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结直肠癌后心理困扰的轨迹。

Trajectories of psychological distress after colorectal cancer.

机构信息

Griffith Health Institute, Griffith University, Brisbane, Queensland, Australia.

出版信息

Psychooncology. 2013 Aug;22(8):1759-65. doi: 10.1002/pon.3210. Epub 2012 Nov 5.

Abstract

OBJECTIVE

Heightened psychological distress after cancer is common but likely highly heterogeneous. This raises potential challenges in how and when to target services; however, data describing longitudinal patterns of distress are limited. This study describes the long term psychological outcomes for colorectal cancer (CRC) survivors and trajectories of adjustment over time.

METHODS

A prospective survey of a population-based sample of 1966 CRC survivors assessed sociodemographic variables, perceived social support and psychological distress, including distress subtypes of anxiety, depression and somatization, at six time points from 5 months to 5 years post-diagnosis.

RESULTS

Over the 5-year trajectory, the prevalence of high overall distress ranged between 44% and 32% but was greater for men compared with women (p < 0.001). Four distress trajectory styles within clusters were identified for overall distress and for each distress subtype with a constant low distress group providing the basis for comparison. Higher distress trajectories varied for overall distress and distress subtypes but were generally differentiated by gender, younger age, lower education, poor socioeconomic advantage, late disease stage and poor social support.

CONCLUSIONS

For global distress, by comparison with women, men with CRC are vulnerable to distress, with men who are younger and with low education and poor social support being a priority for targeted intervention. While distress screening early in the cancer experience will identify those with a constant high distress trajectory, others with late emerging distress or caseness may be missed. On this basis, distress screening through the illness trajectory into long term survivorship seems warranted.

摘要

目的

癌症后心理困扰加剧较为常见,但可能存在高度异质性。这对如何以及何时确定服务目标提出了潜在挑战;然而,描述困扰纵向模式的数据有限。本研究描述了结直肠癌(CRC)幸存者的长期心理结局和随时间调整的轨迹。

方法

对 1966 例基于人群的 CRC 幸存者进行前瞻性调查,评估社会人口统计学变量、感知社会支持和心理困扰,包括焦虑、抑郁和躯体化等困扰亚型,在诊断后 5 个月至 5 年内共 6 个时间点进行评估。

结果

在 5 年的轨迹中,高总体困扰的患病率在 44%至 32%之间波动,但男性高于女性(p<0.001)。确定了总体困扰和每种困扰亚型的四个困扰轨迹类型,以低总体困扰组为基础进行比较。总体困扰和各困扰亚型的较高困扰轨迹存在差异,但通常根据性别、年龄较小、教育程度较低、社会经济地位较差、晚期疾病阶段和社会支持较差来区分。

结论

相比女性,CRC 男性的总体困扰更易受到影响,年龄较小、教育程度较低、社会支持较差的男性是重点干预对象。虽然在癌症早期进行困扰筛查可以识别出具有持续高困扰轨迹的患者,但可能会错过后期出现困扰或确诊的患者。在此基础上,通过疾病轨迹进入长期生存的困扰筛查似乎是合理的。

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