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Canadian Family Physician logoLink to Canadian Family Physician
. 2017 Nov;63(11):853–858.

Knowledge translation tools in preventive health care

Ainsley Elizabeth Moore 1, Sharon E Straus 2, Danielle Kasperavicius 3,, Neil R Bell 4, James A Dickinson 5, Roland Grad 6, Harminder Singh 7, Guylène Thériault 8, Brett D Thombs 9, Heather Colquhoun 10
PMCID: PMC5685446  PMID: 29138155

Seemingly simple decisions about a screening test can have unexpected consequences. Understanding the balance of such consequences, including benefits and harms, can be confusing for patients and clinicians, but it is central to informed decision making. Clinicians must effectively communicate the likelihood that a patient might benefit because an undetected condition is found and effectively treated, as well as possible harms from false-positive findings or from overdiagnosis, which occurs when conditions that would never have affected a patient are diagnosed. Such numerical details are difficult to remember. Notably, explaining the likelihood of benefits and harms is only the first step in the shared decision-making process. This process must also identify and integrate a patient’s perceptions, values, and preferences about screening consequences in order to make a decision. Knowledge translation (KT) tools can simplify complex discussions between clinicians and patients, and improve patients’ knowledge of options, as well as the accuracy of their risk perception, among other benefits.

Knowledge translation tools are resources and products that are meant to facilitate moving evidence into practice.1 The ability to simplify and support information exchange between clinicians and patients in order to reach evidence-informed health decisions that are congruent with a patient’s values and preferences is especially important in the context of weak preventive health recommendations (in contrast to strong). For weak recommendations, the balance between benefits and harms is less clear, and shared decision making is essential to understanding where that balance lies for an individual patient. Most preventive screening recommendations from the Canadian Task Force on Preventive Health Care (CTFPHC) are graded as weak. As per the GRADE (Grading of Recommendations Assessment, Development and Evaluation) system, a weak recommendation is made when the harms and benefits are closely balanced, the quality of evidence is low, or there is uncertainty or variability in patient values and preferences.2

An increasing variety of tools are available to support shared decision making. In this article, we present a case that illustrates the value of KT tools in shared decision making. In the presented case, a clinician perceives a conflict between patient preferences and the preventive health guideline recommendation. Along the way, we will introduce a variety of KT tools produced by the CTFPHC to support preventive health decision making, describe why KT tools are helpful, and explain what makes a KT tool useful.

Kip’s case and KT tools in action

“I need to know my prostate cancer number,” says Kip as he walks into your office. Kip is a 55-year-old man with no relevant family history of prostate cancer. He has heard from a friend, a survivor of prostate cancer, that all men older than age 40 should have the prostate-specific antigen (PSA) test. Kip has visited numerous prostate cancer–related websites and watched online videos about PSA screening shared by his friends.

For men like Kip, who are between the ages of 55 and 69, with no relevant family history of prostate cancer, the CTFPHC provides a weak recommendation against screening for prostate cancer with the PSA test based on moderate-quality evidence. Various tools developed by the CTFPHC can help Kip to make a decision that is right for him.

Diversity of available KT tools

Knowledge translation tools can be broadly organized into 3 areas: implementation tools (eg, point-of-care tools), resource planning tools (eg, equipment or technology needed to support implementation), and evaluation tools (eg, quality indicators).3 Most CTFPHC KT tools are implementation tools. The most common types of implementation tools are printed educational materials and decision aids, which can have a range of uses, target audiences, delivery channels, formats, and components (Table 1).4 Printed educational materials typically refer to printed guidelines, recommendations for clinical care, and peer-reviewed publications,5 but can also include frequently asked questions and other formats. Although traditionally delivered on paper, printed educational materials are increasingly available via electronic applications. They are typically considered passive implementation tools. Decision aids, on the other hand, translate evidence into user-friendly formats in order to actively inform conversations with patients about their decision options, help clarify their values related to possible benefits and harms of options, and guide them through the decision-making process.6 However, Gagliardi and colleagues’ classification of KT tools does not separate passive dissemination and active implementation tools.3 Thus, the term implementation tool as used here, and shown in Table 1,4 refers to a tool (or its components) that can be used for either a passive or an active implementation process. For example, Figure 14 shows an infographic on screening, a popular component of decision aids, which provides visual representation of information that can actively guide a decision-making process or be distributed passively, such as through mass mailings to clinicians or patients.

