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MINI REVIEW article

Front. Pediatr., 07 July 2022
Sec. Pediatric Pulmonology
This article is part of the Research Topic Difficult and Severe Asthma in Children, Volume II View all 11 articles

Frontiers Review: Severe Asthma in Adolescents

  • Department of Respiratory Pediatrics, Royal Brompton Hospital, London, United Kingdom

Asthma remains the most prevalent chronic respiratory disease of childhood. Severe asthma accounts for a minority group of patients but with substantial morbidity burden. It may reflect disease which is resistant to treatment or that which is difficult to treat, or a combination of both. The adolescent patient cohort denote a unique group and are the focus of this review. This group of patients embody transitioning priorities and evolving health beliefs, all of which may influence the management and burden of disease. Factors of importance include the influence of physiological parameters such as sex and race, which have confer implications for medical management and non-physiological factors, such as adherence, risk-taking behavior, and vaping. The holistic approach to management of severe asthma within this group of patients must acknowledge the evolving patient independence and desire for autonomy and strive for a collaborative, patient tailored approach. This review will focus on the factors that may pose a challenge to the management of severe adolescent asthma whilst offering suggestions for changes in practice that might harness patient priorities and shared clinical decision-making.

Introduction

Asthma is the most prevalent chronic lung disease of childhood (1). Most children with asthma achieve good symptom control with low-moderate dose inhaled corticosteroids (ICS). However, a small group with severe disease and poor control despite maximal treatment need further escalation in support and intervention.

The European Respiratory Society (ERS) /American Thoracic Society (ATS) defines severe asthma in those over 6 years of age, as that which obligates treatment with high dose ICS and another maintenance agent, or use of systemic steroids, for more than half of the previous year to achieve control (2).

Along with high treatment burden, severe asthma confers significant morbidity and mortality. Within pediatrics, the National Review of Asthma deaths in the UK revealed that mortality in this population remains alarmingly high (3). Asthma control may be rendered difficult due to a variety of factors that demand recognition (4, 5), particularly within the adolescent group (6).

The Adolescent With Severe Asthma

The World Health Organization (WHO) defines adolescence to be within the ages of 10 and 19 years (7) whilst others propose a more extended length of 10–24 years a more accurate representation (8). Certainly, adolescence embodies young adulthood and a challenging time of transition, marked by the pursuit for independence (9) and autonomy with transformations in social, emotional, and physical domains (10). Ownership of health and self-care sharpens into focus, becoming a greater priority.

Marked differences can exist in the manifestation, exacerbating factors, and management strategies for asthma at different age groups (11). Furthermore, challenges in management lay bare the influence of disparities in socio-economic status, education, exposure to pollution and healthcare access, categories recognized by the Global Initiative for Asthma as obstacles to decreasing the disease burden (12). Ethnic differences in asthma outcomes have also been postulated, with implications for biologics and therapeutic possibilities (13). A study in pediatric minority populations revealed that higher IgE levels were significantly associated with severe asthma, poor control, and exacerbations in the Puerto Rican group whilst none of these outcomes were observed in Mexican Americans. Furthermore, eosinophilic asthma had links with greater asthma severity and exacerbations in the Puerto Rican group, inferring that eosinophil-targeting therapies may confer an advantage in this group (13). Additionally, influence of sex differences are documented, with notable reference to symptomology within the adolescent period (6). A shift in higher prevalence from males to females during the pubertal period is recognized, with greater occurrence of wheeze and more severe asthma in females (6). In an European Community Respiratory Health Survey study of adult female population, lower lung function and higher likelihood of asthma were observed in those with early menarche, implicating hormonal factors (14). Furthermore, asthma in pregnancy has been linked with obstetric complications (15), which may have significant implications for our female cohort of patients. Therefore, as our patients transition to young adults, the growing relevance of such findings should be considered.

This review will explore the multifaceted parameters that bear significance to the management of severe asthma in the adolescent group.

Confirming The Diagnosis

The Diagnostic Label

The WHO categorizes severe asthma into three groups; (1) inadequately treated (2) that which is difficult-to-treat and (3) severe treatment-resistant asthma (STRA), the last of which represents asthma for which the highest level of management is necessitated to achieve control, or which does not despite this (16).

A crucial initial step is in ensuring the diagnostic labeling is accurate and should begin with addressing the basics. A multidisciplinary approach is paramount (5) in diagnosing, initiating, and maintaining treatment.

STRA may warrant the use of biologics and in the UK currently omalizumab and mepolizumab are licensed for use in children aged above 6 years and dupilumab for children aged above 12 years, with the caveat that the patient has not shown an adequate response or is not eligible for mepolizumab (17). The US Food and Drug Administration (FDA) and European Medicines Agency (EMA) have licensed all three biologics for children above age 6 years. In addition, Benralizumab is licensed by the FDA and EMA for children aged 12 years and above with severe eosinophilic asthma. Difficult-to-treat asthma, however, necessitates a broader approach, one that embraces extra-pulmonary influences such as obesity, adherence, family values, and symptom perception (18). Moreover, several conditions might present an asthma-like façade and should addressed (5).

Investigations

A thorough history and appropriate investigations facilitate diagnostic clarity. Investigations include blood tests for full blood count, total IgE and specific IgE to aeroallergens, as severe childhood asthma has associations with atopy and increased blood eosinophilia (19). Spirometry with bronchodilator reversibility is useful for diagnosis, although it is important to note that some children with asthma may have non-obstructive spirometry when not acutely unwell. Fractional exhaled nitric oxide (FeNO) is a surrogate measure of eosinophilic airway inflammation and a good predictor of corticosteroid response. Additional investigations such as inhaled methacholine challenge, eucapnic voluntary hyperventilation and cardiopulmonary exercise tests can provide further clarity. Flexible bronchoscopy may be indicated, to assess for anatomical variations including airway malacia and vascular rings (20). Analysis of the bronchoalveolar lavage (BAL) for cytology and culture growth is beneficial and children with STRA are noted to have a higher eosinophil count in the BAL compared to control subjects (21). Further exclusionary investigations including sweat chloride testing, immunoglobulin levels, testing for reflux, and video fluoroscopy for swallow assessment may be useful (20).

Factors Of Influence In Adolescent Severe Asthma And Management

Breathing Pattern Disorders

Several comorbidities may confound the presentation and diagnosis of asthma and should be considered. Of note are breathing pattern disorders. These are best described as chronic or recurrent changes in breathing pattern that cause respiratory symptoms such as breathlessness and non-respiratory symptoms such as anxiety, light-headedness, and fatigue. The prevalence of some breathing pattern disorders in adolescents with asthma may be as high as 25% (22). Disruption of an optimal breathing pattern can contribute to multiple distressing and debilitating symptoms that impact significantly on the quality of life. The symptoms can masquerade as asthma or worsen asthma symptoms particularly in those with exercise induced dyspnoea and during an acute asthma attack. Breathing pattern retraining can therefore be useful in the management of severe asthma.

Obesity

Obesity, a global health concern, is a significant risk factor for severe asthma and is associated with poor asthma control and increased health care utilization (23). Systemic corticosteroid responsiveness is also impaired in obese children with asthma and is accompanied by heightened patterns of systemic inflammation and metabolites of oxidative stress (24). Additionally, obesity may be associated with other co-morbidities which may impact the holistic quality of life and influence management.

Adherence

The aim of any asthma management strategy should be to achieve symptom control, with minimal therapeutic intervention. The WHO suggests adherence to be “the extent to which a person's behavior—taking medication, following a diet, and/ or executing lifestyle changes, corresponds with agreed recommendations from a health care provider” (25). Contrary to any paternalistic approach, a collaborative effort between the patient and professional, one which embraces the patient priorities, will likely underpin successful adherence. This is particularly relevant since this modifiable factor is recognized as a challenge among adolescents (26), contributing to uncontrolled disease. The National Review of Asthma Deaths in the UK highlighted that over half of asthma deaths were preventable through addressing avoidable factors, including non-adherence and missed appointments (3).

A compendium of factors sway adherence in adolescents (26) and in turn influence the management of severe asthma especially as they transition. Examples of such influences include the determination for greater independence and resistance to parental monitoring (26) paradoxically accompanied by forgetfulness and struggles with organization of time (26). This may also be augmented by social stigma and risk-taking behaviors.

Conflicting and changing priorities and attitudes to health play a key role in this age group (9, 26) and therefore, exploring and accommodating for factors that matter to adolescents may be critical in mitigating the burden of severe disease.

