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Quarterly Updates: Evidence Based Practice For Public Health Nurses Session III

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Title: Quarterly Updates: Evidence Based Practice For Public Health Nurses Session III


1
Quarterly UpdatesEvidence Based Practice For
Public Health NursesSession III
  • Public Health Nursing Section, Evidence Based
    Practice Committee

2
EVIDENCE BASED PUBLIC HEALTH NURSING PRACTICE
CLIENT VALUES/ PREFERENCES
CLINICAL EXPERTISE/ JUDGMENT
KNOWLEDGE/ RESEARCH
3
http//www.youtube.com/watch?v2BzCXDZ1NRk
4
  • One of the greatest discoveries a man makes, one
    of his great surprises, is to find he can do what
    he was afraid he couldnt do.
  • Henry Ford

5
Objectives
  • Develop an understanding of the meaning of
    critical appraisal of evidence
  • Describe how levels of evidence are used in
    appraisal of evidence
  • Explore how other methods (e.g. statistics) can
    be used to appraise evidence
  • Apply the process for appraising evidence to
    public health nursing

6
Evidence Based Practice
  • Uses highest quality of knowledge in providing
    care to produce the greatest impact on health
    status and health care

7
Critical Appraisal of Evidence
  • Key characteristic of evidence based practice
  • Core skill needed to use evidence to support
    nursing practice decisions

8
Critical Appraisal of Evidence
  • Ensures relevance and transferability of evidence
    from the search to the specific population for
    whom the care will be provided

9
Critical Appraisal of Evidence Defined
  • 1) Assessing the strength of the scientific
    evidence
  • 2) Evaluating the research for its quality and
    applicability to health care decision making

10
1) Strength of Evidence
  • Grading of strength of evidence should
    incorporate
  • Quality
  • The extent to which bias was minimized (internal
    validity)
  • Quantity
  • The extent of the magnitude of effect, numbers of
    studies, and sample size or power.
  • Consistency
  • The extent to which similar and different study
    designs report similar findings

11
1) Strength of Evidence
  • Evidence exists on a continuum of rigor
  • Amount of research attention or maturity of
    science varies, therefore evidence varies
  • Type of research design reflects the strength of
    the evidence known as levels of evidence

Stevens Ledbetter, 2000
12
Levels of Evidence
  • Ranking as to how well the evidence informs
    clinical interventions
  • The stronger the level of evidence, the greater
    the confidence that the probability of applying
    the evidence in practice will be effective
  • Levels of evidence are based on research design

Stevens Ledbetter, 2000
13
Levels of Evidence
  • Experts have developed a number of taxonomies to
    rate strength of evidence
  • Most are organized around research designs


14
Levels of Evidence
  • National Guidelines Clearinghouse
  • Ia Evidence obtained from meta-analysis or
    systematic review of randomized controlled trials
  • Ib Evidence obtained from at least one randomized
    controlled trial
  • IIa Evidence obtained from at least one
    well-designed controlled study without
    randomization
  • IIb Evidence obtained from at least one other
    type of well-designed quasi-experimental study,
    without randomization
  • III Evidence obtained from well-designed
    non-experimental descriptive studies, such as
    comparative studies, correlation studies, and
    case studies
  • IV Evidence obtained from expert committee
    reports or opinions and/or clinical experiences
    of respected authorities

15
Levels of Evidence
  • Rating System for the Hierarchy of Evidence
  • Level I Evidence from a systematic review or
    meta-analysis of all relevant randomized
    controlled trials (RCTs), or evidence based
    clinical practice guidelines based ons systematic
    reviews of RCTs
  • Level II Evidence obtained from at least one
    well-designed RCT
  • Level III Evidence obtained from well-designed
    controlled trials without randomization
    (quasi-experimental)
  • Level IV Evidence from well-designed
    case-control and cohort studies (studies of
    prognosis)
  • Level V Evidence from systematic reviews of
    descriptive and qualitative studies
  • Level VI Evidence form a single descriptive or
    qualitative study
  • Level VII Evidence from the opinion of
    authorities and/or reports of expert committees


(Melnyk Fineout-Overholt, 2005)
16
Levels of Evidence
  • RATING SYSTEM FOR LEVELS OF EVIDENCE
  • Type of evidence
  • I. Meta analysis or comprehensive systematic
    review of multiple experimental research studies
    (Cochrane , National Guidelines Clearinghouse
    (AHRQ), The Joanna Briggs Institute, Other
    groups)
  • II. Well designed experimental study
  • III. Well designed quasi-experimental study
    (Non-randomized controlled, Single group pre-post
    design, Cohort, Time series (one group of
    subjects over time), Matched case-controlled
    studies (two or more groups are matched on
    certain variables)
  • IV. Well designed non-experimental study
    (Correlational or comparative descriptive
    studies, Case study design, Qualitative studies)
  • V. Clinical examples and expert opinion (Text
    books, Non-research journal articles, Verbal
    report, Non-research based professional
    standards/guidelines/
  • group article) 
  • Strength of evidence
  • A. Type I evidence or consistent findings from
    multiple studies from levels II, III, or IV.
  • B. Multiple studies with evidence types II, III,
    or IV that are generally consistent.
  • C. Multiple studies with evidence types II, III,
    or IV that are inconsistent.
  • D. Limited research evidence or one type II
    study only.
  • E. Type IV or V evidence only
  •  
  •  
  •  
  •  

Adapted from Joanna Briggs Institute and
AHCPR Eilers Heerman, 2005
17
The U.S. Preventive Services Task Force (2008)
18
Level of Certainty Description
High The available evidence usually includes consistent results from well-designed, well conducted studies in representative primary care populations. Thee studies assess the effects of the preventive service on health outcomes. This conclusion is therefore unlikely to be strongly affected by the results of future studies.
Moderate The available evidence is sufficient to determine the effects of the preventive service on health outcomes, but confidence in the estimate is constrained by such factors as The number, size, or quality of individual studies Inconsistency of findings across individual studies Limited generalizability of findings to routine primary care practice Lack of coherence in the chain of evidence As more information becomes available, the magnitude or direction of the observed effect could change, and this change may be large enough to alter the conclusion.
Low The available evidence is insufficient to assess effects on health outcomes. Evidence is insufficient because The limited number or size of studies Important flaws in study design or methods Inconsistency of findings across individual studies Gaps in the chain of evidence Findings not generalizable to routine primary care practices Lack of information on important health outcomes More information may allow estimation of effects on health outcomes
19
Systematic Reviews
  • Provides state of the science conclusions about
    evidence supporting benefits and risks of a given
    healthcare practice (Stevens, 2001)
  • Most powerful and useful evidence available
  • Refers to summary that uses a rigorous scientific
    approach to combine results from a body of
    original research studies into a clinically
    meaningful whole

Systematic Reviews Meta Analysis
20
Meta-Analysis
  • Statistical approach to synthesizing the results
    of a number of studies summarizes results of
    all studies included in the review
  • Produces a larger sample size and thus greater
    power to determine the true magnitude of an
    effect, yields a summary statistic

Systematic Reviews Meta Analysis
21
Randomized Controlled Trial
  • Experimental studies are the gold standard of
    research design (randomization of participants to
    treatment and control, rigorous methods used to
    minimize bias)
  • Provides most valid, dependable research
    conclusion about clinical effectiveness of an
    intervention and establishing cause and effect
  • Allows us to say with a high degree of certainty
    that the intervention we used was the cause of
    the outcome

Randomized Controlled Trials
Systematic Reviews Meta Analysis
22
Quasi-Experimental
  • Differs from RCTs only in that participants are
    NOT randomized to treatment and control groups

Quasi-Experimental
Systematic Reviews Meta Analysis
Randomized Controlled Trials
23
Non-Experimental
  • Cohort participants are studied over time,
    study population shares common characteristics
  • Case-Control studies that address questions
    about harm or causation, investigates why some
    people develop a disease or behave the way they
    do vs others who do not
  • Descriptive main objective is to describe some
    phenomena
  • Qualitative - "any kind of research that produces
    findings not arrived at by means of statistical
    procedures or other means of quantification"
    (Strauss and Corbin, 1990, p. 17).

