Background
Haemophilia is a genetic disorder characterised by a deficiency of a clotting factor in the blood, leading to prolonged bleed events. The disease is carried on the X chromosome and primarily affects males, though female carriers of the gene may exhibit symptoms of mild haemophilia. The two forms of the condition are Haemophilia A (Factor VIII (FVIII) deficiency) and Haemophilia B (Factor IX (FIX) deficiency); Haemophilia A is approximately four times more common than Haemophilia B [
1]. The global incidence of haemophilia is approximately 1 per 4,000–5,000 male births; in a given year, approximately 400 boys are born with haemophilia in Europe [
1].
Individuals with severe haemophilia – representing approximately one-third of the haemophilia population in Europe [
2,
3] – have factor levels less than 1% of that expected in a healthy person. Such individuals will experience recurrent, spontaneous bleeds, often in the absence of any trauma event [
4]; four-fifths of bleed events occur within the musculoskeletal system [
5]. Approximately 90% of people with severe haemophilia experience chronic haemophilic joint disease, characterised by chronic inflammation and progressive joint deformity, in one or more major joints by the age of 30 [
5]. As well as joint stiffness and diminished range of motion, individuals with haemophilia experience significant acute pain during bleed events and chronic pain due to arthropathy, leading to disability and impaired quality of life in more than half of cases [
6].
Prior to the 1960s, when clotting factor replacement therapy (CFRT) became widely available, life expectancy of persons with haemophilia (PWH) was very low (<30 years) in comparison to that of the general male population, with haemorrhage as the most prevalent cause of death [
2]. Innovations in factor production mean that PWH in nations with developed healthcare systems can now expect a near-normal quality of life and an average lifespan no more than 10 years shorter than that of an unaffected individual [
3,
4]. In this current “golden era” of haemophilia care [
5], management of age-related conditions has become a novel necessity for clinicians and PWH [
6,
7]. Nevertheless, a continuing major risk associated with the use of CFRT is the development of inhibitors, so-called due to the development of antibodies that inhibit factor uptake. Affected individuals experience poor bleed control and subsequently higher levels of morbidity and mortality [
8] and reduced HRQoL [
9,
10]. The cost of treating an individual with an inhibitor can exceed EUR 1 million per year, with regimens of immune tolerance induction (ITI) therapy lasting more than 3 years in rare cases [
11,
12].
The objective of the CHESS study was to estimate and extrapolate resource use, costs, and health-related quality of life (HRQOL) for adults with severe haemophilia in the five largest European economies (EU5: France, Germany, Italy, Spain and the United Kingdom (UK)). The psychological, societal, and economic burden of haemophilia has been documented for a number of European countries [
13‐
17]; few studies have taken a standardised methodology across multiple countries simultaneously [
18], and sought to amalgamate all three levels of burden for severe disease. The overall aim of the CHESS study was to capture the annualised economic and psychosocial burden of severe haemophilia in the EU5.
Methods
Study cohort
The study population is a sample of adult patients (18 years and over) with severe inherited haemophilia A or B (FVIII/FIX level <1 IU dL
−1), drawn approximately in proportion to the population of individuals with haemophilia in each of the five countries participating. Individuals with acquired haemophilia or other clotting factor deficiencies (e.g. von Willebrand disease (VWD), haemophilia C) were excluded, as symptoms of vWD are generally comparable to that of mild or moderate haemophilia [
19], and our sample size would preclude meaningful conclusions for other rare coagulation disorders.
Study design
A retrospective, cross-sectional methodology was employed. Data was collected by means of two questionnaires, designed specifically for specialists and patients: the web-based case record forms (CRFs) were used to collect information on direct medical resource utilisation and clinical data based on recorded notes; and the paper patient self-completion form (PSC), given to patients following the consultation, provided complimentary socio-economic information. One hundred and thirty-nine haematologists (and haemophilia care providers (HCPs) in France) based in hospitals and clinics completed up to eight patient CRFs, with a small number providing information for up to 16 patients. In order to minimise the risk of selection bias, physicians were encouraged to recruit the next eligible patients with whom they consulted, irrespective of their reason for consultation.
