Specifying sickle cell disease interventions: a study protocol of the Sickle Cell Disease Implementation Consortium (SCDIC)-Reference-Cited by-同舟云学术

Specifying sickle cell disease interventions: a study protocol of the Sickle Cell Disease Implementation Consortium (SCDIC)

Published:2018-06-27 Issue:1 Volume:18 Page:
ISSN:1472-6963
Container-title:BMC Health Services Research
language:en
Short-container-title:BMC Health Serv Res

Author:

Baumann Ana A.^ORCID, ,Belle Steven H.,James Aimee,King Allison A.

Funder

National Heart, Lung, and Blood Institute

Publisher

Springer Science and Business Media LLC

Subject

Health Policy

Link

http://link.springer.com/content/pdf/10.1186/s12913-018-3297-1.pdf

Reference58 articles.

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2. Hassell KL. Population estimates of sickle cell disease in the U.S. Am J Prev Med. 2010;38(4):S512–21. https://doi.org/10.1016/j.amepre.2009.12.022 .

3. Adams RJ, McKie VC, Hsu L, et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial doppler ultrasonography. N Engl J Med. 1998;339(1):5–11. https://doi.org/10.1056/NEJM199807023390102 .

4. The Henry J Kaiser Family Foundation. State health facts - life expectancy at birth (in years), by race/ethnicity 2015. http://kff.org/other/state-indicator/life-expectancy-by-re/ . Accessed 19 Mar 2018.

5. Charache S, Terrin ML, Moore RD, et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. N Engl J Med. 1995;332(20):1317–22. https://doi.org/10.1056/NEJM199505183322001 .

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