Comparison of phenobarbital monotherapy to a benzodiazepine-based regimen for management of alcohol withdrawal syndrome in trauma patients

被引:2
|
作者
Fleenor, Lori Montana [1 ]
Beavers, Jennifer R. [1 ]
Tidwell, William P. [1 ]
Atchison, Leanne [1 ]
Woo, Edward [2 ]
Medvecz, Andrew J. [3 ]
Beyene, Robel T. [3 ]
Kast, Kristopher [4 ]
Marcovitz, David [4 ]
Dennis, Bradley M. [3 ]
Guillamondegui, Oscar D. [3 ]
Smith, Michael C. [3 ]
机构
[1] Vanderbilt Univ, Dept Pharmaceut Sci, Med Ctr, 1211 Med Ctr Dr,B151, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Pharm Portfolio HealthIT, Med Ctr, Nashville, TN USA
[3] Vanderbilt Univ, Div Acute Care Surg, Med Ctr, Nashville, TN USA
[4] Vanderbilt Univ, Dept Psychiat & Behav Sci, Med Ctr, Nashville, TN USA
来源
关键词
Alcohol withdrawal syndrome; delirium tremens; trauma; phenobarbital; CIWA-AR;
D O I
10.1097/TA.0000000000004116
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: Alcohol withdrawal syndrome (AWS) is associated with increased morbidity and mortality in the trauma population. Benzodiazepines (BZDs) are standard of care for AWS; however, given the risk of delirium with BZDs and reports of BZD-refractory withdrawal, phenobarbital (PHB) has emerged as an alternative therapy for AWS. Safety and efficacy studies of PHB for AWS in trauma patients are lacking. Our aim was to compare a BZD versus PHB protocol in the management of AWS in trauma patients. METHODS: We performed a retrospective cohort study at a level 1 trauma center of patients at risk for AWS managed with either a BZD or a low-dose oral PHB regimen. Patients were excluded if they were taking BZDs or barbiturates before admission, received propofol or dexmedetomidine before initiation of the study drug, presented with delirium tremens or seizures, or died or discharged within 24 hours of presentation. The primary outcome was complicated AWS (seizures or alcohol withdrawal delirium/delirium tremens). Secondary outcomes included uncomplicated AWS; therapy escalation; oversedation; delirium-, intensive care unit-, and ventilator-free days; and length of stay. RESULTS: A total of 411 patients were identified; 118 received BZD, and 293 received PHB. The odds of developing complicated AWS with PHB versus BZD-based therapy were not statistically significant (odds ratio [OR], 0.52; 95% confidence interval [CI], 0.21-1.39); however, patients receiving PHB were less likely to develop uncomplicated AWS (OR, 0.08; 95% CI, 0.04-0.14) and less likely to require escalation of therapy (OR, 0.45; 95% CI, 0.24-0.84). The PHB group had a length of stay 3.1 days shorter than the BZD group (p = 0.002). There was no difference in intensive care unit-, ventilator-, or delirium-free days. CONCLUSION: A PHB-based protocol for the management of AWS is a safe and effective alternative to BZD-based regimens in trauma patients.
引用
收藏
页码:493 / 498
页数:6
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