Showing 1 – 50 of 282 results.
Curated
ABC News HMO Poll, November 1995 (ICPSR 6683)
Released/updated on: 2006-11-15
Geographic coverage: United States
This special topic poll sought respondents' views on Health Maintenance Organizations (HMOs) and a range of other issues. Respondents were asked to rate their current health insurance coverage based on the quality of care received, cost, personal attention received from the doctor, ability to make an appointment, ability to see medical specialists when necessary, and ability to receive the most sophisticated medical treatments. Respondents were also asked for their opinions of President Bill Clinton and his handling of the presidency, the economy, and foreign policy. They were also queried about the 1996 presidential and congressional elections, the recent Republican budget proposal, and with whom they placed the blame for the looming federal government shutdown. The situation in Bosnia was addressed, with questions covering the sending of U.S. troops to Bosnia, Congressional approval of the troop deployment, and whether America's vital interests were at stake. In addition, respondents were asked to name their favorite traditional Thanksgiving dinner food and to specify if they preferred white or dark meat. Demographic variables include age, race, sex, education, political party, political orientation, family income, voter registration history, and health insurance coverage.
Curated
Alameda County [California] Health and Ways of Living Study, 1994 and 1995 Panels (ICPSR 3083)
Released/updated on: 2006-03-06
Geographic coverage: United States, California
This collection provides a 30-year follow-up with respondents from Alameda County who were originally interviewed in 1965 for the first wave of the Health and Ways of Living Study. The purpose of the survey was to explore the influences of health practices and social relationships on the physical and mental health of a typical sample of the population. The first wave of the study, HEALTH AND WAYS OF LIVING STUDY, 1965 PANEL: [ALAMEDA COUNTY, CALIFORNIA] (ICPSR 6688), collected information for 6,928 respondents (including approximately 500 women aged 65 years and older) on chronic health conditions, health behaviors, social involvements, and psychological characteristics. The second wave, the 1974 panel (ALAMEDA COUNTY [CALIFORNIA] HEALTH AND WAYS OF LIVING STUDY, 1974 PANEL [ICPSR 6838]), collected information from 4,864 of the original respondents. The third and fourth waves (1994 and 1995 panels, respectively), provided in this collection, explore some new topics. The third wave provides a follow-up of 2,729 original 1965 and 1974 respondents and examines health behaviors such as alcohol consumption and smoking habits, along with social activities. Also included is information on health conditions such as diabetes, osteoporosis, hormone replacement, and mental illness. Another central topic investigated is activities of daily living (including self-care such as dressing, eating, and shopping), along with use of free time and level of involvement in social, recreational, religious, and environmental groups. The fourth wave is a follow-up to the 1994 panel, and contains 2,569 cases. This wave examines changes in functional abilities such as self-care activities, employment, involvement in community activities, visiting friends/family, and use of free time since 1994.
Curated
Alameda County [California] Health and Ways of Living Study, 1999 Panel (ICPSR 4432)
Released/updated on: 2006-11-16
Geographic coverage: United States, California
This fifth wave of data, collected in 1999, provides follow-up with 2,123 respondents from Alameda County who were originally interviewed in 1965 for the first wave of the Health and Ways of Living Study. The purpose of the survey was to explore the influences of health practices and social relationships on the physical and mental health of a typical sample of the population. Part 2 of this collection contains mortality data including cause and year of death. The first wave of the study, HEALTH AND WAYS OF LIVING STUDY, 1965 PANEL: [ALAMEDA COUNTY, CALIFORNIA] (ICPSR 6688), collected information for 6,928 respondents (including 360 men and 530 women aged 65 years and older) on chronic health conditions, health behaviors, social involvements, and psychological characteristics. The second wave, the 1974 panel, ALAMEDA COUNTY [CALIFORNIA] HEALTH AND WAYS OF LIVING STUDY, 1974 PANEL (ICPSR 6838), collected information from 4,864 of the original respondents. The third and fourth waves, ALAMEDA COUNTY [CALIFORNIA] HEALTH AND WAYS OF LIVING STUDY, 1994 and 1995 PANELS (ICPSR 3083), provided a follow-up of 2,729 original 1965 and 1974 respondents. The fourth wave is a follow-up to the 1994 panel and contains 2,569 cases.
Curated
Australian [Adelaide] Longitudinal Study of Aging, Wave 6: [1999-2000] (ICPSR 3679)
Released/updated on: 2006-01-18
Geographic coverage: Australia, Global
Time period: 1999-01-01--2000-01-01
The general purpose of the Australian [Adelaide] Longitudinal Study of Aging (ALSA) is to gain further understanding of how social, biomedical, and environmental factors are associated with age-related changes in the health and well-being of persons aged 70 years and older. Emphasis is given to the effects of social and economic factors on morbidity, disability, acute and long-term care service use, and mortality. The aim is to analyze the complex relationships between individual and social factors and changes in health status, health care needs, and service utilization dimensions. Components of Wave 6 (1999-2000) (Part 1) include a comprehensive personal interview conducted via the Computer-Assisted Personal Interview (CAPI) system, a home-based assessment of physiological functions, self-completed questionnaires, and additional clinical studies. In Part 2, Wave 6 Clinical Data, information about the health histories of the respondents was elicited, including information on medication, blood pressure, and physical and mental disabilities.
Curated
Bicol Community Survey (BCS), 1981: [Philippines] (ICPSR 6888)
Released/updated on: 2006-03-30
Geographic coverage: Philippines, Global
During 1981, the Bicol Community Survey gathered data from 100 barangays located in the same provinces of the Philippines that were sampled by the BICOL MULTIPURPOSE SURVEY (BMS), 1978: [PHILIPPINES] (ICPSR 6878): Albay, Camarines Sur, and Sorsogon. Barangays are political subdivisions equivalent to villages in rural areas and to neighborhoods in urban areas. Data were gathered at the community level from barangay heads, health care providers (both public and private), traditional birth practitioners (hilots), traditional healers (herbolario), and barangay residents using a questionnaire divided into six different sections, each with its own particular focus. The six sections correspond to the six data files in this collection. Part 1, Infant Food Prices, contains information from one store in each barangay on content, availability, and price information of infant foods. Part 2, Health Services: Availability and Distance, contains one observation for each barangay from either barangay captains, barangay officials, or housewives regarding the time and cost of travel to health providers, both public and private. Part 3, Health Services: Prices and Quality, provides information from 518 heads of health care facilities, private health care professionals, traditional birth practitioners, and traditional healers about travel costs, costs per visit, and costs for prescribed medication. Part 4, Promotional Practices of Infant Food Companies, offers responses from hilots, heads of health facilities, and private professionals about brands of infant formula available, whether free samples and pamphlets were provided, and whether supplies such as pads, pencils, equipment, or posters were donated. Part 5, Environmental Sanitation, provides data from sanitary inspectors on water availability, water conditions, and garbage disposal within the barangay. For Part 6, Health Professionals Survey Data, heads of facilities and private professionals were given a self-administered survey regarding the demographic, educational, and employment characteristics of workers, along with their knowledge of and attitude toward breast-feeding. Interviews conducted with hilots by field workers using the same questionnaire are also included.
