References

Anderson KA, Morrice-West AV, Wong ASM Poor association between facial expression and mild lameness in Thoroughbred trotup examinations. Animals (Basel). 2023; 13:(11) https://doi.org/10.3390/ani13111727

Ask K, Andersen PH, Tamminen LM, Rhodin M, Hernlund E Performance of four equine pain scales and their association to movement asymmetry in horses with induced orthopedic pain. Front Vet Sci. 2022; 9 https://doi.org/10.3389/fvets.2022.938022

Auer U, Kelemen Z, Vogl C Development, refinement, and validation of an equine musculoskeletal pain scale. Front Pain Res (Lausanne). 2024; 4 https://doi.org/10.3389/fpain.2023.1292299

Barreto da Rocha P, Driessen B, McDonnell SM A critical evaluation for validation of composite and unidimensional postoperative pain scales in horses. PLoS One. 2021; 16:(8) https://doi.org/10.1371/journal.pone.0255618

Bussières G, Jacques C, Lainay O Development of a composite orthopaedic pain scale in horses. Res Vet Sci. 2008; 85:(2)294-306 https://doi.org/10.1016/j.rvsc.2007.10.011

Dalla Costa E, Minero M, Lebelt D, Stucke D, Canali E, Leach MC Development of the Horse Grimace Scale (HGS) as a pain assessment tool in horses undergoing routine castration. PLoS One. 2014; 9:(3) https://doi.org/10.1371/journal.pone.0092281

Dalla Costa E, Pascuzzo R, Leach MC Can grimace scales estimate the pain status in horses and mice? A statistical approach to identify a classifier. PLoS One. 2018; 13:(8) https://doi.org/10.1371/journal.pone.0200339

Dalla Costa E, Dai F, Lecchi C Towards an improved pain assessment in castrated horses using facial expressions (HGS) and circulating miRNAs. Vet Rec. 2021; 188:(9) https://doi.org/10.1002/vetr.82

de Oliveira MGC, de Paula VV, Mouta AN Validation of the Donkey Pain Scale (DOPS) for assessing postoperative pain in donkeys. Front Vet Sci. 2021a; 8 https://doi.org/10.3389/fvets.2021.671330

de Oliveira AR, Gozalo-Marcilla M, Ringer SK Development and validation of the facial scale (FaceSed) to evaluate sedation in horses. PLoS One. 2021b; 16:(6) https://doi.org/10.1371/journal.pone.0251909

Dyson S, Berger J, Ellis AD, Mullard J Development of an ethogram for a pain scoring system in ridden horses and its application to determine the presence of musculoskeletal pain. J Vet Behav. 2018; 23:47-57 https://doi.org/10.1016/j.jveb.2017.10.008

Eerdekens A, Papas M, Damiaans B Automatic early detection of induced colic in horses using accelerometer devices. Equine Vet J. 2024; 56:(6)1229-1242 https://doi.org/10.1111/evj.14069

Evangelista MC, Monteiro BP, Steagall PV Measurement properties of grimace scales for pain assessment in nonhuman mammals: a systematic review. Pain. 2022; 163:(6)e697-e714 https://doi.org/10.1097/j.pain.0000000000002474

Ferlini Agne G, May BE, Lovett A Horse Grimace Scale does not detect pain in horses with equine gastric ulcer syndrome. Animals (Basel). 2023; 13:(10) https://doi.org/10.3390/ani13101623

Fonseca BPA, Alves ALG, Nicoletti JLM, Thomassian A, Hussni CA, Mikail S Thermography and ultrasonography in back pain diagnosis of equine athletes. J Equine Vet Sci. 2006; 26:(11)507-516 https://doi.org/10.1016/j.jevs.2006.09.007

Fuller CJ, Bladon BM, Driver AJ, Barr AR The intra- and inter-assessor reliability of measurement of functional outcome by lameness scoring in horses. Vet J. 2006; 171:(2)281-286 https://doi.org/10.1016/j.tvjl.2004.10.012

Gleerup KB, Lindegaard C Recognition and quantification of pain in horses: a tutorial review. Equine Vet Educ. 2016; 28:(1)47-57 https://doi.org/10.1111/eve.12383

Goodrich LR Strategies for reducing the complication of orthopedic pain perioperatively. Vet Clin North Am Equine Pract. 2008; 24:(3)611-ix https://doi.org/10.1016/j.cveq.2008.10.008

Graubner C, Gerber V, Doherr M, Spadavecchia C Clinical application and reliability of a post abdominal surgery pain assessment scale (PASPAS) in horses. Vet J. 2011; 188:(2)178-183 https://doi.org/10.1016/j.tvjl.2010.04.029

Guedes JRB, Vendruscolo CP, Tokawa PKA, Carvalho AM, Johnson PJ, Faleiros RR The detection of thoracolumbar spine injuries in horses with chronic laminitis using a novel clinical-assessment protocol and ultrasonographic examination. Animals (Basel). 2024; 14:(9) https://doi.org/10.3390/ani14091364

Guesgen MJ, Beausoleil NJ, Leach M, Minot EO, Stewart M, Stafford KJ Coding and quantification of a facial expression for pain in lambs. Behav Processes. 2016; 132:49-56 https://doi.org/10.1016/j.beproc.2016.09.010

