Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Vertex Pharmaceuticals, Boston, Massachusetts, USA.
Clin Pharmacol Ther. 2023 Nov;114(5):1050-1057. doi: 10.1002/cpt.3019. Epub 2023 Aug 25.
Gabapentin is prescribed for pain and is perceived as safe generally. However, gabapentin can cause respiratory depression, exacerbated by concomitant central nervous system depressants (e.g., opioids), a concern for vulnerable populations. We compared mortality rates among new users of either gabapentin or duloxetine with or without concurrent opioids in the 20% Medicare sample. We conducted a new-user design retrospective cohort study, in Medicare enrollees ages 65-89 years with noncancer chronic pain and no severe illness who filled prescriptions between 2015 and 2018 for gabapentin (n = 233,060) or duloxetine (n = 34,009). Daily opioid doses, estimated in morphine milligram equivalents (MMEs), were classified into none, low (0 < MME < 50), and high (≥ 50 MME), based on Centers for Disease Control and Prevention (CDC) recommendations. The outcomes were all-cause mortality (primary) and out-of-hospital mortality (secondary). We used inverse probability of treatment weighting to adjust for differences between gabapentin and duloxetine users. During 116,707 person-years of follow-up, 1,379 patients died. All-cause mortality rate in gabapentin users was 12.16 per 1,000 person-years vs. 9.94 per 1,000 in duloxetine users. Risks were similar for users with no concurrent opioids (adjusted hazard ratio (aHR) = 1.03, 95% confidence interval (CI): 0.80-1.31) or low-dose daily opioids (aHR = 1.06, 95% CI: 0.63-1.76). However, gabapentin users receiving concurrent high-dose daily opioids had an increased rate of all-cause mortality compared with duloxetine users on high-dose opioids (aHR = 2.03, 95% CI: 1.19-3.46). Out-of-hospital mortality yielded similar results. In this retrospective cohort study of Medicare beneficiaries, concurrent use of high-dose opioids and gabapentin was associated with a higher all-cause mortality risk than that for concurrent use of high-dose opioids and duloxetine.
加巴喷丁用于治疗疼痛,一般认为是安全的。然而,加巴喷丁可引起呼吸抑制,与同时使用中枢神经系统抑制剂(如阿片类药物)时会加重这种抑制,这是脆弱人群的一个关注点。我们比较了在 20%的医疗保险样本中,新使用加巴喷丁或度洛西汀(无论是否同时使用阿片类药物)的患者的死亡率。我们进行了一项新使用者设计的回顾性队列研究,纳入了年龄在 65-89 岁之间、患有非癌症慢性疼痛且无严重疾病的医疗保险参保者,他们在 2015 年至 2018 年间开具了加巴喷丁(n=233060)或度洛西汀(n=34009)的处方。根据疾病预防控制中心(CDC)的建议,以吗啡毫克当量(MME)估计的每日阿片类药物剂量分为无(0<MME<50)、低(0<MME<50)和高(≥50 MME)剂量。主要结局为全因死亡率(一级终点)和院外死亡率(二级终点)。我们使用逆概率治疗加权来调整加巴喷丁和度洛西汀使用者之间的差异。在 116707 人年的随访期间,有 1379 名患者死亡。加巴喷丁使用者的全因死亡率为 12.16/1000 人年,度洛西汀使用者为 9.94/1000 人年。无同时使用阿片类药物(调整后的危险比[aHR]=1.03,95%置信区间[CI]:0.80-1.31)或低剂量每日阿片类药物(aHR=1.06,95% CI:0.63-1.76)的使用者风险相似。然而,与使用高剂量度洛西汀的患者相比,同时使用高剂量加巴喷丁和阿片类药物的患者全因死亡率的发生率更高(aHR=2.03,95% CI:1.19-3.46)。院外死亡率得出了类似的结果。在这项对医疗保险受益人的回顾性队列研究中,与同时使用高剂量度洛西汀和阿片类药物相比,同时使用高剂量加巴喷丁和阿片类药物与全因死亡率风险增加相关。