Curated
Bicol Multipurpose Survey (BMS), 1978: [Philippines] (ICPSR 6878)
Released/updated on: 2005-11-04
Geographic coverage: Philippines
The Bicol Multipurpose Survey (BMS) was designed to assess the impact of the Bicol River Basin Development Project (BRBDP) on one of the poorest regions in the Philippines. Using data collected from both semi-urban and rural areas of the Bicol Region, the BMS sought to examine the impact not only of the various development projects of the BRBDP such as irrigation, electricity, and road repair, but also the economic, social, and health issues faced by the residents of the Bicol Region. The survey gathered data for 17 project areas and 3 cities in the provinces of Albay, Camarines Sur, and Sorsogon. Household-level information (Part 1) covers household characteristics, physical environment, income and expenditures, distance from schools, and respondents' feelings about household conditions and the progress of the barangay in which they lived (a barangay is a political subdivision equivalent to a village in rural areas and to a neighborhood in urban areas). Information on topics such as attitudes about foods during pregnancy, infant and child care, prenatal care, community involvement, and work history are contained in a separate Mothers Data file (Part 2). The individual-level data (Parts 3-5) contain demographic information such as age, sex, and education, and include time spent on household and occupational tasks. Information was collected from persons as young as 6 years of age, but was coded for individuals 15 years and older for tasks such as selling, food preparation, farm work, raising livestock and poultry, and the type and amount of fishing. Morbidity data from over 17,000 individuals are also included. The Household Production files (Parts 6-11) cover agriculture and business, crop production, rice farming, raising livestock and poultry, type of fishing done, and quantity of fish caught. Also included are income figures, assets, and liabilities. The Barangay Survey (Part 12) examines the physical aspects of the barangay and the use of social services in the area to determine the impact of the BRBDP and outside influences. The barangay captain or official records provided information on the physical characteristics, community services, medical services, social services, sanitation, and educational systems available within the barangay. The Extension Workers Survey (Part 13) asked 324 workers about their knowledge and activities regarding agricultural practices such as fertilizer use, pest and disease control, and other aspects of planting and transplanting. Through the Medical Practitioners Survey (Part 14), 426 practitioners were asked questions on their education and training, general health knowledge and experience, and knowledge and attitudes about birth control. Data collected in 1978, 1983, and 1994 can be used individually or merged together on a unique household identifier found in Part 15 (with the exception of the Medical Practitioners and Extension Workers data).
Curated
Bicol Multipurpose Survey (BMS), 1983: [Philippines] (ICPSR 6889)
Released/updated on: 2006-01-12
Geographic coverage: Philippines, Global
Time period: 1978-01-01--1982-01-01
The 1983 Bicol Multipurpose Survey (BMS) was designed to revisit the residents of the Bicol Region of the Philippines who were surveyed during 1978 in an effort to review the progress of the Bicol River Basin Development Project (BRBDP). The Bicol Multipurpose Survey (BMS) was designed to assess the impact of the BRBDP on one of the poorest regions in the Philippines. Using data collected from both semi-urban and rural areas of the Bicol Region, the BMS sought to examine the impact not only of the various development projects of the BRBDP such as irrigation, electricity, and road repair, but also the economic, social, and health issues faced by the residents of the Bicol Region. The survey gathered data for 17 project areas and 3 cities in the provinces of Albay, Camarines Sur, and Sorsogon. The 1983 BMS follows the same design as BICOL MULTIPURPOSE SURVEY (BMS), 1978: [PHILIPPINES] (ICPSR 6878), with the data being organized into 31 "blocks" or series of questions. A total of 1,901 households were surveyed in 1983, most of which were previously surveyed in 1978. An additional replacement sample of 420 was drawn from the 1978 rosters for the 1983 survey. Respondents were again asked about income, employment, education, health status, and health services. Additionally, the 1983 survey gathered extensive information on fishing, business expenses, and small business activities, along with fertility, pregnancy, and mortality histories. Due to time and cost considerations, detailed questions on credit, some health-related items regarding beliefs, chronic illnesses, and breast-feeding, and detailed questions on crops were not included in the 1983 BMS. Section I, Household Data (Parts 1-32), focused on background information, transportation, environment, morbidity, and health services. Information was gathered about people living in the household six months prior to the survey as well as people who had left the household five years prior to the survey. Expenditure data on schooling were gathered for individuals 6-30 years of age. Marriage and pregnancy histories were elicited from women aged 15-49 along with family planning and birth interval information. Section II, Agriculture/Income/Labor Data (Parts 33-87), posed questions on employment, wages, and hired labor for men, women, and children aged 6-15. Data on coconut, sugar cane, and abaca crop production were also gathered, along with information about livestock and poultry, and extensive data were collected about fishing activities. Fishing boat owners were interviewed, along with capture fisherman who fished both inland and marine waters. The Barangay Survey (Parts 88-96) provided information about characteristics of the barangay in which the respondent lived (a barangay is a political subdivision equivalent to a village in rural areas and to a neighborhood in urban areas), services available in the community, types of social services or practitioners, the availability of public utilities and transportation, different types of organizations present within the barangay, employment conditions, and environmental sanitation conditions.
Curated
Brazilian Survey on Nutrition and Health, 1989 (ICPSR 2294)
Released/updated on: 1998-05-11
Geographic coverage: Brazil, Global
The Brazilian Survey on Nutrition and Health, 1989 (PNSN-1989) provides information on various measures of nutrition and health for the Brazilian population, including anthropometric measures, health conditions, access to public health services, food supplementation, and obstetrical data. Evaluation of nutritional conditions is based upon measures of weight and height. Demographic and socioeconomic variables included in the survey cover population, housing conditions, level of education, household income, and occupation.
