Pulmonary and systemic arterial pressure in hyaline membrane disease.
Open Access
- 1 April 1992
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 67 (4 Spec No) , 366-373
- https://doi.org/10.1136/adc.67.4_spec_no.366
Abstract
Systolic pulmonary arterial pressure was determined serially over the first 10 days of life in 33 babies with hyaline membrane disease by measuring the peak velocity of pansystolic tricuspid valve regurgitation, using Doppler ultrasound, and applying the Bernoulli equation. Results are presented in age groups 0-12, 13-36, 37-72, and 73-96 hours respectively. The incidence of tricuspid valve regurgitation was 92, 97, 80, and 64% (falling to 35% by day 10) compared with 53, 50, 31, and 0% in 17 healthy premature infants. In comparing healthy babies with those with hyaline membrane disease, no allowance was made for right atrial pressure. The derived 'right ventricle to right atrial (RV-RA) pressure difference', was expressed as a ratio of systemic arterial (systolic) pressure. Over the first three days, this ratio fell much faster in the healthy babies. Values were 0.78:1, 0.77:1, and 0.72:1 in babies with hyaline membrane disease and 0.87:1, 0.53:1, and 0.44:1 in healthy babies. Ductal patency was prolonged in babies with hyaline membrane disease (75% on day 4 compared with 6% in healthy babies). The incidence of bidirectional ductal flow, indicating balanced pulmonary and systemic arterial pressures, was 79, 53, 30, and 20%, and in healthy babies was 41% at 0-12 hours and zero thereafter. Pulmonary arterial pressure was then calculated by adding a right atrial pressure estimate of 5 mm Hg to the RV-RA difference when the babies were ventilated. Babies of lower gestation had lower values. The pulmonary: systemic arterial pressure ratio showed considerable temporal variability, but fell with age and was raised by high mean airway pressure and pneumothorax (through a reduction in systemic pressure), and less noticeably by carbon dioxide tension. It did not correlate significantly with other indices of disease severity. Hyaline membrane disease is associated with delayed postnatal circulatory adaptation characterized by pulmonary hypertension, systemic hypotension, and prolonged ductal patency.Keywords
This publication has 27 references indexed in Scilit:
- Central venous pressure in the ventilated neonate.Archives of Disease in Childhood, 1992
- Predicting death from initial disease severity in very low birthweight infants: a method for comparing the performance of neonatal units.BMJ, 1990
- Doppler flow characteristics in the assessment of pulmonary artery pressure in ductus arteriosus.Heart, 1989
- Noninvasive determination of pulmonary arterial systolic pressure by continuous wave DopplerInternational Journal of Cardiology, 1987
- Effect of mechanical ventilation and volume loading on left ventricular performance in premature infants with respiratory distress syndromeCritical Care Medicine, 1986
- Noninvasive estimation of right ventricular systolic pressure by Doppler ultrasound in patients with tricuspid regurgitation.Circulation, 1984
- Effect of tolazoline in severe hyaline membrane disease.Archives of Disease in Childhood, 1979
- Physiologic factors affecting pulmonary artery pressure in infants with persistent pulmonary hypertensionThe Journal of Pediatrics, 1978
- Disturbances of the transitional circulation: Spectrum of pulmonary hypertension and myocardial dysfunctionThe Journal of Pediatrics, 1976
- Circulatory Studies in Clinical Hyaline Membrane DiseaseNeonatology, 1972