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Program Performance Report

Overview

The Department of Health and Human Services (HHS) manages over 300 programs. It is one of the largest Federal agencies, the Nation’s largest health insurer, and the Federal Government’s largest grant-making agency. The HHS mission is to protect and promote the health and well-being of all Americans while providing world-class leadership in the areas of biomedical research, public health, and social services. HHS programs impact all Americans on a daily basis, through direct services and funding, scientific advances, and educational information that allow people to choose better health care options, medicine, and even food. Through numerous grants and other financing arrangements with both public and private service providers, HHS is committed to improving overall health and human service outcomes and the economic independence of individuals and families throughout the United States.

In FY 2004, HHS published an updated Strategic Plan, which outlines the HHS strategic direction over the next 5 years. The eight strategic goals in the plan guide HHS for FY 2004 - FY 2009 in accomplishing its’ mission of protecting and improving the health and well-being of the American public. These eight goals provide a focus point for HHS program investments and serve as a framework for the measures that track the Department’s overall performance. The Office of the Secretary is responsible for providing overall policy guidance and direction to the Operating Divisions (OPDIVs) to help achieve the Department’s strategic goals.

The strategic goals, performance goals, and program results reflect the combined commitment and effort of HHS programs, and their state, local, Federal, Tribal and non-government partners. These program partners will spend the overwhelming majority of the funds expended for HHS programs in FY 2005 to better the lives of all Americans. A copy of the updated HHS Strategic Plan for FY 2004 - FY 2009 is available at http://aspe.hhs.gov/hhsplan/.

Data and Performance Measurement

Sound information and data are essential to fulfilling the HHS mission of enhancing the health and well-being of every American. Information provided is the main ingredient to success for every HHS performance measure. Whether providing for effective health and human services, or fostering sustained advances in the sciences or public health system, reliable information is an essential tool used in planning, measuring results, and making sound decisions. Accordingly, the Department plays an essential role in producing the necessary data for program decision making, both as a direct producer and a partner in data collection with the states, grantees, and other governmental agencies. The HHS Data Council maintains a directory of all the major data systems supported by HHS OPDIVs, and all surveys on its website (http://aspe.hhs.gov/datacncl/index.shtml.) These data systems support most of the performance measurement objectives within HHS programs, as well as various broad health and social outcome indicators.

HHS’ programs and OPDIVs rely upon accurate data in program management, policy decision making, and intervention development. The Government Performance and Results Act of 1993 (GPRA) emphasizes the importance of data for decision making and creates an incentive for staff throughout HHS to refine the Department’s data systems. HHS programs work extensively with partners in state, local, and Tribal governments; grantees; and Medicare contractors in program implementation and data collection to help meet these standards. The Department continuously identifies system enhancements that improve the timeliness, completeness, and accuracy of data and enables employees to implement more sophisticated performance measures.

HHS has taken a number of steps to address key data needs in a coordinated fashion, promote a HHS-wide strategy on data issues, and strengthen the Department’s ability to work in collaboration with private sector entities, state and local governments, and other partners. The HHS Data Council serves as the principal senior level internal forum on data policy, and serves as the focal point for HHS data policy initiatives. Currently, the Data Council and its working groups are focusing efforts on the following:

  • HHS data collection strategy, priorities, and planning;
  • Cross-HHS budget review, prioritization, and coordination of data collection investments in the budget planning process;
  • Internal and external HHS-wide policy coordination in data policy;
  • Data improvement initiatives in the areas of prescription drugs, health insurance, state level data, income and assets, and race/ethnicity data;
  • National health data standards (e.g., Health Insurance Portability and Accountability Act standards, clinical data standards, and statistical standards);
  • Privacy and confidentiality issues, policies, and best practices in health and human services data;
  • Serving as a focal point for the Coordination with the National Committee on Vital and Health Statistics; and
  • Selected data aspects of national health information infrastructure issues.

As a result, HHS had made improvements in many data collection systems and in HHS-wide data planning and integration process. In addition, integrated, user-friendly access to and availability of the vast data resources in HHS is being improved through the creation of the Data Council’s Gateway to Data and Statistics on the Internet. Additional Department-wide initiatives developed by the Council include the HHS data quality initiative, improvements in geocoding standards and practices, data access and dissemination, statistical confidentiality, and coordination of data collection activities.

However, new data needs for performance measurement are arising, and a number of critical data gaps remain. Additional challenges for performance related data include:

  • Producing data on a more timely basis and with a frequency relevant to the periods over which performance is being measured;
  • Continuously appraising and updating systems to reflect innovations and changes in the delivery of health and human services to the American public;
  • Systematically obtaining accurate, reliable data at the state and local level where many HHS programs are implemented;
  • Developing appropriate performance measurement methodologies to capture the progress of program efforts to produce measurable results;
  • Producing information with sufficient quality and precision to detect what may be relatively small but important changes in key performance indicators; and
  • Achieving major changes in complex data collection systems in a timely and affordable manner.

To address these needs from the Department-wide perspective in the annual budget process, the HHS Data Council works closely with the Office of Budget to review, coordinate, and prioritize all proposed investment requests to improve data and information for decision making. This process helps to ensure that data systems are responsive to performance measurement needs and the Secretary’s priorities. In addition, the Council also continually reviews plans for major data collection activities.

Similarly, throughout HHS, data are being made available to OPDIVs and partners for planning, decision making, and measuring results. These efforts include developing new data collection systems, enhancing current data collection systems, eliminating systems that are no longer relevant, combining reporting where possible, and building the capacity to collect data at the state and local levels.

Throughout this report, when current year performance data are unavailable, a date that the data will become available is provided. As required by Office of Management and Budget (OMB) guidance, HHS will report the results of all performance measures in future reports submitted to Congress.

Guide to Section II

The pages that follow provide an overview of performance measurement at HHS. The Department manages hundreds of programs, and the ones included in this report highlight the many ways that HHS is leading Americans to better health, safety, and well-being. This section highlights the efforts and accomplishments of dedicated program staff in a sample of program areas and provides information on the measures and goals of selected HHS programs. HHS selected programs that represent each of the Department’s eight strategic goals, and each of the OPDIVs that make up the Department. For a comprehensive view of all HHS performance goals and program activities, including the latest performance results, see the FY 2006 performance plans and reports included in the budget justification to Congress for the individual HHS OPDIVs or the FY 2007 performance budgets that will be submitted to Congress in February 2006.

Qualified staff with a thorough knowledge of program content and current operations, including financial and management control procedures, performed the review process on the data for Section II. Assurance of the accuracy of data for Section II was achieved through data verification processes inherent in the recurring usage and updates of the data and tables. Analysts, managers, and executives in the HHS OPDIVs and in the Office of Budget verified the data reported on an ongoing basis. Section II data and narratives received a thorough review within the Office of Budget by budget and program branch chiefs with budget and performance responsibilities. Performance management and assessment activities related to GPRA, the Performance Assessment Rating Tool (PART), and other performance related activities include assurances of the accuracy of data in the Data Verification and Validation section of the OPDIVs’ annual performance plans and reports. These assurances are achieved through a first-level evaluation of data by Agency and Department GPRA and PART coordinators, followed by a second-level review and verification by specifically appointed managers and evaluators.

In developing the programs and measures reported in the FY 2005 Performance and Accountability Report (PAR), HHS attempted to provide the best set of representative measures for HHS programs. Staff developed side-by-side comparisons of the strategic plan indicators and the FY 2006 performance plan measures and engaged OPDIVs and Office of Budget analysts and managers in discussions regarding what measures and programs should be included in the PAR. Budget and performance coordinators compared the strategic plan indicators to the priorities of the President and the Secretary to ensure that all HHS OPDIVs and all major priorities were included on the FY 2005 PAR list. This effort resulted in selecting measures for the FY 2005 PAR that best represent the work and activities of HHS OPDIVs that occurred during FY 2005. However, the selected measures do not always match up neatly with either the Department's Strategic Plan or the FY 2005 Performance Plan. This is because at the time the FY 2005 Performance Plan was prepared, HHS was still developing performance budget plans and had not completed the current FY 2004 - 2009 Strategic Plan. In some cases, measures found in the FY 2006 Performance Plan were more representative of the work and direction the Agency was moving in FY 2005. This process resulted in the list of highlighted programs reported in Section II.

In this section of the PAR, HHS presents detailed performance information for 22 highlighted programs organized by the Department’s eight strategic goals. Each goal overview includes an introduction to the goal and a list of the selected programs and performance measures supporting the goal. Following the overview is a description of the program; a snapshot of the program’s performance targets and results for 4 fiscal years; a discussion of the program performance and results; a description of the data sources; and, if applicable, a summary of the results program evaluations and PART reviews for each program. The PART is an evaluation tool developed by OMB used for reviewing program performance. As a result of a PART review, a program receives a rating as well as OMB recommendations for program improvements. In many cases these recommendations may involve a more comprehensive program evaluation or changes in program legislation. For information on the PART ratings for all HHS programs assessed during the FY 2004 - FY 2006 budget processes, see the section on the PART following the discussion of strategic goal 8.

Strategic Goal 1:

Reduce the Major Threats to the Health and Well-being of Americans

Each year, HHS renews its commitment to reduce health threats and promote healthy behaviors, and this commitment remains a critical priority. This goal supports the Department's vision to improve the health and well-being of people in this country and throughout the world. HHS recognizes that this vision can only be accomplished through coordination across the Department, and through partnerships with states, communities, and health professionals.

