GLUTAMIC-OXALACETIC TRANSAMINASE OF SERUM IN INFANCY AND CHILDHOOD

PEDIATRICS ◽  
1959 ◽  
Vol 24 (3) ◽  
pp. 362-366
Author(s):  
Robert E. Stanton ◽  
Howard A. Joos

Activity of glutamic-oxalacetic transaminase in serum (S-GOT) has been evaluated in normal infants and children and in a wide variety of diseases, including convalescent rheumatic fever, renal disease, hemolytic disease, infections and various hepatic disorders. In 46 normal children, the observed range was 7-41 units. The range of normal values in newborn infants was somewhat wider, 29-79 units. Convalescent rheumatic fever and infections not involving the liver were associated with normal S-GOT. S-GOT was normal with the hemolytic diseases in the absence of fulminant hemolysis. It was frequently exceptionally low in association with renal disease, and slightly elevated for a few days after major surgery. S-GOT is elevated in diseases of the liver, but the results are too variable for specific differentiation of hepatic diseases in early life. The test is best employed in conjunction with careful clinical evaluation and with other measures of liver function.

PEDIATRICS ◽  
1960 ◽  
Vol 25 (1) ◽  
pp. 171-172
Author(s):  
SIMON KOVE

I have read with interest the paper "Glutamic-oxalacetic transaminase of serum in infancy and childhood" by Stanton and Joos (Pediatrics, 24:362, 1959). The statement is made that "S-GOT is elevated in diseases of the liver, but the results are too variable for specific differentiation of hepatic diseases in early life." This conclusion is in sharp contrast to the reported findings of my colleagues (Goldstein, S., Perry, R., and Wróblewski, F.) and myself and some clarification of these divergent views appears to be in order.


2020 ◽  
Vol 14 (2) ◽  
pp. 106-111 ◽  
Author(s):  
Ronghua Gui ◽  
Federico Canavese ◽  
Shuang Liu ◽  
Lianyong Li ◽  
Lijun Zhang ◽  
...  

Purpose Early diagnosis and prevention of lateral growth disturbance of the capital femoral epiphysis is challenging after treatment for developmental dysplasia of the hip (DDH). The aim of the study was to evaluate the radiographic changes of the Alsberg angle (AA) in normal children and those with DDH, and to assess the role of AA as a potential predictor of lateral growth disturbance of the capital femoral epiphysis. Methods AA was measured on the anterior-posterior pelvic radiographs of 1000 normal children ranging in age from one to ten years and in 66 children (92 hips) with DDH treated by closed reduction (CR). A comparative analysis was performed. Results In the normal children, mean AA decreased linearly with age, from 76° at age one year to 65° at age ten years, irrespective of gender and laterality. In children with DDH, the average AA was 81.5°(sd 3.9°; 74° to 87°) prior to CR; it was 75.9° (sd 4.5°; 68° to 83°) in normal children of the same age (p < 0.001). Among the 42 children (64 hips) with successfully and uneventfully treated DDH, AA reached normal values between the ages of five and six years. In contrast, children with lateral growth disturbance of the proximal femur physis (24 children, 28 hips) showed significantly higher AA values in comparison with the age-matched controls. Conclusion In DDH patients with successful CR, AA could be expected to match normal values in children between the ages of five and six years. On the other hand, AA can be used as an early predictor for lateral growth disturbance of the capital femoral epiphysis. Level of Evidence Level III


PEDIATRICS ◽  
1962 ◽  
Vol 30 (1) ◽  
pp. 27-31
Author(s):  
Ralph H. Kunstadter ◽  
Harvey Buchman ◽  
Morad Jacobson ◽  
Leo Oliner

The in vitro erythrocyte uptake studies of radioactive 1-triiodothyronine in 70 normal children, ranging in age from newborn infants to 13 years, are presented. The data reveal elevated uptake values in these children as compared to adults, indicating alteration in binding capacity of thyroxin-binding serum protein carriers, in all probability a reduction in thyroxin-binding prealbumin capacity.


PEDIATRICS ◽  
1958 ◽  
Vol 22 (6) ◽  
pp. 1110-1114
Author(s):  
E. G. Murphy ◽  
Morris M. Cherniak

Serum activities of the enzyme glutamic oxalacetic transaminase were measured in 57 infants and children with various neuromuscular disorders. High values were obtained in 20 out of 32 patients with the Duchenne type of muscular dystrophy. The 12 cases with normal or borderline activities were mainly older children usually with advanced disease. Of the 10 patients with other varieties of muscular dystrophy, all but one had normal values. Normal values were invariably present in primary neuropathies. In the polymyositic group a small series of five cases had normal or borderline activities. The measurement of activity of this enzyme in the serum is a useful diagnostic aid in neuromuscular disorders, particularly in the younger child.