Table 1.

Factors to consider about common implementation tools

FACTORS TO CONSIDER IMPLEMENTATION TOOLS

PRINTED EDUCATIONAL MATERIAL* DECISION AIDS
Target audiences (Who is using the tool?)
  • Patients

  • Patients and clinicians

  • Patients, clinicians, and caregivers

  • Patients

  • Patients and clinicians

  • Patients, clinicians, and caregivers

Format (How is information presented?)
  • Infographic (eg, 1000-person diagram)

  • Frequently asked questions

  • Peer-reviewed publication of a clinical practice guideline

  • Infographic (eg, 1000-person diagram)

  • Algorithms

  • Decision trees

Content (What information is presented?)
  • Health outcomes of clinical interventions

  • Benefits and harms

  • Clinical risk scores

  • Best practices for the topic

  • Guideline recommendations

  • Decision under consideration is explicitly stated

  • Information on test or intervention

  • Benefits and harms

  • Prompt to consider values and preferences

  • Clinical risk scores

Passive dissemination (Examples of 1-way distribution of information to patients or physicians; no dialogue)
  • Review articles such as the following: CTFPHC. Recommendations on screening for developmental delay. CMAJ 2016;188(8):579–87.

  • Read the CTFPHC 1000-person handout that was distributed at a conference (eg, the Prostate Cancer—1000-Person Tool in Figure 1)4

  • Hospital distributes decision tree on surgical options to newly diagnosed patients with prostate cancer

Active implementation (Examples of 2-way exchange of information between patients and physicians; active dialogue)
  • Discuss the printed CTFPHC 1000-person handout with a patient as part of a discussion on screening (eg, Figure 1)4

  • Review a CTFPHC infographic with a patient as part of a screening decision discussion (eg, Figure 1)4

CTFPHC—Canadian Task Force on Preventive Health Care.

*

Printed educational materials can also be delivered through videos, online applications, etc.

A diagram that shows a picture of 1000 individuals and the outcomes of screening for a condition for each person individually.

Figure 1.

Figure 1.

A 1000-person diagram illustrating the results of screening 1000 men with a PSA test

PSA—prostate-specific antigen.

Reprinted from the Canadian Task Force on Preventive Health Care with permission.4

Working with the 1000-person diagram

As the CTFPHC 1000-person diagram shows (Figure 1),4 for men like Kip the risk of dying from prostate cancer is 5 per 1000 men screened compared with 6 per 1000 men not screened.

While considering Kip’s request for PSA testing, you recall that the CTFPHC website has KT tools that can help facilitate shared decision making. You refer Kip to the short video by Canadian physician Mike Evans on PSA testing,7 provide him with the CTFPHC tool entitled PSA Screening: Patient FAQ,8 and book a follow-up appointment to discuss further.

Before Kip’s next visit, you review the CTFPHC clinician-directed KT tools. You refresh your knowledge on the CTFPHC guideline, using the CTFPHC tool Prostate Cancer—Clinician Summary.9 You also watch the CTFPHC screening video for clinicians.10 Your question about screening for different age groups is answered in the Primary Care Practitioner FAQ tool.11 You also review the metrics of the CTFPHC 1000-person diagram (Figure 1).4

Figure 14 shows that screening 1000 men for prostate cancer with the PSA test would save 1 life over 13 years. The overall reduction in prostate cancer mortality is 1 per 1000; although not shown in the infographic, there is no reduction in all-cause mortality.12 The infographic also shows possible harms from screening. It shows that among 1000 men screened, 178 men with positive PSA test results will have follow-up testing that does not identify prostate cancer (false-positive findings) and 4 of those 178 men will experience biopsy complications.

