TY - JOUR
T1 - Treatment and outcomes of an Australian cohort of outpatients with bipolar I or schizoaffective disorder over twenty-four months: implications for clinical practice
AU - Kulkarni, Jayashri
AU - Filia, Sacha Louise
AU - Berk, Lesley
AU - Filia, Kate
AU - Dodd, Seetal
AU - De Castella, Rolet Anthony
AU - Brnabic, Alan
AU - Lowry, Amanda J
AU - Kelin, Katarina
AU - Montgomery, William
AU - Fitzgerald, Paul Bernard
AU - Berk, Michael
PY - 2012
Y1 - 2012
N2 - Background: The Bipolar Comprehensive Outcomes Study (BCOS) is a 2-year, prospective, non-interventional, observational study designed to explore the clinical and functional outcomes associated with `real-world? treatment of participants with bipolar I or schizoaffective disorder. All participants received treatment as usual. There was no study medication.
Methods: Participants prescribed either conventional mood stabilizers (CMS; n = 155) alone, or olanzapine with, or without, CMS (olanzapine ? CMS; n = 84) were assessed every 3 months using several measures, including the Young Mania Rating Scale, 21-item Hamilton Depression Rating Scale, Clinical Global Impressions Scale ? Bipolar Version, and the EuroQol Instrument. This paper reports 24-month longitudinal clinical, pharmacological, functional, and socioeconomic data.
Results: On average, participants were 42 (range 18 to 79) years of age, 58 were female, and 73 had a diagnosis of bipolar I. Polypharmacy was the usual approach to pharmacological treatment; participants took a median of 5 different psychotropic medications over the course of the study, and spent a median proportion of time of 100 of the study on mood stabilizers, 90 on antipsychotics, 9 on antidepressants, and 5 on benzodiazepines/hypnotics. By 24 months, the majority of participants had achieved both symptomatic and syndromal remission of both mania and depression. Symptomatic relapse rates were similar for both the CMS alone (65 ) and the olanzapine ? CMS (61 ) cohorts.
Conclusions: Participants with bipolar I or schizoaffective disorder in this study were receiving complex medication treatments that were often discordant with recommendations made in contemporary major treatment guidelines. The majority of study participants demonstrated some clinical and functional improvements, but not all achieved
remission of symptoms or syndrome.
AB - Background: The Bipolar Comprehensive Outcomes Study (BCOS) is a 2-year, prospective, non-interventional, observational study designed to explore the clinical and functional outcomes associated with `real-world? treatment of participants with bipolar I or schizoaffective disorder. All participants received treatment as usual. There was no study medication.
Methods: Participants prescribed either conventional mood stabilizers (CMS; n = 155) alone, or olanzapine with, or without, CMS (olanzapine ? CMS; n = 84) were assessed every 3 months using several measures, including the Young Mania Rating Scale, 21-item Hamilton Depression Rating Scale, Clinical Global Impressions Scale ? Bipolar Version, and the EuroQol Instrument. This paper reports 24-month longitudinal clinical, pharmacological, functional, and socioeconomic data.
Results: On average, participants were 42 (range 18 to 79) years of age, 58 were female, and 73 had a diagnosis of bipolar I. Polypharmacy was the usual approach to pharmacological treatment; participants took a median of 5 different psychotropic medications over the course of the study, and spent a median proportion of time of 100 of the study on mood stabilizers, 90 on antipsychotics, 9 on antidepressants, and 5 on benzodiazepines/hypnotics. By 24 months, the majority of participants had achieved both symptomatic and syndromal remission of both mania and depression. Symptomatic relapse rates were similar for both the CMS alone (65 ) and the olanzapine ? CMS (61 ) cohorts.
Conclusions: Participants with bipolar I or schizoaffective disorder in this study were receiving complex medication treatments that were often discordant with recommendations made in contemporary major treatment guidelines. The majority of study participants demonstrated some clinical and functional improvements, but not all achieved
remission of symptoms or syndrome.
U2 - 10.1186/1471-244X-12-228
DO - 10.1186/1471-244X-12-228
M3 - Article
SN - 1471-244X
VL - 12
JO - BMC Psychiatry
JF - BMC Psychiatry
M1 - 228
ER -