Animal-assisted therapy for patients in a minimally conscious state: A randomized two treatment multi-period crossover trial
Autoři:
Karin Hediger aff001; Milena Petignat aff001; Rahel Marti aff001; Margret Hund-Georgiadis aff002
Působiště autorů:
Department of Psychology, Division of Clinical Psychology and Psychotherapy, University of Basel, Basel, Switzerland
aff001; REHAB Basel, Clinic for neurorehabilitation and paraplegiology, Basel, Switzerland
aff002; Department of Epidemiology and Public Health, Human and Animal Health Unit, Swiss Tropical and Public Health Institute, Basel, Switzerland
aff003; Institute for Interdisciplinary Research on the Human-Animal Relationship Switzerland, Basel, Switzerland
aff004
Vyšlo v časopise:
PLoS ONE 14(10)
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pone.0222846
Souhrn
Objective
To investigate if animal-assisted therapy (AAT) leads to higher consciousness in patients in a minimally conscious state during a therapy session, measured via behavioral reactions, heart rate and heart rate variability.
Methods
In a randomized two treatment multi-period crossover trial, 10 patients in a minimally conscious state participated in eight AAT sessions and eight paralleled conventional therapy sessions, leading to 78 AAT and 73 analyzed control sessions. Patients’ responses during sessions were assessed via behavioral video coding and the Basler Vegetative State Assessment (BAVESTA), heart rate and heart rate variability (SDNN, RMSSD, HF and LF). Data were analyzed with generalized linear mixed models.
Results
Patients showed more eye movements (IRR = 1.31, 95% CI: 1.23 to 1.40, p < 0.001) and active movements per tactile input during AAT compared to control sessions (IRR = 1.13, 95% CI: 1.02 to 1.25, p = 0.018). No difference was found for positive emotions. With BAVESTA, patients’ overall behavioral reactions were rated higher during AAT (b = 0.11, 95% CI: 0.01 to 0.22, p = 0.038). AAT led to significantly higher LF (b = 5.82, 95% CI: 0.55 to 11.08, p = 0.031) and lower HF (b = -5.80, 95% CI: -11.06 to -0.57, p = 0.030), while heart rate, SDNN, RMSSD did not differ.
Conclusions
Patients in a minimally conscious state showed more behavioral reactions and increased physiological arousal during AAT compared to control sessions. This might indicate increased consciousness during therapeutic sessions in the presence of an animal.
Trial registration
ClinicalTrials.gov NCT02629302.
Klíčová slova:
Dogs – Behavior – Animal behavior – Emotions – Consciousness – Heart rate – Traumatic brain injury – Eye movements
Zdroje
1. Covelli V, Sattin D, Giovannetti AM, Scaratti C, Willems M, Leonardi M. Caregiver’s burden in disorders of consciousness: a longitudinal study. Acta Neurol Scand. 2016;134:352–359. doi: 10.1111/ane.12550 26748540
2. Pisa FE, Biasutti E, Drigo D, Barbone F. The prevalence of vegetative and minimally conscious states: a systematic review and methodological appraisal. J Head Trauma Rehabil. 2014;29:E23–30. doi: 10.1097/HTR.0b013e3182a4469f 24052091
3. Fingelkurts AA, Fingelkurts AA, Bagnato S, Boccagni C, Galardi G. Life or death: prognostic value of a resting EEG with regards to survival in patients in vegetative and minimally conscious states. PLoS One. 2011;6(10):e25967. doi: 10.1371/journal.pone.0025967 21998732
4. La Gattuta E, Corallo F, Lo Buono V, De Salvo S, Cminiti F., Rifici C, et al. Techniques of cognitive rehabilitation in patients with disorders of consciousness: a systematic review. Neurol Sci. 2018;39:1–5.
5. Pistarini C, Maggioni G. Early rehabilitation of Disorders of Consciousness (DOC): management, neuropsychological evaluation and treatment. Neuropsychol Rehabil. 2018;28:1319–1330. doi: 10.1080/09602011.2018.1500920 30033818
6. Perrin F, Castro M, Tillmann B, Luaute J. Promoting the use of personally relevant stimuli for investigating patients with disorders of consciousness. Front Psychol. 2015;6:1102. doi: 10.3389/fpsyg.2015.01102 26284020
7. Sun Y, Wang J, Heine L, Huang W, Wang J, Hu N, et al. Personalized objects can optimize the diagnosis of EMCS in the assessment of functional object use in the CRS-R: a double blind, randomized clinical trial. BMC Neurol. 2018;18:38. doi: 10.1186/s12883-018-1040-5 29649978
8. Borgi M, Cirulli F. Pet Face: Mechanisms Underlying Human-Animal Relationships. Front Psychol. 2016;7:298. doi: 10.3389/fpsyg.2016.00298 27014120
9. IAHAIO. IAHAIO White Paper 2014, updated for 2018. The IAHAIO definitions for animal-assisted intervention and guidelines for wellness of animals involved in AAI. http://iahaio.org/wp/wp-content/uploads/2018/04/iahaio_wp_updated-2018-final.pdf2018. Accessed February 21, 2019.
10. Bardl S, Bardl M, Kornhuber ME. [Dog-based multi-sensorial therapy of a patient with a "persistent vegetative state"—a case report]. Rehabilitation. 2013;52:399–405. doi: 10.1055/s-0033-1334915 24217875
11. Giacino JT, Kezmarsky MA, DeLuca J, Cicerone KD. Monitoring rate of recovery to predict outcome in minimally responsive patients. Arch Phys Med Rehabil. 1991;72:897–901. doi: 10.1016/0003-9993(91)90008-7 1929808
12. Giacino JT, Kalmar K, Chase R. The JFK Coma Recovery Scale: Further Evidence for Applicability in Grading Level of Neurobehavioral Responsiveness Folowwing Severe Brain Injury. Arch Phys Med Rehabil. 1993;74:662.
