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OCR for page 257
Assessing the Quality of Cancer Care: An Approach to Measurement in Georgia
APPENDIX B
Sources of Data: Surveys and Datasets
The data sources for the measures recommended in this report include a variety of established surveys and datasets. This appendix describes the following:
Behavioral Risk Factor Surveillance System;
Consumer Assessment of Health Plans Study;
Health Plan Employer Data and Information Set;
National Home and Hospice Care Survey;
National Vital Statistics System—Mortality; and
Youth Risk Behavior Survey.
OCR for page 258
Assessing the Quality of Cancer Care: An Approach to Measurement in Georgia
Behavioral Risk Factor Surveillance System (BRFSS)
Sponsor
U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotio
Description
Population-based survey. Objective is to collect uniform, state-specific, data on preventive health practices and risk behaviors that are linked to chronic diseases (including cancer), injuries, and preventable infectious diseases in the adult population
Mode of administration/data collection
Telephone interview. Data are collected separately by each state.
Sample design
State-level, random-digit-dialed probability samples
Primary survey content
A rotating core of questions asked every other year in all states, standardized optional questions on selected topics that are administered at the state’s discretion, and state-added questions developed to address state-specific needs. Questions cover behavioral risk factors (e.g., alcohol and tobacco use), preventive health measures including cancer screening, health status, limitation of activity, and health care access and utilization.
Population targeted
U.S. civilian, noninstitutionalized population 18 years of age and older in households with telephones
Demographic data
Gender, age, education, race/ethnicity, household income, employment status, and marital status
Years
Since 1984
Schedule
Annual
Geographic estimates
National; state; smaller area estimates possible in some states
Contact information
http://www.cdc.gov/brfss
OCR for page 259
Assessing the Quality of Cancer Care: An Approach to Measurement in Georgia
Consumer Assessment of Health Plans Study (CAHPS)
Sponsors
U.S. Department of Health and Human Services, including the Agency for Healthcare Research and Quality; Center for Medicare and Medicaid programs, State Medicaid agencies, and State Children’s Health Insurance Programs; public and private employers, individual health plans, and the U.S. Department of Defense
Description
Survey designed to develop and test questionnaires that assess health plans and services, to produce easily understandable reports for communicating survey information to consumers, and to evaluate the usefulness of these reports for consumers in selecting health care plans and services
Mode of administration/data collection
Mail or telephone questionnaire
Sample design
Random sample of health plan members by independent survey vendors following standardized procedures
Primary survey content
Consumer experiences in obtaining health care, including five major areas: getting needed care; getting care without long waits; how well doctors communicate; courteous and helpful office staff; customer service.
Population targeted
Surveys are tailored for various groups, including adults; children; children with chronic conditions; insured populations including commercial, Medicaid, Medicare, and Medicare managed care.
Demographic data
Age, gender, education, race, ethnicity, region, insurance coverage, health status
Years
Since 1998
Schedule
Annual
Geographic estimates
State, census bureau regions
Contact information
http://ncbd.cahps.org
Other
The National CAHPS Benchmarking Database is a national repository of CAHPS survey data that is available to researchers and others interested in using comparative CAHPS survey results for benchmarking and research. Information available at http://ncbd.cahps.org/Home/index.asp.
OCR for page 260
Assessing the Quality of Cancer Care: An Approach to Measurement in Georgia
Health Plan Employer Data and Information Set (HEDIS)
Sponsor
National Committee for Quality Assurance (NCQA)
Description
A set of standardized performance measures designed to provide purchasers and consumers with the ability to evaluate the quality of different health plans.
Mode of administration/data collection
NCQA collects and maintains HEDIS data directly from its member managed-care organizations and preferred provider organizations. All HEDIS data are maintained in a central database.
Sample design
NA
Primary survey content
Effectiveness of care (e.g. cancer screening, immunization status, etc.), access/availability of care, member satisfaction with the experience of care, cost of care, health plan stability, informed health care choices, use of services
Population targeted
Health plan members including children and adults enrolled in Medicaid, Medicare, and commercial health plans
Demographic data
Age, sex, race, education
Years
Since 1993
Schedule
Annual
Geographic estimates
By health plan
Contact information
http://www.ncqa.org/Programs/HEDIS/
NA = not applicable.
OCR for page 261
Assessing the Quality of Cancer Care: An Approach to Measurement in Georgia
National Home and Hospice Care Survey
Sponsor
U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Health Statistics
Description
Survey of home and hospice care agencies concerning agency management and current and discharged patients
Mode of administration/data collection
Personal interviews with administrators and staff are used to complete questionnaires for samples of current and discharged patients.
Sample design
Stratified two-stage probability sample of patients served by Medicare- or Medicaid-certified agencies
Primary survey/database content
Referral and length of service, diagnoses, number of visits, patient charges, health status, reason for discharge, and types of services provided
Population targeted
Patients of U.S. home health and hospice care agencies
Demographic
Gender, age, educational attainment, race/ethnicity, marital data status and health status
Years
For individual years from 1992-1994, 1996, 1998, and 2000
Schedule
Periodically, based on funding availability
Geographic estimates
U.S. Bureau of Census regions and metropolitan statistical areas
Contact information
http://www.cdc.gov/nchs/about/major/nhhcsd/nhhcsd.htm
OCR for page 262
Assessing the Quality of Cancer Care: An Approach to Measurement in Georgia
National Vital Statistics System—Mortality
Sponsor
U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Health Statistics
Description
An intergovernmental collaboration between the National Center for Health Statistics and the 50 states, two cities, and five territories organized to collect and disseminate mortality statistical information from death certificates
Mode of administration/data collection
Death certificates are completed by physicians, coroners, medical examiners, and funeral directors and filed with state vital statistics offices.
Sample design
All deaths (nationally, about 2.2 to 2.3 million annually)
Primary survey/database content
Year of death, underlying and multiple causes of death, place of decedent’s residence, place death occurred, age at death, day and month of death, selected demographic data
Population targeted
U.S. deaths
Demographic data
Detailed race and ethnicity, marital status, place of birth, gender, educational attainment for selected states, and occupation and industry for selected states
Years
Complete since 1933
Schedule
Annual
Geographic estimates
National, regional, and state. Selected data are available for counties with more than 100,000 persons.
Contact information
http://www.cdc.gov/nchs/about/major/dvs/mortdata.htm
OCR for page 263
Assessing the Quality of Cancer Care: An Approach to Measurement in Georgia
Youth Risk Behavior Survey (YRBS)
Sponsor
U.S. Department of Health and Human Services, Centers for Disease Control and Prevention (CDC)
Description
YRBS, a component of the Youth Risk Behavior Survey Surveillance System, is a national school-based survey of high school students that is conducted by CDC. It is designed to monitor national progress toward achieving the Healthy People 2000 and 2010 objectives and to track health risk behaviors among youth. States can receive federal funding to conduct the YRBS for state and local purposes. The state version of the survey uses different sampling and other procedures.
Mode of administration/data collection
Self-administered questionnaire. Students record their responses on a computer-scannable booklet or answer sheet.
Sample design
Three-stage, cluster sample design
Primary survey content
Risk behaviors such as tobacco use, inadequate physical activity, alcohol and drug use, and sexual behavior
Population targeted
9th–12th grade students. States have the option of also surveying middle school students or those in juvenile justice facilities.
Demographic Data
Gender, age, grade in school
Years
Since 1991
Schedule
The national YRBS is conducted every 2 years.
Geographic estimates
National-level estimates only from the national survey
Contact information
http://www.cdc.gov/HealthyYouth/yrbs/
NA = not applicable.
Representative terms from entire chapter:
health plans