Hostname: page-component-89b8bd64d-b5k59 Total loading time: 0 Render date: 2026-05-12T07:45:52.750Z Has data issue: false hasContentIssue false

Investigating the association of opioid prescription with the incidence of psychiatric disorders: nationwide cohort study in South Korea

Published online by Cambridge University Press:  27 May 2024

Tak Kyu Oh
Affiliation:
Department of Anesthesiology and Pain Medicine, College of Medicine, Seoul National University, South Korea; and Department of Anesthesiology and Pain Medicine, Seoul National University Bundang Hospital, South Korea
Hye Yoon Park
Affiliation:
Department of Psychiatry, Seoul National University Hospital, South Korea; and Department of Psychiatry, College of Medicine, Seoul National University, South Korea
In-Ae Song*
Affiliation:
Department of Anesthesiology and Pain Medicine, College of Medicine, Seoul National University, South Korea; and Department of Anesthesiology and Pain Medicine, Seoul National University Bundang Hospital, South Korea
*
Correspondence: In-Ae Song. Email: songoficu@outlook.kr
Rights & Permissions [Opens in a new window]

Abstract

Background

The relationship between opioid use and the incidence of psychiatric disorders remains unidentified.

Aims

This study examined the association between the incidence of psychiatric disorders and opioid use.

Method

Data for this population-based cohort study were obtained from the National Health Insurance Service of South Korea. The study included all adult patients who received opioids in 2016. The control group comprised individuals who did not receive opioids in 2016, and were selected using a 1:1 stratified random sampling procedure. Patients with a history of psychiatric disorders diagnosed in 2016 were excluded. The primary end-point was the diagnosis of psychiatric disorders, evaluated from 1 January 2017 to 31 December 2021. Psychiatric disorders included schizophrenia, mood disorders, anxiety and others.

Results

The analysis included 3 505 982 participants. Opioids were prescribed to 1 455 829 (41.5%) of these participants in 2016. Specifically, 1 187 453 (33.9%) individuals received opioids for 1–89 days, whereas 268 376 (7.7%) received opioids for ≥90 days. In the multivariable Cox regression model, those who received opioids had a 13% higher incidence of psychiatric disorder than those who did not (hazard ratio 1.13; 95% CI 1.13–1.14). Furthermore, both those prescribed opioids for 1–89 days and for ≥90 days had 13% (hazard ratio 1.13, 95% CI 1.12–1.14) and 17% (hazard ratio 1.17, 95% CI 1.16–1.18) higher incidences of psychiatric disorders, respectively, compared with those who did not receive opioids.

Conclusions

This study revealed that increased psychiatric disorders were associated with opioid medication use. The association was significant among both short- and long-term opioid use.

Information

Type
Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press on behalf of Royal College of Psychiatrists
Figure 0

Fig. 1 Flow chart depicting the study participant selection process.

Figure 1

Table 1 Clinicopathological characteristics of the study population (N = 3 505 982)

Figure 2

Table 2 Clinicopathological features of those who did and did not use opioids

Figure 3

Table 3 Diagnosis of psychiatric illness during 2017–2021 for those who did and did not use opioids

Figure 4

Table 4 Multivariable Cox regression model for the diagnosis of psychiatric diseases

Figure 5

Table 5 Multivariable Cox regression model for psychiatric diseases in detail

Supplementary material: File

Oh et al. supplementary material 1

Oh et al. supplementary material
Download Oh et al. supplementary material 1(File)
File 16.3 KB
Supplementary material: File

Oh et al. supplementary material 2

Oh et al. supplementary material
Download Oh et al. supplementary material 2(File)
File 17.9 KB
Supplementary material: File

Oh et al. supplementary material 3

Oh et al. supplementary material
Download Oh et al. supplementary material 3(File)
File 15 KB
Submit a response

eLetters

No eLetters have been published for this article.