Paolo Bottau1*†
Lucia Liotti2†
Eleonora Laderchi3†Alessandra Palpacelli2†
Elisabetta Calamelli1†Carlotta Colombo3Laura Serra1‡Salvatore Cazzato2‡- 1Pediatric and Neonatology Unit, Imola Hospital, Imola, Italy
- 2Pediatric Unit, Department of Mother and Child Health, Salesi Children's Hospital, Ancona, Italy
- 3Postgraduate School of Pediatrics, University of Bologna, Bologna, Italy
Acute Viral Bronchiolitis is one of the leading causes of hospitalization in the first 12–24 months of life. International guidelines on the management of bronchiolitis broadly agree in recommending a minimal therapeutic approach, not recommending the use of bronchodilators. Guidelines, generally, consider bronchiolitis as a “unique disease” and this runs the risk of not administering therapy in some patients who could benefit from the use of bronchodilators, for instance, in those who will develop asthma later in their life and face first episode in the age of bronchiolitis. Today, there is growing evidence that bronchiolitis is not a single illness but can have different “endotypes” and “phenotypes,” based on age, personal or family history of atopy, etiology, and pathophysiological mechanism. There is evidence that some phenotypes of bronchiolitis are more strongly associated with asthma features and are linked to higher risk for asthma development. In these populations, possible use of bronchodilators might have a better impact. Age seems to be the main feature to suggest a good response to a bronchodilator-trial, because, among children > 6 months old with bronchiolitis, the presence of a subset of patients with virus-induced wheezing or the first episode of asthma is more likely. While waiting for new research to define the relationship between therapeutic options and different phenotypes, a bronchodilator-trial (using short-acting β2 agonists with metered-dose inhalers and valved holding chambers) seems appropriate in every child with bronchiolitis and age > 6 months.
Introduction
Acute Viral Bronchiolitis is one of the leading causes of lower respiratory tract infection and hospitalization in the first 12–24 months of life (1, 2). Several guidelines have been published on the diagnosis and management of bronchiolitis; these guidelines have different reference ages in the diagnosis (<24 months in United States and <12 months in Europe), but basically agree in recommending a minimal therapeutic approach without the use of bronchodilators (3–6).
Accumulating evidence has revealed that bronchiolitis is not a single disease but can have different “endotypes” and “phenotypes” based on age of presentation, personal or family history of atopy, etiology, pathophysiological mechanism and clinical presentation (7–10). Therefore, today something seems changing in the viral infant bronchiolitis approach: in some phenotypes, drug treatment may be effective.
In this review, we try to address these topics, evaluating the different etiopathogenetic, clinical and therapeutic aspects of acute viral bronchiolitis.
Pathogenetic Mechanisms
Bronchiolitis is more often described as inflammation and oedema of the bronchioles caused by respiratory viruses that invade the epithelial cells of the small airways. Although the exact mechanism is unknown, epithelial cells become necrotic and are sloughed off with an excessive amount of mucus. This condition leads to obstruction of the bronchioles and varying degrees of bronchospasm and air trapping (11).
Bronchiolitis is mostly associated with respiratory syncytial virus (RSV), that is detected in 50–80% of the hospitalized bronchiolitis cases (1, 12, 13). Other viruses can also be associated with bronchiolitis: rhinovirus (RV), human bocavirus, metapneumovirus, parainfluenza virus, influenza virus, adenovirus, coronavirus. Viral co-infections (usually with RSV and RV) are detected in 10–40% of severe cases (12). RSV is an RNA virus with two antigenically different subtypes (A with 11 genotypes and B with 23 genotypes) (14). RSV infection can be transmitted through direct inoculation of contaminated secretions in the nasal and conjunctival mucosa or by inhalation of large respiratory droplets (2, 15). Reinfections in young children are possible and are usually mild, although severe cases have been reported (16).
RSV binds to epithelial cells and replicates, causing epithelial necrosis and ciliary destruction. After being infected by RSV, the epithelial cells are sloughed to lower respiratory tract, where the virus infects the ciliated epithelial cells of the bronchioles mucosa and pneumocytes in the alveoli. Viral attachment to the target cell is mediated by F and G RSV surface glycoproteins. Epithelial cells necrosis results in the inflammatory response, by increasing the production of cytokines, including alarmins, chemokines, and growth factors. This inflammatory milieu attracts innate lymphoid cells, dendritic cells, and granulocytes to the site of infection (17, 18).
