NR 439 Literature and Levels of Evidence DQ
NR 439 Literature and Levels of Evidence DQ
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- Reflect on your practice, and identify a significant nursing clinical issue or change project that you would like to search for evidence in online sources. Formulate searchable, clinical questions in the PICO(T) format for your nursing clinical issue.
- Next, review the guidelines for the PICOT Assignment due Week 3. Use your PICOT elements to search for one report of a single, original study that has been published within the last 5 years from the CCN Library that is relevant to your nursing clinical issue.
- Briefly describe how it is relevant to your nursing clinical issue. Remember to give a complete reference to the study.
Is All Evidence Created Equal?
The medical literature is immense, but only a small portion of it is immediately useful in answering clinical questions. The literature reports the whole spectrum of the scientific research process — the long journey from in-vitro studies to double-blind randomized controlled trials. This has been called the “wedge of evidence” or the “pyramid of evidence.” (for a visual representation see More Information)
An understanding of how various levels of evidence are reported and how this literature is organized will help the searcher retrieve the highest levels of evidence for a particular clinical question. High levels of evidence may not exist for all clinical questions because of the nature of medical problems and research and ethical limitations.
Adding METHODOLOGY terms and CLINICAL FILTERS to SUBJECT terms will result in the most efficient and optimal retrieval in terms of finding the highest level of evidence in answering clinical questions.
Study Design Concepts
Studies can be descriptive (or observational), such as :
- case reports (a detailed description of a single case)
- case series (descriptions of groups of patients with a disease)
- cohort studies (defined populations which are followed in an attempt to determine distinguishing subgroup characteristics)
Or evaluative (interventional), such as a:
- randomized/controlled clinical trials (a clinical trial involving one or more test treatments, at least one control treatment, specified outcome measures for evaluating the studied intervention, and a bias-free method for assigning patients to the test treatment)
Levels of Clinical Evidence in the Primary Literature
Type of Question
Type of Study Methodology
MEDLINE Filters
Therapy: information needed about
treatments (effectiveness, cost, etc.)Double-Blind
Randomized Controlled TrialRandomized Controlled Trial [PT]
double [TW] and blind [TW]Diagnosis: information needed about a
diagnostic test (sensitivity, accuracy, etc.)Controlled Trial Sensitivity and Specificity [MH]
Diagnosis [SH]Prognosis: information needed about the
course of the disease over time, expected
complications, etc.Cohort Studies
Case Control
Case SeriesCohort Studies [MH]
Prognosis [MH]
Survival Analysis [MH]Etiology/Harm: information needed about
causes of disease or contributing factors of diseaseCohort Studies Cohort Studies [MH]
Risk [TW]Prevention: information needed about the
prevention of disease (immunization,
social factors, etc.)Randomized Controlled Trial
Cohort StudiesRandomized Controlled Trial [PT]
Cohort Studies [MH]
Prevention and Control [SH]Quality Improvement: information needed
about clients’ and health professionals’
experiences and concernsRandomized Controlled Trial Randomized Controlled Trial [PT]
Practice Guideline [PT]
Consensus Development Conference [PT](Abbreviations: MH=Medical Subject Heading; PT=Publication Type; SH=Subheading; TW=Text Word)
Secondary Literature
The practice and teaching of Evidence-Based Medicine has outcome products which help the health care provider and consumer keep up with the medical literature and assess the evidence. This secondary literature synthesizes, filters, and evaluates the primary research literature. Dissemination and incorporation of valid clinical research findings into medical practice is the ultimate goal.
Filtered or Synthesized Information
Description/Definition
How to Find This Type of Information
Systematic Reviews
- differ from traditional review articles in that conclusions are evidence-based rather than commentary
- start with a clearly articulated question
- use explicit, rigorous methods to identify, critically appraise, and synthesize relevant studies
- appraise relevant published and unpublished evidence before combining and analyzing data
- include description of how primary data sources are identified
- assess individual studies for validity
Use Cochrane Collaboration - Cochrane Database of Systematic Reviews
- York Database of Abstracts of Reviews of Effectiveness
- Cochrane Controlled Trials Register
- Cochrane Review Methodology Database
Use PubMed/MEDLINE searching
- Review [PT] AND medline [TW]
- (Quantitative OR Systematic OR Methodologic) AND (Review OR Overview)
Use PubMed Clinical Queries
- “Systematic Review” is available as a limit option
Meta-Analyses
- specific methodologic and statistical technique for combining quantitative data
- type of systematic overview
Use Cochrane Collaboration
Use PubMed/MEDLINE searching- Meta-analysis [PT]
- meta-anal* [TW] OR
- metaanal* [TW]
Evidence-Based Practice Guidelines
- gather, appraise, combine evidence systematically
- include statements designed to assist practitioner and patient decisions
- developed by professional groups, government agencies, local practices
- include a structured abstract: objective, option, outcomes, evidence, values, benefits/harms/costs, recommendation, validation, sponsors
Use National Guideline Clearinghouse Critically Appraised Topics (CATs)
- scan literature for clinically relevant studies
- critically appraise the studies
- provide commentary on strength of study and clinical significance
- provided in a one-page format
Use EBM Reviews Use Essential EvidencePLUS (UIC affiliate access)
- InfoPOEMS
Decision Analyses/Decision Tools
- studies that analyze decisions faced by clinicians for an individual patient, about clinical policy, or a global health care policy
- application of explicit, quantitative methods to analyze decisions under conditions of uncertainty
- risks and benefits of a decision are made fully explicit
- decision tree is included
Use PubMed/MEDLINE searching - Decision Support Techniques [MH]
- Cost-Benefit Analysis [MH]
- decision analysis [TI]
Consensus Development Reports
- assessments of emerging or critical health issues based on available research and expert opinion to identify needs for policy development and further research (description based on information from the NIH Consensus Development Program now ‘retired’ in light of “many other organizations that conduct [evidence] reviews”)
Use PubMed/MEDLINE searching - “consensus statement” [TW] OR “consensus report” [TW]
Study Design Terminology
- Control Group – the group that does not receive the treatment, etc.
- Randomization – assigns participants by chance to either the treatment group or the control group.
- Blinding – the participants and/or some of the researchers do not know the groups to which the participants have been assigned.
- Loss to Follow-up/Intention to Treat – all of the participants should be accounted for even if they did not fully participate.
- P Value – the probability of any observed differences having happened by chance. The convention is that .05 is required.
- Power – the likelihood that a study will detect a statistically significant difference. The convention is that a power of at least 80% is required.
- See also Scientific Experiment Terminology from the Appraisal tab.
More Information
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SUNY Downstate Medical Center EBM Course: A Guide to Research Methods.A visual “evidence pyramid”