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Frontiers in veterinary science2024; 11; 1399815; doi: 10.3389/fvets.2024.1399815

Functional infrared thermography imaging can be used to assess the effectiveness of Maxicam Gel® in pre-emptively treating transient synovitis and lameness in horses.

Abstract: Diagnosing and treating lameness in horses is essential to improving their welfare. In equine orthopedic practice, infrared thermography (IRT) can indirectly detect soreness. Non-steroidal anti-inflammatory drugs can treat painful and inflammatory processes in horses. Using IRT, the efficacy of meloxicam (Maxicam Gel) was evaluated in pre-treating transient synovitis in horses induced by a middle carpal joint injection of lipopolysaccharides (LPS) from 055:B5 at a dose of 10 endotoxin units. Unassigned: In a cross-over design, six healthy horses were randomly assigned to receive either 0.6 mg/kg of oral Maxicam Gel (MAXVO) or a mock administration (control group, C) following a two-week washout period. IRT of the middle carpal joint, visual lameness assessment and joint circumference were recorded over time. Clinical and hematological evaluations were performed. Synovial fluid aspirates were analyzed for total nucleated cell count, total protein, and prostaglandin E. A mixed effects analysis of variance was performed for repeated measures over time, followed by Tukey's test. A multinomial logistic regression was conducted to determine whether there is a relationship between a thermography temperature change and the lameness score. Unassigned: There were no changes in joint circumference. The MAXVO group showed a lower rectal temperature 4 h after synovitis induction. The C group presented an increase in neutrophils and a decrease in total hemoglobin and hematocrit 8 h after induction. No changes were observed in the synovial fluid between groups. The horses that received meloxicam did not show clinically significant lameness at any time, while the C group showed an increase in lameness 2, 4, and 8 h after synovitis induction. Unassigned: IRT indicated that the skin surface temperature of the middle carpal joint was lower in horses who received meloxicam, suggesting a reduction in the inflammatory process induced by LPS. It was observed that the maximum temperature peaks in the dorsopalmar and lateropalmar positions can be utilized to predict the severity of lameness, particularly when the temperature rises above 34°C. Horses pre-treated with meloxicam showed either reduced or no indication of mild to moderate pain and presented a lowehr thermographic temperature, which indicates the effectiveness of Maxicam Gel as an anti-inflammatory.
Publication Date: 2024-06-11 PubMed ID: 38919154PubMed Central: PMC11197459DOI: 10.3389/fvets.2024.1399815Google Scholar: Lookup
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  • 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 shows that Maxicam Gel, an anti-inflammatory medication, can be used to proactively treat inflammation and pain known as transient synovitis in horses, by using infrared thermography imaging to measure its effectiveness.

Research Design and Methodology

  • The study used a cross-over design, allowing each horse to function as its own control over different periods.
  • Six healthy horses were randomly chosen to receive either an oral dose of Maxicam Gel or a placebo, after a two-week washout period.
  • The researchers induced temporary synovitis (inflammation of the joint) by injecting lipopolysaccharides into the middle carpal joint.
  • Infrared thermography was used to assess the affected joint’s temperature at specified intervals. Other measurements taken were visual lameness assessment, joint circumference, and blood tests.
  • Synovial fluid, the fluid present in the joint, was sampled and analysed for total nucleated cell count, total protein, and prostaglandin E (a marker for inflammation).
  • Data analysis included a repeated measures analysis of variance, Tukey’s test, and multinomial logistic regression to identify any relationship between temperature change and lameness score.

Main Findings

  • No change in joint circumference was observed, suggesting the inflammation had not led to gross swelling.
  • Maxicam administered horses showed a lower rectal temperature 4 hours after synovitis induction, suggesting a drop in systemic inflammatory response.
  • There was an increase in neutrophils count and a decrease in total hemoglobin and hematocrit in the control group, indicating an inflammatory response.
  • Synovial fluid analysis did not vary significantly between treatment groups.
  • Variations in lameness were observed, with the control group showing increased lameness, while those administered meloxicam did not exhibit clinically significant lameness at any time.
  • Infrared thermography revealed that horses treated with meloxicam had reduced skin surface temperature of the middle carpal joint, suggesting inflammation reduction after LPS induction.
  • The work found that when the temperature exceeds 34°C at the dorsopalmar and lateropalmar positions, it could predict the severity of lameness.
  • The results show pre-treatment with meloxicam efficaciously reduces or eliminates mild to moderate pain and lowers thermographic temperature, underlining Maxicam Gel’s anti-inflammatory action.

Cite This Article

APA
de Carvalho JRG, Del Puppo D, Littiere TO, de Sales NAA, Silva ACY, Ribeiro G, de Almeida FN, Alves BG, Gatto IRH, Ramos GV, Ferraz GC. (2024). Functional infrared thermography imaging can be used to assess the effectiveness of Maxicam Gel® in pre-emptively treating transient synovitis and lameness in horses. Front Vet Sci, 11, 1399815. https://doi.org/10.3389/fvets.2024.1399815

Publication

ISSN: 2297-1769
NlmUniqueID: 101666658
Country: Switzerland
Language: English
Volume: 11
Pages: 1399815
PII: 1399815

Researcher Affiliations

de Carvalho, Júlia Ribeiro Garcia
  • Laboratory of Equine Exercise Physiology and Pharmacology (LAFEQ), Department of Animal Morphology and Physiology, School of Agricultural and Veterinary Sciences, São Paulo State University, FCAV/UNESP, São Paulo, Brazil.
Del Puppo, Debora
  • Research and Development Department, Ourofino Animal Health Company, São Paulo, Brazil.
Littiere, Thayssa de Oliveira
  • Laboratory of Equine Exercise Physiology and Pharmacology (LAFEQ), Department of Animal Morphology and Physiology, School of Agricultural and Veterinary Sciences, São Paulo State University, FCAV/UNESP, São Paulo, Brazil.
de Sales, Nathali Adrielli Agassi
  • Laboratory of Equine Exercise Physiology and Pharmacology (LAFEQ), Department of Animal Morphology and Physiology, School of Agricultural and Veterinary Sciences, São Paulo State University, FCAV/UNESP, São Paulo, Brazil.
Silva, Ana Carolina Yamamoto
  • Laboratory of Equine Exercise Physiology and Pharmacology (LAFEQ), Department of Animal Morphology and Physiology, School of Agricultural and Veterinary Sciences, São Paulo State University, FCAV/UNESP, São Paulo, Brazil.
Ribeiro, Gesiane
  • Veterinary and Animal Research Centre (CECAV), Faculty of Veterinary Medicine, Lusófona University - Lisbon University Centre, Lisbon, Portugal.
de Almeida, Ferdinando Nielsen
  • Research and Development Department, Ourofino Animal Health Company, São Paulo, Brazil.
Alves, Bruna Gomes
  • Research and Development Department, Ourofino Animal Health Company, São Paulo, Brazil.
Gatto, Igor Renan Honorato
  • Research and Development Department, Ourofino Animal Health Company, São Paulo, Brazil.
Ramos, Gabriel Vieira
  • Equine Sports Medicine Laboratory, Department of Veterinary Medicine and Surgery, School of Agricultural and Veterinary Sciences, São Paulo State University, FCAV/UNESP, São Paulo, Brazil.
Ferraz, Guilherme de Camargo
  • Laboratory of Equine Exercise Physiology and Pharmacology (LAFEQ), Department of Animal Morphology and Physiology, School of Agricultural and Veterinary Sciences, São Paulo State University, FCAV/UNESP, São Paulo, Brazil.

Conflict of Interest Statement

DD, FA, BA, and IG were employed by company Ourofino Animal Health Company. The authors declare that this study received funding from Ourofino Animal Health Company. The funder was involved in the study’s design, writing of this article, and the decision to submit it for publication. The meloxicam was formulated and manufactured by Ourofino Animal Health Company for commercial use in Brazil, and the study was designed to meet Brazilian regulations. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

