You are on page 1of 12

Bell Palsy

Last Updated: March 5, 2007

Rate this Article Email to a Colleague Get CME/CE for article

Synonyms and related keywords: Bell's palsy, facial nerve paralysis, facial paralysis, idiopathic facial paralysis, unilateral facial paralysis, cranial nerve VII paralysis, seventh cranial nerve paralysis, neurologic disorder, paralysis on one side of face, weakness on one side of face, drooling, tearing from eyes, upper respiratory infection, URI, viral infection, herpes simplex virus, HSV, Bell palsy AUTHOR INFORMATION
Section 1 of 10
Author Information Introduction Clinical Differentials Workup Treatment Medication Follow-up Pictures Bibliography

Author: Michael Lambert, MD, Fellowship Director of Emergency Ultrasound, Clinical Assistant Professor, Department of Emergency Medicine, Resurrection Medical Center Michael Lambert, MD, is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Institute of Ultrasound in Medicine, and Society for Academic Emergency Medicine Editor(s): Edward Bessman, MD, Chairman, Department of Emergency Medicine, John Hopkins Bayview Medical Center; Assistant Professor, Department of Emergency Medicine, Johns Hopkins University; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; J Stephen Huff, MD, Associate Professor of Emergency Medicine and Neurology, Department of Emergency Medicine, University of Virginia Health System; John Halamka, MD, Chief Information Officer, CareGroup Healthcare System, Assistant Professor of Medicine, Department of Emergency Medicine, Beth Israel Deaconess Medical Center; Assistant Professor of Medicine, Harvard Medical School; and Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School Disclosure INTRODUCTION
Section 2 of 10

Author Information Introduction Clinical Differentials Workup Treatment Medication Follow-up Pictures Bibliography

Background: Bell palsy is one of the most common neurologic disorders affecting the cranial nerves. It is an abrupt, unilateral, peripheral facial paresis or paralysis without a detectable cause. This syndrome of idiopathic facial paralysis was first described more than a century ago by Sir Charles Bell, yet much controversy still surrounds its etiology and management. Bell palsy is certainly the most common cause of facial paralysis worldwide. Keeping in mind that Bell palsy is a diagnosis of exclusion is imperative. Other disease states or conditions that present with facial palsies are often misdiagnosed as idiopathic.

Patients with Bell palsy frequently present to the ED before seeing any other health care professional. The appearance of a distorted face and the abrupt functional impairment are the driving forces that prompt emergency evaluation. Patients often fear they have had a stroke or have a tumor and that their distorted facial appearance will be permanent. The emergency physician's role consists of the following:

Exclude other causes of facial paralysis. Initiate appropriate treatment. Protect the eye. Arrange appropriate medical follow-up care.

Pathophysiology: Actual pathophysiology is unknown; this is an area of interminable debate. A popular theory champions inflammation of the facial nerve. During this process, the nerve increases in diameter and becomes compressed as it courses through the temporal bone. The facial nerve courses through a portion of the temporal bone commonly referred to as the facial canal. The first portion of the facial canal (the labyrinthine segment) is narrowest. The tiny opening (about 0.66 mm in diameter) in this segment is known as the meatal foramen. The facial nerve is subjected to tight confines on its journey through the facial canal. It seems logical that various inflammatory, demyelinating, ischemic, or compressive processes may impair neural conduction at this unique anatomic site. Anatomy The facial nerve (seventh cranial nerve) has 2 components. The larger portion comprises efferent fibers that stimulate the muscles of facial expression. The smaller portion contains taste fibers to the anterior two thirds of the tongue, secretomotor fibers to the lacrimal and salivary glands, and some pain fibers. Pathway The path of the facial nerve is very complex; this may be the reason the nerve is vulnerable to injury. Two portions of the facial nerve leave the brain at the cerebellopontine angle, traverse the posterior cranial fossa, dive into the internal acoustic meatus, pass through the facial canal in the temporal bone, then angle sharply backwards, where they pass behind the middle ear and exit the cranium at the stylomastoid foramen. From here, the facial nerve bisects the parotid gland, and then terminal branches burst out from the parotid plexus to supply the muscles of facial expression. Frequency:

In the US: The incidence of Bell palsy in the United States is approximately 23 cases per 100,000 persons. The condition affects approximately 1 person in 65 in a lifetime.

Internationally: The incidence is the same as in the United States.

Mortality/Morbidity: Bell palsy can cause aesthetic, functional, and psychological disturbances in patients who have residual nerve dysfunction during their recovery phase or in patients with incomplete healing.

