Rees G, Martin P R, Macrae F A
Centre for Eye Research Australia, University of Melbourne, Victoria, Australia.
Eur J Cancer Care (Engl). 2008 May;17(3):221-32. doi: 10.1111/j.1365-2354.2007.00834.x.
Literature regarding screening behaviour in individuals with a family history of colorectal cancer was reviewed, in order to determine the prevalence of screening in this population and identify factors associated with screening participation. Four electronic databases were searched from 1994. Thirty papers met the inclusion criteria, including 3 community surveys, 13 studies on first-degree relatives of colorectal cancer patients, and 14 studies on genetic services for colorectal cancer risk assessment. Individuals with a family history of colorectal cancer, who have not received risk assessment, frequently have never had any form of screening for colorectal cancer. Uptake of endoscopic screening when offered to individuals identified as being at increased risk was generally high (often >60% participation). Having a medical recommendation to screen, a stronger family history and perceiving fewer barriers to screening were identified as predictors of screening behaviour. Existing data suggest that use of screening tests in individuals with a family history of colorectal cancer is variable, and our understanding of factors associated with screening behaviour is limited. A number of methodological problems in research to date were identified, and further research is needed in order to inform interventions to support sustained screening participation in this population.
为了确定有结直肠癌家族史人群的筛查率,并找出与筛查参与相关的因素,我们对有关这部分人群筛查行为的文献进行了综述。自1994年起检索了四个电子数据库。30篇论文符合纳入标准,包括3项社区调查、13项关于结直肠癌患者一级亲属的研究以及14项关于结直肠癌风险评估基因服务的研究。有结直肠癌家族史但未接受风险评估的个体,通常从未进行过任何形式的结直肠癌筛查。当为被确定为风险增加的个体提供内镜筛查时,其接受率通常较高(参与率通常>60%)。接受医学筛查建议、家族史更强以及认为筛查障碍更少被确定为筛查行为的预测因素。现有数据表明,有结直肠癌家族史个体的筛查测试使用情况各不相同,而且我们对与筛查行为相关因素的了解有限。已确定了迄今为止研究中的一些方法学问题,需要进一步开展研究,以便为支持这部分人群持续参与筛查的干预措施提供依据。