Propofol for Treatment of Refractory Alcohol Withdrawal Syndrome: A Review of the Literature
The authors evaluated all available evidence on the use of propofol as an adjuvant for the treatment of resistant alcohol withdrawal syndrome (AWS) in comparison to other therapies. A comprehensive PubMed search (1966–December 2015) was conducted using the search terms propofol, alcohol withdrawal,...
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description | The authors evaluated all available evidence on the use of propofol as an adjuvant for the treatment of resistant alcohol withdrawal syndrome (AWS) in comparison to other therapies. A comprehensive PubMed search (1966–December 2015) was conducted using the search terms propofol, alcohol withdrawal, and drug therapy. Articles were cross‐referenced for other citations. Clinical studies, case series, and case reports published in the English language assessing the use of propofol in adult patients for treatment of AWS were reviewed for inclusion. Propofol is a sedative‐hypnotic that exerts its actions through agonism of GABAA receptors at a different binding site than benzodiazepines and reduces glutamatergic activity through N‐methyl‐d‐aspartase (NMDA) receptor blockade. Dosages from 5 to 100 μg/kg/minute reduced AWS symptoms with frequent development of hypotension and requirement for mechanical ventilation. Patients on propofol often experienced longer durations of mechanical ventilation and length of stay, which may be attributed to more‐resistant cases of AWS. When propofol was compared with dexmedetomidine as adjuncts in AWS, both agents showed similar benzodiazepine‐ and haloperidol‐sparing effects. Dexmedetomidine was associated with more numerical rates of bradycardia, while propofol was associated with more numerical instances of hypotension. Dexmedetomidine was used more frequently in nonintubated patients. The available data assessing the utility of propofol for AWS exhibited significant heterogeneity. Propofol may be useful in a specific population of patients with AWS, limited to those who are not clinically responding to first‐line therapy with benzodiazepines. Specifically, propofol should be considered in patients who are refractory to or not candidates for other adjuvant therapies, patients already requiring mechanical ventilation, or those with seizure activity or refractory delirium tremens. In severe, refractory AWS, adjuvant therapy with propofol may be considered but requires further research to recommend its use either preferentially or as monotherapy. |
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Grace ; Hammond, Drayton A.</creator><creatorcontrib>Brotherton, Amy L. ; Hamilton, Eric P. ; Kloss, H. Grace ; Hammond, Drayton A.</creatorcontrib><description>The authors evaluated all available evidence on the use of propofol as an adjuvant for the treatment of resistant alcohol withdrawal syndrome (AWS) in comparison to other therapies. A comprehensive PubMed search (1966–December 2015) was conducted using the search terms propofol, alcohol withdrawal, and drug therapy. Articles were cross‐referenced for other citations. Clinical studies, case series, and case reports published in the English language assessing the use of propofol in adult patients for treatment of AWS were reviewed for inclusion. Propofol is a sedative‐hypnotic that exerts its actions through agonism of GABAA receptors at a different binding site than benzodiazepines and reduces glutamatergic activity through N‐methyl‐d‐aspartase (NMDA) receptor blockade. Dosages from 5 to 100 μg/kg/minute reduced AWS symptoms with frequent development of hypotension and requirement for mechanical ventilation. Patients on propofol often experienced longer durations of mechanical ventilation and length of stay, which may be attributed to more‐resistant cases of AWS. When propofol was compared with dexmedetomidine as adjuncts in AWS, both agents showed similar benzodiazepine‐ and haloperidol‐sparing effects. Dexmedetomidine was associated with more numerical rates of bradycardia, while propofol was associated with more numerical instances of