Article Text
Abstract
Objective To estimate the cost of paediatric asthma from a UK National Health Service (NHS) and societal perspective and explore determinants of these costs.
Design Cost analysis based on data from a large clinical trial between 2017 and 2019. Case report forms recorded healthcare resource use and productivity losses attributable to asthma over a 12-month period. These were combined with national unit cost data to generate estimates of health service and indirect costs.
Setting Asthma clinics in primary and secondary care in England and Scotland.
Main outcome measures Cost per asthma attack stratified by highest level of care received. Total annual health service and indirect costs. Modelled effect of sex, age, severity, number of attacks and adherence on total annual costs.
Results Of 506 children included in the analysis, 252 experienced at least one attack. The mean (SD) cost per attack was £297 (806) (median £46, IQR 40–138) and the mean total annual cost to the NHS was £1086 (2504) (median £462, IQR 296–731). On average, children missed 6 days of school and their carers missed 13 hours of paid work, contributing to a mean annual indirect cost of £412 (879) (median £30, IQR 0–477). Health service costs increased significantly with number of attacks and participant age (>11 years). Indirect costs increased with asthma severity and number of attacks but were found to be lower in older children.
Conclusions Paediatric asthma imparts a significant economic burden on the health service, families and society. Efforts to improve asthma control may generate significant cost savings.
Trial registration number ISRCTN 67875351.
- Health Care Economics and Organizations
- Child Health
- Respiratory Medicine
- Paediatrics
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WHAT IS ALREADY KNOWN ON THIS TOPIC
Direct and indirect costs of paediatric asthma in the UK have not been estimated for many years.
Older data indicate that costs to the health service are higher for those with more severe and uncontrolled asthma due to an increased requirement for hospital care.
The condition is associated with considerable indirect costs arising from days missed from school and carers having to take time off work to care for children.
WHAT THIS STUDY ADDS
This study provides detailed contemporary healthcare resource use and productivity loss estimates resulting from paediatric asthma over a 1-year period, and quantifies their relationship with patient and disease characteristics.
Annual costs to the health service are more than threefold higher for children who experience three to four attacks compared with those with no attacks.
Productivity losses are 1.7 times higher for families of participants with more severe (British Thoracic Society (BTS)/Scottish Intercollegiate Guidelines Network (SIGN) step 4) versus less severe (BTS/SIGN step 2) disease, and 6.7 times higher for those who experience three to four attacks per year compared with no attacks.
HOW THIS STUDY MIGHT AFFECT RESEARCH, PRACTICE OR POLICY
This study highlights the potential economic savings of improved asthma treatment to reduce the number of attacks.
The estimates of resource use and cost can serve as key inputs to service planning and future economic modelling studies of asthma interventions and initiatives.
Introduction
Asthma affects between 5% and 10% of children in the UK.1–3 Asthma attacks are common, can be life threatening and impose a considerable economic burden on the health service, families and society.4–7 It has been estimated that provision of care for all patients with asthma costs the National Health Service (NHS) £3.03 billion per year.6
The cost of asthma is known to be associated with severity and control; more severe and less controlled asthma is linked to the greatest healthcare resource use (HCRU).8–10 There is a lack of recently published studies that have quantified the economic burden that paediatric asthma imposes on the health system and society in the UK. This may limit the ability of planners and commissioners to accurately budget for the delivery of asthma services or determine the potential value of initiatives to improve its control. To address this evidence gap, we use data collected from a randomised controlled trial (RCT) which recruited children with asthma between 2017 and 2019 to describe the direct and indirect costs of childhood asthma in the UK.
Methods
Study design
The Reduced Asthma Attacks in Children using Exhaled Nitric Oxide (RAACENO) trial recruited 509 children from centres across the UK between 2017 and 2019, the majority (97%) from secondary care. Participants were aged 6–15 years, diagnosed with asthma, treated with inhaled corticosteroids and had at least one asthma attack in the past year. The trial found no evidence for a difference in clinical outcomes or costs between the randomised treatment groups (FeNO plus symptom-guided treatment or symptom-guided treatment alone), justifying the pooling of data for this cost analysis. Full details of the trial results, objectives and design are available elsewhere.11
Data collection
Data were collected retrospectively from parent-held diaries and case report forms (CRFs) completed during four clinic assessments at 3-month intervals throughout the follow-up period. The information relevant to this analysis included asthma medications, treatment adherence, number of asthma attacks and associated healthcare use, other asthma-related healthcare use and participant and carer time lost from usual activities.
