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Veterinary surgery : VS2009; 38(6); 762-769; doi: 10.1111/j.1532-950X.2009.00564.x

Acute phase response to surgery of varying intensity in horses: a preliminary study.

Abstract: To evaluate the postoperative inflammatory response of horses to elective surgery of varying intensity. Methods: Prospective longitudinal study. Methods: Horses referred to 2 hospitals for either arthroscopic removal of a unilateral osteochondritic lesion in the tibiotarsal joint (minimal surgical trauma, n=11), correction of recurrent laryngeal neuropathy by laryngoplasty and ventriculectomy (intermediate surgical trauma, n=10) or removal of an ovarian tumor by laparotomy (major surgical trauma, n=5). Methods: Horses had a thorough clinical examination every day. White blood cell (WBC) counts and concentrations of serum amyloid A (SAA), fibrinogen, and iron were assessed in blood samples obtained before, and 1-3, 5, 7, 9, and 11 days after surgery. Differences in levels of the inflammatory markers between the 3 surgical groups were analyzed using repeated measures ANOVA. Results: Postoperative concentrations of SAA and fibrinogen were significantly higher in horses that had laparotomy and ovariectomy than in horses that had laryngoplasty and ventriculectomy, or arthroscopy. Iron concentrations decreased to lower levels after intermediate and major surgical trauma than after small surgical trauma. WBC count did not differ between the 3 groups. Conclusions: Levels of SAA, fibrinogen, and iron reflected the intensity of the surgical trauma, whereas WBC count did not. Conclusions: Postoperative measurements of SAA, fibrinogen, and iron may be useful for comparing surgical trauma associated with new and established surgical techniques. Moreover, knowledge of the normal postoperative acute phase response is essential, if acute phase reactants are to be used for monitoring occurrence of postoperative infections.
Publication Date: 2009-08-14 PubMed ID: 19674420DOI: 10.1111/j.1532-950X.2009.00564.xGoogle Scholar: Lookup
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  • Journal Article
  • Multicenter Study
  • Research Support
  • Non-U.S. Gov't

Summary

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This research examines the postoperative inflammation response in horses after different types of surgeries ranging from minimal to major surgical trauma. The study compares the levels of several inflammation markers such as serum amyloid A, fibrinogen, iron, and white blood cell counts. The findings show a distinct correlation between the severity of the surgical trauma and changes in the levels of certain markers; however, the white blood cell count wasn’t significantly varied.

Research Methodology

  • The researchers conducted a prospective longitudinal research involving horses who had been referred to two veterinary hospitals for different intensities of surgeries. These included arthroscopic removal of a unilateral osteochondritic lesion in the tibiotarsal joint (considered as minimal surgical trauma, with 11 horses), correction of recurrent laryngeal neuropathy by laryngoplasty and ventriculectomy (intermediate surgical trauma, with 10 horses), or removal of an ovarian tumor by laparotomy (major surgical trauma, with 5 horses).
  • Each horse was carefully examined on a daily basis. Blood samples were drawn before the surgeries and 1-3, 5, 7, 9, and 11 days afterward. These samples were used to assess white blood cell counts and concentration levels of serum amyloid A (SAA), fibrinogen, and iron.
  • Differences in the levels of inflammatory markers between the three groups were analyzed using repeated measures ANOVA (analysis of variance), a statistical method for comparing the means of three or more groups.

Results and Findings

  • In the postoperative period, horses that went through laparotomy and ovariectomy showed significantly higher concentrations of SAA and fibrinogen compared to horses who underwent laryngoplasty, ventriculectomy, or arthroscopy.
  • Iron concentrations declined to lower levels following intermediate and major surgical traumas than after small surgical trauma.
  • There was no significant variation in the white blood cell counts across the three groups regardless of the intensity of the surgical trauma.
  • The levels of SAA, fibrinogen, and iron mirrored the intensity of the surgical trauma, implying these markers could be accurately used to measure the level of surgical trauma.

Conclusions and Implications

  • Postoperative measurements of SAA, fibrinogen, and iron may prove useful in comparing the extent of surgical trauma associated with new and conventional surgical techniques.
  • Understanding the normal postoperative acute phase response is critical when using acute phase reactants such as SAA, fibrinogen, and iron for the monitoring of postoperative infections occurrence.

Cite This Article

APA
Jacobsen S, Nielsen JV, Kjelgaard-Hansen M, Toelboell T, Fjeldborg J, Halling-Thomsen M, Martinussen T, Thoefner MB. (2009). Acute phase response to surgery of varying intensity in horses: a preliminary study. Vet Surg, 38(6), 762-769. https://doi.org/10.1111/j.1532-950X.2009.00564.x

Publication

ISSN: 1532-950X
NlmUniqueID: 8113214
Country: United States
Language: English
Volume: 38
Issue: 6
Pages: 762-769

Researcher Affiliations

Jacobsen, Stine
  • Department of Large Animal Sciences, Faculty of Life Sciences, University of Copenhagen, DK-2630 Taastrup, Denmark. stj@life.ku.dk
Nielsen, Jon Vedding
    Kjelgaard-Hansen, Mads
      Toelboell, Trine
        Fjeldborg, Julie
          Halling-Thomsen, Maj
            Martinussen, Torben
              Thoefner, Martin Bang

                MeSH Terms

                • Acute-Phase Reaction / blood
                • Acute-Phase Reaction / veterinary
                • Animals
                • Biomarkers
                • Female
                • Fibrinogen / metabolism
                • Horse Diseases / blood
                • Horse Diseases / surgery
                • Horses
                • Iron / blood
                • Leukocyte Count / veterinary
                • Male
                • Serum Amyloid A Protein / metabolism
                • Surgical Procedures, Operative / adverse effects
                • Surgical Procedures, Operative / veterinary

                Citations

                This article has been cited 31 times.
                1. Satué K, Fazio E, La Fauci D, Medica P. Changes of Hepcidin, Ferritin and Iron Levels in Cycling Purebred Spanish Mares.. Animals (Basel) 2023 Mar 31;13(7).
                  doi: 10.3390/ani13071229pubmed: 37048485google scholar: lookup
                2. Blangy-Letheule A, Vergnaud A, Dupas T, Rozec B, Lauzier B, Leroux AA. Spontaneous Sepsis in Adult Horses: From Veterinary to Human Medicine Perspectives.. Cells 2023 Mar 30;12(7).
                  doi: 10.3390/cells12071052pubmed: 37048125google scholar: lookup
                3. Peixoto Rabelo I, Barroco de Paula V, Carvalho Bustamante C, Santana AM, Gomes da Silva D, Baldassi AC, Canola PA, Araújo Valadão CA. Acute phase proteins levels in horses, after a single carbohydrate overload, associated with cecal alkalinization.. Front Vet Sci 2023;10:1043656.
                  doi: 10.3389/fvets.2023.1043656pubmed: 36816195google scholar: lookup
                4. Murakami Y, Tsukano K, Hirata H, Suzuki K. Evaluation of blood serum iron concentration as an alternative biomarker for inflammation in dairy cows.. Biol Trace Elem Res 2023 Oct;201(10):4710-4717.
                  doi: 10.1007/s12011-022-03544-5pubmed: 36622523google scholar: lookup
                5. Thurston CC, Stefanovski D, MacKinnon MC, Chapman HS, Richardson DW, Levine DG. Serum amyloid A and fibrinogen as markers for early detection of surgical site infection associated with internal fixation in the horse.. Front Vet Sci 2022;9:960865.
                  doi: 10.3389/fvets.2022.960865pubmed: 36299628google scholar: lookup
                6. Przewoźny M, Senderska-Płonowska M, Rząsa A, Wierzbicki H, Borkowski J, Swagemakers JH, Żak-Bochenek A, Stefaniak T. Usefulness of Selected Acute-Phase Proteins in the Postsurgical Monitoring of Arthroscopy and Splint Bone Removal in Horses.. Animals (Basel) 2021 Oct 13;11(10).
                  doi: 10.3390/ani11102952pubmed: 34679973google scholar: lookup
                7. Arfuso F, Giudice E, Di Pietro S, Piccione G, Giannetto C. Modulation of Serum Protein Electrophoretic Pattern and Leukocyte Population in Horses Vaccinated against West Nile Virus.. Animals (Basel) 2021 Feb 11;11(2).
                  doi: 10.3390/ani11020477pubmed: 33670395google scholar: lookup
                8. Del Romero A, Cuervo B, Peláez P, Miguel L, Torres M, Yeste M, Rivera Del Alamo MM, Rubio CP, Rubio M. Changes in Acute Phase Proteins in Bitches after Laparoscopic, Midline, and Flank Ovariectomy Using the Same Method for Hemostasis.. Animals (Basel) 2020 Nov 27;10(12).
                  doi: 10.3390/ani10122223pubmed: 33260846google scholar: lookup
                9. Yoshimura S, Koziy RV, Dickinson R, Moshynskyy I, McKenzie JA, Simko E, Bracamonte JL. Use of serum amyloid A in serum and synovial fluid to detect eradication of infection in experimental septic arthritis in horses.. Can J Vet Res 2020 Jul;84(3):198-204.
                  pubmed: 32801454
                10. Wilmink JM, Ladefoged S, Jongbloets A, Vernooij JCM. The evaluation of the effect of probiotics on the healing of equine distal limb wounds.. PLoS One 2020;15(7):e0236761.
                  doi: 10.1371/journal.pone.0236761pubmed: 32726347google scholar: lookup
                11. Sinovich M, Villarino NF, Singer E, Robinson CS, Rubio-Martínez LM. Can blood serum amyloid A concentrations in horses differentiate synovial sepsis from extrasynovial inflammation and determine response to treatment?. Vet Rec 2020 Sep 19;187(6):235.
                  doi: 10.1136/vr.105153pubmed: 32098906google scholar: lookup
                12. Long A, Nolen-Walston R. Equine Inflammatory Markers in the Twenty-First Century: A Focus on Serum Amyloid A.. Vet Clin North Am Equine Pract 2020 Apr;36(1):147-160.
                  doi: 10.1016/j.cveq.2019.12.005pubmed: 32007299google scholar: lookup
                13. Hooijberg EH, Cray C, Steenkamp G, Buss P, Goddard A, Miller M. Assessment of the Acute Phase Response in Healthy and Injured Southern White Rhinoceros (Ceratotherium simum simum).. Front Vet Sci 2019;6:475.
                  doi: 10.3389/fvets.2019.00475pubmed: 31998761google scholar: lookup
                14. Tothova C, Novotny J, Nagy O, Hornakova P, Zert Z, Varga M, Medvecky L, Vdoviakova K, Danko J, Petrovova E. Changes in the Acute-Phase Protein Concentrations and Activities of Some Enzymes in Pigs Following the Repair of Experimentally Induced Articular Cartilage Defects Using Two Types of Biocement Powder.. Animals (Basel) 2019 Nov 7;9(11).
                  doi: 10.3390/ani9110931pubmed: 31703315google scholar: lookup
                15. Stack JD, Cousty M, Steele E, Handel I, Lechartier A, Vinardell T, David F. Comparison of Serum Amyloid A Measurements in Equine Synovial Fluid With Routine Diagnostic Methods to Detect Synovial Infection in a Clinical Environment.. Front Vet Sci 2019;6:325.
                  doi: 10.3389/fvets.2019.00325pubmed: 31632987google scholar: lookup
                16. Tsukano K, Shimamori T, Fukuda T, Nishi Y, Otsuka M, Kitade Y, Suzuki K. Serum iron concentration as a marker of inflammation in young cows that underwent dehorning operation.. J Vet Med Sci 2019 Apr 27;81(4):626-628.
                  doi: 10.1292/jvms.19-0002pubmed: 30828032google scholar: lookup
                17. Tothova C, Mihajlovicova X, Novotny J, Nagy O, Giretova M, Kresakova L, Tomco M, Zert Z, Vilhanova Z, Varga M, Medvecky L, Petrovova E. The Serum Protein Profile and Acute Phase Proteins in the Postoperative Period in Sheep after Induced Articular Cartilage Defect.. Materials (Basel) 2019 Jan 3;12(1).
                  doi: 10.3390/ma12010142pubmed: 30609876google scholar: lookup
                18. Witkowska-Piłaszewicz OD, Żmigrodzka M, Winnicka A, Miśkiewicz A, Strzelec K, Cywińska A. Serum amyloid A in equine health and disease.. Equine Vet J 2019 May;51(3):293-298.
                  doi: 10.1111/evj.13062pubmed: 30565319google scholar: lookup
                19. Kaiser M, Jacobson M, Andersen PH, Bækbo P, Cerón JJ, Dahl J, Escribano D, Jacobsen S. Inflammatory markers before and after farrowing in healthy sows and in sows affected with postpartum dysgalactia syndrome.. BMC Vet Res 2018 Mar 12;14(1):83.
                  doi: 10.1186/s12917-018-1382-7pubmed: 29530043google scholar: lookup
                20. Musk GC, Jacobsen S, Hyndman TH, Lehmann HS, Tuke SJ, Collins T, Gleerup KB, Johnson CB, Laurence M. Objective Measures for the Assessment of Post-Operative Pain in Bos indicus Bull Calves Following Castration.. Animals (Basel) 2017 Sep 28;7(10).
                  doi: 10.3390/ani7100076pubmed: 28956843google scholar: lookup
                21. Andreassen SM, Vinther AML, Nielsen SS, Andersen PH, Tnibar A, Kristensen AT, Jacobsen S. Changes in concentrations of haemostatic and inflammatory biomarkers in synovial fluid after intra-articular injection of lipopolysaccharide in horses.. BMC Vet Res 2017 Jun 19;13(1):182.
                  doi: 10.1186/s12917-017-1089-1pubmed: 28629364google scholar: lookup
                22. Haltmayer E, Schwendenwein I, Licka TF. Course of serum amyloid A (SAA) plasma concentrations in horses undergoing surgery for injuries penetrating synovial structures, an observational clinical study.. BMC Vet Res 2017 May 22;13(1):137.
                  doi: 10.1186/s12917-017-1057-9pubmed: 28532514google scholar: lookup
                23. Turło A, Cywińska A, Czopowicz M, Witkowski L, Niedźwiedź A, Słowikowska M, Borowicz H, Jaśkiewicz A, Winnicka A. The Effect of Different Types of Musculoskeletal Injuries on Blood Concentration of Serum Amyloid A in Thoroughbred Racehorses.. PLoS One 2015;10(10):e0140673.
                  doi: 10.1371/journal.pone.0140673pubmed: 26466121google scholar: lookup
                24. Pihl TH, Scheepers E, Sanz M, Goddard A, Page P, Toft N, Andersen PH, Jacobsen S. Influence of disease process and duration on acute phase proteins in serum and peritoneal fluid of horses with colic.. J Vet Intern Med 2015 Mar-Apr;29(2):651-8.
                  doi: 10.1111/jvim.12542pubmed: 25644457google scholar: lookup
                25. Hooijberg EH, van den Hoven R, Tichy A, Schwendenwein I. Diagnostic and predictive capability of routine laboratory tests for the diagnosis and staging of equine inflammatory disease.. J Vet Intern Med 2014 Sep-Oct;28(5):1587-93.
                  doi: 10.1111/jvim.12404pubmed: 25056342google scholar: lookup
                26. Kristensen L, Buhl R, Nostell K, Bak L, Petersen E, Lindholm M, Jacobsen S. Acute exercise does not induce an acute phase response (APR) in Standardbred trotters.. Can J Vet Res 2014 Apr;78(2):97-102.
                  pubmed: 24688170
                27. Bundgaard L, Jacobsen S, Sørensen MA, Sun Z, Deutsch EW, Moritz RL, Bendixen E. The Equine PeptideAtlas: a resource for developing proteomics-based veterinary research.. Proteomics 2014 Mar;14(6):763-73.
                  doi: 10.1002/pmic.201300398pubmed: 24436130google scholar: lookup
                28. Cywinska A, Witkowski L, Szarska E, Schollenberger A, Winnicka A. Serum amyloid A (SAA) concentration after training sessions in Arabian race and endurance horses.. BMC Vet Res 2013 May 1;9:91.
                  doi: 10.1186/1746-6148-9-91pubmed: 23634727google scholar: lookup
                29. Cray C. Acute phase proteins in animals.. Prog Mol Biol Transl Sci 2012;105:113-50.
                30. Hansson M, Lundeheim N, Nyman G, Johansson G. Effect of local anaesthesia and/or analgesia on pain responses induced by piglet castration.. Acta Vet Scand 2011 May 31;53(1):34.
                  doi: 10.1186/1751-0147-53-34pubmed: 21627797google scholar: lookup
                31. Hillström A, Tvedten H, Lilliehöök I. Evaluation of an in-clinic Serum Amyloid A (SAA) assay and assessment of the effects of storage on SAA samples.. Acta Vet Scand 2010 Feb 2;52(1):8.
                  doi: 10.1186/1751-0147-52-8pubmed: 20122257google scholar: lookup