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Bronchiolitis

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Virtually all children have been exposed to respiratory syncytial virus (RSV) ... from parainfluenza virus, adenovirus, rhinovirus, influenza or mycoplasma pneumonia ... – PowerPoint PPT presentation

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Title: Bronchiolitis


1
Bronchiolitis
  • Dr Rajesh
  • 07/11/07

2
Introduction
  • Bronchiolitis is the most common lower
    respiratory tract infection in infants.
  • Virtually all children have been exposed to
    respiratory syncytial virus (RSV), the cause of
    most bronchiolitis cases, by their second
    birthday.
  • Clinically identical disease can occur with
    infections from parainfluenza virus, adenovirus,
    rhinovirus, influenza or mycoplasma pneumonia
  • Up to 3 of all children are hospitalized with
    bronchiolitis in their first year of life.
  • Despite the high prevalence of bronchiolitis,
    little consensus exists on the optimal management
    of the disease.

3
Pathology
  • Direct viral invasion, an increase in goblet cell
    mucous production, and subsequent necrosis and
    desquamation of the ciliated respiratory
    epithelium, particularly in bronchioles
  • Cellular debris and fibrin form plugs in the
    bronchioles resulting in air flow obstruction
  • As the respiratory epithelium regenerates, the
    new, non-ciliated cells are poorly equipped to
    clear the products of inflammation.
  • Thus, airway oedema, necrosis and mucous plugging
    are the predominant pathological features in
    bronchiolitis

4
Bronchiolitis
5
Definition
  • Bronchiolitis is an acute, highly communicable
    lower respiratory tract infection characterized
    by
  • cough, coryza (runny nose),
  • fever,
  • expiratory wheezing,
  • grunting,
  • tachypnea (fast breathing),
  • retractions
  • air trapping

6
(No Transcript)
7
Complications
  • Acute respiratory distress syndrome (ARDS)
  • Bronchiolitis obliterans
  • Congestive heart failure
  • Secondary infection
  • Myocarditis
  • Arrhythmias
  • Chronic lung disease

8
Indications for admission
  • Oxygen saturation monitored by pulse oximetry
    below 92 in room air
  • Younger than 6 months and unable to maintain oral
    hydration
  • Markedly elevated respiratory rate
  • History of chronic cardiorespiratory disease
  • Extra pulmonary symptoms

9
Utility of CXR
  • large numbers of infants with bronchiolitis have
    abnormalities on chest x-ray films.
  • However, chest x-ray films do not discriminate
    well between bronchiolitis and other forms of
    LRTI
  • In mild disease, chest x-ray films offer no
    information that is likely to affect treatment
    and should not be routinely performed.
  • Chest x-ray films may lead to the use of
    antibiotics.
  • It could be argued that chest x-ray films are
    more likely to lead to inappropriate antibiotic
    use than to improved clinical outcomes

10
Bronchodilators
  • Bronchodilators have been commonly used in the
    management of bronchiolitis.
  • A Canadian study (Law 1993) found that 78 of
    those hospitalized with bronchiolitis received
    bronchodilators. A survey of pediatric allergists
    and pulmonologists in the United States (Newcomb
    1989) found that 86 recommended a trial of
    bronchodilators for this condition. Similarly, in
    a survey of pediatric infectious disease
    specialists in Europe, the majority used
    bronchodilators for treatment of bronchiolitis
    (Kimpen 1997)
  • Three prior meta-analyses (Flores 1997 Hartling
    2003 Kellner 1996) and a systematic review (King
    2004) have shown that bronchodilators may improve
    clinical symptom scores but they do not affect
    disease resolution, need for hospitalization or
    length of stay.

11
Bronchodilators
  • Bronchodilators are very effective in the
    treatment of asthma, where airway obstruction is
    caused by inflammation, bronchospasm and
    bronchial hyperreactivity
  • The pathophysiology of bronchiolitis consists of
    terminal bronchiolar and alveolar inflammation
    with airway swelling and luminal debris, which
    lead to airway obstruction
  • In addition, mediators of bronchospasm have been
    shown to be present in variable amounts in
    children with bronchiolitis
  • Not all children with bronchiolitis are likely to
    have the same propensity to have bronchospasm and
    bronchial hyperreactivity.

