Severity Score, and others. All of these are strengths in the study. Other than the limitations described in the discussion, however, we noted several issues in this study that were not addressed well. First, the area under the curve for NPS was used as primary endpoint for group comparison. Besides, the pain regimen was not standardized; however, the authors did not clearly describe whether an NPS goal of satisfied pain control was included in their design. Given that the mean areas under the curve for NPS at 12 hours to 24 hours and 24 hours to 48 hours were greater than 5 in both groups, we were concerned that a satisfied pain control was not achieved in all patients. Most importantly, it was unclear how opiate and non-opiate-based medical treatments were given and if two groups were comparable with patients' satisfaction for pain control. Thus, we argue that no significant difference in NPS for overall cohort should be attributable to the lack of standardized pain regimen and satisfied pain control goal, rather than failure of low-dose ketamine for pain control.
机译:通过Carver及其同事1评估氯胺酮输注在成年患者患者中的氯胺酮输注进行了多个肋骨骨折的止痛药,他们表明,低剂量氯胺酮未能降低数值疼痛评分(NPS)或口服吗啡等当量(OME)整体队列,但伤病严重成绩的患者中指出了欧姆的减少,大于15.这项研究的许多事情都是正确的。作者使用了一项前瞻性,随机的双盲安慰剂对照试验,其具有一致的研究受试者(多个肋骨骨折)。此外,他们试图控制影响疼痛控制的大多数因素,如年龄,性别,伤害严重程度和其他人。所有这些都是研究中的优势。然而,除了在讨论中描述的局限性之外,我们还注意到这项研究中的几个问题并未得到解决。首先,使用NPS曲线下的区域被用作组比较的主要终点。此外,疼痛方案没有标准化;然而,作者没有明确描述他们的设计中是否包含满足疼痛控制的NPS目标。鉴于两组NPS在12小时至24小时和24小时至48小时的NPS下的平均区域大于5,我们担心所有患者都未实现满意的疼痛控制。最重要的是,目前尚不清楚给予鸦片和非鸦片基础的医疗治疗,如果两组与患者对疼痛控制的满意相当。因此,我们认为整体队列的NPS没有显着差异,应归因于缺乏标准化的疼痛方案和满意的疼痛控制目标,而不是低剂量氯胺酮用于疼痛控制的失效。

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