No benefit from the addition of low-dose ketamine infusion to standard evidence-based care of patients with multiple rib fractures.

IF 2.9 2区 医学 Q2 CRITICAL CARE MEDICINE
Chad Macheel, Joseph Farhat, Jonathan Gipson, Peter Lindbloom, Michaela A West
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引用次数: 0

Abstract

Background: Multiple rib fractures from blunt thoracic trauma cause significant morbidity. Optimal current management includes multimodal analgesia, pulmonary hygiene, and early mobilization. Low-dose ketamine infusion (LDKI) has been proposed as an adjunctive analgesic in this setting. A prior study reported decreased pain scores with LDKI in patients with multiple rib fractures. We hypothesized that LDKI would decrease morphine milligram equivalents (MMEs) in patients with multiple rib fractures.

Methods: A prospective randomized placebo-controlled trial was performed in adult (18 years or older) patients with three or more rib fractures. A prestudy power analysis calculated an 80% chance of identifying a 15% decrease in MMEs with 50 subjects. The study was approved by the institutional review board and informed consent obtained in all subjects. Demographic (age, sex) and injury specific information (Injury Severity Score, number of rib fractures) were obtained. Subjects were randomized 1:1 to receive continuous LDKI (0.1 mg/kg/h) or placebo infusion (0.9% NaCl) for ≤48 hours. All patients received a standard evidence-based multidisciplinary protocol for rib fractures management. Primary outcome measure was MME use or pulmonary complications. Statistical comparison of LDKI versus placebo was performed using the Mann-Whitney U test.

Results: All 50 enrolled subjects (placebo, 25; LDKI, 25) received study drug infusion. The two groups were well matched for age, Injury Severity Score, and number of rib fractures. We observed no differences in the Day 1 (p = 0.961), Day 2 (p = 0.373), or total MMEs (p = 0.946) between groups. Similar total MME use was observed when subjects who received ≥40 hours of study drug and were compared (p = 0.924). Use of LDKI did not alter subsequent need for opiate analgesics postinfusion, hospital length of stay, pulmonary complications, or need for readmission.

Conclusion: The addition of LDKI to an established multimodal, evidence-based protocol for management of multiple rib fractures did not decrease opiate usage or impact pulmonary complications.

Level of evidence: Therapeutic/Care Managaement; Level I.

在对多发性肋骨骨折患者进行标准循证护理的基础上,增加低剂量氯胺酮输注的治疗效果不佳。
背景:胸部钝性创伤造成的多发性肋骨骨折会导致严重的发病率。目前的最佳治疗方法包括多模式镇痛、肺部卫生和早期活动。在这种情况下,低剂量氯胺酮输注(LDKI)被认为是一种辅助镇痛剂。之前有研究报告称,多发性肋骨骨折患者使用 LDKI 后疼痛评分降低。我们假设 LDKI 会降低多发性肋骨骨折患者的吗啡毫克当量(MMEs):我们在有三根或更多肋骨骨折的成年(18 岁或以上)患者中进行了一项前瞻性随机安慰剂对照试验。根据研究前的功率分析计算,50 名受试者有 80% 的机会发现 MMEs 下降了 15%。该研究获得了机构审查委员会的批准,并获得了所有受试者的知情同意。研究人员获得了受试者的人口统计学信息(年龄、性别)和受伤具体信息(受伤严重程度评分、肋骨骨折数量)。受试者按 1:1 随机分配,接受持续输注 LDKI(0.1 毫克/千克/小时)或安慰剂(0.9% 氯化钠)≤48 小时。所有患者都接受了标准的循证多学科肋骨骨折治疗方案。主要结果指标为MME的使用或肺部并发症。LDKI 与安慰剂的统计比较采用 Mann-Whitney U 检验:所有 50 名入选者(安慰剂,25 人;LDKI,25 人)都接受了研究药物输注。两组受试者的年龄、受伤严重程度评分和肋骨骨折数量完全匹配。我们观察到,两组患者在第 1 天(p = 0.961)、第 2 天(p = 0.373)或 MME 总用量(p = 0.946)方面没有差异。如果对接受研究药物治疗时间≥40 小时的受试者进行比较,也能观察到类似的 MME 总用量(p = 0.924)。使用LDKI不会改变输液后对阿片类镇痛药的需求、住院时间、肺部并发症或再入院需求:结论:在治疗多发性肋骨骨折的既定多模式循证方案中加入 LDKI 并未减少阿片类药物的使用,也未对肺部并发症产生影响:证据级别:治疗/护理管理;I级。
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来源期刊
CiteScore
6.00
自引率
11.80%
发文量
637
审稿时长
2.7 months
期刊介绍: The Journal of Trauma and Acute Care Surgery® is designed to provide the scientific basis to optimize care of the severely injured and critically ill surgical patient. Thus, the Journal has a high priority for basic and translation research to fulfill this objectives. Additionally, the Journal is enthusiastic to publish randomized prospective clinical studies to establish care predicated on a mechanistic foundation. Finally, the Journal is seeking systematic reviews, guidelines and algorithms that incorporate the best evidence available.
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