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POSITION STATEMENT

Bronchiolitis: Recommendations for diagnosis, monitoring and management of children one to 24 months of age

Posted: Nov 3 2014 Reaffirmed: Jan 30 2017

The Canadian Paediatric Society gives permission to print single copies of this document from our website. For permission to reprint or reproduce multiple copies, please see our copyright policy.

Principal author(s)

Jeremy N Friedman, Michael J Rieder, Jennifer M Walton; Canadian Paediatric Society, Acute Care Committee, Drug Therapy and Hazardous Substances Committee
Paediatr Child Health 2014;19(9):485-91

Abstract

Bronchiolitis is the most common reason for admission to hospital in the first year of life. There is tremendous variation in the clinical management of this condition across Canada and around the world, including significant use of unnecessary tests and ineffective therapies. This statement pertains to generally healthy children ≤2 years of age with bronchiolitis. The diagnosis of bronchiolitis is based primarily on the history of illness and physical examination findings. Laboratory investigations are generally unhelpful. Bronchiolitis is a self-limiting disease, usually managed with supportive care at home. Groups at high risk for severe disease are described and guidelines for admission to hospital are presented. Evidence for the efficacy of various therapies is discussed and recommendations are made for management. Monitoring requirements and discharge readiness from hospital are also discussed.

Key Words: Respiratory distress; RSV; URTI; Wheezing

Bronchiolitis is a viral lower respiratory tract infection characterized by obstruction of small airways caused by acute inflammation, edema and necrosis of the epithelial cells lining the small airways as well as increased mucus production.[1] Respiratory syncytial virus (RSV) is responsible for most cases.[2][3] However, other viruses, including human metapneumovirus (HMPV), influenza, rhinovirus, adenovirus and parainfluenza can all cause a similar clinical picture.[4] Coinfection with multiple viruses occurs in 10% to 30% of young hospitalized children.[5] Primary infection does not confer protective immunity and reinfections continue to occur into adulthood, with repeat infections being generally milder. In Canada, RSV season usually begins between November and January, and persists for four to five months.[6]

Bronchiolitis affects more than one-third of children in the first two years of life and is the most common cause for admission to hospital in their first year. Over the past 30 years, hospitalization rates have increased from 1% to 3% of all infants.[1][7][8] Rising admissions have been costly for the health care system,[9] and reflect significant morbidity[10] and impact on families.

Despite the existence of numerous clinical practice guidelines, including the often-quoted American Academy of Pediatrics (AAP) clinical practice guideline published in 2006,[1] there is tremendous variation[11] in approaches to diagnosis, monitoring and management. Initiatives to standardize care for bronchiolitis[12] have demonstrated decreased use of diagnostic testing and resource utilization, along with cost reduction and improved outcomes.[7][13] However, while there has been some decrease in testing and treatments since the release of the AAP recommendations,[14] uptake has not been widespread.

The goals of this statement are to build on the comprehensive peer-reviewed AAP statement[1] by incorporating new evidence published over the past eight years, while providing the clinician with recommendations to help guide diagnosis, monitoring and management of previously healthy children one to 24 months of age who present with signs of bronchiolitis (Figure 1). These recommendations are intended to support a decrease in the use of unnecessary diagnostic studies and ineffective medications and interventions. This statement does not apply to children with chronic lung disease, immunodeficiency or other serious underlying chronic disease. The prevention of and potential long-term effects from bronchiolitis are beyond the scope of this statement but are well described in the literature and other statements from the Canadian Paediatric Society.[4][6]

Diagnosis

Bronchiolitis is a clinical diagnosis based on a directed history and physical examination. Bronchiolitis may present with a wide range of symptoms and severity, from a mild upper respiratory tract infection (URTI) to impending respiratory failure (Table 1). Bronchiolitis typically presents with a first episode of wheezing before the age of 12 months. The course begins with a two-to-three-day viral prodrome of fever, cough and rhinorrhea progressing to tachypnea, wheeze, crackles and a variable degree of respiratory distress. Signs of respiratory distress may include grunting, nasal flaring, indrawing, retractions or abdominal breathing. There may or may not be a history of exposure to an individual with a viral URTI.

TABLE 1
History, symptoms and signs of viral bronchiolitis
Preceding viral upper respiratory tract infection, cough and/or rhinorrhea
Exposure to an individual with viral upper respiratory tract infection

Signs of respiratory illness may also include:

  • Tachypnea
  • Intercostal and/or subcostal retractions
  • Accessory muscle use
  • Nasal flaring
  • Grunting
  • Colour change or apnea
  • Wheezing or crackles
  • Lower O2 saturations
TABLE 2
Differential diagnosis for wheezing in young children
Viral bronchiolitis
Asthma
Other pulmonary infections (eg, pneumonia)
Laryngotracheomalacia
Foreign body aspiration
Gastroesophageal reflux
Congestive heart failure
Vascular ring
Allergic reaction
Cystic fibrosis
Mediastinal mass
Tracheoesophageal fistula
Adapted from reference 7

Physical examination findings of importance include increased respiratory rate, signs of respiratory distress, and crackles and wheezing on auscultation. Measurement of oxygen saturation often shows decreased saturation levels. Signs of dehydration may be present if respiratory distress has been sufficient to interfere with feeding.

While the majority of wheezing infants who present acutely between November and April most likely have viral bronchiolitis, clinicians should consider a broad differential diagnosis, especially in patients with atypical presentations such as severe respiratory distress, no viral URTI symptoms and/or frequent recurrences (Table 2).[7]

Investigations

Diagnostic studies are not indicated for most children with bronchiolitis (Table 3). Tests are often unhelpful and can lead to unnecessary admissions, further testing and ineffective therapies. Evidence-based reviews have not supported the use of diagnostic testing in typical cases of bronchiolitis.[1][7]

Chest radiograph (CXR) of infants with bronchiolitis often reveals nonspecific, patchy hyperinflation and areas of atelectasis,[4] which may be misinterpreted as consolidation. This can lead to increased and inappropriate use of antibiotics.[15] In infants with typical bronchiolitis, a recent prospective study found CXR findings inconsistent with bronchiolitis in only two of 265 infants, and in no case did the results change acute management.[16] While routine CXR is not supported by current evidence, it should be considered when the diagnosis of bronchiolitis is unclear, the rate of improvement is not as expected or the severity of disease raises other diagnostic possibilities such as bacterial pneumonia.

Nasopharyngeal swabs for respiratory viruses generally are not helpful from a diagnostic perspective and do not alter management in most cases. They are not routinely recommended unless required for infection control (ie, the cohorting of hospitalized patients). Recently, however, the high rate of coinfection with multiple viruses has called even this indication into question.[17]

Complete blood count has not been found to be useful in predicting serious bacterial infections (SBI).[18]

Bacterial cultures: The incidence of concomitant SBI is believed to be very low, but not insignificant, in febrile infants with bronchiolitis.[7][19]-[21] Infants in their first two months of life have the greatest risk of SBI, especially urinary tract infection.[19]-[22] Rates vary from 0% to 6.1%. Bacteremia is rare (<1%) in most studies. Meningitis complicating bronchiolitis is also extremely rare. A study in the office setting of febrile infants with bronchiolitis found no cases of SBI out of 125 patients with bronchiolitis, compared with 212 of 1933 (11%) in a febrile group of similar age without bronchiolitis.[19]

TABLE 3
Role of diagnostic studies in typical cases of bronchiolitis
TypeSpecific indications
Chest radiographOnly if severity or course suggests alternate diagnosis
(Table 2)
Nasopharyngeal swabsOnly if required for cohorting admitted patients
Complete blood countGenerally not helpful in diagnosis or monitoring of routine cases
Blood gasOnly if concerned about potential respiratory failure
Bacterial culturesNot recommended routinely; may be required based on clinical findings and a child’s age.

Decision to admit

The decision to admit should be based on clinical judgment and consider the infant’s respiratory status, ability to maintain adequate hydration, risk for progression to severe disease and the family’s ability to cope (Tables 4 and 5). Physicians should keep in mind that the disease tends to worsen over the first 72 h when deciding whether to hospitalize.[23] Clinical scores and individual findings on physical examination cannot be relied on in isolation to predict outcomes. Severity scoring systems exist; however, none are widely used and few have demonstrated predictive validity. Respiratory rate, subcostal retractions and oxygen need may be the most helpful parameters used in the various bronchiolitis severity scores.[24]

Repeated observations over a period of time are important because there may be significant temporal variability. Consistent predictors of hospitalization in outpatient populations[7][25] include age (<3 months) and history of prematurity (<35 weeks’ gestation). Another study found that patients with any three of the following four factors – decreased hydration, accessory muscle score >6 of 9, O2 saturation <92% and respiratory rate >60 breaths/min – had a 13-fold increase in hospitalization rate.[26]

The role of pulse oximetry in clinical decision-making remains controversial. While oxygen saturations of <94% are associated with a more than five-fold increase in likelihood of admission,[25] it is important to recognize that setting arbitrary thresholds for oxygen therapy will influence admission rates. This effect was illustrated in a survey of emergency department physicians that showed a significant increase in the likelihood of recommending admission by simply reducing saturation from 94% to 92% in clinical vignettes.[27]

TABLE 4
Groups at higher risk for severe disease
Infants born prematurely (<35 weeks’ gestation)
<3 months of age at presentation
Hemodynamically significant cardiopulmonary disease
Immunodeficiency
TABLE 5
Guidelines for admission may include
Signs of severe respiratory distress (eg, indrawing, grunting, RR >70/min)
Supplemental O2 required to keep saturations >90%
Dehydration or history of poor fluid intake
Cyanosis or history of apnea
Infant at high risk for severe disease (Table 4)
Family unable to cope

Management

Bronchiolitis is a self-limiting disease. Most children have mild disease and can be managed with supportive care at home. For those requiring admission, supportive care with assisted feeding, minimal handling, gentle nasal suctioning and oxygen therapy still forms the mainstay of treatment (Table 6).

TABLE 6
Treating bronchiolitis
RecommendedEvidence equivocalNot recommended

Oxygen

Hydration

Epinephrine nebulization

Nasal suctioning

3% hypertonic saline nebulization

Combined epinephrine and dexamethasone

Salbutamol (Ventolin; GlaxoSmithKline, USA)

Corticosteroids

Antibiotics

Antivirals

Cool mist therapies or therapy with saline aerosol

TABLE 7
Discharge from hospital
Tachypnea and work of breathing improved
Maintain O2 saturations >90% without supplemental oxygen OR stable for home oxygen therapy
Adequate oral feeding
Education provided and appropriate follow-up arranged

Therapies recommended based on evidence

Oxygen

Supplemental oxygen therapy is a mainstay of treatment in hospital. Oxygen should be administered if saturations fall below 90% and used to maintain saturations at ≥90%.[1] To minimize handling, oxygen is usually administered via nasal cannulae, face mask or a head box. A recent alternative is humidified high-flow nasal cannula therapy,[28] which may be better tolerated and potentially decrease the need for mechanical ventilation.[29][30] At this point, there is insufficient evidence to determine effectiveness.[31] There are, however, ongoing studies investigating this question, which will likely help to guide practice in the near future.

Hydration

Some degree of fluid supplementation is required in 30% of hospitalized patients with bronchiolitis.[32]

Frequent feeds should be encouraged and breastfeeding supported; both may be facilitated by providing supplemental oxygen. Infants with a respiratory rate >60 breaths/min, particularly those with nasal congestion, may have an increased risk of aspiration and may not be safe to feed orally.[1] When supplemental fluids are required, a recent randomized trial found nasogastric (NG) and intravenous (IV) routes to be equally effective, with no difference in length of hospital stay.[33] NG insertion may require fewer attempts and have a higher success rate than IV placement. If NG bolus feeds are not tolerated, slow continuous feeds are an option. If the IV route is used, isotonic fluids (0.9% NaCl/5% dextrose) are preferred for maintenance, with regular monitoring of serum Na[34] because of the risk of hyponatremia.[35]

Therapies for which evidence is equivocal

Epinephrine

Some studies have shown that epinephrine nebulization may be effective for reducing hospital admissions,[36] and one trial showed that combined treatment with epinephrine and steroids reduced admissions.[37] However, the evidence remains insufficient to support routine use of epinephrine in the emergency department. It may be reasonable to administer a dose of epinephrine and carefully monitor clinical response; however, unless there is clear evidence of improvement, continued use is not appropriate. A systematic review of 19 studies evaluating the use of epinephrine in bronchiolitis shows no effect on length of hospital stay[36] and there is insufficient evidence to support its routine use in admitted patients.

Nasal suctioning

As for many long-standing and commonly used therapies for children, there is scant evidence supporting the use of nasal suctioning in the management of bronchiolitis. While it appears that suctioning mucus out of blocked nares would be a harmless procedure, one recent study has suggested that deep suctioning and long intervals between suctioning are associated with increased length of stay.[38] This suggests that if suctioning is performed, it should be done superficially and reasonably frequently.

3% hypertonic saline nebulization

The value of nebulized 3% hypertonic saline is being strongly debated and definitive recommendations will likely require further accumulation of evidence. It is hypothesized that hypertonic saline increases mucociliary clearance and rehydrates airway surface liquid, and there is evidence of reduced clinical severity scores in both inpatient and outpatient populations with no reports of significant adverse events.[39] A Cochrane review of 11 trials found that nebulized hypertonic saline was associated with a reduced length of stay of one day in settings where the admission was longer than three days. The optimal treatment regimen remains unclear. The most commonly used regimen in most trials has been 3% saline with or without added bronchodilator by jet nebulizer three times daily, with an interval of 8 h between treatments. Further studies since the Cochrane review have shown mixed results.[40][41] Nebulized 3% saline may be helpful in the inpatient setting; this treatment appears primarily to benefit patients with a longer length of stay. Evidence does not currently support its routine use in the outpatient setting.

Combination epinephrine and dexamethasone

One publication from the Pediatric Emergency Research Canada group found an unexpected synergism between the administration of nebulized epinephrine with oral dexamethasone. The combination appeared to result in a reduced hospitalization rate, with a number needed to treat of 11. However, these results were rendered nonsignificant when adjusted for multiple comparisons.[37] More research is needed to assess the role of combination therapies. Pending better definition of its risks and benefits, this combination is not recommended for the therapy of otherwise healthy children with bronchiolitis.

Therapies not recommended based on evidence

Salbutamol (Ventolin; GlaxoSmithKline, USA)

Children with bronchiolitis present with a wheeze that is clinically similar to that observed with asthma. However, the pathophysiology of bronchiolitis is such that the airways are obstructed[7][42] rather than constricted. Furthermore, infants appear to have inadequate β-agonist lung receptor sites and immature bronchiolar smooth muscles.[43] While studies have shown small improvements in clinical scores, bronchodilators have not been shown to improve O2 saturation, do not reduce admission rates and do not shorten the duration of stay in hospital.[42] When the diagnosis of bronchiolitis is clear, a trial of salbutamol is not currently recommended.[1]

Corticosteroids

Corticosteroids, such as dexamethasone, prednisone or inhaled glucocorticoids, are not associated with a clinically significant improvement in disease, as measured by reduction in clinical scores, rates of hospitalization and length of hospital stay.[1][23][44]-[46] Furthermore, any small benefit that corticosteroids may offer must be weighed against the risks of steroid treatment. Corticosteroids are not recommended for routine use in bronchiolitis.

Antibiotics

Many children with acute bronchiolitis are prescribed an antibiotic. However, bacterial infection in otherwise healthy children with bronchiolitis is exceedingly rare.[46] Research on the role of antibiotics in bronchiolitis is limited and has, to date, failed to identify any benefit. Further research is needed to develop criteria for identifying the minority of patients at high risk for secondary bacterial infection.[46] Currently, antibiotics should not be used except in cases in which there is clear, documented evidence of a secondary bacterial infection.[1]

Antivirals

Antiviral therapies, such as ribavirin, are expensive, cumbersome to administer, provide limited benefit and are potentially toxic to care providers and, thus, are not recommended for the routine treatment of bronchiolitis in otherwise healthy children.[1] In patients with or at risk for particularly severe disease, antivirals could be considered, but this decision should be made on an individual basis in consultation with appropriate subspecialists.[1][47][48]

Chest physiotherapy

Nine clinical trials comparing physiotherapy with no treatment were reviewed.[49] Neither vibration and percussion nor passive expiratory techniques were shown to improve clinical scores or to reduce hospital stay or duration of symptoms. Chest physiotherapy is not recommended for the treatment of bronchiolitis.[1][49]

Cool mist therapies or aerosol therapy with isotonic saline

Cool mist and other aerosol therapies have been used for some time to manage bronchiolitis, with scant evidence supporting their efficacy. A recent Cochrane review concluded that there is no evidence supporting or refuting the use of cool mist and other aerosols for managing bronchiolitis.[50]

Other therapies used for critically ill infants with severe bronchiolitis, such as helium/oxygen, nasal continuous positive airway pressure, mechanical ventilatory support and surfactant, are beyond the scope of this statement.[51]-[53]

Monitoring in hospital

Patients with bronchiolitis should be cared for in an environment with ready access to suction equipment and supplemental oxygen that can be delivered at measurable rates. Close attention must be devoted to infection control processes. Respiratory contact isolation may reduce nosocomial transmission, but there is conflicting evidence regarding the benefits of cohorting patients.[2][8][54][55]

The most important component of monitoring infants admitted with bronchiolitis is regular and repeated clinical assessments by staff with appropriate expertise in the respiratory assessment of young children. Monitoring should include assessment and documentation of respiratory rate, work of breathing, oxygen saturation, findings on auscultation and general condition, including feeding and hydration status. Scoring tools have been developed in an attempt to standardize assessments and facilitate communication among caregivers. However, there is insufficient evidence of impact on patient outcomes to recommend using any specific tool.[56]-[58]

The use of electronic monitoring of vital signs and oxygen saturation should not be considered to be a substitute for regular clinical assessments by experienced personnel. Furthermore, there is growing evidence to suggest that continuous monitoring may prolong length of stay, particularly if staff react to normal transient dips in oxygen saturation or changes in heart and respiratory rates with interventions such as restarting oxygen therapy.[59] The accuracy of pulse oximetry is relatively poor, particularly at saturations <90%.[60]

The primary rationale for cardiac and respiratory monitoring is to detect episodes of apnea requiring intervention. The incidence of apnea in RSV bronchiolitis may be lower than previously believed. In a large study involving 691 infants <6 months of age, only 2.7% had documented apnea, and all had risk criteria of either a previous apneic episode or young age (<1 month or <48 weeks postconception in premature infants).[61] Continuous electronic cardiac and respiratory monitoring may be useful for high-risk patients in the acute phase of illness but are not necessary for the vast majority of patients with bronchiolitis.

Determining oxygen saturation can aid in decisions about escalating or weaning oxygen therapy. However, the issue of continuous versus intermittent monitoring of oxygen saturation is controversial. Continuous monitoring may be more sensitive for identifying patients who are deteriorating and need escalation of treatment. At the same time, many healthy infants exhibit typical transient O2 saturation dips[62][63] and length of stay may be prolonged if oxygen therapy is based on arbitrary saturation targets. Several clinical trials currently underway are attempting to determine best practices in this area. Until clear evidence is available, a reasonable approach is to adjust the intensity of oxygen saturation monitoring according to the patient’s clinical status. Continuous saturation monitoring is appropriate for high-risk patients early in the course of disease, while intermittent monitoring is most appropriate for lower-risk patients and for all patients once they are feeding well, weaning from supplemental oxygen and showing improvement in work of breathing.

Figure 1) Algorithm for medical management of bronchiolitis. D/C Discharge; F/U Follow-up; IV Intravenous; NG Nasogastric; SaO2 Oxygen saturation. Adapted with permission from reference 12

Readiness for discharge from hospital should be based on clinical judgement and consider the family’s ability to recognize and respond to signs of deterioration. In general, patients may be safely discharged from hospital once they are improving clinically and meet criteria listed in Table 7.

Conclusions

The optimal management of bronchiolitis for otherwise healthy children has been debated for some time. In a seminal review published in 1965, the admonition was made to use patience and avoid unnecessary and futile therapy.[64] This prudent advice has been ignored frequently over the past 50 years.[65] The optimal management of bronchiolitis in otherwise healthy children remains nested, first and foremost, in excellent supportive care. While trials investigating other modalities are ongoing, the health care provider is reminded that ‘primum non nocere’ should remain the key dictum in the treatment of otherwise healthy children with bronchiolitis.

Recommendations

  • Bronchiolitis is a clinical diagnosis based on history and physical examination. Diagnostic studies, including chest radiograph, blood tests and viral/bacterial cultures, are not recommended in typical cases.
  • The decision to admit to hospital should be based on clinical judgment, factoring in the risk for progression to severe disease, respiratory status, ability to maintain adequate hydration and the family’s ability to cope at home.
  • Management is primarily supportive including hydration, minimal handling, gentle nasal suctioning and oxygen therapy.
  • If using IV fluids for hydration, an isotonic solution (0.9% NaCl/5% dextrose) is recommended, together with routine monitoring of serum Na.
  • The use of epinephrine is not recommended in routine cases. If a trial of epinephrine inhalation is attempted in the emergency department, ongoing treatment should only occur if there are clear signs of clinical improvement.
  • Current evidence does not support a firm recommendation for hypertonic 3% sodium chloride. There is insufficient evidence to support its use in an ambulatory setting, but some evidence suggesting potential benefit in children hospitalized >3 days.
  • The use of salbutamol (Ventolin) is not recommended in routine cases.
  • The use of corticosteroids is not recommended in routine cases.
  • The use of antibiotics is not recommended unless there is suspicion of an underlying bacterial infection.
  • The use of chest physiotherapy is not recommended.
  • Thoughtful use of oxygen saturation monitoring in hospitalized patients is recommended. Continuous saturation monitoring may be indicated for high-risk children in the acute phase of illness, and intermittent monitoring or spot checks are appropriate for lower-risk children and patients who are improving clinically.

Acknowledgements

This position statement was reviewed by the Community Paediatrics Committee and the Hospital Paediatrics and Emergency Medicine Sections of the Canadian Paediatric Society, as well as by representatives of the College of Family Physicians of Canada.

CPS ACUTE CARE COMMITTEE
Members:
Laurel Chauvin-Kimoff MD (Chair), Isabelle Chevalier MD (Board Representative), Catherine A Farrell MD, Jeremy N Friedman MD, Angelo Mikrogianakis MD (past Chair), Oliva Ortiz-Alvarez MD
Liaisons: Dominic Allain MD, CPS Paediatric Emergency Medicine Section; Tracy MacDonald BScN, Canadian Association of Paediatric Health Centres; Jennifer M Walton MD, CPS Hospital Paediatrics Section

CPS DRUG THERAPY AND HAZARDOUS SUBSTANCES COMMITTEE
Members: Mark L Bernstein MD, François Boucher MD (Board Representative), Ran D Goldman MD, Geer’t Jong MD, Philippe Ovetchkine MD, Michael J Rieder MD (Chair),
Liaisons: Daniel Louis Keene MD, Health Canada; Doreen Matsui MD (past Chair)
Principal authors: Jeremy N Friedman MD, Michael J Rieder MD, Jennifer M Walton MD

References

  1. American Academy of Pediatrics, Subcommittee on Diagnosis and Management of Bronchiolitis. Diagnosis and management of bronchiolitis. Pediatrics 2006;118(4):1774-93.
  2. Hall CB, Weinberg GA, Iwane MK, et al. The burden of respiratory syncytial virus infection in young children. N Engl J Med 2009;360(6):588-98.
  3. Henrickson KJ. Advances in the laboratory diagnosis of viral respiratory disease. Pediatr Infect Dis J 2004;23(1 Suppl):S6-10.
  4. Smyth RL, Openshaw PJ. Bronchiolitis. Lancet 2006;368(9532):312-22.
  5. Paranhos-Baccalà G, Komurian-Pradel F, Richard N, Vernet G, Lina B, Floret D. Mixed respiratory virus infections. J Clin Virol 2008;43(4):407-10.
  6. Robinson J; Canadian Paediatric Society, Infectious Diseases and Immunization Committee. Preventing respiratory syncytial virus infections. Paediatr Child Health 2011;16(8):487-8: http://www.cps.ca/en/documents/position/preventing-rsv (Accessed September 18, 2014).
  7. Zorc JJ, Hall CB. Bronchiolitis: Recent evidence on diagnosis and management. Pediatrics 2010;125(2):342-9.
  8. Shay DK, Holman RC, Newman RD, Liu LL, Stout JW, Anderson LJ. Bronchiolitis-associated hospitalizations among US children, 1980-1996. JAMA 1999;282(15):1440-6.
  9. Stang P, Brandenburg N, Carter B. The economic burden of respiratory syncytial virus-associated bronchiolitis hospitalizations. Arch Pediatr Adolesc Med 2001;155(1):95-6.
  10. Leader S, Yang H, DeVincenzo J, Jacobson P, Marcin JP, Murray DL. Time and out-of-pocket costs associated with respiratory syncytial virus hospitalization of infants. Value Health 2003;6(2):100-6.
  11. Christakis DA, Cowan CA, Garrison MM, Molteni R, Marcuse E, Zerr DM. Variation in inpatient diagnostic testing and management of bronchiolitis. Pediatrics 2005;115(4):878-84.
  12. Bronchiolitis Guideline Team, Cincinnati Children’s Hospital Medical Center, November 2010. Evidence-based care guideline for management of bronchiolitis in infants one year of age or less with a first time episode. 1-16: http://www.cincinnatichildrens.org/WorkArea/DownloadAsset.aspx?id=87885 (Accessed September 24, 2014).
  13. Todd J, Bertoch D, Dolan S. Use of a large national database for comparative evaluation of the effect of a bronchiolitis/viral pneumonia clinical care guideline on patient outcome and resource utilization. Arch Pediatr Adolesc Med 2002;156(11):1086-90.
  14. Parikh K, Hall M, Teach SJ. Bronchiolitis management before and after the AAP guidelines. Pediatrics 2014;133(1):e1-7.
  15. Swingler GH, Hussey GD, Zwarenstein M. Randomised controlled trial of clinical outcome after chest radiograph in ambulatory acute lower-respiratory infection in children. Lancet 1998;351(9100):404-8.
  16. Schuh S, Lalani A, Allen U, et al. Evaluation of the utility of radiography in acute bronchiolitis. J Pediatr 2007;150(4):429-33.
  17. Mansbach JM, Piedra PA, Teach SJ, et al. Prospective, multicenter study of viral etiology and hospital length-of-stay in children with severe bronchiolitis. Arch Pediatr Adolesc Med 2012;166(8):700-6.
  18. Purcell K, Fergie J. Lack of usefulness of an abnormal white blood cell count for predicting a concurrent serious bacterial infection in infants and young children hospitalized with respiratory syncytial virus lower respiratory tract infection. Pediatr Infect Dis J 2007;26(4):311-5.
  19. Luginbuhl LM, Newman TB, Pantell RH, Finch SA, Wasserman RC. Office-based treatment and outcomes for febrile infants with clinically diagnosed bronchiolitis. Pediatrics 2008;122(5):947-54.
  20. Levine DA, Platt SL, Dayan PS, et al. Risk of serious bacterial infection in young febrile infants with respiratory syncytial virus infections. Pediatrics 2004;113(6):1728-34.
