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NCHDA Report 2019 RVBThe National Congenital Heart Disease Audit DatabaseData Quality Audit for CONGENITAL HEART DISEASE Apr 2018 Mar 2019The Royal Victoria Hospital, Belfast2 August 2019 performed

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Who needs national congenital heart disease?

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Individuals diagnosed with congenital heart disease

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Health organizations and government agencies to track prevalence and outcomes

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What is national congenital heart disease?

National congenital heart disease refers to a group of conditions that affect the heart's structure and function that are present at birth. These conditions can range from simple defects, such as small holes in the heart, to more complex issues requiring surgical intervention.

Who is required to file national congenital heart disease?

Medical institutions, healthcare providers, and public health agencies are typically required to file reports related to national congenital heart disease, particularly when documenting cases for statistics, research, and treatment purposes.

How to fill out national congenital heart disease?

To fill out national congenital heart disease documentation, one needs to collect relevant patient data, including the type of congenital heart defect, treatment provided, and patient outcomes, and submit this information through the designated reporting system or form required by health authorities.

What is the purpose of national congenital heart disease?

The purpose of national congenital heart disease reporting is to monitor, analyze, and improve the care and treatment of individuals affected by congenital heart defects, enhance awareness and research, and inform public health policies.

What information must be reported on national congenital heart disease?

The information that must be reported includes details about the patient's demographics, specifics of the congenital heart defect, treatments undertaken, outcomes, and any follow-up care provided.

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