Developing an evidence-based practice

CHAPTER 20


Developing an evidence-based practice


Marita Titler




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Go to Evolve at http://evolve.elsevier.com/LoBiondo/ for review questions, critiquing exercises, and additional research articles for practice in reviewing and critiquing.


Evidence-based health care practices are available for a number of conditions. However, these practices are not always implemented in care delivery settings. Variation in practices abound, and availability of high-quality research does not ensure that the findings will be used to affect patient outcomes (Centers for Medicare and Medicaid Services, 2008; Institute of Medicine, 2001). The use of evidence-based practices is now an expected standard as demonstrated by recent regulations from the Centers for Medicare and Medicaid Services (CMS) regarding not paying for nosocomial events such as injury from falls, Foley catheter-associated urinary tract infections, and stage 3 and 4 pressure ulcers. These practices all have a strong evidence base and when enacted, can prevent these nosocomial events. However, implementing such evidence-based safety practices is a challenge and requires use of strategies that address the systems of care, individual practitioners, senior leadership, and, ultimately, changing health care cultures to be evidence-based practice environments (Leape, 2005).


Translation of research into practice (TRIP) is a multifaceted, systemic process of promoting adoption of evidence-based practices in delivery of health care services that goes beyond dissemination of evidence-based guidelines (Berwick, 2003; Rogers, 2003; Titler & Everett, 2001). Dissemination activities take many forms, including publications, conferences, consultations, and training programs, but promoting knowledge uptake and changing practitioner behavior requires active interchange with those in direct care (Scott et al., 2008; Titler et al., 2008).This chapter presents an overview of evidence-based practice, and the process of applying evidence in practice to improve patient outcomes.




Overview of evidence-based practice


The relationships among conduct, dissemination, and use of research are illustrated in Figure 20-1. Conduct of research is the analysis of data collected from subjects who meet study inclusion and exclusion criteria for the purpose of answering research questions or testing hypotheses. Traditionally, the conduct of research has included dissemination of findings via research reports in journals and at scientific conferences.



Evidence-based practice is the conscientious and judicious use of current best evidence in conjunction with clinical expertise and patient values to guide health care decisions (Sackett et al., 2000). When enough research evidence is available, practice should be guided by research evidence in conjunction with clinical expertise and patient values. In some cases, however, a sufficient research base may not be available, and health care decision making is derived principally from nonresearch evidence sources such as expert opinion and scientific principles. As illustrated in Figure 20-1, application of research findings in practice may not only improve quality care but create new and exciting questions to be addressed via conduct of research.


The terms research utilization and evidence-based practice are sometimes used interchangeably. Although these two terms are related, they are not the same. Adopting the definition of evidence-based practice as the conscious and judicious use of the current “best” evidence in the care of patients and delivery of health care services; research utilization is a subset of evidence-based practice that focuses on the application of research findings. Evidence-based practice is a broader term that not only encompasses research utilization but also includes use of case reports and expert opinion in deciding the practices to be used in health care.



Models of evidence-based practice


Multiple models of evidence-based practice and translation science are available. Common elements of these models are syntheses of evidence, implementation, evaluation of the impact on patient care, and consideration of the context/setting in which the evidence is implemented. For a summary of models, the review by Grol and colleagues (2007) is recommended.


Although review of these models is beyond the scope of this chapter, implementing evidence in practice must be guided by a conceptual model to organize the strategies being used and to clarify extraneous variables (e.g., behaviors, facilitators) that may influence adoption of evidence-based practices (e.g., organizational size, characteristics of users).



The iowa model of evidence-based practice

An overview of the Iowa Model of Evidence-Based Practice as an example of an evidence-based practice model is illustrated in Figure 20-2. This model has been widely disseminated and adopted in academic and clinical settings (Titler et al., 2001).


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FIGURE 20-2  The Iowa model of evidence-based practice to promote quality care. (Redrawn from Titler, M., et al. (2001). The Iowa model of evidence-based practice to promote quality care. Critical Care Nursing Clinics of North America, 13(4), 497–509.)

In this model, knowledge- and problem-focused “triggers” lead staff members to question current nursing practice and whether patient care can be improved through the use of research findings. If, through the process of literature review and critique of studies, it is found that there is not a sufficient number of scientifically sound studies to use as a base for practice, consideration is given to conducting a study. Findings from such studies are then combined with findings from existing scientific knowledge to develop and implement these practices. If there is insufficient research to guide practice, and conducting a study is not feasible, other types of evidence (e.g., case reports, expert opinion, scientific principles, theory) are used and/or combined with available research evidence to guide practice. Priority is given to projects in which a high proportion of practice is guided by research evidence. Practice guidelines usually reflect research and nonresearch evidence and therefore are called evidence-based practice guidelines (see Chapter 11).


