Diagnostic approaches, aetiological agents and their associations with short-term survival and laminitis in horses with acute diarrhoea admitted to referral institutions.
Abstract: An international description of the diagnostic approaches used in different institutions to diagnose acute equine diarrhoea and the pathogens detected is lacking. Objective: To describe the diagnostic approach, aetiological agents, outcome, and development of laminitis for diarrhoeic horses worldwide. Methods: Multicentre retrospective case series. Methods: Information from horses with acute diarrhoea presenting to participating institutions between 2016 and 2020, including diagnostic approaches, pathogens detected and their associations with outcomes, were compared between institutions or geographic regions. Results: One thousand four hundred and thirty-eight horses from 26 participating institutions from 4 continents were included. Overall, aetiological testing was limited (44% for Salmonella spp., 42% for Neorickettsia risticii [only North America], 40% for Clostridiodes difficile, and 29% for ECoV); however, 13% (81/633) of horses tested positive for Salmonella, 13% (35/262) for N. risticii, 9% (37/422) for ECoV, and 5% (27/578) for C. difficile. C. difficile positive cases had greater odds of non-survival than horses negative for C. difficile (OR: 2.69, 95%CI: 1.23-5.91). In addition, horses that were positive for N. risticii had greater odds of developing laminitis than negative horses (OR: 2.76, 95%CI: 1.12-6.81; p = 0.029). Conclusions: Due to the study's retrospective nature, there are missing data. Conclusions: This study highlighted limited diagnostic investigations in cases of acute equine diarrhoea. Detection rates of pathogens are similar to previous reports. Non-survival and development of laminitis are related to certain detected pathogens. Unassigned: Eine internationale Beschreibung der in verschiedenen Institutionen verwendeten diagnostischen Vorgehensweisen in der Diagnostizierung von akuten Durchfallerkrankungen beim Pferd und der nachgewiesenen Pathogene ist nicht vorhanden. Unassigned: Die Beschreibung der diagnostischen Vorgehensweise, ätiologischen Erreger, klinischer Ergebnisse und Aufkommen von Hufrehe bei Pferden mit Durchfallerkrankung weltweit. Methods: Multizentrisch retrospektive Fallserie. Methods: Informationen von Pferden mit akuter Durchfallerkrankung, welche bei teilnehmenden Institutionen zwischen 2016 und 2020 vorstellig waren, inklusive diagnostischer Vorgehensweise, identifizierter Pathogene und deren Assoziationen zu klinischen Ergebnissen, wurden zwischen Institutionen und geographischen Regionen verglichen. Unassigned: 1438 Pferde von 26 teilnehmenden Institutionen aus vier Kontinenten wurden erfasst. Ätiologische Tests waren insgesamt eingeschränkt (44% für Salmonella spp., 42% für Neorickettsia risticii (nur Nordamerika), 40% für Clostridiodes difficile, und 29% für ECoV); allerdings testeten 13% (81/633) der Pferde positiv für Salmonella, 13% (35/262) für N. risticii, 9% (37/422) für ECoV, und 5% (27/578) für C. difficile. C. difficile‐positive Fälle wiesen eine höhere Wahrscheinlichkeit des Nicht‐Überlebens auf als C. difficile‐negative Pferde (OR: 2.69, 95%CI: 1.23 – 5.91). Außerdem hatten N. risticii‐positive Pferde eine höhere Wahrscheinlichkeit, Hufrehe zu entwickeln als negativ getestete Pferde (OR: 2.76, 95%CI: 1.12 ‐ 6.81; P = 0.029). HAUPTEINSCHRÄNKUNGEN: Durch den retrospektiven Charakter der Studie waren nicht alle Daten für alle Pferde verfügbar. Unassigned: Diese Studie zeigt limitierte diagnostische Untersuchungen bei Fällen von akuter Durchfallerkrankung auf. Erfassungsraten von Pathogenen sind mit vorherigen Berichten vergleichbar. Nicht‐Überleben und Aufkommen von Hufrehe sind mit bestimmten nachgewiesenen Pathogenen assoziiert.
© 2023 The Authors. Equine Veterinary Journal published by John Wiley & Sons Ltd on behalf of EVJ Ltd.
Publication Date: 2023-11-20 PubMed ID: 37984355DOI: 10.1111/evj.14024Google Scholar: Lookup
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- Journal Article
- Multicenter Study
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 is about the diagnostic procedures used in different institutions for acute equine diarrhoea. It focuses on the techniques used, the pathogens detected, the horses’ survival rates, and the development of a condition known as laminitis in horses worldwide.
Study Methodology
- The research was a multicentre retrospective case series and collected data from horses diagnosed with acute diarrhoea between 2016 and 2020.
- The participating institutions were located globally, spread across 4 continents with a total of 1438 horses from 26 institutions included in the study.
- Within the scope of the study, researchers compared the diagnostic approaches, the pathogens found in the horses, and their effects on the survival rates between different institutions and geographic regions.
Results
- The results of the research highlighted that the extent of etiological testing, a method used to determine the disease’s cause, was limited. For instance, 44% were tested for Salmonella spp., 42% for Neorickettsia risticii, 40% for Clostridiodes difficile, and 29% for ECoV.
- However, the pathogens’ detection rates were comparatively consistent with previous findings, where 13% of horses tested positive for both Salmonella and N. risticii, 9% for ECoV, and 5% for C. difficile
- The study identified horses tested positive for C. difficile to have 2.69 times greater odds of non-survival than horses negative for C. difficile.
- Similarly, horses tested positive for N. risticii had 2.76 times greater chances of developing laminitis than negative horses.
Conclusions and Limitations
- Despite its valuable insights, the research had its limitations, mainly due to its retrospective nature leading to incomplete data sets.
- However, the study indeed shed light on the limited scope of diagnostic investigations performed globally in cases of acute equine diarrhoea.
- Moreover, the research highlighted that non-survival rates and the onset of laminitis in horses were linked to the detection of certain pathogens, thereby highlighting a potential focus area for future preventive strategies.
Cite This Article
APA
Gomez DE, Arroyo LG, Schoster A, Renaud DL, Kopper JJ, Dunkel B, Byrne D, Toribio RE.
(2023).
Diagnostic approaches, aetiological agents and their associations with short-term survival and laminitis in horses with acute diarrhoea admitted to referral institutions.
Equine Vet J, 56(5), 959-969.
https://doi.org/10.1111/evj.14024 Publication
Researcher Affiliations
- Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada.
- Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada.
- Vetsuisse Faculty, Equine Department University of Zurich, Zurich, Switzerland.
- Ludwig-Maximilians-University Munich, Equine Clinic, Oberschleissheim, Germany.
- Department of Population Medicine, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada.
- Department of Veterinary Clinical Sciences, Iowa State University College of Veterinary Medicine, Ames, Iowa, USA.
- Department of Clinical Science and Services, The Royal Veterinary College, Hertfordshire, UK.
- College of Veterinary Medicine, Murdoch University, Perth, Western Australia, Australia.
- College of Veterinary Medicine, The Ohio State University, Columbus, Ohio, USA.
MeSH Terms
- Animals
- Horses
- Horse Diseases / diagnosis
- Horse Diseases / microbiology
- Horse Diseases / mortality
- Diarrhea / veterinary
- Diarrhea / diagnosis
- Diarrhea / microbiology
- Diarrhea / mortality
- Retrospective Studies
- Foot Diseases / veterinary
- Foot Diseases / mortality
- Foot Diseases / diagnosis
- Foot Diseases / microbiology
- Male
- Female
- Acute Disease
- Hoof and Claw / pathology
- Hoof and Claw / microbiology
- Inflammation / veterinary
References
This article includes 72 references
- Arroyo L, Arnold CE, Barham M, Costa MC, Greiman SE, Magdesian G. Science‐in‐brief: report on the Havemeyer Foundation workshop on acute colitis of the adult horse.. Equine Vet J 2020;52(2):163–164.
- Shaw SD, Stämpfli H. Diagnosis and treatment of undifferentiated and infectious acute diarrhea in the adult horse.. Vet Clin North Am Equine Pract 2018;34(1):39–53.
