St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Department of Clinical Pharmacy and Translational Science, The University of Tennessee Health Science Center College of Pharmacy Memphis, Memphis, Tennessee, USA.
Pediatr Blood Cancer. 2021 Nov;68(11):e29215. doi: 10.1002/pbc.29215. Epub 2021 Jul 15.
Despite a more robust experience with lidocaine infusions for pain management in adults and general pediatric population, there is limited evidence of efficacy of lidocaine infusions for pain management in patients with pediatric hematology and oncology diagnoses.
Data pertaining to continuous intravenous lidocaine infusions prescribed between January 2009 and June 2019 were reviewed, including patients' demographic characteristics, hematology/oncology and pain diagnoses, concurrent pain medications, and lidocaine infusion dose regimens and duration. Pain scores and opioid consumption calculations based on morphine equivalent doses (mg/kg/day) of patient-controlled analgesia were collected 1 day before infusion (D1), during infusion (D2), and 1 day after infusion (D3).
The mean opioid consumption on D3 was significantly lower than that on D2 (p = .01). The pain scores on D3 were significantly lower than those on D1 when measured as average pain scores per 24 hours (p < .001) or as single pain scores immediately before and after infusions (p < .001). No significant associations were found between cumulative doses of lidocaine (loading dose plus total infusion dose) and either a decrease in the opioid consumption or a decrease in pain scores.
In this retrospective series of pediatric hematology and oncology cases, we report positive outcomes in reducing opioid consumption and pain scores after lidocaine infusions. Prospective investigations designed in a collaborative, multi-institutional fashion, including a variety of pediatric populations are needed to further investigate the efficacy of lidocaine infusions.
尽管利多卡因输注在成人和普通儿科人群中的疼痛管理方面有更丰富的经验,但对于利多卡因输注在儿科血液学和肿瘤学患者中的疼痛管理的疗效,证据有限。
回顾了 2009 年 1 月至 2019 年 6 月期间开具的连续静脉内利多卡因输注的数据,包括患者的人口统计学特征、血液学/肿瘤学和疼痛诊断、同时使用的止痛药物以及利多卡因输注剂量方案和持续时间。在输注前 1 天(D1)、输注期间(D2)和输注后 1 天(D3),收集基于患者自控镇痛的等效吗啡剂量(mg/kg/天)的疼痛评分和阿片类药物消耗计算值。
D3 的阿片类药物消耗明显低于 D2(p=.01)。当以 24 小时平均疼痛评分(p<0.001)或输注前后单次疼痛评分(p<0.001)衡量时,D3 的疼痛评分明显低于 D1。未发现利多卡因累积剂量(负荷剂量加总输注剂量)与阿片类药物消耗减少或疼痛评分降低之间存在显著关联。
在本回顾性儿科血液学和肿瘤学病例系列中,我们报告了利多卡因输注后阿片类药物消耗和疼痛评分降低的积极结果。需要以协作、多机构的方式设计前瞻性研究,包括各种儿科人群,以进一步调查利多卡因输注的疗效。