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The harm minimization movement is concerned to ensure that developments in genetic research are of benefit to wider society. However, whether harm reduction strategies are actually productive of positive consequences for the community is currently unclear, and harm reduction rhetoric often masks a deeper underlying agenda. The purpose of this study was to examine the extent to which the harm reduction movement embraces ideas of unintended consequences. Thirty-five members of the UK Genetic Society attended a one-day workshop exploring the implications of the advent of genetic screening for monogenic disorders and cancer predisposition. Participants met for one session to discuss the topics covered in the course-booklets. The findings from the focus groups indicate that the majority of the participants felt that the genetic screening agenda was largely concerned with facilitating the uptake of DNA testing and that risk assessment was a key part of the harm minimization agenda. However, the attendees’ attitudes were more ambivalent towards the engagement of the genetic profession in adoption of a harm minimization agenda. This study reveals the existence of a powerful lobby representing the genetic testing industry that is willing to exert influence on ‘evidence-based’ policies.Impact of a patient-navigator program on colonoscopy completion rates in patients referred for colorectal cancer screening.
Colonoscopy has emerged as the most common test ordered for colorectal cancer screening in the United States, with approximately 50% of patients having screening colonoscopies each year. Colonoscopy is a more expensive test than fecal immunochemical testing (FIT), yet completion rates have remained low. A patient-navigator program aimed at increasing rates of completion was developed and implemented at an academic colorectal cancer screening clinic.
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