13. Giacino JT, Ashwal S, Childs N, Cranford R, Jennett B, Katz DI, et al. The minimally conscious state: definition and diagnostic criteria. Neurology. 2002;58:349–353. doi: 10.1212/wnl.58.3.349 11839831
14. Bruno MA, Vandenhause A, Thibaut A, Moonen G, Laureys S. From unresponsive wakefulness to minimally consious PLUS and functional locked-in syndromes: recent advances in our understanding of disorders of consiousness. J Neurol. 2011;258:1373–1384. doi: 10.1007/s00415-011-6114-x 21674197
15. Affolter F, Bischofberger W, Stockman IJ. Nonverbal perceptual and cognitive processes in children with language disorder. Toward a new framework for clinical intervention. Mahwah, NJ: Lawrence Erlbaum Associates 2000.
16. Huber M, Koch S, Hund-Georgiadis M, Mäder M, Borgwardt S. Stieglitz RD. Diagnostic Validity of the Basler Vegetative State Assessment—BAVESTA. International Journal of Health Professions. 2014;1:50–60.
17. Jones MG, Rice SM, Cotton SM. Incorporating animal-assisted therapy in mental health treatments for adolescents: A systematic review of canine assisted psychotherapy. PloS one. 2019; 14(1), e0210761. doi: 10.1371/journal.pone.0210761 30653587
18. Eapen BC, Georgekutty J, Subbaro B, Bavishi S, Cifu DX. Disorders of Consiousness. Phys Md Rehabil Clin N Am. 2017;28:245–258.
19. Laureys S. The neural correlate of (un)awareness: lessons from the vegetative state. Trends Cogn Sci. 2005;9:556–559. doi: 10.1016/j.tics.2005.10.010 16271507
20. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Heart rate variability. Standards of measurement, physiological interpretation, and clinical use. Eur Heart J. 1996;17:354–381. 8737210
21. Thomas BL, Claassen N, Becker P, Viljoen M. Validity of Commonly Used Heart Rate Variability Markers of Autonomic Nervous System Function. Neuropsychobiology. 2019;5:1–13.
22. Hjortskov N, Rissen D, Blangsted AK, Fallentin N, Lundberg U, Søgaard K. The effect of mental stress on heart rate variability and blood pressure during computer work. Eur J Appl Physiol. 2004;92:84–89. doi: 10.1007/s00421-004-1055-z 14991326
23. Kim HG, Cheon EJ, Bai DS, Lee YH, Koo BH. Stress and Heart Rate Variability: A Meta-Analysis and Review of the Literature. Psychiatry Investig. 2018;15:235–245. doi: 10.30773/pi.2017.08.17 29486547
24. Kreibig SD. Autonomic nervous system activity in emotion: a review. Biol Psychol. 2010;83:394–421.
25. Zupan M, Buskas J, Altimiras J, Keeling LJ. Assessing positive emotional states in dogs using heart rate and heart rate variability. Physiol Behav. 2016;155:102–111. doi: 10.1016/j.physbeh.2015.11.027 26631546
26. Silva K, Lima M, Santos-Magalhaes A, Fafiaes C, de Sousa L. Can Dogs Assist Children with Severe Autism Spectrum Disorder in Complying with Challenging Demands? An Exploratory Experiment with a Live and a Robotic Dog. J Altern Complement Med. 2018;24:238–242.
27. Schretzmayer L, Kotrschal K, Beetz A. Minor Immediate Effects of a Dog on Children’s Reading Performance and Physiology. Front Vet Sci. 2017;4:90. doi: 10.3389/fvets.2017.00090 28674695
28. Motooka M, Koike H, Yokoyama T, Kennedy NL. Effect of dog-walking on autonomic nervous activity in senior citizens. Med J Aust. 2006;184:60–63. 16411869
29. Ein N, Li L, Vickers K. The effect of pet therapy on the physiological and subjective stress response: A meta-analysis. Stress Health. 2018; 34:477–489. doi: 10.1002/smi.2812 29882342
30. Kaminski M, Pellino T, Wish J. Play and pets: The physical and emotional impact of child-life and pet therapy on hospitalized children. Children’s Health Care. 2002;31:321–335.
Článok vyšiel v časopise
PLOS One
2019 Číslo 10
- Metamizol jako analgetikum první volby: kdy, pro koho, jak a proč?
- Nejasný stín na plicích – kazuistika
- Masturbační chování žen v ČR − dotazníková studie
- Těžké menstruační krvácení může značit poruchu krevní srážlivosti. Jaký management vyšetření a léčby je v takovém případě vhodný?
- Fixní kombinace paracetamol/kodein nabízí synergické analgetické účinky
Najčítanejšie v tomto čísle
- Correction: Low dose naltrexone: Effects on medication in rheumatoid and seropositive arthritis. A nationwide register-based controlled quasi-experimental before-after study
- Combining CDK4/6 inhibitors ribociclib and palbociclib with cytotoxic agents does not enhance cytotoxicity
- Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning
- Risk factors associated with IgA vasculitis with nephritis (Henoch–Schönlein purpura nephritis) progressing to unfavorable outcomes: A meta-analysis