- Open Access
The use of inhaled corticosteroids in pediatric asthma: update
World Allergy Organization Journal volume 9, Article number: 26 (2016)
Despite the availability of several formulations of inhaled corticosteroids (ICS) and delivery devices for treatment of childhood asthma and despite the development of evidence-based guidelines, childhood asthma control remains suboptimal. Improving uptake of asthma management plans, both by families and practitioners, is needed. Adherence to daily ICS therapy is a key determinant of asthma control and this mandates that asthma education follow a repetitive pattern and involve literal explanation and physical demonstration of the optimal use of inhaler devices. The potential adverse effects of ICS need to be weighed against the benefit of these drugs to control persistent asthma especially that its safety profile is markedly better than oral glucocorticoids. This article reviews the key mechanisms of inhaled corticosteroid action; recommendations on dosage and therapeutic regimens; potential optimization of effectiveness by addressing inhaler technique and adherence to therapy; and updated knowledge on the real magnitude of adverse events.
Despite advances in care, asthma still imposes a significant burden on the pediatric population. Mortality, hospitalization rates, acute exacerbations and symptom control remain sub-optimal. In controlled trials, most patients gain high levels of control but in ‘real-life’ clinical practice, most patients do not . Communication between clinicians and patients is sometimes poor, and it should be noted that in low income countries, an important obstacle to proper asthma management is the cost of medications .
Inhalation therapy is the cornerstone of asthma treatment in the pediatric age group . The concern about adverse effects induced by systemic CS in children has been much reduced, but not eliminated, with the use of the inhalation route . In this document, the current literature concerning strategies to improve outcome from inhaled corticosteroid (ICS) use is reviewed with the goal of highlighting the potentials and pitfalls encountered.
Mechanisms of action of ICS
Inhaled corticosteroids are the most effective drugs used in asthma to suppress airway inflammation. This occurs mainly by down regulation of pro-inflammatory proteins [5, 6]. Also, corticosteroids seem to reverse components of the asthma-induced structural changes (airway remodeling), including the increased vascularity of the bronchial wall .
At a cellular level, ICS reduce the number of inflammatory cells in the airways, including eosinophils, T lymphocytes, mast cells, and dendritic cells. These remarkable effects of corticosteroids are produced by suppressing the production of chemotactic mediators and adhesion molecules and by inhibiting the survival of these inflammatory cells in the airways. Epithelial cells may be a major cellular target for ICS, which are the mainstay of modern asthma management .
The broad anti-inflammatory profile of corticosteroids probably accounts for their marked clinical effectiveness in asthma . More specific treatment options such as single mediator inhibitors have usually been unsuccessful, emphasizing the importance of simultaneously inhibiting many inflammatory targets .
The anti-inflammatory actions of ICS are divided into considerably delayed actions (taking hours or days) through genomic mechanisms required to change the protein expression and rapid actions (within seconds or minutes) probably mediated through membrane-bound glucocorticoids receptor and direct interaction with the airways vasculature by non-genomic mechanisms . (Table 1; Fig 1).
Genomic mechanism of action of inhaled corticosteroids
These are genomic actions mediated by intracellular receptors; glucocorticoid receptors (GRs), which ultimately alter transcription through direct DNA binding or indirectly through transcription factor inactivation .
The lipophilic corticosteroid molecules easily cross the lipid bilayer of the cell membrane to enter into the cell and bind to specific receptors . Glucocorticoid receptor-α binds corticosteroids, whereas glucocorticoid receptor-β is an alternatively spliced form that binds to DNA but is not activated by corticosteroids .
Direct genomic effects
After corticosteroids have bound to GRs, changes in the receptor structure result in dissociation of molecular chaperone proteins, thereby exposing nuclear localization signals on GRs. This results in rapid transport of the activated glucocorticoid receptor-corticosteroid complex into the nucleus, where it binds to DNA at specific sequences in the promoter region of steroid-responsive genes known as glucocorticoid response elements (GRE) . A pair of GRs (GR homodimer) bind to GRE in the promoter region of steroid-responsive genes and this interaction switches on (and sometimes switches off) gene transcription .
The major action of corticosteroids is to switch off multiple activated inflammatory genes that encode for cytokines, chemokines, adhesion molecules inflammatory enzymes and receptors . Repression of genes occurs through reversal of the histone acetylation that switches on inflammatory genes . Activated GRs may bind to cyclic adenosine monophosphate response element–binding protein (CBP) or other co-activators like p300/CBP-activating factor (PCAF) directly to inhibit their histone acetyl transferase (HAT) activity , thus reversing the unwinding of DNA around core histones and thereby repressing inflammatory genes. Reduction of histone acetylation also occurs through the recruitment of histone deacetylase-2 (HDAC2) to the activated inflammatory gene complex by activated glucocorticosteroid receptor, thereby resulting in effective suppression of all activated inflammatory genes within the nucleus .
Corticosteroids may suppress inflammation by increasing the synthesis of anti-inflammatory proteins, such as annexin-1, secretory leukoprotease inhibitor, interleukin-10, and an inhibitor of nuclear factor-kB (IkB-α) (transactivation)  However, this mechanism seems to have a minor role in the suppression of inflammation. For instance, corticosteroids have been reported to repress inflammation efficiently in mice with a defective glucocorticoid receptor, which cannot bind DNA . Also, therapeutic doses of ICS have not been shown to increase annexin-1 concentrations in bronchoalveolar lavage fluid . It has been proposed that transactivation is responsible for some side effects (e.g. diabetes induction, skin atrophy) caused by corticosteroids .
Indirect genomic effects
Corticosteroids have been shown to have post-transcriptional regulatory effect on gene expression through increasing messenger RNA (mRNA) degradation, and thus block the production of several of pro-inflammatory cytokines and other proteins (transrepression) . Corticosteroids reduce the stability of mRNA for some inflammatory genes, such as cyclooxygenase-2, through an inhibitory action on p38 mitogen-activated protein kinase (p38 MAP kinase) . This inhibitory effect is mediated via the induction of a potent endogenous inhibitor of p38 MAP kinase called MAP kinase phosphatase-1 .
GRs probably bind only to coactivators that are activated by pro-inflammatory transcription factors, such as nuclear factor-kB (NF-kB) and activator protein-1 (AP-1). Also, it is likely that several specific coactivators interact with GRs. This might explain why corticosteroids switch off only inflammatory gene and are well tolerated as a therapy .
Non-genomic mechanism of action of inhaled corticosteroids
Non-genomic actions are initiated by specific interactions with membrane-bound or cytoplasmic GRs, or nonspecific interactions with the cell membrane . Membrane-bound GRs are also present in various human cells and peripheral blood mononuclear cells . Also, membrane binding sites for corticosteroids have been demonstrated in smooth muscle cells isolated from human airway blood vessels . Membrane receptor activation has been shown to induce rapid effects on a variety of second messenger systems (Calcium, adenosine 3ʹ, 5ʹ-monophosphate, inositol trisphosphate, protein kinase C) to alter cellular processes .
Corticosteroids may cause rapid effects by changing the physicochemical properties of the cell membrane. The lipophilic corticosteroid molecules intercalate into the phospholipid bilayers of cellular membranes. Corticosteroids acutely inhibit extraneuronal uptake of norepinephrine in the smooth muscle cells isolated from human bronchial arteries  which will probably increase the duration of the norepinephrine/vasoconstrictor signal, and consequently decreases airway blood flow as seen in healthy and asthmatic subjects after inhalation of corticosteroids .
ICS have been shown to acutely suppress airway hyperperfusion associated with asthma. A single dose of inhaled fluticasone propionate has been shown to decrease airway mucosal blood flow in healthy and asthmatic subjects with a maximal effect, 30 min after inhalation, and a return to baseline at 90 min . The blood flow effect increased in a dose-dependent manner up to 880 mg of fluticasone propionate, with a significantly greater effect in asthmatics than in healthy controls. The acute vasoconstrictor action has also been demonstrated after inhalation of beclomethasone dipropionate and budesonide .
Moreover, ICS has been shown to suppress the increased microvascular permeability and plasma leakage into the airway lumen, which adds to the airway obstruction in asthma, as determined by measuring concentrations of high molecular weight proteins (e.g. alpha-2-macroglobulin) in induced sputum [29, 30] and bronchoalveolar lavage fluid [31, 32].
Based on interventional studies, the inhaled daily doses and the length of therapy seem to be the critical determinants of the vascular effects of ICS. Furthermore, the inhibitory effects on the remodeling process seem to occur only with long-term therapy with corticosteroids. Whereas a 6-month treatment with a daily dose of 800 mg beclomethasone dipropionate reduced the number of blood vessels and the vascular area , a 6-week treatment with fluticasone propionate was only effective at a daily inhaled dose of 1000 mg, and not at 200 mg, to reduce significantly the number of blood vessels and the vascular area .
Functional effects of inhaled corticosteroids
ICS prevents the late but not the early allergic response. However, prolonged treatment with ICS is found to be effective in reducing the early response to an allergen challenge in a time-dependent and probably dose-dependent way [35, 36]. Moreover, ICS do not protect against bronchoconstriction when given immediately before exercise . Regular treatment with ICS is effective in reducing bronchial responsiveness to direct and indirect stimuli  and reduces the prevalence and the severity of exercise-induced asthma .
Interaction of inhaled corticosteroids with some asthma medications
Corticosteroids increase the expression of β2-adrenergic receptors in the lung and prevent their down regulation and uncoupling in response to β2-agonists . The corticosteroid-induced decrease in airway blood flow is likely to enhance the action of inhaled bronchodilators by diminishing their clearance from the airway. Since the corticosteroid-induced vasoconstriction peaks rapidly (~30 min after drug inhalation), simultaneous administration of ICS and bronchodilators is likely to be of clinical significance .
β2-agonists enhance the action of corticosteroids, with an increase in nuclear translocation of GRs in vitro  and enhanced suppression of inflammatory genes . Nuclear localization of GRs is also enhanced after treatment of asthmatic patients with a combination inhaler compared with the same dose of inhaled steroid given alone .
Low doses of theophylline significantly increase histone deacetylase (HDAC) activity in bronchial biopsy specimens from asthmatic patients, and the increase in HDAC activity is correlated with the reduction in airway eosinophils. Because corticosteroids also activate HDAC, but via a different mechanism, theophylline should enhance the anti-inflammatory actions of corticosteroids; this enhancement occurs because the HDAC recruited to the inflammatory gene will be more effective at switching off the gene. Indeed, therapeutic concentrations of theophylline markedly potentiate the anti-inflammatory effects of corticosteroids in vitro . This effect may explain why adding a low dose of theophylline is more effective than increasing the dose of ICS in patients whose asthma is not adequately controlled [44, 45].
Inhaled corticosteroid resistance
Relative resistance is seen in patients who require high doses of inhaled and oral steroids (steroid-dependent asthma). Biopsy studies have demonstrated the typical eosinophilic inflammation of asthma in those patients .
Persistent immune activation and airway inflammation, which to varying degrees is resistant to glucocorticoid therapy, appears to define the immunologic abnormality underlying steroid-resistant asthma . Certain cytokines (particularly interleukin-2, interleukin-4, and interleukin-13, which show increased expression in bronchial biopsy samples from patients with steroid-resistant asthma) may induce a reduction in affinity of GRs in inflammatory cells, such as T-lymphocytes, resulting in local resistance to the anti-inflammatory actions of corticosteroids [46, 48]. Moreover, the inhibitory effect of corticosteroids on cytokine release is reduced in peripheral blood mononuclear cells from patients with steroid-resistant and steroid-dependent asthma .
Other mechanisms involved include impaired nuclear localization of GRs in response to a high concentration of corticosteroids and defective acetylation of histone-4, interfering with the anti-inflammatory actions of corticosteroids .
Dosage and therapeutic regimens
Inhaled corticosteroids are the mainstay of pharmacotherapy for asthma control. Multiple national and international guidelines on asthma have been published [2, 3, 51–60] (Table 2), each with varying recommendations and level of detail regarding the use and rationale of ICS. In some, recommendations on the dose of ICS for initiation and step-up therapy are age-group based. What is common to these guidelines are:
The need for step-up therapy based on poor asthma control
Recognition that preschoolers are different from older children in terms of diagnostic and treatment procedures
A recommended step-down interval of three months of good asthma control
The consideration of ICS dose pertaining to growth.
Perhaps the best-known guideline is that of the Global Initiative for Asthma (GINA), which was last updated in April 2015. As one of the most recent and comprehensive guidelines, it details 
The range of low, moderate and high doses of ICS for children aged up to 5 years, 6–11 years, and 12 years or older separately (Table 3)
Of all the guidelines, only that of the SIGN  mentions a recommended ICS dosing frequency of twice-daily rather than once-daily, for reasons of superior efficacy. The other guidelines make no recommendations regarding dosing frequency.
In general, the consensus is the need to establish the diagnosis of asthma. In cases where this is unclear (such as in preschool children) and other known causes such as chronic infection, a therapeutic 2–3 month-long trial of low-dose ICS appropriate to age and formulation type can be initiated to assess the response of symptoms to this treatment.
Low-dose daily ICS is the first-line controller therapy for mild persistent asthma. None of the guidelines espouse intermittent ICS as an option; this is borne out by a recent meta-analysis  in children aged 1 year and older with suspected persistent asthma. The authors found similar rates in use of rescue oral corticosteroids; however, daily ICS was superior to intermittent ICS in several parameters of lung function, airway inflammation, asthma control, and reliever use.
The TREXA trial  demonstrated both the superiority of daily ICS over intermittent ICS. Of note was the suggestion that intermittent ICS was superior to no ICS in children with asthma that had been controlled through recent ICS use, though this second finding did not reach statistical significance (hazard ratio 0.62, 95 % CI 0.37–1.05, p = 0.073). These results arose from the 4-week run in period to establish asthma control before the participants were randomized to the 4 arms that led to the abovementioned results.
Recent guidelines advocate that when low-dose daily ICS is insufficient, increasing the dose of ICS is the preferred step-up therapy compared to add-on therapy with other agents in children less than 12 years of age. Where the child is 12 years and older, addition of a long-acting beta-agonist (LABA) to the existing ICS dose is preferred.
Small-particle ICS in children
Amirav et al  has described the differences in the airways and air flow between infants, older children, and adults. The importance of mass median aerodynamic diameter of delivered aerosol particles to children – specifically, small particles may improve lung deposition and thus, efficacy – was described theoretically as well as summarized from existing in-vitro and in-vivo studies. The limitation of these studies was the absence of an in-vivo, comparative study on the efficacy of small-particle ICS on asthma control. van Aalderen et al  recently demonstrated better asthma control and lower severe exacerbation rates in a matched retrospective cohort analyses of children aged 5–11 years, when using small-particle beclomethasone dipropionate hydrofluoroalkane compared to fluticasone propionate, in both initiation as well as step-up therapy. When a higher dose of small-particle beclomethasone was compared to addition of LABA as step-up therapy for asthma control, outcomes were generally similar, though the use of short-acting beta-agonists (SABA) was lower in the small-particle beclomethasone group. Among the limitations of this study was the lack of information on side effects, such as growth, which would be a potential concern in the cohort using higher doses of ICS.
Role of long acting ẞ2 agonists and leukotriene receptor antagonists in initiation of controller therapy
In a meta-analysis that compared initiation of LABA/ICS, versus ICS of the same dose in steroid-naïve adults and children aged 6 years and above for asthma control, the LABA/ICS group had slight reduction in symptoms and rescue β2-agonist use but there was no difference to exacerbations requiring oral corticosteroids or rate of hospital admissions .
Various clinical trials [66–71] have demonstrated that ICS is superior to LTRA as monotherapy for asthma control; most of these studies were in children aged 6 years and older, with the exception of Szefler et al.  who demonstrated the superiority of ICS over LTRA in children aged 2–8 years. In contrast, in a large retrospective cohort study in children aged 4–17 years, LTRA appeared to be as effective as ICS upon initiation for asthma control. The authors acknowledged that this result could have been confounded by the ICS group having had more severe asthma at baseline .
The use of Budesonide/Formoterol as a single-inhaler therapy (SiT; also known as Symbicort Maintenance and Reliever Therapy SMART) for asthma control as well as as-needed relief is licensed and has been advocated in patients 12 years and above. A Cochrane meta-analysis  concluded that SiT was superior to fixed-dose combination inhalers in terms of reducing the number of exacerbations requiring oral steroids, hospitalizations and emergency room visits, whilst using a lower mean daily dose of ICS. In terms of reducing exacerbations, SiT proved superior to the other treatment groups: fixed-dose budesonide/formoterol with as-needed terbutaline, and four-times-as-high daily ICS dose (320micrograms of budesonide) with as-needed terbutaline. In addition, growth was superior in the SiT group compared to the higher-dose budesonide group [73, 74].
In summary, for initiation, ICS is preferable to LTRA as monotherapy, with no significant difference between LABA/ICS versus ICS of the same dose. Among the options for LABA/ICS, SiT seems promising, but more studies need to be conducted in children less than 12 years of age.
Step-up controller therapy
In a meta-analysis that compared the addition of LABA to ICS versus ICS of the same dose in adults and children aged 4 years and above with persistent asthma, revealed that LABA/ICS was superior to same-dose ICS alone in markers of lung function. For the whole group, LABA/ICS was also superior to a higher ICS dose in terms of peak expiratory flow and growth rate. However, in children aged 4–18 years (mean 10 years), there was a higher risk of hospitalization and of exacerbations requiring oral steroids in the LABA/ICS compared to higher ICS dose, but this did not reach statistical significance; the authors urged that further studies in this area are needed . A more recent clinical trial showed no difference between salmeterol-fluticasone compared to a double dose of fluticasone in children aged 6–16 years with symptomatic asthma despite the double-dose group receiving 200 micrograms twice daily of fluticasone propionate .
Another meta-analysis that compared addition of LTRA to ICS, compared to ICS of the same or higher dose, was limited by the few trials available, with data available only in children aged 6 years and above . Three trials compared LTRA + ICS to ICS of the same dose, with no significant clinical benefit of the addition of LTRA. Only one triple-crossover trial in children aged 6–17 years compared LTRA + ICS to a higher dose of ICS, again with no difference in hospitalizations or need for oral steroids observed between the two groups. Most significant in that same study was the finding that LABA + ICS was superior to LTRA + ICS; the authors used a composite endpoint comprising less need for oral prednisone, better asthma control or superior FEV1 but did not show the breakdown of results for each separate endpoint. This study also highlighted the importance of follow-up and customizing pharmacotherapy, as there may be a differential response in children to different options of step-up therapy .
A third meta-analysis that compared LABA to LTRA as adjunctive therapy supports the use of LABA/ICS over LTRA as an adjunct, as evidenced by reduction of exacerbations requiring oral corticosteroids, rescue therapy use, and symptoms; and superior lung function and quality of life. However, most of the trials included were in adults and adolescents; there was a lack of data in children aged 5 years and below .
In summary, LABA/ICS appears superior to ICS or LTRA as step-up therapy. However, this requires further study, especially in preschoolers.
Role of ICS in acute asthma exacerbations
The GINA  and Canadian [52, 53] guidelines discuss the benefit of ICS during an acute asthma exacerbation. Current evidence in children does not support dose escalation of ICS in patient self-management of an acute asthma exacerbation. Studies in adults had suggested early dose escalation of existing ICS to double, or even four to five times the original, may be of benefit during an asthma exacerbation [80, 81], but did not significantly reduce the need for oral corticosteroids . Studies in children did not demonstrate any reduction in hospitalization or use of oral corticosteroids, though there was suggestion of symptomatic improvement with higher doses of ICS [83–86]. A recent Cochrane review  did not find a significant reduction in the need for oral corticosteroids in older school-aged children, which were drawn from the TREXA study;  intermittent ICS did show symptomatic improvement and lower likelihood of requiring oral corticosteroids in preschoolers, but the authors acknowledged that this was a distinct group that might not necessarily have long-term asthma. Given the lack of safety information of very high doses of ICS in children, especially if administered frequently, we do not recommend that children be given high doses of ICS to try to mitigate an acute asthma exacerbation.
The role for ICS in the setting of asthma exacerbations presenting to the emergency department, is more promising. Edmonds et al  that showed that ICS reduced hospitalizations in acute asthma where patients did not receive systemic steroids. The addition of ICS to standard asthma treatment that included systemic corticosteroids, also helped prevent hospitalizations. There were no significant adverse effects from the use of ICS in this situation. However, there was wide variation in the type and doses of ICS used, with the most frequent ICS used being Budesonide at a median dose of 900 micrograms each, and a median cumulative dose of 2000 micrograms over up to 6 h. Two, more recent meta-analyses that compared ICS to systemic corticosteroids in the emergency department for children presenting with acute asthma exacerbations, found no difference between ICS and systemic corticosteroids in hospitalization rates [89, 90]. Beckhaus et al  also found no difference between ICS and systemic corticosteroids in the outcomes of unscheduled visits for asthma symptoms (relative risk 9.55; 95 % CI: 0.53–170.52), or need for additional courses of systemic corticosteroids (relative risk 1.45; 95 % CI: 0.28–7.62). However, there was significant heterogeneity between the primary studies including route, type and dose of ICS; and these additional results had extremely wide confidence intervals.
