Geographical Effects on Adult Sickle Cell Disease Treatments, Morbidity, and Mortality
A small percentage of patients with sickle cell disease (SCD) have experienced an increase in life span by 10 years, while others with the same disease continue to die prematurely. The purpose of the study was to evaluate whether or not regional location was a barrier to care for adults with SCD in...
| Main Author: | |
|---|---|
| Format: | Others |
| Language: | en |
| Published: |
ScholarWorks
2016
|
| Subjects: | |
| Online Access: | https://scholarworks.waldenu.edu/dissertations/2641 https://scholarworks.waldenu.edu/cgi/viewcontent.cgi?article=3744&context=dissertations |