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Analysis of the cost-effectiveness of thrombolysis with alteplase in stroke

Abstracts

BACKGROUND: The cerebrovascular accident (CVA) or stroke is the main cause of death in Brazil and little information is available on the cost of treatment. OBJECTIVE: To carry out a cost-effectiveness analysis of thrombolysis in stroke, up to three hours after symptom onset, comparing the treatment with alteplase versus the conservative treatment, under the perspective of the Brazilian Public Health System (SUS). METHODS: A decision analysis model was developed to compare the two types of treatment. Cycles were considered, during which the patients would go through five stages of disability post-stroke, based on the modified Rankin scale. The probability to present intracranial hemorrhage in the first year was obtained from the NINDS trial. For the subsequent years, one-year cycles were considered to calculate patients' mortality. The outcome was expressed as quality-adjusted life years (QALY). Both direct and indirect costs were considered in the analysis. Costs and outcomes were discounted at 5% a year. RESULTS: In the first year, the QALY gained was 0.06 for both sexes, with an incremental cost of R$ 2,558 for men and R$ 2,312 for women. The incremental cost-effectiveness ratio (ICER) in one year was R$ 40,539 / QALY (USD 28,956) for men and R$ 36,640 / QALY (USD 26,171) for women. After the second year, the treatment with alteplase reduced the cost of treatment (Purchasing Power Parity index: US$ 1 = R$ 1.4). CONCLUSION: The thrombolytic therapy with alteplase within the first three hours following a stroke is cost-effective in the Brazilian Public Health System scenario.

Health care costs; stroke; tissue plasminogen activator


FUNDAMENTO: Acidente Vascular Cerebral (AVC) é a principal causa de óbito no Brasil e pouca informação está disponível sobre custo do tratamento. OBJETIVO: Elaborar análise de custo-efetividade da trombólise no AVC, até três horas após o início dos sintomas, comparando o tratamento com alteplase versus conservador, sob a perspectiva do Sistema Único de Saúde (SUS). MÉTODOS: Modelo de análise de decisão foi desenvolvido para comparar os dois tratamentos. Ciclos foram considerados, durante os quais pacientes poderiam transitar entre cinco estágios de incapacidade pós-AVC, baseados na escala modificada de Rankin. A probabilidade de apresentar hemorragia intracerebral no primeiro ano foi obtida do ensaio NINDS. Para os anos subsequentes, ciclos de um ano foram considerados, para contabilizar a mortalidade dos pacientes. O desfecho foi expresso em Anos de Vida Ajustados pela Qualidade (QALY). Tanto os custos diretos quanto os indiretos foram considerados na análise. Custos e desfecho foram descontados em 5% ao ano. RESULTADOS: No primeiro ano, o QALY ganho foi de 0,06 para ambos os gêneros, com custo incremental de R$ 2.558 para homens e R$ 2.312 para mulheres. A razão de custo-efetividade incremental em um ano foi de R$ 40.539 / QALY (USD 28.956) para homens e R$ 36.640 / QALY (USD 26.171) para mulheres. Após o segundo ano, o tratamento com alteplase reduziu o custo do tratamento (índice de Paridade do Poder de Compra US$ 1 = R$ 1,4). CONCLUSÃO: Terapia trombolítica com alteplase nas primeiras três horas após o AVC é custo-efetiva no cenário do Sistema Único de Saúde.

Custos de cuidados da saúde; acidente vascular cerebral; ativador de plasminogênio tecidual


