review sheet for final term 3 FPU EBP Flashcards

(62 cards)

1
Q

Clinical Prediction Rules (CPRs)

A

Utility of CPRs in physical therapist practice

Therapist tool = make decision based on predictable things from history and exam:

Includes:

Making a diagnosis, prognosis, making patients to best interventions, predict response to treatment for an individual patient

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2
Q
  • Ottawa Ankle Rules (OARs) - diagnosis
    ✓Should a patient with acute ankle pain be evaluated with an X-ray?
  • Rule for Shoulder Pain – prognosis
    ✓What is the risk of persistent symptoms in a patient with shoulder
    pain?
  • Rule for Neck Pain - response to treatment
    ✓Which patients with neck pain will benefit from thoracic spine thrust
    manipulation?
    ✓Note: this is different from effect of intervention-
    EXAMPLES of ….
A

CLINCAL PREDICTION RULES (CPR’s)

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3
Q
  • Combinations of clinical findings that are
    ✓systematically derived or developed
    ✓statistically tested
  • Stepwise logistic regression is often used to develop
    the most economic model
  • Which combination of predictors (variables) will provide
    most accurate diagnosis?
A

clinical prediction rule

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4
Q

3 steps for clinical prediction rule?

A

derive
validate
impact

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5
Q

derive

A

ID factors with predictive power

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6
Q

validate

A

evidence of reproducibility accuracy
Narrow or broad

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7
Q

impact

A

evidence that rule changes physician behavior and improves patient outcomes and/or reduces cost

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8
Q

Levels of CPRS

A

Level 1 best – impact analysis – influencing clinician behavior and improving outcomes

Level 2 Broad – varying setting – used with confidence

Level 3 narrow – similar setttings as study – used with caution

Level 4 – things that have predictive power – rules need more info to be applied

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9
Q

level 3 CPR

A

Level 3 narrow – similar setttings as study – used with caution

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10
Q

level 1 CPR (is the best level for CPR?)

A

Level 1 best CPR – impact analysis – influencing clinician behavior and improving outcomes

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11
Q

level 4 CPR ? worst ?

A

Level 4 – things that have predictive power – rules need more info to be applied

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12
Q
  • Look for factors that potentially contribute to diagnosis
  • Sn and Sp: good for ruling dx in or out?
    ✓ OARs: Sn = 95%; Sp = 50% (better for ruling out fx)
  • Analyzed using stepwise logistic regression to use the least number
    of predictors that can most accurately predict the outcome. (Refer
    to concept of ROC curve)

WHICH step of CPR process does this look like?

A

step 1 derive the model

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13
Q
  • Confirm accuracy on different samples in different settings to show that the model is robust

Which step of CPR does this look like?

A

step 2 - validation portion of CPR

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14
Q
  • Has the CPR been widely adopted, and has it improved diagnosis,
    and has it been shown to reduce cost or risk?
    ✓ OARs have significantly reduced number of X-rays

Which step of the CPR does this look like ?

A

step 3 - the impact portion

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15
Q

1.Operationally define the SAMPLE?
Sample homogeneity? Inclusion/exclusion criteria (age, UL pain)
2.Subjects representative of the population ?
Address issue of SAMPLE bias
3.Include all relevant predictive factors in development process?
Compare to gold standard, all the factors?
4.Predictive factors operationally defined?
A clear definition of these variables is necessary to correctly identify
which subjects have these characteristics and to optimize the
accuracy of the prediction rule.
5.Large enough sample size to accommodate the predictive factors?
Statistical POWER
6.Outcomes of operationally defined?
A clear definition of outcomes is necessary to avoid misidentification
7.Outcomes masked?
Masking tester/assessor reduces an opportunity for BIAS
8.Collect info from ALL subjects?

Questions to ask when looking at _______ of articles about the _____ development

A

validity
derivation / rule
Assessment of study credibility – CPR derivation

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16
Q

Is it good, need to show in different samples and in different settings

Did you compare?

CPR vs gold standard, CPR vs outcomes

Were ALL subjects Measures by gold stanard, outcomes

Blinded?