Guyatt GH, Oxman AD, Vist GE GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008; 336:(7650)924-926 https://doi.org/10.1136/bmj.39489.470347.AD

Hernandez-Avalos I, Mota-Rojas D, Mora-Medina P Review of different methods used for clinical recognition and assessment of pain in dogs and cats. Int J Vet Sci Med. 2019; 7:(1)43-54 https://doi.org/10.1080/23144599.2019.1680044

Hewetson M, Christley RM, Hunt ID, Voute LC Investigations of the reliability of observational gait analysis for the assessment of lameness in horses. Vet Rec. 2006; 158:(25)852-857 https://doi.org/10.1136/vr.158.25.852

Howard DL, Lancaster B, de Grauw J Development and preliminary validation of an equine brief pain inventory for owner assessment of chronic pain due to osteoarthritis in horses. Animals (Basel). 2024; 14:(2) https://doi.org/10.3390/ani14020181

Ireland JL, Clegg PD, McGowan CM, McKane SA, Chandler KJ, Pinchbeck GL Comparison of owner-reported health problems with veterinary assessment of geriatric horses in the United Kingdom. Equine Vet J. 2012; 44:(1)94-100 https://doi.org/10.1111/j.2042-3306.2011.00394.x

Jodzio D, DeNotta S, Plummer C, Sanchez C Pain scoring systems in hospitalized horses with ocular disease. J Vet Intern Med. 2024; 38:(1)388-397 https://doi.org/10.1111/jvim.16933

Jönsson L, Roepstorff L, Egenvall A, Näsholm A, Dalin G, Philipsson J Prevalence of clinical findings at examinations of young Swedish warmblood riding horses. Acta Vet Scand. 2013; 55:(1) https://doi.org/10.1186/1751-0147-55-34

Lanci A, Benedetti B, Freccero F Development of a composite pain scale in foals: a pilot study. Animals (Basel). 2022; 12:(4) https://doi.org/10.3390/ani12040439

Lencioni GC, de Sousa RV, de Souza Sardinha EJ, Corrêa RR, Zanella AJ Pain assessment in horses using automatic facial expression recognition through deep learning-based modeling. PLoS One. 2021; 16:(10) https://doi.org/10.1371/journal.pone.0258672

Lesimple C, Fureix C, De Margerie E, Sénèque E, Menguy H, Hausberger M Towards a postural indicator of back pain in horses (Equus caballus). PLoS One. 2012; 7:(9) https://doi.org/10.1371/journal.pone.0044604

Lorena SE, Luna SP, Lascelles BD, Corrente JE Attitude of Brazilian veterinarians in the recognition and treatment of pain in horses and cattle. Vet Anaesth Analg. 2013; 40:(4)410-418 https://doi.org/10.1111/vaa.12025

Malmkvist J, Poulsen JM, Luthersson N Behaviour and stress responses in horses with gastric ulceration. Appl Anim Behav Sci. 2012; 142:(3–4)160-167 https://doi.org/10.1016/j.applanim.2012.10.002

Maskato Y, Dugdale AHA, Singer ER, Kelmer G, Sutton GA Prospective feasibility and revalidation of the Equine Acute Abdominal Pain Scale (EAAPS) in clinical cases of colic in horses. Animals (Basel). 2020; 10:(12) https://doi.org/10.3390/ani10122242

Matsubara LM, Teixeira LR, Mesquita LR, Landeira-Fernandez J, Anunciação L, Luna SPL Psychometric properties of the Brazilian version of the Canine Brief Pain Inventory (CBPI) for dogs with clinical signs of osteoarthritis and preliminary evidence of its clinical utility. Arq Bras Med Vet Zootec. 2022; 74:(4)592-602 https://doi.org/10.1590/1678-4162-12542

Mayaki AM, Abdul Razak IS, Adzahan NM, Mazlan M, Rasedee A Clinical assessment and grading of back pain in horses. J Vet Sci. 2020; 21:(6) https://doi.org/10.4142/jvs.2020.21.e82

McDonnell SM Practical review of self-mutilation in horses. Anim Reprod Sci. 2008; 107:(3–4)219-228 https://doi.org/10.1016/j.anireprosci.2008.04.012

Millares-Ramirez EM, Le Jeune SS Girthiness: retrospective study of 37 horses (2004–2016). J Equine Vet Sci. 2019; 79:100-104 https://doi.org/10.1016/j.jevs.2019.05.025

Mokkink LB, Terwee CB, Patrick DL The COSMIN study reached international consensus on taxonomy, terminology, and definitions of measurement properties for health-related patient-reported outcomes. J Clin Epidemiol. 2010; 63:(7)737-745 https://doi.org/10.1016/j.jclinepi.2010.02.006

Oliveira MC, de Lima MT, Trindade PHE, Luna SPL The impact of using pain scales by untrained students on the decision to provide analgesia to multiple species. Vet Anaesth Analg. 2024; 51:(5)548-557 https://doi.org/10.1016/j.vaa.2024.06.010

