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Impact of an alcohol withdrawal screening and treatment protocol for hospitalized patients.
Schonewald, Brian; Hunter, Krystal; Ely, Alice V; Heil, Jessica; Ganetsky, Valerie; Milburn, Christopher; Rafeq, Rachel; Salzman, Matthew.
Afiliación
  • Schonewald B; Cooper Medical School of Rowan University, United States of America.
  • Hunter K; Cooper Medical School of Rowan University, United States of America; Cooper Research Institute, United States of America.
  • Ely AV; Cooper Medical School of Rowan University, United States of America; Cooper University Healthcare Center for Healing, United States of America.
  • Heil J; Cooper University Healthcare Center for Healing, United States of America.
  • Ganetsky V; Cooper University Healthcare Center for Healing, United States of America.
  • Milburn C; Cooper Medical School of Rowan University, United States of America; Cooper University Healthcare Center for Healing, United States of America.
  • Rafeq R; Cooper University Health Care, Department of Emergency Medicine, United States of America.
  • Salzman M; Cooper Medical School of Rowan University, United States of America; Cooper University Healthcare Center for Healing, United States of America. Electronic address: salzman-matthew@cooperhealth.edu.
J Subst Use Addict Treat ; 164: 209443, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38871256
ABSTRACT

INTRODUCTION:

Alcohol Withdrawal Syndrome (AWS) is a potentially life-threatening complication of alcohol use disorder (AUD) that can be challenging to recognize in hospitalized patients. Our institution implemented universal AUD screening for all patients admitted to a non-critical care venue using the Prediction of Alcohol Withdrawal Severity Scale (PAWSS). At risk patients were then further assessed, utilizing the Glasgow Modified Alcohol Withdrawal Scale (GMAWS), and medicated according to a predetermined protocol. This study sought to determine whether this protocol decreased hospital length of stay, lowered the total benzodiazepine dose administered, and decreased adverse events attributable to AWS.

METHODS:

This retrospective cohort study was conducted over a 6-year period from 2014 to 2020. The study included patients with an ICD-10 code diagnosis of AWS and subsequently divided them into two groups pre- and post-protocol introduction. Outcome measures were compared pre- versus post-protocol introduction.

RESULTS:

There were 181 patient encounters pre- and 265 patient encounters post-protocol. There was no statistically significant difference in median length of stay between the two groups (2.956 days pre and 3.250 days post-protocol, p = 0.058). Post-protocol, there was a statistically significant reduction in median total benzodiazepine dose (13.5 mg and 9 mg lorazepam equivalents pre- and post-protocol, p < 0.001) and in occurrence of delirium tremens (7.7 % pre and 2.3 % post-protocol, p = 0.006).

CONCLUSION:

Protocol implementation did not reduce length of stay in patients with AUD but was associated with a significant reduction in total benzodiazepine dose and, when adjusted, a non-statistically significant decrease in progression to delirium tremens in hospitalized patients, after applying Bonferroni adjustment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Abstinencia a Sustancias / Benzodiazepinas / Alcoholismo / Hospitalización / Tiempo de Internación Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Subst Use Addict Treat Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Abstinencia a Sustancias / Benzodiazepinas / Alcoholismo / Hospitalización / Tiempo de Internación Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Subst Use Addict Treat Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos