Key result
Uncorrected congenital cyanotic heart disease is linked to pathological proteinuria in ~44% of patients.
Why the study?
Patients with congenital cyanotic heart disease may develop glomerulopathy with proteinuria and impaired renal function, but the characteristics and progression of this renal involvement are not well defined.
Observational (n=27)
Patients with persistent congenital cyanotic heart disease have a substantial risk of developing glomerulopathy if cyanosis remains uncorrected for more than ten years.
Suggests age-related proteinuria risk in uncorrected cyanotic heart disease; leaves open need for prospective renal outcome studies before screening changes practice.
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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Krull et al. (1991) conducted an observational in Congenital cyanotic heart disease (n=27). Uncorrected congenital cyanotic heart disease was evaluated on Pathological proteinuria (>150 mg/day/1.73 m2 body surface).
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