Skip to main content
  • Research article
  • Open access
  • Published:

Social and economic costs and health-related quality of life in non-institutionalised patients with cystic fibrosis in the United Kingdom

Abstract

Background

This study aimed to determine the societal economic burden and health-related quality of life (HRQOL) of cystic fibrosis (CF) patients in the UK.

Methods

A bottom-up cost-of-illness, cross-sectional, retrospective analysis of 74 patients was conducted aiming to estimate the economic impact of CF. Data on demographic characteristics, health resource utilisation, informal care, productivity losses and HRQOL were collected from questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D) instrument.

Results

Using unit costs for 2012 we found that the average annual cost for a CF patient was €48,603, with direct health care costs amounting to €20,854 (42.9 % of total costs), direct non-health care costs being €21,528 (44.3 %) and indirect costs attributable to productivity losses being €6,222 (12.8 %). On average, the largest expenditures by far were accounted for by informal care (44.1 %), followed by medications (14.5 %), acute hospitalisations (13.9 %), early retirement (9.1 %) and outpatient and primary health care visits (7.9 %). Sharp differences existed depending on whether CF patients were in need of caregiver help (€76,271 versus €26,335). In adult CF patients, mean EQ-5D index scores were 0.64 (0.93 in the general population) and mean EQ-5D visual analogue scale scores were 62.23 (86.84 in the general population); among caregivers, these scores were 0.836 and 80.85, respectively.

Discussion

Our analysis highlights the importance of the economic and quality of life consequences of CF from a societal perspective. The results highlight that beyond conventional costs such as acute hospitalisations, medication and outpatient and primary care visits, indirect costs related to informal care and early retirement, have significant societal implications. Similarly, our analysis showed that the average EQ-5D index score of adult CF patients was significantly lower than in the general population, an indication that a methodological bias may exist in using the latter in economic analyses.

Conclusion

CF poses a significant cost burden on UK society, with non-health care and indirect costs representing 57 % of total average costs, and HRQOL being considerably lower than in the general population.

Peer Review reports

Background

Cystic fibrosis (CF) is one of the most prevalent, fatal, inherited rare disorders among people of Caucasian descent. The European prevalence ranges between 1/8,000 and 1/10,000 individuals [1]. Data from the UK CF neonatal screening NHS newborn blood spot-screening programme, suggest that 1 in 2,500 babies are born with the disease [2]. The natural course of the disease involves a gradual and progressive deterioration in lung function due to the deranged chloride transport, leading to thick and viscous secretions not only in the lung but also in pancreas, liver, intestine and reproductive tract [3]. Complications due to chronic colonisation by bacteria, lead to destruction of lung architecture and respiratory failure and are the most common causes of death among CF patients [4].

A dramatic improvement in survival among CF patients has been observed in recent years [5] and, as a result, CF is no longer a major mortality cause among children [6, 7]. Despite its low disease prevalence, CF exerts a potentially important economic impact on health care resources, and other social costs [8, 9] and has significant impact on patients’ health-related quality of life (HRQOL) [1012].

The issue of total costs related to the treatment of CF and the HRQOL for CF patients is poorly understood. Although a number of recent studies have measured independently the economic and HRQOL impact on CF patients [816], a comprehensive study in the UK that examines all cost dimensions (direct medical, direct non-medical and indirect costs) and links cost with HRQOL is missing [17].

In this study we report and analyse CF patient-level primary data from the UK collected under the auspices of the BURQOL-RD initiative [18]. The study objectives are twofold: first, to estimate the societal costs of CF by accounting for all direct health, direct non-health care and indirect costs, and, second, to assess the HRQOL of patients with CF.