FUNDAMENTO: Accidente Vascular Cerebral (AVC) es la principal causa de óbito en el Brasil y poca información está disponible sobre el costo del tratamiento. OBJETIVO: Elaborar análisis de costo-efectividad de la trombólisis en el AVC, hasta tres horas después del comienzo de los síntomas, comparando el tratamiento con alteplase versus conservador, bajo la perspectiva del Sistema Único de Salud (SUS). MÉTODOS: Modelo de análisis de decisión fue desarrollado para comparar los dos tratamientos. Ciclos fueron considerados, durante los cuales pacientes podrían transitar entre cinco niveles de incapacidad post-AVC, basados en la escala modificada de Rankin. La probabilidad de presentar hemorragia intracerebral en el primer año fue obtenida del ensayo NINDS. Para los anos subsecuentes, ciclos de un año fueron considerados, para contabilizar la mortalidad de los pacientes. El desenlace fue expresado en Años de Vida Ajustados por la Calidad (QALY). Tanto los costos directos como los indirectos fueron considerados en el análisis. Costos y desenlace fueron descontados 5% al año. RESULTADOS: En el primer año, la ganancia de QALY fue de 0,06 para ambos géneros, con un costo incremental de R$ 2.558 para hombres y de R$ 2.312 para mujeres. La razón de costo-efectividad incremental en un año fue de R$ 40.539 / QALY (USD 28,956) para hombres y R$ 36.640 / QALY (USD 26,171) para mujeres. Después del segundo año, el tratamiento con alteplase redujo el costo del tratamiento (índice de Paridad del Poder de Compra US$ 1 = R$ 1,4). CONCLUSIÓN: Terapia trombolítica con alteplase en las primeras tres horas después del AVC es costo-efectiva en el escenario del Sistema Único de Salud.

Costos de cuidados de la salud; accidente cerebral vascular; activador de plasminógeno tisular


ORIGINAL ARTICLE

Analysis of the cost-effectiveness of thrombolysis with alteplase in stroke

Denizar Vianna AraújoI, III; Vanessa TeichII; Roberta Benitez Freitas PassosII; Sheila Cristina Ouriques MartinsIII, IV

IUniversidade do Estado do Rio de Janeiro - UERJ

IIMedInsight - Decisions in Health Care, Rio de Janeiro, RJ

IIIInstituto Nacional de Ciência e Tecnologia para Avaliação de Tecnologias em Saúde (IATS) - CNPq

IVHospital de Clínicas de Porto Alegre, Porto Alegre, RS - Brazil

Mailing address Mailing address: Denizar Vianna Araújo Avenida Visconde de Albuquerque 1400/501 - Leblon 22450-000 - Rio de Janeiro, RJ - Brazil E-mail: denizar@cardiol.br, denizarvianna@medinsight.com

ABSTRACT

BACKGROUND: The cerebrovascular accident (CVA) or stroke is the main cause of death in Brazil and little information is available on the cost of treatment.

OBJECTIVE: To carry out a cost-effectiveness analysis of thrombolysis in stroke, up to three hours after symptom onset, comparing the treatment with alteplase versus the conservative treatment, under the perspective of the Brazilian Public Health System (SUS).

METHODS: A decision analysis model was developed to compare the two types of treatment. Cycles were considered, during which the patients would go through five stages of disability post-stroke, based on the modified Rankin scale. The probability to present intracranial hemorrhage in the first year was obtained from the NINDS trial. For the subsequent years, one-year cycles were considered to calculate patients' mortality. The outcome was expressed as quality-adjusted life years (QALY). Both direct and indirect costs were considered in the analysis. Costs and outcomes were discounted at 5% a year.

RESULTS: In the first year, the QALY gained was 0.06 for both sexes, with an incremental cost of R$ 2,558 for men and R$ 2,312 for women. The incremental cost-effectiveness ratio (ICER) in one year was R$ 40,539 / QALY (USD 28,956) for men and R$ 36,640 / QALY (USD 26,171) for women. After the second year, the treatment with alteplase reduced the cost of treatment (Purchasing Power Parity index: US$ 1 = R$ 1.4).

CONCLUSION: The thrombolytic therapy with alteplase within the first three hours following a stroke is cost-effective in the Brazilian Public Health System scenario.

Key words: Health care costs; stroke; tissue plasminogen activator.

Introduction

The cerebrovascular accident (CVA) or stroke is one of the main causes of death among the Brazilian adult population, varying between the first and the third positions, according to the year and state of the Federation1. Mortality is only one of the public health measurements of stroke impact, with sequelae being equally important, and, consequently, lack of productivity, loss of quality of life and premature retirement. It is estimated that 85% of the strokes are of ischemic origin and 15% of hemorrhagic origin2.

