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Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review)
Madhok VB, Gagyor I, Daly F, Somasundara D, Sullivan M, Gammie F, Sullivan F
Madhok VB, Gagyor I, Daly F, Somasundara D, Sullivan M, Gammie F, Sullivan F.

Corticosteroids for Bell's palsy (idiopathic facial paralysis).
Cochrane Database of Systematic Reviews 2016, Issue 7. Art. No.: CD001942.
DOI: 10.1002/14651858.CD001942.pub5.
www.cochranelibrary.com

Copyright © 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
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TABLE OF CONTENTS
HEADER......................................................................................................................................................................................................... 1
ABSTRACT..................................................................................................................................................................................................... 1
PLAIN LANGUAGE SUMMARY....................................................................................................................................................................... 2
SUMMARY OF FINDINGS.............................................................................................................................................................................. 3
BACKGROUND.............................................................................................................................................................................................. 5
OBJECTIVES.................................................................................................................................................................................................. 5
METHODS..................................................................................................................................................................................................... 5
RESULTS........................................................................................................................................................................................................ 7
Figure 1.................................................................................................................................................................................................. 8
Figure 2.................................................................................................................................................................................................. 11
Figure 3.................................................................................................................................................................................................. 12
Figure 4.................................................................................................................................................................................................. 13
Figure 5.................................................................................................................................................................................................. 13
Figure 6.................................................................................................................................................................................................. 14
DISCUSSION.................................................................................................................................................................................................. 14
AUTHORS' CONCLUSIONS........................................................................................................................................................................... 15
ACKNOWLEDGEMENTS................................................................................................................................................................................ 15
REFERENCES................................................................................................................................................................................................ 16
CHARACTERISTICS OF STUDIES.................................................................................................................................................................. 18
DATA AND ANALYSES.................................................................................................................................................................................... 28
Analysis 1.1. Comparison 1 Corticosteroid (OS) versus placebo or no treatment (OO), Outcome 1 Incomplete recovery ≥ 6 months 28
after randomisation..............................................................................................................................................................................
Analysis 1.2. Comparison 1 Corticosteroid (OS) versus placebo or no treatment (OO), Outcome 2 Cosmetically disabling 29
persistent sequelae ≥ 6 months after randomisation.........................................................................................................................
Analysis 1.3. Comparison 1 Corticosteroid (OS) versus placebo or no treatment (OO), Outcome 3 Motor synkinesis and crocodile 29
tears........................................................................................................................................................................................................
Analysis 1.4. Comparison 1 Corticosteroid (OS) versus placebo or no treatment (OO), Outcome 4 Adverse effects....................... 29
APPENDICES................................................................................................................................................................................................. 30
WHAT'S NEW................................................................................................................................................................................................. 32
HISTORY........................................................................................................................................................................................................ 32
CONTRIBUTIONS OF AUTHORS................................................................................................................................................................... 32
DECLARATIONS OF INTEREST..................................................................................................................................................................... 33
SOURCES OF SUPPORT............................................................................................................................................................................... 33
DIFFERENCES BETWEEN PROTOCOL AND REVIEW.................................................................................................................................... 33
INDEX TERMS............................................................................................................................................................................................... 34
Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) i

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[Intervention Review]
Corticosteroids for Bell's palsy (idiopathic facial paralysis)
Vishnu B Madhok1,2, Ildiko Gagyor3, Fergus Daly4, Dhruvashree Somasundara2, Michael Sullivan5, Fiona Gammie2, Frank Sullivan6
1Park House Surgery, Bagshot, UK. 2Centre for Primary Care and Population Research, Division of Clinical and Population Sciences and
Education, University of Dundee, Dundee, UK. 3Department of General Practice/Family Medicine, University of Göttingen, Göttingen,
Germany. 4Frontier Science (Scotland) Ltd, Kingussie, UK. 5School of Clinical Sciences, University of Edinburgh, Edinburgh, UK.
6Department of Family and Community Medicine, North York General Hospital, University of Toronto, Toronto, Canada
Contact address: Vishnu B Madhok, Park House Surgery, Park Street, Bagshot, Surrey, GU19 5AQ, UK. vishnumadhok@nhs.net,
vmadhok@doctors.org.uk.
Editorial group: Cochrane Neuromuscular Group.

Publication status and date: New search for studies and content updated (no change to conclusions), published in Issue 7, 2016.
Citation: Madhok VB, Gagyor I, Daly F, Somasundara D, Sullivan M, Gammie F, Sullivan F. Corticosteroids for Bell's palsy (idiopathic facial
paralysis). Cochrane Database of Systematic Reviews 2016, Issue 7. Art. No.: CD001942. DOI: 10.1002/14651858.CD001942.pub5.
ABSTRACT
Background
Inflammation and oedema of the facial nerve are implicated in causing Bell's palsy. Corticosteroids have a potent anti-inflammatory action
that should minimise nerve damage. This is an update of a review first published in 2002 and last updated in 2010.
Objectives
To determine the effectiveness and safety of corticosteroid therapy in people with Bell's palsy.
Search methods
On 4 March 2016, we searched the Cochrane Neuromuscular Specialised Register, the Cochrane Central Register of Controlled Trials
(CENTRAL), MEDLINE, EMBASE and LILACS. We reviewed the bibliographies of the randomised trials and contacted known experts in the
field to identify additional published or unpublished trials. We also searched clinical trials registries for ongoing trials.
Selection criteria
Randomised trials and quasi-randomised trials comparing different routes of administration and dosage schemes of corticosteroid or
adrenocorticotrophic hormone therapy versus a control group receiving no therapy considered effective for this condition, unless the same
therapy was given in a similar way to the experimental group.
Data collection and analysis

We used standard Cochrane methodology. The main outcome of interest was incomplete recovery of facial motor function (i.e. residual
facial weakness). Secondary outcomes were cosmetically disabling persistent sequelae, development of motor synkinesis or autonomic
dysfunction (i.e. hemifacial spasm, crocodile tears) and adverse effects of corticosteroid therapy manifested during follow-up.
Main results
We identified seven trials, with 895 evaluable participants for this review. All provided data suitable for the primary outcome meta-analysis.
One of the trials was new since the last version of this Cochrane systematic review. Risk of bias in the older, smaller studies included some
unclear- or high-risk assessments, whereas we deemed the larger studies at low risk of bias. Overall, 79/452 (17%) participants allocated
to corticosteroids had incomplete recovery of facial motor function six months or more after randomisation; significantly fewer than the
125/447 (28%) in the control group (risk ratio (RR) 0.63, 95% confidence interval (CI) 0.50 to 0.80, seven trials, n = 895). The number of people
who need to be treated with corticosteroids to avoid one incomplete recovery was 10 (95% CI 6 to 20). The reduction in the proportion of
Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 1

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participants with cosmetically disabling sequelae six months after randomisation was very similar in the corticosteroid and placebo groups
(RR 0.96, 95% CI 0.40 to 2.29, two trials, n = 75, low-quality evidence). However, there was a significant reduction in motor synkinesis during
follow-up in participants receiving corticosteroids (RR 0.64, 95% CI 0.45 to 0.91, three trials, n = 485, moderate-quality evidence). Three
studies explicitly recorded the absence of adverse effects attributable to corticosteroids. One trial reported that three participants receiving
prednisolone had temporary sleep disturbances and two trials gave a detailed account of adverse effects occurring in 93 participants, all
non-serious; the combined analysis of data from these three trials found no significant difference in adverse effect rates between people
receiving corticosteroids and people receiving placebo (RR 1.04, 95% CI 0.71 to 1.51, n = 715).
Authors' conclusions
The available moderate- to high-quality evidence from randomised controlled trials showed significant benefit from treating Bell's palsy
with corticosteroids.
PLAIN LANGUAGE SUMMARY
Corticosteroids for Bell's palsy
Review question
What are the effects of corticosteroids on Bell's palsy?
Background
Bell's palsy is a paralysis or weakness of muscles in the face, usually on one side, with no certain cause. Symptoms usually recover, although
not always. Reducing inflammation of the facial nerve using corticosteroid medicines (steroids) is thought to limit nerve damage. This is
an update of a review first published in 2002 and last updated in 2010.
Study characteristics
We identified seven clinical trials involving 895 people with one-sided mild, moderate or severe Bell's palsy of unknown cause. All of these
trials reported rates of incomplete recovery (the proportion of people left with facial weakness) and we were able to combine the results.
People in the studies were aged from 2 to 84 years. They were treated with corticosteroids or placebo (inactive treatment), either alone
or in combination with other therapies. One trial only involved children, from 24 months to 74 months old. The duration of the included
studies for adults and children ranged from 157 days to 12 months.
Key results and quality of the evidence
Incomplete recovery
According to moderate quality to high quality evidence, corticosteroids reduced the number of people left with facial weakness after Bell's
palsy compared to placebo (a pretend medicine). This finding was based on data from seven studies involving 895 participants with Bell's
palsy of varying degrees of severity. We calculated that to stop one person from being left with facial weakness, 10 people need to be
treated.
Five studies provided data on long-term after-effects of Bell's palsy following treatment. Two of the studies (75 participants) looked
at persistent effects on facial appearance after six months or more. The effect was nearly the same for corticosteroids and placebo,
showing that participants who had corticosteroids benefited slightly, although this evidence was low quality. Data from three studies (485
participants) showed clearly that people who received corticosteroids developed less motor synkinesis (unwanted facial movements) and
crocodile tears (watery eyes when eating or chewing), compared with people who received placebo alone. This finding was based on
moderate-quality evidence.
Side effects
Three studies reported that no side effects could be attributed to corticosteroid treatment. Based on moderate-quality evidence from three
studies (715 participants), numbers experiencing side effects were similar with corticosteroids and placebo.
The evidence is current to March 2016.

