Ketorolac Dosing and Outcomes in Neonates Following Congenital Heart Surgery: A Retrospective Analysis

Amy L. Kiskaddon, Neil A. Goldenberg, Trent Abel, Jamie L. Fierstein, Delia Khayat, James A. Quintessenza, Arabela Stock
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Abstract

BACKGROUND: Pain management is essential for postoperative surgery. Given the association of opioids with adverse outcomes, interest in the use of nonopioid analgesics, such as ketorolac, has increased. Published data on use in neonates are limited. OBJECTIVES: To describe ketorolac dosing and safety and efficacy outcomes in the first 48 hours postcardiac surgery in neonates. DESIGN: We performed a single-center retrospective cohort study of neonates (ages < 28 d) who received ketorolac following cardiac surgery from November 2020 to July 2023 (inclusive). The primary safety outcome was a clinically significant decline in renal function, as defined by the composite of an increase in serum creatinine by greater than or equal to 0.3 mg/dL from baseline within 96 hours of ketorolac initiation and urine output less than or equal to 0.5 mL/kg/hr for 6 hours. The secondary safety outcome was clinically significant bleeding, defined as the composite of major bleeding by the International Society on Thrombosis and Hemostasis pediatric criteria and severe/fatal bleeding by the criteria of Nellis et al (2019). Efficacy was measured by opioid utilization based on a standardized pain score-driven analgesia protocol. INTERVENTIONS: Ketorolac was administered at 0.5 mg/kg every 6 hours as per an institutional clinical management algorithm. MEASUREMENTS AND MAIN RESULTS: Thirty-nine patients met the eligibility criteria. The median ketorolac dose was 0.5 mg/kg/dose, and median (interquartile range [IQR]) duration of therapy was 48 hours (6–48 hr). No patients experienced a significant decline in renal function, and there were no clinically significant bleeding events. The median (IQR) IV morphine milligram equivalents (MMEs)/kg/d of opioid administration was 0.2 MME/kg/d (0.1–0.25 MME/kg/d) at the time of ketorolac initiation and 0.1 MME/kg/d (0.1–0.2 MME/kg/d) at 48 hours post-ketorolac initiation. CONCLUSIONS: If validated prospectively, these findings suggest that a ketorolac regimen of 0.5 mg/kg/dose every 6 hours in neonates postcardiac surgery may be safe with regard to renal function and bleeding risk. Additional randomized studies would be needed to determine efficacy with regard to opioid-sparing capacity.
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先天性心脏病手术后新生儿的酮咯酸剂量和疗效:回顾性分析
背景:疼痛管理是术后手术的关键。鉴于阿片类药物与不良后果之间的关联,人们对使用非阿片类镇痛药(如酮咯酸)的兴趣与日俱增。已公布的新生儿使用数据有限。目的描述酮咯酸在新生儿心脏手术后 48 小时内的剂量、安全性和疗效。设计:我们对 2020 年 11 月至 2023 年 7 月(含)期间接受心脏手术后酮咯酸治疗的新生儿(年龄小于 28 d)进行了单中心回顾性队列研究。主要安全性结果是肾功能临床显著下降,即在开始使用酮咯酸的 96 小时内,血清肌酐比基线升高大于或等于 0.3 mg/dL,且 6 小时内尿量小于或等于 0.5 mL/kg/hr。次要安全性结果为临床重大出血,即国际血栓与止血学会儿科标准中的大出血和 Nellis 等人标准(2019 年)中的严重/致命出血。疗效通过基于标准化疼痛评分驱动的镇痛方案的阿片类药物使用情况来衡量。干预:根据机构临床管理算法,每 6 小时给予 0.5 mg/kg 的酮咯酸。测量和主要结果:39 名患者符合资格标准。酮咯酸的中位剂量为 0.5 毫克/千克/剂量,中位(四分位数间距 [IQR])治疗时间为 48 小时(6-48 小时)。没有患者出现肾功能明显下降的情况,也没有发生临床意义重大的出血事件。开始使用酮咯酸时,静脉注射吗啡毫克当量(MMEs)/千克/天的中位数(IQR)为0.2 MMEs/千克/天(0.1-0.25 MMEs/千克/天),开始使用酮咯酸后48小时的中位数(IQR)为0.1 MMEs/千克/天(0.1-0.2 MMEs/千克/天)。结论:如果经过前瞻性验证,这些研究结果表明,对于心脏手术后的新生儿,每 6 小时服用 0.5 毫克/千克/次的酮咯酸治疗方案在肾功能和出血风险方面可能是安全的。还需要进行更多的随机研究,以确定阿片类药物的疗效。
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CiteScore
5.70
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审稿时长
8 weeks
期刊最新文献
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