Value Conflicts in Evidence-Based Practice

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Value Conflicts in Evidence-Based Practice Jeanne Grace Corresponding author: J. Grace E-mail: jeanne_grace@urmc.rochester.edu Jeanne Grace RN PhD Emeritus Clinical Professor of Nursing, University of Rochester, Rochester, New York, USA. Abstract: Ethical dilemmas about care arise when the persons involved in care decisions have conflicting values. Evidence-based practice clarifies the nature of some ethical concerns about care because it sets three explicit values for clinical decision-making: effectiveness of care, efficiency of care, and incorporation of patient values. Defining effectiveness involves establishing relative values for outcomes and determining whose values must be considered. Defining efficiency involves establishing relative values for resources used and determining whose resources must be included. Incorporation of patient values involves balancing those values against the values of other members of society or the strength of the evidence supporting a clinical recommendation. An evidence-based practice perspective that focuses on identifying conflicting values about outcomes, resources, and patient input into decision-making may be helpful in defining, discussing and resolving ethical care dilemmas. J Nurs Sci 2010;28(2): 8-12 Keywords: evidence-based practice, ethics, effectiveness, efficiency, values Ethical dilemmas about care arise when the persons involved in care decisions have conflicting values. Patients, health care providers and society in general all have an interest in health care decisions and may not share the same values. The values and abilities of the care provider must be balanced with the values and needs of the patient. When care decisions are made, the values about the possible outcomes both desired and undesired -- for the patient and others must be weighed. Because health care resources have limits, the values and needs of an individual patient may have to be reconciled with the values and needs of others in the community. Value conflicts, moreover, may exist within groups of patients, providers and community members as well as between these groups. In all these circumstances, conflicts of personal, provider and societal values must be identified and resolved to determine what should be done. Evidence-based practice brings some of the value conflicts about care into sharper focus because of the standards set for clinical decision-making. First, care should be effective. Second, care should be efficient. Third, care decisions should incorporate the patient s values. The use of should language alerts us 8 that these standards are actually explicit provider values incorporated into the evidence-based practice paradigm. Evidence, which is objective and observable, is brought to bear to achieve goals that are valued subjectively. Effectiveness Effective care is care that achieves desirable health outcomes. While evidence can tell us to what extent any diagnostic test or therapy achieves a specified outcome, the desirability of that outcome is value-laden. Patients, providers and society would generally agree that preserving life is a desirable outcome of health care, but what if that preservation comes at the cost of continuing severe pain? Such questions suggest that we implicitly recognize varying levels of desirability, with some outcomes being more valued than others. Whenever outcomes are being ranked in terms of desirability or value, value conflicts may arise. Is length of life more valuable than quality of life? Is regaining function more valuable than relieving pain? Are outcomes for some classes of patients, for example healthy newborns, more valuable than outcomes for others, for example chronically ill elders? Who should make decisions about the relative value of outcomes? Patients? Health care providers? Family members? Society in general?

In the United States, the state of Oregon proposed an unusual approach to health care insurance coverage 1. Faced with a large number of persons who could not afford health care insurance and a limited budget for funding government-supported coverage, Oregon policy makers decided to provide care funding on the basis of procedures, not people. The intent was to provide coverage for all persons in need, not just the poorest, but to limit coverage for everyone to treatments which were most effective. To accomplish this goal, the Oregon Health Services Commission established a prioritized list of diagnosis and treatment pairs and ranked those pairs according to their effectiveness. State lawmakers then determined where a line would be drawn in the rankings, separating therapies that would receive insurance reimbursement (above the line) from those that were considered not valuable enough to pay for (below the line). The Oregon Health Plan was never fully implemented 2, but the priority list offers an example of one set of explicit societal values for effectiveness. Table 1 presents the Oregon Health Plan rankings for seventeen general service categories 3. The rankings combine values about the outcomes of treatment (full recovery from an acute, potentially fatal illness is valued over return to previous health status from an acute, non-fatal illness) with values about the recipients of treatment (preventive care for children is valued over preventive care for adults). Individual patients and providers may or may not agree with the societal values embodied in the Oregon Health Plan rating scheme, but the choices illustrate the dimensions of the moral complexity of defining outcomes for effectiveness. Should outcomes for the person with the most immediate need for care be valued more or less than outcomes for the person who is likely to Table 1 Rankings of seventeen service categories under the Oregon Health Plan Rank Category Outcome Essential Services 1 Acute fatal Treatment prevents death, with full recovery 2 Maternity care Maternity and most newborn care 3 Acute fatal Treatment prevents death, without full recovery 4 Preventive care for children Example: immunizations 5 Chronic fatal Treatment improves lifespan and quality of life 6 Reproductive services Example: contraceptive management 7 Comfort care Palliative therapy for conditions in which death is imminent 8 Preventive dental care Example: cleaning and fluoride applications 9 Proven effective preventive care for adults Example: mammograms Very important services 10 Acute nonfatal Treatment causes return to previous health status 11 Chronic nonfatal One-time treatment improves quality of life 12 Acute nonfatal Treatment without return to previous health status 13 Chronic nonfatal Repetitive treatment improves quality of life Services valuable to certain individuals 14 Acute nonfatal Treatment expedites recovery from self-limiting condition 15 Infertility services Example: in-vitro fertilization 16 Less effective preventive care for adults Example: screening of nonpregnant adults for diabetes 17 Fatal or nonfatal Treatment causes minimal improvement in quality of life Source: United States Office of Technology Assessment 3. 9