SUMMARY OF FINDINGS

Summary of findings for the main comparison. Corticosteroids compared to placebo or no treatment for Bell's palsy
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Corticosteroids compared to placebo or no treatment for Bell's palsy
Patient or population: people with Bell's palsy

Settings: primary and secondary care
Intervention: corticosteroids
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Comparison: placebo or no treatment
Outcomes Illustrative comparative risks* (95% Relative effect No of partici- Quality of the Comments
CI) (95% CI) pants evidence
(studies) (GRADE)
Assumed risk Corresponding risk
Placebo or no Corticosteroids
treatment
Incomplete recovery ≥ 6 months after randomisa- 281 per 1000 177 per 1000 RR 0.63 895 ⊕⊕⊕⊕ NNTB 10,
tion (140 to 225) (0.50 to 0.80) (7 studies) high 1
House-Brackmann grading system and Sunnybrook 95% CI 6 to 20
scale
Follow-up: 157 days to 12 months
Cosmetically disabling persistent sequelae ≥ 6 216 per 1000 208 per 1000 RR 0.96 75 ⊕⊕⊝⊝ -
months after randomisation (86 to 495) (0.4 to 2.29) (2 studies) low 2,3
Clinical assessment
Follow-up: mean 6 months
Motor synkinesis and crocodile tears 260 per 1000 167 per 1000 RR 0.64 485 ⊕⊕⊕⊝ -
Clinical assessment (117 to 237) (0.45 to 0.91) (3 studies) moderate 4
Follow-up: 9 to 12 months

Adverse effects 127 per 1000 133 per 1000 RR 1.04 715 ⊕⊕⊕⊝ 3 other studies
Follow-up: 9 to 12 months (0.71 to 1.51) (3 studies) moderate 5 recorded that
(91 to 192) no adverse ef-
fects occurred
with corticos-
teroid treat-
ment
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is
based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
3

CI: confidence interval; NNTB: number needed to treat for an additional beneficial outcome; RR: risk ratio.
GRADE Working Group grades of evidence
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High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.
1 Two trials excluded participants who were found to have clinical evidence of herpes zoster infection (Lagalla 2002; Taverner 1954). In addition, two studies did not use a scoring
Better health.
Informed decisions.
Trusted evidence.
system such as the House-Brackmann or Sunnybrook scale to assess facial motor function, relying upon clinical examination, electromyographic tests or photographs (May 1976;
Taverner 1954). Taverner 1954 reported outcomes at five months rather than at six months or more. However, we felt that these limitations did not compromise the generalisability
of the findings.
2 We downgraded twice: first for imprecision - there was a low number of events and pooled RR allowed the possibility of both no effect and the chance of harm; second for
publication bias - of the seven included studies, five did not provide data on the presence of cosmetically disabling sequelae six months or more after randomisation.
3 We downgraded once for imprecision. There was a low number of events.
4 We downgraded the quality of the evidence to moderate because of publication bias.
5 We downgraded for publication bias - only three of seven studies provided data on adverse effects.


4

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BACKGROUND How the intervention might work
Description of the condition Corticosteroids are known to have an anti-inflammatory mode of

action, which reduces oedema and inflammation of the facial nerve
Bell's palsy is an acute, generally unilateral, paralysis or weakness in the acute presentation of Bell's palsy.
of facial musculature consistent with peripheral facial nerve
dysfunction, of no detectable cause (Niparko 1993). Additional Why it is important to do this review
symptoms frequently include pain around or behind the ear
The purpose of this systematic review was to collect and
sometimes extending into the occipital or cervical region. Impaired
analyse the available evidence from randomised controlled trials
tolerance to ordinary levels of noise and disturbed sense of taste on
concerning the use of corticosteroids for improving the outcome
the same side may also be present (Burgess 1984).
of people with Bell's palsy. This is an update of a review first
Epidemiological studies have reported an annual incidence of 23 published in 2002 and last updated in 2010. We updated the review
to 25 per 100,000 per year (Martyn 1997; Victor 1994), but one to assess the quality of the evidence regarding the benefit of
study using a general practitioner (GP) database has suggested it corticosteroids in Bell's palsy using current methodology, integrate
may be even higher at 37 per 100,000 per year (Morales 2013). any new evidence and to determine whether further research
Bell's palsy affects men and women more or less equally. Until would be likely to change the estimate of effect or its certainty.
recently was thought to be most common in the 30- to 45-
year age group (Bateman 1992; Brandenberg 1993; Katusic 1986; OBJECTIVES
Peitersen 1982; Peitersen 2002; Yanagihara 1988), although the
To determine the effectiveness and safety of corticosteroid therapy
one more recent primary care database study suggested a peak in
in people with Bell's palsy.
people over 70 years of age (Morales 2013). The condition presents
disproportionately among pregnant women and people who have METHODS
diabetes, influenza, a cold, or some other upper respiratory
ailment. On average, every year a British GP will see one or two Criteria for considering studies for this review
people who have developed the condition. Both sides of the face
are affected equally often (Prescott 1988). Types of studies
Trials of the use of corticosteroid therapy for the treatment of
The aetiology of Bell's palsy is still debated. A viral infection,
recent-onset Bell's palsy in which an attempt had apparently been
vascular ischaemia, autoimmune inflammatory disorders and
made to conduct a randomised or quasi-randomised comparison
heredity have been proposed as underlying causes (Adour 1982;
between corticosteroid therapy and a placebo, or open control
Burgess 1984; Lackner 2010). A viral aetiology has gained popularity
group. As in the previous version of the review, we used study
since the isolation of herpes simplex virus-1 (HSV-1) genome from
quality as an exclusion criteria excluding trials with a high risk of
the facial nerve endoneurial fluid of people with Bell's palsy
bias in several domains.
(Lackner 2010; Murakami 1996). The prognosis is on the whole
favourable. One of the largest series of people with Bell's palsy Types of participants
including those who were not receiving specific therapy, showed
that 85% of people with Bell's palsy began to recover within Participants of any age with clinically diagnosed Bell's palsy,
three weeks of onset (Peitersen 1982). For the remaining 15%, irrespective of the time of evolution of symptoms. We included
partial recovery occurred three to six months later. The same all participants considered to have Bell's palsy or acute idiopathic
series showed that normal facial expression reappeared in 71% facial nerve paralysis by the study authors, irrespective of the
of cases, 13% had insignificant sequelae, and the remaining 16% ancillary studies they performed to rule out other causes of facial
had permanently diminished function with aberrant innervation paralysis. We included in the analysis all participants considered
(expressed as motor synkinesis or autonomic dysfunction) and eligible by the authors of the studies, irrespective of associated
post-paralytic spasms. conditions.
Description of the intervention Types of interventions
The treatment of Bell's palsy used to be highly controversial. We included trials using any corticosteroid or adrenocorticotrophic
Corticosteroids were the treatment of choice, based mainly hormone therapy, irrespective of the route of administration
on non-randomised comparisons (Adour 1972). The authors (oral or parenteral) and length of therapy. We excluded trials
of numerous clinical series both espoused and condemned in which a drug considered 'effective' for this condition was
corticosteroid therapy with, what appeared to them, equally given to the control group, unless it was given in a similar
convincing arguments (Burgess 1984). Four systematic reviews way to the experimental group. The exception was studies in
found a significant trend favouring corticosteroid treatment in which control and treatment groups received concomitant antiviral
improving the recovery of facial motor function (de Almeida 2009; therapy; these are not included in this review, but in the updated
Grogan 2001; Ramsey 2000; Williamson 1996). However, their Cochrane review 'Antiviral treatment for Bell's palsy (idiopathic
conclusions were affected by including trials of poor quality in the facial paralysis)' (Gagyor 2015).
pooled estimate. de Almeida 2009, a state-of-the-art, high-quality
We excluded trials comparing different types of corticosteroids
systematic review, differed from our methodology in the way they
or different dosage schemes, unless the trial included a placebo
collected data, in the inclusion of a non-randomised trial that we
group.
excluded (Martinez 1990), and in the exclusion of a trial that we
included in our analysis (Taverner 1954).

Informed decisions.

Types of outcome measures • Notes: funding for trial and notable conflicts of interest of trial
authors.
Primary outcomes
• Incomplete recovery of facial motor function six months or more All six review authors had a selection of papers to read, review for
after randomisation. quality and extract data from. At least two review authors assessed
each trial. All review authors agreed data extraction.
Secondary outcomes
Two review authors (IG and VM) inputted data into Review Manager
• Cosmetically disabling persistent sequelae of facial paralysis 5 (RevMan 2014).
(poor recovery of facial motor function as defined by the authors
of the studies) six months or more after randomisation. Assessment of risk of bias in included studies
• Motor synkinesis or autonomic dysfunction during follow-up IG completed the 'Risk of bias' table. FS and FD individually
(including facial spasm, motor synkinesis and crocodile tears). reviewed the 'Risk of bias' assessments. We assessed bias by
• Adverse effects attributable to the use of corticosteroids. scoring studies as at high, low or unclear risk of bias using methods
described in the Cochrane Handbook for Systematic Reviews of
Search methods for identification of studies Interventions (Higgins 2011).
Electronic searches
Measures of treatment effect
On 4 March 2016, we searched the Cochrane Neuromuscular
When comparing studies using different symptom scores to assess
Specialised Register, the Cochrane Central Register of Controlled
outcomes, we used the House-Brackmann scale when available as
Trials (CENTRAL in the Cochrane Register of Studies Online),
this was the most widely used or had comparisons to other scales
MEDLINE (January 1966 to February 2016), EMBASE (January
available. When assessing adverse effects, we reported the number
1980 to February 2016) and LILACS (January 1982 to February
of participants affected, as opposed to the number of events, to
2016). The detailed search strategies are in the appendices:
facilitate data comparison.
Cochrane Neuromuscular Specialised Register (Appendix 1),
CENTRAL (Appendix 2), MEDLINE (Appendix 3), EMBASE (Appendix We used dichotomous outcomes and we analysed data as risk
4) and LILACS (Appendix 5). ratios (RR) with a corresponding 95% confidence interval (CI). We
calculated a treatment effect using the Mantel-Haenszel method
On 21 June 2016, we searched ClinicalTrials.gov and the World
(Egger 2007).
Health Organization International Clinical Trials Registry Platform
(ICTRP) (who.int/trialsearch/) for ongoing studies. We searched Unit of analysis issues
both using the term "Bell's Palsy".
Where a single trial included multiple trial arms, we included only
Searching other resources arms relevant to this review. If two comparisons (e.g. drug A versus
placebo and drug B versus placebo) had been combined in the
We reviewed the bibliographies of the randomised trials and
same meta-analysis, our preference would be to combine groups
contacted the study authors and known experts in the field to
to create a single comparison if appropriate, or otherwise use one
identify additional published or unpublished data.
of the other approaches described in Chapter 16 of the Cochrane
Data collection and analysis Handbook for Systematic Reviews of Interventions (Higgins 2011).
Selection of studies Dealing with missing data

Six review authors scrutinised published and unpublished papers One of the trial authors, who is also a review author (FS), provided
retrieved by the literature searches to select papers for inclusion. unpublished trial data. We also contacted a previous study team
At least two review authors independently assessed each paper member (P Lockhart) for additional information on other studies
for relevance, eligibility and quality. There were no disagreements and received a response. We either extracted the number of
about inclusion. We applied no language limitations. participants who completed a treatment originally allocated and
the number with the outcome, and considered the potential effect
Data extraction and management of missing data when presenting results, or reported intention-
to-treat analyses as presented in trial reports. Where data were
Review authors collected and analysed data in pairs (FG and VM, DS
unavailable we contacted the original authors, when there was
and MS, IG and FS). We collected data on the following.
no response, we calculated the numbers from the rates and
• Methods: study design, study duration, number of study centres percentages presented in the papers. We undertook no sensitivity
and location, study setting, withdrawals, and date of study. analyses for missing values. For some trials, we calculated either
• Participants: number (n), mean age, age range, gender, severity number in the analysis or the number experiencing an event using
of condition, diagnostic criteria, baseline characteristics, the percentage experiencing an event.
inclusion criteria and exclusion criteria. Assessment of heterogeneity
• Interventions: intervention, comparison, concomitant
medications. We used the I2 statistic to measure heterogeneity among the trials
• Outcomes: primary and secondary outcomes specified and in each analysis, using the thresholds in the Cochrane Handbook for
collected, and time points reported; definition of recovery Systematic Reviews of Interventions as guidance (Higgins 2011):
status.
• 0% to 40%: might not be important;

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• 30% to 60%: may represent moderate heterogeneity; Handbook for Systematic Reviews of Interventions (Higgins 2011).
• 50% to 90%: may represent substantial heterogeneity; We used GRADEpro software (GRADEpro 2008). We have justified
• 75% to 100%: considerable heterogeneity. all decisions to downgrade or upgrade the quality of studies using
footnotes and have made comments to aid readers' understanding
We interpreted the I2 statistic in the context of its CI, the Chi2 test, of the review where necessary.
P value and the size of the effect.
Subgroup analysis and investigation of heterogeneity
Assessment of reporting biases We did not undertake any subgroup analyses for this review. The
Since we were unable to pool more than 10 trials, we could not protocol detailed possible subgroup analyses, although none were
create a funnel plot to explore possible small-study biases. appropriate for the included studies.
Data synthesis Sensitivity analysis
We used a fixed-effect model for our analysis and performed a We carried out the following sensitivity analyses.
sensitivity analysis with a random-effects model.
• Repeated the analyses excluding smaller and underpowered
If the review had included more than one comparison that could studies.
not be included in the same analysis, we would have reported the • Repeated the analyses excluding studies with short-term follow-
results for each comparison separately. up (less than nine months).
Throughout we have utilised the following notations: RESULTS

OS: corticosteroid treatment alone Description of studies
OO: placebo or no treatment only Results of the search
Using these notations, we conducted the following comparison: OS In the updated searches for this review, we found 59 references in
versus OO. the Cochrane Neuromuscular Specialised Register, 81 in CENTRAL,
818 in MEDLINE, 117 in EMBASE and 15 in LILACS.
'Summary of findings' table
There were seven completed randomised controlled trials
At this update, we added a 'Summary of findings' table. We used the comparing corticosteroids with no active control when this review
following outcomes: incomplete recovery, cosmetically disabling was first written. In subsequent updates, review authors identified
persistent sequelae six months or more after randomisation, motor five other potentially relevant trials (Austin 1993; Bento 1991;
synkinesis and crocodile tears, and adverse effects. Engström 2008; Lagalla 2002; Sullivan 2007).
Under the GRADE approach, the levels of quality of evidence In all, seven trials including 895 evaluable participants met our
are high, moderate, low or very low. Assessors start at high inclusion criteria (Austin 1993; Engström 2008; Lagalla 2002; May
quality and may downgrade the evidence for the pre-specified 1976; Sullivan 2007; Taverner 1954; Unuvar 1999).
outcomes depending on five GRADE considerations, which are:
study limitations, consistency of effect, imprecision, indirectness See Figure 1 for a flow chart illustrating the study selection process
and publication bias. We used methods and recommendations for this update.
described in Section 8.5 and Chapter 12 of the Cochrane


Informed decisions.

Figure 1. Study flow diagram illustrating the study selection process for this update. 1. The previous version of this
review listed comparisons involving participants treated with antiviral therapy from Sullivan 2007 and Engström
2008 as two additional separate studies. These two comparisons are not included in this update.

The previous update of this review, Salinas 2010, listed seven Included studies
excluded studies (Akpinar 1979; Austin 1993; Bento 1991; Bento
Summary details of the included trials are given in Characteristics
1994; Brown 1982; Martinez 1990; Wolf 1978). We have linked two
of included studies.
references previously listed as separate trials (Bento 1991 and
Bento 1994) under one trial identifier in this update (Bento 1991). Austin 1993 recruited 107 participants whose symptoms had
We included Austin 1993, previously excluded because of potential occurred within five days of presentation to the study centre.
attrition bias, as current practice is to include all trials eligible Of these, 31 participants did not return for initial follow-up. The
according to the selection criteria. 76 remaining participants subsequently entered a double-blinded
randomised controlled study allocating them to a corticosteroid
Authors of the last version of this review included groups receiving
treatment group (prednisone) or a placebo group. The trial authors
antiviral therapy and considered the different comparisons from
gave no details about binding or randomisation. Assessment
Engström 2008 and Sullivan 2007 as separate studies (Engström
of participants occurred within five days of onset and at
2008b and Sullivan 2007b). We did not consider the two antiviral-
"regular intervals until they experienced recovery from their acute
treated participant groups from those trials in this updated review.
paralysis". Final follow-up was at six months after recovery. The
These comparisons are included in the companion Cochrane
trial authors stated, "to be included in the analysis, patients must
review, 'Antiviral treatment for Bell's palsy (idiopathic facial
have completed follow up until their acute recovery occurred."
paralysis)' (Gagyor 2015). In this update, we included only the
Investigators measured disease status using the House-Brackmann
comparisons of corticosteroid versus placebo or corticosteroids
grading system. At first evaluation, participants underwent various
versus no treatment.
tests including blood tests, an audiogram, a nerve excitability
test using the maximal stimulation technique and, if indicated,

Informed decisions.

electroneurography. Treatment with prednisone was started at 30 photographic documentation without a validated scoring system.
mg twice daily for the first five days followed by a reducing dose The trial report did not specify the age range of participants in
stated by the trial authors. this double-blinded study. In the intervention group, participants
received prednisone 410 mg in descending doses over 10 days. The
The study reported final outcomes on 53 participants at six placebo intervention was vitamins. Trialists excluded people with
months after recovery. The primary outcome was time to chronic otitis media, trauma, loss of lacrimation, or recurrent or
recovery, for which trial authors found no statistically significant bilateral palsy.
difference between the two groups. Secondary outcomes included
facial paralysis grade at onset versus grade at recovery. There May 1976 was the only study that stated that there was no benefit
was a statistically significant difference in incomplete recovery from corticosteroids for the recovery of Bell's palsy (RR 1.16, 95% CI
rates favouring the treatment group: 5/23 participants receiving 0.57 to 2.36).
prednisone had incomplete recovery at six months versus 10/30
participants receiving placebo (RR 0.65, 95% CI 0.26 to 1.65). Sullivan 2007 recruited 551 participants to be treated within
Investigators found no significant difference in persistence of pain 72 hours of onset. Participants were randomised by a
during recovery, with 3/23 participants in the prednisone group still dedicated remote telephone-computerised mechanism in a
experiencing pain at six months, compared with 4/30 participants two-stage process into four treatment groups in a factorial
in the placebo group (RR 0.98, 95% CI 0.24 to 3.95). design: prednisolone with placebo, prednisolone with aciclovir,
aciclovir with placebo or double placebo. Participants received
Engström 2008 had a factorial design that randomised prednisolone 25 mg twice daily for 10 days. The trial was blinded
829 participants into four treatment groups using a two- for administrator, participant and assessment of recovery status
stage computerised process. The four treatment groups were until the end of follow-up. Assessments took place at onset,
prednisolone with placebo, prednisolone with valaciclovir, after three months and, if participants were still unwell, again
valaciclovir with placebo, and double placebo. Treatment started after nine months. The investigators measured recovery status on
within 72 hours of symptom onset. The trial was double-blind the House-Brackmann scale, with complete recovery defined as
(administrator and participant) for assessment of recovery status House-Brackmann grade I. Data analysis included an assessment of
until the end of follow-up. Participants were assessed at onset, after treatment interaction.
two weeks (11 to 17 days) and after 1, 2, 3, 6 and 12 months. Trialists
measured disease status using the House-Brackmann grading Sullivan 2007 reported final outcomes on 496 completed
system and the Sunnybrook scale, defining complete recovery participants at three and nine months. In the corticosteroid (OS)
status as a Sunnybrook score of 100 and a House-Brackmann grade group, 5/127 participants had incomplete recovery, compared with
of I. Data analysis included an assessment of treatment interaction. 18/122 participants in the placebo (OO) group (RR 0.27, 95% CI 0.10
to 0.70).
The study reported a positive effect on recovery time due to
prednisolone (comparing recovery rates at 12 months in the Taverner 1954 was a double-blind trial that included 26 participants
prednisolone group with the placebo group). For this review, we with a range of ages from 12 to 76 years within 10 days of
analysed the corticosteroid-placebo combination (OS) versus the onset of Bell's palsy. Participants received either oral cortisone
double placebo combination (OO) 12 months after the onset of acetate 1 g in descending doses over eight days or placebo tablets.
facial palsy. Using the Sunnybrook definition, 50/210 participants Participants were monitored for up to 157 days. The trial excluded
had an incomplete recovery with prednisolone compared with a participants with other neurological conditions or diseases of
greater proportion (73/206) in the placebo group (RR 0.67, 95% CI the ear. Taverner 1954 included participants with herpes zoster
0.50 to 0.91). oticus. These participants were allocated in equal numbers to each
treatment arm, and trial authors excluded them from the analyses.
Lagalla 2002 randomised 62 participants within three days of The trialists did not used a validated scoring system to measure
onset of Bell's palsy to high-dose prednisone, 1 g daily for three outcomes.
days, then 0.5 g daily for three days, administered intravenously,
using saline solution as a placebo. The age range was 15 to 84 Taverner 1954 used the recovery of facial motor function as the
years. Exclusion criteria included peptic ulcer disease, pregnancy, main outcome measure and reported a small, non-significant
severe hypertension, other neurological conditions, diseases of benefit of corticosteroids compared with placebo; CIs allowed for
the ear and previous treatment. As in Taverner 1954, investigators effects in either direction (RR 0.86, 95% CI 0.27 to 2.71).
excluded participants with herpes zoster oticus from the analyses
Unuvar 1999 conducted a non-blinded, randomised controlled
(four of the participants initially randomised in Lagalla 2002). The
trial on children with severe to complete presentation of Bell's
investigators monitored participants for 12 months. They assessed
palsy (House-Brackmann grades IV to V). They randomised 42
recovery of facial motor function using the House-Brackmann
children with an age range of 24 to 74 months using a computer-
scale. The trial authors reported the development of disabling
generated random sequence into two groups. All participants
synkinesis at 12-month follow-up.
entered the trial within three days of onset of Bell's palsy and
Lagalla 2002 reported final outcomes on 58 participants at received either methylprednisolone 1 mg/kg daily for 10 days
12 months. In the prednisolone group, 5/30 participants had then gradually withdrawn over three to five days or no specific
incomplete recovery, compared with 8/28 participants in the treatment. They excluded participants with other neurological
placebo group (RR 0.58, 95% CI 0.22 to 1.57). conditions, diseases of the ear or systemic diseases. The primary
outcome was the recovery of facial motor function measured on the
May 1976 included 51 participants within two days of Bell's House-Brackmann facial grading system.
palsy onset and reported outcomes using clinical assessment and

