评估癌症患者诊断为结直肠癌癌症后调节障碍的时间限制和持续症状:一项纵向观察研究

L. M. Wijnhoven, L. Kwakkenbos, I. V. Verdonck‐de Leeuw, J. Prins, J. Custers
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引用次数: 0

摘要

摘要背景:癌症(CRC)患者在癌症诊断和治疗后可能出现调节障碍(AD)症状。如果压力源或其后果在6个月后仍未消失,AD的限时症状可能会持续,但关于AD症状过程的证据很少。这项纵向观察性研究调查了CRC患者在诊断后第一年内出现有时限和持续AD症状的比例,与人口统计学、临床和心理因素以及健康相关的生活质量(HRQoL)有关。方法:从232名参与者中检索知情同意书,194名参与者在基线、诊断后3、6和12个月完成问卷调查。医院焦虑和抑郁量表总分(HADS-T)被归类为无精神障碍症状(MD)(HADS-T≤10)、AD症状(HADS-T11-14)和其他MD症状(HADS-T≥15)的指征。随着时间的推移,症状亚组是先验定义的:无MD、时限性AD、持续性AD、其他MD和波动性症状。结果:81名参与者(41.4%)获得了完整的数据。随着时间的推移,38.3%的参与者没有MD症状,8.6%的参与者有限时AD症状,1.2%的参与者有持续性AD症状,4.9%的参与者还有其他MD症状,46.9%的参与者有波动性症状。与没有MD症状的参与者相比,患有AD和波动症状的参与者对癌症复发的恐惧更高,HRQoL更低,癌症特异性痛苦更高(P<.5)。结论:在CRC诊断后的第一年,只有一小部分患者表现出时间有限和持续的AD症状,大多数患者表现出波动症状。需要更多的前瞻性研究来确定AD症状升高的重复评估与通过诊断访谈确定的AD诊断之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating time-limited and persistent symptoms of adjustment disorder in cancer patients after a colorectal cancer diagnosis: a longitudinal observational study
Abstract Background: Patients with colorectal cancer (CRC) may experience symptoms of adjustment disorder (AD) after cancer diagnosis and treatment. Time-limited symptoms of AD may become persistent if the stressor or its consequences have not disappeared after 6 months, but evidence on the course of AD symptoms is scarce. This longitudinal observational study investigates the proportion of patients with CRC with time-limited and persistent AD symptoms within the first year after diagnosis, in relation to demographic, clinical, and psychological factors and health-related quality of life (HRQoL). Methods: Informed consent was retrieved from 232 participants, and 194 participants completed questionnaires at baseline, 3, 6, and 12 months postdiagnosis. Hospital Anxiety and Depression Scale total scores (HADS-T) were categorized as indication for no symptoms of a mental disorder (MD) (HADS-T ≤10), AD symptoms (HADS-T 11–14), and other MD symptoms (HADS-T ≥15). Symptom subgroups over time were a priori defined: no MD, time-limited AD, persistent AD, other MD, and fluctuating symptoms. Results: Complete data were available for 81 participants (41.4%). Over time, 38.3% had no MD symptoms, 8.6% had time-limited AD symptoms, 1.2% had persistent AD symptoms, 4.9% had other MD symptoms, and 46.9% had fluctuating symptoms. Participants with AD and fluctuating symptoms reported higher fear of cancer recurrence, lower HRQoL, and higher cancer-specific distress than participants without MD symptoms (P < .5). Conclusions: During the first year after CRC diagnosis, only a small proportion of the patients showed time-limited and persistent AD symptoms and most showed fluctuating symptoms. More prospective research is needed to determine how repeated assessments for elevated AD symptoms relate to an AD diagnosis established with a diagnostic interview.
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