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Biomedical subjects

W W Fox

Publications and source records attributed to W W Fox.

At least 37 records · Page 2Linked to original sources

Continuous intracranial pressure monitoring and serial electroencephalographic recordings in severely asphyxiated term neonates.

We report our observations from intensive intracranial pressure (ICP) monitoring and serial clinical neurologic and electroencephalographic examinations in ten asphyxiated full-term neonates, of whom five died and at least two survivors had multiple severe neurologic handicaps. Direct measurements of ICP were obtained by a newly developed infant subarachnoid bolt and/or a transfontanelle pressure transducer. Simultaneous ICPs were recorded and correlated when possible. We noted a dependence of transfontanelle ICP values on application technique and force. In infants with no bleeding diathesis, the subarachnoid bolt was safe and no complications were encountered. Only six infants experienced pathologic elevations of ICP following birth asphyxia, and of these infants only two had sustained, marked increases of ICP. We also noted abundant fluctuations of cerebral perfusion pressure (mean arterial blood pressure minus ICP), but the majority of fluctuations were accounted for by mean arterial pressure changes rather than ICP changes. We found no deterioration of clinical neurologic function as measured by serial mental status examinations and electroencephalogram samples at the time the maximum ICP was measured. We also noted very little change in ICP during most electrographic seizures. In these infants ICP did increase after birth but major ICP elevations were uncommon and did not appear to introduce any acute functional neurologic disturbances. Most changes in cerebral perfusion pressure were attributed to blood pressure rather than ICP changes. It appears unlikely that cerebral edema and elevated ICP play a major role in determining neurologic outcome in some asphyxiated term infants.

Asphyxia Neonatorum↗

Predicting survival in infants with persistent pulmonary hypertension of the newborn.

Since persistent pulmonary hypertension of the newborn (PPHN) often occurs as a life-threatening illness, it would be advantageous to identify the highest-risk infants within the first 24 hours of life so that transfer to centers with extracorporeal membrane oxygenation (ECMO) or high-frequency ventilation can be facilitated. Fifty-three infants with PPHN were evaluated retrospectively. A multivariate discriminant analysis of risk factors determined that lowest pH, critical PaCO2, highest inspiratory pressure (PI), maximum ventilator rate, and 5-minute Apgar score were significantly different between the 35 survivors (66%) and the 18 infants (34%) who had died when examined within the first 24 hours of life. A clinical scoring system was designed based on these five criteria, which predicted outcome accurately in 93% of infants. A logistic regression analysis was performed as a check on these results and found that lowest pH, critical PaCO2, and PI predicted outcome with great accuracy. These results suggest that the use of these scoring systems within the first 24 hours of age may help predict outcome in infants with PPHN.

Apgar Score↗

Pulmonary hypertension and persistent fetal circulation in the newborn.

Despite these infants' very significant medical instabilities, which require vigorous therapeutic intervention, we have seen a population of infants with little in the way of persistent residual problems. Although many of their pulmonary complications persist after hospital discharge, most resolve within the first year of life. In addition, there are few neurodevelopmental disabilities encountered in such a high-risk population of children.

Epoprostenol↗

Infant apnea.

This review provides an understanding of current problems related to apnea of infancy. Methods for diagnosis, evaluation, and treatment of apnea are discussed.

Airway Obstruction↗

Inductive plethysmography--a facilitated postural calibration technique for rapid and accurate tidal volume determination in low birth weight premature newborns.

Inductive plethysmography is a noninvasive method of measuring lung volumes in infants. This technique, however, has had very limited use in premature newborns because of the difficulty of calibrating the device with regard to the small tidal volumes (VT) in such infants. The present study describes a facilitated calibration of the inductive plethysmograph in low birth weight infants. The technique depends on generating significantly different compartmentalization of VT into rib cage and abdominal components by changing the infant's position from supine to upright. Linear regression analyses were performed to compare VT measurements made in 9 premature infants with the inductive plethysmograph and the pneumotachygraph; an overall Z-transformed correlation of 501 breath-to-breath comparisons yielded an r value of 0.80; the mean VT (pneumotachygraph) was 13.9 +/- 4.7 ml SD; the mean VT (inductive plethysmograph) was 14.3 +/- 5.1 ml SD. It is concluded that inductive plethysmography is an accurate method to measure VT in small premature infants. Moreover, the ease of the two-position technique for calibration of the device gives the inductive plethysmograph greater utility as a clinical and research tool for measuring lung volumes in premature infants.

Calibration↗

Transition phase during hyperventilation therapy for persistent pulmonary hypertension of the neonate.

It is important for the clinician who is hyperventilating infants with persistent pulmonary hypertension (PPHN) to recognize a transition phase during therapy when pulmonary hypertension is no longer the primary cause of hypoxemia, because infants who are hyperventilated develop parenchymal lung disease after 2 to 3 days. This study reports ten infants who showed PaO2 lability early in the course of PPHN, with an inverse relationship between PaO2 and PaCO2. At a mean age of 79 +/- 14 (SEM) there was a transition phase, after which PaO2 lability decreased and the infants did not require hyperventilation. The mean change in PaO2 per change in PaCO2 was significantly (p less than .05) higher pretransition (22.4 +/- 5.2) compared to during transition (5.1 +/- 1.4) or post-transition (1.9 +/- 1.2). Mean alveolar-arterial oxygen gradient was higher (p less than .05) pretransition (495 +/- 36) vs. post-transition (405 +/- 52) and was more labile relative to PaCO2 change pretransition (20.3 +/- 5.9) compared to post-transition (.3 +/- 2.4). When ventilator settings were reduced after the transition phase, PaCO2 rose by 12.2 torr.

Carbon Dioxide↗

Preterm infants: ventilation and P100 changes with CO2 and inspiratory resistive loading.

The ventilatory effects of inspiratory flow-resistive loading and increased chemical drive were measured in ten neonates during progressive hypercapnia in control and loaded states. Hypercapnia (mean increase PCO2 = 15-20) resulted from inspiring 8% CO2 in room air and inspiratory loading by a flow-resistive load = 100 cmH2O X l-1) X s. Hypercapnia produced an increase in group minute ventilation secondary to increasing tidal volumes and breathing frequencies. Loading shifted the minute ventilation-CO2 response to the right, and slopes decreased significantly (P less than 0.05) consequent to a significant decrease in the frequency-CO2 slopes (P less than 0.05), which became negative in four of the ten subjects. Mouth pressure measured at 100 ms after onset of inspiratory effort (P100) occlusion pressure-CO2 slopes measured in five subjects showed no significant increase with load application. Resistive loading produced significant increases in inspiratory time (P less than 0.02) and the inspiratory time/total breath time ratio (P less than 0.01). Airway occlusion elicited the Hering-Breuer reflex, with a significant increase in inspiratory time-to-total breath time ratio (P less than 0.01). The results show that the inspiratory resistive load produced ventilatory compromise in newborns and insufficient compensatory augmentation of central drive.

Airway Resistance↗

A newly recognized profile in neonatal lung disease with maternal diabetes.

A radiographic pattern associated with respiratory distress, distinct from hyaline membrane disease and transient tachypnea of the newborn, is described in eight infants of diabetic mothers. The radiographic findings demonstrate a regional distribution of reticulogranular densities accompanied by increased lung volumes. Clinical features were gestationally mature infants in moderate respiratory distress with tachypnea, hypercapnia, and hypoxemia requiring supplemental oxygen, with steady improvement and uneventful recovery within 2 weeks. There was no bacteriologic evidence of infection or radiographic evidence of delayed lung fluid absorption. The mothers had mild diabetes. These features characterize a newly recognized entity in diabetes-related idiopathic lung disease of the newborn. Possible causative factors are discussed.

Female↗

Awake apnea associated with gastroesophageal reflux: a specific clinical syndrome.

Fifteen infants with a specific clinical history including awake apnea were evaluated and compared with a control group of infants, using 24-hour studies of esophageal pH, nasal thermistor, impedance pneumography, and heart rate. Thirteen of the 15 children with awake apnea had clearly documented episodes of airway obstruction in associated with gastroesophageal reflux occurring at least twice during the study (mean 3.9 +/- 0.7, range 2 to 9). The control group did not show similar findings. All 15 children with awake apnea had frequent episodes of gastroesophageal reflux. Treatment with home monitoring and reflux precautions was successful in 10 of 15. Five children received therapy with urecholine hydrochloride because of continuing episodes of reflux-associated apnea. Two children subsequently required Nissen fundoplication, primarily for symptoms of severe esophagitis. Our data suggest that in children with awake apnea, the apnea is associated with gastroesophageal reflux. Medical management is usually successful, but fundoplication may be needed in refractory cases.

Apnea↗

Long-term follow-up of newborns with persistent pulmonary hypertension.

Persistent pulmonary hypertension of the newborn (PPHN) is a syndrome associated with high morbidity and mortality. Mechanical ventilation attempts to maintain a PaCO2 less than 30 torr and a pH greater than 7.5 until pulmonary hypertension resolves. To assess whether the disease or its therapy adversely affects neurodevelopmental or cardiorespiratory outcome, 11 infants diagnosed and treated for PPHN were evaluated at a mean age of 31 months. Nine had normal developmental quotients (DQs) and 2 had mildly delayed DQs. Eight children were entirely normal neurologically, 2 had slightly increased lower-extremity tone, and 1 had unilateral hypertonia. All cardiac exams, echocardiograms, and ECGs were normal. Four children had chronic lung disease requiring either daily or intermittent bronchodilator therapy; however, their activity levels were unaffected. These results suggest that subsequent normal development with little significant medical compromise may be expected in this group of critically ill infants.

