Evaluation of Eosinopenia as a SIRS Biomarker in Critically Ill Horses

Animals (Basel). 2022 Dec 15;12(24):3547. doi: 10.3390/ani12243547.

Abstract

Systemic inflammatory response syndrome (SIRS) is a very common finding in critically ill patients. To accurately identify patients with SIRS and those who need intensive care, several markers have been evaluated, including cortisol, WBC or lactate. It is widely known that a stress leukogram includes eosinopenia as one of its main markers (neutrophilia, eosinopenia, lymphopenia and mild monocytes). It is known that cortisol concentration in plasma is the main stress biomarker and is strongly correlated with the severity of disease in horses. However, it is not possible to measure this parameter routinely in clinical conditions. Hence, in this study it was hypothesized that the eosinophil count could be a reliable parameter to identify critically ill horses. Horses included in this study were divided into three groups: Group A (sick horses received at the Emergency Unit which did not fulfil the criteria for SIRS), Group B (horses that meet two or more criteria for inclusion in the definition of SIRS) and a control group of healthy horses. In this study, horses with SIRS showed lower eosinophil counts than healthy horses. Moreover, non-surviving horses exhibited lower eosinophil counts than survivors. Eosinopenia could be used to identify horses with SIRS and can be useful as a prognostic marker.

Keywords: SIRS; WBC; eosinophils; horse; lactate; prognosis.

Grants and funding

This research was partially supported by grant GR21085 funded by the Regional Ministry of Economy and Infrastructure, Extremadura Government (Spain), and the European Regional Development Fund “A way to make Europe” and by the grant “Ayudas a grupos de la Universidad de Extremadura”. Beatriz Macías-García was recipient of a “Ramón y Cajal” grant from the Ministry of Economy, Industry and Competitiveness (Spain) and the “Fondo Europeo de Desarrollo Regional” (AEI/FEDER/UE); Reference RYC-2017-21545.