12
Bronchodilator Cochrane
  • No improvement in clinical score for 43 of those
    treated with bronchodilators compared to 57 of
    those treated with placebo (odds ratio (OR) for
    no improvement 0.45, 95 confidence interval (CI)
    0.15 to 1.29).
  • There was a statistically significant but
    clinically modest improvement in the overall
    average clinical score.
  • No statistically significant improvement in
    oxygenation overall (weighted mean difference
    (WMD) -0.57, 95 CI -1.17 to 0.03).

13
  • Subgroup analyses showed a slightly greater
    effect size in outpatient studies

14
Bronchodilator Cochrane
  • Authors' conclusions
  • Bronchodilators produce small short-term
    improvements in clinical scores. This small
    benefit must be weighed against the costs and
    adverse effects of these agents

15
Bronchodilators
  • Two groups of patients
  • Responds to bronchodilator ( ? HRAD)
  • Do not respond to bronchodilator

16
Role of Salbutamol
  • Although evidence about the efficacy of
    bronchodilators in bronchiolitis is conflicting,
    administering a beta-agonist, such as albuterol
    (0.15 mg/kg/dose), on a trial basis to patients
    with bronchiolitis and assessing the clinical
    response in 10-15 minutes is reasonable.
  • If improvement in retractions, respiratory rate,
    and wheezing is noted, scheduled aerosol
    treatments may be continued, with additional
    treatments administered as needed.

17
Epinephrine
18
Epinephrine versus Placebo Cochrane
  • There were five inpatient studies that compared
    epinephrine and placebo.
  • Only one out of ten inpatient outcomes
    demonstrated a significant difference between
    treatment groups change in clinical score at 60
    minutes showed a SMD of -0.52 favouring
    epinephrine (95 CI -1.00,-0.03).

19
Epinephrine versus Placebo
  • Three studies compared epinephrine and placebo
    among outpatients.
  • Five of 10 outcomes were significant. Change in
    clinical score at 60 minutes, change in oxygen
    saturation at 30 minutes , respiratory rate at 30
    minutes , and "improvement" (OR 25.06 95 CI
    4.95,126.91).
  • Admission rates, change in clinical score at 30
    minutes, change in oxygen saturation at 60
    minutes, and heart rate at 30 minutes
    post-treatment were not significantly different
    between the treatment arms.

20
Epinephrine versus Salbutamol
  • Four studies compared epinephrine to salbutamol
    among inpatients.
  • Only one of the seven outcomes evaluated was
    statistically significant respiratory rate at 30
    minutes favoured epinephrine over salbutamol (WMD
    -5.12 95 CI -6.83,-3.41).
  • Changes in clinical score, oxygen saturation,
    heart rate, and length of stay were not
    significantly different between the treatment
    groups

21
Epinephrine versus Salbutamol
  • Four studies compared epinephrine to salbutamol
    among outpatients.
  • Four out of sixteen outcomes favoured epinephrine
    over salbutamol change in oxygen saturation at
    60 minutes post-treatment ,heart rate at 90
    minutes post-treatment respiratory rate at 60
    minutes post-treatment "improvement" (OR 4.51
    95 CI 1.93,10.53).
  • Sensitivity analyses using fixed-effects models
    found significant differences favouring
    epinephrine for an additional two outcomes
    change in clinical score at 60 minutes and
    admissions.