Prevention remains at the forefront of the HHS approach to fighting Human Immunodeficiency Virus (HIV)/Acquired Immunodeficiency Syndrome (AIDS), sexually transmitted diseases, and tuberculosis. HHS is making considerable progress toward slowing the transmission of HIV from pregnant women to their children and preventing the spread of tuberculosis. Similarly, childhood immunization rates are at record high levels, but a substantial number of children in the United States are not adequately protected from vaccine-preventable diseases. Further immunization work will continue this year to help ensure that no child, adolescent, or adult will needlessly suffer from a vaccine-preventable disease.

HHS continues to work with the Office of National Drug Control Policy to implement an effective drug strategy that will increase the number of individuals provided with effective substance abuse treatment. Programs such as Access to Recovery promote client choice, expand access to broad array of clinical treatment and recovery support services, including services provided by faith and community based programs, and increase the overall substance abuse treatment capacity. The programs listed highlight Departmental goals and measures representative of the Department's work to reduce the major threats to the health and well-being of Americans.

Highlighted Programs

  • 1a: Centers for Disease Control and Prevention (CDC) National Immunization Program
  • 1b: CDC HIV/AIDS Prevention in the U.S.
  • 1c: Substance Abuse and Mental Health Services Administration (SAMHSA) Substance Abuse Prevention and Treatment Block Grant

1a National Immunization Program
Centers for Disease Control and Prevention (CDC)

Program Description

The mission of CDC’s Immunization program is to prevent disease, disability, and death in children and adults through vaccination. Many life-threatening and/or debilitating infectious diseases, including diphtheria, measles, mumps, and pertussis, were once common in this country. Now, widespread use of vaccines, particularly among children, has resulted in continuing low levels of these diseases.

Appropriate administration of safe and effective vaccines is one of the most successful and cost-effective public health tools in preventing disease, disability, and death and reducing economic costs resulting from vaccine-preventable diseases. To maintain this success, CDC provides national leadership in the ongoing effort to protect children and adults from vaccine-preventable diseases and to ensure the safety of vaccines. The responsibilities are many and varied to focus on the goal of ensuring that every person, of every age, in every part of the country is protected from vaccine-preventable diseases.

CDC strives to ensure control of vaccine-preventable diseases by working with partners to develop national immunization policy, ensure high quality immunization services, increase community participation, education and partnerships, improve systems to monitor disease and vaccination coverage, and improve vaccines and vaccine use.

Snapshot

Performance Measure: Achieve or sustain immunization coverage of at least 90% in children 19- to 35-months of age for: 4 doses DTaP vaccine1, 3 doses Hib vaccine, 1 dose MMR vaccine2, 3 doses hepatitis B vaccine, 3 doses polio vaccine, 1 dose varicella vaccine, 4 doses pneumococcal conjugate vaccine (PCV7)3

Year

Target

Result

2005

90% coverage

Data available 8/2006

2004

90% coverage

DTaP 86%; Hib 94%; MMR 93%; Hepatitis B 92%; Polio 92%; Varicella 88%
(exceeded with the exception of DTaP and Varicella)

2003

90% coverage

DTaP 96%; Hib 94%; MMR 93%; Hepatitis B 92%; Polio 92%; Varicella 85%
(exceeded with the exception of Varicella)

2002

90% coverage

DTaP 95%; Hib 93%; MMR 91 %; Hepatitis B 90%; Polio 90%; Varicella 81%
(exceeded with the exception of Varicella)

Data Source: Data are collected through the National Immunization Survey (NIS) and reflect calendar years.

Data Validation: The NIS uses random-digit-dialing to find households with children aged 19 to 35 months. Parents or guardians are asked to provide verbally the vaccines-with dates-that appear on the child’s "shot card" kept in the home, and demographic and socioeconomic information is also asked. At the end of the interview, permission is asked to contact the child's vaccination providers. Providers are then contacted by mail to verify each child’s vaccinations. The NIS uses a nationally representative sample, and provides estimates of coverage that are weighted to represent the entire population, nationally, and by region, state, and selected large metropolitan areas. The large sample size allows for stratification of the data so that vaccination rates among different groups, for instance, by income level, race, education level of mothers, and other factors can be examined.

Performance Budget Reference: FY 2006 Congressional Justification, pages 260 - 261.

1 Due to a shortage of vaccine and temporary change in recommendations, reported 3 doses from 2002 - 2003.
2 Includes any measles-containing vaccine.
3 Performance targets for newly recommended vaccines, such as pneumococcal conjugate vaccine and influenza vaccine, are reported in GPRA 5 years after Advisory Committee on Immunization Practices recommendation. Measures for pneumococcal conjugate vaccine (PCV7) will begin in 2006 and influenza in 2009.

Discussion of Results and Performance

One of CDC’s immunization goals is to ensure that 2-year-olds are appropriately vaccinated. New cases of most vaccine-preventable disease have decreased approximately 99 percent from peak pre-vaccine levels, which have saved lives and reduced treatment and hospitalization costs. As CDC’s immunization activities increase childhood immunization coverage, the incidence of vaccine-preventable diseases declines significantly. Vaccination coverage levels are at 90 percent or higher for most individual vaccines such as measles, polio, Haemophilus influenzae type b (Hib), and hepatitis B. Examples of the success of immunizations include:

  • Measles is no longer endemic in the United States.
  • Only one child in the United States was born with Congenital Rubella Syndrome in 2003.
  • In March 2005, the CDC announced that rubella is no longer an endemic disease in the United States.
  • Hib cases have dropped more than 99 percent among children younger than age 5 since the Hib vaccine was introduced in 1990.
  • No cases of paralytic polio due to indigenous transmission of wild polio virus have been reported in the United States since 1979.

The target of 90 percent coverage was met in 2004 for most of the vaccines, except for varicella and Diphtheria-Tetanus-Pertussis (DTaP) containing vaccine.

In 2004, the coverage rate for four doses of DTaP did not achieve the 90 percent goal. In 2002 and 2003, CDC modified reporting on the measure for DTaP from four doses to three doses because vaccine shortages limited the availability of the fourth dose to children. This change was made because the Advisory Committee on Immunization Practices (ACIP) recommends that if this vaccine is in short supply, or not available, the fourth dose of DTaP may be dropped. The first three doses are considered the most critical to prevent disease. The change was temporary and reporting for the fourth dose has now been implemented.

The coverage rate for the fourth dose has increased steadily since the change to a four-dose schedule, as recommended by the ACIP in 1991. This goal will be difficult to achieve because it requires that the fourth dose be given to the child between 15 and 18 months of age. The administration of DTaP tends to coincide with regular well-baby visits through the third dose; however, the fourth dose does not, thus requiring a visit specifically for this purpose. Coverage rates are 96 percent for the first three DTaP doses. Although the first three doses are considered to be most critical, CDC and the ACIP feel strongly that the fourth and fifth doses are important for full vaccination. Varying state requirements for the four-dose vaccine schedule may have also led to a slower increase in coverage.

In 2004, the coverage rate for varicella vaccine did not yet achieve the 90 percent goal. Varicella is the most recently introduced vaccine that has a measurable target. Varicella vaccination rates are rising with coverage at only 43 percent in 1998, and reaching 88 percent in 2004. CDC is close to meeting the 90 percent varicella vaccines coverage goal which is especially impressive this soon after the introduction of this particular vaccine, since a child that has already been exposed to chickenpox does not receive the varicella vaccine.

Conjugate vaccines for the prevention of Hib are highly effective. Hib is no longer the leading cause of meningitis among children younger than 5 years of age in the United States.

In 2001, the ACIP added pneumococcal conjugate vaccine (PCV) to the Recommended Childhood Immunization Schedule. Accountability for PCV performance targets begins in FY 2006. PCV already is impacting the incidence of invasive pneumococcal disease. According to a recently published study, the incidence of invasive pneumococcal disease was 77 percent lower among white children less than 2 years of age and 89 percent lower among African American children less than 2 years of age in 2002, as compared to the 1998-1999 averages. Overall, this vaccine is projected to prevent more than 1 million episodes of childhood illness and approximately 120 deaths among children annually.

Data Reliability

Data for the immunization coverage performance come from the National Immunization Survey (NIS), which uses a nationally representative sample and provides estimates of vaccination coverage rates that are weighted to represent the entire population nationally, and by region, state, and selected large metropolitan areas. The NIS was established to provide an ongoing, consistent data set for analyzing vaccination coverage among young children in the United States and disseminating this information to interested public health partners. The NIS uses random-digit dialing to find households with children aged 19 to 35 months. Parents or guardians are asked to provide verbally the vaccines with dates that appear on the child’s "shot card" kept in the home, and demographic and socioeconomic information is also asked. At the end of the interview, permission is asked to contact the child's vaccination providers. Providers are then contacted by mail to verify each child’s vaccinations.

Program Assessments and Evaluations

In response to the PART assessment, CDC is undergoing a comprehensive independent evaluation of the 317 grant program.  An independent contractor will provide recommendations to improve the efficiency of the 317 grant program.  The comprehensive evaluation has three phases.  In phase one, the program mission, performance measures, and objectives, and how the mission and objectives are being implemented by CDC and grantees will be evaluated.  In phase two, the operations and management procedures, including the grant allocation decision-making process, will be evaluated.  In the final phase, the program efficiency and accountability will be evaluated, and methods for improving efficiency of management and operations will be identified. The independent evaluation will be completed in August 2006.

