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This document presents the results of a national survey conducted to assess the availability of data on congenital anomalies across Canadian provinces and territories, identifying common data variables
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How to fill out Congenital Anomalies Surveillance in Canada

01
Gather patient information including demographics and medical history.
02
Identify any congenital anomalies present at birth or diagnosed shortly after.
03
Use standardized definitions and classifications for congenital anomalies.
04
Fill out the required surveillance forms with accurate data.
05
Submit the completed forms to the designated health authorities.
06
Ensure that all data privacy and confidentiality regulations are followed.

Who needs Congenital Anomalies Surveillance in Canada?

01
Healthcare providers who care for pregnant women and newborns.
02
Researchers studying congenital anomalies and their impact.
03
Public health officials monitoring and planning for healthcare resources.
04
Policy-makers developing health programs aimed at improving maternal and child health.
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Congenital Anomalies Surveillance in Canada is a systematic approach to monitor, track, and report the occurrence of congenital anomalies (birth defects) in infants across the country. It aims to collect comprehensive data to understand their prevalence, identify trends, and inform public health strategies.
Healthcare professionals such as obstetricians, pediatricians, and hospitals are required to file Congenital Anomalies Surveillance reports. Additionally, public health agencies and registries may also participate in the collection and reporting process.
To fill out the Congenital Anomalies Surveillance form, healthcare providers must gather information regarding the diagnosed congenital anomaly, maternal health history, and any relevant diagnostic tests or imaging results. The form typically includes sections for patient demographics, details about the anomaly, and follow-up information.
The purpose of Congenital Anomalies Surveillance in Canada is to monitor the incidence and types of congenital anomalies, to identify risk factors, and to enhance the understanding of these conditions for improved prevention and care strategies.
Information that must be reported includes the type of congenital anomaly, date of diagnosis, maternal age, relevant medical history, ethnicity, and any associated complications. Additionally, it's important to include information on prenatal care and any interventions required.
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