Depression, quality of life, and medical resource utilization in sickle cell disease-Reference-Cited by-同舟云学术

Depression, quality of life, and medical resource utilization in sickle cell disease

Published:2017-10-12 Issue:23 Volume:1 Page:1983-1992
ISSN:2473-9529
Container-title:Blood Advances
language:en
Short-container-title:

Author:

Adam Soheir S.¹²^ORCID,Flahiff Charlene M.¹,Kamble Shital³,Telen Marilyn J.¹,Reed Shelby D.¹³,De Castro Laura M.⁴

Affiliation:

1. Department of Medicine, Duke University, Durham, NC;

2. Hematology Department, King Abdulaziz University, Jeddah, Saudi Arabia;

3. Duke Clinical Research Institute, Durham, NC; and

4. Department of Medicine, University of Pittsburgh, Pittsburgh, PA

Abstract

Key Points Depression was found in 35.2% of adult SCD patients and was strongly associated with worse physical and mental quality-of-life outcomes. Total health care costs for adult SCD patients with depression were more than double those of SCD patients without depression.

Publisher

American Society of Hematology

Subject

Hematology

Link

http://ashpublications.org/bloodadvances/article-pdf/1/23/1983/878854/advances006940.pdf

Reference55 articles.

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4. Using chronic pain to predict depressive morbidity in the general population;Ohayon;Arch Gen Psychiatry,2003

5. Sickle cell disease: a stigmatizing condition that may lead to depression;Jenerette;Issues Ment Health Nurs,2005

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