Curated
Community Hospital Program (CHP) Access Impact Evaluation Surveys, 1978-1979, 1981 (ICPSR 8245)
Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1978-01-01--1979-01-01
This data collection evaluates group medical practices and the ways in which they affect both access to and use of medical services. Group practices, sponsored by the Robert Wood Johnson Foundation Community Hospital Program (CHP), were selected for use in this assessment. The data were collected by the Center for Health Administration Studies at the University of Chicago, with the assistance of Chilton Research Services. Two surveys were conducted for the study: a baseline survey in 1978-1979 and a follow-up in 1981. Community residents and CHP patients in 12 communities were interviewed. Demographic and medical care data were collected for selected individuals and families in the survey areas. Data on regular sources of medical care for individuals include the type of organization used, type of practice, accessibility, frequency of visits, types of health care professionals seen, cost, and satisfaction. Also in the collection are data on perceived health, episodes of illness (including symptoms, duration, disability days, and doctors consulted), use of preventive health care services, and insurance coverage. Demographic data for individuals and families include age, sex, race, educational attainment, employment, and income. Of the 198 files in this collection, 88 are "raw" data files and 110 are frequencies. The data files consist of four types. The first type are Sample Person files. These contain the responses of group practice patients and community members. The second type are Doctor Episode files, which record doctors and episodes of illness. Family files make up the third type of file, and consist of family members' responses to the survey. Analysis files, linking patient and doctor data, are the fourth type of file. The SPSS frequency files correspond to the data files: two per file for the Sample Person files, and one per file for the remaining three types of files.
Curated
Partially restricted
Community Tracking Study Household Survey, 1996-1997, and Followback Survey, 1997-1998: [United States] (ICPSR 2524)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1996-07-01--1997-07-01, 1997-10-01--1998-08-01
This data collection comprises two components of the Community Tracking Study (CTS), the Household Survey and the Followback Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and their effects on care delivery and individuals. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The Household Survey was administered to households in the 60 CTS sites and to a supplemental national sample of households. At the beginning of each interview, a household informant was identified and queried about the composition of the household. With this information, individuals in the household were grouped into family insurance units (FIU). An FIU reflects family groupings typically used by insurance carriers. It includes an adult household member, his or her spouse, if any, and any dependent children 0-17 years of age (or 18-22 years of age if a full-time student). Family informants, selected from each FIU in the household, provided information on health insurance coverage, health care use, usual source of care, and the general health of all persons in the FIU. These informants also provided information on family income and out-of-pocket expenses for health care, as well as employment, race, and Hispanic origin for all adult FIU members. Each adult in the household, including the FIU informants, responded through a self-response module to questions regarding unmet health care needs, patient trust, satisfaction with physician choice, limitations in daily activities, smoking behaviors, and last doctor visit. In FIUs with more than one child under 18, only one child was randomly selected for inclusion in the survey. The family informant responded on behalf of the child regarding unmet needs and satisfaction with physician choice. The adult family member who took this child to his or her last doctor visit responded to questions about the visit. The Followback Survey was designed to obtain detailed information on private health insurance coverage reported in the Household Survey. It was administered to health plans and other organizations that offered or administered the comprehensive private health insurance policies covering Household Survey respondents in the 60 CTS sites. Information on private health insurance policies collected by the Followback Survey includes product type, gatekeeping, consumer cost sharing, provider payment methods, and coverage of mental health and/or substance abuse services.
Curated
Partially restricted
Community Tracking Study Household Survey, 1998-1999, and Followback Survey, 1998-2000: [United States] (ICPSR 3199)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1998-01-01--2000-01-01
This collection comprises the second round of the Community Tracking Study (CTS) Household Survey and the second round of the CTS Followback Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and their effects on care delivery and individuals. Fifty-one metropolitan areas and nine nonmetropolitan areas were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first round of the Household Survey (COMMUNITY TRACKING STUDY HOUSEHOLD SURVEY, 1996-1997, AND FOLLOWBACK SURVEY, 1997-1998: [UNITED STATES] (ICPSR 2524)), the second round of the Household Survey was administered to households in the 60 CTS sites and to a supplemental national sample of households. Respondents provided information about household composition and demographic characteristics, health insurance coverage, use of health services, unmet health care needs, out-of-pocket expenses for health care, usual source of care, patient trust and satisfaction, last visit to a medical provider, health status and presence of chronic health conditions, risk behaviors and smoking, and employment, earnings, and income. The purpose of the Followback Survey was to obtain detailed information on private health insurance coverage reported in the Household Survey. It was administered to the health plans and other organizations (managed care organizations, third-party administrators, employer or union plans, and employers) that offered or administered the respondents' comprehensive private health insurance policies. Information on private health insurance policies collected by the Followback Survey includes product type, gatekeeping, consumer cost sharing, provider payment methods, and coverage of mental health and/or substance abuse services.
Curated
Partially restricted
Community Tracking Study Household Survey, 2000-2001: [United States] (ICPSR 3764)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2000-01-01--2001-01-01
This collection comprises the third round of the Community Tracking Study (CTS) Household Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and the effects of those changes on people. Fifty-one metropolitan areas and nine nonmetropolitan areas were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first two rounds of the Household Survey (ICPSR 2524 and 3199), the third round was administered to households in the 60 CTS sites and to a supplemental national sample of households. Respondents provided information about household composition and demographic characteristics, health insurance coverage, use of health services, unmet health care needs, out-of-pocket expenses for health care, usual source of care, patient trust and satisfaction, last visit to a medical provider, health status and presence of chronic health conditions, risk behaviors and smoking, and employment, earnings, and income. A new set of sample design variables was added to the third round data for variance estimation by statistical software packages other than SUDAAN.
Curated
Partially restricted
Community Tracking Study Household Survey, 2003: [United States] (ICPSR 4216)
Released/updated on: 2007-12-03
Geographic coverage: United States
Time period: 2003-01-01--2004-01-01
This collection contains data and documentation for the fourth round of the Community Tracking Study (CTS) Household Survey. Sponsored by the Robert Wood Johnson Foundation, the CTS is a national study designed to track changes in the United States' health care system and their effects. The fourth round was administered to households in the 60 CTS sites: 51 metropolitan areas and nine nonmetropolitan areas which were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The first round of the CTS Household Survey was conducted in 1996-1997 (ICPSR 2524), the second round in 1998-1999 (ICPSR 3199), and the third in 2000-2001 (ICPSR 3764). Respondents to the fourth round provided information about health insurance coverage, use of health services, unmet needs for health care, children's special health care needs, out-of-pocket medical costs, patient trust in physicians, sources of health information, attitudes about medical care, and satisfaction with health care and health plans. Health status, chronic conditions, and risk attitudes and smoking behavior were additional topics covered by the fourth round questionnaire. The data include variables on height and weight, employment, income, ethnicity, race, United States citizenship, household composition, and demographic characteristics.
Curated
Partially restricted
Community Tracking Study Physician Survey, 1996-1997: [United States] (ICPSR 2597)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1996-08-01--1997-08-01
Sponsored by the Robert Wood Johnson Foundation, this survey is one component of the Community Tracking Study (CTS), a national study designed to track changes in the health care system and the effects of the changes on care delivery and on individuals. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The Physician Survey was administered to physicians in the 60 CTS sites and to a supplemental national sample of physicians. Information gathered by the survey instrument includes physician supply and specialty distribution, practice arrangements and physician ownership of practices, sources of practice revenue, level and determinants of physician compensation, effects of care management strategies, and physicians' allocation of time, provision of charity care, career satisfaction, and perceptions of their ability to deliver care. For primary care physicians, the survey instrument also provided vignettes of various clinical presentations for which there was no prescribed method of treatment. These physicians were asked to indicate the percentage of patients for whom they would recommend the course of action specified in each particular vignette. Part 3, the Site and County Crosswalk Data File, describes which counties constitute each site. Part 4, the Physician Survey Summary File, contains site-level averages and percentages and standard errors of these estimates for selected attributes, e.g., the percentage of physicians who were foreign medical school graduates, average age of physicians, average percentage of patient care practice revenue from Medicaid, etc.
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Partially restricted
Community Tracking Study Physician Survey, 1998-1999: [United States] (ICPSR 3267)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1998-01-01--1999-01-01
This study comprises the second round of the physician survey component of the Community Tracking Study (CTS) sponsored by the Robert Wood Johnson Foundation. The CTS is a national study designed to track changes in the American health care system and the effects of the changes on care delivery and on individuals. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first round of the physician survey (COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1996-1997: [UNITED STATES] (ICPSR 2597)), the second round was administered to physicians in the 60 CTS sites and to a supplemental national sample of physicians. The survey instrument collected information on physician supply and specialty distribution, practice arrangements and physician ownership of practices, physician time allocation, sources of practice revenue, level and determinants of physician compensation, provision of charity care, career satisfaction, physicians' perceptions of their ability to deliver care, views on care management strategies, and various other aspects of physicians' practice of medicine. In addition, primary care physicians (PCPs) were asked to recommend courses of action in response to some vignettes of clinical presentations for which there was no prescribed method of treatment.
Dataset 3, the Site and County Crosswalk Data File, identifies the counties that constitute each CTS site.
Dataset 4, the Physician Survey Summary File, contains site-level estimates and standard errors of the estimates for selected physician characteristics, e.g., the percentage of physicians who were foreign medical school graduates, the mean age of physicians, and the mean percentage of patient care practice revenue from Medicaid.
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Partially restricted
Community Tracking Study Physician Survey, 2000-2001: [United States] (ICPSR 3820)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2000-01-01--2001-01-01
This study comprises the third round of the physician survey component of the Community Tracking Study (CTS). Sponsored by the Robert Wood Johnson Foundation, the CTS is a large-scale investigation of changes in the health care system and their effects on people. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first two rounds of the physician survey, COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1996-1997: [UNITED STATES] (ICPSR 2597) and COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1998-1999: [UNITED STATES] (ICPSR 3267), the third round was administered to physicians in the 60 CTS sites and to a supplemental national sample of physicians. The survey instrument collected information on physician supply and specialty distribution, practice arrangements and physician ownership of practices, physician time allocation, sources of practice revenue, level and determinants of physician compensation, provision of charity care, career satisfaction, physicians' perceptions of their ability to deliver care, effects of care management strategies, and various other aspects of physicians' practice of medicine. Part 3, the Site and County Crosswalk Data File, identifies the counties that constitute each CTS site. Part 4, Physician Survey Summary File, contains site-level estimates and standard errors for selected physician characteristics, e.g., the average age of physicians, the percentage of physicians who were either very or somewhat dissatisfied with their overall career in medicine, and the average percentage of patients with prescription coverage that included the use of a formulary.
Curated
Decision-Related Research on the Organization of Service Delivery Systems in Metropolitan Areas: Public Health (ICPSR 7374)
Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1970-01-01--1975-01-01
This study represents one of four research projects on service delivery systems in metropolitan areas, covering fire protection (DECISION-RELATED RESEARCH ON THE ORGANIZATION OF SERVICE DELIVERY SYSTEMS IN METROPOLITAN AREAS: FIRE PROTECTION [ICPSR 7409]), police protection (DECISION-RELATED RESEARCH ON THE ORGANIZATION OF SERVICE DELIVERY SYSTEMS IN METROPOLITAN AREAS: POLICE PROTECTION [ICPSR 7427]), solid waste management (DECISION-RELATED RESEARCH ON THE ORGANIZATION OF SERVICE DELIVERY SYSTEMS IN METROPOLITAN AREAS: SOLID WASTE MANAGEMENT [ICPSR 7487]), and public health (the present study). All four projects used a common unit of analysis, namely all 200 Standard Metropolitan Statistical Areas (SMSAs) that, according to the 1970 Census, had a population of less than 1,500,000 and were entirely located within a single state. In each project, a limited amount of information was collected for all 200 SMSAs. More extensive data were gathered within independently drawn samples of these SMSAs, for all local geographical units and each administrative jurisdiction or agency in the service delivery areas. Two standardized systems of geocoding -- the Federal Information Processing Standard (FIPS) codes and the Office of Revenue Sharing (ORS) codes -- were used, so that data from various sources could be combined. The use of these two coding schemes also allows users to combine data from two or more of the research projects conducted in conjunction with the present one, or to add data from a wide variety of public data files. The delivery of public health services was investigated in 200 SMSAs plus Minneapolis and St. Paul. The basic data collection effort involved the use of public data sources as well as proprietary data from the American Medical Association (AMA) and the Commission on Professional and Hospital Activities (CPHA). Because of the proprietary nature of some of the data and for the preservation of confidentiality, all analyses were performed at the SMSA level. Unlike the other three related research projects, the present study does not provide disaggregated units of analysis such as the administrative jurisdiction, the individual hospital, or other facilities. Variables describe the characteristics of available professionals and facilities, regulatory factors reflecting the impact of federal and state programs available in the area, and financing factors, including the coverage of state Medicaid programs, Blue Cross and Blue Shield, and Medicare programs. Information is also provided regarding the demographic and socioeconomic characteristics of the population served in each SMSA.
