european cystic fibrosis society patient registry...
TRANSCRIPT
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European Cystic Fibrosis Society Patient Registry
Organization and achievements
Lutz Naehrlich
Director ECFSPR
Consultant, Departement of Pediatrics
University Giessen/Germany
Email: [email protected]
Polish Cystic Fibrosis Society Meeting—Warsaw- 24.05.2018
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Patient Advocacy groups
Introduction Value of a Patient Registry
Patients & their families
CF centres
Industry
Researchers
Healthcare authorities
Preparation landscape for clinical trials
Monitor effectivess & safety of new therapies
Information about CF and CF-care in country
Longitudinal and large-scale epidemiological research
Identify disease modifying factors
Monitor quality of care & identify areas for improvement
Improve CF-care
Lobby for CF-care with heathcare authorities and other parties
Information about outcomes in country => discuss with doctor
Enhance CF-care, access to new therapies
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Introduction
COMMITTMENT – TRUST – GOVERNANCE – INDEPENDENCY - SUSTAINABILITY
• Harmonization of data fields and definitions
International comparison based on harmonization
Keep the balance between quality and quantity - Data collection resources
• Data collection method (webbased software tool)
• Data management and data quality controls
• Use of data and dissemination of the results (Annual report)
Essential Registry tools
Viviani et al. Orphanet Journal of Rare Diseases 2014, 9:81
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ECFSPR
Background:
Start in 2003
Part of the European Cystic Fibrosis Society
A platform for the collection of CF data
Anonymised data
Consenting patients with CF
Agreed inclusion criteria, variables and definitions
Cooperation with national and rare disease registries (ERN)
Introduction
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ECFSPR
Encourage new standards
of CF care
Inform public health
planning
Enable research
Mission
Compare aspects of CF and its treatment to…
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ECFSPR Agreed Inclusion Criteria
2 Sweat tests with values > 60 mmol/L chloride
1 sweat test value > 60 mmol/L chloride + 2 identified disease
causing CF mutations
Sweat test values ≤ 60 mmol/L chloride:
DNA analysis: 2 identified disease causing CF mutations
Nasal Potential difference
Clinical presentation: typical CF features
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Demographic
Diagnosis
Transplant
Microbiology
Growth / lung function
Therapy
Genotype
age, gender, status of patient
age at diagnosis, sweat test, meconium Ileus, neonatal screening
Pseudomonas aeruginosa, Staphylococcus aureus, Burkholderia cepacia
Diabetes, liver disease, pancreatic status, malignancy
antibiotic, bronchodilators, oxygen therapy, pancreatic enzymes
ECFSPR
Complications
1st and 2nd mutation
value of best FEV1 and FVC, height and weight at best FEV1
Lung / liver transplant
Agreed Variables, Definitions, References
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CF- Registries in Europe
National registry
20021996
1992
1988
19951999
2007
A.D. Jackson, C. Goss., J Cyst Fibros 2017 in press; RU: Krasovskiy S, J Cyst 2014: S 124; SE: http://kvalitetsregister.se; DK: Nguyen-Nielsen M, Clin Epidemiol, 2013: 249
2011
1992
2001
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ECFSPR:Longitudinal data29 (+6) countries>42.000 patients
Reference: ECFSPR Annual Data Report 2015 + Update (20.05.2018)
National registry
Indivdual centres
Coming soon
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ECFSPR
Model 1 _ Uploading countries
Own governance
Own data management and software
Own budget to maintain this services
Model 2 _ ECFS - Tracker User
• Own governance/country coordinator
• Free use of ECFS-tracker, ECFS-PR service desk/data management
• Option to adapt own variables
• Maintenance cost covered by ECFS
Cooperation with National registries
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ECFSPR
Model 1 _ Uploading countries
Most are established before the ECFSPR started
Own budget (for example D 5000000 € per year)
Data collection/management/software development
Uploading annual ECFSPR dataset
Model 2 _ ECFS-Tracker User
• Own governance/country coordinator – reassure about data use
• Concentration on data collection and reporting (esp. national report)
• Center are owner of the data
Cooperation with National registries
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Software General Features
Web-based and open source
Designed for the collection of CF data
User friendly
Remotely managed
Data quality checks on different levels
Additional variables
Possibility add-on modules for data-collection
A platform for the collection of CF data
for all purposes
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Software Data Protection – Security
Advanced Security Technology
Controlled user access
De-identification of data:
encryption of data during transmission
Identification only at a center level
Compliant with EU data protection regulations
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Software ECFSTracker - homepage
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Software ECFSTracker - dashboard
Data-input once a year
sent to Europe
For clinical use
Real-time data-input of
individual patient visits
throughout the year
patient
centre
country
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Software Annual Summary
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Software Encounters
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Software Centre Reports
Categories of report
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Software Patient Reports
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Software Development
Benchmarking
Encounter Data Collection
Pharmaco-vigilance
Specificresearch
etc.