- Macías‐Rioseco M, Hill AE, Uzal FA. Fatal intestinal inflammatory lesions in equids in California: 710 cases (1990–2013).. J Am Vet Med Assoc 2020;256(4):455–462.
- Schoster A, Kunz T, Lauper M, Graubner C, Schmitt S, Weese JS. Prevalence of Clostridium difficile and Clostridium perfringens in Swiss horses with and without gastrointestinal disease and microbiota composition in relation to Clostridium difficile shedding.. Vet Microbiol 2019;239:108433.
- Weese JS, Staempfli HR, Prescott JF. A prospective study of the roles of Clostridium difficile and enterotoxigenic Clostridium perfringens in equine diarrhoea.. Equine Vet J 2001;33(4):403–409.
- Willette JA, Kopper JJ, Kogan CJ, Seguin MA, Schott HC. Effect of season and geographic location in the United States on detection of potential enteric pathogens or toxin genes in horses ≥6‐mo‐old.. J Vet Diagn Invest 2021;34(3):407–411.
- Acute diarrhea in horses: a multicenter Canadian retrospective study (2015 to 2019)—PubMed [Internet]. [cited 2022 Nov 12]. Available from: https://pubmed.ncbi.nlm.nih.gov/36185796/
- Berryhill EH, Magdesian KG, Aleman M, Pusterla N. Clinical presentation, diagnostic findings, and outcome of adult horses with equine coronavirus infection at a veterinary teaching hospital: 33 cases (2012–2018).. Vet J 2019;248:95–100.
- Nomura M, Kuroda T, Tamura N, Muranaka M, Niwa H. Mortality, clinical findings, predisposing factors and treatment of Clostridioides difficile colitis in Japanese thoroughbred racehorses.. Vet Rec 2020;187(2):e14.
- Mattei DN, Kopper JJ, Sanz MG. Equine coronavirus‐associated colitis in horses: a retrospective study.. J Vet Intern Med 2020;35(4):102906.
- Ruby R, Magdesian KG, Kass PH. Comparison of clinical, microbiologic, and clinicopathologic findings in horses positive and negative for Clostridium difficile infection.. J Am Vet Med Assoc 2009;234(6):777–784.
- Arroyo LG, Moore A, Bedford S, Gomez DE, Teymournejad O, Xiong Q. Potomac horse fever in Ontario: clinical, geographic, and diagnostic aspects.. Can Vet J 2021;62(6):622–628.
- Kopper JJ, Willette JA, Kogan CJ, Seguin A, Bolin SR, Schott HC 2nd. Detection of pathogens in blood or feces of adult horses with enteric disease and association with outcome of colitis.. J Vet Intern Med 2021;35(5):2465–2472.
- Luethy D, Feldman R, Stefanovski D, Aitken MR. Risk factors for laminitis and nonsurvival in acute colitis: retrospective study of 85 hospitalized horses (2011–2019).. J Vet Intern Med 2021;35(4):2019–2025.
- Bertin FR, Reising A, Slovis NM, Constable PD, Taylor SD. Clinical and clinicopathological factors associated with survival in 44 horses with equine neorickettsiosis (Potomac horse fever).. J Vet Intern Med 2013;27(6):1528–1534.
- Rikihisa Y, Reed SM, Sams RA, Gordon JC, Pretzman CI. Serosurvey of horses with evidence of equine monocytic ehrlichiosis.. J Am Vet Med Assoc 1990;197(10):1327–1332.
- Mott J, Rikihisa Y, Zhang Y, Reed SM, Yu CY. Comparison of PCR and culture to the indirect fluorescent‐antibody test for diagnosis of Potomac horse fever.. J Clin Microbiol 1997;35(9):2215–2219.
- Landis JR, Koch GG. The measurement of observer agreement for categorical data.. Biometrics 1977;33(1):159–174.
- Gomez DE, Dunkel B, Renaud DL, Arroyo LG, Schoster A, Kopper JJ. Survival rates and factors associated with survival and laminitis of horses with acute diarrhoea admitted to referral institutions.. Equine Vet J 2024;56(5):970–981.
- Diab SS, Kinde H, Moore J, Shahriar MF, Odani J, Anthenill L. Pathology of Clostridium perfringens type C enterotoxemia in horses.. Vet Pathol 2012;49(2):255–263.
