Professional Documents
Culture Documents
CHAPTER 11
Getting evidence
into practice
LEARNING OBJECTIVES
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Greenhalgh, Trisha M.. Understanding Research Methods for Evidence-Based Practice in Health, 2nd Edition, Wiley, 2019. ProQuest Ebook Central,
http://ebookcentral.proquest.com/lib/ecu/detail.action?docID=5880746.
Created from ecu on 2023-02-22 12:52:58.
© John Wiley & Sons Australia, Ltd. Not for resale or distribution. Any unauthorised distribution or use will result in legal action.
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OPENING SCENARIO
Individual barriers
Before health professionals can use evidence, they need to know how to find it and how to understand it.
Some lack the ability to find evidence resources (because computers weren’t common in healthcare settings
until relatively recently), and they don’t have the IT skills to access or search specialist databases.3 They
may also be unfamiliar with how research is carried out and have never had an opportunity to learn about it,
which makes the whole concept seem very alien — something for doctors and scientists rather than nurses
or allied health professionals. Others lack confidence in how to read research articles, interpret findings
or adapt guidelines, so they avoid them altogether. Lack of time is also a commonly mentioned barrier —
heavy workloads and busy lives mean few health professionals have the luxury of time to explore resources
during work hours or at home.4
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Perhaps the strongest individual barriers, however, are personality based. Some clinicians dislike the
entire concept of EBP and place little value on research.5 Like the RN in the opening scenario, they think
that it’s unnecessary or irrelevant to their practice. Even for those who aren’t completely against EBP,
readiness to adopt healthcare innovations can depend on several factors. These include their attitudes to
change; for example, some people are trendsetters and like to try new things, others prefer to follow once
a new practice has become established, and some will resist change under any circumstance. Change is
risky, and it takes effort to move out of your comfort zone and learn new things.
New evidence can also seem quite threatening on a personal level. Being told that the way you have
been practising isn’t the best way can be very challenging to a person’s self-esteem and feelings of
competence — and the more experienced you are, the more threatening it is. The RN or therapist who
has a wealth of knowledge may greatly resent having this brushed aside for new ideas.
Organisational barriers
While there are many individual barriers to using EBP, the main reasons why clinicians don’t use evidence
tend to be down to the organisations they work for.6 The major organisational barriers to EBP include a
lack of resources and support, and a workplace culture that devalues research. Time is again a problem;
many facilities are short-staffed and workloads are heavy, so health professionals have little opportunity to
research new ways to treat clients. While most workplaces are now computerised, staff don’t always have
access to these resources, or to the databases that hold the evidence. Subscriptions to some databases are
very expensive, and smaller organisations in particular may not be able to afford it. Even in workplaces
with good resources, staff often need support to find and use evidence, from knowledge workers and from
management. If this support is missing, or if the organisation has no interest in becoming evidence-based,
the clinician will find it hard, if not impossible, to implement EBP themselves.
information quickly and easily. Abstraction journals such as Evidence-Based Nursing, which summarise
high-level studies and systematic reviews into a single page, make understanding the research even more
straightforward. Researchers are also moving away from the statistics and jargon-heavy format they once
used in their articles, towards a more readable and understandable way of writing. Some databases, such
as the Cochrane Library, insist that all systematic reviews include a summary in layman’s language, and
most journals now require authors to make their conclusions and implications for practice explicit, so it’s
easier for readers to put the findings into practice.
Motivation is also an important factor in whether a clinician chooses to make changes. When they can
see the benefits of the new evidence, whether it’s a clear improvement in client health outcomes, or a
personal advantage such as reduction in workload or greater ease of use, they are more likely to adopt a
new practice.
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Input from local teams is not about reinventing the wheel in terms of summarising the evidence, but about
taking account of local practicalities and circumstances. For example, a nationally produced guideline
about epilepsy care might recommend an epilepsy specialist nurse in every district. However, in one district,
the healthcare teams might have advertised for such a nurse but failed to recruit one. The ‘local input’ might
be about how best to provide what the epilepsy nurse would have provided, in the absence of a person in
the position. Figure 11.3 presents an abstract from a journal article that outlines the implementation of
Copyright © 2019. Wiley. All rights reserved.
