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1.
AJNR Am J Neuroradiol ; 37(9): 1745-51, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27151752

ABSTRACT

BACKGROUND AND PURPOSE: Infants with congenital diaphragmatic hernia are reported to have evidence of brain MR imaging abnormalities. Our study aimed to identify perinatal clinical factors in infants with congenital diaphragmatic hernia that are associated with evidence of brain injury on MR imaging performed before hospital discharge. MATERIALS AND METHODS: MRIs performed before hospital discharge in infants with congenital diaphragmatic hernia were scored for brain injury by 2 pediatric neuroradiologists. Perinatal variables and clinical variables from the neonatal intensive care unit stay were analyzed for potential associations with brain MR imaging findings. RESULTS: Fifty-three infants with congenital diaphragmatic hernia (31 boys) were included. At least 1 abnormality was seen on MR imaging in 32 infants (60%). The most common MR imaging findings were enlarged extra-axial spaces (36%), intraventricular hemorrhage (23%), ventriculomegaly (19%), white matter injury (17%), and cerebellar hemorrhage (17%). The MR imaging brain injury score was associated with extracorporeal membrane oxygenation (P = .0001), lack of oral feeding at discharge (P = .012), use of inotropes (P = .027), and gastrostomy tube placement before hospital discharge (P = .024). The MR imaging brain injury score was also associated with a large diaphragmatic defect size (P = .011). CONCLUSIONS: Most infants with congenital diaphragmatic hernia have at least 1 abnormality identified on MR imaging of the brain performed before discharge. The main predictors of brain injury in this population are a requirement for extracorporeal membrane oxygenation, large diaphragmatic defect size, and lack of oral feeding at discharge.


Subject(s)
Brain Injuries/diagnostic imaging , Hernias, Diaphragmatic, Congenital/diagnostic imaging , Brain Hemorrhage, Traumatic/diagnostic imaging , Diaphragm/abnormalities , Extracorporeal Membrane Oxygenation/adverse effects , Female , Humans , Infant , Infant, Newborn , Infant, Premature , Intracranial Hemorrhages/diagnostic imaging , Intubation, Gastrointestinal/adverse effects , Magnetic Resonance Imaging , Male , Pregnancy , White Matter/diagnostic imaging
2.
J Perinatol ; 32(4): 293-8, 2012 Apr.
Article in English | MEDLINE | ID: mdl-21760588

ABSTRACT

OBJECTIVE: High-risk infant follow-up programs have the potential to act as multipurpose clinics by providing continuity of clinical care, education of health care trainees and facilitating outcome data research. Currently there are no nationally representative data on high-risk infant follow-up practices in the United States. The objective of this study is to collect information about the composition of high-risk infant follow-up programs associated with academic centers in the United States, with respect to their structure, function, funding resources and developmental assessment practices, and to identify the barriers to establishment of such programs. STUDY DESIGN: Staff neonatologists, follow-up program directors and division directors of 170 Neonatal Intensive Care Units (NICU) associated with pediatric residency programs were invited to participate in an anonymous online survey from October 2009 to January 2010. RESULT: The overall response rate was 84%. Ninety three percent of the respondents have a follow-up program associated with their NICU. Birth weight, gestational age and critical illness in the NICU were the major criteria for follow-up care. Management of nutrition and neurodevelopmental assessments was the most common service provided. Over 70% have health care trainees in the clinic. About 75% of the respondents have the neurodevelopmental outcome data available. Most of the respondents reported multiple funding sources. Lack of personnel and funding were the most common causes for not having a follow-up program. CONCLUSION: High-risk infant follow-up programs associated with academic centers in the United States are functioning as multidisciplinary programs providing clinical care, trainee education and facilitating outcomes research.


Subject(s)
Academic Medical Centers/organization & administration , Aftercare/organization & administration , Continuity of Patient Care/organization & administration , Health Services Research/organization & administration , Infant, Premature, Diseases/therapy , Intensive Care Units, Neonatal/organization & administration , Birth Weight , Capital Financing , Cooperative Behavior , Fellowships and Scholarships , Follow-Up Studies , Gestational Age , Health Services Accessibility/organization & administration , Humans , Infant, Newborn , Interdisciplinary Communication , Internship and Residency , Neonatology/education , Ohio , Patient Care Team/organization & administration , Pediatrics/education , Treatment Outcome
3.
FEBS Lett ; 291(2): 336-40, 1991 Oct 21.
Article in English | MEDLINE | ID: mdl-1936284

ABSTRACT

Mastoparan, which has been shown to active G proteins, inhibits the ADP-ribosylation of 20 kDa human platelet membrane proteins catalyzed by Clostridium botulinum exoenzyme C3 half-maximally and maximally (90%) at 20 and 100 microM concentrations, respectively. Inhibition of ADP-ribosylation was enhanced by GTP-gamma S. Mastoparan increased GTP hydrolysis by porcine brain rho protein and stimulated GTP binding in a concentration dependent manner. The data suggest that mastoparan not only interacts with heterotrimeric G proteins but also with low molecular mass GTP-binding proteins of the rho/rac family.


Subject(s)
Botulinum Toxins , GTP-Binding Proteins/physiology , Membrane Proteins/physiology , Wasp Venoms/pharmacology , ADP Ribose Transferases/antagonists & inhibitors , Adenosine Diphosphate Ribose/metabolism , Animals , Clostridium botulinum/enzymology , GTP-Binding Proteins/chemistry , GTP-Binding Proteins/drug effects , Humans , Intercellular Signaling Peptides and Proteins , Membrane Proteins/chemistry , Molecular Weight , Peptides , Protein Binding , Swine , Wasp Venoms/chemistry , rac GTP-Binding Proteins , rhoB GTP-Binding Protein
5.
Drug Chem Toxicol ; 4(2): 133--46, 1981.
Article in English | MEDLINE | ID: mdl-7198574

ABSTRACT

6-Mercaptopurine monohydrate was injected sc at 2 mg base/kg/day from 2 to 22 days of age to four litters of rat pups (four females, four males per litter). Control neonates were injected sc with basic saline (pH 8). Daily observations for signs of toxicity were made during the treatment period and once weekly thereafter until the rats were 6 months of age. The pups were weighed at 2, 12, 23, 34, 100, and 480 days of age. Fertility was tested at 3 to 6 months of age. From 6 months of age on, the rats were examined for tumors at 3-month intervals until the experiment was terminated at 16 months of age. A reduction in body weight of treated rats began between 34 and 100 days of age and became more pronounced by 16 months of age. Fertility was similar in treated and control groups and there were no detectable tumors in either group. The major finding in treated rats was a delayed onset of hind leg paresis that was first detected at 12 months of age. Light microscopic examination of tissues taken from the hind quarters of these rats at 16 months of age revealed a severe atrophic degeneration with fatty infiltration of sublumbar and thigh muscles.


Subject(s)
Mercaptopurine/toxicity , Muscular Atrophy/chemically induced , Animals , Animals, Newborn , Body Weight/drug effects , Female , Fertility/drug effects , Hindlimb , Male , Muscles/pathology , Paralysis/chemically induced , Rats , Rats, Inbred Strains
6.
Crit Care Med ; 4(5): 223-9, 1976.
Article in English | MEDLINE | ID: mdl-975846

ABSTRACT

The application of a medical mass spectrometer for the monitoring of respired gases in the respiratory intensive care unit of a community hospital is reviewed. This monitoring system is routinely used with intubated patients for periodic monitoring of end-tidal CO2 tensions (PETCO2), FIO2, and PETO2 dead space to tidal volume ratios, and the determination of AaDO2; the value of these measurements is discussed. It is especially useful for continuous monitoring at critical points in the patient's course such as weaning from the ventilator, determining optimal ventilator settings, monitoring, unstable nonintubated patients, and in better defining the pathophysiological disturbances impeding patient progress, examples of which are presented. Preliminary observations suggest it may also provide a simple technique for determining optimal expiratory retard settings. The initial cost of such a system is justified by the benefit to the patient, i.e., reduction in the frequency of nonessential arterial blood gas determinations, shortened weaning period, and early detection of potentially dangerous trends. Technical problems encountered with this system and potential future uses are also discussed.


Subject(s)
Carbon Dioxide , Mass Spectrometry , Monitoring, Physiologic , Oxygen , Respiratory Care Units , California , Humans , Pulmonary Ventilation , Respiration, Artificial , Respiratory Insufficiency/diagnosis , Ventilation-Perfusion Ratio
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