ABSTRACT
AIM: To show the effects of a single course of antenatal betamethasone on cardiac measurements and systolic functions in premature newborn infants. METHODS: Seventy six newborn infants with a gestational age of 25-33 weeks were included in the study. They were first classified according to their gestational age: 25-29 weeks (n = 28) and 30-33 weeks (n = 48). They were then reclassified as betamethasone positive (mother received one course of betamethasone) or betamethasone negative (mother did not receive any antenatal glucocorticoid treatment). Cross sectional M mode echocardiographic scans were performed during the first three postnatal days and at the end of the first and third weeks. Left interventricular septum (IVS), left ventricular posterior wall (LVPW), left ventricular end diastolic (LVED), and left ventricular end systolic (LVES) dimensions, aortic root (AO), and left atrial diameters (LAs) were measured. The IVS to LVPW ratio was calculated to identify asymmetrical septal hypertrophy. RESULTS: In neither group was any statistically significant difference noted in IVS, LVED, LVES, LVPW, LA, and AO measurements during the three cardiac ultrasonography scans. Systolic function, as assessed by fractional shortening, was not significantly different in infants who received betamethasone antenatally, in either age group. There was no difference in the IVS/LVPW ratios between those who received antenatal steroid and those who did not for the 25-29 week and 30-33 week groups during these three consecutive scans. CONCLUSION: One course of antenatal betamethasone did not affect the cardiac wall thicknesses and systolic function in premature infants.
Subject(s)
Betamethasone/pharmacology , Glucocorticoids/pharmacology , Heart/drug effects , Prenatal Care/methods , Prenatal Exposure Delayed Effects , Aging/physiology , Anti-Inflammatory Agents/pharmacology , Female , Gestational Age , Heart/anatomy & histology , Heart Septum/anatomy & histology , Heart Septum/diagnostic imaging , Heart Septum/drug effects , Humans , Infant, Newborn , Infant, Premature , Pregnancy , Statistics, Nonparametric , Systole/drug effects , UltrasonographyABSTRACT
BACKGROUND: Transient tachypnea of the newborn (TTN) is usually a benign self-limiting respiratory disorder in the immediate neonatal period. The lipophilic surfactant-associated protein B (SP-B) was demonstrated to be the most relevant structural component of the surfactant system for immediate postnatal pulmonary adaptation. We hypothesized genetic variations of surfactant protein B (heterozygous 121 ins 2 mutation er intron 4 polymorphisms) to be related to TTN. PATIENTS AND METHOD: We screened genomic DNA of 83 healthy term neonates (gestational age: 39 (37 - 41) completed weeks [median and range]; birth weight: 3325 +/- 541 grams [mean +/- SD]) and 75 infants presenting with TTN (gestational age: 38 (37 - 41) completed wecks [median and range]; birth weight: 3091 +/- 435 grams [mean +/- SD]) by means of PCR-amplification, fragment length and sequence analysis. TTN was diagnosed an the basis of the clinical signs with respiratory rate > 60 breaths/minute, fraction of inspired oxygen > 0.21, and characteristic radiographic findings within less than 24 hours after birth. Newborns with any infection, pulmonary or cardiac congenital malformations, postnatal asphyxia and infants born to diabetic mothers were excluded. RESULTS: In TTN-group the frequency of male infants (68.4 % versus 44.6 %, p < 0.05) and caeserian section were significantly higher (68.4 % versus 30.1 %, p < 0.05). We did not find any statistical difference in frequency of intron 4 variations between controls and TTN-group (8.4 % versus 10.7 %). None of the infants were heterozygous for the 121ins2 SP-B mutation. CONCLUSIONS: WC conclude polymorphisms of intron 4 and heterozygous 121 ins 2 mutation not to associated with TTN.
Subject(s)
Polymorphism, Genetic , Pulmonary Surfactant-Associated Protein B/genetics , Respiration Disorders/genetics , Age Factors , Birth Weight , Cesarean Section , Female , Genetic Variation , Gestational Age , Heterozygote , Humans , Infant, Newborn , Introns/genetics , Male , Mutation , Polymerase Chain Reaction , Respiration Disorders/diagnosis , Respiration Disorders/etiology , Respiratory Distress Syndrome, Newborn/genetics , Risk Factors , Sex Factors , Time FactorsABSTRACT
Intraventricular hemorrhage (IVH) originating from germinal matrix is the major brain injury of the premature. We studied IVH incidence and risk factors which are implied in this pathology in newborns, hospitalized in the neonatal intensive care unit (NICU) of istanbul University Cerrahpasa Faculty of Medicine. Ninety-seven premature newborns with a birth weight of less than 2500 g were examined systematically with cranial ultrasonography (CU). Mean birthweight was 1540 +/- 430 g (720-2450) and gestational age 31.6 +/- 2.4 weeks (26-37). IVH was diagnosed in 40 cases (41%). The significant risk factors are prematurity (gestational age < 33 weeks), artificial ventilation and infusion of fresh frozen plasma.
Subject(s)
Cerebral Hemorrhage/etiology , Cerebral Ventricles , Infant, Premature, Diseases/etiology , Adult , Birth Weight , Blood Component Transfusion/adverse effects , Cerebral Hemorrhage/diagnostic imaging , Gestational Age , Humans , Incidence , Infant, Newborn , Infant, Premature, Diseases/diagnostic imaging , Plasma , Respiration, Artificial/adverse effects , Retrospective Studies , Risk Factors , Sensitivity and Specificity , Severity of Illness Index , Ultrasonography, Doppler, TranscranialABSTRACT
Meckel-Gruber syndrome is a congenital disorder characterized by occipital encephalocele, polydactyly and polycystic kidneys. This rare syndrome has been reported in the literature as incompatible with life. We present the case of a newborn afflicted with the clinical triad of Meckel-Gruber syndrome. Appropriate treatment instituted in our case led to a good early outcome.