Methods

Research design and sample

This was a bottom-up, retrospective, cross-sectional study of non-institutionalised patients diagnosed with CF, receiving outpatient care. Because of the lack of a publicly available, NHS-based CF registry in the UK, a convenience sample of patients was recruited from the Cystic Fibrosis Trust (CFT) that holds its own anonymised register of patients. The survey was anonymous and patients were contacted by the Trust. A CF diagnosis, non-institutionalised status and membership of CFT determined patient eligibility. Questionnaire responses received by the research team had no identification information (name, address/postcode, e-mail or telephone). All patients and caregivers were informed about the study objective, data confidentiality and were asked to indicate their understanding of the study conditions and agreement to participate. The study protocol was submitted to the London School of Economics (LSE) Research Ethics Committee and received an exemption.

Information and variables of interest

Following the identification of the patient sample, CFT sent questionnaires electronically and by post to eligible patients at the end of February 2013. The questionnaire comprised two parts, the first identifying costs and the second including HRQOL. The data collection was carried out between end-February and end-May 2013, with reminders sent at the end of April and May. Demographic, clinical and resource use data were collected from CF patients and their caregivers. The questionnaire was detailed enough to reduce either exaggeration or underestimation.

Following receipt of completed questionnaires, patients were divided into two groups: first, high severity or disability, needing caregiver assistance in order to perform basic (dressing, hygiene, eating, etc.) or instrumental (meal preparation, shopping, laundry) daily activities; and, second, low severity or disability, if they did not need such assistance.

Costing methodology

We used the prevalence approach to estimate resource use and, subsequently, costs from a societal perspective. Disease prevalence takes into account all direct health care resources used for prevention, treatment and rehabilitation, other non-health care resources used (formal and informal care), and indirect costs (productivity loss) within a given year (in a population or in a sample of patients) as a consequence of the illness considered. Prevalence-based cost-of-illness analysis has the advantage of incorporating measurements of total annual health care expenditure, which is particularly relevant for chronic conditions such as CF requiring long-term treatment. In this context, a bottom-up costing approach was used to estimate total and average annual costs.

Data on resource utilisation were collected for each patient and, where appropriate, caregiver. To estimate resource utilisation, the questionnaire solicited information covering the 6-month period prior to the study (12 months for hospital admissions). Data for the preceding 6 months were extrapolated to the entire year. We considered 6 months to be an appropriate recall period [19]. Patients and caregivers were asked about reductions in working time (temporary and permanent sick leave or early retirement), and these data were used to calculate productivity losses. Non-professional caregivers were also asked about informal care time. A list of basic domestic activities (e.g. dressing, bathing, feeding, etc.) and other non-domestic activities (e.g. travelling, shopping, socialising, etc.) was provided, and carers had to specify the approximate daily or weekly time they spent on these activities.

Direct medical costs were derived from health care utilisation. The cost of resources used by patients was calculated based on the relevant unit costs and the average utilisation per patient in the sample. Information about the number of hospital admissions, the number of emergency visits and data for the volume of outpatient care (rehabilitation, medical tests and examinations, visits to health professionals and home medical care) were obtained from the questionnaires.

Unit costs were obtained mostly from the UK payment by results database [20]; additional publicly available resources were used to fill in any remaining data gaps [21, 22]. Unit costs were then multiplied by the respective resource quantities to derive the annual cost per patient, using 2012 as the reference year. In a similar way, resource utilisation information relating to consumption of prescription drugs and medical support devices was obtained from the questionnaires. When no information concerning the number of units per pack was available, we assumed the largest dispensing pack for prescription drugs. Prescription drug unit costs were obtained from the National Drug Tariff database [23] and the British National Formulary [24], whereas unit costs for medical support devices were obtained from major electronic commerce websites.

Direct non-health care costs were the result of aggregating three items: non-health care transportation, social care services (formal care) and caregiver’s time (informal care, provided by non-professional caregivers, who are often relatives, but could also be friends or neighbours and who are not paid for the care provided). Informal care concerned the time spent helping the patient with their basic activities of daily living (ADL), and the time spent helping with necessary instrumental activities of daily living (IADL). The approach used to value care hours was the proxy good method, which values time as an output and values the care provided by the informal caregiver considering that if they did not provide these services, their presence would have to be substituted by a professional caregiver who could provide them [25].

Information on formal (paid) care provided by professional caregivers and other social services was obtained from the questionnaires and is included under the social services category.

Indirect costs were obtained from physical units (days of sick leave and early retirement) converted into monetary units based on the human capital approach [26], using worker gross average earnings from the Annual Survey of Hours and Earnings [27] conducted by the Office for National Statistics to proxy productivity losses.

Patient and caregiver outcomes

Patient and caregiver outcomes were obtained via the EQ-5D-5 L questionnaire [28], the Barthel Index [29] and the Zarit Burden Interview [30]. The EQ-5D-5 L is a generic instrument of HRQOL, commonly used in economic evaluations and routinely included in health technology assessments. Its five dimensions (mobility, self-care, everyday activities, pain/discomfort and anxiety/depression), enable a total of 245 possible health states to be defined, taking values from 0 (death) to 1 (perfect health). The second part of the EQ-5D consists of a vertical 20-cm, 0–100 Visual Analogue Scale (VAS), where 0 represents the worst and 100 represents the best imaginable health states. Respondents mark a point on the scale to reflect their overall health on the day of the interview [28]. Evaluations of these health states have been reported for the general population [31].

The Barthel Index is widely used to assess physical disability and measures the ability of a person to perform ten basic ADL, obtaining a quantitative estimate of the subject’s degree of dependence. Total possible scores for the UK range between 0 and 20, with lower scores indicating increased disability [29].

Finally, the Zarit Burden Interview (22-item version) measures the subjective burden among caregivers. Each item is a statement to which the caregiver is asked to respond using a 5-point scale, with options ranging from 0 (never) to 4 (nearly always). The total score ranges from 0 to 88, with scores under 21 corresponding to little or no burden and scores over 61 to severe burden [30].

Results

Of the 234 questionnaires sent, 131 questionnaires (56 %) were returned from CF patients. Of these, 57 questionnaires were excluded because the information they contained was deemed to be insufficient or inadequate. Therefore, the valid sample totalled 74 patient questionnaires.

Table 1 summarises the main characteristics of the sample. Patients were equally divided between adult and non-adult (37 patients each) and average patient age was 18 years; 52.7 % of patients were male and 44.6 % (33 patients) had a caregiver, whose average age was 37.3 years. The total average time spent on informal caregiving, assuming at least one caregiver, was 74.8 hours per week, (3,900 hours per year).

Table 1 Sample characteristics of interviewed CF patients (n = 74, SD in brackets)

Estimated average annual cost per patient in 2012 was €48,603, and the median was €34,883 (Table 2). Direct non-health care cost was the largest component (44.3 % of the total average cost per patient), followed by direct health care costs (42.9 %) and productivity loss (12.8 %) (Fig. 1). The most important categories of health care costs were medications, (33.8 % of health care and 14.5 % of total costs), followed by acute hospitalizations (32.4 % of health care and 13.9 % of total costs) and outpatient and primary health care visits (18.3 % of health costs and 7.9 % of total costs) (Fig. 2). The most relevant category of direct non-health care cost was informal care, averaging €21,447 (99.6 % of direct non-health care and 44.1 % of total costs), with a special mention given to the cost related to main caregivers (75.8 % of direct non-health care cost and 33.6 % of total costs). Social services only accounted for 0.2 % of direct non-health care cost and 0.1 % of total costs, and non-health care transport represented 0.2 % of direct non-health costs and 0.1 % of total costs respectively. Finally, sick leave accounted for 29 % of productivity loss and 3.7 % of total costs, whereas early retirement accounted for 71 % of productivity loss and 9.1 % of total costs.

Table 2 Average annual costs per CF patient (2012, in €)
Fig. 1
figure 1

Breakdown of costs according to all CF patients, CF patients with carers, and CF patients without carers (2012, €)

Fig. 2
figure 2

Average costs per CF patient broken down by type of cost (2012, €)

The results differ significantly depending on whether CF patients needed the help of a caregiver. A CF patient with caregiver help had a total average annual cost of €76,271 (median €70,641), compared with €26,335 (median €16,591) for a patient who did not require personal care.

