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All (4)

All (4) ((4 results))

  • 1. Cancer in First Nations people in Ontario, Canada: Incidence and mortality, 1991 to 2010
    Articles and reports: 82-003-X202100600002
    Description:

    This study aims to measure cancer incidence and mortality rates of Registered First Nations people in Ontario and to look at trends over time, particularly in cancer rates that are targeted by screening programs (cervical, breast, colorectal) or public health interventions (smoking). The federal Indian Register, the Ontario Cancer Registry and the Registered Persons Database were linked to develop a cohort of First Nations people diagnosed with cancer in Ontario.

    Release date: 2021-06-16
  • 2. Birth outcomes among First Nations, Inuit and Métis populations Archived
    Articles and reports: 82-003-X201701154886
    Description:

    This study examines perinatal outcomes among First Nations, Inuit and Métis. The objective is to describe and compare rates of preterm birth, small-for-gestational age birth, large-for-gestational age birth, stillbirth and infant mortality in the three Indigenous groups and the non-Indigenous population.

    Release date: 2017-11-15
  • 3. Missing paternal data and adverse birth outcomes in Canada Archived
    Articles and reports: 82-003-X201601214686
    Description:

    This study examines birth and death registration data and census data to compare rates of preterm birth, small-for-gestational-age birth, stillbirth and infant mortality, based on the presence or absence of paternal data on the birth registration and in census results, while controlling for maternal characteristics.

    Release date: 2016-12-21
  • 4. The 2006 Canadian Birth-Census Cohort Archived
    Articles and reports: 82-003-X201600114306
    Description:

    This article is an overview of the creation, content, and quality of the 2006 Canadian Birth-Census Cohort Database.

    Release date: 2016-01-20
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Articles and reports (4)

Articles and reports (4) ((4 results))

  • 1. Cancer in First Nations people in Ontario, Canada: Incidence and mortality, 1991 to 2010
    Articles and reports: 82-003-X202100600002
    Description:

    This study aims to measure cancer incidence and mortality rates of Registered First Nations people in Ontario and to look at trends over time, particularly in cancer rates that are targeted by screening programs (cervical, breast, colorectal) or public health interventions (smoking). The federal Indian Register, the Ontario Cancer Registry and the Registered Persons Database were linked to develop a cohort of First Nations people diagnosed with cancer in Ontario.

    Release date: 2021-06-16
  • 2. Birth outcomes among First Nations, Inuit and Métis populations Archived
    Articles and reports: 82-003-X201701154886
    Description:

    This study examines perinatal outcomes among First Nations, Inuit and Métis. The objective is to describe and compare rates of preterm birth, small-for-gestational age birth, large-for-gestational age birth, stillbirth and infant mortality in the three Indigenous groups and the non-Indigenous population.

    Release date: 2017-11-15
  • 3. Missing paternal data and adverse birth outcomes in Canada Archived
    Articles and reports: 82-003-X201601214686
    Description:

    This study examines birth and death registration data and census data to compare rates of preterm birth, small-for-gestational-age birth, stillbirth and infant mortality, based on the presence or absence of paternal data on the birth registration and in census results, while controlling for maternal characteristics.

    Release date: 2016-12-21
  • 4. The 2006 Canadian Birth-Census Cohort Archived
    Articles and reports: 82-003-X201600114306
    Description:

    This article is an overview of the creation, content, and quality of the 2006 Canadian Birth-Census Cohort Database.

    Release date: 2016-01-20
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