Health

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Income of individuals by disability status, age group, sex and income source, Canada, annual.

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Distribution of employment income of individuals by disability status, sex and work activity, Canada, annual.

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Poverty and low-income statistics by disability status, age group, sex and economic family type, Canada, annual.

Description: Number and percentage of persons by household food security status and economic family type, Canada and provinces.

Description: Number and percentage of persons by household food security status, age group, sex, visible minority group, Indigenous group and immigration status, Canada and provinces.

Description: Number and percentage of persons aged 16 years and over with unmet health care needs by sex (Canada and provinces) and age group (Canada only).

Description: This infographic examines the early child care experiences of children with long-term conditions or disabilities using data from the 2023 Survey on Early Learning and Child Care arrangements – Children with Long-term Conditions and Disabilities (SELCCA – CLCD). It explores the types of extra support needed while in child care, the common difficulties they experienced as well as the impacts on the parent or guardian having difficulty finding a child care arrangement.

Description: Using data from the 2023 Survey on Early Learning and Child Care arrangements – Children with Long-term Conditions and Disabilities (SELCCA – CLCD), this American Sign Language video examines the early child care experiences of children with long-term conditions or disabilities.

Description: Oral health is a crucial component of overall health, influencing both physical and mental well-being. Yet, despite the important role that access to and use of oral health care services play in maintaining optimal oral health, substantial disparities remain in access to oral health care services across population groups in Canada. Using data from the 2022 Canadian Community Health Survey, this study examines the association of dental insurance with oral health care access and use in Canada while accounting for income and sociodemographic factors. It contributes to a baseline of oral health care disparities before the implementation of the Canadian Dental Care Plan.

Description: Children’s oral health can affect functional capacities, psychological well-being, and social integration. Additionally, health behaviours established in childhood extend into adulthood and can influence oral health outcomes later in life. Using data from the 2019 Canadian Health Survey on Children and Youth, this study investigates the association between dental insurance, income, and dental care access for Canadian children and youth aged 1 to 17 years. It contributes to a baseline understanding of oral health care use before the implementation of the Canadian Dental Care Plan.

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: Monthly indexes and percentage changes for selected sub-groups of the health and personal care component of the Consumer Price Index (CPI), not seasonally adjusted, for Canada, provinces, Whitehorse and Yellowknife. Data are presented for the corresponding month of the previous year, the previous month and the current month. The base year for the index is 2002=100.

Description: Percentage of persons aged 15 years and over by level of life satisfaction, by gender, for Canada, regions and provinces.

Description: Percentage of persons aged 15 years and over by level of life satisfaction, by gender and other selected sociodemographic characteristics: age group; immigrant status; visible minority group; Indigenous identity; persons with a disability, difficulty or long-term condition; LGBTQ2+ people; highest certificate, diploma or degree; main activity; and urban and rural areas.

Description: Percentage of persons aged 15 years and over by level of sense of meaning and purpose, by gender, for Canada, regions and provinces.

Description: Percentage of persons aged 15 years and over by level of sense of meaning and purpose, by gender and other selected sociodemographic characteristics: age group; immigrant status; visible minority group; Indigenous identity; persons with a disability, difficulty or long-term condition; LGBTQ2+ people; highest certificate, diploma or degree; main activity; and urban and rural areas.

Description: Percentage of persons aged 15 years and over by frequency with which they have a hopeful outlook, by gender, for Canada, regions and provinces.

Description: Percentage of persons aged 15 years and over by frequency with which they have a hopeful outlook, by gender and other selected sociodemographic characteristics: age group; immigrant status; visible minority group; Indigenous identity; persons with a disability, difficulty or long-term condition; LGBTQ2+ people; highest certificate, diploma or degree; main activity; and urban and rural areas.

Description: Percentage of persons aged 15 years and over by frequency with which they feel lonely, by gender, for Canada, regions and provinces.

Description: Percentage of persons aged 15 years and over by frequency with which they feel lonely, by gender and other selected sociodemographic characteristics: age group; immigrant status; visible minority group; Indigenous identity; persons with a disability, difficulty or long-term condition; LGBTQ2+ people; highest certificate, diploma or degree; main activity; and urban and rural areas.

