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Allergy Documentation Audit

Audit whether allergy status is recorded, verified, coded, visible, clinically meaningful and safely communicated across prescribing, handover and discharge.

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Overview

This project audits whether allergy status is documented reliably and safely in the clinical record and prescribing systems. It reviews whether allergy status is recorded and categorised, checked with the person, carer or a reliable source, described with substance, reaction, timing and severity, distinguished from intolerance, visible and consistent across systems, reviewed at medicines reconciliation, considered in prescribing, updated when new information emerges, communicated at discharge and escalated for specialist advice where local policy requires it.

Specialties, services & categories

Clinical specialties:Acute MedicineEmergency MedicineGeneral Internal MedicineGeriatric MedicineSurgeryTrauma and OrthopaedicsAnaestheticsCritical CarePharmacyPrimary Care
Healthcare services:PharmacyNursing & AHPsClinical Governance
Categories:Patient SafetyGovernance

Who should use it

  • Doctors, nurses, pharmacists and pharmacy technicians
  • Medicines optimisation, antimicrobial stewardship and perioperative teams
  • Acute medicine, emergency department and primary care teams
  • Digital, EPR and ePMA teams where allergy coding is audited
  • QI leads, governance teams, supervisors and educators

Objectives

  • Measure whether allergy status is documented, categorised and verified
  • Assess the clinical meaningfulness of recorded allergy detail
  • Identify visibility, coding, duplication and consistency problems across systems
  • Review whether allergy status is considered at reconciliation, prescribing and discharge
  • Generate governance-ready and ARCP-ready evidence and a re-audit cycle

Data collected

  • Anonymous case identifier
  • Inclusion / eligibility decision
  • Anonymised context (age band, sex/gender recorded, care setting, assessment context)
  • Clinical area / location and optional specialty / service
  • Eighteen allergy documentation 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 documentation review only. It does not provide patient-specific prescribing advice and does not diagnose or de-label allergy.
  • Allergy coding frameworks, alert configuration, ePMA workflows and medicine-specific rules are locally configurable and are not presented here as national standards.
  • Use anonymous case identifiers only — never patient-identifiable information.

Lazomis QI supporting resources