Literature DB >> 21721916

Unmet treatment needs in schizophrenia patients: is asenapine a potential therapeutic option?

Maurizio Pompili1, Gianluca Serafini, Marco Innamorati, Elisa Ambrosi, Ludovica Telesforo, Paola Venturini, Gloria Giordano, Michele Battuello, David Lester, Paolo Girardi.   

Abstract

Adverse metabolic events, such as increased adiposity, hyperglycemia, diabetes mellitus and dyslipidemia, have been associated with treatment using atypical antipsychotic medications. However, the complexity of some of the reports on this problem and marketing efforts in this area may make it difficult for psychiatrists to remain fully and accurately informed about the metabolic complications of atypical antipsychotic therapy. Little is currently known about how psychiatrists view what they have read or heard, how they perceive the available information and how this affects their management of patients with schizophrenia. A number of studies have demonstrated that nonadherence to the medication regimen in schizophrenia is associated with poor symptomatic outcome, increased risk of relapse, more frequent use of compulsory treatment and increased risk of suicide and severe self-harm. Suicide is a major cause of death among schizophrenic patients, and their attitude toward medication can make the difference between a proper therapeutic regimen that protects patients from suicide risk versus discontinuation of treatments that are associated with disabling symptoms, some of which are risk factors for suicide. We review the characteristics of a new drug, asenapine, that may improve adherence in patients as a result of a distinctive receptor profile that may be associated with fewer side effects than other second-generation antipsychotic drugs.

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Year:  2011        PMID: 21721916     DOI: 10.1586/ern.11.82

Source DB:  PubMed          Journal:  Expert Rev Neurother        ISSN: 1473-7175            Impact factor:   4.618


  2 in total

1.  Efficacy and safety of asenapine in Asian patients with an acute exacerbation of schizophrenia: a multicentre, randomized, double-blind, 6-week, placebo-controlled study.

Authors:  Toshihiko Kinoshita; Ya-Mei Bai; Jong-Hoon Kim; Mutsuo Miyake; Nobuyuki Oshima
Journal:  Psychopharmacology (Berl)       Date:  2016-06-08       Impact factor: 4.530

2.  Persistent akathisia masquerading as agitated depression after use of ziprasidone in the treatment of bipolar depression.

Authors:  Thomas M Penders; Salina Agarwal; Rachel Rohaidy
Journal:  Neuropsychiatr Dis Treat       Date:  2013-04-04       Impact factor: 2.570

  2 in total

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