Cost-effectiveness of enzyme replacement therapy with alglucosidase alfa in classic-infantile patients with Pompe disease
© Kanters et al.; licensee BioMed Central Ltd. 2014
Received: 1 November 2013
Accepted: 7 April 2014
Published: 16 May 2014
Infantile Pompe disease is a rare metabolic disease. Patients generally do not survive the first year of life. Enzyme replacement therapy (ERT) has proven to have substantial effects on survival in infantile Pompe disease. However, the costs of therapy are very high. In this paper, we assess the cost-effectiveness of enzyme replacement therapy in infantile Pompe disease.
A patient simulation model was used to compare costs and effects of ERT with costs of effects of supportive therapy (ST). The model was filled with data on survival, quality of life and costs. For both arms of the model, data on survival were obtained from international literature. In addition, survival as observed among 20 classic-infantile Dutch patients, who all received ERT, was used. Quality of life was measured using the EQ-5D and assumed to be the same in both treatment groups. Costs included the costs of ERT (which depend on a child’s weight), infusions, costs of other health care utilization, and informal care. A lifetime time horizon was used, with 6-month time cycles.
Life expectancy was significantly longer in the ERT group than in the ST group. On average, ST receiving patients were modelled not to survive the first half year of life; whereas the life expectancy in the ERT patients was modelled to be almost 14 years. Lifetime incremental QALYs were 6.8. Incremental costs were estimated to be € 7.0 million, which primarily consisted of treatment costs (95%). The incremental costs per QALY were estimated to be € 1.0 million (range sensitivity analyses: € 0.3 million - € 1.3 million). The incremental cost per life year gained was estimated to be € 0.5 million.
The incremental costs per QALY ratio is far above the conventional threshold values. Results from univariate and probabilistic sensitivity analyses showed the robustness of the results.
Since the introduction of orphan drug regulations, the number of orphan drugs (i.e. drugs for rare diseases) has grown vastly. This confronts policy makers with a trade-off between access and affordability. On the one hand, the overall proportion of orphan drugs in health care expenditures is substantial and continues to grow . On the other hand, healthcare authorities would like to provide rapid access to promising new treatments, even when the evidence base might not be mature yet. To deal with this trade-off, policy makers can turn to ‘coverage with evidence development schemes’, which enable patients to obtain access to the treatment while effectiveness is simultaneously studied in a real-world setting [2, 3]. When a cost-effectiveness analysis is performed at the same time, policy makers also gain insight in the economic consequences of the new treatment. In 2006, such a scheme was installed in the Netherlands for high-priced in-hospital orphan drugs. During a coverage with evidence development period of four years, effectiveness and cost-effectiveness were studied for orphan drugs listed on a specific policy rule .
One of the drugs reimbursed through this policy rule is a drug to treat Pompe disease. Pompe disease is a rare metabolic disease and presents as a broad clinical spectrum, with the rapidly progressive classic-infantile form at the most severe end and late-onset or adult-onset Pompe disease at the least severe end [5, 6]. In all cases, the disease is caused by a deficiency of the enzyme acid α-glucosidase. The incidence of classic-infantile Pompe disease is 1 in 138,000 births . In classic-infantile Pompe disease, symptoms present in the first months of life and involve respiratory and feeding problems, airway infections, and generalized muscle weakness. Patients also show progressive thickening of the heart (hypertrophic cardiomyopathy) which eventually leads to heart failure. These children generally die before the first year of age from cardiorespiratory failure and the median age of death has been estimated to be 6 to 9 months [8, 9].
Enzyme replacement therapy (ERT) with alglucosidase alfa (Myozyme®, Genzyme corp.) was developed as a treatment for Pompe disease. ERT has proven to have a substantial effect on survival in classic-infantile Pompe patients, reducing the 3-year mortality risk by 95% compared to an untreated historical control group [10, 11]. Cardiac, respiratory and motor functions of patients have been shown to improve by therapy.