Recommendations for practice are developed based on evidence synthesis. The recommended practices, based on evidence, are compared to current practice and a decision is made about the necessity for a practice change. If a practice change is warranted, changes are implemented using a planned change process. The practice is first implemented with a small group of patients, and an evaluation is conducted. The evidence-based practice is then refined based on evaluation data and the change is implemented with additional patient populations for which it is appropriate. Patient/family, staff, and fiscal outcomes are monitored.



Steps of evidence-based practice


The Iowa Model of Evidence-Based Practice to Promote Quality Care (Titler et al., 2001) (see Figure 20-2), in conjunction with Rogers’ diffusion of innovations model (Rogers, 2003) provide steps for actualizing evidence-based practice. A team approach is most helpful in fostering a specific evidence-based practice.



Selection of a topic


The first step in conducting an evidence-based practice project is to select a topic. Ideas for evidence-based practice come from several sources categorized as problem- and knowledge-focused triggers. Problem-focused triggers are those identified by staff through quality improvement, risk surveillance, benchmarking data, financial data, or recurrent clinical problems. An example of a problem-focused trigger is increased incidence of central line occlusion in pediatric oncology patients.


Knowledge-focused triggers are ideas generated when staff read research, listen to scientific papers at research conferences, or encounter evidence-based practice guidelines published by federal agencies or specialty organizations. This includes those evidence-based practices that CMS expects are implemented in practice and have now based reimbursement of care on adherence to indicators of the evidence-based practices. Examples include treatment of heart failure, community-acquired pneumonia, and prevention of nosocomial pressure ulcers. Each of these topics includes a nursing component, such as discharge teaching, instructions for patient self care, or pain management. Sometimes topics arise from a combination of problem- and knowledge-focused triggers, such as the length of bed rest time after femoral artery catheterization. In selecting a topic, it is essential that nurses consider how the topic fits with organization, department, and unit priorities to garner support from leaders within the organization and the necessary resources to successfully complete the project. Criteria to consider when selecting a topic are outlined in Box 20-1.






Forming a team


A team is responsible for development, implementation, and evaluation of the evidence-based practice. A task force approach also may be used, in which a group is appointed to address a practice issue. The composition of the team is directed by the topic selected and should include interested stakeholders in the delivery of care. For example, a team working on evidence-based pain management should be interdisciplinary and include pharmacists, nurses, physicians, and psychologists. In contrast, a team working on the evidence-based practice of bathing might include a nurse expert in skin care, assistive nursing personnel, and staff nurses.


In addition to forming a team, key stakeholders who can facilitate the evidence-based practice project or put up barriers against successful implementation should be identified. A stakeholder is a key individual or group of individuals who will be directly or indirectly affected by the implementation of the evidence-based practice. Some of these stakeholders are likely to be members of the team. Others may not be team members but are key individuals within the organization or unit who can adversely or positively influence the adoption of the evidence-based practice. Questions to consider in identification of key stakeholders include the following:



Failure to involve or keep supportive stakeholders informed may place the success of the project at risk because they are unable to anticipate and/or defend the rationale for changing practice, particularly with resistors (nonsupportive stakeholders) who have a great deal of influence among their peer group.


An important early task for the evidence-based practice team is to formulate the PICO question. This helps set boundaries around the project and assists in evidence retrieval. This approach is illustrated in Table 20-1 (see Chapters 1, 2, 3, and 19).




Evidence retrieval


Once a topic is selected, relevant research and related literature need to be retrieved, including clinical studies, meta-analyses, and existing evidence-based practice guidelines (see Chapters 3 and 11). AHRQ (www.AHRQ.gov) sponsors the Evidenced-Based Practice Centers and a National Guideline Clearinghouse where abstracts of evidence-based practice guidelines are available. Current best evidence from specific studies of clinical problems can be found in an increasing number of electronic databases such as the Cochrane Library (www.thecochranelibrary.com), the Centers for Health Evidence (www.cche.net), and Best Evidence (www.acponline.org) (see Chapter 3). Once the literature is located, it is helpful to classify the articles as clinical (nonresearch), theory articles, research articles, systematic reviews, and evidence-based practice guidelines. Before reading and critiquing the research, it is useful to read background articles to have a broad view of the topic and related concepts, and to then review existing evidence-based practice guidelines. It is helpful to read articles in the following order:




Schemas for grading the evidence


There is no consensus among professional organizations or across health care disciplines regarding the best system to use for denoting the type and quality of evidence, or the grading schemas to denote the strength of the body of evidence (Guyatt et al., 2008a; Institute of Medicine, 2011). See Tables 20-2 and 20-3 for grading and assessing quality of research studies. The important domains and elements to include in grading the strength of the evidence are defined in Table 20-4.



