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  • 1
    ISSN: 1432-198X
    Keywords: Parathyroid hormones ; Kidney failure, chronic ; Ionised calcium ; Hyperparathyroidism, secondary ; Renal osteodystrophy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report our experience of the use of an immunoradiometric assay for intact parathyroid hormone (i-PTH) and the measurement of plasma ionised calcium concentration (PCa2+) in 73 children with chronic renal insufficiency (CRI); plasma creatinine concentration (PCr) 52–856 μmol/l. There was a poor correlation between i-PTH and PCr (r=0.10,n=552) compared with that for C-terminal PTH and PCr (r=0.60,n=248), suggesting that the i-PTH assay is independent of renal function in this group of treated children. A clear response of i-PTH to a low total plasma Ca (tPCa) and PCa2+ was observed. There was a significant positive correlation between both tPCa and PCa2+ (r=0.50,n=389) and the fraction of Ca2+ (the fraction of tCa which was ionised) and PCa2+ (r=0.50,n=389). The finding of a low or normal PCa2+ with a low calculated fraction of Ca2+ was frequently observed, i. e. the measured tPCa was unexpectedly high, suggesting complexing of Ca2+ by accumulated anions in CRI. There was a poor relationship between the plasma albumin concentration and both bound plus complexed Ca (tPCa minus PCa2+) and the fraction of Ca2+ (r=0.15 and −0.17, respectively). The positive predictive value for a raised i-PTH of a tubular reabsorbtion of phosphate of less than 80% was 0.87, and of an alkaline phosphatase greater than 800 U/l was 0.37. We conclude that the immunoradiometric assay for i-PTH should replace indirect assessments of secondary hyperparathyroidism, and that measurement of the Ca2+ concentration is necessary to evaluate the true Ca status in children with CRI.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric nephrology 3 (1989), S. 43-49 
    ISSN: 1432-198X
    Keywords: Polycystic kidneys ; Congenital hepatic fibrosis ; Hypertension ; Hyponatraemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The clinical features of 55 cases of autosomal recessive polycystic kidney disease (ARPCKD) have been reviewed. Each had evidence of ARPCKD. The outcomes of 87% were known; 24 had died. Twenty-four of 31 were seen between 1980 and 1986; 7 could not be traced. Forty-five percent presented under 1 month; 38% between 1 month and 1 year; and 9 cases over 1 year. Hyponatraemia occurred in 15 out of 19 aged less than 3 months; hypertension occurred in 65%; splenomegaly in 47% of those surviving more than 3 months. Portocaval shunts were done in 5 aged 2–12 years. Thirteen died of renal failure, 6 under 1 year, and 7 between 1 year and 13 years. Life-table survival rates calculated from birth revealed that 86% were alive at 3 months, 79% at 1 year, 51% at 10 years, and 46% at 15 years. Calculations based on patients who survived to 1 year of age showed that 82% were alive at 10 years and 79% at 15 years. These results reveal an improved prognosis for a condition once assumed to be fatal.
    Type of Medium: Electronic Resource
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