West Midlands Familial Hypercholesterolaemia Service

Similar documents
Identification and management of familial hypercholesterolaemia (FH) - An overview

Developing General Practice and Web-Based Toolkits for the Familial Hypercholesterolaemia (FH) Case Ascertainment Tool (FAMCAT)

The identification and management of heterozygous familial hypercholesterolaemia in adults, young people and children (QS41)

Cost effectiveness of cascade testing for FH:

GOVERNING BODY REPORT

Familial hypercholesterolaemia

Familial Hypercholesterolaemia: Finding FH and Primary Prevention. Rob Gingell FH Specialist Nurse (North Wales)

Costing report: Lipid modification Implementing the NICE guideline on lipid modification (CG181)

Prescribing Policy: Lipid Modification - Primary Prevention

Delivering NDPP in a super diverse population

Lipid Lowering in patients with High Risk of Cardiovascular Disease (Primary Prevention)

NHS England Getting Serious About Prevention

Getting Serious About CVD Prevention What does this mean for Primary Care?

Low-density lipoproteins cause atherosclerotic cardiovascular disease (ASCVD) 1. Evidence from genetic, epidemiologic and clinical studies

Appendix E Health Economic modelling

APPENDIX 2F Management of Cholesterol

Appendix F Simon Broome Diagnostic criteria for index individuals and relatives

Appendix E Health Economic modelling

Outcomes of diabetes care in England and Wales. A summary of findings from the National Diabetes Audit : Complications and Mortality reports

Four Years of NHS Health Checks in Barnsley - Outcomes and Inequalities

National Dementia Policy in England Responding to the Prime Ministers Challenge

SCHEDULE 2 THE SERVICES. A. Service Specifications

Royal Wolverhampton Hospital Adult Lipid Lowering Therapy Guidelines Lipid Lowering Therapy for the Prevention of Cardiovascular Disease

Primary Prevention Patients aged 85yrs and over

Vascular checks a vascular risk assessment and management. Heather White Deputy Branch Head Vascular Programme

NATIONAL INSTITUTE FOR HEALTH AND CARE EXCELLENCE General practice Indicators for the NICE menu

NATIONAL INSTITUTE FOR HEALTH AND CLINICAL EXCELLENCE

NHS ENGLAND BOARD PAPER

2. Quality and Outcomes Framework: new NICE recommendations

South East Mental Health and Dementia Clinical Network Charlotte Clow, CN Manager Jill Rasmussen, Dementia Clinical Lead

Southern Derbyshire Shared Care Pathology Guidelines. Dyslipidaemia

CVD Prevention Optimal Value Pathway

Reducing smoking in pregnancy in the West Midlands

National Chronic Kidney Disease Audit

Proof of Concept: NHS Wales Atlas of Variation for Cardiovascular Disease. Produced on behalf of NHS Wales and Welsh Government

Saving Lives, Saving Families: The health, social and economic advantages of detecting and treating familial hypercholesterolaemia (FH)

Optimising Hypertension Management Clair Huckerby Pharmaceutical Adviser- Medicines Optimisation Lead

FORTH VALLEY. LIPID LOWERING GUIDELINE v5 2016

Dementia West Midlands Towards Timely Diagnosis & Quality Post-diagnostic support

Dementia Programme Kevin Mullins Head of Mental Health Services

Familial Hypercholesterolemia What a cardiologist should know

Getting serious about preventing cardiovascular disease

Dementia: Post Diagnostic Support Project

CEO Report 2017/ This report reviews and summarises Healthwatch Cambridgeshire and Peterborough activities for 2017/18.