All patient participants provided informed consent. The study protocol was approved by the Research Ethics Sub Committee of the Faculty of Health and Social care within the University of Chester. The approval stipulated that the study was to be carried out in correspondence with regional and relevant guidelines.
Data collected from clinicians included clinical economic and demographic information, while data collected from patients included indirect and direct non-medical resource use, HRQOL (via the EuroQol EQ-5D-3 L), work productivity impact (via the Work Productivity and Activity Impairment (WPAI) Questionnaire), and therapy adherence (via the Morisky Medication Adherence Scale 8-item (MMAS-8)).
Data was collected between December 2014 and April 2015 and captured a period of 12 months retrospectively. Estimates of healthcare utilisation and costs were then calculated for the 12-month period. The online format of the CRFs ensured that numeric responses were kept within reasonable boundaries, and that infeasible responses (such as the ability to provide two mutually exclusive responses, for instance) were kept to a minimum. Nevertheless, a small amount of post-hoc data processing was conducted based on expert clinical guidance.
Statistical analysis
All direct medical and non-medical costs were sourced from publically available data (Table
1). Choice of resources to be included in the CHESS study was defined by the societal and participant/family perspectives [
20]. To investigate the distribution of direct costs, resource use was separated into four categories:
Table 1
National costs for CHESS resource units
Direct costs |
Ambulatory care |
Haematologist visit (per visit) | 25.99–45.99 | 20.88 | 27.32–23.17 | 65.69–113.54 | 124.71–228.57 |
Nurse visit (per visit) | 81.74 | 34.28–38.42 | 15.11 | 20.92–37.46 | 19.36 |
Other specialist visit (per visit) | 14.99–45.99 | 7.30–228.88 | 18.21–27.32 | 16.42–160 | 65.91–612.03 |
Blood test (per test) | 1.89–53.96 | 0.50–112.50 | 2.11–17.22 | 4.78–98.37 | 4.29–7.67 |
Other test/examination (per test) | 10.79–69.00 | 5.50–124.60 | 2.19–134.27 | 7.49–249.21 | 1.69–228.24 |
Drug (per IU)a
| 0.72 | 0.85–2.08 | 0.62–1.23 | 0.39–0.90 | 0.44–0.84 |
Hospitalisation |
Target joint (per procedure) | 28.81–534.40 | 12.02–1,719.43 | 33.48–1,032.91 | 169.75–2,156.33 | 1,161.93–8,397.52 |
Bleed event: ward stay (per day) | 290.85 | 514.29 | 265 | 708.71 | 562.88 |
Bleed event: ICU stay (per day) | 1,174.60 | 1,265 | 366 | 1,559.24 | 1,056.82 |
Professional caregiver (per hour) | 8.30 | 27.43 | 7.39 | 13.66 | 24.56 |
Indirect costsb
|
Wage (patient/caregiver) (per hour) | 24.64 | 27.15 | 17 | 16.35 | 27.75 |
Petrol (per mile) | 0.53 | 0.54 | 0.63 | 0.50 | 0.63 |
Scheduled ambulance (per mile) | 1.36 | - | - | - | - |
(1)
Ambulatory activity, including: haemophilia-related visits to haematologists and other specialists, paramedical practitioners (nurse specialists, physiotherapists, diet and nutritional support, etc.), and all tests and procedures (e.g. blood tests, diagnostic imaging);
(2)
Haemophilia-related admissions to hospital, based on length of stay, including admission to ICU, and surgical procedure/diagnosis (where applicable):
a.
bleed-related hospital admissions; and
b.
procedures on ‘target’ joints – defined here as areas of chronic synovitis [
21] – including arthroscopy, arthrodesis, arthroplasty, arthrocentesis, and synovectomy;
(4)
Use of a professional (paid) care provider.
All factor consumption was reported by the physician. For on-demand regimens, factor consumption for the most recent 3-month period was annualised. For prophylaxis regimens, mean IU per infusion was multiplied by the weekly infusion rate, and annualised.