Clinical trials
Annual Data Collection
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Software Benchmarking
A powerful tool to enhance improvement of CF care
A module in ECFSTracker to allow cross-comparison of indicators of quality of care (= benchmarks).
Direct feedback to Centre Staff
Identify areas for improvement
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Software Benchmarking
Compare results between:
Your country with another country / other countries
Your centre with another country / other countries
Your centre with other centres in your country
Agreement between centres!
Compare with previous years
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Software Benchmarking
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Software Upgrade to version 2.0
Planning:
Development: 2017
Test in pilot countries
Launch in Europe: 2018
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Annual Data ReportsOutput
Deadline future years: 1 May Reference: ECFSPR Annual Data Report 2015
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Distribution of F508del in Europe
0-40%60-80%>80% unknown40-59% .
Reference: ECFSPR Annual Data Report 2015
82%
24%
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Complication: Chronic Pseudomonas in children
10-20%>20% unknown< 10 %
Reference: ECFSPR Annual Data Report 2015
6,9%
63,0%
REASONS:
Health care system
Diagnostic tools
Therapeutic options
Strategy
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Outcome: Lung function in patients 6-17 year
Reference: ECFSPR Annual Data Report 2015
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Outcome: Proportion of adults
< 40%50-59%>60% unknown40-49%
Reference: ECFSPR Annual Data Report 2015
61,7%
18%
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Output
www.ecfs.eu/projects/ecfs-patient-registry
/data-request-application
Applications for data
Researchers, patient organisations, Industry
Title + Aim + Description of the (research) project
Handling:
Review by Scientific Committee
Final Approval by Steering Group for use of data
Use of data (free for ECFS-PR participants)
Publication policy
Research
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Output Research
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Future Trends in CF demographicsERS/ECFFS Task force
Burgel P, ERJ 2015:133. Based on data 2010
Increase in the CF population by 50% corresponding by 25% in children and 75% in adultsImpact on care structures
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Output Manuscripts in the pipeline
International and pan-European comparison of survival in CF.
Changes in demography and clinical outcomes in CF in Europe.
Mortality during pediatric age in patients with CF in Europe.
The effect of CFTR nonsense mutations on phenotype and mortality in patients with CF.
The effect of DNase on longitudinal lung function in patients with CF.
Clinical characteristics of CFRD: Lessons from the ECFSPR.
The effect of Allergic Bronchopulmonary Aspergillosis on lung function in children and
adolescents with CF: analysis of the ECFSPR data.
CF-specific reference equations for FEV1 and BMI : an updated analysis.
Cancer in adult people with CF in Europe.
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Output At-a-Glance Reports
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Projects Overview
Definitions GroupReview variables and definitions
Global CF harmonisation project Harmonise variables & definitions to allow comparison ww
Patient awareness projectJoint effort with CF Europe to bring data closer to patients
Data Quality Group Ensure accuracy and quality of data
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Governance Organisation
Contributors Steering Group
Coordinator
Statisticians
Service Desk
StaffExecutive
Committee
Interaction
CF centres
national registries
Country
representatives
Steering Group
representatives
Scientific Comm.
Steering Group
representatives
Data custodian
StrategyData
Management
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Governance Organisation
Terms of Reference: Registry’s structure
Code of Conduct: roles and responsibilities
Standard Operating Procedures:
• Data Collection & Error reporting
• Data Access • Use of data
Business Plan 2018 - 2020
Objectives Strategy Actions
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Governance Cooperation with rare disease registries
European rare network (ERN /ERN-LUNG)
Registry overarching disease areas
Based on disease-specific registries
Interaction to fullfill these goals
No substitute for disease-specific registries
CFTR 2
Regular data request - cooperation
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Governance Clinical trials
Pharmavigilance _ Longterm safety/efficiency
Cooperation with EMA and industry
„Rare events meet large populations“
Guidance for decison making
Specific problem follow-up
Toolbox registry
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Registry How to join the ECFSPR?
Legal and Ethical approval
Informed Patients Consents
ECFSPR templates on website
Meet requirements of your local legal and ethics
laws
Translate to your own language
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ECFSPR
ECFS-PR offer a whole registry infrastructure for free
FLEXIBLE (National registry/Individual centres)
Including options for national adaptation
Including options for national reporting
Including handling of data requests
Alternative to own national registries with upload of data
Need for own data collection tools/data management/reporting
Start-ups costs – Governance – Maintenance costs
Conclusion
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Partners & Sponsors
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Thank you!