This edition highlights national CJRR coverage, data submission deadlines, data quality reminders and recent releases.
Report based on summary statistics received from 9 organ procurement organizations across Canada. Latest available data is for 2017.
Read the latest annual report from the Canadian Joint Replacement Registry (CJRR) to learn about clinical information and patient outcomes for hip and knee replacements in Canada.
A summary of information for external users of the data. The document helps users assess whether the quality of the data fits their intended use.
Assists organ procurement organization and transplant hospital staff to submit data to CORR.
Reference manuals on submitting data to CORR, for staff at organ procurement organizations, transplant hospitals and hospitals providing renal replacement therapy.
2016 Summary Statistics, January 1 to December 31, 2016
Topics that supplement the tables and figures: CORR board of directors; list of transplant hospitals, renal programs and organ procurement organizations; glossary and acronyms; analytical methods; and primary diagnoses captured by CORR.
Take a closer look at donors, both living and deceased, trends over the last decade, relationships to transplant recipients and donor rates across Canada.
Trends for lung, heart, liver, pancreas (including islet cell) and intestinal transplant recipients, patients on waiting lists and patient outcomes.
Annual release of data from the Canadian Organ Replacement Register (CORR), including statistics on dialysis, organ transplantation and donation characteristics, trends and patient outcomes in Canada between 2007 and 2016.
Information on the types of data captured in CORR, data supply chain, coverage, under-reporting, non-response, reliability/response bias, methodological changes and revision history.
This edition highlights upcoming changes to CJRR, the data submission deadlines, and developments coming in 2018–2019 and beyond.
Information on coverage, non-response, collection processes, data quality control, methodological changes and revision history.
This product uses data from the Hospital Morbidity Database (HMDB), National Ambulatory Care Reporting System (NACRS) and Canadian Joint Replacement Registry (CJRR). Data for the HMDB and NACRS is provided by Canada's provinces and territories. Data for CJRR is provided by provincial ministries of health, regional authorities, orthopedic surgeons, nurses, medical records staff and others across Canada.
CJRR Data Quality Documentation for Users is a summary of information for external users of the data. The document helps users assess whether the quality of the data fits their intended use.
This toolkit includes resources related to the use of patient-centred measurement data.
This report describes current and future patient-centred measurement and reporting in Canada. It presents a 5-year plan to achieve the desired future state.
Tools and guidelines on submitting data to the Canadian Joint Replacement Registry.
Information on the availability of 2015 CORR data and upcoming analytical products.