Occurrence of somnolence and respiratory depression induced by pregabalin and mirogabalin use and the influence of opioid treatment using the Japanese adverse drug event report database.

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL
Pharmazie Pub Date : 2024-08-01 DOI:10.1691/ph.2024.4528
H Kato, T Koseki, M Kondo
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引用次数: 0

Abstract

Background: Gabapentinoid anticonvulsants are standard treatment for neuropathic pain and are often combined with opioids for treating cancer. It is assumed that this combination may heighten somnolence and respiratory depression due to the inhibitory effects of opioids on the central nervous system. Although pregabalin, a gabapentinoid, is known to increase somnolence frequency during opioid therapy, whether mirogabalin exerts similar effects on somnolence frequency under opioid therapy remains unknown. This study examined the signals of somnolence and respiratory depression in response to pregabalin and mirogabalin use by utilizing data from the Japanese Adverse Drug Event Report database and assessed their interaction with strong opioid analgesics. Methods: Information was obtained from the JADER database from April 2004 to August 2023 via the Pharmaceuticals and Medical Devices Agency website. The study focused on neuropathic pain medications, specifically "pregabalin" and "mirogabalin besilate." Adverse events were defined using preferred terms (PTs) from the Medical Dictionary for Regulatory Activities version 26.1. The PTs considered were "Somnolence (10041349)" and "Respiratory depression (10038678)." To investigate the effect of the combination of strong opioid analgesics with pregabalin and mirogabalin on the occurrence of somnolence, a multivariable logistic regression analysis was conducted. Results: Signals for somnolence were detected with the use of both drugs (pregabalin: information component (IC) [95% confidence intervals (CIs)]: 2.89 [2.70 to 3.08]; mirogabalin: IC [95% CIs] 2.50 [1.85 to 3.16]). When evaluating respiratory depression, a typical and serious adverse event of opioid analgesic use, a signal was detected with pregabalin use but not with mirogabalin use (pregabalin: (IC [95% CIs] 1.28 [0.83 to 1.73]; mirogabalin: IC [95% CIs] -0.15 [-2.20 to 1.89]). Multivariable analysis indicated that the use of strong opioid analgesics increased the occurrence of somnolence when combined with pregabalin but not when combined with mirogabalin (p = 0.004). Conclusion: While the safety of concomitant administation of mirogabalin with opioids remains controversial, caution should be exercised when using pregabalin, especially in combination with opioids for neuropathic pain, compared to that for mirogabalin.

使用普瑞巴林和米瑞巴林引起的嗜睡和呼吸抑制的发生率以及阿片类药物治疗的影响,使用日本药物不良事件报告数据库。
背景:加巴喷丁类抗惊厥药是治疗神经性疼痛的标准药物,通常与阿片类药物联合用于治疗癌症。据推测,由于阿片类药物对中枢神经系统的抑制作用,这种联合用药可能会加重嗜睡和呼吸抑制。虽然已知普瑞巴林(一种加巴喷丁类药物)在阿片类药物治疗过程中会增加嗜睡频率,但米罗加巴林在阿片类药物治疗过程中是否会对嗜睡频率产生类似影响仍是未知数。本研究利用日本药物不良事件报告数据库的数据,研究了使用普瑞巴林和米罗格巴林时的嗜睡和呼吸抑制信号,并评估了它们与强阿片类镇痛药的相互作用。研究方法通过药品和医疗器械管理局网站从 JADER 数据库中获取 2004 年 4 月至 2023 年 8 月期间的信息。研究重点是神经痛药物,特别是 "普瑞巴林 "和 "苯磺酸米罗加巴林"。不良事件的定义采用了《监管活动医学词典》26.1 版中的首选术语 (PT)。考虑的首选术语为 "嗜睡(10041349)"和 "呼吸抑制(10038678)"。为了研究强阿片类镇痛药与普瑞巴林和米罗格巴林联用对嗜睡发生率的影响,进行了多变量逻辑回归分析。结果发现使用这两种药物均可检测到嗜睡信号(普瑞巴林:信息成分(IC)[95% 置信区间(CIs)]:2.89 [2.70 至 3.08];米罗格巴林:IC [95% CIs] 2.50 [1.85 至 3.16])。呼吸抑制是使用阿片类镇痛药的典型严重不良反应,在对呼吸抑制进行评估时,发现使用普瑞巴林会出现信号,而使用米瑞巴林则不会(普瑞巴林:(IC [95% CIs] 1.28 [0.83 to 1.73];米瑞巴林:IC [95% CIs] -0.15 [-2.20 to 1.89])。多变量分析表明,与普瑞巴林合用时,使用强阿片类镇痛药会增加嗜睡发生率,但与米罗格巴林合用时不会(p = 0.004)。结论虽然米罗卡巴林与阿片类药物联合用药的安全性仍存在争议,但与米罗卡巴林相比,在使用普瑞巴林,尤其是与阿片类药物联合治疗神经病理性疼痛时应谨慎。
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来源期刊
Pharmazie
Pharmazie 医学-化学综合
CiteScore
3.10
自引率
0.00%
发文量
56
审稿时长
1.2 months
期刊介绍: The journal DiePharmazie publishs reviews, experimental studies, letters to the editor, as well as book reviews. The following fields of pharmacy are covered: Pharmaceutical and medicinal chemistry; Pharmaceutical analysis and drug control; Pharmaceutical technolgy; Biopharmacy (biopharmaceutics, pharmacokinetics, biotransformation); Experimental and clinical pharmacology; Pharmaceutical biology (pharmacognosy); Clinical pharmacy; History of pharmacy.
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