Update on extended release quetiapine fumarate in schizophrenia and bipolar disorders.

作者: Nizar El-Khalili

DOI: 10.2147/NDT.S14369

关键词:

摘要: The atypical antipsychotic quetiapine fumarate is available both as an immediate release (IR) and extended (XR) formulation allowing flexibility of dosing for individual patients. Approved uses XR include the treatment schizophrenia (including maintenance therapy prevention relapse), bipolar disorder (manic depressive episodes), recurrence in patients with who respond to XR. This narrative review provides update on these indications. pharmacological profile quetiapine, including a moderate affinity dopamine D2 receptors higher serotonin 5-hydroxytryptophan (5-HT)2A receptors, may explain its broad efficacy low propensity extrapyramidal symptoms (EPS). has similar bioavailability but prolonged plasma levels compared IR formulation, less frequent (once-daily) dosing. Clinical studies have confirmed relieving acute during short-term trials, reducing risk relapse long-term studies. Direct switching from same dose did not reveal any loss or tolerability issues, conventional other antipsychotics (for reasons insufficient tolerability) also proved be beneficial generally well tolerated. In disorder, proven effective manic symptoms. Adverse events either are those associated most common being sedation, dry mouth, somnolence, dizziness, headache. EPS maintained formulation. Overall, evidence clinical trials suggests that well-tolerated option disorder.

参考文章(64)
Didier Meulien, Martin Brecher, Sherry Liu, David Brown, Jean-Pierre Lindenmayer, The efficacy and tolerability of once-daily extended release quetiapine fumarate in hospitalized patients with acute schizophrenia: a 6-week randomized, double-blind, placebo-controlled study. Psychopharmacology Bulletin. ,vol. 41, pp. 11- 35 ,(2008)
Didier Meulien, Sergiy Malyarov, Joseph Peuskens, Ola Svensson, Martin Brecher, Inger Persson, Frank Miller, Jitendra Trivedi, Prevention of schizophrenia relapse with extended release quetiapine fumarate dosed once daily: a randomized, placebo-controlled trial in clinically stable patients. Psychiatry (Edgmont (Pa. : Township)). ,vol. 4, pp. 34- 50 ,(2007)
Philip Seeman, Atypical Antipsychotics: Mechanism of Action: The Canadian Journal of Psychiatry. ,vol. 47, pp. 27- 38 ,(2002) , 10.1177/070674370204700106
C. Lindsay DeVane, Charles B. Nemeroff, Clinical pharmacokinetics of quetiapine: an atypical antipsychotic. Clinical Pharmacokinectics. ,vol. 40, pp. 509- 522 ,(2001) , 10.2165/00003088-200140070-00003
S Kapur, P Seeman, Antipsychotic agents differ in how fast they come off the dopamine D2 receptors. Implications for atypical antipsychotic action. Journal of Psychiatry & Neuroscience. ,vol. 25, pp. 161- 166 ,(2000)
Charles B. Nemeroff, Jeffrey Goldstein, Becky Kinkead, Quetiapine: preclinical studies, pharmacokinetics, drug interactions, and dosing. The Journal of Clinical Psychiatry. ,vol. 63, pp. 5- 11 ,(2002)
Richard Weisler, J. Mark Joyce, Lora McGill, Arthur Lazarus, Johan Szamosi, Hans Eriksson, , Extended release quetiapine fumarate monotherapy for major depressive disorder: results of a double-blind, randomized, placebo-controlled study. Cns Spectrums. ,vol. 14, pp. 299- 313 ,(2009) , 10.1017/S1092852900020307
Charles L. Bowden, Heinz Grunze, Jamie Mullen, Martin Brecher, Björn Paulsson, Martin Jones, Mårten Vågerö, K. Svensson, A Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Quetiapine or Lithium as Monotherapy for Mania in Bipolar Disorder The Journal of Clinical Psychiatry. ,vol. 66, pp. 111- 121 ,(2005) , 10.4088/JCP.V66N0116
Luca Pani, Luigi Pira, Giorgio Marchese, Antipsychotic efficacy: relationship to optimal D2-receptor occupancy. European Psychiatry. ,vol. 22, pp. 267- 275 ,(2007) , 10.1016/J.EURPSY.2007.02.005