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Information on cost-effectiveness of interventions to treat schizophrenia can assist health policy decision making, particularly given the lack of health resources in developing countries like Thailand. This study aims to determine the optimal treatment package, including drug and non-drug interventions, for schizophrenia in Thailand.
A Markov model was used to evaluate the cost-effectiveness of typical antipsychotics, generic risperidone, olanzapine, clozapine and family interventions. Health outcomes were measured in disability adjusted life years. We evaluated intervention benefit by estimating a change in disease severity, taking into account potential side effects. Intervention costs included outpatient treatment costs, hospitalization costs as well as time and travel costs of patients and families. Uncertainty was evaluated using Monte Carlo simulation. A sensitivity analysis of the expected range cost of generic risperidone was undertaken.
Generic risperidone is more cost-effective than typicals if it can be produced for less than 10 baht per 2 mg tablet. Risperidone was the cheapest treatment with higher drug costs offset by lower hospital costs in comparison to typicals. The most cost-effective combination of treatments was a combination of risperidone (dominant intervention). Adding family intervention has an incremental cost-effectiveness ratio of 1,900 baht/DALY with a 100% probability of a result less than a threshold for very cost-effective interventions of one times GDP or 110,000 baht per DALY. Treating the most severe one third of patients with clozapine instead of risperidone had an incremental cost-effectiveness ratio of 320,000 baht/DALY with just over 50% probability of a result below three times GDP per capita.
There are good economic arguments to recommend generic risperidone as first line treatment in combination with family intervention. As the uncertainty interval indicates the addition of clozapine may be dominated and there are serious side effects, treating severe patients with clozapine is advisable only for patients who do not respond to risperidone and only in the presence of a stricter side effect monitoring system than currently exists.
Schizophrenia generally begins in early adulthood and causes long term mental and physical impairment . It has a significant impact on individuals, families and countries in terms of both health and economic loss. In the 1999 Thai Burden of Disease and Injury study, schizophrenia was responsible for 5% of all non-fatal health loss measured in years lived with disability . The direct health care costs of schizophrenia account for between 1% and 3% of total national health care expenditure worldwide [3-5]. Indirect costs related to lost productivity are estimated to be higher or at least equivalent to direct costs, in the range of 1 to 7 times the direct costs [3,5-7]. The evidence, however, indicates that Asian countries have a larger proportion of indirect costs (87% in Taiwan, 83% in Korea, and 63% in India) [5,8,9] than those reported in Western countries (47% to 70%) .
Thailand has limited health resources for mental disorders, including schizophrenia. The government devoted only 3.0% of health expenditure to mental health in 2008 . It is therefore paramount that decision makers have access to cost-effectiveness information to prioritise allocation of resources within their budget constraints.
Medications are the standard treatment to control acute psychotic symptoms of schizophrenia. The newer 'atypical' antipsychotics have a similar effect on psychotic symptoms as first-generation 'typical' antipsychotics but cause different side effects and are much more expensive [11-13]. The key problems with using medications alone are poor adherence and a partial improvement in functional outcomes only . A combination of drug and non-drug interventions is commonly recommended [15-17].
To our knowledge, there are no cost-effectiveness studies indicating what should be the first and second line drug treatments in Thailand. This study aims to provide policy makers with evidence on the optimal package of drug and non-drug interventions for schizophrenia. We undertook the current study as part of the Setting Priorities using Information on Cost-Effectiveness (SPICE) project which aimed to provide comparable cost-effectiveness results across various disease areas to assist policy makers in priority setting decision making.
We selected interventions for analysis based on: a) efficacy and/or effectiveness in published literature; b) availability of evidence on clinical effectiveness, resource utilization and costs; c) feasibility of implementation in Thailand based on discussions with 10 local mental health experts; and d) relevance to current policy-making. Four drug interventions (typicals, risperidone, olanzapine and clozapine) and family interventions were chosen for analysis. The comparator was a hypothetical 'do nothing' scenario using generalized cost-effectiveness. This required a back-calculation from current practice to the 'partial null', i.e. a hypothetical scenario where we removed the effect of all currently implemented interventions [18,19]. An 'intervention pathway' was calculated to determine the most cost-effective mix of interventions.