The mortality of the ischemic stroke during the first 30 days is approximately 10%, mainly associated with neurological sequelae3 and can reach 40% at the end of the first year. Among the patients that survive the acute phase of the stroke, most present neurological deficits that require rehabilitation4. Around 70% of these individuals will not return to work and 30% will need help to walk.

An epidemiological enquiry carried out the Brazilian Public Health System (SUS)5 with stroke patients, at the productive age of 20 to 59 years, demonstrated that 80% referred some type of persistent functional disability after the first episode. After the stroke, 70% of the patients became unemployed or retired prematurely.

Up to the last decades, the ischemic stroke outcome was determined by the natural evolution and support measures. In July 1996, the Food and Drug Administration (FDA) approved the use of recombinant tissue plasminogen activator (rt-PA) for the treatment of stroke at the acute stage.

In ischemic stroke, the probability of the affected tissue to develop necrosis depends on the residual brain blood flow in the affected region as much as on the duration of ischemia6. The main objective of the thrombolytic drugs is to restore blood flow in the affected area as early as possible, with a consequent decrease in ischemia and limitation of the neurological injury7.

The objective of the present study was to carry out a cost-effectiveness analysis of thrombolysis in stroke up to three hours after symptom onset, comparing the treatment strategy with rt-PA with the conservative treatment, under the perspective of the Brazilian Public Health System (SUS).

Methods

The first phase of the study consisted in the review and critical analysis of the literature. The review was carried out by searching the databases Medline, Cochrane and LILACS for all studies published in Portuguese, English or Spanish that had evaluated the use of rt-PA in ischemic stroke treatment during the last ten years, until May 2008. The inclusion criteria were: type of study (randomized clinical trial, review articles, systematic reviews and meta-analyses) and study population (individuals older than 18 years with ischemic stroke). The studies were limited to those carried out with human beings. The main keywords used in the search were: alteplase, rt-PA, stroke, efficacy. After the search had been carried out, their references were analyzed to locate new publications of interest. The search selected, initially, articles according to the title and/or summary and then, the article was read and critically analyzed, if it were relevant to the objective of the study.

The initial search identified 67 articles. Of these, 28 met the inclusion criteria. Sixteen of them were review articles and 10 reported results of controlled clinical trials. A systematic Cochrane8 review was found on the use of thrombolytic drugs in general, including rt-PA. A summary of this review was published in the Lancet in 19979; however, in 2003 this review underwent alterations, and therefore, it was updated.

Four randomized double-blind clinical trials were carried out to assess the effectiveness and safety of rt-PA use in ischemic CVA: National Institute of Neurological Disorders and Stroke (NINDS) trial10, the first and second European cooperative Acute Stroke Studies (ECASS I11 e ECASSII12) and Alteplase Thrombolysis for Acute Non-interventional Therapy in Ischemic Stroke (ATLANTIS) Study13.

Cochrane Collaboration performed a systematic review, of which last update was carried out in March 2003, to evaluate the effectiveness and safety of the thrombolytic agents in general, in ischemic stroke. A total of 18 clinical trials were assessed, totaling 5,727 patients assessed, testing urokinase, streptokinase, recombinant tissue plasminogen activator (rt-PA) or recombinant pro-urokinase (r-pro-UK). Approximately half of the data referred to rt-PA.

Table 1 summarizes the results of the clinical trials and the meta-analyses that evaluated the efficacy of rt-PA.

Perspective of the analysis

The estimates of the use of resources and value appraisal were guided by the perspective of the Brazilian Public Health System (SUS).

Target-population

Two groups of patients were analyzed, older than 18 years, of both sexes: the first received treatment with rt-PA and the second received the conservative treatment. Only patients treated within three hours since stroke symptom onset were analyzed.

Model design

The type of analysis selected was the analysis of cost-effectiveness, more specifically, the cost-utility analysis, as the model compared the direct and indirect costs involved in the treatment and follow-up of stroke patients and the health outcome in terms of quality-adjusted life years (QALY).

