MRSA
Methicillin-resistant Staphylococcus aureus is a major healthcare-associated pathogen resistant to flucloxacillin and all beta-lactams via the mecA gene (PBP2a). Causes skin/soft tissue infections, bacteraemia, endocarditis, and surgical site infections. UK rates have declined >80% since mandatory screening and decolonisation programmes.
Key Facts
mecA gene encodes altered penicillin-binding protein (PBP2a) → resistance to ALL beta-lactams (penicillins, cephalosporins, carbapenems) UK mandatory screening: all elective and emergency admissions screened with nasal swab ± other sites Decolonisation: mupirocin 2% nasal ointment TDS for 5 days + chlorhexidine 4% body wash for 5 days MRSA bacteraemia: treat with IV vancomycin 15–20mg/kg BD (target trough 15–20 mg/L) or IV daptomycin 6–10mg/kg OD MRSA-related deaths in UK: declined >80% since 2007 mandatory surveillance and screening programmes Community-acquired MRSA (CA-MRSA): Panton-Valentine leukocidin (PVL) producing strains — recurrent boils, skin abscesses, necrotising pneumonia in young healthy individuals Linezolid 600mg BD: oral option for MRSA soft tissue infection; monitor FBC weekly (myelosuppression) Hand hygiene and isolation are the most important infection prevention measures
Overview
Key Facts
MRSA is one of the most important healthcare-associated pathogens worldwide. UK programmes of mandatory screening, decolonisation, and antimicrobial stewardship have achieved dramatic reductions in MRSA bacteraemia.
Epidemiology
- UK MRSA bacteraemia: ~780 cases/year (2022) — down from >7,000/year in 2007
- MRSA accounts for ~5–10% of S. aureus bacteraemia in UK (historically >40%)
- Healthcare-associated MRSA declining; community-acquired strains increasingly recognised
- PVL-MRSA: particular concern in young, otherwise healthy individuals
Aetiology
- S. aureus carrying SCCmec (staphylococcal cassette chromosome mec) with mecA gene
- HA-MRSA: hospital-acquired, often multi-drug resistant
- CA-MRSA: community strains, often PVL-positive, may be susceptible to more agents (e.g. doxycycline, trimethoprim)
- Carriage: nasal carriage in ~2–5% of UK population; higher in healthcare workers, IVDU, prisoners
Pathophysiology
- PBP2a: altered penicillin-binding protein with low affinity for beta-lactams → resistance
- Same virulence factors as MSSA: protein A, coagulase, toxins
- PVL (Panton-Valentine leukocidin): pore-forming toxin → leucocyte lysis → tissue necrosis; associated with CA-MRSA
- Biofilm formation: important in prosthetic device infections
Clinical Presentation
HA-MRSA
- Surgical site infection
- Bacteraemia (often line-related)
- Pneumonia (ventilator-associated)
- Prosthetic joint/device infection
- Wound infections
CA-MRSA (PVL-positive)
- Recurrent skin boils/abscesses (buttocks, axillae, groin)
- Necrotising pneumonia: young, previously healthy; post-influenza; haemoptysis, multi-lobar cavitating consolidation — high mortality
- Necrotising fasciitis
- Bone and joint infections
Red Flags
- S. aureus bacteraemia not responding to flucloxacillin (suspect MRSA)
- Recurrent skin abscesses (PVL-MRSA)
- Young healthy patient with cavitating pneumonia post-flu illness
- Prosthetic device with persistent infection
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| MSSA infection | Same clinical features, susceptible to flucloxacillin | Culture and sensitivity |
| PVL-positive MSSA | Recurrent boils, necrotising pneumonia (same as PVL-MRSA) | Culture + PVL gene testing |
| Streptococcal infection | Cellulitis, impetigo, pharyngitis | Wound/blood culture |
| Fungal skin infection | Chronic, non-purulent, scaling | KOH prep, culture |
