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Open Access Highly Accessed Research article

One-year risk of psychiatric hospitalization and associated treatment costs in bipolar disorder treated with atypical antipsychotics: a retrospective claims database analysis

Edward Kim1, Min You1, Andrei Pikalov2, Quynh Van-Tran2 and Yonghua Jing1*

Author Affiliations

1 Bristol-Myers Squibb, Plainsboro, NJ, USA

2 Otsuka America Pharmaceutical, Inc., Rockville, MD, USA

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BMC Psychiatry 2011, 11:6  doi:10.1186/1471-244X-11-6

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-244X/11/6


Received:30 October 2009
Accepted:7 January 2011
Published:7 January 2011

© 2011 Kim et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

This study compared 1-year risk of psychiatric hospitalization and treatment costs in commercially insured patients with bipolar disorder, treated with aripiprazole, ziprasidone, olanzapine, quetiapine or risperidone.

Methods

This was a retrospective propensity score-matched cohort study using the Ingenix Lab/Rx integrated insurance claims dataset. Patients with bipolar disorder and 180 days of pre-index enrollment without antipsychotic exposure who received atypical antipsychotic agents were followed for up to 12 months following the initial antipsychotic prescription. The primary analysis used Cox proportional hazards regression to evaluate time-dependent risk of hospitalization, adjusting for age, sex and pre-index hospitalization. Generalized gamma regression compared post-index costs between treatment groups.

Results

Compared to aripiprazole, ziprasidone, olanzapine and quetiapine had higher risks for hospitalization (hazard ratio 1.96, 1.55 and 1.56, respectively; p < 0.05); risperidone had a numerically higher but not statistically different risk (hazard ratio 1.37; p = 0.10). Mental health treatment costs were significantly lower for aripiprazole compared with ziprasidone (p = 0.004) and quetiapine (p = 0.007), but not compared to olanzapine (p = 0.29) or risperidone (p = 0.80). Total healthcare costs were significantly lower for aripiprazole compared to quetiapine (p = 0.040) but not other comparators.

Conclusions

In commercially insured adults with bipolar disorder followed for 1 year after initiation of atypical antipsychotics, treatment with aripiprazole was associated with a lower risk of psychiatric hospitalization than ziprasidone, quetiapine, olanzapine and risperidone, although this did not reach significance with the latter. Aripiprazole was also associated with significantly lower total healthcare costs than quetiapine, but not the other comparators.

Background

Bipolar disorder is a chronic, recurring disorder associated with periodic disruptions in mood regulation, with annual treatment costs of $7,200 to $12,100 per year, 20% of which are attributable to hospitalizations [1,2]. Acute mania may require hospitalization for stabilization of behavioral dyscontrol, irritability, and risk-taking behavior. Despite the availability of multiple approved medication therapies, more than 75% of patients with bipolar disorder report at least one lifetime psychiatric hospitalization [3].

Medication treatment patterns are variable in the acute and long-term management of bipolar disorder, with 42-64% of patients receiving mood stabilizers, such as lithium, valproate or carbamazapine, and 44-60% receiving adjunctive antipsychotics [4-6]. Atypical antipsychotics are used alone or in combination with mood stabilizers for more severe manic episodes [7-11]. Moreover, adjunctive mood stabilizer-atypical antipsychotic combination treatments may help to prevent psychiatric hospitalization in bipolar disorder [12].

In a recent commercial claims database study, adjunctive aripiprazole was found to be associated with a longer time to initial psychiatric hospitalization than ziprasidone, olanzapine, quetiapine and risperidone during the first 90 days following initiation [13]. A subsequent analysis found that total healthcare expenditures were lower for aripiprazole than ziprasidone, olanzapine and risperidone, and mental health expenditures were lower for aripiprazole than all comparators [14].

The objective of the current study was to assess the 1-year risk of psychiatric hospitalization and associated treatment costs in commercially insured patients with bipolar disorder newly treated with aripiprazole, ziprasidone, olanzapine, quetiapine or risperidone, alone or in combination with mood stabilizers.

