Introduction
Bronchiolitis is an acute inflammatory condition of the bronchioles that is a result of virusinduced injury.
Etiology
Respiratory syncytial virus (RSV) is the most common viral agent isolated in about 75% (30–70% in Indian studies).
Other viruses: Rhinovirus, parainfluenza, adenovirus, human metapneumovirus, and bocavirus are the other viruses commonly causing the condition. Mycoplasma is more frequently implicated in older children with bronchiolitis.
Diagnosis
· Persistent cough, following a prodrome of coryza lasting 1–3 days, with tachypnea with or without chest recessions and wheeze and/or crackles occurring in a child <2 years of age (usually below 1 year of age, with a peak between 3 and 6 months).
· Associated fever, usually below 39°C, in around 30% cases and poor feeding, vomiting usually after 3–5 days of illness.
· Apnea may be the only presenting feature, particularly below 6 weeks of age.
· The chest may appear hyperexpanded and may be hyper-resonant to percussion. Wheezes and fine crackles may be heard throughout the lungs.
Indications for Hospitalization
· Persistent tachypnea >60 breaths/minute or respiratory distress in form of grunting, recessions
· Inadequate oral intake, inability to feed, dehydration, and inadequate fluid intake (50–75% of usual volume)
· Oxygen saturation (SpO2) <92% in room air
· Child appears seriously unwell to the healthcare provider
· Skill and confidence of the caregiver to look after the child at home and distance from the hospital
Signs of Severe Bronchiolitis
· Apnea, observed/reported
· Marked respiratory distress (severe grunting/chest indrawing/tachypnea
>70/minute)
· Central cyanosis, or SpO2 below 90% (age > 6 weeks) or below 92% (age < 6 weeks, or any age with underlying health conditions)
Risk Factors for Severe Bronchiolitis
Predictors of severe bronchiolitis are presented in Table 1
TABLE 1: Predictors of severe bronchiolitis. | ||
A. Host-related risk factors | B. Environmental risk factors | C. Clinical predictors |
· Prematurity, especially <32 weeks of gestation · Low birth weight · Age <6–12 weeks · Chronic lung disease including BPD · Hemodynamically significant congenital heart disease (e.g., moderate-to-severe pulmonary hypertension, cyanotic heart disease, or congenital heart disease that requires medication to control heart failure) · Immunodeficiency · Neuromuscular disorders | · Having older siblings · Passive smoke · Household crowding · Child care attendance · Lower socioeconomic status | · Toxic or ill appearance · Oxygen saturation <95% by pulse oximetry while breathing room air · Respiratory rate 70 breaths per minute · Moderate/severe chest retractions · Atelectasis on chest radiograph |
Differential Diagnosis
· Pneumonia: Fever >39°C with persistent focal crackles
· Episodic viral wheeze: Persistent wheeze without crackles, or recurrent episodes with or without a family history of atopy
Investigations
· Is a clinical diagnosis based on age, seasonal occurrence, typical clinical presentation, and physical examination?
· Blood investigations and radiology is routinely not indicated.
· A pulse oximetry reading helps to identify hypoxia and need for admission.
· Investigations in admitted patients to rule out alternate diagnosis such as bacterial pneumonia, congenital heart disease with failure, or sepsis might occasionally be indicated.
· Admitted babies may need an arterial blood gas (ABG) analysis, complete blood count, C-reactive protein (CRP), serum electrolytes, and chest radiography for managing the more serious patients.
· Measurement of lactate dehydrogenase (LDH) concentration in the nasal-wash fluid has been proposed as an objective indicator of bronchiolitis severity (Table 2).
· Identification of viral agents does not affect management in the majority of patients. However, in the hospital setting, to avoid antibiotic abuse and prevent nosocomial transmission may be done by:
· Antigen detection, immunofluorescence, polymerase chain reaction (PCR), and culture of respiratory secretions obtained by nasal wash or nasal aspirate.
· New techniques such as real-time PCR, nested PCR, and multiplex PCR have improved the virologic diagnosis of bronchiolitis immensely.
TABLE 2: Severity of bronchiolitis. | |||
| Mild | Moderate | Severe |
Feeding ability | Normal ability to feed | Appear short of breath during feeding | May be reluctant or unable to feed |
Respiratory distress | Little or no respiratory distress | Moderate distress with some chest wall retractions and nasal flaring | *Severe distress with marked chest wall retractions, nasal flaring and grunting *Can have frequent and prolonged apnea |
Saturation | Saturation >92% | Saturation <92%, correctable with O2 | Saturation <92%, may or may not be correctable with O2 |
Management
· Treatment is focused on symptomatic relief and maintaining hydration and oxygenation.
