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

DiagnosisKey FeaturesInvestigation
MSSA infectionSame clinical features, susceptible to flucloxacillinCulture and sensitivity
PVL-positive MSSARecurrent boils, necrotising pneumonia (same as PVL-MRSA)Culture + PVL gene testing
Streptococcal infectionCellulitis, impetigo, pharyngitisWound/blood culture
Fungal skin infectionChronic, non-purulent, scalingKOH prep, culture
Hidradenitis suppurativaRecurrent abscesses in flexures, sinus tractsClinical, 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

InfectionFirst-Line Treatment
BacteraemiaIV vancomycin (trough 15–20) or daptomycin
EndocarditisIV vancomycin ± gentamicin (or daptomycin)
PneumoniaIV vancomycin or linezolid (NOT daptomycin)
Skin/soft tissueDoxycycline, trimethoprim, or linezolid PO
OsteomyelitisIV vancomycin then oral (rifampicin + another agent)
DecolonisationMupirocin nasal + chlorhexidine body wash