Depression, disease severity, and sickle cell disease
| Autor: | J J, Wison Schaeffer, K M, Gil, M, Burchinal, K D, Kramer, K B, Nash, E, Orringer, D, Strayhorn |
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| Rok vydání: | 1999 |
| Předmět: |
Adult
Male Psychiatric Status Rating Scales Chi-Square Distribution Self Disclosure Psychometrics Depression Pain Anemia Sickle Cell Comorbidity Health Surveys Sensitivity and Specificity Severity of Illness Index Sampling Studies Sex Factors Socioeconomic Factors Risk Factors Odds Ratio Humans Regression Analysis Female Sex Distribution |
| Zdroj: | Journal of behavioral medicine. 22(2) |
| ISSN: | 0160-7715 |
| Popis: | The present study examined depressive symptomatology in 440 adults with sickle cell disease (SCD). Participants completed the Center for Epidemiologic Studies--Depression scale (CES-D) as part of their yearly routine visits to the Duke University--University of North Carolina Comprehensive Sickle Cell Center. They also completed questions regarding demographics, disease severity, pain, and health care use. Data analyses revealed that the percentage of patients with SCD exhibiting significant depressive symptomatology dropped from 43 to 18% when a more stringent cutoff was used on the CES-D, suggesting that future studies should determine the most valid cutoff score for identifying depression in patients with SCD. Gender and family income were positively and significantly associated with depressive symptomatology. Also, patients who reported more frequent painful episodes were more likely to report depressive symptoms. Implications for assessment and treatment of depression in adults with SCD are discussed. |
| Databáze: | OpenAIRE |
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