Consequences of long-term oral corticosteroid therapy and its side-effects in severe asthma in adults: a focused review of the impact data in the literature

Timm Volmer, Timo Effenberger, Christoph Trautner, Roland Buhl
European Respiratory Journal 2018 52: 1800703; DOI: 10.1183/13993003.00703-2018

Abstract

This review provides an overview of the role of long-term treatment of severe asthma with oral corticosteroids (OCS) and its associated side-effects in adults. It is based on a systematic literature search conducted in MEDLINE, Embase and the Cochrane Library to identify relevant studies. After a short overview of severe asthma and its treatment we present studies showing a dose–response relationship in asthmatic patients treated with OCS and then consider by organ systems the undesired effects demonstrated in clinical and epidemiological studies in patients with OCS-dependent asthma. It was found that the risk of developing various OCS-related complications, including infections, diabetes and osteoporosis as well as psychiatric disorders, was higher for patients with long-term exposure to OCS compared with control groups. In addition, studies showed a significant increase in healthcare resource utilisation due to OCS treatment. Therefore, it is incumbent on every clinician to carefully weigh the potential benefit of preventing loss of asthma control against this risk before opting to prescribe long-term OCS therapy. Effective corticosteroid-sparing strategies must be used and should aim at short-term use with the lowest effective dose and start tapering as soon as possible until OCS therapy is terminated.

Abstract

Although oral corticosteroids are effective, due to side-effects corticosteroid-sparing strategies must be used and one should aim at short-term use with the lowest effective dose and start tapering as soon as possible until OCS therapy is terminated http://ow.ly/F8wU30ltEXc

Background

Asthma is a chronic inflammatory airway disease affecting ∼235 million people worldwide [1]. In ∼4–8% of asthma patients, symptoms remain uncontrolled and exacerbations occur frequently despite high-intensity treatment, or they need systemic corticosteroid treatment for sustained symptom control [2, 3]. Systemic corticosteroids, usually administered orally, are widely used, both intermittently and long-term, in this population regardless of side-effects that may develop during an extended period of exposure [4], which are associated with a tremendous economic burden [5]. According to data from the Healthcare Cost and Utilization Project [6], corticosteroids in general were the most common cause of drug-related complications in 2004, accounting for 10% of all drug-related complications and 141 000 hospital stays in the USA. The Global Initiative for Asthma (GINA) guidelines therefore recommend use of oral corticosteroids (OCS) for maintenance therapy only in patients with uncontrolled severe asthma despite treatment with all available controller drugs including biologics if appropriate, and only as low-dosed and as short-term as possible [7]. Most studies investigating the side-effects of OCS observed patients receiving this medication for various underlying illnesses, often rheumatoid diseases. An overview of the typical side-effects of OCS found in these studies was presented by Schäcke et al. [8]. OCS treatment can affect skin, skeleton, muscles, eyes, central nervous system, metabolism, cardiovascular system, immune system and gastrointestinal system. In these studies, asthma is mostly only one of the possible indications for OCS treatment in the patients analysed. Relatively few data are available from well-described cohorts of patients with severe asthma only. The purpose of this review is to systematically assess the potential side-effects of long-term OCS treatment in patients with severe asthma and to compare dosing schemes recommended by the GINA guidelines with published data from studies analysing dose–response relationships.

The role of OCS in severe asthma

Because asthma is a chronic inflammatory airway disease, corticosteroids are a very effective therapy. Consequently, maintenance therapy with inhaled corticosteroids (ICS) is recommended for all asthma patients and mandatory for patients with more than just occasional symptoms (more than twice a week) [7, 9]. Most patients need additional bronchodilation. Therefore, long-acting β-agonists (LABA) are added, for compliance reasons typically in a fixed combination with ICS for inhalation. Inhalation as an aerosol or powder delivers the corticosteroids to the bronchial and lung tissue, optimising local anti-inflammatory effects, while minimising undesirable systemic effects.

