You are in: eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease Bacterial TracheitisArticle Last Updated: Oct 19, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Sujatha Rajan, MD, Assistant Professor of Pediatrics, Albert Einstein School of Medicine; Consulting Staff, Department of Pediatrics, Division of Pediatric Infectious Diseases, Schneider's Children's Hospital, North Shore-Long Island Jewish Health System Sujatha Rajan is a member of the following medical societies: American Academy of Pediatrics, Infectious Diseases Society of America, and Pediatric Infectious Diseases Society Coauthor(s): Kathryn Clark Emery, MD, Associate Professor, Department of Pediatrics, University of Colorado Health Sciences Center; Consulting Staff, Department of Emergency Medicine, Children's Hospital of Denver; Sunil K Sood, MD, Professor of Clinical Pediatrics, Department of Pediatrics, Albert Einstein College of Medicine; Chief, Pediatric Infectious Disease, Schneider Children's Hospital at North Shore University Hospital Editors: David Jaimovich, MD, Chief Medical Officer, Joint Commission International and Joint Commission Resources; 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, Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine Author and Editor Disclosure Synonyms and related keywords: bacterial tracheitis, bacterial croup, membranous croup, membranous laryngotracheobronchitis, pseudomembranous croup, tracheitis, acute upper airway obstruction INTRODUCTIONBackgroundBacterial tracheitis is an uncommon infectious cause of acute upper airway obstruction. Patients may present with crouplike symptoms, such as barking cough, stridor, and fever; however, patients with bacterial tracheitis do not respond to standard therapy and may experience acute respiratory decompensation. PathophysiologyBacterial tracheitis is a diffuse inflammatory process of the larynx, trachea, and bronchi with adherent or semiadherent mucopurulent membranes within the trachea. The major site of disease is at the cricoid cartilage level, the narrowest part of the trachea. Acute airway obstruction may develop secondary to subglottic edema and sloughing of epithelial lining or accumulation of mucopurulent membrane within the trachea. Signs and symptoms are usually intermediate between those of epiglottitis and croup. Bacterial tracheitis may be more common in the pediatric patient because of the size and shape of the subglottic airway. The subglottis is the narrowest portion of the pediatric airway, assuming a funnel-shaped internal dimension. In this smaller airway, relatively little edema can significantly reduce the diameter of the pediatric airway, increasing resistance to airflow and work of breathing. With appropriate airway support and antibiotics, most patients improve within 5 days. FrequencyUnited StatesTan and Manoukian reported that 500 children were hospitalized for croup at one pediatric hospital over a 32-month period. Approximately 98% had viral croup, and 2% had bacterial tracheitis. Cases usually occur in the fall or winter months, mimicking the epidemiology of viral croup. Mortality/MorbidityThe predominant morbidity and mortality is related to the potential for acute upper airway obstruction and induced hypoxic insults. The mortality rate has been estimated at 4-20%. In the acute phase, patients generally do well if the airway is adequately managed and if antibiotic therapy is promptly initiated. SexIn most epidemiologic studies, male cases are preponderant. Gallagher et al reported a male-to-female predominance of 2:1. AgeBacterial tracheitis may occur in any pediatric age group. Gallagher et al reported 161 cases of patients younger than 16 years. The age range was from 3 weeks to 16 years, with a mean age of 4 years. This is in contrast to viral laryngotracheobronchitis, which occurs in patients aged 6 months to 3 years. CLINICALHistory
Physical
Causes
DIFFERENTIALSAngioedema Candidiasis Croup Diphtheria Epiglottitis Peritonsillar Abscess Retropharyngeal Abscess Tuberculosis
|
| Drug Name | Oxacillin (Bactocill, Prostaphlin) |
|---|---|
| Description | Provides empiric therapy against etiologic agents, specifically penicillinase-producing strains of Staphylococcus. |
| Adult Dose | 250 mg to 2 g IV q6h |
| Pediatric Dose | 150 mg/kg/d IV divided q6h |
| Contraindications | Documented hypersensitivity |
| Interactions | Oxacillin decreases effects of contraceptives and tetracycline; administered concomitantly with disulfiram and probenecid, may increase oxacillin levels; effect of anticoagulants increase when large IV doses of oxacillin given |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Use with caution in patients with severe renal impairment; use with caution in patients with a documented hypersensitivity to cephalosporins |
| Drug Name | Cefotaxime (Claforan) |
|---|---|
| Description | Provides empiric therapy, especially against H influenzae, and modest activity against anaerobes. |
| Adult Dose | 1-2 g IV q8h |
| Pediatric Dose | 150 mg/kg/d IV divided q6h |
| Contraindications | Documented hypersensitivity |
| Interactions | Probenecid may increase cefotaxime levels; coadministration with furosemide or aminoglycosides may increase nephrotoxicity |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Dosage modification in patients with CrCl is <20 mL/min |
| Drug Name | Vancomycin (Vancocin) |
|---|---|
| Description | May be used in severe cases or in cases with a history of allergies instead of oxacillin for coverage of gram-positive organisms (eg, S aureus, S pyogenes). |
| Adult Dose | 40 mg/kg/d IV divided q6-24h; not to exceed 2 g/d |
| Pediatric Dose | 40 mg/kg/d IV divided q6h |
| Contraindications | Documented hypersensitivity; avoid in patients with previous hearing loss |
| Interactions | The neuromuscular blockade may be enhanced when used concurrently with nondepolarizing muscle relaxants |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Dosage modification required for patients with impaired renal function; red man syndrome is considered a function of the infusion rate |
| Drug Name | Clindamycin (Cleocin) |
|---|---|
| Description | Use in combination with chloramphenicol in patients who are allergic to penicillin. Clindamycin in combination with cefuroxime is an acceptable regimen for patients who are not allergic. |
| Adult Dose | 600-1200 mg/d IV divided bid-qid |
| Pediatric Dose | 25-40 mg/kg/d IV divided q6-8h |
| Contraindications | Documented hypersensitivity to clindamycin or any component; previous pseudomembranous colitis; hepatic impairment |
| Interactions | Increases duration of neuromuscular blockade induced by tubocurarine or pancuronium; CYP450 3A4 inhibitors (eg, saquinavir, ketoconazole) may decrease clearance |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Dosage adjustment may be necessary in patients with severe hepatic dysfunction; no change is necessary with renal insufficiency |
Article Last Updated: Oct 19, 2006