Ortolani F, Scilimati N, Gialletti R, Menchetti L, Nannarone S Development and preliminary validation of a pain scale for ophthalmic pain in horses: the Equine Ophthalmic Pain Scale (EOPS). Vet J. 2021; 278 https://doi.org/10.1016/j.tvjl.2021.105774

Pinho RH, Justo AA, Cima DS Effects of human observer presence on pain assessment using facial expressions in rabbits. J Am Assoc Lab Anim Sci. 2023; 62:(1)81-86 https://doi.org/10.30802/AALAS-JAALAS-22-000056

Price J, Catriona S, Welsh EM, Waran NK Preliminary evaluation of a behaviour-based system for assessment of post-operative pain in horses following arthroscopic surgery. Vet Anaesth Analg. 2003; 30:(3)124-137 https://doi.org/10.1046/j.1467-2995.2003.00139.x

Reed RA, Krikorian AM, Reynolds RM Post-anesthetic CPS and EQUUS-FAP scores in surgical and non-surgical equine patients: an observational study. Front Pain Res (Lausanne). 2023; 4 https://doi.org/10.3389/fpain.2023.1217034

Reid J, Nolan AM, Scott EM Measuring pain in dogs and cats using structured behavioural observation. Vet J. 2018; 236:72-79 https://doi.org/10.1016/j.tvjl.2018.04.013

Rowland AL, Glass KG, Grady ST, Cummings KJ, Hinrichs K, Watts AE Influence of caudal epidural analgesia on cortisol concentrations and pain-related behavioral responses in mares during and after ovariectomy via colpotomy. Vet Surg. 2018; 47:(5)715-721 https://doi.org/10.1111/vsu.12908

Schanz L, Krueger K, Hintze S Sex and age don't matter, but breed type does – factors influencing eye wrinkle expression in horses. Front Vet Sci. 2019; 6 https://doi.org/10.3389/fvets.2019.00154

Sidwell AE, Duz M, Hill B, Freeman S, Hole SL Application of the horse grimace scale in horses with dental disease: preliminary findings. Vet Rec. 2025; 196:(3) https://doi.org/10.1002/vetr.4800

Sorge RE, Martin LJ, Isbester KA Olfactory exposure to males, including men, causes stress and related analgesia in rodents. Nat Methods. 2014; 11:(6)629-632 https://doi.org/10.1038/nmeth.2935

Taffarel MO, Luna SP, de Oliveira FA Refinement and partial validation of the UNESP-Botucatu multidimensional composite pain scale for assessing postoperative pain in horses. BMC Vet Res. 2015; 11 https://doi.org/10.1186/s12917-015-0395-8

Torcivia C, McDonnell S Equine discomfort ethogram. Animals (Basel). 2021; 11:(2) https://doi.org/10.3390/ani11020580

Trindade PHE, Taffarel MO, Luna SPL Spontaneous behaviors of postorchiectomy pain in horses regardless of the effects of time of day, anesthesia, and analgesia. Animals (Basel). 2021; 11:(6) https://doi.org/10.3390/ani11061629

Trindade PHE, Barreto da Rocha P, Driessen B Predictive modeling toward refinement of behavior-based pain assessment in horses. Appl Anim Behav Sci. 2023; 267 https://doi.org/10.1016/j.applanim.2023.106059

Van Dierendonck MC, van Loon JP Monitoring acute equine visceral pain with the Equine Utrecht University Scale for Composite Pain Assessment (EQUUS-COMPASS) and the Equine Utrecht University Scale for Facial Assessment of Pain (EQUUS-FAP): a validation study. Vet J. 2016; 216:175-177 https://doi.org/10.1016/j.tvjl.2016.08.004

van Loon JPAM, Van Dierendonck MC Objective pain assessment in horses (2014–2018). Vet J. 2018; 242:1-7 https://doi.org/10.1016/j.tvjl.2018.10.001

van Loon JPAM, Macri L Objective assessment of chronic pain in horses using the Horse Chronic Pain Scale (HCPS): a scale-construction study. Animals (Basel). 2021; 11:(6) https://doi.org/10.3390/ani11061826

van Loon JPAM, Van Dierendonck MC Pain assessment in horses after orthopaedic surgery and with orthopaedic trauma. Vet J. 2019; 246:85-91 https://doi.org/10.1016/j.tvjl.2019.02.001

van Loon J, Verhaar N, van den Berg E, Ross S, de Grauw J Objective assessment of acute pain in foals using a facial expression-based pain scale. Animals (Basel). 2020; 10:(9) https://doi.org/10.3390/ani10091610

van Weeren PR, Back W Musculoskeletal disease in aged horses and its management. Vet Clin North Am Equine Pract. 2016; 32:(2)229-247 https://doi.org/10.1016/j.cveq.2016.04.003

Wagner AE Effects of stress on pain in horses and incorporating pain scales for equine practice. Vet Clin North Am Equine Pract. 2010; 26:(3)481-492 https://doi.org/10.1016/j.cveq.2010.07.001

Wathan J, Burrows AM, Waller BM, McComb K EquiFACS: the equine facial action coding system. PLoS One. 2015; 10:(8) https://doi.org/10.1371/journal.pone.0131738

