Pramipexole in treatment-resistant depression: a 16-week naturalistic study
Autor: | Lorenzo Lattanzi, Annalisa Bassi, Marianna Abelli, Stefano Pini, A. Gemignani, Liliana Dell'Osso, Giovanni B. Cassano, Paola Rucci, Giulia Battistini, Patricia R. Houck, Paolo Cassano |
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Rok vydání: | 2002 |
Předmět: |
medicine.medical_specialty
Pramipexole medicine.medical_treatment medicine.disease Psychiatry and Mental health Electroconvulsive therapy Tolerability Internal medicine medicine Clinical Global Impression medicine.symptom Adverse effect Psychology Psychiatry Major depressive episode Treatment-resistant depression Biological Psychiatry Depression (differential diagnoses) medicine.drug |
Zdroj: | Bipolar Disorders. 4:307-314 |
ISSN: | 1398-5647 |
DOI: | 10.1034/j.1399-5618.2002.01171.x |
Popis: | Lattanzi L, Dell'Osso L, Cassano P, Pini S, Rucci P, Houck PR, Gemignani A, Battistini G, Bassi A, Abelli M, Cassano GB. Pramipexole in treatment-resistant depression: a 16-week naturalistic study. Bipolar Disord 2002: 4: 307–314. © Blackwell Munksgaard 2002 Objective: To assess the antidepressant efficacy and tolerability of adjunctive pramipexole, a D2–D3 dopamine agonist, in patients with drug-resistant depression. Methods: The study sample consisted of in-patients with major depressive episode, according to the DSM-IV, and drug resistance. Pramipexole was added to antidepressant treatment with TCA or SSRI, at increasing doses from 0.375 to 1.0 mg/day. Two independent response criteria were adopted: a >50% reduction of the Montgomery–Asberg Depressive Rating Scale (MADRS) total score and a score of 1 or 2 on the Clinical Global Impression scale (CGI-I) at endpoint. Side-effects were assessed by the Dosage Record Treatment Emergent Symptom Scale (DOTES). Results: Thirty-seven patients were enrolled. Of these, 16 had unipolar depression and 21 had bipolar depression. Six patients dropped out in the first week. Of the 31 patients included in the analyses, 19 completed the 16-week follow-up. Mean maximal dose of pramipexole was 0.95 mg/day. Mean scores on MADRS decreased from 33.3 ± 8.4 at baseline to 13.9 ± 11.5 at endpoint (p |
Databáze: | OpenAIRE |
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