Use of bupivacaine liposomal injectable suspension in children aged 2 to 6 years undergoing cardiac surgery does not accelerate recovery

Lindsay J. Nitsche BS , Paul J. Devlin MD, MSc , Sarah J. Bond MS, PA-C , Jeremy A. Friedman MD , Kaitlyn R. Rubnitz PA-C , Emily Schwartz MSN, CRNP , Colleen E. Bontrager BA , Lauren I. Karel PharmD , Susan C. Nicolson MD , Stephanie M. Fuller MD, MS
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Abstract

Objective

Bupivacaine liposomal injectable suspension is proven safe and effective for selective postsurgical analgesia in children older than 6 years. We evaluated if intraoperative bupivacaine liposomal injectable suspension administration decreases postoperative opioid use, peak pain scores, and length of stay in children aged 2 to 6 years undergoing cardiac surgery via median sternotomy.

Methods

Serial patients aged 2 to 6 years undergoing cardiac surgery received 4 mg/kg bupivacaine liposomal injectable suspension mixed with 0.25% bupivacaine hydrochloride and 0.9% sodium chloride via local infiltration at the conclusion of their procedure. They were matched with controls who underwent operation within the past 5 years by procedure, age, gender, and weight. Postoperative opioid use was converted into morphine milligram equivalents, and pain severity was measured using the Face, Legs, Activity, Cry, and Consolability scale. Paired t tests, chi-square tests, and descriptive statistics were used depending on the nature of the data.

Results

A total of 100 patients receiving bupivacaine liposomal injectable suspension and matching historical control patients aged 2 to 6 years were analyzed. There were no significant differences in preoperative variables. Patients receiving bupivacaine liposomal injectable suspension received an average of 3.6 (95% CI, 1.2-6.0) fewer morphine milligram equivalents (P = .003). However, there was no significant difference in peak pain score (P = .4), time to first enteral intake (P = .5), intensive care unit length of stay (P = 1), or hospital length of stay (P = .2). The median cost of bupivacaine liposomal injectable suspension was higher than that of bupivacaine hydrochloride (P < .001).

Conclusions

Intraoperative bupivacaine liposomal injectable suspension use in children aged 2 to 6 years undergoing cardiac surgery showed statistically but not clinically significant decreases in postoperative opioid use. Bupivacaine liposomal injectable suspension use had no impact on intensive care unit or hospital length of stay but was substantially more expensive.
2至6岁接受心脏手术的儿童使用布比卡因脂质体注射混悬液不会加速康复
目的研究布比卡因脂质体注射混悬液用于6岁以上儿童术后选择性镇痛的安全性和有效性。我们评估术中布比卡因脂质体注射悬浮液是否减少术后阿片类药物的使用、峰值疼痛评分和2至6岁儿童胸骨正中切开心脏手术的住院时间。方法对2 ~ 6岁心脏手术患者行手术结束后,经局部浸润给予4 mg/kg布比卡因脂质体注射混悬液,混合盐酸0.25%布比卡因和0.9%氯化钠。根据手术方式、年龄、性别和体重将他们与过去5年内接受过手术的对照组相匹配。术后阿片类药物使用转换为吗啡毫克当量,疼痛严重程度采用面部、腿部、活动、哭泣和安慰量表测量。根据数据的性质,使用配对t检验、卡方检验和描述性统计。结果对100例接受布比卡因脂质体注射混悬液治疗的2 ~ 6岁患者进行分析。术前各项指标差异无统计学意义。接受布比卡因脂质体注射悬液的患者平均减少3.6毫克吗啡当量(95% CI, 1.2-6.0) (P = 0.003)。然而,两组在疼痛峰值评分(P = 0.4)、首次肠内摄入时间(P = 0.5)、重症监护病房住院时间(P = 1)和住院时间(P = 0.2)方面无显著差异。布比卡因脂质体注射混悬液的中位成本高于盐酸布比卡因(P <;措施)。结论术中使用布比卡因脂质体注射混悬液对2 ~ 6岁儿童心脏手术后阿片类药物的使用有统计学意义,但无临床意义。布比卡因脂质体注射悬浮液的使用对重症监护病房或住院时间没有影响,但实质上更昂贵。
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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CiteScore
1.70
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