Article Text


Refractory asthma in the UK: cross-sectional findings from a UK multicentre registry
  1. Liam G Heaney1,
  2. Chris E Brightling2,
  3. Andrew Menzies-Gow3,
  4. Michael Stevenson4,
  5. Rob M Niven5,
  6. on behalf of the British Thoracic Society Difficult Asthma Network
  1. 1Centre for Infection and Immunity, Queen's University of Belfast, UK
  2. 2Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, UK
  3. 3Royal Brompton Hospital, London, UK
  4. 4School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, UK
  5. 5North West Lung Centre, University of Manchester, Manchester, UK
  1. Correspondence to Dr Liam Heaney, Centre for Infection and Immunity, Queen's University of Belfast, Level 8, Belfast City Hospital, Lisburn Road, Belfast BT9 7AB, UK; l.heaney{at}


Introduction Refractory asthma represents a significant unmet clinical need where the evidence base for the assessment and therapeutic management is limited. The British Thoracic Society (BTS) Difficult Asthma Network has established an online National Registry to standardise specialist UK difficult asthma services and to facilitate research into the assessment and clinical management of difficult asthma.

Methods Data from 382 well characterised patients, who fulfilled the American Thoracic Society definition for refractory asthma attending four specialist UK centres—Royal Brompton Hospital, London, Glenfield Hospital, Leicester, University Hospital of South Manchester and Belfast City Hospital—were used to compare patient demographics, disease characteristics and healthcare utilisation.

Results Many demographic variables including gender, ethnicity and smoking prevalence were similar in UK centres and consistent with other published cohorts of refractory asthma. However, multiple demographic factors such as employment, family history, atopy prevalence, lung function, rates of hospital admission/unscheduled healthcare visits and medication usage were different from published data and significantly different between UK centres. General linear modelling with unscheduled healthcare visits, rescue oral steroids and hospital admissions as dependent variables all identified a significant association with clinical centre; different associations were identified when centre was not included as a factor.

Conclusion Whilst there are similarities in UK patients with refractory asthma consistent with other comparable published cohorts, there are also differences, which may reflect different patient populations. These differences in important population characteristics were also identified within different UK specialist centres. Pooling multicentre data on subjects with refractory asthma may miss important differences and potentially confound attempts to phenotype this population.

  • Refractory asthma
  • National registry
  • clinical assessment
  • asthma phenotypes
  • asthma epidemiology
  • asthma
  • Received 22 February 2010
  • Accepted 25 May 2010

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Patients with difficult asthma (persistent symptoms and/or frequent exacerbations despite treatment at step 4/5 of British Thoracic Society (BTS) management guidelines1) represent a significant unmet clinical need2 3; however, the evidence base for the assessment and management of this group of patients is small.1 4

In 2006, the BTS Research Committee together with physicians with a specialist interest in difficult asthma established a National Registry for dedicated UK Difficult Asthma Services. The aims were to standardise specialist clinical services, to further define and characterise clinical phenotypes in subjects with well characterised severe asthma and to facilitate research into the assessment and clinical management of difficult asthma.

Observational studies have suggested that after detailed systematic evaluation, ∼50% of patients referred with difficult to control asthma do not have refractory disease, but have multiple other mechanisms for persistent symptoms5–7 The National Registry includes UK centres operating established dedicated multidisciplinary assessment protocols to ensure identification of patients with well characterised refractory asthma. The aim of this paper is to describe the clinical features of a well characterised UK refractory asthma population from the National Difficult Asthma Registry and compare patient groups from individual centres.


There are currently seven UK dedicated Specialist Difficult Asthma Services submitting data to the UK Registry, but the data presented in this paper are from the four pilot UK centres—Royal Brompton Hospital, London, Glenfield Hospital, Leicester, University Hospital of South Manchester and Belfast City Hospital.

The Registry is hosted online by Dendrite Clinical Systems and admits password-protected anonymised data, after fully informed written consent; individual centre data can be downloaded locally by registered users for audit purposes.