Adherence Monitoring

Adherence to treatment may be viewed in stages; initiation (taking the first dose), implementation (the actual dosing by the patient in comparison to what is prescribed) and persistence (time from starting to eventually stopping treatment) (27). In the context of severe adolescent asthma, which may be subject to variable triggers and alterations to treatment regimens, these stages may be in a dynamic state, especially if compounded by non-adherence. Adherence is considered good if over 80% of the prescribed doses are taken with an appreciation that higher treatment observance is associated with reduced exacerbations (28). Adherence is acknowledged as lower in adolescents (26) and a study of 15–18 year olds with moderate to severe asthma, showed a median adherence of 43% detected through electronic monitoring (29). It is important to recognize that whilst non-adherence may be intentional, it may also be non-intentional (30), creating scope for a change in practice.

Furthermore, monitoring adherence may itself pose a challenge. A combination of history and investigations, including trends in spirometry and FeNO measurements, and prescription uptakes offer some indication. Subjective tools to ascertain treatment observance include self-reporting questionnaires, such as the Medicine's Adherence Report Scale (31). However, over reporting may be observed. Objective monitoring tools include data on prescriptions issued, weighing canisters and directly observed therapy (DOT) (31). Aside from DOT, the former measures do not, in fact, reveal the actual dosing of the treatment. Novel electronic monitoring devices (EMD) may enable clinicians to circumvent this challenge (32).

Mental Health and Risk-Taking Behavior

Symptoms of depression and anxiety are documented in adolescents with asthma (33, 34) and are associated with lower quality of life (35). Post-hoc analysis of the IDEAL study noted that 81% of the patients with severe asthma had uncontrolled disease, which was associated with reduced lung function and worsened health related quality of life (35). Furthermore, greater acute healthcare utilization is also observed in adolescents suffering from depression (36, 37).

Worryingly, a higher percentage of risk taking behavior has been described in adolescents with severe asthma (26, 33) including smoking and substance misuse (33). A multi-state survey by the Centers for Disease Control and Prevention revealed that cigarette smoking, cocaine use and low mood were more prevalent in youths with asthma than without (38). Moreover, factors were recognized to co-influence, and where suicidal ideation was reported in those with asthma, there was an association with binge drinking and more than 60% of smoking marijuana (38).

These represent important potential confronts in managing adolescent severe asthma and an integrative approach, which interlocks different tiers of support including school and psychology, is imperative in providing holistic management.

Symptom Perception

Finally, it is important to consider that whilst symptom severity has been described above, poor symptom perception and tolerance to high levels of symptoms is another challenge and may contribute to poor control (26). Poorer symptom control in adolescents has been observed, with the International Study of Asthma and Allergies in Childhood (ISAAC) noting a higher year-long prevalence for symptoms of exercise induced wheeze, severe wheeze limiting speech and night-time cough in adolescents, compared to younger children with asthma (39).

A Growing Threat: E-Cigarettes and Electronic Nicotine Delivery Systems

The Unbiased Biomarkers for the Prediction of Respiratory Disease Outcomes (U-BIOPRED) study reiterate the deleterious impact of smoking on symptomology, noting the association of exhaled smoke with severe wheeze (40). However, vaping is another growing threat and E-cigarettes and Electronic Nicotine Delivery Systems (ENDS) are described as up to two-three times more popular amongst adolescents and young adults in comparison to older adults, despite the original ambition to support smoking cessation in adults (41). A study of young adults in school and colleges (42) revealed that the top promotive factors for e-cigarette experimentation included inquisitiveness, enticing flavors, and peer influences. Interestingly, the perception that these were a healthier alternative to traditional smoking promoted their use, whilst having health concerns was a deterrent (42). This highlights the unassailable influence of education on adolescent health behaviors, to facilitate a more informed transition into adult health care.

Whilst extensive research is lacking, the present understanding on vaping effects on the lungs highlights the associations with increased severe asthma attacks, airway inflammation, increased risk of acute lung injury and reduction in lung function (41). Two case descriptions of adolescents with severe asthma exacerbations resulting in veno-venous extracorporeal membrane oxygenation (VV-ECMO) with earlier ENDS exposure have been described (43), reinforcing the urgency in understanding the adverse effects.