Direct non-medical and indirect costs were defined based on seven categories of resource use:
(1)
Loss of earnings by the patient (due to absenteeism and/or early retirement);
(2)
Loss of earnings by an informal caregiver (family or friend) (as above);
(3)
Transfer payments (e.g. financial aid, state allowances);
(4)
Over-the-counter (OTC) medications;
(5)
Other medical device, personal aid, or home alteration costs (e.g. walking aids, orthotics);
(6)
Alternative therapies (e.g. yoga/Pilates, massage, nutritionist); and
(7)
Transport to/from hospital attendances.
Costs associated with temporary and long-term work absence (including early retirement) were valued using the traditional human capital approach (HCA), due to its benefits in terms of transparency and comparability versus that of the newer friction cost approach (FCA) [
22]. Patients who reported early retirement due to haemophilia, or who reported that they were unable to work due to haemophilia in the 3 months prior to responding, were costed at the average annual salary (stratified by country). For patients in employment, days of work lost due to bleeds across the preceding 3 months was reported and extrapolated. Whilst information regarding comorbidities was captured in the questionnaire, all direct and indirect costs were limited to those resulting directly from haemophilia-related activity.
All local currency total costs were converted to Euros using the official conversion rate as of 30
th May, 2015. Per-patient costs were calculated by multiplying the quantities of the resource used with the national unit price of each resource. To extrapolate the sample costs to country population level, the per-patient costs were multiplied by national prevalence weights [
23]:
$$ \begin{array}{l}-{\mathrm{P}}_i\mathrm{x}\ {\mathrm{Q}}_i = \mathrm{Cos}{\mathrm{t}}_i\\ {}-\mathrm{Cos}{\mathrm{t}}_i\mathrm{x}\ \mathrm{prevalence}\ \mathrm{weights} = \mathrm{population}\ \mathrm{cost}\\ {}-\mathrm{P} = \mathrm{price},\ \mathrm{Q} = \mathrm{resource}\ \mathrm{use},\ \mathrm{and}\ \mathrm{i} = 1\hbox{--} n\left(\mathrm{wheren} = \mathrm{number}\ \mathrm{of}\ \mathrm{cost}\ \mathrm{i}\mathrm{tems}\right)\end{array} $$
Patient outcomes were obtained by means of the self-administered EQ-5D-3 L, a non-disease specific instrument covering the areas of mobility, self-care, everyday activities, pain/discomfort and anxiety/depression [
24]. A three-level rating scale is applied to each dimension, with a total of 245 possible health states defined. The questionnaire has been validated in many countries in Europe and is commonly used in economic evaluation and health technology assessment [
25]. The values or utilities are indicated on a scale on which death has a value of 0 and perfect health a value of 1, with negative values being possible. Validated country-specific adult value sets obtained via the EuroQol website were used, with the exception of Italy, for which values were taken from literature [
26].
Discussion
With an overall population of more than 300 million, the EU5 is home to approximately 8,123 people with severe haemophilia A and 1,370 people with severe haemophilia B. The CHESS study aimed to provide a snapshot view of the economic, societal, and psychological burden of severe haemophilia in adults within the EU5. We estimated the mean per-patient annual direct cost of severe haemophilia at EUR 173,102, EUR 313,068, EUR 210,025, EUR 132,329, and EUR 116,963 for France, Germany, Italy, Spain, and the UK, approximately 48, 79, 87, 65, and 34 times higher than the mean per-capita health expenditure in these countries, respectively [
27]. Direct medical resource use was the predominant cost driver, with more than 97% of direct costs taken by CFRT, reflecting previous research suggesting that costs of CFRT account for the vast majority of the cost burden [
15,
16,
28]. Annual indirect costs averaged just over EUR 6,000 per patient, with marginal variation between countries (range EUR 4,850–8,651). The total economic and societal cost of severe haemophilia in the EU5 in 2014 was estimated at EUR 1.4 billion.
