Title: Quarterly Updates: Evidence Based Practice For Public Health Nurses Session III
1Quarterly UpdatesEvidence Based Practice For
Public Health NursesSession III
- Public Health Nursing Section, Evidence Based
Practice Committee
2EVIDENCE BASED PUBLIC HEALTH NURSING PRACTICE
CLIENT VALUES/ PREFERENCES
CLINICAL EXPERTISE/ JUDGMENT
KNOWLEDGE/ RESEARCH
3http//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
5Objectives
- 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
6Evidence Based Practice
- Uses highest quality of knowledge in providing
care to produce the greatest impact on health
status and health care
7Critical Appraisal of Evidence
- Key characteristic of evidence based practice
- Core skill needed to use evidence to support
nursing practice decisions
8Critical Appraisal of Evidence
- Ensures relevance and transferability of evidence
from the search to the specific population for
whom the care will be provided
9Critical 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
101) 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
111) 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
12Levels 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
13Levels of Evidence
- Experts have developed a number of taxonomies to
rate strength of evidence - Most are organized around research designs
14Levels 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
15Levels 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)
16Levels 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
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Adapted from Joanna Briggs Institute and
AHCPR Eilers Heerman, 2005
17The U.S. Preventive Services Task Force (2008)
18Level 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
19Systematic 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
20Meta-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
21Randomized 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
22Quasi-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
23Non-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
252) 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?
26What 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?
27Are 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?
28Is 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?
29Other 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.
30Other 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
31Other 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
33EBP 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
34Agency 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
35EBP Rich Resources for P/CHN
- Guide to Community Preventive Services
- http//www.thecommunityguide.org/index.html
36Centers for Disease Control Prevention
- CDC for Public Health Professionals
- http//www.cdc.gov/CDCForYou/public_health_profess
ionals.html
37Association of State and Territorial Health
Officials
- Evidence Based Practice
- http//www.astho.org/?templateevidence_based_ph_p
ractice.html
38National 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
39EBP 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
40EBP 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
41EBP 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.
42Evidence 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/
43EBP Rich Resources for P/CHN
44Application 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?
45Cochrane 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
46National 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
47National 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.
48National 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.
49CDC 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)
50CDC 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.
51CDC 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.
53Schecter, 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.
54Application 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?
55Source Level of Evidence
Cochrane Review ?
National Guidelines Clearinghouse ?
CDC Advisory Committee on Immunization Practices ?
Evidence Based Review ?
56Cochrane Review
Did the Evidence Answer our PICO Question?
National Guidelines Clearinghouse
CDC ACIP
Evidence Based Review
57RECOMMENDATIONS?