Health

Description: Statistics Canada is conducting a test of new survey modules on mental health stigma and discrimination. In addition to the new modules, the test questionnaire includes Canadian Community Health Survey modules on general health, health status, income and sociodemographic characteristics.

Description: The purpose of the Survey on Living with Chronic Diseases in Canada (SLCDC) is to provide information on the impact of chronic disease on individuals, as well as how people with chronic disease manage their health condition.

Description: This is a national longitudinal survey that collects information on the transition from military to civilian life, general health and well-being, chronic conditions, labour force participation and other related information. An important goal of the survey is to understand the transition period from military to civilian life and health outcomes in Canadian Veterans.

Description: The purpose of the Survey on Living with Neurological Conditions in Canada is to collect new information about Canadians' experiences with chronic neurological conditions. The survey will report on various factors that impact on health for individuals living with these conditions, their families and caregivers.

Description: This pilot survey asks both smokers and non-smokers about their past and present smoking habits, their attitudes towards smoking, and other related issues.

Description: The purpose of the Childhood National Immunization Coverage Survey is to collect information on national immunization coverage for childhood vaccines.

Description: This survey collects data on the prevalence of several neurological conditions in long-term care facilities.

Description: The objectives of the BCPCHC Survey are: - To provide more information on how people manage their chronic conditions; - To identify barriers to care for those living with chronic conditions including economic and travel related barriers; - To identify barriers to self-management of chronic conditions.

Description: The health effects reported by individuals living in communities in close proximity to noise sources such as traffic, airports, railways and wind turbine installations are not fully understood due to limited scientific research in this area. The CNHS was developed to address this gap by investigating the prevalence of health effects or health indicators among a sample of Canadians exposed to these noise sources using both self-reported and objective health measures.

Description: This survey collects data on non-acute health care facilities that provide medical or professional nursing supervision or some higher level of care to residents.

Description: This table provides Canadians and researchers with provisional data to monitor weekly death trends by age and sex in Canada. Given the delays in receiving the data from the provincial and territorial vital statistics offices, these data are considered provisional. Data in this table will be available by province and territory.

Description:

This table provides Canadians and researchers with provisional data to monitor weekly death trends in Canada. Given the delays in receiving the data from the provincial and territorial vital statistics offices, these data are considered provisional. Data in this table will be available by province and territory.

Description:

This table provides Canadians and researchers with provisional data to monitor weekly death trends by selected grouped causes of death in Canada. Given the delays in receiving the data from the provincial and territorial vital statistics offices, these data are considered provisional. Data in this table will be available by province and territory.

Description: The table displays weekly age standardized mortality rates for every province in Canada (excluding territories), by sex, since 2019. The standardization is done using the 2011 Canadian population.

Description: This dashboard presents data that are relevant for monitoring mortality in Canada. The interactive visualization within the dashboard features insights on weekly death trends from the Canadian Vital Statistics - Death (CVSD) database.

Description: Number and percentage of children and youth with changes or no change in their functional difficulties between 2019 and 2023 by gender and age group, Canada (excluding territories) and provinces.

Description: Number and percentage of youth who report changes or no change in their health characteristics between 2019 and 2023 by gender and age group, Canada (excluding territories) and provinces.

Description: Drug metabolites in wastewater, presented as load per capita, in select Canadian cities, by type of drug. The 95% confidence interval, standard error, and imputation rate of the load per capita of the drug metabolites in wastewater are included.

Description: This dashboard presents provisional monthly estimates of the levels of amphetamine, cannabis, cocaine (benzoylecgonine), codeine, fentanyl (norfentanyl), ecstasy, methadone, methamphetamine, morphine, and oxycodone in the wastewater of Halifax, Montréal, Toronto, Saskatoon, Prince Albert, Edmonton, and Metro Vancouver. The data that are relevant for monitoring the use of these substances in Canadian cities.

Description: The Canadian Statistical Geospatial Explorer empowers users to discover geo enabled data holdings of Statistics Canada at various levels of geography including at the neighbourhood level. Users are able to visualize, thematically map, spatially explore and analyze, export and consume data in various formats. Users can also view the data superimposed on satellite imagery, topographic and street layers.

