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Biomedical subjects

F Pohlandt

Publications and source records attributed to F Pohlandt.

133 records · Page 8Linked to original sources

The protein requirement of preterm infants.

The daily fetal protein accretion rate (g/kg b.w.) was calculated from the daily fetal weight gain and the protein content of the fetus. Taking the net protein utilization of 80% in preterm infants (Snyderman et al., 1969) we calculated the protein requirement of preterm infants from the fetal protein accretion rate to be at a maximum of 2.7 g/kg b.w. day for the fetus growing on the 50th weight centile during the 30th to 31st postconceptional week. The more preterm infant has lower requirements.

Dietary Proteins↗

[Central venous air embolism in an artificially respirated premature infant with respiratory distress syndrome].

We report a 935 g 27 weeks gestational age male infant born to a 30 year old mother on chronic intermittent hemodialysis for three years prior to the pregnancy. Immediately after birth the infant presented with severe respiratory distress requiring mechanical ventilation. Chest x-ray showed severe hyaline membrane disease with interstitial emphysema. The infant developed a left tension pneumothorax and systemic air embolism of the right heart, the inferior and superior vena cava and the hepatic vein, from which it subsequently died about 12 h later.

Embolism, Air↗

[Olivo-ponto-cerebral hypoplasia--case report of a neurodegenerative disease manifesting at birth with a fatal outcome].

We report on a boy with pontocerebellar hypoplasia Type II according to the classification of Barth. The clinical signs were noted at birth and consisted of muscular hypertonus, central hypopnoe requiring artificial ventilation, chorea, hyperthermia above 40 degrees C and myoclonic seizures resistant to all therapeutic modalities. At birth, the boy was noted to have macrocephaly, but was microcephalic by 3 months of age. He failed to develop any mental or motor facilities. After cessation of all therapy the child died at the age of 3 1/2 months. Postmortem examination of the brain revealed loss of neurons and gliosis affecting the olivo-ponto-cerebellar system, signs characteristic of PCH.

Child Development↗

[Necrotizing enterocolitis: a 12-year retrospective study].

UNLABELLED: Necrotizing enterocolitis (NEC) is the most relevant intestinal acquired complication during the neonatal period. Due to the improvements in perinatal medicine during the last decade, we wanted to work out possible differences in the incidence, diagnosis and clinical courses of NEC during a 12 years period. PATIENTS AND METHODS: All premature or term newborns were eligible for the study, if a necrotizing enterocolitis > or = stage 2a according to Bell was diagnosed between January 1980-December 1991. RESULTS: During the study period, 90 preterm or term newborns were treated for necrotizing enterocolitis, 19 infants were admitted to our hospital for therapy of established NEC from other hospitals. Forty-five infants had a birthweight of < or = 1500 g. During the years 1987-1991 there was an increase in the incidence (4-12/year, median 9/year, compared to 0-6, median 3/year during the period 1980-1986). This was paralleled by an increase in very low birthweight infants admitted to the NICU (1980-1986: 35-45/year, 1987-1991: 83-108/year). Prominent clinical signs: abdominal distension (85 infants), increased gastric residuals (72), bright blood from rectum (56). Median time of manifestation in infants < or = 30 weeks was 17 days, for infants of 31-34 weeks 8 days and for infants of > or = 35 weeks of gestation 4 days. Eleven infants were fed parenterally exclusively before NEC, 12 infants received exclusively breast milk, 67 formula. Surgical treatment was indicated in 51 infants (indication: intestinal perforation or peritonitis diagnosed by abdominal paracentesis). Seventy-one infants survived, in 17 infants who died, NEC or secondary disorders were the main cause. CONCLUSION: With increasing numbers of very preterm infants, the relevance of NEC becomes more and more important. Concepts of prevention and early diagnosis further have to be worked out.

Birth Weight↗

[Emergency therapy of neonatal hyperammonemia with high dosage glucose].

In severe neonatal hyperammonemia, therapy must be started immediately to prevent irreversible CNS damage. Endogenous ammonia production can be quickly reduced if an anabolic condition is induced by means of high-dose glucose infusion. We applied this treatment to four newborn infants with hyperammonemia, this being a symptom of an inborn error of metabolism. The dangerous metabolic dysfunction was brought under control without dialysis within 24-48 hours in all four patients.

Ammonia↗