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Bacterial Tracietis
Bacterial Tracietis
ORIGINAL ARTICLE
acterial tracheitis is an uncommon cause of upper airway In this review, the important distinguishing features and the
B obstruction that can potentially result in a life threaten-
ing situation. Bacterial tracheitis was initially described in
pathophysiology will be presented. The differential diagnosis
and approach to treatment of the child with bacterial tra-
the medical literature in the late 1920s, when it was generally cheitis will be discussed.
referred to as acute laryngotracheobronchitis (1). Although
investigators described this as a bacterial illness in the early PATHOPHYSIOLOGY
studies (2-4), the name bacterial tracheitis was not coined In bacterial tracheitis, pathogenic bacteria invade the tra-
until much later when Jones et al (5) reported a case series chea and stimulate both local and systemic inflammatory
of infants with the disorder. Membranous croup, responses. Locally, this results in production of thick,
pseudomembranous croup, bacterial croup, purulent tra- mucopurulent exudates, ulceration and sloughing of the
cheobronchitis and membranous laryngotracheobronchitis tracheal mucosa (5,8). This can result in a variable degree
are other medical terms applied to this disease complex in of upper airway obstruction. The severity of the upper air-
the literature (6). Bacterial tracheitis most frequently affects way obstruction depends on the location and extent of the
preschool and early school-aged children, however, it has damage to the tracheal mucosa, the age and underlying
also been reported in infants as well as adults (5,7). Bacterial medical condition of the patient and the size of the airway.
invasion of the tracheal mucosa results in the formation of Bacterial tracheitis often presents as a secondary illness
mucopurulent exudates which can cause acute upper airway following an acute respiratory viral infection (3,5,9). The
obstruction. The clinical features of bacterial tracheitis are viral illness is believed to cause transient local or systemic
similar to those of both common viral croup and epiglottitis. alterations in the immune response that predispose the host
1Pediatric
Respiratory Medicine;and 2Department of Paediatrics, Faculty of Medicine, University of Calgary, Calgary, Alberta
Correspondence: Dr Valerie Kirk, Alberta Children’s Hospital, 1820 Richmond Road SW, Calgary, Alberta T2T 5C7. Telephone 403-943-2923,
fax 403-943-7059, e-mail val.kirk@calgaryhealthregion.ca
Paediatr Child Health Vol 9 No 1 January 2004 ©2004 Pulsus Group Inc. All rights reserved 25
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to bacterial infection (3,8,10,11). This theory is strongly sup- with a peak incidence around three to eight years of age
ported by the observation that bacterial tracheitis cases occur (5,8,9,12,17-20). The reported male to female ratio is
most often during upsurges of winter viral epidemics in the quite variable, between 1:1 and 5:1. Most published case
community, including that of viral croup (9,12,13). The iso- series, however, clearly show males are more commonly
lation of both viral and bacterial pathogens in the tracheal affected than females, with only a single large series show-
secretions of children with bacterial tracheitis has been ing no sex differences (5,8,9,12,17-19). There are no spe-
reported by a number of investigators. Edwards et al (14) cific risk groups identified to date. Bacterial tracheitis is
reported on the coexistence of Staphylococcus aureus, Group A an uncommon cause of hospital admissions, with an over-
Streptococcus and Influenza B/Hong Kong virus in one child all reported incidence of 0.4 per 1000 paediatric admis-
with bacterial tracheitis and S aureus with parainfluenza type 2 sions (18). The incidence rate at the authors’ institution
in another. A separate and larger case series published around over the last 10 years has ranged from one to two cases per
the same time described the coexistence of parainfluenza 1000 paediatric admissions. These data are based on dis-
type 1 with several pathogenic bacterial species including S charge diagnoses entered into a global computerized data-
aureus, α-Hemolytic Streptococcus species, and Haemophilus base and do not explicitly include bronchoscopy-proven
influenzae type b (9). More recently, Bernstein et al (12) iso- cases. This may account for the discrepancy with pub-
TABLE 1
Typical features of croup, epiglottitis and bacterial tracheitis
Epiglottis
Croup laryngotracheobronchitis Bacterial tracheitis
Incidence Common Rare Less common
Age 6 months – 3 years 2 – 7 years 6 months – 14 years
Etiology Parainfluenza type 1 Haemophilus influenza type b Staphylococcus aureus,
Moraxella catarrhalis,
Streptococcus pneumoniae
Onset of stridor Insidious, common Very rapid, less common Rapid, common
Fever Low grade High High
Cough Common Less common Common
Voice Hoarse Muffled Very hoarse
Drooling Absent Present Absent
Preferred position Supine Tripod Supine
Respiratory distress Common Common Common
*Radiographs are not indicated in the initial management of a child with suspected epiglottitis; †Narrowing of subglottic area; ‡Thickening and rounding of epiglottis.
AP Anteroposterior; CXR Chest x-ray
INVESTIGATIONS epiglottitis until the diagnosis has been confirmed and the
The diagnosis of bacterial tracheitis is most often made on airway stabilized.
the basis of the history and physical examination, combined Chest radiograph abnormalities are common in children
with findings from laboratory and bronchoscopic examina- with bacterial tracheitis. In most case series, at least 50% had
tion. Some authors have used diagnostic criteria that radiological findings suggestive of pneumonia (13).
included clinical signs of upper airway obstruction and at Concurrent pneumonia is often associated with increased
least two of the following: radiographic evidence of intra- disease severity; the largest case series reported that only
tracheal membranes; laryngotracheal inflammation and those patients with pulmonary infiltrates on chest radiograph
mucopurulent secretions noted by direct visualization dur- required endotracheal intubation (12,16,21). Lobar atelecta-
ing bronchoscopy; or a tracheal aspirate positive for leuko- sis due to mucous plugging with compensatory hyperinflation
cytes on gram staining and a positive bacterial culture is another, less frequent, radiographic finding (22).
(12,18).
Results of laboratory investigations including the com- LARYNGOBRONCHOSCOPY
plete blood count with differential and blood cultures are Direct visualization of the airway is the most definitive way
generally nonspecific. Leukocytosis may or may not be pres- to diagnose bacterial tracheitis. Bronchoscopy is also help-
ent; however, most case series do report an increase in ful for the exclusion of other diagnoses such as epiglottitis.
immature cells on the differential. Blood cultures infre- The typical bronchoscopic findings of bacterial tracheitis
quently yield positive identification of the responsible bac- include subglottic narrowing, diffuse erythema and mucopu-
terium (5,9,12,17). rulent exudates that may partially occlude the airway.
Exudates may also be seen extending into the right and/or
RADIOGRAPHIC FINDINGS left main bronchi. Importantly, the epiglottis usually
The anteroposterior radiograph of the cervical airway in appears normal or only slightly inflamed.
children with bacterial tracheitis frequently shows narrow- Pulmonary toilet can be effectively performed via the
ing of the subglottic area (5,13,17,20). Less frequently, dif- bronchoscope, and secretions can be easily obtained and sent
fuse haziness and irregularity of the anterior wall of the for culture and sensitivity to allow for targeted antibiotic
trachea may be seen on the lateral neck radiograph (candle- therapy. Identification of the pathogen is usual (62% to 87%)
dripping sign). This finding, although less common, is more presuming no prior treatment with antibiotics (12).
specific for bacterial tracheitis (5,13,17,20). Radiographs The decision to perform bronchoscopy should be indi-
are contraindicated in any child suspected of having vidualized. Factors to consider include the severity of upper
TABLE 2
Clinical features of other causes of acute upper airway obstruction
Fever Cough Voice Stridor Specific features
Peritonsillar abscess Present Absent Muffled +/– • Sore throat
• Trismus
• Dysphagia
• Torticollis(sometimes)
• Unilateral peritonsillar swelling
• Uvula displaced to opposite side
Retropharyngeal abscess Present Absent +/– muffled +/– • Dysphagia
• Drooling
• Sore throat
• Meningismus
• Increased retropharyneal space on lateral neck x-ray
Angioedema Absent Absent Normal +/– • Urticaria
airway obstruction, the level of clinical suspicion for the Endotracheal intubation is frequently required for stabi-
presence of epiglottitis, accessibility of skilled broncho- lization of the airway, management of acute respiratory fail-
scopists and the age of the child. ure, or pulmonary toilet. The decision to intubate should be
individualized and will depend on the severity of the upper
TREATMENT airway obstruction as well as the likelihood of further dete-
Broad spectrum intravenous antibiotics should be initiated rioration while awaiting a clinical response to antimicrobial
as soon as the clinical diagnosis of bacterial tracheitis is therapy. Clearance of airway secretions is more effective
made. Empirical antimicrobial agents should be targeted to with an endotracheal tube in situ because suctioning can be
the most frequently isolated organisms including S aureus, done frequently and aggressively, preventing occlusion of
M Catarrhalis, S pneumoniae and H influenzae. A third gen- the airway by thick exudates. Younger children are more
eration cephalosporin agent combined with a beta-lacta- likely to require intubation due to the small size of their air-
mase resistant penicillin (eg, cloxacillin) is appropriate for way (20). The level of comfort of the attending physician
first line therapy. If methicillin-resistant S aureus is a con- and availability of ready access to a skilled bronchoscopist
cern at the admitting institution, coverage should be also play major roles in the decision regarding intubation.
