Department of Neurosurgery, University of Duisburg-Essen, Hufelandstrasse 55, 45147, Essen, Germany.
Department of Neurosurgery, University of Erlangen-Nuremberg, Schlossplatz 4, 91054, Erlangen, Germany.
Pituitary. 2016 Dec;19(6):590-600. doi: 10.1007/s11102-016-0750-1.
Quality of life (QoL) and psychosocial well-being are substantially impaired in patients with Cushing's disease (CD), not only at the acute illness stage but also after therapy; however, the reason for these impairments remains unclear.
In this cross-sectional, patient-reported outcome study, we conducted a postal survey on psychosocial impairment and coping strategies in patients after surgical treatment of CD in three large tertiary referral centers. In total, 176 patients with CD completed a compilation of self-assessment inventories pertaining to depression (Hospital Anxiety and Depression Scale, HADS), QoL (Short Form SF-36, Tuebingen CD; Tuebingen CD-25), coping style (Freiburg questionnaire on coping with illness, FKV-LIS), and embitterment (Bern Embitterment Inventory), on average 6.8 ± 6.66 years after surgery. Regression analyses were performed to identify predictors of psychosocial impairment.
At the time of the study, 21.8 % of patients suffered from anxiety, 18.7 % experienced an above-average feeling of embitterment, and 13.1 % suffered from depression. Maladaptive coping styles (FKV-LIS subscales depressive coping and minimizing importance) emerged as robust and strong predictors of psychosocial impairment in all inventories; while age, sex, and hydrocortisone intake failed to explain the variance in these measures.
Similar to several studies in non-pituitary patient cohorts (e.g., patients with multiple sclerosis or lower back pain), our results indicate that psychosocial impairment in CD is significantly influenced by how the patient deals with the illness. Therefore, psychological training of positive coping styles could be a helpful complementary therapy in the overall treatment strategy of CD.
库欣病(Cushing's disease,CD)患者的生活质量(quality of life,QoL)和心理社会健康状况严重受损,不仅在急性疾病阶段,而且在治疗后也是如此;然而,这些损害的原因仍不清楚。
在这项横断面、患者报告结局研究中,我们在三个大型三级转诊中心对接受 CD 手术治疗后的患者进行了一项关于心理社会损害和应对策略的邮寄调查。共有 176 名 CD 患者完成了一系列自我评估量表,包括抑郁(医院焦虑和抑郁量表,HADS)、QoL(Tübingen CD 短表 SF-36、Tübingen CD-25)、应对方式(弗莱堡疾病应对问卷,FKV-LIS)和苦闷(伯尔尼苦闷量表),平均在手术后 6.8±6.66 年。进行回归分析以确定心理社会损害的预测因素。
在研究时,21.8%的患者患有焦虑症,18.7%的患者有明显的苦闷感,13.1%的患者患有抑郁症。适应性应对方式(FKV-LIS 子量表抑郁应对和最小化重要性)是所有量表中心理社会损害的强大且稳健的预测因素;而年龄、性别和氢化可的松摄入并不能解释这些指标的差异。
与多项针对非垂体患者队列的研究(例如,多发性硬化症或腰痛患者)类似,我们的结果表明,CD 患者的心理社会损害受患者处理疾病的方式显著影响。因此,积极应对方式的心理训练可能是 CD 整体治疗策略的一种有益的补充治疗方法。