Informed decisions.

Unuvar 1999 reported a benefit from the treatment with and the other received placebo. It was unclear who diagnosed
corticosteroids although wide CIs allowed for the possibility of both the participants with Bell's palsy and there were varying dosage
no effect and a large effect (RR 0.14, 95% CI 0.01 to 2.61). regimens of corticosteroids used. Two studies were not randomised
or quasi-randomised (Brown 1982; Martinez 1990). It was not
Ongoing studies possible to extract complete information on the specified outcomes
We identified one trial report on the World Health Organization for one study (Wolf 1978). Finally, we excluded Bento 1991 as
International Clinical Trials Registry Platform search portal (Babl number of participants and outcome events by treatment groups
2015). From the website, it appeared that the study has now started was not provided; in addition, 50% of the participants were lost to
recruitment; we will assess this trial fully in future review updates. follow-up.
See Characteristics of ongoing studies.
Risk of bias in included studies
Excluded studies Figure 2 summarises the 'Risk of bias' assessment for each included
Akpinar 1979 compared three groups of 10 participants each; study.
two groups received different dosage regimens of corticosteroids,


Informed decisions.

Figure 2. 'Risk of bias' summary: review authors' judgements about each methodological quality item for each
included study. Green (+) = low risk of bias; yellow (?) = unclear risk of bias; red (-) = high risk of bias.

Allocation and another used a computer-based program (Unuvar 1999). It
was not clear from the reports if there was adequate allocation
All included trials reported the method of randomisation. Four
concealment in Lagalla 2002 or Unuvar 1999. We considered none of
used randomisation centralised at a pharmacy, in accordance
the trials to be at high risk of bias for random sequence generation
with a master sheet of random numbers (May 1976; Taverner
or allocation concealment.
1954), or an automated permuted block technique (Engström 2008;
Sullivan 2007). One study used a random number list (Lagalla 2002),

Informed decisions.

Blinding Other potential sources of bias

Five trials were double-blind, using placebo in the control group We identified no other potential sources of bias.
(Engström 2008; Lagalla 2002; May 1976; Sullivan 2007; Taverner
1954). Two of these trials used lactose as the placebo (Sullivan Effects of interventions
2007; Taverner 1954), one used vitamins (May 1976), and one used
See: Summary of findings for the main comparison
a saline solution (Lagalla 2002). Two trials did not specify what was
Corticosteroids compared to placebo or no treatment for Bell's
used as placebo, but they stated that this was formulated to have
palsy
the same size, smell and colour (Engström 2008; Unuvar 1999). In
the trial using vitamins as placebo, the experimental group received As all trials reported different intervals and lengths of follow-up,
similar looking capsules containing prednisone plus vitamins. The we performed analyses on data reported at the end of the study
trial using saline solution as placebo gave intramuscular vitamins periods. These were 157 days (Taverner 1954), six months (May
to all participants for 15 days (Lagalla 2002). In one trial, it was 1976; Austin 1993), nine months (Sullivan 2007), and 12 months
not clear from the report if the physicians administering the drug (Engström 2008; Lagalla 2002; Unuvar 1999).
were blinded (Lagalla 2002). There were no serious imbalances in
baseline prognostic factors between groups. Primary outcome
Incomplete outcome data Incomplete recovery of facial motor function six months or more
after randomisation
Engström 2008, Sullivan 2007; and Taverner 1954 had drop-out
rates of less than 10%. No participants dropped out in May 1976. All seven trials, with 895 participants, provided data for the
Lagalla 2002 included drop-outs in analyses on an intention-to- outcome complete recovery of facial motor function at six months'
treat basis, by assuming that drop-outs had a poor outcome. Austin follow-up or more (we included data from Taverner 1954, which
1993 had a drop-out rate of 50% for outcomes six months after reported at five months). The number of people with incomplete
recovery. Unuvar 1999 did not report on attrition. recovery at six months' follow-up was lower in the corticosteroid
group compared to the control group (RR 0.63, 95% CI 0.50 to 0.80)
Selective reporting (Analysis 1.1; Figure 3).
All studies reported their intended primary outcomes. Engström
2008 reported all primary outcomes, with secondary outcomes
reported in subsequent publications (Axelsson 2012; Berg 2012).

Figure 3. Forest plot of comparison: 1 Corticosteroid (OS) versus placebo or no treatment (OO), outcome: 1.1
Incomplete recovery ≥ 6 months after randomisation.

The tests for statistical heterogeneity were marginally significant Taverner 1954; Unuvar 1999). There were better outcomes in two of
(Chi2 = 7.32, P value = 0.29, I2 = 18%). This small degree of the studies (Engström 2008; Sullivan 2007).
heterogeneity was due to the differences in the findings between
the large studies (Engström 2008; Sullivan 2007), and small, The number of people who need to be treated with steroids to avoid
underpowered studies (Austin 1993; Lagalla 2002; May 1976; one person with incomplete recovery was 10 (95% CI 6 to 20).

Informed decisions.

Sensitivity analyses Secondary outcomes

We removed smaller underpowered studies (Austin 1993; Lagalla Cosmetically disabling persistent sequelae six months or more
2002; May 1976; Taverner 1954; Unuvar 1999) from the main after randomisation
analysis leaving the two largest studies (Engström 2008; Sullivan
2007). This analysis confirmed the size and direction of effect, but Two trials with 75 participants provided data on the number of
with higher statistical heterogeneity (RR 0.59, 95% CI 0.44 to 0.79, participants with severe paralysis, or what may be judged as
cosmetically disabling sequelae, at six months' follow-up or more
Chi2 = 3.32, I2 = 70%).
(May 1976; Taverner 1954). When we combined the data, the
We analysed the main outcome for the studies that had the longest number of participants with cosmetically disabling sequelae was
follow-up (i.e. between nine and 12 months) (Engström 2008; similar in the corticosteroid group and the control group (RR 0.96,
Lagalla 2002; Sullivan 2007). This did not significantly change the 95% CI 0.40 to 2.29) (Analysis 1.2; Figure 4)
result.

Figure 4. 1.2 Cosmetically disabling persistent sequelae ≥ 6 months after randomisation.

Motor synkinesis or crocodile tears during follow-up months' follow-up (Austin 1993). After pooling these data, we
found a significant reduction in the number of people with motor
Three trials, with 485 evaluable participants, reported separate
synkinesis in the corticosteroid group (40/241) compared to the
data on motor synkinesis or crocodile tears during follow-up
placebo group (64/248) (RR 0.64, 95% CI 0.45 to 0.91) (Analysis 1.3;
(Austin 1993; Engström 2008; Lagalla 2002). Two trials reported
Figure 5). We found no statistical heterogeneity (Chi2 = 0.42, df = 2
the occurrence of disabling synkinesis at 12 months' follow-up
(Engström 2008; Lagalla 2002); the other trial reported at six (P = 0.81), I2 = 0%).

Figure 5. Forest plot of comparison: 1 Corticosteroid (OS) versus placebo or no treatment (OO), outcome: 1.3 Motor
synkinesis and crocodile tears.

Informed decisions.

Adverse effects attributable to the use of corticosteroids (Austin 1993). Two trials gave a detailed account of 93 adverse
effects (Engström 2008; Sullivan 2007), all of them non-serious, with
Three studies explicitly recorded the absence of adverse effects
no significant difference between people receiving corticosteroids
attributable to the experimental treatment (May 1976; Taverner
and people receiving placebo (RR 1.04, 95% CI 0.71 to 1.51). Three
1954; Unuvar 1999). One trial reported that three participants
deaths occurred; all were deemed to be unrelated to treatment,
receiving prednisone had temporary sleep disturbances (Lagalla
all were in the groups not receiving prednisolone. One man with a
2002). Another reported "no severe side effects of steroid therapy",
history of recurrent atrial fibrillation had a transient relapse while
although there were single reported cases of mood swings,
taking prednisolone and valaciclovir (Figure 6).
dyspepsia and minor conjunctivitis by individual participants

Figure 6. Forest plot of comparison: 1 Incomplete recovery of facial motor function, outcome: 1.4 Adverse effects.

