Shiraishi Chihiro, Matsuda Hiroko, Ogura Toru, Iwamoto Takuya
Department of Pharmacy, Mie University Hospital, 2-174 Edobashi, Tsu, Mie, 514-8507, Japan.
Clinical Research Support Center, Mie University Hospital, Tsu, Japan.
J Pharm Health Care Sci. 2021 Feb 2;7(1):7. doi: 10.1186/s40780-021-00190-2.
Phenobarbital (PB) is commonly used as elixir and powder formulations in pediatric care. Its dose adjustment is performed based on individual drug concentration monitoring. Few studies have comprehensively analyzed the variation factors for serum PB concentration. In this study, we retrospectively investigated the factors that influence serum PB concentration and assessed the impacts of dosage formulation and administration route.
This retrospective cohort study covered clinical data from January 2007 to September 2019 at Mie University Hospital. The present study included 60 pediatric patients administered the elixir and powder of PB through oral route and enteral tube. Simple and multiple linear regression analyses were performed to identify the risk factors that affect the weight-corrected PB serum concentration/dose (C/D) ratio in pediatric patients. Six subgroups were also established according to the concomitant use of drugs that potentially inhibit PB metabolism, dosage formulation, and administration route to investigate the difference in the PB C/D ratio among the subgroups.
A significant regression equation to predict the PB C/D ratio was found through simple and multiple linear regression analyses, with an adjusted coefficient of determination of 0.53 (p < 0.001). Further, the concomitant uses of valproic acid (VPA) or amiodarone, which were the only two drugs seen in this study as potential inhibitors of PB, was found to have the greatest effect on the PB C/D ratio (standardized partial regression coefficient (β) = 0.543, p < 0.001). Furthermore, a significant difference in the PB C/D ratio was found between the subgroups classified by the concomitant use of VPA or amiodarone (p = 0.002). However, there were no significant correlations between the PB C/D ratio, dosage formulation, and administration route.
The most influential factor on the PB C/D ratio was the concomitant use of VPA or amiodarone with PB. This result could provide an important perspective in pediatric drug therapy where elixir and powder formulations are administered via the oral route and enteral tube.
苯巴比妥(PB)在儿科护理中常用其酏剂和散剂剂型。其剂量调整是根据个体药物浓度监测进行的。很少有研究全面分析血清PB浓度的变化因素。在本研究中,我们回顾性调查了影响血清PB浓度的因素,并评估了剂型和给药途径的影响。
这项回顾性队列研究涵盖了2007年1月至2019年9月在三重大学医院的临床数据。本研究纳入了60例通过口服途径和鼻饲管给予PB酏剂和散剂的儿科患者。进行简单和多元线性回归分析,以确定影响儿科患者体重校正后的PB血清浓度/剂量(C/D)比值的危险因素。还根据可能抑制PB代谢的药物的联合使用、剂型和给药途径建立了六个亚组,以研究亚组间PB C/D比值的差异。
通过简单和多元线性回归分析发现了一个预测PB C/D比值的显著回归方程,调整后的决定系数为0.53(p<0.001)。此外,丙戊酸(VPA)或胺碘酮的联合使用,这是本研究中仅有的两种被视为PB潜在抑制剂的药物,被发现对PB C/D比值影响最大(标准化偏回归系数(β)=0.543,p<0.001)。此外,在根据VPA或胺碘酮的联合使用分类的亚组之间发现PB C/D比值存在显著差异(p=0.002)。然而,PB C/D比值与剂型和给药途径之间没有显著相关性。
对PB C/D比值影响最大的因素是VPA或胺碘酮与PB的联合使用。这一结果可为通过口服途径和鼻饲管给予酏剂和散剂剂型的儿科药物治疗提供重要的参考。