Child Development↗

Infant apnea. An approach to management.

Apnea of infancy represents a problem that is commonly encountered by the practicing pediatrician; yet, few publications have outlined a practical approach to the care of such infants. In addition, the somewhat controversial aspects of infant apnea and sudden infant death syndrome (SIDS) have resulted in the belief on the part of many physicians that the care of children with apnea or "near-miss" SIDS is either very difficult or of little value. This article, which is based upon the program at The Children's Hospital of Philadelphia, describes an effective management plan for identifying children at risk, lists appropriate evaluation studies, and presents a series of protocols for treating infants with apnea. The initiation of this program has helped to demystify the care of children with apnea and has been very well received by both parents and physicians.

Apnea↗

Effect of external inspiratory loading on ventilation of premature infants.

The ventilatory response of 11 growing premature infants to external inspiratory resistive loads was evaluated. Air flow, tidal volume, minute ventilation, inspiratory duration and total breath duration were measured before and after application of a flow resistive load. A significant (P less than 0.001) immediate decrease in minute ventilation and tidal volume was observed in all infants after load application. Minute ventilation and tidal volume remained decreased throughout the 10-min study period. Minute ventilation and tidal volume for the group decreased to 48 and 50% of control mean value, respectively. In addition, there was a significant (P less than 0.001) sustained increase in inspiratory time resulting in an increase in the ratio of inspiratory time/total respiratory time.

Airway Obstruction↗

Episodic airway obstruction in premature infants.

Seventy-six premature infants with clinical apnea, bradycardia, or cyanosis were studied with polygraph recordings of heart rate, nasal thermistor detection of airflow, and impedance pneumography. Pathologic apnea was defined by cessation of breathing for greater than 20 s or less than 20 s with bradycardia (heart rate, less than 100 beats per minute). Apnea was classified as central, obstructive, or mixed. Four hundred thirty-three apnea episodes were demonstrated: 238 (55.0%) were central, 53 (12.2%) showed obstructive apnea, and 142 (32.8%) were mixed. Fifty-two infants (68.5%) demonstrated some degree of obstructive apnea, while 24 infants (31.5%) had central apnea only. Bradycardia did not occur in any patient unless preceded by apnea. In premature infants, a significant percentage of apnea was associated with airway obstruction.

Airway Obstruction↗

Persistent pulmonary hypertension in the neonate: diagnosis and management.

PPHN should be recognized as a clinical condition associated with a number of pulmonary and systemic diseases. Present therapy has resulted in increased survival, but the aggressive methods required to produce improvement necessitate a clear understanding of the underlying pathophysiology in order to minimize sequelae.

Cardiac Catheterization↗

Changes in pulmonary function during the diuretic phase of respiratory distress syndrome.

To evaluate the relationship between improvement in pulmonary function and spontaneous diuresis in respiratory distress syndrome, nine premature infants requiring mechanical ventilation for RDS were studied at a mean age of 11.9 hours prior to the onset of diuresis, at onset of diuresis, at maximum urine output (mean age 44.9 hours), and at 24 hours after maximum urine output. Prior to diuresis functional residual capacity decreased from mean +/- SEM of 16.2 +/- 2 to 13.3 +/- 1.2 ml/kg, and dynamic lung compliance decreased from 2.5 +/- 0.3 to 1.8 +/- 0.3 ml/cm H2O (P less than 0.05), indicating that the respiratory disease was worsening. There was no significant change in alveolar-arterial oxygen gradient, peak inflating pressure, or rate of intermittent mandatory ventilation over this period. At the time of maximum urine output, however, FRC had increased 36% (P less than 0.05). CL had increased by 60% to 2.8 +/- 0.4 ml/cm H2O (P less than 0.025), AaDO2 had decreased from 246 +/- 27 to 184 +/- 30 torr (P less than 0.005), and PIP had decreased from 14.9 +/- 2.2 to 11.3 +/- 2.1 cm/H2O (P less than 0.05). On follow-up study 24 hours after maximum urine output, there was no further significant improvement in FRC, CL or PIP, but IMV rate and AaDO2 continued to decrease. These data show that the pulmonary function in RDS deteriorates until the onset of diuresis, after which it rapidly improves. This diuresis may represent the removal of excess lung liquid and seems necessary for improvement in RDS.

Diuresis↗