Chapter 6. AHRQ Program Objectives (continued)

Goal 3—Efficiency

AHRQ continues to support research on ways to overcome barriers to care, provide more efficient and effective care, and improve access to care for all Americans. Research in these areas has become more important than ever, as health care costs continue to rise.

Expenditures for health care constitute a substantial portion of the Nation's gross domestic product. For example, data from AHRQ's Medical Expenditure Panel Survey (MEPS) show that total outpatient drug expenses for the Nation's community population grew from $65.3 billion in 1996 to $94.2 billion in 1999, an increase of 44 percent.

In addition, MEPS data show that employee contributions for employer-sponsored health insurance are also on the rise. In 2001, average employee contributions were $498 for single health insurance coverage and $1,741 for family coverage. Employee contributions increased 10.8 percent and 7.8 percent, respectively, over the 2000 levels, continuing the trend from previous years.

Given the increasing costs of health care, it is vitally important for us to find ways to become more efficient and effective in providing high-quality health care. AHRQ research is at the forefront of this effort to improve health care efficiency and effectiveness. For example:

Surgeon's Experience Linked to Patient Outcomes

Seeking out surgeons who frequently perform certain cardiac or cancer-related operations may increase older patients' odds of surviving major surgery, according to this recent AHRQ-supported study.

Previous research has suggested that outcomes are better when certain types of surgery are performed in high-volume hospitals, but little is known about the relationship between hospital volume and surgeon volume in relation to patient death rates. This study was conducted by researchers at Dartmouth Medical School.

Addressing Challenges to Care

The combination of rapid advances in medical knowledge and increased use of evidence-based decisionmaking in medicine holds great promise for improving health care. Developments in genomics, pharmaceuticals, informatics, and other technologies promise increased longevity and better health and functioning. Health care, however, can only be as good as the systems that provide it.

Much of the health care provided in the United States is delivered within large and often fragmented systems with complex funding streams. While the United States has an excellent health care system in many ways, it also exhibits waste and inefficiency which in turn exacerbates health care costs, affects affordability, and creates access problems. Low-income individuals, from both rural and urban areas, and those who lack health insurance are particularly likely to experience these problems. In addition, the current health care system lacks the continuity of services that chronically ill patients need.

One byproduct of the current health care system is an increased incidence of injuries to patients from the care that is intended to help them. Problems with patient safety represent only a small part of the unfolding story of problems with quality in American health care. The current health care system also has an impact on other dimensions of quality, such as efficiency, effectiveness, equity, timeliness, and patientcenteredness.

In this complex and sometimes confusing health care marketplace, all participants in the health care system—employers, insurers, providers, consumers, and Federal and State policymakers—need objective, science-based information they can rely on to help them make critical decisions about health care costs and financing and ways to enhance access to care.

For many years, AHRQ has been supporting research to meet this need. The Agency addresses critical health policy issues through ongoing development and updating of nationally representative databases, the production of public use data products, and research analyses conducted by AHRQ staff and extramural researchers.

Impact of Payment and Organization on Cost, Quality, and Equity

In order to be successful, efforts to improve the quality and efficiency of health care in the United States must be based on a thorough understanding of how the Nation's health systems work and how different organizational and financial arrangements affect health care. AHRQ's research initiatives address these issues by asking questions such as:

To answer these and other related questions, AHRQ issued a Program Announcement on the effects of payment and organization on the cost, quality, and equity of health care. Examples of projects funded under this program announcement include:

Research on Lowering Health Care Costs

AHRQ has a broad portfolio of research focused on identifying ways to lower health care costs without negatively affecting the quality and safety of care. Particular attention is given to initiatives that have the potential to lower costs to the Medicare and Medicaid programs. Examples of findings from recent AHRQ research on lowering health care costs include:

Improving Access to Care

Identifying ways to improve access to care—particularly for low-income individuals, minorities, and other priority populations—has been a major focus for AHRQ research for many decades. Examples of AHRQ-supported research on access to care include:

Recent findings from AHRQ research on access to care include:

Factors Affecting Access To and Use of Hospice Care

Local preferences and factors other than market structure influence county differences in hospice use. Use of hospice care varied more than 11-fold across U.S. metropolitan statistical areas in 1996, but differences in the major components of the health care infrastructure—such as the availability of hospitals, nursing homes, or doctors—did not explain the differences in hospice use.

Rather, the difference seemed to be due to local factors, such as local preferences, differences in the mix of services available from local hospice providers, and differences in community leadership on end-of-life issues. Three demographic factors were significant: individuals living in counties with more white collar employees, people living in the least densely populated counties, and those living in counties with relatively more cancer deaths were more likely to use hospice care.

Medical Expenditure Panel Survey

AHRQ's Medical Expenditure Panel Survey (MEPS) is the only national source for annual data on the specific health services that Americans use, how frequently the services are used, the cost of the services, and the methods of paying for these services. In addition to collecting detailed information from American households, MEPS also collects data from medical providers and establishments. As a result, the survey is unparalleled in its degree of detail.

MEPS is designed to help us understand how the growth of managed care, changes in private health insurance, and other dynamics of today's market-driven health care delivery system have affected, and are likely to affect, the kinds, amounts, and costs of health care that Americans use. No other survey provides the foundation for estimating the impact of changes on different economic groups or special populations such as the poor, elderly, veterans, the uninsured, or racial/ethnic groups.

Since 1977 when data from the first expenditure survey became available, AHRQ's expenditure surveys have been an important and unique resource for public and private-sector decisionmakers. Over the years, this rich data source has become more comprehensive and timely. Design enhancements have improved the survey's analytic capacities, allowing for analyses over an extended period of time with greater statistical power and efficiency. The ability of MEPS to examine differences in the cost, quality, and access to care for minorities, ethnic groups, and low-income individuals provided critical data for the National Healthcare Quality Report and the National Healthcare Disparities Report, which present baseline views of the quality of health care and differences in use of services.

Findings Based on MEPS Data

MEPS data have been used by researchers both within and outside the Federal Government to examine issues of importance to policymakers, consumers, and providers. For example, in a recent study published in Health Affairs, researchers used MEPS data to estimate the medical costs attributable to overweight and obesity and found that they may account for as much as 9.1 percent of total U.S. medical expenditures. In 2003, researchers also used MEPS data to:

According to new MEPS data released in 2003, expenses for outpatient prescribed medicines increased from $72.3 billion in 1997 to $103 billion in 2000. Specifically:

During the last few years, AHRQ has developed a series of statistical briefs using MEPS data. These briefs, which are on the MEPS Web site, offer timely statistical estimates on topics of current interest to policymakers, medical practitioners, and the public at large.

Topics in 2003 included smoking, asthma treatment, trends in antibiotic use among children, expenditures, and insurance. For example, more than 25 million Americans have been told by a physician or other health care provider that they have asthma according to data collected in 2000 by the MEPS. In the 12 months prior to their interview, 6.5 million adults and 3.2 million children had an asthma attack. Asthma attacks—caused by inflammation of the lower airways and obstruction of airflow—can vary from mild to life-threatening. Further, the data showed that:

MEPS Data are Comprehensive and Widely Used and Quoted

The Consumers' Checkbook 2003 Guide to Health Plans used MEPS data to display the level of expenses by health plan. According to the Guide, MEPS data were the most important data used to compare the likely dollar cost to the consumer by plan. Consumers' Checkbook is an independent, non-profit consumer authority that rates local service firms.

Collecting MEPS Data

AHRQ fields a new MEPS panel each year. Two calendar years of information are collected from each household in a series of five rounds of data collection over a 2-½-year period. These data are linked with additional information collected from respondents' medical providers and employers. This series of data collection activities is repeated each year on a new sample of households, resulting in overlapping panels of survey data.

The data from earlier surveys have quickly become a linchpin for the Nation's economic models and projections of health care expenditures and use. The level of detail these surveys supply permits the development of public and private-sector economic models to project national and regional estimates of the impact of changes in financing, coverage, and reimbursement, as well as estimates of who benefits and who bears the cost of a change in policy.

MEPS establishment surveys have been coordinated with the National Compensation Survey conducted by the Bureau of Labor Statistics through AHRQ's participation in the Inter-Departmental Work Group on Establishment Health Insurance Surveys. Based on the Department's survey integration plan, MEPS linked its household survey and the National Center for Health Statistics' National Health Interview Survey, achieving savings in sample frame development and enhancements in analytic capacity.

AHRQ has moved from conducting a medical expenditure survey every 10 years to following a cohort of families on an ongoing basis. Doing so has four primary benefits. It:

MEPS data are used:

In the public sector: Entities such as the Office of Management and Budget, the Congressional Budget Office, the Medicare Payment Advisory Commission, the Treasury Department, and State and local governments rely on MEPS data to evaluate health reform policies, the effect of tax code changes on health expenditures and tax revenue, and proposed changes in government health programs such as Medicare.

