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患者、照料者及肿瘤学家对癌症相关疲劳的认知:一项三方评估调查的结果。疲劳联盟。

Patient, caregiver, and oncologist perceptions of cancer-related fatigue: results of a tripart assessment survey. The Fatigue Coalition.

作者信息

Vogelzang N J, Breitbart W, Cella D, Curt G A, Groopman J E, Horning S J, Itri L M, Johnson D H, Scherr S L, Portenoy R K

机构信息

University of Chicago, IL 60637-1463, USA.

出版信息

Semin Hematol. 1997 Jul;34(3 Suppl 2):4-12.

PMID:9253778
Abstract

Although fatigue is the most common symptom reported by cancer patients and has serious adverse effects on quality of life, it remains poorly understood. A survey was designed to characterize the epidemiology of cancer-related fatigue from the perspectives of the patient, primary caregiver, and oncologist. A telephone survey included 419 cancer patients recruited from 100,000 randomly selected households nationwide. Patients provided access to 200 primary caregivers (usually family members) who were also interviewed by telephone. In a separate mail survey, 197 of 600 randomly sampled oncologists (unrelated to the patients) responded to a questionnaire that assessed perceptions and attitudes concerning fatigue in cancer patients who had received chemotherapy or radiotherapy and their caregivers. The median patient age was 65 years, and the principal cancer diagnoses were breast (females) and genitourinary (males). Fifty-nine percent of the patients had received chemotherapy, 63% radiation therapy, and 24% both; 20% of patients received their last treatment within 6 weeks, 31% within 7 weeks to 1 year, and 49% more than 1 year ago. More than three quarters of patients (78%) experienced fatigue (defined as a general feeling of debilitating tiredness or loss of energy) during the course of their disease and treatment. Thirty-two percent experienced fatigue daily, and 32% reported fatigue significantly affected their daily routines. Caregivers reported observing fatigue in 86% of the index patients, and oncologists perceived that 76% of their patients experienced fatigue. Although oncologists believed that pain adversely affected their patients to a greater degree than fatigue (61% v 37%), patients felt that fatigue adversely affected their daily lives more than pain (61% v 19%). Most oncologists (80%) believed fatigue is overlooked or undertreated, and most patients (74%) considered fatigue a symptom to be endured. Fifty percent of patients did not discuss treatment options with their oncologists, and only 27% reported that their oncologists recommended any treatment for fatigue. When used, treatments for fatigue were generally perceived by patients and caregivers to be successful. These data confirm the high prevalence and adverse impact of cancer-related fatigue, although it is seldom discussed and infrequently treated. For patients and oncologists, improving the quality of life of cancer patients requires a heightened awareness of fatigue, a better understanding of its impact, and improve communication and familiarity with interventions that can reduce its debilitating effects.

摘要

尽管疲劳是癌症患者报告的最常见症状,且对生活质量有严重不良影响,但人们对其仍知之甚少。一项调查旨在从患者、主要照料者和肿瘤学家的角度描述癌症相关疲劳的流行病学特征。一项电话调查纳入了从全国10万户随机抽取的家庭中招募的419名癌症患者。患者让200名主要照料者(通常是家庭成员)参与调查,这些照料者也接受了电话访谈。在另一项邮件调查中,600名随机抽取的肿瘤学家(与患者无关)中有197人回复了一份问卷,该问卷评估了他们对接受过化疗或放疗的癌症患者及其照料者疲劳情况的看法和态度。患者的年龄中位数为65岁,主要癌症诊断为乳腺癌(女性)和泌尿生殖系统癌(男性)。59%的患者接受过化疗,63%接受过放疗,24%两者都接受过;20%的患者在6周内接受了最后一次治疗,31%在7周内至1年,49%在1年多以前。超过四分之三的患者(78%)在疾病和治疗过程中经历过疲劳(定义为一种使人虚弱的疲倦或精力丧失的总体感觉)。32%的患者每天都感到疲劳,32%的患者报告疲劳严重影响了他们的日常生活。照料者报告称,86%的索引患者存在疲劳,肿瘤学家认为76%的患者经历过疲劳。尽管肿瘤学家认为疼痛对患者的不良影响程度大于疲劳(61%对37%),但患者觉得疲劳对其日常生活的不良影响大于疼痛(61%对19%)。大多数肿瘤学家(80%)认为疲劳被忽视或治疗不足,大多数患者(74%)认为疲劳是一种需要忍受的症状。50%的患者没有与肿瘤学家讨论治疗方案,只有27%的患者报告他们的肿瘤学家推荐过任何治疗疲劳的方法。当使用这些方法时,患者和照料者普遍认为对疲劳的治疗是成功的。这些数据证实了癌症相关疲劳的高患病率和不良影响,尽管它很少被讨论且很少得到治疗。对于患者和肿瘤学家来说,提高癌症患者的生活质量需要提高对疲劳的认识,更好地理解其影响,并改善沟通以及熟悉能够减轻其使人虚弱影响的干预措施。

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