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European Heart Journal (2010) 31, 1220 1229 DOI:10.1093/eurheartj/ehq032 CLINICAL RESEARCH Congenital heart disease Mortality in adult congenital heart disease Marianne L. Overheat 1,2,3, Juno S.P.M.
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Collect and review relevant medical records and data related to the patient's condition.
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Assess the patient's demographic information and medical history, including any previous surgeries or interventions.
03
Document and analyze any symptoms or complications the patient has experienced.
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Use appropriate medical coding systems to accurately code the patient's condition and any relevant procedures or treatments.
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Conduct a thorough physical examination and perform any necessary diagnostic tests to assess the severity of the patient's condition.
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Collaborate with a multidisciplinary team, including cardiologists, surgeons, and other specialists, to gather comprehensive information about the patient and their prognosis.
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Utilize validated risk prediction models or scoring systems, such as the Congenital Heart Adult Mortality Estimation (CHAMP) score, to estimate the patient's risk of mortality.
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Consider the patient's quality of life and individual preferences when discussing treatment options and making decisions.
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Document all findings, assessments, and treatment plans accurately and thoroughly in the patient's medical record.

Who needs mortality in adult congenital:

01
Healthcare professionals specialized in adult congenital heart disease, such as cardiologists, internists, and cardiac surgeons, require mortality information to evaluate the outcomes of their patients and provide appropriate care.
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Researchers and scientists studying adult congenital heart disease need mortality data to better understand the long-term effects and prognosis of different conditions.
03
Health policy makers and administrators use mortality information to assess the impact of adult congenital heart disease on public health and allocate resources accordingly.
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Mortality in adult congenital refers to the measure or rate of death among adults who have congenital heart defects.
Healthcare providers, hospitals, and medical institutions that treat adults with congenital heart defects are responsible for filing mortality in adult congenital.
To fill out mortality in adult congenital, healthcare providers need to report the relevant information about the adult patients with congenital heart defects who have died. This includes details such as age, cause of death, and any contributing factors.
The purpose of mortality in adult congenital is to monitor and analyze the death rates among adults with congenital heart defects. This information is used for research, improving healthcare practices, and developing necessary interventions.
The information that must be reported on mortality in adult congenital includes the demographic details of the deceased adult patients with congenital heart defects, the cause of death, any contributing factors, and relevant medical history.
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