Professional Documents
Culture Documents
Martineau Et Al 2024 Comparison of Objective Facial Metrics On Both Sides of The Face Among Patients With Severe Bell S
Martineau Et Al 2024 Comparison of Objective Facial Metrics On Both Sides of The Face Among Patients With Severe Bell S
Martineau Et Al 2024 Comparison of Objective Facial Metrics On Both Sides of The Face Among Patients With Severe Bell S
Abstract
Objective: The extent to which the healthy hemiface dynamically contributes to facial synchronization dur-
ing facial rehabilitation has been largely unstudied. This study compares the synchronization of both hemi-
faces in severe Bell’s palsy patients who either received facial rehabilitation called ‘‘Mirror Effect Plus
Protocol’’ (MEPP) or basic counseling.
Methods: Baseline and 1-year postonset data from 39 patients (19 = MEPP and 20 = basic counseling) were
retrospectively analyzed using Emotrics+, a software that generates facial metrics with artificial intelligence
(AI) algorithms. Paired t-tests were used for intrasubject comparisons of hemifaces, and mixed model anal-
ysis were used to compare between groups.
Results: For voluntary movements, a significant difference in favor of the MEPP group was only found for
smiling ( p = 0.025*). However, at 1-year postonset, the control group showed significant variability between
hemifaces for most synkinesis measurements [nasolabial fold ( p = 0.029*); eye area ( p = 0.043*); palpebral
fissure ( p = 0.011*)].
Conclusion: In this study, a better synchronization of both hemifaces was found in the MEPP group. Inter-
estingly, motor adaptation in movement amplitude of the healthy hemiface seemed to contribute to this
synchronization in MEPP patients. Further studies are needed to standardize the procedure of AI measure-
ments and to adapt it for clinical use.
1
Département de chirurgie et Direction des Services Multidisciplinaires, Hôpital Maisonneuve-Rosemont, Montréal, Québec, Canada.
2
Centre de recherche du Centre intégré universitaire de santé et services sociaux du Nord-de-l’ı̂le-de-Montréal, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada.
3
École d’Orthophonie et d’Audiologie, Faculté de Médecine, Université de Montréal, Montréal, Québec, Canada.
4
Département universitaire d’enseignement et de formation en orthophonie, Faculté de Médecine, Université de Sorbonne, Paris, France.
*Address correspondence to: Sarah Martineau, PhD, Direction des Services Multidisciplinaires, Maisonneuve-Rosemont Hospital, 5415 boul. De l’Assomption, Montréal H1T 2M4,
Canada, Email: sarah.martineau.2@umontreal.ca
172
MEPP AND EMOTRICS+ 173
(https://mirroreffectplus.org/#/login) that duplicates the group during a specific movement (i.e., differences of
healthy side of the face. This should encourage nonforced nasolabial angles during brow raise, differences of naso-
and symmetrical natural facial movement. Patients labial angles during eye closure, and differences in eye
attended four in-clinic therapy sessions during the first 2 areas and palpebral fissures during pucker). For greater
weeks following baseline and then monthly for follow- clarity, all parameters analyzed in this study, with their
up. They also completed two daily 15-min home sessions, appropriate units and visual representations, are summa-
which is thought to promote motor learning and avoid rized in Supplementary Data S1.
muscular fatigue.17
Participants in the control group did not attend therapy
sessions. However, they received instructions to avoid
excessive facial movements. Their concerns or questions
were addressed if needed.