Description:

The National Health and Nutrition Examination Surveys (NHANES) is one of a series of health-related programs sponsored by the United States National Center for Health Statistics. A unique feature of NHANES is the administration of a complete medical examination for each respondent in the sample. To standardize administration, these examinations are carried out in mobile examination centers (MECs). The examination includes physical measurements, tests such as eye and dental examinations, and the collection of blood and urine specimens for laboratory testing. NHANES is an ongoing annual health survey of the noninstitutionalized civilian population of the United States. The major analytic goals of NHANES include estimating the number and percentage of persons in the U.S. population and in designated subgroups with selected diseases and risk factors. The sample design for NHANES needs to create a balance between the requirements for efficient annual and multiyear samples and the flexibility that allows changes in key design parameters to make the survey more responsive to the needs of the research and health policy communities. This paper discusses the challenges involved in designing and implementing a sample selection process that satisfies the goals of NHANES.

Description:

In the last two decades, considerable international effort has been put into the development of summary measures of population health that integrate information of mortality and non-fatal health outcomes and international policy interest in such indicators is increasing. There are two main classes of summary measures of population health: health gaps and health expectancies. The Disability-Adjusted Life Year (DALY) is the best known health gap measure and quantifies the gap between a population's actual health and a normative health goal, defined in terms of a global standard life table specifying the healthy years of life lost due to a death at any given age.

This paper gives an overview of the Global Burden of Disease (GBD) conceptual framework, the relationship of the DALY to other measures of population health, and the GBD analytical approach, with particular attention to issues in (1) dealing with biased and missing data, (2) dealing with uncertainty and (3) specific technical issues in ensuring cross-population comparability. The latter include dealing with variations in quality and completeness of cause of death information, explicit use of a comprehensive framework and internal consistency checks for improving comparability of estimates of incidence, prevalence and mortality for causes, the assessment of disability weights, and techniques for improving the comparability of the assessment of the disease burden attributable to risk factors.

Description:

During the last three decades, there has been general acceptance of an approach to describing health states of individuals in terms of multiple domains of health, and in developing self-report instruments that seek information on each of these domains. A health state is thus a multi-dimensional attribute of an individual that reflects his or her levels on the various components or domains of health. Thus, a health state differs from pathology, risk factors or etiology, and from health service encounters or interventions.

How to describe health states, is a central challenge in undertaking the measurement of health. The relationship of health states to other aspects of health such as future non-fatal health outcomes or risk of mortality need to be examined. The way people report their own health varies consistently with factors such as education, sex, age, or other cultural factors. Various people use different response category cut-points across cultures or population sub-groups, and this 'response shift' implies that self-report categorical data are not comparable across individuals. The responses cannot be directly used to measure health without adjustment.

In recognition of this the WHO World Health Surveys (WHS), used a set of questions across a core set of domains to measure health states and employed vignettes to detect and correct for biases in self-report in order to adjust for response category cut-point shifts. This paper will describe the instrument used in the WHS and the methods used to provide cross population comparable data. It will present results from the WHS demonstrating the existence of systematic reporting biases, the ability of respondents to rate vignettes and their use to adjust for biases in order to make data more comparable. Future strategies to address these problems will be discussed.

Description:

In this presentation, Mr. Murray discusses the notion of functional health status and proposes an agenda for developing comparable methods of measuring this concept.

Description:

We describe statistical disclosure control methods (SDC) developed for a public release Canadian Hospitals Injury Reporting and Prevention Program (CHIRPP) micro-data file. CHIRPP is a national injury surveillance database managed by the Public Health Agency of Canada (PHAC). After describing CHIRPP, the paper includes a brief overview of basic SDC concepts, as an introduction to the process for selecting and developing the appropriate SDC methods for CHIRPP given its specific challenges and requirements. We then summarize some key results. The paper concludes with a discussion of the implication of this work for the health information field and closing remarks with respect to the some methodological issues for consideration.

