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Polypharmacy Review Audit

Audit whether people with polypharmacy have a structured, person-centred medicines review that is properly documented.

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Overview

This project audits whether polypharmacy is recognised, reviewed and documented through a structured, person-centred medicines optimisation process. It reviews whether people who may benefit from structured medication review are identified, whether the medicines list is reconciled, whether indication, ongoing need, high-risk medicines, monitoring, adverse effects, interactions, cumulative burden, frailty and organ function are considered, whether the person's priorities and any carer involvement are documented, whether deprescribing or continuation rationale is recorded, and whether follow-up, responsible reviewer and transfer-of-care communication are complete.

Specialties, services & categories

Clinical specialties:Pharmacy / Medicines OptimisationGeneral PracticeGeriatric Medicine / FrailtyAcute MedicineGeneral Internal MedicineEmergency MedicineCommunity ServicesNursingAllied Health ProfessionalsRehabilitation MedicineStroke / NeurologyPsychiatry / Older Adult Mental HealthLearning Disability ServicesRenal MedicineCardiologyRespiratory MedicineDiabetes / EndocrinologyPalliative Care
Healthcare services:PharmacyClinical GovernancePatient Safety
Categories:Patient Safety

Who should use it

  • Pharmacists, pharmacy technicians and medicines optimisation teams
  • GP practice teams, care-home clinical leads and community teams
  • Doctors, nurses, ACPs and PAs completing structured medication reviews
  • Frailty, geriatric medicine, acute medicine, mental health and rehabilitation teams
  • QI leads, governance teams, supervisors and educators

Objectives

  • Measure identification of people who may benefit from structured medication review
  • Assess reconciliation, indication review, high-risk medicines review and monitoring
  • Review shared decision-making, treatment burden and carer involvement
  • Test deprescribing consideration, continuation rationale, follow-up and transfer communication
  • 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, review context, medicine burden category)
  • Clinical area / location and optional specialty / service
  • Twenty-two structured medication review 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 and medication-review quality assurance only. It does not provide patient-specific prescribing, deprescribing, substitution, monitoring, tapering or withdrawal advice.
  • Polypharmacy thresholds, high-risk medicine lists, STOPP/START outcomes, anticholinergic burden thresholds, deprescribing rules, tapering schedules, monitoring frequencies and review intervals are locally configured and are not presented here as national standards.
  • Use anonymous case identifiers only — never patient-identifiable information, and never identifiable detail about prescribers, carers or family members.

Lazomis QI supporting resources