Curated
Do Older Adults Know Their Spouses' End-of-Life Treatment Preferences? (ICPSR 25701)
Released/updated on: 2009-06-23
Geographic coverage: United States
When terminally ill patients become mentally incapacitated, their surrogates often make treatment decisions in collaboration with health care providers. The authors examined how surrogates' errors in reporting their spouses' preferences are affected by their gender, status as durable power of attorney for health care (DPAHC), whether they and their spouses discussed end-of-life preferences, and their spouses' health status. Structural equation models were applied to data from married couples in their mid-60s from the 2004 wave of the Wisconsin Longitudinal Study. Surrogates reported their spouses' preferences incorrectly 13 percent and 26 percent of the time in end-of-life scenarios involving cognitive impairment and physical pain, respectively. Surrogates projected their own preferences onto their spouses'. Similar patterns emerged regardless of surrogate gender and status as DPAHC, marital discussions about end-of-life preferences, or spousal health status. Implications for the process of surrogate decision-making and for future research are discussed.
Curated
Geriatric Home Care Utilization: San Francisco, 1968-1975 (ICPSR 7853)
Released/updated on: 2006-03-30
Geographic coverage: San Francisco, United States, California
Time period: 1968-01-01--1975-01-01
This data collection reported on geriatric clients served by San Francisco Home Health Services, Inc. (SFHHS) between 1968 and 1975. The study was designed to document and analyze the natural history of home care service use from entry to exit, noting what types of users were in a home care agency's program and how intensively services were utilized. The study also identified outcome categories useful for response to public policy questions on the effectiveness of various service types in meeting geriatric needs. Also examined was the relationship of home care use to nursing home entry, and to the need for other services. In Part 1, data for 2,435 clients were gathered from case records at SFHHS. Variables used in the analysis include entry characteristics (e.g, age, sex, condition, living arrangement, and contextual variables such as referral source, prior source of care, and payment type), duration, intensity, and type of service utilization, as well as discharge or exit status. Some of these are calculated variables derived from each case's accumulated monthly service records (found in their raw form in Part 2). Part 2 contains 35,729 client monthly service records, which are distributed as raw data as received from SFHHS. Variables include billing date, pay plan, and frequency and intensity of assistance.
Curated
Health Interview Survey, 1963 (ICPSR 28381)
Released/updated on: 2010-11-11
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are six types of records in this year's survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Family file (Part 2) includes information on family size, sex, race, education, health status of family members, and total health expenses for the family. The Person file (Part 3) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 4) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 5) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Health Expenditure file (Part 6) includes medical and health related expenses, such as hospital bills, medicine costs, dental bills, doctor bills, as well as insurance coverage and costs.
Curated
Health Interview Survey, 1964 (ICPSR 28663)
Released/updated on: 2010-07-06
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this year's survey, each in a separate data file. The Family file (Part 1) includes information on family size, sex, race, education, health status of family members, and total health expenses for the family. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The X-ray file (Part 5) includes information on X-ray records, doctor visits, height and weight, and total medical X-ray visits.
Curated
Health Interview Survey, 1965 (ICPSR 28761)
Released/updated on: 2010-07-13
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are six types of records in the 1965 survey, each in a separate data file. The Person file (Part 1) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and occupation. These variables are found in the Condition and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 2) contains information for each reported health condition, with specifics on injury and accident reports. The Prescribed Medicine file (Part 3) contains general demographic information, cost of medications, when medications were obtained, and conditions for which medications were prescribed. The Non-prescribed Medicine file (Part 4) contains general demographic information, where medications were obtained and purchased, as well as short-stay hospital episodes. The Diabetes file (Part 5) includes information regarding symptoms of diabetes, genetic variables, and treatment regimen variables. The Hospital Episode file (Part 6) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed.
Curated
Health Interview Survey, 1966 (ICPSR 28801)
Released/updated on: 2010-07-15
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this year's survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition file (Part 3) and the Hospital Episode file (Part 4) as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Medical Care Cost file (Part 5) includes information regarding short-stay hospital visits, family income, and total medical bill costs.
Curated
Health Interview Survey, 1967 (ICPSR 28862)
Released/updated on: 2010-07-16
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are six types of records in the 1967 survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and occupation. These variables are found in the Condition file (Part 3) and the Hospital Episode file (Part 4) as well. The Person file (Part 2) also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit file (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. The Home Care file (Part 6) documents basic demographic information, eating habits, in-home mobility, hospital visits, and the extent that basic living activities and needs are performed with or without aid.
Curated
Health Interview Survey, 1968 (ICPSR 28881)
Released/updated on: 2010-09-30
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. This 1968 study was a transition for the National Health Interview Survey (NHIS) from fiscal year (July 1 to June 30) to calendar year. The 1968 files include both fiscal year files and calendar year files, with some overlap between corresponding fiscal year and calendar year files. During the fiscal year, the NHIS sample was split and two types of questionnaires were administered to approximately half of the overall sample: the "condition approach" questionnaire and the "person approach" questionnaire. During the second half of calendar year 1968, the entire NHIS sample was interviewed using the person approach questionnaire. During this time period, five NHIS files are referred to as "core" files because they were administered each year (through 1996). The five core files are Household, Person, Condition, Doctor Visit, and Hospital. No evidence of a fiscal year Household file was found, and the existing calendar year Household file had too many anomalies to be included in this release. Thus, this release consists of fiscal year and calendar year versions of four out of the five core files, and three supplement files, for a total of eleven files. The eleven types of records in this year's survey are each in a separate data file. The Person Calendar and Fiscal Year files (Part 1 and Part 6) include information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. The Person files also supply data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition Calendar and Fiscal Year files (Part 2 and Part 7) contain information for each reported health condition, with specifics on injury and accident reports. The Hospital Calendar and Fiscal Year files (Part 3 and Part 8) provide information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit Calendar and Fiscal Year files (Part 4 and Part 8) document doctor visits within the time period and identify acute or chronic conditions. The Motor Vehicle Person Accident Calendar and Fiscal Year files (Part 5 and Part 10) contain information regarding types of motor accidents, how many vehicles were involved in a given accident, injuries acquired from a given accident, time of day the accident occurred, and treatments given as a result of a given accident. The Home Care Fiscal Year file (Part 11) documents basic demographic information, eating habits, in-home mobility, hospital visits, and the extent to which basic living activities and needs are performed with or without aid.
