What is the recommended assessment and management of pneumonia in children, including severity classification, antibiotic choice and dosing, and supportive care?

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Management of Community-Acquired Pneumonia in Children

For children with community-acquired pneumonia, use high-dose oral amoxicillin 90 mg/kg/day divided twice daily for 7 days as first-line therapy, reserve chest radiographs for hospitalized patients or those with hypoxemia/respiratory distress, and admit any child with oxygen saturation <92% or significant respiratory distress. 1, 2

Initial Assessment and Severity Classification

Mandatory Clinical Measurements

  • Perform pulse oximetry on every child with suspected pneumonia—oxygen saturation directly determines site of care and guides all subsequent management decisions. 1, 2

  • Assess respiratory rate using WHO age-specific thresholds: >70 breaths/min in infants, >50 breaths/min in children 1-5 years, and >40 breaths/min in older children. 1, 2

  • Evaluate work of breathing by documenting presence of retractions, nasal flaring, grunting, or dyspnea—these findings indicate moderate to severe disease. 1, 2

Criteria for Outpatient Management (All Must Be Present)

  • Oxygen saturation ≥92% on room air 1, 2
  • No significant respiratory distress or increased work of breathing 1, 2
  • Able to tolerate oral fluids and medications 1, 2
  • Reliable caregivers who can ensure follow-up within 48 hours 1, 2
  • Fully immunized child with no toxic appearance 2

Criteria for Hospital Admission (Any One Present)

  • Oxygen saturation <92% on room air 1, 2
  • Moderate to severe respiratory distress with increased work of breathing 1, 2
  • Inability to tolerate oral intake or medications 1, 2
  • Age <3 months with fever and respiratory symptoms 1
  • Suspected community-acquired MRSA infection 2
  • Concerns about safe home observation or inability to secure follow-up 1, 2

ICU Admission Criteria

Transfer to intensive care if ≥1 major criterion OR ≥2 minor criteria are present: 1, 2

Major criteria:

  • Need for invasive mechanical ventilation 1
  • Fluid-refractory shock requiring vasopressors 1
  • Acute need for non-invasive positive pressure ventilation 1
  • Hypoxemia requiring FiO₂ >0.50 or flow not feasible on general ward 1

Minor criteria:

  • Altered mental status from hypercarbia or hypoxemia 1
  • Hypotension or requirement for vasopressor support 1
  • Multilobar infiltrates on chest radiograph 1
  • Presence of parapneumonic effusion 1
  • PaO₂/FiO₂ ratio <250 1

Diagnostic Testing Strategy

Outpatient Setting

  • Do NOT obtain routine chest radiographs in well-appearing children who can be managed as outpatients—this leads to overdiagnosis and unnecessary antibiotic use. 1, 2

  • Do NOT obtain routine blood cultures in non-toxic, fully immunized children managed as outpatients—yield is extremely low. 1, 2

  • Do NOT measure acute-phase reactants (CRP, ESR, procalcitonin) routinely in outpatients—they cannot distinguish viral from bacterial pneumonia and do not change management. 1, 2

  • Obtain chest radiograph (PA and lateral) only if: 1, 2

    • Documented or suspected hypoxemia (oxygen saturation <92%)
    • Significant respiratory distress present
    • Failed initial antibiotic therapy after 48-72 hours
    • Suspicion of complications (effusion, pneumothorax, necrotizing pneumonia)

Inpatient Setting

  • Obtain PA and lateral chest radiograph on all hospitalized children to document infiltrate characteristics and identify complications requiring intervention beyond antibiotics. 1, 2

  • Obtain blood cultures in all children with moderate to severe pneumonia requiring hospitalization. 1, 2

  • Consider complete blood count for severe pneumonia, though it does not reliably distinguish bacterial from viral etiology. 2

  • Acute-phase reactants may be used in conjunction with clinical findings to monitor response to therapy in hospitalized patients with more serious disease. 1

Follow-Up Imaging

  • Do NOT obtain routine follow-up chest radiographs in children who recover uneventfully—radiographic abnormalities lag behind clinical improvement. 1

  • Obtain repeat chest radiograph if: 1

    • No clinical improvement or deterioration within 48-72 hours of antibiotic initiation
    • Persistent fever not responding to therapy over 48-72 hours
    • Worsening respiratory distress in complicated pneumonia
  • Obtain follow-up chest radiograph 4-6 weeks after diagnosis if: 1

    • Recurrent pneumonia involving the same lobe
    • Lobar collapse at initial radiography with suspicion of anatomic anomaly, chest mass, or foreign body aspiration

Antibiotic Selection and Dosing

First-Line Outpatient Therapy

Prescribe high-dose oral amoxicillin 90 mg/kg/day divided into 2 doses (maximum 4 g/day) for 7 days as first-line therapy for all children >3 months with presumed bacterial community-acquired pneumonia. 1, 2, 3, 4

  • This high-dose regimen achieves adequate drug levels against penicillin-resistant Streptococcus pneumoniae with MICs up to 2-4 mg/L. 2, 3

  • S. pneumoniae remains the most common bacterial pathogen causing community-acquired pneumonia across all pediatric age groups. 2, 3

  • Calculate total daily dose by multiplying weight (kg) × 90 mg/kg/day, then divide into two equal doses given every 12 hours. 2, 3

  • Do NOT exceed 2 g per single dose or 4 g per day regardless of weight. 2

When to Add Macrolide Coverage

Add azithromycin to β-lactam therapy in the following situations: 2, 5, 3

  • Children ≥5 years when clinical, laboratory, or radiographic findings cannot reliably differentiate typical from atypical pneumonia 2
  • No clinical improvement within 48-72 hours of amoxicillin monotherapy 2, 3
  • Mycoplasma pneumoniae or Chlamydia pneumoniae suspected based on epidemiology (school-age children, prolonged cough, lack of toxic appearance) 2, 5

Azithromycin dosing: 10 mg/kg (maximum 500 mg) on day 1, then 5 mg/kg (maximum 250 mg) once daily on days 2-5 for a total 5-day course. 2, 5

Critical caveat: Do NOT use macrolide monotherapy in children <5 years due to inadequate coverage of S. pneumoniae—always combine with β-lactam or use β-lactam alone. 2

Alternative Regimens for Specific Situations

For penicillin-allergic patients (non-anaphylactic reactions):

  • Use second- or third-generation cephalosporin (cefdinir, cefuroxime, cefpodoxime) under medical supervision. 2

For penicillin-allergic patients with type I hypersensitivity (anaphylaxis):

  • Use respiratory fluoroquinolone (levofloxacin for growth-mature adolescents) or linezolid. 2

For suspected β-lactamase-producing organisms (H. influenzae, M. catarrhalis) or incomplete immunization:

  • Prescribe amoxicillin-clavulanate 90 mg/kg/day of amoxicillin component (maximum 4 g/day) divided twice daily. 2, 3

Inpatient Parenteral Therapy

For fully immunized children in areas with minimal penicillin resistance:

  • Ampicillin 150-200 mg/kg/day IV divided every 6 hours OR penicillin G 200,000-250,000 units/kg/day IV divided every 4-6 hours. 2

For incompletely immunized children or areas with high penicillin resistance:

  • Ceftriaxone 50-100 mg/kg/day IV divided every 12-24 hours OR cefotaxime 150 mg/kg/day IV divided every 8 hours. 2

If community-acquired MRSA suspected (necrotizing pneumonia, empyema, severe sepsis):

  • Add vancomycin 40-60 mg/kg/day IV divided every 6-8 hours OR clindamycin 40 mg/kg/day IV divided every 6-8 hours. 2

For suspected atypical pneumonia in hospitalized patients:

  • Add azithromycin 10 mg/kg IV (maximum 500 mg) once daily on days 1-2, then transition to oral therapy. 2, 5