Separate from evaluation activities initiated following the 317 grant program PART review, efforts are underway to improve the Vaccines for Children (VFC) program. CDC has initiated a business process improvement project to strengthen the efficiency and accountability of vaccine management systems.  Once implemented, the new systems will ultimately automate and integrate vaccine ordering and management by centralizing distribution of all public purchased vaccines. Although the 317 grant program and the VFC program serve two distinct groups who would not otherwise be immunized, the project focuses on the vaccine delivery, program management, and service delivery functions of the VFC program, which are similar to the Section 317 immunization grant program. Thus far, a set of recommendations have been developed to improve the business processes.  Business process improvements should result in improved efficiencies, accountability, and cost savings for the VFC program and the 317 grant program.

PART Review and Recommendations

The Section 317 Immunization Grant program received an Adequate rating through the PART review. Specifically, the PART assessment determined the program has strong management practices and was successful in improving vaccination coverage levels among children. The PART assessment identified the areas of program management and planning in order to improve the programs ability to demonstrate program outcomes and results. Specific PART recommendations for this program are:

  • Undergo an independent evaluation on a regular basis, or as needed, to fill gaps in performance information to support program improvement and evaluate effectiveness.
  • Establish processes and procedures to measure and/or improve program efficiency.
  • Improve mechanisms linking the program’s budget for state immunization program and operations activities to program performance.

Program improvements and management initiatives are underway to address each of these recommendations.

1b HIV/AIDS PREVENTION IN THE U.S. Centers for Disease Control and Prevention (CDC)

Program Description

HIV remains a deadly infection for which there is no cure. Over 500,000 Americans have died of AIDS and an estimated 1,039,000 to 1,185,000 are currently infected with the virus. CDC has been involved in the fight against HIV and AIDS from the earliest days of the epidemic and remains a leader in HIV/AIDS prevention and control. While HIV incidence has decreased substantially, from an estimated 150,000 new infections per year in the late 1980s, new infections remain unacceptably high at an estimated 40,000 per year. CDC, as the Federal agency charged with preventing HIV infection, works with an array of partners including other Federal agencies, state and local health and education departments, HIV prevention community-planning groups, academic institutions, community-based and other nonprofit groups, and the private sector. CDC's core set of HIV prevention activities includes surveillance, research, intervention, capacity building, and evaluation. Surveillance provides demographic, laboratory, clinical, and behavioral data that are used to identify populations at greatest risk for HIV infection. These data also help CDC estimate the size and scope of the epidemic.

Snapshot

Performance Measure: Reduce the number of HIV infection cases diagnosed each year among people under 25 years of age.

Year

Target

Result

2005

Overall: 1800 reported cases in 25 areas

Data available 11/2006

2004

Overall: 1900 reported cases in 25 areas

Data available 11/2005

2003

Not applicable.

2331* in 25 areas

2002

Not applicable.

2926* in 25 areas

Data Source: Adult and Pediatric Confidential HIV/AIDS Case Reports (OMB Control No. 0920-0573)

Data Validation: HIV data collection systems vary between areas (e.g., name-based code, coded identifier, name-to-code data collection systems). On July 5, 2005, CDC sent a letter to all states and territories recommending that all states and territories adopt confidential name-based surveillance systems to report HIV infections. Currently 43 state and local health departments use confidential name-based reporting of HIV infection while 14 other state, territorial, and local health departments used code-based or name-to-code methods. The period of time between a diagnosis of HIV or AIDS and the arrival of a case report at CDC is called the "reporting delay". In order to provide the best estimates of trends in incidence, HIV and AIDS surveillance data are analyzed by the data of diagnosis and are mathematically adjusted in more recent periods to adjust for reporting delays and incomplete information on some cases. CDC requires a minimum of 18 months after the end of a calendar year to provide accurate estimates of trends for that year.

Performance Budget Reference: FY 2006 Congressional Justification, pages 91 - 93, 247 - 248.

*CDC will continue to revise baseline and targets when data from more states with adequate HIV reporting systems are available.

Performance Measure: Decrease the number of perinatally-acquired AIDS cases from the 1998 base of 235 cases.

Year

Target

Result

2005

<100 cases

Data available 11/2006

2004

<100 cases

Data available 11/2005

2003

<139 cases

58 (Exceeded)

2002

141 cases

90 (Exceeded)

Data Source: Adult and Pediatric Confidential HIV/AIDS Case Reports (OMB Control No. 0920-0573)

Data Validation: HIV data collection systems vary between areas (e.g., name-based code, coded identifier, name-to-code data collection systems). On July 5, 2005, CDC sent a letter to all states and territories recommending that all states and territories adopt confidential name-based surveillance systems to report HIV infections. Currently 43 state and local health departments use confidential name-based reporting of HIV infection while 14 other state and local health departments used code-based or name-to-code methods. The period of time between a diagnosis of HIV or AIDS and the arrival of a case report at CDC is called the "reporting delay". In order to provide the best estimates of trends in incidence, HIV and ADS surveillance data are analyzed by the data of diagnosis and are mathematically adjusted in more recent periods to adjust for reporting delays and incomplete information on some cases. CDC requires a minimum of 18 months after the end of a calendar year to provide accurate estimates of trends for that year.

Performance Budget Reference: FY 2006 Congressional Justification, pages 91 - 93, 248.

Discussion of Results and Performance

CDC's overarching goal in HIV is to reduce by 25 percent the number of new HIV infections in the U.S. as measured by the number of HIV infections diagnosed each year among people less than 25 years of age, from 2,100 in 2000 to approximately 1,600 in 2010. The following measures indicate CDC's progress toward achieving this overarching goal.

HIV Diagnoses Among People Under 25 Years of Age:

The number of HIV infection cases among persons under 25 years of age diagnosed each year is the best data available to monitor new HIV infections. HIV infections occurring in this group are likely to have been acquired recently and thus are a relatively good proxy measure of HIV incidence. In addition, these data enable CDC to look at yearly trends in a meaningful way. Data are from a national surveillance system that collects demographic, clinical, and behavioral information on all AIDS cases diagnosed in the U.S. as well as HIV cases diagnosed in states with HIV reporting requirements. FY 2004 targets were set when only 25 states had stable, confidential name-based HIV reporting. Beginning in 2006, data will be reported from 30 areas with confidential name-based HIV reporting. This measure continues to be refined and has undergone revisions in previously reported data. In 2003, there were 2,331 cases reported in 25 areas with confidential name-based reporting. Data for 2004 will be available in November 2005.

Perinatally-Acquired AIDS:

A dramatic reduction in perinatal (mother-to-child) HIV transmission cases has been noted in the U.S., a result of the widespread implementation of the Public Health Service recommendations made in 1994 and 1995. Recommendations included routinely counseling and voluntarily testing pregnant women for HIV, and offering zidovudine to infected women during pregnancy and delivery, and their infants post-partum. Further decreasing perinatal HIV transmission is one of four strategies included in CDC's Advancing HIV Prevention Initiative. To support this key strategy, CDC issued recommendations that clinicians routinely screen all pregnant women for HIV infection and that jurisdictions with statutory barriers to such routine prenatal screening consider revising them. Surveillance data reported through December 2003 show sharply declining trends in perinatal AIDS cases. This decline was strongly associated with increasing zidovudine use in pregnant women who were aware of their HIV status. More recently, improved treatment also has likely delayed onset of AIDS for HIV-infected children. With efforts to maximally reduce perinatal HIV transmission and increase treatment of those infected, the number of cases is likely to remain low. However, declines may be affected by treatment failures and missed opportunities to prevent transmission. Data for 2003 continues to show low levels of perinatally-acquired AIDS cases, from 90 in 2002 to 58 in 2003. Data for 2004 will be available in November 2005.

Data Reliability

Adult and Pediatric Confidential HIV/AIDS data collection systems vary between areas (e.g., name-based code, coded identifier, name-to-code data collection systems). On July 5, 2005, CDC sent a letter to all states and territories recommending that all states and territories adopt confidential name-based surveillance systems to report HIV infections. Currently 43 state and local health departments use confidential name-based reporting of HIV infection while 14 other state, territorial, and local health departments used code-based or name-to-code methods. The period of time between a diagnosis of HIV or AIDS and the arrival of a case report at CDC is called the "reporting delay". In order to provide the best estimates of trends in incidence, HIV and AIDS surveillance data are analyzed by the data of diagnosis and are mathematically adjusted in more recent periods to adjust for reporting delays and incomplete information on some cases.

Program Evaluations

In 2000, the Institute of Medicine reviewed CDC and other HHS Agencies’ HIV prevention activities to provide recommendations to CDC and other Agencies on how to improve their activities. Twice in the past 10 years, CDC has convened an external review panel to look at CDC’s existing activities and provide recommendations for the future. The first led to reorganization (merging surveillance with prevention programs), and the most recent one led to the current HIV prevention strategic plan. CDC also has some ongoing studies, including HHS’ Office of Inspector General audit of HIV prevention programs.

PART Review and Recommendations

CDC's domestic HIV/AIDS prevention program received a rating of Results Not Demonstrated from the PART review during the FY 2004 budget process. As a result of that review, CDC is working to implement the following action items:

  • Develop methods to estimate the level of resources required to reach program goals;
  • Hold Federal managers accountable for program performance;
  • Develop incentives and procedures to measure and achieve efficiencies and cost effectiveness in program execution;
  • Improve oversight of grantee activities; and
  • Collect data on program performance and make it available publicly.

CDC is working to implement the PART recommendations and reports regularly to OMB on achieving milestones established for each recommendation.