To estimate the treatment costs and outcomes, a Markov model was created, which simulated the treatment of stroke in the acute phase and the transition of patients between the different levels of severity of post-stroke sequelae, characterized by the different states of Markov. The analysis compared the two treatment strategies considered in the NINDS study10: use of rt-PA and placebo, in this case, considered as the conservative treatment. The structure used in the model is shown in Figure 1.


In the present study, the patients were included in the model after an ischemic stroke event. When included in the model, it is assumed that the patient will receive treatment with rt-PA or the conservative treatment. During the treatment, the patient can experience an intracranial bleeding event.

After the stroke treatment, the patients pass through different health stages, according to the degree of sequelae as a consequence of the stroke. In the first year, three-month cycles were considered, at the end of which the patient's status was reassessed and classified according to the modified Rankin scale. The possible states were: R0 (no symptoms), R1 (no significant disability), R2 (minimal disability), R3 (moderate disability), R4 (moderate to severe disability), R5 (severe disability) or death.

After the first year, one-year cycles started to be considered, after which the patients remained at the state they were at the end of the first year or died.

Considered outcomes

The considered health outcome was quality-adjusted life years (QALY). This outcome evaluates the disability caused by the sequelae that impair the quality of life of patients post-stroke. Due to the absence of Brazilian estimates of utility for post-stroke patients, we chose to adopt the utility values of the systematic review created by Post et al14. These authors selected 23 articles that measured utilities for the post-stroke health status. Patients that presented risk for stroke reported utilities, with the time trade-off method, of 0.26 (lower limit of 0.11 and upper limit of 0.39) and 0.55 (lower limit of 0.39 and upper limit of 0.75) for major stroke (Rankin scale from 4 to 5) and minor stroke (Rankin scale from 2 to 3), respectively. For the Rankin scale de 0 to 1, a value of 0.75 was considered.

The economic outcomes considered were "direct and indirect costs". Direct costs refer to the resources used for the patient's treatment, such as cost of medication, hospitalization and rehabilitation treatments. These were collected under the perspective of SUS. The indirect costs refer to the onus derived from the loss of productivity of individuals that retire prematurely due to the stroke sequelae.

Both costs and years of life were discounted at a rate of 5% a year. The impact of this percentage on the results of the model was assessed by analysis of sensitivity.

The results were calculated for different time horizons, varying from 1 to 30 years.

Data collection

Effectiveness Data

The probabilities of transition between the degrees of severity of the post-stroke sequelae every three months were extracted from the NINDS study10 for the first year of the model, as shown in Table 2. The values for nine months were obtained by interpolating the 6-month and the 12-month data. The choice of the NINDS study was due to the fact that this was the only study that assessed patients who received treatment within three hours after stroke symptom onset, with the approved dose of 0.9 mg/kg.

After this period, the model considered that the patients would remain at the same health status or would die due to other causes at each one-year cycle. The mortality rate due to all causes was extracted from IBGE (The Brazilian Institute of Geography and Statistics) for men15 and women16. The model also considered that, after the stroke, the mortality rate of the patients would be 2.67-fold17 higher than that of the general population.

After the first year of the model, similar mortality rates were considered for all patients, varying only between men and women, regardless of the degree of severity of the sequelae that the patient presented. Moreover, the probabilities of intracerebral bleeding during the stroke treatment were also obtained from the NINDS study10, which were 6.40% with rt-PA and 0.60% with the conservative treatment.

The mean age of the patients being treated with rt-PA at the NINDS study10 was 67 years. Due to the absence of similar studies segmented by age range, the model assumed that the effectiveness obtained at the NINDS study could be extrapolated to other age ranges.

Direct cost data

For the first cycle of the model, the costs of treatment of stroke patients were considered. The use of resources was considered to be equivalent for men and women, except for the amount of rt-PA used. The latter varies according to the patient's weight, as the treatment protocol of 0.9 mg/kg was considered, as well as different mean weights for men and women, 75 kg and 65 kg, respectively. Moreover, the difference between the treatment with rt-PA and the conservative treatment also includes the cost of hospitalization. The NINDS study10 showed a difference regarding the mean duration of hospitalization of patients undergoing treatment with rt-PA or placebo. However, as the SUS reimbursement is calculated by procedure and not by daily hospitalization cost, this difference could not be incorporated in the model, with conservative results being attained for rt-PA, as the benefit of the decrease in the mean duration of hospitalization in days was not considered.