Cost estimation methods
The analysis took a UK NHS perspective for HCRU and a societal perspective for time losses. All costs are expressed in 2019/2020 UK sterling using the NHS inflation indices where necessary.12 The costs incurred during each quarterly time interval were summed at the individual level across all observations over the 1-year follow-up period.
Three categories of asthma-related HCRU were identified from the CRFs: (1) HCRU associated with attacks; (2) HCRU not associated with attacks; and (3) medication. Direct NHS costs under each category were calculated by multiplying the reported HCRU by nationally representative unit costs (online supplemental table 1).12–14 Staff time required for pharmacist and NHS 111 contacts were informed by external literature.15 16 The cost of medications was sourced from the British National Formulary (BNF) and combined with the prescribed dose (online supplemental table 2).17 An NHS confidential discount is available for omalizumab injections. For this analysis we used the list price.18
Supplemental material
Indirect costs were measured using the human capital approach.19 Time displaced was categorised as: school, leisure, study and paid or unpaid work. Details of the unit costs applied to time losses are presented in online supplemental material 1.
Statistical analysis
Data were summarised using the mean, SD, median and IQR for continuous variables, and numbers and percentages for categorical variables. While healthcare cost data are often right skewed, whereby a minority of high-resource patients lift the mean above the median, the analysis and interpretation focuses on the mean as the most relevant measure of budgetary impact.20 All analyses were conducted using STATA V.15.21
Missing data were minimised by asking about patient-reported resource use and time losses at each attended clinical assessment visit, covering the time elapsed since the last attended visit. If patients failed to attend their final follow-up assessment, they were followed by phone to collect data on all attacks and associated resource use. We assessed the sensitivity of results to missing data using multiple imputation with chained equations.22
Generalised linear models (GLM) were used to explore the effect on total cost of several covariates: age, sex, asthma severity, number of attacks and treatment adherence. Age was categorised as per the minimisation criteria used in the RAACENO trial (<11 years; ≥11 years). Asthma severity was categorised by level of asthma medication using the British Thoracic Society (BTS) / Scottish Intercollegiate Guidelines Network (SIGN) step system.23 Adherence was measured on a scale between 0 and 1 (online supplemental material 2 and online supplemental table 3), with a value of ≥70% defined as adherent. The number of attacks was categorised as 0, 1–2, 3–4 or ≥5, to allow for non-linearity in the relationship between number of attacks and cost. The cost of study assessment visits was excluded from the GLM analysis of direct health service costs, as these were potentially protocol driven and invariable between patients. GLM results are expressed in terms of the average effect of each variable on the model’s predicted cost. Given the skewed nature of the data, gamma family and log link functions were specified based on findings of modified Park and Box-Cox tests of functional form.24 25 A high proportion of zero values were observed for indirect costs, which creates challenges for statistical modelling. A two-part model was specified with a probit model first used to predict the probability of reporting time losses combined with a GLM model to predict costs among those with time losses.26 These models are combined to estimate the effects of covariates on total indirect costs. Both models used robust SEs clustered by centre number. The trial was registered with the ISRCTN registry (ISRCTN 67875351).
Results
Baseline characteristics
There were 509 participants recruited of whom 506 were included in the analysis. We have previously shown that the RAACENO participants were comparable to children attending secondary care asthma clinics in the UK.11 Most patients (85%) were on step 3 or step 4 BTS/SIGN treatment levels and 56% had an inpatient admission for asthma in the year preceding recruitment (table 1).
Direct cost to the health service
Attacks
There were 509 attacks observed in 252 participants during follow-up. Associated HCRU data were available for 244 participants (497 attacks), with 49 (61 attacks) requiring inpatient hospital admission. The mean cost per attack was £297 (SD: 806) and the median was £46 (IQR: 40, 138). Table 2 presents the cost per attack overall and by the highest level of care received. The average number of healthcare contacts is provided in online supplemental table 4. Most attacks (n=291) were treated in primary care, predominantly by a general practitioner. Where secondary care was required, participants were typically treated in the emergency department, followed by hospital inpatient admissions. No healthcare contact was made for 46 attacks (29 participants) which were treated with a course of oral steroids available at home. Results by treatment group are provided in online supplemental table 5.
Total HCRU
Besides attack-related HCRU and study follow-up assessments, a large proportion of participants (n=225/443) did not report any additional HCRU. Table 3 reports the mean total cost of asthma-related HCRU over the trial follow-up period. The mean cost of asthma is driven by participants who had multiple attacks, required inpatient hospitalisation and were prescribed high-cost omalizumab (n=13/432). All participants used a preventer (inhaled corticosteroid±long-acting beta agonist) and reliever inhaler. Other medication use included leukotriene receptor antagonist (n=287/432), theophylline (n=50/432) and ciclosporin (n=6/432). A detailed breakdown of cost by treatment group and corresponding HCRU is found in online supplemental tables 6 and 7.
Indirect cost
Table 4 summarises participant-reported time losses from productive activities and corresponding indirect costs for those reporting time losses. Most participants reported missing days of school due to asthma. Approximately half (52%) of adult family and carers reported time losses, mostly from paid employment. The mean indirect cost in the population, inclusive of those reporting zero time losses, was £412 (SD: 879). The median was £30 (IQR: 0, 477). On average, participants reported missing 5.9 (SD: 8.5) days of school. Results by treatment allocation group are provided in online supplemental table 8.
Determinants of total direct and indirect costs
The results from GLMs of direct and indirect costs are presented in table 5, in terms of the effect of each explanatory variable on modelled cost. The direct cost model predicts costs of £2841 (SE: 658) for patients ≥11 years old with more severe asthma (BTS step 4) who experience ≥5 attacks in the year. Patients <11 years old, with less severe asthma (BTS step 2), who experience no attacks, are predicted to cost the NHS £521 (SE: 137). A similar pattern was observed for indirect cost, but with a negative association for age. The probability of reporting no time losses was 0.65 (SE: 0.04, p<0.01) if the participant experienced no attacks.
The mean adherence was 72.5% (SD: 20.0). Adherence was found to be predictive of direct cost (p=0.03); adherent patients were projected to cost £464 (SE: 298) more than non-adherent. Previous asthma studies27 28 defined ‘adherent’ as ≥80%. Under this definition, adherence was not found to be a predictor of direct cost (p=0.93). The estimates were robust to missing data assumptions, with similar results obtained using multiple imputation. In a further sensitivity analysis which removed participants who received omalizumab, the effects of age and adherence on direct costs were no longer significant, and the predicted annual direct costs were substantially lower (£728) (online supplemental table 9).
Discussion
This study provides detailed estimates of the cost of paediatric asthma from both the NHS and societal perspective, for a population prone to attacks, followed up mainly in secondary care. The cost per attack to the health service (£297) was driven by hospital inpatient admissions, despite only 12% of attacks leading to admission. The mean cost to the health service was £1086 per participant over the 12-month follow-up period, inclusive of £647 for medication, £296 of attack-related resource use and £145 for other resource use. Participants missed on average 5.9 (SD: 8.5) days of school and parents and carers missed 13.0 (SD: 30.6) hours of work in relation to the child’s asthma. These findings highlight the often unrecognised costs of asthma to children and families.
The higher direct cost for older relative to younger children and the unexpected finding of higher cost for adherent compared with non-adherent children can be explained by omalizumab prescribing being clustered in more adherent children over the age of 11, at a cost of up to £18 078 per year based on the list price. Just 13 participants received this medication, 10 of whom were >11 years old and had adherence >70%. Adherence and age were no longer predictive of direct costs when these participants were removed from the analysis. The finding of lower indirect costs for older participants may be explained by families becoming more knowledgeable of the condition as children age, and therefore better able to manage it without taking time off work. We also know that severity and control improve as children age,29 30 so we may be observing a mediation between asthma severity and age.
A strength of this analysis is that it is based on data from a large multicentre RCT conducted in England and Scotland. A high degree of complete data was achieved, particularly in relation to attack-related resource use. The number of attacks, hospitalisations and school days missed were substantially higher in the year preceding randomisation. It is unclear if such improvement would be achieved outside the trial setting, meaning that ‘real world’ costs might be higher. Data may be subject to protocol biases as participants attended clinical assessments more regularly than in routine practice and may have had better control as a result. It would be of value to externally validate these findings using observational data. Nevertheless, our estimated cost per attack, and effects of covariates on direct and indirect costs, should be generalisable to the wider paediatric asthma population. A further weakness is that our study did not collect information regarding attack severity. There is scope to better understand the determinants of attack cost to the NHS given the high variability observed. There are also limitations of how adherence was measured and defined, with some discrepancies between different sources leading to uncertainty regarding its accuracy. Finally, our estimate of indirect costs is restricted to productivity losses arising from absenteeism. It does not capture presenteeism so may underestimate the full indirect costs of asthma.