Furthermore, E-cigarette use has been shown to be a risk factor for future smoking, not simply a marker for future smoking (44). Data on e-cigarettes from the Children's Health Study (45) reported that 40% of e-cigarette users commenced cigarette smoking, noting a 6 times higher odds of starting cigarettes smoking if they were e-cigarette users, compared to having never-used. More alarmingly, the relationship was stronger for those who had not planned to commence smoking prior to the e-cigarette use. Therefore, E-cigarettes and Electronic Nicotine Delivery Systems are a growing health threat for adolescents and holistic management should include this understanding.

Discussion: Severe Adolescent Asthma Management—A Collaborative Approach

Family Dynamic and Peers: Support Networks

Family dynamics and influence of peers is consistently recognized as an important factor. Stress at the family level is associated with adverse asthma outcomes (46) and parents of adolescents with severe asthma are recognized as more anxious than those without (47). The pursuit for a new equilibrium, in establishing new responsibility for medication adherence, may be subject to confusion in roles where the adolescent may reject the parental support but also rely on it (26). Parents can support the practicalities of management e.g., prescriptions (28) and are in a position to explain rationale and reasoning to the transitioning young adult (28), which would be beneficial.

Furthermore, peer interactions are a significant factor of influence and clinical management should seek to harness this stimulus positively. Emotions of embarrassment are recognized to influence adherence (28). More than half of non-adherent episodes were amongst friends in one study (48) and hesitation in participating in social activities has also been noted (28). Moreover, social media influences are a very relevant entity for the current adolescent cohort and the influence should be explored in clinical consultations.

Motivational Interviewing and Co-design: Greater Ownership of Care

Approach to severe adolescent asthma should embrace clinical necessity with adolescent priority, to cultivate relevant and sustainable interventions. Acknowledging that management does not rely simply on medical interventions but embraces the multifaceted influences discussed thus far in this review, offers key insight. Creating greater ownership of care should be a priority and listening to and engaging the adolescent patient should underpin all clinical consultations. Shared decision-making with patients has shown to enhance adherence amongst adults with poorly controlled asthma, as it accounts for their priorities (49). This is very relevant for our adolescent cohort, as they embrace greater autonomy in health care decisions. Figure 1 summarizes the proposed interplay between factors of influence and collaborative working with the adolescent patient.

FIGURE 1
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Figure 1. Illustration of the interplay between factors of influence for the adolescent patient with severe asthma and collaborative working.

The Health Belief Model (50) proposes that the actions of individuals balance their beliefs about the perceived health risk with the benefits of the behavioral changes required to address the threat. The susceptibility to the disease and the challenges to overcome in achieving the intended behavior change are important considerations and have been described in the context of asthma in adolescents (29). This study reviewed the perceptions around inhaled steroids and their impact on health, challenges to taking medications (e.g., taste, fear of addiction) and suggested prompts for progress (e.g., audio and visual reminders and incentives) (29).

Understanding adolescent health beliefs is therefore a crucial pedagogical step. Motivational interviewing (MI) may be employed, exploring individual priorities and promoting positive health behavior (30). It has been used with success in different settings amongst the adolescent cohort, including diabetes (51). Furthermore, when paired with social media, online support and other supportive adjuncts such as family contributions, MI outcomes are more effective (30).

Creating a bridge between patient held beliefs and accurate knowledge of disease and treatment is an important next step. Experiencing episodes of severe asthma exacerbations and decline in asthma control, has shown to emphasize the importance of maintenance therapy and motivate greater adherence in adolescents (28). This offers an example of health consequence and subsequent modification of behavior. In one study, despite regular attendances at medical appointments, some youths did not appreciate the rationale for medication use and whilst feeling involved, many did not take the ownership of their healthcare visit (52). This highlights an opportunity for timely engagement in self-care, mitigating learning through negative clinical experiences.

A further example where collaborative working may yield a more effective outcome may be seen in school attendance and symptom perception. School and educational establishments are likely to play an integral role in adolescent lives and educational accomplishments are recognized as a priority for adolescents (6). However, poor awareness of symptoms has a considerable impact on adolescent school attendance, with up to nine times greater chance of hospital admissions and four times greater likelihood of school absenteeism, in one study (53). Therefore, greater knowledge around symptom presentation and benefits of better control for the priorities that matter to adolescents, will enable shared clinical goals. This may also be harnessed within the practical components, such as inhaler technique, with poor technique shown to contribute to poor adherence and control (54).

