π₯ Hospital-acquired infections (HAIs), also called nosocomial infections, occur β₯48 hours after admission and are a major cause of morbidity, mortality, and cost in healthcare.
They prolong recovery, drive antimicrobial resistance, and are key targets for NHS patient safety initiatives.
π‘ The βbig 5β HAIs: UTI, SSI, BSI, VAP, and C. difficile colitis.
π¦ Common Hospital-Acquired Infections
- π§ Urinary Tract Infection (UTI)
β Commonest HAI, usually catheter-associated.
β Pathogens: E. coli, Klebsiella, Pseudomonas.
β Risk factors: prolonged catheterisation, diabetes, dehydration, poor hygiene.
β Prevention: Aseptic insertion, closed drainage, daily review β βIf you donβt need it, donβt leave it.β
- πͺ Surgical Site Infection (SSI)
β Occurs within 30 days (or 90 if prosthesis).
β Pathogens: skin flora, esp. S. aureus.
β Risk factors: long/emergency surgery, obesity, diabetes, immunosuppression.
β Prevention: Antibiotic prophylaxis, sterile technique, normothermia, glycaemic control, meticulous wound care.
- π Bloodstream Infection (BSI)
β Often from central lines, cannulae, TPN, dialysis.
β Pathogens: coagulase-negative staphylococci, S. aureus, Gram-negatives.
β Prevention: Full sterile precautions at insertion, chlorhexidine skin prep, daily line review, early removal.
- π¬οΈ Ventilator-Associated Pneumonia (VAP)
β Usually >48h after intubation.
β Pathogens: Pseudomonas, Acinetobacter, MRSA, Enterobacteriaceae.
β Prevention (βVAP bundleβ): Head up 30β45Β°, daily sedation breaks, early extubation, chlorhexidine oral care, subglottic suction tubes if long-term ventilation expected.
- π§» Clostridioides difficile Colitis
β Follows broad-spectrum antibiotics (esp. cephalosporins, clindamycin, fluoroquinolones).
β Risk factors: age >65, PPIs, immunosuppression, recent hospitalisation.
β Prevention: Antibiotic stewardship, soap & water hand hygiene (alcohol gel ineffective vs spores), isolation, chlorine-based cleaning.
π Assessment of Suspected HAI
- π History: Recent procedures, device use (catheter, central line, ventilation), prior antibiotics, immunosuppression.
- π©Ί Examination: Sepsis screen: fever, tachycardia, hypotension, altered mental status. Inspect wounds, lines, drains.
- π§ͺ Investigations: Blood/urine/wound cultures, CXR if pneumonia, stool PCR/toxin assay for C. diff.
- π§€ Infection control: Hand hygiene, PPE, patient isolation, notify infection control team.
- π Antibiotic stewardship: Culture before antibiotics, de-escalate promptly.
π§ Diagnostic & Management Pathway
- β οΈ Clinical suspicion: New fever, raised CRP/WCC, localising signs (dysuria, wound erythema, new infiltrates, diarrhoea).
- π§ͺ Investigations: Take cultures before antibiotics (blood, urine, sputum, wound, stool).
- π Empiric therapy:
β Start within 1 hr if sepsis suspected.
β IV piperacillinβtazobactam or meropenem if resistant risk.
β Add MRSA cover (vancomycin/linezolid) if indicated.
β Fluids, oxygen, and source control (remove line, drain abscess).
- π¬ Targeted therapy: Narrow spectrum once cultures return. Shortest effective course (5β7d uncomplicated).
- π‘οΈ Prevention: Catheter, line, and ventilator βbundlesβ. Daily device review. Antimicrobial stewardship ward rounds. HAI surveillance + reporting for QI.
π Key NHS Prevention Bundles
- π§ Catheter Care Bundle: aseptic insertion, daily review, prompt removal.
- π Central Line Bundle: full sterile barrier, chlorhexidine, documented line necessity review.
- π¬οΈ Ventilator Bundle: head elevation, sedation breaks, oral hygiene, extubation as soon as possible.
π‘ Pearls:
β Culture before antibiotics. π§ͺ
β βDevice out is as important as antibiotic in.β π«π
β HAIs = β₯48 hrs after admission (exclude community-acquired).
β Surveillance + multidisciplinary prevention are as important as treatment.
π References