In conclusion, there is insufficient evidence to recommend that ICS can replace systemic corticosteroids in the emergency department attendance for a child with an acute asthma exacerbation.
Future needs in research
Small-particle ICS and SiT represent two promising approaches that warrant further study. Small-particle ICS appears superior to LABA/ICS in both initiation and step-up therapy, but this inference is restricted to a single retrospective cohort analysis, and a single comparator (fluticasone propionate); prospective randomized controlled studies are required. SiT may be ideal when considering LABA/ICS, both in terms of evidence as well as convenience, but it is licensed and studied mainly in children 12 years and older; promising results in younger children should be substantiated with further study.
Methods of ICS delivery
Inhaled medications are only effective if they are used properly. The correct use of an inhaler device delivers the medication right to the lungs insuring a better response. The proper inhalation technique is not followed by most of asthma individuals. By training and practice, one can learn and adhere to proper inhalation techniques and practice.
Choosing the appropriate device
Currently available devices for delivering inhaled medications include jet nebulizers, ultrasonic nebulizers, metered dose inhalers (MDIs) with and without a spacer device, and dry powder inhalers (DPIs). An important factor is the cooperation between the child and caregiver. Jet nebulizers may be more easy to use in infants and toddlers as they need no active cooperation. With the improvement of cooperation throughout childhood, MDIs with holding chambers and masks should be used. Finally, MDIs with holding chambers or DPIs can be used in fully cooperative older children and adolescents.
To date, there is no ideal device for delivering inhaled medications. Characteristics for the perfect device include reproducible dose delivery to the lungs across a wide range of inspiratory flows; this is important due to the uneven inspiratory rate by children. The optimum size of the particles (2–5 microns) is necessary to optimize drug delivery. Particles larger than 10 microns deposit in the oropharynx, particles 5–10 microns deposit in the trachea and large bronchi, and particles less than one micron are exhaled. Other desirable characteristics include ease of use, portability, and the availability of dose counters. There is capacity of dispensing single dose by DPIs, but multiple dose capacity devices are also used [54, 59].
Infants and young children (below 5 years of age) represent a unique subpopulation with significant difficulties and challenges for aerosol delivery due to peculiar anatomic, physiological, and emotional factors. Infants are obligate nose breathers and this may lead to less effective lung deposition of aerosols and particles. They also fail to hold their breath leading to exhalation of a great proportion of the inhaled medication. Crying is another important factor that may cause deposition of the drug in the upper respiratory tract and affect the seal between the mask and face . Even a 1-cm gap between the mask and the face may reduce the dose delivered to the respiratory tract by 50 %  It was suggested that large-particle corticosteroid aerosols are not likely to be effective in infants and young children  and that small particles may offer better lung deposition [63, 64].
Data comparing different inhalation devices
A systematic review was conducted to determine the clinical effectiveness of pressurized MDIs with or without spacer compared with other hand held inhaler devices for the delivery of corticosteroids in stable asthma. Twenty four randomized controlled trials were included. There was no evidence pertaining to the effectiveness of alternative inhaler devices (DPIs, breath actuated pressurized MDIs, or hydrofluoroalkane pressurized MDIs) when compared to the pressurized MDIs for delivery of inhaled corticosteroids. Hence, in the first line delivery devices pressurized MDIs remain the most cost effective . A Cochrane systematic review assessed the efficacy and safety of inhaled corticosteroids delivered via nebulizer versus holding chamber for the treatment of chronic asthma. The only double-blinded study included revealed that high dose of budesonide delivered by the particular nebulizer was more effective than budesonide 1600 ug delivered via a large volume spacer .
There was equal efficacy, acceptable safety and tolerability profile when beclomethasone dipropionate (BDP) suspension for nebulization 3000–4000 μg day-1 given via a nebulizer was compared with BDP spray 1500–2000 μg day-1 given via a metered dose inhaler in steroid-dependent adult patients with moderate to severe asthma . The results from another study attested to the efficiency of jet-nebulized budesonide suspension and indicated that nebulized budesonide is equipotent to standard budesonide therapy delivered by pressurized metered dose inhaler, provided nebulization is synchronized with inspiration and no loss of aerosol occurs during expiration . On the other hand, a randomized placebo-controlled study compared the relative lung delivery of fluticasone propionate (FP), using adrenal suppression as a surrogate for the respirable dose, when administered via large volume spacer or nebulizer in healthy adults. The spacer produced about a sevenfold higher relative lung dose than the nebulizer. The authors suggested that very little of the labeled nebulized dose is actually respirable . In a double-blind cross-over study, 40 children with childhood asthma were randomized to receive 400 micrograms BDP as aerosol or powder. The peak flow performance in the morning was more benefited in the aerosol group with severe asthma. However there was no difference in evening peak flow and symptom scores .
In the short-term treatment of mild to moderate asthma in children, BDP delivered by Clickhaler was a well-tolerated and therapeutically equivalent alternative to BDP delivered by a conventional MDI plus spacer . A randomized cross over study showed that in 3- to 4-year-old children, budesonide dose delivery was higher and/or more consistent from the pMDI Nebuhaler than from the Turbuhaler . One hundred thirty seven patients received FP 250 μg twice daily from a Diskus inhaler and 140 received budesonide 600 μg twice daily from a Turbuhaler inhaler for 4 weeks. The Diskus inhaler was generally rated more highly by patients than the Turbuhaler .
The electrostatic and non electrostatic properties of metal inhalers also regulate the amount of inhalation. There is greater delivery of aerosol to the mouth by the metal valved holding chamber (VHC) having non electrostatic properties compared to the plastic polypropylene VHC. In young children, when budesonide was used (400 ug/day) under real life conditions, the metal VHC was not associated with greater hypothalamus pituitary axis (HPA) suppression . The metal VHC was not more effective than the Aero Chamber despite a greater total dose delivered to the mouth .
The type of spacer did not influence the state of asthma control in 141 patients 5–57 months old but the parents’ preference made a difference in choice . There was improved perception by parents of their children’s asthma control by better Pediatric Asthma Caregiver’s Quality of Life (PACQLQ) scores when the valved holding chamber has been enhanced to include a Flow-Vu inspiratory flow indicator that provides visual inhalation feedback during use although there was no actual change in asthma control . A recent trial demonstrated that Salmeterol/fluticasone combination given through the breath actuated inhaler (BAI) produces comparable efficacy and safety endpoints as metered dose inhaler. Additionally, BAI was more preferred by patients compared to conventional MDI . This shows that there is individual preference in choosing the inhaler device that could be an influential factor in decision making by the health care professional.
In summary, age and cooperation between the child and caregiver are important determinants of effective inhalation therapy. Other important factors include the particle size, device portability, and the availability of dose counters. Due to the relatively flat dose–response relationship in asthma, significant benefit in terms of symptom and lung function improvement is usually seen at low to moderate doses of different ICS.
