Health

Description: Differences in the number and proportion of persons with disabilities in terms of the reasons for experiencing difficulty in finding work, by age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities in terms of those who used and did not use the Internet for personal use from any location, during the past 12 months.

Description: Differences in the number and proportion of employees with disabilities in terms of their perceived qualification level for their current job, by age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities who are not in the labour force, by main reason for not looking for work (grouped), aged 15 years and over, Canada.

Description: Differences in the number and proportion of persons with disabilities who are employed in part-time work by main reason (grouped) for working less than 30 hours a week and age group.

Description: Differences in the number and proportion of youth with disabilities who are not in employment, education, or training (NEET) by province or territory and gender.

Description: Differences in the number and proportion of current or recent students with disabilities in terms of requirements for different educational accommodations or modifications (grouped) and if these needs are met or unmet.

Description: Differences in the number and proportion of persons with disabilities in terms of those who have the potential to work, or no potential to work (based on an updated definition) by age group and gender.

Description: Differences in the number and proportion of employed persons with disabilities in terms of met and unmet needs for required workplace accommodations by age group and gender.

Description: Differences in the number and proportion of persons with disabilities in terms of those who use or do not use information and communication technology-related (ICT-related) assistive aids, devices, or technologies by province, age group and gender.

Description:

Private nursing and residential care facilities, summary statistics, by North American Industry Classification System (NAICS) 623, which includes all members under Summary statistics, annual, (dollars unless otherwise noted), Canada and provinces, five years of data.

Description: Estimated annual number of deaths by 5-year age groups and gender for Canada, provinces and territories.

Description: Estimated annual number of births by gender for Canada, provinces and territories.

Description: Number and percentage of Canadians aged 12 and older, by age group and gender, who had a visit to a dental professional in the past year, as well as their coverage by dental insurance.

Description: Number and percentage of Canadians aged 12 and older, by adjusted family net income quintile, who had a visit to a dental professional in the past year, as well as their coverage by dental insurance.

Description:

Number and rate of new cancer cases diagnosed annually from 1992 to the most recent diagnosis year available. Included are all invasive cancers and in situ bladder cancer with cases defined using the Surveillance, Epidemiology and End Results (SEER) Groups for Primary Site based on the World Health Organization International Classification of Diseases for Oncology, Third Edition (ICD-O-3). Random rounding of case counts to the nearest multiple of 5 is used to prevent inappropriate disclosure of health-related information.

Description:

The number of new cases, age-standardized rates and average age at diagnosis of cancers diagnosed annually from 1992 to the most recent diagnosis year available. Included are all invasive cancers and in situ bladder cancer with cases defined using the Surveillance, Epidemiology and End Results (SEER) Groups for Primary Site based on the World Health Organization International Classification of Diseases for Oncology, Third Edition (ICD-O-3). Cancer incidence rates are age-standardized using the direct method and the final 2011 Canadian postcensal population structure. Random rounding of case counts to the nearest multiple of 5 is used to prevent inappropriate disclosure of health-related information.

Description: Socioeconomic characteristics of the population aged 15 and older that is Two-Spirit, lesbian, gay, bisexual, transgender, and queer or who use other terms related to gender or sexual diversity (2SLGBTQ+), by gender, age group and geographic region. Marital status, presence of children under age 12 in the household, education, employment, personal income, Indigenous identity, the visible minority population, immigrant status, language(s) spoken most often at home, place of residence (population centre/rural), self-rated general health, and self-rated mental health. Estimates are obtained from combined cycles of the Canadian Community Health Survey, 2019 to 2021.

Description: Selected socioeconomic characteristics of the transgender or non-binary population aged 15 and older, by age group. Marital status, presence of children under age 12 in the household, education, employment, personal income, Indigenous identity, the visible minority population, immigrant status, language(s) spoken most often at home, place of residence (population centre/rural), self-rated general health, and self-rated mental health. Estimates are obtained from combined cycles of the Canadian Community Health Survey, 2019 to 2021.

Description: Socioeconomic characteristics of the population aged 15 and older whose reported sexual orientation is lesbian or gay, bisexual or pansexual, or another sexual orientation that is not heterosexual (LGB+), by gender, age group and geographic region. Marital status, presence of children under age 12 in the household, education, employment, personal income, Indigenous identity, the visible minority population, immigrant status, language(s) spoken most often at home, place of residence (population centre/rural), self-rated general health, and self-rated mental health. Estimates are obtained from combined cycles of the Canadian Community Health Survey, 2019 to 2021.

Description:

Analyses based on census data, vital statistics, and data from the Health and Activity Limitation Surveys show that immigrants, especially those from non-European countries, had a longer life expectancy and more years of life free of disability and dependency than did the Canadian-born. But while immigrants were less likely than the Canadian-born to be disabled, they were only slightly less likely to be dependent on others for help with activities of daily living. The reasons for immigrants' longevity and good health are likely related to the "health immigrant effect"

Description:

From 1974 to 1994, the number of children Canadian women are likely to have during their lifetime decreased. This downturn in fertility meant that the annual number of live births rose only slightly during this period, even though it marked the prime childbearing years for the baby-boom generation. As they pursued higher education and employment in the paid workforce, women have postponed childbearing. Consequently, the average age of women giving birth has risen. More than a quarter of women over age 30 who have a baby are first-time mothers. And by starting families later in life, women tend to have fewer children. In addition, largely because of the growing number of common-law relationships, over a quarter of all births are to unmarried women. Using data provided by the provincial and territorial Vital Statistics Registries, this article examines national and provincial/territorial trends in births and fertility from 1974 to 1994.

