The Research Unit for General Practice, Section of General Practice, Department of Public Health, University of Copenhagen, Copenhagen K, Denmark.
Department of Communication and Psychology, Centre for Applied Ethics and Philosophy of Science, Aalborg University Copenhagen, Denmark.
Eur J Public Health. 2021 Feb 1;31(1):200-206. doi: 10.1093/eurpub/ckaa158.
Health authorities can influence citizens in subtle ways that render them more likely to participate in cancer screening programmes, and thereby possibly increase the beneficial effects. If the influences become too severe, the citizens' ability to make a personal choice may be lost on the way. The purpose of this analysis was to identify and categorize the influences while questioning whether they still permit the citizens to make their own choices regarding participation.
A two-stringed approach was used to obtain empirical examples of systematic influences that aim to raise participation rates in cancer screening programmes: First, a systematic literature search was conducted on three databases. Second, relevant experts were contacted via internationally based e-mail lists and asked for examples of systematic influences in cancer screening. The present analysis was based on direct, conventional content analysis to address different categories of systematic influences.
The literature search yielded 19 included articles and the expert inquiry yielded 11 empirical examples of which content analysis of the empirical examples generated six major categories of systematic influence: (i) misleading presentation of statistics, (ii) misrepresentation of harms vs. benefits, (iii) opt-out systems, (iv) recommendation of participation, (v) fear appeals and (vi) influencing the general practitioners and other healthcare professionals.
The six categories of identified influences work through psychological biases and personal costs and are still in widely use. The use of these types of influence remains ethically questionable in cancer screening programmes since they might compromise informed decision making.
卫生当局可以以微妙的方式影响公民,使他们更有可能参与癌症筛查计划,从而可能增加有益的效果。如果这些影响变得过于严重,公民做出个人选择的能力可能会在这个过程中丧失。本分析的目的是识别和分类这些影响,同时质疑它们是否仍然允许公民自行选择参与。
采用双管齐下的方法来获取旨在提高癌症筛查计划参与率的系统影响的实证例子:首先,在三个数据库中进行了系统的文献搜索。其次,通过国际电子邮件列表联系了相关专家,要求他们提供癌症筛查中系统影响的例子。本分析基于直接的常规内容分析,以解决不同类别的系统影响。
文献搜索产生了 19 篇纳入文章,专家查询产生了 11 个实证例子,对这些实证例子的内容分析产生了系统影响的六个主要类别:(i)对统计数据的误导性呈现,(ii)对危害与益处的错误描述,(iii)退出系统,(iv)推荐参与,(v)恐惧诉求,以及(vi)影响全科医生和其他医疗保健专业人员。
已确定的影响类别通过心理偏见和个人成本发挥作用,并且仍在广泛使用。在癌症筛查计划中使用这些类型的影响在伦理上仍存在疑问,因为它们可能会影响知情决策。