hypotension. Dexmedetomidine was used more frequently in nonintubated patients. The available data assessing the utility of propofol for AWS exhibited significant heterogeneity. Propofol may be useful in a specific population of patients with AWS, limited to those who are not clinically responding to first‐line therapy with benzodiazepines. Specifically, propofol should be considered in patients who are refractory to or not candidates for other adjuvant therapies, patients already requiring mechanical ventilation, or those with seizure activity or refractory delirium tremens. In severe, refractory AWS, adjuvant therapy with propofol may be considered but requires further research to recommend its use either preferentially or as monotherapy.</description><identifier>ISSN: 0277-0008</identifier><identifier>EISSN: 1875-9114</identifier><identifier>DOI: 10.1002/phar.1726</identifier><identifier>PMID: 26893017</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adrenergic alpha-2 Receptor Agonists - administration & dosage ; Adrenergic alpha-2 Receptor Agonists - adverse effects ; Adrenergic alpha-2 Receptor Agonists - therapeutic use ; Adult ; Alcohol ; alcohol withdrawal syndrome ; Alcohol-Induced Disorders, Nervous System - drug therapy ; Alcohol-Induced Disorders, Nervous System - physiopathology ; Alcohol-Induced Disorders, Nervous System - therapy ; benzodiazepine ; Bradycardia - chemically induced ; Bradycardia - physiopathology ; Chemotherapy, Adjuvant - adverse effects ; dexmedetomidine ; Dexmedetomidine - administration & dosage ; Dexmedetomidine - adverse effects ; Dexmedetomidine - therapeutic use ; Dose-Response Relationship, Drug ; Drug Resistance ; Evidence-Based Medicine ; GABA-A Receptor Agonists - administration & dosage ; GABA-A Receptor Agonists - adverse effects ; GABA-A Receptor Agonists - therapeutic use ; Humans ; Hypnotics and Sedatives - administration & dosage ; Hypnotics and Sedatives - adverse effects ; Hypnotics and Sedatives - therapeutic use ; Hypotension - chemically induced ; Hypotension - physiopathology ; Hypotension - therapy ; Length of Stay ; Practice Guidelines as Topic ; Precision Medicine ; propofol ; Propofol - administration & dosage ; Propofol - adverse effects ; Propofol - therapeutic use ; Respiration, Artificial ; Severity of Illness Index</subject><ispartof>Pharmacotherapy, 2016-04, Vol.36 (4), p.433-442</ispartof><rights>2016 Pharmacotherapy Publications, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4576-1c1c68aef55791b44f64c01bd20814005987f2fbf6acd11ce8173678dc217dc73</citedby><cites>FETCH-LOGICAL-c4576-1c1c68aef55791b44f64c01bd20814005987f2fbf6acd11ce8173678dc217dc73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fphar.1726$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fphar.1726$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26893017$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brotherton, Amy L.</creatorcontrib><creatorcontrib>Hamilton, Eric P.</creatorcontrib><creatorcontrib>Kloss, H. Grace</creatorcontrib><creatorcontrib>Hammond, Drayton A.</creatorcontrib><title>Propofol for Treatment of Refractory Alcohol Withdrawal Syndrome: A Review of the Literature</title><title>Pharmacotherapy</title><addtitle>Pharmacotherapy</addtitle><description>The authors evaluated all available evidence on the use of propofol as an adjuvant for the treatment of resistant alcohol withdrawal syndrome (AWS) in comparison to other therapies. A comprehensive PubMed search (1966–December 2015) was conducted using the search terms propofol, alcohol withdrawal, and drug therapy. Articles were cross‐referenced for other citations. Clinical studies, case series, and case reports published in the English language assessing the use of propofol in adult patients for treatment of AWS were reviewed for inclusion. Propofol is a sedative‐hypnotic that exerts its actions through agonism of GABAA receptors at a different binding site than benzodiazepines and reduces glutamatergic activity through N‐methyl‐d‐aspartase (NMDA) receptor blockade. Dosages from 5 to 100 μg/kg/minute reduced AWS symptoms with frequent development of hypotension and requirement