Caga, J and Ramsey, E and Hogden, A and Mioshi, E and Kiernan, MC, A longer diagnostic interval is a risk for depression in amyotrophic lateral sclerosis, Palliative and Supportive Care, 13 pp. 1019-1024. ISSN 1478-9523 (2015) [Refereed Article]
Copyright Cambridge University Press, 2014
Method: Structured medical and psychiatric history questionnaires and a validated depression scale (Depression, Anxiety, Stress Scale–21) were completed by 27 ALS patients (60% female; 59% limb onset; age 65.11±SE 2.21) prior to their initial review at a multidisciplinary clinic. Physical function was assessed with the Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS–R).
Results: At the time of initial assessment, 44% of patients had a previous psychiatric history, although the majority (62%) reported no symptoms of depression. The mean ALSFRS–R score was 37.78±SE 1.22, with an average diagnostic interval of 16.04±SE 2.39 months. Logistic regression analysis revealed that the length of the diagnostic interval alone predicted depressive symptoms (x2 (3, n = 26) = 9.21, Odds Ratio (OR) = 1.12, p , 0.05.
Significance of Results: The illness experiences of ALS patients rather than established mental health risk factors influence the manifestation of depressive symptoms in the early stages of the disease, with clinical implications for the assessment and treatment of psychological morbidity. Patients with lengthy diagnostic intervals may be prime targets for psychological assessment and intervention, especially in the absence of ALS-specific tests and biomarkers.
|Item Type:||Refereed Article|
|Keywords:||depression, risk factors, diagnostic interval, grief|
|Research Division:||Medical and Health Sciences|
|Research Field:||Neurology and Neuromuscular Diseases|
|Objective Group:||Health and Support Services|
|Objective Field:||Palliative Care|
|UTAS Author:||Hogden, A (Dr Anne Hogden)|
|Deposited By:||Australian Institute of Health Service Management|
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