Non-Experimental
Systematic Reviews Meta Analysis
Randomized Controlled Trials
Quasi-Experimental
24
. Clinical Examples Expert Opinion
  • Expert Opinion arriving at a value judgement
    which incorporates the main information available
    on the subject as well as previous experiences
  • Clinical examples
  • The 5 rights

Clinical Examples Expert Opinion
Systematic Reviews Meta Analysis
Randomized Controlled Trials
Quasi-Experimental
Non-Experimental
25
2) Evaluating Quality Applicability
  • What are the results?
  • Are the results valid?
  • Can the results be applied to the targeted
    population and/or public health practice and
    intervention?

26
What are the results?
  • Were the results similar from study to study (if
    systematic review or meta-analysis)?
  • What are the overall results?
  • How precise were the results?
  • Can a causal relationship be inferred from the
    data?

27
Are the Results Valid?
  • Does this article explicitly address our public
    health question?
  • Was the search for our article detailed and
    exhaustive? Is it likely that important, relevant
    studies were missed?
  • Does the study selected appear to be of high
    methodological quality?
  • Do you feel the study selected is reproducible?

28
Is the Evidence Applicable?
  • How can the results be interpreted and applied
    to public health practice and intervention?
  • Are study subjects similar to clients to whom
    care is to be delivered?
  • Were all important outcomes considered?
  • Are the benefits worth the costs and potential
    risks?

29
Other Methods Used to Appraise Evidence
  • Fineout-Overholt, E., Melynk, B.M. (2004).
    Evaluation of studies of prognosis. Evidence
    Based Nursing, 7, 4-8.
  • Melynk, B.M. (2003). Finding and appraising
    systematic reviews of clinical interventions
    Critical skills for evidence-based practice.
    Pediatric Nursing, 29(2), 147-149.
  • Melynk, B.M., Fineout-Overholt, E. (2005).
    Rapid critical appraisal of randomized controlled
    trials An essential skill for evidence-based
    practice. Pediatric Nursing, 31(1), 50-52.
  • Melynk, B.M., Fineout-Overholt, E. (2002). Key
    steps in implementing evidence-based practice
    Asking compelling, searchable questions and
    searching for the best evidence. Pediatric
    Nursing, 22(3), 262-266.

30
Other Methods Used to Appraise Evidence
  • Statistical Evaluation, for example calculating
    effect size
  • Effect size measures the magnitude or strength
    of the treatment or intervention effect (how
    well the intervention worked in the group who
    received the intervention vs the group that did
    not receive the intervention)
  • Small, medium and large effects are designated as
    .2, .5, and .8 respectively
  • Several formulas to use depending on statistical
    analysis used (e.g. t-tests, etc)
  • Thalheimer, W., Cook, S. (2002, August). How to
    calculate effect sizes from published research
    articles A simplified methodology. Retrieved
    April 29, 2009 from http//www.work-learning.com/w
    hite_papers/effect_sizes/Effect_Sizes_pdf5.pdf

31
Other Methods Used to Appraise Evidence
  • AGREE instrument (AGREE Collaboration, London)
  • http//www.agreecollaboration.org/instrument/
  • AGREE is an international collaboration of
    researchers and policy makers who seek to improve
    the quality and effectiveness of clinical
    practice guidelines by establishing a shared
    framework for their development, reporting and
    assessment shared framework is the AGREE
    instrument (Appraisal of Guidelines for Research
    Evaluation).
  • CATmaker (Centre for Evidence Based Medicine,
    Oxford, U.K.)
  • http//www.cebm.net/index.aspx?o1216
  • Is a software tool which helps you create
    Critically Appraised Topics, or CATs, for
    articles found when searching for evidence (free
    download)
  • Rapid (Joanna Briggs Institute, University of
    Adelaide, Australia)
  • http//www.joannabriggs.edu.au/services/rapid.php
  • On-line critical appraisal of evidence training
    program
  • Rap Maker is a program to appraise a study, its
    methods, findings and applicability. RAP maker
    facilitates construction of a final report, which
    may then be submitted on-line to the RAPid
    library for independent critique, then uploading
    for world wide access.

32
  • Search evidence rich resources first

33
EBP Rich Resources for P/CHN
  • Cochrane review http//www.cochrane.org/reviews/
  • DARE Database of Abstracts of Reviews of
  • Effectiveness http//www.mrw.interscience.wiley.co
    m/cochrane/cochrane_cldare_articles_fs.html

34
Agency for Healthcare Research and Quality (AHRQ)
  • National Guidelines Clearinghouse
    www.guidelines.gov
  • Guide to Clinical Preventive Services (2008)
    http//www.ahrq.gov/clinic/pocketgd.htm
  • Evidence reports ahrq www.ahrq.gov/clinic/epcix.ht
    m

35
EBP Rich Resources for P/CHN
  • Guide to Community Preventive Services
  • http//www.thecommunityguide.org/index.html

36
Centers for Disease Control Prevention
  • CDC for Public Health Professionals
  • http//www.cdc.gov/CDCForYou/public_health_profess
    ionals.html

37
Association of State and Territorial Health
Officials
  • Evidence Based Practice
  • http//www.astho.org/?templateevidence_based_ph_p
    ractice.html

38
National Association of City and County Public
Health Officials
  • The Model Practices Database
  • http//www.naccho.org/topics/modelpractices/
  • http//archive.naccho.org/modelPractices/
  • Online searchable collection of
    practices across public health areas.
  • Allows you to benefit from colleagues'
    experiences, to learn what works, and to ensure
    that resources are used wisely on effective
    programs that have been implemented with good
    results.
  • The database features practices in the following
    areas
  • Community Health
  • Environmental Health
  • Public Health Infrastructure
  • Emergency Preparedness

39
EBP Rich Resources for P/CHN
  • Health Services/Technology Assessment Text
    (HSTAT)
  • http//hstat.nlm.nih.gov
  • Searchable collection of large, fulltext practice
    guidelines, technology assessments and health
    information

40
EBP Rich Resources for P/CHN
  • Health Policy Guide
  • http//www.healthpolicyguide.org/
  • evidence-based policies to improve the publics
    health
  • 150 policy topics to support advocacy and
    decision making at the state and local levels

41
EBP Rich Resources for P/CHN
  • http//guides.nursinglibrary.yale.edu/content.php?
    pid14371sid96991
  • National Institute for Health clinNICE is an
    independent organisation responsible for
    providing national guidance on promoting good
    health and preventing and treating ill health.

42
Evidence Based Public Health Nursing
  • http//www.uic.edu/depts/lib/projects/ebphn/
  • http//www.uic.edu/depts/lib/projects/ebphn/module
    smain.html
  • http//www.uic.edu/nursing/aphne/

43
EBP Rich Resources for P/CHN
44
Application Exercise
  • PICO QUESTION
  • For the 4 year old pre-K age group, are there
    fewer injection site complications with giving
    the immunizations in the thigh as compared to
    giving the immunizations in the arm?

45
Cochrane Review
  • Tinnion O, Hanlon M. Acellular vaccines for
    preventing whooping cough in children. Cochrane
    Database of Systematic Reviews 1999, Issue 2.
    Art. No. CD001478. DOI 10.1002/14651858.CD001478
    .pub2
  • Differences in trial design precluded pooling
    of the efficacy data and results should be
    interpreted with caution. Most systemic and local
    adverse events were significantly less common
    with acellular than with whole cell pertussis
    vaccines.
  • Emailed page to print off

46
National Guidelines Clearinghouse
  • 1) General recommendations on immunization
    recommendations of the Advisory Committee on
    Immunization Practices (ACIP). 2) Update
    recommendations from the Advisory Committee on
    Immunization Practices (ACIP) regarding
    administration of combination MMRV vaccine.

http//www.guidelines.gov/summary/summary.aspx?doc
_id12325nbr006390stringvaccineANDadministra
tionANDsiteANDroute
47
National Guidelines Clearinghouse
  • Injection Route and Injection Site
  • With the exception of Bacillus Calmette-Guerin
    (BCG) vaccine, injectable vaccines are
    administered by the intramuscular and
    subcutaneous route. The method of administration
    of injectable vaccines is determined, in part, by
    the presence of adjuvants in some vaccines. The
    term adjuvant refers to a vaccine component
    distinct from the antigen that enhances the
    immune response to the antigen. The majority of
    vaccines containing an adjuvant (e.g., DTaP, DT,
    Td, Tdap, PCV, Hib, HepA , HepB, and HPV) should
    be injected into a muscle because administration
    subcutaneously or intradermally can cause local
    irritation, induration, skin discoloration,
    inflammation, and granuloma formation.

48
National Guidelines Clearinghouse
  • Routes of administration are recommended by the
    manufacturer for each immunobiologic. Deviation
    from the recommended route of administration
    might reduce vaccine efficacy or increase local
    adverse reactions.

49
CDC Advisory Committee on Immunization Practices
  • Route
  • Administering a vaccine by the recommended route
    is imperative. Deviation from the recommended
    route of administration might reduce vaccine
    efficacy or increase the risk of local reactions.
    (p. D5)

50
CDC Advisory Committee on Immunization Practices
  • Site
  • Although there are several IM injection sites on
    the body, the recommended IM sites for vaccine
    administration are the vastus lateralis muscle
    (anterolateral thigh) and the deltoid muscle
    (upper arm). The site depends on the age of the
    individual and the degree of muscle development.
  • The usual sites for vaccine administration
    subcutaneously are the thigh (for infants lt12
    months of age) and the upper outer triceps of the
    arm (for persons gt12 months of age). If
    necessary, the upper outer triceps area can be
    used to administer subcutaneous injections to
    infants.

51
CDC Advisory Committee on Immunization Practices
  • Injectable Vaccine Administration for Children
    Birth to 6 years
  • IM
  • anterolateral thigh or deltoid Use of deltoid
    muscle in children 18 monts and older (if
    adequate muscle mass) is an option for IM
    injections (p. D22)
  • SC
  • anterolateral thigh or lateral upper arm (p. D22)

52
  • Schecter, Zempsky, Cohen, McGrath, McMurtry,
    Bright (2007). Pain reduction during pediatric
    immunizations evidence-based review and
    recommendations. Pediatrics, 119(5), e1184-98.
  • Evidence is limited and somewhat controversial..
  • The limited data available suggests that
    intramuscular administration of immunizations
    should occur in the anterolateral thigh or
    vastus lateralis for children lt 18 months of age
    and in the upper arm or deltoid for those gt 36
    months of age.
  • Controversy exists in site selection for 18 to
    36 month old children.

53
Schecter, Zempsky, Cohen, McGrath, McMurtry,
Bright (2007). Pain reduction during pediatric
immunizations evidence-based review and
recommendations. Pediatrics, 119(5), e1184-98.
  • The shift from thigh to arm should occur when the
    upper arm has adequate muscle mass to allow
    injection. This shift is driven by research with
    18month old infants that suggests that injection
    in the thigh is more painful and causes more
    incapacitation (decreased movement of the
    extremity, limping) than injection in the arm.
    However, redness and swelling was found to occur
    more frequently when given in the arm.

54
Application Exercise
  • PICO QUESTION
  • For the 4 year old pre-K age group, are there
    fewer injection site complications with giving
    the immunizations in the thigh as compared to
    giving the immunizations in the arm?

55
Source Level of Evidence
Cochrane Review ?
National Guidelines Clearinghouse ?
CDC Advisory Committee on Immunization Practices ?
Evidence Based Review ?
56
Cochrane Review
Did the Evidence Answer our PICO Question?
National Guidelines Clearinghouse
CDC ACIP
Evidence Based Review
57
RECOMMENDATIONS?
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