Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
1 Polypharmacy and medicines optimisation Dr Martin Duerden [email protected] 2 Polypharmacy is not new! We dislike polypharmacy as much as it is possible, and we would never exhibit a remedy of any kind unless we had a scientific reason for so doing and unless we were prepared to defend our method of treatment. W Newnham, Provincial Medical and Surgical Journal, 1848 Defining polypharmacy • Appropriate polypharmacy is prescribing for an individual for complex conditions or for multiple conditions in circumstances where medicines use has been optimised and the medicines are prescribed according to best evidence. The overall intent for the combination of medicines prescribed should be to maintain good quality of life, improve longevity and minimise harm from drugs. • Problematic polypharmacy is where multiple medications are prescribed inappropriately, or where the intended benefit of the medication is not realised, or where one or more of the following apply… 4 Problematic….where one or more of the following apply… • The drug combination is hazardous because of interactions. • The overall demands of medicine-taking, or ‘pill burden’, are unacceptable to the patient. • These demands make it difficult to achieve clinically useful medication adherence (reducing the ‘pill burden’ to the most essential medicines is likely to be more beneficial). • Medicines are being prescribed to treat the side effects of other medicines where alternative solutions are available to reduce the number of medicines prescribed. 5 Defining medicines optimisation NICE, Medicines Optimisation Guideline NG1, March 2015. • A person-centred approach to safe and effective medicines use, to ensure people obtain the best possible outcomes from their medicines. • Applies to people who may or may not take their medicines effectively. • Shared decision-making is an essential part of evidence-based medicine, seeking to use the best available evidence to guide decisions about the care of the individual patient, taking into account their needs, preferences and values. “Social prescriptions” • Exercise (on prescription) • Arts (on prescription) • Educational programmes • Social contact for isolation and loneliness • Links to voluntary organisations • Community activities • Alleviating boredom • Consider alcohol problems • etc. 7 What’s the problem? The growth of multimorbidity and associated polypharmacy (and guidelines and targets!) 8 Estimated and projected age structure of the United Kingdom population, mid-2014 and mid-2039 (Report, October 2015) www.ons.gov.uk/ons/rel/npp/national-population-projections/2014-based-projections/index.html 9 Percentage age distribution, UK, year ending mid-1971 to year ending mid-2089 (Report, October 2015) www.ons.gov.uk/ons/rel/npp/national-population-projections/2014-based-projections/index.html 10 Number of chronic disorders by age group Barnett K et al. Lancet 2012; 380: 37-43. 11 Comorbidity of 10 common conditions among UK primary care patients Guthrie B et al. BMJ 2012;345:e6341 Prescribing is increasing Guthrie et al. BMC Medicine (2015) 13:74 DOI 10.1186/s12916-015-0322-7 13 Prevalence of polypharmacy in a Scottish primary care population. Payne et al. Eur J Clin Pharmacol 2014; DOI 10.1007/s00228013-1639-9 14 A nation of pill takers? Health Survey for England, 2013 Report 2015: www.hscic.gov.uk/catalogue/PUB16076 • 43% men and 50% women reported that they had taken at least 1 prescribed medicine in the last week • 22% men and 24% women reported that they had taken at least 3 prescribed medicines in the last week • More than 50% of participants aged 65-74 and more than 70% of those aged >75 had taken at least 3 prescribed medicines. • The most frequently reported prescribed medicine classes were: • lipid-lowering medicines – 16% men and 12% women • antihypertensive medicines (14% and 15% respectively) • for women, analgesics and/or NSAIDs (12%). A nation of pill takers? Health Survey for England, 2013 Report 2015: www.hscic.gov.uk/catalogue/PUB16076 A nation of pill takers? Health Survey for England, 2013 Report 2015: www.hscic.gov.uk/catalogue/PUB16076 17 Polypharmacy – identifying high risk • A pragmatic approach to identifying higher-risk polypharmacy in practice is to focus on patients at particularly high risk. • For example: • Those receiving 10 or more regular medicines, or • Those receiving 4 to 9 regular medicines together with other unfavourable factors (examples include: a contraindicated drug; where there is potential for drug-drug interaction; or where medicine taking has proved a problem in the past). 