EM@3AM: Bacterial Tracheitis

Authors: Jacob Tauferner, MD (EM Resident Physician, UTSW/ Dallas, TX) and Mihir Patel, MD (EM Attending Physician, Dallas, TX) // Reviewed by: Sophia Görgens, MD (EM Physician, BIDMC, MA); Cassandra Mackey, MD (Assistant Professor of Emergency Medicine, UMass Chan Medical School); Alex Koyfman, MD (@EMHighAK); Brit Long, MD (@long_brit)

Welcome to EM@3AM, an emDOCs series designed to foster your working knowledge by providing an expedited review of clinical basics. We’ll keep it short, while you keep that EM brain sharp.


A 3-year-old male with no previous past medical history, born full term, and unvaccinated presents after 6 days of cough, fever, myalgias, and rhinorrhea. His mother states that he appeared improved until today when he developed high-pitched inspiratory noises and appeared overall unwell. Vitals are as follows: HR 105 bpm, BP 83/54, SpO2 92%, Temperature 39.1, RR 55 rpm. On exam the patient is ill appearing with tachypnea, retractions, and stridor at rest.

Question: What’s the next step in your evaluation and treatment, and what is the potentially life-threatening diagnosis?


Answer: Bacterial tracheitis

 

Introduction

  • Bacterial tracheitis (BT), also known as bacterial croup or laryngotracheobronchitis, is a potentially lethal infection of the subglottic trachea. [2]
    • Bacterial infection usually preceded by viral infection.
    • Typically in children less than 6 years of age. [3]
    • Can be rarely seen spontaneously in adults.
    • Tracheostomy dependent patients of any age are also at risk. [2]
  • There is a mainstay concern for airway protection in the setting for BT due to thick mucopurulent secretions causing narrowing and obstruction of the airway. [2-4]

 

Etiology

  • The most common preceding viruses include:
    • Influenza A and B
    • Respiratory syncytial virus (RSV)
    • Parainfluenza virus
    • Measles virus
    • Enterovirus [2][3]
  • In BT bacteria invade the trachea and stimulate local and systemic inflammatory responses leading to production of thick, mucopurulent exudates, ulceration and sloughing of the tracheal mucosa and upper airway obstruction. [2][3][5]
  • Implicated bacteria most commonly include:
    • Staphylococcus aureus (including MRSA)
    • Streptococcus pneumoniae,
    • Streptococcus pyogenes,
    • Moraxella catarrhalis,
    • Haemophilus influenzae type B (HiB),
    • Haemophilus influenzae (non-typeable), and less commonly,
    • Pseudomonas aeruginosa,
    • Escherichia coli,
    • Klebsiella pneumonia,
    • Anaerobic organisms [2-4]
  • Long-term tracheostomy patients are presumed to be colonized by a single or multi-bacterial species predisposing them to BT caused most commonly by S. aureus, Gram-negative bacilli, Pseudomonas aeruginosa, and Streptococcus pneumoniae.
  • Meticulous tracheostomy care is imperative in minimizing risk of BT in this population. [2][6][7]

 

Epidemiology

  • Annual incidence of bacterial tracheitis has an estimated incidence of 0.1 to 1 case per 100,000 children.
    • A peak incidence is seen in ages 3 to 8. [2][3]
    • The incidence rises in the fall and winter months, coinciding with seasonal viral epidemics (influenza, parainfluenza, and RSV). [2-4]

 

Presentation

  • BT most commonly presents as prodromal symptoms that suggest a viral respiratory tract infection (rhinorrhea, post-nasal drip, cough, fever, myalgia, and sore throat) presenting a week before the acute worsening of the patient.
    • Patients then develop acute airway deterioration, high fevers, hoarseness, toxic appearance, and increased mucopurulent cough.
  • Signs and symptoms include stridor (inspiratory or expiratory), fever, productive and painful cough, thick secretions, and tenderness of the trachea. [2-4]
  • Tracheostomy-dependent patient symptoms of BT include high fevers, productive cough, thick mucopurulent secretions, hemoptysis, peristomal skin breakdown or cellulitis, high ventilatory peak pressures, and/or tracheostomy obstruction. [2][3]

 

Evaluation

  • Labwork
    • CBC: A white blood cell count is variable and nonspecific. Leukocytosis, as well as mild leukopenia, are common.
    • ESR, CRP: Erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) are also nonspecific but are estimated to be elevated in 68% of patients.
    • Blood cultures: Blood cultures are rarely positive; however, should be obtained if suspicion for sepsis is present or if the patient is immunocompromised. [2][3]
  • Imaging
    • X-ray images of the lateral or anteroposterior neck can show subglottic or tracheal narrowing (steeple sign), typically seen with croup. The epiglottis will appear normal. [2][3]
    • Chest x-rays are poorly diagnostic but can show concurrent pneumonia in approximately 50% of cases.
    • CT scans are typically not recommended in pediatric patients, but can be useful in adults with concern for tracheal stenosis or recurrent tracheitis, however airway stabilization takes precedence. [2][3]
  • Definitive diagnosis is made by laryngoscopy or bronchoscopy showing normal or mildly erythematous epiglottis and an erythematous, edematous trachea with thick mucopurulent exudates. [3]

