Guan Qi, Men Siyu, Lunsky Yona, Juurlink David N, Bronskill Susan E, Wunsch Hannah, Gomes Tara
Institute of Health Policy, Management and Evaluation, University of Toronto, Canada; ICES, Toronto, Canada; and Li Ka Shing Knowledge Institute, St Michael's Hospital, Toronto, Canada.
ICES, Toronto, Canada.
BJPsych Open. 2022 Nov 28;8(6):e208. doi: 10.1192/bjo.2022.612.
Individuals with intellectual and developmental disability (IDD) can have a high prevalence of pain, which can be managed with prescription opioids. However, the prevalence of substance use disorder is also high in this population, raising concern about opioid-related adverse events.
To assess the risk of opioid-related adverse events following opioid initiation among adults with versus without IDD.
We conducted a population-based, propensity score matched cohort study on all adults starting prescription opioid therapy in Ontario, Canada, between January 2013 and December 2018. The outcomes of interest were opioid toxicity, new opioid use disorder (OUD) diagnosis and dose escalation (≥90 mg morphine or equivalent) in the year after opioid initiation. We used Cox proportional hazards models to assess the association between IDD diagnosis and each outcome.
The hazards of opioid toxicity and OUD were significantly higher in those with IDD compared with those without IDD in unmatched analyses (opioid toxicity hazard ratio 3.19, 95% CI 2.81-5.18; OUD hazard ratio 2.36, 95% CI 2.10-2.65), whereas the hazard of dose escalation was significantly lower (hazard ratio 0.76, 95% CI 0.66-0.88). Findings were no longer significant in propensity score matched models for opioid toxicity and dose escalation, whereas the hazard of OUD diagnosis was attenuated substantially in those with IDD (hazard ratio 0.79, 95% CI 0.68-0.91).
IDD diagnosis is not a driver of opioid-related harm. The increased risk we observed is likely driven by various risk factors often present in this population.
智力和发育障碍(IDD)患者的疼痛发生率较高,可使用处方阿片类药物进行治疗。然而,该人群中物质使用障碍的发生率也很高,这引发了对阿片类药物相关不良事件的担忧。
评估有和没有IDD的成年人开始使用阿片类药物后发生阿片类药物相关不良事件的风险。
我们对2013年1月至2018年12月在加拿大安大略省开始处方阿片类药物治疗的所有成年人进行了一项基于人群的倾向评分匹配队列研究。感兴趣的结局是阿片类药物毒性、新的阿片类药物使用障碍(OUD)诊断以及开始使用阿片类药物后一年内的剂量增加(≥90毫克吗啡或等效剂量)。我们使用Cox比例风险模型来评估IDD诊断与每个结局之间的关联。
在未匹配分析中,IDD患者发生阿片类药物毒性和OUD的风险显著高于无IDD患者(阿片类药物毒性风险比3.19,95%置信区间2.81 - 5.18;OUD风险比2.36,95%置信区间2.10 - 2.65),而剂量增加的风险显著较低(风险比0.76,95%置信区间0.66 - 0.88)。在倾向评分匹配模型中,阿片类药物毒性和剂量增加的结果不再显著,而IDD患者中OUD诊断的风险大幅降低(风险比0.79,95%置信区间0.68 - 0.91)。
IDD诊断并非阿片类药物相关伤害的驱动因素。我们观察到的风险增加可能是由该人群中经常存在的各种风险因素驱动的。