1c Substance Abuse Prevention and Treatment Block Grant
Substance Abuse and Mental Health Services Administration (SAMHSA)

Program Description

The goal of SAMHSA’s Substance Abuse Prevention and Treatment Block Grant is to improve the health of the Nation by bringing effective alcohol and drug treatment and prevention services to every community through a block grant to the states. The effects of substance use disorders are seen in permanent damage to the Nation’s children, the transmission of HIV/AIDS and other communicable diseases, criminal involvement, premature and preventable deaths, and economic and social consequences estimated to cost the Nation more than $2941 billion per year. The block grant supports and expands substance abuse prevention and treatment, while providing maximum flexibility to the states. States and territories may expend block grant funds only for the purpose of planning, carrying out, and evaluating activities related to these services. The block grant is the cornerstone of states’ substance abuse programs and is an integral part of the President’s drug treatment initiative. States are heavily dependent upon block grant funding for urgently needed substance abuse services.

Snapshot

  • Performance Measure: Number of clients served
  • Year
  • Target
  • Result
  • 2005
  • 1,963,851 clients
  • Data available 10/2007
  • 2004
  • 1,925,345 clients
  • Data available 10/2006
  • 2003
  • 1,884,654 clients
  • 1,840,275 clients [3]
  • 2002
  • 1,751,537 clients
  • 1,882,584 clients [2]
  • 2001
  • 1,635,422 clients
  • 1,739,796 clients [1]
  • Data Source: SAMHSA, Office of Applied Studies. Treatment Episode Data Set (TEDS). Specific references below.
  • Data Validation: Treatment Episode Data Set data represent admissions to treatment, not the total number of individual clients served, and are used as a proxy for this measure. Detailed instructions for data submission, review, and cleaning are available at http://wwwdasis.samhsa.gov/dasis2/teds.htm.
  • Performance Budget Reference: SAMHSA Congressional Justification: FY 2006, pages SI-30 through SI-32; FY Year 2005, pages GPRA 44 through GPRA 49

[1] Source: SAMHSA, Office of Applied Studies. Treatment Episode Data Set (TEDS): 1992-2001. National Admissions to Substance Abuse Treatment Services, Drug Abuse Services Information System (DASIS) Series: S-20, HHS Publication No. (SMA) 03-3778, Rockville, MD, 2003. p. 79. (Issued as proxy for this measure)
[2] Source: SAMHSA, Office of Applied Studies. Treatment Episode Data Set (TEDS): 1992-2002. National Admissions to Substance Abuse Treatment Services, DASIS Series: S-23, HHS Publication No. (SMA) 04-3965, Rockville, MD, 2004, p. 71 (Issued as a proxy for this measure)
[3] SAMHSA, Office of Applied Studies, Treatment Episode Data Set (TEDS):1993-2003. National Admissions to Substance Abuse Treatment Services, DASIS Series: S-29, DHHS Publication No. (SMA)05-4118, Rockville, MD, 2005, p. 73. (Issued as a proxy for this measure)

Results and Performance

Although the FY 2001 and 2002 targets for increasing the number of clients served were exceeded, the FY 2003 target was missed slightly. Data collected by the Drug Abuse Services Information System-Treatment Episode Data Set (DASIS-TEDS) information system showed SAMHSA served 1,840,275 clients in FY 2003, about 2 percent below the target. FY 2003 is the most recent year for which data are currently available, because of the time required for states to report data on the number of admissions in any given year. FY 2004 data will be available in October 2006, and FY 2005 data will be available in October 2007. DASIS-TEDS is a proxy for this measure, representing treatment admissions rather than the total number served. This measure is one of SAMHSA’s National Outcome Measures, which, when fully implemented by the end of FY 2007, will provide more direct and accurate data on number of clients served by reporting an unduplicated count of clients. The unduplicated reporting will be phased in among the States. As States begin to report unduplicated counts, DASIS-TEDS might show that that the number of admissions has gone down, since readmissions of the same individual in the reporting period would be counted as a single client served. Targets may be adjusted to reflect this change.

Data Reliability

The proxy data reported represent treatment admissions data. These data are used as a proxy for persons served because many states currently are unable to employ a unique client identifier, which is necessary in order to track unduplicated numbers of clients served. States are working toward providing unduplicated counts of the number of clients served. SAMHSA expects that the 2004 and 2005 goals will be met. Limitations to DASIS-TEDS data fall into two broad categories: those related to the scope of the data collection system (e.g., the fact that DASIS-TEDS collects data on admissions rather than individuals), and those related to the difficulties of aggregating data from highly diverse state data collection systems. A more detailed discussion of data limitations is available at http://www.nationaloutcomemeasures.samhsa.gov/new_reserve/teds.asp#teds_limitations

The following external factors affect the performance of the block grant:

  • The status of the national economy, including changes in employment and insurance coverage for substance abuse and mental health services;
  • The amount of resources that states and communities are able to allocate to prevention and treatment of substance abuse; and
  • The variation in the supply of (and demand for) illegal drugs such as heroin and cocaine, as well as new addictive substances.

Program Assessments and Evaluations

The block grant received a PART rating in the FY 2005 budget cycle of Ineffective. The review identified strengths, such as program purpose, need for program, and program design. The review identified a number of areas for improvement, with the main area related to performance measures. The assessment found that SAMHSA faces continuing challenges in collecting performance data. SAMHSA will address this problem over time by implementing the National Outcome Measures, and has established the goal of all states reporting on all National Outcome Measures by the end of FY 2007. At that point, the data source will change to the State Outcomes Measurement and Management System, which will collect data on all the National Outcome Measures.

An evaluability assessment of the Substance Abuse Prevention and Treatment Block Grant was completed in December 2004. A comprehensive evaluation is under development, with results expected in late 2006.

Strategic Goal 2

Enhance the Ability of the Nation’s Health Care System to Effectively Respond to Bioterrorism and Other Public Health Challenges

HHS has a number of initiatives and programs directed at protecting Americans from bioterrorist attacks and other public health challenges. The events of September 11, 2001, and subsequent anthrax attacks have reinforced the lead role HHS plays in protecting Americans from attacks on the Nation’s health and food supply. The HHS role in enhancing the Nation’s level of preparedness and overall response capabilities is absolutely vital to helping maintain vigilance and security.

The Office of Public Health Emergency Preparedness (OPHEP) was established to direct the Department's efforts in preparing for, protecting against, responding to, and recovering from bioterrorism and other public health emergencies that could affect the civilian population. OPHEP serves as the focal point for these activities, directing and coordinating the development and implementation of a comprehensive HHS strategy.

Several OPDIVs have major rolls in helping meet this strategic goal. The Food and Drug Administration works to provide responsive regulatory review of new biodefense medical countermeasures and plays a major role by inspecting high-risk domestic food manufacturers and enhancing food import inspections to protect our Nation's food supply and prevent food borne illness. The Health Resources and Services Administration works to prepare hospitals and other medical facilities for health consequences of bioterrorism and other mass casualty events. The Centers for Disease Control and Prevention has played an integral role in strengthening state and local public health infrastructure to respond effectively to emergencies. The measures described in this section are representative of progress HHS has made in building the necessary infrastructure to respond to bioterrorist and other public health challenges.

Highlighted Programs

  • 2a: FDA Field Foods Program
  • 2b: HRSA Bioterrorism Hospital Preparedness
  • 2c: CDC Terrorism Preparedness and Emergency Response, Strategic National Stockpile

2a Field Foods Program
Food and Drug Administration

Program Description

FDA’s Prior Notice Center (PNC) was established in response to regulations promulgated in conjunction with the Public Health Security and Bioterrorism Preparedness Act of 2002. Its mission is to identify imported food products that may be intentionally contaminated with biological, chemical, or radiological agents, or which may pose significant health risks to the American public, from entering into the United States. The PNC targets food and animal feed commodities that have been identified as high-risk based on either threat assessments that have been conducted or the receipt of specific intelligence indicating the items may cause death or serious injury due to terrorism or other food related emergencies.

Snapshot

Performance Measure: Perform prior notice import security reviews on food and animal feed line entries considered to be at risk for bioterrorism and/or present the potential of a significant health risk.

Year

Target

Result

2005

38,000

86,187

2004

Not applicable

33,111

2003

Not applicable

Not applicable

2002

Not applicable

Not applicable

Data Source: Field Data Systems

Data Validation: The prior notice security review process involves multiple levels of validation and verification that culminate in a manual review of shipments deemed to be of the highest public health risk based on risk analysis assessments and contemporary intelligence reports. A brief outline of the progressive validation process follows:

  1. Verification that the mandatory Prior Notice data requirements have been fulfilled.
    All prior notice data are submitted electronically via the Automated Broker Interface of Customs and Border Protection’s (CBP) Automated Commercial System and/or FDA’s web-based Prior Notice System Interface. Both systems are set to perform data checks to assure that the minimal submission requirements are met. Unless data are provided for the all the mandatory prior notice elements, the next validation step is not conducted and a prior notice confirmation number is not issued. Once information has been provided for the mandatory prior notice elements, the system conducts a series of validation edits to identify discrepancies, conflicts, and errors in the submitted data. The validation process includes but is not limited to determining if an appropriate bill of lading or airway bill has been provided, if the manufacturer data matches registration and shipping records, and if a US-based consignee has been provided when appropriate. It is not until the prior notice contains the minimal data element requirements and has passed the internal validation edits that the prior notice is considered adequate and a prior notice confirmation number is issued electronically to the submitter.
  2. Application of screening criteria to identify and flag high-risk shipments.
    Once the initial prior notice data are accepted, high-risk products are identified by applying screening criteria that reflect current risk-based assessments of food vulnerability and threats based on contemporary intelligence reports. PNC personnel set and adjust the screening criteria in real time in response to intelligence and changes in threat levels while the screening process operates via FDA’s Operational and Administrative System for Import Support data system. Prior notice submissions containing data that match the screening criteria are filtered and flagged for manual review.
  3. Manual risk-based assessment of prior notice information.
    The hands-on security review encompasses additional validation, verification, and risk-assessment processes that constitute a threat matrix analysis of the shipment. The prior notice data are reviewed for accuracy and verified in historic and contemporary shipping and law enforcement databases to uncover derogatory information and potential shipment discrepancies. For example, the manufacturer and manufacturer's registration number contained in the prior notice are verified to assure the subject manufacturer is properly identified and registered.
    The Prior Notice data and any additional data about the shipment that is obtained from the databases are sorted through an automated targeting system. The targeting system assimilates the shipment data and associates it with sensitive derogatory information contained in law enforcement databases maintained by CBP, the Department of Homeland Security and other agencies. In addition, suspicious patterns and activities associated with terrorist or criminal activity are identified and together the information is scored against a set of risk-based rules developed by FDA and CBP personnel with terrorism, targeting, and food security expertise to provide an initial risk indicator. Since the targeting system does not reference FDA's databases, the indicator is used in combination with historical and current FDA information.
    Along with information obtained from FDA, CBP, and Department of Homeland Security systems, the prior notice research and risk assessment is complemented by using other authenticated databases utilized at the National Targeting Center and external sources such as web-based state or city business records, firm websites, news sources, and Internet research.
  4. Threat assessment review.
    Based on the comprehensive outcome of this research, a decision is made whether to allow the shipment to proceed to FDA general admissibility status or to classify the shipment as a potential bioterrorism threat and stop the shipment for examination prior to entering the country.

Performance Budget Reference: FY 2006 Congressional Justification, Pages 501, 504 and 505.

Results and Performance

This is a new goal since the Bioterrorism Act became effective in December 2003. In FY 2005, FDA achieved this goal by collaborating with the Department of Homeland Security’s Customs and Border Protection to direct field personnel to conduct 86,187 intensive security reviews of prior notice submissions in order to intercept contaminated products before they entered the food supply. This exceeded the FY 2005 target by 48,187.

However, it should be noted that the import security reviews that are performed by the Prior Notice Center are performed on all prior notice submissions that are selected after intelligence, known risk factors, and information available about the shipper and consignee are applied to the prior notice submission data.   FDA is not able to know in advance how many of the prior notices submitted will need to have a security review since the candidates are not selected in relation to the volume of submissions; they are selected on the basis of risk factors. The 38,000 estimate of the number of security reviews to be performed was simply an estimate based on the first 6 months of the Prior Notice Center's operation in FY 2004.

Data Reliability

The reliability and completeness of the prior notice security review can be assessed at each level of the review process described in the Data Validation segment. The first step is to ensure that the prior notice minimally contains data for all the required fields while the next step subjects the data to a series of validation edits. These two steps are entirely electronic and are ascertained for accuracy routinely by the contractors. Adjustments to the editing and rejection process can be tested on the reporting data for effectiveness prior to implementation. Likewise, the segregation of high-risk products from the entire pool of prior notice submissions involves establishing electronic criteria that target and mark elements of the prior notice data that coincide with intelligence and prevailing risk assessments.

The manual review of prior notice information involves the evaluation and assimilation of the adequacy, accuracy, and risk assessment of the shipment by a PNC Reviewer. When a shipment is associated with a Treasury Enforcement Communication System (TECS) record that involves terrorism or a terrorist action or the research cannot discount a terrorist or public health concern, the prior notice data are brought to the attention of a PNC Watch Commander or supervisor. The information is vetted in conjunction with CBP using internal, external and classified sources. If possible terrorist activity or public health concerns cannot be discounted at this level, the situation is brought to the attention of the PNC Deputy Director, and/or PNC Director, and/or the Director of the Division of Import Operations and Policy. Regardless, the Reviewers complete a research sheet and check list for each shipment that they review.

Program Assessments and Evaluations

The PNC was established in December 12, 2003, and began its operations under a period of enforcement discretion of the prior notice requirements. Since that time, major changes in the enforcement of the prior notice elements were coupled with changes in the electronic processing and analysis of the prior notice and introduced to the import community in stages. Since the quality of the prior notice data and the effectiveness of the computer processing and analysis are directly tied to the review process, FDA’s methods of conducting risk-based assessments have evolved. Although the basic threat assessment matrix and determination process has not changed, the accuracy and quantity of the data obtained in the prior notice itself and from research sources has improved. In addition, recent enhancements in the specificity of the screening criteria improve the ability to target, review and respond to dynamic and emerging public health threats.

FDA was evaluated as an entire Agency during the FY 2005 PART assessment and achieved an overall rating of Moderately Effective.

2b National Bioterrorism Hospital Preparedness Program
Health Resources and Services Administration (HRSA)

Program Description

The goal of the Bioterrorism Hospital Preparedness program, which is part of the President’s Homeland Security Initiative, is to ready hospitals and supporting health care entities to deliver coordinated and effective care to victims of terrorism and other public health emergencies. The Nation has lacked adequate plans and infrastructure to respond to challenges that terrorist acts and other events with mass casualties may pose. A GAO investigation (Report 03-373), conducted late in 2002, found widespread deficiencies in capacity, communication, and coordination elements essential to preparedness and response.

The Hospital Preparedness program, established in FY 2002, enables state and regional planning among local hospitals, emergency medical services systems, health centers, poison control centers, and other health care facilities, to improve their capability to respond to the healthcare consequences of terrorist attacks and address infectious disease epidemics and other mass public health emergencies. This program works in concert with CDC’s Public Health Emergency Preparedness program and the Metropolitan Medical Response System program of the Department of Homeland Security.

Snapshot

Performance Measure: Percent of awardees that have developed plans to address surge capacity.

Year

Target

Result

2005

100%

100%

2004

90%

89%

2003

Not applicable

59% (estimated baseline)

2002

Not applicable

Not applicable [1]

Data Source: Grantees’ semi-annual progress reports and continuation applications.

Data Validation: Validated by project officers through review of plans and site visits.

Performance Budget Reference: FY 2006 Congressional Justification, page 438.

[1]This program was established in FY 2002.
Results and Performance
A terrorist attack or other large-scale public health emergency could result in a demand for health care that could rapidly overwhelm the resources in a specific region. Surge capacity is the ability to evaluate and care for a markedly increased volume of patients. The requirement to develop plans to address surge capacity in response to potential terrorist and other threats is based on the concept that improved outcomes can be achieved when critical components of preparedness are formalized in a plan and organized into a system of care.

Plans for surge capacity must address the following issues: (1) hospital bed capacity for adults and children; (2) the capability for isolation and decontamination; (3) appropriate staffing; (4) appropriate medical prophylaxis and treatment for hospital staff and their family members; (5) personal protective equipment; (6) capacity for trauma and burn care; (7) capacity for mental health care; (8) communications and information technology and (9) hospital laboratory connectivity and capacity.

By FY 2005, 100 percent of Hospital Preparedness program awardees had developed surge capacity plans. This represents an increase from 89 percent in FY 2004. In the future, the program will track various aspects of the implementation of these plans.
Data Reliability
Performance information for this program is obtained through three principal means: (1) grantees’ semi-annual reports, (2) grantees’ continuation applications, and (3) a survey of hospitals. Semi-annual report data and information from continuation applications are validated through reviews and site visits by project officers.
Program Assessments and Evaluations
An HHS Office of Inspector General report on “Hospital Bioterrorism Surge Capacity: Status of Early Implementation” is forthcoming.

2c Terrorism Preparedness and Emergency Response Program (Strategic National Stockpile)
Centers for Disease Control and Prevention (CDC)

Program Description

The health and security of the United States depends on our preparedness against terrorism. CDC’s mission in this area is to prevent death, disability, disease and injury associated with urgent health threats. CDC contributes to the enhancement of the Nation’s public health care ability to effectively respond to bioterrorism and other public health challenges by:

  • Investing in preparedness and response efforts;
  • Developing new, and maintaining traditional and non-traditional, partnerships;
  • Working with provider and first responder organizations to link personal and community health to enhance early intervention activities; and
  • Expanding technology.

Another key mechanism for advancing national preparedness is the bioterrorism preparedness cooperative agreement awarded to 62 state and local grantees.

CDC's comprehensive terrorism preparedness and emergency response program comprises three key components: Detection activities assure the ability to detect an event so intervention can begin as early as possible to minimize mass trauma; Investigation and response activities ensure plans and systems are in place to respond to and investigate a public health event; and Control, containment, and recovery activities ensure, among other activities, state and local government's ability to receive and distribute the Strategic National Stockpile, a national repository of life-saving pharmaceuticals, medical material, and equipment.

CDC, through the Strategic National Stockpile (SNS), acquires, manages and deploys the Nation's stockpile of life saving pharmaceuticals and other medical assets for a response to a terrorist event or other type public health emergency. Portions of the stockpile are configured in 50-ton, 12-Hour Push Packages that contain supplemental medicine and medical supplies designed to be deployed rapidly and used in the event of mass casualty incidents. These packages can be delivered to any point in the country within 12 hours. Additionally, SNS assists state and local planners with the receipt, staging, storage, distribution and dispensing of SNS assets.

Snapshot


Performance Measure: 100% of state public health agencies improve their capacity to respond to exposure to chemicals or category A agents by annually exercising scalable plans and implementing corrective action plans to minimize any gaps identified

Year

Target

Result

2005

25%

Data available 12/2005

2004

Not applicable

Not applicable

2003

Not applicable

Not applicable

2002

Not applicable

Not applicable

Data Source: Self-reported data as part of required progress reports.