Description: This article examines differences in health status and health determinants between residents of the North (Yukon and Northwest Territories) and of the provinces, and between Aboriginal and non-Aboriginal territorial residents. The use of health services and medications is also analyzed.

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This paper demonstrates the utility of a multi-stage survey design that obtains a total count of health facilities and of the potential client population in an area. The design has been used for a state-level survey conducted in mid-1995 in Uttar Pradesh, India. The design involves a multi-stage, areal cluster sample, wherein the primary sampling unit is either an urban block or rural village. All health service delivery points, either self-standing facilities or distribution agents, in or formally assigned to the primary sampling unit are mapped, listed, and selected. A systematic sample of households is selected, and all resident females meeting predetermined eligibility criteria are interviewed. Sample weights for facilities and individuals are applied. For facilities, the weights are adjusted for survey response levels. The survey estimate of the total number of government facilities compares well against the total published counts. Similarly the female client population estimated in the survey compares well with the total enumerated in the 1991 census.

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This article provides an overview of trends from 1974 to 1994 in the pregnancies among women aged 15 to 19.

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This article examines the marital status of women who obtained abortions between 1974 and 1994, with particular attention to those who were married or in common-law relationships.

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For people living in the community, this article explores selected health problems and personal characteristics that are associated with having been hospitalized.

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This article examines trends in infant mortality and the incidence of low birthweight from 1975 to 1995.

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This article focuses on the prevalence of diabetes mellitus among Canadians, the health status of those with the disease, their socioeconomic characteristics, personal health behaviours, and use of health services.

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This article illustrates analytical uses of multiple-cause-of-death data, which reflect all causes entered on the death certificate, not only the single, underlying cause. Heart diseases are used as an example.

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This article investigates whether, compared with younger women, those aged 30-34 and 35 and older experienced a higher risk of adverse pregnancy outcomes and maternal complications, and whether their infants faced an increased risk of perinatal complications and congenital anomalies.

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For historical reasons, the best known life tables and those most often used are period tables. They are built using death rates by age for a short period of observation (often a single year) and have as their purpose to represent the status of mortality for this period. The survivors and deaths appearing in their columns are in a way abstractions rather than reality. It is thus erroneous to believe that the life table for a given year (for example, 1995) serves in any way whatever to predict the rate at which those born that year will pass away and, hence, of the average length of the life that they have just begun. With rare exceptions, the average number of years lived by individuals has always been longer than the life expectancy found in the life table constructed for the year of their birth. This is due to the fact that period tables are established using the risks of death by age prevailing in that year. But the ceaseless battle against death reduces these risks year after year for these ages and, by growing older, people benefit from these successive gains.

To reconstitute (or foresee) the rate at which the members of a cohort have (or will) really pass away, it is necessary to deploy very long series of death rates by age and to possess reliable indicators of missing data, and then to adjust them to establish the actual experience of the persons in a cohort. Built in exactly the same way as period tables, these tables are naturally called cohort tables, but comparing observations of their parameters yields conclusions of a different kind.

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Introductory video for the survey provided to respondents at the household and posted on the Canadian Health Measures Survey Respondent relations (Statcan) website.

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The Canadian Survey on Disability (CSD) is a national survey of Canadians aged 15 and over whose everyday activities are limited because of a long-term condition or health-related problem.

The 2012 CSD Concepts and Methods Guide is designed to assist data users by providing relevant information on survey content and concepts, sampling design, collection methods, data processing, data quality and product availability. Chapter 1 of this guide provides an overview of the 2012 CSD by introducing the survey's background and objectives. Chapter 2 explains the key concepts and definitions and introduces the indicators measured by the CSD questionnaire modules. Chapters 3 to 6 cover important aspects of survey methodology, from sampling design to data collection and processing. Chapters 7 and 8 cover issues of data quality, including the approaches used to minimize and correct errors throughout all stages of the survey. Users are cautioned against making comparisons with data from previous Participation and Activity Limitations Surveys. Chapter 9 outlines the survey products that are available to the public, including data tables, a fact sheet and reference material. Appendices provide more detail on survey indicators as well as a glossary of terms.