Partial paralysis Motor synkinesis (involuntary movement accompanying a voluntary movement) Autonomic synkinesis (involuntary lacrimation after a voluntary muscle movement)

Race: Incidence of Bell palsy appears to be slightly higher in persons of Japanese descent. Sex: No difference exists in sex distribution in patients with Bell palsy. Age: Age affects the probability of contracting Bell palsy. The incidence is highest in persons aged 15-45 years. Bell palsy is less common in those younger than 15 years and in those older than 60 years.

CLINICAL

Section 3 of 10

Author Information Introduction Clinical Differentials Workup Treatment Medication Follow-up Pictures Bibliography

History: Most patients presenting to the ED suspect they have suffered a stroke or have an intracranial tumor. The most common complaint is of weakness on one side of their face.

Postauricular pains: Almost 50% of patients experience pain in the mastoid region. The pain frequently occurs simultaneously with the paresis, but precedes the paresis by 2-3 days in about 25% of patients. Tear flow: Two thirds of patients complain about tear flow. This is due to the reduced function of the orbicularis oculi in transporting the tears. Fewer tears arrive at the lacrimal sac and overflow occurs. The production of tears is not accelerated. Altered taste: While only one third of patients complain about taste disorders, four fifths of patients show a reduced sense of taste. This may be explained by only half the tongue being involved. Dry eyes Hyperacusis: Impaired tolerance to typical levels of noise due to an increased irritability to the sensory neural mechanism.

Physical: Findings of facial paralysis are easily recognizable on physical examination. A careful, complete examination excludes other possible causes of facial paralysis. Strongly consider other etiologies if all branches of the facial nerve are not affected.

The classic definition of Bell palsy describes mononeuric involvement of the facial nerve, yet other cranial nerves are probably affected. The facial nerve is the only cranial nerve eliciting obvious findings on physical examination because of its unique anatomical course from the brain to the lateral face. Remember that weakness and/or paralysis from involvement of the facial nerve manifests as weakness of the entire face (upper and lower) on the affected side. Focus attention on the voluntary movement of the upper part of the face on the affected side. In supranuclear lesions such as a cortical stroke (upper motor neuron; above the facial nucleus in the pons), the upper third of the face is spared while the lower two thirds are paralyzed. The orbicularis, frontalis, and corrugator muscles are innervated bilaterally, which explains the pattern of facial paralysis. Test other cranial nerves; their examination results should be normal. Tympanic membranes should not be inflamed; presence of infection raises possibility of complicated otitis media.

Causes: "All that glitters is not gold" (William Shakespeare) The etiology of Bell palsy remains unclear, although vascular, infectious, genetic, and immunologic causes have all been proposed. Patients with other diseases or conditions sometimes develop a peripheral facial nerve palsy, but these are not classified as Bell palsy (see Differentials).

Viral infections: Clinical and epidemiologic data lend credence to an infectious origin, which triggers an immunologic response, resulting in damage to the facial nerve. Pathogens leading the list include herpes simplex virus type 1 (HSV-1); herpes simplex virus type 2 (HSV-2); human herpesvirus (HHV); varicella zoster virus (VZV); Mycoplasma pneumoniae; Borrelia burgdorferi; influenza B; adenovirus; coxsackievirus; Ebstein-Barr virus; hepatitis A, B, and C; cytomegalovirus (CMV); and rubella virus. Pregnancy: Bell palsy is uncommon in pregnancy; however, the prognosis is significantly worse in pregnant women with Bell palsy than among nonpregnant women with palsy. Genetics: Recurrence rates (4.5-15%) and familial incidence (4.1%) have been addressed in various studies. Genetics may have a role in Bell palsy, but which factors are inherited is unclear.

DIFFERENTIALS

Diabetes Mellitus, Type 1 - A Review Diabetes Mellitus, Type 2 - A Review Fractures, Mandible Herpes Zoster Multiple Sclerosis Tick-Borne Diseases, Lyme Other Problems to be Considered: Herpes zoster Pregnancy (especially third trimester) Polyneuritis Acute otitis Chronic otitis Temporal bone fracture Infectious mononucleosis Parotid tumors Sarcoidosis Cholesteatoma of the middle ear Aneurysm of vertebral, basilar artery, or carotid arteries Carcinomatous meningitis Facial trauma (blunt, penetrating, iatrogenic) Leukemic meningitis Leprosy Melkersson-Rosenthal syndrome Middle ear surgery Osteomyelitis of the skull base Skull base tumor Lab Studies:

