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

IF 1.1 Q4 HEALTH CARE SCIENCES & SERVICES
Palliative medicine reports Pub Date : 2024-08-05 eCollection Date: 2024-01-01 DOI:10.1089/pmr.2023.0061
Tetsumi Sato, Shigeki Ono, Tetsu Sato, Rei Tanaka, Yoshiko Kamo, Tomomi Suzuki
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引用次数: 0

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.

将纯μ-阿片类激动剂与曲马多联合注射作为阿片类药物诱导剂用于阿片类药物过敏的癌症患者的安全性和有效性
背景:众所周知,曲马多与吗啡联合使用可产生协同镇痛作用:众所周知,曲马多与吗啡联合使用可提供协同镇痛作用:本研究的目的是(1)引入一种阿片类药物联合疗法,使用纯μ-阿片受体激动剂(OPI)+曲马多注射液(OPI+曲马多);(2)阐明这种联合疗法对阿片类药物无效癌痛患者的安全性和有效性:对转诊到我们姑息治疗团队(日本)的无法口服药物并接受 OPI + 曲马多作为阿片类药物诱导剂的阿片类药物无效患者的电子病历进行了回顾性调查。OPI+曲马多的剂量根据患者的疼痛程度进行调整,即数字评分量表≤4/10或支持团队评估表-日语≤1。对患者的人口统计学资料、OPI和曲马多的用药剂量以及不良反应进行了分析:结果:共纳入 44 例患者。结果:共纳入 44 例患者,主要恶性肿瘤器官为胰腺(11 例)、胃(5 例)、肺(4 例)、乳腺(4 例)、肝(4 例)及其他(13 例)。注射的 OPI 包括氢吗啡酮(39)、吗啡(6)、羟考酮(1)和芬太尼(1)。OPI(吗啡当量)和曲马多的起始剂量分别为 6.05 ± 1.63 毫克/天和 67.8 ± 13.6 毫克/天,OPI(吗啡当量)和曲马多的最终剂量分别为 8.14 ± 3.85 毫克/天和 80.0 ± 28.5 毫克/天。所有患者都达到了治疗目标。有3名患者因镇痛效果不佳而更换了OPI,除了服用OPI或曲马多时已知会出现的副作用外,没有出现其他新的副作用:研究结果表明,这种创新而独特的阿片类药物疗法可以安全有效地应用于未使用过阿片类药物的癌症患者,这些患者的生命相对接近终结。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.20
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