22
Epinephrine versus Salbutamol
  • Epinephrine appears to be a better choice than
    salbutamol

23
Nebulisation Dose
  • Epinephrine 0.03mg/kg/dose
  • Salbutamol
  • Ipratropium

24
Epinephrine
  • Constriction of capillary arterioles
  • For croup
  • Racemic Epinephrine11 mixture of the d- and
    l-isomers of epinephrine (2.25), dose
    0.25ml-0.75 ml in saline
  • L-isomer (0.1) 4mg, 4-5 ml 2ml saline
  • Racemic for bronchiolitis 0.05 mL/kg diluted in
    3 mL NS given via nebulizer over 15 min q1-2h

25
L-Epinephrine
  • Dose of L-epinephrine
  • 2-3 ml diluted to 5 ml with NS

26
Inhaled corticosteroid for post bronchiolitic
wheezing Cochrane
  • It has been shown that RSV is an independent risk
    factor for post-bronchiolitic wheezing (Stein
    1999). The vast majority of patients included in
    the studies of this review suffered from RSV
    bronchiolitis. In a post-hoc analysis we were
    unable to show a beneficial effect of inhaled
    steroids on hospital re-admissions in patients
    who suffered from bronchiolitis caused by RSV.

27
Systemic Steroid
  • Theoretically steroid should have effect in
    bronchiolits, especially in the early phase of
    diseasae
  • Evidence ?

28
Systemic Corticosteroid Cochrane
  • Limited current evidence is unable to show any
    benefit of corticosteroid use in infants and
    young children with bronchiolitis.
  • Widespread use is not recommended until the
    benefits and harms can be clarified further.
  • The expected benefits appear to be limited to a
    shorter length of hospital stay in admitted
    patients of up to, but less than, one day.
  • There is no supporting evidence to show
    improvements in clinical score, respiratory rate
    or haemoglobin oxygen saturation in treated
    infants and young children compared to those
    receiving placebo.

29
Systemic Corticosteroid Cochrane
30
Steroids Hospital stay pediatrics
31
Systemic Corticosteroid Cochrane
32
Additive effects of dexamethasone in nebulized
salbutamol or L-epinephrine treated infants with
acute bronchiolitis.Pediatr Int. 2004
Oct46(5)539-44
  • either nebulized L-epinephrine (3 mg) or
    salbutamol (0.15 mg/kg) and 15 min later, either
    dexamethasone 0.6 mg/kg or placebo (PLA),
    intramuscularly
  • CONCLUSIONS A single dose of intramuscular
    dexamethasone added to nebulized L-epinephrine,
    or salbutamol therapies resulted in better
    outcome measures than bronchodilators alone in
    the late phase (fifth day) of mild to moderate
    degree bronchiolitis attack. However, effects of
    EPI DEX combination was not different from SAL
    DEX combination.

33
RIBAVARIN
  • The current recommendations of the Academy of
    Pediatrics are that ribavirin aerosol therapy may
    be considered selected infants and young children
    at high risk for serious RSV disease.
  • This includes patients with complicated
    congenital heart disease, including pulmonary
    hypertension patients with bronchopulmonary
    dysplasia, cystic fibrosis, and other chronic
    lung disease patients with underlying
    immunosuppressive disease patients who are
    severely ill with or without mechanical
    ventilation and hospitalized patients who are
    younger than 6 weeks or who have underlying
    conditions such as multiple congenital anomalies
    or certain neurological and metabolic diseases.

34
RIBAVARIN
  • 20 mg/mL as starting solution using continuous
    aerosol administration for 12-18 h/d for 3-7 d

35
Prevention Palivizumab
  • Intramuscular injection, of 15 mg/kg every 30
    days from October through February or according
    to the local RSV season.
  • In a multi-institutional, randomized,
    placebo-controlled study of 1502 high-risk,
    preterm infants in 139 centers in the US and
    Canada during the 1996-1997 RSV season,
    hospitalizations were decreased by 55. Hospital
    length of stay, days on oxygen, and intensive
    care unit admissions all were reduced. Adverse
    effects were uncommon. Unfortunately, while cost
    effective, per-patient cost is approximately
    3000, thus restricting availability to only
    high-risk patients.

36
Conclusion
  • OPD treatment Steroid ?
  • Borderline cases Epinephrine nebulisation
    Dexona (?)
  • Admitted cases Epinephrine nebulisation
    Steroid (?)

37
RSV and Parainfluenza virus
38
RSV immunity
39
Bronchiolitis Obliterans
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