Pregabalin as adjunctive therapy in benzodiazepine discontinuation

PURPOSE.The available evidence for the use of pregabalin as adjunctive therapy in the discontinuation of benzodiazepines is reviewed. SUMMARY.Pregabalin has been studied as an adjunctive pharmacologic treatment for the discontinuation of long-term benzodiazepine use. Unlike carbamazepine, pregabalin...

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Veröffentlicht in:American journal of health-system pharmacy 2018-01, Vol.75 (2), p.67-71
Hauptverfasser: Caniff, Kaylee, Telega, Emily, Bostwick, Jolene R, Gardner, Kristen N
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container_end_page 71
container_issue 2
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container_title American journal of health-system pharmacy
container_volume 75
creator Caniff, Kaylee
Telega, Emily
Bostwick, Jolene R
Gardner, Kristen N
description PURPOSE.The available evidence for the use of pregabalin as adjunctive therapy in the discontinuation of benzodiazepines is reviewed. SUMMARY.Pregabalin has been studied as an adjunctive pharmacologic treatment for the discontinuation of long-term benzodiazepine use. Unlike carbamazepine, pregabalin has little potential for drug interactions, and its adverse effects are mostly mild and transient. Pregabalin reduces the release of excitatory neurotransmitters by binding to regulatory subunits of voltage-activated calcium channels. The majority of studies evaluated failed to find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparator groups. The long-term efficacy of pregabalin in benzodiazepine discontinuation is also unknown, as patients were only followed for 0–12 weeks after discontinuing the benzodiazepines. Most studies, however, did observe consistent improvement in withdrawal symptoms, anxiety symptoms, and cognitive function with pregabalin use in benzodiazepine discontinuation. Studies varied in design elements, such as whether past benzodiazepine discontinuation attempts occurred, baseline benzodiazepine use characteristics (agent, dose, duration), benzodiazepine discontinuation strategies previously used, and the use of comorbid psychiatric diagnoses and concurrent psychotropics as exclusion criteria. In addition, the literature does not clearly describe whether patients successfully discontinued pregabalin, for which there are reports of substance abuse. CONCLUSION.Based on the current available evidence, pregabalin is not recommended for use in benzodiazepine discontinuation, as the majority of studies did not find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparatory groups despite an improvement in withdrawal and anxiety symptoms.
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SUMMARY.Pregabalin has been studied as an adjunctive pharmacologic treatment for the discontinuation of long-term benzodiazepine use. Unlike carbamazepine, pregabalin has little potential for drug interactions, and its adverse effects are mostly mild and transient. Pregabalin reduces the release of excitatory neurotransmitters by binding to regulatory subunits of voltage-activated calcium channels. The majority of studies evaluated failed to find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparator groups. The long-term efficacy of pregabalin in benzodiazepine discontinuation is also unknown, as patients were only followed for 0–12 weeks after discontinuing the benzodiazepines. Most studies, however, did observe consistent improvement in withdrawal symptoms, anxiety symptoms, and cognitive function with pregabalin use in benzodiazepine discontinuation. Studies varied in design elements, such as whether past benzodiazepine discontinuation attempts occurred, baseline benzodiazepine use characteristics (agent, dose, duration), benzodiazepine discontinuation strategies previously used, and the use of comorbid psychiatric diagnoses and concurrent psychotropics as exclusion criteria. In addition, the literature does not clearly describe whether patients successfully discontinued pregabalin, for which there are reports of substance abuse. CONCLUSION.Based on the current available evidence, pregabalin is not recommended for use in benzodiazepine discontinuation, as the majority of studies did not find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparatory groups despite an improvement in withdrawal and anxiety symptoms.</description><identifier>ISSN: 1079-2082</identifier><identifier>EISSN: 1535-2900</identifier><identifier>DOI: 10.2146/ajhp160712</identifier><identifier>PMID: 29317396</identifier><language>eng</language><publisher>England: Copyright American Society of Health-System Pharmacists, Inc. 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SUMMARY.Pregabalin has been studied as an adjunctive pharmacologic treatment for the discontinuation of long-term benzodiazepine use. Unlike carbamazepine, pregabalin has little potential for drug interactions, and its adverse effects are mostly mild and transient. Pregabalin reduces the release of excitatory neurotransmitters by binding to regulatory subunits of voltage-activated calcium channels. The majority of studies evaluated failed to find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparator groups. The long-term efficacy of pregabalin in benzodiazepine discontinuation is also unknown, as patients were only followed for 0–12 weeks after discontinuing the benzodiazepines. Most studies, however, did observe consistent improvement in withdrawal symptoms, anxiety symptoms, and cognitive function with pregabalin use in benzodiazepine discontinuation. Studies varied in design elements, such as whether past benzodiazepine discontinuation attempts occurred, baseline benzodiazepine use characteristics (agent, dose, duration), benzodiazepine discontinuation strategies previously used, and the use of comorbid psychiatric diagnoses and concurrent psychotropics as exclusion criteria. In addition, the literature does not clearly describe whether patients successfully discontinued pregabalin, for which there are reports of substance abuse. CONCLUSION.Based on the current available evidence, pregabalin is not recommended for use in benzodiazepine discontinuation, as the majority of studies did not find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparatory groups despite an improvement in withdrawal and anxiety symptoms.