According to GINA, severe asthma is asthma that requires step 4 or 5 treatment, e.g. high-dose ICS+LABA with or without a third controller, to maintain control or asthma that remains uncontrolled despite this treatment [7]. It is important to distinguish severe asthma from asthma that is insufficiently controlled due to inappropriate treatment, lack of treatment adherence, psychosocial factors or insufficiently controlled comorbidities. This definition is in line with the international European Respiratory Society/American Thoracic Society [10] guidelines on severe asthma.

The majority of patients with severe asthma that is insufficiently controlled by ICS and LABA and additional anti-inflammatory drugs (e.g. leukotriene antagonists) and bronchodilators (e.g. anticholinergics such as tiotropium) will be escalated to treatment with systemic corticosteroids [2, 3]. Systemic application of corticosteroids increases the desired anti-inflammatory effect, while the typical undesired side-effects of systemic corticosteroids may co-occur, depending on dose, duration of treatment and individual susceptibility. Two different uses of OCS in asthma need to be distinguished: as a “controller option” for severe asthma, and as short-term treatment of exacerbations. The focus of this article is on the use of OCS as controller therapy in patients with severe asthma.

OCS as controller therapy for severe asthma

In step 5 of national [11] and international [7] guidelines different add-on treatments to ICS+LABA, e.g. tiotropium as well as anti-IgE and anti-interleukin (IL)-5 antibodies are recommended and, as a second-choice option, low-dose OCS. This represents a downgrading of the role of OCS by GINA, in line with increasing clinical evidence supporting the use of tiotropium as additional bronchodilator in severe asthma as well as omalizumab in severe allergic asthma and monoclonal antibodies against IL-5 in severe eosinophilic asthma. Until 2012, GINA recommended in step 5 the addition of an oral glucocorticosteroid (lowest dose) or anti-IgE treatment in severe allergic asthma on top of step 4 treatment (ICS+LABA) as controller options without giving explicit preference to either [12]. Starting in 2014, the GINA guidelines recommended add-on treatment, e.g. anti-IL-5 and anti-IgE, as the preferred controller choice and low dose OCS as “other” controller option only [13]. GINA based this recommendation on the substantial side-effects of OCS, although they may be effective for some patients [7].

Recommended duration of OCS treatment as a controller option

OCS should be considered a temporary option only. Recommendations by GINA emphasise the need to step down or terminate OCS treatment when it is no longer needed or proves to be ineffective. In most patients, reduction of OCS doses or a step-down trial is indicated and feasible after some time. Any step-down of asthma treatment should be considered a therapeutic trial, with the response evaluated in terms of both symptom control and exacerbation frequency. Several options for stepping down from existing OCS treatment levels are recommended by GINA including slowly tapering OCS dose, or switching to alternate-day OCS treatment, while continuing treatment with high-dose ICS+LABA with or without additional controller(s) [7].

Common OCS doses in clinical practice

Systemic corticosteroids are usually administered orally in a wide range of doses, starting at 1 mg [14, 15]. In recent randomised trials of anti-IL-5 antibodies as an add-on to the existing maintenance therapy of severe eosinophilic asthma, patients received at baseline daily OCS doses within a range of 5–70 mg. This might be a realistic range of OCS doses that patients with severe asthma receive in many parts of the world [15–17]. European real-life data showed a range of 14.3–26.5 mg [18].

A summary of product characteristics for prednisone defines a low OCS dose as 10–40 mg·day−1, and a “very low dose” as 1.5–7.5 mg·day−1, possibly up to 10 mg·day−1. This is in line with the defined daily dose recommended by the World Health Organization of 10 mg per day. The same summary of product characteristics allows a dose of up to 100 mg per day while recommending tapering the dose soon after clinical response, and a maintenance dose independent of specific indications that is as low as possible, usually 5–15 mg·day−1 of prednisone [19]. The consequences resulting from “very low dose” or “low dose” OCS asthma treatment was investigated using a systematic literature review.

Methods

A systematic literature search for studies reporting primary data on side-effects of maintenance therapy with OCS in adults with asthma was performed in MEDLINE, Embase, and the Cochrane Library (online supplementary material). Studies focusing on acute short-term therapy for exacerbations were excluded, as the side-effects of high-dose burst treatment differ from those of long-term exposure. In addition, studies in paediatric populations were excluded, as the side-effects of OCS in children are well known and described in comparison to those in adult patients. An additional hand search of the references of cited publications was performed to complete the results.