No specific laboratory tests exist to confirm the diagnosis of Bell palsy. Clinical setting determines tests that may be of value. Other potential causes in the differential diagnosis may be confirmed or suspected based on the following diagnostic laboratory tests:
o o o o o

Complete blood count Erythrocyte sedimentation rate Thyroid function studies Lyme titer Serum glucose level

Rapid plasma reagin (RPR) or Venereal Disease Research Laboratory (VDRL) test Human immunodeficiency virus (HIV) Cerebral spinal fluid analysis Immunoglobulin M (IgM), immunoglobulin G (IgG), and immunoglobulin A (IgA) titers for CMV, rubella, HSV, hepatitis A, hepatitis B, hepatitis C, VZV, M pneumoniae, and B burgdorferi.

o o o

Imaging Studies:

Bell palsy remains a clinical diagnosis. Imaging studies are not indicated in the ED. Excluding other causes of facial palsy may require one of the following imaging studies depending on clinical setting.
o

Facial CT scan or plain radiographs: Perform to rule out fractures or bony metastasis. CT scan is indicated when stroke, or acquired immunodeficiency syndrome (AIDS)-CNS involvement is considered in differential diagnosis MRI: For a suspected neoplasm of the temporal bone, brain, parotid gland, or other structure, or to evaluate for multiple sclerosis, MRI is the superior method of imaging. The course of the facial nerve through the intratemporal and extratemporal regions from the brain to the facial muscles and glands can be followed on MRI. MRI also may be considered in lieu of CT scan.

Other Tests:

Electrodiagnosis of the facial nerve: These studies assess the function of the facial nerve. These tests are rarely performed on an emergent basis.
o

Electromyography (EMG) and nerve conduction velocities produce a graphic readout of the electrical currents displayed by stimulating the facial nerve and recording the excitability of the facial muscles it supplies. Comparison to the contralateral side helps determine the extent of nerve injury and has prognostic implications. This is not part of the acute workup. In the nerve excitability test, the threshold of the electrical stimulus producing visible muscle twitching is determined. Electroneurography (ENoG) compares evoked potentials on the paretic side versus the healthy side.

TREATMENT

Section 6 of 10

Author Information Introduction Clinical Differentials Workup Treatment Medication Follow-up Pictures Bibliography

Emergency Department Care: The primary treatment of patients with Bell palsy in the ED is pharmacologic management. The remainder of care focuses on reassurance, eye care instructions, and appropriate follow-up care.

Steroids
o

Treatment of Bell palsy with steroids remains controversial. Numerous research articles have been written on the benefit or uselessness of steroids to treat patients with Bell palsy. Researchers seem to lean more toward using steroids as a means to optimize outcomes. Once the decision to use steroids is made, the consensus is to start immediately.

Antiviral agents: Although there is insufficient research evaluating the efficacy of antiviral medicines in Bell palsy, most experts believe in a viral etiology. Therefore, antiviral agents seem a logical choice for pharmacologic management and are commonly recommended. Eye care: The eyes are frequently unprotected in patients with Bell palsy. This leaves the eyes at risk for corneal drying and foreign body exposure. Manage with tear substitutes, lubricants, and eye protection.
o

Artificial tears: Use these during waking hours to replace diminished or absent lacrimation. Lubricants are used during sleep. They may be used during waking hours if artificial tears cannot provide adequate protection. One disadvantage is blurred vision during waking hours. Eyeglasses or shields protect the eye from injury and reduce drying by decreasing the air currents that come directly in contact with the exposed cornea.

Consultations: The patient's primary care physician or consultant should provide close follow-up care. Documentation should chart the progress of the patient's recovery. Opinions vary widely on referral to a specialist. Some specific referral indications are listed below:

Neurologist: When other neurologic signs are identified on physical examination and for an atypical presentation of Bell palsy, referral is indicated.

MEDICATION

Section 7 of 10

Ophthalmologist: For any unexplained ocular pain or abnormal findings on physical examination of the eyes, the patient should be referred for further workup. Otolaryngologist: In patients with persistent paralysis, prolonged weakness of the facial muscles, or recurrent weakness, referral is warranted. Surgeon: Surgery to decompress the facial nerve is recommended occasionally for patients with Bell palsy. Patients with a poor prognosis identified by facial nerve testing or persistent paralysis appear to benefit the most from surgical intervention.

Since most patients recover without medication, physicians may be able to manage patients without prescribing medication. This watchful waiting plan is an option; however, some individuals with Bell palsy never completely recover. Both medications listed below have clinical trials that support and dispute their efficacy.

