Croup Medication

  • Author: Germaine L Defendi, MD, MS, FAAP; Chief Editor: Russell W Steele, MD   more...
 
Updated: Oct 5, 2011
 

Medication Summary

As previously mentioned, the current cornerstones in the treatment of croup are corticosteroids and nebulized epinephrine; steroids have proven beneficial in severe, moderate, and even mild croup. The anti-inflammatory action of corticosteroids reduces laryngeal mucosal edema and decreases the need for salvage nebulized epinephrine.

Nebulized racemic epinephrine (mixture of dextro isomers and levo isomers) or L-epinephrine is typically reserved for patients in moderate to severe distress. Epinephrine constricts the precapillary arterioles through adrenergic stimulation, thereby decreasing capillary hydrostatic pressure. This leads to fluid resorption from the interstitium and improvement in the laryngeal mucosal edema.

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Corticosteroids

Class Summary

Steroids are thought to decrease airway edema via their anti-inflammatory effect. Although a subject of controversy throughout the 1980s and 1990s, corticosteroids have since become a routine part of ED management of croup. Corticosteroids have been shown to reduce hospitalization rates by 86%, and in mild disease, they have been proven to reduce the number of children returning to the ED for further treatment.

In moderate to severe disease, corticosteroids improve croup scores within 12-24 hours and decrease hospitalization rates. Most trials have used dexamethasone at 0.6 mg/kg (intramuscular or oral), but oral doses as low as 0.15 mg/kg are effective.[29] Oral and intramuscular routes appear equally beneficial. Prednisolone (1 mg/kg) has been proven effective but may be associated with a greater return of children to the ED.

Inhaled corticosteroids also have demonstrated efficacy, with most trials using budesonide. According to most authors, however, the relative ease, speed, and cost of administration make systemic corticosteroids preferable to nebulized formulations.

Dexamethasone (Baycadron)

 

Several studies have shown improvement in clinical symptoms and croup score in hospitalized and ED patients who received dexamethasone. The drug exerts a beneficial effect via anti-inflammatory action that decreases laryngeal mucosal edema. The onset of action occurs within 6 hours after oral or intramuscular administration. Dexamethasone has a long pharmacodynamic effect of 36-56 hours. No studies have evaluated the effect of multiple doses of the drug.

Prednisone

 

Several studies have shown improvement in clinical symptoms and croup score in patients who were treated while hospitalized or in the ED. Corticosteroids exert beneficial effect via anti-inflammatory action in which laryngeal mucosal edema is decreased. In calculating an appropriate prednisone dose, it is important to know that dexamethasone is 6.67 times more potent and has a long half-life of 36-56 hours, versus a median half-life of 18-36 hours for prednisone.

Prednisolone (Prelone, Pediapred, Millipred)

 

Corticosteroids exert beneficial effect via anti-inflammatory action in which laryngeal mucosal edema is decreased. Like with prednisone, in calculating an appropriate prednisolone dose, it is important to know that dexamethasone is 6.67 times more potent and has a long half-life of 36-56 hours, versus a median half-life of 18-36 hours for prednisolone.

Budesonide inhaled (Pulmicort Respules, Pulmicort Flexhaler)

 

Clinical studies have documented improvement in symptoms and decrease in hospital admissions with nebulized budesonide in children with croup. Inhaled budesonide has been shown in several studies to be equivalent to oral dexamethasone.

Corticosteroids exert beneficial effect via anti-inflammatory action in which laryngeal mucosal edema is decreased.

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Nebulized Vasoconstrictors

Class Summary

Epinephrine stimulates alpha receptors and beta2 receptors. It constricts the precapillary arterioles, thus decreasing airway edema. Because of the potential adverse effects of tachycardia and hypertension, it is reserved for children with moderate to severe disease.[11]

The effects of epinephrine are transient, and most trials show alleviation of symptoms for no longer than 2 hours. In the 1980s and early 1990s, a rebound phenomenon was thought to occur, necessitating admission of all children who received the drug. However, patient discharge after 3-4 hours of observation has since become acceptable, as long as the patient has no stridor at rest, normal air entry, normal color, and normal consciousness and has received a dose of steroids.

Epinephrine (Adrenalin)

 

This agent is a levo isomer. It stimulates alpha-, beta1-, and beta2-adrenergic receptors, which results in bronchodilatation, increased peripheral vascular resistance, hypertension, increased chronotropic cardiac activity, and positive inotropic effects. Epinephrine causes alpha-adrenergic receptor–mediated vasoconstriction of edematous tissues, thus reversing upper airway edema.

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Contributor Information and Disclosures
Author

Germaine L Defendi, MD, MS, FAAP  Associate Clinical Professor, Department of Pediatrics, Olive View-UCLA Medical Center

Germaine L Defendi, MD, MS, FAAP is a member of the following medical societies: American Academy of Pediatrics

Disclosure: Nothing to disclose.

Coauthor(s)

Antonio Muñiz, MD  Professor of Emergency Medicine and Pediatrics, University of Texas Medical School at Houston; Medical Director of the Pediatric Emergency Department, Children's Memorial Hermann Hospital

Antonio Muñiz, MD is a member of the following medical societies: American Academy of Emergency Medicine, American Academy of Pediatrics, American College of Emergency Physicians, American Heart Association, American Medical Association, Society for Academic Emergency Medicine, and Southern Medical Association

Disclosure: Nothing to disclose.

Rona E Molodow, MD, JD  Clinical Professor, Department of Pediatrics, Olive View-UCLA Medical Center

Rona E Molodow, MD, JD is a member of the following medical societies: American Academy of Pediatrics and American Professional Society on the Abuse of Children

Disclosure: Nothing to disclose.

Chief Editor

Russell W Steele, MD  Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine

Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association

Disclosure: Nothing to disclose.

Additional Contributors

Joseph Domachowske, MD Professor of Pediatrics, Microbiology and Immunology, Department of Pediatrics, Division of Infectious Diseases, State University of New York Upstate Medical University

Joseph Domachowske, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Phi Beta Kappa

Disclosure: Nothing to disclose.

Mary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

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Child with croup. Note the steeple or pencil sign of the proximal trachea evident on this anteroposterior film. Courtesy of Dr. Kelly Marshall, CHOA at Scottish Rite.
Steeple sign on radiograph.
 
 
 
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