News Release

Benzodiazepine and gabapentinoids are contributing to Scottish drug-related deaths

In the last decade, use of “designer” drugs in Scotland may have driven polydrug use and increased drug-related deaths

Peer-Reviewed Publication

PLOS

Systematic review: The relationship between gabapentinoids, etizolam, and drug related deaths in Scotland

image: 

Percentage of Scottish cases where specific benzodiazepines were mentioned in the cause of death between 2013–2020. Source: Adapted from Corkey et al., (2022) original table. Licensed under CC BY 4.0.

view more 

Credit: Ciesluk et al., 2024, PLOS ONE, CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/)

Etizolam and gabapentinoids, central nervous system drugs with sedative effects and high potential for abuse, may be both driving a culture of polydrug use and contributing to an increasing pattern of drug-related deaths in Scotland, according to a new study published October 9, 2024, in the open-access journal PLOS ONE by a team of researchers at the University of the West of Scotland, U.K., and colleagues.

In recent years, Scotland has been experiencing a disproportionally high number of drug-related deaths compared to other European countries, with the Scottish Parliament unanimously voting the issue to be a public health emergency in 2021. One distinct feature of the recent rise in drug-related deaths is the increase in polydrug use and in “designer” benzodiazepines and gabapentinoids, substances designed to mimic the effects of traditional medications.

In the new study, researchers analyzed 18 previously-published studies that included data on the role of etizolam (one designer benzodiazepine) and gabapentinoids among drug-related deaths in Scotland as well as data on the drugs’ use and abuse. Although both drugs are unlikely to cause death on their own, they can cause adverse reactions when being used alongside each other or other opioids.

The study found that both drugs are increasingly cited as contributing factors to drug-related deaths. Gabapentinoid-related deaths in Scotland, for instance, increased from 2 to 367 deaths between 2008 to 2018, accounting for almost 1 in 3 (31 percent) of all drug-related deaths by 2018. Concurrent use of opioids and other substances is the most common determinant of both etizolam- and gabapentinoid- related adverse effects and fatality in Scotland.

Data also revealed a rise in gapapentinoid prescriptions, especially their off-label use, which has been associated with misuse and illicit-market availability. This prescription trend is likely attributed to efforts to limit prescribing of opioids and benzodiazapines. Data on the use of etizolam, on the other hand, suggested an illicitly-manufactured etizolam supply in Scotland, which can contribute to inaccurate dosing.

Finally, data on the characteristics of individuals using these drugs was limited but suggested a higher rate of gabapentinoid prescriptions among older women. Etizolam-related deaths were more likely to be accidental among men and intentional among women. These conclusions both support a possible vulnerability among older women.

The authors call for further research into the prevalence and risk of etizolam and gabapentinoids use in Scotland, but note that their study suggests that both substances may drive polydrug use and contribute to Scottish drug-related deaths.

The authors add: “It is essential that we understand the role that polydrug use, especially prescription drugs and designer benzodiazepines, play in drug related deaths to be able to effectively reduce risk from harm in people who use drugs.”

#####

In your coverage please use this URL to provide access to the freely available article in PLOS ONE: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0310655

Citation: Ciesluk B, Inglis DG, Parke A, Troup LJ (2024) Systematic review: The relationship between gabapentinoids, etizolam, and drug related deaths in Scotland. PLoS ONE 19(10): e0310655. https://doi.org/10.1371/journal.pone.0310655

Author Countries: U.K.

Funding: BC & LJT received PhD Scholarship funding from The Carnegie Trust for the Universities of Scotland. Charity Number: SC015600 https://carnegie-trust.org/carnegie-phd-scholarships/. The funders played NO part in the design data collection and analysis of this work and were NOT involved in the decision to publish or preparation of this manuscript.


Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.