Public Reporting in Health Care: How Do Consumers Use Quality-of-Care Information? (original) (raw)

Consumer Use of Provider Quality Report Cards

Medical Care, 2019

Objective: The objective of this study was to measure the dissemination of comparative provider quality information (CPQI) and evaluate its impact on consumers’ awareness and use of CPQI. Data Sources: Two-period, random-digit-dial panel survey of chronically ill consumers residing in 14 regions of the United States; summaries of CPQI dissemination activities of regional multistakeholder alliances; and the LexisNexis Academic and Access World News databases. Study Design/Methods: Fixed effects regression to isolate the effect of CPQI producers’ dissemination activities and the print media’s CPQI coverage on chronically ill consumers’ self-reported awareness and use of CPQI. Principal Findings: Direct CPQI dissemination had no overall effect on either awareness or use of CPQI. One unit increase in the media coverage of an Aligning Forces for Quality (AF4Q) multistakeholder alliance report increased consumer awareness and use of CPQI by 1.4 percentage points (P=0.049) and 1.1 percenta...

Consumer Information about Health Plan Quality: Evidence Prior to the National Medicare Education Program

The Center for Medicare & Medicaid Services (CMS) initiated the National Medicare Education Program (NMEP) in 1998, aiming to collect information of quality from contracted managed care plans and disseminate it to Medicare beneficiaries. Before evaluating these CMS efforts, it is necessary to understand what quality information was publicly available before the NMEP, how such information affected Medicare enrollment during pre-NMEP periods, and how such information correlated with the information collected by CMS. This paper answers these questions by examining the publicly available information from the National Committee of Quality Assurance (NCQA). Specifically, we find that (1) CMS efforts provide extra information on managed care quality but do not replace the public-accessible NCQA information; (2) although NCQA information already had a strong correlation with Medicare enrollment during pre-NMEP periods, it was not utilized to the full extent. In particular, publicly released NCQA data on plan performance contributed to the enrollment shift from fee-for-service to managed care, but did not draw clear distinction among competing managed care plans. These findings suggest that NMEP may have great potential in separating good managed care plans from bad ones, but will have a limited ability in generating further switches from fee-for-service to managed care.

Is Anyone Paying Attention to Physician Report Cards? The Impact of Increased Availability on Consumers' Awareness and Use of Physician Quality Information

Health services research, 2016

To determine if the release of health care report cards focused on physician practice quality measures leads to changes in consumers' awareness and use of this information. Data from two rounds of a survey of the chronically ill adult population conducted in 14 regions across the United States, combined with longitudinal information from a public reporting tracking database. Both data were collected as part of the evaluation for Aligning Forces for Quality, a nationwide quality improvement initiative funded by the Robert Wood Johnson Foundation. Using a longitudinal design and an individual-level fixed effects modeling approach, we estimated the impact of community public reporting efforts, measured by the availability and applicability of physician quality reports, on consumers' awareness and use of physician quality information (PQI). The baseline level of awareness was 12.6 percent in our study sample, drawn from the general population of chronically ill adults. Among tho...

The Effect of Publicized Quality Information on Home Health Agency Choice

Medical care research and review : MCRR, 2016

We examine consumers' use of publicized quality information in Medicare home health care markets, where consumer cost sharing and travel costs are absent. We report two findings. First, agencies with high quality scores are more likely to be preferred by consumers after the introduction of a public reporting program than before. Second, consumers' use of publicized quality information differs by patient group. Community-based patients have slightly larger responses to public reporting than hospital-discharged patients. Patients with functional limitations at the start of their care, at least among hospital-discharged patients, have a larger response to the reported functional outcome measure than those without functional limitations. In all cases of significant marginal effects, magnitudes are small. We conclude that the current public reporting approach is unlikely to have critical impacts on home health agency choice. Identifying and releasing quality information that is m...

Role of consumer information in today's health care system

Health care financing review, 1996

This overview discusses articles published in this issue of the Health Care Financing Review, entitled "Consumer Information in a Changing Health Care System." The overview describes several trends promoting more active consumer participation in health decisions and how consumer information facilitates that role. Major issues in developing consumer information are presented, stressing how orientation to consumer needs and use of social marketing techniques can yield improvement. The majority of the articles published in this issue of the Review discuss different aspects of information for choice of health plan, ranging from consumer perspectives on their information needs and their comprehension of quality indicators, to methods used for providing such information, such as direct counseling and comparative health plan performance data. The article concludes with thoughts on how we will know if we succeed in developing effective consumer health information.

Consumer perspectives on information needs for health plan choice

Health care financing review, 1996

The premise that competition will improve health care assumes that consumers will choose plans that best fit their needs and resources. However, many consumers are frustrated with currently available plan comparison information. We describe results from 22 focus groups in which Medicare beneficiaries, Medicaid enrollees, and privately insured consumers assessed the usefulness of indicators based on consumer survey data and Health Employer Data Information Set (HEDIS)-type measures of quality of care. Considerable education would be required before consumers could interpret report card data to inform plan choices. Policy implications for design and provision of plan information for Medicare beneficiaries and Medicaid enrollees are discussed.

Americans’ Growing Exposure To Clinician Quality Information: Insights And Implications

Health Affairs, 2019

For two decades, various initiatives have encouraged Americans to consider quality when choosing clinicians, both to enhance informed choice and to reduce disparities in access to highquality providers. The literature portrays these efforts as largely ineffective. But this depiction overlooks two factors: the dramatic expansion since 2010 in the availability of patients' narratives about care and the growth of information seeking among consumers. Using surveys fielded in 2010, 2014, and 2015, we assessed the impact of these changes on consumers' awareness of quality information and sociodemographic differences. Public exposure to any quality information doubled between 2010 and 2015, while exposure to patient narratives and experience surveys tripled. Reflecting a greater propensity to seek quality metrics, minority consumers remained better informed than whites over time, albeit with differences across subgroups in the types of information encountered. An education-related gradient in quality awareness also emerged over the past decade. Public policy should respond to emerging trends in information exposure, establish standards for rigorous elicitation of narratives, and assist consumers' learning from a combination of narratives and quantified metrics on clinician quality.