The costs considered for the treatment of stroke, including the cost of treatment of a bleeding event, using rt-PA or conservative treatment is shown in Table 3.

After the stroke, the patients started the follow-up period, and could be assigned to five different states, classified according to the degree of sequelae, based on the modified Rankin scale, or die. Depending on the post-stroke patient's status, different percentages of patients needed rehabilitation. This percentage was obtained based on a cost-utility study developed under the Canadian perspective18, which considered the percentage of patients that needed support at a specific structure after the stroke (rehabilitation hospital or long-term care institution) or went back home.

In the current model, we considered that the patient would need or not rehabilitation treatment, but in both cases, he or she would return home. The rehabilitation treatment considered was a daily home visit to assist the patient.

All patients being followed also received treatment with antiaggregants and anti-hypertensive drugs and had a consultation with a neurologist very two months. No differences were considered regarding the use of resources by sex and age range.

Indirect cost data

The indirect costs considered in the model referred to the loss of productivity and early withdrawn of the retirement funds due to the premature retirement of patients, depending on the severity of the stroke sequelae.

In order to do that, we obtained from IBGE19 the mean rate of unemployment of the population and the mean monthly income of the employed population. Thus, the mean loss of work per year was calculated.

Moreover, a mean monthly retirement of one minimum wage was considered to calculate the additional cost per year of premature retirement.

The model considered, therefore, that, if the patients were younger than the mean age of retirement and were in a state of the Rankin scale < R3 (R3, R4 or R5), the consequence would be the costs caused by the loss of productivity and additional costs concerning the social security. In case of death, only the costs concerning the loss of productivity would apply.

The parameters considered for the calculation of indirect costs are shown in Table 4.

Results

The comparative results of the alternative strategies of treatment were measured by the incremental cost-effectiveness ratio. That is defined, for two specific alternatives of treatment, as the additional cost of treatment divided by the additional health benefit. This "benefit" was expressed in terms of QALY.

The model base case considered a rate of discount of 5% a year and an initial mean age of the patients of 50 years. Additionally, mean retirement ages of 60 and 65 years, for women and men, respectively, were considered.

The one-year results for men and women are shown in Table 5. Table 6 shows the results for different time horizons, from 1 to 30 years.

It can be observed that, for a one-year result, for men, the cost of treatment with rt-PA is higher than the cost of the conservative treatment. This result is mainly directed by the cost of the medication. Part of this additional cost is compensated by the lower cost of rehabilitation and the smaller losses of productivity as early as the two first years, as the patients treated with rt-PA present fewer sequelae than those who receive the conservative treatment.

After the second year post-stroke, for men and women, the treatment with rt-PA starts to present a lower cost when compared to the conservative treatment, when direct and indirect costs are considered. From this time horizon onward, the additional cost of the medication starts to be more than compensated by the smaller losses of productivity and lower social security and patient rehabilitation costs.

The analysis of cost-effectiveness measures the cost in monetary units divided by a non-monetary unit, called the natural unit, for instance, "years of life saved". It allows the estimation of the cost per unit of effectiveness. A healthcare intervention is called cost-effective if it produces a clinical benefit that is justifiable for its cost.

The calculation of how much the additional effectiveness justifies the additional cost is determined by society and depends on social values and the availability of resources. Although the explicit quantification of the acceptable cost for certain effectiveness ("clinical benefit") is difficult to define, valuable levels of reference are the medical interventions that the society chooses to incorporate20. The World Health Organization (WHO) recommends a 3-fold value of the Gross Domestic Product (GDP) per capita of the country where the analysis was carried out, as the limit of cost-effectiveness justifiable for that context.

Analysis of sensitivity

Univariate analyses of sensitivity were carried out to evaluate the impact of key-parameter variation on the results of the model.

