The Effect of Preoperative Exposure to Benzodiazepines on Opioid Consumption After One and Two-level Anterior Cervical Discectomy and Fusion

被引:0
作者
Meade, Matthew H. [1 ,3 ]
Schultz, Matthew J. [1 ]
Radack, Tyler [2 ]
Michael, Mark [1 ]
Hilibrand, Alan S. [2 ]
Kurd, Mark F. [2 ]
Hsu, Victor [2 ]
Kaye, Ian David [2 ]
Schroeder, Gregory D. [2 ]
Kepler, Christopher [2 ]
Vaccaro, Alexander R. [2 ]
Woods, Barrett I. [2 ]
机构
[1] Jefferson Hlth NJ, Div Orthoped Surg, Stratford, NJ USA
[2] Thomas Jefferson Univ, Rothman Inst, Dept Orthopaed Spine Surg, Philadelphia, PA USA
[3] 1 Med Ctr Dr, Stratford, NJ 08084 USA
来源
CLINICAL SPINE SURGERY | 2023年 / 36卷 / 10期
关键词
opioid; benzodiazepine; ACDF; pain; LOW-BACK-PAIN; RISK-FACTORS; SEX-DIFFERENCES; SURGERY; HEALTH; PRESCRIPTION; ASSOCIATION; DISABILITY; EVENTS; GENDER;
D O I
10.1097/BSD.0000000000001481
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Design:Retrospective cohort.Objective:Investigate the relationship between preoperative benzodiazepine exposure and postoperative opioid use in patients undergoing primary 1 or 2-level anterior cervical discectomy and fusion (ACDF).Background:Little is known about the effect of preoperative benzodiazepine exposure on postoperative opioid use in spine surgery.Patients and Methods:Patients undergoing primary 1 or 2-level ACDF at a single institution from February 2020 to November 2021 were identified through electronic medical records. The prescription drug monitoring program was utilized to record the name, dosage, and quantity of preoperative benzodiazepines/opioids filled within 60 days before surgery and postoperative opioids 6 months after surgery. Patients were classified as benzodiazepine naive or exposed according to preoperative usage, and postoperative opioid dose and duration were compared between groups. Regression analysis was performed for outcomes that demonstrated statistical significance, adjusting for preoperative opioid use, age, sex, and body mass index.Results:Sixty-seven patients comprised the benzodiazepine-exposed group whereas 90 comprised the benzodiazepine-naive group. There was no significant difference in average daily morphine milligram equivalents between groups (median: 96.0 vs 65.0, P = 0.11). The benzodiazepine-exposed group received postoperative opioids for a longer duration (median: 32.0 d vs 12.0 d, P = 0.004) with more prescriptions (median: 2.0 vs 1.0, P = 0.004) and a greater number of pills (median: 110.0 vs 59.0, P = 0.007). On regression analysis, preoperative benzodiazepine use was not significantly associated with postoperative opioid duration [incidence rate ratio (IRR): 0.93, P = 0.74], number of prescriptions (IRR: 1.21, P = 0.16), or number of pills (IRR: 0.89, P = 0.58).Conclusions:While preoperative benzodiazepine users undergoing primary 1 or 2-level ACDF received postoperative opioids for a longer duration compared with a benzodiazepine naive cohort, preoperative benzodiazepine use did not independently contribute to this observation. These findings provide insight into the relationship between preoperative benzodiazepine use and postoperative opioid consumption.Level of Evidence:Level III.
引用
收藏
页码:E410 / E415
页数:6
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