ArticleFrontiers in pharmacology2025
Incident gabapentin prescribing associated with opioid and benzodiazepine/Z-drug prescribing - a population-based longitudinal study in primary care.
Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Benzodiazepines in Epilepsy: A US Perspective on Clinical Use, Pharmacology, Abuse Methods, and Public Health Considerations.Neurology and therapy · 2026Review
- Real-world effectiveness of medication-assisted treatment and psychotherapy for opioid use disorder: a national multi-health care organization analysis.Frontiers in psychiatry · 2026Article
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Authors and funding
4 authors.
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Abstract
Aim: To investigate the association between long-term prescribing of opioids, benzodiazepines and Z-drugs, and the incidence of gabapentin prescribing. Methods: From January 2009 to December 2012, 219,800 patients contacted primary healthcare centres in the Reykjavik metropolitan area. Of these, 94,840 patients aged 10-69 years, met the inclusion criteria. Data on relevant ICD-10 conditions related to multimorbidity were retrieved from a comprehensive medical records database for the primary healthcare centres in the area run by the Primary Healthcare of the Capital Area. Information on redeemed prescriptions for the relevant drugs was obtained from the Medicines Registry of the Directory of Health. The subjects were divided into four groups based on long-term use of opioids, benzodiazepines (BZDs) and Z-drugs (Defined Daily Doses, DDDs). The incidence rate ratio (IRR) of gabapentin was assessed using Cox regression. The effect of certain chronic conditions and long-term use of selective serotonin reuptake inhibitors (SSRIs) was also explored. Finally, the amount and duration of future gabapentin use were examined. Results: Long-term use of opioids, BZDs or Z-drugs was associated with an increased risk of future gabapentin use. Individuals with the highest use of opioids and benzodiazepines or Z-drugs, i.e., ≥30 DDDs BZDs or Z-drugs were most likely to initiate gabapentin therapy (IRR 7.18: 95% CI 6.50-7.93). These individuals also had the longest average duration of future gabapentin use. Conclusion: The rise in gabapentin prescriptions must be carefully monitored as prior history of opioids, benzodiazepines and Z-drugs may pose a risk of problematic gabapentin use.
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