Treatment of Morganella morganii Infections
For Morganella morganii infections, use fluoroquinolones (ciprofloxacin) or trimethoprim-sulfamethoxazole as first-line therapy for uncomplicated infections, reserving carbapenems for severe infections or documented resistance, with treatment duration of 4 months for complicated skin/soft tissue infections and 6 months for bone infections. 1, 2, 3
Antibiotic Selection by Clinical Scenario
Urinary Tract Infections
- Ciprofloxacin is FDA-approved for M. morganii urinary tract infections and represents an excellent first-line choice given the organism's susceptibility profile 2
- Trimethoprim-sulfamethoxazole is also FDA-approved and effective for M. morganii UTIs 3
- Avoid ampicillin-clavulanate and first-generation cephalosporins due to ubiquitous resistance (100% resistance documented) 4
Skin and Soft Tissue Infections
- Ciprofloxacin is FDA-approved for M. morganii skin and skin structure infections and should be considered first-line 2
- Piperacillin-tazobactam demonstrates excellent susceptibility (98.2% susceptible) and is appropriate for moderate-to-severe infections 4
- Complicated skin/soft tissue infections require a minimum of 4 months of therapy 1
- Skin and soft tissue infections represent the most common manifestation (54% of cases) 5
Intra-Abdominal Infections
- Ciprofloxacin combined with metronidazole is FDA-approved for complicated intra-abdominal infections involving M. morganii 2
- Avoid tigecycline due to intrinsic resistance 1
- Hepatobiliary tract infections account for 27.5% of bacteremia cases 4
Bone and Joint Infections
- Ciprofloxacin is FDA-approved for M. morganii bone and joint infections 2
- Treatment duration must be 6 months for bone infections 1
- Consider combination therapy for severe osteomyelitis
Bacteremia and Severe Infections
- Reserve carbapenems (imipenem or meropenem) for critically ill patients or documented resistance to first-line agents 1
- Gentamicin demonstrates 69.7% susceptibility and is the most frequently used antibiotic in systematic reviews 6, 4
- Combination therapy with gentamicin plus third-generation cephalosporin is recommended for invasive infections after testing for AmpC β-lactamase production 6, 7
- Amikacin shows excellent susceptibility and should be considered for severe infections 6
Antimicrobial Susceptibility Profile
High Susceptibility (>90%)
- Piperacillin-tazobactam (98.2% susceptible) 4
- Imipenem (universally susceptible) 6
- Ceftazidime (highly susceptible) 6
- Amikacin (highly susceptible) 6
Moderate Susceptibility (70-90%)
Universal Resistance (Avoid)
- First-generation cephalosporins (100% resistant) 4
- Ampicillin-clavulanate (100% resistant) 4
- Tigecycline (intrinsic resistance) 1
Special Considerations
Polymicrobial Infections
- M. morganii is part of polymicrobial infections in 58% of cases 5
- Add metronidazole for intra-abdominal infections to cover anaerobes 2
- Consider broader coverage when clinical context suggests mixed flora 5
Resistance Concerns
- Test all isolates for AmpC β-lactamase production before using third-generation cephalosporins 6
- Emerging resistance includes blaNDM-1 and qnrD1 genes, posing serious challenges 8
- Perform susceptibility testing to guide definitive therapy, especially in nosocomial infections 6
Surgical Source Control
- Surgical debridement, drainage, or removal of infected foreign material is essential for treatment success in invasive infections 1
- Medical therapy alone has high failure rates without adequate source control 1
- Consider surgical intervention for abscesses, gangrenous appendicitis, and deep tissue infections 5
Prognostic Factors
High-Risk Features
- APACHE II score is the only independent predictor of mortality (OR 1.55 per point increase) 4
- Elevated blood urea nitrogen values (OR 5.26) 4
- ICU admission requirement (OR 4.4) 4
- Overall 14-day mortality is 14.7%, with 8% mortality in general series 5, 4
Patient Populations at Risk
- Elderly patients with multiple comorbidities (hypertension 62.4%, diabetes 38.5%) 4
- Debilitated patients have higher mortality risk 5
- Nosocomial and postoperative settings increase infection risk 6
- Immunosuppressed patients and young children are vulnerable 6
Common Pitfalls to Avoid
- Never use ampicillin-clavulanate or first-generation cephalosporins due to universal resistance 4
- Do not delay surgical source control in favor of medical therapy alone 1
- Avoid tigecycline for M. morganii infections 1
- Do not undertake treatment without adequate duration (4-6 months for complicated infections) 1
- Always consider polymicrobial infection and provide appropriate coverage 5