Since 2000, data on premium costs from the MEPS Insurance Component have been used by the Bureau of Economic Analysis to produce Estimates of the Gross Domestic Product (GDP) for the Nation. The GDP represents the total goods and services produced over a given period, usually 1 year.

In the private sector: MEPS data are used by many private businesses, foundations, and academic institutions—such as RAND, the Heritage Foundation, Lewin-VHI, and the Urban Institute—to develop economic projections.

By researchers: MEPS data are a major resource for the health services research community at large.

Public Use Data Files and Other MEPS Products

AHRQ ensures that MEPS data are readily available, consistent with privacy policies, for use in research and policymaking. MEPS data are released in a variety of ways:

Recent Key Findings from the MEPS Household Component
Recent Key Findings from the MEPS Insurance Component
Healthcare Cost and Utilization Project

As health care costs in the United States escalate and concerns about quality of care become more pronounced, the need for accurate and timely health care data has increased dramatically. Policy analysts, administrators, and the research community require comprehensive and precise data resources in order to evaluate cost, quality, and access to care. The AHRQ-sponsored Healthcare Cost and Utilization Project (HCUP) is a resource comprising a family of databases that meets this need for reliable data.

HCUP develops and maintains a family of health care databases, related software tools, support services, and products whose information resources are grounded in vital partnerships among Federal, State, and industry associations. HCUP databases integrate the data collected by State governments, hospital associations, private data organizations, and the Federal government (a mosaic of "Partners") to create a national health care information resource of hospital, ambulatory surgery center, and emergency department data. HCUP features the largest collection of hospital care data collected over a period of time in the United States. All-payer, encounter-level information is available beginning in 1988.

The multi-State databases contain discharge-level information in a uniform format designed to ensure patient privacy. The resulting HCUP databases facilitate research on a broad range of health policy and health services issues, including:

Because of their large size and scope, HCUP databases enable analyses, such as investigating specific medical conditions and procedures (including rare events); tracking use for population subgroups, such as minorities, children, women, and the uninsured; and analyzing different geographic levels (national, regional, State, and community) within the United States. To augment the HCUP databases, software tools and Web-based products are publicly available for use by audiences with varying levels of research experience.

The collaboration of Federal, State, and industry partners creates a mutually beneficial opportunity for sharing data and building a national resource. HCUP research benefits extend to a diversity of institutions and individuals:

Policy analysts: HCUP data enable policy analysts and decisionmakers to develop effective and informed recommendations on crucial health care policy issues such as cost, use, quality, and access to health care.

Hospital industry: HCUP provides hospital associations, hospitals, and provider alliances with access to national health care databases. Hospital industry members are able to make national comparisons of efficiency, cost, value, and quality of service.

Statewide data organizations: Participants in this national project can contribute to the health care knowledge base and reinforce the value of their data collection efforts. States are also able to compare their health care statistics to other States and to regional and national indicators. Those States that are just starting data collection programs may benefit from HCUP technical assistance and the experience of other organizations already collecting these data.

Researchers: The comprehensive data available in HCUP databases enable researchers to conduct health services research in many different areas, including but not limited to quality of care, medical practice patterns, and treatment outcomes.

HCUP databases include:

AHRQ expands the HCUP databases each year by adding new States that will improve national and regional representation and by expanding the number of partners that contribute ambulatory surgery and emergency department data. In the last year AHRQ added Minnesota, Nebraska, Rhode Island, and Vermont to HCUP. Each of the four new States supplied data beginning with the 2001 data year. AHRQ also added three new ambulatory surgery databases and three new emergency department databases. Currently, 33 Statewide data organizations participate in HCUP.

Over the past 2 years, AHRQ has implemented a multifaceted effort to make HCUP data more accessible to researchers and other interested users. A centerpiece of this effort is HCUPnet, an interactive tool for identifying, tracking, analyzing, and comparing statistics on hospital care. HCUPnet queries generate statistics in a table format using data from the NIS and SID databases for those States that have agreed to participate. New data have recently been added from the Kids' Inpatient Database (KID). Aggregate statistics from HCUPnet are made available to the public on the AHRQ HCUPnet Web site at http://www.ahrq.gov/data/hcup/hcupnet.htm.

Another means instituted by AHRQ to enhance access to HCUP data is the HCUP Central Distributor, which was developed by AHRQ to prepare and distribute HCUP data for use by researchers outside of AHRQ on behalf of participating HCUP partner organizations. Participation in the HCUP Central Distributor is voluntary, and it includes only the partner organizations that agree to release their HCUP data to public and private users.

