BMC Psychiatry | |
Early reduction in painful physical symptoms is associated with improvements in long-term depression outcomes in patients treated with duloxetine | |
Research Article | |
Harald Weigmann1  Deborah Quail2  Edith Schneider3  Hans-Peter Hundemer3  Thomas Wagner3  Michael Linden4  | |
[1] Boehringer Ingelheim Pharma GmbH & Co KG, A Medizinische Wissenschaft, Ingelheim am Rhein, Germany;Dept European Medical Information Sciences, Eli Lilly and Co Ltd, Windlesham, UK;Lilly Deutschland GmbH, Medical Department, Bad Homburg, Germany;Research Group Psychosomatic Rehabilitation at the Charité, University Medicine Berlin and the Rehabilitation Centre Seehof, Teltow/Berlin, Germany; | |
关键词: Depression; painful physical symptoms; non-interventional study; duloxetine; | |
DOI : 10.1186/1471-244X-11-150 | |
received in 2011-03-08, accepted in 2011-09-20, 发布年份 2011 | |
来源: Springer | |
【 摘 要 】
BackgroundTo investigate the association of the change of painful physical symptoms (PPS) after 4 weeks, with the 6-month treatment outcomes of depressive symptoms in patients treated with duloxetine in clinical practice.MethodsMulticenter, prospective, 6-month, non-interventional study in adult outpatients with a depressive episode and starting treatment with duloxetine. Depression severity was assessed by the clinician (Inventory for Depressive Symptomatology [IDS-C]) and patient (Kurz-Skala Stimmung/Aktivierung [KUSTA]). Somatic symptoms and PPS were assessed using the patient-rated Somatic Symptom Inventory (SSI) and visual analog scales (VAS) for pain items. Association of change in PPS with outcomes of depressive symptoms was analyzed based on mean KUSTA scores (mean of items mood, activity, tension/relaxation, sleep) and achievement of a 50% reduction in the total IDS-C score after 6 months using linear and logistic regression models, respectively.ResultsOf the 4,517 patients enrolled (mean age: 52.2 years, 71.8% female), 3,320 patients (73.5%) completed the study. 80% of the patients had moderate to severe overall pain (VAS > 30 mm) at baseline. A 50% VAS overall pain reduction after 4 weeks was associated with a 13.32 points higher mean KUSTA score after 6 months, and a 50% pain reduction after 2 weeks with a 6.33 points improvement. No unexpected safety signals were detected in this naturalistic study.ConclusionPain reduction after 2 and 4 weeks can be used to estimate outcomes of long-term treatment with duloxetine. PPS associated with depression have a potential role in predicting remission of depressive symptoms in clinical practice.
【 授权许可】
CC BY
© Schneider et al; licensee BioMed Central Ltd. 2011
【 预 览 】
Files | Size | Format | View |
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RO202311096268898ZK.pdf | 465KB | download |
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