  21. Bilavsky E, Shouval DS, Yarden-Bilavsky H, Fisch N, Ashkenazi S, Amir J. A prospective study of the risk for serious bacterial infections in hospitalized febrile infants with or without bronchiolitis. Pediatr Infect Dis J 2008;27(3):269-70.
  22. Melendez E, Harper MB. Utility of sepsis evaluation in infants 90 days of age or younger with fever and clinical bronchiolitis. Pediatr Infect Dis J 2003;22(12):1053-6.
  23. Wainwright C. Acute viral bronchiolitis in children: A very common condition with few therapeutic options. Paediatr Respir Rev 2010;11(1):39-45; quiz 45.
  24. Destino L, Weisgerber MC, Soung P, et al. Validity of respiratory scores in bronchiolitis. Hosp Pediatr 2012;2(4):202-9.
  25. Mansbach JM, Clark S, Christopher NC, et al. Prospective multicenter study of bronchiolitis: Predicting safe discharges from the emergency department. Pediatrics 2008;121(4):680-8.
  26. Parker MJ, Allen U, Stephens D, Lalani A, Schuh S. Predictors of major intervention in infants with bronchiolitis. Pediatr Pulmonol 2009;44(4):358-63.
  27. Mallory MD, Shay DK, Garrett J, Bordley WC. Bronchiolitis management preferences and the influence of pulse oximetry and respiratory rate on the decision to admit. Pediatrics 2003;111(1):e45-51.
  28. Mayfield S, Bogossian F, O’Malley L, Schibler A. High-flow nasal cannula oxygen therapy for infants with bronchiolitis: Pilot study. J Paediatr Child Health 2014;50(5):373-8.
  29. McKiernan C, Chua LC, Visintainer PF, Allen H. High-flow nasal cannulae therapy in infants with bronchiolitis. J Pediatr 2010;156(4):634-8.
  30. Hilliard TN, Archer N, Laura H, et al. Pilot study of vapotherm oxygen delivery in moderately severe bronchiolitis. Arch Dis Child 2012;97(2):182-3.
  31. Beggs S, Wong ZH, Kaul S, Ogden KJ, Walters JA. High-flow nasal cannula therapy for infants with bronchiolitis. Cochrane Database Syst Rev 2014;(1):CD009609.
  32. Kennedy N, Flanagan N. Is nasogastric fluid therapy a safe alternative to the intravenous route in infants with bronchiolitis? Arch Dis Child 2005;90(3):320-1.
  33. Oakley E, Borland M, Neutze J, et al. Nasogastric hydration versus intravenous hydration for infants with bronchiolitis: A randomised trial. Lancet Respir Med 2013;1(2):113-20.
  34. Friedman JN; Canadian Paediatric Society, Acute Care Committee. Risk of acute hyponatremia in hospitalized children and youth receiving maintenance intravenous fluids. Paediatr Child Health 2013;18(2):102-7.
  35. Wang J, Xu E, Xiao Y. Isotonic versus hypotonic maintenance IV fluids in hospitalized children: A meta-analysis. Pediatrics 2014;133(1):105-13.
  36. Hartling L, Bialy LM, Vandermeer B, et al. Epinephrine for bronchiolitis. Cochrane Database Syst Rev 2011(6):CD003123.
  37. Plint AC, Johnson DW, Patel H, et al. Epinephrine and dexamethasone in children with bronchiolitis. N Engl J Med 2009;360(20):2079-89.
  38. Mussman GM, Parker MW, Statile A, Sucharew H, Brady PW. Suctioning and length of stay in infants hospitalized with bronchiolitis. JAMA Pediatr 2013;167(5):414-21.
  39. Zhang L, Mendoza-Sassi RA, Wainwright C, Klassen TP. Nebulised hypertonic saline solution for acute bronchiolitis in infants. Cochrane Database Syst Rev 2013;(7):CD006458.
  40. Wu S, Baker C, Lang ME, et al. Nebulized hypertonic saline for bronchiolitis: A randomized clinical trial. JAMA Pediatr 2014;168(7):657-63.
  41. Florin TA, Shaw KN, Kittick M, Yakscoe S, Zorc JJ. Nebulized hypertonic saline for bronchiolitis in the emergency department: A randomized clinical trial. JAMA Pediatr 2014;168(7):664-70.
  42. Gadomski AM, Scribani MB. Bronchodilators for bronchiolitis. Cochrane Database Syst Rev 2014;(6):CD001266.
  43. Anil AB, Anil M, Saglam AB, Cetin N, Bal A, Aksu N. High volume normal saline alone is as effective as nebulized salbutamol-normal saline, epinephrine-normal saline, and 3% saline in mild bronchiolitis. Pediatr Pulmonol 2010;45(1):41-7.
  44. Fernandes RM, Bialy LM, Vandermeer B, et al. Glucocorticoids for acute viral bronchiolitis in infants and young children. Cochrane Database Syst Rev 2013;(6):CD004878.
