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Self-report and clinician-rated measures of depression severity : can one replace the other? (CROSBI ID 202935)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Uher, R. ; Perlis, R.H. ; Placentino, A. ; Dernovšek, M.Z. ; Henigsberg, Neven ; Mors, O. ; Maier, W. ; McGuffin, P. ; Farmer, A. Self-report and clinician-rated measures of depression severity : can one replace the other? // Depression and anxiety, 29 (2012), 12; 1043-1049. doi: 10.1002/da.21993

Podaci o odgovornosti

Uher, R. ; Perlis, R.H. ; Placentino, A. ; Dernovšek, M.Z. ; Henigsberg, Neven ; Mors, O. ; Maier, W. ; McGuffin, P. ; Farmer, A.

engleski

Self-report and clinician-rated measures of depression severity : can one replace the other?

It has been suggested that clinician-rated scales and self-report questionnaires may be interchangeable in the measurement of depression severity, but it has not been tested whether clinically significant information is lost when assessment is restricted to either clinician-rated or self-report instruments. The aim of this study is to test whether self-report provides information relevant to short-term treatment outcomes that is not captured by clinician-rating and vice versa. METHODS: In genome-based drugs for depression (GENDEP), 811 patients with major depressive disorder treated with escitalopram or nortriptyline were assessed with the clinician-rated Montgomery-Åsberg Depression Rating Scale (MADRS), Hamilton Rating Scale for Depression (HRSD), and the self-report Beck Depression Inventory (BDI). In sequenced treatment alternatives to relieve depression (STAR*D), 4, 041 patients treated with citalopram were assessed with the clinician-rated and self-report versions of the Quick Inventory of Depressive Symptomatology (QIDS-C and QIDS-SR) in addition to HRSD. RESULTS: In GENDEP, baseline BDI significantly predicted outcome on MADRS/HRSD after adjusting for baseline MADRS/HRSD, explaining additional 3 to 4% of variation in the clinician-rated outcomes (both P < .001). Likewise, each clinician-rated scale significantly predicted outcome on BDI after adjusting for baseline BDI and explained additional 1% of variance in the self-reported outcome (both P < .001). The results were confirmed in STAR*D, where self-report and clinician-rated versions of the same instrument each uniquely contributed to the prediction of treatment outcome. CONCLUSIONS: Complete assessment of depression should include both clinician-rated scales and self-reported measures.

depression; assessment/diagnosis; clinical trials; antidepressants; treatment; mood disorders

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Podaci o izdanju

29 (12)

2012.

1043-1049

objavljeno

1091-4269

10.1002/da.21993

Povezanost rada

Kliničke medicinske znanosti

Poveznice
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