Salivary Immunoglobulins: Absence of γA in Saliva Following Exchange Transfusions in Neonatal Period

PEDIATRICS ◽  
1967 ◽  
Vol 40 (3) ◽  
pp. 452-454
Author(s):  
JOHN C. SELNER ◽  
DEBORAH A. MERRILL ◽  
HENRY N. CLAMAN

The possible transport of serum γA into saliva was studied in the newborn period. Five infants with erythroblastosis fetalis and undetectable γA in serum or saliva had two-volume exchange transfusions. Serum γA rose to "adult" levels after transfusion, but no detectable γA appeared in serial samples of saliva, as measured by electroimmunodiffusion (EID). The data support the thesis that salivary γA is not transported from the serum and tends to confirm the findings of Haworth and Dilling who previously described the absence of salivary γA following exchange transfusions in newborn infants.

PEDIATRICS ◽  
1957 ◽  
Vol 20 (4) ◽  
pp. 584-589
Author(s):  
Simon Kove ◽  
Stanley Goldstein ◽  
Felix Wróblewski

The activity of glutamic oxaloacetic transaminase (GOT) in the serum was determined by the spectrophotometric method in 63 normal term newborn infants, varying from birth to 11 days of age. The normal range of activity in the newborn period varied from 13 to 105 units (with the exception of one infant in whom the level was 160 units). This is a considerably wider range than that of 5 to 45 units found in normal adults. Allowing for an error of about ±10% inherent in the method of determination of GOT, activity as great as approximately 120 units, which in adults would be indicative of some pathologic state, must be considered physiologic in the newborn infant. The activity of GOT was not related to the age of the infant within the neonatal period studied, and varied widely in different infants for each day of age, without any distinctive pattern. Variations of the activity of GOT in specimens of cord blood studied ranged below 59 units, which was lower than for any other day of the neonatal period adequately investigated. No infants were studied repeatedly. No relation was found between the concentration of bilirubin and the activity of GOT in the serum.


Neonatology ◽  
2021 ◽  
pp. 1-8
Author(s):  
Nestor E. Vain ◽  
Florencia Chiarelli

Neonatal hypoglycaemia is a common metabolic disorder presenting in the first days of life and one potentially preventable cause of brain injury. However, a universal approach to diagnosis and management is still lacking. The rapid decrease in blood glucose (BG) after birth triggers homeostatic mechanisms. Most episodes of hypoglycaemia are asymptomatic, and symptoms, when they occur, are nonspecific. Therefore, neonatologists are presented with the challenge of identifying infants at risk who might benefit from a rapid and effective therapy while sparing others unnecessary sampling and overtreatment. There is much controversy regarding the definition of hypoglycaemia, and one level does not fit all infants since postnatal age and clinical situations trigger different accepted thresholds for therapy. The concentration and duration of BG which cause neurological damage are unclear. Recognizing which newborn infants are at risk of hypoglycaemia and establishing protocols for treatment are essential to avoid possible deleterious effects on neurodevelopment. Early breastfeeding may reduce the risk of hypoglycaemia, but in some cases, the amount of breast milk available immediately after birth is insufficient or non-existent. In these situations, other therapeutic alternatives such as oral dextrose gel may lower the risk for NICU admissions. Current guidelines continue to be based on expert opinion and weak evidence. However, malpractice litigation related to neurodevelopmental disorders is frequent in children who suffered hypoglycaemia in the neonatal period even if they had other important factors contributing to the poor outcome. This review is aimed to help the practicing paediatricians and neonatologists to comprehend neonatal hypoglycaemia from physiology to therapy, hoping it will result in a rational decision-making process in an area not sufficiently supported by evidence.


PEDIATRICS ◽  
1958 ◽  
Vol 22 (4) ◽  
pp. 785-845
Author(s):  
Shirley G. Driscoll ◽  
David Yi-Yung Hsia

PEDIATRIC literature and clinical experience contain abundant indications of physiologic immaturity in newborn infants, especially in those born prior to term. Functional immaturity of brain, liver, kidney, immune response and blood coagulation are among the well-recognized peculiarities of the newborn period. Exaggerations of these usually mild, transitory phenomena may contribute to grave disorders and possibly prove to be lethal. In addition to apparent derangements of particular systems or organs, there are occasional infants, notably the delicate offspring of diabetic mothers, whose general response and appearance suggest immaturity disproportionate to size and gestational age. In this group, general metabolic disturbances are suspected which await biochemical localization and characterization. Conventional post-mortem examinations may be discouragingly unrevealing in these babies. For example, one of the most commonly encountered problems is that of infants dying following unexplained respiratory distress. Pathologically, only so-called "hyaline membranes" with atelectasis have been found. This pattern can be noted in at least half of all infants of diabetic mothers and prematures and occasionally in a full-term baby, and constitutes one of the most baffling problems in clinical pediatrics today. In contrast, the increasing availability of biochemical methods of study are providing a rapidly growing fund of information concerning the normal fetus and newborn. From studies on the chemical embryology of other species and from limited similar work with human material, characteristic patterns of chemical differentiation are emerging. Extension of such observations may be expected to permit the establishment of new metabolic parameters by which to assess the developing fetus and infant.