Results

The search resulted in nine publications with studies of seven large datasets from registers or health insurance claims. The studies by Sweeney et al. [14] and Barry and co-workers [20, 21] used partly the same dataset. The results of the studies are summarised in tables 1 and 2 presented separately by the different organ classes to facilitate the comparison of effect sizes.

View this table:
TABLE 1

Summary of results from included studies by oral corticosteroid (OCS) dose

View this table:
TABLE 2

Summary of results from included studies by disease severity

Tables 1 and 2 show an increased susceptibility of a wide range of investigated side-effects after exposure to OCS in comparison to the control groups.

Dose–response relationship

To investigate whether there is a dose–response relationship between long-term treatment with OCS and OCS-related side-effects, Dalal et al. [23] performed a subgroup analysis based on the extent of OCS exposure (figure 1).

FIGURE 1
FIGURE 1

Risk of developing oral corticosteroid (OCS)-related complications by OCS dose exposures. OCS doses <5 mg·day−1 are considered low, 5–10 mg·day−1 medium and >10 mg·day−1 high. OR >1 describes a higher risk for developing OCS-related side-effects. Reproduced and modified from [23] with permission.

The analysis reflects a statistically significant linear relationship between increasing OCS exposure in terms of dose and duration and increasing risk of developing OCS-related complications. Patients taking OCS had a higher risk of complications than patients without OCS exposure, independent of the dose. Infections, bone/muscle diseases and skin diseases were significantly more frequent in patients receiving OCS, even if they had received <5 mg of prednisone-equivalent during the observation period. In addition, patients receiving <5 mg·day−1 showed an elevated risk of acute complications (OR 1.72). For the “any OCS-related complications” category, the odds ratio was 2.50. In patients receiving an OCS dose ≥5 mg·day−1, there was a statistically significant increase in the odds of experiencing acute and chronic complications, with reported odds ratios for infections of 2.25 (2.43 for >10 mg) and for bone/muscle disease of 2.28 (2.42 for >10 mg).

In patients with severe asthma who received >5 mg OCS per day, healthcare resource utilisation was increased, with odds ratios for inpatient visits of 2.40 (3.37 for >10 mg) and for emergency room visits of 1.78 (2.17 for >10 mg). Consequently, the costs per patient of OCS-related complications increased relative to no exposure, with additional annual costs of USD 2670, USD 4639 and USD 9162 for low- (<5 mg·day−1), medium- (5–10 mg·day−1) and high-dose (>10 mg·day−1) OCS treatment, respectively [23]. In a British study, the estimated direct healthcare treatment costs from a National Health Service perspective were 43% higher for patients on maintenance OCS than for those not receiving maintenance OCS [28].

The Lefebvre et al. [24] study showed similar results, with a significant dose–response relationship found for side-effects in patients with severe asthma who received OCS. Infections, as well as gastrointestinal, bone and muscle, cardiovascular, metabolic, psychiatric and ocular complications were significantly more frequent in patients with asthma receiving an OCS treatment of >6 mg·day−1 than in patients receiving <6 mg·day−1. Patients receiving >12 mg·day−1 showed the same pattern as those receiving 6–12 mg·day−1, but in most cases with a numerically higher risk of OCS-related complications.

The study by Curtis et al. [29] surveyed the use of OCS by patients, of whom 12% had asthma, and patient-reported adverse events. The study showed that the proportion of patients reporting side-effects of OCS as “bothersome” or “very bothersome” increased with increasing cumulative dose. Regular treatment with 5 mg prednisolone-equivalent per day for 1 year already resulted in an increase in adverse events of ∼40% for mood problems, ~45% for sleep problems, ~40% for skin bruising and ~60% for weight gain, and in various other adverse events such as cataracts (~10%), high blood sugar (~5%) and bone fractures (~10%). If 12.5 mg were ingested daily, the frequencies of adverse events, such as mood problems (~55%), sleep problems (~60%), weight gain (~75%), cataracts (~15%), and bone fractures (~15%), were even higher. It was concluded that the prevalence of eight commonly attributed self-reported corticosteroid-associated adverse events was significantly associated with increasing average corticosteroid dose in a dose-dependent fashion [29].