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to be less effective if approaches are singular and do not address issues of participation by those groups
who have the greatest stake in improved health outcomes. This paper presents a multifaceted framework,
which has been developed in New Zealand to ensure health inequalities experienced by Maori ̄ (the
indigenous population within New Zealand) are addressed when developing evidence-based guidance.
The framework has two overarching goals. These are: (i) to ensure the explicit identification of Maori ̄
health needs occurs during each formal stage of guideline development; and (ii) to ensure there is full
̄
Maori participation in the guidance development process. The steps to achieving these two goals are
described in detail. The framework presented is evolving and intended to be flexible dependent upon
healthcare environments and resourcing. This paper is intended to provide some focus and discussion
for the role of evidence-based guidance in both addressing and entrenching health inequalities in
vulnerable groups.
Source: Berentson-Shaw 2012.9
The quality of guidelines can be variable, so it is important for practitioners to be able to evaluate
them properly (see the chapter on reviewing literature). A flawed guideline can lead to inappropriate care,
particularly for clients who have multiple morbidities and may need more than one guideline applied. (This
is covered in more detail in the chapter on challenges to evidence-based practice.)
far, they have mainly been used in medical research, but are becoming more popular in studies carried out
in other health disciplines.11
Shared decision-making
While PROMs are important, they only tell us what patients or clients, on average, value most, not what
the client in front of us values most. To find that out, you would have to ask the client — and there is now a
science and a methodology for this.12 The idea is based on the notion of the client as a rational chooser, able
and willing (perhaps with support) to join in the deliberation over options and make an informed choice.
Not every client will want to do this; many prefer to let the clinician as expert decide for them. For
those who do wish to be involved, health professionals need to help them understand the situation as
clearly as possible, and know their options and the consequences of these. One challenge is maintaining
equipoise — that is, holding back on what you feel the course of action should be and setting out the
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different options with the pros and cons presented objectively, so the client can make their own decision.13
Using a decision aid is a good way to do this.
Many decision aids are available online, allowing the client to click through different steps in the
algorithm (with or without support from a health professional). The best way to get your head round
shared decision-making tools is to look at a few — and, if possible, put them to use in practice. The
Australian Commission on Safety and Quality in Health Care website (www.safetyandquality.gov.au) has
more information on decision aids and a link to a comprehensive range of decision tools.
Option grids
Most discussions about treatment options do not require — and may even be hindered by — an exhaustive
analysis of probabilities, risks and preference scores. What most people want is a brief but balanced list
of the options, setting out the costs and benefits of each and including an answer to the question ‘What
would happen if I went down this route?’
The option grid does just this.15 The information is presented in a table with the different options
appearing as columns, with each row answering a different question such as ‘What does the treatment
involve?’, ‘How soon would I feel better?’ and ‘How would this treatment affect my ability to work?’ The
grid can be used online or printed off and given to the client so they can go away and consider the options
before returning for a further consultation. And unlike the previous generation of shared decision-making
tools, they are very simple and easy to use.
Table 11.1 shows an option grid to help clients and practitioners decide what treatment they would like
to undertake for tonsillitis.
Copyright © 2019. Wiley. All rights reserved.
Frequently asked
questions Tonsillectomy Active management
What does it involve? The tonsils are removed under general Your GP will prescribe appropriate
anaesthetic. treatment if your child has further
tonsillitis. Your child will be referred for
a tonsillectomy if necessary.
How long does it The operation will take about 30 minutes. Until other treatment is considered
take? Your child may need to stay in the necessary.
hospital for one night.
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How long does it About two weeks. During this time your As with previous episodes, it will take
take to recover? child will need to stay at home to prevent 3–7 days to recover from each event.
infection.
