Rasmus Wentzer Licht
Aalborg University
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Publication
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American Journal of Psychiatry | 2013
Isabella Pacchiarotti; David J. Bond; Ross J. Baldessarini; Willem A. Nolen; Heinz Grunze; Rasmus Wentzer Licht; Robert M. Post; Michael Berk; Guy M. Goodwin; Gary S. Sachs; Leonardo Tondo; Robert L. Findling; Eric A. Youngstrom; Mauricio Tohen; Juan Undurraga; Ana González-Pinto; Joseph F. Goldberg; Ayşegül Yildiz; Lori L. Altshuler; Joseph R. Calabrese; Philip B. Mitchell; Michael E. Thase; Athanasios Koukopoulos; Francesc Colom; Mark A. Frye; Gin S. Malhi; Konstantinos N. Fountoulakis; Gustavo H. Vázquez; Roy H. Perlis; Terence A. Ketter
OBJECTIVE The risk-benefit profile of antidepressant medications in bipolar disorder is controversial. When conclusive evidence is lacking, expert consensus can guide treatment decisions. The International Society for Bipolar Disorders (ISBD) convened a task force to seek consensus recommendations on the use of antidepressants in bipolar disorders. METHOD An expert task force iteratively developed consensus through serial consensus-based revisions using the Delphi method. Initial survey items were based on systematic review of the literature. Subsequent surveys included new or reworded items and items that needed to be rerated. This process resulted in the final ISBD Task Force clinical recommendations on antidepressant use in bipolar disorder. RESULTS There is striking incongruity between the wide use of and the weak evidence base for the efficacy and safety of antidepressant drugs in bipolar disorder. Few well-designed, long-term trials of prophylactic benefits have been conducted, and there is insufficient evidence for treatment benefits with antidepressants combined with mood stabilizers. A major concern is the risk for mood switch to hypomania, mania, and mixed states. Integrating the evidence and the experience of the task force members, a consensus was reached on 12 statements on the use of antidepressants in bipolar disorder. CONCLUSIONS Because of limited data, the task force could not make broad statements endorsing antidepressant use but acknowledged that individual bipolar patients may benefit from antidepressants. Regarding safety, serotonin reuptake inhibitors and bupropion may have lower rates of manic switch than tricyclic and tetracyclic antidepressants and norepinephrine-serotonin reuptake inhibitors. The frequency and severity of antidepressant-associated mood elevations appear to be greater in bipolar I than bipolar II disorder. Hence, in bipolar I patients antidepressants should be prescribed only as an adjunct to mood-stabilizing medications.
World Journal of Biological Psychiatry | 2009
Heinz Grunze; Eduard Vieta; G M Goodwin; Charles L. Bowden; Rasmus Wentzer Licht; Hans-Jürgen Möller; Siegfried Kasper
These updated guidelines are based on a first edition that was published in 2003, and have been edited and updated with the available scientific evidence until end of 2008. Their purpose is to supply a systematic overview of all scientific evidence pertaining to the treatment of acute mania in adults. The data used for these guidelines have been extracted from a MEDLINE and EMBASE search, from the clinical trial database clinicaltrials.gov, from recent proceedings of key conferences, and from various national and international treatment guidelines. Their scientific rigor was categorised into six levels of evidence (A–F). As these guidelines are intended for clinical use, the scientific evidence was finally asigned different grades of recommendation to ensure practicability.
World Journal of Biological Psychiatry | 2010
Heinz Grunze; Eduard Vieta; G M Goodwin; Charles L. Bowden; Rasmus Wentzer Licht; Hans-Jürgen Möller; Siegfried Kasper
Abstract Objectives. These guidelines are based on a first edition that was published in 2002, and have been edited and updated with the available scientific evidence until September 2009. Their purpose is to supply a systematic overview of all scientific evidence pertaining to the treatment of acute bipolar depression in adults. Methods. The data used for these guidelines have been extracted from a MEDLINE and EMBASE search, from the clinical trial database clinicaltrials.gov, from recent proceedings of key conferences, and from various national and international treatment guidelines. Their scientific rigor was categorised into six levels of evidence (A–F). As these guidelines are intended for clinical use, the scientific evidence was finally assigned different grades of recommendation to ensure practicability. Results. We identified 10 pharmacological monotherapies or combination treatments with at least limited positive evidence for efficacy in bipolar depression, several of them still experimental and backed up only by a single study. Only one medication was considered to be sufficiently studied to merit full positive evidence. Conclusions. Although major advances have been made since the first edition of this guideline in 2002, there are many areas which still need more intense research to optimize treatment. The majority of treatment recommendations is still based on limited data and leaves considerable areas of uncertainty.
World Journal of Biological Psychiatry | 2013
Heinz Grunze; Eduard Vieta; Guy M. Goodwin; Charles L. Bowden; Rasmus Wentzer Licht; Hans-Jürgen Möller; Siegfried Kasper
Abstract Objectives. These guidelines are based on a first edition that was published in 2004, and have been edited and updated with the available scientific evidence up to October 2012. Their purpose is to supply a systematic overview of all scientific evidence pertaining to the long-term treatment of bipolar disorder in adults. Methods. Material used for these guidelines are based on a systematic literature search using various data bases. Their scientific rigor was categorised into six levels of evidence (A–F) and different grades of recommendation to ensure practicability were assigned. Results. Maintenance trial designs are complex and changed fundamentally over time; thus, it is not possible to give an overall recommendation for long-term treatment. Different scenarios have to be examined separately: Prevention of mania, depression, or an episode of any polarity, both in acute responders and in patients treated de novo. Treatment might differ in Bipolar II patients or Rapid cyclers, as well as in special subpopulations. We identified several medications preventive against new manic episodes, whereas the current state of research into the prevention of new depressive episodes is less satisfactory. Lithium continues to be the substance with the broadest base of evidence across treatment scenarios. Conclusions. Although major advances have been made since the first edition of this guideline in 2004, there are still areas of uncertainty, especially the prevention of depressive episodes and optimal long-term treatment of Bipolar II patients.