· Fever should be controlled with paracetamol.
· Nose block should be cleared with saline nasal drops and gentle suctioning.
· Child should be made to lie in a propped up or head end elevated positioning.
· Orogastric tube feeding may be indicated in admitted patients. Intravenous
(IV) fluids in children with impending respiratory failure or who do not tolerate orogastric/nasogastric (OG/NG) fluids.
· Suctioning of the upper airway in children with apnea, respiratory secretions, and feeding difficulties due to upper airway secretions
· Supplemental oxygen in children with SpO2 below 90% (>6 weeks) or below 92% (<6 weeks or with underlying health issues)
· Continuous positive airway pressure (CPAP) in babies with impending respiratory failure (limited low-quality evidence)
· High-flow nasal cannula (HFNC) oxygen may have a role as a rescue therapy to reduce proportion of those requiring intensive care
· Drugs with questionable value might reduce need for admission or length of hospital stay, but broad consensus is lacking.
§ Nebulized hypertonic saline: In children hospitalized for >3 days
§ Nebulized adrenaline: 0.1–0.3 mL/kg/dose of 1:1,000 as a potential rescue medication; however inconsistent and short-lived improvement
§ Beta-agonists: Optional single trial; may be continued if there is clinical response (a trial of bronchodilator therapy may be initiated, but should be discontinued if there is no objective improvement)
· No role of:
· Chest physiotherapy
· Antibiotics
· Antivirals
· Montelukast
· Ipratropium bromide
· Systemic or inhaled steroids
· Steam inhalation
· RSV polyclonal immunoglobulin/palivizumab (no roll in acute management but useful in prophylaxis)
· Inhaled furosemide/inhaled interferon alfa-2a/inhaled recombinant human deoxyribonuclease (DNase)
· Interventions which are possibly effective for most severe cases:
§ CPAP
§ Surfactant
§ Heliox
§ Aerosolized ribavirin
Criteria for Discharge
§ Clinically stable
§ Taking adequate oral feeds, at least 75% of usual
§ Maintaining SpO2 above 90% (>6 weeks) and 92% (<6 weeks or with health issues) in room air
§ Ability of the caregiver to look after at home and distance from the hospital, and have understood the “red flag” signs Red flag signs for the caregiver at home:
§ Increased work of breathing (e.g., grunting, nasal flaring, and chest retractions)
§ Fluid intake <50–75% of normal or no urine for 12 hours
§ Apnea or cyanosis
§ Exhaustion (i.e., not responding normally to social cues and responds only with prolonged stimulation)
Prevention
§ Breastfeeding: Three-fold greater risk in non-breastfed infant
§ Hand hygiene
§ Avoid passive smoking
§ Immune prophylaxis:
•• Palivizumab: Monoclonal antibody, monthly injections during seasonal epidemics
Indications: Infants <12 months with prematurity <29 weeks; CLD of prematurity; hemodynamically significant heart disease
Palivizumab is administered intramuscularly at a dose of 15 mg/kg monthly (every 30 days) during the RSV season. A maximum of five doses is generally sufficient prophylaxis during one season.
•• Nirsevimab: On trial; single dose for 5 months
•• Motavizumab, a second-generation mAb, and Numax-YTE, a third- generation mAb—under trial
Complications
· Acute respiratory distress syndrome (ARDS)
· Myocarditis
· Congestive heart failure
· Arrhythmias
· Bronchiolitis obliterans
· Secondary bacterial infection
· Predisposition to childhood asthma
Summary
Flowchart 1: Summary of viral bronchiolitis.
(ABG: arterial blood gas; ICU: intensive care unit; IV: intravenous; SpO2: oxygen saturation)
Further Reading
· Gupta S, Shamsundar R, Shet A, Chawan R, Srinivasa H. Prevalence of respiratory syncytial virus infection among hospitalized children presenting with acute lower respiratory tract infections. Indian J Pediatr. 2011;78:1495- 7.
· National Institute for Health and Care Excellence. (2015). Bronchiolitis in children: diagnosis and management. [online] Available from www.nice.org.uk/guidance/ng9. [Last accessed March, 2022].
· 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(5): e1474-502.
References
- Gupta S, Shamsundar R, Shet A, Chawan R, Srinivasa H. Prevalence of respiratory syncytial virus infection among hospitalized children presenting with acute lower respiratory tract infections. Indian J Pediatr. 2011;78:1495- 7.
- National Institute for Health and Care Excellence. (2015). Bronchiolitis in children: diagnosis and management. [online] Available from www.nice.org.uk/guidance/ng9. [Last accessed March, 2022].
- 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(5): e1474-502.