Table 7 presents the results of the variation of the types of costs considered in the analysis. The base results considered in the analysis are the five-year results.

Discussion

Our study suggests that the early intervention in the stroke evolution can be a cost-effective strategy for the Brazilian Public Health System (SUS), using the limits recommended by the WHO. The GDP per capita of Brazil in 2007 was US$ 9,700, equivalent to the cost- effectiveness threshold of US$ 29,100 (3x the GDP per capita) per QALY.

The NINDS clinical trial showed that patients treated with rt-PA within three hours after symptom onset, when compared to the placebo group, had at least a 30% higher probability of presenting minimal disability or none at all after 3 months. This benefit, although associated with an increased risk of intracranial bleeding, was not related to an increase in mortality.

The treatment of stroke patients implies elevated costs, estimated in 1994 in the United States as 20 billion dollars of direct costs and 46 billion dollars of indirect costs21. Therefore, an intervention capable of preventing the consequent unfavorable stroke outcomes will have an important economic impact.

Christensen et al estimated the cost of the acute treatment of ischemic and hemorrhagic stroke in two Brazilian public hospitals22. The authors used a retrospective analysis of medical files and identified 316 patients with a mean hospital stay duration of 12.0±8.8 days for ischemic stroke and 13.3±23.4 days for hemorrhagic stroke. The mean cost of hospitalization for the treatment of ischemic stroke was US$ 1,902. In our study, for the group of hypothetical patients allocated at the alteplase group, it was US$ 2,262 for men and US$ 2,058 for women (Table 3). The same Purchasing Power Parity index: was used: 1 US$ = 1.4 reais1.

The analysis of cost-effectiveness of thrombolysis in Acute Myocardial Infarction (AMI) has also been recently estimated in our country, in the Public Health System scenario23. The researchers concluded that the strategy of pre-hospital thrombolysis of the AMI can save lives and reduce costs related to the treatment of AMI and its complications.

Our study has some limitations, a characteristic of the cost-effectiveness analyses carried out with decision analysis models. The data used in the model are obtained from controlled clinical trials, that is, it refers to efficacy data, instead of effectiveness data that portray the "real world". The result expresses the mean cost of a usual patient, does not portray the cost of patients that present complications and require a long-term hospitalization. No median values were used for the monthly income, as healthcare decision-makers and policy-makers are more familiarized with the use of means for monetary values.

The proposed treatment is based on the guidelines of the Specialty Medical Societies, which does not necessarily express the usual treatment of patients in the Public Health System. The models are probabilistic estimates of the natural history of the disease and their interventions and hardly incorporate all uncertainties inherent to biology and thus, should be always critically analyzed regarding the capacity of generalization for "real-world" patients.

Conclusion

The use of rt-PA thrombolytic therapy within the first three hours of the CVA evolution can change the natural history of the disease. It is noteworthy the fact that this is the only effective intervention available in the current therapeutic arsenal, substituting the conservative and expectant treatment. This intervention can minimize direct costs, by reducing hospitalization time and rehabilitation duration and, especially, it can reduce the indirect costs (loss of productivity, absenteeism, premature death), with a significant socioeconomic impact.

When the loss or gain of productivity can be measured in monetary units, due to a treatment that has been applied, the health policy makers can make more conscious decisions, based on consistent information.

Potential Conflict of Interest

No potential conflict of interest relevant to this article was reported.

Sources of Funding

There were no external funding sources for this study.

Study Association

This study is not associated with any post-graduation program.

References

Manuscript received June 10, 2009; revised manuscript received December 23, 2009; accepted March 3th, 2010.

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  • Mailing address:
    Denizar Vianna Araújo
    Avenida Visconde de Albuquerque 1400/501 - Leblon
    22450-000 - Rio de Janeiro, RJ - Brazil
    E-mail:
  • Publication Dates

    • Publication in this collection
      11 June 2010
    • Date of issue
      July 2010

    History

    • Reviewed
      23 Dec 2009
    • Received
      10 June 2009
    • Accepted
      03 Mar 2010
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