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Dr Brenda Dooley, Managing Director, AXIS Healthcare Consulting Ltd.

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Does Economic Evaluation lead to increased uptake of new medical technologies? Brenda Dooley March 25 th 2015
Transcript

Does Economic Evaluation lead to

increased uptake of new medical

technologies?

Brenda Dooley March 25th 2015

For consideration today

• What is Economic Evaluation?

• Methodological approaches in current use?

• Impact of evaluation decisions made in one jurisdiction

• Relevance for Ireland

What is an Economic Evaluation?

• Formal assessment of the major health effects a

new technology will have on the patient and the

health care system.

• Purpose is to inform decision making & meet the

needs of the decision maker.

• Assessment methods and practices need to fit

the technologies to be assessed, specific to the

decision to inform.

• Positive outcome should lead to funding and

uptake of new technology.

Differences between health innovations?

• Process of innovation for medical

devices and pharmaceuticals

differs greatly

• Dissimilar mechanism of action

• Product lifecycle

• Provision of robust clinical

evidence – v challenging for

medical devices

• Ready established pathways for

evaluation of pharmaceuticals not

entirely suitable for medical

technologies.

HTA in Practice

Medical Technologies Evaluation Programme (MTEP)

• MTEP provides a single entry point for manufacturers to submit

products for evaluation – then routed to appropriate evaluation

programme

• Overall objectives threefold – to simplify access to, speed up and

increase evaluation capacity for medical devices

• Products must have a CE mark, be new or represent a significant

modification and have clear benefits for patients of NHS

• 1st MTEP guidance published in 2010

• Recommended technologies not subject to mandatory funding

Methodological Approach by MTEP

• Cost Consequence Analysis – no attempt to summarise the benefits into

a single outcome measure.

• Subjective decision making - relative value of each outcome

considered.

• Limitations of the CCA - a medical device is only more beneficial than

current practice if it is resource releasing.

• Approach to evidence synthesis.

• “it (NICE) may discriminate against technologies that would ultimately

provide a net benefit to the NHS” 1

1. Greene W and Hutton J . Health technology assessments in England: an analysis of

the NICE Medical Technologies Evaluation Programme. Eur J Health Econ. 2014 .

Has MTEP been successful to date ?

• Medical Technology Guidance ( MTG ) published for 15 technologies in

initial 3 years of MTEP.

• Target for year 1 = 15 50 in future years

• 4 MTG published in 1st year

Overall

Evaluations

( 2010-2013 )

Recommended ,

some with

specific

circumstances

Further

research

required

Not

Recommended

15 12 2 1

Has MTEP been successful ?

2. Chapman, A.M., Taylor, C.A., & Girling, A.J., 2014. Are the UK Systems of Innovation and

Evaluation of Medical Devices Compatible? The Role of NICE's Medical Technologies Evaluation

Programme (MTEP). Appl Health Econ Health Policy, 12(4), pp.347-357.

Has MTEP been successful to date ?

2.Chapman, A.M., Taylor, C.A., & Girling, A.J., 2014. Are the UK Systems of Innovation and

Evaluation of Medical Devices Compatible? The Role of NICE's Medical Technologies

Evaluation Programme (MTEP). Appl Health Econ Health Policy, 12(4), pp.347-357.

By mid 2014,

nearly 2/3

exceeded

target with avg

of 16.7 mo’s 2

Has MTEP been successful to date ?

• While MTEP provides an accessible entry point for companies wishing to

submit a product for evaluation, barriers exist

• The current process at NICE attracts a small subset of mainly large

device manufacturers.

• Due to current evaluation timelines, high risk of guidance being

outdated prior to uptake.

• No Mandatory uptake of MTEP guidance in England.

NICE efforts to support uptake of new technologies

• Health Technologies Adoption Program (HTAP)

• Develops resources to aid the adoption of NICE guidance

• Topics selected are those identified as having potential adoption

barriers in England

• HTAP teams works with the NHS with a) demonstrator projects or

b) adoption projects

An Example

• Ambu aScope2 system; sterile, single-

patient use endoscope and reusable

monitor for complex intubations.

• During development of NICE guidance -

Ambu aScope3 launched

• HTAP developed a site demonstrator

pack to aid implementation & uptake

of usage : including info on new design

• One major limitation : no metrics on

impact of HTAP

Copyright Ambu Ltd

2013

Copyright Ambu Ltd 2013

Relevance for Ireland

• AdvaMed report recommends “use of value based criteria should be

routine in medical device procurement vs simplistic recourse to

procurement based on lowest price” 3

• IMSTA has called for a multi disciplinary Professional Evaluation Group

to be established to standardise medical technology Evaluation in

Ireland

• Also conducting a piece of work examining the issues associated with

how clinical investigations are currently conducted here

• Objective is a list of recommendations to help standardise how

evidence is collected in clinical investigations

3. IMSTA publication “New Approaches for procuring effective healthcare solutions”

published with permission of AdvaMed 2014

Conclusions

• The MTEP experience would suggest that evaluation of medical

technologies to date has not led to increased uptake

• Partly due to design of the MTEP

• Recent developments indicate willingness to address gaps in uptake

• Key learnings for Ireland if economic evaluation is to be introduced

• Appropriate timelines central coupled with appropriate methodologies

that are fit for purpose of evaluating medical technologies

• NB. A link should be established between guidance and uptake

THANK YOU


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