Confirm findings with a new set of people ?

Validated for a population other than the one it was made for ?

These are questions for what process?

A

validating CPR

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17
Q

✓Sensitivity, specificity, predictive values,
positive/negative likelihood ratios (LR+, LR-)

A

diagnostic categories

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18
Q

✓Odds ratios, risk ratios, hazard ratios

A

prognostic categories

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19
Q

odds ratio

A

The OR is calculated by comparing the odds of an event happening in one group to the odds of it happening in another group

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20
Q

Interpreting the Odds Ratio:

A

An OR of 1 indicates that the odds are the same in both groups, meaning there’s no difference in the likelihood of the event.

An OR greater than 1 suggests that the event is more likely to occur in the first group compared to the second.

An OR less than 1 suggests that the event is less likely to occur in the first group compared to the second.

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21
Q

Risk ratio

A

When risks are computed in a study, the risk ratio is the measure that compares the Risk exposed to the Risk unexposed . The risk ratio is defined as the risk in the exposed cohort (the index group) divided by the risk in the unexposed cohort (the reference group). A risk ratio may vary from zero to infinity

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22
Q

hazard ratio (HR)

A

a measure in survival analysis that compares the probability of an event occurring in one group to the probability of the same event occurring in another group, over a specified period of time. It’s a ratio of the hazard rate in one group to the hazard rate in another. The hazard rate is the instantaneous probability of an event occurring at a given time, assuming that the event has not already occurred

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23
Q

likelihood ratios

A

Likelihood ratios are used for assessing the value of performing a diagnostic test

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24
Q

sensitivity and specificity

A

They use the sensitivity and specificity of the test to determine whether a test result usefully changes the probability that a condition exists