Since September 2002, AHRQ has been building an HCUP user support infrastructure that includes telephone and E-mail access to technical support staff and a publicly available Web site that features database documentation and HCUP product information. The goal of HCUP user support is to increase awareness of the strengths and uses of HCUP data and to enhance the skills of those using HCUP data and tools for their work in research, education, and policy analysis.

In 2003, HCUP launched a new toll-free dedicated technical assistance phone line (1-866-290-HCUP) and a new dedicated E-mail service (hcup@ahrq.gov). A new Web site has also been established at http://www.hcup-us.ahrq.gov/home.jsp. This Web resource offers general information regarding the HCUP databases, available technical support, project contact information, and background information on the technical support team.

Other HCUP-related activities currently underway at AHRQ include the development of a new fact book that addresses potentially avoidable hospitalizations using the AHRQ Prevention Quality Indicators. This fact book will describe ambulatory care sensitive conditions—that is, conditions that usually can be avoided through timely and effective outpatient care. The fact book will use graphs and tables to describe these conditions, including priority conditions such as asthma, diabetes, congestive heart failure, and hypertension, as well as the incidence of low birthweight infants. Specifically, the fact book evaluates time trends between 1994 and 2000; variations across regions of the United States; and differences among priority populations, including children, the elderly, women, low-income individuals, and rural residents.

Another new resource is Care of Children and Adolescents in U.S. Hospitals, a fact book that examines hospital care for children and adolescents, providing insight into the types of conditions for which children are hospitalized, the types of procedures they receive, who is billed for the stays, the resource use associated with children's hospital stays, and where children are discharged to when they leave the hospital. The fact book begins with an overview of hospital care for children overall and, to put this care into perspective, compares information about children to information about adults' hospital stays. It then provides more detailed information for three major subgroups of pediatric hospital stays:

Use of HCUP Data

The HCUP databases are being used by a variety of Federal agencies and national health care organizations to examine practices and trends and guide health care decisionsmaking. For example:

Quality Indicators

AHRQ's Quality Indicators (QIs) are measures of health care quality that make use of readily available hospital inpatient administrative data, such as diagnoses and procedures, along with information on a patient's age, sex, source of admission, and discharge status. The first QIs were developed in the early 1990s and came out of HCUP through the data partnership among the Agency, the health care industry, and States. These original HCUP QIs, which were created in response to requests for assistance from State-level data organizations and hospital associations, enabled these entities to use their administrative data for quality improvement and tracking.

In preparation for the National Healthcare Quality Report, AHRQ worked in partnership with the University of California, San Francisco (UCSF)/Stanford Evidence-based Practice Center to refine, expand, and risk adjust these measures. The resulting updated AHRQ QIs include three modules: the Prevention Quality Indicators (PQIs), the Inpatient Quality Indicators (IQIs), and the Patient Safety Indicators (PSIs). The AHRQ QI software analyzes administrative data on inpatient stays to produce information about potentially avoidable adverse hospital outcomes such as postsurgical pneumonia, potentially inappropriate and over used hospital procedures such as cesarean section deliveries, and potentially preventable hospital admissions such as pediatric asthma. The AHRQ QIs are designed to highlight probable quality concerns, identify areas that need further study and investigation, and track changes over time. Users include hospitals, managed care organizations, business-health coalitions, researchers, and others at the Federal, State, and local levels. The software is available free on the AHRQ QI Web site at http://www.qualityindicators.ahrq.gov.

The first three AHRQ QI modules—the Prevention Quality Indicators (PQIs), the Inpatient Quality Indicators (IQIs), and the Patient Safety Indicators (PSIs)—include a total of 73 indicators. These QIs are designed for use with inpatient hospital discharge data and primarily apply to the inpatient setting. However, the PQIs are pertinent to outpatient care, since the indicators represent hospitalization rates for events that potentially could be prevented by improvements in access to and/or delivery of outpatient care.

The AHRQ QIs are being used by a variety of providers, purchasers, and State agencies as an integral part of quality improvement programs. Their use has exceeded all Agency estimates. Each month AHRQ responds to an average of 30 user requests, supports 1,920 LISTSERV subscribers, and logs between 3,500 and 6,000 visits to the Web site and more than 1,000 downloads of QI documentation and software. The rapid uptake of the QIs has been due to many factors including a demand for standardized measures using readily available data for both quality improvement and comparative quality reporting, an increased emphasis on public reporting, and efforts to link payment to quality. Examples of QI use:

Return to Contents
Proceed to Next Section