Differential

  • Epiglottitis can also present with fever, upper airway obstruction, and toxic appearance. However, these patients often present with drooling and a preference for the tripod position, which is uncommon in bacterial tracheitis. [2][3]
  • Bacterial tracheitis should be suspected over croup if nebulized racemic epinephrine or steroids do not improve the clinical course. [2][3][8]
  • Peritonsillar or retropharyngeal abscesses will demonstrate fever, drooling, and muffled voice, associated with limited mobility of the neck. [2][8]
  • Other etiologies including but not limited to: angioedema, foreign body aspiration, caustic ingestion, laryngeal malignancies, diphtheria, bacterial pneumonia. [2][3]

 

Management/Disposition

  • ABCs and resuscitation if indicated
    • Assessment for need of definitive airway is imperative as rate of intubation is high (38-100%) in various studies. [2][3][9] Hypoxia, respiratory muscle retractions, fatigue, altered mental status, and decreased breath sounds are signs indicative of impending airway failure. [2]  If intubation is indicated, endotracheal tubes one or two sizes smaller than expected for the patient should be selected due to airway narrowing. [2]
  • Antibiotics
    • Antibacterial management should be prompt and include broad-spectrum coverage, including MRSA. [2]
    • Suggested antibiotics include: ceftriaxone or cefotaxime + vancomycin or clindamycin.
    • Patients with true cephalosporin allergy may be treated with vancomycin or clindamycin + levofloxacin or ciprofloxacin. [2][3][9]

  • Glucocorticoid were not shown to alter clinical course or patient outcomes. [2][3]
  • Consultations:
    • Intensive care physicians for ICU placement
    • Otolaryngology to prevent morbidity and mortality and potential for help with intubation in the OR [2][9]
  • Complications:
    • Acute respiratory distress syndrome (ARDS)
    • Airway obstruction
    • Anoxic encephalopathy
    • Disseminated intravascular coagulation (DIC)
    • Sepsis, septic shock
    • Tracheal stenosis
    • Death

 

Pearls

  • Bacterial Tracheitis is a rare, potentially fatal disease that is not exclusive to children, and can affect immunocompromised and tracheostomy-dependent adult patients.
  • BT typically presents with days of viral prodromal symptoms followed by acute decline with stridor, respiratory distress, and overall toxic appearance.
  • Labs and x-ray can be nonspecific, and definitive diagnosis is made with direct visualization.
  • Assessment of necessity for definitive airway takes precedence in BT in conjunction with appropriate antibiotics.

A 6-year-old girl presents to the ED with 1 day of fevers up to 104.1°F (40.1°C), cough with thick sputum production, and a sore throat. She has had a dry cough and rhinorrhea for 10 days, which had been improving over 2 days until she awoke this morning feeling worse. On examination, biphasic stridor is appreciated, and she appears in moderate respiratory distress. What is the most appropriate empiric antimicrobial therapy for the most likely diagnosis?

A) Ampicillin-sulbactam

B) Ceftriaxone and azithromycin

C) Ceftriaxone and vancomycin

D) Clindamycin

 

 

 

Answer: C

Bacterial tracheitis is an uncommon life-threatening upper airway infection that can lead to airway obstruction. It most often affects children between 5 and 8 years of age. The most likely organisms causing bacterial tracheitis include Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Moraxella catarrhalis, Haemophilus influenzae, and anaerobes. The classic presentation occurs after a recent viral upper respiratory infection, followed by the sudden onset of worsening fever, stridor (e.g., often biphasic), and cough with thick mucopurulent sputum production. Children may be toxic appearing and have early airway obstruction from thick mucopurulent secretions. The diagnosis is based on clinical signs and symptoms, aided by plain radiographs of the neck, which may demonstrate subglottic narrowing and irregular tracheal margins. Empiric treatment includes vancomycin or clindamycin in addition to a third-generation cephalosporin (e.g., ceftriaxone, cefotaxime) or a penicillin beta-lactamase inhibitor (e.g., ampicillin-sulbactam). Definitive airway management should be pursued early.

Ampicillin-sulbactam (A) appropriately covers gram-positive organisms, anaerobes, and oral flora responsible for bacterial tracheitis but would not provide sufficient Staphylococcus aureus coverage.

Ceftriaxone and azithromycin (B) is the appropriate empiric treatment for community-acquired pneumonia and common microbes, including Streptococcus pneumoniae and atypical pathogens (e.g., Mycoplasma pneumonia, Legionella pneumoniae). This coverage would not suffice for bacterial tracheitis.

Clindamycin (D) provides gram-positive coverage against pathogens such as Staphylococcus aureus that cause bacterial tracheitis but provides insufficient coverage for oral flora.


References

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