确定美沙酮诱导癌症患者日间嗜睡的因素,并提出从其他阿片类药物到口服美沙酮的转换比率:一项回顾性队列研究。

IF 1.1 Q4 HEALTH CARE SCIENCES & SERVICES Palliative medicine reports Pub Date : 2023-01-01 DOI:10.1089/pmr.2023.0007
Miho Takemura, Kazuyuki Niki, Yoshiaki Okamoto, Yoshinobu Matsuda, Makie Kohno, Mikiko Ueda
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引用次数: 0

摘要

背景:当美沙酮用于治疗癌痛时,日本医保系统建议根据国家综合癌症网络提出的既往阿片类药物吗啡当量日剂量(MEDD)的等效转换表确定起始剂量。由于转换表的变异性范围很大,美沙酮增加了白天嗜睡的发生率。目的:确定与白天嗜睡相关的因素,并提出从预处理MEDD到口服美沙酮的转换比率,以降低白天嗜睡的风险。设计:回顾性队列研究。背景/受试者:纳入2013年1月1日至2022年8月31日在日本兵库县石谷市立医院(Ashiya Municipal Hospital, Hyogo, Japan)口服美沙酮缓解癌性疼痛的100例患者。测量方法:主要终点,从预处理MEDD到口服美沙酮无日间嗜睡的转化率,采用受试者特征曲线(ROC)分析确定。结果:美沙酮起始7天内白天嗜睡发生率为40.0%。结论:美沙酮剂量相对于预处理MEDD较高时,会发生白天嗜睡。据我们所知,这是第一个提出从预处理MEDD到口服美沙酮的转化率而不引起白天嗜睡的研究。
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Identification of Factors Contributing to Methadone-Induced Daytime Sleepiness in Cancer Patients and Proposal of the Conversion Ratio from Other Opioids to Oral Methadone: A Retrospective Cohort Study.

Background: 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.

Objective: 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.

Design: 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.

Measurements: The primary endpoint, the conversion ratio from pretreatment MEDD to oral methadone without daytime sleepiness, was determined using receiver operator characteristic (ROC) curve analysis.

Results: 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, p <0.001) and methadone dose (OR: 1.395, 95% CI: 1.178-1.652, p <0.001). The conversion ratio from pretreatment MEDD to oral methadone was 0.24, with an area under the ROC curve of 0.909 (p <0.001).

Conclusions: 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.

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