Table 1. Mean Values (Standard Deviation) of Symmetry During Facial Expressions (From a Rest Position to the Targeted
Movement) Representing Hemifaces’ Synchronization with Intrasubject Analysis for Evolution of Each Hemiface and Mixed
Model Analyses for Differences Between Groups
Table 2. Intrasubject Comparison of Affected Versus Healthy Side Synchronization at 12 Months for Voluntary Movements
with Paired t-Tests with Their 95% Confidence Intervals
MEPP Controls
Variation in commissure position during smiling 0.511 ( 1.893 to 3.104) 0.308 1.981 ( 11.116 to 5.255) 0.031
Variation in nasolabial angle during smiling 0.182 ( 7.711 to 6.479) 0.429 0.403 ( 12.092 to 8.191) 0.346
Variation in brow height during brow raise 1.361 ( 8.024 to 1.748) 0.096 1.831 ( 13.876 to 0.950) 0.042
Variation in commissure position during pucker 1.208 (0.880 to 0.785) 0.121 0.462 (1.056 to 2.708) 0.325
Facial symmetry and dynamic synchronization which suggests that synchronization between both hemi-
in voluntary movements faces tended to be greater for the MEPP group.
Figure 1 represents the evolution of the facial expressions
Downloaded by University of Cape Town from www.liebertpub.com at 05/19/24. For personal use only.
for each hemiface in the control and MEPP groups for the Co-contractions and synkinesis
three following voluntary movements: smiling, brow raise, Table 3 and Figure 2 report the mean values of potential
and pucker. Results of the dynamic synchronization in co-contractions (for the healthy side) or synkinesis of the
these three voluntary movements are reported in Table 1. affected side for both groups at 12 months.
Overall, the healthy side did not significantly vary over Measures of co-contractions were expected to show very
time in both groups, except for the pucker (MEPP: little variation on the healthy side, because synkinesis only
t = 3.234; p = 0.005 and controls: 4.273; p = 0.001). occurs as a result of the reinnervation process on the affected
The pucker showed a larger negative (under 0) variation side. However, variations in movements of the healthy side
at 12 months, which could be interpreted as a generally are depicted here alongside synkinetic movements, because
more ample commissure movement bilaterally toward they convey information about general movement ampli-
midline. As expected, the affected side tended to show sig- tude and patients’ overall tendency to harmonize move-
nificant variation over time, demonstrating greater move- ments between their hemifaces. Importantly, amplitude of
ment at 12 months. In addition, results of the mixed the healthy side movement during synkinesis is information
model analysis for comparison between treatment modali- that could not be analyzed in our previous work.
ties demonstrated no significant differences between con- In Figure 2, when comparing groups, the nasolabial
trols and MEPP patients over time regarding symmetry angle of the affected side tended to augment during
of voluntary movements, except for the commissure posi- brow raise and eye closure only in the control group,
tion in smiling. which is representative of a cheek synkinesis. During
In Table 2, intrasubject analyses demonstrated no sig- pucker, the percentage of eye area and palpebral fissure
nificant differences between the healthy and affected decreased in both groups, demonstrating an eye synkinesis
sides of the face for the MEPP group at 12-month poston- in both groups. The control group showed significantly
set. However, the control group demonstrated a signifi- more variation between hemifaces than the MEPP
cant difference across hemifaces for commissure group, for measures of synkinesis during eye closure
position during smiling (t = 1.981; p = 0.031) and (nasolabial angle variation: t = 2.032; p = 0.029*), and
brow height during brow raise (t = 1.361; p = 0.042), pucker (eye area: t = 1,814; p = 0.043* and palpebral
Table 3. Mean Values (Standard Deviation) of Synkinesis at 12-Month Postonset and Intrasubject Comparisons of Affected
Versus Healthy Side Synchronization in Both Groups
MEPP Controls
Variation in nasolabial angle during brow raise in degrees 0.55 (3.218) 0.64 (2.05) 0.99 (3.98) 0.35 (4.58)
Paired t-test values ( p values) t = 0.073 ( p = 0.471) t = 0.526 ( p = 0.303)
Variation in nasolabial angle during eye closure in degrees 1.16 (1.63) 0.52 (2.61) 0.60 (2.94) 0.80 (1.84)
Paired t-test values ( p values) t = 1.032 ( p = 0.158) t = 2.032 (p = 0.029)
Variation in eye area during pucker in % 25.76 (27.83) 20.89 (26.45) 27.39 (32.41) 11.21 (21.99)
Paired t-test values ( p values) t = 0.918 ( p = 0.185) t = 1.814 (p = 0.043)
Variation in palpebral fissure width during pucker in % 24.15 (26.78) 15.58 (26.54) 30.86 (27.32) 11.45 (17.68)
Paired t-test values ( p values) t = 1.445 ( p = 0.083) t = 2.5 (p = 0.011)
between the healthy and affected hemiface, which is a Khawla Kharra, Nadim T. Saydy, Laurence Gascon,
key component that affects the perception of facial Ariane Poulin, and Stéphanie Des Ormeaux.