Adverse effects of ICS
Adverse effects resulting from the use of ICS are often underestimated in daily clinical practice. Although ICS treatment is generally considered safe in children, the potential adverse effects related to its regular use have been and continue to be a matter of concern. ICS are reported to cause some local and systemic adverse effects  (Table 6). This seems to be dose-dependent being most common in individuals receiving high dose ICS with or without oral corticosteroids (OCS).
Local adverse effects
Relatively few studies sought to evaluate local side effects of ICS as they are generally viewed as minor complications of therapy. Nevertheless, approximately 5–10 % of subjects treated with ICSs report adverse effects in the oral cavity. The local effects can be clinically significant, affect patient quality of life, and hinder compliance with therapy [108–110]. Local deposition of glucocorticoids is, thus, an important risk factor for oropharyngeal candidiasis [111, 112].
A meta-analysis revealed that the ICS MDI device was associated with a 5-fold greater risk of oral candidiasis versus MDI placebo (OR, 5.40). In contrast, the ICS DPI device had a 3-fold greater risk for oral candidiasis versus DPI placebo (OR, 3.24). A similar trend was observed with regard to dysphonia. Both ICS MDI and DPI were associated with an approximately 2-fold greater risk of pharyngitis compared with placebo .
Oropharyngeal candidiasis clinically presents as white soft plaques that leave a painful erythematous, eroded, or ulcerated surface. Common sites are the buccal mucosa, oropharynx, and lateral aspects of tongue. Patients may complain of tenderness, burning, and dysphagia once the pseudo-membrane gets disrupted [112, 114]. The mechanism of oral candidiasis induced by ICS remains obscure. Predictive factors identified by multivariate logistic regression were higher daily dose of ICS and concomitant use of OCS .
Inhaled fluticasone use and dysphonia were reported in association with posterior pharyngeal candidiasis at bronchoscopy even in the absence of clinically overt oral involvement . Isolated Candida was significantly greater in patients with oral symptoms than asymptomatic patients .
Esophageal candidiasis was reported with the use of dry powder budesonide which might have favored esophageal drug deposition . This occurred in an 18-month old girl who received ICS therapy for bronchial asthma who presented with coffee-ground emesis and melena. The diagnosis was based on the presence of pseudohyphae in endoscopic biopsy and the identification of candida species by culture . The prevalence of esophageal candidiasis was 37 % among a group of Japanese patients treated with inhaled fluticasone propionate, compared to 0.3 % of the control patients. A reduction in the daily dose eliminated the infection . Nevertheless; another investigation revealed that subclinical esophageal and oropharyngeal Candida colonization was statistically comparable between asthma patients on ICS and steroid naive asthmatic controls suggesting that the risk of esophageal candidiasis due to ICS is low .
Rachelefsky et al.  analyzed data from 23 studies published from 1966 through 2004 and noted that ICS at all dosages was associated with a 5.2-fold greater risk of dysphonia as compared with placebo. Causes of dysphonia associated with ICS therapy have been poorly investigated, and the origins of dysphonia may have multiple confounding factors. It may likely result from deposition of active ICS in the oropharynx during inhalation resulting in chemical inflammation [122, 123]. Candidiasis of the larynx was infrequently observed in patients with voice complaints after ICS therapy .
Using the lowest effective dosage of ICS and administering it with a spacer may decrease oropharyngeal deposition of inhaled aerosols. After using a spacer, it must be washed with tap water and allowed to air dry. Patients should be instructed to rinse the mouth, gargle, and wash the face after inhalation . Switching to another ICS was also suggested .
Other local complications
Xerostomia may associate inhalation therapy and is clinically presented as oral fissuring, ulceration, and epithelial atrophy. As a consequence of diminished salivary flow, food retention and an acidic environment is encouraged. This in turn encourages the growth of aciduric bacteria and dental caries . Caries was detected in mixed or permanent dentition of children receiving various forms of inhalation therapy [125, 126]. However, the causal relationship to ICS in particular and long-term effects have yet to be established.
Inhaled drugs in general can also alter the taste perception due to interaction of drug metabolite and saliva, or secondary to xerostomia and/or candidiasis . Halitosis and gingivitis could also happen due to oral infections and xerostomia [127, 128]. Mouth breathing habit in these patients further increases gingivitis due to dehydration of the alveolar mucosa .
Immediate mouth washing after inhalation was found to be most useful for prevention of oral complications and the amount of drugs removed by mouth washing is significantly associated with the time lag between inhalation and mouth washing .
Systemic adverse effects
Asthma as a chronic disease by itself has growth-suppressing effects probably due to growth-suppressing influence of endogenous cytokines and glucocorticoids produced in response to illness and inflammation and this can confound studies of the effect of ICS on growth. Any resulting delay in the growth process is associated with delays in pubertal development and pronounced growth deceleration in late childhood . Normal childhood growth can be divided conceptually into three phases according to primary growth-supporting factors: nutrition-dependent growth of infancy, growth hormone (GH)-dependent childhood growth, and sex steroid/GH stimulation of pubertal growth. Susceptibility to glucocorticoid-induced growth suppression appears to increase during periods of transition from one phase to another, particularly in the immediate prepubertal years . The effect of ICS on growth velocity and final adult height has been a subject of debate.
Table 7 displays some studies that sought to investigate this adverse effect [132–141]. Growth suppression was considered both a sensitive and relatively specific indicator of systemic corticosteroid effect. Regular use of ICS at low or medium daily doses was associated with a mean reduction of 0.48 cm/year in linear growth velocity and a 0.61-cm change from baseline in height during a one-year treatment period in children with mild to moderate persistent asthma . An evidence-based analysis revealed that there is ICS dose-dependent reduction in growth velocity in prepubescent school-aged children with mild to moderate persistent asthma whatever the ICS molecule (mometasone, ciclesonide or fluticasone) consumed . Flunisolide hydrofluoroalkane has not been associated with reduced growth velocity in a 12 month study . In a randomized controlled trial on 4–9 year old children, one year of treatment with a daily dose of 200 μg of mometasone furoate DPI in the morning resulted in some changes in growth velocity when compared with placebo .
The effect of childhood ICS use on final adult height is conflicting . The Childhood Asthma Management Program (CAMP) trial is the only prospective study that was started at childhood and followed the subjects to adulthood. Although the attained height was not a primary objective of this trial, the height was monitored regularly, frequently, and precisely with a stadiometer . A larger daily dose of inhaled glucocorticoid in the first 2 years was associated with a lower adult height (−0.1 cm for each microgram per kilogram of body weight; p = 0.007) . Loke et al.  recently noted a slight reduction of about one cm in final adult height which when interpreted in the context of average adult height in England represented a 0.7 % reduction compared to non-ICS users.
In spite of these measurable effects of ICS on the linear growth, it is important to recall that the safety profile of all ICS preparations, which focus anti-inflammatory effects on the lung, is markedly better than the oral glucocorticoids . Published data support growth retardation, not suppression, in adult heights of children who were treated with ICSs; however, the effect is sustained and not cumulative . Furthermore, it is unknown if the reductions in growth represent a permanent effect or a temporary 1- to 2-year slowing in growth velocity. ICS induced growth suppression seems to be maximal during the first year of therapy and less pronounced in subsequent years of treatment. However, physicians prescribing ICS to children should be aware of this possibility and carefully monitor linear growth . Additional studies are needed to better characterize the ICS molecule dependency of growth suppression, particularly with newer molecules (mometasone, ciclesonide).
Adrenal suppression (AS) due to exposure of the HPA axis to exogenous glucocorticoids is the most common cause of secondary adrenal insufficiency (AI). This is a well-recognized complication of most forms of steroid therapy (e.g., oral, inhaled, parenteral, or intranasal) . ICS at high doses and long duration appear to be a significant independent risk factor for AI [149, 150]. Also, changing the type of ICS or reducing the dose could potentially trigger AI [151–153]. Adrenal insufficiency may cause a spectrum of presentations varying from vague symptoms of fatigue to potentially life threatening acute adrenal crises . Characteristic hyperpigmentation of the skin and orthostatic hypotension usually do not occur in secondary AI .
HPA deficiency and AS have been considered rare in children receiving low or medium dose ICS for a short period of time . Schwartz et al. , noted that 14 children out of 93 cases of symptomatic AI that were reported in PubMed were in fact using a moderate dose of 500 mcg or less/day of fluticasone propionate. They, therefore, recommended that pre-adolescent children who are receiving 400 mcg or more of fluticasone propionate or equivalent per day should be quarterly tested for HPA axis suppression. A Cohort study by Smith et al.  determined the prevalence of HPA axis suppression to be 9.3 % of 214 children using ICS. They concluded that children on low to moderate doses of ICS were still at risk of HPA axis suppression.
Screening for adrenal suppression was recommended in children taking high dose ICS (≥500 μg/day of fluticasone propionate or equivalent; ≥400 μg/day under age 12) for more than 6 months as well as considering screening in those on medium dose (251–500 μg/day of FP or equivalent; 201–400 μg/day under age 12) when there is concomitant use of nasal and topical corticosteroids, recent or frequent short courses OCS, high level of adherence to therapy, or smaller body mass for age . Other indications for screening may include patients with symptoms suggestive of AS regardless of ICS dose, concomitant use of drugs that increases the bioavailability of ICS such as ritonavir or ketoconazole, recurrent respiratory infections with slow recovery, any planned surgical procedure, unexplained hypoglycemia, gastroenteritis, chronic nausea and vomiting, dehydration, heat stress, or any condition where AI might result in acute adrenal crisis .
Morning serum cortisol level can be used as a screening tool and abnormal results should be confirmed with low-dose ACTH stimulation tests . Scalp hair cortisol was suggested as a non-invasive biomarker of HPA suppression and a sensitive tool for monitoring adherence to ICS. Its median level was found lower in 10 asthmatic children treated with ICS as compared to a healthy control group . Again, hair cortisol levels of 18 asthmatic children were two fold lower compared with the period of no ICS use . Salivary cortisol is increasingly used to assess patients with suspected hypo- and hypercortisolism. Measurement of salivary cortisol and cortisone responses offers an alternative to those of serum cortisol during a synacthen test in the investigation of adrenal hypofunction due to the ease of collection and independence of binding proteins allowing for determination of the free hormone [159–161].
In case of AI, oral physiologic corticosteroid replacement therapy should be prescribed and written instructions for stress corticosteroid dosing should be provided until the adrenal suppression resolves. The use of a medical identification tag is also advisable .
Effect on bone mineral accretion
Corticosteroids have adverse effects on function and survival of osteoblasts and osteocytes, and with the prolongation of osteoclast survival, induce metabolic bone disease . Overall, existing data suggest that the relationship between ICS use and bone mineral density (BMD) in children is conflicting and confounded by numerous other variables . The conflict is probably due to various study designs, duration of use, outcome measures, and population demographics of research trials .
There is some concern that prolonged treatment with high doses of ICS reduces bone mass in prepubertal asthmatic children [166–168]. In children aged 4 to 17 years, the relative risk for a non-vertebral fracture appeared to increase with larger daily doses of ICS, with a relative risk of 1.1 for an average beclomethasone dose of less than 200 μg/day, 1.2 for doses of 201–400 μg/day, and 1.3 for doses greater than 400 μg/day. However, the excess risk disappeared after adjusting for markers of asthma severity, suggesting that the observed effect might result partially from the respiratory disease rather than ICS use alone . The CAMP study group reported that no significant differences in BMD were noted between budesonide, nedocromil or placebo therapy . In a follow up study for a median of 7 years of children with mild to moderate asthma initially randomized into the CAMP trial, cumulative ICS use was associated with a small decrease in bone mineral accretion in males not females, but with no increased risk of osteopenia. The authors concluded that this effect on BMD is outweighed by the ability to reduce the amount of OCS used .
Another study of asthmatic children receiving long-term, high-dose fluticasone propionate (average 771.2 μg/d) showed no significant changes in bone metabolism or BMD compared with control subjects . A similar conclusion was observed by Gregson et al.  in children with moderate-to-severe asthma treated with fluticasone propionate (200 μg/d) or beclomethasone dipropionate (400 μg/d) for 82 weeks. Some drugs may potentiate the effect of ICS on bone including the highly active anti-retroviral drug ritonavir  and the antifungal drug ketoconazole  due to the potential for increasing the serum levels of ICS.
Corticosteroid use and worsening airflow limitation are associated with lower Vitamin D serum levels in asthmatic patients. Vitamin D supplementation might potentiate anti-inflammatory function of corticosteroids in asthmatic patients and thereby improve asthma control . A significant inverse association was reported between vitamin D levels and the use of ICS in some populations .
The risk of osteopenia and osteoporosis seems negligible in patients receiving low to moderate dose ICS treatment, especially in the absence of co-existent conditions that affect bone mineral accretion. Those receiving high dose ICS with intermittent systemic steroids such as patients with poorly controlled asthma are particularly vulnerable to developing ICS induced bone disease [163, 165]. Impairment of BMD as a result of HPA-axis suppression from long-term high-dose ICS use also requires further study . Nutritional supplementation (e.g. calcium and vitamin D) should blunt the effects of ICS on bone mineral density. Also, ICS therapy should always aim to reach the lowest effective dose that gives asthma control .
Effect on immunity
Several studies assessed the effects of high dose ICS on cell mediated immunity by using delayed type hypersensitivity skin testing as the measure of impaired cellular immunity and did not find any impairment compared with asthmatics on medications other than ICS  or healthy subjects . The prolonged use of low dose ICS in asthmatic children has not been shown to affect cell mediated immunity either . On the other hand, some recent studies have reported the association between ICS therapy and increased risk of pneumonia in adult COPD patients [180, 181]. Also, some case reports have suggested that ICS may aggravate tuberculosis (TB)  A nested case–control study from Korea concluded that ICS use increases the risk of TB and that clinicians should be aware of the possibility of TB development among patients who are long-term high-dose ICS users .
It was suggested that combinations of drugs commonly used in asthma therapy inhibit both early pro-inflammatory cytokines and key aspects of the type I interferon pathway and may curtail excessive inflammation induced by rhinovirus infections in patients with asthma, but whether this inhibits viral clearance in vivo remains to be determined . ICS therapy was also found to inhibit T-helper 17 mediated immunity which may be involved in the airway inflammation of allergic asthma in children .
