Bell’s palsy is facial nerve paralysis of unknown cause. Left untreated, 70–75% of patients make a full recovery.
Early treatment with prednisolone increases the chance of complete recovery of facial function to 82%. Eleven people need to be treated for one extra complete recovery at six months.
There may be benefit in adding an antiviral drug to prednisolone in some cases. Additional research is needed on this treatment.
The palsy may leave the surface of the eye exposed. Early eye protection with lubrication and a patch is crucial to prevent long-term complications.
Bell’s palsy, also called idiopathic facial paralysis, is defined as an acute-onset, isolated, unilateral, lower motor neurone facial weakness. The reported annual incidence varies in different parts of the world with estimates varying between 11 and 40 per 100 000 people.1 It is more common in people with diabetes.2
The underlying pathophysiology observed in post mortem cases of Bell’s palsy is vascular distension, inflammation and oedema with ischaemia of the facial nerve. The aetiology remains unclear. Various causes have been proposed including viral, inflammatory, autoimmune and vascular. However, reactivation of herpes simplex virus or herpes zoster virus from the geniculate ganglion is suspected to be the most likely cause.3,4 Despite advances in neuroimaging, the diagnosis of Bell’s palsy is mainly clinical.5
- upper motor neurone lesion – based on innervation, absence of forehead wrinkling is a reliable way of differentiating Bell’s palsy from an upper motor neuron lesion
- herpes zoster oticus (Ramsay Hunt syndrome)
- rarer causes including otitis media, HIV infection, sarcoidosis, autoimmune disorders or tumours of the parotid gland.
In addition to ocular problems, complications of Bell’s palsy include:
- motor synkinesis (involuntary movement of muscles occurring at the same time as deliberate movement, e.g. involuntary mouth movement during voluntary eye closure)
- crocodile tears (tears when eating due to misdirection of regenerating gustatory fibres destined for the salivary glands, so that they become secretory fibres to the lacrimal gland and cause ipsilateral tearing while the patient is eating)
- incomplete recovery
- contracture of facial muscles
- reduction or loss of taste sensation
- problems with dysarthria due to facial muscle weakness.
Possible signs of Bell's palsy
Box - Clinical features of Bell’s palsy
Weakness or paralysis of the upper and lower facial muscles of the affected side
Drooping of ipsilateral eyelids
Inability to close the eye completely
Dry eye due to inability to close eyes completely
Excessive tearing of the eye (epiphora)
Drooping of the corner of the mouth
Ipsilateral impaired/loss of taste sensation
Difficulty with eating due to ipsilateral muscle weakness causing food to be trapped on the affected side of the mouth
Dribbling of saliva
Altered sensation on the affected side of the face
Pain in or behind the ear
Increased sensitivity to sound (hyperacusis) on affected side if stapedius muscle is involved
The severity of symptoms of Bell’s palsy varies from mild weakness to severe paralysis, but the prognosis is generally good. The Copenhagen Facial Nerve Study found that around 71% of patients recover normal function without treatment. Around 13% are left with slight weakness and around 4% with severe weakness resulting in major facial dysfunction. Contracture of the facial muscles on the affected side was found in 17% and associated movements were found in 16%.6 Scoring systems such as the House–Brackmann scale used in randomised controlled trials and systematic reviews may be helpful to monitor progress.7
Although the study was underpowered to detect significant differences in recovery between patients with different degrees of severity, the recovery rate in one randomised controlled trial was significantly higher for those with moderate severity at onset compared to those with severe Bell’s palsy. Recovery was 90% with those moderately affected and 78% in those severely affected.8
The frequency of review depends on the individual patient and the severity of their symptoms. If there is no improvement after a month the patient should be referred. A referral is also indicated if there is only partial recovery after 6–9 months.
The palsy recurs in 7% of patients, with equal incidence of ipsilateral and contralateral recurrence. There are insufficient data on whether treatment affects the rate of recurrence.
The treatment of Bell’s palsy aims to speed recovery and reduce long-term complications. An inability to close the eye on the affected side increases the risk of corneal complications. Eye protection is crucial so an eye patch and lubricants are used to prevent drying of the cornea. Eye drops, such as hypromellose drops, should be applied for lubrication during the day and ointment at night. In severe cases, the eye may have to be taped or partially sutured shut.