palsy severity and quality of life in patients.27
Based on our previous10,28 and present studies, we next Authors’ Contributions
hypothesized that the better synchronization of both hem- S.M. was responsible for study design, literature review,
ifaces by the MEPP participants could be partly data collection, data analysis, and was a major contributor
explained by an accentuation of the natural neurophysio- in writing and revising the manuscript. L.P. and H.K. con-
logical organization of the facial motor system, thanks to tributed to data collection and revising the manuscript.
its mirror therapy component.29 The present results are A.R. contributed largely to study design, to literature
also consistent with that of Ross et al.,30 who found ro- reviewing, and revising the manuscript. K.M. contributed
bust evidence for a predominantly independent hemi- largely to study design, literature review, data collection,
spheric motor control of the lower versus upper face. data analysis, and revising the manuscript.
This independence leads to a relative easiness in execut-
ing asymmetrical (or emotionally distinctive) movements Author Disclosure Statement
in the inferior versus superior quadrant of the face. How- The authors declare no conflict of interest.
ever, those asymmetrical movements were not easily pro-
Downloaded by University of Cape Town from www.liebertpub.com at 05/19/24. For personal use only.
duced across the sagittal plane (right vs. left) of the face. Funding Information
Clinically, for BP patients, this could mean that a rehabil- The authors disclose receipt of the following financial
itation focusing on the synchronization at the horizontal support for the research, authorship, and/or publication
axis, such as the MEPP, could sustain natural recovery. of this article: This work was supported by REPAR-
This study does have some limitations. Data of one OOAQ grant (No. 5080); a La Division ORL grant; and
MEPP patient could not be analyzed due to low-quality Fonds de Recherche du Québec—Santé grants (Nos.
pictures gathered during the pandemic. In addition, 266532 and 33310).
while AI is a promising tool to automate analysis and
minimize human bias, not all pictures completely con-
Supplementary Material
formed to the criteria of those used for training the algo- Supplementary Data S1
rithm, for example, blue background,14 which led to Supplementary Data S2
manual adjustments of the reference points in some pic-
tures by blinded judges. Finally, very little research References
until now has used Emotrics+ to calculate dynamic sym- 1. Steinhäuser J, Volk GF, Thielker J, et al. Multidisciplinary care of patients
with facial palsy: Treatment of 1220 patients in a German Facial Nerve
metry and synkinesis following an intervention; thus, the Center. J Clin Med 2022;11(2):427. doi:10.3390/jcm11020427
procedure described in the methodology has not yet been 2. Basić-Kes V, Dobrota VD, Cesarik M, et al. Peripheral facial weakness (Bell’s
palsy). Acta Clin Croat 2013;52(2):195–202.
standardized and should be replicated in further studies. 3. Shokri T, Azizzadeh B, Ducic Y. Modern management of facial nerve dis-
However, the results can be the basis for future power orders. Semin Plast Surg 2020;34(4):277–285. doi:10.1055/s-0040-
calculations about mirror therapy. 1721824
4. Ferreira M, Marques EE, Duarte JA, Santos PC. Physical therapy with drug
treatment in Bell palsy: a focused review. Am J Phys Med Rehabil
Conclusion 2015;94:331–340. doi:10.1097/phm.0000000000000255
5. Monini S, Buffoni A, Romeo M, et al. Kabat rehabilitation for Bell’s palsy in
The results in this study suggest that AI facial metrics the elderly. Acta Otolaryngol 2016;137:646–650. doi:10.1080/00016489
could be used to successfully differentiate between intra- .2016.1262553
individual differences in hemifaces’ evolution in two 6. Nicastri M, Mancini P, De Seta D, et al. Efficacy of early physical therapy in
severe Bell’s palsy: a randomized controlled trial. Neurorehabil Neural
groups of BP patients. Furthermore, a slightly greater Repair 2013;27:542–551. doi:10.1177/1545968313481280
motor adaptation of the healthy hemiface was seen in pa- 7. Barth JM, Stezar GL, Acierno GC, Kim TJ, Reilly MJ. Mirror book therapy for
the treatment of idiopathic facial palsy. Ear Nose Throat J
tients who benefited from the MEPP, a facial retraining 2020:145561320913211. doi:10.1177/0145561320913211
program that includes a mirror therapy component, 8. Adhikari SP, Chaudhary M, Rubee D. Kabat Interventions integrated with
which could have led to improved synchronization of facial expressive and functional exercises for better and speedy re-
covery in Bell’s Palsy: a pre-post design. J Chitwan Med College
both hemifaces. 2020;10(34):71–76.
9. Paolucci T, Cardarola A, Colonnelli P, et al. Give me a kiss! An integrative
Acknowledgments rehabilitative training program with motor imagery and mirror therapy
for recovery of facial palsy. Eur J Phys Rehabil Med 2020;56(1):58–67.
We deeply thank our participants and their families for doi:10.23736/s1973-9087.19.05757-5
their commitment to this project. We are also grateful 10. Martineau S, Rahal A, Piette E, Moubayed S, Marcotte K. The ‘‘Mirror Effect
Plus Protocol’’ for acute Bell’s palsy: a randomized controlled trial with a
to the Massachusetts Eye and Ear Center who kindly one-year follow-up. Clin Rehabil 2022;36(10):1292–1304. doi:10.1177/
shared their Emotrics+ software with the SCBS commu- 02692155221107090
nity. We also thank our collaborators who participated 11. Ross ED, Gupta SS, Adnan AM, Holden TL, Havlicek J, Radhakrishnan S.
Neurophysiology of spontaneous facial expressions: I. Motor control of
either in recruitment, analysis, or as blind judges: the upper and lower face is behaviorally independent in adults. Cortex
Anne-Marie Chouinard, Camille Rivest, Marie Julien, 2016;76:28–42. doi:10.1016/j.cortex.2016.01.001
MEPP AND EMOTRICS+ 179
12. Ross ED, Gupta SS, Adnan AM, Holden TL, Havlicek J, Radhakrishnan S. 22. Streiner DL, Norman GR. Health Measurement Scales: A Practical Guide to
Neurophysiology of spontaneous facial expressions: II. Motor control of Their Development and Use. 4th ed. Oxford, UK: Oxford University Press;
the right and left face is partially independent in adults. Cortex 2008.
2019;111:164–182. doi:10.1016/j.cortex.2018.10.027 23. Martineau S, Rahal A, Dufour-Fournier C, Marcotte K. Post lengthening
13. Greene JJ, Guarin DL, Tavares J, et al. The spectrum of facial palsy: The temporalis myoplasty facial rehabilitation by speech-language pathol-
MEEI facial palsy photo and video standard set. Laryngoscope ogists: A study of three patients [In French]. Revue Canadienne
2020;130(1):32–37. doi:10.1002/lary.27986 d’Orthophonie et d’Audiologie 2018;42:117–126.