TABLE 20-2   


EXAMPLES OF EVIDENCE-BASED PRACTICE RATING SYSTEMS




















GRADE WORKING GROUP (GRADE WORKING GROUP, 2004; GUYATT et al., 2008b) U.S. PREVENTATIVE SERVICES TASK FORCE AFTER MAY 2007 (HARRIS et al., 2001; U.S. PREVENTIVE SERVICES TASK FORCE, 2008)
Strength of Evidence: Quality of the Evidence Levels of Certainty Regarding Net Benefit
High: Further research is very unlikely to change confidence in the estimate of effect. Scientific evidence provided by well-designed, well-conducted, controlled trials (randomized and nonrandomized) with statistically significant results that consistently support the recommendation.
Moderate: Further research is likely to have an important impact on confidence in the estimate of effect and may change the estimate.
Low: Further research is very likely to have an important impact on confidence in the estimate of effect and is likely to change the estimate
Very Low: Any estimate of effect is very uncertain.
Note: The type of evidence is first ranked as follows:
Randomized trial = high.
Observational study = low.
Any other evidence = very low.
Limitations in study quality, important inconsistency of results, uncertainty about the directness of the evidence, imprecise or sparse data, and high probability of reporting bias can lower the evidence grade. Expert opinion that supports the guideline recommendation because the available scientific evidence did not present consistent results or because controlled trials were lacking. Grade of evidence can be increased if there is (1) strong evidence of association—significant relative risk of >2.0 (< 0.5) based on consistent evidence from two or more observational studies, with no plausible confounders (1); (2) very strong evidence of association—significant relative risk of >5.0 (<0.2) based on direct evidence with no major threats to validity (2); (3) evidence of a dose response gradient (1); and (4) all plausible confounders would have reduced the effect (1).
High: Available evidence usually includes consistent results from well-designed, well-conducted studies in representative primary care populations. These studies assess 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 of one or more of the following:
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 practice.
Lack of information on important health outcomes.
More information may allow estimation of effects on health outcomes.
Strength of Recommendations Recommendation Grades
 Strong: confident that desirable effects of adherence to a recommendation outweigh undesirable effects.
Weak: desirable effects of adherence to a recommendation probably outweigh the undesirable effects, but developers are less confident.
Note: Strength of recommendation is determined by the balance between desirable and undesirable consequences of alternative management strategies, quality of evidence, variability in values and preferences, and resource use.


USPSTF recommends the service. There is high certainty that the net benefit is substantial. Practice: Offer or provide this service.


USPSTF recommends the service. There is high certainty that the net benefit is moderate or there is moderate certainty that the net benefit is moderate to substantial. Practice: Offer or provide this service.


USPSTF recommends against routinely providing the service. There may be considerations that support providing the service in an individual patient. There is at least moderate certainty that the net benefit is small. Practice: Offer or provide this service only if other considerations support the offering or providing the service in an individual patient.


USPSTF recommends against the service. There is moderate or high certainty that the service has no net benefit or that the harms outweigh the benefits. Practice: Discourage the use of this service.


The USPSTF concludes that the current evidence is insufficient to assess the balance of benefits and harms of the service. Evidence is lacking, of poor quality, or conflicting, and the balance of benefits and harms cannot be determined. Practice: Read the clinical considerations section of USPSTF Recommendation Statement. If the service is offered, patients should understand the uncertainty about the balance of benefits and harms.



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FIGURE 20-3  Implementation model. (Redrawn from Rogers, E. M. (2003). Diffusion of innovations (5th ed.). New York, NY: Free Press; Titler, M. G., & Everett, L. Q. (2001). Translating research into practice: considerations for critical care investigators. Critical Care Nursing Clinics of North America, 13(4), 587–604.)

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Feb 15, 2017 | Posted by in NURSING | Comments Off on Developing an evidence-based practice

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