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Delirium Screening Audit

Audit whether delirium risk, screening, recognition, documentation, escalation and communication are completed reliably.

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Overview

This project audits the quality, completeness and reliability of delirium screening and documentation. It reviews whether delirium risk factors, screening tool use, results, escalation, prevention and care planning and onward communication are documented clearly enough to support safe care, in line with NICE CG103 and QS63 and local policy.

Specialties, services & categories

Clinical specialties:Acute MedicineEmergency MedicineGeneral Internal MedicineGeriatric MedicineFrailtyOrthogeriatricsDementia and Cognitive ImpairmentLiaison Psychiatry
Healthcare services:Clinical GovernanceNursing & AHPsPharmacy
Categories:Patient SafetyGovernance

Who should use it

  • Acute medicine, emergency medicine and general internal medicine teams
  • Frailty, geriatric medicine and orthogeriatric teams
  • Nurses, pharmacists, ACPs and physician associates
  • Care home clinical leads, community and hospice teams where locally relevant
  • QI leads, governance teams and educators

Objectives

  • Measure documentation of delirium risk assessment and screening in eligible records
  • Assess use and recording of the locally approved screening tool and its result
  • Assess escalation, senior or MDT review where delirium is suspected or identified
  • Identify variation by clinical area / location and optional specialty / service
  • Generate governance-ready and ARCP-ready evidence

Data collected

  • Anonymous case identifier
  • Inclusion / eligibility decision
  • Anonymised biodata (age band, recorded sex/gender, care setting, delirium screening context)
  • Clinical area / location and optional specialty / service
  • Twenty delirium recognition, screening, assessment, management and communication criteria (met / not met / not applicable)
  • Free-text learning points and any project custom fields

Outputs generated

  • Live dashboard
  • Audit report (Word)
  • Executive summary (Word)
  • Excel workbook
  • PowerPoint presentation
  • Conference poster
  • ARCP evidence summary

Standards and guidance

This ready-built project is developed using the guidance, standards and authoritative sources listed below, so you can see what is being measured and why. Lazomis QI does not publish or own this guidance, and inclusion here does not imply endorsement or approval by any of these organisations.

Governance notes

  • Designed to use anonymised or pseudonymised audit identifiers.
  • This tool supports, but does not replace, clinical judgement.
  • Local policy, formulary and specialist advice should be followed.
  • Organisations remain responsible for local governance arrangements.
  • This tool supports, but does not replace, clinical judgement. Follow local policy, formulary and specialist advice.
  • Use anonymous case identifiers only — never patient-identifiable information.

Lazomis QI supporting resources