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首页> 外文期刊>Journal of Clinical Oncology >Symptom Burden in the First Year After Cancer Diagnosis: An Analysis of Patient-Reported Outcomes
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Symptom Burden in the First Year After Cancer Diagnosis: An Analysis of Patient-Reported Outcomes

机译:癌症诊断后第一年的症状负担:分析患者报告的结果

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PurposeImprovement in the quality of life of patients with cancer requires attention to symptom burden across the continuum of care, with the use of patient-reported outcomes key to achieving optimal care. Yet there have been few studies that have examined symptoms in the early postdiagnosis period during which suboptimal symptom control may be common. A comprehensive analysis of temporal trends and risk factors for symptom burden in newly diagnosed patients with cancer is essential to guide supportive care strategies.MethodsA retrospective observational study was performed of patients who were diagnosed with cancer between January 2007 and December 2014 and who survived at least 1 year. Patient-reported Edmonton Symptom Assessment System scores, which are prospectively collected at outpatient visits, were linked to provincial administrative health care data. We described the proportion of patients who reported moderate-to-severe symptom scores by month during the first year after diagnosis according to disease site. Multivariable logistic regression models were constructed to identify risk factors for moderate-to-severe symptom scores.ResultsOf 120,745 patients, 729,861 symptom assessments were recorded within 12 months of diagnosis. For most symptoms, odds of elevated scores were highest in the first month, whereas nausea had increased odds of elevated scores up to 6 months after diagnosis. On multivariable analysis, cancer site, younger age, higher comorbidity, female sex, lower income, and urban residence were associated with significantly higher odds of elevated symptom burden.ConclusionA high prevalence of moderate-to-severe symptom scores was observed in cancers of all sites. Patients are at risk of experiencing multiple symptoms in the immediate postdiagnosis period, which underscores the need to address supportive care requirements early in the cancer journey. Patient subgroups who are at higher risk of experiencing moderate-to-severe symptoms should be targeted for tailored supportive care interventions.
机译:癌症患者的生活质量的目的性质需要注意在关注的连续性上的症状负担,使用患者报告的结果关键来实现最佳护理。然而,几乎没有研究过迟交期的早期症状期间的研究可能是常见的。对新诊断的癌症患者症状负担的综合分析对于指导支持性护理策略至关重要..对诊断为2007年1月至2014年12月诊断癌症的患者进行了患者的患者,并且至少幸存下来1年。患者报告的Edmonton症状评估系统得分,这些评估系统分数在门诊访问中,与省级行政卫生保健数据相关联。根据疾病现场,我们描述了在诊断后的第一年期间报告中度至严重症状分数的患者的比例。构建多变量逻辑回归模型以确定中度至严重症状评分的危险因素。诊断12个月内120,745名患者,729,861名症状评估记录。对于大多数症状,升高的分数在第一个月最高的可能性最高,而恶心在诊断后6个月内增加了升高的分数。在多变量分析,癌症网站,较年轻的年龄,更高的合并症,女性性别,较低的收入和城市住所的升高的升高几率明显较高有关。在所有的癌症中观察到中度至严重的症状分数的高度普及网站。患者有可能在后诊断期间经历多种症状,强调了在癌症旅程中早期满足支持性护理要求的必要性。在体验中度至严重症状的风险较高风险的患者亚组应该针对量身定制的支持性护理干预措施。

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