Key result
Mandatory sickle cell trait screening of collegiate athletes raises ethical concerns regarding stigmatization, and should be improved with universal precautions and genetic counseling.
Mandatory sickle cell trait screening in NCAA athletes raises ethical concerns regarding stigmatization, suggesting a shift towards universal precautions and genetic counseling.
May prompt policy review of mandatory SCT screening in athletes; leaves open optimal integration of precautions with counseling.
The National Collegiate Athletic Association (NCAA) requires all student-athletes have their sickle cell trait (SCT) status confirmed prior to athletic participation. The NCAA approved the screening program in 2010 for institutions participating in Division I athletics and extended it in subsequent years to institutions at Division II and III levels. Ethical concerns about the controversial policy focus on its mandatory nature and potential impact on student-athletes, particularly through stigmatization of and discrimination against those with SCT. Organizations, such as the American Society of Hematology (ASH), oppose the imposition of SCT testing and instead recommend universal precautions that would protect the entire student-athlete population without revealing student-athletes' SCT statuses. This paper discusses these issues and offers recommendations, including genetic counseling, which would improve the current SCT screening program. It argues that implementation of universal precautions would ensure that the most ethically sound practices are afforded to every student-athlete.
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Ferrari et al. (2015) conducted a review in Sickle cell trait. Mandatory sickle cell trait screening vs. Universal precautions was evaluated. Mandatory sickle cell trait screening of collegiate athletes raises ethical concerns regarding stigmatization, and should be improved with universal precautions and genetic counseling.
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