The Impact of Different Feeding Strategies During Packed Red Cell Transfusion on Intestinal Oxygenation

Sponsor
Marmara University (Other)
Overall Status
Unknown status
CT.gov ID
NCT02733718
Collaborator
(none)
20
1
3
22
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Study Details

Study Description

Brief Summary

This study aims to compare the differences between three different feeding regimens on intestinal oxygenation during packed red blood cell (PRBC) transfusion in premature babies.

Condition or Disease Intervention/Treatment Phase
  • Device: NIRS (near-infrared spectroscopy)
N/A

Detailed Description

Necrotizing enterocolitis is an important cause of mortality and morbidity in neonates. Especially neonates, who are smaller than 32 weeks of gestational, need transfusions during their hospital stay. Recent evidences suggest a relation between antecedent PRBC transfusions and an increase in necrotizing enterocolitis (NEC). It has been reported that transfusion related NEC (TR-NEC) tend to occur immediately and up to 48 hours post-transfusion. Although the underlying mechanism of this relationship is still overinvestigation, altered oxygenation of the mesenteric vasculature during PRBC transfusion has been hypothesized to contribute to NEC development. But pathophysiology of this has not been cleared, yet. Nowadays, due to the increased risk of NEC during PRBC transfusion, different nutrition protocols are implemented in different units. These protocols contain permanent discontinuation, reducement or continuation of nutrition during the transfusion. As a result, there is still no evidence -based practice recommendation in this regard.

"Restricted Transfusion Guidelines" will be used for the decision of transfusion in premature infants. Patients will be divided into three different groups, according to their feeding regimen during transfusion.

Group 1: No enteral feeding before (two hours), during (3 hours) and after (two hours) red blood cell transfusion.

Group 2: Enteral feeding is reduced by %50 before, during and after the red blood cell transfusion.

Group 3: The same feeding volume will be continued without decreasing or stopping.

Groups will be determined with randomization. It was targeted to be at least twenty infants in each group. In all patients, mesenteric oxygenation will be compared before-during and after blood transfusion. Mesenteric oxygenation will be measured with Near Infrared Spectroscopy (NIRS), that is a non-invasive NIRS conducted technology. Cerebral oxygenation and peripheral oxygen saturations will be measured at the same timeline.

The investigators primary aim is to show the best method of feeding during transfusion that causes less feeding intolerance and NEC. The secondary outcomes will be the risk factors associated with feeding intolerance and NEC during PRBC transfusion, in premature babies.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
The Impact of Different Feeding Strategies During Packed Red Cell Transfusion on Intestinal Oxygenation
Study Start Date :
Nov 1, 2015
Anticipated Primary Completion Date :
Jun 1, 2017
Anticipated Study Completion Date :
Sep 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Other: Group 1: no enteral feeding

intervention: NIRS (near-infrared spectroscopy)

Device: NIRS (near-infrared spectroscopy)
mesenteric oxygenisation measurement

Other: Group 2: Feeding is reduced by %50

intervention: NIRS (near-infrared spectroscopy)

Device: NIRS (near-infrared spectroscopy)
mesenteric oxygenisation measurement

Other: Group 3: Feeding will be continued

intervention: NIRS (near-infrared spectroscopy)

Device: NIRS (near-infrared spectroscopy)
mesenteric oxygenisation measurement

Outcome Measures

Primary Outcome Measures

  1. mesenteric oxygenisation (number of participants that has low mesenteric oxygenisation after transfusion) [48 hours]

    number of participants that has low mesenteric oxygenisation after transfusion

Secondary Outcome Measures

  1. Feeding intolerance (number of participants that has feeding intolerance after transfusion) [starting with transfusion until discharge, assessed up to 12 weeks]

    number of participants that has feeding intolerance after transfusion

  2. NEC (number of participants that has occurred transfusion related NEC) [starting with transfusion until discharge, assessed up to 12 weeks]

    number of participants that has occurred transfusion related NEC

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 4 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Prematurity (<32 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

  • Intraventricular hemorrhage >Grade 3

  • Hemodynamically significant patent ductus arteriosus

  • Infants requiring vasopressor support

  • Skin disruption precluding application of sensors

Contacts and Locations

Locations

Site City State Country Postal Code
1 Marmara University School of Medicine Istanbul Turkey

Sponsors and Collaborators

  • Marmara University

Investigators

  • Study Director: Hülya Selva Bilgen, MD, professor

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marmara University
ClinicalTrials.gov Identifier:
NCT02733718
Other Study ID Numbers:
  • MR-01022016
First Posted:
Apr 11, 2016
Last Update Posted:
Apr 11, 2016
Last Verified:
Apr 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Marmara University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 11, 2016