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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Renal involvement in patients with congenital cyanotic heart disease
F Krull1, J H Ehrich, U Wurster
1Department of Paediatric Nephrology, Medizinische Hochschule, Hannover, Germany.
Insights
Congenital cyanotic heart disease can lead to kidney damage, specifically glomerulopathy. Prolonged hypoxemia, especially over ten years, significantly increases the risk of developing this condition in children.
Area of Science:
- Nephrology
- Cardiology
- Pediatrics
Background:
- Congenital cyanotic heart disease (CCHD) is associated with potential renal complications.
- Glomerulopathy, characterized by proteinuria and reduced renal function, can occur in CCHD patients.
Purpose of the Study:
- To investigate the prevalence and characteristics of glomerulopathy in patients with uncorrected CCHD.
- To determine the relationship between disease duration, hypoxemia, and renal impairment.
Main Methods:
- Study included 27 patients with uncorrected CCHD (age 1 day to 25 years).
- Assessed proteinuria (mg/day/1.73 m2), hematocrit, creatinine clearance, and erythrocyte count.
- Analyzed data based on patient age groups.
Main Results:
- Proteinuria was observed in 12 patients, increasing with age.
- Patients over 20 years old exhibited significant glomerular proteinuria and impaired creatinine clearance.
- Pathological proteinuria correlated with higher erythrocyte counts and longer duration of hypoxemia.
Conclusions:
- Persistent CCHD carries a substantial risk of developing glomerulopathy.
- The risk increases significantly with disease duration exceeding ten years.
- Early detection and management of hypoxemia may be crucial for preventing renal damage in CCHD.
Abstract:
Patients with congenital cyanotic heart disease may develop a glomerulopathy with proteinuria and impaired renal function. In order to investigate this problem we conducted a study on 27 patients with uncorrected cyanotic heart disease who were between 1 day and 25 years old. As a consequence of hypoxaemia haematocrit was elevated to 57%. Proteinuria was above 150 mg/day/1.73 m2 body surface in 12 patients. Only one of 9 children under 10 years of age had pathological proteinuria presenting as isolated albuminuria. Seven out of 10 patients between 11 and 20 years had an elevated proteinuria with a glomerular pattern. Creatinine clearance was normal in these patients. All four patients above 20 years of age had a considerable glomerular proteinuria with a mean excretion of 5.7 g/24 h/1.73 m2 body surface. These patients suffered additionally from chronic cardiac failure and creatinine clearance was below the normal range. There was a clear relationship between pathological proteinuria and age of the patients and thus duration of hypoxaemia. Patients with pathological proteinuria had a significant higher erythrocyte count (7.3 +/- 1.3 vs 5.6 +/- 1.4 10(12)/l p less than 0.01) and a lower mean corpuscular haemoglobin. In summary, children with persistent congenital cyanotic heart disease have substantial risk of developing a glomerulopathy if the cyanosis remains unchanged for more than ten years.
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