Inhaled steroids reduce pain and sVCAM levels in individuals with sickle cell disease: A triple-blind, randomized trial

Author:

Glassberg Jeffrey1,Minnitti Caterina2,Cromwell Caroline3,Cytryn Lawrence3,Kraus Thomas4,Skloot Gwen S.5,Connor Jason T.6,Rahman Adeeb H.7,Meurer William J.8

Affiliation:

1. Department of Emergency Medicine; Icahn School of Medicine at Mount Sinai; New York

2. Department of Oncology; Montefiore Medical Center; Bronx New York

3. Department of Hematology and Oncology; Icahn School of Medicine at Mount Sinai Beth Israel; New York

4. Center for Therapeutic Antibody Development, Icahn School of Medicine at Mount Sinai; New York

5. Department of Pulmonary, Critical Care and Sleep Medicine; Icahn School of Medicine at Mount Sinai; New York

6. Berry Consultants; Austin Texas

7. Department of Genetics and Genomic Sciences; Icahn School of Medicine at Mount Sinai; New York

8. Departments of Emergency Medicine and Neurology; University of Michigan; Ann Arbor Michigan

Funder

National Heart Lung and Blood Institute

Publisher

Wiley

Subject

Hematology

Reference40 articles.

1. Mortality in children and adolescents with sickle cell disease. Cooperative Study of Sickle Cell Disease;Leikin;Pediatrics.,1989

2. Wheezing in children with sickle cell disease;Glassberg;Curr Opin Pediatr.,2014

3. [Complications of sickle-cell anemia];Petrov;Klin Med (Mosk).,1966

4. Pulmonary function abnormalities in childhood sickle cell disease;Pianosi;J Pediatr.,1993

5. Pulmonary manifestations of sickle cell disease;Siddiqui;Postgrad Med J.,2003

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