| Hidradenitis suppurativa | Recurrent abscesses in flexures, sinus tracts | Clinical, biopsy |
Diagnosis / Investigation
Screening
- Nasal swab (bilateral nares): standard MRSA screening
- Additional sites: groin, axillae, wounds, catheter sites, throat
- Enrichment culture or PCR: for rapid detection
Infection Diagnosis
- Wound swab/pus: culture and sensitivity
- Blood cultures: essential in suspected bacteraemia
- Susceptibility testing: determines antibiogram (e.g. vancomycin MIC)
- PVL gene testing: request if recurrent abscesses or necrotising infection
Bloods
- FBC, CRP, lactate: infection markers
- Vancomycin trough levels: target 15–20 mg/L for serious infections
Imaging
- Echocardiography: all S. aureus bacteraemia (TEE preferred) — endocarditis occurs in ~10–25%
- CT/MRI: metastatic infection (bone, joints, epidural abscess)
- CXR/CT chest: pneumonia
Special Tests
- Repeat blood cultures at 48–72 hours: all S. aureus bacteraemia to confirm clearance
- Removable source identification: lines, prosthetics, abscesses
Management
Non-pharmacological
- Contact precautions: isolation in single room, gown and gloves
- Hand hygiene: soap and water (MRSA spores resistant to alcohol gel — though MRSA is not spore-forming; hand hygiene with alcohol gel is effective but soap and water preferred)
- Environmental cleaning: enhanced cleaning of patient environment
- Source removal: remove/replace infected lines, drain abscesses
Decolonisation (MRSA carriers)
- Mupirocin 2% nasal ointment TDS for 5 days (both nares)
- Chlorhexidine 4% body wash OD for 5 days
- Chlorhexidine mouthwash: if throat carriage
- Re-screen 48 hours after completion; repeat if still positive
Pharmacological
MRSA bacteraemia:
- IV vancomycin 15–20mg/kg BD (target trough 15–20 mg/L) for minimum 14 days (28 days if endocarditis)
- IV daptomycin 6–10mg/kg OD: alternative (NOT for pneumonia — inactivated by surfactant)
- Duration: minimum 14 days for uncomplicated bacteraemia; 4–6 weeks for endocarditis, osteomyelitis
MRSA skin/soft tissue:
- Oral: doxycycline 200mg then 100mg OD, trimethoprim 200mg BD, or linezolid 600mg BD (guided by sensitivities)
- IV: vancomycin, daptomycin, or linezolid
- Linezolid: monitor FBC weekly (thrombocytopenia, anaemia); max 28 days
MRSA pneumonia:
- IV vancomycin or IV linezolid 600mg BD (linezolid achieves higher lung concentrations)
Incision and drainage:
- Essential for abscesses — antibiotics alone insufficient
Referral Criteria
- Infectious diseases/microbiology: all MRSA bacteraemia
- Cardiology: echocardiography for S. aureus bacteraemia
- Surgery: abscess drainage, prosthetic device removal
- Infection prevention team: all MRSA-positive patients
Prognosis
- MRSA bacteraemia: mortality 20–30% (similar to MSSA bacteraemia when appropriately treated)
- PVL-necrotising pneumonia: mortality 30–75%
- Endocarditis: mortality 20–40%
- Skin/soft tissue MRSA: generally good prognosis with appropriate drainage and antibiotics
- UK MRSA bacteraemia rates reduced >80% since mandatory surveillance (2007)
- Decolonisation: effective in ~75% of carriers with single course
- Recurrent MRSA carriage: common; may need repeated decolonisation or systemic antibiotics
Other Relevant Information
MRSA Treatment Summary
| Infection | First-Line Treatment |
|---|---|
| Bacteraemia | IV vancomycin (trough 15–20) or daptomycin |
| Endocarditis | IV vancomycin ± gentamicin (or daptomycin) |
| Pneumonia | IV vancomycin or linezolid (NOT daptomycin) |
| Skin/soft tissue | Doxycycline, trimethoprim, or linezolid PO |
| Osteomyelitis | IV vancomycin then oral (rifampicin + another agent) |
| Decolonisation | Mupirocin nasal + chlorhexidine body wash |