Richard Watson, Chief Transformation Officer. Dr P Holloway, GP Clinical Lead for Cancer Lisa Parrish, Senior Transformation Lead

ESSENTIAL SHARED CARE AGREEMENT FOR Risperidone, Olanzapine, Quetiapine, Aripiprazole, Amisulpride (South Staffordshire Only)

NHS Diabetes Prevention Programme Briefing Paper. May 2016

Project Initiation Document Meeting the Dementia Challenge Timely Diagnosis (Phase 1)

The National Quality Standards for Chronic Kidney Disease

NHS NATIONAL DIABETES PREVENTION PROGRAMME. Tom Newbound, NHS DPP Programme Manager

Volume 2; Number 11 July 2008

Lincolnshire JSNA: Cancer

POTENTIAL LINKAGES BETWEEN THE QUALITY AND OUTCOMES FRAMEWORK (QOF) AND THE NHS HEALTH CHECK

National Diabetes Audit

Diabetes Network

NHS England Impact Analysis of implementing NHS Diabetes Prevention Programme, 2016 to 2021

Knee Replacement Surgery Criteria Based Access Protocol Supporting people in Dorset to lead healthier lives

Delivery of An Evolving Well Established Community Diabetes Service in South Sefton

Cheshire & Merseyside Cardiovascular Programme

THE CVD CHALLENGE IN NORTHERN IRELAND. Together we can save lives and reduce NHS pressures

NHS Health Check Training for Healthy Living Centre Staff and Colleagues. June 2015 Amanda Chappell

Datix Ref:

Integrated Diabetes Care in Oxfordshire -patient's perspective. Avril Surridge

SECONDARY PREVENTION OF CORONARY HEART DISEASE AND ISCHAEMIC STROKE/TIA

Yorkshire and the Humber Strategic Clinical Networks

Hepatitis C Strategy. About us. What is hepatitis C?

The British Cardiovascular Society 2014 Workforce Survey. A report to the BCS October 2014

British Academy of Audiology Heads of Service Day

Understanding new international guidelines to tackle CV Risk: A practical model John Deanfield, MD UCL, London United Kingdom s

NHS DIABETES PREVENTION PROGRAMME: Preventing Type 2 Diabetes in England

CYNLLUN CODI CALON/UPLIFTING HEART PROJECT

Commissioning for value focus pack

Evaluation Report Executive Summary

Orthodontics Service Specification

The reduced cost of providing a nationally recognised service for familial hypercholesterolaemia

Sudden death and inherited heart disease: a national plan. Dr Paul Brennan Lead Consultant in Cardiac Genetics Northern Genetics Service, UK

NHS DIABETES PREVENTION PROGRAMME: Preventing Type 2 Diabetes in England

Bariatric Surgery Questionnaire

Cardiovascular disease profile

Cardiovascular disease profile

Sandwell & West Birmingham integrated community care diabetes model (DICE) the future of diabetes services?

Number of people with diabetes

NHS Bowel Cancer Screening Programme

ESSENTIAL SHARED CARE AGREEMENT FOR Risperidone, Olanzapine, Quetiapine, Aripiprazole, Amisulpride or Asenapine

Modifiable and non-modifiable risk factors

South Tyneside Exercise Referral and Weight Management Programme

Type 2 Diabetes. Stopping Smoking. Consider referral to smoking cessation. Consider referring for weight management advice.

Improving Value in Chemotherapy

Let s Talk About Weight: A step-by-step guide to brief interventions with adults for health and care professionals

SCHEDULE 2 THE SERVICES

DESIGNED TO TACKLE RENAL DISEASE IN WALES DRAFT 2 nd STRATEGIC FRAMEWORK for

Optimizing risk assessment of total cardiovascular risk What are the tools? Lars Rydén Professor Karolinska Institutet Stockholm, Sweden

Insert logo. Linda Main, Dietetic Adviser

South Tyneside Diabetic Screening One Stop Clinic

Service Specification: Bristol and South Gloucestershire Specialist Substance Misuse Treatment Service January 2016

POSITION STATEMENT. Diabetic eye screening April Key points

Shared Decision Making screening for abdominal aortic aneurysm. Deciding whether to get screened for an abdominal aortic aneurysm (AAA)

Deciding whether to get screened for an abdominal aortic aneurysm (AAA)

Evaluation of the Health and Social Care Professionals Programme Interim report. Prostate Cancer UK

In 2008 NICE issued guidelines on lipid modification. Key points are summarised below.