Wennerstrand J, Johnston C, Roethlisberger-Holm K, Erichsen C, Eksell P, Drevemo S Kinematic evaluation of the back in the sport horse with back pain. Equine Vet J. 2004; 36:(8)707-711 https://doi.org/10.2746/0425164044848226

A review of pain behaviour assessment scales in horses

02 May 2025
15 mins read
horse’s facial expression

Abstract

Most clinical problems involve pain, and there are a greater number of pain assessment scales available for horses than any other species. Identifying pain is vital to assist with the analgesic strategy. This review guides the clinician in selecting the most appropriate equine full-body or facial pain assessment scales, based on the type (somatic or visceral), progression (acute and chronic) and location of pain (limbs, thoracolumbar, head, soft tissue, abdomen), applied to horses and foals through information on the usability, limitations, reliability and validity attributes of each scale. The confounding factors influencing pain assessment, suggestions for the future and free resources available for assessing pain in horses are presented in a practical and ready-to-use way.

Horses express pain in an obvious and particular way, and the behavioural signs they demonstrate for abdominal pain are unique, ranging from mild to severe as a result of the horse's specific gastrointestinal anatomy, physiology and behaviour. Therefore, it is not a surprise that, even compared to small animals, there are a greater number of scales to assess pain in horses (Reid et al, 2018; Hernandez-Avalos et al, 2019; Barreto da Rocha et al, 2021; Ortolani et al, 2021; Lanci et al, 2022). Horses are also the most privileged large animal species when considering treatment with painkillers, as they receive more analgesics than ruminants and pigs (Lorena et al, 2013).

Most clinical problems involve pain, and although the under-treatment of pain is still a reality, pain relief therapy has evolved both qualitatively and quantitatively in the last 3 decades. This may be credited to a better understanding of physiopathology and the development of pain assessment methods. Pain assessment is the cornerstone for deciding whether to provide analgesia and select the most appropriate analgesic therapy (Barreto da Rocha et al, 2021), so pain identification, following attitudes for adequate analgesia, is imperative to guarantee and improve animal welfare.

Methods to assess clinical pain

Pain can only be treated after it has been detected, but the decision to provide analgesic treatment is not only driven by whether pain is present or not. Identifying the type and intensity of pain are key to guiding the choice of the best analgesic therapy for a horse experiencing pain. To do this, the pain needs to be scored and allocated a ‘number’. After that, the success or failure of a given analgesic can be checked by determining if, following analgesia, the score has reduced below the cut-off point of the pain scale.

So, how is clinical pain measured in horses? There are a number of objective and subjective methods available to assess pain in horses. Objective methods, including physiological data (appetite, heart and respiratory rates, blood pressure and temperature), endocrine changes, nociceptive tests and locomotor activity, are less affected by the observer's judgment. However, they are non-specific and may be intrusive or invasive, costly (if they require equipment) and time-consuming, and the results may not be available immediately (Graubner et al, 2011; Barreto da Rocha et al, 2021).

Physiological parameters correlated poorly with the total visceral pain score (Graubner et al, 2011) and their contribution for somatic pain is also questionable. Physiological and neuroendocrine responses are limited for assessing orthopaedic pain if it is not combined with behavioural indicators (Price et al, 2003).

Unlike humans, who can self-report any pain, horses express unpleasant experiences through their behaviour. Although pain-related behaviour assessment is a subjective method, it is non-invasive, does not require equipment, is free of cost and may be performed remotely by video cameras (Torcivia and McDonnell, 2021). Considering convenience, cost, practicality and efficacy, behaviour is the ‘gold standard’ method to assess clinical pain when it is evaluated by a validated pain scale, because it is feasible in all scenarios, including the field, farms, hospitals and experimental environments.

Behavioural pain scales

The most common equine pain-related behaviours under different conditions are well documented (Bussières et al, 2008; Taffarel et al, 2015; Gleerup and Lindegaard, 2016), and the efforts of different research groups to develop numerous scales to assess pain in horses are summarised in Table 1.


Age indication Adult horses Foals Adult horses
Type of scales Facial Full body behaviour Facial Limb
Type of pain Somatic and soft tissue Colic Ocular Chronic musculoskeletal Somatic and ST Laminitis
Scales/type of pain HGS EQUUS FAP CPS UHAPS EAAPS EQUUS COMPASS PASPAS EOPS MPS EBPI HCPS FCPS EQUUS FAP Foal Obel Mod Obel
Orthopaedic surgery
Soft tissue surgery
Emergency Gl surgery
Orquiectomy
Ovariectomy
Orthopaedic trauma
Thoracolumbar injury
Laminitis
Head
Dental
Ocular
Colic
Chronic musculoskeletal
Osteoarthritis
Acute abdominal and MS
Number of items 6 9 13 10 10 14 9 13 7 15 15 11 11 4 5
Number of sub-items 18 27 52 27 27 56 31 44 25 15 60 29 29 4 15
Maximal score 12 18 39 17 5 42 30 31 26 140 45 22 22 4 15
Response to palpation
Physiological variables
Reliability
Repeatability
Reproducibility
Measurement error
Internal consistency
Responsiveness
Validity
Content
Criterium/convergent
Construct
Face
Cut-off scores >4 ≥7 ≥5 ≥0.6 ≥7 ≥7 >3
Available in Vetpain

Reliability is given by repeatability (intra-rater reliability), reproducibility (inter-rater reliability) and measurement error which includes accuracy and/or sensitivity and/or specificity and/or test-retest and/or cut-off score (the score corresponding to the highest sensitivity and specificity)

Validity is given by responsiveness (changes in time in response to pain or analgesia), content validity (based on ethogram and/or literature and/or experts), criterium/convergent (correlation with another pain assessment method), construct validity (differences of scores between control and pain groups) and face validity (feasibility)

Physiological variables: HR-heart rate, RR-respiratory rate, GI-digestive sounds, T-temperature and A-appetite

Legend for the type of pain: A-anaesthesia only, C-control, CO-colic, COD-chronic orthopaedic diseases, CS-colic surgery, D-dental disease; EOA-experimental induced osteoarthritis, H-head; L-laminitis, N-normal, MS-musculoskeletal, OA-osteoarthritis, OD-ocular diseases, OQ-orquiectomy, OS-orthopaedic surgery, OT-orthopaedic trauma, OV-ovariectomy, P-pain, PO-postoperative, ST-soft tissue surgery, TL-thoracolumbar injuries, VP-visceral pain (colic)

Legend of pain scales with the literature (in bold are the articles that contain the description of the scales), number of horses and pain conditions.

CPS-Composite Pain Scale: Bussières et al (2008) 18 EOA; Van Loon et al (2010) 80 OQ, CS, OS, ST, 14 C; van Loon et al (2014), 48 CS; van Loon and Van Dierendonck (2019) 43 OT, 34 C; Barreto da Rocha et al (2021) 40 OS and ST. Physiological variables: HR, RR, GI, T and A

EAAPS-Equine Acute Abdominal Pain Scale: Sutton et al (2013a; 2013b); Sutton et al (2019) 35 CO, 5 C; Maskato et al (2020) 231 CO

EBPI-Equine Brief Pain Inventory for Owner Assessment of Chronic Pain Due to Osteoarthritis: Howard et al (2024) 23 OA

EOPS-Equine Ophthalmic Pain Scale: Ortolani et al (2021) 8 OD, 15 C. Physiological variables: HR, RR, GI, and T

EQUUS COMPASS-Equine Utrecht University Scale for Composite Pain Assessment: van Loon and Van Dierendonck (2015) 25 VP, 25 C; Van Dierendonck and van Loon (2016) 23 VP, 23 C. Physiological variables: HR, RR, GI, T

EQUUS-FAP-Equine Utrecht University Scale for Facial Assessment of Pain: van Loon and Van Dierendonck (2015), 25 VP, 25 C; Van Dierendonck and van Loon (2016) 23 VP, 23 C; van Loon and Van Dierendonck (2017) 23 H, 23 C; van Loon and Van Dierendonck (2019) 43 OT, 34 C

EQUUS-FAP FOAL: van Loon et al (2020) 42 L, OT, P0, VP 17 C

FCPS-Foal Composite Pain Scale: Lanci et al (2022) 15 P, 35 C

HCPS-Horse Chronic Pain Scale: van Loon and Macri (2021) 26 MS, 27 C

HGS-Horse Grimace Scale: Dalla Costa et al (2014) 40 OQ, 6 A; Dalla Costa et al (2016), 10 L; Dalla Costa et al (2021) 11 OQ; Rowland et al (2018) 9 OV; Guedes et al (2024) 60 TL; Jodzio et al (2024) 65 OD; Sidwell et al (2024) 12 D

Modified Obel: Meier et al (2019) 37 L

MPS-Musculoskeletal Pain Scale: Auer et al (2023) 154 COD

Obel: Menzies-Gow et al (2010), 38 N and L ponies; Viñuela-Fernández et al (2011) 12 L

PASPAS: Graubner et al (2011) 34 CS, 8 A. Physiological variables: HR, RR, A

UHAPS-Unesp-Botucatu Horse Pain Scale: Taffarel et al (2015) 12 OQ, 12 A; Barreto da Rocha et al (2021) 40 OS and ST. Physiological variables: HR

This Table is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en

The simplest scales for assessing pain are unidimensional scales, like the simple descriptive scale (1 – no pain, 2 – mild pain, 3 – moderate pain and 4 – intense pain), numerical scale (from 1 – no pain; to 10 – the worst possible pain) and visual analogue scale. The visual analogue scale uses a 10 cm long straight line, where the left extreme is no pain and the right extreme is the worst possible pain; the score score is defined by measuring the distance in millimetres from the left extreme to the point marked by the observer. These scales may be simpler and faster when compared to composite alternatives, but they do not encompass the complexity of pain, have limited reproducibility and are not accurate when used by inexperienced evaluators (Graubner et al, 2011; van Loon and Van Dierendonck, 2018). In horses with visceral pain, the visual analogue scale showed lower inter-observer agreement than composite scales (van Loon and Van Dierendonck, 2018). Composite multidimensional scales embrace the sensorial, cognitive and emotional attributes of pain, have greater sensitivity and indicate the most appropriate pain behaviours to be assessed (Graubner et al, 2011; van Loon and Van Dierendonck, 2018).