This article includes 61 references
  1. Whittaker AL, Muns R, Wang D, Martinez-Burnes J, Hernández-Ávalos I, Casas-Alvarado A. Assessment of pain and inflammation in domestic animals using infrared thermography: a narrative review.. Animals (2023) 13:2065.
    doi: 10.3390/ani13132065pmc: PMC10340041pubmed: 37443863google scholar: lookup
  2. Jacobs CC, Schnabel LV, Mcllwraith CW, Blikslager AT. Non-steroidal anti-inflammatory drugs is equine orthopaedics.. Equine Vet J (2022) 54:636–48.
    doi: 10.1111/evj.13561pmc: PMC9304133pubmed: 35076950google scholar: lookup
  3. Knych HK. Nonsteirodal anti-inflammatory drug use in horses.. Vet Clin N Am Equine Pract (2017) 33:1–15.
    doi: 10.1016/j.cveq.2016.11.001pubmed: 28190614google scholar: lookup
  4. Bonnesen K, Schmidt M. Recategorization on non-aspirin nonsteroidal anti-inflammatory drugs according to clinical relevance: abandoning the traditional NSAID terminology.. Can J Cardiol (2021) 37:1707.
    doi: 10.1016/j.cjca.2021.06.014pubmed: 34182020google scholar: lookup
  5. UCVM Class of 2016, Banse H, Cribb AE. Comparative efficacy of oral meloxicam and phenylbutazone in 2 experimental pain models in the horse.. Can Vet J (2017) 58:157–67.
    pmc: PMC5234315pubmed: 28216685
  6. Ziegler A, Fogle C, Blikslager A. Update on the use of cyclooxygenase-2-selective nonsteroidal anti-inflammatory drugs in horses.. J Am Vet Med Assoc (2017) 250:1271–4.
    doi: 10.2460/javma.250.11.1271pmc: PMC5588883pubmed: 28509650google scholar: lookup
  7. Khalil NY, Aldosari KF. Meloxicam. Profiles of drug substances, excipients and related methodology London: Academic Press; (2020). 159–97.
    pubmed: 32164967
  8. Yuan Y, Cui D, Zhang Y. Preemptive meloxicam achieves a better effect on postoperative pain control and similar tolerance compared with postoperative meloxicam in patients receiving arthroscopic knee surgery.. Inflammopharmacology (2019) 27:1091–100.
    doi: 10.1007/s10787-019-00614-4pubmed: 31254137google scholar: lookup
  9. Toutain PL, Cester CC. Pharmacokinetic-pharmacodynamic relationships and dose response to meloxicam in horses with induced arthritis in the right carpal joint.. Am J Vet Res (2004) 65:1533–41.
    doi: 10.2460/ajvr.2004.65.1533pubmed: 15566092google scholar: lookup
  10. de Grauw JC, van de Lest CHA, Brama PAJ, Rambags BPB, van Weeren PR. In vivo effects of meloxicam on inflammatory mediators, MMP activity and cartilage biomarkers in equine joints with acute synovitis.. Equine Vet J (2009) 41:693–9.
    doi: 10.2746/042516409x436286pubmed: 19927589google scholar: lookup
  11. van de Water E, Oosterlinck M, Korthagen NM, Duchateau L, Dumoulin M, van Weeren PR. The lipopolysaccharide model for the experimental induction of transient lameness and synovitis in Standardbred horses.. Vet J (2021) 270:105626.
    doi: 10.1016/j.tvjl.2021.105626pubmed: 33641810google scholar: lookup
  12. van de Water E, Oosterlinck M, Dumoulin M, Korthagen NM, van Weeren PR, van den Broek J. The preventive effects of two nutraceuticals on experimentally induced acute synovitis.. Equine Vet J (2017) 49:532–8.
    doi: 10.1111/evj.12629pmc: PMC5484312pubmed: 27554764google scholar: lookup
  13. Redaelli V, Bergero D, Zucca E, Ferrucci F, Costa LN, Crosta L. Use of thermography techniques in equines: principles and applications.. J Equine Vet (2014) 34:345–50.
  14. Soroko M, Howell K. Infrared thermography: current applications in equine medicine.. J Equine Vet (2018) 60:90–6.
  15. Schiavon G, Capone G, Frize M, Zaffagnini S, Candrian C, Filardo G. Infrared thermography for the evaluation of inflammatory and degenerative joint diseases: a systematic review.. Cartilage (2021) 13:1790S–801S.
    doi: 10.1177/19476035211063862pmc: PMC8804782pubmed: 34933442google scholar: lookup
  16. Kruljc P. Thermographic examination of the horse.. Acta Vet (2023) 73:289–316.
    doi: 10.2478/acve-2023-0023google scholar: lookup
