Dysphagia associated with presumed pharyngeal dysfunction in 16 neonatal foals.
Abstract: Dysphagia due to pharyngeal dysfunction occurs in human neonates and is associated with prematurity and hypoxic episodes. This syndrome probably occurs in neonatal foals but has not been reported. Objective: The objectives of this study were to describe 1) a series of neonatal foals with dysphagia due to pharyngeal dysfunction; 2) the progression, treatment and resolution of the dysphagia; 3) the comorbidities; and 4) the prognosis for life and athleticism for affected foals. Methods: Records from 3 referral equine hospitals were reviewed from neonatal foals with dysphagia of pharyngeal origin. Inclusion criteria were a normal to strong suckle, dysphagia evidenced by milk at the nostrils after nursing the dam, and endoscopic examination of the airway. Foals with mechanical reasons for dysphagia, botulism or hyperkalaemic periodic paralysis were not included. Results: Sixteen neonatal foals qualified for the study. Eight (50%) were premature and/or diagnosed with hypoxic ischaemic encephalopathy. Twelve (75%) had aspiration pneumonia. Fifteen foals were discharged alive from the hospital, nursing the mare with no evidence of dysphagia (n = 14), or mild dysphagia (n = 1), a mean +/- s.d. of 7 +/- 6 days (median = 6.3 days, range 0-22 days) after hospital admission. One foal was subjectedto euthanasia in hospital. Follow-up nformation was available for 14 animals. Thirteen of 16 (81%) were alive and included one yearling and 12 horses >2 years old. Seven of the 14 (50%) were racing, training or in work, and 6 horses were pets, breeding animals or had unknown athletic status. Two had laryngeal deficits. One foal was subjected to euthanasia within weeks of discharge from the hospital due to aspiration pneumonia. Conclusions: Dysphagia related to pharyngeal dysfunction occurs in equine neonates and can resolve, but may require days to weeks of supportive care. Prognosis for life is favourable and for athleticism fair.
Publication Date: 2012-05-19 PubMed ID: 22594037DOI: 10.1111/j.2042-3306.2011.00451.xGoogle Scholar: Lookup
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Summary
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The study examines dysphagia, a condition characterized by difficulty swallowing, due to pharyngeal dysfunction in newborn foals. It elaborates on the symptoms, progression, associated conditions, and prognosis of the affected foals, data of which was collected from three different equine hospitals.
Study Objective and Methods
- The main goal of this study was to delineate the characteristics, progression, and potential treatments of dysphagia in newborn foals resulting from pharyngeal dysfunction. The study also aimed to shed light on accompanying conditions—the comorbidities—and the life and athletic prognosis for the affected foals.
- To achieve these objectives, the researchers reviewed records from three different equine hospitals, focusing solely on newborn foals exhibiting dysphagia of pharyngeal origin.
- The inclusion criteria for the study centered on healthy suckling behavior, evidence of dysphagia, i.e. milk residue at the nostrils after nursing, and endoscopic examination of the airway.
- Foals with mechanical causes for dysphagia or those suffering from botulism or hyperkalemic periodic paralysis were not featured in the study.
Research Findings
- A total of 16 newborn foals conformed to the study criteria. Out of these, eight (50%) were premature and/or were diagnosed with hypoxic-ischemic encephalopathy.
- Most of these foals (75%) developed aspiration pneumonia as a complication.
- Fifteen foals successfully recovered and were discharged from the hospital showing no or mild signs of dysphagia on an average of seven days after admission. One of them was euthanized during the hospital stay.
- Follow-up information was available for 14 of the released animals. It showed that 81% of the study foals were alive, among which one was a yearling, and 12 were over two years old.
- Half of the surviving foals were involved in racing or training, and the others lived as pets, breeding animals, or didn’t have a defined athletic status. However, two of them had laryngeal defects.
- One of the foals was euthanized in the weeks following discharge due to a recurrence of aspiration pneumonia.
Conclusions
- The study concludes that newborn foals can experience dysphagia associated with pharyngeal dysfunction, mirroring occurrences in human neonates.
- With the right supportive care over a few days to weeks, there are high chances of recovery and disappearance of dysphagia symptoms.
- Lastly, the paper notes that the prognosis for life is generally positive, while the prospects for athleticism are fair, implying that the condition does not majorly impact the foals’ ability to live normally or partake in athletic activities. However, they remain susceptible to associated issues like aspiration pneumonia and laryngeal defects.
Cite This Article
APA
Holcombe SJ, Hurcombe SD, Barr BS, Schott HC.
(2012).
Dysphagia associated with presumed pharyngeal dysfunction in 16 neonatal foals.
Equine Vet J Suppl(41), 105-108.
https://doi.org/10.1111/j.2042-3306.2011.00451.x Publication
Researcher Affiliations
- Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, USA. holcombe@cvm.msu.edu
MeSH Terms
- Animals
- Animals, Newborn
- Deglutition Disorders / pathology
- Deglutition Disorders / veterinary
- Horse Diseases / diagnosis
- Horse Diseases / pathology
- Horses
- Pharyngeal Diseases / pathology
- Pharyngeal Diseases / veterinary
Citations
This article has been cited 3 times.- Delvescovo B, Mullen KR, Eicker SW, Ivanek R, Ainsworth DM. The effect of neonatal dysphagia on subsequent racing performance in Standardbred horses. Equine Vet J 2021 May;53(3):481-487.
- Arnold C. From Canaries to Cats: Domestic Animals as Sentinels for Human Exposure Effects. Environ Health Perspect 2023 Nov;131(11):112001.
- van der Vossen N, Cavalcante P, Glynn S, Achappa D, Mehmood W, Oikawa M, Vinardell T, Jamieson C. A case-control study of atypical guttural pouch empyema in Arabian foals. Vet Med Sci 2023 Jul;9(4):1599-1609.
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