Therefore, collaborative working with the adolescent patient and their families, one which endeavors to codesign clinically appropriate but patient-focused management regimens, may offer a bridge to more effective management of severe, difficult to manage asthma.

Transition

Transition from pediatric to adult services is an important phase in the management of severe adolescent asthma and should endeavor to acknowledge the influence of the various aspects discussed in this review. The transition process should involve a named asthma nurse and consultant from the pediatric and adult services for better outcomes. Whilst a consensus on a set age for transition is lacking, it usually between the ages of 16 and 18. However, the conversations around transition should start early (11, 55), aiming for a gradual process rather than an abrupt event and offering time for readiness. Transition to adult services may be a worrying time for parents and carers, especially when their child's asthma has been difficult to control and they need to be supported in letting their adolescent have control over their asthma before transitioning to adult services. The emphasis should be on self-management by the adolescent with caregiver engagement, whilst acknowledging vulnerabilities (11). Co-production of relevant and informed transition services with young people and their carers is strongly advocated (55) and exploring patients' beliefs and goals is recognized as vital in enabling smooth transition (56). These interactions offer opportunities to identify and address potential challenges and barriers. Therefore, transition should embrace the priorities of the adolescent and family and aim to work in collaboration with all groups, including adult services, to achieve successful transfer of priorities, goals, and care.

Future Directions and Challenges

Despite greater understanding, asthma mortality remains high and there are associations that need further exploration. The authors recognize that one such area is the contribution of ethnic differences in asthma subtypes and outcomes, with recent findings suggesting the influence of race and ethnic differences in asthma outcomes and severity (13). These findings expose the need for further research into the role of racial and ethnic differences in severe asthma disease management.

Summary

Severe asthma in the adolescent requires a broader perspective and demands recognition of the components that are relevant to this unique age group. Table 1 summarizes the key learning points. Adolescence marks a period of transition and is subject to a variety of influences. Escalation in support may be medical such as the use of biologic therapy but may also warrant a wider approach, which nurtures collaborative decision making with the adolescent cohort and strives for more patient-relevant management regimens.

TABLE 1
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Table 1. Summary of key learning points.

Author Contributions

SW wrote the first draft. Both authors reviewed, revised, made contributions to all subsequent drafts, and contributed to the work of this manuscript.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. World Health Organization. Asthma: Key Facts. (2022). Available online at: https://www.who.int/news-room/fact-sheets/detail/asthma (accessed March 21, 2022).

Google Scholar

2. Chung KF, Wenzel SE, Brozek JL, Bush A, Castro M, Sterk PJ, et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur Respir J. (2014) 43:343–73. doi: 10.1183/09031936.00202013

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Healthcare Quality Improvement Partnership, Royal Royal College of Physicians of London. Why Asthma Still Kills: The National Review of Asthma Deaths (NRAD). Confidential Enquiry Report May 2014 Confidential Enquiry Report May 2014. London: Royal College of Physicians (2014). Available online at: https://www.asthma.org.uk/support-us/campaigns/publications/national-review-of-asthma-deaths/ (accessed March 9, 2022).

Google Scholar

4. Bush A. This child's asthma appears to be severe: but where actually is the severe problem? Acta Med Acad. (2020) 49:103–16. doi: 10.1007/978-3-030-27431-3_3

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Bush A, Fitzpatrick AM, Saglani S, Anderson WC, Szefler SJ. Difficult-to-treat asthma management in school-age children. J Allergy Clin Immunol Pract. (2022) 10:359–75. doi: 10.1016/j.jaip.2021.11.010

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Bitsko MJ, Everhart RS, Rubin BK. The adolescent with asthma. Paediatr Respir Rev. (2014) 15:146–53. doi: 10.1016/j.prrv.2013.07.003

PubMed Abstract | CrossRef Full Text | Google Scholar

7. World Health Organization. Adolescent Health. (2022). Available online at: https://www.who.int/health-topics/adolescent-health#tab=tab_1 (accessed April 19, 2022)

Google Scholar

8. Sawyer SM, Azzopardi PS, Wickremarathne D, Patton GC. The age of adolescence. Lancet Child Adolesc Health. (2018) 2:223–8. doi: 10.1016/S2352-4642(18)30022-1

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Costello RW, Foster JM, Grigg J, Eakin MN, Canonica W, Yunus F, et al. The seven stages of man: the role of developmental stage on medication adherence in respiratory diseases. J Allergy Clin Immunol Pract. (2016) 4:813–20. doi: 10.1016/j.jaip.2016.04.002