Transcription:

Elaine George WMFHS Clinical Programme Manager West Midlands Familial Hypercholesterolaemia Service Elaine George WMFHS Clinical Programme Manager PCCS Conference November 2018 1

Presentation Objectives What is Familial Hypercholesterolaemia (FH) What is the difference between FH and Hypercholesterolaemia. National Policy Case for change in the West Midlands Implementing a systems approach to the detection and management of FH in the West Midlands Challenges of implementation Case Studies 2

What is Familial Hypercholesterolaemia (FH)? FH is an autosomal dominant Lipid Disorder affecting approximately 1:250 people DEFINITION (SWAN UK) - Some conditions are passed on through families in a dominant way. This means that if a person inherits one normal copy of a gene and one changed (mutated) copy, the changed (mutated) gene is dominant over, or overrides, the normal copy. This causes the individual to become affected by the genetic condition

Inheritance Pattern (Heterozygous) 4

Familial Hypercholesterolaemia Confers a lifelong risk of premature cardiovascular disease because of lifelong raised LDL-Cholesterol 1 (Low Density Lipoprotein Cholesterol). Untreated FH leads to markedly increased risk of CHD. Greater than 50% risk of CHD in men by the age of 50 2. At least 30% risk of CHD in women by the age of 60 2. Effective treatment reduces risk of mortality to almost that of the general population, especially in those that have not developed CHD 3. FH is a modifiable risk factor for cardiovascular disease 1. Watts et al. Int J Cardiology. 2014; 171: 2. NICE clinical guideline 71. Available at http://guidance.nice.org.uk/cg71. Accessed April 2015 3. Brice P, et al. Atherosclerosis, 2013; 231:223-226 5

Scope of the problem Most people with FH are undiagnosed (~8-15% cases known nationally) and are therefore untreated. Based on prevalence of 1 in 250 to 1 in 500 people; 130,000 260,000 are affected in the UK. Children of an individual with FH have a 50% chance of inheritance. Families are trapped in a cycle of: premature heart disease/premature death. No standard delivery model nationally. Variation of services locally, regionally nationally. 6

National Policy and Guidance NICE Guideline CG71 (2008 and updated in 2017). NICE Quality Standard on FH (2013). DoH CVD Outcomes Strategy 2013. NHS Health Checks Best Practice Guidance (2017 edition). NHS RightCare CVD Prevention Pathway. NHS England Improving outcomes through personalised medicine (September 2016). PHE Implementing a systems approach to detection and management of FH (August 2018). 7

Former West Midlands Model Variation across region. Some availability of genetic testing. Lacked regional co-ordination. Patients referred to secondary care if (total) cholesterol elevated. Generally good uptake of NHS HC programme. No systematic case finding service. No systematic cascade screening service. Ambition for service redesign for many years. 8

West Midlands Region - Population of 5.6 million - Approx. 750 GP practices - 20 CCG s -11 acute trusts DIVERSE! 9

West Midlands FH Prevalence Total Population 5.6 million 1:500 11,000 1:250 22,000 identified1,650 7.5% (1:250)

West Midlands Case for Change 2015 - Business case developed by NHSE for regional FH service. Ambition for Primary Care delivery model. Grant application to BHF for nurse funding approved. All 20 West Midlands CCG s approved case for change and agreed funding (1:500). Nurses recruited in 2016. Open tender for genetic testing contract awarded to Bristol Genetics Laboratory. Service mobilisation 1 st November 2017.

FH Service - Areas Covered Area Covered Birmingham and Solihull No of CCG s Population Estimated number of FH cases 1:500 Estimated number of FH cases 1:250 1 1,215,000 2430 4860 Black Country 4 1,376,000 2752 5502 Staffordshire and Shropshire Hereford and Worcester Coventry and Warwickshire 8 1,306,000 2612 5224 4 756,000 1512 3024 3 914,000 1828 3656 TOTALS 20 5,567.000 11,134 22,266 12

Systematic approach to commissioning FH services There are broadly five objectives of an FH service:- To identify those at risk of carrying an FH gene (detection). To undertake genetic testing for those considered appropriate. To undertake cascade genetic testing for appropriate relatives of those with confirmed monogenic FH. To manage those with monogenic FH (treat) and to do so with most cost-effective use of primary and specialist care. To manage the majority of those with polygenic hypercholesterolaemia in primary care (as per NICE guidance).

