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Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals
BACKGROUND: Sparse information regarding plasma iron concentration in neonatal foals and its utility as an inflammatory marker in this population has been published. OBJECTIVES: To determine the physiologic plasma iron concentration in neonatal foals. To assess its utility as an inflammatory marker...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255657/ https://www.ncbi.nlm.nih.gov/pubmed/32297679 http://dx.doi.org/10.1111/jvim.15770 |
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author | Sanmartí, Júlia Armengou, Lara Viu, Judit Alguacil, Eduardo Civit, Sandra Ríos, José Jose‐Cunilleras, Eduard |
author_facet | Sanmartí, Júlia Armengou, Lara Viu, Judit Alguacil, Eduardo Civit, Sandra Ríos, José Jose‐Cunilleras, Eduard |
author_sort | Sanmartí, Júlia |
collection | PubMed |
description | BACKGROUND: Sparse information regarding plasma iron concentration in neonatal foals and its utility as an inflammatory marker in this population has been published. OBJECTIVES: To determine the physiologic plasma iron concentration in neonatal foals. To assess its utility as an inflammatory marker to predict systemic inflammatory response syndrome (SIRS) and as a prognostic marker. ANIMALS: Forty‐seven ill neonatal foals admitted to a referral equine hospital were divided in 2 groups based on the SIRS criteria (24 SIRS and 23 non‐SIRS). Two control groups of 43 hospital and 135 stud farm healthy neonatal foals were also included. METHODS: Observational prospective study. Data were summarized by mean and its 95% confidence interval and absolute frequency and percentage for quantitative andqualitative variables. One‐way ANOVA, ANCOVA (group and age effects) and Dunnett as posthoc analysis were used to compare plasma iron concentration among groups. RESULTS: Neonatal foals with SIRS did not have had any statistically significant different plasma iron concentrations compared to non‐SIRS (P = .56) and stud farm control group (P = .99), 172.8 μg/dL (95% CI; 126.0‐219.6), 193.1 μg/dL (139.1‐247.2), and 181.8 μg/dL (171.3‐192.4), respectively. Plasma iron concentration had a large variability in healthy neonatal foals, and was negatively correlated with age in hospital controls (rho = −0.387) and sick neonatal foals (rho = −0.598) (P < .001). CONCLUSIONS AND CLINICAL IMPORTANCE: Plasma iron was not a useful marker of SIRS in neonatal foals and was not associated with outcome. |
format | Online Article Text |
id | pubmed-7255657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72556572020-06-01 Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals Sanmartí, Júlia Armengou, Lara Viu, Judit Alguacil, Eduardo Civit, Sandra Ríos, José Jose‐Cunilleras, Eduard J Vet Intern Med EQUID BACKGROUND: Sparse information regarding plasma iron concentration in neonatal foals and its utility as an inflammatory marker in this population has been published. OBJECTIVES: To determine the physiologic plasma iron concentration in neonatal foals. To assess its utility as an inflammatory marker to predict systemic inflammatory response syndrome (SIRS) and as a prognostic marker. ANIMALS: Forty‐seven ill neonatal foals admitted to a referral equine hospital were divided in 2 groups based on the SIRS criteria (24 SIRS and 23 non‐SIRS). Two control groups of 43 hospital and 135 stud farm healthy neonatal foals were also included. METHODS: Observational prospective study. Data were summarized by mean and its 95% confidence interval and absolute frequency and percentage for quantitative andqualitative variables. One‐way ANOVA, ANCOVA (group and age effects) and Dunnett as posthoc analysis were used to compare plasma iron concentration among groups. RESULTS: Neonatal foals with SIRS did not have had any statistically significant different plasma iron concentrations compared to non‐SIRS (P = .56) and stud farm control group (P = .99), 172.8 μg/dL (95% CI; 126.0‐219.6), 193.1 μg/dL (139.1‐247.2), and 181.8 μg/dL (171.3‐192.4), respectively. Plasma iron concentration had a large variability in healthy neonatal foals, and was negatively correlated with age in hospital controls (rho = −0.387) and sick neonatal foals (rho = −0.598) (P < .001). CONCLUSIONS AND CLINICAL IMPORTANCE: Plasma iron was not a useful marker of SIRS in neonatal foals and was not associated with outcome. John Wiley & Sons, Inc. 2020-04-16 2020-05 /pmc/articles/PMC7255657/ /pubmed/32297679 http://dx.doi.org/10.1111/jvim.15770 Text en © 2020 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | EQUID Sanmartí, Júlia Armengou, Lara Viu, Judit Alguacil, Eduardo Civit, Sandra Ríos, José Jose‐Cunilleras, Eduard Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals |
title | Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals |
title_full | Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals |
title_fullStr | Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals |
title_full_unstemmed | Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals |
title_short | Plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals |
title_sort | plasma iron concentrations and systemic inflammatory response syndrome in neonatal foals |
topic | EQUID |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255657/ https://www.ncbi.nlm.nih.gov/pubmed/32297679 http://dx.doi.org/10.1111/jvim.15770 |
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