Key result
High-dose benzodiazepines show no association with QTc prolongation across polysubstance user groups.
Why the study?
The relationship between benzodiazepine use and QTc prolongation is currently unclear, especially considering polysubstance use and risk factors.
Does high-dose benzodiazepine use increase the risk of QTc interval prolongation in adults with BDZ dependence?
Cross-Sectional (n=216)
No
Does high-dose benzodiazepine use increase the risk of QTc interval prolongation in adults with BDZ dependence?
High-dose and long-term benzodiazepine use does not appear to be associated with an increased risk of QTc prolongation in patients with benzodiazepine dependence.
Answers are grounded in this paper and cite their sources.
No QTc signal with high-dose benzodiazepines in dependence; hypothesis-generating and should not yet change practice.
Benzodiazepine (BDZ) addiction is a widespread and multifaceted phenomenon. For many patients, especially females, the concomitant use of other drugs also increases their risk of QTc prolongation, possibly leading to complications such as seizures and even sudden death. However, the relationship between BDZ use and QTc prolongation is currently unclear. The present study aims to examine patterns of polysubstance use among a sample of Italian adults with BDZ dependence in relation with their QTc prolongation risk. We used Latent Class Analysis (LCA) on data collected from 251 inpatients of the Addiction Medicine Unit in Verona to group patients into three classes according to their substance use and their QTc prolongation risk. Results showed no significant relationship between QTc prolongation and BDZ use in any of the classes considered. We conclude that BDZs, even if used long-term and at high dosages, can be considered safe in terms of cardiovascular complications for patients.
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Zamboni et al. (2024) conducted a cross-sectional in Benzodiazepine addiction (n=216). High-dose benzodiazepine use was evaluated on QTc interval prolongation. High-dose benzodiazepine use was not significantly associated with QTc interval prolongation in any of the identified latent classes of polysubstance users.
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