  17. Daglish J, Le Jeune SS, Pypendop BH, Ramirez EM, Turner TA. Use of infrared thermography to detect jugular venipuncture in the horse.. J Equine Vet (2017) 59:1–6.
  18. Prochno HC, Barussi FM, Bastos FZ, Weber SH, Bechara GH, Rehan IF. Infrared thermography applied to monitoring musculoskeletal adaptation to training in thoroughbred race horses.. J Equine Vet (2020) 87:102935.
    doi: 10.1016/j.jevs.2020.102935pubmed: 32172920google scholar: lookup
  19. Silva CJFL, Trindade KTG, Cruz RKS, Vilela CF, Coelho CS, Ribeiro-Filho JD. Association between infrared thermography, blood count and creatine kinase in the evaluation of the welfare of Vaquejada horses.. Open J Vet Med (2023) 13:53–67.
    doi: 10.4236/ojvm.2023.136006google scholar: lookup
  20. Witkowska-Piłaszewicz O, Masko M, Domino M, Winnicka A. Infrared thermography correlates with lactate concentration in blood during race training in horses.. Animals (2020) 10:2072.
    doi: 10.3390/ani10112072pmc: PMC7695344pubmed: 33182281google scholar: lookup
  21. Janczarek I, Wiśniewska A, Tkaczyk E, Wnuk-Pawlak E, Kaczmarek B, Liss-Szczepanek M. Effect of different water-cooling treatments on changes in rectal and surface body temperature in leisure horses after medium-intensity effort.. Animals (2022) 12:525.
    doi: 10.3390/ani12040525pmc: PMC8868132pubmed: 35203233google scholar: lookup
  22. Verdegaal ELJMM, Howarth GS, McWhorter TJ, Delesalle CJG. Thermoregulation during field exercise in horses using skin temperature monitoring.. Animals (2024) 14:136.
    doi: 10.3390/ani14010136pmc: PMC10777899pubmed: 38200867google scholar: lookup
  23. Kim SM, Cho GJ. Validation of eye temperature assessed using infrared thermography as an indicator of welfare in horses.. Appl Sci (2021) 11:7186.
    doi: 10.3390/app11167186google scholar: lookup
  24. Domino M, Borowska M, Kozlowska N, Zdrojkowski L, Jasinski T, Smyth G. Advances in thermal image analysis for the detection of pregnancy in horses using infrared thermography.. Sensors (2022) 22:191.
    doi: 10.3390/s22010191pmc: PMC8749616pubmed: 35009733google scholar: lookup
  25. Urayama S, Tanaka A, Kusano K, Sato H, Muranaka M, Mita H. Oral administration of meloxicam and flunixin meglumine have similar analgesic effects after lipopolysaccharide-induced inflammatory response in thoroughbred horses.. J Equine Vet (2023) 121:104205.
    doi: 10.1016/j.jevs.2022.104205pubmed: 36586521google scholar: lookup
  26. Lisboa BRF, Silva JAR, Silva WC, Barbosa AVC, Silva LKX, Lourenço-Júnior JB. Evaluation of thermoregulation of horses (Equus caballus) submitted to two methods of post-exercise cooling, in hot and humid climate conditions, in the Eastern Amazon.. Front Vet Sci (2023) 10:1150763.
    doi: 10.3389/fvets.2023.1150763pmc: PMC10149968pubmed: 37138916google scholar: lookup
  27. Carvalho JRG, Conde G, Antonioli ML, Dias PP, Vasconcelos RO, Taboga SR. Biocompatibility and biodegradation of poly (lactic acid)(PLA) and an immiscible PLA/poly (ε-caprolactone) (PCL) blend compatibilized by poly (ε-caprolactone-b-tetrahydrofuran) implanted in horses.. Polym J (2020) 52:629–43.
    doi: 10.1038/s41428-020-0308-ygoogle scholar: lookup
  28. Carvalho JRG, Trindade PHE, Conde G, Antonioli ML, Funnicelli MIG, Dias PP. Facial expressions of horses using weighted multivariate statistics for assessment of subtle local pain induced by polylactide-based polymers implanted subcutaneously.. Animals (2022) 12:2400.
    doi: 10.3390/ani12182400pmc: PMC9495041pubmed: 36139260google scholar: lookup
  29. Ioannou S. Functional infrared thermal imaging: a contemporary tool in soft tissue screening.. Sci Rep (2020) 10:9303.
    doi: 10.1038/s41598-020-66397-9pmc: PMC7283266pubmed: 32518287google scholar: lookup
  30. Branco JHL, Branco RLL, Siqueira TC, Souza LC, Dalago KMS, Andrade A. Clinical applicability of infrared thermography in rheumatic diseases: a systematic review.. J Therm Biol (2022) 104:103172.