18 Guidelines everywhere… 2008 • • • • • • • • • • • • • • • • • • Prostate cancer Osteoarthritis Surgical management of OME Irritable bowel syndrome Antenatal care Diabetes in pregnancy Prophylaxis against infective endocarditis Perioperative hypothermia (inadvertent) Type 2 diabetes Lipid modification Stroke Respiratory tract infections Induction of labour Familial hypercholesterolaemia Attention deficit hyperactivity disorder (ADHD) Chronic kidney disease Surgical site infection Metastatic spinal cord compression 2009 • • • • • • • • • • • • • • • • Medicines adherence Antisocial personality disorder Borderline personality disorder (BPD) Rheumatoid arthritis Breast cancer (early & locally advanced) Breast cancer (advanced) Schizophrenia Critical illness rehabilitation Diarrhoea and vomiting in children under 5 Glaucoma Coeliac disease Type 2 Diabetes - newer agents Low back pain When to suspect child maltreatment Depression in adults Depression with a chronic physical health problem 2010 • • • • • • • • • • • • • • • • • • • • • Venous thromboembolism reducing the risk Donor breast milk banks Unstable angina and NSTEMI Chest pain of recent onset Neuropathic pain pharmacological management Lower urinary tract symptoms Neonatal jaundice Constipation in children and young people Alcohol-use disorders: physical complications Chronic obstructive pulmonary disease Bacterial meningitis and meningococcal septicaemia Delirium Metastatic malignant disease of unknown primary origin Motor neurone disease - noninvasive ventilation Barrett's oesophagus - ablative therapy Hypertension in pregnancy Chronic heart failure Transient loss of consciousness in adults and young people Pregnancy and complex social factors Nocturnal enuresis - the management of bedwetting in children and young people Sedation in children and young people 2011 • • • • • • • • • • • • • • • • • • • • • • • • Anxiety Anaemia management in people with CKD Alcohol dependence and harmful alcohol use Food allergy in children and young people Tuberculosis Colonoscopic surveillance for prevention of colorectal cancer Diabetic foot problems - inpatient management Psychosis with coexisting substance misuse Lung cancer Ovarian cancer Common mental health disorders Hip fracture Peritoneal dialysis Stable angina Hypertension Autism in children and young people Multiple pregnancy Hyperglycaemia in acute coronary syndromes Colorectal cancer Caesarean section Self-harm (longer term management) Anaphylaxis Organ donation Service user experience in adult mental health 2012 • • • • • • • • • • • • • • • • • • Epilepsy Patient experience in adult NHS services Infection control Opioids in palliative care Acute upper GI bleeding Autism in adults Sickle cell acute painful episode Venous thromboembolic diseases Spasticity in children and young people Osteoporosis fragility fracture Lower limb peripheral arterial disease Urinary incontinence in neurological disease Antibiotics for early-onset neonatal infection Headaches Neutropenic sepsis Crohn’s disease Psoriasis Ectopic pregnancy and miscarriage 20 Potentially serious drug-drug interactions between drugs recommended by clinical guidelines for three index conditions and drugs recommended by each of other 11 other guidelines. Dumbreck et al. BMJ 2015;350:bmj.h949 21 Guidelines also rarely tell us when to stop… The challenge of ‘deprescribing’ (see WeMeReC Bulletin 2010 and eNotes, www.wemerec.org ) • Is the drug still needed? • Has the condition changed? • Can the patient continue to benefit? • Has the evidence changed? • Have the guidelines changed? • Is the drug to treat an iatrogenic problem? • What are the ethical issues about withholding care? • Would discontinuation cause problems? – opioids, antidepressants, BDPs/Z-drugs, corticosteroids, beta-blockers etc. • [+ Do ‘End of Life’ considerations apply? ] 22 Pharmacology and older people Milton et al. BMJ 2008;336:606-609. • Reduction in renal clearance • Reduction in liver size and metabolism, reduced albumin • Reduction in lean body mass • Increased pharmacodynamic/sensitivity to drugs – partic. CNS • Increased morbidity and co-morbidities • Polypharmacy – risk of ADRs, interactions • (+ FALLS!) 23 Polypharmacy Some key points (from the KF report) 24 Key points – choosing to prescribe (KF) • For many people, appropriate polypharmacy will extend life expectancy and improve their quality of life. Where there is no evidence of benefit from the drugs being prescribed, polypharmacy should be avoided. • The evidence for choosing treatment where there is polypharmacy should ideally be clearly stated. Prescribers should record the rationale for nonevidence-based prescriptions, for example, through patient choice. 