Patients were recruited to the CHESS study via their haematologist or HCP, with a response rate of 43% across the pooled sample. Participation in the study by clinicians and patients was voluntary, and we therefore cannot rule out a degree of selection bias. Because the cost of illness for non-responding patients remains unknown, it is also not possible to assess the extent of the potential bias. The ratio of haemophilia A patients relative to that of haemophilia B in the CHESS cohort (approximately 1:3.5) is more narrow than current epidemiological studies, which place the ratio closer to 1:5 in severe disease [
29]. The differential burden between haemophilia A and B is a topic of ongoing research; current evidence suggests that any overrepresentation by haemophilia B may generate more conservative estimates of disease burden, due to milder disease symptoms [
30].
The proportion of patients receiving prophylaxis in the study cohort (57%) broadly matches that of a recent retrospective audit of haemophilia care in the EU5 [
31]; prevalence of diagnosed inhibitors (4.5%) is almost identical to that of a recent study in Portugal (4.7%) [
16], though the study included children (more than half of inhibitors present before the age of 9 years [
32]), as well as mild and moderate haemophilia patients, who are at lower risk of inhibitor development [
33].
Five percent of the CHESS cohort have recorded HCV comorbidity, with the highest rate in Italy (8%); results from the World Federation of Hemophilia Annual Global Survey [
34] suggests that prevalence of HCV among haemophilia patients is upwards of one in ten, with almost half of patients in Germany co-diagnosed. Furthermore, approximately 7% of PWH in the EU5 are HIV-positive [
34‐
36]; we find prevalence in CHESS to be less than half this amount. We suggest that a sampling bias towards non-infected patients may be present to some extent in this study. The implications of any underrepresentation for our burden estimates are uncertain: the extent to which HIV/HCV coinfection impact upon costs of haemophilia is of some dispute in current literature [
37,
38], but may be more than 50% higher compared to those with haemophilia alone.
By profiling consulting patients, we draw from a cohort of patients who consult more frequently – maybe because they have difficulty with bleed control, due to joint degeneration, suboptimal therapy, or adherence. It is possible, therefore, that our sample is biased towards those older, more costly, and less adherent patients, and that our extrapolated costs may be an overestimate of the actual disease burden. However, the age distribution of the CHESS cohort is similar to that of another recent study that sourced data directly from haemophilia treatment centres and data registers across the EU5, Belgium and Sweden [
31].
Our study is limited in its cost estimates by the need to use publically available reimbursement data, particularly for hospital admissions, rather than actual costs to hospital providers and patients. Any divergence between these costs may lead to an under- or over-estimate of the actual realised costs. Recall bias regarding consultations and outpatient visits may be present for clinicians, particularly for consultations with other specialists. Smaller payments by patients may also be overlooked when reporting use of devices, aids, and OTC medications. Costs of informal care provision are limited to that of the primary caregiver; informal care and household burden cost estimates were consequently underestimated for households in which additional individuals contributed to informal care.
Randomized controlled trials (RCTs) are the gold standard of evidence generation for health interventions. However, design of RCTs in rare diseases such as haemophilia is difficult due to the limited size of the patient population [
39]. Further, there is often disparities between the highly structured environment of an RCT and ‘real world’ practice, particularly in the absence of formal clinical guidelines. Instead, much of the available evidence for rare diseases is based on larger-scale registries, post-authorisation surveillance studies, and observational studies such as CHESS, which have in recent years produced major insights into the treatment and management of individuals with haemophilia [
40].
PWH in the five CHESS countries benefit from major investment of resources for their care and treatment. These patients are likely to obtain first access to novel long-acting and gene-based therapies in haemophilia, and it is therefore important to understand the continuing unmet need within these populations and where these new therapies will fit with current treatment approaches. The estimates of resource use and cost burden within this study are less translatable outside of Western Europe, where haemophilia often remains underdiagnosed and undertreated [
41]. In countries where access to CFRT is restricted and many PWH experience major joint damage and deformity by adolescence, the burden of disease will be weighted more towards the psychosocial and employment impact resulting from severe disability and premature mortality [
42].
Acknowledgements
Kind thanks to Ian Jacob (HCD Economics), Andi Mabhala (University of Chester), Declan Noone (European Haemophilia Consortium), and Janice Gidman (University of Chester) for reviewing the manuscript drafts.