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Nanzer AM, Lawton A, D'Ancona G, Gupta A. Transitioning asthma care from adolescents to adults: severe asthma series. Chest. (2021) 160:1192–9. doi: 10.1016/j.chest.2021.05.019

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Withers ALi, Green R. Transition for adolescents and young adults with asthma. Front Pediatrics. (2019) 7:301. doi: 10.3389/fped.2019.00301

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Masoli M, Fabian D, Holt S, Beasley R, Global Initiative for Asthma (GINA) program. The global burden of asthma: executive summary of the GINA dissemination committee report. Allergy. (2004) 59:469–78. doi: 10.1111/j.1398-9995.2004.00526.x

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Wohlford EM, Huang PF, Elhawary JR, Millette LA, Contreras MG, Witonsky J, et al. Racial/ethnic differences in eligibility for asthma biologics among pediatric populations. J Allergy Clin Immunol. (2021) 148:1324–31.e12. doi: 10.1016/j.jaci.2021.09.005

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Macsali F, Real FG, Plana E, Sunyer J, Anto J, Dratva J, et al. Early age at menarche, lung function, and adult asthma. Am J Respir Crit Care Med. (2011) 183:8–14. doi: 10.1164/rccm.200912-1886OC

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Bonham CA, Patterson KC, Strek ME. Asthma outcomes and management during pregnancy. Chest. (2018) 153:515–27. doi: 10.1016/j.chest.2017.08.029

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Bousquet J, Mantzouranis E, Cruz AA, Aït-Khaled N, Baena-Cagnani CE, Bleecker ER, et al. Uniform definition of asthma severity, control, and exacerbations: document presented for the World Health Organization consultation on severe asthma. J Allergy Clin Immunol. (2010) 126:926–38. doi: 10.1016/j.jaci.2010.07.019

PubMed Abstract | CrossRef Full Text | Google Scholar

17. National Instituite for Clinical Excellence. Dupilumab for Treating Severe Asthma With Type 2 Inflammation: Technology Appraisal Guidance. (2021). Available online at: https://www.nice.org.uk/guidance/ta751/resources/dupilumab-for-treating-severe-asthma-with-type-2-inflammation-pdf-82611370398661 (accessed April 19, 2022).

Google Scholar

18. Agusti A, Bel E, Thomas M, Vogelmeier C, Brusselle G, Holgate S, et al. Treatable traits: toward precision medicine of chronic airway diseases. Eur Respir J. (2016) 47:410–9. doi: 10.1183/13993003.01359-2015

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Jarjour NN, Erzurum SC, Bleecker ER, Calhoun WJ, Castro M, Comhair SAA, et al. Severe asthma. Am J Respir Crit Care Med. (2012) 185:356–62. doi: 10.1164/rccm.201107-1317PP

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Ramratnam SK, Bacharier LB, Guilbert TW. Severe asthma in children. J Allergy Clin Immunol Pract. (2017) 5:889–98. doi: 10.1016/j.jaip.2017.04.031

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Bossley CJ, Fleming L, Gupta A, Regamey N, Frith J, Oates T, et al. Pediatric severe asthma is characterized by eosinophilia and remodeling without TH2 cytokines. J Allergy Clin Immunol. (2012) 129:974–82.e13. doi: 10.1016/j.jaci.2012.01.059

PubMed Abstract | CrossRef Full Text | Google Scholar

22. D'Alba I, Carloni I, Ferrante AL, Gesuita R, Palazzi ML, de Benedictis FM. Hyperventilation syndrome in adolescents with and without asthma. Pediatr Pulmonol. (2015) 50:1184–90. doi: 10.1002/ppul.23145

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Lee DS, Gross E, Hotz A, Ngo KC, Rastogi D. Impact of obesity on asthma morbidity during a hospitalization. Hosp Pediatr. (2018) 8:538–46. doi: 10.1542/hpeds.2017-0265

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Fitzpatrick AM, Mutic AD, Mohammad AF, Stephenson ST, Grunwell JR. Obesity is associated with sustained symptomatology and unique inflammatory features in children with asthma. J Allergy Clin Immunol Pract. (2022) 10:815–26.e2. doi: 10.1016/j.jaip.2021.10.020

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Sabaté E, World Health Organization eds. Adherence to Long-Term Therapies: Evidence for Action. Geneva: World Health Organization (2003). p. 198.

