Analyze Diet
Animals : an open access journal from MDPI2023; 13(21); 3387; doi: 10.3390/ani13213387

A Longitudinal Analysis of Equine Asthma Presentation and Response to Treatment Using Lung Function Testing and BAL Cytology Analysis in Combination with Owner Perception.

Abstract: (1) Background: Equine asthma (EA) is a pervasive and important cause of poor performance and respiratory morbidity in horses. Diagnosis of EA includes an owner complaint, clinical scoring, lung function testing, and cytological analysis of bronchoalveolar lavage (BAL) cytology. There is a paucity of information about the longitudinal course of the disease using these outcome assessments; thus, this study sought to describe and quantify, in horses with more than one visit to a specialty pulmonary clinic in New England, the type and range of clinical presentations with an eventual diagnosis of EA. It also aimed to develop and compare the outcomes of scoring systems for owner complaints and veterinary assessments, document and assess the diagnostic methods used, and evaluate the response of the horses to treatment and time. (2) Methods: This study was a retrospective, cross-sectional, STROBE-compliant observational analysis of equine patients who visited the Tufts Cummings Hospital for Large Animals (HLA) for evaluation of equine asthma (EA) from 1999-2023. The horses were categorized as having mild-moderate (mEA) or severe EA (sEA) using the ACVIM consensus statement guidelines. After excluding those with inadequate documentation or only one visit ( = 936), a total of 76 horses were included in the study. Of the 197 visits, 138 (70.0%) resulted in a diagnosis of mEA and 45 (22.8%) resulted in a diagnosis of sEA. Demographic information, owner complaints, clinical examination and scoring, lung function testing, BAL cytology, and recommendations for environmental remediation and pharmacologic treatment were recorded for all the visits. The data were analyzed for agreement between owner complaints (complaint score, CS) and clinical examination findings (examination score, ES), changes in CS and ES, lung function testing, and BAL cytology over time, with 197 visits recorded. (3) Results: A comparison between the CS and ES showed that the owners were more likely than veterinarians to detect cough, and a decrease in cough was the most common owner observation after treatment. The response to the histamine challenge, used to detect airway hyperreactivity, was significantly improved with treatment or time in the horses with mEA, whereas baseline lung function did not significantly change in mEA or sEA. (4) Conclusions: Owners can be astute observers of clinical signs, especially cough, in EA. Tests of airway hyperreactivity are more successful in detecting changes in mEA than are baseline lung function testing and assessment of BAL cytology.
Publication Date: 2023-11-01 PubMed ID: 37958142PubMed Central: PMC10649418DOI: 10.3390/ani13213387Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article focuses on an evaluation of how horses suffering from Equine Asthma (EA) respond to treatment and their progression over time. The study also examines how perceptions between horse owners and veterinarians differ when it comes to identifying symptoms of EA.

Background of the Study

  • The paper presents a research on Equine Asthma, a respiratory condition common in horses that often leads to poor performance and respiratory diseases.
  • The study aims to develop a comprehensive understanding of the disease and the effectiveness of its treatments by considering both, clinical tests and owners’ observations.
  • The study also focuses on identifying the various symptoms of the disease and how they evolve over time in response to treatments.

Methodology

  • The researchers conducted a longitudinal analysis involving 76 horses who visited the Tufts Cummings Hospital for Large Animals between 1999 and 2023.
  • All the horses were evaluated based on the guidelines of the ACVIM consensus statement, with the severity of their condition categorized as mild-moderate or severe.
  • Data collected included demographic information, owner complaints, clinical scoring, lung function testing results, BAL cytology and recommended treatments.
  • The researchers sought to compare the complaint score – based on owners’ feedback, with the exam score – based on clinical examination findings.

Results

  • Results showed a significant difference in the perception of EA symptoms between horse owners and veterinarians. Owners were more likely to notice symptoms such as coughing in horses, which was also the most common observation post treatment.
  • Through a histamine challenge test – used to detect respiratory hypersensitivity, improvements were noted in horses suffering from mild to moderate EA, but no such improvements were seen in the base lung functions of horses with either mild-moderate or severe EA.

Conclusions

  • From the findings, it is clear that horse owners can be good observers of clinical signs of EA, especially in detection of symptoms like coughing.
  • Airway hyperreactivity tests have proven to be more successful in detecting changes in EA than baseline lung function testing and BAL cytology assessments.

Cite This Article

APA
Robins TJ, Bedenice D, Mazan M. (2023). A Longitudinal Analysis of Equine Asthma Presentation and Response to Treatment Using Lung Function Testing and BAL Cytology Analysis in Combination with Owner Perception. Animals (Basel), 13(21), 3387. https://doi.org/10.3390/ani13213387

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 13
Issue: 21
PII: 3387

Researcher Affiliations

Robins, Tyler-Jane
  • Cummings School of Veterinary Medicine, Tufts University, North Grafton, MA 01536, USA.
Bedenice, Daniela
  • Cummings School of Veterinary Medicine, Tufts University, North Grafton, MA 01536, USA.
Mazan, Melissa
  • Cummings School of Veterinary Medicine, Tufts University, North Grafton, MA 01536, USA.