Methods

Study design

The study was a retrospective cohort study utilizing the Ingenix I3/LabRx claims dataset from 1/1/2003 through 12/31/2006. The dataset is a proprietary sample of individuals receiving health insurance benefits from United Health Care (UHC). UHC data include the inpatient, outpatient and prescription drug claims of more than 15 million of covered lives across the United States. The index date was the date of the first prescription claim for an atypical antipsychotic. Patients were followed for up to 1 year post-index. Because the dataset in this study was derived from an insurance claim database and the data conform to the Health Insurance Portability and Accountability Act of 1996 confidentiality requirements, the study did not require informed consent or institutional review board approval.

Inclusion criteria

The study included outpatients aged 18-65 years with an ICD-9 code for bipolar disorder, manic, mixed or hypomanic (296.0x, 296.1, 296.4x, 6x, 7x, 8x). Eligible patients required at least 180 days or continuous health plan enrollment before, and 365 days after, the index date. Patients were included only if they were treated on a single atypical antipsychotic at index.

Exclusion criteria

Patients were excluded from the analysis if they resided in a nursing home, hospice, or another type of long-term care facility, received mail-order prescriptions, or were diagnosed with a schizophrenia spectrum disorder (295.xx) during the pre- or post-index study period. Patients were also excluded if they used any atypical antipsychotic in the 180-day pre-index period, or had prescriptions for more than one atypical antipsychotic at index. Additionally, patients were also excluded if they were hospitalized within 7 days of their index antipsychotic prescription, in order to reduce treatment selection bias based on extreme agitation or instability.

Assessments and statistical analyses

The primary outcome of interest was the first psychiatric hospitalization in the follow-up period. Patients were censored for the following events: medical hospitalization, discontinuation of index antipsychotic (>15 days gap in coverage), or a prescription for a different antipsychotic during the follow-up period.

In order to control for treatment selection bias, we employed propensity score matching to construct comparison groups that shared similar demographic and clinical characteristics. Propensity score matching is a robust means of controlling for observed confounding in observational data [15]. Propensity scores were calculated for each patient using logistic regression with independent variables of age, sex, region, pre-index diagnosis or treatment of diabetes or hyperlipidemia, pre-index psychiatric hospitalization, pre-index lipid or glucose laboratory claims, choice of pre-index mood stabilizer exposure and Charlson comorbidity index. The propensity score was the predicted probability of treatment calculated for each patient in the regression model. Patients in comparison treatment groups were matched 1:1 if their propensity scores were within 0.25 standard deviations of the logit of the propensity score. All analyses were conducted in propensity score-matched cohorts of the study sample.

The primary analysis used Cox proportional hazards regression to assess time-dependent risk of post-index psychiatric hospitalization with a pre-specified threshold for statistical significance of p < 0.05. Covariates for adjustment in the models included age, sex, diagnosis or treatment for diabetes or hyperlipidemia diagnosis, pre-index psychiatric hospitalization, pre-index lipid or glucose laboratory claims, choice of pre-index mood stabilizer and the Deyo Charlson comorbidity index [16]. Intent-to-treat analysis was used for the cost analysis. Monthly treatment costs during the follow-up period were compared using generalized gamma regression controlling for pre-index costs in patients with positive post-index healthcare costs. First, we calculated the mean for each of the numeric covariates, and gave equal share of the categorical covariates, and then calculated the log mean of the fitted gamma distribution based on these covariate values and the parameter estimates and then exponentiated the log mean to get the cost in dollars. Gamma regressions were used to compare outcomes because gamma distribution is suggested by many as a close approximation of cost data. For example, Diehr and colleagues compared different methods to model healthcare cost data and concluded that, for understanding the effect of individual covariates on total costs, the gamma distribution might be preferred because it is a multiplicative model [17]. Generalized gamma regression has been found to be a more robust estimator than traditional ordinary least squares regression in the analysis of healthcare expenditure data due to the distributional qualities of healthcare costs [18]. Only patients with positive healthcare costs in the follow-up period were included in the analysis, which categorized costs into mental health (inpatient/ER and outpatient), medical (inpatient/ER and outpatient) and pharmacy (all medications used). We excluded patients with non-positive costs based on the assumption that patients taking medications were also receiving billable services and that the absence of such costs reflected aberrant data.

As a sensitivity analysis, we also replicated all multivariate regression analyses on the full unmatched samples.