Orphan drugs are often very expensive and this is also true for ERT to treat Pompe disease . As of 2006, ERT for Pompe disease is reimbursed in the Netherlands under a coverage with evidence development scheme, during which the cost-effectiveness of the treatment needs to be assessed, even though this was expected to be unfavorable upfront. This study reports on the cost-effectiveness of ERT in classic-infantile Pompe disease.
Patients and treatments
All Dutch patients with classic-infantile Pompe disease were enrolled in an observational study. Diagnosis of Pompe disease was confirmed by enzyme assay in leukocytes or fibroblasts and/or mutation analysis. All patients were treated by the Erasmus MC Center for Lysosomal and Metabolic Diseases, Rotterdam, the Netherlands. The Institutional Review Board approved the studies. Written informed consent was provided by parents.
Currently ERT is the only available registered treatment for Pompe disease. In this study, the comparative treatment therefore consisted of usual supportive therapy (ST), including for example (nightly) ventilation, surgical correction of scoliosis, or nutritional support.
The registered dose of ERT is 20 mg/kg/2 weeks. Patients in the Netherlands received doses ranging from 20 mg/kg/2 weeks to 40 mg/kg/week. Since 2008 the majority of patients use the higher dose. The majority of the Dutch data was collected in patients using this dose. In the base case analyses of the model we therefore used the maximum dose of 40 mg/kg/week.
Study design and model structure
A patient simulation model was used to compare costs and effects of ERT with costs and effects of ST for patients with classic-infantile Pompe disease. The model was filled with data on survival, utilities and costs. For both treatment arms, the model generated costs, survival, quality of life and quality adjusted life years (QALYs). In addition, the model generated an estimate of the cost-effectiveness of treatment, expressed as cost per QALY.
Patient characteristics for patients in survival analyses
Age at end study in months [range]
Patients using ventilation
Dosage (every other week)
Quality of life
Quality of life was assessed in Dutch patients using the Euroqol-5D (EQ-5D), completed by parents of patients every six months. The EQ-5D is a validated instrument for measuring and valuing generic health related quality of life . The instrument describes 245 health states, and each health state is associated with a utility using a scoring formula. Utility scores typically range from zero (death) to 1 (perfect health). Utility scores were estimated using the Dutch tariff . Only observations for patients above the age of two years were included (n = 6; median follow-up 24 months). The average utility was 0.62, ranging from 0.24 to 0.82. For five patients, multiple observations were available; their average utility was used in the analyses.
Costs were calculated from a societal perspective. This implies that all costs are included, no matter to whom they accrue. Total costs for patients treated with ERT consisted of four components: the cost of the drug alglucosidase alfa, infusion-related costs, costs related to other health care use and informal care costs. Patients receiving ST did not incur costs of the drug and infusion-related costs. Costs were expressed in 2009 euro values.
Costs of the drug alglucosidase alfa are dependent on patient’s weight. In the Netherlands, costs per vial (50 mg) are €556.50. In the Netherlands the doses applied in infants with classic-infantile Pompe disease range from 20 mg/kg/2 weeks to 40 mg/kg/week bodyweight (since 2008 the majority of patients use the higher dose). For the model we used the maximum dose of 40 mg/kg/week so drug costs per kilo bodyweight were €445.20. With weekly infusions (52 infusions per year), yearly medication costs per kilo are €445.20*52 = €23,150.40. Data from the Dutch cohort were collected between May 2007 and October 2012. Patients’ weights were estimated on the basis of available data on Dutch patients (n = 17; median follow-up 35 months), and increased with the patient’s age to a maximum of 75 kilograms.
Infusion-related costs were based on detailed time studies using the methodology described in the Dutch costing manual . The total costs for infusion consisted of cost associated to physician and nursing time during infusion, overhead, capital, materials, informal care and travel time. A distinction was made with respect to treatment location of patients; patients receive infusions at home or in hospital. The estimated mean cost per infusion at home was € 426 compared to € 520 per infusion at the hospital. A total percentage of 68% of the Dutch patients were treated in the home situation. Based on weekly infusions (52 infusions per year), the annual infusion costs were estimated to be € 23.710.
Cost components and associated unit costs (2009 prices)
Cost per unitb
Hospital day visits
General practitioner visit
€ 14 - € 91
Home care per hour
€ 29 - € 65
Other medical costs
Tests & procedures
€ 54 - € 181
Respiratory support per day
€ 18 - € 1,500
Informal care costs per hour
Other health care utilization costs were estimated using a generalized estimated equation (GEE) model, a logarithmic link function and a gamma distribution (n = 12). Age was the only predictor variable used in this model.
No data was available on health related quality of life (utility) for patients receiving ST. Utilities were therefore assumed to be equal in the two treatment arms. Hence, differences in QALYs only resulted from differences in life expectancy between the two treatment arms. Health care utilization costs were only available for patients receiving ERT. We assumed that patients receiving ST incurred the same costs as ERT-treated patients with the exception of treatment costs. Differences in costs therefore only resulted from treatment costs and differences in life expectancy between the two treatment arms.
Cost-effectiveness was expressed in incremental cost per QALY gained and incremental cost per life year gained. Costs were discounted at a rate of 4% and effects were discounted at a rate of 1.5% in accordance with Dutch guidelines for pharmacoeconomic research . A lifetime time horizon was used and a cycle length of ½ year was used.
Univariate sensitivity analyses were performed to examine the impact of the assumptions of the model on the results. We varied the following input variables: ERT dosage (the registered dose of 20 mg/kg/2 weeks as opposed to the mostly used dose in the Netherlands of 40 mg/kg/week in the base case analysis); costs of treatment (€ 11,575.20 per kilo per infusion as opposed to € 23,150.40 per kilo per infusion); time horizon (5 years as opposed to lifetime in the base case); quality of life (0.49 and 0.74 in both cohorts and 0.31 in the ST cohort combined with 0.62 in the ERT cohort – implying a treatment effect on quality of life – as opposed to 0.62 in both cohorts); survival in the ERT cohort (varying the distributions used in the parametric survival analyses); and costs incurred by the ST cohort (double costs and no costs for the ST-cohort instead of assuming that ‘other healthcare costs’ were the same as the costs seen in ERT-treated patients).
Next to the univariate sensitivity analyses, probabilistic sensitivity analyses were performed to examine the impact of the uncertainty around the values of the input variables on the estimated effectiveness and cost-effectiveness of ERT. For this purpose, 1,000 populations were randomly drawn from relevant distributions in a Monte Carlo simulation procedure. The results from the probabilistic sensitivity analyses were presented in a cost-effectiveness plane (CE-plane). The CE-plane shows total incremental costs and total incremental effects of ERT against ST.
Estimates for health care utilization costs were based on data of 12 Dutch classic-infantile patients; 8 male patients and 4 female patients. At first measurement, average age of these patients was 3.5 years. Data on quality of life was available for six patients; four male patients, average age 6.1 years (range 2.2 – 11.1) at baseline.
Total and incremental costs and effects
[95% confidence interval]
Life expectancy (years)
[1.55 – 25.23]
[2.32 – 11.19]
[1,869,635 – 12,130,422]
- ERT costs
[1,615,059 – 11,645,991]
- Infusion costs
[121,477 – 304,108]
- Other costs
[131,728 – 181,694]
Table 3 also shows the total and incremental costs for classic-infantile patients. The majority of the incremental costs consisted of drug costs (95% of incremental costs). In addition, infusion costs were estimated to be € 212,793 (3.0%). ERT-treated patients incurred higher costs than ST-treated patients not simply because of the ERT treatment they received but also because they lived much longer. Incremental costs were estimated to be € 7.0 million.