Our study design was cost-effectiveness analysis using a Markov model with cycles of one year. Patients with schizophrenia in Thailand in the year 2005 were the target population. Each year patients could remain alive with schizophrenia, recover or die from disease-related or other causes (Figure (Figure1).1). To reflect the chronic course of schizophrenia, costs and effects were assessed until age 80 or death. The annual transition probabilities were based on local and overseas data (See Additional file 1: Transition probability estimates).
The model was analyzed from a government costing perspective. Our survey showed that 75% of patients with schizophrenia used the universal coverage health care system . However, because schizophrenia has significant impacts outside the health sector [1,3], we also considered costs to patients and families (time and travel costs). Discounting at 3% was applied to both costs and benefits to be consistent with the study of Burden of Disease in Thailand and in line with recommendations from the Panel on Cost-Effectiveness in Health and Medicine [2,21]. Our model was constructed using Microsoft Excel.
Health outcomes from the drug and non-drug interventions were measured in disability-adjusted life years (DALYs) averted using identical methods. Intervention effect size was measured as a change in disability weight (DW) using a method described by Magnus et al  to translate pooled effect sizes from the international literature into a change in DW. To combine effect sizes, Hedges' g test was applied to determine the mean difference in standard deviation units including an adjustment to correct for small sample sizes . Because the psychiatric literature usually reports efficacy measures based on different psychometric scales , we calculated the effect sizes based on the Brief Psychiatric Rating Scale (BPRS) and the Positive and Negative Syndrome Scale (PANSS) in our meta-analyses since they are the most common scales for scoring psychiatric symptoms. Our analyses relied heavily on the information on intervention effects from Cochrane systematic reviews [25-30]. The standardized effect sizes were then pooled using the random effects meta-analysis method to deal with variation around some overall average treatment effect . The method used in the Australian Assessing Cost Effectiveness - Mental Health (ACE-MH) project [22,24] to transfer the pooled effect sizes into a change in disability weight was adjusted to include the spread of the Brief Psychiatric Rating Scale-Expanded (BPRS-E) scores from our survey, a cross-sectional descriptive study including 307 people with schizophrenia in Thailand (279 outpatients and 28 inpatients) [20,31]. We mapped each BPRS-E score (ranging from 24 = least severe to 134 = most severe) to the Dutch lowest and highest DWs for schizophrenia (0.21-0.98) using the methods developed by the ACE-MH Study [24,32]. Note that the lowest disability weight for schizophrenia still means a substantial loss of health reflecting the disability associated with a stigmatized illness as well as some residual symptoms. Across the survey sample we calculated the standard deviation of the BPRS scores and estimated the average health loss (in disability weight) associated with a 1 SD change in severity . As the effect sizes for the impact of interventions are expressed in standard deviation units, we could then impute the average change in disability weight given an effect size for each intervention. The impact of a change in extrapyramidal (EPS) adverse effect was estimated separately and transferred into an additional change in DW. We borrowed data on the proportions of patients with moderate and severe EPS due to typicals (25%) and atypicals (13%), as well as the DW of each severity level, i.e. 0.422 and 0.453 for moderate and severe EPS, respectively from the Australian study  to calculate the DW change due to less EPS on atypicals. Due to lack of data we had to assume that all the atypicals induced EPS equally.
Apart from accounting for the EPS side effects in the change in DW, we also estimated the mortality and morbidity risks associated with the average weight gain associated with each drug using the potential impact fraction RiskIntegral add-in for Excel (http://www.epigear.com). The benefit of preventing suicide was taken into account for clozapine, the only antipsychotic drug with evidence of this effect . The weighted average relative risk of suicide for people taking clozapine was 0.53, calculated using data from studies by Munro  and Harris . Table Table11 shows the input parameters used to estimate intervention benefits.
