Gish Emily C, Harrison Donald, Gormley Andrew K, Johnson Peter N
Department of Pharmacy, Primary Children's Medical Center, Salt Lake City, Utah.
J Pediatr Pharmacol Ther. 2011 Jan;16(1):39-46.
The purpose of this study was to assess the appropriateness of weight-based dosing of continuous intravenous infusion of fentanyl in overweight/obese versus normal-weight children admitted to the pediatric intensive care unit (PICU).
This retrospective, pilot study included 5- to 12-year-old children admitted to the PICU over a 2-year period who received continuous intravenous infusion fentanyl for ≥ 4 days. The overweight/obese group included children with a body mass index (BMI) ≥ 85th percentile, while the control group included children with BMI < 85th percentile. The primary objective was to compare the number of fentanyl continuous intravenous infusion dosage changes required per day to achieve adequate sedation between groups. Secondarily, opioid withdrawal symptoms following the discontinuation of fentanyl and concomitant sedative/analgesic regimens were analyzed between groups. Student t tests and chi-square analyses were performed as appropriate, with an a priori alpha of p≤0.05.
Sixteen normal-weight and 15 overweight/obese patients with 18 and 16 individual infusions were identified, respectively. No statistical difference was found between groups for the number of dosage changes per day, 0.92 versus 0.69 (p=0.16). Five patients in each group experienced withdrawal (p=0.71). The total number of concomitant bolus doses received was greater in the overweight/obese group but did not reach statistical significance.
There was a numerical, but statistically nonsignificant difference in the number of sedative/analgesic bolus doses and dosing changes per day between groups. Larger studies are warranted to determine the optimal dosing strategy for continuous intravenous infusion fentanyl in overweight/obese children.
本研究旨在评估儿科重症监护病房(PICU)收治的超重/肥胖儿童与正常体重儿童中,基于体重的芬太尼持续静脉输注剂量是否合适。
这项回顾性试点研究纳入了在2年期间入住PICU且接受芬太尼持续静脉输注≥4天的5至12岁儿童。超重/肥胖组包括体重指数(BMI)≥第85百分位数的儿童,而对照组包括BMI <第85百分位数的儿童。主要目的是比较两组之间为达到充分镇静每天所需的芬太尼持续静脉输注剂量变化次数。其次,分析两组在停用芬太尼及伴随的镇静/镇痛方案后出现的阿片类药物戒断症状。根据情况进行学生t检验和卡方分析,先验α水平为p≤0.05。
分别确定了16名正常体重和15名超重/肥胖患者,分别有18次和16次个体输注。两组之间每天的剂量变化次数没有统计学差异,分别为0.92次和0.69次(p = 0.16)。每组有5名患者出现戒断症状(p = 0.71)。超重/肥胖组接受的伴随推注剂量总数更多,但未达到统计学意义。
两组之间在镇静/镇痛推注剂量次数和每天的剂量变化方面存在数值差异,但无统计学意义。需要进行更大规模的研究来确定超重/肥胖儿童芬太尼持续静脉输注的最佳给药策略。