Curated
Health Interview Survey, 1970 (ICPSR 7838)
Released/updated on: 2010-09-21
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit file (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. The Health Insurance file (Part 6) includes information on education level, family income, hospital visits and length of stay, and also data on medical coverage, hospital coverage, medicare coverage, and doctor visit coverage. The Medical Care Cost file (Part 7) includes information on hospital bill expenses, doctor and dental bill expenses, optical bill expenses, and total personal and family expenses. The X-Ray file (Part 8) includes information on x-ray records, doctor visits, height, weight, and total medical x-ray visits.
Curated
Health Interview Survey, 1971 (ICPSR 8336)
Released/updated on: 2010-09-30
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The variables in the Household File (Part 2) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth file has been added, along with the five core files. The Person Supplement File (Part 6) provides information on health conditions, hearing quality, doctor visits, and hospital stay information.
Curated
Health Interview Survey, 1972 (ICPSR 8337)
Released/updated on: 2010-09-30
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth file has been added, along with the five core files. The Health Insurance File (Part 6) documents basic demographic information along with medical coverage and health insurance plans, as well as differentiates between hospital, doctor visit, and surgical insurance coverage.
Curated
Health Interview Survey, 1973 (ICPSR 8338)
Released/updated on: 2010-11-29
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth and seventh file have been added, along with the five core files. The Condition Supplement File (Part 6) documents past bed days, duration of limitation of the condition, whether or not a doctor was seen, the type of injury incurred, satisfaction with treatment, whether or not a prescription was given or filled, and if applicable, the reason why medical attention was not sought. The Pregnancy File (Part 7) documents activity restriction, bed disability, work or school loss days, doctor and dental visits within the last two weeks to twelve months, number of chronic conditions, time since routine physical exams have been completed, and the number of times pregnancies have been terminated in the past twelve months, as well as how many live births have occurred over one's lifetime, and routine pregnancy related doctor visits.
Curated
Health Interview Survey, 1974 (ICPSR 8339)
Released/updated on: 2010-11-29
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in the core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth and seventh file have been added along with the five core files. The Condition Supplement File (Part 6) provides further information regarding injuries, health status, medical advice received, travel time and waiting time for care, and satisfaction with health services provided. The Health Insurance File (Part 7) provides general demographic information as well as type of care obtained through insurance plans, work loss because of current conditions, and whether or not the patient has any type of insurance or no insurance coverage at all.
Curated
Health Interview Survey, 1975 (ICPSR 7672)
Released/updated on: 2010-11-15
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode File as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions.
Curated
Health Interview Survey, 1976 (ICPSR 8340)
Released/updated on: 2010-12-03
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions.
Curated
Health Interview Survey, 1977 (ICPSR 7839)
Released/updated on: 2010-12-14
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) in this collection include type of living quarters, size of family, and geographic region. The Person File (Part 2) variables include sex, age, race, marital status, veteran status, education, income, occupation, and limits on activity. The Condition File (Part 3) contains variables on the incidence of illness or injury within the past year. The Hospital Episode File (Part 4) contains variables on the incidence of hospitalizations and presence of chronic conditions. The Doctor Visit File (Part 5) includes variables regarding frequency of doctor visits, type of doctor seen, and reasons for each visit. A sixth, seventh, eighth, and ninth file have been provided. The Disability Supplement File (Part 6) contains variables on the need for help, services, and environment modifications. The H1 Supplement File (Part 7) includes basic demographic variables, medical information, health variables, doctor visits, medical insurance, work days lost, and activity level variables. The Special Aids Supplement File (Part 8)includes basic demographic variables, special aids onset and amount needed, medical information, health variables, and doctor visits. The Influenza Supplement File (Part 9) includes basic demographic variables, flu, grippe, or fever onset, work and school days lost, hospital visits, length of stay, and cost of care.
Curated
Health Interview Survey, 1978 (ICPSR 8044)
Released/updated on: 2011-01-05
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) in this collection include type of living quarters, size of family, and geographic region. The Person File (Part 2) variables include sex, age, race, marital status, veteran status, education, income, occupation, and limits on activity. The Condition File (Part 3) contains variables on the incidence of illness or injury within the past year. The Hospital Episode File (Part 4) contains variables on the incidence of hospitalizations and presence of chronic conditions. The Doctor Visit File (Part 5) includes variables regarding frequency of doctor visits, type of doctor seen, and reasons for each visit. A sixth and seventh file have been provided. The Family Medical Expenses File (Part 6) provides variables including sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. Other variables include amounts paid for personal, family, and outside family dental bills, doctor bills, hospital bills, optical bills, prescription medicine, health insurance, and other medical expenses. Other questions include total personal, family, and outside family medical expenses, including and excluding health insurance, and the sex and race of the family head. The Immunization File (Part 7) includes basic demographic variables, hospital stay length, doctor visit periods, types of immunizations received, and when they were obtained.
Curated
Health Interview Survey, 1981 (ICPSR 8319)
Released/updated on: 2011-04-25
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in the core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth file has been provided. The Child Health Supplement File (Part 6) provides detailed data on child health and development. This supplement offers information on age of child, sex, birth-date, physical and social development, family relationships, prenatal care, hospitalization and illness, behavior, schooling, and seat-belt usage.
Curated
Health Interview Survey, 1982 (ICPSR 8460)
Released/updated on: 2011-04-06
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in the 1982 core survey, each in a separate data file. The variables in the Household File (Part 1) in this collection include type of living quarters, size of family, region, condition list assigned, and type of PSU. The Person File (Part 2) variables include sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. The Condition File (Part 3), Doctor Visit File (Part 4), and Hospital Episode File (Part 5) contain information on each reported condition, two-week doctor visit, or hospitalization (twelve-month recall), respectively. A sixth and seventh file have been provided. The Health Insurance Supplement File (Part 6) contains questions about health insurance plans pertaining to the type of plan, including private, Medicare, Medicaid, military and other plans, and coverage or reasons for lack of coverage are provided. The Preventive Care Supplement File (Part 7) contains variables that chronicle when routine tests, physicals, and preventative examinations have last been performed.
