BMC Psychiatry | |
Hospital stay in patients admitted for acute bipolar manic episodes prescribed quetiapine immediate or extended release: a retrospective non-interventional cohort study (HOME) | |
Antonello Bellomo2  Esteban Medina1  Miguel Angel Gonzalez3  Miriam Moreno-Manzanaro1  Domingo Gonzalez6  Murad Atmaca5  Andreas Reif7  Oğuz Karamustafalıoğlu4  | |
[1] AstraZeneca Farmaceutica Spain, Madrid, Spain;Department of Clinical and Experimental Sciences, Section of Psychiatry and Clinical Psychology, University of Foggia, Foggia, Italy;Quintiles, Parque Empresarial Cristalia, Madrid, Spain;Department of Psychiatry, Şişli Etfal Teaching and Research Hospital, Istanbul, Turkey;Department of Psychiatry, Firat University School of Medicine, Elazig, Turkey;Assertive Outreach, Birmingham & Solihull Mental Health Trust, Birmingham, UK;Department of Psychiatry, Psychosomatics and Psychotherapy, Head Psychiatric Neurobiology and Bipolar Disorder Program, University of Würzburg, Würzburg, Germany | |
关键词: Length of stay; Hospitalisation; Quetiapine; Acute mania; Bipolar disorder; | |
Others : 1123369 DOI : 10.1186/s12888-014-0246-3 |
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received in 2013-08-21, accepted in 2014-08-19, 发布年份 2014 | |
【 摘 要 】
Background
Bipolar manic episodes often require hospital admission to ensure patient safety. The antipsychotic quetiapine is a common treatment for bipolar mania and is available in immediate release (IR) and extended release (XR) formulations; however, outcomes in patients receiving these different formulations have not been directly compared in an acute hospital setting.
Methods
We conducted a multinational, observational, retrospective cohort study to describe and compare hospital stay in patients admitted for an acute bipolar manic episode treated with quetiapine IR or XR from 1 October 2009–1 October 2010. The primary outcome measure was comparison of length of stay (LOS) using zero-truncated negative binomial regression.
Results
In total, 1230 patients were included (659 in the IR cohort; 571 in the XR cohort). The median LOS (interquartile range) was 18.0 days (12.0, 28.0) in the IR cohort and 20.0 days (12.0, 34.0) in the XR cohort, respectively. LOS was not significantly associated with quetiapine formulation irrespective of whether or not clinical characteristics were taken into account (p = 0.820 and p = 0.386, respectively). Overall, 84.2% and 84.4% of patients in the IR and XR cohorts, respectively, had not previously used quetiapine; of these patients, 78.7% and 68.9% received one total daily dose, and 14.4% and 23.9% received dose titration. Over half of patients received antipsychotic monotherapy (53.1% and 58.3% in the IR and XR cohorts, respectively) and most received a daily quetiapine dose ≥ 400 mg (64.9% and 71.8%, respectively, for quetiapine monotherapy and 59.9% and 80.3%, respectively, for combination treatment).
As a secondary outcome, multivariate analysis was used to identify other factors that affect LOS. Factors associated with a longer hospital stay included public funding versus private, maximum number of new medications administered, did not receive lithium and did not receive anxiolytics, sedatives/hypnotics (all p < 0.0001). Factors associated with a shorter hospital stay included presence of drug/alcohol abuse, living accompanied and having a psychiatric medical history (all p < 0.05).
Conclusions
LOS was not found to be associated with quetiapine formulation. However, most patients received only one total daily dose of quetiapine without dose titration, which was unexpected and contrary to current recommendations.
Trial registration
Trial registration: NCT01239589 webcite
【 授权许可】
2014 Karamustafalioglu et al.; licensee BioMed Central Ltd.
【 预 览 】
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Figure 1. | 48KB | Image | download |
【 图 表 】
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