Long-term efficacy and safety of lamotrigine for all types of bipolar disorder

Yoshinori Watanabe,1,2 Seiji Hongo2 1Himorogi Psychiatric Institute, Tokyo, 2Nanko Clinic of Psychiatry, Shirakawa city, Fukushima, Japan Background: We investigated whether the long-term efficacy and safety of lamotrigine (LTG) for bipolar disorder (BP) differs between disease types (BP-I, BP-II,...

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Autores principales: Watanabe Y, Hongo S
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Publicado: Dove Medical Press 2017
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spelling oai:doaj.org-article:42823fff5f74466fa131bfdc537654dc2021-12-02T02:32:17ZLong-term efficacy and safety of lamotrigine for all types of bipolar disorder1178-2021https://doaj.org/article/42823fff5f74466fa131bfdc537654dc2017-03-01T00:00:00Zhttps://www.dovepress.com/long-term-efficacy-and-safety-of-lamotrigine-for-all-types-of-bipolar--peer-reviewed-article-NDThttps://doaj.org/toc/1178-2021Yoshinori Watanabe,1,2 Seiji Hongo2 1Himorogi Psychiatric Institute, Tokyo, 2Nanko Clinic of Psychiatry, Shirakawa city, Fukushima, Japan Background: We investigated whether the long-term efficacy and safety of lamotrigine (LTG) for bipolar disorder (BP) differs between disease types (BP-I, BP-II, or BP not otherwise specified [BP-NOS]), and the efficacy of the concomitant use of antidepressants (ADs).Methods: For >1 year, we observed 445 outpatients with BP (diagnosed by DSM-IV criteria) who initiated LTG treatment between July 1 and October 31, 2011, using the Himorogi Self-rating Depression (HSDS) and Anxiety Scales and the Clinical Global Impression-Improvement scale and also recorded adverse events.Results: Treatment efficacy was observed at week 4, with the improved HSDS scores sustained until week 52 for all types of BP; 50% of the patients with any type of BP could be treated with LTG for 1 year, whereas ~40% could be treated for >1.5 years. However, 25% of the patients were withdrawn within the first 4 weeks. The overall incidence of adverse events was 22.9% (104/455): 34.1% (14/41) for BP-I, 22.7% (15/66) for BP-II, and 22.2% (75/338) for BP-NOS. The most common adverse event was skin rash: 22.0% for BP-I, 16.7% for BP-II, and 12.1% for BP-NOS.Limitations: There was no control group. Data were collected retrospectively.Conclusion: With careful and adequate titration, long-term treatment with LTG is possible for any type of BP, with BP-NOS patients, the largest population in clinical practice, responding particularly well. Symptoms can improve with or without ADs. Large-scale prospective studies of the efficacy of ADs in bipolar treatment are warranted. Keywords: lamotrigine, bipolar disorder, long-term efficacy, antidepressant, skin rash, anxietyWatanabe YHongo SDove Medical Pressarticlelamotriginebipolar disorderlong-term efficacyantidepressantskin rashanxietyNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol Volume 13, Pp 843-854 (2017)
institution DOAJ
collection DOAJ
language EN
topic lamotrigine
bipolar disorder
long-term efficacy
antidepressant
skin rash
anxiety
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
spellingShingle lamotrigine
bipolar disorder
long-term efficacy
antidepressant
skin rash
anxiety
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
Watanabe Y
Hongo S
Long-term efficacy and safety of lamotrigine for all types of bipolar disorder
description Yoshinori Watanabe,1,2 Seiji Hongo2 1Himorogi Psychiatric Institute, Tokyo, 2Nanko Clinic of Psychiatry, Shirakawa city, Fukushima, Japan Background: We investigated whether the long-term efficacy and safety of lamotrigine (LTG) for bipolar disorder (BP) differs between disease types (BP-I, BP-II, or BP not otherwise specified [BP-NOS]), and the efficacy of the concomitant use of antidepressants (ADs).Methods: For >1 year, we observed 445 outpatients with BP (diagnosed by DSM-IV criteria) who initiated LTG treatment between July 1 and October 31, 2011, using the Himorogi Self-rating Depression (HSDS) and Anxiety Scales and the Clinical Global Impression-Improvement scale and also recorded adverse events.Results: Treatment efficacy was observed at week 4, with the improved HSDS scores sustained until week 52 for all types of BP; 50% of the patients with any type of BP could be treated with LTG for 1 year, whereas ~40% could be treated for >1.5 years. However, 25% of the patients were withdrawn within the first 4 weeks. The overall incidence of adverse events was 22.9% (104/455): 34.1% (14/41) for BP-I, 22.7% (15/66) for BP-II, and 22.2% (75/338) for BP-NOS. The most common adverse event was skin rash: 22.0% for BP-I, 16.7% for BP-II, and 12.1% for BP-NOS.Limitations: There was no control group. Data were collected retrospectively.Conclusion: With careful and adequate titration, long-term treatment with LTG is possible for any type of BP, with BP-NOS patients, the largest population in clinical practice, responding particularly well. Symptoms can improve with or without ADs. Large-scale prospective studies of the efficacy of ADs in bipolar treatment are warranted. Keywords: lamotrigine, bipolar disorder, long-term efficacy, antidepressant, skin rash, anxiety
format article
author Watanabe Y
Hongo S
author_facet Watanabe Y
Hongo S
author_sort Watanabe Y
title Long-term efficacy and safety of lamotrigine for all types of bipolar disorder
title_short Long-term efficacy and safety of lamotrigine for all types of bipolar disorder
title_full Long-term efficacy and safety of lamotrigine for all types of bipolar disorder
title_fullStr Long-term efficacy and safety of lamotrigine for all types of bipolar disorder
title_full_unstemmed Long-term efficacy and safety of lamotrigine for all types of bipolar disorder
title_sort long-term efficacy and safety of lamotrigine for all types of bipolar disorder
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/42823fff5f74466fa131bfdc537654dc
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