World Journal of Biological Psychiatry | 2002
Heinz Grunze; Siegfried Kasper; Guy M. Goodwin; Charles L. Bowden; David S. Baldwin; Rasmus Wentzer Licht; Eduard Vieta; Hans-Jürgen Möller
Summary: These practice guidelines for the biological, mainly pharmacological treatment of bipolar depression were developed by an international task force of the World Federation of Societies of Biological Psychiatry (WFSBP). Their purpose is to supply a systematic overview of all scientific evidence pertaining to the treatment of bipolar depression. The data used for these guidelines have been extracted from a MEDLINE and EMBASE search, and from recent proceedings of key conferences and various national and international treatment guidelines. Their scientific rigor was categorised into four levels of evidence (A-D). As these guidelines are intended for clinical use, the scientific evidence was not only graded, but also commented on by the experts of the task force to ensure practicability.
World Journal of Biological Psychiatry | 2003
Heinz Grunze; Siegfried Kasper; Guy M. Goodwin; Charles L. Bowden; David S. Baldwin; Rasmus Wentzer Licht; Eduard Vieta; Hans Jürgen Möller
Identical to the preceding guidelines of this series, these practice guidelines for the biological, mainly pharmacological treatment of acute bipolar mania were developed by an international Task Force of the World Federation of Societies of Biological Psychiatry (WFSBP). Their purpose is to supply a systematic overview of all scientific evidence pertaining to the treatment of acute mania. The data used for these guidelines have been extracted from a MEDLINE and EMBASE search, from recent proceedings of key conferences, and from various national and international treatment guidelines. Their scientific rigor was categorised into four levels of evidence (A-D). As these guidelines are intended for clinical use, the scientific evidence was finally not only graded, but has also been commented by the experts of the task force to ensure practicability.
World Journal of Biological Psychiatry | 2004
Heinz Grunze; Siegfried Kasper; Guy M. Goodwin; Charles L. Bowden; Hans Jürgen Möller; Hagop S. Akiskal; Hervé Allain; José L. Ayuso-Gutiérrez; David S. Baldwin; Per Bech; Otto Benkert; Michael Berk; István Bitter; Marc Bourgeois; Graham D. Burrows; Joseph R. Calabrese; Giovanni Cassano; Marcelo Cetkovich-Bakmas; John C. Cookson; Delcir da Costa; Mihai George; Frank Goodwin; Gerado Heinze; Teruhiko Higuchi; Robert M. A. Hirschfeld; Cyril Höschl; Edith Holsboer-Trachsler; Kay Jamison; Cornelius Katona; Martin B. Keller
Summary As with the two preceding guidelines of this series, these practice guidelines for the pharmacological maintenance treatment of bipolar disorder were developed by an international task force of the World Federation of Societies of Biological Psychiatry (WFSBP). Their purpose is to supply a systematic overview of all scientific evidence relating to maintenance treatment. The data used for these guidelines were extracted from a MEDLINE and EMBASE search, from recent proceedings from key conferences and various national and international treatment guidelines. The scientific justification of support for particular treatments was categorised into four levels of evidence (A-D). As these guidelines are intended for clinical use, the scientific evidence was not only graded, but also reviewed by the experts of the task force to ensure practicality.
Therapeutic Drug Monitoring | 1998
Ole Vendelin Olesen; Rasmus Wentzer Licht; Erik Thomsen; Troels Bruun; Jens Emil Viftrup; Kristian Linnet
Steady state serum concentrations of risperidone and 9-hydroxyrisperidone (9-OH-risperidone), the active moiety, were measured in 42 patients. The concentration-to-dose ratios (C/D) varied by a factor of 20, from 1.8 to 36.8 (nmol/l)/(mg/24 hours), and 90% of the active moiety was constituted of 9-OH-risperidone. No correlation between the serum concentration of the active moiety and the side effects evaluated by the UKU Side Effect Scale was found. The absence of CYP2D6 (poor metabolizers) or the coadministration of drugs other than benzodiazepines increased the ratio between parent compound and metabolite but did not significantly influence the C/D of the total active moiety. A therapeutic range for serum risperidone has not been established, but 6 mg/day is considered the optimum dose for most patients. The authors found that in 90% of 22 patients administered 6 mg/day risperidone, the serum levels were within 50 to 150 nmol/l.
Acta Psychiatrica Scandinavica | 2008
Rasmus Wentzer Licht; H. Gijsman; Willem A. Nolen; Jules Angst
Objective: To address whether switch of depression into hypomania or mania or cycle acceleration in patients with bipolar disorder is caused by antidepressants or whether this phenomenon is attributable to the natural history of bipolar disorder itself.
Acta Psychiatrica Scandinavica | 2005
Rasmus Wentzer Licht; S. Qvitzau; P. Allerup; Per Bech
Objective: Evaluation of antidepressant drug efficacy requires adequate rating scales for measuring the severity of depression. However, to measure the illness severity by such a total score, the scale needs to fulfil criteria of unidimensionality. On this background, we aimed at comparing the unidimensionality of the Bech–Rafaelsen Melancholia Scale (MES) and the 17‐item Hamilton Depression Rating Scale (HAM‐D17).
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University of Texas Health Science Center at San Antonio
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