Baillie Samantha, Saxena Sonia, Jayasooriya Nishani, Bottle Alex, Petersen Irene, Blackwell Jonathan, Pollok Richard
Institute for Infection and Immunity, City St George's University of London, London, UK.
School of Public Health, Imperial College London, London, UK.
Aliment Pharmacol Ther. 2025 Oct;62(7):732-742. doi: 10.1111/apt.70247. Epub 2025 Jul 2.
Individuals with inflammatory bowel disease (IBD) often experience pain, mood disturbances, and sleep disruption, which may lead to greater use of pain-relieving and sedative medications compared with the general population. These are associated with increased mortality, paradoxical worsening of pain, and inappropriate IBD treatment discontinuation. Chronic prescribing and co-prescribing increase the risk of respiratory depression, dependence, and overdose.
Using Clinical Practice Research Datalink, a large nationally representative dataset, we examined the annual prevalence of total, chronic (> 90 days opioids; > 28 days sedatives), and co-prescribed opioids, gabapentinoids and sedatives in adults with incident IBD from January 2010 to December 2019. Multivariable regression identified predictors of chronic or co-prescribing.
Among 17,388 individuals, over 20% were prescribed a pain or sedative medication each year. Annual prevalence for opioids and gabapentinoids increased (13.6%-14% and 2.5%-5.6%, respectively) while sedative prevalence remained stable (8.4%). Chronic prescribing increased for strong opioids (3.6%-4.6%), weak opioids (3.6%-3.7%) and sedatives (4.2%-4.4%). Between 4.2% and 6.9% of individuals per year were co-prescribed opioids, gabapentinoids, and/or sedatives. Female sex, smoking, older age at diagnosis, Crohn's disease, and a diagnosis of inflammatory arthropathy, irritable bowel syndrome, fibromyalgia, or anxiety/depression were significantly associated with chronic and/or co-prescriptions of opioids or sedatives.
A substantial proportion of individuals with IBD are prescribed pain and sedative medications, including long-term and co-prescriptions. Identifying high-risk patients is essential to ensure they are prioritised for limited resources, such as psychological therapies, as alternatives to harmful prescriptions.
炎症性肠病(IBD)患者常经历疼痛、情绪障碍和睡眠中断,与普通人群相比,这可能导致更多地使用止痛和镇静药物。这些与死亡率增加、疼痛反常恶化以及不适当的IBD治疗中断有关。长期开药和联合开药会增加呼吸抑制、药物依赖和药物过量的风险。
利用临床实践研究数据链(Clinical Practice Research Datalink)这一具有全国代表性的大型数据集,我们调查了2010年1月至2019年12月间新发IBD成年患者中,阿片类药物、加巴喷丁类药物和镇静剂的总体、慢性(阿片类药物>90天;镇静剂>28天)及联合使用的年患病率。多变量回归分析确定了长期或联合用药的预测因素。
在17388名患者中,每年超过20%的人开具了止痛或镇静药物。阿片类药物和加巴喷丁类药物的年患病率有所上升(分别从13.6%升至14%和从2.5%升至5.6%),而镇静剂的患病率保持稳定(8.4%)。强阿片类药物(从3.6%升至4.6%)、弱阿片类药物(从3.6%升至3.7%)和镇静剂(从4.2%升至4.4%)的长期开药率增加。每年有4.2%至6.9%的患者联合使用阿片类药物、加巴喷丁类药物和/或镇静剂。女性、吸烟、诊断时年龄较大、克罗恩病以及诊断为炎性关节病、肠易激综合征、纤维肌痛或焦虑/抑郁与阿片类药物或镇静剂的长期和/或联合用药显著相关。
相当一部分IBD患者开具了止痛和镇静药物,包括长期用药和联合用药。识别高危患者对于确保他们能够优先获得有限的资源(如心理治疗)至关重要,这些资源可作为有害处方的替代方案。