Improving Outcomes for Patients With Sickle Cell Disease in the United States-Reference-Cited by-同舟云学术

Improving Outcomes for Patients With Sickle Cell Disease in the United States

Published:2021-10-29 Issue:10 Volume:2 Page:e213467
ISSN:2689-0186
Container-title:JAMA Health Forum
language:en
Short-container-title:JAMA Health Forum

Author:

Kanter Julie¹,Meier Emily R.²,Hankins Jane S.³,Paulukonis Susan T.⁴,Snyder Angela B.⁵

Affiliation:

1. Division of Hematology and Oncology, University of Alabama Birmingham, Birmingham

2. Indiana Hemophilia and Thrombosis Center, Indianapolis

3. Department of Hematology, St. Jude Children’s Research Hospital, Memphis, Tennessee

4. Tracking California Program, Public Health Institute, Richmond, California

5. Georgia Health Policy Center and the Department of Public Management and Policy, Andrew Young School of Policy Studies, Georgia State University, Atlanta

Publisher

American Medical Association (AMA)

Subject

General Earth and Planetary Sciences,General Environmental Science

Link

https://jamanetwork.com/journals/jama-health-forum/articlepdf/2785579/kanter_2021_sc_210006_1635438772.74641.pdf

Reference50 articles.

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2. Decreased median survival of adults with sickle cell disease after adjusting for left truncation bias: a pooled analysis.;DeBaun;Blood,2019

3. Risk factors for mortality in adult patients with sickle cell disease: a meta-analysis of studies in North America and Europe.;Maitra;Haematologica,2017

4. Definitions of the phenotypic manifestations of sickle cell disease.;Ballas;Am J Hematol,2010

5. The risk of acute events among patients with sickle cell disease in relation to early or late initiation of care at a specialist center: evidence from a retrospective cohort study.;Rankine-Mullings;BMC Pediatr,2020

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