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Childrenscolorado.org/CCHDScreening p: 7207776820 Critical Congenital Heart Disease Screening Program COMPETENCY CHECKLIST Competency Title: Critical CHD Screening Process Competency Criteria includes
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01
Start by gathering all the necessary information about the individual with the congenital heart disease. This includes their personal details, medical history, and any relevant documents or reports.
02
Consult with medical professionals, such as pediatric cardiologists or healthcare providers specializing in congenital heart diseases, to ensure accuracy and completeness of the information.
03
Begin by documenting the specific diagnosis of critical congenital heart disease. This typically includes information about the specific heart defects present and their severity.
04
Provide a detailed description of the symptoms or signs that led to the diagnosis of critical congenital heart disease. This may include information about abnormal heart sounds, difficulty breathing, poor feeding, or other associated symptoms.
05
Include any previous medical interventions or surgeries that have been performed to address the congenital heart disease. This could involve surgical repairs, heart catheterizations, or the use of medications or devices to manage the condition.
06
Document any ongoing treatments or medications that the individual is currently receiving to manage their critical congenital heart disease. This should include dosage information, frequency of usage, and any specific instructions or precautions.
07
Note any additional medical conditions or complications that may be present alongside the critical congenital heart disease. It is important to capture a comprehensive picture of the individual's health status.
08
Provide details about the recommended treatment plan for the individual, including any scheduled surgeries, follow-up appointments, or ongoing medical management. This could also include information about lifestyle recommendations, such as dietary restrictions or activity modifications.
09
Remember to adhere to any specific guidelines or templates provided by relevant healthcare organizations or regulatory bodies when filling out the critical congenital heart disease documentation.

Who needs critical congenital heart disease?

01
Infants and children who are born with significant structural abnormalities in their heart.
02
Individuals who require ongoing medical management or surgical interventions to address their heart condition.
03
Families or caregivers of individuals with critical congenital heart disease who need access to their medical history and treatment plans for accurate and coordinated care.
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Critical congenital heart disease is a condition present at birth that affects the structure of a baby's heart and the way it functions.
Healthcare providers, hospitals, and public health departments are required to file critical congenital heart disease cases.
Critical congenital heart disease is typically reported through a standardized form provided by the relevant health department.
The purpose of reporting critical congenital heart disease is to track and monitor cases, improve treatment outcomes, and conduct research.
Information such as the baby's date of birth, diagnosis, treatment, and outcomes must be reported on critical congenital heart disease.
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