1987 ◽  
Vol 9 (3) ◽  
pp. 89-94
Author(s):  
William B. Weil

Some of the difficulties of obtaining surrogate decisions that are in the children's best interests, the extension of this problem to the newborn period, and the political and social derivatives of these difficulties have been reviewed. The 1984 child abuse and neglect amendments have been summarized and their impact on the care of newborns has been discussed. The outcomes of this entire process have been described and the potential extension of these issues to the prenatal period has been mentioned. Although not everything that has transpired or will transpire as the result of the Baby Doe issue is salutary, it seems likely that the care of newborn infants has changed and will continue to change, and these changes will ultimately impact on medical care for everyone.


PEDIATRICS ◽  
1961 ◽  
Vol 28 (5) ◽  
pp. 850-851
Author(s):  
GLORIA S. BAENS ◽  
WILLIAM OH ◽  
EVELYN LUNDEEN ◽  
MARVIN CORNBLATH

To the Editor: Recently, there has been a renewed interest in the level of blood sugar in the newborn period, with very low or zero blood sugars being reported1, 2 In some of these reports there is no mention of how the blood was collected, how long it was permitted to stand, how it was precipitated, or analyzed. As reviewed by Peters and Van Slyke,3 the disappearance of sugar from blood in vitro has been well documented since the time of Claude Bernard.


2021 ◽  
Vol 28 (4) ◽  
pp. 153-156
Author(s):  
Gyu Min Yeon ◽  
Yu Jin Jung

Incidence of human herpesvirus-6 (HHV-6) infection in the neonatal period has been reported in few cases. HHV-6, commonly responsible for roseola, is known to establish infection during infancy and early childhood. A 14-day-old neonate, presented with a fever of 38.3℃, primarily due to an HHV-6 infection, was admitted to our neonatal intensive care unit. A polymerase chain reaction (PCR) of his cerebrospinal fluid was positive for HHV-6. Additionally, serology for HHV-6 PCR was positive. We believe that HHV-6 can cause infection in febrile newborn infants.


1996 ◽  
Vol 33 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Margit Bacher ◽  
Gernot Göz ◽  
Thinh Pham ◽  
Thomas Ney ◽  
Michael Ehrenfeld

Congenital decubital ulcers were found in 94% of newborn infants with unilateral cleft lip and palate in the course of a systematic study of a large cohort study (N = 52). The procedures for diagnosis, documentation, and follow-up are described. The ulceration area at birth varied over a wide range. The ulcerations were usually located in the posterior part of the vomer. Sonographic evidence supports the hypothesis that the ulcerations are caused mechanically by the motor activity of the tongue during the fetal and newborn period. The decubital ulcer disappeared in each case within 5 days following the implementation of a palatal plate.


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 ◽  
1950 ◽  
Vol 6 (5) ◽  
pp. 737-742
Author(s):  
HAROLD S. MEDOFF ◽  
GIULIO J. BARBERO

A total of 262 eosinophil counts were done on a series of 57 infants. The mean level was 267 at birth and 483 at 1 month of age. The eosinophil count rose significantly in the first week of life in 75% of 44 infants. Eighty-two per cent of 28 infants showed a significant rise in eosinophils from 5 to 30 days of age. The marrow of newborn infants was relatively rich in myelocytic and rubrocytic elements and low in lymphocytes. At 30 days of age the marrow showed a significant and reciprocal change in the relative proportions of these elements. The infant's eosinophil pattern in the first week after birth was variable and erratic. It differed quantitatively and qualitatively from that of his mother.


PEDIATRICS ◽  
1989 ◽  
Vol 83 (5) ◽  
pp. 785-789
Author(s):  
D. A. FISHER ◽  
B. L. FOLEY

Mass population screening of newborn infants for congenital hypothyroidism was introduced in 1974 and now is a routine and effective means of early diagnosis of congenital hypothyroidism throughout most of the industrialized world. A large number of affected infants and children have been treated with replacement thyroid hormone, and several reports of IQ measurements and functional assessments of 5-to 7-year-old treated children now are available. These reports document normal mean IQ values, satisfactory school performance, and minimal motor dysfunction in treated children. However, there have been reported correlations between lower IQ values and biologic parameters of the hypothyroid state in the neonatal period among several reported studies, and it is not yet clear whether early adequate treatment will reverse all of the effects of congenital hypothyroidism.


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