The treatments considered for Bell’s palsy include oral corticosteroids (prednisolone) and antiviral drugs. Although the aetiology of Bell’s palsy is uncertain, it is known that inflammation and oedema of the facial nerve are responsible for the symptoms. Corticosteroids have therefore been used for their anti-inflammatory effect.
The maximum benefit is seen when steroids are commenced within 72 hours of the onset of symptoms. There is no optimum regimen, but in adults 50–60 mg prednisolone daily for 10 days has been commonly used.6,7 Prednisolone has been used at a dose of 1 mg/kg/day up to a maximum of 80 mg in some studies. Doses of more than 120 mg/day have been used safely in patients with diabetes.9
In a randomised controlled trial the recovery rate at nine months with prednisolone was 94%. It was 81.6% in patients who did not receive prednisolone.7
A systematic review of trials that used prednisolone showed that at six months 17% of patients had incomplete recovery compared with 28% of patients who received no treatment. There was also a significant reduction in motor synkinesis in those who received prednisolone. There was no significant reduction in cosmetically disabling sequelae.10
The antiviral drugs used in trials were aciclovir (400 mg five times daily for five days) or valaciclovir (1000 mg/day for five days).11 There is currently no evidence to support the use of either antiviral drug on its own,12,13 and there is uncertainty regarding the benefit of adding them to corticosteroids.
A randomised controlled trial found that at nine months of diagnosis, facial function had recovered in 94.4% of patients who took prednisolone alone, 85.4% of those who took aciclovir alone and 92.7% of those who received both. There were no serious adverse effects in any group. The study concluded that early treatment with prednisolone alone increases the likelihood of complete recovery and there was no additional benefit of treatment with aciclovir alone or combining with prednisolone.7 However, a systematic review also found that treatment with prednisolone reduced the chances of incomplete recovery but using an antiviral drug had an additional benefit.14
There have been several studies looking at the benefit of antiviral drugs with or without prednisolone. A randomised prospective study found that a combination of an antiviral and a steroid was more effective in treating severe to complete Bell’s palsy than steroid alone.15 A guideline development group found that there was low-quality evidence of benefit from adding antivirals. Patients who are offered them in addition to corticosteroids should be counselled that the increase in recovery is less than 7%.16
A Cochrane review in 2015 found that antivirals combined with corticosteroids improved rates of incomplete recovery compared with corticosteroids alone, but this was not significant and the evidence was low quality. There was moderate-quality evidence that the combination reduced long-term sequelae such as excessive tear production and synkinesis. The outcome for patients who received corticosteroids alone was significantly better than for those who received antivirals alone. Antiviral drugs alone had no benefit over placebo. None of the treatments had significant differences in adverse effects, but the evidence was again of low quality.12
The optimum management of children with Bell’s palsy is also unknown. A major trial (BellPIC) in Australia is addressing this question.17
Adverse effects of treatment
Treatment courses are short, but can cause adverse effects.
Prednisolone should be used with caution in immunosuppression and sepsis. It may lead to:
- induction or worsening of peptic ulcer disease
- hyperglycaemia especially in diabetics, however higher doses may be required in diabetes
- malignant hypertension
- hepatic and renal dysfunction.
Antiviral drugs may cause:
- nausea and vomiting
- abdominal pain
- neurological reactions – dizziness, convulsions (more common with higher doses)
- very rarely, hepatitis and jaundice.
Physical therapies including tailored facial exercises, acupuncture to affected muscles, massage, thermotherapy and electrical stimulation have been used to hasten recovery. However, there is no evidence for any significant benefit. A Cochrane review concluded from poor-quality evidence that tailored facial exercises can help improve facial function, mainly for moderate paralysis and chronic cases. Early facial exercise may reduce recovery time, long-term paralysis and number of chronic cases.18
The symptoms of Bell’s palsy vary from mild to severe. The aetiology is still unclear, but it is known that the symptoms are caused by swelling and inflammation of the facial nerve. Eye protection remains crucial in preventing long-term eye complications.
Drug treatment is controversial, given that over 70% of patients will eventually recover normal facial function without treatment. Early treatment with prednisolone can hasten recovery and reduce long-term sequelae. Although the quality of evidence is low to moderate, there may be some benefit in adding antiviral drugs to prednisolone.12 It is, however, important to discuss the harms and benefits with patients, given the potential adverse effects of prednisolone and antiviral drugs.
Conflict of interest: none declared
- De Diego-Sastre JI, Prim-Espada MP, Fernández-García F. [The epidemiology of Bell’s palsy]. Rev Neurol 2005;41:287-90.