Quality of life

The influence of OCS on quality of life (QoL) is multifaceted. At a first glance, it seems obvious that patients with severe uncontrolled asthma benefit initially from long-term treatment with OCS due to better asthma control. Conversely, the multitude of side-effects developing over time as a consequence of OCS therapy make improvements in QoL at least questionable [30]. Newer treatments with a “steroid-sparing” effect proved to be associated with a reduction in corticoid exposure and a simultaneous rise in QoL [16, 31–35]. A mere reduction of OCS is not responsible, as a trial with tapering the dose of OCS while maintaining asthma control (without medication with a steroid-sparing effect) showed no significant impact on QoL despite the dose reduction of OCS [36]. In the British Thoracic Society (BTS) registry study, quality of life scores were significantly better in the non-corticosteroid dependent group, although many values (44–46%) were missing [14]. Those partly contradictory results can be explained by the fact that the currently available scales for the assessment of QoL in clinical trials are insufficient for measuring the treatment burden of long-term therapy with OCS [37], and that most steroid-sparing interventions in asthma have an impact on QoL independent of their steroid-sparing potential. Furthermore, the perception of treatment burden may not be adequately measured by commonly used tools for the assessment of QoL as patients could adapt to the chronic use of OCS. For a final assessment of the relationship between long-term treatment with OCS and QoL in asthma patients, development of more sensitive, valid and reliable asthma-specific scales for determination of the treatment burden is necessary.

Discussion

The results of this literature overview support the recommendation by GINA [7] and other asthma guidelines [11] to increase asthma treatment intensity with inhaled drugs such as ICS, LABAs, tiotropium and monoclonal antibodies (e.g. anti-IgE, anti-IL-5) before considering OCS long-term use.

All long-term OCS therapies, independent of the dose, have been reported to elevate the risk of comorbidity and complications. Even “low” doses of OCS (according to guidelines) lead to complications, as described in the analysed literature. If OCS are used following the guidelines, they should be given as maintenance therapy in the lowest possible dose and as short-term as possible. The results of the review highlight that a comprehensive look into OCS long-term safety is urgently warranted as part of clinical management (not only) in severe asthma. It also has a cost component, shown for instance in the Optimum Patient Care Research Database (OPCRD) dataset. The health economic impact of severe asthma, showing mean annual total costs of GBP 560–1324 for non-asthmatic patients compared to GBP 978–2072 for mild/moderate asthma and GBP 2603–4533 for severe asthma [21]. Lefebvre et al. [22] calculated that the costs for patients with low-, medium- and high-dose intensity were USD 678, USD 1181 and USD 2140 higher, respectively, than those of OCS non-users due to OCS-related complications. Another important conclusion of our literature review is that clinicians ought to pay high attention to prevention of OCS side-effects (e.g. substitution with calcium, vitamin D, recommend physical exercise, etc.), as they occur more consistently and widely and are more costly than previously thought.

This review is limited to adult patients, and can therefore not be generalised to paediatric populations. Additionally, a purely systematic literature search seemed not to be appropriate to better capture the diverse nature of the study designs. As publications retrieved by hand search were included in the review, a total of seven datasets and nine publications were finally consulted to summarise the effects of OCS treatment-related side-effects in asthmatic patients.

The study by Dalal et al. [23] based on US claims data from two Truven Health MarketScan Research databases provided data on the side-effects of OCS in a large cohort of patients with severe asthma, showing that the risk of corticosteroid-related complications increases with increasing dose of OCS. The findings were confirmed in the studies by Lefebvre et al. [22, 24], who based their research on Medicaid claims data in the US, but also used a longitudinal observational cohort study design. Zazzali et al. [26] used US commercial healthcare claims in a matched cohort study and Zeiger et al. [27] presented administrative pharmacy and healthcare utilisation data gathered from the Kaiser Permanente Southern California Research Data Warehouse in a retrospective observational cohort study. All the above data sources would have been missed by focussing on randomised evidence from clinical trials only.