Subgroup analyses reduces, making the likelihood of adverse effects in practical use
less than in longer-term indications.
In this updated version of the review, we did not perform any
subgroup analyses. Overall completeness and applicability of evidence
DISCUSSION No new studies have been published since the previous Cochrane
review (Salinas 2010). The two most recent, well-powered studies
Summary of main results (Engström 2008; Sullivan 2007), with five smaller studies (Austin
1993; Lagalla 2002; May 1976; Taverner 1954; Unuvar 1999),
High-quality evidence from randomised controlled trials indicated
provided a significant result based on the evidence provided. These
benefit from the use of corticosteroids in Bell's palsy.
studies sufficiently address the objectives of this review in that they
Two trials reached a statistically significant difference favouring the investigate all relevant participants, interventions and outcomes.
use of prednisolone (Engström 2008; Sullivan 2007). Meta-analysis The findings are in accordance with suggested current clinical
of the complete high-quality randomised controlled trial literature practice (Madhok 2009).
convincingly supported a beneficial effect of prednisolone for
reducing the numbers of participants with incomplete recovery. Quality of the evidence
For the main outcome of this review (incomplete recovery
Moderate-quality evidence indicated that participants who
six months or more after randomisation), all seven studies
received corticosteroid treatment had less motor synkinesis and
combined provided high-quality evidence. In addition, for motor
crocodile tears than the placebo group.
synkinesis and crocodile tears, data from three studies provided
Based on these two studies, low-quality evidence revealed no moderate-quality evidence. Cosmetically disabling persistent
important differences between corticosteroids and placebo in sequelae six months or more after randomisation was the only
cosmetically disabling persistent sequelae, but wide CIs allowed for analysis performed where the quality of evidence was low. For
the possibility of an effect in either direction. adverse effects, the evidence was moderate quality. Reasons for
downgrading the quality of evidence were that in one study
The included studies did not report differences in the occurrence participants and assessors were not blinded to the treatment
of adverse effects between corticosteroids and placebo and that they received (Unuvar 1999), and in another study, loss
additionally no serious adverse effects were reported. However, to follow-up was 50%, representing incomplete outcome data
corticosteroids have well-known adverse effects, of which the (Austin 1993). Two studies excluded participants who were found
incidence rises markedly with prolonged dosages above 10 mg after randomisation to have clinical evidence of herpes zoster
of prednisolone or its equivalent per day (Dollery 1999). Usually infection (Lagalla 2002; Taverner 1954). Two studies did not use
corticosteroid courses in Bell's palsy are short and the dose quickly a standardised scale for assessment of facial motor function (May
Informed decisions.

1976; Taverner 1954). We considered the effects of these factors on corticosteroids were safe and probably effective in improving facial
the quality of the evidence insufficient for further downgrading for functional outcomes in people with Bell's palsy (Grogan 2001). This
indirectness of evidence. The results of the majority of studies in Practice Parameter was published, also, before the publication of
this review were consistent with each other, apart from those of one Sullivan 2007 and Engström 2008.
older, smaller study (May 1976).
AUTHORS' CONCLUSIONS
Potential biases in the review process
Implications for practice
To help ensure that decisions about which studies to include in
this review were reproducible, two review authors repeated the According to high-quality evidence, 10 people with Bell's palsy
process (we divided the studies into three groups). There was no need to be treated with corticosteroids to avoid one incomplete
distinction made on the experience and expertise of each author recovery. The available evidence from randomised controlled trials
in the reviewing pairs. On applying the eligibility criteria and shows that corticosteroids significantly reduce the frequency of
assessing the relevance of studies, review authors were aware of incomplete recovery from Bell's palsy.
the names of the study authors, institutions, journal of publication
and results. FS and FD did not assess their own trial (Sullivan 2007). Implications for research
There were no final disagreements about which studies should be Further research on Bell's palsy treatment should consider giving
included. According to previous practice in this review, we excluded corticosteroids to those participants acting as controls.
several studies and a published abstract that provided insufficient
information. Therefore, there might be some risk of publication There should be no further studies that do not include
and selective reporting bias due to data from some studies being corticosteroids as a treatment for Bell's palsy. No participants
unavailable. should be given placebo or no treatment in any future studies.
There is an adequate body of evidence to support the use of
Agreements and disagreements with other studies or corticosteroids in the treatment of Bell's palsy.
reviews
ACKNOWLEDGEMENTS
Our results are coincident with three previous systematic reviews,
which found that corticosteroids significantly improved the We would like to thank the authors of previous editions of this
prognosis of people with Bell's palsy (de Almeida 2009; Ramsey review and we are very grateful for their hard work and enthusiasm.
2000; Williamson 1996). All three reviews, even though of good Our thanks are also extended to Angela Gunn who provided the
quality, included a study that lost 50% of participants to follow- search results and to Cochrane Neuromuscular for their extensive
up (Bento 1991). Only one of them, de Almeida 2009, was carried technical assistance and support.
out after the publication of the largest trials included in our
review (Engström 2008; Sullivan 2007). Two of them (de Almeida The review has some sections in common with the Cochrane
2009; Ramsey 2000) also included a non-randomised study in the review 'Antiviral treatment for Bell's palsy (idiopathic facial
analyses (Martinez 1990; Shafshak 1994). A Practice Parameter paralysis)' (Gagyor 2015), which has been completed in parallel
published by the American Academy of Neurology concluded that with this review by the same authors.

Informed decisions.

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CHARACTERISTICS OF STUDIES
Characteristics of included studies [ordered by study ID]

Austin 1993
Methods Double-blind, randomised, controlled study
Participants 107 people were initially randomised; 76 completed follow-up until acute recovery and were included
in the study analyses
Participants were treated within 5 days of onset
Sex: male 39 (51%), female 37 (49%)
Age: mean 36.8 years, range 18 to 70 years
37 cases (49%) right side palsy and 39 cases (51%) left side palsy
Interventions • Prednisone (n = 35): in a scheduled dosage (30 mg twice daily for 5 days reducing to 20 mg twice daily
on day 6, 15 mg twice daily on day 7, 10 mg twice daily on day 8, 5 mg twice daily on day 9, and 5 mg
once daily on day 10)
• Equivalent placebo (n = 31)
Outcomes Primary outcome:
• time to resolution in days of facial function as defined by the House-Brackmann scale
Secondary outcomes:
• distribution of facial nerve grade at 6 months after recovery, in addition to

• crocodile tears and
• anxiety during follow-up
Follow-up up to 9 months
Funding Not stated

Informed decisions.

Austin 1993 (Continued)
Conflicts of interest Not stated
Date conducted 1 October 1989 to 31 December 1990
Notes Good recovery defined as grade I or II of the House-Brackmann scale
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence genera- Unclear risk Stated to be randomised at the pharmacy but details not given
tion (selection bias)
Allocation concealment Unclear risk Allocation of participants not described

(selection bias)
Blinding of participants Unclear risk Quote: "The study was blinded to both the patient and the clinical investiga-
and personnel (perfor- tors". Further details of blinding not given
mance bias)
All outcomes
Blinding of outcome as- Unclear risk Quote: "The study was blinded to both the patient and the clinical investiga-
sessment (detection bias) tors". Further details of blinding not given
All outcomes
Incomplete outcome data High risk 107 participants randomised, 31 did not attend for follow-up assessment. 76
(attrition bias) allocated to prednisone or placebo
All outcomes
Analysis 6 months after resolution of Bell's palsy included 53 participants (23
prednisolone and 30 placebo), representing over 50% loss to follow-up at this
point. Reasons for additional drop-outs at 6 months not described
Selective reporting (re- Low risk All primary outcomes reported

porting bias)
Other bias Low risk Single-centre study

Engström 2008
Methods Randomised, placebo-controlled trial with 4 treatment groups
Participants 829 participants randomised within 72 hours of facial palsy onset
No contraindications to corticosteroid or antiviral use
Sex: male 341 (41%), female 488 (59%)
Age: mean 40 years, range 31-54 years
Interventions Participants allocated into 1 of 4 treatment groups:
• prednisolone with placebo

• valaciclovir with prednisolone
• valaciclovir with placebo
• double placebo

Informed decisions.

Engström 2008 (Continued)
Dosages: valaciclovir 1000 mg 3 times daily for 7 days; prednisolone 60 mg daily for 5 days
• recovery of facial function, as assessed at visits with the Sunnybrook scale and the House-Brackmann
scale
Complete recovery was taken as Sunnybrook scale 100 and House-Brackmann scale grade I
Other outcomes:
• degree of pain, as recorded during the first 2 months

• adverse effects recorded for the first month
• frequency of severe pain, synkinesis, facial spasm and residual facial symptoms at 12 months
Follow-up at 2 weeks, and 1, 2, 3, 6 and 12 months after randomisation, according to recovery
Final outcomes reported at 12 months
Funding Uppsala University; GlaxoSmithKline (Sweden); Pfizer AB (Sweden); Acta Otolaryngologica Foundation;
Rosa and Emanuel Nachmanssons Foundation; Stig and Ragna Gorthon Foundation; Torsten Birger
Segerfalk Foundation; Margit Arstrups Foundation; County Council of Skane;
̊ Helsinki University Central
Hospital Research Funds
Conflicts of interest One author was paid by GlaxoSmithKline for a lecture on Bell's Palsy
Date conducted May 2001 to September 2006
Notes Multicentre
Risk of bias
Random sequence genera- Low risk Generated by computer number generator. Sequentially numbered identical
tion (selection bias) containers allocated to participants on entry into the trial, by the recruiting
physician
Allocation concealment Low risk Allocation sequence double-blind and generated by a computer number gen-
(selection bias) erator in random permuted blocks of 8
Blinding of participants Low risk Study drugs issued in identical containers. All participants blinded to treat-
and personnel (perfor- ment group until study completion. All study personnel and data analysts
mance bias) blinded to treatment group until study completion
All outcomes
Blinding of outcome as- Low risk All study personnel and data analysts blinded to treatment group until study
sessment (detection bias) completion
All outcomes
Incomplete outcome data Low risk Numbers lost to follow-up and reasons given:
(attrition bias)
All outcomes • 213 randomised to corticosteroids: 3 did not receive the drug, 24 lost to fol-
low-up at 12 months (12.7%); 210 analysed
• 209 randomised to placebo: 3 did not receive the placebo; 18 lost to follow-up
at 12 months; 206 analysed
'Modified' intention-to-treat analyses used. All randomised participants who

received at least 1 dose of study medication included, but participants who did
not start therapy excluded. Last observation carried forward method used for

Informed decisions.