achieve the greatest health gains as a result of care? How should outcomes for acute, chronic and potential health threats be ranked in value? Is care to achieve temporary outcomes only valued when permanent outcomes cannot be achieved? How consistently must care achieve a desired outcome to be valued as effective? As we discuss these issues, values conflicts between and among patients, providers and society are likely to emerge. Efficiency Efficient care is care that makes the best possible use of resources to achieve desirable outcomes. The implicit societal definition for best in this context means using the fewest resources possible to achieve an acceptable level of outcome. Ethical debates about the value of health and life are not unique to evidence-based practice. Whenever a society decides that access to health care should not be completely limited by the individual s ability to pay for that care, value conflicts are likely to arise: How much of my money is your health worth? How much of your money is my health worth? Who needs to benefit from the desired health outcomes to justify expenditure of shared resources? These are ethical questions that often inform political decision-making. The explicit evidence-based practice standard of efficiency, however, leads to a consideration of what resources and whose resources will be included in evaluating this goal. While patients, providers and society would generally agree that money paid directly for care from whatever source should be part of the measurement of efficiency, what other costs should be included? In a series of randomized clinical trials, Brooten and associates 4 have demonstrated that a model of transitional care managed by advanced practice nurses safely reduces length of hospital stay and overall medical costs for selected high risk patient groups. The groups studied included women with high-risk pregnancies, low birth weight infants, and elders with cardiac disease or other common health problems. The hospital and physician charges for inpatient care were considered as evidence for the cost-effectiveness (efficiency) of this model, as were medical insurance payments for services following hospital discharge. Costs of family caregiving following discharge were not considered. We cannot determine, therefore, whether any of the savings claimed for this model are really only shifts from use of health care system resources to use of family resources when patients are discharged early or managed at home. Suppose, for example, that a woman had to take unpaid leave from her job to provide care for a frail elderly relative, who is discharged home earlier under the transitional care model. Considering the loss of family income, there is apt to be a value conflict between this patient s family and providers about the efficiency of this model. The nature of evidence introduces an additional dimension into considerations of efficiency for disease screening programs, like mammography for early detection of breast cancer. Evidence represents generalized experience; that is, it tells us what the likely benefits and costs of any intervention will be across a group of individuals. Evidence cannot, however, allow us to identify with complete certainty which specific individuals will reap the benefits and which ones will bear the costs. Thus, societal and provider values about resource use in general may be in conflict with those of individual patients. The recent change in recommendations of the United States Preventive Services Task Force (USPTF) about screening mammography for women in their forties illustrates this dilemma 5. In essence, the task force concluded, following review of current evidence, that routine annual mammography was effective, but not efficient, for early detection of breast cancer among women in this age group. This recommendation is consistent with societal and provider values about what counts as efficient use of common resources for other health screening activities. Most of us, however, know at least one woman whose breast cancer was successfully treated because it was detected by screening mammogram done when she was in her forties. For what values does a care provider, making recommendations to a patient in situations like these, advocate? Those of society? Those of the individual patient? Incorporating patient values There are many stakeholders in defining health care effectiveness and efficiency. The Oregon prioritized list was developed on the basis of health policy research and public input 1. The USPTF is funded by an agency of the United States federal government, but the members are primary care physicians and nurses who are not government employees. Partners of the task force include organizations representing health insurance plans and health care professionals 6. Brooten s research on transitional care models was funded by grants from 10