A behaviour-based pain scale must have proven reliability and validity before being applied in clinical practice or research. Validity guarantees that the instrument measures what it is designed for, and reliability ensures repeatability and reproducibility. Other important properties of a pain assessment instrument are item interrelation, mutual association and homogeneity, to guarantee a good relationship between items and the contribution of each item. Finally, a cut-off score to provide decision-making for analgesic intervention must be defined (Mokkink et al, 2010; Barreto da Rocha et al, 2021).

Table 1 presents the most important scales according to the validation criteria established by the COnsensusbased Standards for the selection of health Measurement INstruments (COSMIN) (Mokkink et al, 2010) and GRADE (Grading of Recommendations, Assessment, Development and Evaluations) (Guyatt et al, 2008) guidelines, which are well-recognised methods supporting the recommendation of a given instrument considering the quality of evidence and strength.

Assessment of somatic pain

Changes in the locomotor system are the main causes of somatic pain, and lameness is the most common clinical sign in horses with orthopaedic injury (Goodrich, 2008), especially in athletic animals (Wagner, 2010).

Unidimensional scales, like numerical scales, present low reliability when used for assessing lameness (Hewetson et al, 2006). However, the repeatability and reproducibility of an overall score (given by comparing the method −1 – worse, 0 – equal, 1 – better and 2 – improvement in all movements) showed better results than the classical lameness score from 0–10 in horses with osteoarthritis (Fuller et al, 2006).

Back pain is a common cause of somatic pain, especially in competition horses (Fonseca et al, 2006). Objective assessments like electromyography (Lesimple et al, 2012), kinematics (Wennerstrand et al, 2004), thermography and ultrasonography (Fonseca et al, 2006) can facilitate recognition and quantification of pain and enable an efficient diagnosis of thoracolumbar spinal injuries. However, these methods can have a high cost, are impractical and are not applicable in the field.

A protocol has been proposed to grade back pain based on the pain response, muscular hypertonicity, thoracolumbar joint stiffness and overall physical dysfunction of the horse, but it still requires validation (Mayaki et al, 2020). Multidimensional pain scales are more sensitive for assessing pain of variable intensity and chronic pain, which is difficult to diagnose, including head and/or dental pain.

The instruments that are closest to meeting the COSMIN (Mokkink et al, 2010) and GRADE (Guyatt et al, 2008) guidelines are the Horse Grimace Scale (Dalla Costa et al, 2014), the Composite Pain Scale (Bussières et al, 2008), and the Unesp-Botucatu Horse Acute Pain Scale (Taffarel et al, 2015; Barreto da Rocha et al, 2021) (Table 1). The Horse Grimace Scale was initially developed in horses undergoing orchiectomy (Dalla Costa et al, 2014) and was later used for ovariectomy (Rowland et al, 2018), laminitis and thoracolumbar spine injury (Guedes et al, 2024), and ophthalmic (Jodzio et al, 2024) and dental disorders (Sidwell et al, 2025). The Horse Grimace Scale failed to identify pain in horses experiencing equine gastric ulcer syndrome (Ferlini Agne et al, 2023); therefore, other signs like increased girth sensitivity (Millares-Ramirez and Le Jeune, 2019), pawing and aggressiveness before alimentation (Malmkvist et al, 2012), self-mutilation (McDonnell, 2008) and decreased athletic performance might be indicative of equine gastric ulcer syndrome.

In a systematic review, the Horse Grimace Scale showed the highest level of evidence compared to all other facial scales developed for horses (Evangelista et al, 2022); however, a cut-off point indicative of providing analgesia has not yet been calculated. In addition, the association between the Horse Grimace Scale and the Equinosis Lameness Locator was inconsistent in predicting mild orthopaedic pain through lameness assessment before races (Anderson et al, 2023).

The Composite Pain Scale (Bussières et al, 2008) was shown to be the most accurate and reliable pain scale compared to the Horse Grimace Scale (Dalla Costa et al, 2014), Equine Utrecht University Scale of Facial Assessment of Pain (Van Dierendonck and van Loon, 2016) and Equine Pain Scale (Gleerup and Lindegaard, 2016), for correctly identifying horses submitted to experimentally-induced acute arthritis, according to movement asymmetry, using objective gait analysis in horses. However, Composite Pain Scale scores may underestimate pain, as they did not coincide with movement asymmetry in mild lameness (Ask et al, 2022).

Assessment of visceral pain

The most validated and easiest scale to assess acute abdominal pain syndrome is the Equine Acute Abdominal Pain Scale (Maskato et al, 2020). This is a simple and straight-to-the-point instrument that meets the demand for a quick evaluation in emergency cases. The score to discriminate colic cases vs controls is 0.6, mild vs severe pain is 2.8, surgical treatment is 3.5 and death is 4.5 out of 5, providing relevant information regarding clinical conduct, prognosis and therapeutic strategies; a table demonstrating this was produced by Maskato et al (2020). A more complex and time-consuming instrument that can be used to assess acute colic pain is EQUUS-COMPASS (van Loon and van Dierendonck, 2016).