Description:

The increase in life expectancy that would result from the elimination of certain diseases and the resulting change in hospital utilization vary, depending on the disease. In some cases, life expectancy would rise and total days spent in hospital would decline, while in others, the gain in life expectancy would be accompanied by a increase in hospital days. For instance, if mental health disorders were eliminated, the increase in life expectancy at age 45 would be minimal: from 34.9 to 35.3 years, but time spent in hospital would decline from 168 to 151 days. By contrast, if diseases of the circulatory system were eliminated, life expectancy at age 45 would rise from 34.9 to 41.6 years, but time spent in hospital would also rise: from 168 to 290 days. Elimination of not only mental illnesses but also injuries and poisoning and diseases of the nervous system has the potential of both increasing life expectancy and reducing hospital use.

Description:

Abridged life tables centred on 1991 were produced from the 1991 Canadian census, net census undercoverage estimates, and death data from 1990 to 1992. The sensitivity of life table values to differing methods of estimation and population estimates was investigated. The results from four methods by Greville, Chiang, and Keyfitz were compared, and population undercoverage, were used to test the effects of method and type of population estimate on life table values. The results indicate that the method used to derive the estimates had much less influence on the life table values than did the choice of population estimate. The change life expectancy at birth due to the method of calculation chosen was at most 15 days, whereas the change due to the population estimate chosen was about 73 days. Since there are age, sex and provincial variations in net undercoverage rates, life expectancies differed accordingly.

Description: The official 1990-92 detailed life tables show a continuation of the trend toward longer life expenctancy for Canadians. Life expectancy at birth has reached an all-time high: 80.89 years for females and 74.55 years for males. Recent improvements in life expectancy are attributable to many factors, including declines in infant mortality, cerebrovascular and cardiovascular disease, and mortality from accidents and poisoning.

Description:

As the population ages, discussion increasingly focuses on how to keep people in the community and out of health care instituions. But when health fails, the only option may be long-term residential care.

Description:

This paper evaluates the results of the questions related to activity limitation and its impact on labour market activity from the January 1993 Survey of Labour and Income Dynamics (SLID) test.

Description:

Using data from Statistics Canada's 1988 and 1993 General Social Survey (GSS), this article examines the incidence and consequences of accidents in Canada and the characteristics of respondents aged 15 and over who were involved in them. In 1993, an estimated 3.9 million Canadians reported that they had been involved in 4.8 million accidents in the previous 12 months. Motor vehicle accidents and sports accidents were the most frequent, each accounting for about 27% of incidents, followed by accidents at work (21%) and at home (14%). Accidents were most common among young people, particularly men. However, from 1988 to 1993, there was a decline in the proportion of adults reporting accidents, and the sharpest drop was for the age group most at risk - 15-to 24-year-olds. Most of the downturn was attributable to a decrease in the motor vehicle accident rate. Since alcohol is known to be associated with accidents, reduced consumption during the same period may have been partly responsible for the decline in accident rates. Other factors that may have contributed include stricter enforcement of impaired driving legislation and speeds limits, and improvements in automobile safety. Nonetheless, despite the decline in accidents rates, the toll taken by accidents reported in 1993 was considerable: 80% of accidents caused personal injury, and almost half of these resulted in medical attention in a hospital. Overall, 62% of accidents resulted in activity-loss days, and 29% involved bed-disability days. Hospital utilization costs associated with these accidents in 1993 were about $1.5 billion. As well, about one-third of accidents involved out-of-pocket expenses, totalling $791 million. Moreover, accidents continue to be the leading cause of death among persons under age 44.

Description:

Indicators based on the registration of vital events are used to determine the health status of populations. The need for these indicators at the regional and community levels has grown with the trend toward decentralization in the delivery of health services. Such indicators are important because they affect funding and the types of service that are provided. Health status indicators tend to be associated with variables such as the level of urbanization or socioeconomic status. According to four indicators - mortality ratios for all causes of death, mortality ratios for external causes of death, infant mortality ratios, and low birth weight live birth ratios - some areas of British Columbia, specifically along the border with Alberta, have relatively good health, although the characteristics of these regions suggest that this should not be the case. However, a much different picture emerges when vital event data registered in Alberta for residents of these areas of British Columbia are considered. This article shows that for adequate health planning and program implementation, some communities need data from neighbouring provinces. It illustrates the effect of incorporating Alberta data into the development of health status indicators for British Columbia. It also suggests that similar adjustments may be necessary for data compiled in other provinces.

Description:

The positive relationship between socioeconomic status (SES) and longevity has long been established. Comparable evidence exists for SES and morbidity, but observations of this relationship tend to be limited to specific health indicators. In this article, a comprehensive quantitative measure of health status, the Health Utility Index (HUI), is applied to an analysis of the relationship between SES the health status of people aged 25 and over in Ontario. The HUI, based on a set of questions included in the 1990 Ontario Health Survey (OHS), provides a summary index of the health of each respondent. The OHS data show that lower levels of education, income, and occupation are associated with lower HUI values. Health status differences across SES groups are greater in late middle-age than at younger or older ages, a pattern consistent with the findings of other studies. The development of summary indicators like the HUI is part of a larger effort to construct measures for monitoring the health of Canadians.

Description:

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

Description:

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.

Description:

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.

Description:

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.

Description:

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.

Description:

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.

Description:

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.

Description:

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.

Description:

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.

Description:

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.