Delivery Model Clinical Programme Manager and 5 FH Specialist Nurses funded by British Heart Foundation. Eligibility Criteria TC >9.0 mmol/l and/or Simon Broome criteria*. Referrals from all specialities. Patient invited to appointment at location of their choice. A bespoke West Midlands FH database is currently in use. Assessment includes family history, family pedigree drawing, medications, physical presentation, lifestyle etc., BP, pulse, BMI. Give lifestyle advice. Receive written consent and obtain blood sample for genetic testing. *CG71 (2008) 15

Physical presentation of FH 16

Genetic Results FH Confirmed. FH Not Confirmed. Low Likelihood of Polygenic Hypercholesterolaemia. Medium Likelihood of Polygenic Hypercholesterolaemia. High Likelihood of Polygenic Hypercholesterolaemia. Variant of Uncertain Significance (VUS) 17

FH Confirmed 18

Genetic Test Results FH Confirmed If +ve TREAT in accordance with NICE CG71(2017) guidelines (Managing FH). MECC, lifestyle advice and refer to relevant lifestyle services. Refer to lipid clinic for cardiac risk assessment; (echocardiogram, calcium scoring if indicated, prescription of additional lipid lowering therapy (in addition to statins e.g. PCSK9-inhibitor drugs). Manage majority in General Practice. INITIATE FAMILY CASCADE SCREENING. 19

FH Not Confirmed 20

FH Not Confirmed If ve TREAT in accordance with NICE CG181 guidelines (CVD Risk Assessment and Reduction). MECC, lifestyle advice and refer to relevant lifestyle services. Offered referral to 100,000 genome project (if eligible). Manage in General Practice but refer to lipid clinic where lipid lowering therapy does not reduce to TC to <5.0 mmol/l or LDLc to <2.5 mmol/l. Advise family members to have cholesterol checked. 21

Patient Eligibility Identify Patients via data extraction or opportunistic review of GP clinical Systems. Criteria TC greater than or equal to 9.0 mmol/l & triglyceride <5.0 mmol/l. AND NO HISTORY OF Diagnosis/Treatment for nephrotic syndrome. Diagnosis/Treatment for CKD 4 and above. Diagnosis/Treatment for chronic liver disease. TC 7.5 8.9 mmol/l risk stratify using Welsh Scoring Criteria 22

12 months on. Paediatric service developed in conjunction with Birmingham Children's Hospital. First paediatric patient seen on 21 st June 2018. Service delivered from 60 sites across West Midlands. Patient experience surveys positive. Engaged with a wide range of stake holders. Nominated for Building Healthier Lives award. Multiple abstracts accepted for presentation. 23

12 months on In excess of 1520 referrals to date (since 1 st November 2017). 52% from General Practice. 48% from Consultants. 664 genetic tests sent. 526 results received. 115+ve (22%). 16 Paediatric samples sent; 12 results, 4+ve (33%). 49 Cascade samples sent; 23 +ve (47%). 111 referred to 100 000 genome project (results awaited!). 14 VUS. 24

Challenges to implementation IT. Clinic space. Administration. Incomplete referral information. 25

Case Study 2 26

Case Study 1 27

Paediatric Case Study* Seconds after finishing a cross country run and telling her friend "Oh God, I think I am going to die", 11 year old Rianna Wingett's heart stopped beating. Despite her positive family history, Rianna had undiagnosed FH. Estimated 56,000 children with FH in the UK. *HEART UK Case study 28

Acknowledgements WMFHS Specialist Nurses. Dr Robert Cramb Clinical Adviser WMFHS. NHS England Midlands and East. University Hospitals Birmingham NHS foundation Trust. Dr Kiran Patel Medical Director NHSE Midlands and East. British Heart Foundation. Bristol Genetics Laboratory. Heart UK. National FH Colleagues. westmidlands.fhnurses@nhs.net 29

Questions. 30