A strong induction of antiviral type I and type III interferons and interferon-induced genes is the primary response of the RSV infected mucosa, but RSV has developed the capacity to evade this innate interferon (INF) response through RSV-NS1/2 proteins, which are able to reduce both IFN-I and INF-III responses (19, 20). The disease state following RSV infection is associated with an increase in IL-17 production. This cytokine is more prominent in neonates, thus contributing to more severe clinical aspects (21, 22).
Intraluminal airway obstruction is caused by cellular infiltration of the peribronchiolar tissue, mucus overproduction, sloughing of infected epithelial cells and inefficient ciliary beating (15). Air trapping and varying degrees of lobar collapse can be caused by plugs composed of cellular debris and mucus in the bronchiole lumens (1). Viral clearance is permitted by innate and adaptive immune responses and the bronchiolar epithelium begins to regenerate within 3–4 days after the symptoms resolution. Currently, many studies indicate an association between RSV bronchiolitis and subsequent development of asthma (8).
Three RSV genotypes have been identified: NA1, ON1, and BA, respectively. The NA1 genotype infects young infants and is related to a more severe clinical course; the BA genotype is associated with eosinophilia and family history of asthma, while, in general, the ON1 genotype is associated with less severe symptoms (23). Interestingly, Harford et al. found that RSV infection resulted in dysregulation of β2-adrenergic receptor (β2AR) function, position and number. This dysregulation can explain the ineffectiveness of β2 agonists in treating obstruction in RSV infected patients (24).
The second most common virus causing bronchiolitis during infancy is RV. Its detection frequently occurs in children over 12 months of age. RV is an RNA Enterovirus belonging to the Picornaviridae family.
Lower respiratory tract infections are typically due to a RSV infection, particularly in very young children; on the contrary, RV infections are more common in slightly older children, in those with atopic predisposition in particular, and can cause severe wheezing (17). Lower respiratory tract infection is usually caused by RV type A, while severe wheezing is more commonly linked to RV type C infection (13, 25).
A partial defect in mucosal antiviral innate interferon responses may be related to a higher risk of severe RV infection and wheezing in young children with a family history of allergy and asthma. Cadherin-related family member 3 (CDHR3) has recently been identified as a unique receptor for RV-C (26), thus explaining the high pathogenic potential of RV-C. It is important to underline that an increased risk of childhood asthma has been associated with a polymorphism in the CDHR3 gene (27). RV infections seem to induce a milder epithelial inflammation than RSV, but in RV infections the expression of IFN type I decreases, with a predominant Th2 immune response (28).
Recently, a group of Italian researchers has demonstrated the presence of differing Th1/Th2 balance in patient hospitalized during the peak epidemic months or out of this period. The latter group was found to have a higher Th2 polarization in the immune response with a greater production of IL-4 and lower levels of IFNγ; therefore, they hypothesize the presence of two phenotypes of bronchiolitis: the first with RSV infection during the peak period and the second with a possible genetic predisposition to atopy and hospitalized during the non-peak season (29).
In conclusion, bronchiolitis is due to direct viral cytotoxic injury in conjunction with a robust host inflammatory response, but the relative contribution remains uncertain and is probably related to the type of virus involved and to the variability of the individual immune response. The role of the underlying genetic mechanisms is not yet clearly understood.
Clinical Presentation
Diagnosis of acute bronchiolitis is clinical, supported by epidemiological and virological data. The term is generally applied to the first episode of wheezing in infants younger than 12–24 months of age (2, 5, 8). Peak incidence occurs between 3 and 6 months of age (1). After an incubation period of 4–6 days, infants show signs of upper respiratory tract infection (2): cough, runny nose, and fever are followed by lower respiratory distress characterized by nasal flaring, tachypnea, increased work of breathing with intercostal, subcostal or supraclavicular retractions, use of abdominal muscles and grunting in the next 1–3 days (1, 8). Multiple respiratory sounds can be heard: respiratory crackles and bilateral wheezing are typical (1). Acute viral bronchiolitis is a quite dynamic disease: clinical severity usually peaks around 3–5 days from the symptoms onset, and the minute-to-minute variation in clinical findings is characteristic, as mucus and debris are cleared from the airways by coughing or as the child becomes asleep or agitated; thus, several examinations are recommended (1). Clinical assessment is also possibly confounded by nasal congestion, the resolution of which, with nasal discharge, can help ascertain whether respiratory sounds come from lower respiratory tract (2). Fever can be present in almost 30% of infants and usually occurs early in the course of disease (30).