Engström 2008 (Continued)
the modified intention-to-treat analysis, and missing data points imputed in
the post-baseline follow-up visits from the last observation available for each
participant
Selective reporting (re- Low risk All primary outcomes reported. Other outcomes reported in another paper
porting bias) due to space constrictions
Other bias Low risk No other biases identified

Lagalla 2002
Methods Randomised, placebo-controlled, double-blind trial
Participants 62 participants within 3 days of onset of onset of Bell's palsy; 4 people excluded after randomisation
because of acute herpes zoster infection
Sex: male 34, female 28
Age: mean (± SD) 47.5 (± 19) years, range 15 to 84 years
Participants with contraindications to corticosteroids (peptic ulcer disease, pregnancy, severe hyper-
tension), or previously treated excluded. No losses to follow-up
34 cases left palsy, 28 cases right palsy
Interventions • Prednisone: 1 g daily intravenously in saline solution for 3 days and then 0.5 g for the other 3 days
• Placebo: saline solution
All participants received intramuscular vitamins for 15 days
• recovery of facial function
Used House-Brackmann scale for assessment. "Good recovery" was grades I or II
Secondary outcomes:
• motor synkinesis and crocodile tears
Follow-up at 1, 3, 6 and 12 months
Final outcomes reported at 6 and 12 months
Funding Not stated
Date conducted Not stated
Notes Single centre
Risk of bias
Random sequence genera- Low risk Random list used to generate random sequence

Informed decisions.

Lagalla 2002 (Continued)
Allocation concealment Unclear risk Not stated by authors
(selection bias)
Blinding of participants Low risk Participants were blinded to the treatment. Saline solution was used as a
and personnel (perfor- placebo
mance bias)
All outcomes
Blinding of outcome as- Unclear risk Not stated if assessors were blinded
sessment (detection bias)
All outcomes
Incomplete outcome data Low risk Numbers lost to follow-up and reasons given: 62 people randomised, 4 exclud-
(attrition bias) ed after randomisation (2 in each group) because of herpes zoster infection;
All outcomes the remaining 58 completed study
Trial authors stated: "Comparative statistics was carried out on an inten-

tion-to-treat basis, by assuming that drop-outs had a poor outcome. Data
analysis concerning basal features included all patients enrolled. The analysis
of clinical grading changes included data from only 58 subjects"
Selective reporting (re- Low risk Primary and secondary outcomes reported
porting bias)
Other bias Low risk No other bias identified

May 1976
Methods Double-blind, placebo-controlled, randomised trial with 2 treatment groups
Participants 51 participants within 2 days of onset of Bell's palsy
People with chronic otitis, trauma, loss of lacrimation, and bilateral or recurrent palsy, and herpes
zoster excluded
Age: ranges not clearly stated "30 years or less and 31 years or older"
Interventions • Prednisone: 410 mg in descending doses over 10 days, plus vitamins

• Placebo: vitamins alone
• complete recovery of facial function
Assessment made clinically using photographs (examples given in the paper) at 6 months after onset
Secondary outcomes:
• pain
• taste
• hyperacusis
• time to recovery
No adverse effects reported

Informed decisions.

May 1976 (Continued)
Funding Not stated
Date conducted 1972 to 1974
Notes Single centre
Risk of bias
Random sequence genera- Low risk Random stratified sequence generated by a statistician, administered in a
tion (selection bias) pharmacy
Allocation concealment Low risk Allocation of treatment group unknown to both participants and physicians
(selection bias)
Blinding of participants Low risk Double-blinded. Placebo was similar-looking tablets containing vitamins
and personnel (perfor-
mance bias)
All outcomes
Blinding of outcome as- Low risk Assessors blinded to treatment group

All outcomes
Incomplete outcome data Unclear risk No information on loss to follow-up rates

(attrition bias)
All outcomes
Selective reporting (re- Unclear risk Primary outcomes reported, adverse effects not reported
porting bias)

Sullivan 2007
Methods Double-blind, placebo-controlled, randomised, factorial trial
Participants 552 participants randomised and 496 included in final outcome assessment
Referred for assessment and treatment within 72 hours of paralysis onset.
All participants aged ≥ 16 years and no contraindications to corticosteroids or antiviral therapy
Sex: male 253 (51%), female 243 (49%)
Age: mean (± SD) 44 (± 16.4) years
Interventions Participants allocated to 1 of 4 treatment groups to receive:
• aciclovir
• prednisolone
• aciclovir with prednisolone
• placebo

Informed decisions.

Sullivan 2007 (Continued)
Participants received prednisolone 25 mg twice daily for 10 days or aciclovir 400 mg 5 times daily for 10
days, both treatments or neither treatment, depending on allocation
• recovery rated on House-Brackmann scale, where recovery was grade I
Secondary outcomes:
• health-related quality of life

• Health Utilities Index Mark 3
• facial appearance (Derriford Appearance Scale)
• pain
• adverse effects
• frequency of incomplete recovery at end of study
Follow-up at 3 and 9 months
Final outcomes reported at 9 months
Funding Supported by a grant (02/09/04) from the Health Technology Assessment Programme of the Nation-
al Institute for Health Research (Department of Health, England). The Scottish Executive (Chief Scien-
tist Office and National Health Service Education for Scotland) funded the Scottish School of Primary
Care during the study. Practices were reimbursed for their contributions through national Support for
Science mechanisms
Conflicts of interest Drs Sullivan and Donnan reported receiving grant support from GlaxoSmithKline for projects unrelated
to the trial. No other potential conflict of interest relevant to this article reported
Date conducted June 2004 to June 2006
Notes Multicentre: 17 hospitals
Risk of bias
Random sequence genera- Low risk Quote: "... patient was randomly assigned to a study group by an independent,
tion (selection bias) secure, automated telephone randomisation service"
Allocation concealment Low risk All parties blinded to allocation

(selection bias)
Blinding of participants Low risk Participants not receiving active drug received placebo. All administered med-
and personnel (perfor- ication was identical and in identical containers
mance bias)
All outcomes
Blinding of outcome as- Low risk Assessors blinded to treatment group

All outcomes
Incomplete outcome data Low risk Frequency and reason for drop-outs documented:
(attrition bias)
All outcomes 138 assigned to prednisolone, of whom 127 completed the trial: 3 received an
incorrect drug and 11 were lost to follow-up (4 withdrew consent, 2 sought ac-
tive treatment, 1 did not provide primary outcome data, 4 could not be con-
tacted after the 1st visit)

Informed decisions.

Sullivan 2007 (Continued)
141 assigned to placebo of whom 122 completed the trial: 19 were lost to fol-
low-up (6 withdrew consent, 3 could not be contacted, 3 sought active treat-
ment, 1 did not provide primary outcome data, 3 could not be contacted after
the 1st visit, 2 died, 1 withdrawn by investigator)
Selective reporting (re- Low risk All planned outcome measures reported
porting bias)
Other bias Low risk No other potential sources of bias identified

Taverner 1954
Methods Double-blind, randomised controlled trial
Participants 26 participants within 10 days of onset of Bell's palsy
Sex: male 13 and female 13
Age: range 12 to 76 years
Interventions • Cortisone acetate: orally in descending doses over 8 days (200 mg in divided doses daily for the first
3 days, 100 mg daily for 3 days and 50 mg daily for 2 days)
• Placebo: same number of lactose tablets for the same period
Outcomes Primary outcomes:
• recovery of facial function (clinical assessment)

• signs of denervation on electromyographic examination
Secondary outcome:
• duration of recovery
Final outcome reported at 157 days
Funding Medical Research Council supplied cortisone acetate
Date conducted August 1953 to June 1954
Notes Single-centre study
Risk of bias
Random sequence genera- Low risk Randomisation centralised in pharmacy, in accordance with a master sheet of
tion (selection bias) random numbers
Allocation concealment Low risk Central allocation in pharmacy

(selection bias)
Blinding of participants Low risk Assessors and participants both blinded

mance bias)
All outcomes

Informed decisions.

Taverner 1954 (Continued)
Blinding of outcome as- Low risk Assessors and participants both blinded (the point to which assessors were
sessment (detection bias) blinded was not clear)
All outcomes
Incomplete outcome data Low risk 2 people excluded from analysis because of herpes of the external meatus
(attrition bias)
All outcomes
Selective reporting (re- Unclear risk Adverse effects not reported

porting bias)

Unuvar 1999
Methods Randomised controlled trial
Participants 42 children within 3 days of onset of Bell's palsy
Age: mean (± SD) 56.9 (± 4.7) months, range 24 to 74 months
Children with chronic neurological conditions, other reasons for facial palsy and acute otitis media ex-
cluded
Interventions • Oral methylprednisolone: 1 mg/kg daily, for 10 days, and then withdrawn in 3 to 5 days
• Control: no specific treatment (no placebo used)
• recovery of facial motor function (House-Brackmann scale)
Secondary outcome:
• adverse effects
Follow-up at 4, 6 and 12 months
Funding Not stated
Date conducted Not stated
Notes Single-centre study
Risk of bias
Random sequence genera- Low risk Computer-generated random sequence

Allocation concealment Low risk Participants allocated to groups by concealed computer-generated random
(selection bias) sequence

Informed decisions.

Unuvar 1999 (Continued)
Blinding of participants High risk Participants not blinded to the treatment that they were receiving
mance bias)
All outcomes
Blinding of outcome as- High risk Assessors not blinded to the treatment that participants were receiving
All outcomes
Incomplete outcome data Unclear risk Losses to follow-up not reported

(attrition bias)
All outcomes
Selective reporting (re- Low risk Outcomes given by authors

porting bias)
Other bias Low risk No other potential biases were identified
n: number of participants; SD: standard deviation.