Where a caregiver was present, implying higher severity patients, the most relevant cost category was informal care with an average cost of €48,092 (63.1 % of total costs). Direct medical and direct non-medical costs represented 31.5 and 63.1 % of total costs respectively. In terms of direct medical cost categories, hospitalisations ranked highest (26.2 % of direct medical costs, and 18.2 % of total costs), followed by medications (35.5 % of direct medical costs and 24.7 % of total costs), and outpatient and primary health care visits (19.1 % of direct medical costs and 13.3 % of total costs). Social services only accounted for 0.2 % of direct non-medical costs and 0.1 % of total costs, whereas non-healthcare transport only represented 0.2 % of the direct non-medical costs and a 0.7 % of total costs. Productivity loss accounted for 5.4 % of total costs, with sick leave and early retirement separately accounting for 29 and 71 % of indirect costs, and 3.7 and 9.1 % of total costs respectively.

For patients without a caregiver, direct medical and direct non-medical costs represented 69.5 and 0.4 % of total costs respectively, while indirect costs represented 30.1 % of total costs. The most important categories of direct medical costs were medications (35.3 % of medical costs and 24.7 % of total costs), acute hospitalizations (26.2 % of medical costs and 18.2 % of total costs) and outpatient visits (19.1 % of medical costs and 13.3 % of total costs). Social health services and non-health care transport accounted for 0.2 % and 0.15 % of total costs, respectively. Sick leave and early retirement accounted for 39.1 and 60.3 % of indirect costs and 12 and 18.2 % of total costs, respectively.

Further analysis was conducted to explore the differences in costs between adults and children (Table 3). Average total annual costs per adult and adolescent patient were €44,583 (median €31,511) and €52,624 (€46,356) respectively, of which direct and indirect costs comprised 72.1 (€32,140) and 27.9 % (€12,443) in the adult group, with no indirect costs in the adolescent group. Direct health care costs were much higher than direct non- health care costs among adult patients (€26,439 vs. €5,701), compared with the adolescent patients group, where the opposite trend was observed (€15,268 vs. €37,355), indicating a much higher impact of informal care on total costs in the adolescent group.

Table 3 Average annual costs (main groups only) for adult and adolescent CF patients, (2012, in €)

With regards to HRQOL of adult patients the EQ-5D index score was 0.64 out of 1, and the EQ-5D visual analogue scale score was 62.23 out of 100 (Table 1). These scores are lower than the EQ-5D values for the UK adult general population (0.93 and 86.84, respectively) after controlling for age [32]. For caregivers, the mean EQ-5D index and VAS scores were 0.836 and 80.85 respectively (Table 1), which are lower than in the UK general population (0.91 and 86.56 respectively). Among adult patients, the average Barthel index was 19.27 reflecting very low dependence, while the average Zarit burden interview score burden was 29.03, indicating a moderate burden for caregivers (Table 1).

Discussion

In this study we have provided a descriptive rather than quantitative analysis of total cost and HRQOL among patients with CF. Among rare diseases, CF represents a health problem with important societal impact in high-income countries, including the UK [8, 9, 33]. The incidence and prevalence of CF and its health and social impact in terms of mortality, morbidity, economic cost and quality of life justify the attention received from health authorities and society. A recently published systematic review studying the socioeconomic impact of ten rare diseases identified in total 29 costing studies related to CF, four of which investigated aspects of CF management in the UK mainly relating to direct health care costs [17]. The first ever CF costing study in the UK investigated the direct medical costs of patients served at a regional adult CF centre [34]. To date however, this is the first UK-based study attempting to quantify the total (direct medical, direct non-medical and indirect) cost for CF patients together with estimates of quality of life. Studies conducted in different settings prove testament to the high costs associated with CF. For example, annual cost per patient amounted to €41,468 in Germany [33], whereas annual mean direct health care costs per patient were shown to vary across countries. In Germany these were found to range from €17,219 per patient per year, increasing to €21,782 allowing for IV therapy [35]. In the USA, one study showed average annual treatment costs per patient to be $63,127 in 2006 (€50,299) [36], whereas another study suggested a mean annual cost of $43,000 per CF patient in 2008 (€29,378) [15]; however the latter is most likely to be an underestimate mainly because direct non-medical costs were not extensively investigated to the same extent as in our study. In France the direct costs were found to be €22,725 in 2003 [37], whereas in Australia national registry data have indicated that the presence of chronic infections increases cost of care by 70–164 % [16].