Pain assessment in foals

There are two reasonably well-validated pain assessment instruments in foals. The Foal Composite Pain Scale (Lanci et al, 2022) is currently the most widely validated full-body behaviour instrument available to assess pain in neonates (13±12 [1–47] months old). The items were included according to the literature and expertise and resemble previously reported instruments in adults, complemented with the foal's specific behaviours. The analgesic intervention score was included to guide decision-making to provide analgesia (Table 1).

The Equine Utrecht University Scale for Facial Assessment of Pain in Foals assesses acute pain using facial expressions in neonates (<14 days old) and older foals (15–180 days old), with a cut-off point of >3 (van Loon et al, 2020).

Assessment of chronic pain

If acute pain assessment is a challenge, chronic pain assessment is more so. Like in other animal species, musculoskeletal disease is the principal source of chronic pain in horses and, consequently, lameness is the most frequent clinical sign (Jönsson et al, 2013; van Weeren and Back, 2016; Dyson et al, 2018). Musculoskeletal disorders are generally age-dependent and under-treated (van Weeren and Back, 2016).

Behavioural changes elicited by chronic pain are gradual and subtle, which is why the owners or caregivers are important allies for chronic pain assessment in companion animals (Matsubara et al, 2022). This scenario may be different in horses because owner-reported lameness is low (Ireland et al, 2012).

The Equine Brief Pain Inventory for Owner Assessment of Chronic Pain Due to Osteoarthritis may fill this gap. This scale showed face validity and readability, for use in 5 minutes by owners with limited veterinary knowledge. It shows promise as a tool for assessing osteoarthritis-related chronic pain once fully validated (Howard et al, 2024).

To date, the Musculoskeletal Pain Scale has the highest level of validation to assess musculoskeletal pain. This scale can be used by caretakers and veterinarians, and it incorporates facial expression, posture, head height, weight-bearing and shifting (Auer et al, 2024).

Limitations of behaviour-based pain scales and suggested improvements

The literature makes clear the questionable contribution of some real-time physiological variables (appetite, heart and respiratory rates, digestive sounds and temperature) to assess pain in horses (Bussières et al, 2008; Barreto da Rocha et al, 2021), and their importance requires further investigation. It seems that some of these variables, if not all, might be excluded from pain scales without compromising the construct because they are usually intrusive, time-consuming and cumbersome, and are sometimes not measurable according to the horse's behaviour. Their exclusion would facilitate pain assessment without disturbing the horse.

The second decision is to make the scales as short as possible. The Horse Grimace Scale, Unesp-Botucatu Horse Acute Pain Scale and Equine Acute Abdominal Pain Scale for acute pain and Musculoskeletal Pain Scale for chronic pain are already heading in this direction (Table 1). Conversely, the Composite Pain Scale and Equine Utrecht University Scale for Composite Pain Assessment are long and demand more time. The Equine Utrecht University Scale for Composite Pain Assessment items have not been investigated in isolation to check if they are deemed necessary. In fact, some of the Composite Pain Scale items are redundant and could be excluded (Barreto da Rocha et al, 2021).

Both the Composite Pain Scale and Unesp-Botucatu Horse Acute Pain Scale were critically tested to assess pain after orthopaedic and soft tissue surgery. Although they showed intra- and inter-observer reliability and some validity attributes that met COSMIN criteria, their items were poorly associated and their sensitivity was weak, suggesting that they did not achieve the ideal standards of COSMIN. However, they are the only full-body postoperative pain behaviour instruments to which the COSMIN checklist has been applied to date. The takehome message for the Composite Pain Scale and Unesp-Botucatu Horse Acute Pain Scale is that they require further refinement by excluding redundant or unnecessary items.

Based on this premise, the Composite Pain Scale and Unesp-Botucatu Horse Acute Pain Scale behavioural items were merged, mined and weighted in a single instrument using a predictive model (Trindade et al, 2023). The diagnostic capacity of the short model, including 25% of behaviours from both instruments, was excellent (area under the curve 99% vs 85% for the Unesp-Botucatu Horse Acute Pain Scale and 89% for the Composite Pain Scale). This approach was an encouraging method to ameliorate the current instruments.

The Horse Grimace Scale showed a high level of evidence for measurement properties (Evangelista et al, 2022). A classifier used to estimate the pain status based on the Horse Grimace Scale showed that some facial action units (like ear position and orbital tightening) contributed to identifying pain in horses, while mouth strain and strained nostrils did not (Dalla Costa et al, 2018). Therefore, the Horse Grimace Scale may require refinement, like the Composite Pain Scale and Unesp-Botucatu Horse Acute Pain Scale. Studies on the Horse Grimace Scale also used high-quality images (Dalla Costa et al, 2021) that do not express locum live situations. The horse's face should be accessible without manipulation of the animal to avoid disturbances. Facial scales are liable to missing data when some facial action units are not assessable, or the quality of the images is unsatisfactory as a result of restricted visibility. Facial expression can vary quickly and may not represent the real-time evaluation. Facial scales may also not be effective in detecting certain types of pain, because they do not encompass more complex behaviour repertoires related to different anatomical, sensory, motor, emotional and cognitive dimensions in the way that full-body behavioural pain scales do. Another limitation of facial pain scales is that breed influences superior eye wrinkles in horses, and tension above the eye is one of the items included in Horse Grimace Scale scores (Schanz et al, 2019).

