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The Healthcare Effectiveness Data and Information Set, more commonly called HEDIS, consists of compiled reports from managed-care organizations concerning their health plan performance on a broad range of clinical and nonclinical measures. The National Committee for Quality Assurance (NCQA) developed and released the initial version of the measures in 1993. Although most participation in HEDIS is voluntary, more than 90% of U.S. health plans submit HEDIS data, in part to increase their competitiveness but also, often, as part of accreditation or certification activities. Health services researchers also use HEDIS measures to conduct studies of the access, cost, quality, and outcome of care.

HEDIS measures are divided into eight categories: (1) effectiveness of care, (2) access to and availability of care, (3) satisfaction with the experience of care, (4) use of services, (5) cost of care, (6) health plan descriptive information, (7) health plan stability, and (8) informed-care choices. Of these, effectiveness of care is the largest category and includes measures dealing with highly specific standards of care such as appropriate medication for asthma patients and the use of medical-imaging studies for lower-back pain. Measures in other categories evaluate other aspects of patients' experiences (e.g., the number of customer service calls abandoned) and the business aspects of the health plans (e.g., financial stability). Over time, HEDIS has evolved to meet changing standards of healthcare and in response to regulatory changes, and NCQA now publishes changes to HEDIS measures on an annual basis.

Development and Evaluation of HEDIS Measures

NCQA uses an ongoing process to develop new HEDIS measures, evaluate existing ones, and retire those that have outlived their usefulness. Proposals for new measures first are examined through expert Measurement Advisory Panels (MAPs) tasked with evaluating them using three criteria: (1) relevance (e.g., health importance, cost-effectiveness, and potential for improvement); (2) feasibility (e.g., cost and ability to be audited); and (3) scientific soundness (e.g., basis in evidence and reproducibility). Once approved by an MAP, the proposed measures move through a process of technical development and field testing before being released for public comment. Measures subsequently reviewed and accepted by NCQA's Committee on Performance Measurement (CPM) are added as first-year measures in the new HEDIS set. NCQA does not provide public reporting on new measures during their first-year status, allowing time for reporting organizations to evaluate the initial results and address any technical issues. In subsequent years, MAPs evaluate the measures under a continuous improvement process, which may result in their alteration or removal from the HEDIS set.

New Measurement Controversies

Although NCQA earns broad respect for its measurements, its processes sometimes draw criticism. For example, the 2006 addition to HEDIS (after 5 years of debate) of specific blood pressure and glycemic-control outcome benchmarks for patients with diabetes mellitus met with resistance from some areas of the medical establishment. Most clinical HEDIS measures focus on process rather than clinical benchmarks: Some felt that adding such specific measurements failed to adequately account for comorbidities and other individual patient variations.

Uses of NCQA's Published HEDIS Reports

NCQA makes HEDIS information available in a variety of forms to meet the needs and goals of its constituencies, chiefly accreditation and certification activities, delivering information to organizational purchasers of health plans, and delivering information to healthcare consumers.

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