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国际专家和丹麦公民对公民参与癌症筛查做出知情选择所需的“相关知识”的看法:定性研究。

Perspectives of international experts and the Danish citizens on the 'relevant knowledge' that citizens need for making informed choices about participation in cancer screening: Qualitative study.

机构信息

University Research Clinic for Cancer Screening, Department of Public Health Programmes, Randers Regional Hospital, Randers, Denmark; Department of Clinical Medicine, Aarhus University, Denmark.

University Research Clinic for Cancer Screening, Department of Public Health Programmes, Randers Regional Hospital, Randers, Denmark; Department of Clinical Medicine, Aarhus University, Denmark.

出版信息

Patient Educ Couns. 2025 Jan;130:108479. doi: 10.1016/j.pec.2024.108479. Epub 2024 Oct 24.

DOI:10.1016/j.pec.2024.108479
PMID:
39488032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11980426/
Abstract

OBJECTIVES

This study aimed to investigate the perspectives of international experts and Danish citizens on relevant knowledge about population-based breast, colorectal and cervical cancer screening.

METHODS

This was a qualitative interview study with focus group interviews with experts and Danish citizens eligible for breast, colorectal and/or cervical cancer screening. Data were collected using semi-structured interview guides, audio-recorded and transcribed verbatim. A thematic analysis was conducted.

RESULTS

Participants were nine international experts from Germany, Canada, the USA, Sweden, the Netherlands and Australia, and 54 citizens from Denmark. Most citizens had 'adequate' or 'problematic' levels of health literacy. Themes that experts and citizens agreed on were: knowledge about the disease and symptoms, practical information about screening, benefits of screening, the option of non-participation and the importance of having numeric information of possible screening outcomes. Experts agreed on the importance of knowledge about the harms of screening, but only a minority of citizens considered this important.

CONCLUSIONS

The experts and citizens disagreed on the relevance of knowledge about harms of screening and agreed on other relevant knowledge.

PRACTICE IMPLICATIONS

What experts and citizens find important may not align when making informed decisions. Therefore, experts and citizens needs to be involved when developing questionnaires.

摘要

目的

本研究旨在调查国际专家和丹麦公民对基于人群的乳腺癌、结直肠癌和宫颈癌筛查相关知识的看法。

方法

这是一项定性访谈研究,采用焦点小组访谈的形式对有资格接受乳腺癌、结直肠癌和/或宫颈癌筛查的专家和丹麦公民进行访谈。使用半结构化访谈指南收集数据,录音并逐字转录。进行了主题分析。

结果

参与者包括来自德国、加拿大、美国、瑞典、荷兰和澳大利亚的 9 名国际专家以及来自丹麦的 54 名公民。大多数公民的健康素养水平为“足够”或“有问题”。专家和公民一致认为的主题有:疾病和症状知识、筛查的实用信息、筛查的益处、不参与的选择以及获得可能的筛查结果的数字信息的重要性。专家们一致认为了解筛查的危害很重要,但只有少数公民认为这很重要。

结论

专家和公民对筛查危害知识的相关性存在分歧,但对其他相关知识的看法一致。

实践意义

在做出知情决策时,专家和公民认为重要的内容可能并不一致。因此,在开发问卷时需要专家和公民的参与。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23c/11980426/77a1e5c214a7/nihms-2068633-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23c/11980426/77a1e5c214a7/nihms-2068633-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23c/11980426/77a1e5c214a7/nihms-2068633-f0001.jpg

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