Most infants have a mild clinical form that resolves in 10–14 days and can be managed at home; cough usually resolves within 2–3 weeks (31). Infant aged <3 months, born pre-term or with cardiopulmonary (e.g., chronic lung disease or congenital heart disease), immunodeficiency or neuromuscular disorders are at greater risk of severe disease, with complications including apnoea or bacterial infection (32). In particular, preterm infants are at a higher risk of apnoea (with a reported rate from 1 to 24%) (2), especially if with a corrected age of <2 weeks, birth weight <2.3 kg, respiratory rate <30 or >70 at presentation, and SpO2 of 90% or less at presentation (33).
RSV infection is typically associated with an increased severity of presentation, while other viruses cause milder phenotypes (26, 34). In a retrospective cohort of previously healthy RSV-infected patients, respiratory failure was associated with lethargy, grunting, and a PaCO2 ≥ 65 mmHg at initial emergency department presentation (35, 36).
Hospitalization is usually recommended when children present with poor feeding, severe retractions, oxygen saturation of 92% or less, a respiratory rate higher then 60/min and in the presence of significant social risk factors (e.g., poor parental reliability or inadequate home environment) (35). Severity Scoring tools have been developed and validated to be used in clinical settings and can be useful for an objective measure. In general, these scores should be integrated with other measures and repeated to obtain clinical assessment to guide practical decisions (1, 7).
Finally, attempts have recently been made to characterize the clinical phenotype of bronchiolitis. Dumas et al. identified several clinical profiles from a multicenter study on children admitted to hospital with bronchiolitis: Profile A with high probability of RV etiology, history of wheezing and wheezing at presentation, eczema, and older age of the patient; profile B: wheezing at presentation, but no history of wheezing or eczema and high probability of RSV infection; profile C: the most severely ill group, with a longer hospital stay, and a high probability of RSV infection; profile D: the less severe illness, including non-wheezing children with a shorter length of hospitalization (26). A clinical respiratory assessment of the first bronchiolitis episode based on lung-X-rays, respiratory outcomes (hypoxemia, wheezing, and/or sub-costal retractions), nasal protein levels of antiviral and type 2 cytokines (IFNγ, IL-10, IL-4, IL-13, IL-1β, and TNFα) was conducted also by Arroyo et al. (37) in 2020 to define mild, hypoxemia or wheezing phenotypes.
These studies provide informations about outcomes, disease patterns and underlying airway immunobiology and, above all, they may be the evidence of the need of a tailored clinical and therapeutic approach (8, 27).
Therapeutic Options
Among international guidelines, there is broad agreement on the role of support therapy; it is well-established that bronchiolitis management should be focused on guarantying proper hydration and oxygenation of the child. Intravenous or nasogastric fluid administration is recommended to ensure hydration whenever oral route is non-viable. Moreover, the enteral route should be preferred to the intravenous route (1). Oxygen therapy is recommended in children with peripheral oxygen saturation below 92% (1, 38) and should be performed through standard oxygen therapy (SOT) or via high flow nasal cannula (HFNC), providing heated and humidified air (39, 40).
Drug administration is ground for controversy, as corticosteroids, nebulized hypertonic saline, and nebulized epinephrine are mostly not recommended, while β2 agonist bronchodilators are contemplated in some guidelines and object of a long-lasting debate (1, 41–43). Although several guidelines advise against bronchodilators administration (4–6), in some countries, such as in Italy (3), the β2 agonist trial is considered as a possibility in selected cases as well. The recommendation of some guidelines on minimal handling of bronchiolitis (3–6) may result in several concerns of pediatric care providers and in the lack of adherence to the guidelines themselves (7, 44).
The indication on the utility of bronchodilators is mainly based on Gadomski and Scribani Chochrane systematic review, which states that albuterol administration does not result in a significant reduction in hospitalization or disease duration in non-hospitalized children. However, these same authors point out that some children may benefit from the administration of bronchodilators (45). As Wall suggests (42), it may be possible that some children, who will develop asthma later in their life, may experience their first episode in the age range of bronchiolitis and, thus, be indistinguishable from children with “pure” bronchiolitis (4, 42). This could be the reason why older patients (>6–12 months) with history of personal or familiar atopy, moderate to severe respiratory distress and wheeze as predominant auscultatory feature (i.e., no crackles) may improve with an asthma type therapy (42). Common practice as well suggests that clinical features of bronchiolitis in infants under 3 months of age are quite different from infants 8–12 months old. These data have been confirmed by two Italian studies, that noted how bronchiolitis in infants under 6 months of age is different from that in infants older than 6 months (46, 47).