- Burgess BA. Salmonella in horses.. Vet Clin North Am Equine Pract 2023;39:25–35.
- Bierbaum M, Rapport F, Arnolda G, Nic Giolla Easpaig B, Lamprell K, Hutchinson K. Clinicians' attitudes and perceived barriers and facilitators to cancer treatment clinical practice guideline adherence: a systematic review of qualitative and quantitative literature.. Implement Sci 2020;15(1):39.
- Gohari IM, Arroyo L, Macinnes JI, Timoney JF, Parreira VR, Prescott JF. Characterization of Clostridium perfringens in the feces of adult horses and foals with acute enterocolitis.. Can J Vet Res 2014;78(1):1–7.
- Mehdizadeh Gohari I, Unterer S, Whitehead AE, Prescott JF. NetF‐producing Clostridium perfringens and its associated diseases in dogs and foals.. J Vet Diagn Invest 2020;32(2):230–238.
- Uzal FA, Arroyo LG, Navarro MA, Gomez DE, Asín J, Henderson E. Bacterial and viral enterocolitis in horses: a review.. J Vet Diagn Invest 2021;34(3):354–375.
- Nyaoke AC, Navarro MA, Fresneda K, Diab SS, Moore J, Lyras D. Paeniclostridium (Clostridium) sordellii‐associated enterocolitis in 7 horses.. J Vet Diagnost Invest 2020;32(2):239–245.
- Zakia LS, MacNicol JL, Borges AS, Yu S, Boerlin P, Gomez DE. Fecal prevalence of Clostridium innocuum DNA in healthy horses and horses with colitis.. Anaerobe 2022;79:102681.
- Zakia LS, Gomez DE, Caddey BB, Boerlin P, Surette MG, Arroyo LG. Direct and culture‐enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis.. PloS One 2023;18(4):e0284193.
- Burgess BA, Morley PS. Risk factors for shedding of salmonella enterica among hospitalized large animals over a 10‐year period in a veterinary teaching hospital.. J Vet Intern Med 2019;33(5):2239–2248.
- Ekiri AB, MacKay RJ, Gaskin JM, Freeman DE, House AM, Giguère S. Epidemiologic analysis of nosocomial Salmonella infections in hospitalized horses.. J Am Vet Med Assoc 2009;234(1):108–119.
- Ernst NS, Hernandez JA, MacKay RJ, Brown MP, Gaskin JM, Nguyen AD. Risk factors associated with fecal Salmonella shedding among hospitalized horses with signs of gastrointestinal tract disease.. J Am Vet Med Assoc 2004;225(2):275–281.
- Roberts MC, O'Boyle DA. The prevalence and epizootiology of salmonellosis among groups of horses in south East Queensland.. Aust Vet J 1981;57(1):27–35.
- Palmer J, Benson C. Salmonella shedding in the equine.. International symposium on Salmonella; 1985.
- Pusterla N, Byrne BA, Mapes S, Akana N, Wademan C, Fielding LC. Investigation of the use of pooled faecal and environmental samples following an enrichment step for the detection of Salmonella enterica by real‐time PCR.. Vet Rec 2014;174(10):252.
- Pusterla N, Madigan JE, Chae JS, DeRock E, Johnson E, Pusterla JB. Helminthic transmission and isolation of Ehrlichia risticii, the causative agent of Potomac horse fever, by using trematode stages from freshwater stream snails.. J Clin Microbiol 2000;38(3):1293–1297.
- Pusterla N, Leutenegger CM, Sigrist B, Chae JS, Lutz H, Madigan JE. Detection and quantitation of Ehrlichia risticii genomic DNA in infected horses and snails by real‐time PCR.. Vet Parasitol 2000;90(1–2):129–135.
- Madigan JE, Rikihisa Y, Palmer JE, DeRock E, Mott J. Evidence for a high rate of false‐positive results with the indirect fluorescent antibody test for Ehrlichia risticii antibody in horses.. J Am Vet Med Assoc 1995;207(11):1448–1453.