Drug Category: Corticosteroids -- Have anti-inflammatory properties and cause


profound and varied metabolic effects. Modify the body's immune response to diverse stimuli. Prednisone (Deltasone, Orasone, Sterapred) -Pharmacologic success may be the result of antiinflammatory effect, which presumably decreases compression of the facial nerve in the facial canal. 1 mg/kg/d PO for 7 d Administer as in adults Documented hypersensitivity; viral, fungal, connective tissue, and tubercular skin infections; peptic ulcer disease; hepatic dysfunction; GI disease Coadministration with estrogens may decrease prednisone clearance; concurrent use with digoxin may cause digitalis toxicity secondary to hypokalemia; phenobarbital, phenytoin, and rifampin may increase metabolism of glucocorticoids (consider increasing maintenance dose); monitor for hypokalemia with coadministration of diuretics B - Usually safe but benefits must outweigh the risks. Abrupt discontinuation of glucocorticoids may cause adrenal crisis; hyperglycemia, edema, osteonecrosis, myopathy, peptic ulcer disease, hypokalemia, osteoporosis, euphoria, psychosis, myasthenia gravis, growth suppression, and infections may occur with glucocorticoid use

Drug Name Adult Dose Pediatric Dose Contraindications

Interactions

Pregnancy

Precautions

Drug Category: Antiviral -- Herpes simplex infections may be a common cause of


Bell palsy. Acyclovir is the most-used treatment, but other antiviral agents may be appropriate. Acyclovir (Zovirax) -- Has demonstrated inhibitory activity directed against both HSV-1 and HSV-2, and infected cells selectively take it up. 4000 mg/24 h PO for 7-10 d <2 years: Not recommended >2 years: 1000 mg PO divided qid for 10 d Documented hypersensitivity Concomitant use of probenecid or zidovudine prolongs half-life and increases CNS toxicity of acyclovir C - Safety for use during pregnancy has not been established. Caution in renal failure or when using nephrotoxic drugs
Section 8 of 10

Drug Name Adult Dose Pediatric Dose Contraindications Interactions Pregnancy Precautions FOLLOW-UP

Author Information Introduction Clinical Differentials Workup Treatment Medication Follow-up Pictures Bibliography

In/Out Patient Meds:

Consider prednisone at an initial dose of 1 mg/kg/day.


o

Prednisone is a potent drug with a high risk of side effects. The evidence of its usefulness continues to come under scrutiny in the literature. Until efficacy can be clearly defined, it should not be perceived as a standard of care. With no contraindications and if the physician chooses to administer steroids, the best choice is prednisone at a high dose, as early as possible in the disease course. (Consider tapering on day 5 to 5 mg bid for 5 d.)

Administer acyclovir (Zovirax) 800 mg PO 5 times/d for 10 d; 20 mg/kg in patients younger than 2 years. Recent evidence supports HSV as the presumed cause in more than 70% of Bell palsy cases.

Complications:

Most patients with Bell palsy recover without any cosmetically obvious deformities; however, approximately 5% are left with an unacceptably high degree of sequelae. Incomplete motor regeneration
o

The largest portion of the facial nerve comprises efferent fibers that stimulate muscles of facial expression. If the motor portion achieves

suboptimal regeneration, paresis of all or some of these facial muscles results. This manifests as (1) oral incompetence, (2) epiphora (excessive tearing), and (3) nasal obstruction.

Incomplete sensory regeneration


o o o

Dysgeusia (impairment of taste) may result. Ageusia (loss of taste) may result. Dysesthesia (impairment of sensation or disagreeable sensation to normal stimuli) may result.

Aberrant reinnervation of the facial nerve


o

After the impaired neural conduction of the facial nerve begins the regeneration and repair process, some nerve fibers take an unusual course and connect to neighboring fibers. This aberrant reconnection produces unusual neurologic pathways. When voluntary movements are initiated, they are accompanied by involuntary movements (eg, the movement of a closed eye following that of the uncovered one). These involuntary movements accompanying voluntary movement are termed synkinesis.

Prognosis:

The natural course of Bell palsy varies from early complete recovery to substantial nerve injury with permanent sequelae. Prognostically, patients fall into 3 groups with roughly equal numbers in each group.
o

Group 1 regains complete recovery of facial motor function without sequelae. Group 2 experiences incomplete recovery of facial motor function, but no cosmetic defects are apparent to the untrained eye. Group 3 experiences permanent neurologic sequelae that are cosmetically and clinically apparent.

Most patients develop an incomplete facial paralysis during the acute phase. This group has an excellent prognosis for full recovery. Patients demonstrating complete paralysis are at higher risk for severe sequelae. Of patients with Bell palsy, 85% achieve complete recovery. Ten percent are bothered by some asymmetry of facial muscles, while 5% experience severe sequelae.