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25
Sensitivity & specificity refer to groups of people whereas likelihood ratios (LRs) can be applied to individual patients.
yup
26
lack of impact analysis, limited applicability to diverse populations, insufficient patient understanding, inadequate outcome measurement, biases in predictor or outcome variable definition and measurement, and barriers to clinician acceptance and implementation
threats to CPR's
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Is the study high quality? Does the design minimize bias/ Are the results important enough to use? Is your patient/client represented in the study sample? Patient/client values and preferences regarding: ✓Desire to know the future regardless of its nature ✓Belief in the value of scientific evidence ✓Previous experiences
considerations relevant to deciding whether to use evidence with the patient/client
28
“... statements that include recommendations intended to optimize patient care. They are informed by a systematic review of evidence and an assessment of the benefits and harms of alternative care options.”
Clinical Practice Guidelines
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Rationale for “Quality of Evidence = Level of Evidence” and Strength of Recommendation used to classify the CPGs (GRADE); Levels of Evidence * Central to a CPG creation is the quantity and quality of the evidence relating to the topic of CPGs. * The studies located may have varying degree of bias associated with different research designs. * As a result, authors of CPGs typically rely on “Levels of Evidence” to characterize the strength of the recommendation in the Guideline
The GRADE working group Quality of evidence high, mod, low, very low High further research unnecessary, mod further research will be good for confidence, low further research would be very good to improve our confidence, very low uncertain The GRADE guidelines strong for, weak for, weak against, strong against 1st two feel the desirable consequences outweigh the undesirable consequences 2nd two feel the desirable consequences do not out weight the undesirable RCTS help rate things high but can be downgraded a level if 1.Bias of study design and implementation 2.Population, intervention, control, outcome issues 3.Unexplained heterogeneity or inconsistent findings 4.Very wide confidence intervals, imprecision 5.Publication bias
30
A considerable variability in hierarchy definitions (or classifications) may lead to inconsistencies among the Guidelines that address the same topic.
Grading of Recommendations Assessment, Development and Evaluation (GRADE) working group has been organized to deal with this issue. The GRADE working group Quality of evidence high, mod, low, very low The GRADE guidelines strong for, weak for, weak against, strong against
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RCTS help rate things high in GRADE but can be downgraded if....
Bias of study design and implementation Population, intervention, control, outcome issues Unexplained heterogeneity or inconsistent findings Very wide confidence intervals, imprecision Publication bias
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Perform an exhaustive literature search? Inclusion and exclusion criteria for studies? Evaluate the quality of studies? Have conclusions based on findings of the quality review?
Evaluating clinical practice guidelines (CPGs) with appropriate questions to ask about their design
33
The appraisal of guidelines resarch and eval collaboration – guidelines rating system
AGREE
34
The International standard for reporting the development and eval of CPGS, AGREE, has 6 domains (things to ask) . what are they?
1. Scope and purpose “overall aim of CPG, clinical focus, target population” 2. Stakeholder involvement “extent to which the CPG was developed by the appropriate stakeholders and represents the views of its intended users” 3. Rigor of development – the process used to gather & synthesize the evidence: Methods (search, selection, appraisal ) to formulate and update the recommendations 4. Clarity and presentation – language, structure and format of the guidelines 5. Applicability – the likely barriers and facilitators to implementation; strategies to improve uptake; resource implications of applying the guidelines 6. Editorial independence – formulation of recommendations not being unduly biased with competing interest
35
how often should CPG's be updated?
every 3 years
36
consider the 3 pillars of EBP when using CPG's
clinical Expertise, Best evidence, Patient values
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questions to ask about a CPG article
Perform an exhaustive literature search? Inclusion and exclusion criteria for studies? Eva8luate the quality of studies? Have conclusions based on findings of the quality review?
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CONSORT
Consolidated Standards of Reporting Trials Randomized trials N or 1 trials reporting of harms, pragmatic trials, non inferiority trials for RCTS
40
RCTS use which reporting standards
CONSORT
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STROBE
strengthening the reporting of observational studies in epidemiology corhort studies, case control studies, cross sectional studies
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Observational studies like cohort studies, case control studies and cross sectional studies use which REPORTING standard
STROBE
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PRISMA
Preferred reporting items for systematic reviews and meta analyses systematic reviews and meta analyses, scoping reviews, improving harms
44
systematic reviews and meta analyses scoping reviews improving harms which reporting standard would these things use?
PRISMA
45
Standards for Reporting of Diagnostic Accuracy (STARD) Transparent Reporting of a multivariable Prediction model for individual Prognosis Or Diagnosis (TRIPOD)
Diagnostic accuracy and prognostic studies
46
diagnostic accuracy and prognostic studies Standard reporting?
STARD/TRIPOD
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qualitative research reporting standards
SRQR ( standards for reporting qualitative research) COREQ (consolidated criteria for reporting qualitative research)
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SRQR
standards for reporting Qualitative research
49
COREQ
consolidated criteria for reporting Qualitative research
50
CASE reports reporting standard
CARE Consensus based clinical case reporting
51
Consensus based clinical case reporting
CARE (for case studies)
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clinical practice guidelines (reporting standards?)
AGREE (appraisal of guidelines, research and eval) RIGHT (Reporting tool for practice guidelines in health care)
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Reporting tool for practice guidelines in health care
RIGHT (for CPG's)
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appraisal of guidelines, research and eval
AGREE for CPG's
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Study protocols (reporting standards)
SPIRIT (standard protocol items: recommendations for intervention trials) PRISMA - P (preferred reporting items for sys reviews and meta analysis protocols )
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preferred reporting items for sys reviews and meta analysis protocols
PRISMA - P (for study protocol standards)
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SPIRIT?
for study protocols standard protocol items: recommendations for intervention trials
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quality and economic guidelines (standards for reporting?)
SQUIRE (standards for quality improvement reporting excellence) CHEERS (consolidated health economic eval reporting standards)
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SQUIRE CHEERS for what ?
economic and quality guidelines
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journal editors role
editors assess submitted papers to determine if they fit the journal's scope and are suitable for peer review.
61
peer reviewers role
A peer reviewer evaluates submitted research papers or scholarly works, providing feedback to improve the quality and validity of the manuscript before publication. They assess the validity, significance, and originality of the research, offering constructive criticism and suggestions for improvement. Reviewers also determine if the research aligns with the journal's scope and recommend whether the paper should be accepted, rejected, or revised.
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