Limitations of the above data sources result from the typically reported challenges well known for claims data studies: conversion of claims into unique visits, identification of incomplete claims data, categorisation of providers and locations of service and selecting the most useful measures of utilisation and expenditures [38]. The study by Daugherty et al. [25] was longitudinal in design, but did not use claims data. Instead, the study was based on the UK Clinical Practice Research Datalink database.

Unlike the longitudinal studies, the studies by Sweeney et al. [14] and Barry and co-workers [20, 21] were cross-sectional in design, so that the point prevalence can be measured, but reliable incidence rates are not available. In these two studies, the risks of complications for patients with severe asthma compared with non-asthmatic controls seem to be greater than those of patients with mild/moderate asthma. Higher risks of concomitant disease in patients with asthma than in people without asthma may contribute to the above findings. The significantly higher prevalence of comorbidities such as diabetes and hypertension in asthmatics versus non-asthmatics reported by Su et al. [39] may explain the increased risk of chronic kidney disease found in patients with severe asthma by Sweeney et al. [14], as diabetes and hypertension have a negative impact on kidney function. An increase in depression, anxiety, mood disorders and sleep disorders may in part be explained by an increased severity of the disease. The same is true for the detrimental impact on quality of life. All these limitations suggest that some of the apparently increased risks of patients with severe asthma may in fact be due to the severity of the disease, and not only the detrimental effects of long-term OCS treatment.

Taken together, all the identified studies demonstrate a substantially increased risk for “typical” steroid-induced side-effects in patients with severe asthma who take OCS long-term. In line with these findings, the GINA guidelines recommend counselling about potential side-effects, regular checks of blood pressure as well as monitoring for risk of corticosteroid-induced osteoporosis in patients with asthma who receive OCS as maintenance therapy and appropriate prevention of osteoporosis for patients expected to be treated for ≥3 months [7].

Comparison of the OCS doses received by patients in included studies with the recommended GINA dose for treatment of severe asthma revealed that the GINA recommendation (≤7.5 mg·day−1) was already regarded as medium [22–24] or high exposure [25, 27].

A different approach was used by Zazzali et al. [26]: high OCS use was defined as more than >30 days of OCS supply per year resulting in a median daily dose of ∼3.5 mg·day−1 in the included patients. This is comparable with the low-dose groups defined by Dalal et al. [23] and Lefebvre et al. [22, 24].

Patients with severe asthma in the BTS registry took on average 15 mg·day−1 OCS [14]. Obviously, most patients with severe asthma in the BTS registry therefore received much more than the recommended GINA dose of ≤7.5 mg·day−1 [14]. Most patients in the comparator group probably received the equivalent of an average daily dose of 1–5 mg·day−1. To interpret the results of the BTS study, two facts need to be considered: the doses taken by the patients with severe asthma were considerably higher than those taken by the patients in the other included studies. However, whereas the comparator groups in the OPCRD (non-asthma) and the studies by Dalal et al. [23], Daugherty et al. [25], Lefebvre et al. [22, 24] and Zazzali et al. [26] were not exposed to any OCS, the comparator group in the BTS study received a considerable average dose due to rescue medications during periods of exacerbation.

Conclusion

Several independent studies demonstrate that the exposure of side-effects of long-term OCS treatment of severe asthma is associated with the level of the daily dose used. Side-effect severity of chronic OCS exposure presents as a continuum, starting even at very low doses <5 mg·day−1. We could not find a well-founded threshold for side-effects of OCS or a dosing window for a “safe” long-term use. On the basis of these findings, the advantage of better asthma control with OCS must be thoroughly weighed against the risk of side-effects. Effective corticosteroid-sparing strategies must be used to reduce side-effects. If OCS treatment is needed, it should aim at short-term use with the lowest effective dose and start tapering as soon as possible until OCS therapy is terminated.

The GINA guidelines now recommend steroid-sparing therapies such as omalizumab, benralizumab, reslizumab and mepolizumab as a preferred treatment choice over the use of OCS. German guidelines already recommend initiating an OCS therapy only after all other step 5 treatments (tiotropium, anti-IgE or anti-IL-5) have failed or are not suitable because of side-effects [11]. Patients with severe asthma may benefit from disease phenotyping in terms of disease control and treatment-related adverse events [7].

