A Double-Blind Trial of Gabapentin Versus Lorazepam in the Treatment of Alcohol Withdrawal

被引:120
作者
Myrick, Hugh [1 ,2 ]
Malcolm, Robert
Randall, Patrick K.
Boyle, Elizabeth
Anton, Raymond F.
Becker, Howard C. [2 ]
Randall, Carrie L.
机构
[1] Med Univ S Carolina, Inst Psychiat 4N, Dept Psychiat & Behav Sci, Alcohol Res Ctr, Charleston, SC 29425 USA
[2] Vet Affairs Med Ctr, Ralph H Johnson Dept, Charleston, SC 29403 USA
关键词
Gabapentin; Alcohol Dependence; Alcohol Withdrawal; Lorazepam; BRAIN; ANTICONVULSANT; DEPENDENCE; MECHANISMS; PLACEBO; ABUSE; ACID;
D O I
10.1111/j.1530-0277.2009.00986.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Introduction: Some anticonvulsants ameliorate signs and symptoms of alcohol withdrawal, but have an unacceptable side effect burden. Among the advantages of using anticonvulsant agents in this capacity is their purported lack of interaction with alcohol that could increase psychomotor deficits, increase cognitive impairment, or increase intoxication. The aim of this study was to evaluate alcohol use and symptom reduction of gabapentin when compared with lorazepam in the treatment of alcohol withdrawal in a double-blinded randomized clinical trial. Methods: One hundred individuals seeking outpatient treatment of alcohol withdrawal with Clinical Institute Withdrawal Assessment for Alcohol-Revised (CIWA-Ar) ratings >= 10 were randomized to double-blind treatment with 2 doses of gabapentin (900 mg tapering to 600 mg or 1200 tapering to 800 mg) or lorazepam (6 mg tapering to 4 mg) for 4 days. Severity of alcohol withdrawal was measured by the CIWA-Ar on days 1 to 4 of treatment and on days 5, 7, and 12 post-treatment and alcohol use monitored by verbal report and breath alcohol levels. Results: CIWA-Ar scores decreased over time in all groups; high-dose gabapentin was statistically superior but clinically similar to lorazepam (p = 0.009). During treatment, lorazepam-treated participants had higher probabilities of drinking on the first day of dose decrease (day 2) and the second day off medication (day 6) compared to gabapentin-treated participants (p = 0.0002). Post-treatment, gabapentin-treated participants had less probability of drinking during the follow-up post-treatment period (p = 0.2 for 900 mg and p = 0.3 for 1200 mg) compared to the lorazepam-treated participants (p = 0.55). The gabapentin groups also had less craving, anxiety, and sedation compared to lorazepam. Conclusions: Gabapentin was well tolerated and effectively diminished the symptoms of alcohol withdrawal in our population especially at the higher target dose (1200 mg) used in this study. Gabapentin reduced the probability of drinking during alcohol withdrawal and in the immediate postwithdrawal week compared to lorazepam.
引用
收藏
页码:1582 / 1588
页数:7
相关论文
共 40 条
[1]  
[Anonymous], STRUCTURES CLIN INTE
[2]  
[Anonymous], 1994, NEUROLOGY S5
[3]  
Anton RF, 1999, ALCOHOL RES HEALTH, V23, P165
[4]   Novel role for gabapentin in neuroprotection of central nervous system in streptozotocine-induced diabetic rats [J].
Baydas, G ;
Sonkaya, E ;
Tuzcu, M ;
Yasar, A ;
Donder, E .
ACTA PHARMACOLOGICA SINICA, 2005, 26 (04) :417-422
[5]   AN INVENTORY FOR MEASURING DEPRESSION [J].
BECK, AT ;
ERBAUGH, J ;
WARD, CH ;
MOCK, J ;
MENDELSOHN, M .
ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) :561-&
[6]   The acute effects of gabapentin in combination with alcohol in heavy drinkers [J].
Bisaga, Adam ;
Evans, Suzette M. .
DRUG AND ALCOHOL DEPENDENCE, 2006, 83 (01) :25-32
[7]   Randomized double-blind pilot trial of gabapentin versus placebo to treat alcohol dependence and comorbid insomnia [J].
Brower, Kirk J. ;
Kim, Hyungjin Myra ;
Strobbe, Stephen ;
Karam-Hage, Maher A. ;
Consens, Flavia ;
Zucker, Robert A. .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2008, 32 (08) :1429-1438
[8]   Activation of two types of brain glutamate dehydrogenase isoproteins by gabapentin [J].
Cho, SW ;
Cho, EH ;
Choi, SY .
FEBS LETTERS, 1998, 426 (02) :196-200
[9]  
CIRAULO DA, 1988, AM J PSYCHIAT, V145, P1501
[10]   Functional biology of the α2δ subunits of voltage-gated calcium channels [J].
Davies, Anthony ;
Hendrich, Jan ;
Van Minh, Alexandra Tran ;
Wratten, Jack ;
Douglas, Leon ;
Dolphin, Annette C. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2007, 28 (05) :220-228