Augmentin IV Treatment Protocol for Severe Bacterial Infections
For severe bacterial infections requiring intravenous therapy, administer Augmentin (co-amoxiclav) at 30 mg/kg every 8 hours, with the dose doubled to 60 mg/kg every 8 hours (maximum 4 g/day) in severe infections, particularly for community-acquired pneumonia, intra-abdominal infections, and complicated skin/soft tissue infections. 1
Dosing by Age and Severity
Pediatric Dosing (1 month to 18 years)
- Standard severe infections: 30 mg/kg IV every 8 hours 1
- Life-threatening infections: 60 mg/kg IV every 8 hours (maximum 4 g/day) 1
- Children >3 months with severe infections: Frequency can be increased to every 6 hours (4 times daily) 1
Adult Dosing (12-18 years and older)
Primary Indications for IV Augmentin
Community-Acquired Pneumonia
- Use when oral therapy is not tolerated or in severe disease with hypoxemia, respiratory rates ≥70 breaths/min in infants, or significant chest recession 1
- Duration: 7-10 days, may extend to 14 days based on clinical response 1
Intra-Abdominal Infections
- Mild to moderate community-acquired IAI: Augmentin provides adequate coverage for mixed aerobic-anaerobic infections 1
- Severe IAI: Consider 30 mg/kg every 6 hours (4 times daily) for enhanced coverage 1
- Duration: 5-7 days after adequate source control 1
Complicated Skin and Soft Tissue Infections
- Particularly effective for polymicrobial infections including animal/human bites and contaminated traumatic wounds 2, 3
- First-line for infections involving axilla or perineum 1
Critical Administration Principles
Timing and Loading
- Sepsis/septic shock: Administer within 1 hour of recognition 1
- Loading dose: Use higher initial doses in critically ill patients due to "third spacing phenomenon" affecting hydrophilic beta-lactams 1
Infusion Strategy
- Extended infusion: Consider prolonged infusion over 3 hours for beta-lactam antibiotics to maximize time above MIC, particularly in severe infections 1
- Standard infusion: Over 30-60 minutes 4
Administration with Food
- When transitioning to oral therapy, administer with meals to reduce gastrointestinal upset 4
Duration of Therapy
Standard Durations
- Respiratory tract infections: 7-10 days, up to 14 days if slow clinical response 1
- Intra-abdominal infections: 3-7 days after adequate source control in stable patients 1
- Bacteremia: 7-14 days depending on source 1
Transition to Oral Therapy
- Switch to oral formulation (same total daily dose) when patient demonstrates clinical improvement, can tolerate oral intake, and hemodynamically stable 1
- Typical transition occurs after 3 days of IV therapy 5
Resistance Considerations and Limitations
Appropriate Use
- Effective against beta-lactamase-producing organisms including H. influenzae, M. catarrhalis, and many Enterobacteriaceae 6
- NOT appropriate for: ESBL-producing organisms (use carbapenems instead), carbapenem-resistant Enterobacteriaceae, or MRSA 1
When to Avoid or Escalate
- Do not use as empirical monotherapy for nosocomial infections in critically ill patients 1
- Escalate to carbapenems if patient has known ESBL colonization within 3 months AND presents with severe sepsis/septic shock 1
- Consider alternatives for hospital-acquired infections with prior third-generation cephalosporin or fluoroquinolone exposure in last 3 months 1
Common Pitfalls to Avoid
Dosing Errors
- Do not underdose: In severe infections, failure to double the standard dose (from 30 to 60 mg/kg) may lead to treatment failure 1
- Maximum daily dose: Do not exceed 4 g/day total amoxicillin component 1
Inappropriate Spectrum
- Avoid for suspected Pseudomonas infections—Augmentin lacks anti-pseudomonal activity 1
- Do not use for vancomycin-resistant enterococci—requires linezolid or daptomycin 1
Duration Mistakes
- Do not continue beyond 5-7 days without reassessing for uncontrolled source or treatment failure 1
- Avoid prolonged courses without documented indication, as this drives resistance 1
Monitoring and De-escalation
Clinical Assessment
- Evaluate for improvement within 48-72 hours 1
- If no improvement by 48 hours, consider diagnostic workup for alternative diagnosis or resistant pathogen 1
Culture-Directed Therapy
- Narrow to targeted therapy once culture results available 1
- Discontinue if cultures negative and clinical improvement evident 1
Adverse Effects and Tolerance
Common Side Effects
- Gastrointestinal upset (vomiting, diarrhea) occurs in minority of patients 5, 7
- Local IV site reactions are rare with proper administration 5, 7
- Overall tolerance is excellent even at high doses up to 1.0 g/day clavulanic acid 8