14. Guarin D, Dusseldorp J, Hadlock T, Jowett N. A machine learning ap- 24. Blanchin T, Martin F, Labbe D. Reeducation des paralysies faciales apres
proach for automated facial measurements in facial palsy. JAMA Facial myoplastie d’allongement du muscle temporal. Interet du protocole
Plast Surg 2018;20(4):335–337. doi:10.1001/jamafacial.2018.0030 ‘‘effet-miroir’’ [Lengthening temporalis myoplasty: A new approach to
15. Gagyor I, Madhok VB, Daly F, et al. Antiviral treatment for Bell’s palsy facial rehabilitation with the ‘‘mirror-effect’’ method]. Ann Chir Plast
(idiopathic facial paralysis). Cochrane Database Syst Rev Esthet 2013;58:632–637. doi:10.1016/j.anplas.2013.03.001
2015;(11):CD001869. doi:10.1002/14651858.CD001869.pub8 25. Garmi R, Labbe D, Coskun O, Compere JF, Benateau H. Lengthening
16. Nasreddine ZS, Phillips NA, Bedirian V, et al. The Montreal Cognitive temporalis myoplasty and brain plasticity: a functional magnetic reso-
Assessment, MoCA: a brief screening tool for mild cognitive impair- nance imaging study. Ann Chir Plast Esthet 2013;58(4):271–276. doi:10
ment. J Am Geriatr Soc 2005;53(4):695–699. doi:10.1111/j.1532-5415 .1016/j.anplas.2013.03.002
.2005.53221.x 26. Martin F, Belleme S, Leon S. Le biofeedback électromyographique
17. Martineau S, Martel-Sauvageau V, Piette E, Chouinard A-M, Rahal A, appliqué aux fonctions oro-faciales. Rééducation Orthophonique
Marcotte K. A Pilot Study on the Mirror Effect PLUS Protocol: a stan- 2002;210:129–137.
dardized and adapted facial rehabilitation for acute Bell’s palsy. Canad J 27. Dey JK, Ishii M, Boahene KD, Byrne PJ, Ishii LE. Changing perception: facial
Speech Lang Pathol Audiol 2020;44(2):57–72. reanimation surgery improves attractiveness and decreases negative
Downloaded by University of Cape Town from www.liebertpub.com at 05/19/24. For personal use only.
18. Martineau S, Rahal A, Piette É, Chouinard A-M, Marcotte K. The Mirror facial perception. Laryngoscope 2014;124(1):84–90. doi:10.1002/lary
Effect Plus Protocol for acute Bell’s palsy: a randomised and longitudi- .24262
nal study on facial rehabilitation. Acta Otolaryngol 2021;141(2):203–208. 28. Martineau S, Rivest C, Rahal A, Marcotte K. Development of an open-
doi:10.1080/00016489.2020.1842905 source and free facial rehabilitation website for severe bell’s palsy: a
19. Miller MQ, Hadlock TA, Fortier E, Guarin DL. The Auto-eFACE: machine within-subject study on user experience and patient’s compliance with
learning-enhanced program yields automated facial palsy assessment the MEPP-website. Disabil Rehabil 2022;44(26):8357–8366. doi:10.1080/
tool. Plast Reconstr Surg 2021;147(2):467–474. doi:10.1097/prs 09638288.2021.2012846
.0000000000007572 29. Sessle BJ, Adachi K, Avivi-Arber L, et al. Neuroplasticity of face primary
20. Guarin DL, Yunusova Y, Taati B, et al. Toward an automatic system for motor cortex control of orofacial movements. Arch Oral Biol
computer-aided assessment in facial palsy. Facial Plast Surg Aesthet Med 2007;52(4):334–337. doi:10.1016/j.archoralbio.2006.11.
2020;22(1):42–49. doi:10.1089/fpsam.2019.29000.gua 002
21. Koo TK, Li MY. A guideline of selecting and reporting intraclass correlation 30. Ross ED, Prodan CI, Monnot M. Human facial expressions are organized
coefficients for reliability research. J Chiropr Med 2016;15(2):155–163. functionally across the upper-lower facial axis. Neuroscientist
doi:10.1016/j.jcm.2016.02.012 2007;13(5):433–446. doi:10.1177/1073858407305618