  45. Corneli HM, Zorc JJ, Mahajan P, et al. A multicenter, randomized, controlled trial of dexamethasone for bronchiolitis. N Engl J Med 2007;357(4):331-9.
  46. Spurling GK, Doust J, Del Mar CB, Eriksson L. Antibiotics for bronchiolitis in children. Cochrane Database Syst Rev 2011(6):CD005189.
  47. Li L, Avery R, Budev M, Mossad S, Danziger-Isakov L. Oral versus inhaled ribavirin therapy for respiratory syncytial virus infection after lung transplantation. J Heart Lung Transplant
  48. 2012;31(8):839-44.
  49. Turner TL, Kopp BT, Paul G, Landgrave LC, Hayes D Jr, Thompson R. Respiratory syncytial virus: Current and emerging treatment options. Clinicoecon Outcomes Res 2014;6:217-25.
  50. Roqué i Figuls M, Giné-Garriga M, Granados Rugeles C, Perrotta C. Chest physiotherapy for acute bronchiolitis in paediatric patients between 0 and 24 months old. Cochrane Database Syst Rev 2012;(2):CD004873.
  51. Umoren R, Odey F, Meremikwu MM. Steam inhalation or humidified oxygen for acute bronchiolitis in children up to three years of age. Cochrane Database Syst Rev 2011(1):CD006435.
  52. Essouri S, Laurent M, Chevret L, et al. Improved clinical and economic outcomes in severe bronchiolitis with pre-emptive nCPAP ventilatory strategy. Intensive Care Med 2014;40(1):84-91.
  53. Essouri S, Durand P, Chevret L, et al. Optimal level of nasal continuous positive airway pressure in severe viral bronchiolitis. Intensive Care Med 2011;37(12):2002-7.
  54. Donlan M, Fontela PS, Puligandla PS. Use of continuous positive airway pressure (CPAP) in acute viral bronchiolitis: A systematic review. Pediatr Pulmonol 2011;46(8):736-46.
  55. Madge P, Paton JY, McColl JH, Mackie PL. Prospective controlled study of four infection-control procedures to prevent nosocomial infection with respiratory syncytial virus. Lancet 1992;340(8827):1079-83.
  56. Krasinski K, LaCouture R, Holzman RS, Waithe E, Bonk S, Hanna B. Screening for respiratory syncytial virus and assignment to a cohort at admission to reduce nosocomial transmission. J Pediatr 1990;116(6):894-898.
  57. Liu LL, Gallaher MM, Davis RL, Rutter CM, Lewis TC, Marcuse EK. Use of a respiratory clinical score among different providers. Pediatr Pulmonol 2004;37(3):243-8.
  58. Rödl S, Resch B, Hofer N, et al. Prospective evaluation of clinical scoring systems in infants with bronchiolitis admitted to the intensive care unit. Eur J Clin Microbiol Infect Dis 2012;31(10):2667-72.
  59. Duarte-Dorado DM, Madero-Orostegui DS, Rodriguez-Martinez CE, Nino G. Validation of a scale to assess the severity of bronchiolitis in a population of hospitalized infants. J Asthma 2013;50(10):1056-61.
  60. Schroeder AR, Marmor AK, Pantell RH, Newman TB. Impact of pulse oximetry and oxygen therapy on length of stay in bronchiolitis hospitalizations. Arch Pediatr Adolesc Med 2004;158(6):527-30.
  61. Ross PA, Newth CJ, Khemani RG. Accuracy of pulse oximetry in children. Pediatrics 2014;133(1):22-9.
  62. Willwerth BM, Harper MB, Greenes DS. Identifying hospitalized infants who have bronchiolitis and are at high risk for apnea. Ann Emerg Med 2006;48(4)441-7.
  63. Hunt CE, Corwin MJ, Lister G, et al. Longitudinal assessment of hemoglobin oxygen saturation in healthy infants during the first 6 months of age. Collaborative Home Infant Monitoring Evaluation (CHIME) Study Group. J Pediatr 1999;135(5):580-6.
  64. Poets A, Urschitz MS, Poets CF. Intermittent hypoxia in supine versus side position in term neonates. Pediatr Res 2009;65(6):654-6.
  65. Wright FH, Beem MO. Diagnosis and treatment: Management of acute viral bronchiolitis in infancy. Pediatrics 1965;35:334-7.
  66. Schroeder AR, Mansbach JM. Recent evidence on the management of bronchiolitis. Curr Opin Pediatr 2014;26(3):328-33.

Disclaimer: The recommendations in this position statement do not indicate an exclusive course of treatment or procedure to be followed. Variations, taking into account individual circumstances, may be appropriate. Internet addresses are current at time of publication.