- Teymournejad O, Lin M, Bekebrede H, Kamr A, Toribio RE, Arroyo LG. Isolation and molecular analysis of a novel Neorickettsia species that causes Potomac horse fever.. MBio 2020;11(1):e03429‐19.
- Donaldson MT, Palmer JE. Prevalence of Clostridium perfringens enterotoxin and Clostridium difficile toxin A in feces of horses with diarrhea and colic.. J Am Vet Med Assoc 1999;215(3):358–361.
- Båverud V, Franklin A, Gunnarsson A, Gustafsson A, Hellander‐Edman A. Clostridium difficile associated with acute colitis in mares when their foals are treated with erythromycin and rifampicin for Rhodococcus equi pneumonia.. Equine Vet J 1998;30(6):482–488.
- Weese JS, Toxopeus L, Arroyo L. Clostridium difficile associated diarrhoea in horses within the community: predictors, clinical presentation and outcome.. Equine Vet J 2006;38(2):185–188.
- Medina‐Torres CE, Weese JS, Staempfli HR. Prevalence of Clostridium difficile in horses.. Vet Microbiol 2011;152(1–2):212–215.
- Båverud V, Gustafsson A, Franklin A, Aspán A, Gunnarsson A. Clostridium difficile: prevalence in horses and environment, and antimicrobial susceptibility.. Equine Vet J 2003;35(5):465–471.
- Medina‐Torres CE, Weese JS, Staempfli HR. Validation of a commercial enzyme immunoassay for detection of Clostridium difficile toxins in feces of horses with acute diarrhea.. J Vet Intern Med 2010;24(3):628–632.
- Silva ROS, Vilela EG, Neves MS, Lobato FCF. Evaluation of three enzyme immunoassays and a nucleic acid amplification test for the diagnosis of Clostridium difficile‐associated diarrhea at a university hospital in Brazil.. Rev Soc Bras Med Trop 2014;47(4):447–450.
- Ramos CP, Lopes EO, Oliveira Júnior CA, Diniz AN, Lobato FCF, Silva ROS. Immunochromatographic test and ELISA for the detection of glutamate dehydrogenase (GDH) and a/B toxins as an alternative for the diagnosis of Clostridioides (Clostridium) difficile‐associated diarrhea in foals and neonatal piglets.. Braz J Microbiol 2020;51(3):1459–1462.
- Arroyo LG, Kruth SA, Willey BM, Staempfli HR, Low DE, Weese JS. PCR ribotyping of Clostridium difficile isolates originating from human and animal sources.. J Med Microbiol 2005;54(Pt 2):163–166.
- Schoster A, Staempfli HR, Arroyo LG, Reid‐Smith RJ, Janecko N, Shewen PE. Longitudinal study of Clostridium difficile and antimicrobial susceptibility of Escherichia coli in healthy horses in a community setting.. Vet Microbiol 2012;159(3–4):364–370.
- Schoster A, Arroyo LG, Staempfli HR, Shewen PE, Weese JS. Presence and molecular characterization of Clostridium difficile and Clostridium perfringens in intestinal compartments of healthy horses.. BMC Vet Res 2012;8:94.
- Ossiprandi MC, Buttrini M, Bottarelli E, Zerbini L. Preliminary molecular analysis of Clostridium difficile isolates from healthy horses in northern Italy.. Comp Immunol Microbiol Infect Dis 2010;33(6):e25–e29.
- Båverud V, Gustafsson A, Franklin A, Lindholm A, Gunnarsson A. Clostridium difficile associated with acute colitis in mature horses treated with antibiotics.. Equine Vet J 1997;29(4):279–284.
- Madewell BR, Tang YJ, Jang S, Madigan JE, Hirsh DC, Gumerlock PH. Apparent outbreaks of Clostridium difficile‐associated diarrhea in horses in a veterinary medical teaching hospital.. J Vet Diagn Invest 1995;7(3):343–346.
- Oue Y, Ishihara R, Edamatsu H, Morita Y, Yoshida M, Yoshima M. Isolation of an equine coronavirus from adult horses with pyrogenic and enteric disease and its antigenic and genomic characterization in comparison with the NC99 strain.. Vet Microbiol 2011;150(1–2):41–48.
- Nemoto M, Oue Y, Murakami S, Kanno T, Bannai H, Tsujimura K. Complete genome analysis of equine coronavirus isolated in Japan.. Arch Virol 2015;160(11):2903–2906.
- Pusterla N, James K, Mapes S, Bain F. Frequency of molecular detection of equine coronavirus in faeces and nasal secretions in 277 horses with acute onset of fever.. Vet Rec 2019;184(12):385.
- Goodrich EL, Mittel LD, Glaser A, Ness SL, Radcliffe RM, Divers TJ. Novel findings from a beta coronavirus outbreak on an American miniature horse breeding farm in upstate New York.. Equine Vet Educ 2020;32(3):150–154.
- Hierweger MM, Remy‐Wohlfender F, Franzen J, Koch MC, Blau D, Schoster A. Outbreak of equine coronavirus disease in adult horses, Switzerland 2021.. Transbound Emerg Dis 2022;69(4):1691–1694.
- Zhao S, Smits C, Schuurman N, Barnum S, Pusterla N, van Kuppeveld F. Development and validation of a S1 protein‐based ELISA for the specific detection of antibodies against equine coronavirus.. Viruses 2019;11(12):1109.
- Miszczak F, Tesson V, Kin N, Dina J, Balasuriya UBR, Pronost S. First detection of equine coronavirus (ECoV) in Europe.. Vet Microbiol 2014;171(1–2):206–209.
- Nemoto M, Schofield W, Cullinane A. The first detection of equine coronavirus in adult horses and foals in Ireland.. Viruses 2019;11(10):946.
- Pusterla N, Vin R, Leutenegger CM, Mittel LD, Divers TJ. Enteric coronavirus infection in adult horses.. Vet J 2018;231:13–18.
- Pusterla N, Mapes S, Wademan C, White A, Ball R, Sapp K. Emerging outbreaks associated with equine coronavirus in adult horses.. Vet Microbiol 2013;162(1):228–231.
- Oue Y, Morita Y, Kondo T, Nemoto M. Epidemic of equine coronavirus at Obihiro Racecourse, Hokkaido, Japan in 2012.. J Vet Med Sci 2013;75(9):1261–1265.
- Nemoto M, Oue Y, Higuchi T, Kinoshita Y, Bannai H, Tsujimura K. Low prevalence of equine coronavirus in foals in the largest thoroughbred horse breeding region of Japan, 2012–2014.. Acta Vet Scand 2015;57(1):53.
- Slovis NM, Elam J, Estrada M, Leutenegger CM. Infectious agents associated with diarrhoea in neonatal foals in central Kentucky: a comprehensive molecular study.. Equine Vet J 2014;46(3):311–3116.
- Pusterla N, Vin R, Leutenegger C, Mittel LD, Divers TJ. Equine coronavirus: an emerging enteric virus of adult horses.. Equine Vet Educ 2016;28(4):216–223.
- Fielding CL, Higgins JK, Higgins JC, McIntosh S, Scott E, Giannitti F. Disease associated with equine coronavirus infection and high case fatality rate.. J Vet Intern Med 2015;29(1):307–310.
- Nemoto M, Oue Y, Morita Y, Kanno T, Kinoshita Y, Niwa H. Experimental inoculation of equine coronavirus into Japanese draft horses.. Arch Virol 2014;159(12):3329–3334.
- Hart KA, Linnenkohl W, Mayer JR, House AM, Gold JR, Giguère S. Medical management of sand enteropathy in 62 horses.. Equine Vet J 2013;45(4):465–469.
- Kilcoyne I, Dechant JE, Spier SJ, Spriet M, Nieto JE. Clinical findings and management of 153 horses with large colon sand accumulations.. Vet Surg 2017;46(6):860–867.
- Niinistö K, Hewetson M, Kaikkonen R, Sykes BW, Raekallio M. Comparison of the effects of enteral psyllium, magnesium sulphate and their combination for removal of sand from the large colon of horses.. Vet J 2014;202(3):608–611.
- Husted L, Andersen MS, Borggaard OK, Houe H, Olsen SN. Risk factors for faecal sand excretion in Icelandic horses.. Equine Vet J 2005;37(4):351–355.
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