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Risk minimisation in the Australian context
Dr Claire Larter
Acting Co-Director, Risk Management Plan Evaluation Section,
Pharmacovigilance & Special Access Branch
Medicines Regulation Division, TGA
ARCS Scientific Congress Canberra 2016
11 August 2016
Presentation overview
• What is risk minimisation?
• General principles for risk minimisation plans
• Tools available for risk minimisation
• How to describe your risk minimisation plan in the ASA
Presentation title 1
What is risk minimisation?
• Part of risk management → described in the RMP
• Intended to improve patient outcomes
– Optimise risk: benefit
– Minimise harm
• Includes both risk prevention and risk mitigation
– Some risks are neither preventable or able to be mitigated
– May be acceptable depending on benefit
Risk minimisation in the Australian context 2
Risk minimisation requires understanding the
risks of the product
• Inherent risks, including:
• Likelihood
• Severity (including reversibility)
• Preventability
• Risk factors in the population
• Intended and potential use
Risk minimisation in the Australian context 3
General risk minimisation principles
• Iterative process that continues throughout the lifecycle of the product
– Pre-registration → plan to minimise risks identified during development,
know where the gaps are
– Post-registration → address emerging risk
• Consider the burden of risk minimisation
– On patients and the healthcare system
– Burden should be proportionate to risk
Risk minimisation in the Australian context 4
Developing an effective risk minimisation plan
• Appropriate tool selection
– Choose most effective tool to achieve an objective
• Must be well planned
– Clear goals
– More likely to succeed if integrated into the health system
– What success is should be well defined and measurable
 Process indicators
 Outcome indicators
– Plan should be adapted as necessary
Risk minimisation in the Australian context 5
Risks requiring additional risk minimisation should
be carefully selected
• Are there risks that cannot be minimised by routine measures?
• This requires knowledge of the medicine:
– Indication, population, risks
– Overall risk-benefit
– Setting of use
– Will “real-world” use likely differ from intended use?
– Potential for misuse
Need to consider how these factors may interact
Risk minimisation in the Australian context 6
Risk minimisation tools
Routine Additional
Product Information Patient education
Consumer Medicine Information Patient Alert Cards
Product labeling Healthcare profession education
Legal (prescription) status Dear healthcare professional letter
Pack size & design Safety device design
Restricted access
Patient registry
Risk minimisation in the Australian context 7
Selecting the appropriate tools
• Will depend on the following factors:
– Risk identification: recognition (existence of a risk) and
characterisation (level of risk)
– Goal setting: goals, objectives and targets
– Health care system integration: adaptation to local requirements
– Evidence-based activities: based on scientific literature or other evidence
– Proportionality/Burden considerations: reasonable minimisation-burden
balance
• A comprehensive strategy may require a range of interventions
Risk minimisation in the Australian context 8
Commonly used tools in Australia
• 37 RMPs were evaluated for
new chemical entities in
2015.
• 26 included additional risk
minimisation activities
• Education was the most
common activity
0
2
4
6
8
10
12
14
Patient
education
Health
professional
education
Controlled
access
scheme
Pregnancy
prevention
program
Risk minimisation in the Australian context 9
Patient Education
• Patient brochures, websites for patients
• Targeted to specific patient populations
Useful for products where patient behaviors can influence safety
Advantages Disadvantages
Promote appropriate use Requires periodic assessment ± updating
May increase early detection of AEs Can be a burden for dispensers
Reinforce instructions given by healthcare
professionals
May be dependent on health literacy
May be perceived as marketing
Risk minimisation in the Australian context
10
Healthcare professional communication
Dear healthcare professional letters
• Useful for:
– Medicines that require adherence to special guidance to manage risks
– Changes in indication that may involve a different dosing regimen
– Emerging safety concerns
Advantages = Broad and rapid dissemination of information
Disadvantages = Effect can fade over time
Can be overlooked
Risk minimisation in the Australian context 11
Healthcare professional communication
• Prescribing/ dispensing guides
– Useful for complicated dosing regimens, managing drug-drug interactions or
medicines that may require dose adjustments, etc…
• Targeted education
– Useful for medicines that require additional monitoring (e.g. renal function), different use in
different populations, etc…
Advantages Disadvantages
Enhance prescriber knowledge Requires periodic assessment ± updating
Clinically useful – can keep for future reference Can be a burden for dispensers
Can be integrated into continuing professional
development activities
May be perceived as marketing
Risk minimisation in the Australian context
12
Restricted access schemes
• Less commonly used
• Different models
– Patient registration
– Prescriber/ dispenser certification
– Dispensing linked to test confirmation
– Certain types of prescribers
• Detailed documentation critical
– How the system will work
– How it will be checked for effectiveness
TGA
Risk minimisation in the Australian context 13
Describing risk minimisation in the ASA
• Follow the template
Australian-Specific Annex template
3. Risk minimisation plan
3.1. How risk minimisation activities will be implemented in Australia.
3.2 Potential for medication errors or other risks if applicable
3.3 How risk minimisation activities will be evaluated in Australia
4. Summary of the RMP
Risk minimisation in the Australian context 14
Consider what is different about Australia?
What are the features of our health system, medical
practice, geography, population and culture that could
influence how risk minimisation tools are selected and
implemented?
• Indigenous population
• Large Asian population
• Rurality/ lack of access to specialist services
• State vs federal control over some aspects of how
medicines are used
• Access to health professionals and information
Risk minimisation in the Australian context 15
Key areas in the ASA for risk minimisation
• Compare activities between EU and Australia for all safety concerns
– Identify and justify differences
– Describe local implementation
– Include exact wording of PI statements
• Include evaluation plan
• Include any proposed educational materials as an appendix
Risk minimisation in the Australian context 16
Presentation: Risk minimisation in the Australian context

