Goal 2—Quality

Making Quality Count

Millions of Americans receive high-quality health care services. The United States has many of the world's finest health care professionals, academic health care centers, and other institutions. Yet, too often, patients receive substandard care. Sometimes they receive too many services or unnecessary services that undermine the quality of care and needlessly increase costs. At other times they do not receive needed services that have been proven to be effective.

The research that provided much of the basis for the 2001 report by the Institute of Medicine (IOM), Crossing the Quality Chasm, goes back several decades to early studies on quality of care, most of which were supported by AHRQ and its predecessor agencies. In its report, the IOM pointed out that quality problems occur across all types of cancer care and in all aspects of the process of care. For example, the IOM report described "underuse of mammography for early cancer detection, lack of adherence to standards for diagnosis, inadequate patient counseling regarding treatment options, and underuse of radiation therapy and adjuvant chemotherapy following surgery."

Poor quality care leads to patients who are sicker, have more disabilities, incur higher costs, and have lower confidence in the Nation's health care system. There is great potential to improve the quality of health care provided to Americans, and AHRQ is committed to this goal. We are working to develop and test measures of quality, identify the best ways to collect, compare, and communicate data on quality, and widely disseminate information about effective strategies to improve the quality of care.

Following are examples of AHRQ-supported research now in progress that focuses on improving health care quality:

Examples of recent findings from AHRQ-supported research on improving health care quality include:

Using Research Findings to Improve Quality of Care

Thousands of Medicare patients with atrial fibrillation (AF) can benefit from a new quality improvement tool developed with support from AHRQ. Findings from a second study can be used to improve end-of-life care by encouraging more discussions between terminally ill HIV patients and their doctors.

Atrial fibrillation. Researchers found that their new CHADS2 method for predicting risk of stroke in patients with AF is more accurate than existing methods. CHADS2 may be especially helpful for identifying low-risk patients who, by taking aspirin, can avoid the office visits, expense, and risks associated with warfarin, which carries a risk of bleeding.

End-of-life discussions. Half of all HIV-infected people in the United States—especially blacks, Hispanics, injection drug users, and people with low education—never talk about end-of-life care with their doctors. Such discussions could improve physicians' understanding of the types of care their patients want when they are very ill and close to death, and they may lead to designation of a surrogate to make decisions when the patient is too ill to do so.

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Patient Safety and Reducing Errors in Medicine

The November 1999 report of the Institute of Medicine (IOM), To Err is Human: Building a Safer Health System, focused a great deal of attention on the issues of medical errors and patient safety and showed that a wide gap exists in the quality of care people receive and the quality of care that we as a Nation are capable of providing. The report indicated that as many as 44,000 to 98,000 people die in hospitals each year as at the result of medical errors. Even using the lower estimate, this would make medical errors the eighth leading cause of death in this country.

More people die from medical errors than from automobile accidents (43,458), breast cancer (42,297), or AIDS (16,516). It is estimated that about 7,000 people each year die from medication errors alone—about 16 percent more deaths than the number attributable to work-related injuries.

Although the increased public attention on this issue is a recent phenomenon, AHRQ has recognized for some time that reducing medical errors is critically important for improving the quality of health care. In 1993, the Agency published one of the first reports focused on medical errors. This landmark report noted that 78 percent of adverse drug reactions were due to system failures, such as the misreading of handwritten prescriptions. Subsequent studies sponsored by AHRQ have focused on the detection of medical errors, investigation of diagnostic inaccuracies, the relationship between nurse staffing and adverse events, computerized adverse drug event monitoring, and computer-assisted decisionmaking tools to reduce the potential for errors and improve safety.

Americans are very concerned about medical errors. According to a national poll conducted by the National Patient Safety Foundation:

  • 42 percent of respondents had been affected by a medical error, either personally or through a friend or relative.
  • 32 percent of the respondents indicated that the error had a permanent negative effect on the patient's health.

The results of an AHRQ/Kaiser Family Foundation survey found that more than 60 percent of the respondents believe there is a role for government in promoting, monitoring, and providing information about the quality of care provided by doctors, hospitals, and health plans.

In FY 2001, AHRQ invested $50 million in 94 new research grants, contracts, and other projects to reduce medical errors and improve patient safety. This effort represents the Federal government's largest single investment in research on medical errors. These projects will address key unanswered questions about when and how errors occur and provide science-based information on what patients, clinicians, hospital leaders, policymakers, and others can do to make the health care system safer. The results of this research will identify improvement strategies that work in hospitals, doctors' offices, nursing homes, and other health care settings across the Nation. AHRQ's $50 million investment is the first phase of a multiyear effort.

Examples of funded projects in the six major categories of AHRQ's FY 2001 patient safety initiative follow.

