Analyze Diet
BMC veterinary research2022; 18(1); 149; doi: 10.1186/s12917-022-03248-x

Clinical features and treatment response to differentiate idiopathic peritonitis from non-strangulating intestinal infarction of the pelvic flexure associated with Strongylus vulgaris infection in the horse.

Abstract: Peritonitis in horses secondary to non-strangulating infarction (NSII) has a guarded prognosis, even after intestinal resection. In contrast, horses with idiopathic peritonitis respond well to medical treatment. Affected horses in both cases often show signs of both colic and systemic inflammation, but early diagnosis is crucial for optimal treatment and an accurate prognosis. One cause of NSII is thrombus formation secondary to Strongylus vulgaris larval migration. There has been a documented increase in S. vulgaris prevalence in Sweden since the implementation of selective anthelmintic treatment in 2007, which subsequently could result in a rise in NSII cases. In a retrospective clinical study, medical records from cases diagnosed with NSII of the pelvic flexure or idiopathic peritonitis from three equine referral hospitals in Sweden during 2017-2020 were reviewed. Information including demographic data, relevant medical history, and clinical- and laboratory parameters were obtained from patient records. To facilitate the differentiation between cases of idiopathic peritonitis and cases with confirmed NSII of the pelvic flexure, the aim of the study was to compare clinical and laboratory parameters, clinical progression and initial response to antimicrobial treatment. A secondary aim was to compare survival-rates. Results: Horses with NSII (n = 20) were significantly more likely to present during the winter months with a poorer response to medical treatment within 48 h. Cases of idiopathic peritonitis (n = 107) had a 100% survival rate with medical treatment, although one case required surgical correction of a colon displacement. In comparison, all confirmed NSII cases were non-responsive to antimicrobial treatment, with a survival rate to discharge of 50% after colon resection. Specific rectal findings and peripheral blood neutropenia were strongly associated with NSII. Conclusions: In Sweden, idiopathic peritonitis cases still predominate over S. vulgaris associated NSII cases and have an excellent survival rate with antimicrobial treatment. However, horses presenting with septic peritonitis during the winter months with a palpable rectal mass and displaying fever and colic signs beyond 48 h of medical treatment are likely to suffer from NSII of the pelvic flexure and should be considered for abdominal surgery.
Publication Date: 2022-04-23 PubMed ID: 35461295PubMed Central: PMC9034621DOI: 10.1186/s12917-022-03248-xGoogle 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 study focuses on differentiating idiopathic peritonitis from non-strangulating intestinal infarction (NSII) in horses, highlighting the clinical features and response to treatments. It presents a comparative analysis between the two conditions and acknowledges the significant role of early diagnosis in determining the course of treatment and prognosis.

Research Methodology

  • The study is a retrospective clinical review of medical records from cases diagnosed with NSII of the pelvic flexure or idiopathic peritonitis. This data was taken from three equine referral hospitals in Sweden from 2017 to 2020.
  • The researchers obtained various pieces of information for their study, including demographical data, relevant medical history, and clinical laboratory parameters from the patient records.
  • The primary aim of this research was to distinguish between cases of idiopathic peritonitis and NSII of the pelvic flexure by comparing various factors such as clinical and laboratory parameters, clinical progression, and the initial response to antimicrobial treatment.
  • The secondary aim was to evaluate and compare the survival rates of the two conditions.

Research Findings

  • The research found that horses with NSII are more likely to show up during winter and they generally have a less favorable response to medical treatment within the first 48 hours.
  • Horses suffering from idiopathic peritonitis had a 100% survival rate with medical treatment, though surgical intervention was necessary in one case for rectifying a colon displacement.
  • On the contrary, horses with NSII were not responsive to antimicrobial treatments and had a survival rate of 50% after undergoing colon resection.
  • Particular rectal findings and the presence of a lesser number of neutrophils in the blood i.e., neutropenia, were strongly associated with NSII.

Conclusions

  • The study concludes that in Sweden, the cases of idiopathic peritonitis are still greater in number as compared to NSII cases related to S.vulgaris. However, those horses that exhibit septic peritonitis during the winter months and exhibit persistence of symptoms like a palpable rectal mass, fever, and colic signs, despite more than 48 hours of medical treatment, are more likely to have NSII of the pelvic flexure. Therefore, they should be considered for abdominal surgery.
  • The study emphasizes the importance of early diagnosis for optimizing the treatment plan and achieving accurate prognosis.

