Treatment and Prognosis of Facial Palsy on Ramsay Hunt Syndrome: Results Based on a Review of the Literature

Abstract

Introduction Ramsay Hunt syndrome is the second most common cause of facial palsy. Early and correct treatment should be performed to avoid complications, such as permanent facial nerve dysfunction.

Objective The objective of this study is to review the prognosis of the facial palsy on Ramsay Hunt syndrome, considering the different treatments proposed in the literature.

Data Synthesis We read the abstract of 78 studies; we selected 31 studies and read them in full. We selected 19 studies for appraisal. Among the 882 selected patients, 621 (70.4%) achieved a House-Brackmann score of I or II; 68% of the patients treated only with steroids achieved HB I or II, versus 70.5% when treated with steroids plus antiviral agents. Among patients with complete facial palsy (grades V or VI), 51.4% recovered to grades I or II. The rate of complete recovery varied considering the steroid associated with acyclovir: 81.3% for methylprednisolone, 69.2% for prednisone; 61.4% for prednisolone; and 76.3% for hydrocortisone.

Conclusions Patients with Ramsay-hunt syndrome, when early diagnosed and treated, achieve high rates of complete recovery. The association of steroids and acyclovir is better than steroids used in monotherapy.

Keywords

prognosis - facial palsy - ramsay hunt syndrome - varicela zoster - house-brackmann

Introduction

Ramsay Hunt syndrome (RHS) is an infectious disease caused by the varicella zoster virus (VZV).[1] The main clinical symptoms are facial palsy, inner ear dysfunction, periauricular pain, and herpetiform vesicles on the pinna. J. Ramsay Hunt, in 1907, was the first author to describe the disease, which now represents the second most common cause of peripheral facial palsy. The incidence of RHS is 5 cases/100,000 people.[2] It affects mostly patients between the ages of 20 and 30, with no gender predilection.[1] Spontaneous remission of the facial palsy caused by VZV occurs only in a few cases - without proper treatment, only 20% achieve complete recovery.[3]

The physiopathological mechanism is the reactivation of the VZV in the geniculate ganglion, with subsequent inflammation, edema, and compression of the VII cranial nerve.[2] Viral demyelination may also contribute to further damage of the nerve.[3] [4] A viral prodrome or an upper respiratory tract infection might be the first symptoms,[5] evolving into severe pain in the pinna, acute facial hypotonia, and a herpetiform vesicular eruption on the pinna, external acoustic meatus, face, tongue, hard palate, neck, larynx, and oral mucosa.[2] Cochleovestibular impairment such as hypoacusis, tinnitus, and vertigo may occur. The involvement of other cranial nerves, such as V, IX, X, XI, and XII is rare.[1] [6] [7] [8] Permanent facial deformity and other possible sequelae of RHS substantially impact patientś social life. Thus, early diagnosis and treatment of this clinical entity is essential to avoid such sequels.[6]

Another clinical presentation of the disease is the “Ramsay Hunt syndrome sine herpete,” characterized by peripheral facial paralysis without ear or mouth rash, and the presence of either a 4-fold rise in antibody to VZV or the detection of VZV DNA in skin, blood mononuclear cells, or middle ear fluid. Thus, some patients diagnosed with idiopathic facial palsy could be suffering from zoster sine herpete.[9] [10]

The objective of this study was to evaluate the prognosis of facial palsy in RHS after different treatments proposed in the literature, and to determine the best treatment option for these patients.

Materials and Methods

We performed a systematic review of the literature. The Ethics Committee of the Banco de Olhos de Sorocaba hospital approved this manuscript. We searched the LILACS, SciELO, and PUBMED databases from January to June 2015. The keywords used were: (Ramsay AND hunt) OR (“varicella”) AND (“facial paralysis” OR (“facial” AND “paralysis”) OR “facial paralysis” OR (“facial nerve” OR (“facial” AND “nerve”). Additional filters used were: period of publication: 1995–2014; human subjects; with abstracts available; Spanish, English, and Portuguese languages. We read the resulting studies in full, and the criteria for study selection were as follows:

a) Inclusion Criteria

• Case reports and prospective and retrospective studies referring to the prognosis and treatment of facial palsy in RHS.

b) Exclusion Criteria

• Studies of patients with tumors; traumatic lesions; ear infections; diseases that cause recurrent facial palsy; facial paralysis secondary to intracranial lesions such as cerebrovascular disease.

• Studies that did not classify the facial palsy on the House-Brackmann (HB) scale.

• Studies of patients with RHS that did not mention the type of treatment, results, or prognosis.

[Fig. 1] shows a flowchart of the decision process regarding the study selection.

Fig. 1 Flowchart of the decision criteria involved in the selection of the studies.

Review of the Literature

Results

The database search resulted in 259 studies. After reading all the resulting manuscripts in full by two of the authors, we selected 19 studies for appraisal, and included 13 in the quantitative analysis. The studies included a total of 882 patients with facial paralysis caused by RHS[1] [2] [3] [4] [5] [6] [7] [8] [11] [12] [13] [14] [15] [16] [17] ([Table 1]). The duration of follow-up extended from 73 days to one year among the different studies.