extended to cover this organsim (eg, vancomycin). If the Overall rates of intubation for airway management of bac-
anaerobic culture is positive, additional or alternative ther- terial tracheitis reported in published case series are variable
apy such as clindamycin or metronidazole may be consid- and range from 38% to 100%, depending on the centre
ered, particularly in a child who is not responding to first (5,8,9,17-20). When intubation is indicated, the endotra-
line therapy. However, contamination of tracheal aspirate cheal tube size needs to be modified to a smaller size than
secretions with oral anaerobes is not uncommon when the that normally required for the age to account for the airway
specimens are obtained via bronchoscopy. Antibiotic cov- inflammation present. In Bernstein et al’s case series (12), 26
erage can then be modified according to culture and sensi- of 46 children (54%) were managed with intubation using
tivity results. A total 10 to 14 day course of antibiotics endotracheal tubes that were smaller than that normally
(intravenous plus oral) is recommended based on previous required for the age (mean of –1.7 mm) (12). In this particu-
case series; however, there have been no formal studies to lar series, the mean duration of intubation was 3.2 days.
establish the optimum duration of antimicrobial therapy for However, there was a high yield of positive viral cultures in
bacterial tracheitis. Intravenous therapy is recommended this patient population, raising the possibility that some
until the child is afebrile for at least 48 h, the tracheal ten- subjects may not have had true bacterial tracheitis. Indeed,
derness has resolved and the voice has recovered normal the diagnostic criteria used for this case series did not neces-
quality. sarily include positive bronchoscopic findings, and although
all their patients underwent bronchoscopy, these findings Diagnostic approach to acute airway obstruction in children
were not discussed in the paper. Other case series report a Acute upper airway obstruction
mean duration of intubation of between 1.5 to 7.6 days
(8,12,18,19). Identify
Response to racemic: epinephrine
Indications for extubation include indicators of general •Laryngeal foreign body
clinical improvement such as reduced fever, decreased tra- •Angioedema (see Table 2)
egy is particularly helpful for older children who may be sup- •Airway clearance
pressing cough due to discomfort. •Observation and monitoring in close proximity to personnel
skilled at airway management (arrange transport if appropriate)
Unlike viral croup, there is currently no data to suggest
that inhaled or systemic steroids provide any clinical bene-
Figure 1) Diagnostic approach to acute airway obstruction in chil-
fit in the treatment of bacterial tracheitis. Concern regard- dren. IV Intravenous
ing adverse effects in the absence of documented clinical
efficacy prohibits the recommendation that steroids be used
for routine management. Racemic epinephrine, used com- slowly with time, and the most recent and largest case series
monly to treat symptoms of upper airway obstruction in reported no mortality associated with the illness
children with viral croup, is not very effective in relieving (9,12,18,19). The improvement in mortality rate is likely
airway obstruction related to bacterial tracheitis (9,12,17-19). due to the early recognition and improved treatment of the
An algorithm outlining the approach to a child with acute disorder with aggressive airway clearance techniques and
upper airway obstruction is presented in Figure 1. early initiation of broad spectrum antibiotics.
