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Physical Therapy Reviews

ISSN: 1083-3196 (Print) 1743-288X (Online) Journal homepage: http://www.tandfonline.com/loi/yptr20

Effectiveness of electrical stimulation for


rehabilitation of facial nerve paralysis

Katie A Fargher & Susan E Coulson

To cite this article: Katie A Fargher & Susan E Coulson (2017): Effectiveness of electrical
stimulation for rehabilitation of facial nerve paralysis, Physical Therapy Reviews, DOI:
10.1080/10833196.2017.1368967

To link to this article: http://dx.doi.org/10.1080/10833196.2017.1368967

Published online: 31 Aug 2017.

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Download by: [Australian Catholic University] Date: 20 September 2017, At: 00:02
Effectiveness of electrical stimulation for
rehabilitation of facial nerve paralysis
Katie A Fargher, Susan E Coulson 
Discipline of Physiotherapy, Faculty of Health Sciences, University of Sydney, Sydney, Australia

Background: Despite no significant advantage being demonstrated for its use and no standardization of treatment
guidelines, electrical stimulation is still applied by therapists to treat facial paralysis. The aim of this investigation
was to determine whether electrical stimulation therapy for patients with acute or chronic facial nerve paralysis
improves time to, and rates of full recovery and facial function compared with no intervention.
Method: A systematic review of randomized and quasi-randomized controlled trials through Scopus, Medline,
Downloaded by [Australian Catholic University] at 00:02 20 September 2017

PEDro, Embase, CINAHL, Pubmed, and Cochrane Library search engines for studies published up until August
2016. Reference lists were reviewed for further studies. Review Manager was used to extract data and review
quality of the studies. Studies were assessed for randomization of participants, allocation concealment, blinding
of participants, assessors and physiotherapists, presence and reporting of outcome data.
Results: Five studies were included for analysis – four during acute recovery and one in chronic facial nerve
paralysis. In acute facial nerve paralysis, two studies found no benefit of electrical stimulation and two studies
found improvement. A meta-analysis on changes in the House–Brackmann Score after treatment, rates of full
recovery and time to full recovery showed no statistically significant difference between intervention and control
groups. In chronic facial nerve paralysis, one study found improvements after extensive electrical stimulation on
the Facial Paralysis Recovery Profile.
Conclusions: There is no evidence to support the use of electrical stimulation during the acute phase of recovery
after Bell’s palsy and there is low-level evidence for patients with chronic symptoms. Furthermore, there is no
evidence available on the use of electrical stimulation for other causes of facial nerve paralysis.
Keywords:  Bell palsy, Facial nerve, Electrical stimulation therapy, Facial paralysis, Physiotherapy, Rehabilitation

Introduction and trauma vary depending upon the site and severity of
Facial nerve paralysis (FNP) affects social interaction, the injury.
communication, and self-esteem, leading to long-lasting Along with pharmacology8 and surgery, physiotherapy
negative impacts on daily life.1 Idiopathic Bell’s palsy is undertaken after FNP to improve function. Patients are
accounts for 75% of all cases, with trauma and Herpes referred to physiotherapists during acute and chronic
Zoster Oticus the next most common causes.2,3 There is a phases of recovery. Electrical stimulation has been used
variable degree of recovery after FNP without intervention since the 1950s with the goal of improving facial function
and this is dependent on the severity, cause, and location and minimizing sequelae.9 The aim of electrical stimula-
of the nerve damage.4 With neuropraxia, or partial degen- tion is to encourage nerve regeneration,10 and to main-
eration of the nerve, clinically observable facial move- tain muscle bulk and contractile properties.10–12 In animal
ment usually begins within a few weeks.4 When complete studies, the quality of the muscle reinnervation is also
degeneration of the nerve occurs, as with axonotmesis or examined on a cellular level, with electrical stimulation
neurotmesis, movement only begins after the nerve regen- aiming to minimize polyinnervation, collateral branching,
erates.2,5 The nerve grows at a rate of 0.5 to 3 mm per day6 interstitial fibrosis,13 Wallerian degeneration and demyeli-
and reinnervation may be disordered due to scar tissue nation.14 The types of electrical stimulation that have been
and disruption of nerve fibers.5 Regeneration can lead to used by therapists include galvanic,9 eutrophic,15 mono-
altered patterns of muscle contraction, salivation, and tear- phasic,11 biphasic,12 subthreshold,13 and contraction level.11
ing (motor and autonomic synkinesis).7 Earlier recovery of A systematic review in 200316 concluded that using
function indicates a milder injury with better prognosis.2 electrical stimulation was beneficial, however it included
All patients with Bell’s palsy experience some recovery, case studies and case series which do not control for nat-
with 71% achieving full recovery. Outcomes after surgery ural recovery. A Cochrane Review in 201117 addressed
multiple physiotherapy modalities for acute Bell’s palsy
Correspondence to: Susan E Coulson, Discipline of Physiotherapy Faculty
of Health Sciences, University of Sydney, Sydney, Australia. Email: susan. and concluded no benefits of electrical stimulation at
coulson@sydney.edu.au

