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Volume
3:
No. 3, July 2006
REVIEW
A Review of Studies Examining Stated Preferences for Cancer Screening
Kathryn A. Phillips, PhD, Stephanie Van Bebber, MSc, Deborah Marshall, PhD, Judith Walsh, MD, MPH, Lehana Thabane, PhD
Suggested citation for this article: Phillips KA, Van Bebber S, Marshall D, Walsh J, Thabane L. A review of studies examining stated preferences for cancer screening. Prev Chronic Dis [serial online] 2006 Jul [date cited]. Available from: URL:
http://www.cdc.gov/pcd/issues/2006/
jul/05_0208.htm.
PEER REVIEWED
Abstract
Introduction
Stated preference studies for cancer screening programs are used to understand how the programs can be improved to maximize usage. Our objectives were to
conduct a systematic review of stated preference studies for cancer screening,
identify gaps in the literature, and determine which types of research should be conducted in the future.
Methods
We considered all studies in the PubMed database through May 2005 that measured utility-based stated preferences for cancer screening using contingent valuation or conjoint analysis. We abstracted data on 1) study characteristics and 2) study results and policy implications.
Results
We found eight (of 84 identified) preference studies for cancer screening. The most commonly studied cancer was breast cancer, and the most commonly used method was contingent valuation. We found no studies
for prostate cancer or physician preferences. Studies demonstrated that although individuals are able to state their preferences for cancer screening, they
do not weigh test benefits and harms, and a significant percentage would choose to have no screening at all. Several studies found that test accuracy and reduction in mortality risk were important
for determining preferences.
Conclusion
Few studies of cancer screening preferences exist. The available studies examine only a few
types of cancer and do not explore practice and policy implications in depth. The results
of this review will be useful in identifying
the focus of future research, identifying which screening methods may be more preferred to increase use of the programs, and developing interventions and policies that could facilitate
informed and shared decision making for screening.
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Introduction
In the United States, several types of cancer screening have been recommended, and increasing the number of individuals who receive recommended cancer screenings is a health priority. Therefore, it is important to understand
individual screening preferences and how the preferences can be used to develop future programs and policies. The objectives of this study
were as follows:
- Conduct a systematic review of the PubMed database for stated preference studies on cancer screening
by using contingent valuation or conjoint analysis approaches to identify the numbers and types of published studies
- Identify gaps in the literature and assess which types of research should be conducted in the future to better assess the influence of
individual preferences on cancer screening decisions, clinical practice, and health policy.
Previous studies have found that patient preferences for health care interventions can have a large impact on their willingness to use services and on the resulting outcomes (1). Understanding preferences is also important because of the increasing emphasis on involving patients in decisions about their care. However, measurement, or valuation, of individuals’ preferences for
health care interventions such as cancer screening programs is a significant challenge for health care researchers because this type of information is typically obtained from surveys. The most commonly used approaches to valuation are attitude surveys, which ask respondents to rate their opinion about individual
health care services, and utility-based preference surveys, which use more complex
approaches that are based on economic theory. Although the terms attitudes and preferences are occasionally used interchangeably, the term preferences in this article refers to preferences based on economic theory — patients have preferences for health care, and they seek to maximize usefulness
within the constraints of a budget. Understanding preferences,
rather than simply attitudes, is particularly important for understanding the use of cancer screening because preference studies provide insights into how individuals
weigh harms and benefits of tests and quantify preferences into dollars.
This review focuses on stated preference studies — or studies of cancer screening preferences that were measured using a theoretically based, economic approach
and that used contingent valuation or conjoint analysis approaches. To our knowledge, no review of these types of preference studies of cancer screening has been done. The results will be useful in identifying areas for future
research, identifying which screening methods may be preferred to increase usage, and developing interventions and policies that could facilitate informed and shared decision making
about screening.
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Methods
Definition of preference study
Several approaches are available for measuring preferences, and much confusion in the literature exists about the terms used to describe different types of studies. In this study, we limited our analyses to utility-based preference studies using contingent valuation surveys (also called willingness-to-pay surveys) or conjoint analysis surveys (also called choice format stated
preferences or discrete choice experiments). Thus, we did not include attitude studies or preference studies used to develop health-state utility weights for use in quality-adjusted life years or other utility approaches. Contingent valuation and conjoint analysis approaches are often the most relevant to cancer screening and thus are the focus of our study. These methods measure the
value of screening programs and the process of care as well as outcomes, not just health states. Furthermore, the use of these methods is increasing because of their strengths in realistically measuring choices
and the harms and benefits of screening.
