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儿童癌症幸存者报告的晚期效应、寻求生存护理的动机以及就诊模式。

Childhood Cancer Survivors' Reported Late Effects, Motivations for Seeking Survivorship Care, and Patterns of Attendance.

机构信息

Kids Cancer Centre, Sydney Children's Hospital, Randwick, NSW, Australia.

Discipline of Paediatrics & Child Health, School of Clinical Medicine, UNSW Sydney, NSW, Australia.

出版信息

Oncologist. 2023 May 8;28(5):e276-e286. doi: 10.1093/oncolo/oyad004.

Abstract

BACKGROUND

Childhood cancer survivors are vulnerable to long-term treatment-related health conditions, which can lead to poor quality of life. Little data exist on the overall health of long-term Australian and New Zealand childhood cancer survivors or on survivors' motivations for attending survivorship clinics.

METHODS

This study administers a cross-sectional questionnaire to long-term survivors ≥5 years from their primary diagnosis. We compared participant-reported number of late effects by a cancer diagnosis, and identified clinical (eg, treatment) and demographic (eg, age) factors that were associated with late effects burden and engagement in cancer survivorship care.

RESULTS

A total of 634 participants completed questionnaires (48% male, mean age = 21.7 years). Most participants (79%) reported at least one cancer-related late effect, most commonly fatigue (40%) and memory/learning difficulties (34%). Brain tumor survivors reported a higher total number of late effects than survivors with other diagnoses (mean = 5.7 vs. 3.2, P < .001). Participants' most commonly reported motivators for engaging in care were to understand problems that may occur later in life because of their cancer and/or treatment (98.5%) and to get reassurance about one's health (97.4%). The proportion of survivors endorsing each motivating factor was similar across cancer diagnoses, with the exception of learning more about insurance and pensions (highest in brain tumor survivors = 80%). In multivariable analyses, survivors were more likely to report being engaged in survivorship care if they were younger (P < .001), less time had elapsed since their diagnosis (P < .001), or they reported a higher number of motivating factors (P = .016).

CONCLUSION

Survivors report a range of health problems decades after treatment completion. Understanding the burden of late effects, and motivators for seeking survivorship care to manage these health problems, is important for ensuring that tailored interventions or services are available to meet the needs of this growing population and to design effective models of survivorship care.

摘要

背景

儿童癌症幸存者易受到长期治疗相关健康问题的影响,从而导致生活质量下降。关于澳大利亚和新西兰长期儿童癌症幸存者的整体健康状况,以及幸存者参加生存随访诊所的动机,数据很少。

方法

本研究对主要诊断后≥5 年的长期幸存者进行横断面问卷调查。我们比较了参与者报告的按癌症诊断划分的晚期影响数量,并确定了与晚期影响负担和参与癌症生存随访护理相关的临床(例如治疗)和人口统计学(例如年龄)因素。

结果

共有 634 名参与者完成了问卷调查(48%为男性,平均年龄为 21.7 岁)。大多数参与者(79%)报告至少有一种癌症相关的晚期影响,最常见的是疲劳(40%)和记忆力/学习困难(34%)。脑肿瘤幸存者报告的晚期影响总数高于其他诊断的幸存者(平均为 5.7 比 3.2,P<.001)。参与者报告参与护理的最常见动机是了解因癌症及其治疗可能在以后的生活中出现的问题(98.5%),并对自己的健康状况感到安心(97.4%)。在不同癌症诊断中,对每个激励因素的认可比例相似,但了解更多关于保险和养老金的信息除外(脑肿瘤幸存者中最高,为 80%)。在多变量分析中,如果幸存者年龄较小(P<.001)、诊断后时间较短(P<.001)或报告的激励因素较多(P=.016),则更有可能报告正在接受生存随访护理。

结论

幸存者在治疗完成后几十年会报告一系列健康问题。了解晚期影响的负担以及寻求生存随访护理以管理这些健康问题的动机,对于确保提供针对这一不断增长的人群的定制干预措施或服务以及设计有效的生存随访护理模式非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c5/10166180/43fc6a4e0523/oyad004_fig1.jpg

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