  31. Marziani L, Boffa A, Angelelli L, Andriolo L, Di Martino A, Zaffagnini S. Infrared thermography in symptomatic knee osteoarthritis: joint temperature differs based on patient and pain characteristics.. J Clin Med (2023) 12:2319.
    doi: 10.3390/jcm12062319pmc: PMC10055129pubmed: 36983319google scholar: lookup
  32. Warner R, Kleinhenz M, Ydstie J, Schleining J, Wulf L, Coetzee J. Comparison of analgesics for control of lameness-associated pain in lactating dairy cattle.. J Anim Sci (2019) 97:162–3.
    doi: 10.1093/jas/skz122.287pubmed: 33309349google scholar: lookup
  33. Alves JC, Santos A, Jorge P, Lavrador C, Carreira LM. Evaluation of digital thermography imaging to assess and monitor treatment of police working dogs with naturally occurring hip osteoarthritis.. BMC Vet Res (2021) 17:180.
    doi: 10.1186/s12917-021-02876-zpmc: PMC8088695pubmed: 33933090google scholar: lookup
  34. National Academies of Sciences, Engineering, and Medicine; Division on Earth and Life Studies; Board on Agriculture and Natural Resources; Committee on a Review of Methods for Detecting Soreness in Horses. A review of methods for detecting soreness in horses.. National Academies Press Washington, DC; (2021). 624–6242.
    pubmed: 34251765
  35. Purohit RC, McCoy MD. Thermography in the diagnosis of inflammatory processes in the horse.. Am J Vet Res (1980) 41:1167–74.
    pubmed: 7447110
  36. Higgins AJ, Lees P, Sedgwick AD, Buick AR, Churchus R. Use of a novel non‐steroidal anti‐inflammatory drug in the horse.. Equine Vet J (1987) 19:60–6.
  37. Urayama S, Tanaka A, Kusano K, Sato H, Nagashima T, Fukuda I. Oral administration of meloxicam suppresses low-dose endotoxin challenge-induced pain in thoroughbred horses.. J Equine Vet (2019) 77:139–43.
    doi: 10.1016/j.jevs.2019.03.001pubmed: 31133308google scholar: lookup
  38. Figueiredo T, Dzyekanski B, Pimpão CT, Silveira AB, Capriglione LG, Michelotto PV Jr.. Use of infrared thermography to detect intrasynovial injections in horses.. J Equine Vet (2013) 33:257–60.
  39. Carregaro AB, Freitas GC, Ribeiro MH, Xavier NV, Dória RGS. Physiological and analgesic effects of continuous-rate infusion of morphine, butorphanol, tramadol or methadone in horses with lipopolysaccharide (LPS)-induced carpal synovitis.. BMC Vet Res (2014) 10:1–8.
    doi: 10.1186/s12917-014-0299-zpmc: PMC4297404pubmed: 25528353google scholar: lookup
  40. Fails AD. Functional anatomy of the equine musculoskeletal system. Adams and Stashak’s lameness in horses Hoboken: John Wiley & Sons, Inc. (2020). 1–65.
  41. Byars TD, Gonda KC. Equine history, physical examination, records, and recognizing abuse or neglect in patients. Large animal internal medicine Riverport Lane: Elsevier; (2015). 14.
  42. Noble G, Edwards S, Lievaart J, Pippia J, Boston R, Raidal SL. Pharmacokinetics and safety of single and multiple oral doses of meloxicam in adult horses.. Vet Intern Med (2012) 26:1192–201.
  43. Lucia JL, Coverdale JA, Arnold CE, Winsco KN. Influence of an intra-articular lipopolysaccharide challenge on markers of inflammation and cartilage metabolism in young horses.. J Anim Sci (2013) 91:2693–9.
    doi: 10.2527/jas.2012-5981pubmed: 23508023google scholar: lookup
  44. Guedes A. Pain management in horses.. Vet Clin North Am Equine Pract (2017) 33:181–211.
    doi: 10.1016/j.cveq.2016.11.006pubmed: 28325179google scholar: lookup
  45. Andreassen SM, Vinther AML, Nielsen SS, Andersen PH, Tnibar A, Kristensen AT. Changes in concentrations of haemostatic and inflammatory biomarkers in synovial fluid after intra-articular injection of lipopolysaccharide in horses.. BMC Vet Res (2017) 13:182.
    doi: 10.1186/s12917-017-1089-1pmc: PMC5477303pubmed: 28629364google scholar: lookup
  46. Martinez RE, Leatherwood JL, Arnold CE, Glass KG, Walter KW, Valigura HC. Responses to an intra-articular lipopolysaccharide challenge following dietary supplementation of Saccharomyces cerevisiae fermentation product in young horses.. J Anim Sci (2021) 99:1–8.
