Health

Health regions are defined by the provinces and represent administrative areas or regions of interest to health authorities. This product contains correspondence files (linking health regions to latest Census geographic codes) and digital boundary files. User documentation provides an overview of health regions, sources, methods, limitations and product description (file format and layout).

In addition to the geographic files, this product also includes Census data (basic profile) for health regions.

The purpose of this working paper is to define the concept of peer groups, to give an overview of how they are created and to demonstrate their usefulness.

The Health Research Working Paper Series publishes: analytical work-in-progress; background documentation for specific research projects (e.g methodological papers); lengthy reports intended for specific clients, and; compendiums of data tables. Publication in this series does not preclude publication of specific aspects of the work in a peer-reviewed journal.

Over 80 indicators measure the health of the Canadian population and the effectiveness of the health care system. Designed to provide comparable information at the health region and provincial/territorial levels, these data are produced from a wide range of the most recently available sources.

This Internet publication is produced by Statistics Canada and the Canadian Institute for Health Information.

This table contains 3552 series, with data for years 2000/2002 - 2010/2012 (not all combinations necessarily have data for all years). This table contains data described by the following dimensions (Not all combinations are available): Geography (148 items: Canada; Newfoundland and Labrador; Eastern Regional Integrated Health Authority, Newfoundland and Labrador; Central Regional Integrated Health Authority, Newfoundland and Labrador; ...);  Sex (3 items: Both sexes; Males; Females);  Infant or perinatal mortality (2 items: Infant mortality; Perinatal mortality);  Characteristics (4 items: Number; Rate; Low 95% confidence interval, rate; High 95% confidence interval, rate).

This table contains 3672 series, with data for years 2000/2002 - 2010/2012 (not all combinations necessarily have data for all years). This table contains data described by the following dimensions (Not all combinations are available): Geography (153 items: Canada; Newfoundland and Labrador; Census metropolitan areas and census agglomerations, Newfoundland and Labrador; Census metropolitan areas, Newfoundland and Labrador; ...); Sex (3 items: Both sexes; Males; Females); Infant or perinatal mortality (2 items: Infant mortality; Perinatal mortality); Characteristics (4 items: Number; Rate; Low 95% confidence interval, rate; High 95% confidence interval, rate).

Number of deaths, by place of residence and place of occurrence, 1991 to most recent year.

Number and percentage of deaths, by month and place of residence, 1991 to most recent year.

Number and percentage of deaths, by age group, sex, and place of residence, 1991 to most recent year.

This table contains 3552 series, with data for years 2000/2002 - 2010/2012 (not all combinations necessarily have data for all years). This table contains data described by the following dimensions (Not all combinations are available): Geography (148 items: Canada; Newfoundland and Labrador; Eastern Regional Integrated Health Authority, Newfoundland and Labrador; Central Regional Integrated Health Authority, Newfoundland and Labrador; ...);  Sex (3 items: Both sexes; Males; Females);  Infant or perinatal mortality (2 items: Infant mortality; Perinatal mortality);  Characteristics (4 items: Number; Rate; Low 95% confidence interval, rate; High 95% confidence interval, rate).

This table contains 3672 series, with data for years 2000/2002 - 2010/2012 (not all combinations necessarily have data for all years). This table contains data described by the following dimensions (Not all combinations are available): Geography (153 items: Canada; Newfoundland and Labrador; Census metropolitan areas and census agglomerations, Newfoundland and Labrador; Census metropolitan areas, Newfoundland and Labrador; ...); Sex (3 items: Both sexes; Males; Females); Infant or perinatal mortality (2 items: Infant mortality; Perinatal mortality); Characteristics (4 items: Number; Rate; Low 95% confidence interval, rate; High 95% confidence interval, rate).

Number of deaths, by place of residence and place of occurrence, 1991 to most recent year.

Number and percentage of deaths, by month and place of residence, 1991 to most recent year.

Number and percentage of deaths, by age group, sex, and place of residence, 1991 to most recent year.

Number of deaths and mortality rates, by age group, sex, and place of residence, 1991 to most recent year.

Number of deaths, by marital status, age group, sex, and place of residence, 1991 to most recent year.

Number of infant deaths and infant mortality rate, by age (neonatal and post-neonatal) and sex, 1991 to most recent year.

Number of infant deaths and infant mortality rates, by age group (neonatal and post-neonatal), 1991 to most recent year.