for mechanical ventilation. Patients on propofol often experienced longer durations of mechanical ventilation and length of stay, which may be attributed to more‐resistant cases of AWS. When propofol was compared with dexmedetomidine as adjuncts in AWS, both agents showed similar benzodiazepine‐ and haloperidol‐sparing effects. Dexmedetomidine was associated with more numerical rates of bradycardia, while propofol was associated with more numerical instances of hypotension. Dexmedetomidine was used more frequently in nonintubated patients. The available data assessing the utility of propofol for AWS exhibited significant heterogeneity. Propofol may be useful in a specific population of patients with AWS, limited to those who are not clinically responding to first‐line therapy with benzodiazepines. Specifically, propofol should be considered in patients who are refractory to or not candidates for other adjuvant therapies, patients already requiring mechanical ventilation, or those with seizure activity or refractory delirium tremens. In severe, refractory AWS, adjuvant therapy with propofol may be considered but requires further research to recommend its use either preferentially or as monotherapy.</description><subject>Adrenergic alpha-2 Receptor Agonists - administration & dosage</subject><subject>Adrenergic alpha-2 Receptor Agonists - adverse effects</subject><subject>Adrenergic alpha-2 Receptor Agonists - therapeutic use</subject><subject>Adult</subject><subject>Alcohol</subject><subject>alcohol withdrawal syndrome</subject><subject>Alcohol-Induced Disorders, Nervous System - drug therapy</subject><subject>Alcohol-Induced Disorders, Nervous System - physiopathology</subject><subject>Alcohol-Induced Disorders, Nervous System - therapy</subject><subject>benzodiazepine</subject><subject>Bradycardia - chemically induced</subject><subject>Bradycardia - physiopathology</subject><subject>Chemotherapy, Adjuvant - adverse effects</subject><subject>dexmedetomidine</subject><subject>Dexmedetomidine - administration & dosage</subject><subject>Dexmedetomidine - adverse effects</subject><subject>Dexmedetomidine - therapeutic use</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Resistance</subject><subject>Evidence-Based Medicine</subject><subject>GABA-A Receptor Agonists - administration & dosage</subject><subject>GABA-A Receptor Agonists - adverse effects</subject><subject>GABA-A Receptor Agonists - therapeutic use</subject><subject>Humans</subject><subject>Hypnotics and Sedatives - administration & dosage</subject><subject>Hypnotics and Sedatives - adverse effects</subject><subject>Hypnotics and Sedatives - therapeutic use</subject><subject>Hypotension - chemically induced</subject><subject>Hypotension - physiopathology</subject><subject>Hypotension - therapy</subject><subject>Length of Stay</subject><subject>Practice Guidelines as Topic</subject><subject>Precision Medicine</subject><subject>propofol</subject><subject>Propofol - administration & dosage</subject><subject>Propofol - adverse effects</subject><subject>Propofol - therapeutic use</subject><subject>Respiration, Artificial</subject><subject>Severity of Illness Index</subject><issn>0277-0008</issn><issn>1875-9114</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10MFv0zAUBnALgVgZO_APoEhc2CGbn5P4OdyqamsRFUxj0y5Ilus8qxlJXRxnpf89iVp2QOL0Lr_v09PH2DvgF8C5uNyuTbgAFPIFm4DCIi0B8pdswgViyjlXJ-xN1z0OFGQuXrMTIVWZccAJ-3ET_NY73yTOh-QukIktbWLiXXJLLhgbfdgn08b69WAe6riugtmZJvm-31TBt_QpmQ7yqabdmIlrSpZ1pGBiH-gte-VM09HZ8Z6y--uru9kiXX6bf55Nl6nNC5QpWLBSGXJFgSWs8tzJ3HJYVYIryDkvSoVOuJWTxlYAlhRgJlFVVgBWFrNT9vHQuw3-V09d1G3dWWoasyHfdxpQZVlWAo70wz_00fdhM3w3KsGRSy4HdX5QNviuC-T0NtStCXsNXI-T63FyPU4-2PfHxn7VUvUs_248gMsD2NUN7f_fpG8W09tjZXpI1F2k388JE35qiRkW-uHrXBdfitkc-UKr7A9GyJkN</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Brotherton, Amy L.</creator><creator>Hamilton, Eric P.</creator><creator>Kloss, H. 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Grace</creatorcontrib><creatorcontrib>Hammond, Drayton A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brotherton, Amy L.</au><au>Hamilton, Eric P.