Furthermore, the infographic shows that 33 per 1000 men screened will be diagnosed with prostate cancer that would not have caused illness or death (overdiagnosis) and will be potentially exposed to treatments and their adverse effects, as well as experience anxiety from knowing this overdiagnosis of prostate cancer.

Use and development of KT tools

Why use KT tools?

Guidelines, which are developed to synthesize evidence into clear recommendations, are foundational for health care planning and delivery, as well as quality improvement; however, the dissemination of guidelines alone rarely results in changes to everyday practice.13 Clinicians need help to clarify the evidence and to elicit their patients’ preferences. Knowledge translation tools are not a panacea, but can improve the uptake of knowledge into practice. A recent Cochrane review of decision aids (105 studies, 31 043 participants) identified benefits for both patients and clinicians. Benefits included improved patient knowledge of options, increased participation in decision making, and better accuracy of risk perception related to available options.14 The review also found that decision aids increased the likelihood that a patient and a clinician would talk about the decision to be made and that using decision aids during consultations added approximately 2.6 minutes (median) to the length of the consultation.14 The review did not identify any adverse effects on health outcomes or patient satisfaction. A recent systematic review that focused on decision aids in prostate cancer screening (13 studies, 6909 men) found that decision aids increased patient knowledge and reduced decisional conflict.15

A Cochrane review (45 studies) of passively distributed printed educational materials (eg, a printed flyer of recommendations on lung cancer screening) suggests that these tools might have a small effect on professional practice outcomes (eg, number of tests ordered and drug prescriptions).16 However, there was insufficient information to reliably estimate any possible effects on patient outcomes (eg, blood pressure, complications after surgery).16

What is a useful KT tool?

Knowledge translation tools are intended to support effective sharing of information so that patients can make the best possible choice for themselves. Not all KT tools are equally effective. Ideal tool characteristics include an explicit statement of objectives, a description of who would use the tool, and instructions on how to use it, among other desirable features (Box 1).3

Box 1. Desirable features of KT tools.

Ideal characteristics of KT tools include the following:

  • Tool objectives are stated

  • Target users are named

  • Instructions on tool use are provided

  • Methods used to develop the tool are described

  • Tool is based on a comprehensive search for content

  • Evidence upon which tool content is based is described

  • Sources of evidence are cited

  • Setting in which the tool was developed and in which the tool will be used is described

  • Those intended to use the tool were involved in tool development

  • Methods used to evaluate the tool are described

  • Tool was pilot-tested with users

  • User feedback about tool use and its effects (eg, on practice) is prospectively collected

KT—knowledge translation.

Data from Gagliardi et al.3

Notably, not all KT tools are equally trustworthy sources of health information. In some cases, KT tools can be misleading. Ideological, financial, intellectual, and other interests might lead to omitting or downplaying of risk, overstating outcome effectiveness, presenting inaccurate risk calculators, or providing misleading statistics, such as reporting ratios but not absolute rates of benefits and harms.17 Trustworthy KT tools should present a balance of harms and benefits, provide references for the evidence presented, and disclose conflicts of interest.18

In order to help clinicians critically appraise available decision aids, the International Patient Decision Aids Standards Collaboration has established quality appraisal criteria for decision aids (Box 2).19 The Ottawa Hospital Research Institute (OHRI) provides an online service that allows clinicians to search by health topic for decision aids produced by a range of organizations.20 Decision aids are rated by the OHRI based on the International Patient Decision Aids Standards criteria to lower the risk of using a biased decision aid.19,20 For more information, including online tutorials and tool kits on using decision aids in practice, visit the OHRI website at https://decisionaid.ohri.ca/index.html.20

Box 2. Criteria for judging the quality of decision aids, as per iPDAS.

The IPDAS criteria are as follows:

  • Balanced Information is presented
    • - Positive and negative features of each option are compared with equal detail (eg, font, order, display of statistics), including the option of doing nothing
  • Decision process is facilitated
    • -Explicitly states the decision that needs to be considered
    • - Includes the methods for clarifying and expressing patient’s values
    • -Asks patients to consider which positive and negative aspects matter most
  • Systematic development process has been used
    • - Methods of finding, appraising, and summarizing evidence are reported
    • -Quality of evidence is reported
    • -Date of evidence update is reported
    • -Evidence sources are referenced
    • - Evidence base of population is consistent with decision aid target user
  • Conflicts of interest are disclosed

IPDAS—International Patient Decision Aids Standards.