Supplementary material

Supplementary Material

Please note: supplementary material is not edited by the Editorial Office, and is uploaded as it has been supplied by the author.

Supplementary material ERJ-00703-2018_Supplement

Footnotes

  • This article has supplementary material available from erj.ersjournals.com

  • Conflict of interest: T. Volmer reports grants from Teva Pharmaceutical Industries Ltd, during the conduct of the study; and personal fees for consultancy from Teva Pharmaceutical Industries Ltd, outside the submitted work.

  • Conflict of interest: T. Effenberger reports grants from Teva Pharmaceutical Industries Ltd, during the conduct of the study; and personal fees for consultancy from Teva Pharmaceutical Industries Ltd, outside the submitted work.

  • Conflict of interest: C. Trautner reports grants from Teva Pharmaceutical Industries Ltd, during the conduct of the study; and personal fees for consultancy from Teva Pharmaceutical Industries Ltd, outside the submitted work.

  • Conflict of interest: R. Buhl reports grants from Teva Pharmaceutical Industries Ltd, during the conduct of the study; and personal fees for consultancy from Teva Pharmaceutical Industries Ltd, outside the submitted work.

  • Support statement: This research was partly funded through a restricted grant from Teva. Funding information for this article has been deposited with the Crossref Funder Registry.

  • Received April 13, 2018.
  • Accepted August 13, 2018.

