Cargando…
Development and validation of the sickle cell stress scale‐adult
Disease‐specific stress can partly explain Sickle Cell Disease (SCD) healthcare utilization. We developed and validated two measures of adult SCD‐specific stress for research and clinical care. A large cohort of adults with SCD completed both the 3‐item Likert‐scale adapted from a previous disease s...
Autores principales: | Smith, Wally R., McClish, Donna K., Bovbjerg, Viktor E., Singh, Harjot K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531901/ https://www.ncbi.nlm.nih.gov/pubmed/35585659 http://dx.doi.org/10.1111/ejh.13789 |
Ejemplares similares
-
Comorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES Project
por: McClish, Donna K., et al.
Publicado: (2017) -
Health related quality of life in sickle cell patients: The PiSCES project
por: McClish, Donna K, et al.
Publicado: (2005) -
Intraindividual pain variability and phenotypes of pain in sickle cell disease: a secondary analysis from the Pain in Sickle Cell Epidemiology Study
por: Bakshi, Nitya, et al.
Publicado: (2022) -
The prevalence of abnormal leukocyte count, and its predisposing factors, in patients with sickle cell disease in Saudi Arabia
por: Ahmed, Anwar E, et al.
Publicado: (2017) -
Health-related quality of life in patients with sickle cell disease in Saudi Arabia
por: Ahmed, Anwar E., et al.
Publicado: (2015)