Cite This Article

APA
Hedberg-Alm Y, Tydén E, Tamminen LM, Lindström L, Anlén K, Svensson M, Riihimäki M. (2022). Clinical features and treatment response to differentiate idiopathic peritonitis from non-strangulating intestinal infarction of the pelvic flexure associated with Strongylus vulgaris infection in the horse. BMC Vet Res, 18(1), 149. https://doi.org/10.1186/s12917-022-03248-x

Publication

ISSN: 1746-6148
NlmUniqueID: 101249759
Country: England
Language: English
Volume: 18
Issue: 1
Pages: 149
PII: 149

Researcher Affiliations

Hedberg-Alm, Ylva
  • Department of Biomedical Science and Veterinary Public Health, Parasitology Unit, Swedish University of Agricultural Sciences, Uppsala, Sweden. ylva.hedberg.alm@uds.slu.se.
  • Equine Clinic, University Animal Hospital, Swedish University of Agricultural Sciences, Uppsala, Sweden. ylva.hedberg.alm@uds.slu.se.
Tydén, Eva
  • Department of Biomedical Science and Veterinary Public Health, Parasitology Unit, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Tamminen, Lena-Mari
  • Department of Clinical Sciences, Veterinary Epidemiology Unit, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Lindström, Lisa
  • Department of Biomedical Science and Veterinary Public Health, Pathology Unit, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Anlén, Karin
  • Specialist Equine Hospital, Evidensia Animal Hospital, Helsingborg, Sweden.
Svensson, Maria
  • Equine Clinic, University Animal Hospital, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Riihimäki, Miia
  • Department of Clinical Sciences, Equine Medicine Unit, Swedish University of Agricultural Sciences, Uppsala, Sweden.

MeSH Terms

  • Animals
  • Colic / veterinary
  • Gastrointestinal Diseases / veterinary
  • Horse Diseases / diagnosis
  • Horse Diseases / drug therapy
  • Horse Diseases / epidemiology
  • Horses
  • Infarction / complications
  • Infarction / diagnosis
  • Infarction / veterinary
  • Peritonitis / diagnosis
  • Peritonitis / drug therapy
  • Peritonitis / veterinary
  • Retrospective Studies
  • Strongylus
  • Vascular Diseases / veterinary

Conflict of Interest Statement

The authors declare that they have no competing interests.

References

This article includes 39 references
  1. Golland LC, Hodgson DR, Hodgson JL, Brownlow MA, Hutchins DR, Rawlinson RJ, Collins MB, McClintock SA, Raisis AL. Peritonitis associated with Actinobacillus equuli in horses: 15 cases (1982-1992).. J Am Vet Med Assoc 1994 Jul 15;205(2):340-3.
    pubmed: 7928617
  2. Matthews S, Dart AJ, Dowling BA, Hodgson JL, Hodgson DR. Peritonitis associated with Actinobacillus equuli in horses: 51 cases.. Aust Vet J 2001 Aug;79(8):536-9.
  3. Odelros E, Kendall A, Hedberg-Alm Y, Pringle J. Idiopathic peritonitis in horses: a retrospective study of 130 cases in Sweden (2002-2017).. Acta Vet Scand 2019 Apr 25;61(1):18.
    doi: 10.1186/s13028-019-0456-2pmc: PMC6485108pubmed: 31023351google scholar: lookup
  4. Pihl TH, Nielsen MK, Olsen SN, Leifsson PS, Jacobsen S. Nonstrangulating intestinal infarctions associated with Strongylus vulgaris: Clinical presentation and treatment outcomes of 30 horses (2008-2016).. Equine Vet J 2018 Jul;50(4):474-480.
    doi: 10.1111/evj.12779pubmed: 29112788google scholar: lookup
  5. White NA 2nd. Intestinal infarction associated with mesenteric vascular thrombotic disease in the horse.. J Am Vet Med Assoc 1981 Feb 1;178(3):259-62.
    pubmed: 7228781
  6. Mair TS, Pearson GR. Multifocal non-strangulating intestinal infarction associated with larval cyathostomiasis in a pony.. Equine Vet J 1995 Mar;27(2):154-5.
  7. Spanton JA, Mair TS, Sherlock CE. Non-strangulating intestinal infarction in horses in the UK: A review of 15 cases. Equine Vet Educ 2019;32:603–610.
    doi: 10.1111/eve.13129google scholar: lookup
  8. Vibe-Petersen G, Nielsen K. [Verminous enteritis and thrombo-embolic colic in the horse. A description of 36 cases (author's transl)].. Nord Vet Med 1979 Sep;31(9):385-91.
    pubmed: 492971
  9. Nielsen MK, Jacobsen S, Olsen SN, Bousquet E, Pihl T. Nonstrangulating intestinal infarction associated with Strongylus vulgaris in referred Danish equine cases.. Equine Vet J 2016 May;48(3):376-9.
    doi: 10.1111/evj.12422pubmed: 25604521google scholar: lookup
  10. Nielsen MK, Vidyashankar AN, Olsen SN, Monrad J, Thamsborg SM. Strongylus vulgaris associated with usage of selective therapy on Danish horse farms-is it reemerging?. Vet Parasitol 2012 Oct 26;189(2-4):260-6.
    doi: 10.1016/j.vetpar.2012.04.039pubmed: 22703964google scholar: lookup
  11. Tydén E, Enemark HL, Franko MA, Höglund J, Osterman-Lind E. Prevalence of Strongylus vulgaris in horses after ten years of prescription usage of anthelmintics in Sweden.. Vet Parasitol X 2019 Nov;2:100013.
    doi: 10.1016/j.vpoa.2019.100013pmc: PMC7458386pubmed: 32904767google scholar: lookup
  12. Hedberg-Alm Y, Penell J, Riihimäki M, Osterman-Lind E, Nielsen MK, Tydén E. Parasite Occurrence and Parasite Management in Swedish Horses Presenting with Gastrointestinal Disease-A Case-Control Study.. Animals (Basel) 2020 Apr 7;10(4).
    doi: 10.3390/ani10040638pmc: PMC7222828pubmed: 32272754google scholar: lookup
  13. McCraw BM, Slocombe JO. Strongylus vulgaris in the horse: a review.. Can Vet J 1976 Jun;17(6):150-7.
    pmc: PMC1697226pubmed: 779947
  14. Borji H, Moosavi Z, Ahmadi F. Cranial Mesenteric Arterial Obstruction Due To Strongylus vulgaris Larvae in a Donkey (Equus asinus).. Iran J Parasitol 2014 Sep;9(3):441-4.
    pmc: PMC4316578pubmed: 25678931
  15. Nielsen MK, Scare J, Gravatte HS, Bellaw JL, Prado JC, Reinemeyer CR. Changes in Serum Strongylus Vulgaris-Specific Antibody Concentrations in Response to Anthelmintic Treatment of Experimentally Infected Foals.. Front Vet Sci 2015;2:17.
    doi: 10.3389/fvets.2015.00017pmc: PMC4672185pubmed: 26664946google scholar: lookup
  16. Stewart AJ. Actinobacillus pleuritis and peritonitis in a quarter horse mare.. Vet Clin North Am Equine Pract 2006 Apr;22(1):e77-93.
    doi: 10.1016/j.cveq.2005.12.023pubmed: 16627097google scholar: lookup
  17. Jacobsen S. Review of Equine Acute-Phase Proteins. AAEP Proceedings Vol 53. 2007.
  18. Enigk K. Zur Entwicklung von Strongylus vulgaris (Nematoden) im Wirtstier. Z Tropenmed Parasitol 1950;2:287–306.
  19. Drudge JH, Lyons ET, Szanto J. Pathogenesis of migrating stages of helmimths, with special reference to Strongylus vulgaris. In: Soulsby EJL, editor. Biology of parasites. Emphasis on veterinary parasites. New York and London: Academic Press Inc; 1966. pp. 199–214.
  20. Duncan JL, Pirie HM. The pathogenesis of single experimental infections with Strongylus vulgaris in foals.. Res Vet Sci 1975 Jan;18(1):82-93.
    doi: 10.1016/S0034-5288(18)33635-Xpubmed: 1118668google scholar: lookup
  21. Drudge JH. Clinical aspects of Strongylus vulgaris infection in the horse. Emphasis on diagnosis, chemotherapy, and prophylaxis.. Vet Clin North Am Large Anim Pract 1979 Nov;1(2):251-65.
    pubmed: 399708doi: 10.1016/s0196-9846(17)30183-0google scholar: lookup
  22. Fjordbakk T, Gunnes G. Circumferential Ileal Rupture due to Verminous Arteritis in a Pony: A Case Report. J Eq Vet Sci 2012;32:638–640.
  23. Lilliehöök I, Tvedten HW, Bröjer J, Edner A, Nostell K. Time-related changes in equine neutrophils after experimental endotoxemia: myeloperoxidase staining, size, and numbers.. Vet Clin Pathol 2016 Mar;45(1):66-72.
    doi: 10.1111/vcp.12334pubmed: 26918552google scholar: lookup
  24. Wallace KD, Selcer BA, Tyler DE, Brown J. Transrectal ultrasonography of the cranial mesenteric artery of the horse.. Am J Vet Res 1989 Oct;50(10):1699-703.
    pubmed: 2679249
  25. Mair TS, Hillyer MH, Taylor FG. Peritonitis in adult horses: a review of 21 cases.. Vet Rec 1990 Jun 9;126(23):567-70.
    pubmed: 2368303
  26. Rycroft AN, Garside LH. Actinobacillus species and their role in animal disease.. Vet J 2000 Jan;159(1):18-36.
    doi: 10.1053/tvjl.1999.0403pubmed: 10640409google scholar: lookup
  27. DIMOCK WW, EDWARDS PR, BRUNER DW. Infections observed in equine fetuses and foals.. Cornell Vet 1947 Apr;37(2):89-99.
    pubmed: 20243963
  28. Coles GC, Bauer C, Borgsteede FH, Geerts S, Klei TR, Taylor MA, Waller PJ. World Association for the Advancement of Veterinary Parasitology (W.A.A.V.P.) methods for the detection of anthelmintic resistance in nematodes of veterinary importance.. Vet Parasitol 1992 Sep;44(1-2):35-44.
    doi: 10.1016/0304-4017(92)90141-Upubmed: 1441190google scholar: lookup
  29. Bellaw JL, Nielsen MK. Evaluation of Baermann apparatus sedimentation time on recovery of Strongylus vulgaris and S. edentatus third stage larvae from equine coprocultures.. Vet Parasitol 2015 Jun 30;211(1-2):99-101.
    doi: 10.1016/j.vetpar.2015.05.001pubmed: 25976635google scholar: lookup
  30. RUSSELL AF. The development of helminthiasis in thoroughbred foals.. J Comp Pathol Ther 1948 Apr;58(2):107-27.
    doi: 10.1016/S0368-1742(48)80009-3pubmed: 18861669google scholar: lookup
  31. Nielsen MK, Peterson DS, Monrad J, Thamsborg SM, Olsen SN, Kaplan RM. Detection and semi-quantification of Strongylus vulgaris DNA in equine faeces by real-time quantitative PCR.. Int J Parasitol 2008 Mar;38(3-4):443-53.
    doi: 10.1016/j.ijpara.2007.07.014pubmed: 17889881google scholar: lookup
  32. Beroza GA, Marcus LC, Williams R. Laboratory diagnosis of Anoplocephala perfoliata infection in horses. Proc Am Assoc Equine Pract 1987;32:435–439.
  33. R Core Team. R: A language and environment for statistical computing. R. Foundation for Statistical Computing, Vienna, Austria. 2020.
  34. Hummel M, Edelmann D, Kopp-Schneider A. Clustering of samples and variables with mixed-type data.. PLoS One 2017;12(11):e0188274.
  35. Hummel M, Edelmann D, Kopp-Schneider A. CluMix R package version 2.3.1. 2019.
  36. Yoshida K, Bartel A. Tableone: Create 'Table 1' to Describe Baseline Characteristics with or without Propensity Score Weights. R package version 0.12.0. 2020.
  37. Schratz P. R package 'oddsratio': Odds ratio calculation for GAM(M)s & GLM(M)s, version: 1.0.2. 2017.
    doi: 10.5281/zenodo.1095472google scholar: lookup
  38. Venables WN, Ripley BD. Modern Applied Statistics with S. 4. New York: Springer; 2002.
  39. Hastie T. gam: Generalized Additive Models. R package version 1.20. 2020.

Citations

This article has been cited 5 times.
  1. Halvarsson P, Tydén E. The complete ITS2 barcoding region for Strongylus vulgaris and Strongylus edentatus. Vet Res Commun 2023 Sep;47(3):1767-1771.
    doi: 10.1007/s11259-022-10067-wpubmed: 36598645google scholar: lookup
  2. Nielsen MK, Pyatt A, Perrett J, Tydén E, van Doorn D, Pihl TH, Schmidt JS, von Samson-Himmelstjerna G, Beasley A, Abbas G, Jabbar A. Global equine parasite control guidelines: Consensus or confusion?. Int J Parasitol Drugs Drug Resist 2025 Aug;28:100600.
    doi: 10.1016/j.ijpddr.2025.100600pubmed: 40472642google scholar: lookup
  3. Tharwat M, Al-Sobayil F. Equine colic: A comprehensive overview of the sonographic evaluation, diagnostic criteria, and management of different categories. Open Vet J 2025 Mar;15(3):1116-1139.
    doi: 10.5455/OVJ.2025.v15.i3.5pubmed: 40276205google scholar: lookup
  4. Hedberg-Alm Y, Tydén E, Tamminen LM, Lindström L, Anlén K, Svensson M, Riihimäki M. Correction: Clinical features and treatment response to differentiate idiopathic peritonitis from non‑strangulating intestinal infarction of the pelvic flexure associated with Strongylus Vulgaris infection in the horse. BMC Vet Res 2025 Apr 14;21(1):265.
    doi: 10.1186/s12917-024-04388-ypubmed: 40223049google scholar: lookup
  5. Hedberg Alm Y, Tydén E, Martin F, Lernå J, Halvarsson P. Farm size and biosecurity measures associated with Strongylus vulgaris infection in horses. Equine Vet J 2025 May;57(3):703-711.
    doi: 10.1111/evj.14212pubmed: 39171858google scholar: lookup