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The impact of an electronic health questionnaire on symptom management and behavior reporting for breast cancer survivors

机译:电子健康调查表对乳腺癌幸存者症状管理和行为报告的影响

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Breast cancer (BC) patients experience multiple symptoms as a result of diagnosis and treatment. While surveillance for detecting cancer recurrence is fundamental to follow-up care, managing symptoms, and promoting health behaviors are equally important. UCSF has implemented a secure online health questionnaire enabling BC patients to provide updates of their health history and symptoms. We randomly selected a sample of stage I–III BC patients (n = 106) who completed a questionnaire before a medical oncology visit between August 2010 and January 2011 and consented to have data used for research. We conducted a chart review calculating the number of symptoms reported in the questionnaire, the clinic note only, and both questionnaire and clinic note, excluding chronic symptoms addressed previously. Self-reported data on exercise and alcohol consumption was compared to documentation of these lifestyle factors in clinic notes. Patients reported significantly more symptoms using the online questionnaire (mean = 3.8, range 0–13) than were documented by the provider in clinic notes (mean = 1.8, range 0–7; p < 0.001 for the difference). A regression plot comparing the percentage of symptoms agreed upon by the patient and provider and the percentage of symptoms addressed yields a slope of 0.56 (95 % CI 0.41–0.71). The number of self-reported symptoms correlates with self-reported Karnofsky scale such that the number of symptoms reported by the patient increases linearly with this score until a threshold and it then plateaus (p < 0.001). Exercise behavior and alcohol consumption were reported in 100 % of the online questionnaires, but was documented in only 30/106 (28 %) and 75/106 (70 %) of charts reviewed. In 19/75 (25 %) charts with alcohol consumption documented, there was substantial discordance between patient and clinician reporting. Electronic data collection of BC patient-reported outcomes has a positive effect on symptom management and identification of opportunities for risk-reducing behavior change.
机译:乳腺癌(BC)患者由于诊断和治疗而出现多种症状。尽管检测癌症复发的监视对于后续护理至关重要,但控制症状和促进健康行为也同样重要。 UCSF已实施了一项安全的在线健康调查表,使卑诗省患者能够提供其健康史和症状的最新信息。我们从2010年8月至2011年1月进行医学肿瘤学访问之前完成问卷调查的I-III期BC患者(n = 106)的样本中随机抽取,并同意将其用于研究。我们进行了图表审查,计算了调查表中报告的症状数(仅适用于临床笔记以及问卷和临床笔记),不包括先前提到的慢性症状。自我报告的运动和饮酒数据与临床记录中这些生活方式因素的文档进行了比较。患者使用在线问卷报告的症状明显多于提供者在临床笔记中记录的症状(平均= 3.8,范围0–13;平均值= 1.8,范围为0–7;差异p <0.001)。回归图比较了患者和提供者同意的症状百分比与所解决症状的百分比,得出的斜率为0.56(95%CI 0.41-0.71)。自我报告的症状数量与自我报告的卡诺夫斯基量表相关,因此患者报告的症状数量随该分数线性增加,直至达到阈值,然后达到平稳状态(p <0.001)。在100%的在线调查表中报告了运动行为和饮酒情况,但在所查看的图表中只有30/106(28%)和75/106(70%)有记录。在记录有酒精消耗的19/75(25%)图表中,患者和临床医生的报告之间存在很大差异。 BC患者报告结果的电子数据收集对症状管理和降低风险行为改变机会的识别具有积极作用。

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