Survival in adults with sickle cell disease in a high-income setting

Author:

Gardner Kate12,Douiri Abdel345,Drasar Emma12,Allman Marlene2,Mwirigi Anne2,Awogbade Moji2,Thein Swee Lay12

Affiliation:

1. Molecular Haematology, Division of Cancer Studies, King’s College London, London, United Kingdom;

2. Department of Haematological Medicine, King’s College Hospital National Health Service (NHS) Foundation Trust, London, United Kingdom;

3. Division of Health and Social Care, King’s College London, London, United Kingdom;

4. National Institute for Health Research (NIHR) Biomedical Research Centre, Guy’s and St. Thomas’ NHS Trust and King’s College London, London, United Kingdom; and

5. NIHR Collaboration for Leadership in Applied Health Research and Care, King’s College Hospital NHS Foundation Trust, London, United Kingdom

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference14 articles.

1. The hereditary haemoglobinopathies. Sickle cell disease and allied syndromes. In: The Haemolytic Anaemias: Congenital and Acquired Part I—The Congenital Anaemias.;Dacie,1960

2. Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London.;Telfer;Haematologica,2007

3. Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines.;Couque;Br J Haematol,2016

4. Improved survival of children and adolescents with sickle cell disease.;Quinn;Blood,2010

5. Mortality in sickle cell disease. Life expectancy and risk factors for early death.;Platt;N Engl J Med,1994

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