The present analysis highlights the importance of studying the economic consequences of CF from a societal perspective and interpreting the results in an international context. Our results provide insights into the distribution of CF costs and their impact on national health expenditure as well as patient and family income. Beyond the average annual total cost of €48,603 (ranging from €26,335 to €76,271 for patients without carers and with carers, respectively), we found that informal care, medication, acute hospitalisations, early retirement and outpatient and primary health care visits represented the highest expenditures.

The high contribution of informal care to the costs identified in this study may have several explanations. First, our methodology may have influenced our estimates. In earlier studies, indirect costs included both job loss and informal care costs. Recently published cost-of-illness studies, however, use more precise classifications of the items that contribute to societal costs. Second, our study design excluded institutionalised patients from the analysis and, therefore, the cost estimates produced in this study are likely to be an under-estimate of the total CF cost due to non-inclusion of institutionalisation and long-term care costs.

HRQOL can be a useful indicator together with other information sources such as incidence, prevalence, mortality and costs to set priorities in health and measure the effectiveness of health interventions on disease management. Our analysis showed that the average EQ-5D index score of adult CF patients was lower than in the general population. Despite its relatively low prevalence, CF is characterized by a substantial economic burden and patients with higher dependence on caregivers, therefore reflecting a higher disability, are more likely to incur higher productivity losses compared to people with lower dependence. Although it would have been of great interest to expand upon the notion of higher disease burden being associated with higher cost by exploring the association of decrements in EQ-5D scores with increases in cost, this would not yield robust estimates because of the relatively small number of patients with available EQ-5D scores in the sample, giving rise to relative few degrees of freedom and, therefore, decreasing the credibility of the results. Instead, the existence or absence of a caregiver was used as a proxy for disability, resulting in a larger sample.

Our study is not without limitations. The first limitation relates to sampling issues. Both the study sample and the recruitment process may limit the external validity of the study. However, other CF studies have used smaller sample sizes due to the low disease prevalence and high rates of participation refusal [3538]. Although the sample was almost evenly distributed between high- and low-severity patients, we cannot guarantee the avoidance of selection bias but this is common in most rare disease studies involving small numbers of patients. There may also be potential recall bias, given that patient-based data were obtained by questionnaire. A second limitation relates to the non-use of disease-specific HRQOL instruments, such as the cystic fibrosis questionnaire (CFQ). However, a recent systematic review of HRQOL instruments used for rare diseases concluded that the EQ-5D-5 L can be considered a cross-sectional valid generic health outcome measure reflecting the progression of CF [39]. In addition, we have used the Barthel Index and the Zarit scale as proxies to measure disability and severity. Finally, our study used cross-sectional data. An ideal study would be a prospective longitudinal study of a CF cohort, but this type of study was beyond our means and no such study has been undertaken in CF.

Despite the limitations of cost-of-illness analysis studies, governments continue to encourage such research, as the information emerging about the financial impact of disease provides a useful input for program planning and public policy design. This information complements epidemiological data on population-level health problems. This study represents the most complete and realistic costing to date of the burden of CF performed in the UK, a key strength being the use of a bottom-up approach to costing. Additionally, estimating costs over a one-year period has provided a more accurate picture of the medium-term burden of CF.

Conclusion

By pursuing a bottom-up cost and HRQOL study, we have shown that direct health care costs of CF are substantial, although other social costs, such as informal care, are even higher proportionately, and that higher disability, as reflected through the existence or absence of a caregiver, is associated with significantly higher CF social costs. Overall, CF represents a significant hidden cost to society and this should be taken into account when considering treatments and support programs for CF patients and their caregivers. The data in this study could form the basis for integrated and harmonised approaches to periodically assess the future impact of new public policies and interventions for rare diseases at national and EU level.

References

  1. Orphanet: Cystic fibrosis. [http://www.orpha.net]. Accessed on 24 May 2013.

  2. NHS Newborn Blood SPOT Screening Programme. [http://newbornbloodspot.screening.nhs.uk/cf]. Accessed on 24 May 2013.

  3. Rowe SM, Miller S, Sorscher EJ. Cystic fibrosis. N Engl J Med. 2005;352(19):1992–2001.

    Article  CAS  PubMed  Google Scholar 

  4. Roberts HJ, Hubbard R. Trends in bronchiectasis mortality in England and Wales. Respir Med. 2010;104(7):981–5.

    Article  PubMed  Google Scholar 

  5. Ratjen F, Doring G. Cystic fibrosis. Lancet. 2003;361(9358):681–9.

    Article  CAS  PubMed  Google Scholar 

  6. Bellis G, Cazes MH, Parant A, Gaimard M, Travers C, Le Roux E, et al. Cystic fibrosis mortality trends in France. J Cyst Fibros. 2006;6:179–86.

    Article  PubMed  Google Scholar 

  7. Dodge JA, Lewis PA. Cystic fibrosis is no longer an important cause of childhood death in the UK. Arch Dis Child. 2005;90(5):547–a.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Joish VN, Spilsbury-Cantalupo M, Operschall E, Luong B, Boklage S. Economic burden of non-cystic fibrosis bronchiectasis in the first year after diagnosis from a US health plan perspective. Appl Health Econ Health Policy. 2013;11(3):299–304.

    Article  PubMed  Google Scholar 

  9. van Gool K, Norman R, Delatycki MB, Hall J, Massie J. Understanding the costs of care for cystic fibrosis: an analysis by age and health state. Value Health. 2013;16(2):345–55.

    Article  PubMed  Google Scholar 

  10. Kianifar HR, Bakhshoodeh B, Hebrani P, Behdani F. Quality of life in cystic fibrosis children. Iran J Pediatr. 2013;23(2):149–53.

    PubMed  PubMed Central  Google Scholar 

  11. Tluczek A, Becker T, Grieve A, Laxova A, Rock MJ, Gershan WM, et al. Health-related quality of life in children and adolescents with cystic fibrosis: convergent validity with parent-reports and objective measures of pulmonary health. J Dev Behav Pediatr. 2013;34(4):252–61.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Tepper LA, Utens EM, Caudri D, Bos AC, Gonzalez-Graniel K, Duivenvoorden HJ, et al. Impact of bronchiectasis and trapped air on quality of life and exacerbations in cystic fibrosis. Eur Respir J. 2013;42(2):371–9.

    Article  PubMed  Google Scholar 

  13. Weiner JR, Toy EL, Sacco P, Duh MS. Costs, quality of life and treatment compliance associated with antibiotic therapies in patients with cystic fibrosis: a review of the literature. Expert Opin Pharmacother. 2008;9(5):751–66.

    Article  CAS  PubMed  Google Scholar 

  14. Groeneveld IF, Sosa ES, Pérez M, Fiuza-Luces C, Gonzalez-Saiz L, Gallardo C, et al. Health-related quality of life of Spanish children with cystic fibrosis. Qual Life Res. 2012;21:1837–45.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Dewitt EM, Grussemeyer CA, Friedman JY, Dinan MA, Lin L, Schulman KA, et al. Resource use, costs, and utility estimates for patients with cystic fibrosis with mild impairment in lung function: analysis of data collected alongside a 48-week multicenter clinical trial. Value Health. 2012;15:277–83.

    Article  PubMed  Google Scholar 

  16. Gu, Y., Perez, S.G., Massie, J., van Gool, K. Cost of care for cystic fibrosis: an investigation of cost determinants using national registry data. Eur J Health Econ in press.

  17. Angelis A, Tordrup D, Kanavos P. Socio-Economic Burden of Rare Diseases: A Systematic Review of Cost of Illness Evidence. Health Policy 2015, DOI: 10.1016/j.healthpol.2014.12.016

  18. Linertová R, Serrano-Aguilar P, Posada-de-la-Paz M, Hens-Pérez M, Kanavos P, Taruscio D, et al. Delphi approach to select rare diseases for a European representative survey. The BURQOL-RD study. Health Policy. 2012;108(1):19–26.

    Article  PubMed  Google Scholar 

  19. Lopez-Bastida J, Monton-Alvarez F, Serrano-Aguilar P, Perestelo-Perez L. The social-economic costs in patients with ataxias cerebelosas in Spain. Mov Disord. 2008;23:212–7.

    Article  PubMed  Google Scholar 

  20. Payment by Results in the NHS: tariff for 2012 to 2013. [https://www.gov.uk/government/publications/confirmation-of-payment-by-results-pbr-arrangements-for-2012-13]. Accessed on 24 May 2013.

  21. Curtis, L. Unit Costs of Health and Social Care 2012. [http://www.pssru.ac.uk/project-pages/unit-costs/2012/]. Accessed on 24 May 2013.

  22. NHS reference costs 2012 to 2013. [https://www.gov.uk/government/publications/nhs-reference-costs-2012-to-2013]. Accessed on 24 May 2013.

  23. NHS Drug Tariff. [http://www.ppa.org.uk/ppa/edt_intro.htm]. Accessed on 24 May 2013.

  24. British National Formulary. [http://www.bnf.org/bnf/index.htm]. Accessed on 24 May 2013.

  25. McDaid D. Estimating the costs of informal care for people with Alzheimer’s disease: methodological and practical challenges. Int J of Geriatr Psychiatry. 2001;16:400–5.

    Article  CAS  Google Scholar 

  26. Hodgson TA, Meiners MR. Cost-of-illness methodology: a guide to assessment practices and procedures. Milbank Mem Fund Q. 1982;60:429–91.

    Article  CAS  Google Scholar 

  27. Annual Survey of Hours and Earnings, 2012. [http://www.ons.gov.uk/ons/rel/ashe/annual-survey-of-hours-and-earnings/2012-provisional-results/index.html]. Accessed on 24 May 2013.

  28. Brooks R. EuroQol: the current state of play. Health Policy. 1996;37:53–72.

    Article  CAS  PubMed  Google Scholar 

  29. Collin C, Wade DT, Davies S, Horne V. The Barthel ADL Index: a reliability study. Int Disabil Stud. 1988;10(2):61–3.

    Article  CAS  PubMed  Google Scholar 

  30. Hérbert R, Bravo G, Préville M. Reliability, validity, and reference values of the Zarit Burden Interview for assessing informal caregivers of community-dwelling older persons with dementia. Can J Aging. 2000;494–507.

  31. Dolan P. Modeling valuations for EuroQol health states. Med Care. 1997;35:1095–108.

    Article  CAS  PubMed  Google Scholar 

  32. Kind P, Hardman G, Macran S. UK Population Norms for EQ-5D. Discussion paper 172, The University of York Centre of Health Economics.

  33. Heimeshoff M, Hollmeyer H, Schreyögg J, Tiemann O, Staab D. Cost of illness of cystic fibrosis in Germany. Pharmacoeconomics. 2012;30:763–77.

    Article  PubMed  Google Scholar 

  34. Robson M, Abbott J, Webb K, Dodd M, Walsworth-Bell J. A cost description of an adult cystic fibrosis unit and cost analyses of different categories of patients. Thorax. 1992;47:684–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Baltin CT, Smaczny C, Wagner TO. Drug treatment of cystic fibrosis – cost patterns and savings potential for outpatient treatment. Med Klin (Munich). 2010;105(12):887–900.