Results

Patient disposition and characteristics

Of 198,919 patients with at least one atypical antipsychotic prescription, 7,169 met full inclusion criteria (Figure 1). Of these, 776 patients were on aripiprazole, 492 on ziprasidone, 1,919 on olanzapine, 2,497 on quetiapine and 1,485 on risperidone. Propensity score-matching enabled matching of: 461 aripiprazole and ziprasidone patients; 737 aripiprazole and olanzapine patients; 770 aripiprazole and quetiapine patients; and 771 aripiprazole and risperidone patients. Baseline characteristics after matching are shown in Table 1, demonstrating that comparable baseline characteristics were seen across all propensity score-matched treatment groups.

Table 1. Baseline and pre-index characteristics of propensity score-matched study sample

Clinical outcomes

Table 2 describes the disposition and dosing for patients in each treatment group. Hospitalization rates among patients treated with aripiprazole ranged from 6.2 to 7.4% depending on the matched cohort, whereas comparators ranged from 9.3 to 12.8%. More than two-thirds of all patients discontinued their index antipsychotic during the 1-year follow-up period, and less than 5% completed a full year of follow-up taking their index antipsychotic medication. The duration of therapy on atypical antipsychotics was comparable across all treatment groups and fairly brief, with a median of 30 days across all treatments. Starting and maximal doses were relatively similar, suggesting limited titration after initiation.

Table 2. Patient disposition and dosing - study sample

Fully adjusted Cox proportional hazards analysis demonstrated that treatment with aripiprazole was associated with a significantly lower risk of hospitalization than ziprasidone, olanzapine and quetiapine, and not significantly different than risperidone. Table 3 summarizes the results of these models, in which pre-index psychiatric hospitalization was significantly associated with risk of post-index hospitalization in all models. The number of pre-index mood stabilizers was not significantly associated with risk of hospitalization. Gender and age were not associated with risk of hospitalization in any cohort. There was variability among matched cohorts regarding the association between post-index mood stabilizer exposure and risk of hospitalization. Results of the analysis in unmatched samples are in Table 4. The effects are directionally the same, statistically significant, with some effect sizes being even larger than in the matched analyses.

Table 3. Adjusted Cox proportionate hazards models (aripiprazole reference)

Table 4. Adjusted Cox proportionate hazards models (aripiprazole reference) for unmatched samples

Economic outcomes

Monthly post-index healthcare cost estimates derived from the gamma regression are summarized in Table 5. Adjusted monthly inpatient/ER mental health costs were significantly lower in the aripiprazole-treated patients compared with those treated with ziprasidone, olanzapine and quetiapine, and numerically lower than risperidone in those patients with inpatient costs. Total mental health costs were lower for aripiprazole compared to ziprasidone and quetiapine, but not significantly different compared to olanzapine and risperidone. Compared to aripiprazole, total medical costs were higher for quetiapine but not significantly different for all other comparators. Pharmacy costs were lower for olanzapine, risperidone and quetiapine, and not significantly different for ziprasidone. Total healthcare costs in the follow-up period were significantly lower for aripiprazole than quetiapine, and not significantly different for the other comparators. Results of the analysis in unmatched samples are in Table 6. The effects are directionally the same.

Table 5. Adjusted monthly post-index costs for patients with positive costs, US dollars

Table 6. Adjusted monthly post-index costs for unmatched patients with positive costs, US dollars

Discussion

This study extends findings of a previous short-term retrospective cohort study that reported reduced risk of hospitalization and lower psychiatric treatment costs of patients with bipolar disorder treated with mood stabilizer and adjunctive aripiprazole compared to adjunctive ziprasidone, olanzapine and quetiapine during a 90-day follow-up period [13,14]. In this 1-year follow-up study, risk of hospitalization was lower in patients treated with aripiprazole with or without mood stabilizer compared to ziprasidone, olanzapine and quetiapine. Duration of therapy on atypical antipsychotic therapy was comparable across all atypical antipsychotics in this study, although the duration was brief relative to the follow-up period, lasting less than 3 months in 75% of cases. However, treatment guidelines recommend regimen simplification after patients are stabilized [7,11]. Therefore, in our sample, it is possible that the short duration of atypical antipsychotic therapy reflects stabilization of patients that allowed discontinuation of the atypical antipsychotic. Gianfrancesco et al. found somewhat longer treatment durations in a study of commercially insured patients treated with antipsychotics, with treatment durations of 7-10 months [19]. However, they allowed a gap of up to 120 days before ending a treatment episode, whereas our threshold of 15 days was much more conservative. To allow for meaningful comparative analysis of the cost data, intent-to-treat analysis was conducted for the cost analysis and patients were followed up for 1 year after their initial atypical antipsychotics treatment.

