scholarly journals Retrospective analysis of Pulmonary Surfactant on Respiratory Distress Syndrome of Late Premature or Full-term Infants Paper Title

Author(s):  
Hui Wu ◽  
Jing Cui ◽  
Dan Dang ◽  
Dongxuan Wang
PEDIATRICS ◽  
1993 ◽  
Vol 92 (1) ◽  
pp. 135-139
Author(s):  
Hatem Khammash ◽  
Max Perlman ◽  
Julian Wojtulewicz ◽  
Michael Dunn

Objective. In light of the paucity of published data on the use of surfactant in full-term infants with respiratory failure due to meconium aspiration syndrome and respiratory distress syndrome, we report our experience with this therapy. Our goal was to explore possible justification for randomized controlled trials of surfactant treatment in similar patients at an earlier, less severe stage of the disease. Methods. Retrospective consecutive case series of 20 infants with severe meconium aspiration syndrome and 29 infants with severe respiratory distress syndrome who received bovine surfactant between March 1990 and December 1992 in three neonatal intensive care units in a regionalized setting. Outcome of treatment was assessed by comparing changes in several respiratory indices including the oxygenation index, between 4 and 6 hours and 1 and 3 hours before and after the first dose of surfactant. Differences were analyzed using analysis of variance for repeated measures, with treatment and time as co-variates. Results. In the meconium aspiration group the mean oxygenation index decreased from 36 ± 12 at 1 to 3 hours presurfactant to 24 ± 14 at 1 to 3 hours postsurfactant (P < .001). In the patients with respiratory distress syndrome the mean oxygenation index fell from 30 ± 17 at 1 to 3 hours presurfactant to 12 ± 6 at 1 to 3 hours postsurfactant (P = .0001). Three of 20 patients with meconium aspiration syndrome and 3 of 29 patients with respiratory distress syndrome received extracorporeal membrane oxygenation. Conclusions. Surfactant therapy in full-term infants with respiratory failure due to the meconium aspiration and respiratory distress syndromes is often effective in improving gas exchange. A randomized controlled trial of surfactant therapy at an earlier stage in the course of the illness should be performed.


PEDIATRICS ◽  
1959 ◽  
Vol 24 (4) ◽  
pp. 562-576
Author(s):  
Robert Usher

A study of 59 premature infants with respiratory distress syndrome has revealed the presence of severe increase in concentration of potassium with electrocardiographic changes. Thirty-six of 37 of these infants examined serially between 12 and 60 hours of age developed electrocardiographic abnormalities. Concentrations of potassium in serum of over 7.0 meq/l were associated with these prolonged conduction times. Concentrations of over 9.0 meq/l occurred in 12 infants, 11 of whom died. Parenteral administration of glucose, insulin, and bicarbonate produced a fall in the concentration of potassium in the serum and a correction of the electrocardiogram. Control premature and full-term infants had concentrations of potassium between 4 and 7 meq/l and never showed electrocardiographic disturbances. Evidence is produced that premature infants with the respiratory distress syndrome develop a toxic degree of hyperkalemia which is reversible.


PEDIATRICS ◽  
1959 ◽  
Vol 24 (6) ◽  
pp. 1069-1101
Author(s):  
L. Stanley James

To improve our understanding of the respiratory distress syndrome, the importance of early examination of the infant, preferably at delivery, cannot be overemphasized. An attempt should be made to estimate clinically the degree of birth asphyxiation by a method such as the Apgar Score. The nature of respirations as well as the rate should be noted, particularly retractions and grunting. Decreased response to stimuli or poor tone, and a low blood pressure are significant signs. In this review, a number of comparisons have been drawn, including evidence from adult medicine or animal experiments. While these may appear unrelated, irrelevant or unduly speculative, they have been introduced for several purposes: to draw attention to aspects of the syndrome other than respiratory distress; to acquaint the general reader with more recent physiology which is deemed pertinent; and to emphasize the importance of relating one system to another, especially respiration to circulation. Many of the studies of respiratory function point to cardiac as well as pulmonary failure, notably the need for oxygen in the presence of a normal tidal and increased minute volume. Other circumstantial evidence of cardiac failure is abundant. Asphyxia appears to play a central role, affecting almost every system in the body and every phase of metabolism. It is probably responsible for the normal or low venous pressures occurring with a failing myocardium. It also accounts for the higher incidence of respiratory distress in the smaller prematures who are unable to achieve and maintain normal lung expansion. The syndrome is uncommon in larger full-term infants and in these instances is associated with obstetrical complications causing more severe degrees of birth asphyxia. The clinical picture includes a number of variations depending upon whether respiratory depression or symptoms relating to the central nervous or gastrointestinal systems predominate. Nevertheless, diagnosis of the respiratory distress syndrome should rely not on the presence or absence of membranes at necropsy, but rather on the history, symptoms and clinical signs. Inasmuch as asphyxia is not a disease, it would seem more logical to regard the syndrome as a failure in adaptation to extrauterine life. Failure to comprehend the many adaptations which newborn infants must make, both cardiopulmonary and biochemical, together with a narrow view centering only around the hyaline membranes, have for so many years cloaked this syndrome with mystery. Physiologic measurements in sick infants are difficult, and many of the determinations and calculations arduous. Some of the studies require confirmation, and others remain to be done, employing new or improved technics which are free from disadvantages of older methods. Because of many variables, caution should be exercised in drawing conclusions from a small number of cases. Early pioneering work has contributed greatly and has paved the way for future investigations. The value of serial studies correlated with careful clinical observations in order that the precise nature of a dynamic process may be more fully revealed has been clearly shown.


PEDIATRICS ◽  
1994 ◽  
Vol 93 (3) ◽  
pp. 538-538
Author(s):  
L. Gortner ◽  
F. Pohlandt ◽  
P. Bartmann

Kammash and co-workers described the effects of natural surfactant (BLSE) in full-term neonates1 suffering from adult respiratory distress syndrome (ARDS)-like disorders.2 Due to paucity of further published data,3 we would like to confirm the aforementioned studies by our observations in neonates. Full-term newborns were eligible for the pilot trial, if severe ARDS-like disorder was diagnosed: Fio2 0.9 to 1.0 for Pao2 >50 mm Hg; peak inspiratory pressure (PIP) 35 cm H2O for Paco2 50 mm Hg.


PEDIATRICS ◽  
1975 ◽  
Vol 55 (4) ◽  
pp. 497-499
Author(s):  
Richard M. Cowett ◽  
Leo Stern

In order to establish whether maternal thyroid hormones cross the placenta and produce surfactant in the fetus, possibly reducing the incidence of respiratory distress syndrome (RDS), a retrospective analysis of low-birthweight infants was undertaken. Results indicate that maternal thyroid hormones play a negligible role and that any thyroid mediation would result from fetal thyroid activity.


1988 ◽  
Vol 34 (10) ◽  
pp. 1976-1982 ◽  
Author(s):  
T Spillman ◽  
D B Cotton ◽  
E Golunski

Abstract Densitometric lecithin/sphingomyelin ratios (LSR) and the presence of phosphatidylglycerol (PG) were determined for 735 consecutively received amniotic fluids. Of the 371 fluids with "mature" LSR between 2.0 and 4.5, more than one-third lacked detectable PG. Clinical outcomes for the 305 of the total group that were delivered within 72 h of sampling were also determined. Respiratory distress syndrome (RDS) did not occur in the 239 cases with LSR greater than or equal to 2.0, even when, as in 43 instances, PG was not detected. When the LSR was greater than or equal to 2.0, transient tachypnea was more prevalent in the absence of detectable PG (PG detected, 3% transient tachypnea; PG undetected, 16% transient tachypnea). Of the 103 cases where PG was undetected, 58% exhibited no respiratory problems. Even in the 60 cases where the LSR was less than 2.0 and PG was not detected, 42% of the cases were free of respiratory problems. RDS did not occur in any case where PG was detected, even in the six where the LSR was less than 2.0. We evaluate these results in light of various contradictory reports in the literature.


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