References

  1. ↵
    World Health Organization (WHO). Asthma Fact Sheet N°307. www.who.int/mediacentre/factsheets/fs307/en/ Date last updated: August 31, 2017.
  2. ↵
    1. Kauppi P,
    2. Peura S,
    3. Salimäki J, et al.
    Reduced severity and improved control of self-reported asthma in Finland during 2001–2010. Asia Pac Allergy 2015; 5: 32–39.
    OpenUrlCrossRefPubMed
  3. ↵
    1. von Bülow A,
    2. Kriegbaum M,
    3. Backer V, et al.
    The prevalence of severe asthma and low asthma control among Danish adults. J Allergy Clin Immunol Pract 2014; 2: 759–767.
    OpenUrl
  4. ↵
    1. Fardet L,
    2. Kassar A,
    3. Cabane J, et al.
    Corticosteroid-induced adverse events in adults: frequency, screening and prevention. Drug Saf 2007; 30: 861–881.
    OpenUrlCrossRefPubMed
  5. ↵
    1. Manson SC,
    2. Brown RE,
    3. Cerulli A, et al.
    The cumulative burden of oral corticosteroid side effects and the economic implications of steroid use. Respir Med 2009; 103: 975–994.
    OpenUrlCrossRefPubMedWeb of Science
  6. ↵
    1. Elixhauser A,
    2. Owens P
    . Adverse Drug Events in U.S. Hospitals, 2004. Agency for Healthcare Research and Quality HCUP Statistical Brief #29. April 2007. www.hcup-us.ahrq.gov/reports/statbriefs/sb29.pdf
  7. ↵
    Global Initiative for Asthma (GINA). 2018 Gina Report, Global Strategy for Asthma Management and Prevention. https://ginasthma.org/2018-gina-report-global-strategy-for-asthma-management-and-prevention/
  8. ↵
    1. Schäcke H,
    2. Döcke WD,
    3. Asadullah K
    . Mechanisms involved in the side effects of glucocorticoids. Pharmacol Ther 2002; 96: 23–43.
    OpenUrlCrossRefPubMedWeb of Science
  9. ↵
    1. Barnes PJ
    . Glucocorticosteroids. Handb Exp Pharmacol 2017; 237: 93–115.
    OpenUrl
  10. ↵
    1. Chung KF,
    2. Wenzel SE,
    3. Brozek JL, et al.
    International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur Respir J 2014; 43: 343–373.
    OpenUrlAbstract/FREE Full Text
  11. ↵
    1. Buhl R,
    2. Bals R,
    3. Baur X, et al.
    S2k-Leitlinie zur Diagnostik und Therapie von Patienten mit Asthma [Guideline for the Diagnosis and Treatment of Asthma – Guideline of the German Respiratory Society and the German Atemwegsliga in Cooperation with the Paediatric Respiratory Society and the Austrian Society of Pneumology]. Pneumologie 2017; 71: 849–919.
    OpenUrl
  12. ↵
    Global Initiative for Asthma (GINA). Global Strategy for Asthma Management and Prevention. GINA, 2012.
  13. ↵
    Global Initiative for Asthma (GINA). Global Strategy for Asthma Management and Prevention. GINA, 2014.
  14. ↵
    1. Sweeney J,
    2. Patterson CC,
    3. Menzies-Gow A, et al.
    Comorbidity in severe asthma requiring systemic corticosteroid therapy: cross-sectional data from the Optimum Patient Care Research Database and the British Thoracic Difficult Asthma Registry. Thorax 2016; 71: 339–346.
    OpenUrlAbstract/FREE Full Text
  15. ↵
    1. Ortega HG,
    2. Liu MC,
    3. Pavord ID, et al.
    Mepolizumab treatment in patients with severe eosinophilic asthma. N Engl J Med 2014; 371: 1198–1207.
    OpenUrlCrossRefPubMed
  16. ↵
    1. Bel EH,
    2. Wenzel SE,
    3. Thompson PJ, et al.
    Oral glucocorticoid-sparing effect of mepolizumab in eosinophilic asthma. N Engl J Med 2014; 371: 1189–1197.
    OpenUrlCrossRefPubMedWeb of Science
  17. ↵
    1. Nair P,
    2. Wenzel S,
    3. Rabe KF, et al.
    Oral glucocorticoid-sparing effect of benralizumab in severe asthma. N Engl J Med 2017; 376: 2448–2458.
    OpenUrl
  18. ↵
    1. Molimard M,
    2. Buhl R,
    3. Niven R, et al.
    Omalizumab reduces oral corticosteroid use in patients with severe allergic asthma: real-life data. Respir Med 2010; 104: 1381–1385.
    OpenUrlCrossRefPubMed
  19. ↵
    Merck Serono GmbH. Zusammenfassung der Merkmale der Arzneimittel – Decortin Tabletten [Summary of Product Characteristics – Decortin Tablets]. 2015.
  20. ↵
    1. Barry LE,
    2. O'Neill C,
    3. Patterson C, et al.
    Age and sex associations with systemic corticosteroid-induced morbidity in asthma. J Allergy Clin Immunol Pract 2018; in press [https://doi.org/10.1016/j.jaip.2018.04.008].
  21. ↵
    1. Barry LE,
    2. Sweeney J,
    3. O'Neill C, et al.
    The cost of systemic corticosteroid-induced morbidity in severe asthma: a health economic analysis. Respir Res 2017; 18: 129.
    OpenUrl
  22. ↵
    1. Lefebvre P,
    2. Duh MS,
    3. Lafeuille MH, et al.
    Burden of systemic glucocorticoid-related complications in severe asthma. Curr Med Res Opin 2017; 33: 57–65.