Contingent valuation studies use questionnaires to estimate the willingness of respondents to pay for projects or programs, typically public programs for which there is no defined market. For example, a contingent valuation of preferences for colorectal cancer screening would describe a possible screening program and ask individuals how much they would be willing to pay
for such a
program. Conjoint analysis studies involve comparing hypothetical scenarios by ranking, rating, or choosing scenarios. For example, respondents may be asked to choose from test A and test B after each test is described
by using a combination of attributes. A conjoint analysis of preferences for colorectal cancer screening might describe different testing methods in terms of process, accuracy, and
cost. Examples of each type of survey are included in Appendices A and B.
Inclusion and exclusion criteria
We included all studies that measured stated patient preferences for cancer screening using conjoint analysis or contingent valuation. Studies that used simple rating scales to measure attitudes or studies that measured utility weights using time trade-off, standard gamble, or rating scales were excluded. A study was considered to be a cancer screening study if it examined a cancer screening
program, test, or method. Studies that focused primarily on methodology of preference measurement, examined preferences for treatment, or focused on diagnosing disease characteristics (such as screening known cancers for genetic mutations) were excluded.
Data source and search strategy
We searched the PubMed (Medline) database for studies that measured patient preferences for cancer screening, using several search strategies to identify all potentially relevant studies. Our search included all English articles through May 2005 with no limitations on start date. To identify search terms, we first reviewed the index for several known studies of quantitative preference
measurement (1-4). Preliminary search results suggested that study indexing is not standardized, possibly because neither terms for preference measurement (e.g., conjoint analysis) nor the term preference are associated with a unique medical subject heading (MeSH) term
in PubMed. Therefore, we combined MeSHs for the four key components of interest. The search strategy combined the following
terms by using Boolean operators — OR within the four categories and AND across the categories:
- Cancer terms. We used the MeSH term neoplasm OR the keyword cancer.
- Screening terms. We used the MeSH terms mass screening OR mass screening/economics and keywords cancer OR screening.
- Preference terms. No MeSH term for preferences exists. Thus, we used a combination of the MeSH terms patient satisfaction/economics OR patient satisfaction/statistics & numerical data OR consumer satisfaction/economics OR consumer satisfaction/statistics & numerical data OR health knowledge, attitudes, practice as well as the keywords
preference(s) OR attitudes.
- Quantitative methods. We used one MeSH term, choice behavior, and keywords conjoint analysis OR contingent valuation OR stated preference OR discrete choice OR willingness to pay to capture the quantitative methods used to measure preferences.
Study selection and coding
Two authors (SVB and KAP) independently reviewed titles and abstracts, and all potential articles were obtained for additional review. The two authors also conducted all data abstraction and reached consensus through discussion
about any disagreement. We abstracted two types of information: 1) study descriptions (cancer site, method used, objectives, and population), and 2) study results and
policy implications.
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Results
We found eight stated preference studies for cancer screening (of 84 identified) (Figure). Three fourths of the studies were excluded based on the abstract or title either because they were not stated preference studies (n = 24) or because they were not relevant to cancer screening (n = 37). Fifteen of the remaining 23 citations were subsequently excluded after a full review: six were not
stated preference studies and one was not relevant to cancer screening. We also excluded eight studies, even though they were cancer screening preference studies, because they focused on methodological issues.
Figure. Flow chart of PubMed database search strategy and results. [A text description of this chart is also available.]
Table 1 describes the included studies (4-11). The most commonly studied types of cancer were breast cancer (n = 4) and colorectal cancer (n = 3). We found no preference studies for prostate cancer screening, even though prostate cancer is the most common cancer among men, and preferences are particularly important because no consensus exists on the appropriateness of prostate cancer
screening. The most commonly used method to assess preference was contingent valuation to determine willingness to pay (n = 5). Most studies administered surveys to a general population (n = 6).
Several policy implications emerged from the study results (Table 2). Studies demonstrated that individuals were able to provide meaningful responses and state their preferences for cancer screening, although many respondents did not consider the potential harms of a particular screening test, and a significant percentage would not choose any type of screening (4,8). Several studies found that
test accuracy and a reduction in mortality risk were important for determining preferences (4,7,9). Researchers generally noted that preference studies could provide useful information for clinicians and policymakers in determining the net benefits of screening programs and which screening types may be most preferred, but none of the studies explored clinical or policy implications in detail.