Subjects were entered into the Registry in a non-selected manner, and centres were asked to have 100 subjects entered by a predefined deadline. The data in this manuscript were utilised as part of an initial service evaluation between clinical centres, and represent subjects, who after detailed assessment, fulfilled the American Thoracic Society (ATS) definition of refractory asthma.8

Statistical analysis

Anonymised data were analysed using Statistical Package for Social Sciences (SPSS, Chicago, Illinois, USA), Version 16. Between-centre comparisons were made using one-way analysis of variance (ANOVA) and Kruksal–Wallis testing, with posthoc comparisons using Bonferroni and Games–Howell comparisons, as appropriate. For categorical variables, comparisons were made using χ2 analysis with exact tests as appropriate. As multiple between-centre comparisons were made, statistical significance was taken as p<0.01 to minimise the number of results exhibiting type 1 error. General linear modelling was used to generate models with the dependent variables unscheduled care visits, rescue oral steroids and hospital admissions (entered as the square root of the index variable to ensure residuals in the model were normally distributed). For intensive care unit (ICU) admission, only 71 of 376 cases had prior ICU admission, so a binary logistic regression model was used. In all modelling, final model selection was parsimonious, with accepted variables having statistical significance of p<0.05.


Group data and between-centre comparisons are shown in tables 1–6.

Table 1

Patient demographic data

Table 2

Medical history

Table 3

Allergen testing

Table 4

Healthcare utilisation and medication

Table 5

Lung function

Table 6

Blood testing and bone density


There was a predominance of females, and more ethnic white Caucasians in all centres (table 1). In three of the centres ∼1/3 of subjects were in full-time employment, but this was significantly higher in Leicester (58.2%). Patients were less likely to record asthma as the reason for not working in Belfast, compared with Manchester and London, which had similar prevalences of full-time employment.

A family history of asthma was more common in Belfast and an atopic history highest in London (71.7%); there were also significant between-centre differences in the recorded prevalence of perennial rhinitis and seasonal rhinitis (table 2). Subjects in Belfast and London were more likely to have had prior nasal surgery compared with Leicester and Manchester. Of note, few premenopausal women recorded significant premenstrual asthma worsening.


The higher atopic prevalence in London was supported by allergen testing (table 3), with greater inhalant allergen sensitisation compared with Belfast (Leicester and Manchester use a clinically targeted allergen testing approach). The higher London atopic prevalence was not explained by younger ‘age of asthma onset’, because in subjects with asthma diagnosis ≥10 years, allergic sensitisation remained higher (eg, house dust mite-positive subjects: Belfast, 18 of 59 (30.5%) vs London, 38 of 41 (92.7%)).

Healthcare utilisation

In terms of healthcare utilisation, unscheduled visits (defined as general practitioner (GP)/hospital unscheduled contact) were higher in Belfast compared with other centres (table 4). Prereferral rescue steroid courses were lower in Manchester, although the hospital admission rate was highest in London, as was prior admission to an ICU.


The number of subjects taking maintenance oral steroids was highest in London, though the median dose was not different between centres (table 4). Inhaled steroid dose was significantly higher in London compared with other centres, and patients were more likely to be receiving theophyllines in London and leukotriene receptor antagonists in London and Belfast. There was a range of nebuliser usage, but again this was highest in London (66%) and lowest in Leicester (24%). Few patients were on anti-immunoglobulin E (IgE) treatment or steroid-sparing medication at referral (three Manchester patients on omalizumab had started in a clinical trial before referral).

Lung function

Prebronchodilator forced expiratory volume in 1 s (FEV1) for all subjects and degree of airflow obstruction was similar in Manchester, London and Belfast; FEV1 was significantly higher and less obstructive in Leicester (table 5). In those subjects where a postbronchodilator study was available, again prebronchodilator spirometry was significantly better in Leicester compared with other centres, and postbronchodilator FEV1 was significantly better in Leicester compared with Belfast. Residual volume and total lung capacity were significantly greater in London compared with Belfast and Manchester, but KCO (carbon monoxide transfer coefficient) was normal and similar in all centres.

