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EMIS NUG conference September 2010 Warwick University Julia Hippisley-Cox Sessional GP Epidemiologist Director QResearch Director ClinRisk Ltd EMIS & EMIS Practices contributing data Many GPs & nurses for suggestions, piloting University of Nottingham Academic colleagues ClinRisk Ltd (software) THIN (validation data) Oxford University – independent validation Update on QSurveillance QFeedback Update on QScores ◦ QIntervention ◦ QFracture ◦ Qcancer General discussion Real time infectious diseases surveillance system Vaccine uptake reporting system History ◦ ◦ ◦ ◦ ◦ ◦ 2004 - Pilot study on QResearch in 2004 2005 - Upgraded to online QFLU 2006 – Separate Flu vaccine service 2007 – Separate Pneumo vaccine service 2007 – upgraded to QSurveillance Avon floods Included prospective consent for data extraction in emergency Key part of HPA and DH emergency response Age/sex aggregated data 100-150 indicators Infectious diseases Vaccine uptake – flu, pneumo, MMR Daily, weekly, monthly, quarterly, annual reports No patients can be identified Counts < 5 suppressed JHC custodian & responsible to practices, profession, ethics etc No patients identifiable Counts < 5 suppressed Process for new indicators: ◦ Practice consent covers additional data extracted to support emergency response ◦ consult with relevant agency re need, ethics and advisory board (including NUG) Practice consent Oversight board/review mechanism with NUG representation Robust safeguards in place to protect patients and practices Practices able to switch it on or off Practice can access and benefit from data extracted Incredibly busy with flu pandemic Daily reporting over 10 months Unexpectedly high demand across NHS Detailed coverage by media Under resourced Need to ensure its scalable, resilient, properly resourced. Decision to industrialise it Ensure practices can access and benefit from data Population level ◦ Risk stratification ◦ Identification of rank ordered list of patients for recall or reassurance Individual assessment ◦ Who is most at risk of preventable disease? ◦ Who is likely to benefit from interventions? ◦ What is the balance of risks and benefits for my patient? ◦ Enable informed consent and shared decisions Disease outcomes QRISK (CVD) QDScore (diabetes) QFracture QKidney (CKD3b+) Qcancer Range of other significant outcomes Status published published published published completed In progress Different approach needed Assess baseline risk of outcomes Then how they change with interventions Use RCTs and meta analyses for benefits Use database analyses for unintended effects Starting with commonly used drugs e.g ◦ ◦ ◦ ◦ ◦ ◦ Statins Antidepressants HRT Warfarin Antipsychotics NSAIDS Identify patients at high risk of vascular disease ◦ CVD ◦ Diabetes ◦ Stage 3b,4, 5 Kidney Disease Assessment of individual’s risk profile Risks and benefits of interventions ◦ ◦ ◦ ◦ Weight loss Smoking cessation BP control Statins Risk of CVD & “Heart age” Extensively reviewed and externally validated Now included in ◦ QOF ◦ DH Vascular Guidance ◦ NICE Widespread use across NHS Nearly all GP systems, many pharmacies, some hospitals, NHS Choices, Supermarkets, Occupational Health etc Also free Open Source and Closed Software Predicts risk of type 2 diabetes Published in BMJ (2009) Independent external validation by Oxford University Needed as epidemic of diabetes & obesity Evidence diabetes can be prevented Evidence that earlier diagnoses associated with better prognosis. Set of algorithms ◦ Identifies those at risk of CKD3b+ End Stage Renal Failure ◦ Published BMC 2010 So we can then ◦ ◦ ◦ ◦ ◦ ◦ Identify high risk Modify risk factors Avoid nephrotoxic drugs Monitor more closely Prevent deterioration Improve outcomes Two recent papers: ◦ Unintended effects statins (BMJ, 2010) ◦ Individualising Risks & Benefits of Statins (Heart, 2010) Conclusions: ◦ New tools to quantify likely benefit from statins ◦ New tools to identify patients who might get rare adverse effects eg myopathy for closer monitoring Many of the risk factors over overlap Many of the interventions overlap But different patients have different risk profiles ◦ Smoking biggest impact on CVD risk ◦ Obesity has biggest impact on diabetes risk ◦ Blood pressure biggest impact on CKD risk Help set individual priorities Development of personalised plans and achievable target Offer information about: • absolute risk of vascular disease • absolute benefits/harms of an intervention Information should: • present individualised risk/benefit scenarios • present absolute risk of events numerically • use appropriate diagrams and text Osteoporosis major cause preventable morbidity & mortality. 2 million women affected in E&W 180,000 osteoporosis fractures each year 30% women over 50 years will get vertebral fracture 20% hip fracture patients die within 6/12 50% hip fracture patients lose the ability to live independently 1.8 billion is cost of annual social and hospital care 29 Not Worth Living In Constant Pain Daily Analgesia Hard to Bend Hard to Stand Wake Early 0 20 40 60 80 % Patients 30 Scane et al, Osteoporosis Int 1994; 4: 89-92. Effective interventions exist to reduce fracture risk Challenge is better identification of high risk patients likely to benefit Avoiding over treatment in those unlikley to benefit or who may be harmed Some guidelines recommend BMD but high cost and low specificity Other guidelines recommend using 10 year risk of fracture Cohort study using patient level QResearch database Similar methodology to QRISK Published in BMJ 2009 Algorithm includes established risk factors Undertook validation against FRAX Developed risk calculator which can - identify high risk patients for assessment - show risk of fracture to patients QFracture Primary care Works better in EMIS Open Source No funding Includes extra risk factors eg ◦ Falls ◦ CVD ◦ Type 2 diabetes ◦ Asthma ◦ Antidepressants ◦ Detail smoking/Alcohol ◦ HRT FRAX Selected cohorts Over-predicts in EMIS Not published Industry sponsored NOGG guidance 64 year old women Heavy smoker Non drinker BMI 20.6 Asthma On steroids Rheumatoid H/O falls 20 15 10 Before After 5 0 Vit D + calcium Bisphosph Hip HRT (out of protectors fashion) Need to quantify risks of interventions Few large long term safety studies Bisphosphonates may increase risk of ◦ ◦ ◦ ◦ ◦ Oesophageal cancer Atrial fibrillation Osteonecrosis of jaw Atypical fracture ? Other outcomes Key thing for my patient is ◦ Baseline risk of fracture ◦ Likely benefit of intervention ◦ risk of adverse effects of intervention What is the overall risk/benefit ratio? Tools to predict risk of range of common cancers Risk stratification: Identify those who need regular screening Identify those who need ad hoc assessment Patient communication Background risk with family history – may be reassuring Risk of cancer with “alarm” symptoms Risks of cancer with smoking as decision aid for smoking cessation Current Ex smoker Non smoker Cancers Breast cancer Prostate Colorectal Oesophageal Renal/bladder Lung Ovary Uterus Alarm symptoms Breast lump Prostatism Rectal bleeding Dysphagia Haematuria Haemoptysis Abdo pain/distension Post menopausal bleeding Information about QResearch database Academic papers Technical & statistical documents Open source software Patient information Clinician information Power points presentations Information on how to contribute to the database (or email [email protected] ) Questions Comments Suggestions Feedback