A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

Pharmacological Treatments in Alcohol Use Disorder and Risk of Alcohol‐Related Hospitalizations: A Register Study




TekijätBach, Patrick; Franck, Johan; Hällgren, Jonas; Widing, Härje; Gissler, Mika; Westman, Jeanette

KustantajaWiley

KustannuspaikkaHOBOKEN

Julkaisuvuosi2025

Lehti: Acta Psychiatrica Scandinavica

Tietokannassa oleva lehden nimiActa Psychiatrica Scandinavica

Lehden akronyymiACTA PSYCHIAT SCAND

Vuosikerta152

Numero2

Aloitussivu94

Lopetussivu103

Sivujen määrä10

ISSN0001-690X

eISSN1600-0447

DOIhttps://doi.org/10.1111/acps.13802

Julkaisun avoimuus kirjaamishetkelläAvoimesti saatavilla

Julkaisukanavan avoimuus Osittain avoin julkaisukanava

Verkko-osoitehttps://doi.org/10.1111/acps.13802

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/491651961


Tiivistelmä

Objectives: Despite the high prevalence of alcohol use disorder (AUD), only a minority of patients receive recommended pharmacological treatments, possibly owing to uncertainty about the real-world effectiveness of these medications. Here, we analyzed nationwide, register-based data to investigate the association between approved AUD medications (naltrexone, acamprosate, disulfiram, and nalmefene) and the risk of alcohol-related hospitalizations among individuals with AUD.

Methods: People aged 18-64 with a registered first-time diagnosis of AUD between 2009 and 2019 (N = 93,727) were identified from the Swedish National Patient Register. Cox regression models were used to analyze the association between AUD medication exposure and the risk of alcohol-related hospitalizations.

Results: Exposure to naltrexone (hazard ratio [HR] = 0.80; 95% confidence interval [CI] = 0.73-0.87) or disulfiram (HR = 0.83, 95% CI = 0.79-0.88) as monotherapy, or a combination of naltrexone/disulfiram (HR = 0.68, 95% CI = 0.49-0.96), or disulfiram/acamprosate (HR = 0.57 95% CI = 0.44-0.74) was significantly associated with a lower risk of alcohol-related hospitalizations compared to periods without exposure to any of these medications. In contrast, no significant associations were observed for acamprosate, nalmefene, or the combination of acamprosate/naltrexone. Sensitivity analyses in individuals with severe AUD and stratified subgroup analyses by different socioeconomic groups confirmed the robustness of the results.

Conclusion: Results indicate a significant association between disulfiram and naltrexone monotherapy, as well as the combination of disulfiram with naltrexone or acamprosate, with a lower risk of alcohol-related hospitalizations among individuals with AUD. Low prescription rates suggest that AUD medications are currently underutilized. Increasing the availability of these medications for individuals with AUD could help reduce alcohol-related hospitalizations.


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Julkaisussa olevat rahoitustiedot
This work was supported by The Swedish Research Council for Health, Working Life and Welfare (FORTE) (Dnr 2020–00467), Karolinska Institutet (KID, Dnr 2020–02653), and Region Stockholm (Dnr. FoUI-977024) to Johan Franck and Jeanette Westman.


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