Description:

The process of public-use micro-data files creation involves a number of components. One of its key elements is RTI International's innovative MASSC methodology. However, there are other major components in this process such as treatment of non-core identifying variables and extreme outcomes for extra protection. The statistical disclosure limitation is designed to counter both inside and outside intrusion. The components of the process are accordingly designed.

Description:

In 1999, the first nationally representative survey of the mental health of children and young people aged 5-15 was carried out in Great Britain. A second survey was carried out in 2004. The aim of these surveys was threefold: to estimate the prevalence of mental disorders among young people, to look at their use of health, social and educational services, and to investigate risk factors associated with mental disorders. The achieved number of interviews was 10,500 and 8,000 respectively. Some key questions had to be addressed on a large number of methodological issues and the factors taken into account to reach decisions on all these issues are discussed.

Description:

In accordance with an effort to design a set of questions for the Current Population Survey (CPS) to measure disability, potential questions were drawn from existing surveys, cognitively and field tested. Based on an analysis of the test data, a set of seven questions was identified, cognitively tested, and placed in the February 2006 CPS for testing. Analysis of the data revealed a lower overall disability rate as measured in the CPS than in the field test, with lower positive response rates for each question. The data did not indicate that there was an adverse effect on the response rates.

Description:

On behalf of Statistics Canada, I would like to welcome you all, friends and colleagues, to Symposium 2006. This the 23rd International Symposium organized by Statistics Canada on survey methodology.

Description:

Now that we have come to the end of a day of workshops plus two very full days of sessions, I have the very pleasant task of offering a few closing remarks and, more importantly, of recognizing the efforts of those who have contributed to the success of this year's symposium. And it has clearly been a success.

Description: As of the 1994/95 data year, the Canadian Institute for Health Information (CIHI) assumed the data collection and dissemination responsibilities for Mental Health Statistics. Public enquiries about Mental Health Statistics should be directed to CIHI at mentalhealth@cihi.ca. The annual information presently collected by this program provides data on separation (discharges) from psychiatric hospitals and general hospitals for inpatients being treated for mental disorders.

Description: The Canadian Cancer Registry (CCR) is a population based registry that includes data collected and reported to Statistics Canada (StatCan) by each provincial/territorial cancer registry (PTCR). The person based CCR collects information about each new primary cancer diagnosed among Canadian residents since 1992. The objective is to produce standardized and comparable incidence data that can be used to assist and support health planners and decision-makers to: identify risk factors; plan, monitor and evaluate cancer screening, treatment and control programs; and conduct research.

Description: Note: Since the 1995-96 data year, the Canadian Institute for Health Information (CIHI) assumed the responsibility for data collection, processing and for the production and custody of the clean data files. A clean analysis file is provided to Health Statistics Division, Statistics Canada for data analysis. This annual survey provides detailed statistics on finances, services and utilization of Canadian hospitals.

Description: The purpose of the Therapeutic Abortion Survey is to provide some basic indicators (for example, counts and rates) on induced abortions. Information from this database is also used in the calculation of pregnancy statistics, especially for teen pregnancies.

Description: This survey collects the financial and operating data needed to develop national and regional economic policies and programs.

Description: This survey provides data on the lifestyle and health of Canadians, complementing existing administrative data bases.

Description: This survey was designed to collect information on the health of the Canadian population and related socio-demographic information.

Description: The central objective of the Canadian Community Health Survey (CCHS) is to gather health-related data at the sub-provincial levels of geography (health region or combined health regions).

Description: This is an administrative survey that collects demographic information annually from all provincial and territorial vital statistics registries on all live births in Canada. 2017 birth and stillbirth data for Yukon are not available. Due to improvements in methodology and timeliness, the duration of data collection has been shortened compared to previous years. As a result, there may have been fewer births and stillbirths captured by the time of the release. The 2017 data are therefore considered preliminary.

Description: This is an administrative survey that collects demographic and medical (cause of death) information annually from all provincial and territorial vital statistics registries on all deaths in Canada.