2019 ◽  
Author(s):  
Emmy Okello ◽  
Meghna Murali ◽  
Joselyn Rwebembera ◽  
Jenifer Atala ◽  
Nada Harik ◽  
...  

AbstractBackgroundCentral to rheumatic fever (RF) diagnosis is evidence of streptococcal exposure, specifically antistreptolysin O (ASO) and antideoxyribonuclease B (ADB) antibodies. It is unknown if these antibody titers should be adjusted to the background exposure rates of GAS or if published standards should be used. Here, we establish the normal values of ASO and ADB in Uganda and examine RF case detection using published vs. population-specific thresholds.MethodsParticipants (age 0-50 years) were recruited. ASO was measured in-country by nephelometric technique. ADB samples were sent to Australia (PathWest) for ADB determination by enzyme inhibition assay, andthe 80% upper limit values by age were established. The published standard values for ASO (200IU/ml) and ADB (375IU/ml) were compared to the Ugandan 80% upper limit of normal values (ULN) for RF case detection in children 5-15 years.FindingsOf the 428 participants, 16 were excluded from analysis (9 sore throat, 1 skin sores, 5 fever, 4 echocardiograms showing occult RHD), and 183 of the remaining were children 5-15 years. The median ASO titer in this age group was 220 IU/ml, with the 80th percentile value of 389 IU/ml. The median ADB titer in this age group was 375 IU/ml, with the 80th percentile value of 568 IU/ml. Application of new Ugandan cutoffs to 528 children enrolled in our prospective RF study, reduced the number of definite RF cases to 120/528 (22·7%), as compared to 173/528 (32·8%) using published normal values.InterpretationThe 80th percentile ULN for ASO and ADB are higher in Uganda than in other countries. Applying these higher values to RF diagnosis in Uganda results in higher diagnostic specificity, but some unknown loss in sensitivity. Implications of over-diagnosis and missed cases will be explored through a longitudinal follow-up study of children in the RF research program.FundingThis work was supported by American Heart Association Grant #17SFRN33670607 / Andrea Beaton / 2017 and DELTAS Africa Initiative.Research in contextEvidence before this studyWe searched PubMed for data on normal values of streptococcal antibody titers within diverse populations between database inception and January 1, 2019, using the search terms (rheumatic fever) OR (streptococcal antibodies). Nine studies were identified, but only one was from sub-Saharan Africa (2018, Ethiopia) and it was limited by vague exclusion criteria and lack of data on anti-DNase B. Given the high burden of rheumatic heart disease in sub-Saharan Africa, further data is needed to determine normal streptococcal antibody titers in this population and to assess the clinical impact of different cutoffs for RF diagnosis.Added value of this studyOur study utilized a rigorous approach to exclude patients with history of recent possible streptococcal exposure including skin and throat infection and employed echocardiography to exclude patients with pre-existing rheumatic heart disease. Additionally, this study was conducted in parallel to a larger epidemiological cohort study of rheumatic fever in Uganda, allowing us, for the first time, to prospectively determine how utilization of different streptococcal antibody titer cutoffs affect diagnosis of rheumatic fever.Implications of all the available evidenceRheumatic fever remains a challenging diagnosis based on a clinical decision rule with imperfect sensitivity and specificity. Improved understanding of streptococcal antibody titers in rheumatic heart disease endemic populations may improve diagnostic performance. Our study also points to the need for development of a rheumatic fever diagnostic test, in order to provide a more definitive assessment of risk.


PEDIATRICS ◽  
1951 ◽  
Vol 7 (5) ◽  
pp. 691-706
Author(s):  
WALTER HEYMANN ◽  
HERBERT Z. LUND