    doi: 10.1093/jas/skab272pmc: PMC8557629pubmed: 34619765google scholar: lookup
  47. Wagner AE. Effects of stress on pain in horses and incorporating pain scales for equine practice.. Vet Clin North Am Equine Pract (2010) 26:481–92.
    doi: 10.1016/j.cveq.2010.07.001pubmed: 21056295google scholar: lookup
  48. de Grauw JC, van Loon JPAM. Systematic pain assessment in horses.. Vet J (2016) 209:14–22.
    doi: 10.1016/j.tvjl.2015.07.030pubmed: 26831169google scholar: lookup
  49. Kahn MK, Coverdale JA, Leatherwood JL, Arnold CE, Dabareiner RA, Bradbery AN. Age-related effects on markers of inflammation and cartilage metabolism in response to an intra-articular lipopolysaccharide challenge in horses.. J Anim Sci (2017) 95:671–80.
    doi: 10.2527/jas2016.1078pubmed: 28380609google scholar: lookup
  50. Anderson SL, Singh B. Equine neutrophils and their role in ischemia reperfusion injury and lung inflammation.. Cell Tissue Res (2018) 371:639–48.
    doi: 10.1007/s00441-017-2770-1pubmed: 29335779google scholar: lookup
  51. Sheats MK. A comparative review of equine SIRS, sepsis, and neutrophils.. Front Vet Sci (2019) 6:69.
    doi: 10.3389/fvets.2019.00069pmc: PMC6424004pubmed: 30931316google scholar: lookup
  52. Meleiro MCZ, Carvalho HJC, Ribeiro RR, Silva MD, Gomes CMS, Miglino MA. Immune functions alterations due to racing stress in thoroughbred horses.. Animals (2022) 12:1203.
    doi: 10.3390/ani12091203pmc: PMC9104563pubmed: 35565629google scholar: lookup
  53. Borzio R, Mulchandani N, Pivec R, Kapadia BH, Leven D, Harwin SF. Predictors of septic arthritis in the adult population.. Orthopedics (2016) 39:e657–63.
    doi: 10.3928/01477447-20160606-05pubmed: 27286047google scholar: lookup
  54. Neuenschwander HM, Moreira JJ, Vandruscolo CP, Fülber J, Seidel SRT, Michelacci YM. Hyaluronic acid has chondroprotective and joint-preserving effects on LPS-induced synovitis in horses.. J Vet Sci (2019) 20:e67.
    doi: 10.4142/jvs.2019.20.e67pmc: PMC6883190pubmed: 31775194google scholar: lookup
  55. Rinnovati R, Bonelli F, Tognetti R, Gallo C, Bassini RF, Marchetti V. Effect of repeated arthrocentesis on cytology of synovial fluid.. J Equine Vet (2017) 57:112–5.
  56. Ross TN, Kisiday JD, Hess T, McIlwraith CW. Evaluation of the inflammatory response in experimentally induced synovitis in the horse: a comparison of recombinant equine interleukin 1 beta and lipopolysaccharide.. Osteoarthr Cartil (2012) 20:1583–90.
    doi: 10.1016/j.joca.2012.08.008pubmed: 22917743google scholar: lookup
  57. van den Boom R, van de Lest CHA, Bull S, Brama PAJ, van Weeren PR, Barneveld A. Influence of repeated arthrocentesis and exercise on synovial fluid concentrations of nitric oxide, prostaglandin E2 and glycosaminoglycans in healthy equine joints.. Equine Vet J (2005) 37:250–6.
    doi: 10.2746/0425164054530740pubmed: 15892235google scholar: lookup
  58. NCR TM, van Weeren PR. How exercise influences equine joint homeostasis.. Vet J (2017) 222:60–7.
    doi: 10.1016/j.tvjl.2017.03.004pubmed: 28392152google scholar: lookup
  59. Bosch S, Serra Bragança F, Marin-Perianu M, Marin-Perianu R, van der Zwaag BJ, Voskamp J. EquiMoves: a wireless networked inertial measurement system for objective examination of horse gait.. Sensors (2018) 18:850.
    doi: 10.3390/s18030850pmc: PMC5877382pubmed: 29534022google scholar: lookup
  60. Hardeman AM, Egenvall A, Serra Bragança FM, Swagemakers JH, Koene MHW, Roepstorff L. Visual lameness assessment in comparison to quantitative gait analysis data in horses.. Equine Vet J (2022) 54:1076–85.
    doi: 10.1111/evj.13545pmc: PMC9786350pubmed: 34913524google scholar: lookup
  61. McManus C, Tanure CB, Peripolli V, Seixas L, Fischer V, Gabbi AM. Infrared thermography in animal production: an overview.. Comput Electron Agric (2016) 123:10–6.

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