Curated
Health Interview Survey, 1983 (ICPSR 8603)
Released/updated on: 2011-04-13
Geographic coverage: United States
The basic purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in household, and geographic region. The variables in the Person File (Part 2) include sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition (Part 3), Doctor Visit (Part 4), and Hospital Episode (Part 5) Files contain information on each reported condition, two-week doctor visit, or hospitalization (twelve-month recall), respectively. A sixth, seventh, eighth, and ninth file have been added, along with the five core files. The Alcohol/Health Practices Supplement File (Part 6) includes information on diet, smoking and drinking habits, and health problems. The Bed Days and Dental Care Supplement File (Part 7) contains information on the number of bed days, the number of and reason for dental visits, treatment(s) received, type of dentist seen, and travel time for visit. The Doctor Services Supplement File (Part 8) supplies data on visits to doctors or other health professionals, reasons for visits, health conditions, and operations performed. The Health Insurance Supplement File (Part 9) documents basic demographic information along with medical coverage and health insurance plans, as well as differentiates between hospital, doctor visit, and surgical insurance coverage.
Curated
Health Maintenance Organizations in the United States, 1984 (ICPSR 8468)
Released/updated on: 2006-01-18
Geographic coverage: United States
The Health Maintenance Organization study was designed to provide an up-to-date report card on how well HMOs are meeting the aspirations and demands of members, employers, and physicians who work in them. This study includes a detailed assessment of the strengths and successes, weaknesses and failures of HMOs as perceived by their key constituencies. This survey also obtained attitudes toward, and knowledge of HMOs among the general public, as well as changes in those attitudes. Other objectives include a comparison of different levels of knowledge, attitudes, and perceptions of HMOs among the public, employers, and physicians both working in HMOs and non-HMO physicians. Variables in the Corporate Employer file include familiarity with HMOs, whether the company offers HMOs to employees, type of experience with HMOs, incentives and drawbacks of HMOs, number of employees, industry of the company, and number of years at present position of the executive being interviewed. The Physicians file contains variables on opinions and attitudes toward HMOs, whether the physician is an HMO practitioner, the number of HMO patients seen in a week, changes in the physician's practice caused by HMOs, primary speciality, number of years in practice, and age. The Members of HMOs and Public Cross-Section files contain variables on HMO membership, opinions on services at HMOs, comparisons between HMOs and traditional services, desire to join an HMO, health of respondent, occupation, education, age, marital and financial status, and race.
Curated
Partially restricted
Hospitalized Older Persons Evaluation (HOPE) Study, 1991-1993: [California] (ICPSR 6560)
Released/updated on: 2006-01-12
Geographic coverage: United States, California
Time period: 1991-03-01--1993-05-31
The HOPE study was a multi-center randomized clinical trial mounted to determine the effects of hospital inpatient consultative comprehensive geriatric assessment (CGA) under typical practice conditions on selected patient health and health services utilization outcomes. The main outcome measures were functional status, health status, mortality, rehospitalization, and total use of health care services for hospital patients 65 years of age and older. Functional status was evaluated by questions about limitations in patients' activities of daily living due to health problems. Also included were items covering living arrangements (with whom and where), ethnicity, education, and marital status. Health status questions covered patients' perceptions of mental health and current physical health. The functional and health status of patients was measured prior to CGA treatment and randomization, again at 3 months post-randomization, and at 12 months post-randomization. Functional and health status data are included in Parts 3-8. Health services utilization data (Parts 9-15) cover patient use of medical services such as urgent care, emergency room, radiology, durable medical equipment, and medications (prescribed and over the counter). Mortality information (Part 17) includes date of lost contact or death, and data source of survival status. Hospitalization measures (Part 18) include date of admission and discharge, admittance source diagnoses and procedures, and inpatient/outpatient status.
Curated
Partially restricted
Local Health Department Infrastructure Study, 1999-2000: [United States] (ICPSR 3185)
Released/updated on: 2024-02-14
Time period: 1999-01-01--2000-01-01
The purpose of this survey was to address the paucity of current data on the United States' local public health infrastructure and to advance understanding of the many ways local public health agencies contribute to keeping the nation's population and environment healthy. The survey collected information on local health department (LHD) characteristics (e.g., type of jurisdiction served, office to which the LHD reported directly, total expenditures, and sources of the LHD's total budget), priority program areas, and public health services provided directly or through contracts with others. Additional data cover LHD workforce composition, staffing needs, workforce training, and partnerships and collaborations with other groups and organizations, such as state or federal agencies, hospitals, HMOs, community health centers, universities, community-based organizations, professional associations, faith communities/churches, and business/private corporations. LHDs also reported on completion of community health assessments and development of community health improvement plans.
Curated
Master Facility Inventory: Hospitals, 1976 (ICPSR 7630)
Released/updated on: 1992-02-16
The Master Facility Inventory (MFI) data collection provides a comprehensive list of hospital facilities in the United States in 1976. The criteria for inclusion were that a facility provided medical, nursing, personal, or custodial care to groups of unrelated persons on an inpatient basis and was licensed or operated by federal or state agencies. The American Hospital Association conducted the survey, supplying the resulting data to the National Center for Health Statistics in order to update its Master Facility Inventory on the number and kinds of hosptals in the United States and the changes in the list since the last MFI survey. Information gathered is for the previous calendar year and includes facility identification information, ownership, number of full- and part-time staff, number of beds per unit, number of adult and pediatric inpatients, numbers in newborn nursery, outpatient utlilization (e.g., emergency care and clinics), major and minor surgical operations, hospital classification (e.g., government, non-government, investor-owned), and finances (e.g., total revenue, expenses, and assets) for 7,271 institutions.
Curated
Master Facility Inventory: Nursing Homes and Other Health Care Facilities, 1976 (ICPSR 7631)
Released/updated on: 1992-02-16
The Master Facility Inventory data collection provides a comprehensive list of nursing, personal care, and domiciliary care facilities in the United States in 1976. The criteria for inclusion were that a facility provided medical, nursing, personal, or custodial care to groups of unrelated persons on an inpatient basis. The survey was conducted by the National Center for Health Statistics in order to update its Master Facility Inventory on the number and kinds of such facilities in the United States and the changes to the list since the last MFI survey. Information gathered is for the previous calendar year and includes facility identification information, ownership and type of facility, capacity and type of beds (i.e., total beds set up and staffed for use and number of beds certified by Medicare or Medicaid as skilled and intermediate), acceptance criteria, and total number of male and female residents (or patients) for 26,748 institutions.