There is a paucity of contemporary studies reporting on the cost of paediatric asthma in the UK.8 10 Kerkhof et al reported a mean annual HCRU cost of £861 (2015 prices) for patients with severe, uncontrolled eosinophilic asthma. Our estimate for secondary care managed paediatric asthma, inclusive of quarterly clinical assessment visits, is higher at £1846. This may be explained by differences between the study populations—only 2% of the population reported by Kerkhof et al were under 18 years of age—and more intensive routine monitoring within the RAACENO trial. Gokhale et al 8 assessed the HCRU of 265 paediatric asthma patients aged 6–17 years in England who had severe refractory asthma. During a 1-year period, 42.6% of patients experienced at least one oral corticosteroids (OCS)-defined attack (excluding attacks treated at home), and 24.5% of attacks resulted in a hospital attendance. In RAACENO, we found that 48.6% (242/498) of participants experienced at least one attack requiring contact with primary or secondary care, with 35.5% of these resulting in secondary care contact.
Our results with respect to productivity losses are broadly consistent with those reported in the literature. Based on a review of published evidence, Nunes et al reported that a child experiencing an exacerbation can expect to miss 3–5 days of school, with parents missing a similar number of days of work.5 RAACENO participants experienced two attacks on average. Those who experienced at least one attack reported missing 9.4 (SD: 10.3) days of school and their carers reported missing 20.9 (SD: 39.2) hours of paid work
The results of this study can support the planning of asthma services for similar populations. This is directly relevant to initiatives to improve asthma care and outcomes in the NHS such as phase 1 of the National Bundle of Care for Children and Young People with Asthma.31 It is estimated there are currently 1.1 million children receiving treatment for asthma in the UK.32 A recent UK-based cohort study of children with asthma in primary care suggests an annual attack rate of at least 0.18 per patient-year.33 Assuming our cost per attack estimate is generalisable to attacks experienced by the wider paediatric asthma population, the expected annual cost of asthma attacks would be in the region of £59.2 million at the population level ( ). Acknowledging the caveats around generalisability of hospitalisation rates for attacks observed in the RAACENO study, this simple calculation illustrates how our results could be used to inform service planning and future modelling initiatives.
In conclusion, paediatric asthma imparts a significant economic burden on the health service, families and society. Our data provide a useful input to future studies that seek to model the broader costs and savings of efforts to improve paediatric asthma control and reduce attack frequency.
Ethics statements
Patient consent for publication
Ethics approval
This study involves human participants and was approved by the North of Scotland Research Ethics Committee (16/NS/0106). Participants gave informed consent to participate in the study before taking part.
Acknowledgments
We thank all the children who took part in the study and their families, and the staff at recruitment sites who facilitated identification, recruitment and follow-up of study participants. We acknowledge Jessica Wood, Victoria Bell and Andrea Fraser from the RAACENO trial office. We also thank Aileen Neilson who initially led the health economic aspects of the RAACENO trial.
Supplementary materials
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Footnotes
Contributors ST was the chief investigator of the RAACENO trial and contributed to the conception and design of the trial, conduct of the trial, recruitment and follow-up of participants, and the interpretation of results. SC was the trial manager and contributed to the design and conduct of the trial, the interpretation of results, and was responsible for the day-to-day management of the trial. GS was the senior health economist on the RAACENO trial and oversaw the health economic analysis and contributed to the interpretation of results. CK was responsible for the health economic analysis of the RAACENO trial and contributed to the interpretation of results. CK, GS, ST and SC contributed to the analysis plans for the cost analysis reported in this paper. CK conducted the data analysis and wrote the first draft of the manuscript. CK, GS, ST and SC revised it critically for important intellectual content and gave approval for final submission. GS is the guarantor for this research and publication.
Funding The study was funded by Efficacy and Mechanism Evaluation (EME) Programme (project number: 15/18/14), a Medical Research Council (MRC) and National Institute for Health Research (NIHR) partnership. The Health Services Research Unit (HSRU) and the Health Economics Research Unit (HERU) were core funded by the Chief Scientist Office of the Scottish Government Health and Social Care Directorate during the time this study was conducted.
Disclaimer The views expressed in this publication are those of the author(s) and not necessarily those of the MRC, NIHR or the Department of Health and Social Care.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.