25 Key points – the patient perspective (KF) • People often do not take medicines in the way that prescribers intend and there is considerable evidence that many dispensed medicines remain unused or are wasted. These problems increase as drug regimens become more complex. • The patient perspective on medicine-taking needs to be determined. Compromise may be needed between the view of the prescriber and the patient’s informed choice. 26 Key points – evidence and guidelines (KF) • Many clinical trials and practice guidelines do not consider polypharmacy in the context of multi-morbidity. A singledisease framework prevails in most health care systems, medical research and medical education. • It is important that pragmatic clinical trials are conducted that include patients with multi-morbidity and polypharmacy. • Guidelines should be developed that take account of longterm conditions that commonly co-exist, such as diabetes, coronary heart disease, heart failure and chronic obstructive pulmonary disease. Lehman and Krumholz. BMJ 2010;340:c580 – when QOF set at <7% 28 The original “polypill” idea? The LODR Salim Yusuf. Lancet 2002:360:2-3 Potential cumulative impact of four simple secondary-prevention treatments: Intervention Relative-risk reduction 2-year event rate .. 8% Aspirin 25% 6% ß-blockers 25% 4·5% Lipid lowering 30% 3.0% 25% 2.3% No intervention (by 1·5 mmol/L) ACE inhibitors Cumulative relative risk reduction if all four drugs are used is about 75% But also….. smoking cessation, BP treatment, etc.….. 29 OK – which 5? 30 Medicalisation, too much medicine, overdiagnosis, Prudent Healthcare, and Choosing Wisely •31 Key points – training, organisation (KF) • Multimorbidity and polypharmacy increase clinical workload. Doctors, nurses and pharmacists need to work coherently as a team, with a carefully balanced clinical skill-mix. • There should be more training in managing complex multimorbidity, polypharmacy and other aspects of medicines management. • This could include GPs, clinicians who specialise in care of older people, orthogeriatricians, clinical pharmacologists, nurse specialists and clinical pharmacists. • Patients with multi-morbidity admitted to hospital under one specialty may require access to a generalist clinician to coordinate their overall care. 32 Key points – adverse effects (KF) • Prescribers may not recognise that symptoms could be iatrogenic and unwittingly prescribe new medication to counter the adverse effects of other drugs. This is known as incremental prescribing or the ‘prescribing cascade’ and should be avoided. • Prescribers should consider whether interactions between drugs where medication is combined will undermine therapeutic benefit. 33 34 Key points – end of life (KF) • Many people stay on medicines beyond the point where they are deriving optimal benefit from an intervention. When reviewing medications, health care professionals should consider if treatment can be stopped and recognise that ‘end-of-life’ considerations apply to many chronic diseases as well as cancer-related conditions. www.goldstandardsframework.org.uk 36 Teams, prescribing systems …and place of decision support 37 Clinical pharmacists in the team • Reviewing systems – repeat prescriptions, drug monitoring protocols, response to hazard/warnings • Significant event reviews, audits • Identifying and targeting those: • on high risk drugs • at risk (polypharmacy, multimorbidity, frail etc.) • on inappropriate/unsafe drugs • Post discharge and reconciliation reviews • Support to care homes • Medication reviews – medicines optimisation • Case management • Supporting Reducing Unplanned Admission Enhanced Service (or equivalent) 38 The PINCER trial Avery A, et al. Lancet 2012; 379:310-319 • The study involved at-risk patients who were being prescribed drugs that are commonly and consistently associated with medication errors • 72 practices, cluster randomisation: Simple feedback - Computergenerated feedback on patients at potential risk from hazardous prescribing (n=36) vs. Pharmacist-led intervention, simple feedback plus educational outreach and dedicated support to correct and prevent potentially hazardous prescribing (n=36) • At 6-months follow-up patients in the PINCER group were: • 42% less likely to have been prescribed a non-selective NSAID if they had a history of peptic ulcer without gastroprotection • 27% less likely to be given a beta blocker if they had asthma • Almost 50% less likely to be prescribed an ACE inhibitor or loop diuretic without appropriate