Factors influencing and confounding behavioural pain assessment

Multiple confounding factors can interfere with pain assessment, including human presence (Torcivia and McDonell, 2021). Human presence may cause under or overestimation of facial pain expression in lambs (Guesgen et al, 2016), rodents (Sorge et al, 2014) and rabbits (Pinho et al, 2023) that are truly experiencing or not experiencing pain respectively, and in full-body behaviour expression in rabbits (Pinho et al, 2023) and horses (Torcivia and McDonell, 2021). Torcivia and McDonell (2021) claimed that the caretaker visits interrupted disturbance behaviour in horses; however, only the effect of a human presence outside the box and the examination or treatment administration were not evaluated separately. These factors may inhibit disturbance behaviour to a greater extent than only the human presence. Analysis only of the human presence effect without concurrent intrusive assessments is necessary to confirm that disturbance behaviours are inhibited. Until this information is available, whenever possible, pain assessment should ideally be performed remotely using video cameras.

Other confounding factors include the presence of insects, which augmented tail, ear and head movements in donkeys (de Oliveira et al, 2021a). The time of day, anaesthesia and analgesia influence spontaneous pain behaviours like walking, looking out the window, resting the pelvic limb and resting standing still (Trindade et al, 2021), and the residual effect of anaesthesia may lead to overestimation of the Composite Pain Scale and Equine Utrecht University scale for facial assessment of pain scores for 3 hours (Reed et al, 2023). Post-anaesthetic sedation may influence both body behaviour (Trindade et al, 2021) and facial scales (de Oliveira et al, 2021b).

Although previous experience or familiarity with the pain assessment instruments is advisable (van Loon and van Dierendonck, 2019), the use of scales optimises the ability of less experienced observers to measure pain. When assessing a horse experiencing intense pain, students indicated less analgesic intervention according to their opinion (66%) than according to their Unesp-Botucatu Horse Acute Pain Scale scores (96%), and when using the Unesp-Botucatu Horse Acute Pain Scale cut-off scores, they perceived pain demanding analgesic intervention similarly to an expert (Oliveira et al, 2024).

The future

Algorithms for merging, mining and weighting pain behaviours have been applied to the Horse Grimace Scale (Dalla Costa et al, 2018), Composite Pain Scale and Unesp-Botucatu Horse Acute Pain Scale (Trindade et al, 2023). Automatic recognition of pain based on artificial intelligence and machine vision algorithms was developed by training a convolutional neural network (Lencioni et al, 2021). A software algorithm accurately recognised the early signs and severity of experimentally-induced visceral pain using accelerometry to detect the activity index (Eerdekens et al, 2024). Although using artificial intelligence is the next logical step, these technologies have not yet been tested in the field.

Useful sources of information on pain assessment

After developing pain assessment scales, the subsequent step is to popularise and facilitate their use beyond the academic and scientific world. To this end, various resources were developed:

  • The website www.animalpain.org
  • The free Vetpain application, which can be used with Android and IOS.
  • The Vetpain app can be used to assess acute and chronic pain in horses and all laboratory and domestic mammals, as well as sedation in horses and dogs. Using Vetpain, veterinarians, students, nurses, animal caretakers and owners can also assess videos demonstrating examples of all behaviours present in the pain scales to improve their learning, accuracy and reliability. Videos are available for training and teaching, where the users can check their knowledge according to the template before using the scales on animals. These resources are also useful for teaching purposes. Users can evaluate pain in their animals or animals they are caring for with automatic calculation of scores. Data may be shared among the staff, and because the data are stored, previous pain assessments can be compared to current ones to verify the efficacy and duration of analgesic therapy. The indicative cut-off scores offer assertive information to orient the clinician's decision to provide analgesia for animals experiencing pain, minimising the risk of insufficient analgesia.

    A further free source for learning and teaching how to assess discomfort behaviours is the Equine Discomfort Ethogram, which comprises a set of 73 illustrative videos of discomfort behaviours of various intensities, anatomical origins and clinical conditions (Torcivia and McDonnell, 2021). A useful free source for training to identify facial expressions is EQUIFACS (Wathan et al, 2015). Ideally, a metrology instrument should be short, and easy and quick to complete; the simpler the instrument is, the easier it will be to use and the greater the chance of it being used in practice.

    Conclusions

    This article provides a comprehensive review of the available pain scales to allow readers to discern which scales are appropriate for each type of pain and choose the best option based on simplicity and validity robustness. Accurate pain recognition guides decision-making towards analgesia. The selection of the most appropriate full-body and facial pain assessment scale in horses and foals should be based on the type, progression and location of pain. The free sources available for equine pain assessment facilitate scoring the pain intensity and choosing the best analgesic technique.

    KEY POINTS

  • Most clinical problems involve pain.
  • Accurate pain identification guides decision-making towards analgesia.
  • The selection of the most appropriate full-body and facial pain assessment scale in horses and foals should be based on the type, progression and location of pain.
  • Confounding factors influence pain assessment.
  • Free sources are available for equine pain assessment.