- Adour K, Wingerd J, Doty HE. Prevalence of concurrent diabetes mellitus and idiopathic facial paralysis (Bell’s palsy). Diabetes 1975;24:449-51.
- Linder T, Bossart W, Bodmer D. Bell’s palsy and Herpes simplex virus: fact or mystery? Otol Neurotol 2005;26:109-13.
- Murakami S, Mizobuchi M, Nakashiro Y, Doi T, Hato N, Yanagihara N. Bell palsy and herpes simplex virus: identification of viral DNA in endoneurial fluid and muscle. Ann Intern Med 1996;124:27-30.
- Seok JI, Lee DK, Kim KJ. The usefulness of clinical findings in localising lesions in Bell’s palsy: comparison with MRI. J Neurol Neurosurg Psychiatry 2008;79:418-20.
- Peitersen E. Bell’s palsy: the spontaneous course of 2,500 peripheral facial nerve palsies of different etiologies. Acta Otolaryngol Suppl 2002;549:4-30.
- Sullivan FM, Swan IR, Donnan PT, Morrison JM, Smith BH, McKinstry B, et al. Early treatment with prednisolone or acyclovir in Bell’s palsy. N Engl J Med 2007;357:1598-607.
- Sullivan FM, Swan IRC, Donnan PT, Morrison JM, Smith BH, McKinstry B, et al. A randomised controlled trial of the use of aciclovir and/or prednisolone for the early treatment of Bell’s palsy: the BELLS study. Health Technol Assess 2009;13(47):1-130.
- Saito O, Aoyagi M, Tojima H, Koike Y. Diagnosis and treatment for Bell’s palsy associated with diabetes mellitus. Acta Otolaryngol Suppl 1994;511:153-5.
- Madhok VB, Gagyor I, Daly F, Somasundara D, Sullivan M, Gammie F, et al. Corticosteroids for Bell’s palsy (idiopathic facial paralysis). Cochrane Database Syst Rev 2016;7:CD001942.
- Hato N, Yamada H, Kohno H, Matsumoto S, Honda N, Gyo K, et al. Valacyclovir and prednisolone treatment for Bell’s palsy: a multicentre, randomized, placebo-controlled study. Otol Neurotol 2007;28:408-13.
- Allen D, Dunn L. Aciclovir or valaciclovir for Bell’s palsy (idiopathic facial paralysis). Cochrane Database Syst Rev 2004;3:CD001869.
- Gagyor I, Madhok VB, Daly F, Somasundara D, Sullivan M, Gammie F, et al. Antiviral treatment of Bell’s palsy (idiopathic facial paralysis). Cochrane Database Syst Rev 2015;11:CD001869.
- de Almeida JR, Al Khabori M, Guyatt GH, Witterick IJ, Lin VY, Nedzelski JM, et al. Combined corticosteroid and antiviral treatment for Bell palsy: a systematic review and meta-analysis. JAMA 2009;302:985-93.
- Lee HY, Byun JY, Park MS, Yeo SG. Steroid-antiviral treatment improves the recovery rate in patients with severe Bell’s palsy. Am J Med 2013;126:336-41.
- Gronseth GS, Paduga R; American Academy of Neurology. Evidence-based guideline update: steroids and antivirals for Bell palsy: report of the Guideline Development Subcommittee of the American Academy of Neurology. Neurology 2012;79:2209-13.
- Research Data Australia [Internet]. Bell’s palsy in children (BellPIC) [2015-2020]. Australian National Data Service. [cited 2017 May 1]
- Teixeira LJ, Valbuza JS, Prado GF. Physical therapy for Bell’s palsy (idiopathic facial paralysis). Cochrane Database Syst Rev 2011;12:CD006283.
- McAllister K, Walker D, Donnan PT, Swan I. Surgical interventions for the early management of Bell’s palsy. Cochrane Database Syst Rev 2013;10:CD007468.
- Grogan PM, Gronseth GS. Practice parameter: Steroids, acyclovir, and surgery for Bell’s palsy (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology 2001;56:830-6.
- de Almeida JR, Guyatt GH, Sud S, Dorion J, Hill MD, Kolber MR, et al.; Bell Palsy Working Group, Canadian Society of Otolaryngology - Head and Neck Surgery and Canadian Neurological Sciences Federation. Management of Bell palsy: clinical practice guideline. CMAJ 2014;186:917-22.