    Article  Google Scholar 

  36. Tur-Kaspa I, Aljadeff G, Rechitsky S, Grotjan HE, Verlinsky Y. PGD for all cystic fibrosis carrier couples: novel strategy for preventive medicine and cost analysis. Reprod Biomed Online. 2010;21(2):186–95.

    Article  CAS  PubMed  Google Scholar 

  37. Huot L, Durieu I, Bourdy S, Ganne C, Bellon G, Colin C, et al. Evolution of costs of care for cystic fibrosis patients after clinical guidelines implementation in a French network. J Cyst Fibros. 2008;7(5):403–8.

    Article  PubMed  Google Scholar 

  38. Eidt-Koch D, Mittendorf T, Greiner W. Cross-sectional validity of the EQ-5D-Y as a generic health outcome instrument in children and adolescents with cystic fibrosis in Germany. BMC Pediatr. 2009;9:55.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Ghatnekar O, Glenngård AH, Olofsson S, Persson U. A literature review of instruments for measuring health-related quality of life in rare diseases. The Swedish Institute for Health Economics. Internal report of BURQOL-RD; April 2011.

Download references

Acknowledgements

We are grateful to the Cystic Fibrosis Trust for assisting with the data collection process and to two anonymous referees for providing very helpful comments. All outstanding errors remain our own.

*Members of the BURQOL-RD Research Network listed in the Appendix

Funding

Supported by the Social Economic Burden and Health-Related Quality of Life in Patients with Rare Diseases in Europe Project, which has received funding from the European Union in the framework of the Health Programme [grant A101205]. The Executive Agency of the European Union is not responsible for any use that may be made of the information contained in this study.

Author information

Authors and Affiliations

Authors

Consortia

Corresponding author

Correspondence to Aris Angelis.

Additional information

Competing interests

The authors declare no conflicts of interests.

Authors’ contributions

All authors were involved in drafting the article or revising it critically for important intellectual content, and all authors approved the final version to be submitted for publication. PK and JLB had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Study conception and design. JLB, RL, PSA, PK. Acquisition of data. PK, EN, AA, JLB, PSA. Analysis and interpretation of data. AA, PK, JLB, RL

Authors’ information

Not applicable.

Availability of data and materials

Not applicable.

Appendix I

Burqol-Rd Research Network

  • Canary Islands Foundation for Research and Health (FUNCIS) (Spain): Pedro Serrano-Aguilar, Renata Linertová

  • Universidad Castilla-La Mancha (Spain): Julio López-Bastida, Juan Oliva-Moreno

  • Research Institute for Rare Diseases, Instituto de Salud Carlos III (Spain): Manuel Posada de la Paz, Manuel Hens Pérez, Ignacio Abaitua

  • National Center for Rare Diseases, Istituto Superiore di Sanità (Italy): Domenica Taruscio, Yllka Kodra

  • Mario Negri Institute for Pharmacological Research (Italy): Arrigo Schieppati

  • Bulgarian Association for Promotion of Education and Science (Bulgaria): Rumen Stefanov, Georgi Iskrov

  • Centre for Public Affairs Studies Foundation (Hungary): László Gulácsi, Márta Péntek

  • Federación Española de Enfermedades Raras (Spain): Rosa Sánchez de Vega García, Claudia Delgado

  • London School of Economics and Political Science (UK): Panos Kanavos, Aris Angelis, Elena Nicod

  • Leibniz University Hannover (Germany): Johann-Matthias Graf von der Schulenburg, Alexander Kuhlmann

  • The Swedish Institute for Health Economics (Sweden): Ulf Persson, Ola Ghatnekar

  • University Paris Est (France): Karine Chevreul, Karen Brigham

  • Universita Commerciale “Luigi Bocconi” (Italy): Giovanni Fattore, Marianna Cavazza

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Angelis, A., Kanavos, P., López-Bastida, J. et al. Social and economic costs and health-related quality of life in non-institutionalised patients with cystic fibrosis in the United Kingdom. BMC Health Serv Res 15, 428 (2015). https://doi.org/10.1186/s12913-015-1061-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12913-015-1061-3

Keywords