From the, Faculty of Epidemiology & Population Health, (CTR), London School of Hygiene & Tropical Medicine, London, UK.
Veterans Aging Cohort Study Coordinating Center, (CTR, ACJ, JPT), VA Connecticut Healthcare System, West Haven, Connecticut, USA.
Alcohol Clin Exp Res. 2020 Sep;44(9):1807-1815. doi: 10.1111/acer.14408. Epub 2020 Jul 28.
Gabapentin is prescribed for seizures and pain and has efficacy for treating alcohol use disorder (AUD) starting at doses of 900 milligrams per day (mg/d). Recent evidence suggests safety concerns associated with gabapentin including adverse neurologic effects. Individuals with hepatitis C (HCV), HIV, or AUD may be at increased risk due to comorbidities and potential medication interactions.
We identified patients prescribed gabapentin for ≥ 60 days for any indication between 2002 and 2015. We propensity-score matched each gabapentin-exposed patient with up to 5 gabapentin-unexposed patients. We followed patients for 2 years or until diagnosed with (i) falls or fractures, or (ii) altered mental status using validated ICD-9 diagnostic codes. We used Poisson regression to estimate incidence rates and relative risk (RR) of these adverse events in association with gabapentin exposure overall and stratified by age, race/ethnicity, sex, HCV, HIV, AUD, and dose.
Incidence of falls or fractures was 1.81 per 100 person-years (PY) among 140,310 gabapentin-exposed and 1.34/100 PY among 431,408 gabapentin-unexposed patients (RR 1.35, 95% confidence interval [CI] 1.28 to 1.44). Incidence of altered mental status was 1.08/100 PY among exposed and 0.97/100 PY among unexposed patients, RR of 1.12 (95% CI 1.04 to 1.20). Excess risk of falls or fractures associated with gabapentin exposure was observed in all subgroups except patients with HCV, HIV, or AUD; however, these groups had elevated incidence regardless of exposure. There was a clear dose-response relationship for falls or fractures with highest risk observed among those prescribed ≥ 2,400 mg/d (RR 1.90, 95% CI 1.50 to 2.40). Patients were at increased risk for altered mental status at doses 600 to 2,399 mg/d; however, low number of events in the highest dose category limited power to detect a statistically significant association ≥ 2,400 mg/d.
Gabapentin is associated with falls or fractures and altered mental status. Clinicians should be monitoring gabapentin safety, especially at doses ≥ 600 mg/d, in patients with and without AUD.
加巴喷丁用于治疗癫痫和疼痛,起始剂量为每天 900 毫克时对治疗酒精使用障碍(AUD)有效。最近的证据表明,加巴喷丁存在安全性问题,包括不良神经影响。患有丙型肝炎(HCV)、艾滋病毒(HIV)或 AUD 的个体由于合并症和潜在药物相互作用,可能面临更高的风险。
我们确定了 2002 年至 2015 年间,任何适应证下使用加巴喷丁治疗≥60 天的患者。我们采用倾向评分匹配,为每个接受加巴喷丁治疗的患者匹配了最多 5 名未接受加巴喷丁治疗的患者。我们对患者进行了 2 年的随访,或直到他们被诊断为(i)跌倒或骨折,或(ii)使用 ICD-9 诊断代码确定为精神状态改变。我们使用泊松回归来估计与加巴喷丁暴露相关的这些不良事件的发生率和相对风险(RR),总体以及按年龄、种族/族裔、性别、HCV、HIV、AUD 和剂量分层。
在 140310 名接受加巴喷丁治疗的患者中,跌倒或骨折的发生率为每 100 人年 1.81 例,而在 431408 名未接受加巴喷丁治疗的患者中,跌倒或骨折的发生率为每 100 人年 1.34 例(RR 1.35,95%置信区间 [CI] 1.28 至 1.44)。在暴露组中,精神状态改变的发生率为每 100 人年 1.08 例,在未暴露组中为每 100 人年 0.97 例,RR 为 1.12(95%CI 1.04 至 1.20)。除了 HCV、HIV 或 AUD 患者外,在所有亚组中都观察到与加巴喷丁暴露相关的跌倒或骨折的风险增加;然而,这些组无论是否暴露,发病率都很高。跌倒或骨折与剂量之间存在明确的剂量反应关系,在接受≥2400 毫克/天的患者中观察到最高风险(RR 1.90,95%CI 1.50 至 2.40)。在 600 至 2399 毫克/天剂量范围内,患者发生精神状态改变的风险增加;然而,由于最高剂量组中的事件数量较少,因此无法检测到统计学上显著的关联(≥2400 毫克/天)。
加巴喷丁与跌倒或骨折和精神状态改变有关。临床医生应监测加巴喷丁的安全性,特别是在 AUD 患者和非 AUD 患者中,剂量为 600 毫克/天及以上。