PRE HOSPITAL
- Oxygen and oxygen saturation monitoring
- Nebulized β-adrenergic agonist: Albuterol
- Intubate for respiratory failure or severe fatigue.
- IV fluids if evidence of dehydration
- Rapid transport and good communication with ED
INITIAL STABILIZATION/THERAPY
- Maintain SaO
2
>90–95%.
- β-adrenergic nebulizer(s): Albuterol
- Intubate for respiratory failure.
- 20 mL/kg 0.9% NS bolus if evidence of dehydration.
ED TREATMENT/PROCEDURES
- Assess patient for signs of potential respiratory failure:
- Cyanosis
- Severe anxiety or irritability
- Lethargy, somnolence, fatigue
- Persistent tachypnea
- Poor air entry, ventilation
- Severe retractions
- Monitor oxygenation; titrate oxygen saturation to SaO
2
>95% (sea level).
- β-adrenergic nebulizer: Albuterol:
- Frequent or continuous for severe asthma
- Levalbuterol may require less frequent dosing and may be associated with less side effects.
- Ipratropium bromide may be added as adjunct to β-adrenergic agonists. Most effective when combined with 1st 3 doses of β-adrenergic agent in moderate to severely ill children
- Steroid therapy:
- Oral for moderate exacerbations in those able to take oral meds
- IV for severe exacerbations or in those unable to take oral meds
- 1 dose of dexamethasone may be equivalent to traditional steroids
- SC epinephrine or terbutaline for severe or refractory asthma (rarely used)
- Magnesium sulfate may be useful in severe disease following standard therapy.
- Intubate for respiratory failure:
- Ketamine is a useful induction agent.
- 20 mL/kg of 0.9% NS bolus if evidence of dehydration
- Heliox (oxygen and helium) may be useful but studies are inconclusive
MEDICATION
- Albuterol (0.5% solution or 5 mg/mL):
- Nebulizer: 0.15 mg/kg per dose, up to 5 mg per dose, q15–30min PRN
- Metered-dose inhaler (MDI) (with spacer) (90 μg/puff): 2 puffs q5–10min, max. 10 puffs
- Also available for nebulizer as 0.083% solution or 2.5 mg/3 mL
- Dexamethasone 0.3 mg/kg/dose (max.: 16 mg)
- Epinephrine (1:1,000) (1 mg/mL): 0.01 mg/kg SC, up to 0.35 mL per dose, q20min for 3 doses
- Ipratropium bromide: Nebulizer (0.02% inhaled sol 500 μg/2.5 mL), 250–500 μg per dose q6h
- Ketamine (for intubation): 1–2 mg/kg IV as induction agent
- Levalbuterol (0.63 and 1.25 mg vials): q6–8h by nebulizer
- Magnesium sulfate: 25 mg/kg per dose IV over 20 min; max. 1.2–2 g per dose
- Methylprednisolone: 1–2 mg/kg per dose IV q6h; max. 125 mg per dose
- Prednisolone: 1–2 mg/kg per dose PO q12h (available as 15 mg/5 mL)
- Prednisone: 1–2 mg/kg per dose PO q6–12h; max. 80 mg per dose
- Terbutaline/ (available as 1 mg/1 mL) (0.01%): 0.01 mL/kg SC q15–20min up to 0.25 mL per dose, q20min for 2 doses
First Line
- Albuterol
- Steroids
- Ipratropium
Second Line
- Epinephrine or terbutaline
- Magnesium sulfate
FOLLOW-UP
DISPOSITION
Admission Criteria
- Need to individualize based upon subjective and objective assessment
- Persistent respiratory difficulty:
- Persistent wheezing
- Increased respiratory rate/tachypnea
- Retraction and use of accessory muscles
- SaO
2
<93% (sea level) on room air
- Peak expiratory flow rate (PEFR) <50–70% predicted levels
- Inability to tolerate oral medicines or liquids
- Prior ED visit in last 24 hr
- Comorbidity:
- Congenital heart disease
- Bronchopulmonary dysplasia
- CF
- Neuromuscular disease
- Concomitant illness:
- Pneumonia or severe viral infection
Intensive Care Unit Criteria