When lung function was compared between smoking groups, only KCO was different (never smokers 105.8±16.7, ex-smokers 97.6±19.4, current smokers 94.7±21.5); posthoc testing confirmed that KCO was lower in ex-smokers compared with never smokers (p=0.020).

Inflammatory markers, immunoglobulins and bone densitometry

The baseline blood eosinophil count was higher in Belfast compared with other centres, and posthoc testing confirmed that this difference was restricted to a difference between Belfast and London. Induced sputum, fractional exhaled nitric oxide (FeNO) and IgE showed no significant differences between centres (table 6).

General linear modelling

General linear models with dependent variables of unscheduled care visits, rescue oral steroids and hospital admission are shown in table 7. For prior ICU admission, binary logistic regression modelling with ever ICU admission as dependent variable demonstrated significant associations with age of asthma diagnosis (OR 0.965 (95% CI 0.948 to 0.984), p<0.001) and inhaled steroid dose per 100 μg increase in beclomethasone dipropronate (BDP) equivalent (OR 1.029 (95% CI, 1.003 to 1.055), p<0.05).

Table 7

General linear models for listed dependent variables: dependent variables were entered as the square root of the index variable to ensure residuals in the model were normally distributed


This UK Difficult Asthma Network aims to standardise clinical assessment across specialist centres and use a Registry to facilitate phenotypic characterisation and research in patients with ‘difficult asthma’. These specialist centres have established assessment protocols, ensuring subjects have well characterised refractory asthma. The numbers of subjects per centre provide further analytical strengths and, when data are consistent across three or four centres, we believe they are representative of the UK refractory asthma population. Between-centre differences are not explained by local referral patterns (60–75% tertiary referrals, the remainder coming from primary/non-specialist physicians); however, this cannot be entirely excluded.

Three other multicentre studies have collated data on ‘difficult asthma’ previously. The TENOR study was a large-scale US observational study (4756 patients, 3489 adults) of difficult asthma (≥2 unscheduled care visits or ≥2 oral steroid bursts plus high dose inhaled steroids)9; 51% were classified as severe asthma by the treating physician. The ENFUMOSA cross-sectional study (12 centres in nine European countries) recruited 163 patients with severe asthma (≥1 exacerbation in the previous year despite ≥1200 μg of BDP equivalent inhaled steroid).10 The SARP study included 204 subjects ≥12 years, fulfilling the ATS definition of refractory asthma (9 US and 1 UK centre).11 In these studies, group data only are presented, whereas our data additionally allow comparison between individual UK centres, which has demonstrated important differences.

Our data confirm the usual female preponderance which remains unexplained,9–11 though catamennial asthma was not a common exacerbating factor.

Age at first assessment was similar between centres, though age at asthma diagnosis was significantly lower in the Brompton cohort. Median body mass index (BMI) was in the non-obese range, and similar to that seen in TENOR (average BMI was 29.9),9 whereas the average BMI in ENFUMOSA was lower (male average 26.5, female average 27.2). Current smoking is infrequent, though 29.8% had previously been smokers, with no difference between centres; these smoking prevalence figures are similar to the TENOR cohort where 4.3% of ‘difficult to control’ adults were current smokers, 32% ex-smokers and 63.7% never smokers.9

In Leicester, more patients were in full-time employment, compared with 33–36% in other centres, but why asthma is less often volunteered as the reason for not working in Belfast remains unclear, though this would significantly impact on costing refractory asthma. Occupational asthma worsening was consistently uncommon, and only appears relevant to a minority of patients.

Three centres recorded a family history of asthma in 42–44%, but in Belfast this was 74%. Retrospective data checking confirmed that the ‘family history’ definition was applied consistently, and a family history appears more common in Northern Ireland, which has traditionally low levels of immigration. Recorded familial asthma death was low, suggesting it is an infrequent event, even in this refractory group; however, this was not well recorded and we cannot exclude that the familial asthma death rate may be higher.