Incremental cost-effectiveness ratios (dosage 40 mg/kg/week unless otherwise specified)
Costs/life year gained
Base case analysis dosage 40 mg/kg/week
Registered dosage regimen (20 mg/kg/2 weeks)
Lower treatment costs (costs divided by 2)
Shorter time horizon (5 years)
Lower utility (0.49) in both cohorts
Higher utility (0.74) in both cohorts
Lower utility in ST-treated patients
Lognormal survival distribution
No costs incurred by ST-treated patients
Double cost incurred by ST-treated patients
Table 4 also provides the results from the sensitivity analyses. The first sensitivity analysis examined the effect of dosage on the ICER. Total costs for ERT-treated patients were considerably lower in the 20 mg/kg/2 weeks analysis than in the base case analysis, because less medication was administered. Incremental costs were estimated to be € 1.9 million. The ICERs at the lower, biweekly dose were about 3.6 times lower than the ICER in the base case analysis.
In a sensitivity analysis, the influence of treatment costs on the ICER was examined by halving these costs. The ICER dropped substantially (47%), indicating the prominent role of treatment costs in the analyses.
When a shorter time horizon of 5 years was used, the ICER was lower relative to the analyses with a lifetime horizon. During this period, patients’ body weights’ were relatively low, which considerably decreased treatment costs leading to more favorable ICERs. Incremental costs in this analysis were estimated to be € 1.2 million and the incremental effects to be 2.20 QALYs.
Since information on utility (quality of life) was limited, we varied the utility value used in the base-case analysis by 20% to determine how much it affected the results (range: 0.49 to 0.74). A change in quality of life can only affect QALY gain and thereby the ICER; it has no impact on the incremental costs. A lower value for quality of life reduced QALY gains and led to an increase in the ICER. When a higher utility value was used, the QALY gain increased and the ICER decreased. The use of a lower utility in the ST-treated patients only (implying a treatment effect on utility) did not change the ICER substantially.
Survival in the ERT-treated patients was based on an exponential survival distribution, because that fitted the data best. Use of the lognormal distribution, which had the second lowest BIC, increased life expectancy from 13.8 to 21.9 years, primarily because the predicted survival later in life was higher. Incremental QALYs increased to 9.3 in this analysis. This longer life expectancy increased the incremental costs to 9.7 million. However, this did not affect the ICER, which remained 1.04 million/QALY. Two other distributions were also tested (Weibull, log-logistic), but they did not have any substantial effect on the ICER (Weibull: life expectancy 14.9 years; ICER 1.05 million/QALY; log-logistic distribution: life expectancy 20.6 years; ICER 1.03 million/QALY).
Since no data was available regarding costs of ST treatment we assumed in the base case analysis that these costs were the same as the costs seen in the ERT-treated group (excluding ERT-related costs). We tested the importance of this assumption by doubling the costs for the ST cohort and by setting the total costs in the ST cohort to zero. However, since the costs for the ST cohort in the base case analysis were limited because of the short life expectancy in this group, changes in the costs for the ST cohort had no appreciable influence on the ICER.
Probabilistic sensitivity analyses
This is one of the first studies to assess the cost-effectiveness of an orphan drug, evaluating the cost-effectiveness of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in classic-infantile Pompe disease. The incremental cost-effectiveness was calculated on the basis of available data, a pharmacoeconomic model and assumptions on disease course. The cost per QALY was estimated to be € 1.0 million; cost per life year gained was € 0.5 million.
The results from the univariate sensitivity analyses and probabilistic sensitivity analyses showed the robustness of the model. Uncertainty with regard to the ICER is limited; in all cases the ICER is beyond any conventionally used cost-effectiveness threshold. While the absolute gains in life years, incremental QALYs, and incremental costs differ between various sensitivity analyses, ICERs are not affected.