Recent evidence noted that several pathogenetic clusters based on age, viral agents, immune phenotype, presence of wheeze and crackles, disease severity and risk of recurrent wheezing and asthma may underlie bronchiolitis (7–10). One group may be formed by very young infants (<6 months of age) with RSV infection and increased risk of recurrent wheezing; instead, another group may comprise older children (>6 months of age) with RV infection, atopic predisposition, high risk of developing asthma (8) and, probably, a better response to bronchodilators. Although much more evidence is required, proposals were put forward for a more personalized treatment, based on the hypothesis of different entities of bronchiolitis (8, 48). An interesting recent study by Rodríguez-Martínez et al. (49) found out that therapeutic options based on a phenotypic-guided strategy are also more cost-effective than a guideline-guided strategy.
Considering all these data, there is evidence that some phenotypes of bronchiolitis are more strongly associated with asthma features and are linked to higher risk for asthma development. In these populations, use of bronchodilators might have a better impact. More specifically, we propose that an inhaled bronchodilator trial could be considered particularly in children older than 6 months of age, but two specific conditions must be advised. The first is that in these infants, that we can consider as “viral wheezers,” bronchodilators should be administrated by metered-dose inhalers and valved holding chambers, as recommended by current guidelines, since this method is more effective and with less side effects than nebulized therapy (50, 51). The second is the indication to observe a clinical improvement with clinical scores after the bronchodilator trial (52). The dose and the time when to re-evaluate the clinical picture are still debated, perhaps the treatment scheme of worsening asthma in children younger than 5 years proposed by the GINA 2021 guidelines (short-acting β2 agonist: 2–4 puff every 20′ for three times in the first hour and review) can be applied (51).
Similarly to bronchodilators, the use of corticosteroid is not recommended in the management of infant bronchiolitis (1), but is part of the treatment of viral wheezing or asthma, so we agree that a course of corticosteroid could be indicated in moderate to severe clinical pictures, when the bronchodilators trial gave a positive result (42, 53–56).
These several data and considerations stress the necessity of subtype-specific studies, in order to evaluate the clinical response to different treatments and meet the need for a more personalized precision therapy.
Discussion and Conclusion
Bronchiolitis is one of the major health problems in infants around the world, but unfortunately, to date, no therapy has been validated for the management of this disease. Many guidelines have been published by various scientific societies, which agree on minimal handling (i.e., hydration and the administration of oxygen as the only treatment options) (3–6). Unfortunately, this approach risks excluding some patients who might benefit from the bronchodilator treatment (48). However, as pointed out by the American Academy of Pediatrics, guidelines are intended to assist clinicians in decision making and are not intended to “replace clinical judgment or establish a protocol for the care of all children with bronchiolitis” (5). In light of the data emerging from the scientific literature, acute bronchiolitis should no longer be considered as a single disease but rather as characterized by different phenotypes and endotypes (7–10, 26). In particular, it seems that the phenotype characterized by older age, type 2 immune response, personal or family (first-degree) history of atopy, RSV genotypes (ON1 and BA) or RV etiology and infection during non-RSV-predominant or non-peak viral months may have a good response to a trial with bronchodilators (48).
Evaluating all the evidence, age seems to be the main feature that may suggest a good response to the bronchodilator-trial. For instance, in the research by Dumas et al., the “profile A” (patient with personal or family history of wheezing and eczema, wheezing at clinical presentation, and RV infection) is often >6 months, probably have initial sign of asthma and may respond to a short-acting β2 agonist-trial (26, 57). Probably, the “true” bronchiolitis (in which therapy is useless) affects the child <6 months. This hypothesis may be supported by epidemiological data (1, 4), showing that bronchiolitis reaches its peak of incidence between 3 and 6 months, and by other studies suggesting that bronchiolitis in infants under 3–6 months of age is quite different from that in infants >6 months old (46, 47).
In a recent multicenter study with the objective of identifying factors associated with the use of albuterol among infants hospitalized for bronchiolitis, Condella et al. found that there is a subgroup of patients to whom clinicians preferentially administer albuterol. Characteristics of these infants mainly include presentation with wheeze and older age (>6 months), and these children may be similar to those affected by viral wheezing or their first episode of asthma (58).