</au><au>Kloss, H. Grace</au><au>Hammond, Drayton A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Propofol for Treatment of Refractory Alcohol Withdrawal Syndrome: A Review of the Literature</atitle><jtitle>Pharmacotherapy</jtitle><addtitle>Pharmacotherapy</addtitle><date>2016-04</date><risdate>2016</risdate><volume>36</volume><issue>4</issue><spage>433</spage><epage>442</epage><pages>433-442</pages><issn>0277-0008</issn><eissn>1875-9114</eissn><abstract>The authors evaluated all available evidence on the use of propofol as an adjuvant for the treatment of resistant alcohol withdrawal syndrome (AWS) in comparison to other therapies. A comprehensive PubMed search (1966–December 2015) was conducted using the search terms propofol, alcohol withdrawal, and drug therapy. Articles were cross‐referenced for other citations. Clinical studies, case series, and case reports published in the English language assessing the use of propofol in adult patients for treatment of AWS were reviewed for inclusion. Propofol is a sedative‐hypnotic that exerts its actions through agonism of GABAA receptors at a different binding site than benzodiazepines and reduces glutamatergic activity through N‐methyl‐d‐aspartase (NMDA) receptor blockade. Dosages from 5 to 100 μg/kg/minute reduced AWS symptoms with frequent development of hypotension and requirement for mechanical ventilation. Patients on propofol often experienced longer durations of mechanical ventilation and length of stay, which may be attributed to more‐resistant cases of AWS. When propofol was compared with dexmedetomidine as adjuncts in AWS, both agents showed similar benzodiazepine‐ and haloperidol‐sparing effects. Dexmedetomidine was associated with more numerical rates of bradycardia, while propofol was associated with more numerical instances of hypotension. Dexmedetomidine was used more frequently in nonintubated patients. The available data assessing the utility of propofol for AWS exhibited significant heterogeneity. Propofol may be useful in a specific population of patients with AWS, limited to those who are not clinically responding to first‐line therapy with benzodiazepines. Specifically, propofol should be considered in patients who are refractory to or not candidates for other adjuvant therapies, patients already requiring mechanical ventilation, or those with seizure activity or refractory delirium tremens. In severe, refractory AWS, adjuvant therapy with propofol may be considered but requires further research to recommend its use either preferentially or as monotherapy.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26893017</pmid><doi>10.1002/phar.1726</doi><tpages>10</tpages></addata></record> |
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subjects | Adrenergic alpha-2 Receptor Agonists - administration & dosage Adrenergic alpha-2 Receptor Agonists - adverse effects Adrenergic alpha-2 Receptor Agonists - therapeutic use Adult Alcohol alcohol withdrawal syndrome Alcohol-Induced Disorders, Nervous System - drug therapy Alcohol-Induced Disorders, Nervous System - physiopathology Alcohol-Induced Disorders, Nervous System - therapy benzodiazepine Bradycardia - chemically induced Bradycardia - physiopathology Chemotherapy, Adjuvant - adverse effects dexmedetomidine Dexmedetomidine - administration & dosage Dexmedetomidine - adverse effects Dexmedetomidine - therapeutic use Dose-Response Relationship, Drug Drug Resistance Evidence-Based Medicine GABA-A Receptor Agonists - administration & dosage GABA-A Receptor Agonists - adverse effects GABA-A Receptor Agonists - therapeutic use Humans Hypnotics and Sedatives - administration & dosage Hypnotics and Sedatives - adverse effects Hypnotics and Sedatives - therapeutic use Hypotension - chemically induced Hypotension - physiopathology Hypotension - therapy Length of Stay Practice Guidelines as Topic Precision Medicine propofol Propofol - administration & dosage Propofol - adverse effects Propofol - therapeutic use Respiration, Artificial Severity of Illness Index |
title | Propofol for Treatment of Refractory Alcohol Withdrawal Syndrome: A Review of the Literature |
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