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Pediatrics: General Medicine > Infectious Disease
Parainfluenza Virus Infections
Article Last Updated: Sep 24, 2007
AUTHOR AND EDITOR INFORMATION
Section 1 of 10
Author: Roy M Vega, MD, Associate Chair, Department of Emergency Medicine, Director, Children's Emergency Care Center, Huntington Hospital
Roy M Vega is a member of the following medical societies: American Academy of Pediatrics
Editors: Ashir Kumar, MBBS, MD, FAAP, Professor, Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University; Consulting Staff, Department of Pediatrics, EW Sparrow Hospital; Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc; Joseph Domachowske, MD, Associate Professor, Department of Pediatrics, Division of Infectious Diseases, State University of New York-Upstate Medical University; Robert W Tolan Jr, MD, Chief of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine; Russell W Steele, MD, Professor and Vice Chairman, Department of Pediatrics, Head, Division of Infectious Diseases, Louisiana State University Health Sciences Center
Author and Editor Disclosure
Synonyms and related keywords:
parainfluenza virus infection, PVI, croup, upper respiratory tract infection, laryngotracheobronchitis, URTI, severe acute respiratory syndrome, SARS, pneumonia, parainfluenza virus, coryza, cough, bronchiolitis, paramyxovirus
Background
Human parainfluenza viruses (PIVs) account for a large percentage of pediatric respiratory infections, including upper respiratory tract infections (URTIs), laryngotracheobronchitis (croup), bronchiolitis, and pneumonia. Human PIV is the major cause of croup (type 1 is most frequent, followed by type 3 and type 2). Human PIVs are divided into 4 types, all of which are classified as paramyxoviruses. Infections from types 1 and 3 account for most disease.
Pathophysiology
The virus colonizes the nose and the nasopharynx; then, it invades the epithelium, resulting in cell damage, edema, and loss of cilia. A fibrinous exudate develops with downward spread of cell damage and edema. The resulting airway obstruction and laryngeal muscle spasm account for the typical symptoms of croup. The incubation period is 1-7 days.
Frequency
United States
Outbreaks of parainfluenza disease occur regularly throughout fall and mid winter. Parainfluenza virus type 1 causes biennial epidemics in the United States.
Mortality/Morbidity
- Most children with croup have mild infections that are usually managed on an outpatient basis.
- Approximately 41,000 individuals per year are admitted to the hospital for PIV infections. Only 1-5% of patients admitted to the hospital need artificial airway support.
Age
- Parainfluenza-related laryngotracheobronchitis commonly affects children aged 3 months to 3 years.
- PIV infection can also account for bronchiolitis in infants and children younger than 2 years.
History
- Patients typically present with a history of coryza and low-grade fever. They then develop the classic barking cough associated with croup.
- Symptoms of croup include the following:
- Fever
- Barking cough
- Coryza
- Stridor
- Retractions
- Tachypnea (when lower airways become involved)
- Irritability
- Children with croup are usually more symptomatic at night. Coughing often awakens them from sleep. The reasons for worsening of symptoms at night are unknown.
- Parainfluenza infections can also present as bronchiolitis. The typical presentation includes fever, coryza, tachypnea, coughing, and wheezing.
Physical
- Croup scoring systems have been developed to aid in grading the severity of infection.
- Factors in such scoring systems include stridor, retractions, air entry, color, and level of consciousness.
- Croup scoring systems were developed prior to the advent of pulse oximetry. Pulse oximetry may be beneficial in grading severity of illness, response to management, and disposition.
Epiglottitis
Retropharyngeal Abscess
Other Problems to be Considered
Tracheitis Pneumonia
Lab Studies
- Viral cultures usually require 4-7 days to yield results, which limits their clinical applicability in the acute setting. Cultures can be helpful from an epidemiological standpoint.
- Immunofluorescent and enzyme immunoassay methods can be performed to test nasopharyngeal washings; however, they are not readily available and vary in sensitivity.
- The WBC count on CBC count samples is usually normal; however, lymphocytosis may be noted.
Imaging Studies
- Posteroanterior (PA) radiography of the neck may reveal the classic steeple sign (ie, narrowing of the proximal portion of the trachea, indicative of subglottic edema); however, this finding is absent in approximately 50% of cases.
- Lateral soft tissue films of the neck are normal in most cases. Lateral neck films can be useful if the diagnosis is unclear, especially if conditions such as foreign body aspiration, retropharyngeal abscess, or epiglottitis are in the differential diagnosis.
Medical Care
Management of croup depends on the severity of disease.
- Prehospital care
- Prehospital care includes fever control and attempts to alleviate respiratory symptoms and patient anxiety.
- Respiratory symptoms commonly improve with benign measures such as sitting in a bathroom with a steaming shower and allowing vapor droplets to soothe inflamed airways. Another option includes exposing the child to the cool night air. Often, the patient's symptoms resolve en route to the hospital. Attempts at calming or distracting the child can be beneficial.
- Antipyretics may assist with fever control. Moderate or severe croup requires medical evaluation in the office or emergency department.
- Emergency department care
- Mild croup: Management of mild croup consists of cool blow-by oxygen mist, fever control, and observation to determine whether the airway appears compromised.
- Moderate croup
- Cool oxygen mist and steroids are common therapies. Controlled trials for the palliation of croup symptoms have yielded conflicting results, and routine use of dexamethasone in this disease remains controversial. Dexamethasone was traditionally intramuscularly administered; however, recent studies have documented the use of oral steroids.
- In patients who fail to improve, administration of racemic epinephrine with a nebulizer has been beneficial. If racemic epinephrine alleviates symptoms, observe the patient for a minimum of 3 hours to ensure the patient's condition does not worsen (eg, due to possible rebound laryngospasm as the racemic epinephrine dose wears off). If asymptomatic at this time, the patient can be discharged with proper follow-up care.
- In patients with moderate croup, oral intake may be lacking; therefore, evaluate the patient's hydration status. Intravenous fluids may be required.
- Severe croup
- Perform the same measures as in moderate croup. Observe for signs of impending respiratory failure.
- Repeat racemic epinephrine nebulization may be needed, in addition to intensive care monitoring. Racemic epinephrine nebulizations can be repeated at 1- to 2-hour intervals as needed. Fortunately, fewer than 5% of patients who are admitted require artificial airway support (endotracheal intubation).
No specific antiviral agents are available for treating parainfluenza virus (PIV) infections; however, medications are available to treat the respiratory symptoms associated with croup. The medications include corticosteroids and nebulized epinephrine to treat airway inflammation and edema.
Drug Category: Glucocorticoids
These agents have anti-inflammatory properties and cause profound and varied metabolic effects. They modify the body's immune response to diverse stimuli. Anti-inflammatory drugs (specifically dexamethasone) help reduce the inflammation and subglottic edema of croup. Despite delayed onset of action, the high potency and prolonged intramuscular half-life of dexamethasone make it the preferred corticosteroid for croup.
| Drug Name | Dexamethasone (Decadron) |
| Description | Criterion standard anti-inflammatory drug for reducing airway edema that occurs in croup. Other glucocorticoids have been used, including prednisone and prednisolone. Dexamethasone is thought to decrease inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability. |
| Adult Dose | 10 mg PO/IV/IM qd |
| Pediatric Dose | 0.6 mg/kg PO/IM qd prn; not to exceed 10 mg/d |
| Contraindications | Documented hypersensitivity; immunosuppressed patients receiving corticosteroids; varicella |
| Interactions | Possible decreased effects with coadministration of barbiturates, phenytoin, or rifampin; decreases effect of salicylates and vaccines |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Caution in hyperthyroidism, osteoporosis, cirrhosis, nonspecific ulcerative colitis, peptic ulcer, diabetes, and myasthenia gravis; tuberculosis; untreated systemic infections; ocular herpes simplex virus |
| Drug Name | Budesonide (Pulmicort Respules) |
| Description | Nebulized budesonide has been found to be beneficial in treating croup. |
| Adult Dose | Not applicable |
| Pediatric Dose | 2-4 mg/d inhaled via nebulizer divided qd/bid |
| Contraindications | Documented hypersensitivity; immunosuppressed patients receiving corticosteroids; varicella; patients may develop PO thrush |
| Interactions | Ketoconazole may increase plasma levels of budesonide; cimetidine may increase bioavailability of budesonide |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Tuberculosis, untreated systemic infections, ocular herpes simplex virus |
| Drug Name | Prednisolone (Delta-Cortef, Pediapred) |
| Description | Many practitioners administer liquid prednisolone for patients with croup in lieu of dexamethasone. Prednisolone has not been proven superior to dexamethasone. |
| Adult Dose | Not applicable |
| Pediatric Dose | 1-2 mg/kg/d PO qd or divided bid |
| Contraindications | Documented hypersensitivity; immunosuppressed patients receiving corticosteroids; varicella |
| Interactions | Decreases effects of salicylates and toxoids (for immunizations); phenytoin, carbamazepine, barbiturates, and rifampin decrease effects of corticosteroids |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Caution in hyperthyroidism, osteoporosis, cirrhosis, nonspecific ulcerative colitis, peptic ulcer, diabetes, and myasthenia gravis; tuberculosis; untreated systemic infections; ocular herpes simplex virus |
Drug Category: Bronchodilators
When delivered by air or oxygen-powered devices, epinephrine is directly delivered to respiratory mucosal surfaces and smooth muscle. Because nebulizers deliver the medication directly to the target organ, fewer systemic adverse effects are encountered in comparison with oral or parenteral administration.
