Takemura Miho, Niki Kazuyuki, Okamoto Yoshiaki, Matsuda Yoshinobu, Kohno Makie, Ueda Mikiko
Department of Clinical Pharmacy Research and Education, Osaka University Graduate School of Pharmaceutical Sciences, Suita, Japan.
Department of Pharmacy, Ashiya Municipal Hospital, Ashiya, Japan.
Palliat Med Rep. 2023 Jul 28;4(1):194-201. doi: 10.1089/pmr.2023.0007. eCollection 2023.
When methadone is used to treat cancer pain, the Japanese health insurance system recommends to determine the starting dose according to the equivalency conversion table based on the morphine-equivalent daily dose (MEDD) of prior opioids proposed by the National Comprehensive Cancer Network. Owing to the wide range in variability of the conversion table, methadone increases the incidence of daytime sleepiness.
To identify the factors associated with daytime sleepiness and propose a conversion ratio from pretreatment MEDD to oral methadone that decreases the risk of daytime sleepiness.
Retrospective cohort study.
SETTING/SUBJECTS: One hundred patients who started oral methadone to relieve cancer pain at Ashiya Municipal Hospital (Hyogo, Japan) from January 1, 2013, to August 31, 2022, were enrolled.
The primary endpoint, the conversion ratio from pretreatment MEDD to oral methadone without daytime sleepiness, was determined using receiver operator characteristic (ROC) curve analysis.
The incidence of daytime sleepiness within seven days of methadone initiation was 40.0%. The factors identified as contributing to daytime sleepiness were pretreatment MEDD (odds ratio [OR]: 0.941, 95% confidence interval [CI]: 0.916-0.966, <0.001) and methadone dose (OR: 1.395, 95% CI: 1.178-1.652, <0.001). The conversion ratio from pretreatment MEDD to oral methadone was 0.24, with an area under the ROC curve of 0.909 ( <0.001).
Daytime sleepiness developed when methadone dose is high relative to pretreatment MEDD. To the best of our knowledge, this is the first study to suggest the conversion ratio from pretreatment MEDD to oral methadone without causing daytime sleepiness.
当使用美沙酮治疗癌症疼痛时,日本医疗保险系统建议根据美国国立综合癌症网络提出的先前阿片类药物的吗啡等效日剂量(MEDD),按照等效转换表来确定起始剂量。由于转换表的变异性范围广泛,美沙酮会增加日间嗜睡的发生率。
确定与日间嗜睡相关的因素,并提出从治疗前MEDD到口服美沙酮的转换率,以降低日间嗜睡的风险。
回顾性队列研究。
设置/研究对象:纳入了2013年1月1日至2022年8月31日期间在日本兵库县芦屋市立医院开始口服美沙酮以缓解癌症疼痛的100名患者。
使用受试者工作特征(ROC)曲线分析确定主要终点,即从治疗前MEDD到无日间嗜睡的口服美沙酮的转换率。
美沙酮起始后7天内日间嗜睡的发生率为40.0%。被确定为导致日间嗜睡的因素是治疗前MEDD(比值比[OR]:0.941,95%置信区间[CI]:0.916 - 0.966,P < 0.001)和美沙酮剂量(OR:1.395,95% CI:1.178 - 1.652,P < 0.001)。从治疗前MEDD到口服美沙酮的转换率为0.24,ROC曲线下面积为0.909(P < 0.001)。
当美沙酮剂量相对于治疗前MEDD较高时会出现日间嗜睡。据我们所知,这是第一项提出从治疗前MEDD到口服美沙酮且不会导致日间嗜睡的转换率的研究。