SMA Flow Patterns in Neonatal Transfusion (SPARTAN)

University of Calgary

Status: Completed

Conditions: Necrotizing Enterocolitis

Treatments: Other: Observational Study

Study type: Observational

Funder types: Other

Identifiers

NCT02347475

14-0312

Details and patient eligibility

About

This study aims to measure the changes induced by packed red blood cell (PRBC) transfusion in the superior mesenteric artery (SMA) flow velocity and intestinal oxygenation indices in premature neonates. These changes will be measured in relation to feeding, before and after a blood transfusion. Overall reduction of intestinal perfusion is a risk factor for necrotizing enterocolitis (NEC) - a condition with significant mortality and long term morbidity. Identifying specific patterns of flow velocity and tissue oxygenation changes will allow for planning, studying and implementing risk avoidance and minimization strategies.

Full description

Hypothesis: In preterm neonates the anticipated physiologic post-prandial increase in each SMA flow and intestinal perfusion is blunted post transfusion. This is worse in SGA infants and/or in the presence of a PDA.

Questions: 1) Does PRBC transfusion alter postprandial SMA flow increases and intestinal oxygenation indices in preterm infants receiving enteral feeds? 2) Is there a difference in postprandial SMA flow and intestinal perfusion changes in recently transfused SGA infants compared to AGA infants, and in those with and without a PDA? Primary Outcome: Post-prandial SMA flows changes before and after PRBC transfusion.

Secondary outcomes: Pre-post prandial changes in near-infrared spectroscopy (NIRS)-measured intestinal oxygenation parameters before and after PRBC transfusion.

Enrollment: 7 patients

Sex: All

Ages: 1 day to 6 months old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Prematurity (<34 completed weeks of gestation at birth)
• Need for PRBC transfusion
• Feeding at least 30ml/kg/day at the time of transfusion

Exclusion criteria

• Neonates previously diagnosed with gastrointestinal problems such as NEC, intestinal perforation or atresia.
• Infants receiving continuous feeds or less than 30ml/kg/day
• Major congenital or chromosomal abnormalities or infants unlikely to survive
• Skin disruption precluding application of sensors