Patient Education:

Eye care
o o o

Protect the eye from foreign objects and sunlight. Keep the eye well lubricated. Educate the patient to report new ocular findings such as pain, discharge, or visual changes.

For excellent patient education resources, visit eMedicine's Brain and Nervous System Center. Also, see eMedicine's patient education article Bell Palsy.
Section 9 of 10

PICTURES Caption: Picture 1. The facial nerve.

Author Information Introduction Clinical Differentials Workup Treatment Medication Follow-up Pictures Bibliography

View Full Size Image

eMedicine Zoom View (Interactive!)

Picture Type: Image BIBLIOGRAPHY


Section 10 of 10
Author Information Introduction Clinical Differentials Workup Treatment Medication Follow-up Pictures Bibliography

Adams RD, Victor M, eds: Diseases of the spinal cord, peripheral nerve, and muscle. In: Principles of Neurology. 5th ed. NY: McGraw Hill; 1993:11751177. Cousin GC: Facial nerve palsy following intra-oral surgery performed with local anaesthesia. J R Coll Surg Edinb 2000 Oct; 45(5): 330-3[Medline]. English JB, Stommel EW, Bernat JL: Recurrent Bell's palsy. Neurology 1996 Aug; 47(2): 604-5[Medline]. Helling TD, Neely JG: Validation of objective measures for facial paralysis. Laryngoscope 1997 Oct; 107(10): 1345-9[Medline]. Morgan M, Moffat M, Ritchie L, et al: Is Bell's palsy a reactivation of varicella zoster virus? J Infect 1995 Jan; 30(1): 29-36[Medline]. Morrow MJ: Bell's Palsy and Herpes Zoster Oticus. Curr Treat Options Neurol 2000 Sep; 2(5): 407-416[Medline]. Niparko JK, Mattox DE: Bell's palsy and herpes zoster oticus. In: Current Therapy in Neurologic Disease. 4th ed. Philadelphia: BC Decker; 1993:355361. O'Halloran HS, Sen HA, Baker RS: Accidental ocular perforation from selfinflicted facial palsy. Retina 1997; 17(2): 164-6[Medline]. O'Rahilly R, Muller F: Basic Human Anatomy: A regional Study of Human Structure. Philadelphia: WB Saunders Co; 1983:391-98.

Olson WH, Brumback RA, Christoferson LA: Practical Neurology for the Primary Care Physician. Springfield, Ill: Thomas Books; 1981:262. Peitersen E: Bell's palsy: the spontaneous course of 2,500 peripheral facial nerve palsies of different etiologies. Acta Otolaryngol Suppl 2002; 430[Medline]. Pulec JL: New horizons in facial nerve therapy. Ear Nose Throat J 1997 Jun; 76(6): 360[Medline]. Qiu WW, Yin SS, Stucker FJ, et al: Time course of Bell palsy. Arch Otolaryngol Head Neck Surg 1996 Sep; 122(9): 967-72[Medline]. Sittel C, Sittel A, Guntinas-Lichius O, et al: Bell's palsy: a 10-year experience with antiphlogistic-rheologic infusion therapy. Am J Otol 2000 May; 21(3): 425-32[Medline]. Smith IM, Cull RE: Bell's palsy--which factors determine final recovery? Clin Otolaryngol 1994 Dec; 19(6): 465-6[Medline]. Smouha EE, Coyle PK, Shukri S: Facial nerve palsy in Lyme disease: evaluation of clinical diagnostic criteria. Am J Otol 1997 Mar; 18(2): 25761[Medline]. Unlu Z, Aslan A, Ozbakkaloglu B, et al: Serologic examinations of hepatitis, cytomegalovirus, and rubella in patients with Bell's palsy. Am J Phys Med Rehabil 2003 Jan; 82(1): 28-32[Medline]. Victor M, Martin J: Disorders of the cranial nerves. WJM 2000; 173: 266-268. Volter C, Helms J, Weissbrich B, et al: Frequent detection of Mycoplasma pneumoniae in Bell's palsy. Eur Arch Otorhinolaryngol 2004 Aug; 261(7): 400-4[Medline]. Wiederholt WC: Bell's palsy. In: Wiederhold WC, ed. Therapy for Neurologic Disorders. NY: Wiley; 1992:257. Williamson IG, Whelan TR: The clinical problem of Bell's palsy: is treatment with steroids effective? Br J Gen Pract 1996 Dec; 46(413):

You might also like