Characteristics of excluded studies [ordered by study ID]

Study Reason for exclusion
Akpinar 1979 Allocation to treatment group was according to the day of admission, which is a method that is
highly susceptible to bias. It was not clear who diagnosed participants with Bell's palsy and they
used varying dosage regimens of corticosteroids. Follow-up 3 weeks
Bento 1991 Did not provide the number of participants and outcome events by treatment groups. 50% of par-
ticipants lost to follow-up
Brown 1982 Not randomised or quasi-randomised. There was no placebo group or open control group
Martinez 1990 Not randomised or quasi-randomised. 27% of participants lost to follow-up
Wolf 1978 Unable to extract complete information on the specified outcomes

Characteristics of ongoing studies [ordered by study ID]

Babl 2015
Trial name or title Bell's palsy in children: a multi-centre, double-blind, randomised, placebo-controlled trial to deter-
mine whether prednisolone improves recovery at 1 month
Methods Randomised control trial (computer-generated randomisation schedule), parallel assignment
Participants Participants aged 6 months to 18 years, weight ≥ 5 kg, diagnosed with Bell's palsy by their treating
doctor and have an acute onset of symptoms of Bell's palsy for < 72 hours prior to randomisation
Interventions • Prednisolone 1 mg/kg/day (dosing based on weight categories) up to a maximum of 50 mg/day

for 10 days
• Placebo: oral liquid with the same ingredients as the intervention solution minus the active drug

Informed decisions.

Babl 2015 (Continued)
• complete recovery at 1-month post-randomisation, where recovery was defined as a House-
Brackmann facial grading score of I. Recovery assessed by a specialist clinician in a face-to-face
setting
Starting date 1 July 2015
Contact information Prof Franz Babl
Emergency Research Department, Murdoch Children's Research Institute, Royal Children's Hospi-
tal, VIC, Australia
+61399366748
franz.babl@rch.org.au
Notes www.anzctr.org.au/Trial/Registration/TrialReview.aspx?ACTRN=12615000563561

DATA AND ANALYSES

Comparison 1. Corticosteroid (OS) versus placebo or no treatment (OO)
Outcome or subgroup title No. of No. of Statistical method Effect size

studies partici-
pants
1 Incomplete recovery ≥ 6 months after 7 895 Risk Ratio (M-H, Fixed, 95% CI) 0.63 [0.50, 0.80]
randomisation
2 Cosmetically disabling persistent se- 2 75 Risk Ratio (M-H, Fixed, 95% CI) 0.96 [0.40, 2.29]
quelae ≥ 6 months after randomisation
3 Motor synkinesis and crocodile tears 3 485 Risk Ratio (M-H, Fixed, 95% CI) 0.64 [0.45, 0.91]
4 Adverse effects 3 715 Risk Ratio (M-H, Fixed, 95% CI) 1.04 [0.71, 1.51]

Analysis 1.1. Comparison 1 Corticosteroid (OS) versus placebo or no treatment
(OO), Outcome 1 Incomplete recovery ≥ 6 months after randomisation.
Study or subgroup OS OO Risk Ratio Weight Risk Ratio
n/N n/N M-H, Fixed, 95% CI M-H, Fixed, 95% CI
Austin 1993 5/23 10/30 6.91% 0.65[0.26,1.65]
Engström 2008 50/210 73/206 58.66% 0.67[0.5,0.91]
Lagalla 2002 5/30 8/28 6.59% 0.58[0.22,1.57]
May 1976 10/25 9/26 7.02% 1.16[0.57,2.36]
Sullivan 2007 5/127 18/122 14.61% 0.27[0.1,0.7]
Taverner 1954 4/14 4/12 3.43% 0.86[0.27,2.71]
Unuvar 1999 0/21 3/21 2.79% 0.14[0.01,2.61]

Total (95% CI) 450 445 100% 0.63[0.5,0.8]
Favours OS 0.005 0.1 1 10 200 Favours OO

Informed decisions.


Total events: 79 (OS), 125 (OO)
Heterogeneity: Tau2=0; Chi2=7.32, df=6(P=0.29); I2=18.05%
Test for overall effect: Z=3.73(P=0)

Analysis 1.2. Comparison 1 Corticosteroid (OS) versus placebo or no treatment (OO),
Outcome 2 Cosmetically disabling persistent sequelae ≥ 6 months after randomisation.
Taverner 1954 3/13 3/11 39.87% 0.85[0.21,3.38]
May 1976 5/25 5/26 60.13% 1.04[0.34,3.16]

Total (95% CI) 38 37 100% 0.96[0.4,2.29]
Heterogeneity: Tau2=0; Chi2=0.05, df=1(P=0.82); I2=0%
Test for overall effect: Z=0.09(P=0.93)

Analysis 1.3. Comparison 1 Corticosteroid (OS) versus placebo or
no treatment (OO), Outcome 3 Motor synkinesis and crocodile tears.
Austin 1993 3/23 4/30 5.47% 0.98[0.24,3.95]
Engström 2008 32/186 53/188 83.11% 0.61[0.41,0.9]
Lagalla 2002 5/30 7/28 11.42% 0.67[0.24,1.86]

Total (95% CI) 239 246 100% 0.64[0.45,0.91]
Heterogeneity: Tau2=0; Chi2=0.42, df=2(P=0.81); I2=0%
Favours OS 0.1 0.2 0.5 1 2 5 10 Favours OS

Analysis 1.4. Comparison 1 Corticosteroid (OS) versus placebo or no treatment (OO), Outcome 4 Adverse effects.
Engström 2008 21/203 25/201 54.57% 0.83[0.48,1.44]
Lagalla 2002 3/32 0/30 1.12% 6.58[0.35,122.21]
Sullivan 2007 24/127 20/122 44.31% 1.15[0.67,1.98]

Total (95% CI) 362 353 100% 1.04[0.71,1.51]

Informed decisions.


Heterogeneity: Tau2=0; Chi2=2.31, df=2(P=0.31); I2=13.43%

APPENDICES
Appendix 1. Cochrane Neuromuscular Specialised Register (CRS) search strategy

#1 MeSH DESCRIPTOR Facial Nerve Diseases [REFERENCE] [STANDARD]
#2 MeSH DESCRIPTOR Bell Palsy [REFERENCE] [STANDARD]
#3 MeSH DESCRIPTOR Facial Paralysis [REFERENCE] [STANDARD]
#4 MeSH DESCRIPTOR Hemifacial Spasm [REFERENCE] [STANDARD]
#5 (((bell* or facial* or hemifacial* or cranial*) NEAR3 (pals* or paralys* or paresi* or spasm*))) AND (INREGISTER) [REFERENCE] [STANDARD]
#6 #1 or #2 or #3 or #4 or #5 [REFERENCE] [STANDARD]
#7 MeSH DESCRIPTOR Steroids [REFERENCE] [STANDARD]
#8 steroid or steroids [REFERENCE] [STANDARD]
#9 MeSH DESCRIPTOR Adrenal Cortex Hormones [REFERENCE] [STANDARD]
#10 MeSH DESCRIPTOR Adrenocorticotropic Hormone [REFERENCE] [STANDARD]
#11 MeSH DESCRIPTOR Prednisone [REFERENCE] [STANDARD]
#12 MeSH DESCRIPTOR Prednisolone [REFERENCE] [STANDARD]
#13 MeSH DESCRIPTOR Glucocorticoids [REFERENCE] [STANDARD]
#14 MeSH DESCRIPTOR Cortisone [REFERENCE] [STANDARD]
#15 corticosteroid* or adrenocorticotroph* or prednisone or prednisolone or glucocorticoid* or cortisone or methylprednisone
[REFERENCE] [STANDARD]
#16 #7 or #8 or #9 or #10 or #11 or #12 or #13 or #14 or #15 [REFERENCE] [STANDARD]
#17 #6 and #16 [REFERENCE] [STANDARD]
Appendix 2. CENTRAL (CRSO) search strategy

Search run on Fri Mar 4 2016
#1 ((Bell or "Bell's" or Bells or facial or hemifacial or cranial) NEAR (palsy or palsies or paralysis or paresis or spasm or spasms)):TI,AB,KY 555
#2 (steroid* or corticosteroid* or adrenocorticotroph* or corticotropin or prednisone or prednisolone or glucocorticoid* or cortisone or
methylprednisone or "adrenal cortex hormone*"):TI,AB,KY 37189
#3 (steroid* or corticosteroid* or adrenocorticotroph* or corticotropin or prednisone or prednisolone or glucocorticoid* or cortisone or
methylprednisone or "adrenal cortex hormone*"):TI,AB,KY 37189
#4 #1 AND #2 98
#5 sr-neuromusc:cc 5823
#6 #4 not #5 44
Appendix 3. MEDLINE (OvidSP) strategy

Database: Ovid MEDLINE(R) <1946 to February Week 4 2016>
Search Strategy:
--------------------------------------------------------------------------------
1 randomized controlled trial.pt. (407164)
2 controlled clinical trial.pt. (90097)
3 randomized.ab. (304430)
4 placebo.ab. (155333)
5 drug therapy.fs. (1823046)
6 randomly.ab. (215472)
7 trial.ab. (313777)
8 groups.ab. (1364056)
9 or/1-8 (3457470)
10 exp animals/ not humans.sh. (4191570)
11 9 not 10 (2944190)
12 facial nerve diseases/ (1409)
Informed decisions.

13 Bell Palsy/ (977)

14 Facial Paralysis/ or hemifacial spasm/ (11784)
15 ((bell$ or facial$ or hemifacial$ or cranial$) adj3 (pals$ or paralys$ or paresi$ or spasm$)).tw. (14759)
16 or/12-15 (19812)
17 steroid$.tw. or steroids/ (195309)
18 corticosteroid$.tw. or adrenal cortex hormones/ (111371)
19 adrenocorticotroph$.tw. or corticotropin/ (47991)
20 prednisone.tw. or prednisone/ (46046)
21 prednisolone.tw. or prednisolone/ (38861)
22 glucocorticoid$.tw. or glucocorticoids/ (87141)
23 cortisone.tw. or cortisone/ (22428)
24 methylprednisone.tw. (209)
25 or/17-24 (448308)
26 11 and 16 and 25 (892)
27 remove duplicates from 26 (886)
Appendix 4. EMBASE (OvidSP) strategy

Database: Embase <1980 to 2016 Week 09>
Search Strategy:
--------------------------------------------------------------------------------
1 crossover-procedure.sh. (46158)
2 double-blind procedure.sh. (126385)
3 single-blind procedure.sh. (21564)
4 randomized controlled trial.sh. (393423)
5 (random$ or crossover$ or cross over$ or placebo$ or (doubl$ adj blind$) or allocat$).tw,ot. (1223922)
6 trial.ti. (193286)
7 or/1-6 (1370827)
8 (animal/ or nonhuman/ or animal experiment/) and human/ (1446761)
9 animal/ or nonanimal/ or animal experiment/ (3498115)
10 9 not 8 (2901774)
11 7 not 10 (1261401)
12 limit 11 to embase (1041826)
13 exp facial nerve paralysis/ (20154)
14 Bell palsy/ (2578)
15 hemifacial spasm/ (2209)
16 ((bell$ or facial$ or hemifacial$ or cranial$) adj3 (pals$ or paralys$ or paresi$ or spasm$)).tw. (18906)
17 or/13-16 (28552)
18 corticosteroid/ or corticosteroid$.tw. (233317)
19 glucocorticoid/ or glucocorticoid$.tw. (101570)
20 corticotropin/ or corticotrophin$.tw. (58083)
21 prednisolone/ or prednisolone.tw. (106302)
22 prednisone/ or prednisone.tw. (142280)
23 or/18-22 (552861)
24 12 and 17 and 23 (133)
25 remove duplicates from 24 (131)
Appendix 5. LILACS IAHx strategy

("Bell palsy" or "paralisis de Bell" or "paralisia de Bell" or "facial paralysis" or "paralisis facial" or "paralisia facial" or "hemifacial
spasm" or "espasmo hemifacial") and (MH:D06.472.040$ or steroids or esteroides or cortisone or cortisona or corticoesteroides or
corticosteroides or corticosteroid$ or glucocorticoid$ or prednisolone or prednisolona or prednisone or prednisona or methylprednisone)
and ((PT:"Randomized Controlled Trial" or "Randomized Controlled trial" or "Ensayo Clínico Controlado Aleatorio" or "Ensaio Clínico
Controlado Aleatório" or PT:"Controlled Clinical Trial" or "Ensayo Clínico Controlado" or "Ensaio Clínico Controlado" or "Random
allocation" or "Distribución Aleatoria" or "Distribuição Aleatória" or randon$ or Randomized or randomly or "double blind" or "duplo-
cego" or "duplo-cego" or "single blind" or "simples-cego" or "simples cego" or placebo$ or trial or groups) AND NOT (B01.050$ AND NOT
(humans or humanos or humanos)))
Appendix 6. Clinical trials registries search strategies

ClinicalTrials.gov and World Health Organization International Clinical trials Registry
Bell's palsy

Informed decisions.

WHAT'S NEW

Date Event Description
4 July 2016 New citation required but conclusions New author team. One new trial was found, with no change to
have not changed previous conclusions. We made the following corrections and re-
visions:
• more detailed documentation of methods and additional sec-

tions to comply with current standards
• amendments and corrections in the results section
• inclusion of additional study data in our primary analysis,
which changed the RR for incomplete recovery from 0.71 (95%
CI 0.61 to 0.83) to 0.63 (95% CI 0.50 to 0.80)
• we largely presented available data analyses, reporting inten-
tion-to-treat data only when trialists used this approach
• removal of comparisons involving antiviral co-medication,
which are analysed in a separate Cochrane review
• inclusion of an analysis of adverse events
• inclusion of a 'Summary of findings' table and of comments on
the quality of evidence in the text of the review
4 March 2016 New search has been performed Searches updated and integrated

HISTORY
Protocol first published: Issue 1, 2000
Review first published: Issue 1, 2002

Date Event Description
25 February 2009 New citation required and conclusions New trials have been added leading to a substantial change in
have changed the conclusion of the review
16 July 2008 Amended Converted to new review format.
23 June 2008 New citation required and conclusions Substantive amendment

have changed
28 February 2006 New search has been performed February 2006

We updated the search of the Cochrane Neuromuscular Disease
Group specialised register (November 2005), MEDLINE (January
1966 to November 2005), EMBASE (January 1980 to November
2005) and LILACS (January 1982 to November 2005). No new ran-
domised controlled trials were found.

CONTRIBUTIONS OF AUTHORS
All six review authors worked in pairs on study selection and data extraction.
IG and VM agreed data input into Review Manager 5.
IG performed risk of bias assessments; FS and FD reviewed them.

Informed decisions.

IG and VM drafted the revised review.
FD assisted with calculations.
VM and IG revised the review after editorial review.
All authors approved the final draft.
DECLARATIONS OF INTEREST
None known.
SOURCES OF SUPPORT
Internal sources
• New source of support, Other.
External sources
• No sources of support supplied
DIFFERENCES BETWEEN PROTOCOL AND REVIEW
A new author team updated this review: Vishnu B Madhok, Ildiko Gagyor, Fergus Daly, Dhruvashree Somasundara, Michael Sullivan, Fiona
Gammie, Frank Sullivan.
The review authors added a 'Summary of findings' table and added some sections to the Methods to comply with current Cochrane
standards.
Changes from the previous update of this review

When looking at Engström 2008 and Sullivan 2007, we excluded participants that were given antiviral therapy with corticosteroids or
antiviral therapy alone as these are reported in a separate review (Gagyor 2015).
As a result, in this update we deleted the comparisons from those trials that the previous review authors designated Sullivan b and
Engström b.
We assume that the total number of events given in Engström a (i.e. 213) was incorrect, and changed the figure to 210.
In the previous Cochrane review, authors used intention-to-treat numbers. We decided to perform available-case analysis unless the
trialists reported intention-to-treat data.
We deleted Sullivan b from Table 1.2 "cosmetically disabling persistent sequelae" for the reasons above. Sullivan a did not contribute data
to this table.
In Analysis 1.3, "motor synkinesis of or autonomic dysfunction during follow up", we deleted Engström b for the reasons above.
In Analysis 1.3, we changed the data for Engström a - the previous Cochrane review correctly gave the number of participants reporting
synkinesis at 12 months in the OS group as 32. We continued to use this event rate, but changed the total sample number from 290 to 186
in accordance with the information given.
We deleted what was previously Analysis 1.4 "incomplete recovery of patients with Bell's Palsy" as the numbers of participants was
negligible (only 22 participants from two studies Sullivan a and May 1976), after we removed the data from Sullivan b.
We checked the numbers for May 1976; Taverner 1954; and Unuvar 1999. We found that the numbers included for Taverner were incorrect
and updated these in Analysis 1.1.
The previous Cochrane review excluded Lagalla 2002 from the main meta-analysis giving the reason that the paper did not provide primary
outcome data on complete recovery. We decided to include this study given that we could use information on page 109 (results section) of
the paper to calculate the data for input into Analysis 1.1. In the prednisolone group, 32 participants, 83%, had complete recovery, hence
17% (five participants) had incomplete recovery. In the placebo group, there were 30 participants, of whom 25% (eight participants) had
incomplete recovery.
Based on our changes to Analysis 1.1, the RR changed from 0.51 (95% CI 0.32 to 0.80) to 0.65 (95% CI 0.50 to 0.83).
We added a table of adverse effects (Analysis 1.4).

Informed decisions.

We checked the data for each of the included studies and made significant amendments and corrections in the Effects of interventions
section.
In the Objectives, we deleted the reference to 'early' use of corticosteroids in Bell's palsy.
INDEX TERMS
Medical Subject Headings (MeSH)

Anti-Inflammatory Agents [*therapeutic use]; Bell Palsy [*drug therapy]; Cortisone [*analogs & derivatives] [therapeutic use];
Glucocorticoids [adverse effects] [*therapeutic use]; Methylprednisolone [therapeutic use]; Prednisolone [therapeutic use];
Prednisone [therapeutic use]; Randomized Controlled Trials as Topic; Recovery of Function; Vitamins [therapeutic use]
MeSH check words

Humans


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Madhok VB, Gagyor I, Daly F, Somasundara D, Sullivan M, Gammie F, Sullivan F

Madhok VB, Gagyor I, Daly F, Somasundara D, Sullivan M, Gammie F, Sullivan F.

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) i

Corticosteroids for Bell's palsy (idiopathic facial paralysis)

Editorial group: Cochrane Neuromuscular Group.

Data collection and analysis

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 1

Corticosteroids for Bell's palsy

What are the effects of corticosteroids on Bell's palsy?

Key results and quality of the evidence

The evidence is current to March 2016.

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 2

Patient or population: people with Bell's palsy

Cochrane Database of Systematic Reviews

GRADE Working Group grades of evidence

Cochrane Database of Systematic Reviews

BACKGROUND How the intervention might work

Description of the condition Corticosteroids are known to have an anti-inflammatory mode of

Description of the intervention Types of interventions

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 5

Selection of studies Dealing with missing data

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 6

Data synthesis Sensitivity analysis

Throughout we have utilised the following notations: RESULTS

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 7

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 8

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 9

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 10

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 11

Blinding Other potential sources of bias

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 12

Sensitivity analyses Secondary outcomes

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 15

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 16

Brandenberg 1993 Madhok 2009

Burgess 1984 Martyn 1997

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 17

Victor 1994 Database of Systematic Reviews 2002, Issue 3. [DOI:

Characteristics of included studies [ordered by study ID]

Participants were treated within 5 days of onset

Sex: male 39 (51%), female 37 (49%)

Age: mean 36.8 years, range 18 to 70 years

Outcomes Primary outcome:

• time to resolution in days of facial function as defined by the House-Brackmann scale

• distribution of facial nerve grade at 6 months after recovery, in addition to

Funding Not stated

Corticosteroids for Bell's palsy (idiopathic facial paralysis) (Review) 18

Date conducted 1 October 1989 to 31 December 1990

Notes Good recovery defined as grade I or II of the House-Brackmann scale

Bias Authors' judgement Support for judgement

Allocation concealment Unclear risk Allocation of participants not described

Selective reporting (re- Low risk All primary outcomes reported

Other bias Low risk Single-centre study

Participants 829 participants randomised within 72 hours of facial palsy onset

No contraindications to corticosteroid or antiviral use

Sex: male 341 (41%), female 488 (59%)

Age: mean 40 years, range 31-54 years

Interventions Participants allocated into 1 of 4 treatment groups:

• prednisolone with placebo