Transition to Oral Therapy

Switch from IV to oral antibiotics when: 2

  • Child is afebrile for 24 hours
  • Improved respiratory rate and work of breathing
  • Tolerating oral intake without vomiting
  • Typically occurs within 48-72 hours of admission

Complete a total antibiotic course of 7 days for uncomplicated community-acquired pneumonia—do not extend beyond 7 days if clinically resolved. 2, 4

Supportive Care Measures

Oxygen Therapy

  • Administer supplemental oxygen via nasal cannula, head box, or face mask to maintain oxygen saturation >92% in all children with documented hypoxemia. 1, 2

  • Monitor oxygen saturation at least every 4 hours in all patients receiving oxygen therapy. 1

Fluid Management

  • Administer intravenous fluids at 80% of basal maintenance requirements if IV hydration is needed, and monitor serum electrolytes closely to avoid hyponatremia. 1

  • Avoid nasogastric tubes in severely ill children, especially infants with small nasal passages, as they may compromise breathing—if necessary, use the smallest tube in the smallest nostril. 1

Symptomatic Management

  • Use antipyretics (acetaminophen or ibuprofen) and analgesics to keep the child comfortable and help with coughing. 1

  • Minimize handling in ill children to reduce metabolic and oxygen requirements. 1

  • Do NOT perform chest physiotherapy—it provides no benefit and should not be used in children with pneumonia. 1

Expected Clinical Response and Re-evaluation

Timeline for Improvement

Children on appropriate antibiotic therapy should demonstrate clinical improvement within 48-72 hours, including: 2, 5, 3

  • Decreased or resolved fever
  • Improved respiratory rate
  • Reduced work of breathing
  • Better oral intake and activity level

Re-evaluation Protocol if No Improvement

If the child remains febrile or unwell 48-72 hours after starting therapy, reassess for: 2, 3

  • Inadequate antibiotic dosing or inappropriate drug selection—verify correct weight-based calculation and consider resistance patterns 2

  • Atypical pathogens requiring macrolide addition—particularly in school-age children with prolonged symptoms 2, 3

  • Complications:

    • Parapneumonic effusion or empyema requiring drainage 1, 2
    • Necrotizing pneumonia 1, 2
    • Pneumothorax 1
    • Lung abscess 2
  • Resistant organisms—consider MRSA, highly resistant S. pneumoniae, or β-lactamase-producing organisms 2

  • Alternative diagnoses—foreign body aspiration, tuberculosis, fungal infection, malignancy, or non-infectious causes 2

Obtain repeat chest radiograph to evaluate for these complications if clinical deterioration or lack of improvement occurs. 1

Common Pitfalls to Avoid

  • Do NOT underdose amoxicillin—the 90 mg/kg/day regimen (not 45 mg/kg/day) is required for adequate pneumococcal coverage in the era of resistant S. pneumoniae. 2, 3

  • Do NOT obtain chest radiographs routinely in well-appearing outpatients—this leads to overdiagnosis, as 55-65% of children with clinical findings suggestive of pneumonia do not have radiographic infiltrates. 6

  • Do NOT use macrolide monotherapy in children <5 years—inadequate S. pneumoniae coverage leads to treatment failure. 2

  • Do NOT confuse azithromycin dosing with other macrolides—azithromycin is dosed once daily, whereas clarithromycin requires twice-daily dosing. 5

  • Do NOT withhold antibiotics in young children with mild symptoms and wheeze—primary bacterial pneumonia is unlikely when wheeze is the predominant finding. 1

  • Do NOT rely solely on acute-phase reactants to distinguish viral from bacterial pneumonia—they lack sufficient specificity and sensitivity for this purpose. 1, 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Community-Acquired Pneumonia Management in Children

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

High‑Dose Amoxicillin Regimen for Pediatric Community‑Acquired Pneumonia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Azithromycin Dosage and Administration Guidelines for Children

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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