Data Validation: Plans for validation of self reported data are under development.

Performance Budget Reference: FY 2006 Congressional Justification, pages 311, 313.

Performance Measure: 100% of state public health agencies are prepared to use materiel contained in the SNS as demonstrated by evaluation of standard functions as determined by CDC.

Year

Target

Result

2005

70% certified

Data available: 12/2005

2004

60% certified

72% (Exceeded)

2003

Not applicable

Not applicable

2004

Not applicable

Not applicable

Data Source: Completed SNS Assessment Tools, based on criteria outlined in A Guide for Preparedness, V 10.00.

Data Validation: All states are reassessed at least annually.

Performance Budget Reference: FY 2006 Congressional Justification, pages 218-220, 316.

Discussion of Results and Performance

The FY 2005 target for the measure is that 25 percent, or 15 states/territories/grantees, will conduct an exercise to evaluate their plans and response systems. As of November 2004, 100 percent of grantees have written response plans that cover at least one of the Category A biological agents and chemical agents. As of May 2005, 94 percent (47/50) of state public health agencies have exercised the plan for at least one of these priority agents.

In future years, grantees will need to implement corrective actions within 90 days of identifying a deficiency through a drill, exercise, or real event.

CDC, in A Guide for Preparedness, V 10.00, describes 12 functions of SNS Preparedness required for the effective management and use of deployed SNS materiel. Based on these functions, grantees are required to develop SNS Preparedness Plans detailing the performance of these functions during an emergency. In an effort to enhance grantee SNS preparedness planning efforts, the SNS Program maintains a staff of Program Services Consultants who provide ongoing technical advice and training assistance to grantees. The Program Services Consultants also evaluate the grantee’s level of preparedness to receive, distribute and dispense SNS assets. As of the third quarter of FY 2005, 78 percent (42/54) of the states and directly-funded cities have met the minimum standards for demonstrating preparedness to use SNS assets and thus received a rating of amber or better.

Data Reliability

Currently, states self-report performance information. Plans for validation of self-reported data are under development.

Program Evaluations

CDC’s Terrorism program, through its Coordinating Office for Terrorism Preparedness and Emergency Response, coordinates in-depth evaluations initiated by GAO, and the Office of Evaluation and Inspections (of the HHS Office of the Inspector General). CDC reports on program status and progress, and uses recommendations to evaluate/improve program effectiveness. Audits and evaluations broadly focus on each component of public health preparedness to include: workforce development, surveillance and epidemiology, laboratory capacity, communication, funding management and accountability, disease reporting systems, and the Strategic National Stockpile.

PART Review and Recommendations

CDC’s Division of State and Local Readiness received a rating of Results Not Demonstrated from the PART review during the FY 2005 budget process. As a result of the PART assessment, the program is implementing an independent program evaluations to inform strategic planning and program management and to link performance and measures. CDC is working to implement additional recommendations for continued program improvement.

Strategic Goal 3:

Increase the Percentage of the Nation’s Children and Adults Who Have Access to Health Care Services, and Expand Consumer Choices

The Department is working to expand health care to all and remains committed to its many efforts aimed at increasing the percentage of the Nation's children and adults who have access to care and expanding consumer choices. The Department will also continue to promote increased access to health care for uninsured and underserved people and for those whose health care needs are not adequately met by the private health care system.

In support of this goal, HHS will continue to promote a wide variety of activities intended to increase access to health care, encourage the development of low-cost health insurance options, reduce health disparities, and to strengthen and improve health care services for targeted populations with special health care needs.

HHS is committed to raising awareness among minority communities about major health risks prevalent in their specific populations and providing access to information on how to reduce these risks. This commitment also includes efforts to promote cultural competence among practitioners, thereby reducing communication barriers between health care providers and their patients. HHS will continue to conduct and support research to find underlying causes of racial and ethnic health disparities and develop and disseminate effective strategies to reduce them.

Highlighted Programs

  • 3a: HRSA Health Centers Program
  • 3b: IHS National Diabetes Program
  • 3c: CMS Medicaid and the State Children’s Health Insurance Program
  • 3d: CMS Medicare
  • 3e: CMS Quality Improvement Organizations

3a Health Centers Program
Health Resources and Services Administration (HRSA)

Program Description

Health centers are a major component of America’s health care safety net for the Nation’s indigent, underserved, and vulnerable populations. This program, which is nearly 40 years old, is a Presidential initiative to increase health care access for those Americans most in need. Millions of Americans are uninsured and lack access to a regular source of health care. These and others also face non-financial barriers to receipt of appropriate care. Health centers provide regular access to high quality, family-oriented, and comprehensive primary and preventive health care regardless of patients’ ability to pay while also reducing other barriers to care. The ultimate goal of Health centers is to contribute to improvements in the health status of underserved and vulnerable populations and to the elimination of health disparities. The program provides grants to a variety of community-based public and private nonprofit organizations for the operation of health centers. These grants provide about 25 percent of health centers’ revenues on average, leveraging $3 for each Health Centers program dollar spent.

Snapshot

Performance Measure: Increase the infrastructure of the Health Center program to support an increase in utilization via new or expanded sites.

Year

Target

Result

2005

153

158

2004

124

129

2003

180

188

2002

260

302

Data Source: HRSA/BPHC’s Bureau of Health Care Delivery and Assistance Network (BHCDANET), which maintains data on health center sites that are included in the grantees’ approved scope of project.

Data Validation: BHCDANET is an agency mainframe system with business rules to generate unique grantee and site identifiers and has hard code editing procedures. Site development is also monitored via Office of Management and Budget Circular A-133 audit reports.

Performance Budget Reference: FY 2006 Congressional Justification, page 320.


Performance Measure: Increase the number of uninsured and underserved persons served by Health Centers.

Year

Target

Result

2005

14.0 million

Data available: 08/2006

2004

13.2 million

13.13 million

2003

12.5 million

12.39 million

2002

11.75 million

11.32 million

Data Source: HRSA/BPHC Uniform Data System (UDS), based on data provided by grantees.

Data Validation: UDS data are validated through edit checks and onsite reviews.

Performance Budget Reference, FY 2006 Congressional Justification, page 320


Performance Measure: Continue to assure access to preventive and primary care for racial/ethnic minorities.

Year

Target

Result

2005

9.07 million (65%)

Data available: 08/2006

2004

8.58 million (65%)

8.3 million (64%)

2003

8.16 million (65%)

7.92 million (64%)

2002

7.64 million (65%)

7.24 million (64%)

Data Source: HRSA/BPHC Uniform Data System (UDS), based on data provided by grantees.

Data Validation: UDS data are validated through edit checks and onsite reviews.

Performance Budget Reference: FY 2006 Congressional Justification, page 321.

Results and Performance

The President’s Health Centers initiative began in FY 2002 with the goal of creating 1,200 new or expanded health center sites and increasing the number of clients served by 6.1 million. A critical element in expanding access to care for the Nation’s most vulnerable populations is the establishment of new health center sites and the expansion of existing sites to provide required facilities, personnel and services, particularly in communities of greatest need. In the first 4 years of the initiative, FY 2002-FY 2005, the program funded 777 new or significantly expanded sites, exceeding the target each year. This total does not include the FY 2006 expansion sites in areas affected by Hurricane Katrina that received accelerated partial funding in September 2005 to initiate the expansions as quickly as possible.

Growth in the number of persons served by health centers is an indicator of expanded access to care for the Nation’s most vulnerable populations. Health centers served 13.1 million persons in 2004, achieving more than 99 percent of its target even though it generally takes several years for newly established sites to become fully operational. This represented a growth of more than 730,000 persons over the previous year and growth has increased by nearly three million persons since the beginning of the President’s initiative.

Access to care is key to eliminating health disparities. The number of racial/ethnic minority individuals served by Health Centers increased from 7.9 million in 2003 to 8.3 million in 2004, continuing a steady growth consistent with the overall growth in program clients. The proportion of racial/ethnic minority individuals has remained steady at 64 percent of total clients, only one percentage point below the target of 65 percent. Maintaining steady percentages of the Nation’s most vulnerable is an important achievement given the growth in the program.

The President’s Health Centers initiative includes expansions for existing centers and development of new service sites. Some of these new sites are or will be in underserved rural areas that do not have large numbers of racial/ethnic minorities. The substantial and rapid increases in the total number of clients served and expansions in areas with relatively small proportions of racial/ethnic minorities impact the program’s ability to maintain and increase the proportion of minority clients served. Therefore, a racial/ethnic minority representation of 65 percent of the Health Centers’ total client population is a challenging performance target.

Data Reliability

A broad range of performance information for the Health Centers program is collected through five principal means: (1) a Uniform Data System collects aggregate administrative, demographic, financial, and utilization data annually from each organization receiving support; (2) information from Health Disparities Collaboratives which includes data on chronic disease treatment and outcomes collected from health centers participating in formal collaboratives to improve quality of care; (3) periodic surveys of a representative sample of health center patients to provide in-depth information on individuals and the care they receive, comparable to the National Health Interview Survey and the National Hospital Ambulatory Medical Care Survey; (4) Sentinel Centers Network data on patient and provider characteristics obtained from a representative group of HRSA-supported health centers; and (5) occasional special evaluation studies. Uniform Data System data are validated through edit checks and onsite reviews conducted during each organization’s project period. All data collection tools have edit checks for internal consistency. To assure representativeness of Sentinel Centers Network and survey data, sociodemographic and organizational characteristics are compared with the Uniform Data System reporting.