Disseminated varicella infection and increased risk of herpes zoster were associated with asthma and systemic corticosteroid therapy in children [186, 187]. However, a retrospective cohort study revealed that varicella vaccine failure and hence chicken pox outbreaks was not associated with asthma or the use of inhaled steroids, but with the use of oral steroids .
As with oral corticosteroids, ICS have been associated with an increased risk of developing diabetes and also worsening glycemic control in patients with known diabetes [189, 190]. A large Canadian study looking at a cohort of adult patients with chronic obstructive pulmonary disease (COPD) treated with ICS found an increased risk of development and progression of diabetes, especially at high doses . However, a small prospective double-blind randomized controlled trial (n = 12) found no difference in HbA1c values in patients with known asthma or COPD and diabetes on inhaled steroids at six weeks . In children, a cross sectional study revealed a statistically significant elevation of the mean HbA1c value (5.44 ± 0.75 %) among non-diabetic children with asthma as compared to the healthy control group (5.14 ± 0.41 %). However, HbA1c levels did not correlate with the cumulative dose of ICS or time of usage .
Despite the paucity of studies in the pediatric age group, data extrapolated from adult studies would indicate blood glucose monitoring in diabetic children on ICS therapy. Longitudinal well controlled studies are warranted in this domain.
Other potential adverse effects of ICS
Ocular complications of glucocorticoids have been a subject of concern. Although the use of systemic corticosteroids poses an increased risk for cataract, it has been difficult to establish a similar link to ICS therapy . Some studies on the effect of ICS on the eyes did not exclude subjects who had been exposed to oral corticosteroids thus confounding their results . The risk of subcapsular and nuclear cataract development related to ICS use seems minimal in asthmatic children, although it may be greater in older patients. The CAMP research group studied the development of posterior subcapsular cataracts associated with long-term budesonide, and only 1 child developed evidence of cataract at the end of the 6-year study period . Studies on the association of glaucoma to ICS therapy showed no evidence of a direct link or increased risk of elevation of intraocular pressure in patients after the initiation of ICS therapy. However, monitoring of ocular pressure may be necessary in patients on prolonged ICS therapy especially the elderly .
Oral as well as inhaled steroids cause a reduction in collagen synthesis by the skin . Thinning of the dermis and increased bruising/purpura have been noted in patients on high dose ICS but this adverse effect is more common in adults [194, 195]. One case report suggested a link between ICS and acne but no subsequent studies have analyzed this association . Hypertrichosis was reported in association with ICS therapy in children. The time between the start of ICS and the occurrence of hypertrichosis varied between one month and three years . Also, hair depigmentation was reported in an Afro-Caribbean girl. The hypothetical explanation may comprise direct cytotoxic effect, changes in ground substance, vasoconstriction, mechanical effects of edema, or a dysregulation of melanogenesis .
It has been difficult to confirm that ICS use is associated with an increased psychiatric morbidity . A study conducted in the Netherlands reported alterations in behavior in the pediatric population . Another study in an adult population suggested that high dose ICS is negatively associated with mental well being. However, it was difficult to confirm its relation to ICS rather than asthma severity . Data from the CAMP study, showed was greater improvement in the total score on the Children’s Depression Inventory in the budesonide group as compared with the placebo group (a decline of 3.2 vs. 2.2, P = 0.01) indicating less depression .
An increased frequency of teeth malocclusion and an open bite in children using ICS has been reported . A slight increase in the risk for gastrointestinal ulceration, gastritis and bleeding in patients taking ICS was also reported. This was reduced on using a spacer .
The ideal inhaled corticosteroid should combine high local activity with minimal systemic adverse events. The therapeutic index of corticosteroids has been improved by inhalation devices and techniques that permit direct delivery of lower doses of steroids, thus reducing systemic exposure. Despite these advances, adverse systemic effects still exist and should be looked for .
Adherence to ICS therapy
Adherence to daily inhaled corticosteroid therapy is a key determinant of asthma control. Achieving good adherence is a complex task, and may require interventions not covered in current guidelines. Poor adherence may persist in children despite a high level of concordance between medical team and parents, even in the absence of socio-economic barriers to good adherence . The cost impact of achieving various levels of increase in ICS adherence levels among school aged asthmatic children (5–12 years) was recently evaluated. It was concluded that effective large-scale interventions can produce substantial cost savings from even modest increases in real-world adherence to ICS therapy among Medicaid enrolled children with asthma .
Factors affecting adherence to ICS therapy
There are two forms of non-adherence; intentional and unintentional. Intentional non-adherence involves choosing not to take the medication based on the patient’s own needs, knowledge, or perception. Unintentional non-adherence can result from the complexity of the treatment regimen or understanding of the medication . Intentional barriers to adherence are common; driven by illness perceptions and medication beliefs, patients and parents deliberately choose not to follow the doctor’s recommendations. Common non-intentional barriers are related to family routines, child-raising issues, and to social issues such as poverty .
Potential factors associated with low adherence to daily ICS within a sample of minority adolescents with persistent asthma were older age and low knowledge of ICS after adjusting for other baseline characteristics. There was an inverse relationship between age and adherence . With increase in age, medication taking responsibility transfers from the parent or guardian to the adolescent . Moreover, complacency with outcomes uncertainty and drive for immediate gratification over delayed benefits may contribute to non-adherence in adolescents .
Beliefs play a crucial role in medication adherence. Two specific medication beliefs can be distinguished namely necessities and concerns. Patients can have specific thoughts related to the necessity of their medication in maintaining their health. On the other hand, patients can also have specific concerns about the possible harmful long-term effects and dependence on their medication . Necessities were positively related to self-reported adherence in a group of asthmatics from the Netherlands suggesting that it could be more important to focus on necessities than on concerns in an attempt to improve adherence .
Taxonomy of barriers and facilitators to long-term ICS therapy adherence was proposed. These were classified into three loci of responsibility and its corresponding domains: (1) patient (cognition; motivation, attitudes and preferences; practical implementation; and parental support); (2) patient-physician interaction (communication and patient-physician relationship); and (3) health care system (resources and services). The quality of interaction with the physician (e.g., shared decision making) and access to key health care resources (e.g., lung function testing) and services (e.g., drug insurance) appear to play crucial roles in enhancing or impeding patients’ adherence, and importantly, to modify patients’ cognition, motivation, attitudes, and behaviors .
In a UK-wide, cross-sectional study, unexpectedly large proportion of people with asthma experienced side effects and had strong concerns about their treatment, which impeded their adherence. There was a disparity between clinicians’ estimates of the frequency of side effects and the frequency reported by asthmatics. For instance, although 46 % of people taking ICS reported sore throat, clinicians estimated that this figure would be 10 % .
The level of caregiver supervision is an important factor affecting adherence to ICS therapy in children with asthma. Maternal educational status was found to affect proper ICS use and adherence in asthmatic children .
Monitoring of adherence
Appropriate assessment of adherence should be done in patients with difficult-to-control asthma, before making decision about increasing the treatment including possible prescription of an expensive biological therapy [218, 219].
