Is a cut-off score a suitable measure of treatment outcome in short-term trials in depression? A methodological meta-analysis
| Autor: | A. Delini-Stula, Jules Angst, Hans H. Stassen, M. Stabl |
|---|---|
| Rok vydání: | 1993 |
| Předmět: |
medicine.medical_specialty
business.industry Treatment outcome Hamilton Rating Scale for Depression Placebo Psychiatry and Mental health Neurology Internal medicine Meta-analysis Moclobemide Hamd medicine Pharmacology (medical) Neurology (clinical) Cut-off business Psychiatry Depression (differential diagnoses) medicine.drug |
| Zdroj: | Human Psychopharmacology: Clinical and Experimental. 8:311-317 |
| ISSN: | 1099-1077 0885-6222 |
| DOI: | 10.1002/hup.470080503 |
| Popis: | In a meta-analysis of short-term (four weeks) trials of antidepressants, two response criteria were compared separately for low- ( 28) scores on the 17-item version of the Hamilton Rating Scale for Depression: (HAMD-17): (a) 50 per cent reduction of the baseline HAMD-17 score and (b) 50 per cent reduction plus a cut-off HAMD score of < 10. The material consisted of the data pool of comparative trials with moclobemide provided by Hoffmann-La Roche, Basle. The analysis showed that, on average, the HAMD-17 scores decrease uniformly in all groups independently of the initial severity of depression. The percentage of score differences between high-score, medium-score and low-score groups remained virtually unchanged over the whole observation period. Furthermore, the criterion combining a 50 per cent decrease with a cut-off score of < 10 gives clear disadvantage for high-scores to become responders since cases of severe depression require a much longer time to reach the threshold of 10 than do milder or moderately severe cases. As to the question of evaluating differences between placebo and drugs, our analyses provided evidence that the simple criterion of 50 per cent reduction of baseline HAMD-17 score is better suited to discriminate between placebo and drug responders in acute trials. |
| Databáze: | OpenAIRE |
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