PubMed Abstract | Google Scholar

26. Kaplan A, Price D. Treatment Adherence in Adolescents with Asthma. J Asthma Allergy. (2020) 13:39–49. doi: 10.2147/JAA.S233268

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Vrijens B, Dima AL, Van Ganse E, van Boven JFM, Eakin MN, Foster JM, et al. What we mean when we talk about adherence in respiratory medicine. J Allergy Clin Immunol Pract. (2016) 4:802–12. doi: 10.1016/j.jaip.2016.05.019

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Simoni AD, Horne R, Fleming L, Bush A, Griffiths C. What do adolescents with asthma really think about adherence to inhalers? Insights from a qualitative analysis of a UK online forum. BMJ Open. (2017) 7:e015245. doi: 10.1136/bmjopen-2016-015245

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Naimi DR, Freedman TG, Ginsburg KR, Bogen D, Rand CS, Apter AJ. Adolescents and asthma: why bother with our meds? J Allergy Clin Immunol. (2009) 123:1335–41. doi: 10.1016/j.jaci.2009.02.022

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Gesinde B, Harry S. The use of motivational interviewing in improving medication adherence for individuals with asthma: a systematic review. Perspect Public Health. (2018) 138:329–35. doi: 10.1177/1757913918786528

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Pearce CJ, Fleming L. Adherence to medication in children and adolescents with asthma: methods for monitoring and intervention. Expert Rev Clin Immunol. (2018) 14:1055–63. doi: 10.1080/1744666X.2018.1532290

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Makhecha S, Chan A, Pearce C, Jamalzadeh A, Fleming L. Novel electronic adherence monitoring devices in children with asthma: a mixed-methods study. BMJ Open Respir Res. (2020) 7:e000589. doi: 10.1136/bmjresp-2020-000589

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Bender BG. Risk taking, depression, adherence, and symptom control in adolescents and young adults with asthma. Am J Respir Crit Care Med. (2006) 173:953–7. doi: 10.1164/rccm.200511-1706PP

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Licari A, Ciprandi R, Marseglia G, Ciprandi G. Anxiety and depression in adolescents with asthma and in their parents: a study in clinical practice. Monaldi Arch. Chest Dis. (2019) 89:15–9. doi: 10.4081/monaldi.2019.1063

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Müllerová H, Cockle SM, Gunsoy NB, Nelsen LM, Albers FC. Clinical characteristics and burden of illness among adolescent and adult patients with severe asthma by asthma control: the IDEAL study. J Asthma. (2021) 58:459–70. doi: 10.1080/02770903.2019.1708095

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Shankar M, Fagnano M, Blaakman SW, Rhee H, Halterman JS. Depressive symptoms among urban adolescents with asthma: a focus for providers. Acad Pediatr. (2019) 19:608–14. doi: 10.1016/j.acap.2018.12.004

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Richardson LP, Russo JE, Lozano P, McCauley E, Katon W. The effect of comorbid anxiety and depressive disorders on health care utilization and costs among adolescents with asthma. Gen Hosp Psychiatry. (2008) 30:398–406. doi: 10.1016/j.genhosppsych.2008.06.004

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Bender BG. Depression symptoms and substance abuse in adolescents with asthma. Ann Allergy Asthma Immunol. (2007) 99:319–24. doi: 10.1016/S1081-1206(10)60547-9

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Worldwide variations in the prevalence of asthma symptoms: the International Study of Asthma and Allergies in Childhood (ISAAC). Eur Respir J. (1998) 12:315–35. doi: 10.1183/09031936.98.12020315

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Fleming L, Murray C, Bansal AT, Hashimoto S, Bisgaard H, Bush A, et al. The burden of severe asthma in childhood and adolescence: results from the paediatric U-BIOPRED cohorts. Eur Respir J. (2015) 46:1322–33. doi: 10.1183/13993003.00780-2015

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Chatziparasidis G, Kantar A. Vaping in asthmatic adolescents: time to deal with the elephant in the room. Children. (2022) 9:311. doi: 10.3390/children9030311

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Kong G, Morean ME, Cavallo DA, Camenga DR, Krishnan-Sarin S. Reasons for electronic cigarette experimentation and discontinuation among adolescents and young adults. Nicotine Tob Res. (2015) 17:847–54. doi: 10.1093/ntr/ntu257

