Treatment of Infectious Colitis
The initial treatment approach for infectious colitis depends critically on disease severity and suspected pathogen, with immediate discontinuation of inciting antibiotics, aggressive supportive care, and pathogen-directed antimicrobial therapy—avoiding antiperistaltic agents entirely due to risk of toxic megacolon. 1, 2
Immediate Assessment and Critical Actions
Severity Stratification
Classify disease severity immediately to guide treatment intensity 1, 2:
- Non-severe disease: Stool frequency <4 times daily, WBC ≤15,000/μL, serum creatinine <1.5 mg/dL 1
- Severe disease: WBC >15,000/μL, serum creatinine ≥1.5 mg/dL (>50% above baseline), fever >38.5°C, hemodynamic instability 3, 2
- Fulminant disease: Hypotension/septic shock, ileus, toxic megacolon, serum lactate >5.0 mmol/L, peritonitis, colonic distension on imaging 3, 2
Universal Management Principles
Avoid antiperistaltic agents (loperamide) and opiates completely—these promote toxin retention, worsen outcomes, and precipitate toxic megacolon. 3, 1, 2
Discontinue the inciting antibiotic immediately if clinically feasible, as this alone resolves symptoms in approximately 25% of mild cases 1, 2
Supportive Care Framework
Fluid and Electrolyte Management
- Oral rehydration for mild to moderate disease 3
- Intravenous fluid resuscitation for severe disease with aggressive electrolyte replacement 3
- Consider albumin supplementation for severe hypoalbuminemia (<2 g/dL) for both supportive and anti-toxin properties 3
Monitoring Requirements
For hospitalized patients with severe disease 3:
- Monitor vital signs including temperature and pulse four times daily
- Serial complete blood counts, electrolyte profiles, serum creatinine, and lactate levels
- Measure intra-abdominal pressure when risk factors for abdominal compartment syndrome exist 3
Pathogen-Specific Treatment
Clostridioides difficile Infection
For initial episode, oral vancomycin 125 mg four times daily for 10 days is first-line treatment for non-severe disease. 1, 2
Non-Severe C. difficile
- Preferred: Oral vancomycin 125 mg four times daily for 10 days 1, 2
- Alternative: Oral fidaxomicin 200 mg twice daily for 10 days (may reduce recurrence risk) 2
- Metronidazole 500 mg three times daily orally for 10 days is now considered inferior 3
Severe C. difficile
- Preferred: Oral vancomycin 125 mg four times daily for 10 days 3
- Alternative: Fidaxomicin 200 mg twice daily for 10 days (increasingly recommended as first-line) 2
Fulminant C. difficile (When Oral Therapy Impossible)
For patients with ileus or inability to take oral medications 3, 2:
- Metronidazole 500 mg IV every 8 hours PLUS
- Intracolonic vancomycin 500 mg in 100 mL normal saline every 4-12 hours via retention enema AND/OR
- Vancomycin 500 mg four times daily via nasogastric tube 3, 1
Recurrent C. difficile
- First recurrence: Treat same as initial episode with vancomycin or fidaxomicin 3, 1, 2
- Second and subsequent recurrences: Vancomycin taper/pulse strategy (decrease daily dose by 125 mg every 3 days, then pulse 125 mg every 3 days for 3 weeks) 3, 1, 2
- Critical warning: Avoid repeated or prolonged metronidazole courses due to cumulative neurotoxicity risk 1, 2
Bacterial Colitis (Salmonella, Shigella, Campylobacter)
Empiric Treatment for Febrile Dysentery
When invasive bacterial pathogens are suspected (fever, bloody diarrhea) 4:
- Azithromycin 1000 mg single dose for empiric treatment in adults 4
- Obtain stool cultures before initiating therapy when possible 4, 5
- Use multiplex PCR followed by guided culture for rapid diagnosis and antibiotic susceptibility testing 5
Pathogen-Specific Considerations
- Initiate pathogen-specific antimicrobial therapy once laboratory diagnosis is confirmed 4
- Narrow antibiotic spectrum after culture and susceptibility results become available 3
Critical Exception: Shiga Toxin-Producing E. coli (STEC)
Do NOT treat STEC with antibiotics—suspect when acute dysentery presents with low-grade or absent fever 4
- Test directly for E. coli O157:H7 and Shiga toxin in stool 4
- Antibiotics increase risk of hemolytic uremic syndrome 4
Diagnostic Workup
Stool Studies
Obtain comprehensive stool evaluation for severe or complicated cases 3:
- Blood in stool
- C. difficile toxin testing
- Bacterial cultures for Salmonella, Shigella, Campylobacter, E. coli 3
- Multiplex PCR is preferred over traditional culture methods 5
Additional Testing
For severe disease, obtain 3:
- Complete blood count with differential
- Comprehensive metabolic panel including creatinine
- Serum lactate (critical prognostic marker) 3
- Imaging if toxic megacolon or perforation suspected 3
Surgical Intervention
Indications for Urgent Colectomy
Obtain early surgical consultation when any of the following are present 3, 1, 2:
- Colonic perforation
- Toxic megacolon or severe ileus
- Systemic inflammation with deteriorating clinical condition despite maximal medical therapy
- Serum lactate >5.0 mmol/L (operate before this threshold when possible) 3, 1
Timing Considerations
- Do not delay surgical consultation when clinical deterioration continues despite antibiotics 1, 2
- Colectomy should be performed before colitis becomes very severe 3
- Early surgery improves survival in fulminant cases 1, 2
Treatment Response Monitoring
Expected Response Timeline
Treatment response is defined as 3:
- Decreased stool frequency or improved consistency after 3 days AND
- No new signs of severe colitis develop 3
Treatment Failure
Consider treatment failure and escalate care if 3, 2:
- No improvement within 3 days of appropriate therapy
- Clinical deterioration at any point
- Development of fulminant features
Common Pitfalls to Avoid
Never use antiperistaltic agents or opiates in infectious colitis—they worsen outcomes and precipitate toxic megacolon 3, 1, 2
Do not use metronidazole for recurrent C. difficile or prolonged courses due to neurotoxicity 1, 2
Do not treat STEC with antibiotics—increases hemolytic uremic syndrome risk 4
Do not delay surgical consultation in deteriorating patients—early intervention saves lives 1, 2
Do not use broad-spectrum antibiotics empirically without considering C. difficile risk—narrow spectrum once pathogen identified 3