Curated
Medicare Current Beneficiary Survey, Access to Care, Calendar Year 1992: [United States] (ICPSR 6332)
Released/updated on: 2006-01-12
Geographic coverage: United States
This data collection is the second in a series of data releases from the Medicare Current Beneficiary Survey (MCBS) relating to beneficiary access to medical care. The MCBS is a continuous, multipurpose survey of a representative sample of the Medicare population, both aged and disabled. Sample persons are interviewed three times a year over several years to form a continuous profile of their health care experience. Interviews are conducted regardless of whether the sample person resides at home or in a long-term care facility, using the questionnaire version appropriate to the setting. The MCBS also collects a variety of information about demographic characteristics (date of birth, sex, race, education, military service, and marital status), health status and functioning, access to care, sources of and satisfaction with care, insurance coverage, financial resources, and family supports. The 1992 interview data were collected during September through December of 1992, the fourth round of data collection. The 1992 data are designed to stand alone for cross-sectional analysis, or they can be used for longitudinal analysis. Weights are provided for both cross-sectional and longitudinal analysis.
Curated
Medicare Current Beneficiary Survey, Access to Care, Calendar Year 1993: [United States] (ICPSR 6637)
Released/updated on: 2006-01-12
Geographic coverage: United States
This data collection is the third in a series of data releases from the Medicare Current Beneficiary Survey (MCBS) relating to beneficiary access to medical care. The MCBS is a continuous, multipurpose survey of a representative sample of the Medicare population, both aged and disabled. Sample persons are interviewed three times a year over several years to form a continuous profile of their health care experience. Interviews are conducted regardless of whether the sample person resides at home or in a long-term care facility, using the questionnaire version appropriate to the setting. The MCBS also collects a variety of information about demographic characteristics (date of birth, sex, race, education, military service, and marital status), health status and functioning, access to care, sources of and satisfaction with care, insurance coverage, financial resources, and family supports. The 1993 interview data were collected during September through December of 1993, the seventh round of data collection. The 1993 data are designed to stand alone for cross-sectional analysis, or they can be used for longitudinal analysis. Weights are provided for both cross-sectional and longitudinal analysis.
Curated
Medicare Current Beneficiary Survey, Calendar Year 1991: [United States] (ICPSR 6118)
Released/updated on: 2006-01-12
Geographic coverage: United States
This data collection is the first in a series of data releases planned from the ongoing Medicare Current Beneficiary Survey (MCBS). The MCBS is a continuous, multipurpose survey of a representative sample of the Medicare population. Sample persons are interviewed three times a year over several years to form a continuous profile of their health care experience. Field work for Round 1 began in September of 1991 and was completed in December. New rounds, which involve reinterviewing the same sample persons (or other appropriate respondents), begin every four months. Interviews are conducted regardless of whether the sample person resides at home or in a long-term care facility, using the questionnaire version appropriate to the setting. This first-round interview captured baseline information about the Medicare population, including their demographic characteristics (date of birth, sex, race, education, military service, and marital status), health status and functioning, insurance coverage, financial resources, and family support. Round 1 of the community interview, which questioned respondents living at home, also included a topical supplement on access to medical care, sources of medical care, and satisfaction with medical care.
Curated
Simple Crosstabs
Medicare Health Outcomes Survey (HOS), 1998-2014 (ICPSR 23380)
Released/updated on: 2016-05-26
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States
Time period: 1998-01-01--2014-01-01
The Medicare Health Outcomes Survey (HOS) is the first patient reported health outcomes measure for the Medicare population in managed care settings. It is a continuous study that measures the physical and mental health and well-being of Medicare beneficiaries over a two-year period. Starting in 1998, a baseline survey was administered to a new cohort of respondents each year in the spring and a follow-up survey was conducted of those same respondents two years later. Cohorts 1-5 include the Baseline Data, the Follow-Up Data, and the Analytic Data file, which contains the merged Baseline and Follow-Up files along with supplemental variables. Beginning with Cohort 6, the Follow-Up Data were included only in the Analytic file. The HOS consists of the SF-36 Health Survey, which yields physical and mental health summary measures, as well as questions on topics such as chronic medical conditions, activities of daily living (ADLs), depression, smoking, physical health symptoms, weight and height, and additional questions corresponding to HEDIS (Health Care Employer Data and Information Set) measures such as urinary incontinence in older adults, osteoporosis testing in older women, and fall risk management. In 2006, CMS implemented the Medicare HOS 2.0 for Medicare Advantage Organizations (MAOs) which evaluates physical and mental health status using the Veteran RAND 12-Item Health Survey (VR-12). The revised instrument contains questions that gather information for case-mix and risk-adjustment variables, and collects information on respondents' physical functioning, bodily pain, social functioning, mental health, vitality, general health, and how respondents' physical and emotional health affects their lives. The survey includes case-mix adjustment variables which may be used to adjust the survey response data for beneficiary characteristics that are known to be related to systematic biases in the way people respond to survey questions. Demographic information includes respondent's age, gender, race, education level, marital status, annual household income, and geographic region.
Curated
National Ambulatory Medical Care Survey, 1973 (ICPSR 9192)
Released/updated on: 2008-09-12
Geographic coverage: United States
Time period: 1973-01-01--1974-01-01
The National Ambulatory Medical Care Surveys (NAMCS) supply data on ambulatory medical care provided in physicians' offices. These national estimates describe the utilization of ambulatory medical care and the nature and treatment of illness among the population seeking ambulatory care. The survey includes data on date of visit, reason for visit, date of birth, sex and race of patient, diagnosis, treatment, disposition of visit, and the physician's specialty.
Curated
National Ambulatory Medical Care Survey, 1975 (ICPSR 9193)
Released/updated on: 2008-09-12
Geographic coverage: United States
The National Ambulatory Medical Care Surveys (NAMCS) supply data on ambulatory medical care provided in physicians' offices. These national estimates describe the utilization of ambulatory medical care and the nature and treatment of illness among the population seeking ambulatory care. The survey includes data on date of visit, reason for visit, date of birth, sex and race of patient, diagnosis, treatment, disposition of visit, and the physician's specialty.
Curated
National Ambulatory Medical Care Survey, 1976 (ICPSR 9194)
Released/updated on: 2008-09-12
Geographic coverage: United States
The National Ambulatory Medical Care Surveys (NAMCS) supply data on ambulatory medical care provided in physicians' offices. These national estimates describe the utilization of ambulatory medical care and the nature and treatment of illness among the population seeking ambulatory care. The survey includes data on date of visit, reason for visit, date of birth, sex and race of patient, diagnosis, treatment, disposition of visit, and the physician's specialty.
Curated
National Ambulatory Medical Care Survey, 1977 (ICPSR 8046)
Released/updated on: 1992-02-16
Geographic coverage: United States
The National Ambulatory Medical Care Survey (NAMCS) contains data on medical care provided in physicians' offices and is a continuously sampled survey based on a nationwide sample of patient records.