© 2017 Informa UK Limited, trading as Taylor & Francis Group


DOI 10.1080/10833196.2017.1368967 Physical Therapy Reviews   2017 1
Fargher and Coulson  A systematic review and meta-analysis of the literature

6 months post onset. This review aims to address the summary is presented in Figure 2. The PRISM-A state-
question ‘Does electrical stimulation therapy for patients ment was followed during data extraction.19 Data analysis
with acute or chronic FNP improve time to full recovery, was completed in Review Manager (RevMan version 5.3;
rates of full recovery and facial function compared to no Copenhagen, Denmark: The Nordic Cochrane Centre, The
intervention?’. Cochrane Collaboration, 2014)18 using mean difference
and odds ratios with 95% confidence intervals. Kim and
Method Choi10 were the only paper to include a standard deviation
Identification and selection of studies in their pre-treatment data. As it was calculated from a
Literature searches were completed on Scopus, Medline, large population (n = 60), it was the best estimate availa-
PEDro, Embase, CINAHL, Pubmed, and Cochrane Library ble and was used across the studies to allow the pooling
search engines. Search terms used were ‘facial nerve’, of data.
‘facial paralysis’, ‘facial palsy’, ‘Bell$ palsy’, ‘electrical
stimulation’, ‘electrotherapy’, ‘physical therapy’, ‘physi- Results
otherapy’, and ‘rehab*’. Reference lists of retrieved arti- Included studies
cles were also reviewed for further relevant studies. All Twenty-one papers were reviewed. Eight studies were
searches were completed between 26 May 2015 and 19 excluded for being case series20–27, two for a lack of rand-
August 2016 by KF. Screening of titles and abstracts for omization28,29 and one for comparing ES to an alternative
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inclusion was completed by KF and SC. Disagreement therapy with no control group.30 Four reviews16,31–33 and
was resolved by discussion. one retrospective chart review3 were also excluded. Five
Wide inclusion criteria were necessary to draw con- studies were found to meet final criteria – four in acute
clusions relevant to variable etiologies and different phase of recovery and one in chronic phase (Figure 3).
phases of rehabilitation (Figure 1). Only human studies
were included. Electrical stimulation delivered through Characteristics of studies
acupuncture needles was excluded. Randomized control Two randomized9,11 and two quasi-randomized controlled
trials and quasi-randomized control trials were included trials10,12 applied electrical stimulation during acute phases
for analysis. Articles were excluded if electrical stimu- of recovery and one quasi-randomized controlled trial15 in
lation was combined with another intervention that the chronic phase. The dominant etiology was Bell’s palsy.
comparison group did not receive. Only published work Full details of included studies are in Table 2. The quality
available in English through the document search were of each study was assessed using individual domains of
used. Studies were excluded if they did not meet one of selection, performance, detection, attrition, and reporting
the inclusion criteria. bias. A lack of blinding of the participants impacted on all
study outcomes. This would likely bias participants in their
Assessment of study characteristics and data compliance with therapy and home programs, as they are
analysis aware that they are in the active therapy group. Conclusions
Variables sought from the studies are listed in Table 1. The of some studies were considered with respect to low partic-
information was extracted by KF and reviewed by SC. The ipant numbers in treatment and control groups. No study
risk of bias analysis was completed in Review Manager used intention-to-treat analysis. The risk of selection bias
(RevMan version 5.3; Copenhagen, Denmark: The Nordic was high in three studies,10,12,15 unclear in one,9 and low
Cochrane Centre, The Cochrane Collaboration, 2014)18 in one.11 The impact of selection bias in unclear. Results
and addressed randomization of participants, allocation may have been affected by participants being preferen-
concealment, blinding of participants, assessors and phys- tially allocated to treatment or control groups depending
iotherapists, presence and reporting of outcome data. The on their prognosis. Blinding of assessors was only clearly
stated in one study.11 This places the other studies at high
risk of bias toward the predispositions of the researchers.

Electrical stimulation parameters


In the acute studies, three used similar therapy parameters
to maintain muscle properties (Table 2).9,11,12 The program
started between two- and four-week post injury and was
administered by a therapist. Minimal muscle contractions
were used during sessions. The frequency of treatment var-
ied from 1 day per week12 to 5 days per week.11 Electrical
stimulation was continued for a variable length of time
from 3 weeks11 to 3 months.12
Kim and Choi10 used electrical parameters that were
Figure 1  Inclusion criteria. different to the other studies. Stimulation was at a

2 Physical Therapy Reviews   2017


Fargher and Coulson  A systematic review and meta-analysis of the literature

Table 1  Variables sought from studies

Patient factors Cause of paralysis, length of injury, specific surgery (if relevant), presence of denervation
Intervention information Machine used, intensity, frequency, length of each session, number of sessions per day/week, length of
total intervention, type of pulse, type of electrical stimulation (galvanic/faradic), pulse duration, interval, pulse
rate, who applied electrical stimulation, size and location of electrodes, time post injury intervention was
started
Comparisons Other treatments used in control and experimental groups
Outcomes Number and type of outcome measures used, functional outcomes, electrophysical results, adverse out-
comes, patient tolerance, dropout rate, blinding of assessors, type of data analysis
Study Size of trial, duration of follow-up, bias including sources of financial assistance, publication location, num-
information ber of times cited, intention to treat

Outcome measures
The outcomes considered were the length of time to full
recovery, rates of full recovery, improvements in facial
function, and rates of complications. The outcomes used in
the studies included the House–Brackmann Facial Nerve
Grading System, the Facial Paralysis Recovery Profile
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(FPRP), the Facial Paralysis Recovery Index (FPRI),


Facial Disability Index, and Sunnybrook Facial Grading
System. Video-based motion analysis and various point
rating systems to grade motion were also used.

Length of time to full recovery


In Mosforth and Taverner’s study,9 participants were
divided into two subgroups: those with and without
nerve degeneration as assessed by EMG data. They
reported no difference in the length of time to full recov-
ery between groups for participants without denerva-
tion (treatment group mean 43 days, range 14–90 days;
Figure 2  Risk of Bias. control group mean 39 days, range 14–134 days). For
participants with denervation, time to initial movement
return in the intervention group was 53 days (range
10–104 days) compared with 66 days (14–90 days) in
the control group. The inclusion of infrared radiation as
part of the intervention protocol, however, confounds
this study’s findings.
Kim and Choi10 included only participants with
less severe forms of Bell’s palsy (House–Brackmann
score < IV). The initial House–Brackmann scores of
some of the patients were higher than the inclusion cri-
terion (mean = 3.5 ± 1.2) and some patients enrolled
after three weeks post onset. There was a faster time to
full recovery in the intervention group (Kruskal-Wallis
one-way ANOVA, p < 0.05). It is unclear whether the
Figure 3  Selection of studies.
assessments were blinded and what confidence intervals
subthreshold level, and applied continuously for the first were used.
2 months of recovery to limit Wallerian degeneration of As Kim and Choi10 were the only researchers to
the nerve. The electrodes were placed near the mastoid include a standard deviation in their initial data, their
process instead of the muscles and the equipment was average standard deviation was used across the studies
applied by the participant. to allow the pooling of data. The time to full recov-
Like the majority of the acute studies, participants in the ery after acute facial nerve injury was also assessed in
chronic stages were instructed to use electrical stimulation Review Manager (RevMan version 5.3; Copenhagen,
at the muscle contraction threshold with the aim being to Denmark: The Nordic Cochrane Centre, The Cochrane
maintain muscles and encourage return of structure and Collaboration, 2014)18 and found to have no significant
function.15 The intervention was used for much longer difference between groups (mean difference −0.79, 95%
durations in the chronic population (see Table 2). CI −2.71–1.13, Figure 4).

 Physical Therapy Reviews  2017 3


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4
Table 2  Characteristics of included studies

Participants and groups


Diagnosis:
Length after injury:
Supports electrical
Study stimulation? Groups: Intervention Electrical stimulation parameters
Mosforth and Tavern- No Diagnosis: Bells palsy, n = 83 Administration: therapist Type: galvanic
er (1958) Saline electrodes
Length of injury: <2 weeks Pulse: 100 ms
Location: 12 muscles Machine: Ritchie-Sneath

Physical Therapy Reviews   2017


Groups: control and electrical stimulation. Sessions: 3 sets of 30 contractions
Both groups: self-massage daily. Sessions per week: 3
Threshold: minimal contraction
Length of intervention: variable, up to
1 year.
Kim and Choi (2016) Yes Diagnosis: Bells palsy; n = 60; House–Brackmann Grade less than IV Administration: self Duration: 10 ms
Frequency: 20 Hz
Length of injury: <3 weeks Location: cathode on main branches of Voltage: 20 MV–10 V
Groups: control and electrical stimulation. facial nerve, anode on mastoid process. Intensity: just below sensory threshold
Sessions: ‘continuous’
Fargher and Coulson  A systematic review and meta-analysis of the literature

Sessions per week: ‘continuous’ Electrodes: 2 cm surface electrodes


Both groups: prednisolone and acyclovir Threshold: subsensory
Length of intervention: 2 months
Tuncay et al. (2014) Yes Diagnosis: Bells palsy; n = 60 Administration: therapist Type: Monophasic
Length of injury: 4 weeks Location: 11 facial muscles Pulse duration: 100 ms
Groups: Control and electrical stimulation. Interval: 300 ms
Both groups: hot pack, facial expression exercises, massage, oral corticoster- Sessions: 3 sets of 30 contractions Pulse rate: 2.5 pulses/sec
oids. Sessions per week: 5 Intensity: muscle contraction
Threshold: minimal contraction Machine: Dynatron 438
Length of intervention: 1 month Delivery: carbon-rubber electrode
Alakram and Puckree No Diagnosis: Bells palsy, n = 16 Administration: therapist Type: Biphasic
(2010) Length of injury: mean 2 weeks Location: 3 facial muscles Pulse duration: 10microsec
Groups: Control and electrical stimulation. Sessions: 30 min. Frequency: 10 Hz Intensity: visible twich
Sessions per week: 1 Machine: EV-803 Digital SD TENS
Both groups: prednisolone, hot pack, massage, and facial expression exercis- Threshold: minimal contraction
es, home exercise program with exercises. Length of intervention: 3 months
Farragher et al. Yes Diagnosis: Bells palsy, n = 39, HZO, n = 1 Administration: self Type: eutrophic 
(1987) Location: 2 facial muscles Delivery: Carbon rubber electrodes
Length of injury: mean 77 months Sessions: 3–5 h Voltage: 18 (muscle contraction
­threshold)
Groups: Initial treatment (n = 20), crossover at 6 weeks15 cross over at Sessions per week: 7 Pulse duration: 80microsec
12 weeks,3 cross over at 18 weeks.2 All groups: advice, mirror exercises, mas- ­compensated rectangular monophasic
sage at beginning of study pulses
Threshold: muscle contraction threshold.
Length of intervention: unknown.
Fargher and Coulson  A systematic review and meta-analysis of the literature

Figure 4  Forest plot of length of time to full recovery.


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Figure 5  Forest plot of rate of full recovery.

Achievement of full recovery groups. The House–Brackmann data were included for
Mosforth and Taverner reported full recovery in 100% of
9 meta-analysis.
participants who had a conduction block without dener- Alakram and Puckree12 reported each patient’s results
vation. In the subgroup with denervation, no participant as a recovery rate by taking their change in House–
achieved full recovery by 12 months. Kim and Choi10 Brackmann score and dividing it by the number of weeks
reported at one-year follow-up, 3 out of 30 participants in to recovery. In order to analyze the data and calculate
the control group and 1 out of 30 in the intervention group mean House–Brackmann scores, the equation used in
had incomplete recovery. Analysis of the data from the the paper was reversed. To retrieve the average recov-
two studies found no difference between the intervention ery time, the treatment time in each group (9 weeks in
and control groups (odds ratio 1.38, 95% CI 0.62–3.08, control, 8 weeks in intervention) was added to the time
Figure 5). to commencement of physiotherapy (2 weeks). Tuncay
et al.11 reported median and range of House–Brackmann
Improvement in facial function values. They tested the difference between the groups
Improvement in facial function was the most commonly at pre-treatment, reported the p-value and did the same
reported outcome in the studies, although each study at post-treatment. It was therefore possible to consider
used a different measure to quantify this outcome. After a parametric test between two means that produced the
acute Bell’s palsy, Mosforth and Taverner9 scored the same p-value, and calculate the difference between the
improvement in function in patients who did not achieve means to determine the treatment effect. The treatment
full recovery (n = 33) and found no difference between effect was entered into Review Manager (RevMan version
the intervention and control groups. Tuncay et al.11 5.3; Copenhagen, Denmark: The Nordic Cochrane Centre,
reported that both control and intervention groups had The Cochrane Collaboration, 2014)18 by setting the control
a statistically significant improvement on the House– group difference to 1 (the difference between the reported
Brackmann Scale. The post-intervention measures median values) and the intervention group difference as
were compared using the Mann–Whitney U test and 1 + Treatment Effect. There was no improvement in facial
the difference was found to be statistically significant function after electrical stimulation found in the pooled
in favor of the intervention group (p = 0.03). The rate House–Brackmann results (mean difference −0.38, 95%
of change in facial function was not statistically deter- CI −0.78 – 0.03, Figure 6).
mined between the two groups. It is unclear how many Farragher et al.15 reported no change in facial function
participants were in each House–Brackmann grade. prior to electrical stimulation treatment in the crossover
Alakram and Puckree12 found no difference in facial groups with chronic FNP. Improvement was reported at 6,
function improvement between control and interven- 12, and 18 weeks after treatment was commenced; how-
tion groups (p = 0.36, Mann–Whitney test rank). Using ever the number of patients assessed declined by over 50%
the House–Brackmann scale, Kim and Choi10 reported (n = 35 at 6 weeks and 11 at 18 weeks). Assessment at
a significantly higher change in facial function in the 6 months after the completion of treatment reported ‘no
intervention group compared to control group at all data decline’, however no data were provided. The FPRP was
collection visits except for 4, 10, and 12 weeks post not reported separately, therefore the stated improvement
symptom onset. The Sunnybrook Facial Nerve Grading in voluntary movement is inseparable from the reported
System scores were not significantly different between complications.

 Physical Therapy Reviews  2017 5


Fargher and Coulson  A systematic review and meta-analysis of the literature

Figure 6  Forest plot of improvement in House–Brackmann Score.

Complications recovery, however, there is variation in frequency of treat-


The rate of development of contracture after FNP was not ment from one to five days per week.9,11,12 The other study
altered by the use of electrical stimulation.9 One study in the acute phase used continuous subthreshold stimula-
reported contact dermatitis in four out of thirty participants tion and placed the electrodes over the main branch of the
in the electrical stimulation group.10 ‘No indications of any facial nerve rather than the muscles.10
adverse response to the treatment’ was reported in one Electrical stimulation does not alter the speed or rate
study12 however overall there was not a comprehensive of full recovery, nor does it improve facial function in the
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and standardized reporting of complications. acute phase. In the chronic phase of recovery, there is low
quality evidence in one study 15 that extensive electrical
Discussion stimulation may have a positive impact on facial function.
The main goal of this review is to examine the efficacy Reasons for this may include extrapolation of study results
of electrical stimulation on recovery after FNP. In the from other areas of the body to the facial region, giving
acute phase of recovery, there are two randomized9,11 and the impression of movement to the patient, and equip-
two quasi-randomized controlled trials.10,12 Alakram and ment manufacture. There is no evidence that electrical
Puckree12 found no benefit in facial function with Tuncay11 stimulation will result in full recovery when used with
presenting positive findings in the electrical stimulation chronic FNP.
group. Kim and Choi10 found improvements in length of There are potential negative outcomes from using
time and rates of return to facial function by adding elec- electrical stimulation. Complications after FNP such as
trical stimulation while Mosforth and Taverner9 reported reinforcing synkinesis34 have been reported in the liter-
no difference. Three studies did not use true randomization ature for human subjects. In studies examining facial
techniques instead using alternate enrollment,12 division nerve regeneration in rats, no change in polyinnervation
by specialist,10 or unclear list methods.9 There was also no or collateral branching was found with axonal projec-
attempt to blind assessors in three studies placing them at tion disorganized in the electrical stimulation and sham
high risk of bias of the predisposition of the researchers, stimulation groups.13 Additionally, the number of motor
likely in favor of active intervention.9,10,12 Tuncay et al.11 endplates in the facial muscles was reduced to 24% of
was the only study to include randomization for group the value of the sham stimulation group,13 leading to
selection and blinding of assessors. The lack of blinding partial innervation instead of complete, which would
of participants potentially biases the intervention group. detrimentally impact on return of facial function. Animal
When the studies were combined for meta-analysis, there studies using electrical stimulation in other areas of the
was no statistically significant difference between treat- body have also demonstrated a halt in growth cone
ment and control groups for improvement in function, advancement,35 prevention of terminal sprouting,36,37
time to full recovery and achievement of full recovery limiting growth of axons and terminal Schwann cells,38
(Figures 4–6). and decreased reinnervation.39
The participants with chronic FNP in Farragher’s This current metanalysis provides no clear evidence
study who were initially enrolled in the control group, of benefit to support patients spending time and money
all received electrical stimulation when they crossed over on electrical stimulation following facial nerve paraly-
into the treatment group, therefore they could not be post- sis. There is, however, evidence of effective interventions
tested to compare with the intervention group.15 As noted which are currently used following FNP such as mime
by Tuncay et al., by losing the control group, it is difficult therapy,40 video self-modeling,41 and tailored facial exer-
to assess whether the positive impacts are due to electri- cises.17 An animal model study has also demonstrated
cal stimulation or intensive attention from a therapist.11 support for manual stimulation in favor of electrical stim-
Additionally, there was a greater than 50% decline in par- ulation for improving outcomes.42
ticipants reported in the results after 18 weeks.
The included studies used a variety of intervention Implications for clinicians
protocols (Table 2). Three studies used similar muscle This review found no evidence to support the use of
contraction electrical stimulation in the acute phase of electrical stimulation in the acute stages of Bell’s palsy