- Severe respiratory distress
- SaO
2
<90% or PaO
2
<60 mm Hg on 40% oxygen
- PaCO
2
>40 mm Hg
- Significant complications:
Discharge Criteria
- Good response to therapy. Observe in ED 60 min after last treatment before discharging:
- PEFR >70% predicted based on age/height
- SaO
2
>93% on room air (sea level)
- Respiratory rate normal
- No retractions
- Clear or minimal wheezing
- No or minimal dyspnea
- Good follow-up and compliance. Reduce exposure to irritants (smoking) or allergens
- Discharge treatment:
- Intensive β-adrenergic regimen for 3–5 days
- Short course (3–5 days) of steroids (2 mg/kg/day) for those presenting with moderate symptoms with consideration of ongoing therapy using nebulized or MDI routes. Patients with moderate or severe exacerbations should have arrangements made for inhaled steroids over a 1–2 mo period such as fluticasone, budesonide, or beclomethasone
- Follow-up appointment 24–72 hr
- Instructions to return for shortness of breath refractory to home regimen
- Long-term therapy should be considered for children with recurrent episodes, persistent symptoms, or activity limitations.
FOLLOW-UP RECOMMENDATIONS
Primary care physician for maintenance therapy, often including nebulized or MDI steroid therapy and education about acute rescue management.
PEARLS AND PITFALLS
- Rapid treatment with continuous re-evaluation to detect any progression of disease is essential.
- When admitting patients, assure that β-adrenergic agent therapy is not interrupted.
ADDITIONAL READING
- Krebs SE, Flood RG, Peter JR, et al. Evaluation of a high dose continuous albuterol protocol for treatment of pediatric asthma in the emergency department.
Pediatr Emerg Care.
2013;29:191–196.
- National Heart, Blood and Lung Institute; National Asthma Education and Prevention Program.
Guidelines for the diagnosis and management of asthma
. Bethesda, MD: NIH; 2007.
- Robinson PD, Van Asperen P. Asthma in childhood.
Pediatr Clin North Am
. 2009;56(1):191–226.
- Scarfone RJ, Friedlaender E. Corticosteroids in acute asthma: Past, present, and future.
Pediatr Emerg Care
. 2003;19(5):355–361.
See Also (Topic, Algorithm, Electronic Media Element)
- Bronchiolitis, Pediatric
- Pneumonia, Pediatric
CODES
ICD9
- 493.00 Extrinsic asthma, unspecified
- 493.02 Extrinsic asthma with (acute) exacerbation
- 493.90 Asthma, unspecified type, without mention of status asthmaticus
ICD10
- J45.901 Unspecified asthma with (acute) exacerbation
- J45.902 Unspecified asthma with status asthmaticus
- J45.909 Unspecified asthma, uncomplicated
ASYSTOLE
David F. M. Brown
•
Calvin A. Lee
BASICS
DESCRIPTION
Absence of ventricular electrical activity
ETIOLOGY
- An end-stage rhythm, sometimes degrading from:
- Prolonged bradycardia
- Prolonged ventricular fibrillation (VF)
- Prolonged pulseless electrical activity
- Patient is extremely unlikely to survive when asystole occurs outside the hospital:
- ∼40% will have return of spontaneous circulation and survive to hospital admission, but <15% survive to hospital discharge.
- Prognosis is similarly poor for those patients who develop asystole after countershock for ventricular tachycardia/VF; <10% survive to hospital discharge.
- Potentially reversible causes include:
- Hypoxia
- Hypovolemia (blood loss)
- Acidosis
- Hyperkalemia
- Hypokalemia
- Drug overdose
- Hypothermia
- Pulmonary embolism
- Myocardial infarction
- Tension pneumothorax
- Cardiac tamponade
DIAGNOSIS