</description><subject>Animals</subject><subject>Anti-Anxiety Agents - administration &amp; dosage</subject><subject>Anti-Anxiety Agents - adverse effects</subject><subject>Anxiety</subject><subject>Benzodiazepines</subject><subject>Benzodiazepines - administration &amp; dosage</subject><subject>Benzodiazepines - adverse effects</subject><subject>Calcium</subject><subject>Calcium channels</subject><subject>Calcium channels (voltage-gated)</subject><subject>Carbamazepine</subject><subject>Cognitive ability</subject><subject>Dosage and administration</subject><subject>Drug abuse</subject><subject>Drug therapy</subject><subject>Drug Therapy, Combination</subject><subject>Humans</subject><subject>Neurotransmitters</subject><subject>Observational Studies as Topic - methods</subject><subject>Pregabalin</subject><subject>Pregabalin - administration &amp; dosage</subject><subject>Randomized Controlled Trials as Topic - methods</subject><subject>Regulatory subunits</subject><subject>Substance withdrawal syndrome</subject><subject>Substance Withdrawal Syndrome - diagnosis</subject><subject>Substance Withdrawal Syndrome - epidemiology</subject><subject>Substance Withdrawal Syndrome - prevention &amp; control</subject><subject>Withdrawal</subject><subject>Withholding Treatment - standards</subject><subject>Withholding Treatment - trends</subject><issn>1079-2082</issn><issn>1535-2900</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkUtv1TAQhSMEog_Y8ANQJDYIKWX8iB_LUkFBqgQLWFuTeNLrS64T7ISq_fX46hYqEJqFR-Nvjo7mVNULBmecSfUWt5uZKdCMP6qOWSvahluAx6UHbRsOhh9VJzlvARg3oJ5WR9wKpoVVx9W7L4muscMxxBpzjX67xn4JP6leNpRwvq3LR0fxbvIB72gOkWofcj_FJcQVlzDFZ9WTAcdMz-_f0-rbh_dfLz42V58vP12cXzW95Fo0XvWdF5K1iLbrDElthNUoFQiPxqLUXkLrCYAL6o3EwRsBypD3Ej3rxGn1-qA7p-nHSnlxu2KExhEjTWt2zBrbKmkVK-irf9DttKZY3DkORVNzJuwDdY0juRCHaUnY70XdectbawU3slBn_6FKedqFcgcaQpn_tfDmsNCnKedEg5tT2GG6dQzcPjD3EFiBX947Xbsd-T_o74QKIA_AzTQulPL3cb2h5DaE47JxACCF4rqkzAww1kID-wOKX4oXnqc</recordid><startdate>20180115</startdate><enddate>20180115</enddate><creator>Caniff, Kaylee</creator><creator>Telega, Emily</creator><creator>Bostwick, Jolene R</creator><creator>Gardner, Kristen N</creator><general>Copyright American Society of Health-System Pharmacists, Inc. 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SUMMARY.Pregabalin has been studied as an adjunctive pharmacologic treatment for the discontinuation of long-term benzodiazepine use. Unlike carbamazepine, pregabalin has little potential for drug interactions, and its adverse effects are mostly mild and transient. Pregabalin reduces the release of excitatory neurotransmitters by binding to regulatory subunits of voltage-activated calcium channels. The majority of studies evaluated failed to find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparator groups. The long-term efficacy of pregabalin in benzodiazepine discontinuation is also unknown, as patients were only followed for 0–12 weeks after discontinuing the benzodiazepines. Most studies, however, did observe consistent improvement in withdrawal symptoms, anxiety symptoms, and cognitive function with pregabalin use in benzodiazepine discontinuation. Studies varied in design elements, such as whether past benzodiazepine discontinuation attempts occurred, baseline benzodiazepine use characteristics (agent, dose, duration), benzodiazepine discontinuation strategies previously used, and the use of comorbid psychiatric diagnoses and concurrent psychotropics as exclusion criteria. In addition, the literature does not clearly describe whether patients successfully discontinued pregabalin, for which there are reports of substance abuse. CONCLUSION.Based on the current available evidence, pregabalin is not recommended for use in benzodiazepine discontinuation, as the majority of studies did not find a significant difference in benzodiazepine discontinuation rates between pregabalin and comparatory groups despite an improvement in withdrawal and anxiety symptoms.</abstract><cop>England</cop><pub>Copyright American Society of Health-System Pharmacists, Inc. All rights reserved</pub><pmid>29317396</pmid><doi>10.2146/ajhp160712</doi><tpages>5</tpages></addata></record>
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subjects Animals
Anti-Anxiety Agents - administration & dosage
Anti-Anxiety Agents - adverse effects
Anxiety
Benzodiazepines
Benzodiazepines - administration & dosage
Benzodiazepines - adverse effects
Calcium
Calcium channels
Calcium channels (voltage-gated)
Carbamazepine
Cognitive ability
Dosage and administration
Drug abuse
Drug therapy
Drug Therapy, Combination
Humans
Neurotransmitters
Observational Studies as Topic - methods
Pregabalin
Pregabalin - administration & dosage
Randomized Controlled Trials as Topic - methods
Regulatory subunits
Substance withdrawal syndrome
Substance Withdrawal Syndrome - diagnosis
Substance Withdrawal Syndrome - epidemiology
Substance Withdrawal Syndrome - prevention & control
Withdrawal
Withholding Treatment - standards
Withholding Treatment - trends
title Pregabalin as adjunctive therapy in benzodiazepine discontinuation
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