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2015 | 15 | 2 | 76-80

Article title

Przegląd interwencji w polekowym przyroście masy ciała podczas leczenia klozapiną

Content

Title variants

EN
An overview of interventions in drug-induced weight gain during clozapine treatment

Languages of publication

EN PL

Abstracts

EN
Aims and methods: Clozapine is an atypical antipsychotic of choice for the treatment of drug-resistant schizophrenia. It is associated with the risk of adverse effects, such as blood dyscrasia, cardiovascular and metabolic disorders, such as insulin resistance and impaired lipid profile, as well as weight gain. The aim of this article is a review of research into methods (both pharmacological and non-pharmacological) of preventing clozapine-induced weight gain. Antipsychotics, other psychotropic drugs, metabolism-regulating agents and appetite suppressants were assessed in groups of patients treated with clozapine (based on medical databases). Among non-pharmacological interventions, the efficacy of cognitive-behavioural therapy, dietary counselling and exercise programmes was assessed in several patient populations. Results: Among the discussed medications aripiprazole, topiramate, fluvoxamine and metformin appear to be efficacious. Orlistat shows efficacy in males. Cognitive-behavioural therapy was shown to be more effective compared to a brief nutrition education. However, pharmacological, psychotherapeutic and dietary interventions were considered insufficient in balancing the total weight gain. Conclusions: Each of the pharmacological interventions should be individually considered in the context of potential benefits and adverse effects. Non-pharmacological methods are recommended in all cases, regardless of the effect. Clinical practice indicates the need to conduct further research and develop management algorithms to prevent excessive weight gain in patients treated with clozapine.
PL
Cel i metody: Klozapina to atypowy lek przeciwpsychotyczny, stosowany z wyboru w schizofrenii lekoopornej. Z przyjmowaniem klozapiny wiąże się prawdopodobieństwo wystąpienia działań niepożądanych w postaci zaburzeń obrazu krwi oraz zaburzeń sercowo-naczyniowych i metabolicznych, takich jak insulinooporność i zaburzenia profilu lipidowego, a także przyrost masy ciała. Celem niniejszego opracowania jest przegląd badań dotyczących metod (zarówno farmakologicznych, jak i niefarmakologicznych) przeciwdziałania przyrostowi masy ciała indukowanemu klozapiną. Wzięto pod uwagę leki przeciwpsychotyczne i inne psychotropowe oraz te regulujące metabolizm i zmniejszające apetyt; poświęconą im część pracy oparto na badaniach grup chorych leczonych klozapiną (informacje z medycznych baz danych). Spośród interwencji niefarmakologicznych na przykładzie kilku grup pacjentów analizowano psychoterapię poznawczo-behawioralną, poradnictwo dietetyczne i programy ćwiczeń fizycznych. Wyniki: Skutecznymi lekami okazały się aripiprazol, topiramat, fluwoksamina i metformina, a u mężczyzn także orlistat. Wykazano przewagę terapii poznawczo-behawioralnej nad wyłączną krótką edukacją żywieniową. Skuteczność interwencji farmakologicznych, psychoterapeutycznych i dietetycznych jest jednak niewystarczająca, gdyż tylko w niewielkim stopniu równoważy przyrost masy ciała. Wnioski: Podjęcie każdej interwencji farmakologicznej powinno zostać rozważone indywidualnie – w kontekście korzyści i działań niepożądanych. Metody niefarmakologiczne, niezależnie od efektu, są polecane w każdym przypadku. Praktyka kliniczna wskazuje na potrzebę przeprowadzenia większej liczby badań i ustalenia algorytmów postępowania związanych z zapobieganiem nadmiernemu przyrostowi masy ciała u osób leczonych klozapiną.

Discipline

Year

Volume

15

Issue

2

Pages

76-80

Physical description

Contributors

  • Klinika Psychiatrii Dorosłych, Gdański Uniwersytet Medyczny
  • Klinika Psychiatrii Dorosłych, Gdański Uniwersytet Medyczny
  • Klinika Psychiatrii Dorosłych, Gdański Uniwersytet Medyczny

References

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Document Type

review

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.psjd-29597928-b918-4c94-b2e4-b0fb089f1cc9
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