1. Chronic renal disease was produced in 235 4 to 5 week-old rats of the Long-Evans strain by the intravenous injection of nephrotoxic sera obtained from rabbits. 2. Massive proteinuria, largely without hematuria, was noted without delay. Severe edema and ascites was observed in 35% of the animals within the first 2 to 3 weeks. Thirty-two per cent died within the first two weeks. A spontaneous cure of the disease occurred in 30% and chronic renal disease that lasted in some instances as long as 13 months, was observed in the remaining animals. 3. From 125 sick rats, 74% remained normotensive. A fluctuating and moderately severe hypertension was noted in the remaining 26%. 4. The blood chemistry revealed marked hypoproteinemia and hyperlipemia in the earliest phase. This subsided slowly as the disease progressed but did not reach normal values as long as the disease persisted. With a few exceptions the creatinine concentration remained normal during all phases of the disease. Marked azotemia was frequently obtained in severe disease at onset. It subsided regularly within the first two months and slight degrees of azotemia in late stages of the disease were noted in approximately 50% of the rats. 5. A histologic analysis was obtained in 119 sick, 12 recovered and 31 control rats. By correlating the chronologic order of clinical evidence with the pathologic picture, the following conclusions were drawn: (a) The nephrotoxin produces primarily a degenerative lesion with changes in glomeruli and tubules; (b) There may be recovery from the degenerative phase or it may be followed at variable intervals by a variable degree of fibrous proliferation in the glomerular tufts and capsules.


PEDIATRICS ◽  
1955 ◽  
Vol 16 (2) ◽  
pp. 184-195
Author(s):  
Robert Stempfel ◽  
Rolf Zetterström

1. Twenty-four full-term, newborn infants, of whom 23 were Rh-isoimmunized, were followed with serial determinations of the serum and spinal fluid bilirubin and spinal fluid total protein during the neonatal period. Of the 51 spinal fluid samples examined, measurable quantities of bilirubin were present in all cases. 2. In the presence of marked indirect hyperbilirubinemia, the spinal fluid bilirubin was predominantly indirect-reacting, though no linear relationship exists between the serum and spinal fluid bilirubin. It is suggested that this is a manifestation of individual variations in blood-brain barrier permeability within the neonatal period. A significant correlation between the spinal fluid indirect bilirubin and the spinal fluid total protein is further evidence to support this view. 3. Spectrophotometric absorption studies of 13 serum and spinal fluid samples from 8 infants with hemolytic disease of the newborn are discussed. These studies tend to confirm the observation that there is no direct correlation between the hyperbilirubinemia and the spinal fluid bilirubin concentration, though the configuration of the absorption pattern of the serum closely follows that obtained from the corresponding spinal fluid. 4. The findings in the Rh-isoimmunized group of infants were not unlike those observed in a single case of "physiologic jaundice" presented. 5. The question of indirect bilirubin neurotoxicity is briefly reviewed.


PEDIATRICS ◽  
1959 ◽  
Vol 23 (6) ◽  
pp. 1063-1084
Author(s):  
Eleanor Colle ◽  
Elsa Proehl Paulsen

Balance data for sodium, potassium, chloride, nitrogen, and water were obtained postoperatively in 15 newborn infants operated upon in the first 4 days of life and in 5 control newborn infants. The infants showed a response in terms of electrolyte and water balances which is significantly different from that reported in adults: The volumes of urine were equal to or greater than those in normal infants of a comparable age. The data suggest a diminished capacity of the newborn to conserve water postoperatively, but a normal capacity to dilute the urine. No evidence of retention of water was observed. The urinary excretion of sodium and chloride was equal to or larger than that of normal infants. The infants who had losses postoperatively from gastrointestinal suction showed no capacity to reduce renal excretion of these ions while they suffered these large extrarenal losses. The concentrations of sodium and chloride in the serum remained normal or became slightly elevated postoperatively. Losses of potassium and nitrogen in the urine were of the same relative magnitude as those in adults. The observed responses are discussed in terms of the function of antidiuretic and adrenocortical hormones in the newborn infant. The application of these data to practical considerations of fluid and electrolyte therapy in the postoperative management of the newborn infant are discussed briefly.


PEDIATRICS ◽  
1948 ◽  
Vol 2 (5) ◽  
pp. 570-576
Author(s):  
ROSE LUBSCHEZ

Electrophoretic analyses of blood plasma or serum of 30 children in apparent health between the ages of two and 11 years revealed that the relative concentration of the various components was in close agreement with adult values, although the individual variation was several times greater. For 27 children in apparent health, but who had experienced various types of infection during a one to four month interval prior to the time the specimen was taken, elevation of the gamma component occurred in about 40% of the determinations. Illness within the month produced the greatest number of abnormalities, although abnormalities were noted in specimens of children who had been free of infection two to three months. A few abnormalities were noted in all components except beta globulin. At younger ages (two to four years) children showed a slightly higher albumen level and a slightly lower gamma globulin level. Normal children susceptible to rheumatic fever on a genetic basis exhibited no specific differences in the electrophoretic pattern.


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