Long-term negative impact on quality of life in patients with successfully treated Cushing's disease
✍ Scribed by Adrian H. Heald; Sandip Ghosh; Stephanie Bray; Christine Gibson; Simon G Anderson; Helen Buckler; Helen L. Fowler
- Book ID
- 108703023
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 197 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0300-0664
No coin nor oath required. For personal study only.
✦ Synopsis
Summary
objective A cohort of pituitary tumour patients, who had undergone definitive treatment within a 15‐year period at a single neuroscience centre, were investigated as to whether there were differences in psychological well‐being and psychosocial functioning, dependent on endocrine pathology and treatment variables.
design A detailed assessment of 114 patients with benign pituitary tumours in relation to primary diagnosis and mode of treatment was carried out. Psychological rating scales used were: the Hospital Anxiety and Depression Scale − UK version (HADS‐UK), the World Health Organization Quality of Life Scale − abbreviated version (WHOQOL‐BREF), General Health Questionnaire 28 (GHQ‐28), the Functional Assessment of Cancer Therapy (FACT) and the Social Adjustment Scale − modified (SAS1 and SAS2; the former completed by the patient and the latter by another person who knows the patient well). All Cushing's patients were biochemically cured as defined by a normal 24‐h urine free cortisol excretion within the previous 6 months.
results Patients with treated Cushing's disease had significantly impaired psychological well‐being and psychosocial functioning across all tested domains compared with all other pituitary tumours, where scores were similar. When participants with Cushing's disease were excluded, patients who had undergone transfrontal surgery scored significantly higher on GHQ and HADS ratings than transsphenoidally treated patients.
conclusion Cushing's disease even when biochemically stable has long‐term adverse effects on mood and social functioning. We hypothesize that this may be related to irreversible changes in central neural function. Further studies are necessary to define the precise pathways involved.
📜 SIMILAR VOLUMES
## Abstract The objective of this study was to evaluate possible relationships between quality of life (QoL) of Polish patients with long‐lasting Parkinson's disease and various demographic and clinical factors. The study comprised 141 patients of Movement Disorders outpatient clinics in Warsaw and
## Abstract Health‐related quality of life (HRQoL) in Wilson's disease (WD) has not been extensively studied. Therefore, the purpose of this cross‐sectional study was to identify clinical and demographic factors influencing HRQoL in 60 treated, clinically stable patients with WD using a generic que