Respiratory, Head, and Neck Infections

Tuberculosis

Patient Population:
Pediatric
Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments
Latent tuberculosis infection (LTBI), positive tuberculosis skin test or interferon gamma release assay without evidence for active TB disease, without known exposure to individual with drug-resistant tuberculosis Mycobacterium tuberculosis 

Rifampin*  
17.5 mg/kg (max 600 mg/dose) enterally daily 

Drug-drug interactions should be evaluated prior to starting therapy (use Lexi-Comp drug-drug interaction checker) 

Isoniazid and Rifapentine* weekly for 12 weeks is the shortest treatment option for children 2 years and older who meet criteria; refer to linked guidelines below and consider ID consultation or discussion with local public health department   

Patient with contraindication to Rifampin (e.g. drug-drug interaction)

Isoniazid
12.5 mg/kg (max 300 mg/dose) enterally  daily 

AND 

Pyridoxine supplementation if exclusively breastfeeding or other risk factors for peripheral neuropathy (refer to linked guidelines below)  

A short course regimen is now preferred for all eligible patients due to higher likelihood of treatment completion and lower risk for adverse effects 

Duration

Rifampin: 4 months 

Isoniazid: 9 months 

Refer to linked guidelines below for detailed recommendations including LTBI diagnosis and monitoring during therapy 

Initiation of LTBI therapy is not recommended during pregnancy unless at high risk for progression - discuss with ID or local public health department as needed  

Latent tuberculosis infection, defined as above, with known exposure to individual with drug-resistant tuberculosis  Mycobacterium tuberculosis, drug-resistant  Consult ID and/or local public health department    Consult ID and/or local public health department 
Active tuberculosis disease  Mycobacterium tuberculosis  Consult ID   Consult ID

References:  

Latent Tuberculosis Infection Guidance for Preventing Tuberculosis in California. California Tuberculosis Controllers Association-California Department of Public Health Joint Guideline (June 2019 revision). 

* Centers for Disease Control and Prevention. Update on Rifamycin Issues  

 

Acute Bacterial Sinusitis

Patient Population:
Pediatric
Condition Major Pathogens  First-choice Therapy Alternative Therapy Comments

Acute bacterial sinusitis 

Diagnosed based on acute upper respiratory illness with: 

Persistent rhinorrhea or daytime cough lasting >=10 days and not improving  

OR 

Substantially worsening course after initial improvement 

OR 

Severe symptoms at onset:  

T >= 39C 

AND  

Purulent nasal discharge for at least 3 consecutive days 

Streptococcus pneumoniae 

Haemophilus influenzae 

Moraxella catarrhalis 

  

Recommend initial observation without antibiotic therapy if diagnosis is made only based on persistence of rhinorrhea or cough - many patients improve without antibiotic therapy 

Non-severe symptoms

Amoxicillin  
45 mg/kg/dose (max 1000 mg/dose)* enterally bid  

------------------------ 

Severe symptoms (see 1st  column)

Amoxicillin-clavulanate (Augmentin)
45 mg amoxicillin/kg/dose (max 2000 mg amoxicillin/dose)*  enterally bid  

Penicillin allergy with lower risk for allergic reaction

Oral cephalosporin (follow link for options) 

--------------------- 

Penicillin allergy with higher risk for allergic reaction

Consult ID/ASP  

Azithromycin is not recommended for this indication. 

Duration: Typical treatment duration is 10 days 

*See guidance on maximum dosing of Amoxicillin and Amoxicillin-Clavulanate 

Refer to Intracranial Abscess section if intracranial complication or Orbital Cellulitis section if orbital extension 

References

Wald, ER, et al. Clinical practice guideline for the diagnosis and management of acute bacterial sinusitis in children aged 1 to 18 years. Pediatrics 2013;132:e262-e280. 

American Academy of Pediatrics. In: Kimberlin DW, Barnett ED, Lynfield R, Sawyer MH, eds. Red Book: 2021 Report of the Committee on Infectious Diseases. 32nd ed. Elk Grove Village, IL: American Academy of Pediatrics; 2021.  

American Academy of Family Physicians Choosing Wisely Recommendation (updated 2018).

American College of Emergency Physicians Choosing Wisely Recommendation (2014).

 

Streptococcal Pharyngitis

Patient Population:
Pediatric
Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments
Streptococcal pharyngitis  Group A streptococcus 

Amoxicillin  
50 mg/kg/dose (max 1000 mg/dose) enterally daily  

------------------------ 

Anticipated difficulty tolerating or adhering to enteral therapy

Weight < 27 kg: Benzathine Penicillin G 600,000 units IM x 1 dose 

Weight > 27 kg: Benzathine Penicillin G 1.2 million units IM x 1 dose 

Penicillin allergy with lower risk for allergic reaction

Cephalexin  
25 mg/kg/dose (max 500 mg/dose) enterally bid  

------------------------- 

Penicillin allergy with higher risk for allergic reaction

Clindamycin  
7 mg/kg/dose (max 300 mg/dose) enterally tid 

Azithromycin is not recommended for this indication.  

Duration for oral beta lactam therapy (not Benzathine Penicillin): 10 days 

Acute Otitis Media

Patient Population:
Pediatric
Condition Major Pathogens  First-choice Therapy Alternative Therapy Comments
Acute otitis media 

Streptococcus pneumoniae 

Haemophilus influenzae 

Moraxella catarrhalis 

----------------------- 

Severe symptoms: moderate or severe otalgia or otalgia > 48 hours, or temperature 39C or higher 

Non-severe symptoms: mild otalgia < 48 hours, temperature <39C 

Recommend initial observation without antibiotic therapy for 48-72 hours in immunocompetent patients with the following criteria: 

6 months-2 years old: unilateral, no otorrhea, non-severe symptoms (see second column) 

OR 

>=2 years old: no otorrhea, non-severe symptoms (see second column) 

Ensure that reassessment and initiation of antibiotic will be feasible if symptoms do not improve during observation 

------------------------- 

For patients not meeting above criteria

Amoxicillin  
45 mg/kg/dose (max 1000 mg/dose)* enterally bid  

 

If patient meets criteria for treatment (same as 3rd column), and has received Amoxicillin within preceding 30 days, has purulent conjunctivitis, history of recurrent AOM not responsive to Amoxicillin, or does not respond to initial therapy with Amoxicillin x 48-72 hours

Amoxicillin-clavulanate (Augmentin)
45 mg amoxicillin/kg/dose (max 1000 mg amoxicillin/dose)* enterally bid   

Penicillin allergy with lower risk for allergic reaction

Oral cephalosporin (follow link for options) 

Penicillin allergy with higher risk for allergic reaction:  

Consult AAP/AAFP guidelines (linked below) or ASP. Azithromycin is not recommended for this indication. 

------------------------- 

Failed oral therapy:  

Consult AAP/AAFP guidelines (linked below) 

Duration for beta lactam therapy

< 2 years old or any age with severe symptoms: 10 days 

2-5 years old: 7 days 

> 5 years old: 5 days 

Pain control recommended for all patients 

*See guidance on Amoxicillin and Amoxicillin-clavulanate maximum dosing and formulation

References

Lieberthal, AS, et al. The diagnosis and management of acute otitis media. Pediatrics 2013;131:e964-e999. 

American Academy of Family Physicians Choosing Wisely Recommendation (updated 2018).

American Academy of Pediatrics. In: Kimberlin DW, Barnett ED, Lynfield R, Sawyer MH, eds. Red Book: 2021 Report of the Committee on Infectious Diseases. 32nd ed. Elk Grove Village, IL: American Academy of Pediatrics; 2021.  

Pertussis

Patient Population:
Pediatric
Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments
Pertussis Bordetella pertussis 

Age < 6 months

Azithromycin 
10 mg/kg/dose enterally or IV daily x 5 days 

------------------------ 

Age >= 6 months

Azithromycin  
10 mg/kg/dose (max 500 mg/dose) once enterally or IV on day 1 , then 5 mg/kg/dose (max 250 mg/dose) enterally or IV daily on days 2-5  

Refer to CDC guidelines below 

Provided regimens can also be used for post-exposure prophylaxis 

Refer to CDC guidelines on post-exposure prophylaxis 

Enteral therapy is preferred once it can be tolerated 

  

Periorbital/Preseptal Cellulitis

Patient Population:
Pediatric
Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments

Periorbital/preseptal cellulitis, suspected to be caused by skin flora (most common) 

Group A streptococcus 

Staphylococcus aureus 

  

Cephalexin
25 mg/kg/dose (max 500 mg/dose) enterally tid  

OR 

Cefazolin
25 mg/kg/dose (max 1000 mg/dose) IV q8h  

Choice of IV vs. enteral depending on illness severity; switch to enteral upon clinical improvement 

Penicillin or cephalosporin allergy with higher risk for allergic reaction:  

Clindamycin
10 mg/kg/dose (max 900 mg/dose) IV q8h  

OR  

Clindamycin
10 mg/kg/dose (max 600 mg/dose) enterally tid 

If patient is ill enough for inpatient care, consider evaluation for Orbital Cellulitis/Abscess, consider Ophthalmology consult 

Duration: 5-7 days or until resolution of inflammation 

Periorbital/preseptal cellulitis, suspected to be caused by sinus flora (patient has associated symptoms of sinusitis)  

Include coverage for:  

Streptococci 

Anaerobes 

Amoxicillin-clavulanate (Augmentin)
45 mg amoxicillin/kg/ dose (max 1000mg amoxicillin/dose)*  enterally bid 

OR 

Ampicillin-sulbactam (Unasyn) 50 mg ampicillin/kg/dose (max 2000 mg ampicillin/dose) IV q6h  

Choice of IV vs. enteral depending on illness severity; switch to enteral upon clinical improvement 

Penicillin or cephalosporin allergy with higher risk for allergic reaction

Clindamycin
10 mg/kg/dose (max 900 mg/dose) IV q8h  

OR  

Clindamycin
10 mg/kg/dose (max 600 mg/dose) enterally tid 

If patient is ill enough for inpatient care, consider evaluation for Orbital Cellulitis/Abscess, consider Ophthalmology consult 

*See guidance on Amoxicillin-Clavulanate maximum dosing and formulations 

Duration: 5-7 days or until resolution of inflammation. Duration may need to be extended to treat associated sinusitis. See Sinusitis section.  

Reference: 

American Academy of Pediatrics. In: Kimberlin DW, Barnett ED, Lynfield R, Sawyer MH, eds. Red Book: 2021 Report of the Committee on Infectious Diseases. 32nd ed. Elk Grove Village, IL: American Academy of Pediatrics; 2021.  

Orbital Cellulitis/Abscess

Patient Population:
Pediatric

Need for drainage/source control of head and neck infections should be evaluated carefully in consultation with Pediatric Otolaryngology, Head and Neck Surgery. If initial non-operative management is chosen, a narrow spectrum regimen (i.e. without vancomycin), is encouraged to facilitate transition to oral therapy. 

ID consultation is recommended for head and neck infections occcurring in immunocompromised patients, and for those with atypical features, chronic course, or lack of response to first line therapy. 

Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments
Orbital cellulitis/abscess 

Streptococci 

Staphylococcus aureus 

Haemophilus influenzae 

Anaerobes 

Ampicillin-sulbactam (Unasyn) 50 mg ampicillin/kg/dose (max 2000 mg ampicillin/dose) IV q6h  

If there is a large abscess (>10mm), anticipated to undergo surgical drainage, toxic appearance, rapidly progressive proptosis or ophthalmoplegia, or patient with history of documented MRSA infection or carriage within the last 6 months: 

ADD Vancomycin  

(follow link for dosing and monitoring)  

Penicillin or cephalosporin allergy with higher risk for allergic reaction:  

Consult ID/ASP 

Urgent OHNS and Ophthalmology consults recommended to evaluate need for source control   

ID consult recommended (see details above) 

For intracranial extension, refer to Intracranial Abscess section for empiric therapy 

Therapy may be tailored based on cultures from I&D. If Vancomycin was started but MRSA not recovered, Vancomycin should be discontinued.  

Duration: Uncomplicated orbital cellulitis/abscess is typically treated first with IV therapy then converted to enteral therapy within days based on clinical improvement, with a total duration of 14-21 days (combined IV and enteral).  

A longer duration may be indicated if there is significant bone destruction or a large abscess that is not drained. 

References: 

Seltz LB, et al. Microbiology and antibiotic management of orbital cellulitis. Pediatrics 2011;127:e566-e572. 

American Academy of Pediatrics. In: Kimberlin DW, Barnett ED, Lynfield R, Sawyer MH, eds. Red Book: 2021 Report of the Committee on Infectious Diseases. 32nd ed. Elk Grove Village, IL: American Academy of Pediatrics; 2021.  

Conjunctivitis (Infants, Children, Adolescents)

Patient Population:
Pediatric

See Ophthalmia Neonatorum section for special considerations in neonates.  

Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments

Conjunctivitis 

This section does not address infectious keratitis associated with contact lens wear (patients with this condition should be managed in consultation with an optometrist or ophthalmologist) 

Often viral 

Streptococcus pneumoniae 

Haemophilus influenzae 

Moraxella catarrhalis 

Staphylococcus aureus 

Supportive care without topical antibiotic therapy is recommended unless bacterial etiology is suspected based on clinical features 

If suspected bacterial etiology

Trimethoprim-Polymyxin B (Polytrim) 0.1%-10,000 units/ml ophthalmic drops 1-2 drops 4 times daily  

Topical therapy is not necessary if patient is on concurrent systemic therapy with coverage against likely causative organisms 

Commonly caused by viruses, consider supportive treatment such as warm compresses or cold saline drops 

Duration: 5-7 days 

Mastoiditis

Patient Population:
Pediatric

Need for drainage/source control of head and neck infections should be evaluated carefully in consultation with Pediatric Otolaryngology, Head and Neck Surgery. If initial non-operative management is chosen, a narrow spectrum regimen (i.e. without vancomycin) is encouraged to facilitate transition to oral therapy. 

ID consultation is recommended for head and neck infections occurring in immunocompromised patients, and for those with atypical features, chronic course, or lack of response to first line therapy.  

Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments

Mastoiditis - acute, immunocompetent patient          

(<1 month duration) 

OR 

Subacute (duration >= 1 month) but with the following distinctions from chronic mastoiditis:  
 
Develops as a complication of acute otitis media 

Patient does not have history of a chronically non-intact tympanic membrane 

Patient does not have history of chronic suppurative otitis media 

Streptococcus pneumoniae 

Group A streptococcus 

Staphylococcus aureus 

Ampicillin-sulbactam (Unasyn) 50 mg ampicillin/kg/dose (max 2000 mg ampicillin/dose) IV q6h  

If patient has history of documented MRSA infection or carriage within the last 6 months:

ADD Vancomycin  

(follow link for dosing & monitoring)  

Penicillin or cephalosporin allergy with higher risk for allergic reaction:  

Consult ID/ASP 

Urgent OHNS consult recommended to evaluate need for source control 

Consider ID consult (see details above) 

For confirmed or suspected intracranial extension, refer to Intracranial Abscess section for empiric therapy 

Therapy may be tailored based on cultures from I&D 

If Vancomycin was started and MRSA not recovered from drained abscess, discontinue Vancomycin 

Duration: Uncomplicated acute mastoiditis is typically treated first with IV therapy then converted to enteral therapy within days based on clinical improvement, with a total duration of 3-4 weeks (combined IV and enteral).  

A longer duration and more IV therapy is indicated for intracranial or other complications.  

Mastoiditis - chronic    

(months-years duration, arising as a complication of chronic suppurative otitis media, with chronically non-intact tympanic membrane) 

Variable depending on risk factors  

  

Individualized treatment guided in consultation with OHNS    

OHNS consult recommended (management is primarily surgical)  

ID consult recommended if patient is presenting with new severe local symptoms and/or signs in the context of history of chronic mastoiditis, or if not responsive to usual management 

Reference: 

American Academy of Pediatrics. In: Kimberlin DW, Barnett ED, Lynfield R, Sawyer MH, eds. Red Book: 2021 Report of the Committee on Infectious Diseases. 32nd ed. Elk Grove Village, IL: American Academy of Pediatrics; 2021.

Lymphadenitis

Patient Population:
Pediatric

Need for drainage/source control of head and neck infections should be evaluated carefully in consultation with Pediatric Otolaryngology, Head and Neck Surgery. If initial non-operative management is chosen, a narrow spectrum regimen (i.e. without vancomycin) is encouraged to facilitate transition to oral therapy. 

ID consultation is recommended for head and neck infections occurring in immunocompromised patients, and for those with atypical features, chronic course, or lack of response to first line therapy. 

Condition Major Pathogens  First Choice Therapy Alternative Therapy Comments

Lymphadenitis - acute, suppurative bacterial, usually unilateral 

Usual presentation, without suspected dental source (e.g. periodontal disease, poor dental hygiene) 

Staphylococcus aureus 

Group A streptococcus 

  

Cephalexin 25 mg/kg/dose (max 500 mg/dose) enterally tid  

OR 

Cefazolin 25 mg/kg/dose (max 1000 mg/dose) IV q8h  

Choice of IV vs. enteral depending on illness severity; switch to enteral route upon clinical improvement 

Penicillin or cephalosporin allergy with higher risk for allergic reaction OR history of documented MRSA infection or carriage within the last 6 months 

Please confirm clindamycin susceptibility if prior cultures are available, tailor antibiotics to past susceptibility:

Clindamycin
10 mg/kg/dose (max 600 mg/dose) enterally tid 

OR  

Clindamycin
10 mg/kg/dose (max 900 mg/dose) IV q8h 

Consider OHNS consult to evaluate need for source control 

If lack of response to empiric therapy, consider need for drainage, or alternative etiology besides typical bacteria - consider ID consult (also see details above) 

Duration: 10 days (or 5-7 days after abscess drainage if applicable) 

Lymphadenitis - acute, suppurative bacterial, usually unilateral 

With suspected dental source (e.g. concurrent periodontal disease) 

Oral streptococci and anaerobes 

Amoxicillin-clavulanate (Augmentin) 22.5 mg amoxicillin/kg/ dose (max 875 mg amoxicillin/dose) enterally bid  

OR 

Ampicillin-sulbactam (Unasyn) 50 mg ampicillin/kg/dose (max 2000 mg ampicillin/dose) IV q6h  

Choice of IV vs. enteral depending on illness severity, switch to enteral route upon clinical improvement

Penicillin or cephalosporin allergy with higher risk for allergic reaction OR history of documented MRSA infection or carriage within the last 6 months 

Please confirm clindamycin susceptibility if prior cultures are available, tailor antibiotics to past susceptibility

Clindamycin
10 mg/kg/dose (max 600 mg/dose) enterally tid 

OR 

Clindamycin
10 mg/kg/dose (max 900 mg/dose) IV q8h  

Consider OHNS consult to evaluate need for source control 

If lack of response to empiric therapy, consider need for drainage, or alternative etiology besides typical bacteria - consider ID consult (also see details above) 

Duration: 10 days (or 5-7 days after abscess drainage if applicable) 

Reference: 

American Academy of Pediatrics. In: Kimberlin DW, Barnett ED, Lynfield R, Sawyer MH, eds. Red Book: 2021 Report of the Committee on Infectious Diseases. 32nd ed. Elk Grove Village, IL: American Academy of Pediatrics; 2021.