    OpenUrl
  23. ↵
    1. Dalal AA,
    2. Duh MS,
    3. Gozalo L, et al.
    Dose–response relationship between long-term systemic corticosteroid use and related complications in patients with severe asthma. J Manag Care Spec Pharm 2016; 22: 833–847.
    OpenUrl
  24. ↵
    1. Lefebvre P,
    2. Duh MS,
    3. Lafeuille MH, et al.
    Acute and chronic systemic corticosteroid-related complications in patients with severe asthma. J Allergy Clin Immunol 2015; 136: 1488–1495.
    OpenUrl
  25. ↵
    1. Daugherty J,
    2. Lin X,
    3. Baxter R, et al.
    The impact of long-term systemic glucocorticoid use in severe asthma: a UK retrospective cohort analysis. J Asthma 2018; 55: 651–658.
    OpenUrl
  26. ↵
    1. Zazzali JL,
    2. Broder MS,
    3. Omachi TA, et al.
    Risk of corticosteroid-related adverse events in asthma patients with high oral corticosteroid use. Allergy Asthma Proc 2015; 36: 268–274.
    OpenUrlCrossRefPubMed
  27. ↵
    1. Zeiger RS,
    2. Schatz M,
    3. Li Q, et al.
    Burden of chronic oral corticosteroid use by adults with persistent asthma. J Allergy Clin Immunol Pract 2017; 5: 1050–1060.
    OpenUrl
  28. ↵
    1. O'Neill S,
    2. Sweeney J,
    3. Patterson CC, et al.
    The cost of treating severe refractory asthma in the UK: an economic analysis from the British Thoracic Society Difficult Asthma Registry. Thorax 2015; 70: 376–378.
    OpenUrlAbstract/FREE Full Text
  29. ↵
    1. Curtis JR,
    2. Westfall AO,
    3. Allison J, et al.
    Population-based assessment of adverse events associated with long-term glucocorticoid use. Arthritis Rheum 2006; 55: 420–426.
    OpenUrlCrossRefPubMedWeb of Science
  30. ↵
    1. Walsh LJ,
    2. Wong CA,
    3. Oborne J, et al.
    Adverse effects of oral corticosteroids in relation to dose in patients with lung disease. Thorax 2001; 56: 279–284.
    OpenUrlAbstract/FREE Full Text
  31. ↵
    1. Noonan M,
    2. Chervinsky P,
    3. Busse WW, et al.
    Fluticasone propionate reduces oral prednisone use while it improves asthma control and quality of life. Am J Respir Crit Care Med 1995; 152: 1467–1473.
    OpenUrlPubMedWeb of Science
    1. Fish JE,
    2. Karpel JP,
    3. Craig TJ, et al.
    Inhaled mometasone furoate reduces oral prednisone requirements while improving respiratory function and health-related quality of life in patients with severe persistent asthma. J Allergy Clin Immunol 2000; 106: 852–860.
    OpenUrlCrossRefPubMedWeb of Science
    1. Schmier J,
    2. Leidy NK,
    3. Gower R
    . Reduction in oral corticosteroid use with mometasone furoate dry powder inhaler improves health-related quality of life in patients with severe persistent asthma. J Asthma 2003; 40: 383–393.
    OpenUrlPubMed
    1. Chipps B,
    2. Buhl R,
    3. Beeh KM, et al.
    Improvement in quality of life with omalizumab in patients with severe allergic asthma. Curr Med Res Opin 2006; 22: 2201–2208.
    OpenUrlPubMed
  35. ↵
    1. Siergiejko Z,
    2. Świebocka E,
    3. Smith N, et al.
    Oral corticosteroid sparing with omalizumab in severe allergic (IgE-mediated) asthma patients. Curr Med Res Opin 2011; 27: 2223–2228.
    OpenUrlPubMed
  36. ↵
    1. Hashimoto S,
    2. Brinke AT,
    3. Roldaan AC, et al.
    Internet-based tapering of oral corticosteroids in severe asthma: a pragmatic randomised controlled trial. Thorax 2011; 66: 514–520.
    OpenUrlAbstract/FREE Full Text
  37. ↵
    1. Hyland ME,
    2. Whalley B,
    3. Jones RC, et al.
    A qualitative study of the impact of severe asthma and its treatment showing that treatment burden is neglected in existing asthma assessment scales. Qual Life Res 2015; 24: 631–639.
    OpenUrlPubMed
  38. ↵
    1. Tyree PT,
    2. Lind BK,
    3. Lafferty WE
    . Challenges of using medical insurance claims data for utilization analysis. Am J Med Qual 2006; 21: 269–275.
    OpenUrlCrossRefPubMed
  39. ↵
    1. Su X,
    2. Ren Y,
    3. Li M, et al.
    Prevalence of comorbidities in asthma and nonasthma patients: a meta-analysis. Medicine 2016; 95: e3459.
    OpenUrl
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Consequences of long-term oral corticosteroid therapy and its side-effects in severe asthma in adults: a focused review of the impact data in the literature
Timm Volmer, Timo Effenberger, Christoph Trautner, Roland Buhl
European Respiratory Journal Oct 2018, 52 (4) 1800703; DOI: 10.1183/13993003.00703-2018
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