This knowledge suggests that among infants >6 months with bronchiolitis, there could be a subset of patients who may have a virus-induced wheezing or their first episode of asthma and may respond to the bronchodilator-trial (4, 42).
To conclude, there is evidence that some phenotypes of bronchiolitis are more strongly associated with asthma features and are also linked to higher risk for asthma development. In these populations, use of bronchodilators might have a better impact.
Looking forward to future RCTs targeted to assess the utility of short-acting β2 agonists in different bronchiolitis phenotypes, a bronchodilator-trial (using short-acting β2 agonists with metered-dose inhalers and valved holding chambers) could be performed in infants with bronchiolitis and age > 6 months.
Author Contributions
PB and LL designed the review. PB, LL, EL, AP, and CC performed literature search and draft the manuscript. PB, LL, and EC review and editing. LS and SC supervision the manuscript. All authors contributed to the article and approved the submitted version.
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
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References
1. Florin TA, Plint AC, Zorc JJ. Viral bronchiolitis. Lancet. (2017) 389:211–24. doi: 10.1016/S0140-6736(16)30951-5
2. Meissner HC. Viral bronchiolitis in children. N Engl J Med. (2016) 374:62–72. doi: 10.1056/NEJMra1413456
3. Baraldi E, Lanari M, Manzoni P, Rossi GA, Vandini S, Rimini A, et al. Inter-society consensus document on treatment and prevention of bronchiolitis in newborns and infants. Italian J Pediatr. (2014) 40:65. doi: 10.1186/1824-7288-40-65
4. Bronchiolitis in Children: Diagnosis Management. National Institute for Health and Care Excellence: Guidelines. London: National Institute for Health and Care Excellence (NICE) (2021). Available online at: http://www.ncbi.nlm.nih.gov/books/NBK573086/ (accessed August 4, 2021).
5. Ralston SL, Lieberthal AS, Meissner HC, Alverson BK, Baley JE, Gadomski AM, et al. Clinical practice guideline: the diagnosis, management, and prevention of bronchiolitis. Pediatrics. (2014) 134:e1474–e502. doi: 10.1542/peds.2014-2742
6. O'Brien S, Borland ML, Cotterell E, Armstrong D, Babl F, Bauert P, et al. Australasian bronchiolitis guideline. J Paediatr Child Health. (2019) 55:42–53. doi: 10.1111/jpc.14104
7. Rodríguez-Martínez CE, Castro-Rodriguez JA, Nino G, Midulla F. The impact of viral bronchiolitis phenotyping: Is it time to consider phenotype-specific responses to individualize pharmacological management? Paediatr Respir Rev. (2020) 34:53–8. doi: 10.1016/j.prrv.2019.04.003
8. Jartti T, Smits HH, Bønnelykke K, Bircan O, Elenius V, Konradsen JR, et al. Bronchiolitis needs a revisit: distinguishing between virus entities and their treatments. Allergy. (2019) 74:40–52. doi: 10.1111/all.13624
9. Polack FP, Stein RT, Custovic A. The syndrome we agreed to call bronchiolitis. J Infect Dis. (2019) 220:184–6. doi: 10.1093/infdis/jiz082
10. Petrarca L, Nenna R, Di Mattia G, Frassanito A, Castro-Rodriguez JA, Rodriguez Martinez CE, et al. Bronchiolitis phenotypes identified by latent class analysis may influence the occurrence of respiratory sequelae. Pediatr Pulmonol. (2022) 57:616–22. doi: 10.1002/ppul.25799
11. Smith DK, Seales S, Budzik C. Respiratory syncytial virus bronchiolitis in children. Am Fam Physician. (2017) 95:94–9.
