1. Knowledge and Awareness of Sickle Cell Trait Among Young African American Adults
- Author
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Tamara D. Warner, Christy M. Walcott, and Sayward E. Harrison
- Subjects
Male ,Health Knowledge, Attitudes, Practice ,medicine.medical_specialty ,Sickle Cell Trait ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Surveys and Questionnaires ,Health care ,Humans ,Medicine ,Medical history ,030212 general & internal medicine ,Misinformation ,Psychiatry ,Health implications ,General Nursing ,Reproductive health ,African american ,Internet ,Sickle cell trait ,030505 public health ,business.industry ,Awareness ,medicine.disease ,Black or African American ,Cross-Sectional Studies ,Trait ,Female ,Self Report ,0305 other medical science ,business ,Clinical psychology - Abstract
Sickle cell trait (SCT) places individuals at risk of passing an abnormal hemoglobin gene to biological children and is associated with rare but serious complications. The present study sought to examine knowledge of SCT and awareness of personal trait status among 258 young African American adults. Participants were surveyed regarding demographics, medical history, and sources of sickle cell information before completing a trait knowledge questionnaire. Overall, participants possessed significant misinformation about the condition. Women and those who had learned about sickle cell from families displayed higher levels of knowledge. Most participants were uncertain of personal trait status, and many did not wish to be informed of it. Health care providers should be alert that individuals with SCT may be unaware of their condition and potential reproductive and health implications. Screening and reporting procedures should be examined to ensure individuals have access to and control of this vital health information.
- Published
- 2016
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