6 Physical Therapy Reviews   2017


Fargher and Coulson  A systematic review and meta-analysis of the literature

as it has not been shown to improve either the rate of PubMed PMID: 111313094. Language: English. Entry Date: 20151207.
Revision Date: 20160428. PublicationType: Article. Journal Subset:
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brackmann scores in early Bells palsy. Physiother Theory Pract.
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support electrical stimulation in the acute phase of facial nerve repair in rats. Ann AnaT. 2009;191(4):356–70. doi:10.1016/j.
aanat.2009.03.004
nerve paralysis. 14 Kim J, Han SJ, Shin DH, Lee WS, Choi JY. Subthreshold continuous
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Quality randomized control trials of humans are needed in 15 Farragher D, Kidd G, Tallis R. Eutrophic electrical stimulation for
the area of chronic FNP of various etiologies using inter- Bell’s palsy. Clin Rehabil. 1987;1:265–71.
16 Quinn R, Cramp F. The efficacy of electrotherapy for Bell’s palsy: a
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palsy (idiopathic facial paralysis). Cochrane Database Syst Rev.


electrical stimulation programs and consistent follow-up. 2011;12:CD006283. doi: 10.1002/14651858.CD006283.pub3
An objective and systematic recording of complications 18 Review Manager (RevMan). 5.3 ed. Copenhagen: The Nordic
Cochrane Centre, the Cochrane Collaboration; 2014.
should be included in all studies. 19 Shamseer L, Moher D, Clarke M, Ghersi D, Liberati A, Petticrew
M, et al. Preferred reporting items for systematic review and meta-
analysis protocols (prisma-p) 2015: elaboration and explanation.
Notes on contributors BMJ. 2015;349. doi:10.1136/bmj.g7647
Katie Fargher, BAppSc, is a clinical physiotherapist, and 20 Wilson CMR SL. Rehabilitation postfacial reanimation surgery after
research interests are in both pediatrics and in rehabilita- removal of acoustic neuroma: a case study. J Neurol Phys Ther.
2010;34(1):41–9. doi:10.1097/NPT.0b013e3181cfc324
tion of facial nerve disorders. 21 Shrode LW. Treatment of facial muscles affected by Bell’s palsy with
Susan Coulson, PhD (Physio); MAppSc(Ex & Sport Sc); high-voltage electrical muscle stimulation. J Manipulative Physiol
Ther. 1993;16(5):347–52.
BAppSc(Physio), is a lecturer discipline of Physiotherapy, 22 Weiss MH. Case report: successful treatment of Bell’s palsy. Dent
Faculty of Health Sciences, The University of Sydney. Surv. 1976;52(8):32–3.
23 Frach JP, Osterbauer PJ, Fuhr AW. Treatment of Bell’s palsy by
Her research interest is in rehabilitation of facial nerve mechanical force, manually assisted chiropractic adjusting and high-
disorders. voltage electrotherapy. J Manipulative Physiol Ther. 1992;15(9):596–
8.
24 Targan RS, Alon G, Kay SL. Effect of long-term electrical stimulation
on motor recovery and improvement of clinical residuals in patients
ORCID with unresolved facial nerve palsy. Otolaryngol Head Neck Surg.
2000;122(2):246–52. PubMed PMID: 10652399.
Susan E Coulson   http://orcid.org/0000-0002-3586-2562 25 Hyvarinen A, Tarkka IM, Mervaala E, Paakkonen A, Valtonen H,
Nuutinen J, et al. Cutaneous electrical stimulation treatment in
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8 Physical Therapy Reviews   2017

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