Nielsen Suzanne, Picco Louisa, Rowland Bosco, Andrew Nadine E, Collyer Taya A, Lalic Samanta, Buchbinder Rachelle, Pearce Christopher, Bell J Simon, Lubman Dan I, Xia Ting
Monash University, Melbourne, VIC.
Turning Point Alcohol and Drug Centre, Eastern Health, Melbourne, VIC.
Med J Aust. 2025 Aug 4;223(3):134-140. doi: 10.5694/mja2.52713. Epub 2025 Jun 26.
To investigate the combined effect of two policies for reducing prescription opioid supply in Australia on hospital use by people prescribed opioids in primary care.
Retrospective data linkage study; controlled interrupted time series analysis of linked primary care electronic medication records and hospital admissions data.
Three Victorian health care networks (Monash Health, Eastern Health, Peninsula Health); pre-intervention period: 1 April 2018 - 31 March 2020; intervention period: 1 April 2020 - 31 March 2022.
People prescribed opioid medications at least twice during the preceding six months (opioid group) and propensity score-matched patients, based on age, gender, comorbidity, and residential postcode-based socio-economic status (control group); matching was undertaken for each month of the study period.
Mandatory prescription drug monitoring (from 1 April 2020); tighter restriction criteria for the subsidisation of opioid medications by the Pharmaceutical Benefits Scheme (PBS) (from 1 June 2020).
Differences between the opioid and control groups in immediate changes after start of the intervention in rates of emergency department (ED) presentation and hospital admission related to opioid use, non-opioid substance use, self-harm, or mental health problems; differences between the two groups in the change in trend for these rates between the pre-intervention and intervention periods.
Propensity matching was undertaken for 179 091 people in the opioid group and a total of 389 061 people in the control group. The opioid-related ED presentation rate for the opioid group had been increasing prior to the intervention, but declined after its introduction at a rate not significantly different from that of the control group. The immediate change in non-opioid substance-related ED presentation rate was greater for the opioid group than the control group (β, 11.1 [95% confidence interval, 1.7-20.5] presentations per 100 000 patients); by 31 March 2022, the rate had declined to below the pre-intervention level. Differences between groups in changes to self-harm- and mental health-related presentations, and in all hospital admission rates, were not statistically significant.
Following implementation of two prescription opioid supply-restricting polices in 2020, the opioid-related ED presentation rate declined among people prescribed opioids; the non-opioid substance-related presentation rate initially increased, but was lower than the pre-intervention level by the end of the study period. Our findings suggest that some opioid-restricting policies can reduce opioid-related harm without increasing long term non-opioid substance- or mental health-related harm.
European post-authorisation study register (EUROPAS), EUPAS104005 (prospective).
研究澳大利亚两项减少处方阿片类药物供应政策对在初级保健中开具阿片类药物处方的人群住院使用情况的综合影响。
回顾性数据关联研究;对关联的初级保健电子用药记录和住院数据进行对照中断时间序列分析。
三个维多利亚州医疗保健网络(莫纳什医疗中心、东部医疗中心、半岛医疗中心);干预前期:2018年4月1日至2020年3月31日;干预期:2020年4月1日至2022年3月31日。
在过去六个月内至少开具过两次阿片类药物处方的人群(阿片类药物组)以及基于年龄、性别、合并症和基于居住邮政编码的社会经济状况进行倾向得分匹配的患者(对照组);在研究期间的每个月进行匹配。
强制处方药物监测(自2020年4月1日起);药品福利计划(PBS)对阿片类药物补贴的更严格限制标准(自2020年6月1日起)。
干预开始后,阿片类药物组和对照组在与阿片类药物使用、非阿片类物质使用、自我伤害或心理健康问题相关的急诊科就诊率和住院率的即时变化差异;干预前期和干预期之间两组在这些率的趋势变化上的差异。
对阿片类药物组的179,091人和对照组的总共389,061人进行了倾向得分匹配。阿片类药物组与阿片类药物相关的急诊科就诊率在干预前一直在上升,但引入干预后下降,下降速度与对照组无显著差异。阿片类药物组与非阿片类物质相关的急诊科就诊率的即时变化大于对照组(β,每100,000名患者11.1次就诊[95%置信区间,1.7 - 20.5]);到2022年3月31日,该率已降至干预前水平以下。两组在与自我伤害和心理健康相关的就诊变化以及所有住院率方面的差异无统计学意义。
2020年实施两项处方阿片类药物供应限制政策后,开具阿片类药物处方的人群中与阿片类药物相关的急诊科就诊率下降;与非阿片类物质相关的就诊率最初上升,但在研究期结束时低于干预前水平。我们的研究结果表明,一些阿片类药物限制政策可以减少与阿片类药物相关的危害,而不会增加长期与非阿片类物质或心理健康相关的危害。
欧洲上市后研究注册库(EUROPAS),EUPAS104005(前瞻性)