12. Mansbach JM, Piedra PA, Teach SJ, Sullivan AF, Forgey T, Clark S, et al. Prospective multicenter study of viral etiology and hospital length of stay in children with severe bronchiolitis. Arch Pediatr Adolesc Med. (2012) 166:700–6. doi: 10.1001/archpediatrics.2011.1669
13. Miller EK, Gebretsadik T, Carroll KN, Dupont WD, Mohamed YA, Morin L-L, et al. Viral etiologies of infant bronchiolitis, croup and upper respiratory illness during 4 consecutive years. Pediatr Infect Dis J. (2013) 32:950–5. doi: 10.1097/INF.0b013e31829b7e43
14. Vandini S, Biagi C, Lanari M. Respiratory syncytial virus: the influence of serotype and genotype variability on clinical course of infection. Int J Mol Sci. (2017) 18:E1717. doi: 10.3390/ijms18081717
16. Lambert L, Sagfors AM, Openshaw PJ, Culley FJ. Immunity to RSV in early-life. Front Immunol. (2014) 5:466. doi: 10.3389/fimmu.2014.00466
17. Jartti T, Gern JE. Role of viral infections in the development and exacerbation of asthma in children. J Allergy Clin Immunol. (2017) 140:895–906. doi: 10.1016/j.jaci.2017.08.003
18. Rossi GA, Colin AA. Infantile respiratory syncytial virus and human rhinovirus infections: respective role in inception and persistence of wheezing. Eur Respir J. (2015) 45:774–89. doi: 10.1183/09031936.00062714
19. Kalinowski A, Galen B, Ueki I, Sun Y, Mulenos A, Osafo-Addo A, et al. Respiratory syncytial virus activates epidermal growth factor receptor to suppress interferon regulatory factor 1-dependent interferon-lambda and antiviral defence in airway epithelium. Mucosal Immunol. (2018) 11:958–67. doi: 10.1038/mi.2017.120
20. Thwaites RS, Coates M, Ito K, Ghazaly M, Feather C, Abdulla F, et al. Reduced nasal viral load and IFN responses in infants with RSV bronchiolitis and respiratory failure. Am J Respir Crit Care Med. (2018) 198:1074–84. doi: 10.1164/rccm.201712-2567OC
21. Mukherjee S, Lindell DM, Berlin AA, Morris SB, Shanley TP, Hershenson MB, et al. IL-17-induced pulmonary pathogenesis during respiratory viral infection and exacerbation of allergic disease. Am J Pathol. (2011) 179:248–58. doi: 10.1016/j.ajpath.2011.03.003
22. de Almeida Nagata DE, Demoor T, Ptaschinski C, Ting H-A, Jang S, Reed M, et al. IL-27R- mediated regulation of IL-17 controls the development of respira- tory syncytial virus-associated pathogenesis. Am J Pathol. (2014) 184:1807–18. doi: 10.1016/j.ajpath.2014.02.004
23. Midulla F, Nenna R, Scagnolari C, Petrarca L, Frassanito A, Viscido A, et al. How respiratory syncytial virus genotypes influence the clinical course in infants hospitalized for bronchiolitis. J Infect Dis. (2019) 219:526–34. doi: 10.1093/infdis/jiy496
24. Harford TJ, Rezaee F, Gupta MK, Bokun V, Naga Prasad SV, Piedimonte G. Respiratory syncytial virus induces b2-adrenergic receptor dysfunction in human airway smooth muscle cells. Sci Signal. (2021) 14:eabc1983. doi: 10.1126/scisignal.abc1983
25. Turunen R, Koistinen A, Vuorinen T, Arku B, Söderlund-Venermo M, Ruuskanen O, et al. The first wheezing episode: respiratory virus etiology, atopic characteristics, and illness severity. Pediatr Allergy Immunol. (2014) 25:796–803. doi: 10.1111/pai.12318
26. Dumas O, Mansbach JM, Jartti T, Hasegawa K, Sullivan AF, Piedra PA, et al. A clustering approach to identify severe bronchiolitis profiles in children. Thorax. (2016) 71:712–8. doi: 10.1136/thoraxjnl-2016-208535
27. Bønnelykke K, Sleiman P, Nielsen K, Kreiner-Møller E, Mercader JM, Belgrave D, et al. A genome-wide association study identifies CDHR3 as a susceptibility locus for early child- hood asthma with severe exacerbations. Nat Genet. (2014) 46:51–5. doi: 10.1038/ng.2830
28. Spann KM, Tran KC, Collins PL. Effects of nonstructural proteins NS1 and NS2 of human respiratory syncytial virus on interferon regulatory factor 3, NF-κB, and proinflammatory cytokines. J Virol. (2005) 79:5353–62. doi: 10.1128/JVI.79.9.5353-5362.2005
29. Nenna R, Frassanito A, Petrarca L, Di Mattia G, Pierangeli A, Scagnolari C, et al. RSV bronchiolitis in infants hospitalized during the epidemic peak and non-peak months: different Th1/Th2 response. Am J Respir Crit Care Med. (2018) 197:A2865.
30. McCulloh R, Koster M, Ralston S, Johnson M, Hill V, Koehn K, et al. Use of intermittent vs continuous pulse oximetry for nonhypoxemic infants and young children hospitalized for bronchiolitis: a randomized clinical trial. JAMA Pediatr. (2015) 169:898–904. doi: 10.1001/jamapediatrics.2015.1746
31. Thompson M, Vodicka TA, Blair PS, Buckley DI, Heneghan C, Hay AD, et al. Duration of symptoms of respiratory tract infections in children: systematic review. BMJ. (2013) 347:f7027. doi: 10.1136/bmj.f7027
32. Karampatsas K, Kong J, Cohen J. Bronchiolitis: an update on management and prophylaxis. Br J Hosp Med (Lond). (2019) 80:278–84. doi: 10.12968/hmed.2019.80.5.278
33. Paluch L. Identifying and managing bronchiolitis. J Am Acad Phys Assist. (2020) 33:12–5. doi: 10.1097/01.JAA.0000694944.22382.39
34. Ramagopal G, Brow E, Mannu A. Demographic, clinical and hematological profile of children with bronchiolitis: a comparative study between respiratory syncytial virus [RSV] and [Non RSV] groups. J Clin Diagn Res. (2016) 10: SC05–S8. doi: 10.7860/JCDR/2016/20331.8262
35. Kou M, Hwang V, Ramkellawan N. Bronchiolitis: from practice guideline to clinical practice. Emerg Med Clin North Am. (2018) 36:275–86. doi: 10.1016/j.emc.2017.12.006
36. Prodhan P, Sharoor-Karni S, Lin J, Noviski N. Predictors of respiratory failure among previously healthy children with respiratory syncytial virus infection. Am J Emerg Med. (2011) 29:168–73. doi: 10.1016/j.ajem.2009.08.020
37. Arroyo M, Salka K, Perez GF, Rodríguez-Martínez CE, Castro-Rodriguez JA, Gutierrez MJ Nino G. Phenotypical sub-setting of the first episode of severe viral respiratory infection based on clinical assessment and underlying airway disease: a pilot study. Front Pediatr. (2020) 8:121. doi: 10.3389/fped.2020.00121
38. Cunningham S, Rodriguez A, Adams T, Boyd KA, Butcher I, Enderby B, et al. Oxygen saturation targets in infants with bronchiolitis (BIDS): a double-blind, randomised, equivalence trial. Lancet. (2015) 386:1041–8. doi: 10.1016/S0140-6736(15)00163-4
39. Franklin D, Babl FE, Schlapbach LJ, Oakley E, Craig S, Neutze J, et al. A Randomized trial of high-flow oxygen therapy in infants with bronchiolitis. N Engl J Med. (2018) 378:1121–31. doi: 10.1056/NEJMoa1714855
40. Lin J, Zhang Y, Xiong L, Liu S, Gong C, Dai J. High-flow nasal cannula therapy for children with bronchiolitis: a systematic review and meta-analysis. Arch Dis Child. (2019) 104:564–76. doi: 10.1136/archdischild-2018-315846
41. Elliott SA, Gaudet LA, Fernandes RM, Vandermeer B, Freedman SB, Johnson DW, et al. Comparative efficacy of bronchiolitis interventions in acute care: a network meta-analysis. Pediatrics. (2021) 147:e2020040816. doi: 10.1542/peds.2020-040816
42. Wall MA. Bronchodilators and steroids should not be given in viral bronchiolitis - CON. Paediatr Respir Rev. (2019) 32:20–2. doi: 10.1016/j.prrv.2019.09.001
43. Brown MA. Bronchodilators and steroids should not be given in viral bronchiolitis - PRO. Paediatr Respir Rev. (2019) 32:18–9. doi: 10.1016/j.prrv.2019.09.002
44. Wolf ER, Richards A, Lavallee M, Sabo RT, Schroeder AR, Schefft M, et al. Patient, provider, and health care system characteristics associated with overuse in bronchiolitis. Pediatrics. (2021) 148:e2021051345. doi: 10.1542/peds.2021-051345
45. Gadomski AM, Scribani MB. Bronchodilators for bronchiolitis. Cochrane Database Syst Rev. (2014) 2014:CD001266. doi: 10.1002/14651858.CD001266.pub4
46. Nenna R, Frassanito A, Petrarca L, Di Mattia G, Midulla F. Age limit in bronchiolitis diagnosis: 6 or 12 months? Front. Pediatr. (2020) 8:144. doi: 10.3389/fped.2020.00144