Will my child stop Yes, but they may still have episodes of Possibly, 30 in every 100 children
having tonsillitis? sore throat. Tonsillectomy can reduce (30%) stop having tonsillitis without
sore throats by up to 9 episodes in the an operation. They may still have
2 years following surgery. sore throats.
What is the risk from As with all operations there is a small Serious complications of tonsillitis are
the procedure or risk of serious complications. More very rare.
process? common problems include pain, vomiting,
bleeding, infection and dental damage.
What is the risk of 1 in every 100 children (1%) will have Bleeding from tonsillitis (haemorrhagic
bleeding? serious bleeding immediately after the tonsillitis) is very rare.
operation. Most of these will need to have
another operation to stop the bleeding.
3 in every 100 children (3%) will have
serious bleeding in the first two weeks
after the operation. Some will need
to have another operation to stop the
bleeding.
Will it reduce the Possibly. It depends on how much time Possibly. As children get older, they often
number of days your child has been missing from school. have fewer attacks of tonsillitis.
missed from school?
Are other parents Yes, studies show that parents are happy Yes, if their child gets better without the
happy with their with the surgery and its effects on their need for an operation.
decisions? child’s health.
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SUMMARY
Despite a legal requirement for health professionals to use evidence to underpin practice, it can still take
time for research findings to filter through to the workplace, due to personal and organisational barriers that
prevent clinicians from implementing evidence-based practice. Personal barriers include lack of knowledge
and skills to find and interpret research, lack of time, and issues of confidence, self-esteem and autonomy.
Organisational barriers include lack of support or resources, and a disregard for the use of EBP. These
barriers can be addressed through education, accessibility of information and support, and the use of tools
such as integrated care pathways and clinical practice guidelines. Client decision aids can also be used to
include the client more fully in their own care.
KEY TERMS
clinical practice guidelines Systematically developed statements to assist practitioner decisions about
appropriate healthcare for specific clinical circumstances.16
decision aid Evidence-based tools designed to help clients to participate in making specific and
deliberated choices among healthcare options. Client decision aids supplement (rather than replace)
clinicians’ counselling about options.17
integrated care pathway A pre-defined plan of client care relating to a specific diagnosis (e.g. suspected
fractured hip) or intervention (e.g. hernia repair), with the aim of making the management more
structured, consistent and efficient.18
option grid A one-page table covering a single topic, to help clients and clinicians compare alternative
treatment options to find the most suitable.
patient-reported outcome measure (PROM) The outcome from a research study that matter most to
the client/patient rather than those the researchers think are the most important. Identified through
qualitative research methods prior to the quantitative study.
WEBSITES
1 Australian Clinical Practice Guidelines (NHMRC): www.clinicalguidelines.gov.au
2 National Institute for Health and Care Excellence (UK): www.nice.org.uk
3 National Guideline Clearinghouse (USA): www.guideline.gov
4 The Effective Practice and Organisation of Care (EPOC): http://epoc.cochrane.org
5 Australian Commission on Safety and Quality in Health Care: www.safetyandquality.gov.au/our-
work/shared-decision-making/other-resources
6 OHRI patient decision aids: http://decisionaid.ohri.ca
7 Option grids for client decisions: www.optiongrid.org
ENDNOTES
1. See the AHPRA (www.ahpra.gov.au) website for Codes of Conduct for 15 health practitioner groups, including Chinese
medicine, occupational therapy, physiotherapy and podiatry, and the NMBA Registered Nurse Standards for Practice.
2. See the New Zealand Nurses Organisation website (www.nursingcouncil.org.nz) for the Code of Conduct and Standards of
Copyright © 2019. Wiley. All rights reserved.
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5. K. E. Harding et al., ‘Not enough time or a low priority? Barriers to evidence-based practice for allied health clinicians,’
Journal of Continuing Education in the Health Professions 34, no. 4 (2014): 224–31.
6. K. Samuelsson and E. Wressle, ‘Turning evidence into practice: barriers to research use among occupational therapists,’
British Journal of Occupational Therapy 78, no. 3 (2015): 175–81; K. A. Abrahamson, R. L. Fox, and B. N. Doebbeling,
‘Facilitators and barriers to clinical practice guideline use among nurses,’ American Journal of Nursing 112, no. 7 (2012):
26–35. doi: 10.1097/01.NAJ.0000415957.46932.bf.
7. M. Laurant et al., ‘Nurses as substitutes for doctors in primary care,’ Cochrane Library of Systematic Reviews 7 (2018). doi:
10.1002/14651858.CD001271.pub3.
8. J. Rycroft-Malone, ‘Evidence-informed practice: from individual to context,’ Journal of Nursing Management 16 (2008):
404–8; A. Thomas and M. Law, ‘Research utilization and evidence-based practice in occupational therapy: a scoping study,’
American Journal of Occupational Therapy 67 (2013): e55–65. doi: 10.5014/ajot.2013.006395.
9. J. Berentson-Shaw, ‘Reducing inequality in health through evidence-based clinical guidance: is it feasible? The New Zealand
experience,’ International Journal of Evidence-Based Healthcare 10 (2012): 146–53.
10. A. Edwards and G. Elwyn, Shared decision-making in health care: achieving evidence-based patient choice (New York:
Oxford University Press, 2009).
11. J. Dawson et al., ‘The routine use of patient reported outcome measures in healthcare settings,’ BMJ: British Medical Journal
(Clinical Research ed.) 340 (2009): c186; K. McGrail, S. Bryan, and J. Davis, ‘Let’s all go to the PROM: the case for routine
patient-reported outcome measurement in Canadian healthcare,’ Healthcare Papers 11, no. 4 (2011): 8–18; K. A. Meadows,
‘Patient-reported outcome measures: an overview,’ British Journal of Community Nursing 16, no. 3 (2011): 146–51.
12. Edwards and Elwyn, Shared decision-making in health care; G. Makoul and M. L. Clayman, ‘An integrative model of shared
decision making in medical encounters,’ Patient Education and Counseling 60, no. 3 (2006): 301–12.
13. G. Elwyn et al., ‘Shared decision making and the concept of equipoise: the competences of involving patients in healthcare
choices,’ The British Journal of General Practice 50, no. 460 (2000): 892–9.
14. D. Stacey et al., ‘Decision aids for people facing health treatment or screening decisions (review),’ Cochrane Database of
Systematic Reviews 4 (2017). doi: 10.1002/14651858.CD001431.pub5.
15. G. Elwyn et al., ‘Option grids: shared decision making made easier,’ Patient Education and Counseling 90 (2013): 207–12.
16. M. J. Field and K. N. Lohr, eds., Guidelines for clinical practice: from development to use (National Academies Press (US),
1992).
17. Stacey et al., ‘Decision aids,’ 7.
18. T. Rotter et al., ‘Clinical pathways: effects on professional practice, patient outcomes, length of stay and hospital costs,’
Cochrane Database of Systematic Reviews 3 (2010). doi: 10.1002/14651858.CD006632.pub2.
ACKNOWLEDGEMENTS
Adapting author for this Australian edition: Elaine Crisp
Photo: © Miriam Doerr Martin Frommherz / Shutterstock.com
Figure 11.1: © M. Laurant et al., ‘Nurses as substitutes for doctors in primary care,’ Cochrane Library of
Systematic Reviews 7 (2018). doi: 10.1002/14651858.CD001271.pub3.
Figure 11.3: © PubMed / Public Domain
Figure 11.4: © D. Stacey et al., ‘Decision aids for people facing health treatment or screening decisions
(review),’ Cochrane Database of Systematic Reviews 4 (2017). doi: 10.1002/14651858.CD001431.pub5.
Table 11.1: © Trustees of Dartmouth College
Copyright © 2019. Wiley. All rights reserved.
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