Self-monitoring at home (e.g. symptoms, peak expiratory flowmetry), as part of a personal management plan is encouraged. Objective measures of adherence are indeed more informative than self reporting. In an ancillary study conducted in three CAMP Clinical Centers, adherence of less than 80 % was seen in 75 % of 140 children when adherence was measured objectively but only in 6 % of children when measured by means of self-report.  The measurement of fractional exhaled nitric oxide (FENO) might unmask non-adherence to ICS therapy. However, in many countries, the capacity to measure FENO is unlikely to be available outside specialized centers .
A review of the studies using electronic adherence monitoring shows that half of them report mean adherence rates of 50 % or below and the majority report rates below 75 %  An observational study in 135 children, 2–12 years of age, with asthma revealed that median (interquartile range) one-year adherence to ICS, as measured by electronic devices, was 84 % (70–92 %). Fifty five children (41 %) did not achieve the pre-defined level of good adherence (≥80 %) and this was associated with poorer asthma control .
In a multivariate analysis conducted in 6 Asian countries, three questions related to patients’ acceptance of inhaler medicines remained significantly associated with poor adherence, after adjusting for potential confounders: “I am not sure inhaler type medicines work well” (p < 0.001), “Taking medicines more than once a day is inconvenient” (p < 0.002), and “Sometimes I skip my inhaler to use it over a longer period” (p < 0.001) .
Potential methods to improve adherence and compliance
To date, efforts to address the problem of non-adherence in childhood asthma have had little success . GINA 2016 noted that only a few adherence interventions have been studied closely in asthma: 
Shared decision-making for medication and dose choice
Inhaler reminders for missed doses
Reduced complexity of the regimen (once versus twice daily)
Comprehensive asthma education with home visits by asthma nurses
Clinicians reviewing feedback on their patients’ dispensing records.
Education should highlight the importance of adherence to prescribed ICS even in the absence of symptoms, and should involve literal explanation and physical demonstration of the optimal use of inhaler devices and peak flow meters. Education should be tailored according to the socio-cultural background of the family .
The use of a single combination inhaler, rather than separate inhalers, is generally recommended, to maximize adherence and efficacy . It was suggested that once-daily ICS therapy provides a practical therapeutic option that did not appear to jeopardize the clinical efficacy of asthma controller therapy . Once-daily dosing strategy was associated with lower costs and higher level of quality-adjusted life-years (QALYs) .
Developing electronic monitoring device technology with reminders might be a key noninvasive resource to address poor adherence in children and adolescents . The Use of an electronic monitoring device with an audiovisual reminder led to significant improvements in adherence to ICS in a group of school-aged children with asthma who attended an emergency department in Auckland, New Zealand . Strong potential was found for low-cost speech recognition adherence programs integrated with an electronic health record in which speech recognition telephone calls to parents were triggered when an inhaled corticosteroid refill was due or overdue .
Efficacy at increasing asthma self-management skills was demonstrated using group interactive learning in the school setting . On the other hand, 34 children (6–11 years old) were randomized to intervention or attention control groups for 10-weeks. The intervention arm participated in weekly coping peer group support sessions and received mp3 peer-recorded asthma messages promoting adherence. At 10 weeks, no statistical difference in objectively measured adherence could be detected between the two arms adjusting for baseline adherence (p = 0.929). Participants’ in both study arms self-reported adherence was significantly higher than their objectively measured adherence at week 10 .
Targeted parenting skills were chosen to address treatment resistance, and included nurturance and autonomy granting, use of positive reinforcement strategies, predictable routines, limit setting, problem solving, taking charge when needed, and staying calm under pressure. After the 6-month intervention, adherence with ICS increased from 72.9 % to 100.0 %, (p = 0.013). The percentage of children with controlled asthma increased from 0 to 62.5 % (p = 0.026) indicating a clinically meaningful change. Parents’ ratings at 6-months suggested that asthma-related tasks and child behaviors were less problematic and their confidence to manage asthma increased .
Conclusions and unmet needs
Despite the availability of several formulations of ICS and delivery devices for treatment of childhood asthma and despite the development of evidence-based guidelines, childhood asthma control remains suboptimal.
ICS are considered the most effective drugs used to suppress airway inflammation in asthma. However, Inhaled medications are only effective if they are used properly. Therefore, choosing the appropriate delivery device and offering competent education about its proper use is mandatory to gain asthma control. It is important to realize the need for step-up therapy based on poor control and step-down at three month intervals whenever good asthma control is achieved. Physicians should recognize that preschoolers are different from older children in treatment strategies. Although ICS treatment is generally considered safe in children, the potential adverse effects related to its regular use continue to be a matter of concern. ICS therapy should always aim to reach the lowest effective dose because most adverse effects are dose-dependent. It is also more common in individuals receiving concomitant oral or nasal corticosteroids. The potential adverse effects of ICS need to be weighed against the benefit of these drugs to control persistent asthma especially that its safety profile is markedly better than oral glucocorticoids.
ICS do not offer cure to asthmatic children and discontinuation leads to deterioration of clinical control, lung function, and airway responsiveness within weeks in a proportion of patients. Therefore, adherence to daily ICS therapy is a key determinant of asthma control. This mandates that asthma education follow a repetitive pattern and involve literal explanation and physical demonstration of the optimal use of inhaler devices. Education should be tailored according to the socio-cultural background of the community.
Breath actuated inhaler
Bone mineral density
Childhood Asthma Management Program
Cyclic adenosine monophosphate response element binding protein
Chronic obstructive pulmonary disease
Dry powder inhalers
Fractional exhaled nitric oxide
Global Initiative for Asthma
Glucocorticoid response elements
Histone acetyl transferase
Hypothalamus pituitary axis
- MAP kinase:
Mitogen-activated protein kinase
Metered dose inhalers
Mometasone furoate/formoterol fumarate
Short Acting beta-agonist
Scottish Intercollegiate Guidelines Network
Single inhaler therapy
Valved holding chamber
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We acknowledge the tremendous efforts of Sofia Dorsano from the World Allergy Organization (WAO) International Headquarters, Milwaukee WI, USA, in organizing the production and formatting of this systematic review. This paper was reviewed and approved by members of the WAO Pediatric Asthma Committee and the WAO Board of Directors and Executive Committee.
This is a review article that did not need or receive any funding.
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This is a review article.
EH initiated the concept and led the development of the document and contributed “Abstract; Introduction; Adverse Effects of ICS in Children; Adherence to ICS Therapy; and Conclusions and Unmet Needs. NR contributed to “Adverse Effects of ICS in Children”. BWL and JYS contributed “Dosage and Therapeutic Regimens”. MS contributed “Methods of ICS Delivery in Children”. DEG contributed “Mechanisms of Action of ICS”. PLS reviewed the manuscript. All authors reviewed and approved the final manuscript.
The authors have no competing interests to declare relevant to this work.
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The manuscript does not report on or involve the use of any animal or human data or tissue.
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Hossny, E., Rosario, N., Lee, B.W. et al. The use of inhaled corticosteroids in pediatric asthma: update. World Allergy Organ J 9, 26 (2016). https://doi.org/10.1186/s40413-016-0117-0
- Inhaled corticosteroids
- Adverse effects