Data from IPDAS 2005: criteria for judging the quality of patient decision aids.19

How does the CTFPHC develop KT tools?

The CTFPHC develops plain-language tools that are intended to guide active conversations or to be reviewed by individual clinicians or patients (passive implementation). Based on desired and trustworthy features of KT tools, the CTFPHC makes use of synthesized evidence from CTFPHC guidelines and other systematically collected evidence from patient-engagement activities. Following a series of development and review stages, a KT tool undergoes usability testing with target end users. Target end users provide feedback on the tool’s content, format, and navigation; aesthetics; and the perceived usefulness of the tool, which is expressed either during one-on-one interviews or focus groups. Feedback from target end users and CTFPHC partners is incorporated into final versions of KT tools.

Back to Kip

Kip is back in your office, and you check if he understands his decision options, which include getting a PSA test or not getting a PSA test. To guide your conversation, you use the CTFPHC 1000-person diagram (Figure 1)4 for men aged 55 to 69 years of age. You help Kip understand the risks of benefits and harms of PSA testing using natural frequencies, which are more understandable than probabilities (eg, 1 less man per 1000 screened over 13 years will die from prostate cancer compared with men who are not screened).

While reviewing portions of the tool with Kip, you seek to understand how much the potential benefits and harms matter to him. He is not impressed with the modestly reduced risk of dying from prostate cancer as a result of PSA screening. He is not that concerned about a prostate biopsy if his PSA is elevated; he has been through worse. On the other hand, Kip is concerned about getting a prostate cancer diagnosis if that cancer was not destined to become a problem in his lifetime.

You then review whether Kip has enough information to make a decision. Kip is confident he has enough information to choose. He decides not to have the PSA test. Kip thanks you and takes a hard copy of the CTFPHC 1000-person diagram to show to friends.

Conclusion

Knowledge translation tools simplify our discussions with patients. They improve preventive health screening conversations by giving patients access to useful resources and helping them to understand relevant information. Knowledge translation tools provide direct benefits to both patients and clinicians in a shared decision-making context.

KEY POINTS

  • Knowledge translation (KT) tools are resources and products that are meant to facilitate shared decision making between patients and clinicians (eg, decision aids). Tools can be clinician centred (eg, clinical practice guidelines) or more patient oriented (eg, plain-language videos).

  • Not all KT tools are equally effective or equally trustworthy sources of health information. Ideal tool characteristics include an explicit statement of objectives, a description of the target audience, and instructions on tool use. Trustworthy KT tools should present a balance of harms and benefits, provide references for the evidence presented, and disclose conflicts of interest.

  • Decision aids are designed to improve patients’ knowledge of their options, increase their participation in decision making, and increase their ability to accurately compare potential benefits and harms of options. They do not advise people to choose one option over another and do not replace counseling from a clinician. Use of a typical decision aid adds approximately 2.6 minutes to the clinical encounter.

Footnotes

This article is eligible for Mainpro+ certified Self-Learning credits. To earn credits, go to www.cfp.ca and click on the Mainpro+ link.

La traduction en français de cet article se trouve à www.cfp.ca dans la table des matières du numéro de novembre 2017 à la page e466.

Competing interests

All authors have completed the International Committee of Medical Journal Editors’ Unified Competing Interest form (available on request from the corresponding author) and declare that they have no competing interests. For additional information on the conflict of interests of the Canadian Task Force on Preventive Health Care, please visit https://canadiantaskforce.ca/.

Suggested additional reading

1. Straus S, Tetroe J, Graham I, editors. Knowledge translation in health care. Moving from evidence to practice. 2nd ed. West Sussex, UK: John Wiley & Sons; 2013.

2. Grimshaw JM, Eccles MP, Lavis JN, Hill SJ, Squires JE. Knowledge translation of research findings. Implementation Sci 2012;7:50.

References


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