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Evaluation of phenobarbital dosing strategies for hospitalized patients with alcohol withdrawal syndrome.
Stallworth, Sara; Stilley, Kelsey; Viriyakitja, Wassamon; Powers, Shelby; Parish, Alice; Erkanli, Alaattin; Komisar, Jonathan.
Afiliação
  • Stallworth S; University of Kentucky College of Pharmacy, 789 S Limestone, Lexington, KY 40508, United States of America. Electronic address: sara.stallworth@uky.edu.
  • Stilley K; Duke University Hospital, 2301 Erwin Road, Durham, NC 27710, United States of America.
  • Viriyakitja W; Duke University Hospital, 2301 Erwin Road, Durham, NC 27710, United States of America.
  • Powers S; Duke University Hospital, 2301 Erwin Road, Durham, NC 27710, United States of America; Department of Psychiatry & Behavioral Sciences, Duke University School of Medicine, 40 Duke Medicine Circle 124 Davison Building, Durham, NC 27710, United States of America.
  • Parish A; Department of Biostatistics & Bioinformatics, Duke University School of Medicine, 40 Duke Medicine Circle 124 Davison Building, Durham, NC 27710, United States of America.
  • Erkanli A; Department of Biostatistics & Bioinformatics, Duke University School of Medicine, 40 Duke Medicine Circle 124 Davison Building, Durham, NC 27710, United States of America.
  • Komisar J; Department of Psychiatry & Behavioral Sciences, Duke University School of Medicine, 40 Duke Medicine Circle 124 Davison Building, Durham, NC 27710, United States of America.
Gen Hosp Psychiatry ; 85: 155-162, 2023.
Article em En | MEDLINE | ID: mdl-37926051
ABSTRACT

OBJECTIVE:

Alcohol remains the fourth­leading preventable cause of death in the U.S. The objective of this study was to compare the incidence of phenobarbital (PHB)-resistant withdrawal and determine risk factors for PHB-resistant alcohol withdrawal syndrome (AWS).

METHODS:

This retrospective cohort study included adults admitted to an academic center with AWS who received PHB as part of an institution-specific treatment protocol. The primary outcome was incidence of AWS resistant to initial protocolized PHB load across two cohorts (standard-dose, 10 mg/kg vs. low-dose, 6 mg/kg).

RESULTS:

Among 176 included patients, there was no difference in the incidence of PHB-resistant AWS based on initial PHB load [low-dose load, 21 (18.3%) vs. standard-dose load, 12 (19.7%), p = 0.82]. There were also no differences in observed PHB-related ADEs between the groups. Total benzodiazepine dose received (mg) in the 24 h prior to initial PHB load was the only risk factor significantly associated with AWS resistant to initial protocolized PHB load [adjusted OR 1.79 (95% CI 1.24, 2.60)]. PHB-resistant withdrawal occurred in 33 (18.8%) patients with a median cumulative PHB dose of approximately 20 mg/kg during hospitalization. CONCLUSION(S) There were no differences in the incidence of PHB-resistant AWS or PHB-related ADEs based on initial PHB loading dose.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Abstinência a Substâncias / Alcoolismo Limite: Adult / Humans Idioma: En Revista: Gen Hosp Psychiatry Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Abstinência a Substâncias / Alcoolismo Limite: Adult / Humans Idioma: En Revista: Gen Hosp Psychiatry Ano de publicação: 2023 Tipo de documento: Article