| Drug Name | Epinephrine, racemic solution (Vaponefrin, microNefrin) |
| Description | Very effective in reversing upper airway edema when administered with a nebulizer. Proposed mechanism of action is alpha-adrenergic receptor-mediated vasoconstriction of edematous tissues. |
| Adult Dose | Mix 0.5 mL with 3 mL 0.9% NaCl (normal saline) and inhale via nebulizer q1-2h prn |
| Pediatric Dose | Mix 0.05 mL/kg with 3 mL 0.9% NaCl (normal saline) and inhale via nebulizer q1-2h prn; not to exceed 0.5 mL/dose |
| Contraindications | Documented hypersensitivity |
| Interactions | Inhaled anesthetics may enhance cardiac irritability; nonselective beta-blockers block the beta effects of epinephrine leaving unopposed alpha effects (eg, hypertension) |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Tachycardia, especially with HR >200 BPM; consider cardiac monitoring if multiple doses required |
| Drug Name | L-epinephrine (Adrenalin) |
| Description | In concentrations of 1:1000, may be substituted for racemic epinephrine for nebulized administration. |
| Adult Dose | 5 mL nebulized q1-2h prn; mix with 3 mL 0.9% NaCl |
| Pediatric Dose | <4 years: Mix 2.5 mL with 3 mL 0.9% NaCl (normal saline) and inhale via nebulizer >4 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Inhaled anesthetics may enhance cardiac irritability; nonselective beta-blockers block the beta effects of epinephrine leaving unopposed alpha effects (eg, hypertension) |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Tachycardia, especially with HR >200 BPM, consider cardiac monitoring if multiple doses required |
Further Inpatient Care
Indications for hospitalization include the following: - Stridor or retractions present at rest despite therapy
- Need for repeated doses of racemic epinephrine
- Rebound laryngospasm in patients who receive racemic epinephrine
- Signs of respiratory distress
- Inadequate oral intake or dehydration
Further Outpatient Care
- Use cool mist vaporizers.
- Administer acetaminophen or ibuprofen for fever.
- Increase oral fluid intake.
Deterrence/Prevention
No vaccine is currently available for parainfluenza virus (PIV). Passively acquired maternal antibodies from breast feeding may be protective in the first few months of life. Handwashing and contact precautions can limit the spread of disease to others.
Complications
Posttransplant PIV is a cause of serious lower respiratory tract involvement in both adults and children who undergo bone marrow transplantation. Long-term ribavirin therapy has been helpful in case reports.1
Prognosis
- Patients with parainfluenza infections generally do well, with resolution of symptoms in 7-10 days.
- On occasion, the infection spreads to the lower respiratory tract, causing bronchiolitis or viral pneumonia.
- Denudation of respiratory epithelium places patients at a slightly increased risk of bacterial superinfection. Evaluate any patient recovering from croup who deteriorates suddenly for possible bacterial tracheitis.
Patient Education
- For excellent patient education resources, visit eMedicine's Lung and Airway Center. Also, see eMedicine's patient education article Croup.
Medical/Legal Pitfalls
- A common occurrence in pediatric emergency department charts concerns varied assessment of the patient. All notes on the chart (eg, triage, nursing, resident) should be examined. If the assessments differ from the physician's assessment, the physician should address said differences in his or her notes. At discharge, ensure that proper discharge instructions, both written and oral, are given to the patient.
- Document an examination at time of discharge. For example, "Patient is breathing comfortably, is alert, consolable, without tachypnea, stridor, or retractions." A pulse oximetry reading can also be included if available.
- If the patient has a pediatrician or other primary care provider, attempt to contact them to ensure proper follow-up care. The pediatrician can also be consulted on management issues if the physician has concerns or doubts.
- For any concerns about stability for discharge, always err on the side of admission.
- Stankova J, Carret AS, Moore D, et al. Long-term therapy with aerosolized ribavirin for parainfluenza 3 virus respiratory tract infection in an infant with severe combined immunodeficiency. Pediatr Transplant. Mar 2007;11(2):209-13. [Medline].
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- Kairys SW, Olmstead EM, O'Connor GT. Steroid treatment of laryngotracheitis: a meta-analysis of the evidence from randomized trials. Pediatrics. May 1989;83(5):683-93. [Medline].
- Klassen TP, Watters LK, Feldman ME, et al. The efficacy of nebulized budesonide in dexamethasone-treated outpatients with croup. Pediatrics. Apr 1996;97(4):463-6. [Medline].
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- Vega R. Rapid viral testing in the evaluation of the febrile infant and child. Curr Opin Pediatr. Jun 2005;17(3):363-7. [Medline].
- Wendt CH, Weisdorf DJ, Jordan MC, Balfour HH Jr, Hertz MI. Parainfluenza virus respiratory infection after bone marrow transplantation. N Engl J Med. Apr 2 1992;326(14):921-6. [Medline].
- Williams JV. The clinical presentation and outcomes of children infected with newly identified respiratory tract viruses. Infect Dis Clin North Am. Sep 2005;19(3):569-84. [Medline].
Parainfluenza Virus Infections excerpt Article Last Updated: Sep 24, 2007
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