Program Assessments and Evaluations

The HHS Office of Inspector General conducted a survey of risk management activities at health centers in FY 2005 (OEI-01-03-00050). The survey results indicated that health centers identified staff training, patient tracking, and peer review as the three most difficult risk management practices to carry out. Lack of financial resources for risk management, lack of a dedicated staff person for risk management, and lack of training were cited as key challenges to conducting risk management. In its response to this report, HRSA identified a goal that by 2010, 100 percent of health centers will participate in structured risk management activities as a strategic element for improving health care quality. Activities aimed at achieving this goal may include holding risk management workshops and developing a comprehensive training agenda.

An article by O’Malley et. al analyzed Health Centers’ most recent visit survey compared to the one conducted in 1994. The study revealed that the number of patients continued to increase and the visit rate per patient was sustained. Continuity of care also improved and there were no disparities in preventive services delivery by race/ethnicity or insurance status. The authors concluded that continued growth under the Presidential initiative is likely to help reduce health disparities and improve care for the underserved. (O'Malley, A., et al. Health Center Trends, 1994-2001: What Do They Portend for the Federal Growth Initiative? Health Affairs, 2005; 2(24(2):465-472.)

3b National Diabetes Program
Indian Health Service (IHS)

Program Description

The IHS Division of Diabetes Treatment and Prevention is an integral part of the IHS Hospitals and Health Clinics program. The mission of the IHS Division of Diabetes Treatment and Prevention (DDTP) is to develop, document, and sustain a public health effort to prevent and control diabetes in American Indian/Alaska Native (AI/AN) people. The program works with communities to prevent and treat diabetes, in addition to overseeing the Special Diabetes Program for Indians grant program (SDPI). Development of the regional Model Diabetes programs is a major achievement of the IHS DDTP. The Model Diabetes programs are designed to expedite care and provide education to people with diabetes, and to translate and develop new approaches to diabetes control that serve as models for other Indian communities facing similar problems. Area diabetes consultants within each IHS Area provide consultation and technical assistance related to clinical activities and programmatic issues to Indian, Tribal, and Urban facilities and SDPI programs. This ongoing emphasis on diabetes care within IHS’ Hospital and Health Clinics budget recognizes the role of diabetes as a major cofactor in morbidity and as well as one of the major causes of mortality among AI/AN people. Meeting performance indicators in this program reflects an increase in the percentage of AI/AN patients who have access to quality clinical care within the IHS system.

Snapshot

Long Term Goal: By 2010 increase the percentage of patients with ideal glycemic control to 40%.

Measure

FY

Target

Result

Address the proportion of patients with diagnosed diabetes that have demonstrated glycemic control at the ideal level (HbA1c<7.0)

2005

34%

Data available: 10/2005;
final 1/2006

2004

32%

34%

2003

30%

31%

2002

>29%

30%

Data Source: Yearly IHS Diabetes Care and Outcome Audit.

Data Validation: Annual aggregation and comparison of data using Clinical Indicator Reporting System and Diabetes Audit results

Performance Budget Reference: FY 2006 Congressional Justification 3,5 (SUP-71); FY 2005 Congressional Justification p 1-33, and B: pg IHS-25, 141

Results and Performance

The FY 2004 indicator was to increase the proportion of AI/AN patients with diabetes that have improved glycemic control by 1 percent. IHS met and surpassed this target. The 2004 performance enabled IHS to improve the FY 2003 performance level for ideal glycemic control in patients with diagnosed diabetes by 3 percent. Two data sources (the diabetic audit of glycemic control as well as an electronic health information system application [Clinical Indicator Reporting System]) provide reliable and consistent performance information; the diabetic audit of over 33,000 diabetic patients substantiates the electronic Clinical Reporting System audit of over 74,000 diabetic patients.

Glycemic control refers to how well blood sugars are controlled in a person with diabetes. It is measured with a blood test called the Hemoglobin A1c. The IHS Diabetes Care and Outcomes Audit process divides these levels of control into “Ideal” (<7 percent); “Good” (7.0-7.9 percent); “Fair” (8.0-9.9 percent); “Poor” (10-11.9 percent); and “Very Poor” (>12 percent) categories, based on national diabetes care standards. The graph below illustrates IHS’ ongoing ability to improve glycemic control in AI/AN populations, as well as improve the percentage of patients in ideal control.

Diabetes Care & Outcomes Audit

HbA1c measures the glucose level (sugar content) of a patient's blood. A lower HbA1c percentage indicates better blood sugar control. This graph illustrates improving glycemic control among the IHS population, broken into age categories for patients 55 years and older, and among the population as a whole.

IHS uses several treatment and prevention strategies to achieve glycemic control in the AI/AN population:

  • Glucose lowering medications: Many glucose-lowering medications have been introduced on the market in recent years. These medications are quite effective.
  • Negotiation of wholesale/at cost purchase of these newer, more effective medications for AI/AN patients with diabetes.
  • Continued emphasis on patient education about nutrition, diet, and exercise, coupled with the efforts of the IHS Health Promotion/ Disease Prevention initiative.
  • Availability of ‘best practice’ guidelines on the IHS website for provider, patient, community, and health care facility guidance.
  • Enhancement of a clinical software application (the Clinical Indicator Reporting System) that allows sites to track and provide timely feedback on the achievement of glycemic control, as well as other diabetic indicators.

IHS targets continue to be ambitious in overcoming the diabetes epidemic in AI/AN populations. There is a historical and projected annual increase in diabetic prevalence of 4 percent. Since 1997, the number of patients with diabetes served by the Indian, Tribal, and Urban system has increased by 45 percent, according to a review of diabetes program data by diabetes statisticians.

Data Reliability

Data for this review is obtained from the annual IHS Diabetes Care and Outcomes Audit. In FY 2004, more than 33,000 charts were reviewed as part of the diabetic audit throughout all 12 Areas. IHS, Tribal, and Urban clinical facilities are encouraged to maintain diabetes registries of all persons with diabetes. Selected clinical variables and interventions are collected annually using a systematic random sample of charts at each facility. In short, a sample size is chosen for each facility that is sufficient to provide an estimate within ten percent of the true rate of adherence for each facility with a confidence of > 90 percent. The abstracted data are then entered into a general-purpose microcomputer-based software program. Data are collected following standardized protocols using fixed definitions and data collection forms. While validation studies of the audit have not been published, some IHS areas have implemented additional audits using different reviewers to audit the same charts and to assure accuracy in data entry procedures. In addition, a comparison study has shown good observed agreement between the manual and electronic audits (0.78 percent - 1.00 percent) at a particular site.

Additional information on the audit is available at:

http://www.ihs.gov/generalweb/webapps/sitelink/site.asp?link=http://www.dmaudit.com/.

The Clinical Indicator Reporting application, a part of RPMS (the IHS Health Information Technology solution) conducts an extensive electronic audit of the diabetic user population. This application is used throughout the facilities to evaluate clinical quality, and includes a sub report on diabetes. In FY 2004, over 78,000 diabetic charts were electronically reviewed. Further information is available at: http://www.ihs.gov/cio/crs/.

Program Assessments and Evaluations

During the FY 2004 budget process, the IHS PART included a review of the IHS Direct Federal programs and the Hospital and Clinics Budget, where the funding for diabetes care resides. The program received a rating of Moderately Effective. IHS shared the PART review results with the clinical providers and healthcare facilities, where quality care improvements are operationalized. These improved trends in diabetes care demonstrate the public health impact made possible when local, program, and Departmental initiatives are focused on a common outcome. The PART review process also has focused attention on the continued importance of assuring valid and reliable performance data addressing diabetic care at all levels of the Indian health system (i.e., IHS, Tribal and Urban); performance data collection, thus, was addressed in both the Urban Indian Health Program and RPMS/IT PART reviews during the FY 2005 budget process. The FY 2006 Facilities PART included this measure as one of its annual and long-term strategic goals for illustrating the impact of new facilities on the health status of communities. The FY 2007 Tribally Operated Health Facilities include this measure as one of the elements of its composite results measure.

3c.1 Medicaid and the State Children’s Health Insurance Program (SCHIP)
Centers for Medicare & Medicaid Services

Program Description

Medicaid is a means-tested health care program for low-income Americans, administered by CMS in partnership with the states. It is the primary source of health care for a large population of medically vulnerable Americans, including poor families, the disabled, and persons with developmental disabilities requiring long-term care. In coordination with the Medicaid program, the State Children’s Health Insurance Program (SCHIP) has stimulated enormous change in the availability of health care coverage for children.

SCHIP was created through the Balanced Budget Act of 1997 to address the fact that nearly 11 million American children (one in seven) were uninsured and at increased risk for preventable health problems. This program represents the largest single expansion of health insurance coverage for children in more than 30 years and improves the quality of life for millions of vulnerable children less than 19 years of age. Many of these children were in working families that earned too little to afford private insurance on their own, but too much to be eligible for Medicaid. The funds allocated for SCHIP cover insurance costs, reasonable administrative costs, and outreach services to get children enrolled.

Title XXI of the Social Security Act gave states the option to expand their Medicaid program, establish a separate SCHIP, or use a combination of both. CMS’ goal is to increase the number of children (up to age 19 for SCHIP; age 21 for Medicaid) enrolled in regular Medicaid or SCHIP.