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Presentation: Risk minimisation in the Australian context

  • 1. Risk minimisation in the Australian context Dr Claire Larter Acting Co-Director, Risk Management Plan Evaluation Section, Pharmacovigilance & Special Access Branch Medicines Regulation Division, TGA ARCS Scientific Congress Canberra 2016 11 August 2016
  • 2. Presentation overview • What is risk minimisation? • General principles for risk minimisation plans • Tools available for risk minimisation • How to describe your risk minimisation plan in the ASA Presentation title 1
  • 3. What is risk minimisation? • Part of risk management → described in the RMP • Intended to improve patient outcomes – Optimise risk: benefit – Minimise harm • Includes both risk prevention and risk mitigation – Some risks are neither preventable or able to be mitigated – May be acceptable depending on benefit Risk minimisation in the Australian context 2
  • 4. Risk minimisation requires understanding the risks of the product • Inherent risks, including: • Likelihood • Severity (including reversibility) • Preventability • Risk factors in the population • Intended and potential use Risk minimisation in the Australian context 3
  • 5. General risk minimisation principles • Iterative process that continues throughout the lifecycle of the product – Pre-registration → plan to minimise risks identified during development, know where the gaps are – Post-registration → address emerging risk • Consider the burden of risk minimisation – On patients and the healthcare system – Burden should be proportionate to risk Risk minimisation in the Australian context 4
  • 6. Developing an effective risk minimisation plan • Appropriate tool selection – Choose most effective tool to achieve an objective • Must be well planned – Clear goals – More likely to succeed if integrated into the health system – What success is should be well defined and measurable  Process indicators  Outcome indicators – Plan should be adapted as necessary Risk minimisation in the Australian context 5
  • 7. Risks requiring additional risk minimisation should be carefully selected • Are there risks that cannot be minimised by routine measures? • This requires knowledge of the medicine: – Indication, population, risks – Overall risk-benefit – Setting of use – Will “real-world” use likely differ from intended use? – Potential for misuse Need to consider how these factors may interact Risk minimisation in the Australian context 6
  • 8. Risk minimisation tools Routine Additional Product Information Patient education Consumer Medicine Information Patient Alert Cards Product labeling Healthcare profession education Legal (prescription) status Dear healthcare professional letter Pack size & design Safety device design Restricted access Patient registry Risk minimisation in the Australian context 7
  • 9. Selecting the appropriate tools • Will depend on the following factors: – Risk identification: recognition (existence of a risk) and characterisation (level of risk) – Goal setting: goals, objectives and targets – Health care system integration: adaptation to local requirements – Evidence-based activities: based on scientific literature or other evidence – Proportionality/Burden considerations: reasonable minimisation-burden balance • A comprehensive strategy may require a range of interventions Risk minimisation in the Australian context 8
  • 10. Commonly used tools in Australia • 37 RMPs were evaluated for new chemical entities in 2015. • 26 included additional risk minimisation activities • Education was the most common activity 0 2 4 6 8 10 12 14 Patient education Health professional education Controlled access scheme Pregnancy prevention program Risk minimisation in the Australian context 9
  • 11. Patient Education • Patient brochures, websites for patients • Targeted to specific patient populations Useful for products where patient behaviors can influence safety Advantages Disadvantages Promote appropriate use Requires periodic assessment ± updating May increase early detection of AEs Can be a burden for dispensers Reinforce instructions given by healthcare professionals May be dependent on health literacy May be perceived as marketing Risk minimisation in the Australian context 10
  • 12. Healthcare professional communication Dear healthcare professional letters • Useful for: – Medicines that require adherence to special guidance to manage risks – Changes in indication that may involve a different dosing regimen – Emerging safety concerns Advantages = Broad and rapid dissemination of information Disadvantages = Effect can fade over time Can be overlooked Risk minimisation in the Australian context 11
  • 13. Healthcare professional communication • Prescribing/ dispensing guides – Useful for complicated dosing regimens, managing drug-drug interactions or medicines that may require dose adjustments, etc… • Targeted education – Useful for medicines that require additional monitoring (e.g. renal function), different use in different populations, etc… Advantages Disadvantages Enhance prescriber knowledge Requires periodic assessment ± updating Clinically useful – can keep for future reference Can be a burden for dispensers Can be integrated into continuing professional development activities May be perceived as marketing Risk minimisation in the Australian context 12
  • 14. Restricted access schemes • Less commonly used • Different models – Patient registration – Prescriber/ dispenser certification – Dispensing linked to test confirmation – Certain types of prescribers • Detailed documentation critical – How the system will work – How it will be checked for effectiveness TGA Risk minimisation in the Australian context 13
  • 15. Describing risk minimisation in the ASA • Follow the template Australian-Specific Annex template 3. Risk minimisation plan 3.1. How risk minimisation activities will be implemented in Australia. 3.2 Potential for medication errors or other risks if applicable 3.3 How risk minimisation activities will be evaluated in Australia 4. Summary of the RMP Risk minimisation in the Australian context 14
  • 16. Consider what is different about Australia? What are the features of our health system, medical practice, geography, population and culture that could influence how risk minimisation tools are selected and implemented? • Indigenous population • Large Asian population • Rurality/ lack of access to specialist services • State vs federal control over some aspects of how medicines are used • Access to health professionals and information Risk minimisation in the Australian context 15
  • 17. Key areas in the ASA for risk minimisation • Compare activities between EU and Australia for all safety concerns – Identify and justify differences – Describe local implementation – Include exact wording of PI statements • Include evaluation plan • Include any proposed educational materials as an appendix Risk minimisation in the Australian context 16

Editor's Notes

  • #4: All medicines have benefits and risks The risk-benefit ratio can be improved by proactively addressing the known risks
  • #14: Examples…