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Screening for sickle-cell trait in the emergency department
S W Wright1, M H Zeldin, K Wrenn
1Department of Emergency Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee.
Journal of General Internal Medicine
|August 1, 1994
Summary
Most young Black adults in the ED know about sickle-cell anemia but not their own sickle-cell trait status. Emergency departments should screen at-risk patients for sickle-cell trait.
Area of Science:
- Medical Genetics
- Public Health
- Emergency Medicine
Background:
- Sickle-cell anemia is a prevalent genetic blood disorder, particularly in individuals of African descent.
- Awareness of sickle-cell anemia and personal trait status is crucial for reproductive planning and disease management.
Purpose of the Study:
- To assess awareness of sickle-cell anemia among young Black adults in an emergency department (ED).
- To determine the proportion of these patients who know their sickle-cell trait status.
Main Methods:
- Interviews were conducted with 147 Black patients in an urban university hospital ED.
- Participants were assessed for knowledge of sickle-cell anemia and their own trait status.
- Sickle-cell trait screening was offered to all participants.
Main Results:
- 98% of patients had heard of sickle-cell anemia, and 73% recognized it as genetic.
- Only 31% knew their own sickle-cell trait status.
- Women were more likely than men to know their status; 4% tested positive for the trait.
Conclusions:
- While awareness of sickle-cell anemia is high among young Black adults, knowledge of personal trait status is low.
- ED physicians should inquire about and offer sickle-cell trait screening or referral for at-risk patients.
- Improved primary care access is needed to enhance routine screening and genetic counseling.
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