Serial plasma vasopressin concentration in healthy and hospitalised neonatal foals.
Abstract: Vasopressin dysregulation occurs in critically ill human patients and in neonatal foals. Limited data about serial plasma vasopressin dynamics exist in sick neonatal foals. Objective: To evaluate serial plasma arginine vasopressin (AVP) concentrations in sick neonatal foals. Methods: Prospective, longitudinal clinical study. Methods: Plasma samples were collected from 7 healthy and 26 sick foals before and after initial fluid resuscitation and 12, 24, 36, 48 and 96 h after presentation. Foals with a modified sepsis score ≥ 11 were considered septic. Results: Admission AVP was increased in septic foals compared to healthy and to sick, nonseptic foals. There were no significant differences between groups on subsequent days. Nonsurvivors had higher AVP concentrations than survivors. Conclusions: Plasma AVP concentrations are higher in septic foals on admission than in healthy and sick nonseptic foals. Higher early plasma AVP concentrations are associated with increased mortality.
© 2013 EVJ Ltd.
Publication Date: 2013-09-11 PubMed ID: 23781864DOI: 10.1111/evj.12121Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research conducted a detailed study on the vasopressin levels in the plasma of newborn foals, comparing the rates between healthy foals and those hospitalized due to sickness or sepsis. The findings indicate a correlation between elevated vasopressin concentrations on admission and higher mortality rates.
Objective and Methodology of the Research
- The primary objective of this research was to examine changes in plasma arginine vasopressin (AVP) concentrations in sick newborn foals over time. Arginine vasopressin is a hormone responsible for maintaining the water balance in the body and its dysregulation can lead to critical illnesses.
- The researchers carried out a prospective, longitudinal clinical study where they collected plasma samples from 33 foals. The cohort consisted of 7 healthy foals and 26 sick foals. They gathered these samples at various intervals – prior and post the preliminary fluid resuscitation, and at 12, 24, 36, 48, and 96 hours after the foals’ presentation.
- Among the 26 sick foals, those with a modified sepsis score (MSS) greater or equal to 11 were classified as septic. This score is an indication of the presence of a severe systemic inflammatory response to infection.
Results of the Research
- The study found that the vasopressin levels on admission were higher in septic foals in comparison to both, healthy foals and sick non-septic foals. However, there were no statistically significant differences noted in the AVP concentrations between these groups in subsequent days.
- Another critical observation made was that foals that didn’t survive had higher AVP concentrations compared to those who survived.
Conclusions drawn from the Research
- The research concluded that plasma AVP concentrations in septic foals on admission are greater than in healthy and sick non-septic foals, suggesting a correlation with illness severity.
- Furthermore, the findings suggest that higher early plasma AVP concentrations are related to increased mortality in foals. This might infer that elevated vasopressin levels could serve as an early indicator of severe illness and potentially predict adverse outcomes in newborn foals.
Cite This Article
APA
Borchers A, Magdesian KG, Schenck PA, Kass PH.
(2013).
Serial plasma vasopressin concentration in healthy and hospitalised neonatal foals.
Equine Vet J, 46(3), 306-310.
https://doi.org/10.1111/evj.12121 Publication
Researcher Affiliations
- William R. Pritchard Veterinary Medical Teaching Hospital, University of California, USA.
MeSH Terms
- Animals
- Animals, Newborn
- Arginine Vasopressin / blood
- Biomarkers / blood
- Horse Diseases / blood
- Horses
- Hospitals, Animal
- Longitudinal Studies
- Sepsis / blood
- Sepsis / veterinary
Citations
This article has been cited 1 times.- Yang J, Zhu J, Pei R, Oliver JA, Landry DW, Stojanovic MN, Lin Q. Integrated Microfluidic Aptasensor for Mass Spectrometric Detection of Vasopressin in Human Plasma Ultrafiltrate. Anal Methods 2016 Jul 14;8(26):5190-5196.
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