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焦虑和抑郁导致炎症性肠病中抗肿瘤坏死因子的停药。

Anxiety and Depression Leads to Anti-Tumor Necrosis Factor Discontinuation in Inflammatory Bowel Disease.

机构信息

Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada; University of Manitoba IBD Clinical and Research Centre, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

Clin Gastroenterol Hepatol. 2021 Jun;19(6):1200-1208.e1. doi: 10.1016/j.cgh.2020.07.013. Epub 2020 Jul 12.

DOI:10.1016/j.cgh.2020.07.013
PMID:32668341
Abstract

BACKGROUND & AIMS: Anxiety and mood disorders (AMDs) are common among persons with inflammatory bowel diseases (IBD) and are associated with increased health care use and lower quality of life. We assessed the effects of AMDs on persistence on anti-tumor necrosis factor (anti-TNF) therapy in patients with IBD, and risk of IBD-related adverse outcomes after therapy initiation.

METHODS

We identified all persons with IBD in Manitoba, Canada who were dispensed an anti-TNF agent from 2001 through 2016 and then identified those with a validated administrative definition of AMD in the 2 years before initiation of therapy. Survival analysis was used to assess the association between active AMDs and anti-TNF discontinuation and the first occurrence of an IBD-related adverse outcome (defined as IBD-related hospitalization or surgery, new or recurrent corticosteroid use, switching to an alternative anti-TNF, or death). We used Cox proportional hazards multivariable regression models to adjust for demographic and clinical factors associated with outcomes.

RESULTS

We identified 1135 persons with IBD who began anti-TNF therapy; 178 of these patients (15.7%) met the diagnostic criteria for an AMD. AMDs significantly increased risk of discontinuation of anti-TNF therapy (adjusted hazard ratio, 1.28; 95% CI, 1.03-1.59) and discontinuation in the 1 year following anti-TNF initiation (hazard ratio, 1.50; 95% CI, 1.15-1.94). There was no association between AMDs and subsequent risk of IBD-related adverse events.

CONCLUSIONS

Patients with IBD and an AMD within 2 years before starting anti-TNF therapy are at increased risk of discontinuing therapy, compared to patients with IBD without AMD. Studies are needed to determine if treatment of AMDs increases compliance with treatment.

摘要

背景与目的

焦虑和情绪障碍(AMDs)在炎症性肠病(IBD)患者中很常见,与增加医疗保健的使用和降低生活质量有关。我们评估了 AMD 对 IBD 患者抗肿瘤坏死因子(anti-TNF)治疗的持续性以及治疗开始后 IBD 相关不良结局的风险的影响。

方法

我们确定了 2001 年至 2016 年期间在加拿大马尼托巴省接受抗 TNF 药物治疗的所有 IBD 患者,然后在治疗开始前的 2 年内确定了那些符合 AMD 验证性行政定义的患者。生存分析用于评估活跃 AMD 与抗 TNF 停药和 IBD 相关不良结局(定义为 IBD 相关住院或手术、新的或复发性皮质类固醇使用、改用替代抗 TNF 或死亡)首次发生之间的关联。我们使用 Cox 比例风险多变量回归模型调整与结局相关的人口统计学和临床因素。

结果

我们确定了 1135 名开始接受抗 TNF 治疗的 IBD 患者;其中 178 名患者(15.7%)符合 AMD 的诊断标准。AMD 显著增加了抗 TNF 治疗停药的风险(调整后的危险比,1.28;95%CI,1.03-1.59)和抗 TNF 治疗开始后 1 年内停药的风险(危险比,1.50;95%CI,1.15-1.94)。AMD 与随后发生的 IBD 相关不良事件的风险之间没有关联。

结论

与没有 AMD 的 IBD 患者相比,在开始抗 TNF 治疗前 2 年内患有 IBD 和 AMD 的患者停止治疗的风险增加。需要研究来确定治疗 AMD 是否会增加对治疗的依从性。

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