Antipsychotic doses observed also tended to be lower than label-recommended doses and demonstrated little titration over the course of treatment. These observations are consistent with other reports on atypical antipsychotic dosing in bipolar disorder [20,21]. Although we are not able to determine the reasons for these dosing patterns, it is possible that, due to concerns regarding tolerability or safety, physicians were reluctant to start patients on higher doses.

Along with the lower risk of psychiatric hospitalizations associated with aripiprazole compared to three of the four comparators, patients who initiated aripiprazole had lower psychiatric inpatient costs. These results suggest that treatment with aripiprazole tends to provide a valuable cost-offset in saving from decreased hospitalization risk and associated inpatient costs. In particular, the lower risk of hospitalization combined with lower total costs compared to quetiapine represent two attractive outcomes for formulary decision-makers responsible for the entire costs of care [22].

Observational studies can provide important insights into the outcomes of clinical practice in real-world settings, where dosing, titration and concomitant medications are not constrained by trial protocols. Such studies evaluate the effectiveness of treatments as they are actually used rather than when optimally dosed. We included the full range of observed dosing in our analysis based on the assumption that, in selecting medications, physicians also use what they believe is the most appropriate dosing and titration for that medication.

This study has several limitations. As a non-randomized retrospective study of observational data, it is possible that despite the use of propensity score matching and multivariate modeling, unobserved treatment selection bias may confound the results. Propensity score matching, however, is a widely accepted method for minimizing the effects of treatment selection bias in observational data [15]. Other approaches such as instrumental variables and Heckman's sample selection bias method may also be used in such settings [23,24], although the potential for residual confounding remains with all such methods. The consistency of our results in propensity score-matched and unmatched samples suggests that these findings are robust. However, the dataset we analyzed consists of patients from a single commercial health plan; results may not be applicable to chronic populations that are more likely to be covered by public sector insurance. Replication in other observational datasets is necessary to validate the robustness of these results.

Additionally, by restricting the analysis to an inception cohort, we were only able to study the effects of the initial choice of medication following an antipsychotic-free period and are thus limited to conclusions on initial antipsychotic selection rather than the effectiveness of a given medication under all circumstances. Based on our results, aripiprazole appears to be the most effective initial choice among atypical antipsychotics for the acute treatment of bipolar disorder, and these effects appear to persist in the post-acute phase. Finally, the study only followed patients until their first psychiatric hospitalization and did not address outcomes following adding, switching, or discontinuing antipsychotics, which may be common in this population. The analysis of such complex treatment patterns within claims data may be subject to high levels of unobservable confounding and difficult to interpret with respect to the contribution of individual medications across complex regimens. Specifically, it may be challenging to account for residual effects of prior medications following a switch, which is why we chose inception cohort design. Moreover, the reasons for adding versus switching antipsychotics would require detailed clinical information not available in this dataset to adjust for treatment selection bias. Therefore, our results are limited to outcomes only while the patient is on their initial antipsychotic medication for that episode of treatment.

Conclusions

In adults with bipolar disorder, treatment with aripiprazole was associated with a lower risk of hospitalization than ziprasidone, olanzapine and quetiapine, and lower mental health costs than ziprasidone and quetiapine in the year following initial prescription. Total healthcare costs of patients treated with aripiprazole were lower than those treated with quetiapine.

Competing interests

Edward Kim MD, MBA, Min You, MS, and Yonghua Jing, PhD, are employees of Bristol-Myers Squibb. Andrei Pikalov, MD, PhD, and Quynh Van-Tran, PharmD, are employees of Otsuka America Pharmaceutical, Inc.

Authors' contributions

All authors contributed to the design and coordination of the study, statistical analysis of results and manuscript preparation.

Acknowledgements

This study was supported by Bristol-Myers Squibb (Princeton, NJ, USA) and Otsuka Pharmaceutical Co., Ltd. (Tokyo, Japan). Editorial support for the preparation of this manuscript was provided by Ogilvy Healthworld Medical Education; funding was provided by Bristol-Myers Squibb.

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Pre-publication history

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