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Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study

Necrotising enterocolitis (NEC) is a potentially serious illness with significant mortality and morbidity in preterm infants. Previous studies have reported association of volume and colour (bile and blood stained) of gastric residuals (GR) with NEC. We aimed to study this association in our cohort...

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Autores principales: Purohit, Gajanan, Mehkarkar, Puja, Athalye-Jape, Gayatri, Nathan, Elizabeth, Patole, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285712/
https://www.ncbi.nlm.nih.gov/pubmed/34272983
http://dx.doi.org/10.1007/s00431-021-04193-x
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author Purohit, Gajanan
Mehkarkar, Puja
Athalye-Jape, Gayatri
Nathan, Elizabeth
Patole, Sanjay
author_facet Purohit, Gajanan
Mehkarkar, Puja
Athalye-Jape, Gayatri
Nathan, Elizabeth
Patole, Sanjay
author_sort Purohit, Gajanan
collection PubMed
description Necrotising enterocolitis (NEC) is a potentially serious illness with significant mortality and morbidity in preterm infants. Previous studies have reported association of volume and colour (bile and blood stained) of gastric residuals (GR) with NEC. We aimed to study this association in our cohort of extremely preterm (EP) infants. In a case–control study using retrospective data (January 2006–December 2011), EP (gestation < 28 weeks) infants with confirmed NEC ≥ stage II (cases) were compared with infants without NEC (controls) matched for birth weight (BW) and gestational age (GA). Forty cases of NEC ≥ stage II diagnosed at a median (IQR) age of 16.5 days (10.3–23) were compared with 40 controls matched for gestation (± 3 days) and birth weight (± 680 g). Median maximum GR volume (GRV) from birth to the day of occurrence of NEC was significantly higher in cases vs. controls (5.9 vs.3.7 ml; p < 0.001). Increased maximum GRV was associated with NEC ≥ Stage II in adjusted analysis (aOR 1.36, 95%CI 1.06–1.75, p = 0.017). There was no significant difference in GRV between cases and controls throughout the clinical course, including 72, 48 and 24 h before the onset of NEC. However, green (65.0% vs. 27.5%, p = 0.001) and haemorrhagic GRs (45.0% vs. 27.5%, p = 0.092) were higher 24 h before the diagnosis of NEC. Conclusion: GRV was not associated with NEC ≥ stage II. However, green and haemorrhagic GRs were significantly higher 24 h before the diagnosis of the illness. Adequately powered prospective studies are needed to confirm the significance of our findings.
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spelling pubmed-82857122021-07-19 Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study Purohit, Gajanan Mehkarkar, Puja Athalye-Jape, Gayatri Nathan, Elizabeth Patole, Sanjay Eur J Pediatr Original Article Necrotising enterocolitis (NEC) is a potentially serious illness with significant mortality and morbidity in preterm infants. Previous studies have reported association of volume and colour (bile and blood stained) of gastric residuals (GR) with NEC. We aimed to study this association in our cohort of extremely preterm (EP) infants. In a case–control study using retrospective data (January 2006–December 2011), EP (gestation < 28 weeks) infants with confirmed NEC ≥ stage II (cases) were compared with infants without NEC (controls) matched for birth weight (BW) and gestational age (GA). Forty cases of NEC ≥ stage II diagnosed at a median (IQR) age of 16.5 days (10.3–23) were compared with 40 controls matched for gestation (± 3 days) and birth weight (± 680 g). Median maximum GR volume (GRV) from birth to the day of occurrence of NEC was significantly higher in cases vs. controls (5.9 vs.3.7 ml; p < 0.001). Increased maximum GRV was associated with NEC ≥ Stage II in adjusted analysis (aOR 1.36, 95%CI 1.06–1.75, p = 0.017). There was no significant difference in GRV between cases and controls throughout the clinical course, including 72, 48 and 24 h before the onset of NEC. However, green (65.0% vs. 27.5%, p = 0.001) and haemorrhagic GRs (45.0% vs. 27.5%, p = 0.092) were higher 24 h before the diagnosis of NEC. Conclusion: GRV was not associated with NEC ≥ stage II. However, green and haemorrhagic GRs were significantly higher 24 h before the diagnosis of the illness. Adequately powered prospective studies are needed to confirm the significance of our findings. Springer Berlin Heidelberg 2021-07-17 2022 /pmc/articles/PMC8285712/ /pubmed/34272983 http://dx.doi.org/10.1007/s00431-021-04193-x Text en © Crown 2021, corrected publication 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Purohit, Gajanan
Mehkarkar, Puja
Athalye-Jape, Gayatri
Nathan, Elizabeth
Patole, Sanjay
Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study
title Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study
title_full Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study
title_fullStr Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study
title_full_unstemmed Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study
title_short Association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study
title_sort association of gastric residual volumes with necrotising enterocolitis in extremely preterm infants—a case–control study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285712/
https://www.ncbi.nlm.nih.gov/pubmed/34272983
http://dx.doi.org/10.1007/s00431-021-04193-x
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