another United States federal government agency 4. Broadly, these stakeholders represent provider and societal values with particular input from those who collect and allocate resources for health care. Any guidance for clinical decision-making, whether explicitly evidence-based or not, embodies implicit or explicit provider and societal values about the goals and means of providing appropriate care. For evidence-based practice guidelines, the values are clear: effectiveness and efficiency. Ideally, an evidence-based practice guideline will clearly identify the goals of care and the persons consulted in establishing those goals. Were the goals identified by knowledgeable care providers? Were patients and families consulted? Similarly, the resources considered in determining efficiency should be identified. Before care recommendations developed in one setting can be implemented in a different setting, it is important to consider whether the personal, provider and societal values for outcomes and resource use in the new setting are consistent with those in the original setting. If not, analysis of the evidence may lead to different conclusions about the way care should be provided. Evidence-based practice includes an explicit value that the patient s values should be incorporated into clinical decision-making. The extent to which patient values should influence the final decision, however, may be a source of patient, provider or societal values conflict. Many evidence-based practice guidelines include rating schemes for the strength of the recommendations, based on the strength of the evidence and the amount of expected benefit to patients. When evidence about a service is rigorous and consistent and the benefit is large and very likely, care providers are encouraged to offer or provide the service routinely. Routine provision means that providers do not actively solicit discussion of individual patient values. In essence, a provider value about the importance of the evidence conflicts with and overrules the provider value about incorporating the patient s values. When the evidence is less rigorous and consistent and the net benefit small, the patient s values about specific harms and benefits may be the deciding factor in the decision. Care providers are then expected to initiate a discussion with the patient to determine what those values are. The strength of recommendation for the current USPTF guideline for women in their forties about screening mammography falls into this discuss category 5. The provider and societal value to incorporate patients values in clinical decision-making implies a further ethical obligation, that of informed consent. What evidence does a patient need to have, in order to make an informed decision about his/her care? Evidence about efficiency? Evidence about effectiveness, only? Patients tend to interpret infrequent outcomes as more likely when they are presented in terms of relative risk (risk ratio) rather than absolute risk (number needed to treat NNT) 7, so even completely accurate evidence can be delivered in ways that may influence patients value judgments. The effect of combined (estrogen and progestin) hormone therapy in preventing hip fractures for postmenopausal women in the large Women s Health Initiative clinical trial offers an example 8. Women who received combined hormone therapy reduced their risk of hip fracture during the five year follow-up period by 33%, compared to women who did not. It is equally accurate to report that 200 women needed to take combined hormone therapy to prevent one hip fracture in that period. Which presentation of the evidence is more likely to influence a menopausal woman to seek combined hormone therapy? Is the care provider ever justified in biasing the presentation of evidence on the basis of his/her own personal values? On the basis of provider or societal values? If so, does it matter whether the conflicting values are related to efficiency, rather than effectiveness? Ethical dilemmas are resolved by reference to ethical standards, identification and consideration of the conflicting values of all those with interests at stake, and application of some decision rule. Common decision rules are do no harm and greatest good for the greatest number. Empirical evidence is unlikely ever to resolve an ethical dilemma. The stated values of evidence-based practice, however, form a useful framework for defining and discussing the nature of value conflicts about care. When we have identified differences of opinion about the goals of care, the valuing of resources for care and the inclusion of patients values into decision making, we have made significant progress toward understanding the viewpoints of all the stakeholders in a ethical dilemma. 11

References 1. Bodenheimer T. The Oregon Health Plan lessons for the nation (first of two parts). NEJM 1997;337:651-655. 2. Saultz JW. Defining basic health benefits: Lessons learned from the Oregon Health Plan. Fam Med 2008;40(6):433-437. 3. United States Office of Technology Assessment. Evaluation of the Oregon Medicaid Proposal. Washington (DC): The author; 1992. 4. Brooten D, Naylor MD, York R, Brown LP, Munro BH, Hollingsworth AO, et al. Lessons learned from testing the Quality Cost Model of Advanced Practice Nursing (APN) Transitional Care. J. of Nurs. Schol. 2002;34(4):369-375. 5. United States Preventive Services Task Force. Screening for breast cancer. [document on the internet]. Washington (DC): Agency for Healthcare Research and Quality; 2009. [updated 2009 December; cited 2010 April 6]. Available from http://www.ahrq.gov/clinic/uspstf/uspsbrca.htm. 6. United States Preventive Services Task Force. About USPSTF. [document on the internet]. Washington (DC): Agency for Healthcare Research and Quality; 2010. [updated 2010 January; cited 2010 April 7]. Available from http://www.ahrq.gov/clinic/uspstfab. htm. 7. Grace, J. Essential skills for evidence-based practice: statistics for therapy questions. J. Nurs Sci 2010; 28(1):12-18. 8. Cauley JA, Robbins J, Chen Z, Cummings SR, Jackson RD, et al. Effects of estrogen plus progestin on risk of fracture and bone mineral density: the Women s Health Initiative randomized trial. JAMA 2003; 290:1729 38. 12