Economic Modelling and Transferring Economic Evaluations Flashcards

(17 cards)

1
Q

what is alongside

A
  • Evaluations where the economic data are prospectively collected from patients within an effectiveness evaluation (sometimes referred to as ‘EEACTs’)
  • The economic and clinical evaluations run concurrently
  • Costs and outcomes are estimated for each individual patient
  • Low bias (if the underlying evaluation is unbiased) and high ‘internal validity’
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2
Q

Issues with alongside

A
  • Comparators are limited to those in the study
  • How many HIV medications are there?
  • Length of follow-up can be too short
  • How long to assess the effectiveness of HIV meds?
  • Low ‘external validity’?
  • Are patients, doctors and hospitals typical?
  • Inadequate sample size for rare events?
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3
Q

Role of models today

A
  • It provides a method for combining data in a structured manner; data are chosen to meet the decision maker’s needs…all relevant comparators, appropriate time horizon and representing the relevant patient population
  • Best estimates of parameters are combined in a ‘base case’ analysis, then altered in sensitivity analyses
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4
Q

what is a model

A

• A model is a simplification of the real world. The world is described by a set of parameters which represent our knowledge of that world and which can be changed to to assess different scenarios

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5
Q

list at least 4 model types

A
  • Decision trees
  • State transition (“Markov”) models
  • Transmission models
  • Discrete event simulation models
  • Hybrid models, e.g. trees with Markov terminal nods
  • All are different types of decision analytic model
  • Unstructured calculations are also sometimes used…are they models? Technically, yes
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6
Q

what types of data do models use

A

patient data

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7
Q

what type of patient data does models use

A
  • Cohort
  • Probabilities relate to averages for the patient population
  • Model is run once using the mean value for each probability
  • Mean costs and outcomes are produced
  • Individual patient
  • Probabilities are specific to each individual, based on baseline characteristics and subsequent events
  • Model is run for each individual in the patient population
  • Mean costs and outcomes are calculated from the distributions produced by each run of the model
  • Sometimes referred to as individual patient simulations
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8
Q

When to use a decision tree

A

For simple models or problems with special characteristics (e.g., very short time horizons, very few outcomes), a decision tree may be appropriate.

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9
Q

when not to use a decision tree

A

Not useful when:
• States ‘recycle’ or there are recurrences of same illness
• Modelling complex problems over a long time
• Timing of events is important
• Need to model interaction

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10
Q

what is the State-transition models

A

model type
Disease is defined by health states (ovals)
Disease progression is modelled by transitions between states (lines)
Transitions occur at end of ‘cycles’ and are ‘memoryless’

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11
Q

when do you use ‘Markov’ models?-

A

more suitable for long term conditions

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12
Q

what are ‘Markov’ models?-

A
  • The conditional probability distribution of future states of the process depends only upon the present state, not on the sequence of events that preceded it.
  • Markov models are memoryless – transition probabilities do not depend on history
  • Markov assumption required in cohort-level state transition models
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13
Q

When to use a state-transition model

A

If the conceptualization involves representing the disease or treatment process as a series of health states, state-transition models are appropriate.

Their primary disadvantage, the Markovian assumption that transition probabilities do not depend on history, can be addressed by increasing the number of states.

Individual state-transition models, which do not require this assumption, are an alternative when the number of states grows too large

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14
Q

when not to use a state-transition model

A

when
• Many events could occur in one time unit
• Transitions are depend on patient history, e.g. number of previous episodes of ill-health or ‘time to….’
• Modelling interactions

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15
Q

what do you need to consider when Choosing a modelling method

A
  • Representation of disease as states or events
  • Recurring events
  • Time horizon
  • Influence of past events
  • Interactions between individuals
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16
Q

Rationale for transferability

A
  • Economic evaluations are time consuming and expensive.
  • Lack of technical expertise and data in some countries
  • Effectiveness is generally generalisable…most big drug trials are multinational
  • Existing studies done elsewhere can be transferred to other contexts
  • Just change the currency?
17
Q

Why is transferability an issue?

A
  • Countries differ in many different ways:
  • Treatment patterns
  • Effectiveness….genetics, case mix, adherence, etc.
  • Costs…price levels, quality of care, etc.
  • Values placed on outcomes….health state utilities
  • Acceptable methods*…discount rates, outcome measures
  • Funding thresholds
  • Some of these can be solved with simple adjustments (e.g unit costs), but some may require additional data collection (e.g. new comparators)