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Mental illnesses largely involve alterations in mood, thinking, and behaviour, as well as other domains of mental functioning, and affect almost all Canadians in some way, either directly or indirectly. They routinely cause significant impairments in emotional functioning, which may lead to social or physical limitations. In some cases, such as in agoraphobia, individuals cannot even leave their homes due to intense anxiety; depression can cause an individual to lose all interest in life. This document describes the mental illnesses that have the greatest impact on Canadians in terms of prevalence or severity of disability, and how they affect the health status of Canadians.

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This report presents the results of the 3rd Consensus Conference on Health Indicators that was convened in March 2009, including information that was presented at the conference, a summary of the consultation process leading up to the event, and the priority health areas deemed most important for future indicator development work.

The conference marked the 10th anniversary of the Health Indicators project, a collaboration between Statistics Canada and Canadian Institute for Health Information (CIHI). The goal of the project is to provide health regions, health care providers and the public in general with reliable and comparable data on the health of Canadians and to assist stakeholders and decision makers in the use and interpretation of the indicator data.

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Since 2007/2008, Statistics Canada has centred analysis of data holdings related to health as well as our program of dissemination of health research within the new Health Information and Research Division (HIRD).

The new division has launched a comprehensive approach to analytical planning including environmental scanning and consultation; establishment of strategic multi-year priorities for health research at Statistics Canada; a process of project selection and review that ensures that analytical effort addresses our priorities; metrics to measure our adherence to priorities and the impact of our analytical effort; and communication and dissemination of analytical plans.

This multi-year analytical plan identifies the key high-level priority areas for Statistics Canada's investment in health research for 2008/2009 to 2010/2011, and serves as a blueprint for subsequent operational research planning.

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This special methodological paper will help readers understand and assess reports that rank the health status or health system performance of a country, province or jurisdiction. The report outlines the components and processes that underlie health rankings, explores why such rankings can be difficult to interpret and includes a plain-language checklist to use as a critical evaluative resource when reading health-ranking reports.

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This report highlights the latest developments and rationale behind recent cycles of the General Social Survey (GSS). Starting with an overview of the GSS mandate and historic cycle topics, we then focus on two recent cycles related to families in Canada: Family Transitions (2006) and Family, Social Support and Retirement (2007). Finally, we give a summary of what is to come in the 2008 GSS on Social Networks, and describe a special project to mark 'Twenty Years of GSS'.

The survey collects data over a twelve month period from the population living in private households in the 10 provinces. For all cycles except Cycles 16 and 21, the population aged 15 and older has been sampled. Cycles 16 and 21 sampled persons aged 45 and older.

Cycle 20 (GSS 2006) is the fourth cycle of the GSS to collect data on families (the first three cycles on the family were in 1990, 1995 and 2001). Cycle 20 covers much the same content as previous cycles on families with some sections revised and expanded. The data enable analysts to measure conjugal and fertility history (chronology of marriages, common-law unions, and children), family origins, children's home leaving, fertility intentions, child custody as well as work history and other socioeconomic characteristics. Questions on financial support agreements or arrangements (for children and the ex-spouse or ex-partner) for separated and divorced families have been modified. Also, sections on social networks, well-being and housing characteristics have been added.

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The Record Linkage Overview describes the process used in annual internal record linkage of the Canadian Cancer Registry. The steps include: preparation; pre-processing; record linkage; post-processing; analysis and resolution; resolution entry; and, resolution processing.

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The compendium of Canadian Cancer Registry procedures manuals set out the rules for reporting cancer data to the CCR for all provincial and territorial cancer registries.

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The Record Linkage Overview describes the process used in annual internal record linkage of the Canadian Cancer Registry. The steps include: preparation; pre-processing; record linkage; post-processing; analysis and resolution; resolution entry; and, resolution processing.