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  • 1
    ISSN: 1432-1076
    Keywords: Mechanical ventilation ; Preterm infant ; Extra-alveolar air leakage ; Randomised trial
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two different ventilation techniques were compared in a seven-centre, randomised trial with 181 preterm infants up to and including 32 completed weeks gestational age, who needed mechanical ventilation because of lung disease of any type. Technique A used a constant rate (60 cycles/min), inspiratory time (IT) (0.33s) and inspiratory: expiratory ratio (I∶E) (1∶2). The tidal and minute volume was only changed by varying peak inspiratory pressure until weaning via continuous positive airway pressure. Technique B used a lower rate (30 cycles/min) with longer IT (1.0s). The I∶E ratio could be changed from 1∶1 to 2∶1 in case of hypoxaemia. Chest X-rays taken at fixed intervals were evaluated by a paediatric radiologist and a neonatologist unaware of the type of ventilation used in the patients. A reduction of at least 20% in extra-alveolar air leakage (EAL) or death prior to EAl was supposed in infants ventilated by method A. A sequential design was used to test this hypothesis. The null hypothesis was rejected (P=0.05) when the 22nd untied pair was completed. The largest reduction in EAL (−55%) was observed in the subgroup 31–32 weeks of gestation and none in the most immature group (〈28 weeks). We conclude that in preterm infants requiring mechanical ventilation for any reason of lung insufficiency, ventilation at 60 cycles/min and short IT (0.33s) significantly reduces EAL or prior death compared with 30 cycles/min and a longer IT of 1s. We speculate that a further increase in rate and reduction of IT would also lower the risk of barotrauma in the most immature and susceptible infants.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 136 (1981), S. 249-262 
    ISSN: 1432-1076
    Keywords: Trisomy ; Autosomal/partial/chromosome no. 12 ; Short arm (p)-inherited ; Familial translocation ; Balanced/unbalanced ; Dysmorphic syndrome ; Malformation syndrome ; Retardation syndrome ; Segregation pattern ; Risk figures ; Genetic counselling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This is the report of two independent families in which a balanced maternal translocation led to trisomy 12p in one of each their offspring. Evaluation of 21 further case reports indicates that this is a phenotypically well defined syndrome which leads to severe developmental retardation. It can be recognized by a characteristic combination of craniofacial anomalies which are summarized in a phantom picture. The gene sequences which produce the typical features in the trisomic state must be localized distally to band 12p 12, which is the breakpoint in the partial trisomies. The specific craniofacial anomalies are not visibly modified by the length of the trisomic segment or additional small monosomies or trisomies of recipient chromosomes. However, the frequency and severity of organ malformations and the resulting probability of survival seem to decrease with increasing degrees of chromosomal imbalance. A cytogenetic classification of the 21 inherited translocations and a segregation analysis from the pedigree data was performed. For the different types of translocations the calculated risk figures are given.
    Type of Medium: Electronic Resource
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