Exam notes Flashcards
(49 cards)
What percentage of patients do not receive care according to present scientific evidence?
Or care provided is not needed or potentially harmful?
- 30-40%
- 20-25%
What are the barriers to EBP
Proffessional barriers?
Social barriers
- lack of financial reimbursement for EB care
- lack of time in consultation
- fear of legal liability
Professional barriers?
- lack of skill
- doctors sense of information overload
Social barriers:
- patient expectations
- advocacy (Advocacy is a political process by an individual or group which aims to influence decisions within political, economic, and social systems and institutions)
Consumers must ask?
Consumers should be able to expect from their doctors?
- What are my options
- What are the expected outcomes
- What is the likelihood of each expected outcome
Consumer expectations?
- know his subject, know what evidence is available and draws on it
- use expertise and experience
- compassionate- every patient is different
What are the 4 challenges that face physicians?
- Reaching correct diagnosis
- selecting management that does more good than harm
- Keeping up with useful advances
What is evidenced based practice?
Extend on each
Integration of best research evidence with clinical expertise and patient values and circumstances
- Best research evidence: patient centred clinical research into accuracy and precision of diagnostic tests, power of prognostic markers, efficacy and safety of therapeutic, rehabilitative and preventative regimes
- Clinical expertise: ability to use clinical skills and past experience to rapidly identify each patient’s unique health state and diagnosis, their individual risks and benefits of potential interventions and the patients personal values and expectations, must be biologically plausible
- Patient values and circumstances: the unique preferences, concerns, expectations and circumstances each patient brings to a clinical encounter and which must be integrated into clinical decisions if they are to serve the patient
What is the P value, what does it mean?
-measure of strength against the null hypothesis
The null hypothesis (H0) is a hypothesis which the researcher tries to disprove, reject or nullify.
eg H0: Tomato plants show no difference in growth rates when planted in compost rather than soil.
-less than 0.05 means that it is clinically significant
The P value or calculated probability is the estimated probability of rejecting the null hypothesis (H0) of a study question when that hypothesis is true.
What a confidence interval?
what are the things that can affect it?
-what does the CI indicate?
So its basically how confident you are that the samples results mimic the true population. A small confidence interval is better. 2 things that effect it is variation within the population- more variation the bigger the CI.
-and the sample size- the bigger the sample the smaller the CI. The smaller the sample the less likely it is to represent the true population.
-so the CI gives a measure of precision or uncertainty of study results for making interferences about population under question.
-95% of such intervals will contain the true population value
-indicate strength of evidence about quantities of direct inter.
If the wisker thing crosses the 0 its bad -worthless- not clinically significant.
Hierarchy of Evidence types?
- Systematic reviews of randomised controlled trials
- systematic reviews use rigorous methods to identify, critically appraise and synthesis relevant studies. - Individual RCT- a randomised controlled trial.
- used in testing the efficacy of medicines - SR of cohort studies
- Individual cohort studies
- Outcomes Research
- SR of case-control studies
- Individual case control study
- case series
- Expert opinion.
EBP needs the following steps?
- Converting info needs from clinical encounters into questions with an answerable format
- Locating best available evidence in order to answer these questions
- Critically appraising the evidence (exam internal validity, assessing important or size of effect, deciding on relevance (exam internal, assessing importance or size of effect, deciding on relevance to your clinical practice
- Applying the information from critical appraisal to care of individual, requires integration of our critical assessment of article with clinical expertise and knowledge about individual patients, their values and circumstances.
What does PICO stand for?
- Population, patient or problem
- Intervention, prognostic factor or exposure
- Comparison
- Outcomes
- In patients with (patient, population, problem) does (intervention) affect (outcome) compared to (comparison)?
- Also, type of question and type of study?
what are the common types of questions related to clinical taste?
- Therapy and prevention: Evidence for question of therapy efficacy, RCT’s, SR’s
- Harm/aetiology: how to identify causes for harm or causes of disorder, cohort, case control studies
- Diagnosis: how to select and interpret diagnostic tests, ‘gold standard’ test
- Prognosis: how to estimate patients likely clinical course over time and anticipate likely complications of disorder
Secondary research?