Due to the absence of Thai data on adherence to drug treatment for schizophrenia, we assumed adherence of 47% (« 7.4%) from a review study by Lacro et.al . A study on depression treatment in Thailand found adherence of 41%, indicating a similar level of adherence within the mental health system . We applied this rate for both people receiving atypical and typical antipsychotics [38,39]. We provide further details of health effect estimation via the online document (See Additional file 1: Health effect estimations)
The cost analyses comprise of: a) intervention cost; b) medical costs for treating or preventing side effects; c) cost of hospitalization; and d) time and travel cost of patients and families. All costs were adjusted to 2005 using the Consumer Price Index (CPI) based on data from the Bank of Thailand website (http://www.bot.or.th).
We estimated the annual drug cost for each of the antipsychotics by combining the unit cost for a standard daily dose with the costs of drug administration (i.e. outpatient visits). Costs of benzhexol, an anticholinergic drug that treats EPS side effects were also included. We separately measured costs of regular blood tests to prevent the fatal adverse effect of clozapine, agranulocytosis . We used a 27% hospitalization rate among patients on typicals based on local data  while adopting the relative reduction in hospitalization rates in patients taking atypicals from Leucht et al. . According to the Cochrane review study, we assumed that by comparison with no treatment typicals reduce the hospitalization rate by 50% .
The costs of family interventions mainly consisted of start-up costs (development and training) and ongoing costs (services, supplies, travel and salary). We assumed that the family intervention protocol would be prepared by 2 specialists employed by the project for 100 hours each and a training program would be conducted for a group of clinicians from all 17 psychiatric hospital across Thailand. One psychiatrist and 20 psychiatric nurses from each hospital would be trained. The family intervention program would consist of 10 weekly 2-hr sessions by a psychiatric nurse . We assumed that each session would have 16 participants (8 patients and 8 family carers). As there is no information on the longer term outcomes of family interventions, we assumed after expert consultation that 2 booster sessions to patients and families every year, would enable the benefit of FI to be maintained over a patient's lifetime.
Time cost was assumed to be 25% of personal income per capita in Thailand in 2005 (http://www.nesdb.go.th) and travel costs of patient and families were computed using patient-reported data from our survey . The cost parameters, values and data sources are described in the online supporting document (See Additional file 1: Assessment of intervention cost).
One way sensitivity analysis was undertaken for (a) intervention costs including and excluding time and travel costs of patients and families; and (b) varying costs of risperidone. Generic risperidone is not yet available in Thailand. However, the Royal College of Psychiatrists of Thailand has urged the Government Pharmaceutical Organization to produce a generic version of risperidone following the expiration of its patent and it is currently in the process of Food and Drug Administration approval . In this sensitivity analysis we modelled risperidone prices ranging from 4 baht (expected generic price ) to 50 baht. We compared risperidone to typicals in this sensitivity analysis.
Probabilistic sensitivity analysis using Monte Carlo simulation was undertaken using an Excel add-in Ersatz (http://www.epigear.com). The uncertainties in all values were considered simultaneously using appropriate distributions and relevant parameters. Additional online information provides the details of input parameters, distributions and data sources used for uncertainty analysis (See Additional file 1: Uncertainty parameters and distributions.
While the initial results were based on cost-effectiveness analysis, broader aspects which may be important in terms of policy, known as "second filter" criteria, were also considered. In Australian 'Assessing Cost-Effectiveness' studies 'strength of evidence', 'equity', 'feasibility', 'acceptability' and sustainability have been considered . Our expert advisory group and the steering committee of the SPICE project played an important role in applying these second filter criteria and formulating policy recommendations.
Atypical antyipsychotics were not significantly more effective than typicals in reducing the severity of disease (Tables (Tables11 and and2).2). Clozapine had an additional benefit of preventing suicide but greater health loss from weight gain than the other drugs (Table (Table2).2). Family intervention had additional health benefits when combined with drug treatment.
At a cost of 4 baht per 2 mg tablet, generic risperidone would be the preferred drug treatment due to lower hospital costs despite higher drug costs (Table (Table3).3). While all atypicals have lower hospital costs than typicals, the drug cost of risperidone, only, was offset by hospital saving. The annual cost of clozapine treatment per individual was about twice that for typicals or risperidone, mostly because of the higher cost of monitoring side effects and the associated time costs of patients. Olanzapine was the most costly drug, approximately 7 times higher than typicals and risperidone. Giving risperidone with family interventions was more expensive than risperidone alone by 4,000 baht in the first year due to higher patient and family costs.
By comparison with 'do nothing', most of the selected interventions, with the exception of clozapine and olanzapine, were cost-saving (Table (Table4).4). The cost-effectiveness ratio of clozapine (12,000 baht/DALY averted) was below Thailand GDP per capita of 110,000 baht which is considered the threshold for very cost-effective health interventions (http://www.dcp2.org). When we included costs of patient and family time in the analyses, all of the interventions were no longer dominant but their cost-effectiveness ratios (except for clozapine and olanzapine) still fell well below the threshold of 110,000 baht. Olanzapine (1,000,000 baht/DALY averted) has an unfavourable cost-effectiveness ratio due to its high cost for at most only a small additional benefit over other drug treatments.
The ideal intervention package would start with generic risperidone, assuming the cost is 4 baht per 2 mg tablet (Figure (Figure22 and Table Table5).5). The next step would be to add family interventions to risperidone with significant health gain at a small net cost (ICER 1,900 baht/DALY; 95%CI: "dominant", 18,000; 100% probability of a result below the one times GDP per capita). Providing clozapine instead of risperidone to the most severe one-third of patients has an ICER of 320,000 baht/DALY (95% CI: 26,000, "dominated"; 51% probability of a result below the three times GDP per capita threshold of 330,000 baht/DALY for cost-effective interventions). We assumed that patients who had a score greater than 40 on the BPRS (this would include about one-third of patients in our survey) would be eligible for clozapine [20,31]. "Dominated" denotes an intervention more costly and less effective than the comparator, while "dominant" means the intervention is more effective and less costly than the comparator.
Analysis of generic risperidone was based on an "expected cost". The actual cost for generic risperidone could have a significant impact on the cost-effectiveness, so we examined potential values in a one-way sensitivity analysis (Figure (Figure3).3). If generic risperidone costs less than 10 baht per 2 mg tablet, it is dominant over typicals. Up to a cost of 19 baht (95% uncertainty interval 15-25 baht) replacing typicals by risperidone would still be considered a very cost-effective intervention against a threshold of 110,000 baht.
Based on the CEA results, the recommended intervention package would be the combination between risperidone, clozapine and family interventions. Providing clozapine for highly severe patients cannot be recommended until it is ensured that its serious side effect of agranulocytosis is prevented: patients receive periodic blood test during this treatment (Table (Table66).
The three main findings from this study are (a) generic risperidone should be used as the first line drug treatment for schizophrenia if the cost is less than 10 baht per 2 mg tablet; (b) combining risperidone with family interventions will substantially increase health gain with lower hospitalization cost; and (c) clozapine could be a second line medication for patients with high severity who fail to respond to risperidone.
The key recommendation of this study is that risperidone should be included in the national drug list while olanzapine should not (Table (Table6).6). Clozapine should be reserved for severe patients who do not respond to risperidone as it may have superior benefits in treatment-resistant schizophrenia and in preventing suicidal behaviour [33,46]. However, the poor compliance with the Clozapine Patient Monitoring Service program in Thailand  means that clozapine cannot be recommended until monitoring has improved.
The stigma of schizophrenia could be a significant barrier to family interventions . More importantly, due to a lack of mental health resources and high travel costs, poor households and people living in rural areas may have limited access. A new stream of long term government funding would be required to provide family interventions across the country and make these services accessible long-term.
This study has several limitations. First, the studies included in our meta-analyses were generally from Western countries not Thailand or other Asian countries. Second, the course of disease varies considerably between patients. Modelling the average cost and impact on the average case of disease could lead to erroneous conclusions . The alternative is to use a microsimulation approach; however, that would require more clinical and epidemiological information on individuals than we had available. Third, the methods used for translating the effect sizes into a change in DW need the assumption that the effect sizes from trials can be directly applied to general health status estimated using a generic measurement. Normally, generic measurements are less relevant to schizophrenia's symptoms by comparison with specific ones as BPRS used in this study. However, this is the only method allowing us to clarify DWs in patients with different treatments. An advantage of using this method is that we could include Thai data on the individual patients into the analysis. We would content that it is not necessarily so that departure from the assumed linear relationship between symptom change and disability change would lead to over-estimation of health benefits in DALYs. Fourth, the assumption that patients remain on the same treatment throughout the course of their illness is in contrast to the common clinical practice of switching patients from one treatment to another treatment based on individual medication responses . However, a large double-blinded randomized clinical trial in the US suggested no difference in rates of improvement between patients with atypical antipsychotics switching to a new medication and patients staying on their initial treatment . Finally, we have not incorporated the costs of treating diseases related to increased body weight due to unavailability of local disease costing data. Because there is only a small difference in weight gain between typicals and risperidone, this limitation is unlikely to affect the findings.
