Clinical Reasoning/EBP/Scientific Method Flashcards

1
Q

What is deductive reasoning?

A

“top down” logic
-creates a linear relationship between pt’s restrictions/impairments etc and their pathology of body structures, personal factors, environment, etc

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2
Q

What is narrative reasoning?

A

using specific observations to draw conclusions
-achieved throughout open ended questions and active listening to gather info about the pt’s personal and environmental factors

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3
Q

What is Bayesian reasoning?

A

basically involves application of probability as data is gathered to identify if something is more or less likely or the probability that something is true or not true

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4
Q

What is the cluster of findings for nociplastic pain(central sensitization)

A

characterized by pain that is disproportionate, non-mechanical, unpredictable, and diffuse

-in the absence of red flag findings

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5
Q

Sensitivity and Specificity of nociplastic pain cluster?

A

sensitivity 91.8%

specificity 97.7%

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6
Q

What is the cluster of findings for peripheral neuropathic pain(radicular or referred)

A

-symptoms that are referred in a dermatomal (radicular) or cutaneous (referred) distribution
-history of nerve injury, pathology, or mechanical compromise of the nerve w/ symptom provocation via mechanical testing

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7
Q

Sensitivity and speficifity of peripheral neuropathic pain cluster?

A

sensitivity 86.3%

specificity 96%

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8
Q

What is the cluster of findings for nociceptive pain?

A

-symptoms localized to an area of injury or dysfunction
-provocation and/or alleviation are clearly identifiable and proportionate
-match known mechanical and anatomical distributions
-symptoms usually intermittent and start w/ onset movement or mechanical provocation
-quality of symptoms may be a constant dull ache or a throb at rest

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9
Q

Sensitivity

A

the ability to identify a condition when it truly exists
-find true positives
-higher sensitivity means you will catch it if it’s there
-most people with the condition will test positive
-lower sensitivity means you will get some false positives

SnNOUT
-negative result rules it out
-only people without the condition get ruled out, but you may have false positives

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10
Q

Specificity

A

the ability to identify when a condition is not present
-find true negatives
-higher specificity means that when the test is negative, you are confident that the condition is not present
-most people with the condition will test positive, but anyone who DOES NOT have it will test negative
-lower specificity means that when test is negative, you are less confident it is a true negative. might be a false negative

SpPIN
-positive result rules it in
-only people WITH the condition will test positive

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11
Q

Type 1 error

A

“backing a loser”

FALSE POSITIVE

concluding that there IS a significant difference when there actually ISNT

-set a stricter alpha level for statistical significant difference to reduce likelihood
-larger sample size also helps
-well defined hypothesis
-replication studies with different samples can help validate findings

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12
Q

Type 2 error

A

“missing a winner”

FALSE NEGATIVE

concluding that there ISNT a significant difference when there actually IS

-increase # of subjects in the study to reduce likelihood of this

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13
Q

Large effect size

A

0.8 and up

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14
Q

Moderate effect size

A

0.5-0.7999

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15
Q

Small effect size

A

0.2-0.4999

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16
Q

Trivial effect size

17
Q

Cohen’s kappa (k)

A

describes how reliable something is

0 = no reliability(no better than chance)
1= perfect reliability

0 no better than chance
<0.4 poor
0.4-0.6 fair
0.6-0.75 good
>0.75 excellent
1 perfect reliability

18
Q

positive likelihood ratio

A

these will be >1

> 10 large shift in probaiblity
5-10 moderate shift
<5 small shift
1 = no change

19
Q

negative likelihood ratio

A

these will be <1

<0.1 large shift
0.1-0.2 moderate shift
>0.2 small shift
1.0 no change

20
Q

Placebo effect

A

individual believes in positive effect, even though no therapeutic value

good research should have placebo group so that test group improves MORE than placebo group

good research should have placebos that look like the real treatment
-placebo group needs to have belief that they actually had real treatment

placebo effect most powerful on outcomes mediated by the brain

21
Q

Nocebo effect

A

negative beliefs about a treatment
-exaggerated when subjects expect negative side effects or negative experiences with treatments in the past

research groups example
-good to have exclusion criteria
-in a research study on spinal manipulation this would exclude those who have positive or negative expectations about it
-randomization also helps reduce this effect

22
Q

Hawthorne effect

A

subjects who know they are observed as part of a research study tend to work harder than they would otherwise
-we find that people change their behavior(positive or negative) due to being observed

23
Q

Observer effect

A

people work harder when being watched
-more improvement in response to more attention

-control for this by making sure all treatment groups get about the same amount of attention from clinician

group that receives more attention likely to improve more

example:
group 1: 30 mins manual
group 2: 30 mins exercise
group 3: 30 mins manual + 30 mins exercise
-60 total minutes, they are likely to improve the most

24
Q

John Henry effect

A

“legend of john henry outcompeting the machine”

control group perceives that they are disadvantaged compared to experimental group
-they seek out additional treatment/help because they think they aren/t getting enough care otherwise

best way to reduce
-blind subjects so that they don’t know if they are in control or experimental group

25
Q

Pygmalion effect

A

AKA “rosenthal effect”

expectations of those in authority shape results of their subjects
-high expectations lead to improved performance
-low expectations lead to poor performance

best way to reduce
-blind clinicians who treat the group and those who assess the group

26
Q

Level 1 evidence

A

high quality diagnostic studies, prospective studies, RCTs, or systematic reviews

27
Q

Level 2 evidence

A

comes from lesser quality diagnostic studies, prospective studies, RCTs, or systematic reviews
-weaker diagnostic criteria
-weaker reference standards
-improper randomization
-no blinding
- <80% follow up

28
Q

Level 3 evidence

A

case control studies or retrospective studies

29
Q

Level 4 evidence

A

case series
-has no control compared to case control study

30
Q

Level 5 evidence

A

expert opinion

31
Q

Grade A recommendation

A

STRONG
-preponderance of level 1 and/or level 2 studies support the recommendation
-includes AT LEAST 1 level 1 study

Obligation
“Should”

32
Q

Grade B recommendation

A

MODERATE
-a single high quality RCT or a preponderance of level 2 studies support the recommendation
-includes studies w/ only short term follow up
(less than 3 months) or small sample size (less 100 subjects)

Obligation
“May”

33
Q

Grade C recommendation

A

WEAK
-single level 2 study supports the recommendation

Obligation
“Can”

34
Q

Grade D recommendation

A

CONFLICTING OR NO EVIDENCE
-level 1 and level 2 studies disagree with respect to their conclusions or provide no evidence of benefit

Obligation
“Should NOT”

35
Q

Incidence vs prevalence

A

incidence = # of NEW cases during a period of time
“10 of 100” people develop LBP during 2024

prevalence = # of cases at a specific point in time
“10 of 100” people have LBP on 12/10/2024
-prevalence includes ALL cases, including new and pre-existing

36
Q

MDC

A

smallest change detected that is not attributed to measurement error

example: moving from 2/10 to 1/10 on VAS, however MCID may be 2 full points

37
Q

MCID

A

smallest change in condition that either pt or clinician may consider important