For instance, using log-normal and log-logistic distributions to estimate survival had a large impact on the life expectancy. This was primarily caused by a higher survival later in life. However, despite the large gains in survival, the ICER was relatively unaffected, due to the significant costs of therapy. This shows the paradoxical situation of performing an economic evaluation with a therapy of such high annual costs; better effectiveness did not lead to a better cost-effectiveness ratio.
This study was performed using currently available information, but the available evidence on (infantile) Pompe disease is increasing as the follow-up period increases. For instance, some patients have already survived to the age of 15 and hope to reach adulthood. Increases in the number of patients and follow-up time will lead to more stable estimates of survival.
Limitations of the study
There are a number of limitations of the study that need to be stressed. Most limitations are due to the relatively scarce availability of data, both with respect to number of patients (due to orphan disease status) and time period involved.
Firstly, survival estimates from various sources were combined to increase sample size. Hence, the implicit assumption was that survival probabilities for patients were comparable, although the doses used in these groups of patients varied. The number of patients was too small to perform subgroup analysis by dosage. Furthermore, survival was modeled using an exponential survival distribution, which assumes a constant hazard over time. The choice of the distribution was made on the basis of visual inspection and best fit of the data . Although a constant hazard might not be a realistic assumption, the sensitivity analyses showed that the choice of the distribution did not have a large influence on the ICER.
Secondly, the pharmacoeconomic model was based on observations of a limited period. We assumed that these results could be extrapolated into the future. Accordingly, we assumed that patients did not change therapy over the course of time. In addition, costs and effectiveness of the treatment were assumed not to change.
A third point of attention concerns the valuation of health related quality of life, which was assessed using a proxy version of the EQ-5D. The use of a proxy to make statements on a subjective measure as quality of life can be difficult. However, for young children alternatives are limited . In addition, we only used the utility observations of children older than two years of age to estimate the utility of the entire group, because of reasons of applicability of the EQ-5D items. The assumption of equal utilities in both treatment arms was made due to these data constraints, and represented a conservative scenario. Sensitivity analyses showed that the utility level in the ST-cohort did not influence the results.
Finally, in the current model we used a base case in which patients received 40 mg/kg/week, since this is the dosage regimen used by the majority of Dutch patients. We also used information on patients receiving other dosages (particularly 20 mg/kg/2 weeks) to build the model. For these patients, treatment costs are lower and effects are likely to be lower. In the sensitivity analyses, the effect of dosage on costs was examined, keeping effectiveness constant. A lower dosage and fewer infusions reduced the ICER substantially. However, it is likely that a lower dosage also leads to a reduction in effects. In that case, the ICER would increase.
The current study assesses the cost-effectiveness of ERT in Pompe disease only in the severe infantile form of the disease; results may differ for other populations.
A lively debate has taken place in the literature as to whether or not orphan drugs should be excluded from any cost-effectiveness assessment [24, 25]. The most prominent question is whether society is willing to pay a premium because of the rarity of a disease. A recent study showed that this might not be the case, at least in Norway . In contrast, the Dutch Health Care Insurance Board seems to place extra value on rarity, judging by the advice to the Minister of Health to reimburse Myozyme® in infantile Pompe disease in 2012. This decision is probably also driven by the relatively small budget impact. Other factors thus play a role in reimbursement decisions. This hints at the potential role for multi-criteria decision analyses in reimbursement decisions of orphan drugs, although deriving weights for the different criteria might be a major challenge.
In this study, the cost-effectiveness of enzyme replacement therapy with Myozyme® in classic-infantile Pompe disease was assessed. Incremental costs per QALY were estimated to be € 1.0 million.
The authors would like to thank the participants of the 5th Low Lands Health Economics Study Group for the fruitful discussion on a draft version of the paper. Furthermore, the authors would like to thank Carin van Gelder and Jan-Dietert Brugma for providing data used in this paper.
- Schey C, Milanova T, Hutchings A: Estimating the budget impact of orphan medicines in Europe: 2010-2020. Orphanet J Rare Dis. 2011, 6: 62-10.1186/1750-1172-6-62.View ArticlePubMedPubMed CentralGoogle Scholar
- Drummond M, Evans B, LeLorier J, Karakiewicz P, Martin D, Tugwell P, MacLeod S: Evidence and values: requirements for public reimbursement of drugs for rare diseases–a case study in oncology. Can J Clin Pharmacol. 2009, 16: e273-e281.PubMedGoogle Scholar
- Hutton J, Trueman P, Henshall C: Coverage with evidence development: an examination of conceptual and policy issues. Int J Technol Assess Health Care. 2007, 23: 425-432.View ArticlePubMedGoogle Scholar
- Garau M, Mestre-Ferrandiz J: Access mechanisms for orphan drugs: a comparative study of selected European countries. Off Health Econ. 2009, 52: 1-30.Google Scholar
- Kishnani PS, Howell RR: Pompe disease in infants and children. J Pediatr. 2004, 144: S35-S43. 10.1016/j.jpeds.2004.01.053.View ArticlePubMedGoogle Scholar
- Van der Ploeg AT, Reuser AJJ: Pompe’s disease. Lancet. 2008, 372: 1342-1353. 10.1016/S0140-6736(08)61555-X.View ArticlePubMedGoogle Scholar
- Ausems MGEM, Verbiest J, Hermans MMP, Kroos MA, Beemer FA, Wokke JHJ, Sandkuijl LA, Reuser AJJ, Van der Ploeg AT: Frequency of glycogen storage disease type II in the Netherlands: implications for diagnosis and genetic counselling. Eur J Hum Genet. 1999, 7: 713-716. 10.1038/sj.ejhg.5200367.View ArticlePubMedGoogle Scholar
- Van den Hout HMP, Hop W, Van Diggelen OP, Smeitink JAM, Smit GPA, Bakker HD, Loonen MCB, de Klerk JBC, Reuser AJJ, Van der Ploeg AT: The natural course of infantile Pompe’s disease: 20 original cases compared with 133 cases from the literature. Pediatrics. 2003, 112: 332-340. 10.1542/peds.112.2.332.View ArticlePubMedGoogle Scholar
- Kishnani PS, Hwu WL, Mandel H, Nicolino M, Yong F, Corzo D: A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr. 2006, 148: 671-676. 10.1016/j.jpeds.2005.11.033.View ArticlePubMedGoogle Scholar
- Kishnani PS, Corzo D, Nicolino M, Byrne B, Mandel H, Hwu WL, Leslie N, Levine J, Spencer C, McDonald M: Recombinant human acid α-glucosidase: major clinical benefits in infantile-onset Pompe disease. Neurology. 2007, 68: 99-109. 10.1212/01.wnl.0000251268.41188.04.View ArticlePubMedGoogle Scholar
- Kishnani PS, Corzo D, Leslie ND, Gruskin D, Van der Ploeg A, Clancy JP, Parini R, Morin G, Beck M, Bauer MS: Early treatment with alglucosidase alfa prolongs long-term survival of infants with Pompe disease. Pediatr Res. 2009, 66: 329-335. 10.1203/PDR.0b013e3181b24e94.View ArticlePubMedPubMed CentralGoogle Scholar
- Vegter S, Rozenbaum MH, Postema R, Tolley K, Postma MJ: Review of regulatory recommendations for orphan drug submissions in the Netherlands and Scotland: focus on the underlying pharmacoeconomic evaluations. Clin Ther. 2010, 32: 1651-1661. 10.1016/j.clinthera.2010.08.006.View ArticlePubMedGoogle Scholar
