Intrauterine growth restriction, visceral blood flow velocity and exocrine pancreatic function

<p>Abstract</p> <p>Background</p> <p>Animal models and observations in human neonates suggest fetal exocrine pancreas vulnerability to reduced maternofetal blood flow. We investigated the relationship between superior mesenteric artery blood flow velocity (sma bfv) and...

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Bibliographic Details
Main Authors: Deenmamode Jean M, Nicholl Richard M, Gamsu Harold R
Format: Article
Language:English
Published: BMC 2008-11-01
Series:BMC Research Notes
Online Access:http://www.biomedcentral.com/1756-0500/1/115
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Summary:<p>Abstract</p> <p>Background</p> <p>Animal models and observations in human neonates suggest fetal exocrine pancreas vulnerability to reduced maternofetal blood flow. We investigated the relationship between superior mesenteric artery blood flow velocity (sma bfv) and exocrine pancreatic function, in a cohort of very low birth weight (VLBW) babies.</p> <p>Group 1: 9 babies < 3rd percentile for birth weight. Antenatally, all had absent or reversed diastolic flow on Doppler ultrasound of the umbilical artery (UA).</p> <p>Group2: 18 babies > 10th percentile for birth weight.</p> <p>Findings</p> <p>All had Doppler ultrasound scan of the superior mesenteric artery (sma), by same operator (RMN), on day 1 of life before commencement of enteral feeding. Stool samples assayed for faecal chymotrypsin and weekly serum samples assayed for amylase and lipase (kinetic colorimetric assay) from days 1 to 14 of life.</p> <p>Growth restricted babies had significantly lower sma bfv values compared with appropriately grown preterm babies. Faecal chymotrypsin levels were also lower but this difference did not achieve statistical significance. Both groups had serum lipase levels detectable in adult concentrations. Serum amylase was undetectable in either group.</p> <p>Conclusion</p> <p>Babies with previous in-utero blood flow redistribution may exhibit altered gut ontogeny with re-setting of mesenteric blood flow velocities and altered exocrine pancreatic function.</p>
ISSN:1756-0500