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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Hospital-acquired pneumonia

Infectious diseases, microbiology and sexual health · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Escalate

Treat shock, rapidly rising oxygen or ventilator need, reduced consciousness, major haemoptysis or suspected necrotising infection as an immediate resuscitation problem. Obtain useful cultures without delaying the sepsis antimicrobial timeframe, critical-care support or drainage of infected pleural fluid.

Synopsis

Decide whether a new hospital-onset pulmonary deterioration is bacterial pneumonia, use prior colonisation and local resistance data to choose proportionate treatment, and de-escalate safely once respiratory microbiology and the clinical trajectory are known.

  • Hospital-acquired pneumonia is considered when symptoms begin at least 48 hours after admission and infection was not incubating on arrival; disease appearing on days 3 to 5 without resistance risk may still follow the community-acquired regimen.
  • Diagnosis requires a new lower-respiratory syndrome and new or progressive imaging change after considering oedema, atelectasis, aspiration pneumonitis, pulmonary embolism, ARDS and alveolar haemorrhage.
  • Endotracheal tubes become colonised quickly. A resistant organism in sputum or tracheal aspirate changes probability but does not prove that it is invading lung tissue.
  • Before empirical treatment, review recent antibiotics, earlier cultures, known MRSA or multidrug-resistant Gram-negative carriage, structural lung disease, immune suppression and the current ward or ICU antibiogram.
  • NICE advises antibiotics as soon as possible after HAP is suspected and within 4 hours; suspected sepsis may require the shorter sepsis-specific timeframe.
  • Use oral treatment first for non-severe low-resistance-risk disease when absorption is reliable; severe illness, VAP or resistance risk requires a locally selected intravenous regimen and microbiology input.
  • At 48 hours revisit whether pneumonia remains credible, then stop, narrow, change route or define an end date. Review after 5 total days and consider stopping when clinically stable.
  • Prevention is cumulative: remove avoidable devices, reduce unnecessary ventilation and sedation, maintain safe oral and airway care, mobilise, prevent aspiration and avoid antimicrobial exposure without an indication.

Key red flags

Ventilator-associated syndrome

After more than 48 hours of intubation, new infiltrates accompany worsening oxygenation or ventilator settings, altered secretion burden and systemic inflammatory change; several findings together are required.

Resistance-enriched presentation

Prior broad-spectrum therapy, previous resistant isolates, known colonisation, bronchiectasis, prolonged critical care or overseas healthcare increases the chance that a narrow default regimen will be inactive.

Necrotising or pleural complication

Cavitation, haemoptysis, persistent bacteraemia, pleuritic pain or a loculated effusion suggests tissue destruction or an infected pleural space requiring urgent imaging, sampling and source control.

Investigation priorities

01
Serial observations and respiratory-support recordFirst step

Define the onset and severity of the new pulmonary deterioration.

Management branches

SuspectEstablish infection and immediate risk

A hospital inpatient develops a new lower-respiratory deterioration after the admission boundary.

  1. Perform ABCDE, prescribe oxygen to an individual target and involve critical care for shock, exhaustion or escalating respiratory support.
  2. Compare current and previous imaging, review aspiration and fluid balance, and examine for pulmonary and non-pulmonary alternatives.
  3. Collect a representative respiratory specimen and blood cultures when indicated, then meet the NICE or sepsis treatment timeframe without waiting for final results.

Key medicines

Co-amoxiclav for low-risk non-severe HAPGive 500/125 mg orally three times daily for 5 days, then review.Avoid in immediate penicillin hypersensitivity or previous co-amoxiclav-associated jaundice or hepatic dysfunction; reduce for renal impairment, monitor liver injury and diarrhoea, and review anticoagulant control when clinically relevant.
Piperacillin with tazobactamGive 4.5 g intravenously three times daily, increasing to four times daily for severe infection under the adopted policy.Avoid after serious beta-lactam hypersensitivity, reduce maintenance in renal impairment and review sodium, potassium, blood counts and liver tests. Concurrent vancomycin and other nephrotoxins increase renal-injury concern; obtain cultures and de-escalate.
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Sources and review status5 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NICE NG250 pneumonia recommendationsCurrent HAP timing, resistance-risk factors, adult regimens, IV review and five-day stopping review.
  • NHS England national infection prevention and control manualStandard and transmission-based precautions for hospital infection prevention.
  • RCPath UK SMI B57 lower respiratory specimensRespiratory specimen quality, processing and interpretation.
  • Piperacillin tazobactam summary of product characteristicsDose, renal modification, contraindications, sodium and laboratory monitoring.
  • Linezolid summary of product characteristicsDose, marrow toxicity, monoamine-oxidase effects and serotonergic interactions.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom