Adverse outcomes associated with concurrent gabapentin, opioid, and benzodiazepine utilization: A nested case-control study

被引:17
作者
Olopoenia, Abisola [1 ]
Camelo-Castillo, Wendy [1 ]
Qato, Danya M. [1 ,2 ]
Adekoya, Adepeju [3 ]
Palumbo, Frank [1 ]
Sera, Leah [4 ]
Simoni-Wastila, Linda [1 ,5 ]
机构
[1] Univ Maryland, Dept Pharmaceut Hlth Serv Res, Baltimore, MD USA
[2] Univ Maryland, Sch Med, Baltimore, MD USA
[3] Johns Hopkins Med, Dept Anesthesiol & Crit Care Med, Div Chron Pain Med, Baltimore, MD USA
[4] Univ Maryland, Dept Pharm Practice & Sci, Baltimore, MD USA
[5] Univ Maryland, Peter Lamy Ctr Drug Therapy & Aging, Baltimore, MD USA
来源
LANCET REGIONAL HEALTH-AMERICAS | 2022年 / 13卷
关键词
Gabapentin; Opioids; Benzodiazepine; Pain; Mental health; ENHANCED RECOVERY; UNITED-STATES; CHRONIC PAIN; ABUSE; RISK; DRUG; PRESCRIPTION; PERFORMANCE; PREGABALIN; DEPENDENCE;
D O I
10.1016/j.lana.2022.100302
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background Gabapentin, opioids, and/or benzodiazepines are commonly prescribed for a variety of pain and psychiatric conditions. Despite the high likelihood of co-prescription of these medications, little is known about co-utilization of gabapentin (GABA), opioids (OP), and benzodiazepines (BZD) and associated public health outcomes. Methods Using Medicare CCW Data, 2013-2016, we conducted a nested case-control study to examine the association between concurrent utilization of GABA, OP, and BZD and respiratory depression, opioid, and substance-related overdose among Medicare disabled beneficiaries. Cases and controls were Fee-for-service disabled beneficiaries who had a diagnosis of acute pain (AP), chronic pain (CP) or mental health conditions (MH) and received GABA, OP or BZD. Cases with respiratory depression, opioid or substance-related overdose were matched with up to 4 controls on socio-demographics, year of cohort entry and disease risk score. Primary exposure was concurrent medication utilization defined as an overlap of at least one day in prescriptions for GABA, OP and BZD. Findings Across all cohorts, the majority of cases and controls were under 65, female, dually eligible and had prior histories of pain and mental health conditions. GABA+OP+BZD use was associated with increased odds of respiratory depression [AOR(95%CI)<inverted exclamation> AP: 1.35 (1.19-1.52), CP:1.24 (1.11-1.38) and MH: 1.16 (1.02-1.32) vs. OP only], opioidrelated overdose [AP: 1.43 (1.04-1.98), CP: 1.47 (1.07-2.00) and MH: 1.44 (1.04-2.00) vs. OP only], and substancerelated overdose [AP: 1.77 (1.26-2.50), CP: 1.70 (1.24-2.34) and MH: 1.92 (1.31-2.82) vs. GABA only]. While there were cohort differences in the association between GABA+OP and both respiratory depression and opioid-related overdose, GABA+OP and GABA+BZD use were associated with significantly higher odds of substance-related overdose across all clinical cohorts. Interpretation Among Medicare disabled beneficiaries, concurrent utilization of gabapentin, opioids, and benzodiazepines is associated with multiple adverse outcomes. Given this, it is imperative that the benefits and risks of coprescribing these medications be comprehensively examined. Copyright (c) 2022 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
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页数:13
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