Ou George, Bressler Brian, Galorport Cherry, Lam Eric, Ko Hin Hin, Enns Robert, Telford Jennifer, Schaffer Nathan, Lee Terry, Rosenfeld Greg
University of British Columbia, Faculty of Medicine, Department of Medicine. St. Paul's Hospital, Vancouver, B.C. Canada.
J Can Assoc Gastroenterol. 2018 Sep;1(3):99-106. doi: 10.1093/jcag/gwy023. Epub 2018 Jun 4.
Corticosteroid is an effective therapeutic option for inflammatory bowel disease flares, but its adverse effects may compromise treatment adherence and reduce patients' quality of life. There is lack of data on the incidence of corticosteroid-induced mood changes in this patient population, which may be underappreciated by healthcare providers in clinical practice and interfere with optimal care. This study aimed to determine the rate of mood changes in this patient population.
In this prospective observational study, adult outpatients treated with prednisone for inflammatory bowel disease flares were considered for inclusion. Participants completed validated questionnaires (Beck Depression Inventory-II and Activation Subscale of Internal State Scale version two) before starting prednisone, after two weeks of prednisone, and at the end of prednisone taper to assess for mood changes. Harvey-Bradshaw Index and Simple Clinical Colitis Activity Index were used to monitor clinical disease activity.
Fifty-three subjects were included in the analyses. The rate of mood change after two weeks of prednisone was 49.1%, primarily driven by increase in mood towards (hypo)mania. Younger age was an independent risk factor. Mood state returned to pretreatment level at the end of treatment. There was no correlation between clinical disease activity change and mood change.
Oral prednisone for inflammatory bowel disease flare is associated with high rate of mood change. As prednisone is a critical part of induction therapy, ways to minimize this adverse event must be studied. For now, healthcare providers should inform patients and monitor closely for this adverse event.
皮质类固醇是治疗炎症性肠病发作的一种有效治疗选择,但其不良反应可能会影响治疗依从性并降低患者的生活质量。关于该患者群体中皮质类固醇诱发情绪变化的发生率的数据尚缺乏,在临床实践中医疗服务提供者可能对此认识不足,从而干扰最佳治疗。本研究旨在确定该患者群体中情绪变化的发生率。
在这项前瞻性观察性研究中,纳入了因炎症性肠病发作而接受泼尼松治疗的成年门诊患者。参与者在开始服用泼尼松前、服用泼尼松两周后以及泼尼松逐渐减量结束时完成经过验证的问卷(贝克抑郁量表-II和内部状态量表第二版的激活子量表),以评估情绪变化。使用哈维-布拉德肖指数和简单临床结肠炎活动指数来监测临床疾病活动。
53名受试者纳入分析。服用泼尼松两周后的情绪变化发生率为49.1%,主要是向(轻)躁狂方向的情绪增加所致。较年轻的年龄是一个独立危险因素。治疗结束时情绪状态恢复到治疗前水平。临床疾病活动变化与情绪变化之间无相关性。
口服泼尼松治疗炎症性肠病发作与高情绪变化发生率相关。由于泼尼松是诱导治疗的关键部分,必须研究将这种不良事件降至最低的方法。目前,医疗服务提供者应告知患者并密切监测这一不良事件。