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Acinar arterial changes with chronic lung disease of prematurity in the surfactant era
Because echocardiographic studies on infants with chronic lung disease (CLD) suggest that pulmonary hypertension (PH) may contribute to its severity, we studied acinar arterial walls in the following surfactant‐era infants: controls (n = 38): 22–41 weeks of gestational age (GA), exposed briefly to o...
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Published in: | Pediatric pulmonology 2003-12, Vol.36 (6), p.482-489 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Because echocardiographic studies on infants with chronic lung disease (CLD) suggest that pulmonary hypertension (PH) may contribute to its severity, we studied acinar arterial walls in the following surfactant‐era infants: controls (n = 38): 22–41 weeks of gestational age (GA), exposed briefly to oxygen and positive pressure ventilation, died within 48 hr of birth; prolonged rupture of fetal membranes (PROM) and persistent pulmonary hypertension (PPHN) (n = 17); and SCORE (integrated area under curve of average daily FiO2 × average daily MAP) groups ( |
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ISSN: | 8755-6863 1099-0496 |
DOI: | 10.1002/ppul.10349 |