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 29 references
  1. Couëtil LL, Cardwell JM, Gerber V, Lavoie JP, Léguillette R, Richard EA. Inflammatory Airway Disease of Horses—Revised Consensus Statement. J. Vet. Intern. Med. 2016;30:503–15.
    doi: 10.1111/jvim.13824pmc: PMC4913592pubmed: 26806374google scholar: lookup
  2. Couetil L, Cardwell JM, Leguillette R, Mazan M, Richard E, Bienzle D, Bullone M, Gerber V, Ivester K, Lavoie JP. Equine Asthma: Current Understanding and Future Directions. Front. Vet. Sci. 2020;7:450.
    doi: 10.3389/fvets.2020.00450pmc: PMC7438831pubmed: 32903600google scholar: lookup
  3. Gerber V, Schott HC II, Robinson NE. Owner assessment in judging the efficacy of airway disease treatment. Equine Vet. J. 2011;43:153–158.
  4. Marti E, Gerber H, Essich G, Oulehla J, Lazary S. The genetic basis of equine allergic diseases 1. Chronic hypersensitivity bronchitis. Equine Vet. J. 1991;23:457–460.
  5. Ivester KM, Couëtil LL, Moore GE. An observational study of environmental exposures, airway cytology, and performance in racing thoroughbreds. J. Vet. Intern. Med. 2018;32:1754–1762.
    doi: 10.1111/jvim.15226pmc: PMC6189343pubmed: 30222207google scholar: lookup
  6. Bullone M, Murcia RY, Lavoie JP. Environmental heat and airborne pollen concentration are associated with increased asthma severity in horses. Equine Vet. J. 2016;48:479–484.
    doi: 10.1111/evj.12559pubmed: 26708931google scholar: lookup
  7. Cardwell JM, Smith KC, Wood JLN, Newton JR. Infectious risk factors and clinical indicators for tracheal mucus in British National Hunt racehorses. Equine Vet. J. 2014;46:150–155.
    doi: 10.1111/evj.12109pubmed: 23738942google scholar: lookup
  8. Fortier G, Richard E, Hue E, Fortier C, Pronost S, Pottier D, Lemaitre L, Lekeux P, Borchers K, Thiry E. Long-lasting airway inflammation associated with equid herpesvirus-2 in experimentally challenged horses. Vet. J. 2013;197:492–495.
    doi: 10.1016/j.tvjl.2012.12.027pubmed: 23433569google scholar: lookup
  9. Hoffman A, Kuehn H, Riedelberger K, Kupcinskas R, Miskovic MB. Flowmetric comparison of respiratory inductance plethysmography and pneumotachography in horses. J. Appl. Physiol. 2001;91:2767–2775.
    doi: 10.1152/jappl.2001.91.6.2767pubmed: 11717245google scholar: lookup
  10. Wichtel M, Gomez D, Burton S, Wichtel J, Hoffman A. Relationships between equine airway reactivity measured by flowmetric plethysmography and specific indicators of airway inflammation in horses with suspected inflammatory airway disease. Equine Vet. J. 2016;48:466–471.
    doi: 10.1111/evj.12482pubmed: 26174367google scholar: lookup
  11. Rossi H, Virtala AM, Raekallio M, Rahkonen E, Rajamäki MM, Mykkänen A. Comparison of Tracheal Wash and Bronchoalveolar Lavage Cytology in 154 Horses with and without Respiratory Signs in a Referral Hospital Over 2009–2015. Front. Vet. Sci. 2018;5:61.
    doi: 10.3389/fvets.2018.00061pmc: PMC5879091pubmed: 29632867google scholar: lookup
  12. Cuschieri S. The STROBE guidelines. Saudi J. Anaesth. 2019;13:S31–S34.
    doi: 10.4103/sja.SJA_543_18pmc: PMC6398292pubmed: 30930717google scholar: lookup
  13. Mazan MR, Vin R, Hoffman AM. Radiographic scoring lacks predictive value in inflammatory airway disease. Equine Vet. J. 2005;37:541–545.
    doi: 10.2746/042516405775314899pubmed: 16295932google scholar: lookup
  14. Gerber V, Straub R, Marti E, Hauptman J, Herholz C, King M, Imhof A, Tahon L, Robinson NE. Endoscopic scoring of mucus quantity and quality: Observer and horse variance and relationship to inflammation, mucus viscoelasticity and volume. Equine Vet. J. 2004;36:576–582.
    doi: 10.2746/0425164044864525pubmed: 15581321google scholar: lookup
  15. Mahalingam-Dhingra A, Bedenice D, Mazan MR. Bronchoalveolar lavage hemosiderosis in lightly active or sedentary horses. J. Vet. Intern. Med. 2023;37:1243–1249.
