Lamotrigine add-on therapy to venlafaxine treatment in adolescent-onset bipolar II disorder: a case report covering an 8-month observation period
dc.contributor.author | Bildik, T. | |
dc.contributor.author | Tamar, M. | |
dc.contributor.author | Korkmaz, S. | |
dc.contributor.author | Gokcen, S. | |
dc.contributor.author | Ozbaran, B. | |
dc.contributor.author | Erermis, S. | |
dc.contributor.author | Aydin, C. | |
dc.date.accessioned | 2019-10-27T19:18:48Z | |
dc.date.available | 2019-10-27T19:18:48Z | |
dc.date.issued | 2006 | |
dc.department | Ege Üniversitesi | en_US |
dc.description.abstract | Observations made with lamotrigine add-on therapy with venlafaxine in this case give clues for some aspects of its use in adolescent-onset bipolar 11 disorder. An 18-year-old adolescent boy with a 3-year history of bipolar 11 disorder had experienced 2 episodes of hypomania and 4 episodes of major depression. He had been depressed for the last 3 months and had taken olanzapine 5 mg daily for over 6 weeks as mood stabilizer but was still depressed at referral. Other aspects of the patient history included anhedonia, psychomotor retardation, poor concentration, a feeling of hopelessness, hypersonmia, overeating, weight gain, low energy and a refusal to attend school. Parents reported that his symptoms had recently become more severe. His medicine was replaced by venlafaxine, which has a more rapid onset of action and is often used in bipolar depression, especially in patients with atypical depression. Since the clinical response at 6 weeks was only partial, lamotrigine was added to this regimen. The patient responded to lamotrigine after 3 weeks of treatment while on a dose of 50 mg/day. After 6 weeks of treatment, whilst on a dose of 75 mg/day, his symptoms remitted completely with no evidence of any adverse effects. At the time of publication of this article, the patient had remained euthymic for a total of 8 months. The present report shows that lamotrigine add-on therapy with venlafaxine facilitated clinical remission and that this combination is well tolerated. | en_US |
dc.identifier.endpage | 206 | en_US |
dc.identifier.issn | 0946-1965 | |
dc.identifier.issue | 5 | en_US |
dc.identifier.pmid | 16724574 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 198 | en_US |
dc.identifier.uri | https://hdl.handle.net/11454/38645 | |
dc.identifier.volume | 44 | en_US |
dc.identifier.wos | WOS:000237829200002 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Dustri-Verlag Dr Karl Feistle | en_US |
dc.relation.ispartof | International Journal of Clinical Pharmacology and Therapeutics | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | lamotrigine | en_US |
dc.subject | bipolar II disorder | en_US |
dc.subject | adolescent | en_US |
dc.subject | venlafaxine | en_US |
dc.title | Lamotrigine add-on therapy to venlafaxine treatment in adolescent-onset bipolar II disorder: a case report covering an 8-month observation period | en_US |
dc.type | Article | en_US |