Zusammenfassung
Definition [7, 17, 28]
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Neugeborene >2,0 mmol/1 = 35 mg/dl innerhalb der ersten 24 h,
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Neugeborene >2,6 mmol/1 = 45 mg/dl nach der 24-h-Grenze.
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Frühgeborene >1,4 mmol/1 = 25 mg/dl in der 1. Lebenswoche,
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Frühgeborene >2,2 mmol/1 = 40 mg/dl danach.
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Literatur
Ausems MG, Verbiest J, Hermans MP et al. (1999) Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling. Eur J Hum Genet 7:713–716
Burton BK (1998) Inborn errors of metabolism in infancy: a guide to diagnosis Pediatrics 102:E69
Chace DH, Sherwin JE, Hillman SL, Lorey F, Cunningham GC (1998) Use of phenylalanine to tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 hours. Clin Chem 44:2405–2409
Chaves-Carballo E (1992) Detection of inherited neurometabolic disorders, a clinical approach. Pediatric Neurology 39:801–820
Cornblath M, Ichord R (2000) Hypoglycemia in the neonate. Semin Peri-natol 24:136–149
Cornblath M, Hawdon JM, Williams AF, Aynsley Green A, Ward Platt MP, Schwartz R, Kalhan SC (2000) Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds. Pediatrics 105: 1141–1145
Cornblath M, Schwartz R, Aynsley-Green A, Lloyd JK (1990) Hypoglycemia in infancy: The need for a rational definition. Pediatrics 85: 834–837
Cowett RM, Howard GM, Johnson J, Vohr B (1997) Brain stem auditory-evoked response in relation to neonatal glucose metabolism. Biol Neonate 71:31–36
Denne SC, Kalhan SC (1986) Glucose carbon recycling and oxidation in human newborns. Am J Physiol 251:E71–E77
Duvanel CB, Fawer CL, Cotting J, Hohlfeld P, Matthieu JM (1999) Long term effects of neonatal hypoglycemia on brain growth and psychomotor development in small-for-gestational age preterm infants J Pediatr 134:492–498
Galloway A, Stevenson J (1996) An audit of the organisation of neonatal screening for phenylketonuria and congenital hypothyroidism in the Northern Region. Public Health 110:119–121
Giacoia GP, Padilla-Luger A (1986) Severe transient neonatal hyperammonemia. Am J Perinatol 3:249–254
Greene CL, Goodman SI (1997) Catastrophic metabolic encephalopathies in the newborn period. Evaluation and management. Clin Perinatol 24:773–786
Lucas A, Morley R, Cole TJ (1988) Adverse neurodevelopmental outcome of moderate neonatal hypoglycaemia. Br Med J 297:1304–1308
Maestri NE, Clissold D, Brusilow SW (1999) Neonatal onset ornithine tran-scarbamylase deficiency: A retrospective analysis. J Pediatr 134:268–272
McCabe ER, McCabe LL (1999) State of the art for DNA technology in newborn screening. Acta Paediatr 88:58–60
Mehta A (1994) Prevention and management of neonatal hypoglycaemia. Arch Dis Child 70:F54–F60
Pang S, Shook MK (1997) Current status of neonatal screening for congenital adrenal hyperplasia. Curr Opin Pediatr 9:419–423
Perrine SP, Greene MF, Faller DV (1985) Delay in the fetal globin switch in infants of diabetic mothers. N Engl J Med 321:334–338
Peterschmitt MJ, Simmons JR, Levy HL (1999) Reduction of false negative results in screening of newborns for homocystinuria. N Engl J Med 341: 1572–1576
Pollitt RJ, Green A, McCabe CJ et al. (1997) Neonatal screening for inborn errors of metabolism: cost, yield and outcome. Health Technol Assess 1:1–202
Relier MD, Tsang RG, Meyer RA, Braun CP (1985) Relationship of prospective diabetes control in pregnancy to neonatal cardiorespiratory function. J Pediatr 106:86–90
Rizzo T, Metzger BE, Burns WJ, Burns K (1991) Correlations between antepartum maternal metabolism and intelligence of offspring. N Engl J Med 325:911–916
Saudubray JM, Touati G, Delonlay P et al. (1999) Liver transplantation in urea cycle disorders. Eur J Pediatr 158:55–59
Schwartz RP (1997) Neonatal hypoglycemia: how low is too low? [editorial; comment] J Pediatr 131:171–173
Scriver CR, Beaudet AL, Sly WS (eds) (1995) The metabolic and molecular basis of inherited disease, 6th edn. McGraw-Hill, New York
Shohat M, Merlob P, Reisner SH (1984) Neonatal polycythemia. I. Early diagnosis and incidence relating to time of sampling. Pediatrics 73:7–10
Sinclair JC (1997) Approaches to the definition of neonatal hypoglycemia. Acta Paediatr Jpn 39 (Suppl 1):S17–S20
Sonntag J, Waltz S, Schollmeyer T, Schuppler U, Schroder H, Weisner D (1996) Morbidity and mortality of discordant twins up to 34 weeks of gestational age. Eur J Pediatr 155:224–229
Spady DW, Saunders LD, Bamforth F (1998) Who gets missed: coverage in a provincial newborn screening program for metabolic disease. Pediatrics 102:E21
Spellacy WN (1984) Evaluation and management of diabetes in pregnancy. Adv Clin Obstet Gynecol 2:34–42
Stanley CA (1997) Hyperinsulinism in infants and children. Pediatr Clin North Am 44:363–374
Uchino T, Endo F, Matsuda I (1998) Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan. J Inherit Metab Dis 21: 151–159
Vannucci RC, Vannucci SJ (2000) Glucose metabolism in the developing brain. Semin Perinatol 24:107–115
Verhoeven AJ, Visser G, van Zwieten R, Gruszczynska B, Tien Poll The DW, Smit GP (1999) A convenient diagnostic function test of peripheral blood neutrophils in glycogen storage disease type lb. Pediatr Res 45:881–885
Verloes A, Massin M, Lombet J et al. (1997) Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form. Am J Med Genet 72:135–142
Visser G, Herwig J, Rake JP, Niezen Koning KE, Verhoeven AJ, Smit GP (1998) Neutropenia and neutrophil dysfunction in glycogen storage disease type 1c. J Inherit Metab Dis 21:227–231
White P (1965) Pregnancy and diabetes. Med Clin North Am 49:1015
Wraith JE (1989) Diagnosis and management of inborn errors of metabolism. Arch Dis Child 64:1410–1415
Yamaguchi Y, Aoki T, Arashima S et al. (1999) Mass screening for Wilson’s disease: results and recommendations. Pediatr Int 41:405–408
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Obladen, M. (2002). Akute metabolische Entgleisungen. In: Bein, G., Maier, R.F., Waldschmidt, J. (eds) Neugeborenenintensivpflege. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-08937-8_16
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