Snapshot

Long Term Goal: Decrease the Number of Uninsured Children by Working with states to Enroll Children in SCHIP and Medicaid

Efficiency Measure

FY

Target

Result

Decrease the number of uninsured children by working with states to enroll children in SCHIP and Medicaid

Baseline: In 1997, the year SCHIP was enacted, there were 21,000,000 children enrolled in Medicaid, and none in SCHIP.

2005

Increase the number of children who are enrolled in regular Medicaid or SCHIP by 3%, or approximately 1,000,000 over the previous year.

Data available:
Spring 2006.

2004

Maintain enrollment at FY 2003 levels.

Goal met.
+2,900,000

2003

Increase enrollment 5% over FY 2002 levels.

Goal met.
+2,200,000/
+7.2 percent

2002

Increase enrollment 1,000,000 over FY 2001 levels.

Goal met.
+3,100,000

Data Source: States are required to submit quarterly and annual SCHIP statistical forms to CMS through the automated Statistical Enrollment Data System (SEDS). Using these forms, states report quarterly on unduplicated counts of the number of children under age 19 who are enrolled in separate SCHIP programs, Medicaid expansion SCHIP programs, and regular Medicaid programs. The enrollment counts presented in this update are the sum of the unduplicated number of children ever enrolled in separate SCHIP programs, Medicaid expansion SCHIP programs, and regular Medicaid programs during the year.
The estimate of 21,000,000 for Medicaid enrollment for FY 1997 is based on CMS-2082 data edited by The Urban Institute and published in December 1999. Although CMS previously reported a 1997 baseline of 22,700,000 children enrolled in Medicaid, this was based on unedited CMS-2082 data and incomplete data reported by the states through SEDS. CMS and states consider the 21,000,000 Medicaid enrollment figure to be a final estimate for 1997. This figure is also cited in the first annual report of the CMS-funded evaluation of SCHIP by Mathematica Policy Research (at website http://www.cms.hhs.gov/schip/sho-letters/mpr12301.asp).

Results and Performance

While this goal focuses on enrolling children in Medicaid and SCHIP rather than on measuring un-insurance rates, there is overwhelming evidence that the rate of un-insurance in children has been reduced since the inception of SCHIP. CMS continues to work with states to assure that their programs are designed to best meet the needs of their children and provides extensive technical assistance to states that need to modify their programs.

In an effort to address budget issues, some states have submitted amendments to increase cost sharing, reduce benefits, reduce the period of coverage from 12 to 6 months, and other programmatic changes, which may lead to decreases in enrollment for some states. CMS has also approved SCHIP state plan amendments to allow some states to implement an enrollment cap and/or waiting list. However, as the budget situation improves some states are making plans to remove these enrollment caps and/or waiting lists and decrease enrollee cost sharing. In addition, many states have eliminated barriers that prevent families from enrolling in Medicaid and SCHIP. For example, many states have simplified application forms and eliminated income verification requirements.

Data Reliability

The program enrollment data that States submit through the Statistical Enrollment Data System are reviewed by CMS every quarter. CMS will measure, to the extent possible, the unduplicated count of the number of children who are enrolled in any of the following programs: regular Medicaid; expansions of Medicaid through SCHIP; and separate SCHIP programs as reported by the States. While CMS considers an unduplicated count to be an appropriate measure for this goal and the unduplicated count we can be measured within each program, some children may be enrolled in Medicaid at one point in the year and in SCHIP at another point, making it difficult to establish an accurate unduplicated count across all programs. Similarly, the SCHIP counts include some double counting of children in States that have combination programs. To the extent the data allows, CMS will closely monitor this issue.

The data for this goal are complete and reliable. This program is audited through the CMS Chief Financial Officer audit.

Program Assessment and Evaluations

There are no program evaluations pertaining to enrollment planned for FY 2005.

Program Assessment Rating Tool (PART) - SCHIP was initially assessed using PART in the FY 2004 cycle and was reassessed as Adequate in the FY 2005 cycle. As a result of the PART findings for FY 2004, CMS developed an SCHIP Action Plan to address certain concerns. CMS continues to develop with states a core set of national performance measures to evaluate the quality of care received by low-income children. A new annual performance goal was established to utilize the information gathered with states to establish formal collaborations that will improve health care delivery and quality for Medicaid and SCHIP populations using reliable and valid performance measures. In addition, CMS expanded the Payment Error Rate Measurement (PERM) program developed to measure and ultimately reduce Medicaid and SCHIP payment error rates, beginning with the Medicaid Fee-For-Service component in FY 2006.

3c.2 Medicaid and the State Children’s Health Insurance Program (SCHIP)Centers for Medicare & Medicaid Services

Program Description

Because of the Federal-state partnership in the Medicaid and SCHIP programs, improvements in the use of performance measures to improve health care quality are best accomplished if jointly identified by CMS and states. As part of the Performance Measurement Partnership Project (PMPP), seven HEDIS® measures were proposed by a work group of state Medicaid and SCHIP officials as performance indicators that states would report annually on a voluntary basis. The following are the seven proposed performance measures (SCHIP-related measures in italics): Adult access to preventive/ambulatory health services; Children’s access to primary care practitioners; Comprehensive diabetes care (HbA1c tests); Prenatal and postpartum care (prenatal visits); Use of appropriate medications for children with asthma; Well child visits for children in the first 15 months of life; and Well child visits in the 3rd, 4th, 5th, and 6th years of life.

Snapshot

Long Term Goal: Improve Health Care Quality Across Medicaid and the State Children’s Health Insurance Program (SCHIP)

Measure

FY

Target

Result

Improve Health Care Quality Across Medicaid

2005

Refine the strategy and work plan for the provision of technical assistance to states in performance measurement calculation and reporting; collect 2002 performance measurement data from a minimum of 10 states; and continue to provide technical assistance to improve state capability for performance measurement calculation and reporting, and to encourage voluntary reporting by additional states.

Goal met

2004

Continue to work with state representatives and update the timeline for implementing recommendations; identify a strategy for improving health care delivery and/or quality and for implementing recommendations.

Goal met

2003

Identify a timeline for implementing recommendations; identify a strategy for improving health care delivery and/or quality, and specify measures for gauging improvement; and initiate action steps for implementing recommendations.

Goal partially met

2002

Not applicable

Not applicable


Long Term Goal: Improve Health Care Quality Across Medicaid and the State Children’s Health Insurance Program (SCHIP)

Improve Health Care Quality Across SCHIP

2005

Continue to collect core performance measurement data from states through the state annual reports;
use the new automated State Annual Report Template System (SARTS) to analyze and evaluate performance data; and provide technical assistance to states on establishing baselines, measurement methodologies, and targets for SCHIP core measures.

Goal met

2004

Refine data submission, methodological processes, and reporting; produce 2002 performance measures in standardized reporting format; and collect 2003 data (baseline) from states.

Goal met

2003

Identify a timeline for implementing recommendations; identify a strategy for improving health care delivery and/or quality, and specify measures for gauging improvement; initiate action steps for implementing recommendations; and begin to implement core SCHIP performance measures.

Goal met

2002

Not applicable

Not applicable

Data Source: Developmental. The current vehicle for SCHIP programs to report Performance Measurement Partnership Project (PMPP) measures to CMS is the SCHIP Annual Report. In addition, CMS created an automated web-based system -- SARTS, which allows states to input and submit their annual reports to CMS via the Internet.

Data Validation: Developmental. CMS will monitor performance measurement data related to the SCHIP core performance measures through SARTS. In addition, state performance data submitted through SARTS will be monitored to assure that individual state goals are consistent with the approved Title XXI SCHIP state plan.

Performance Budget Reference: See the FY 2006 CMS Congressional Justification, page 350, for further information about this goal.

Results and Performance

A data collection tool for states to voluntarily report measurement data on the core set of performance measures as a pilot test was developed and was cleared by OMB in May 2004. Results from the initial data collection effort will support continued technical assistance to states to improve state reporting capability and encourage voluntary reporting of performance measurement data by additional states.

Medicaid:

The project contractor has completed analysis of the feasibility of using Medicaid Statistical Information System (MSIS) data to calculate the Medicaid performance measures. Results from two states targeted for specific reporting analysis suggest that MSIS can be used to calculate a current set of performance measures in states with predominantly fee-for-service Medicaid programs. However, it is recommended that use of MSIS be delayed until MSIS is fully populated with standardized HIPAA compliant data.

SCHIP:

CMS began collecting SCHIP performance measures through the SCHIP annual reports beginning in FY 2003. CMS revised the SCHIP state annual report template in FY 2003 to include the core measures for states to report, to the extent they have data available. CMS received and analyzed the FY 2003 SCHIP annual reports from all states. CMS also amended a contract to enhance the reporting of quality performance measurement for SCHIP, in preparation for the FY 2004 annual reports.

Data Reliability

The program enrollment data that States submit through the Statistical Enrollment Data System are reviewed by CMS every quarter. CMS will measure, to the extent possible, the unduplicated count of the number of children who are enrolled in any of the following programs: regular Medicaid; expansions of Medicaid through SCHIP; and separate SCHIP programs as reported by the States. While CMS considers an unduplicated count to be an appropriate measure for this goal and the unduplicated count we can be measured within each program, some children may be enrolled in Medicaid at one point in the year and in SCHIP at another point, making it difficult to establish an accurate unduplicated count across all programs. Similarly, the SCHIP counts include some double counting of children in States that have combination programs. To the extent the data allows, CMS will closely monitor this issue.

The data for this goal is complete and reliable. This program is audited through the CMS Chief Financial Officer audit.

Program Assessment and Evaluations

SCHIP:

A contractor will prepare an analysis of the state-reported core performance measures by the end of FY 2005.

Medicaid: