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单纯μ阿片类激动剂与曲马多联合注射作为阿片类药物初治癌症患者的阿片类诱导剂的安全性和有效性

Safety and Efficacy of Combined Injection of Pure-μ-Opioid Agonist with Tramadol as an Opioid Induction Agent for Opioid-Naïve Cancer Patients.

作者信息

Sato Tetsumi, Ono Shigeki, Sato Tetsu, Tanaka Rei, Kamo Yoshiko, Suzuki Tomomi

机构信息

Division of Palliative Medicine, Shizuoka Cancer Center, Shizuoka, Japan.

Palliative Care Team, Shizuoka Cancer Center, Shizuoka, Japan.

出版信息

Palliat Med Rep. 2024 Aug 5;5(1):340-349. doi: 10.1089/pmr.2023.0061. eCollection 2024.

Abstract

BACKGROUND

Tramadol is known to provide synergistic analgesia when used in combination with morphine.

OBJECTIVES

The aims of this study were: (1) to introduce an opioid combination therapy using pure-μ-opioid receptor agonist (OPI) + tramadol injections (OPI + tramadol) and (2) to elucidate safety and efficacy of this combination therapy for opioid-naïve cancer pain patients.

METHODS

Opioid-naïve patients referred to our palliative care team (in Japan) who were unable to take oral medications and received OPI + tramadol as opioid induction agents were retrospectively investigated on the electric medical chart. OPI + tramadol dosage was adjusted to achieve the patient's pain as Numerical Rating Scale ≤4/10 or Support Team Assessment Schedule-Japanese ≤1. Patients' demography, doses of OPI and tramadol administered, and adverse events were analyzed.

RESULTS

A total of 44 patients were included. The primary organs of malignancy were pancreas (11), stomach (5), lung (4), breast (4), liver (4), and others (13). OPI injections administered were hydromorphone (39), morphine (6), oxycodone (1), and fentanyl (1). The starting doses of OPI (morphine equivalent) and tramadol were 6.05 ± 1.63 and 67.8 ± 13.6 mg/day, respectively, and the final doses of OPI (morphine equivalent) and tramadol were 8.14 ± 3.85 and 80.0 ± 28.5 mg/day, respectively. Treatment goals were achieved in all patients. There were three patients in whom OPI was switched owing to inadequate analgesia and no new side effects other than those known to occur when OPI or tramadol is administered appeared.

CONCLUSION

The results suggest that this innovative and unique opioid therapy can be safely and effectively introduced to opioid-naïve cancer patients who are relatively close to the end of life.

摘要

背景

已知曲马多与吗啡联合使用时可提供协同镇痛作用。

目的

本研究的目的是:(1)引入一种使用纯μ-阿片受体激动剂(OPI)+曲马多注射液(OPI+曲马多)的阿片类联合治疗方法,以及(2)阐明这种联合治疗方法对未使用过阿片类药物的癌症疼痛患者的安全性和有效性。

方法

回顾性研究转诊至我们姑息治疗团队(在日本)的未使用过阿片类药物、无法口服药物并接受OPI+曲马多作为阿片类诱导剂的患者的电子病历。调整OPI+曲马多的剂量,以使患者的疼痛程度达到数字评分量表≤4/10或日本支持团队评估量表≤1。分析患者的人口统计学特征、给予的OPI和曲马多剂量以及不良事件。

结果

共纳入44例患者。恶性肿瘤的主要器官为胰腺(11例)、胃(5例)、肺(4例)、乳腺(4例)、肝脏(4例)和其他(13例)。给予的OPI注射液为氢吗啡酮(39例)、吗啡(6例)、羟考酮(1例)和芬太尼(1例)。OPI(吗啡等效剂量)和曲马多的起始剂量分别为6.05±1.63和67.8±13.6mg/天,OPI(吗啡等效剂量)和曲马多的最终剂量分别为8.14±3.85和80.0±28.5mg/天。所有患者均实现了治疗目标。有3例患者因镇痛效果不佳而更换了OPI,除使用OPI或曲马多时已知会出现的副作用外,未出现新的副作用。

结论

结果表明,这种创新且独特的阿片类治疗方法可安全有效地应用于相对接近生命末期的未使用过阿片类药物的癌症患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b42f/11319850/c945b995cc1d/pmr.2023.0061_figure1.jpg

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