monitoring = Using GP computer systems to identify patients at risk, combined with a pharmacist intervention, can substantially reduce medication errors 39 (Un)Safety Indicators: PINCER Query Library www.nottingham.ac.uk/primis/tools-audits/list-of-audit-tools/pincer.aspx Query 1: Patients with a history of peptic ulcer who have been prescribed a non-selective NSAID without co-prescription of a PPI Query 2: Patients with a history of asthma who have been prescribed a βblocker Query 3: Patients aged 75 years and older who have been prescribed an ACEI or a loop diuretic long-term who have not had a computer-recorded check of their U&E in the previous 15 months Query 4: Women with a past medical history of venous or arterial thrombosis who have been prescribed combined hormonal contraceptives (CHC) Query 5: Patients receiving methotrexate for at least three months who have not had a recorded FBC or LFT within the previous three months Query 6: Patients receiving warfarin for at least three months who have not had a recorded check of their INR within the previous 12 weeks Query 7: Patients receiving lithium for at least three months who have not had a recorded check of their lithium concentrations in the previous three months Query 8: Patients receiving amiodarone for at least six months who have not had a TFT within the previous six months 40 Much to be done – variation in prescribing safety Stocks et al. BMJ 2015;351:h5501 (see December KINES) • 526 practices across the UK contributing to CPRD up to April 2013. • Anonymised data from patients >18yrs, database of 5 million. • Analysed using indicators developed from PINCER. • 49,927 of the 949,552 patients at risk triggered at least one • • • • prescribing indicator – 5.26% (95% CI 5.21% to 5.30%). 21,501 of 182,721 – 11.8% (95% CI 11.6% to 11.9%) triggered at least one monitoring indicator. The prevalence of potential prescribing hazard ranged from 0 to 10.2%, and for inadequate monitoring ranged from 10.4% to 41.9% = substantial variation. Older patients and those prescribed multiple repeat medications had significantly higher risks of triggering a prescribing indicator. Younger patients with fewer repeat prescriptions had significantly higher risk of triggering a monitoring indicator. 41 STOPP (Screening Tool of Older Person's Prescriptions) and START (Screening Tool to Alert doctors to Right Treatment) www.ucc.ie/en/misl/research/previous/stopp_start • Developed in Cork, Ireland • Delphi Questionnaire – 18 experts, first published 2008 • Widely researched and adopted since then • Version 2 published October 2014, updated with wider European-wide consensus • 87 STOPP rules • 34 START rules • Applies to people >65 years • Distinction from PINCER is that represent indicators of potentially inappropriate prescribing, rather than focused purely on (un)safety 42 STOPP: Some CVS Examples • Digoxin at a long-term dose > 125μg/day with impaired • • • • • • • • renal function Loop diuretic for dependent ankle oedema only i.e. no clinical signs of heart failure Loop diuretic as first-line monotherapy for hypertension Thiazide diuretic with a history of gout Non-cardioselective beta-blocker with COPD Beta-blocker in combination with verapamil Calcium channel blockers with chronic constipation Aspirin at dose > 150mg day Aspirin with no history of coronary, cerebral or peripheral vascular symptoms or occlusive event 43 START: Some CVS Examples • Aspirin or clopidogrel with a history of atherosclerotic • • • • • coronary, cerebral or peripheral vascular disease in patients with sinus rhythm Antihypertensive therapy where systolic BP consistently >160 mmHg Statin therapy with a history of coronary, cerebral or peripheral vascular disease, where functional status remains independent for activities of daily living and life expectancy is > 5 years Angiotensin Converting Enzyme (ACE) inhibitor with chronic heart failure ACE inhibitor following acute myocardial infarction Beta-blocker with chronic stable angina 44 By way of conclusion…. Resources and challenges www.awmsg.org/medman_library.html www.sehd.scot.nhs.uk/dl/DL(2015)04.pdf 47 Medicines optimisation and polypharmacy Many challenges, including…. • Time, resources, manpower – doctors, nurses, pharmacists • Importance of formal medication review • Multidisciplinary assessment (vs. specialism) • ‘One-stop shop’ reviews • Getting evidence of improved patient outcome • Shared decision-making (and recording) • Coding accuracy for decision support • Adaptive guidelines • Alert fatigue • Use of “order sentences” & stating what medication is for • Interfaces, and integrated care; care homes