Cargando…

FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial

BACKGROUND: Necrotising Enterocolitis (NEC) is a devastating neonatal disease. A temporal association between red cell transfusion and NEC has been recognized and there have been concerns about the effects of feeding during transfusion. We aimed to assess the effect of different enteral feeding regi...

Descripción completa

Detalles Bibliográficos
Autores principales: Schindler, Tim, Yeo, Kee Thai, Bolisetty, Srinivas, Michalowski, Joanna, Tan, Alvin Hock Kuan, Lui, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359615/
https://www.ncbi.nlm.nih.gov/pubmed/32664953
http://dx.doi.org/10.1186/s12887-020-02233-3
_version_ 1783559085210206208
author Schindler, Tim
Yeo, Kee Thai
Bolisetty, Srinivas
Michalowski, Joanna
Tan, Alvin Hock Kuan
Lui, Kei
author_facet Schindler, Tim
Yeo, Kee Thai
Bolisetty, Srinivas
Michalowski, Joanna
Tan, Alvin Hock Kuan
Lui, Kei
author_sort Schindler, Tim
collection PubMed
description BACKGROUND: Necrotising Enterocolitis (NEC) is a devastating neonatal disease. A temporal association between red cell transfusion and NEC has been recognized and there have been concerns about the effects of feeding during transfusion. We aimed to assess the effect of different enteral feeding regimens on splanchnic oxygenation in preterm infants receiving red cell transfusions. METHODS: This was an open, multi-arm, parallel-group, randomised controlled trial conducted in a single centre in Australia. We compared three different enteral feeding regimes during a single red cell transfusion in preterm infants < 35 weeks gestational age at birth. Infants were randomised to either: (1) Withholding enteral feeds for 12 h from the start of transfusion or; (2) Continuing enteral feeds or; (3) Restriction of enteral feed volume to 120 ml/kg/day (maximum 20 kcal/30 ml) for 12 h. The primary outcome was mean splanchnic-cerebral oxygenation ratio (SCOR) and mean splanchnic fractional oxygen extraction (FOE) before (1 h prior), during (1 h into transfusion) and after (end of transfusion; 12 and 24 h post) transfusion. RESULTS: There were 60 transfusion episodes (20 transfusion episodes in each group) included in the analysis. 41 infants with a median gestational age at birth of 27 weeks (range 23–32 weeks) were enrolled. The median postnatal age was 43 days (range 19–94 days) and the median pre-transfusion haematocrit was 0.27 (range 0.22–0.32). All three groups were similar at baseline. There were no differences in mean SCOR and mean splanchnic FOE at any of the pre-specified time points. There were also no differences in clinical outcomes. There were no episodes of NEC in any infant. Across all groups the mean SCOR increased from the start to the end of each transfusion (0.97 [CI95% 0.96–0.98] vs 1.00 [CI95% 0.99–1.01]; p = 0.04) and the mean FOE decreased from the start to the end of each transfusion (0.22 [CI95% 0.21–0.23] vs 0.17 [CI95% 0.16–0.18]; p < 0.001). CONCLUSIONS: There were no differences in splanchnic oxygenation when enteral feeds were either withheld, continued or restricted during a transfusion. However, the successful conduct of this study supports the feasibility of a large trial powered to assess clinical outcomes. TRIAL REGISTRATION: ANZCTR, ACTRN12616000160437. Registered 10 February 2016, https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=370069
format Online
Article
Text
id pubmed-7359615
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-73596152020-07-17 FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial Schindler, Tim Yeo, Kee Thai Bolisetty, Srinivas Michalowski, Joanna Tan, Alvin Hock Kuan Lui, Kei BMC Pediatr Research Article BACKGROUND: Necrotising Enterocolitis (NEC) is a devastating neonatal disease. A temporal association between red cell transfusion and NEC has been recognized and there have been concerns about the effects of feeding during transfusion. We aimed to assess the effect of different enteral feeding regimens on splanchnic oxygenation in preterm infants receiving red cell transfusions. METHODS: This was an open, multi-arm, parallel-group, randomised controlled trial conducted in a single centre in Australia. We compared three different enteral feeding regimes during a single red cell transfusion in preterm infants < 35 weeks gestational age at birth. Infants were randomised to either: (1) Withholding enteral feeds for 12 h from the start of transfusion or; (2) Continuing enteral feeds or; (3) Restriction of enteral feed volume to 120 ml/kg/day (maximum 20 kcal/30 ml) for 12 h. The primary outcome was mean splanchnic-cerebral oxygenation ratio (SCOR) and mean splanchnic fractional oxygen extraction (FOE) before (1 h prior), during (1 h into transfusion) and after (end of transfusion; 12 and 24 h post) transfusion. RESULTS: There were 60 transfusion episodes (20 transfusion episodes in each group) included in the analysis. 41 infants with a median gestational age at birth of 27 weeks (range 23–32 weeks) were enrolled. The median postnatal age was 43 days (range 19–94 days) and the median pre-transfusion haematocrit was 0.27 (range 0.22–0.32). All three groups were similar at baseline. There were no differences in mean SCOR and mean splanchnic FOE at any of the pre-specified time points. There were also no differences in clinical outcomes. There were no episodes of NEC in any infant. Across all groups the mean SCOR increased from the start to the end of each transfusion (0.97 [CI95% 0.96–0.98] vs 1.00 [CI95% 0.99–1.01]; p = 0.04) and the mean FOE decreased from the start to the end of each transfusion (0.22 [CI95% 0.21–0.23] vs 0.17 [CI95% 0.16–0.18]; p < 0.001). CONCLUSIONS: There were no differences in splanchnic oxygenation when enteral feeds were either withheld, continued or restricted during a transfusion. However, the successful conduct of this study supports the feasibility of a large trial powered to assess clinical outcomes. TRIAL REGISTRATION: ANZCTR, ACTRN12616000160437. Registered 10 February 2016, https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=370069 BioMed Central 2020-07-14 /pmc/articles/PMC7359615/ /pubmed/32664953 http://dx.doi.org/10.1186/s12887-020-02233-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Schindler, Tim
Yeo, Kee Thai
Bolisetty, Srinivas
Michalowski, Joanna
Tan, Alvin Hock Kuan
Lui, Kei
FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial
title FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial
title_full FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial
title_fullStr FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial
title_full_unstemmed FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial
title_short FEEding DURing red cell transfusion (FEEDUR RCT): a multi-arm randomised controlled trial
title_sort feeding during red cell transfusion (feedur rct): a multi-arm randomised controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359615/
https://www.ncbi.nlm.nih.gov/pubmed/32664953
http://dx.doi.org/10.1186/s12887-020-02233-3
work_keys_str_mv AT schindlertim feedingduringredcelltransfusionfeedurrctamultiarmrandomisedcontrolledtrial
AT yeokeethai feedingduringredcelltransfusionfeedurrctamultiarmrandomisedcontrolledtrial
AT bolisettysrinivas feedingduringredcelltransfusionfeedurrctamultiarmrandomisedcontrolledtrial
AT michalowskijoanna feedingduringredcelltransfusionfeedurrctamultiarmrandomisedcontrolledtrial
AT tanalvinhockkuan feedingduringredcelltransfusionfeedurrctamultiarmrandomisedcontrolledtrial
AT luikei feedingduringredcelltransfusionfeedurrctamultiarmrandomisedcontrolledtrial