The purpose of this working paper is to define the concept of peer groups, to give an overview of how they are created and to demonstrate their usefulness.

The Health Research Working Paper Series publishes: analytical work-in-progress; background documentation for specific research projects (e.g methodological papers); lengthy reports intended for specific clients, and; compendiums of data tables. Publication in this series does not preclude publication of specific aspects of the work in a peer-reviewed journal.

Over 80 indicators measure the health of the Canadian population and the effectiveness of the health care system. Designed to provide comparable information at the health region and provincial/territorial levels, these data are produced from a wide range of the most recently available sources.

This Internet publication is produced by Statistics Canada and the Canadian Institute for Health Information.

The infographic is a short representation of the data findings from the 2017 Canadian Survey on Disability. It highlights points from the sections on demographics, employment and unmet needs.

This video features the highlights of the Canadian Survey on Disability, 2017, using American Sign Language (ASL).

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 2017 CSD Concepts and Methods Guide is designed to assist CSD 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 2017 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 the 2012 CSD. Chapter 9 outlines the survey products that are available to the public, including data tables, an analytical article and reference material. Appendices provide more detail on the survey's indicators and other supporting documents for the CSD.

This profile article is the first main release by Statistics Canada based on findings from the 2017 Canadian Survey on Disability. It is divided into three sections - demographics, employment, and income - and provides a general snapshot on persons with disabilities to inform on emerging government priorities (such as Opportunity for All: Canada's First Poverty Reduction Strategy; Government of Canada, 2018) and community interest in the areas of disability prevalence, labour market participation, and income inequality.

The purpose of this fact sheet is to provide an overview of the evolution of disability in Canada since the mid-1980's. It explains how the federal government, academics and person's with disabilities have worked together to develop survey questions that reflect this evolution and the impact that this evolution has had on the ability to measure change.

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.

Health regions are defined by the provinces and represent administrative areas or regions of interest to health authorities. This product contains correspondence files (linking health regions to latest Census geographic codes) and digital boundary files. User documentation provides an overview of health regions, sources, methods, limitations and product description (file format and layout).

In addition to the geographic files, this product also includes Census data (basic profile) for health regions.

This document presents the methodology underlying the production of the life tables for Canada, provinces and territories, from reference period 1980/1982 and onward.

The 2016 Census Program Content Test was conducted from May 2 to June 30, 2014. The Test was designed to assess the impact of any proposed content changes to the 2016 Census Program and to measure the impact of including a social insurance number (SIN) question on the data quality.

This quantitative test used a split-panel design involving 55,000 dwellings, divided into 11 panels of 5,000 dwellings each: five panels were dedicated to the Content Test while the remaining six panels were for the SIN Test. Two models of test questionnaires were developed to meet the objectives, namely a model with all the proposed changes EXCEPT the SIN question and a model with all the proposed changes INCLUDING the SIN question. A third model of 'control' questionnaire with the 2011 content was also developed. The population living in a private dwelling in mail-out areas in one of the ten provinces was targeted for the test. Paper and electronic response channels were part of the Test as well.

This report presents the Test objectives, the design and a summary of the analysis in order to determine potential content for the 2016 Census Program. Results from the data analysis of the Test were not the only elements used to determine the content for 2016. Other elements were also considered, such as response burden, comparison over time and users’ needs.

This paper describes the process that led to the creation of the new Disability Screening Questions (DSQ), jointly developped by Statistics Canada and Employment and Social Development Canada. The DSQ form a new module which can be put on general population surveys to allow comparisons of persons with and without a disability. The paper explains why there are two versions of the DSQ—a long and a short one—, the difference between the two, and how each version can be used.

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

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.

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.

Before each Census of Population, Statistics Canada carries out a three- to four-year process to review the content of the census questionnaires in consultation with census data users, performing tests and developing questionnaire content to ensure that it takes into account the evolution of Canadian society. Factors considered in developing the content include legislative requirements regarding information, program and policy requirements; the burden placed on respondents to respond to questions; concerns about privacy; feedback from consultations and tests; data quality; costs and operational considerations; the comparability of data with earlier data and the availability of alternative data sources. Before each census, Statistics Canada tests the questionnaire content through an extensive test. The content report presents the analyses conducted from the data collected from this test and the results that are used to fine tune the questionnaires, the methodology and the systems used for the Census Program.

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.

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.