Polypharmacy and Deprescribing

Key points

  • Polypharmacy: the concurrent use of multiple medicines - not inherently wrong, but risk of harm rises sharply as the number of medicines increases, especially beyond 5-10.
  • Appropriate vs problematic polypharmacy: appropriate polypharmacy is prescribed for good reason, reviewed regularly, and the patient can manage; problematic polypharmacy carries more risk than benefit or is unmanageable.
  • STOPP/START: Screening Tool of Older Persons' Prescriptions (potentially inappropriate medicines to stop) and Screening Tool to Alert to Right Treatment (evidence-based medicines to start) - the standard UK structured review tools.
  • Anticholinergic burden: cumulative anticholinergic load from multiple drugs increases falls, cognitive impairment and confusion risk - assessed with a scale such as the ACB, not drug by drug in isolation.
  • Prescribing cascade: a new drug is started to treat a side effect of another drug, rather than recognising and stopping the causative one - a common, avoidable driver of polypharmacy.
  • Deprescribing: a planned, supervised, evidence-based process, not an ad hoc cut - one drug at a time where possible, with monitoring for withdrawal or rebound effects.
  • Shared decision-making: deprescribing decisions should be made with the patient, explaining the rationale and addressing any concern about 'giving up' on their care.
  • Structured medication review: increasingly delivered by clinical pharmacists working within general practice, alongside GP-led review.

Introduction

Polypharmacy - the concurrent use of multiple medicines by one person - is extremely common in older people, most of whom have at least one long-term condition and many of whom have several. It is not inherently a problem: many older people are appropriately prescribed five, ten or more regular medicines, each addressing a genuine indication with net benefit. The clinical skill is distinguishing appropriate from problematic polypharmacy, and having a safe, structured process for reducing the latter.1

This matters because the risk of adverse drug events, drug-drug interactions and drug-disease interactions rises steeply, not linearly, as the number of concurrent medicines increases - and because polypharmacy is one of the most common, and most fixable, contributors to falls, delirium, hospital admission and reduced quality of life in older people.

Appropriate versus problematic polypharmacy

Distinguishing appropriate from problematic polypharmacy.
Appropriate polypharmacyProblematic polypharmacy
Each drug has a clear, current indicationOne or more drugs has no clear ongoing indication, or the original indication has resolved
Prescribed according to best evidence and reviewed regularlyPrescribed reactively over time without structured review ('accretion')
The patient understands and can manage the regimenThe patient cannot manage the regimen safely, or adherence is poor as a result
Benefits outweigh risks and burden for this individualRisk or burden now outweighs benefit for this individual, given their goals and prognosis

Why older people are at higher risk

  • Altered pharmacokinetics: reduced renal and hepatic clearance, altered volume of distribution (reduced lean mass, increased fat), meaning standard adult doses can accumulate to toxic levels
  • Altered pharmacodynamics: increased sensitivity to certain drug classes - for example, greater sedative and hypotensive effect at a given dose, and increased susceptibility to anticholinergic and central nervous system side effects
  • Reduced physiological reserve (frailty): less capacity to compensate for an adverse effect, meaning a modest drug-induced fall in blood pressure or level of consciousness has a disproportionately larger clinical impact - see 2
  • Guideline stacking: applying every relevant single-disease guideline in full generates additive medicine burden - see 3 for the multimorbidity perspective
  • Reduced capacity to manage a complex regimen, particularly with coexisting cognitive impairment

The prescribing cascade

A prescribing cascade occurs when a new drug is started to treat what is actually a side effect of an existing drug, rather than the side effect being recognised and the causative drug reviewed. This is a common, avoidable driver of polypharmacy that is worth naming explicitly in any medication review.

Classic prescribing cascade examples.
Original drugSide effectMistaken new prescription
Amlodipine (or other dihydropyridine CCB)Ankle oedemaA diuretic, rather than reviewing the calcium channel blocker
AntipsychoticDrug-induced parkinsonismAn anti-parkinsonian drug, rather than reviewing the antipsychotic
NSAIDHypertension / fluid retentionAn antihypertensive, rather than stopping the NSAID
Cholinesterase inhibitorUrinary incontinence (cholinergic effect)An anticholinergic bladder drug - which then directly opposes the cholinesterase inhibitor's mechanism

STOPP/START criteria

STOPP (Screening Tool of Older Persons' Prescriptions) and START (Screening Tool to Alert to Right Treatment) are complementary, validated criteria widely used in UK practice to structure medication review in people aged 65 and over.4

STOPP/START at a glance.
ToolPurposeExample
STOPPFlags potentially inappropriate medicines that should usually be stopped or reviewedLong-term NSAID in a patient with CKD or heart failure; benzodiazepines for over 4 weeks; a drug duplicating another's therapeutic class
STARTFlags evidence-based medicines that are indicated but missingNo statin in a patient with established atherosclerotic disease and reasonable life expectancy; no bone protection in a patient on long-term corticosteroids

Using both together avoids the common error of a review that only removes medicines and never considers what evidence-based treatment might genuinely be missing.

Anticholinergic and sedative burden

Many individually 'acceptable' drugs have anticholinergic or sedative properties that are additive when combined - the cumulative anticholinergic burden matters more than any single drug in isolation. Common contributors include tricyclic antidepressants, some antihistamines (particularly older, sedating ones), bladder antimuscarinics (oxybutynin, tolterodine), some antipsychotics, and some Parkinson's drugs.