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Bradford LE, Rebuli ME, Ring BJ, Jaspers I, Clement KC, Loughlin CE. Danger in the vapor? ECMO for adolescents with status asthmaticus after vaping. J Asthma. (2020) 57:1168–72. doi: 10.1080/02770903.2019.1643361

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Wills TA, Sargent JD, Gibbons FX, Pagano I, Schweitzer R. E-cigarette use is differentially related to smoking onset among lower risk adolescents. Tob Control. (2017) 26:534–9. doi: 10.1136/tobaccocontrol-2016-053116

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Barrington-Trimis JL, Urman R, Berhane K, Unger JB, Cruz TB, Pentz MA, et al. E-cigarettes and future cigarette use. Pediatrics. (2016) 138:e20160379. doi: 10.1542/peds.2016-0379

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Landeo-Gutierrez J, Celedón JC. Chronic stress and asthma in adolescents. Ann Allergy Asthma Immunol. (2020) 125:393–8. doi: 10.1016/j.anai.2020.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Licari A, Ciprandi R, Marseglia G, Ciprandi G. Anxiety and depression in adolescents with severe asthma and in their parents: preliminary results after 1 year of treatment. Behav Sci. (2019) 9:78. doi: 10.3390/bs9070078

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Mulvaney SA, Ho Y-X, Cala CM, Chen Q, Nian H, Patterson BL, et al. Assessing adolescent asthma symptoms and adherence using mobile phones. J Med Internet Res. (2013) 15:e141. doi: 10.2196/jmir.2413

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Wilson SR, Strub P, Buist AS, Knowles SB, Lavori PW, Lapidus J, et al. Shared treatment decision making improves adherence and outcomes in poorly controlled asthma. Am J Respir Crit Care Med. (2010) 181:566–77. doi: 10.1164/rccm.200906-0907OC

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Champion V, Skinner CCS. The health belief model. In: Glanz K, Rimer BK, Viswanath K, editors. Health Behaviour and Health Education: Theory, Research and Practice. San Francisco, CA: Jossey-Bass (2008). p. 45–65.

Google Scholar

51. Channon S, Smith VJ, Gregory JW. A pilot study of motivational interviewing in adolescents with diabetes. Arch Dis Child. (2003) 88:680–3. doi: 10.1136/adc.88.8.680

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Edgecombe K, Latter S, Peters S, Roberts G. Health experiences of adolescents with uncontrolled severe asthma. Arch Dis Child. (2010) 95:985–91. doi: 10.1136/adc.2009.171579

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Rhee H, Belyea MJ, Halterman JS. Adolescents' perception of asthma symptoms and health care utilization. J Pediatr Health Care. (2011) 25:105–13. doi: 10.1016/j.pedhc.2009.10.003

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Yawn BP. The role of the primary care physician in helping adolescent and adult patients improve asthma control. Mayo Clin Proc. (2011) 86:894–902. doi: 10.4065/mcp.2011.0035

PubMed Abstract | CrossRef Full Text | Google Scholar

55. NICE. Transition From Children's to Adults' Services for Young People Using Health or Social Care Services. (2016). Available online at: https://www.nice.org.uk/guidance/ng43 (accessed June 13, 2022).

Google Scholar

56. Lugasi T, Achille M, Stevenson M. Patients' perspective on factors that facilitate transition from child-centered to adult-centered health care: a theory integrated metasummary of quantitative and qualitative studies. J Adolesc Health. (2011) 48:429–40. doi: 10.1016/j.jadohealth.2010.10.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: severe childhood asthma, severe adolescent asthma, holistic management, transition, collaborative working

Citation: Warraich S and Sonnappa S (2022) Frontiers Review: Severe Asthma in Adolescents. Front. Pediatr. 10:930196. doi: 10.3389/fped.2022.930196

Received: 27 April 2022; Accepted: 15 June 2022;
Published: 07 July 2022.

Edited by:

Nicola Ullmann, Bambino Gesù Children's Hospital (IRCCS), Italy

Reviewed by:

Kelechi Benjamin Ugonna, Sheffield Children's Hospital, United Kingdom

Copyright © 2022 Warraich and Sonnappa. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Samatha Sonnappa, s.sonnappa@rbht.nhs.uk

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