Our study also has several major strengths. First, the information used for assessing costs and effectiveness of each intervention is documented and transparent, and from Thai sources wherever possible. Second, to our knowledge, there is no previous study including time and travel costs in the cost estimations. Our findings show that these are a significant burden on patients and families, particularly for clozapine and family interventions. Third, we clearly address the issue of uncertainty in the data, presenting our results as a range within which the value is expected to fall. Fourth, we have had regular contact with local policy makers over the five-year span of our work. As a result of this, the food and drug administration in Thailand has already allocated 40 million baht to add generic risperidone to the national essential drug list.
This is the first study of its kind in Thailand. Studies elsewhere have modeled cost-effectiveness of different atypical antipsychotics, with fewer studies addressing both drug and non-drug interventions. Our results are in line with previous research. A study conducted in Slovenia which measured effectiveness as the percentage of patients in remission found that risperidone was more cost-effective than haloperidone and olanzapine for schizophrenia . Studies in Canada, Brazil and Australia consistently found that using risperidone rather than olanzapine would reduce the medical costs of schizophrenia [22,53,54]. In contrast, a number of studies using the method developed by the WHO-CHOICE project suggested using typical antipsychotics in combination with psychosocial interventions . However, the authors discussed that if generic forms of atypical medication would become available, the findings could change  as our sensitivity analysis indicates. Costs associated with drug treatments are a major driver of the results of cost-effectiveness analysis and limit the applicability of our conclusions to other countries.
A combination of psychosocial interventions and medications has been highly recommended as a successful treatment package for schizophrenia . Our results confirm that this package not only provides more health gain to patients, but also could help the government to reduce hospitalization cost by as much as 40% compared to typicals (Table (Table3).3). The hospitalization cost is generally considered to be the most expensive component of direct costs [3,5,8,9].
The cost of medications is the most important factor in the cost-effectiveness of antipsychotic interventions for schizophrenia. Atypicals are more cost-effective than typicals if their generic versions can be produced at a cost level achieved for many other generic medications in Thailand. Family intervention is an additional cost-effective option to help not only improve disease severity, but also reduce hospitalizations thus lessening the economic burden on the government.
The authors declare that they have no competing interests.
PP, TV and HW participated in the study design and data collection. PP, TV and MB conducted the data analysis and contributed to design of the modelling strategy. PP wrote the first draft of the manuscript. All authors have been involved in reviewing the manuscript and have given final approval of this manuscript version
Estimations of transition probabilities, health outcomes and intervention costs. 1) Transition probability estimates - This file explains a Markov cohort model with 3 health states: alive with schizophrenia, alive without schizophrenia and dead due to suicide, increased body weight or other causes. 2) Health effect estimations - This file describes measurement of the health benefit as a change in severity of disease calculated as a change in disability weight. Additionally, it provides details on estimation of the mortality and morbidity risks associated with weight gain. 3) Uncertainty parameters and distributions - This file gives information on uncertainty parameters, distributions used and data sources. 4) Assessment of intervention cost - This file gives details on cost estimates including cost elements, cost value and data sources.
We would like to acknowledge the Department of Mental Health, Thailand. We also would like to thank Dr. Supasit Pannarunothai, Dr. Manit Srisurapanont, Dr. Stephen Lim and Dr. Jan Barendreg for their advice and support. This study was supported by the Setting Priority using information on cost-effectiveness (SPICE), funded by the Wellcome Trust, U.K. (Grant number: 071842/Z/03/Z) and the National Health and Medical Research Council of Australia (Grant number: 301199).