Ketorolac vs. Fentanyl: A retrospective chart review of analgesia in the prehospital environment

Kane Darling , Brandon Wilkinson , Cheyenne Wong , Angela MacFarlane , Camille Brummett , Isain Zapata
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Abstract

Background

With growing concerns on the worsening opioid epidemic and provider hesitation for opioid use, opioid-sparing treatment regimens are being introduced such as ketorolac administration. The primary aims of this study are to compare the safety and efficacy of ketorolac to fentanyl in the prehospital setting and to determine ketorolac's potential as a practical alternative analgesic.

Methods

A retrospective chart review of patient encounters obtained from a prehospital emergency medical services agency in New Mexico was conducted to evaluate the safety and efficacy of ketorolac vs. fentanyl in the prehospital setting. Primary outcomes assessed were the reported medication complications, initial pain, last pain, and pain reduction on a Numerical Rating Scale. Data was evaluated using unadjusted and adjusted (age, gender, and weight of the patient) models.

Results

A total of 4102 records were evaluated (3182 fentanyl cases vs. 920 ketorolac cases). No significant differences in initial, last pain or pain reduction were seen in unadjusted models and for age, gender, or weight adjusted models. However, adjusted models displayed a difference in the number of complications that occurred while all cases of medication complications occurred within the fentanyl group (64 occurrences, P<0.0001). Among the complications seen, nausea and hypoxia are the most frequent with 40.6 and 29.7% of occurrences respectively).

Conclusion

Findings suggest that ketorolac is both effective and safe in the prehospital environment when compared to fentanyl. These findings encourage prehospital agencies to adopt opioid-sparing treatment protocols to encourage increased treatment of pain without potentiating the current opioid epidemic.

酮咯酸与芬太尼:院前环境镇痛的回顾性病历审查
背景随着人们对阿片类药物疫情日益恶化的担忧以及医疗服务提供者对阿片类药物使用的犹豫不决,人们开始采用克罗拉克等阿片类药物替代治疗方案。本研究的主要目的是比较酮咯酸与芬太尼在院前环境中的安全性和疗效,并确定酮咯酸作为一种实用替代镇痛药的潜力。方法 对从新墨西哥州一家院前急救医疗服务机构获得的患者就诊情况进行回顾性病历审查,以评估酮咯酸与芬太尼在院前环境中的安全性和疗效。评估的主要结果是报告的用药并发症、最初疼痛、最后疼痛以及数字评分量表上的疼痛减轻程度。采用未调整和调整(患者年龄、性别和体重)模型对数据进行了评估。结果 共评估了 4102 条记录(芬太尼病例 3182 对酮咯酸病例 920)。在未经调整的模型以及年龄、性别或体重调整模型中,初始疼痛、最后疼痛或疼痛减轻程度均无明显差异。然而,调整后的模型显示出并发症发生数量的差异,而所有药物并发症病例均发生在芬太尼组(64 例,P<0.0001)。结论研究结果表明,与芬太尼相比,酮咯酸在院前环境中既有效又安全。这些研究结果鼓励院前机构采用节省阿片类药物的治疗方案,以鼓励在不加剧当前阿片类药物流行的情况下增加对疼痛的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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