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UHB/QEB NCHDA Report 2022The National Congenital Heart Disease Audit Procedures for CONGENITAL HEART DISEASEData Quality Audit for April 2021 March 2022 University Hospitals Birmingham NHS Foundation
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Who needs national congenital heart disease?
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What is national congenital heart disease?
National congenital heart disease refers to congenital heart defects that are present at birth and includes a range of heart abnormalities. It is a collective term for conditions that affect the structure and function of the heart.
Who is required to file national congenital heart disease?
Health care providers, hospitals, and other entities that diagnose or treat patients with congenital heart disease are often required to file national congenital heart disease reports.
How to fill out national congenital heart disease?
To fill out national congenital heart disease reports, you typically need to gather patient information, details about the diagnosis, treatment provided, and other relevant clinical data. This information should be entered into the designated reporting system or forms as specified by the health authorities.
What is the purpose of national congenital heart disease?
The purpose of national congenital heart disease reporting is to collect data for research, improve patient care, develop guidelines, and track outcomes to enhance the understanding and treatment of congenital heart defects.
What information must be reported on national congenital heart disease?
Information that must be reported includes patient demographics, type of congenital heart defect, treatment received, outcomes, complications, and follow-up care details.
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