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Working Conditions and Quality of Care

Increasing our understanding of how working conditions affect health care workers, the risks for errors, and the quality of services provided to patients is of major importance to the health care industry. Recent efforts to reduce costs and streamline the delivery of care have led to significant changes in the health care workplace. The experiences of other industries demonstrate that differences in the equipment and physical characteristics of the workspace, changes in work responsibility and process, and differences in staffing levels can affect the quality of the products or services provided. For example, research on working conditions in the aviation industry has provided evidence of the relationship between aviation safety and work hours, including the effect of factors such as fatigue, lack of sleep, and shift work.

Despite the importance of these factors, there has been scant research focused on the importance of the quality of the workplace environment—not only for worker satisfaction, worker health, and the avoidance of disability, but also for the quality and productivity of the work performed. Workplace factors, including the way work is organized and staffed, may pose a threat, not only to the health and well-being of workers, but also to the quality of care they provide to patients and the safety of the patients.

In FY 2001, AHRQ funded 30 projects that will examine the effects of working conditions on health care workers' ability to provide safe, high-quality care in ambulatory, inpatient (both hospital and long-term care institutions), and home care settings. Examples of the critical issues to be addressed include:

Working conditions—The characteristics of the health care workplace and workforce, including the physical environment, workflow design, staffing, and organizational culture.

Health care workers—Workers, including physicians, nurses, pharmacists, physician assistants, nursing assistants, and emergency medical technicians who provide direct care to patients in health care settings such as hospitals, ambulatory care settings, and nursing homes.

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Helping Patients and Consumers Use Quality Information

Americans are demanding greater value and quality in their health care. In today's rapidly changing health care environment, consumers need solid, reliable information to help them choose among health care plans, practitioners, and facilities. They also need information to help them participate more actively and effectively in their personal health care decisions. AHRQ is playing a unique role in providing the information consumers want and need to help them get the best possible health care.

Consumer Assessment of Health Plans

The Consumer Assessment of Health Plans Study (CAHPS®) is an easy-to-use kit of survey and reporting tools that provide reliable information to help consumers and purchasers assess and choose among health plans. Some recent CAHPS® accomplishments include:

Making Quality Count for Patients and Consumers

AHRQ has funded three demonstration projects to enhance the health care systems' ability to provide patients with information on health care quality. Total projected funding for these three projects is $3.4 million. The researchers will develop and test methods and models for developing information on quality for consumer and patient use in health care decisions, as well as evaluate the impact of strategies to provide information about quality to consumers and patients. The newly funded projects are:

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National Healthcare Quality Report

AHRQ is developing the first-ever annual report on the quality of health care in the United States, as called for in the Agency's reauthorization legislation, which became law in 1999. The goal of the report, now in its early design phase and due out in 2003, is to provide a clear, easily understood picture of the quality of health care in America. The development of a national report on health care quality is an important step in improving the quality of the Nation's health care system and addressing the health care needs of priority populations. Go to "Research on the Health Care of Priority Populations" in this report to learn about AHRQ's program priorities and activities focused on women, children, and minorities.

The project is being led by AHRQ in collaboration with the Centers for Disease Control and Prevention's (CDC's) National Center for Health Statistics. An interagency work group will develop the final content and design of the report. Other members of the work group include the Department's Office of the Assistant Secretary for Planning and Evaluation, CDC, the Centers for Medicare & Medicaid Services, the National Institutes of Health, and the Substance Abuse and Mental Health Services Administration.

As of FY 2001, work on the National Healthcare Quality Report (NHQR) is proceeding as follows:

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National Healthcare Disparities Report

AHRQ is also developing the first-ever report on prevailing disparities in health care delivery in the United States. A large and consistent body of research, much of it funded by AHRQ, has demonstrated persistent disparities in health care quality and access associated with race, ethnicity, socioeconomic position, sex, age, and place of residence. For example, a recent study of Medicare patients revealed that black patients with congestive heart failure or pneumonia received poorer quality care than whites. Further, these differences are associated with greater mortality among black patients.

The Agency's reauthorization legislation, which became law in late 1999, directed AHRQ to develop a report, beginning with fiscal year 2003, on prevailing disparities in health care delivery as they relate to racial factors and socioeconomic factors in priority populations. AHRQ's priority populations include rural, inner-city, low-income groups, minority groups, women, children, the elderly, and individuals with special health care needs. The National Healthcare Disparities Report (NHDR) will serve as a companion document to the National Healthcare Quality Report, providing greater depth and insights into differences in health care quality for priority populations.

This report will be an unprecedented effort to present a comprehensive picture of prevailing disparities in health care in the United States, and it will identify opportunities for improving care for priority populations. The report also will provide a benchmark for evaluating the success of programs to reduce disparities in health care.

The project is being led by AHRQ and will involve collaboration with multiple components of the Department of Health and Human Services. As of FY 2001, work on the NHDR is proceeding as follows:

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