Nakayama Hirokazu, Echizen Hirotoshi, Ogawa Ryuichi, Akabane Atsuya, Kato Toshiaki, Orii Takao
*Department of Pharmacy, NTT Medical Center Tokyo, Tokyo, Japan; †Department of Pharmacotherapy, Meiji Pharmaceutical University, Tokyo, Japan; and ‡Gamma Knife Center, NTT Medical Center Tokyo, Tokyo, Japan.
Ther Drug Monit. 2017 Jun;39(3):297-302. doi: 10.1097/FTD.0000000000000391.
Phenobarbital is well tolerated and effective for controlling agitation or preventing convulsion at the end of life. No information is available concerning parenteral bioavailability of phenobarbital when induration develops at the injection or infusion site. We investigated whether induration at injection or infusion site is related to phenobarbital bioavailability via parenteral routes of continuous subcutaneous infusion and intermittent subcutaneous or intramuscular injection.
A retrospective analysis was conducted on the medical data obtained from 18 patients who received chronic subcutaneous or intramuscular injections of phenobarbital for the prevention of convulsions and underwent plasma concentration monitoring of the drug. Patients whose concomitant medications were altered during the observation periods were excluded from the analysis. Comparisons were performed for concentration/dose (C/D) ratios obtained from patients with induration at injection or infusion sites (induration group, n = 6) and those without induration (noninduration group, n = 12). P < 0.05 was considered statistically significant.
The induration group showed significantly reduced C/D ratio compared with the noninduration group [median (range): 0.131 (0.114-0.334) versus 0.219 (0.180-0.322) d/L, P < 0.05). Assuming that systemic clearance was constant in our patients, changes in the C/D ratio would have contributed to 40% (median) reduction in bioavailability of the drug from the injection or infusion site.
Our data suggest that absolute bioavailability of phenobarbital may be reduced when induration develops at the injection or infusion site in patients treated parenterally by continuous subcutaneous infusion or intramuscular injection.
苯巴比妥耐受性良好,在生命终末期控制躁动或预防惊厥有效。关于注射或输液部位出现硬结时苯巴比妥的胃肠外生物利用度尚无相关信息。我们研究了注射或输液部位的硬结是否与通过持续皮下输注以及间歇性皮下或肌内注射的胃肠外途径的苯巴比妥生物利用度相关。
对18例接受苯巴比妥慢性皮下或肌内注射以预防惊厥并进行了该药物血浆浓度监测的患者的医疗数据进行回顾性分析。观察期内伴随用药发生改变的患者被排除在分析之外。对注射或输液部位出现硬结的患者(硬结组,n = 6)和未出现硬结的患者(无硬结组,n = 12)的浓度/剂量(C/D)比值进行比较。P < 0.05被认为具有统计学意义。
与无硬结组相比,硬结组的C/D比值显著降低[中位数(范围):0.131(0.114 - 0.334)对0.219(0.180 - 0.322)d/L,P < 0.05]。假设我们的患者全身清除率恒定,C/D比值的变化将导致药物从注射或输液部位的生物利用度降低40%(中位数)。
我们的数据表明,对于通过持续皮下输注或肌内注射进行胃肠外治疗的患者,当注射或输液部位出现硬结时,苯巴比妥的绝对生物利用度可能会降低。