    doi: 10.1111/jvim.16692pmc: PMC10229344pubmed: 36975043google scholar: lookup
  16. Mazan MR, Hoffman AM, Manjerovic N. Comparison of forced oscillation with the conventional method for histamine bronchoprovocation testing in horses. Am. J. Vet. Res. 1999;60:174–180.
    pubmed: 10048547
  17. Robinson NE, Derksen FJ, Olszewski MA, Buechner-Maxwell VA. The pathogenesis of chronic obstructive pulmonary disease of horses. Br. Vet. J. 1996;152:283–306.
    doi: 10.1016/S0007-1935(96)80101-1pubmed: 8762605google scholar: lookup
  18. House AM. Understanding Recurrent Airway Obstruction (RAO) in the Horse. Veterinary Medicine-Large Animal Clinical Sciences Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida; Gainesville, FL, USA: 2010. VM142.
  19. Bedenice D, Mazan MR, Hoffman AM. Association between Cough and Cytology of Bronchoalveolar Lavage Fluid and Pulmonary Function in Horses Diagnosed with Inflammatory Airway Disease. J. Vet. Intern. Med. 2008;22:1022–1028.
  20. Couetil LL, Rosenthal FS, Denicola DB, Chilcoat CD. Clinical signs, evaluation of bronchoalveolar lavage fluid, and assessment of pulmonary function in horses with inflammatory respiratory disease. Am. J. Vet. Res. 2001;62:538–546.
    doi: 10.2460/ajvr.2001.62.538pubmed: 11327461google scholar: lookup
  21. Richard EA, Fortier GD, Denoix JM, Art T, Lekeux PM, Erck VV. Influence of subclinical inflammatory airway disease on equine respiratory function evaluated by impulse oscillometry. Equine Vet. J. 2009;41:384–389.
    doi: 10.2746/042516409X366121pubmed: 19562901google scholar: lookup
  22. Cullimore A, Secombe C, Lester G, Robertson I. Bronchoalveolar lavage fluid cytology and airway hyper-reactivity in clinically normal horses. Aust. Vet. J. 2018;96:291–296.
    doi: 10.1111/avj.12721pubmed: 30129032google scholar: lookup
  23. Ivester KM, Couëtil LL. Management of chronic airway inflammation in the horse: A systematic review. Equine Vet. Educ. 2014;26:647–656.
    doi: 10.1111/eve.12238google scholar: lookup
  24. Bond SL, Greco-Otto P, Macleod J, Galezowski A, Bayly W, Léguillette R. Efficacy of dexamethasone, salbutamol, and reduced respirable particulate concentration on aerobic capacity in horses with smoke-induced mild asthma. J. Vet. Intern. Med. 2020;34:979–985.
    doi: 10.1111/jvim.15696pmc: PMC7096652pubmed: 31953974google scholar: lookup
  25. Derksen FJ, Olszewski MA, Robinson NE, Berney C, Hakala JE, Matson CJ, Ruth DT. Aerosolized albuterol sulfate used as a bronchodilator in horses with recurrent airway obstruction. Am. J. Vet. Res. 1999;60:689–693.
    pubmed: 10376893
  26. Read JR, Boston RC, Abraham G, Bauquier SH, Soma LR, Nolen-Walston RD. Effect of prolonged administration of clenbuterol on airway reactivity and sweating in horses with inflammatory airway disease. Am. J. Vet. Res. 2012;73:140–145.
    doi: 10.2460/ajvr.73.1.140pubmed: 22204300google scholar: lookup
  27. Mazan MR, Lascola K, Bruns SJ, Hoffman AM. Use of a novel one-nostril mask-spacer device to evaluate airway hyperresponsiveness (AHR) in horses after chronic administration of albuterol. Can. J. Vet. Res. 2014;78:214–220.
    pmc: PMC4068413pubmed: 24982553
  28. Falk JA, Minai OA, Mosenifar Z. Inhaled and systemic corticosteroids in chronic obstructive pulmonary disease. Proc. Am. Thorac. Soc. 2008;5:506–512.
    doi: 10.1513/pats.200707-096ETpmc: PMC2645327pubmed: 18453363google scholar: lookup
  29. Thompson JA, Mirza MH, Barker SA, Morgan TW, Bauer RW, McConnico RS. Clenbuterol toxicosis in three Quarter Horse racehorses after administration of a compounded product. J. Am. Vet. Med. Assoc. 2011;239:842–849.
    doi: 10.2460/javma.239.6.842pubmed: 21916768google scholar: lookup

Citations

This article has been cited 0 times.