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患者心理社会困扰的线索和症状:肿瘤临床医生对困扰进行评估和治疗的预测因素是什么?

Patient cues and symptoms of psychosocial distress: what predicts assessment and treatment of distress by oncology clinicians?

作者信息

Sheldon Lisa Kennedy, Blonquist Traci M, Hilaire Dany M, Hong Fangxin, Berry Donna L

机构信息

University of Massachusetts Boston, Boston, MA, USA.

Dana-Farber Cancer Institute, Boston, MA, USA.

出版信息

Psychooncology. 2015 Sep;24(9):1020-7. doi: 10.1002/pon.3689. Epub 2014 Oct 7.

Abstract

OBJECTIVE

Psychosocial concerns arise after a cancer diagnosis and during treatment requiring oncology clinicians to initiate discussions to identify distress. This study examined patient-clinician communication about psychosocial concerns and predictors of assessment and treatment/referral for distress.

METHODS

Secondary analysis of existing dataset coded to explore patient-clinician communication during ambulatory visits in two comprehensive cancer centers was carried out. Sample included adult patients with various cancers and stages. Dataset included audio-recordings and symptom/QOL reports 4-6 weeks after starting treatment from all distressed patients (n = 66) in parent study and random sample of nondistressed patients (n = 23). Distressed patients had moderate-to-severe depression (Patient Health Questionnaire-9 scores ≥10) and/or poor emotional functioning (European Organization for Research and Treatment of Cancer Quality of Life Questionnaire emotional function scores <50). Audio-recordings were coded to describe patient-clinician communication about psychosocial concerns using the coding scheme from the parent study plus Medical Interview Aural Rating System.

RESULTS

The remaining patients gave 222 cues of psychosocial concerns: 183 from 46 distressed patients and 39 from nine nondistressed patients. Distressed patients were younger, were female, had higher symptom burden, and/or gave more cues. Significantly, more distressed patients had at least one cue/visit. Clinicians initiated 62% of discussions overall with no statistical difference between distressed and nondistressed groups. More explicit cues and more than four cues predicted treatment/referral for distress.

CONCLUSIONS

Distressed patients were younger, were female, had higher symptom burden, and/or gave more verbal cues. Clinicians responded to explicit and more frequent cues by providing treatment and/or referrals for distress. Further exploration is needed regarding clinician factors related to assessment of psychosocial concerns.

摘要

目的

癌症诊断后及治疗期间会出现心理社会问题,这要求肿瘤临床医生展开讨论以识别患者的痛苦。本研究考察了医患之间关于心理社会问题的沟通情况以及痛苦评估与治疗/转诊的预测因素。

方法

对两个综合癌症中心门诊就诊期间医患沟通情况进行编码的现有数据集进行二次分析。样本包括患有各种癌症及不同分期的成年患者。数据集包括来自母研究中所有痛苦患者(n = 66)及非痛苦患者随机样本(n = 23)治疗开始后4 - 6周的音频记录和症状/生活质量报告。痛苦患者有中度至重度抑郁(患者健康问卷 - 9得分≥10)和/或情绪功能较差(欧洲癌症研究与治疗组织生活质量问卷情绪功能得分<50)。使用母研究的编码方案加医学访谈听觉评分系统对音频记录进行编码,以描述医患之间关于心理社会问题的沟通。

结果

其余患者给出了222条心理社会问题线索:46名痛苦患者给出183条,9名非痛苦患者给出39条。痛苦患者更年轻、为女性、症状负担更高且/或给出的线索更多。值得注意的是,更多痛苦患者每次就诊至少有一条线索。总体上临床医生发起了62%的讨论,痛苦组和非痛苦组之间无统计学差异。更明确的线索以及超过四条线索可预测痛苦的治疗/转诊。

结论

痛苦患者更年轻、为女性、症状负担更高且/或给出更多言语线索。临床医生通过提供痛苦治疗和/或转诊来回应明确且更频繁的线索。需要进一步探索与心理社会问题评估相关的临床医生因素。

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