47. Ferrante G, Fondacaro C, Cilluffo G, Dones P, Cardella F, Corsello G. Identification of bronchiolitis profiles in Italian children through the application of latent class analysis. Italian J Pediatr. (2020) 46:147. doi: 10.1186/s13052-020-00914-4
48. Rodríguez-Martínez CE, Nino G, Castro-Rodriguez JA, Acuña-Cordero R, Sossa-Briceño MP, Midulla F. For which infants with viral bronchiolitis could it be deemed appropriate to use albuterol, at least on a therapeutic trial basis? Allergol Immunopathol (Madr). (2021) 49:153–8. doi: 10.15586/aei.v49i1.12
49. Rodríguez-Martínez CE, Nino G, Castro-Rodriguez JA, Perez GF, Sossa-Briceño MP, Buendia JA. Cost-effectiveness analysis of phenotypic-guided versus guidelines-guided bronchodilator therapy in viral bronchiolitis. Pediatr Pulmonol. (2021) 56:187–95. doi: 10.1002/ppul.25114
50. Csonka P, Tapiainen T, Mäkelä MJ, Lehtimäki L. Optimal administration of bronchodilators with valved holding chambers in preschool children: a review of literature. Eur J Pediatr. (2021) 180:3101–9. doi: 10.1007/s00431-021-04074-3
51. Global Initiative for Asthma,. Global Strategy for Asthma Management Prevention. (2021). Available online at: http://www.ginasthma.org
52. Rodriguez-Martinez CE, Sossa-Briceno MP, Nino G. Systematic review of instruments aimed at evaluating the severity of bronchiolitis. Paediatr Respir Rev. (2018) 25:43–57. doi: 10.1016/j.prrv.2016.12.006
53. Alansari K, Sakran M, Davidson BL, Ibrahim K, Alrefai M, Zakaria I. Oral dexamethasone for bronchiolitis: a randomized trial. Pediatrics. (2013) 132:e810–6. doi: 10.1542/peds.2012-3746
54. Koistinen A, Lukkarinen M, Turunen R, Vuorinen T, Vahlberg T, Camargo CA, et al. Prednisolone for the first rhinovirus-induced wheezing and 4-year asthma risk: a randomized trial. Pediatr Allergy Immunol. (2017) 28:557–63. doi: 10.1111/pai.12749
55. Jartti T, Nieminen R, Vuorinen T, Lehtinen P, Vahlberg T, Gern J, et al. Short- and long-term efficacy of prednisolone for first acute rhinovirus-induced wheezing episode. J Allergy Clin Immunol. (2015) 135:691–8.e9. doi: 10.1016/j.jaci.2014.07.001
56. Hurme P, Homil K, Lehtinen P, Turunen R, Vahlberg T, Vuorinen T, et al. Efficacy of inhaled salbutamol with and without prednisolone for first acute rhinovirus-induced wheezing episode. Clin Exp Allergy. (2021) 51:1121–32. doi: 10.1111/cea.13960
57. Dumas O, Erkkola R, Bergroth E, Hasegawa K, Mansbach JM, Piedra PA, et al. Severe bronchiolitis profiles and risk of asthma development in Finnish children. J Allergy Clin Immunol. (2021). doi: 10.1016/j.jaci.2021.08.035. [Epub ahead of print].
Keywords: bronchiolitis, guideline, viral bronchiolitis phenotype, bronchodilator, valved holding chambers
Citation: Bottau P, Liotti L, Laderchi E, Palpacelli A, Calamelli E, Colombo C, Serra L and Cazzato S (2022) Something Is Changing in Viral Infant Bronchiolitis Approach. Front. Pediatr. 10:865977. doi: 10.3389/fped.2022.865977
Received: 30 January 2022; Accepted: 23 March 2022;
Published: 14 April 2022.
Edited by:
Renato Cutrera, Bambino Gesù Children's Hospital (IRCCS), ItalyReviewed by:
Raffaella Nenna, Sapienza University of Rome, ItalyHeidi Makrinioti, Chelsea and Westminster Hospital NHS Foundation Trust, United Kingdom
Jose A. Castro-Rodriguez, Pontificia Universidad Católica de Chile, Chile
Copyright © 2022 Bottau, Liotti, Laderchi, Palpacelli, Calamelli, Colombo, Serra and Cazzato. 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: Paolo Bottau, paolo.bottau@gmail.com
†These authors have contributed equally to this work and share first authorship
‡These authors share senior authorship