Hyperuricemia in Congenital Heart Disease
- 1 September 1978
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Pediatrics & Adolescent Medicine
- Vol. 132 (9) , 900-902
- https://doi.org/10.1001/archpedi.1978.02120340076016
Abstract
β Gout is rarely noted as a clinical problem in secondary polycythemia—even if profound polycythemia exists, as in cyanotic congenital heart disease. A retrospective study of 81 patients with congenital heart disease was done to assess the incidence of hyperuricemia. Twenty of 46 patients with cyanotic congenital heart disease had serum levels of uric acid greater than 8 mg/dl. Thirteen of 16 (81%) cyanotic male patients more than 15 years old had serum levels greater than 8 mg/dl. For cyanotic patients, serum levels of uric acid were related directly to the degree of polycythemia (r =.44; P <.02). Impaired renal function or drug therapy did not seem to account for the hyperuricemia. Because levels of uric acid greater than 10 mg/dl probably are nephropathic, many of these patients may be incurring subclinical uric acid nephropathy. (Am J Dis Child 132:900-902, 1978)This publication has 8 references indexed in Scilit:
- The Etiology and Pathogenesis of GoutPublished by Springer Nature ,1976
- Urinary Xanthine Stones-a Rare Complication of Allopurinol TherapyNew England Journal of Medicine, 1969
- Uric Acid Nephrolithiasis in GoutAnnals of Internal Medicine, 1967
- Hyperuricaemia in Polycythaemia VeraAnnals of the Rheumatic Diseases, 1966
- Effect of allopurinol (4-Hydroxypyrazolo-(3,4-d)pyrimidine) on serum and urinary uric acid in primary and secondary goutThe American Journal of Medicine, 1964
- A familial disorder of uric acid metabolism and central nervous system functionThe American Journal of Medicine, 1964
- GOUT IN CYANOTIC CONGENITAL HEART DISEASEHeart, 1961
- GOUT AND BLOOD DYSCRASIASMedicine, 1959