A Scoping Review of Social Determinants of Health and Pain Outcomes in Sickle Cell Disease.
Authors
Darby JE, Akpotu IC, Wi D, Ahmed S, Doorenbos AZ, Lofton S
Abstract
Sickle cell disease (SCD) is a hereditary blood disorder with chronic pain that affects over 100,000 people in the United States. Previous research suggests a complex interaction between SCD pain outcomes and social determinants of health (SDOH).
This website or its third-party tools use cookies, which are necessary to its functioning and required to achieve the purposes illustrated in the cookie policy. If you want to know more or withdraw your consent to all or some of the cookies, please refer to the IASP Privacy Policy. By closing this banner, you agree to the use of cookies.Agree