[Outpatient psychosocial screening in a skin cancer center: acceptance, psychosocial distress and utilization of support : A post hoc analysis in a quality management program].

Dermatologie (Heidelberg, Germany) Pub Date : 2024-08-01 Epub Date: 2024-05-08 DOI:10.1007/s00105-024-05347-2
Alexander Wünsch, Niklas Jeske, Natalie Röderer, Frank Meiss
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Abstract

Background: Psychosocial care of cancer patients is an important aspect throughout the entire course of oncological treatment. Since 2015, psychosocial screening has been implemented in the outpatient clinics of the Skin Cancer Center in Freiburg. We present here a post hoc analysis in the context of a quality management program.

Question: Acceptance, psychosocial distress and desire for counseling were evaluated. Exploratively, we investigated which patient and disease characteristics are related to increased subjective distress.

Materials and methods: In a full survey from 06/2015 to 12/2015, we evaluated acceptance, psychosocial distress by distress thermometer (DT), and desire for counseling.

Results: Of 753 patients, 345 (45.8%) participated in psychosocial screening and data from 310 (174 men, 136 women; 89.7% melanoma patients, mean time since initial diagnosis 4.7 ± 3.9 years) could be analyzed. The mean burden on the DT was 2.97 ± 2.83 (median 2, range 0-10). High distress (DT ≥ 5) was reported by 84 patients (28.8%). Thirty-four patients (11%) indicated a desire for counseling, and 23 patients took up the counseling offer. The patient group with high distress was younger, more often under ongoing or recently completed systemic therapy, and had more often a desire for counseling.

Conclusion: In addition to assessing psychosocial distress with validated screening instruments, the survey of the subjective desire for care represents an important parameter for the identification of patients in need of care. Young patients and patients with ongoing systemic therapy should be the focus of attention.

[一家皮肤癌中心的门诊患者社会心理筛查:接受度、社会心理困扰和对支持的利用:质量管理计划中的事后分析]。
背景:癌症患者的社会心理护理是贯穿整个肿瘤治疗过程的一个重要方面。自 2015 年起,弗莱堡皮肤癌中心的门诊诊所开始实施社会心理筛查。我们在此介绍在质量管理计划背景下进行的事后分析:我们对患者的接受程度、心理压力和咨询愿望进行了评估。我们探索性地研究了哪些患者和疾病特征与主观痛苦的增加有关:在 2015 年 6 月至 2015 年 12 月的一次全面调查中,我们评估了患者的接受程度、通过痛苦温度计(DT)获得的心理社会痛苦以及咨询愿望:在 753 名患者中,有 345 人(45.8%)参加了社会心理筛查,其中 310 人(174 名男性,136 名女性;89.7% 为黑色素瘤患者,平均确诊时间为 4.7 ± 3.9 年)的数据可供分析。DT 的平均负担为 2.97 ± 2.83(中位数为 2,范围为 0-10)。84名患者(28.8%)报告了高度痛苦(DT≥5)。34名患者(11%)表示希望接受心理咨询,23名患者接受了心理咨询。心理困扰程度高的患者群体更年轻,更多正在接受或刚刚完成系统治疗,并且更多希望获得心理咨询:结论:除了使用有效的筛查工具评估心理社会困扰外,主观护理愿望调查也是识别需要护理的患者的一个重要参数。应重点关注年轻患者和正在接受系统治疗的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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