The ORYGEN first episode manila study: an 8 weeks comparison of chlorpromazine and olanzapine in combination with lithium
Détails
ID Serval
serval:BIB_10D0F7831985
Type
Actes de conférence (partie): contribution originale à la littérature scientifique, publiée à l'occasion de conférences scientifiques, dans un ouvrage de compte-rendu (proceedings), ou dans l'édition spéciale d'un journal reconnu (conference proceedings).
Sous-type
Abstract (résumé de présentation): article court qui reprend les éléments essentiels présentés à l'occasion d'une conférence scientifique dans un poster ou lors d'une intervention orale.
Collection
Publications
Institution
Titre
The ORYGEN first episode manila study: an 8 weeks comparison of chlorpromazine and olanzapine in combination with lithium
ISBN
0920-9964
Statut éditorial
Publié
Date de publication
2006
Peer-reviewed
Oui
Volume
86
Série
Schizophrenia Research
Pages
37
Langue
anglais
Notes
SAPHIRID:61529
Résumé
Context: The risk of relapse and disability of Bipolar Disorder increases with multiple episodes. Treatment trials in first episode populations offer an optimal opportunity to study a homogeneous cohort with an early intervention strategy. Additionally, here are currently no clear treatment guidelines for first episode mania. While atypical neuroleptics seem to offer advantages compared to typical neuroleptics, they nevertheless also have side effects.
Aims: Comparison of efficacy, safety and tolerability of chlorpromazine and olanzapine, both in combination with lithium, in the treatment of a first manic episode with psychotic features.
Methods: Individuals presenting to EPPIC were randomised to either a combination of olanzapine and lithium or chlorpromazine and lithium in the treatment of a first episode of psychotic mania. The duration of the acute phase of the trial was 8 weeks, and there is an 18 month follow up period. Outcome measures include the Young Mania Rating Scale, Clinical Global Impression, Global Assessment of Functioning Scale and the Social and Occupational Functioning Assessment Scale. A total of 75 subjects, between the age of 16 and 30 consented to the trial. They were randomised to either olanzapine is started at 5 mg per day or chlorpromazine, started at 100 mg per day, with doses titrated according to need. All individuals were on concurrent treatment with lithium, serum levels between 0.8 and 1.0.
Results: Primary and secondary outcome measures of the trial will be presented.
Aims: Comparison of efficacy, safety and tolerability of chlorpromazine and olanzapine, both in combination with lithium, in the treatment of a first manic episode with psychotic features.
Methods: Individuals presenting to EPPIC were randomised to either a combination of olanzapine and lithium or chlorpromazine and lithium in the treatment of a first episode of psychotic mania. The duration of the acute phase of the trial was 8 weeks, and there is an 18 month follow up period. Outcome measures include the Young Mania Rating Scale, Clinical Global Impression, Global Assessment of Functioning Scale and the Social and Occupational Functioning Assessment Scale. A total of 75 subjects, between the age of 16 and 30 consented to the trial. They were randomised to either olanzapine is started at 5 mg per day or chlorpromazine, started at 100 mg per day, with doses titrated according to need. All individuals were on concurrent treatment with lithium, serum levels between 0.8 and 1.0.
Results: Primary and secondary outcome measures of the trial will be presented.
Création de la notice
10/03/2008 10:00
Dernière modification de la notice
20/08/2019 12:38