- Systematic reviews: focus on a clinical topic and answer a specific question
- Meta-analysis: takes systematic reviews and summarises the results of several studies into a single estimate of their combined result (through statistical analysis)
- Practise guidelines: systematically developed statements to assist practitioner, review and evaluate evidence and then make explicit recommendations for practise
Data bases and resources
- Medline: medicine, nursing, dentistry, vet, health care system
- Pubmed: access to Medline, InProcess citations OldMedline and citations to out-of-scope articles, diagnosis, aetiology, therapy or prognosis, systematic reviews and meta-analysis
- Cochrane: systematic reviews
Describe natural history studies
- The course of disease from onset to resolution
Stages
1: pathological onset
2: pre-symptomatic stage-> from onset to first appearance of symptoms/signs
3: clinically manifest disease, may progress inexorably, be subject to remissions or regress spontaneously - Detection and intervention may alter natural history of disease
- Eg. Sciatica: stage 1 -> silent internal disc disruption from a degenerative process,
Stage 2-> LBP, stage 3-> fully blown leg pain which may regress spontaneously
Disease frequency studies?
- Quantify occurrence of disease
- Need numerator and denominator
- Can put this in terms of incidence and prevalence = rates
- Incidence = number of new cases per unit time
- Prevalence = number of cases present at a particular time/ in a time interval
Descriptive studies
- Describe patterns of disease occurrence in relation to variables eg. Person, place, time
1. Correlation - consider patterns of disease among populations
- look at measures that represent characteristics of populations that are used to describe disease in relation to some factor
- correlation coefficient r: quantifies extent to which there is a linear relations between exposure and disease, +1 - -1
- Limitations: limited ability to link exposure with disease, what is cause and what is effect?
Case report or case series
- describe experience of single patient/ group of patients with similar diagnosis
- may lead to formation of new hypothesis (usually unusual feature of disease or patients history has been identified)
- cannot be used to test for presence of valid statistical association or to demonstrate efficacy in therapy
- commonly used for alerting a potential adverse event or providing an unusual diagnostic presentation
- generally, limited to hypothesis generation (do not show convincing evidence in terms of preventative or therapeutic intervention)
Cross sectional surveys of individuals
- exposure and disease of interest are assessed simultaneously
- provide snapshot in time of condition
- eg. National health surveys, LBP prevalence study
- limitations: cannot determine temporal sequence between exposure and outcome
Ecological studies
- units of analysis are populations or groups
Case control studies (retrospective)
Odds ratio - what is it?
What are the limitations to a retrospective study?
- observational analytic epidemiologic investigation
- subjects are selected of basis of whether they do (cases) or do not (controls) have disease
- cases are uncommon and are selected, then matching controls are assembled for comparison
- retrospective
- statistically results are often quoted as odd ratios with confidence intervals
Odds ratio:
- ratio of odds of having the disorder in question if exposed to the factor in question divided by the odds of having the disorder if not exposed to the factor in question
Limitations:
- limitations: retrospective, recall bias, other factors may have intervened, selection bias, hospital controls are often ill in another way, relying on medical records
Cohort study
- observational analytic study
- group or group of individuals are defined on basis of presence or absence of exposure
- ‘follow up’ study -> subjects followed forward over time (prospectively)
- Subjects have been exposed to risk factor but do not have disease in question, subjects then assessed over time to see if disease manifests
- Useful for rare exposures
- Can use similar statistic to odds ratio -> relative risk = risk of getting disease if exposed vs. risk of getting disease if not exposed
Look at the table of comparison of cohort, case control, prevalence
s
Experimental Studies
- Clinical trial where individuals are randomly allocated to 2+ groups (experimental and control groups)
- Experimental group is given treatment, control group is given another treatment, sham, placebo or no treatment
1. Therapeutic: agent/ procedure given to relieve symptoms or improve survivorship of those with disease
2. Intervention: intervention before disease has developed in individuals with characteristics that increase risk of developing disease
3. Preventative: attempt made to determine efficacy of preventative agent/procedure
View table
Blinding
Single blind study
double blind
triple blind
- Single blind study: subjects not sure what group they are
- Double blind: single blinding plus observer taking data are blind
- Triple blind: double blinding plus analyser is blind