Professional Documents
Culture Documents
n
c
Hospital General de Yajalón, Secretaría de Salud, Yajalón, Chiapas, México
io
rs
Abstract.
ve
BACKGROUND: Up to now there is not enough evidence that supports the use of electrotherapy in the treatment of Bell’s palsy.
OBJECTIVE: Through a systematic review, we aimed to verify whether the use of electrotherapy is effective for treating Bell’s
f
oo
reeducation. Although the effect of electrotherapy alone was not evaluated, the use of electrotherapy combined with other treat-
ments produced a significant improvement in the individuals evaluated.
CONCLUSIONS: Due to the diverse methodologies used and the small number of individuals included in the studies, we
ct
could not fully prove the efficacy of electrotherapy for treating Bell’s Palsy. Future studies with larger samples and homogenous
rre
2 Facial peripheral paralysis, or Bell’s palsy, is an uals with Diabetes Mellitus, immunocompromised pa- 9
3 acute mononeuropathy of the facial nerve. It is of un- tients, individuals with arterial hypertension, patients 10
4 known cause and can affect a single nerve; it starts with who have had a viral infection of the upper respiratory 11
5 pain in the mastoids region and partial or total paral- tract, and pregnant woman [5]. Although Bell’s palsy 12
6 ysis of one side of the face [1,2]. Bell’s palsy affects can happen at any age, there are peaks of incidence 13
ISSN 1053-8127/20/$35.00
c 2020 – IOS Press and the authors. All rights reserved
Galley Proof 19/03/2020; 9:42 File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 2
n
35 review.
36 and some systematic reviews, physical therapy is not
io
37 a highly recommended treatment due to the scarce ev- 2.1.2. Exclusion criteria 68
idence of improvement observed in individuals with Controlled clinical trials that did not include elec- 69
rs
38
39 Bell’s palsy who received any type of physical ther- trotherapy as part of the Bell’s facial paralysis treat- 70
40 apy [3,12–14]. Nonetheless, in a recent systematic re- ment. Protocol articles for future studies were also ex-
ve 71
44 cological treatment alone [15]. Therefore, our system- We performed a search in PUBMED and Web of 74
45 atic review will determine if the use of electrother- Science databases. We used the terms “Bell’s palsy”, 75
apy is recommendable when treating individuals with
pr
46
“electrical stimulation”, “rehabilitation” and combina- 76
47 Bell’s palsy. The objective of this systematic review is tions such as “Bell’s palsy and electrical stimulation” 77
48 to demonstrate the benefits and efficacy of electrother- and “Rehabilitation and facial paralysis”. The search 78
ed
49 apy for treating patients with facial paralysis (Bell’s was concluded in January 2017. Initially, the elec- 79
50 palsy), in comparison to patients who did not receive tronic search generated 1,148 potentiality relevant pa- 80
51 electric stimulation. pers; of those, we excluded 517 because they were du-
ct
81
53
ter reading the abstract. Finally, we considered 24 pa- 86
54 porting Items for Systematic Review and Meta-analysis
pers; however, after reading and analyzing the con- 87
55 (PRISMA) criteria. The protocol of this systematic re-
tents, only 7 papers were included in this systematic 88
56 view was registered in PROSPERO (https://www.crd.
review (Fig. 1). 89
57 york.ac.uk/PROSPERO/index.php), registration num-
58 ber 42014014938. 2.3. Data extraction 90
59 2.1. Inclusion and exclusion criteria Data was extracted by two independent investigators 91
Table 1
Quality assessment of the studies using GRADE system
Reference Design Number of patients Quality of the evidence (GRADE) Publication bias
[23] Gittins J (1998) Cross-sectional 10 ⊕ ⊕ ⊕ Moderate Undetected
[17] Targan R (2000) Case-control 12 ⊕ ⊕ ⊕⊕ High Undetected
[18] Manikadan N (2006) Case-control 29 ⊕ ⊕ ⊕⊕ High Undetected
[22] Hyvärinen A (2008) Cross-sectional 10 ⊕ ⊕ ⊕ Moderate Undetected
[19] Alakram P (2010) Case-control 8 ⊕ ⊕ ⊕ Moderate Undetected
[20] Tuncay F (2015) Case-control 32 ⊕ ⊕ ⊕⊕ High Undetected
[21] Kim J (2016) Case-control 30 ⊕ ⊕ ⊕⊕ High Undetected
99 GRADE system (Grading of Recommendations As- Both groups had the same treatment; however, the ex- 136
100 sessment, Development and Evaluation Scale) (http:// perimental group additionally received 30 minutes of 137
101 www.gradeworkinggroup.org) for quality evaluation electrical stimulation of facial muscles using a TENS 138
102 (Table 1). unit (Frequency 10 Hz, pulse width 10 µsec). Accord- 139
n
103 3. Results trol group (37.6 ± 18.1 versus 29.6 ± 12.5, respec- 142
io
tively); nevertheless, these differences were not statis- 143
104 This systematic review analyzed seven studies re- tically significant (p = 0.36). 144
rs
105 lated to facial paralysis or Bell’s palsy and rehabilita- In a different study [20], individuals with Bell’s 145
106 tive treatment. The descriptive characteristics of each palsy were divided into a group that received elec-
ve 146
107 study are shown in Table 2. tro stimulation (n = 32) and another group that did 147
3.1. Brief description of each study included between the groups when the FDI scale was evalu- 149
f
108
oo
109 The study by Targan et al. in the USA [17] in- improvement of physical function (p = 0.02) and so- 151
cluded twelve individuals with idiopathic facial paral- cial welfare function (p = 0.03). 152
pr
110
111 ysis and five individuals with a history of surgically Finally, in a study performed by Kim et al. in Ko- 153
112 affected nerves were recruited [17]. Diagnoses were rea [21], 60 individuals with Bell’s palsy in early phase 154
155
113 based on latency and the House-Brackmann scale.
114 They obtained the correlation coefficients between (n = 30) and experimental (n = 30). The treat- 156
clinical residuals and nerve conduction latency (r = ment in both groups consisted of drugs, with addi- 157
ct
115
116 0.44). The House-Brackmann scale and nerve conduc- tional electrical stimulation for the experimental group. 158
119 Another study performed in India included 59 indi- ceived acyclovir (1500 mg/day) during five days. The 161
162
120 viduals diagnosed with Bell’s palsy [18]. Patients were
group was 96%, while in the control group was 88%. 163
121 divided into a control group (n = 30) and a group
122 of neuromuscular facial re-education (n = 29). The 3.2. Studies without a comparison group 164
123 control group was treated following a standard proto-
124 col, while the facial neuromuscular re-education group In a study conducted in Finland by Hyvärinen et 165
125 received a treatment that included 3 sets of 5 to 10 al., ten individuals with chronic facial paralysis were 166
126 repetitions of electrical stimulation. The facial scale enrolled [22]. When electrical stimulation was ap- 167
127 ratings in the control group were 32 (9.7–54) in pre- plied in the facial nerve, patients showed improvement, 168
128 treatment, and 54.5 (42.2–71.7) in post-treatment, p 6 and the distal latency obtained improved (p = 0.02). 169
129 0.01. While the group of neuromuscular reeducation Moreover, in a study conducted in the UK, ten indi- 170
130 scored 33 (18–43.5) in pretreatment, and 66 (54–76.7) viduals with chronic paralysis of the seventh cranial 171
131 in post-treatment, p 6 0.01. nerve were recruited [23]. They were assessed with 172
132 In a recent study performed in the region of South EMG system for measuring eyelid function. The re- 173
133 Africa [19], 16 individuals were recruited and divided sults showed that electrical stimulation therapy im- 174
134 into a re-education group (n = 8) and an experimental proved voluntary movement, increasing the displace- 175
135 group (n = 8) within the early phase of Bell’s palsy. ment of the eyebrows in a range of 1.4 mm to 4.1 mm 176
Table 2 4
Descriptive and clinical characteristics of the studies
Galley Proof
Study Location Controls Cases Diagnosis Characteristics of the treatment Additional treatment Result
Gittins J United – 101 Secondary Evolution of the paralysis 12 to 24 months None Voluntary closing of the eyelid
(1998) [23] Kingdom palsy of the 7th Current type and wave Constant voltage currents com- increased an average of 2.5 mm
cranial nerve2 form pensated Monophasic current and improved the speed 0.9 sec-
Frequency 2 Hz–200 Hz onds.
Intensity Not specified Lagophthalmus: 2.9 mm
Pulse width 50 µsec–200 µsec decrease (mean) in 8 patients.
Duration 3 months Eyelid displacement (P <
co
Application time 1 hour daily 0.005)
Combination with drugs None
during treatment
rre
Targan R EE. UU 17 123 Chronic facial Evolution of the paralysis 3.7 (Bell’s palsy group) and None Decreased facial motor nerve la-
(2000) [17] nerve damage 7.2 years for acoustic neuroma tency 1.13 ms (P = 0.001)
caused by group) Improvement on the House-
ct
Bell’s palsy or Electrical stimulation Monophasic current Brackmann Scale (P = 0.003)
19/03/2020; 9:42
Frequency and pulse width Not specified ing flaccid faces plus electri- component in favor of the con-
rs
Intensity Motor level cal stimulation. trol group was observed (P <
Duration 2 weeks (6 days for week) Re-education group: 0.01).
io
Application time 10 visible contractions for mus- Techniques tailored to each There were no significant
cle, 3 times daily
n
patient differences in synkinesis
Combination with drugs None subcomponents.
during treatment
File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 4
Table 2, continued
Study Location Controls Cases Diagnosis Characteristics of the treatment Additional treatment Result
Hyvärinen A Finland – 10 Chronic facial Evolution of the paralysis Chronic 1–24 years None Improvement in motor latency
(2008) [22] nerve palsy of Wave form: Monophasic current of the facial nerve, significantly
Galley Proof
rs
Frequency 2.5 Hz timulation. Significant improvement in the
Pulse width Interpulse in- 100 µsec All patients received amplitude and latency of the fa-
terval 300 µsec
io
corticosteroid treatment for cial nerve motor in the experi-
Duration: 3 weeks (5 day for week) 10 days. mental group.
Application time 3 sets of 30 contractions per
n Improvement in the Facial
treated muscle Disability Index in both
Combination with drugs No. The use of corticosteroids treatment groups, in favor of the
was previous to the treatment experimental group.
with electrical stimulation
5
File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 5
6
Galley Proof
Table 2, continued
co
Study Location Controls Cases Diagnosis Characteristics of the treatment Additional treatment Result
Kim J Korea 305 306 Facial paralysis Evolution of the paralysis One week Control group: Treated An improvement in facial per-
(2016) [21] idiopathic Wave form Monophasic current during the first 5 days with formance was noted in the first
rre
Frequency 20 Hz–5 KHz prednisolone (1 mg/kg/day), 2 weeks in the experimental
Intensity Sub-motor level (Sensory and decreased during 10 days. group, and the time for com-
threshold) They were also treated with plete recovery was significantly
ct
19/03/2020; 9:42
Pulse width 100 µsec every 50 ms acyclovir (1500 mg at day) shorter than that in the control
Duration 6 months during five days. group (P < 0.05).
ed
Combination with drugs Prednisolone (1 mg/kg/day for Experimental group: Same All patients except one showed
the first 5 days, weaned off drug treatment of the control complete recovery in the experi-
within 2 weeks) for 10 days, group plus continuous, low mental group in three months.
plus acyclovir (1500 mg daily) frequency-impulse electrical In the control group, 5 patients
pr
for 5 days stimulation (SCLES). did not recover normal facial
function within 6 months.
oo
1 Voluntary closure of the eyelid was measured only in 7 individuals, but the Lagophthalmus was used in 10 individuals. 2 Eight patients secondary to Neurinoma, one with surgical lesion and
one patient with trauma. 3 Twelve patients with Bell’s palsy and five patients with surgical resection of the facial nerve by acoustic neuroma. 4 11.4 days for control group and 12.5 days for
f
experimental group. 5 30 patients used medical treatment only (control group). 6 30 patients use medical treatment plus electrical stimulator.
ve
E.G. Burelo-Peregrino et al. / Electrotherapy and Bell’s palsy
rs
io
n
File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 6
Galley Proof 19/03/2020; 9:42 File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 7
177 with an average of 2.5 mm. However, due to their ex- increasing the amount of time per day during 6 months 225
178 clusion criteria the study group was reduced to seven until reaching 6 hrs of stimulation. Gittins [23] on 226
179 individuals. Four of them showed significant improve- the other hand, used a frequency of 2 Hz to 200 Hz 227
180 ment in range of motion (p 6 0.01). and 50 µseg–200 µsec pulse length. Clearly, the fre- 228
181 4. Discussion tins [23]; nevertheless, in the study by Hyvärinen [22] 231
182 This study was conducted in order to determine tients showed significant improvement according to the 233
183 if the use of electrotherapy is helpful in the treat- House-Brackmann scale. In the study by Gittins [23] 234
184 ment of Bell’s palsy. The results of this systematic re- however, the entire study population showed no im- 235
n
240
189 Bell’s palsy [24], the results found in this systematic cial muscles stimulation. Although patients showed 241
io
190 review are oriented towards a positive response to the improvement, we must emphasize that electro stim- 242
191 treatment. ulation therapy was combined with facial rehabilita- 243
rs
192 In the present study, we analyzed 131 cases and 113 tion exercises, through which much of this improve- 244
193 controls. We included seven publications, while both of ment was obtained. In more recent studies [19–21], the
ve 245
194 the previous systematic reviews only included three or results of electrical stimulation treatment in the early 246
195 four publications. For instance, the review about physi- phase of Bell’s Palsy demonstrated a significant re- 247
196 cal therapy for treating Bell’s palsy performed by Teix- covery. It is important to mention that this improve-
f
248
oo
197 eira et al. [25], analyzed 3 trials and reported no signif- ment was observed in studies with a considerable n, 249
198 icant improvement in patients who received electrical [20,21] with more than 20 patients in the control and 250
199 stimulation, questioning its cost-effectiveness. In the experimental groups, unlike a recent study with a poor 251
pr
200 update of the same review [14], four trials were ana- n, [19] in which statistical significance was not ob- 252
201 lyzed and the results obtained were similar. It is neces- served. Another important aspect in the methodology 253
202 sary to emphasize that these previous reviews did not 254
203 aim to specifically evaluate electrotherapy, but multi- used a motor level [18–20] others applied sub-motor 255
204 ple physical therapies. In addition, the trials analyzed level (sensory threshold) [17,21,22], this represents 256
ct
205 were not very recent. a controversy, because literature indicates that stim- 257
On the other hand, there are several countries with- ulation at motor level, could favor secondary effects 258
rre
206
207 out an up to date guide for the long term treatment such as synkinesia. It is considered that patients with 259
208 of Bell’s palsy [26]. Although it has been stated that chronic peripheral paralysis receiving daily treatment 260
261
209 receiving electrotherapy in the acute phase of Bell’s
significantly [23]. Nonetheless, depending on the nerve 262
210 palsy is beneficial for patients [19–21,27], and it is
injury and latencies deficiency in nerve conduction, pa- 263
211 highly used in the Mexican clinical practice (for di-
tients with facial paralysis will be considered for a pro- 264
212 agnosis and management of Bell’s palsy), there is not
longed electro stimulation combined with exercise pro- 265
213 enough evidence to support the efficacy of electrother-
grams or drug treatment, in order to increase the suc- 266
214 apy in acute cases. cess of the intervention. 267
215 It is necessary to mention that although patients who Given the importance of the treatment in Bell’s 268
216 received electrical stimulation improved their condi- palsy, our findings suggest that the use of electrother- 269
217 tion in all the studies evaluated, the methodology used apy may play an important role in the improvement 270
218 in each one was different. For instance, in the study by of patients. It would be necessary to develop further 271
219 Tuncay et al. [20], the electro stimulation with a cur- studies with similar characteristics such as parame- 272
220 rent wave phase began four weeks after diagnosis. The ters of frequency, intensity, pulse duration, treatment 273
221 results showed differences in facial re-education ac- time, number of sessions, number of contractions and 274
222 cording to the House-Brackmann scale. Furthermore, even the same area of stimulation, with the purpose of 275
223 Hyvärinen [22] used 20 Hz electro stimulation and clarifying the genuine role that electrotherapy plays in 276
224 100 µseg pulse duration, 30 min/day, for two weeks, Bell’s palsy treatment. 277
Galley Proof 19/03/2020; 9:42 File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 8
278 Conflict of interest [13] Pereira LM, Obara K, Dias JM, Menacho MO, Lavado EL, 322
Cardoso JR. Facial exercise therapy for facial palsy: System- 323
atic review and meta-analysis. Clin Rehabil. 2011; 25: 649- 324
279 The authors have no competing interests to report. 658. 325
[14] Teixeira LJ, Valbuza JS, Prado GF. Physical therapy for Bell’s 326
palsy (idiopathic facial paralysis). Cochrane Database Syst 327
n
291 [4] De Diego JI, Prim MP, Madero R, Gavilan J. Seasonal pat-
on facial symmetry in patients with Bell’s palsy: A random- 341
292 terns of idiopathic facial paralysis: A 16-year study. Otolaryn-
ized controlled trial. Clin Rehabil. 2007; 21: 338-343.
io
342
293 gol Head Neck Surg. 1999; 120: 269-271.
[19] Alakram P, Puckree T. Effects of electrical stimulation on 343
294 [5] Peitersen E. Bell’s palsy: The spontaneous course of 2,500 pe-
House-Brackmann scores in early Bell’s palsy. Physiother
rs
344
295 ripheral facial nerve palsies of different etiologies. Acta Oto-
Theory Pract. 2010; 26: 160-166. 345
296 laryngol Suppl. 2002: 4-30.
[20]
ve Tuncay F, Borman P, Taser B, Unlu I, Samim E. Role of elec- 346
297 [6] Reginald F. Baugh M, Gregory. Basura, MD, PhD, Lisa E.
trical stimulation added to conventional therapy in patients 347
298 Ishii, MD, MHS, Seth R. Schwartz. Clinical Practice Guide-
with idiopathic facial (Bell) palsy. Am J Phys Med Rehabil. 348
299 line: Bell’s Palsy. Otolaryngology-Head and Neck Surgery.
2015; 94: 222-228. 349
300 2013: 1-27.
[21] Kim J, Choi JY. The effect of subthreshold continuous elec-
f
350
301 [7] McCormick DP. Herpes simplex virus as a cause of Bell’s
oo
354
305 plinary care. J Neurol Neurosurg Psychiatry. 2015; 86: 1356-
unresolved facial nerve paralysis: An exploratory study. Am 355
306 1361.
J Phys Med Rehabil. 2008; 87: 992-997. 356
307 [9] McCaul JA, Cascarini L, Godden D, Coombes D, Bren-
[23] Gittins J, Martin K, Sheldrick J, Reddy A, Thean L. Electrical 357
ed
313 Cd001942.
[25] Teixeira LJ, Soares BG, Vieira VP, Prado GF. Physical ther- 363
314 [11] Gagyor I, Madhok VB, Daly F, Somasundara D, Sullivan M,
apy for Bell s palsy (idiopathic facial paralysis). Cochrane 364
315 Gammie F, et al. Antiviral treatment for Bell’s palsy (idio-
Database Syst Rev. 2008: Cd006283. 365
316 pathic facial paralysis). Cochrane Database Syst Rev. 2015:
co
Eligibility criteria 6 Specify study characteristics (e.g., PICOS, length of follow-up) and report characteristics (e.g., years considered, language, publication 4–5
status) used as criteria for eligibility, giving rationale.
ed
Information sources 7 Describe all information sources (e.g., databases with dates of coverage, contact with study authors to identify additional studies) in the 4–5
search and date last searched.
Search 8 Present full electronic search strategy for at least one database, including any limits used, such that it could be repeated. 4–6
Study selection 9 State the process for selecting studies (i.e., screening, eligibility, included in systematic review, and, if applicable, included in the 5–6
pr
meta-analysis).
Data collection process 10 Describe method of data extraction from reports (e.g., piloted forms, independently, in duplicate) and any processes for obtaining and 5–6
oo
confirming data from investigators.
Data items 11 List and define all variables for which data were sought (e.g., PICOS, funding sources) and any assumptions and simplifications made. 4
f
Risk of bias in individual 12 Describe methods used for assessing risk of bias of individual studies (including specification of whether this was done at the study or 4–6
studies outcome level), and how this information is to be used in any data synthesis.
ve
Summary measures 13 State the principal summary measures (e.g., risk ratio, difference in means). NA
Synthesis of results 14 Describe the methods of handling data and combining results of studies, if done, including measures of consistency (e.g., I2 ) for each 5–6
E.G. Burelo-Peregrino et al. / Electrotherapy and Bell’s palsy
meta-analysis.
rs
Risk of bias across studies 15 Specify any assessment of risk of bias that may affect the cumulative evidence (e.g., publication bias, selective reporting within studies). Table 1
Additional analyses 16 Describe methods of additional analyses (e.g., sensitivity or subgroup analyses, meta-regression), if done, indicating which were 6, Table 2
io
pre-specified.
Results
n
Study selection 17 Give numbers of studies screened, assessed for eligibility, and included in the review, with reasons for exclusions at each stage, ideally with 6
a flow diagram.
Study characteristics 18 For each study, present characteristics for which data were extracted (e.g., study size, PICOS, follow-up period) and provide the citations. 6–9, Table 2
Risk of bias within studies 19 Present data on risk of bias of each study and, if available, any outcome level assessment (see item 12). Table 1
Results of individual 20 For all outcomes considered (benefits or harms), present, for each study: (a) simple summary data for each intervention group (b) effect 6–8
studies estimates and confidence intervals, ideally with a forest plot.
Synthesis of results 21 Present results of each meta-analysis done, including confidence intervals and measures of consistency. NA
Risk of bias across studies 22 Present results of any assessment of risk of bias across studies (see Item 15). Table 1
Additional analysis 23 Give results of additional analyses, if done (e.g., sensitivity or subgroup analyses, meta-regression [see Item 16]). NA
9
File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 9
10
Galley Proof
co
Section/topic # Checklist item Reported
on page #
rre
Discussion
Summary of evidence 24 Summarize the main findings including the strength of evidence for each main outcome; consider their relevance to key groups (e.g., 9–11
ct
19/03/2020; 9:42
rs
io
n
File: bmr–1-bmr171031.tex; BOKCTP/xjm p. 10