Several studies showed that test accuracy plays an important role in
preference for screening (4,7,9). Furthermore, our colorectal cancer screening studies
have found that sensitivity (i.e., the ability of the test to identify those with
cancer) is more highly valued than specificity (i.e., the ability of the
test to correctly identify those without cancer) (12). The study by Salkeld et
al (8) highlights another important finding: many people may prefer no
screening at all, thus the currently available methods of screening may actually
provide disutility to some individuals (i.e., they may think the tests
cause more harm than good).
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Discussion
Only a few preference studies for cancer screening have been published; they assess few types of cancer and have a limited range of questions. We were surprised that we did not identify any studies of physicians’ predictions about their patients’ preferences. Physician recommendations for screening have consistently been found to be strong predictors of
screening usage, so it is important to understand how well physicians’ views of preferences actually reflect patients’ preferences. We found in
our ongoing study of colorectal cancer screening that physicians’ views of patients’ preferences were not congruent with what patients reported they preferred (12). In particular, physicians were much more likely to predict that patients
would prefer no screening when the patients actually preferred screening, which may explain why some physicians do not always offer screening to their patients.
Our review suggests that although preference studies can provide useful findings that can improve our understanding of cancer screening, more research needs to be completed. We found that test accuracy plays a role in screening preference. The preference for sensitivity over specificity suggests that individuals tend
to prefer false-positive results over false-negative results. This may help
explain the willingness of individuals to receive complete-body computed tomography scans and for women aged 40 to 50 years to undergo mammography screenings, despite the high rate of false-positives for such procedures. Schiffner et al (9) confirm that patients may not understand the potential drawbacks of having false-positive results. This finding by Salkeld et al (8) that many people prefer
no screening is important from a methodological perspective because it suggests that preference surveys should consider measuring not only preferences for screening but also preferences for
no screening.
Our findings also suggest that it may be necessary to develop new methods of screening that better address patient preferences. Although we recognize the ongoing debate about whether the goal of preventive public health programs is to maximize participation in screening or maximize the usefulness of the screening, our study did not address these issues. Regardless, preference information can be
useful for meeting either goal.
None of the studies explored in detail the implications of their results for clinical practice and health policy. This research gap is surprising given
the current emphasis on more patient participation and shared, or informed, decision making between patients and providers. For example, some guidelines for mammography screening for women aged 40 to 50 years recommend that screening decisions be
based on preferences and shared decision making. In general, research on informed decision making and decision aids is based on attitude data rather than true preference data, although preference data could provide additional insight into what patients want and how to elicit preferences for use in decision making. Thus, one key area for future research is the development of mechanisms
that enable
the use of preference data. During the development of such mechanisms, researchers will need to consider how to simplify the often time-consuming surveys
used to measure preferences and develop efficient ways to use preference data in clinical practice. Similarly, preferences need to be incorporated into health policies. For example, our finding that many people would
prefer colonoscopy over other forms of colorectal cancer screening provides important information, because many private insurers and government health systems do not currently provide coverage for colonoscopies (13).
Our study has limitations. Our literature search may not have identified potentially relevant studies that have not been indexed in PubMed
or published in English. In addition, because the studies we found had varying
methods (e.g., contingent valuation, conjoint analysis), research questions, and
cancer types, we were unable to conduct a quantitative analysis such as a
meta-analysis. We excluded other types of utility studies
because they were not as relevant to this review, but future researchers could examine these studies.
Although we identified only a few studies of cancer screening preferences, the published studies have provided some useful results. More research is needed to identify preferences to help clinicians and decision makers improve screening programs.
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Acknowledgments
We are grateful for comments from F. Reed Johnson at Research Triangle Institute and John Marshall at McMaster University. This work was supported by funding from the Canadian Institutes for Health Research (MOB-53116), the National Cancer Institute (R01 CA 10184), and the Agency for Healthcare Research and Quality (P01 HS10771 and P01 HS 10856).
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Author Information
Corresponding Author: Kathryn A. Phillips, University of California, San Francisco, 3333 California St, UCSF Box 0613, San Francisco, CA 94143-0613. Telephone: 415-502-8271. E-mail:
phillipsk@pharmacy.ucsf.edu.
Author Affiliations: Stephanie Van Bebber, Judith Walsh, University of California, San Francisco, San Francisco, Calif; Deborah Marshall, McMaster University and St. Joseph’s Hospital,
Hamilton, Ontario, Canada; Lehana Thabane, McMaster University, Hamilton,
Ontario, Canada.
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