- Nicolino M, Byrne B, Wraith JE, Leslie N, Mandel H, Freyer DR, Arnold GL, Pivnick EK, Ottinger C, Robinson PH, Loo JA, Smitka M, Jardine P, Tato L, Chabrol B, McCandless S, Kimura S, Mehta L, Bali D, Skrinar A, Morgan C, Rangashari L, Corzo D, Kishnani PS: Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease. Genet Med. 2009, 11: 210-219. 10.1097/GIM.0b013e31819d0996.View ArticlePubMedGoogle Scholar
- Latimer NR: Survival analysis for economic evaluations alongside clinical trials—extrapolation with patient-level data inconsistencies, limitations, and a practical guide. Med Decis Making. 2013, 33: 743-754. 10.1177/0272989X12472398.View ArticlePubMedGoogle Scholar
- Statistics Netherlands: Life Expectancy; age and Gender. 2011, Retrieved 04/10, 2013, from http://statline.cbs.nl/StatWeb/publication/?DM=SLNL&PA=37450&D1=0&D2=a&D3=0-91&D4=l&HDR=T,G1&STB=G2,G3&VW=TGoogle Scholar
- EuroQol Group: EuroQol: a new facility for the measurement of health-related quality of life. Health Policy. 1990, 16: 199-208.View ArticleGoogle Scholar
- Lamers LM, McDonnell J, Stalmeier PFM, Krabbe PFM, Busschbach JJV: The Dutch tariff: results and arguments for an effective design for national EQ‒5D valuation studies. Health Econ. 2006, 15: 1121-1132. 10.1002/hec.1124.View ArticlePubMedGoogle Scholar
- Oostenbrink JB, Bouwmans CAM, Koopmanschap MA, Rutten FFH: Manual for Costing Studies, Methods and Standard Unit Costs for Economic Evaluations in Health Care. Amstelveen, the Netherlands: College voor Zorgverzekeringen;2004.Google Scholar
- Kanters TA, Hagemans MLC, Van der Beek NAME, Rutten FFH, Van der Ploeg AT, Hakkaart L: Burden of illness of Pompe disease in patients only receiving supportive care. J Inherit Metab Dis. 2011, 34: 1045-1052. 10.1007/s10545-011-9320-x.View ArticlePubMedPubMed CentralGoogle Scholar
- College voor Zorgverzekeringen: Pharmacotherapeutic Compass. Diemen, the Netherlands: College voor Zorgverzekeringen; 2009.Google Scholar
- Hoogendoorn EJI, Feenstra TL, Rutten-van Molken M: Inventarisation Health Care Usage and Costs of Asthma and COPD in the Netherlands. Bilthoven, the Netherlands: Rijksinstituut voor Volksgezondheid en Milieu; 2005.Google Scholar
- College voor Zorgverzekeringen: Guidelines for Pharmacoeconomic Research, Updated Version. Diemen, the Netherlands: College voor Zorgverzekeringen;2006.Google Scholar
- Ungar WJ: Challenges in health state valuation in paediatric economic evaluation. Pharmacoeconomics. 2011, 29: 641-652. 10.2165/11591570-000000000-00000.View ArticlePubMedGoogle Scholar
- Drummond MF, Wilson DA, Kanavos P, Ubel P, Rovira J: Assessing the economic challenges posed by orphan drugs. Int J Technol Assess Health Care. 2007, 23: 36-42.View ArticlePubMedGoogle Scholar
- McCabe C, Claxton K, Tsuchiya A: Orphan drugs and the NHS: should we value rarity?. BMJ. 2005, 331: 1016-1019. 10.1136/bmj.331.7523.1016.View ArticlePubMedPubMed CentralGoogle Scholar
- Desser AS, Gyrd-Hansen D, Olsen JA, Grepperud S, Kristiansen IS: Societal views on orphan drugs: cross sectional survey of Norwegians aged 40 to 67. BMJ. 2010, 341: c4715-10.1136/bmj.c4715.View ArticlePubMedPubMed CentralGoogle Scholar
This article is published under license to 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.