Long-term morbidity associated with bacterial tracheitis
COMPLICATIONS AND PROGNOSIS is minimal. As treatment in the acute phase of the illness
Full recovery with no long-term morbidity is expected in frequently requires insertion of an endotracheal tube into
the vast majority of children with bacterial tracheitis, espe- an inflamed airway, the potential for the subsequent devel-
cially if there are no complications during the acute illness. opment of subglottic stenosis is recognized. This complica-
The mean length of stay in hospital varies with reports tion, indeed, has been reported in two papers. Gallagher
between three and 12 days (5,8,12,18,19). One small case (18) reported that three of 18 patients had subglottic steno-
series of children with bacterial tracheitis reported a mean sis, and Kasian (19) reported one case in 14 patients.
duration of hospitalization of 20.8 days (17). The authors
speculated that this was due to complications associated CONCLUSION
with a protracted recovery in several patients (17). Bacterial tracheitis is a potentially life-threatening condi-
The most frequent complication associated with the tion, however, when diagnosed and treated early, complete
acute phase of illness is pneumonia. Other less common recovery is usual. Primary care physicians need to be famil-
complications include acute respiratory distress syndrome, iar with this condition and how the clinical presentation of
septic shock, toxic shock syndrome, pulmonary edema, bacterial tracheitis differs from croup.
pneumothorax, and rarely, cardiorespiratory arrest (21).
The mortality rate due to bacterial tracheitis has decreased ACKNOWLEDGEMENTS: The authors wish to thank Dr Ruth
dramatically with time. In the early twentieth century, the Connors and Dr Abdulla Al-Shamrani for their thoughtful review
of the manuscript and helpful editorial comments.
mortality rate was 10% to 40% (11). This has declined
REFERENCES
1. Baum HL. Acute laryngotracheobronchitis. JAMA 1928;91:1097-102. 13. Han BK. DJ, Striker TW. Membranous laryngotracheobronchitis
2. Orton HB, Smith EL, Bell HO. Acute laryngotracheobronchitis. (membranous croup). AJR Am J Roentgenol
Arch Otolaryngol 1941;33:926-60. 1979;133:53-8.
3. Nelson W. Bacterial croup: A historical perspective. J Pediatr 14. Edwards K, Dundon M, Altemeier W. Bacterial tracheitis as a
1984;105:52-5. complication of viral croup. Pediatr Infect Dis
4. Neffson AH. Acute laryngotracheobronchitis: A 25 year review. 1983;2:390-1.
Am J Med Sci 1944;208:524-47. 15. Wong V, Mason W. Branhamella catarrhalis as a cause of bacterial
5. Jones R, Santos J, Overall Jr J. Bacterial tracheitis. JAMA tracheitis. Pediatr Infect Dis J 1987;6:945-6.
1979;242:721-6. 16. Brook I. Aerobic and anaerobic microbiology of bacterial tracheitis
6. Stern RC. Acute laryngotracheobronchitis, 3rd ed. Philadelphia: in children. Pediatr Emerg Care 1997;13:16-8.
WB Saunders, 1983. 17. Sofer S, Duncan P, Chernick V. Bacterial tracheitis – An old disease
7. Johnson J, Liston S. Bacterial tracheitis in adults. Arch Otolaryngol rediscovered. Clin Pediatr 1983;22:407-11.
Head Neck Surg 1987;113:204-5. 18. Gallagher P. An approach to the diagnosis and treatment of
8. Donnelly B, McMillan J, Weiner L. Bacterial tracheitis: Report of eight membranous laryngotracheobronchitis in infants and children.
new cases and review. Rev Infect Dis 1990;12:729-35. Pediatr Emerg Care 1991;7:337-42.
9. Liston SL, Gehrz RC, Siegel LG, Tilelli J. Bacterial tracheitis. 19. Kasian G, Bingham W, Steingberg J, et al. Bacterial tracheitis in
Am J Dis Child 1983;137:764-7. children. CMAJ 1989;140:46-50.
10. Davidson S, Barzilay Z, Yahav J, Rubinstein E. Bacterial tracheitis – 20. Friedman E, Jorgensen K, Healy G, McGill T. Bacterial tracheitis –
a true entity? J Laryngol Otol 1982;96:173-5. Two-year experience. Laryngoscope 1985;95:9-11.