A structured approach to deprescribing

Deprescribing is the planned, supervised process of stopping or reducing a medicine when its harms or burden now outweigh its benefit, or its original indication no longer applies - a deliberate clinical decision, not a passive drift or crisis reaction.

  1. Compile a complete, accurate medication list, including over-the-counter and herbal remedies, and confirm what the patient is actually taking versus what is prescribed
  2. Identify each drug's indication and whether it is still valid
  3. Assess overall benefit versus harm/burden for this individual, given their frailty, goals and life expectancy
  4. Prioritise which drug to address first - usually starting with the highest-risk, lowest-benefit drug (e.g. one with a known prescribing cascade, or one no longer clearly indicated)
  5. Plan the withdrawal, including tapering where needed and a monitoring plan for withdrawal or rebound effects
  6. Involve the patient in the decision, explaining the rationale clearly - deprescribing can otherwise feel to a patient like their care is being reduced or their doctor is 'giving up'
  7. Review and monitor after each change before making the next one, rather than stopping several drugs simultaneously

Drug classes most often targeted for deprescribing

Certain classes recur repeatedly in deprescribing work because they combine high prevalence, meaningful harm in older people, and frequently absent or expired indications.

Common deprescribing targets and the reasoning.
ClassWhy it is often stoppedWithdrawal consideration
Benzodiazepines and Z-drugsPrescribed for short-term insomnia or anxiety and continued for years; cause falls, cognitive impairment and dependenceTaper slowly - abrupt withdrawal risks seizures, rebound insomnia and severe anxiety
Proton pump inhibitorsFrequently started during an admission or alongside an NSAID that has since stopped, then never reviewed; associated with C. difficile, hypomagnesaemia and fracture riskStep down or stop; rebound acid hypersecretion can occur, so a tapering or on-demand approach helps
Antipsychotics in dementiaOften started for a behavioural crisis and continued indefinitely; increase stroke and mortality riskAttempt withdrawal after a period of stability, with monitoring for recurrence
Anticholinergic bladder drugsModest benefit for urgency, substantial contribution to anticholinergic burden and confusionCan usually be stopped directly; consider mirabegron as an alternative
Statins for primary preventionBenefit accrues over years; may be inappropriate where life expectancy is shortCan be stopped directly; distinguish carefully from secondary prevention, where the case to continue is much stronger
AntihypertensivesTargets set when the patient was fitter; now causing postural hypotension and fallsReduce stepwise with lying and standing blood pressure monitoring; avoid abrupt beta-blocker cessation
BisphosphonatesOften continued indefinitely; benefit plateaus and rare long-term harms accrueReview at 5 years (3 for zoledronic acid) with reassessment of fracture risk

Structured medication review in practice

In UK primary care, structured medication reviews are increasingly delivered by clinical pharmacists integrated into general practice teams, working alongside GPs, and are a formal component of chronic disease review (see 5) and of care for patients identified as frail or on the multimorbidity pathway. Triggers for a structured medication review include: 10 or more regular medicines, a recent hospital admission, a fall, new confusion, a change in renal function, or entry to a care home.

Discussing deprescribing with patients

Deprescribing conversations fail more often for communication reasons than clinical ones. Patients who have been told for years that a medicine is important may hear a proposal to stop it as rationing, as a sign that treatment is being withdrawn because they are near the end of life, or as an implication that they were wrong to take it. Framing matters as much as the pharmacology.

  • Open by asking their view: what they think each medicine does, which ones they feel help, and whether any are a nuisance to take - most patients readily identify candidates themselves
  • Explain the rationale positively: 'this one was helping when your blood pressure was higher, but now it may be causing the dizziness' rather than 'you don't need this any more'
  • Name the trade-off honestly, including any small increase in risk, rather than presenting the decision as risk-free
  • Emphasise reversibility: framing it as a monitored trial that can be reversed if symptoms return substantially reduces anxiety and increases agreement
  • Agree a specific review point and tell the patient what to look out for in the meantime
  • Document the reasoning, so a future clinician does not simply restart the drug without knowing why it was stopped

Common pitfalls

  • Reviewing medication only reactively (after a crisis) rather than proactively at routine intervals
  • Stopping multiple drugs simultaneously, making it hard to identify the cause if something goes wrong
  • Failing to taper drugs that require gradual withdrawal
  • Focusing only on stopping drugs (STOPP) while missing evidence-based treatment that should be started (START)
  • Not involving the patient in the decision, risking loss of trust or non-adherence to the revised plan
  • Assuming problematic polypharmacy only applies to a high absolute number of drugs, missing genuinely harmful combinations at a lower count

Prognosis and impact

Structured deprescribing, done well, reduces adverse drug events, falls, and sometimes hospital admission, while improving quality of life through reduced treatment burden - without evidence of net harm from appropriately selected medication withdrawal. The evidence base for individual deprescribing decisions varies by drug class, but the overall principle - regular, structured, patient-involved review rather than indefinite, unreviewed continuation - is consistently supported and applies across virtually every older patient with multiple medicines.

References

  1. NICE NG5. Medicines optimisation. Available here
  2. British Geriatrics Society. Fit for Frailty guidance. Available here
  3. NICE NG56. Multimorbidity: clinical assessment and management. 2016. Available here
  4. O'Mahony D, O'Sullivan D, Byrne S et al. STOPP/START criteria for potentially inappropriate prescribing in older people: version 2. Age and Ageing. 2015. Available here
  5. NHS England. Structured medication reviews and medicines optimisation. Available here

This article is written for revision and education. It is not clinical guidance and must not be used to make decisions about the care of a patient. Always check current NICE guidance and local protocols.

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