This higher reported atopic prevalence in London was supported by allergen testing (table 3), as subjects were more likely to be allergen positive. The difference is particularly notable between London and Belfast, where all subjects were tested for similar allergens. In Leicester and Manchester, targeted allergen testing is performed, and reported allergen positivity may represent an underestimation. Interestingly, Apergillus sensitivity in Manchester (which is routinely tested) was ‘between’ that of London and Belfast. In SARP, 71% of those with severe asthma were skin prick positive to ≥1 of 14 allergens (85% and 87% for subjects with mild/moderate asthma, respectively).11 In ENFUMOSA, ∼58% of those with severe asthma had positivity ≥1 allergen, (well controlled asthmatics ∼76%), with individual allergen positivity in those with severe asthma varying between ∼10% and 35%.10 Individual centre data are not presented in these studies; however, our data suggest that individual allergen sensitisation appears to vary in different refractory asthma populations in UK specialist centres, possibly reflecting important regional differences even within the UK.

Oral steroid courses in the 12 months before referral were fewer in Manchester compared with other centres, where the median number of rescue steroids was 4–5 per annum; this difference may reflect patient recollection in Manchester, but the similarity in other centres supports significant rescue steroid use in this group. In SARP, 54% of those with severe asthma reported ≥3 steroid bursts per year11 and, in our cohort, 63% used ≥3 courses in the previous year. Unscheduled visits were more common in Belfast, although hospital admissions and ICU usage were higher in London, though they were uncommon events. In SARP, 54% reported ≥1 unscheduled care visit per year,11 whereas this was 86% for this UK cohort. It is unclear if differences are due to different healthcare delivery for exacerbation management, or to differences in exacerbation severity.

Almost twice as many patients in the Brompton were on maintenance steroids, compared with the other centres. Inhaled steroid dose at referral was also higher in the Brompton patients compared with all other centres. The UK cohort average inhaled steroid dose was similar to the ENFUMOSA severe asthma cohort (1676±667 μg BDP equivalent), but comparative data between centres were not presented. Our data suggest that in multicentre studies specifying a minimum steroid dose for inclusion, it is important to examine medication utilisation from individual centres.

Wide variation was noted in nebuliser usage, and patients in Belfast and Brompton were more likely to be on a theophylline and leukotriene receptor antagonist at referral. These differences presumably relate to local prescribing practice and referral pattern, but all patients were on multiple medications at referral. Few patients were on steroid-sparing medication or anti-IgE treatment at referral, suggesting that these medications are not widely used outside specialist centres.

We observed a low prevalence of aspirin/non-steroidal anti-inflammatory drug (NSAID) sensitivity and, while different definitions of aspirin sensitivity probably affect reported prevalence,12 our data are notably different from those of ENFUMOSA, which suggested an association between asthma severity and self-reported aspirin exacerbation.10 Our data are similarly based on self-reported increased asthma symptoms after aspirin/NSAID ingestion, and the difference may reflect differences between the UK and a European population.

Spirometry for the UK group was lower than for the ENFUMOSA study (FEV1 % predicted 71.8% rising to 80.9% postbronchodilator), though it was similar to SARP (FEV1 % predicted 62±22%), consistent with a patient population with more severe asthma. Consistent with better spirometry in ENFUMOSA, total lung capacity in the UK cohort was higher (134.7±42.3%), compared with ENFUMOSA (104.4±15.2%). Of note, KCO was normal and similar in all centres despite the high prevalence of ex-smoking in the UK cohort, though we demonstrated a relationship between KCO and prior smoking. The normal percentage KCO is again different from ENFUMOSA, where KCO was 90.6±19% predicted; the authors suggested that abnormal gas exchange and parenchymal injury may be a feature of severe asthma. However, our data suggest that in a well characterised population with refractory asthma, the transfer factor is well preserved, and any reductions relate to prior smoking history.

Interesting differences between UK centres are seen for spirometry. Prebronchodilator and postbronchodilator spirometry and degree of airflow obstruction were better in Leicester compared with other centres. Allied with other indices—for example, increased numbers in full-time work—it suggests less severe disease in the Leicester cohort compared with other centres. This is despite the fact that all of these patients fulfilled the same definition of refractory asthma, suggesting a spectrum of severity using the ATS definition. Prospective analysis of patient outcome and treatment requirements, which is facilitated by the UK Registry, will help address this issue further. Residual volume % predicted and total lung capacity were significantly greater in the London cohort compared with Belfast and Manchester; however, the absolute differences are small.

Peripheral blood eosinophil count was highest in Belfast, but there was no significant difference in sputum eosinophilia or FeNO between centres. In SARP, FeNO data were available on 135 subjects with severe asthma and FeNO was 40±38 ppb, which is similar to this UK cohort. Mean IgE in ENFUMOSA was 109 (95% CI 85 to 139), and in SARP 100±5.75. We have presented IgE as median (IQR) as this is not normally distributed in this cohort, but our median value of 130 is comparable with other published cohorts. In subjects who had bone density measurements, 18 (10.6%) subjects had either a spinal or femoral neck bone density T score less than or equal to −2.5 (osteoporosis) and 58 (34.3%) subjects had a T score less than or equal to −1.0 (osteopenia). Bone density measurements were not done in all subjects and there may be some selection bias; however, these data are consistent with a significant morbidity in this group.

Important clinical outcomes in this group are unscheduled healthcare visits, rescue steroid use, hospital admission and ICU admission. Hierarchical regression modelling supported important between-centre differences, as this remained a significant factor in the final model for three of the four tested dependent variables (table 7). It is important to note that if this patient group was treated as a homogeneous study population, different regression models were obtained, with other additional significant associations, which were not demonstrated when centre was included as a factor (data not shown). Importantly, however, the factors which remained in our regression models with clinical centre included as a random factor also remained in each regression model, independent of whether centre was included or not.

The association between peripheral blood eosinophils and both steroid exposure and unscheduled visits in this refractory patient group is consistent with other studies which have demonstrated a relationship between blood and/or sputum eosinophilia and asthma exacerbation and loss of asthma control.13–15 Patients who were younger at the time of assessment at the Difficult Asthma Service had higher levels of both unscheduled visits and hospital admissions in the respective models. The association between total number of prior ICU admissions and hospital admission is perhaps not surprising as prior severe asthmatic events are associated with increased risk of asthma death.16 17 Home nebuliser usage and theophylline prescription may also be markers of severity and thus related to increased rescue steroid exposure and unscheduled visits, respectively. The association with female gender and unscheduled visits is interesting, particularly as this gender effect is not translated into either more steroid exposure or hospital admission, and might suggest a lower threshold for healthcare contact in females. The association between dose of inhaled steroids and ICU admission is interesting, particularly as this has previously been shown to be a predictor of treatment-resistant asthma5 and is presumably an index of longer term severity with increasing doses of inhaled steroid over time. The association with age of asthma diagnosis may reflect ICU admission in childhood but, even if this is the case, it does suggest that severe asthma in this group is present from an early stage after the initial diagnosis.

In summary, this paper presents for the first time demographic, physiological and immunological data from a well characterised UK population of subjects with refractory asthma. While similarities exist to other comparable published cohorts, there are also differences which may reflect different patient populations (difficult to control vs refractory vs different levels of asthma severity), and again argues for the production and application of precise definitions for this population of subjects with asthma. In addition, important population characteristics are different between UK specialist centres, suggesting that ‘grouping’ multicentre data (even centres in the same country) may miss important differences and potentially confound attempts to phenotype refractory asthma, giving rise to so-called ‘ecological fallacy’. The differences identified between UK centres warrant further study, but suggest refractory asthma may be more heterogeneous within an individual country than previously known.


We thank the data input staff and medical and nursing staff in the UK Difficult Asthma Centres—Belfast, Jacqui Gamble and Kirsty Graham; Leicester, Sarah Terry, Amisha Singapuri, Beverley Hargadon, Maria Shelley, Ruth Green, Ian Pavord, Andrew Wardlaw and Peter Bradding; London, Debbie Campbell and Suzanne Regan; Manchester, Gill McCumesky and Leanne Holmes.


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  • Funding Pilot funding for the Registry was provided as unrestricted research grants from Astra Zeneca, Glaxo Smith Kline and Novartis. CB is supported by a Wellcome Senior Clinical Fellowship.

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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