Read new SCD publications from CDC
Health scientists study information collected by the Sickle Cell Data Collection (SCDC) program. They often present their findings at scientific conferences and SCD partner meetings. They also publish their findings in peer-reviewed articles and reports. This information is used to improve SCD education, treatments, and policy. This week, we’re sharing some publications that highlight key findings resulting from the analyses of SCDC program data. Visit the SCDC publications page to view the references of all publications developed by the SCDC program.
2020
- Aluc A, Zhou M, Paulukonis ST, Snyder AB, Wong D, Hulihan MM. Using surveillance to determine the number of individuals with sickle cell disease in California and Georgia, 2005-2016. Ped Hem Onc. DOI: 10.1080/08880018.2020.1779886.
- Johnston EE, Adesina OO, Alvarez E, Amato H, Paulukonis S, Nichols A, Chamberlain LJ, Bhatia S. Acute Care Utilization at End of Life in Sickle Cell Disease: Highlighting the Need for a Palliative Approach. J Palliat Med. 2020 Jan;23(1):24-32.
- Kayle M, Valle J, Paulukonis S, Holl JL, Tanabe P, French DD, Garg R, Liem RI, Badawy SM, Treadwell MJ. Impact of Medicaid expansion on access and healthcare among individuals with sickle cell disease. Pediatr Blood Cancer. 2020 May;67(5):e28152.
2019
- Snyder AB, Zhou M, Theodore R, Quarmyne MO, Eckman J, Lane PA. Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease. Public Health Rep. 2019 May/Jun;134(3):274-281. doi: 10.1177/0033354919839072.
- Tang A, Branscomb J, Zhou M, Snyder A, Eckman J. Characterizing complication risk from multisite, intermittent transfusions for the treatment of sickle cell disease. Pediatr Blood Cancer. 2019 Oct;66(10):e27921.
Want to learn more about SCD? Visit our SCD website.
Next week, we will share information on the Sickle Cell Data Collection (SCDC) program.
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