Table 1 Results regarding the evolution of the facial nerve function obtained by different authors on patients with Ramsay Hunt syndrome, by using different treatments

Authors	No. of patients	HB scale and patients		Treatment	Follow-up	Patients with HB I or II AT
		BT	AT
Ryu et al[16]	155	HB III – 24	HB I or II – 22	Prednisolone (80 mg oral methylprednisolone per day for 4 days, 60 mg/d for 2 days, 40 mg/d for 2 days, 20 mg/d for 2 days, and 10 mg/d for 5 days); Acyclovir (4000 mg/d for 7 days)	3 months	91 (58.7%)
		HB IV – 53	HB I or II – 35
		HB V or VI – 78	HB I or II – 34
Zainine et al[4]	15	HB III – 1	HB I – 1	Hydrocortisone (100 mg 3x/day IV for 8 days) Acyclovir (4000 mg/d PO for 8 days)	8 months	10 (66.6%)
		HB IV – 8	HB I – 4 HB II – 2 HB III – 1 HB IV – 1
		HB V – 6	HB II – 3 HB V – 3
Kansu et al[12]	01	HB V – 1	HB IV – 1	Corticosteroid (1 mg/kg/d) Acyclovir (90 mg/kg/d)	4 months	00 (0%)
Donati et al[2]	01	HB V – 1	HB I – 1	Oral valacyclovir (3 g/day, lowered to 1.5 g/day after 1 week) and prednisone 50 mg/day. On day 66–methylprednisolone (1 g/day I.V. for 5 days.	248 days	02 (100%)
	01	HB V – 1	HB I – 1	Oral acyclovir (800 mg/day) for 10 days and prednisone 75 mg/d. On day 37–methylprednisolone, 1 g/day I.V. for 3 days	73 days	–
Shim et al[17]	339	HB II – 40	HB I – 33 HB II – 7	Prednisone (1 mg/kg/d orally for 4 days, tapered to zero until day 10) Acyclovir (400 mg/8h for 5 days)	6 months	225 (66.3%)
		HB III – 95	HB I – 52 HB II – 34 HB III – 9
		HB IV – 137	HB I – 30 HB II – 52 HB III – 26 HB IV – 29
		HB V – 67	HB I- 12 HB II – 5 HB III – 21 HB IV – 13 HB V – 16
Kim et al[13]	11	HB II – 5	HB I – 5	Steroids (40 to 60 mg of prednisolone, or 48 mg of methylprednisolone, orally, for 10 to 37 days Acyclovir (750 to 4800 mg, intravenously, for 5 to 12 days)	6 months	09 (81.8%)
		HB III – 1	HB II – 1
		HB IV – 2	HB II – 2
		HB V – 3	HB II – 1 HB III – 2
Boemo et al[1]	54	HB II – 4	HB I – 4	Acyclovir 250 mg/8h and methylprednisolone 120 mg/d IV for 48h; then acyclovir 850 mg/8h for 10 days and methylprednisolone 30mg/d orally, in a decreasing dosage for 16 days	6 months	33 (61.1%)
		HB III – 8	HB I – 8
		HB IV – 20	HB I – 10 HB III – 8 HB IV – 2
		HB V – 22	HB I – 3 HB II – 8 HB III – 6 HB IV – 5
Gondivkar et al[8]	01	HB V – 1	HB I – 1	Initial dose of acyclovir and steroids I.V., and a 2-week course of oral acyclovir and steroids after discharge; Transcutaneal electrical nerve stimulation and facial neuromuscular exercise.	5 weeks	01 (100%)
Yeo et al[6]	26	HB II – 3	HB I – 2 HB II – 1	Prednisolone (1 mg/kg/d IV for 5 days; then, the dose was tapered for another 5 days); Acyclovir (5 mg/kg/8h IV for 5 days); Famciclovir (500 mg orally for 7 days, after the 5-day cycle of acyclovir); Dextran; Peripheral vasodilators.	6 months	22 (84.6%)
		HB III – 13	HB I – 7 HB II – 4 HB III – 2
		HB IV – 10	HB I – 4 HB II – 4 HB III – 1 HB IV – 1
Furuta et al[7]	37	HB II – 1	HB I – 1	Acyclovir (4000 mg in tablet form or 750 mg per day by infusion) or valacyclovir (3000 mg in tablets) was administered to all patients for 5 to 7 days. Patients with grade IV to VI facial paralysis were usually given 40 to 60 mg prednisone for 4 days.	6 months	27 (72.9%)
		HB III – 3	HB I – 3
		HB IV – 9	HB I – 9
		HB V – 17	HB I – 9 HB II – 2 HB III – 5 HB IV – 1
		HB VI – 7	HB I – 2 HB II – 1 HB III – 1 HB IV – 3
Uri et al[11]	23	HB IV – 3	HB I – 2 HB III – 1	Acyclovir (5 mg/kg/8h intravenously for 7 days) Hydrocortisone (100 mg/8h intravenously for 7 days)	1 year	19 (82.6%)
		HB V – 2	HB I – 2
		HB VI – 18	HB I – 11 HB II – 4 HB III – 1 HB IV – 1 HB V – 1
Kinishi et al[14]	91	HB III – 2	HB I – 82	Dextran (500 mL, for 7 days) Methylprednisolone (500 m on day 1, 250 mg on days 2 and 3 and 100 mg for 4 days thereafter Adenosine triphosphate (ATP) and vitamins B6 and B12 Acyclovir, 4000 mg/d, 7 days	6 months	85 (93.4%)
		HB IV – 17	HB II – 3
		HB V – 33	HB III – 5
		HB VI – 39	HB IV – 1
	47	HB III – 2	HB I – 30	The same protocol described above, but without the acyclovir		32 (68%)
		HB IV – 9	HB II – 2
		HB V – 17	HB III – 10
		HB VI – 19	HB IV – 5
Murakami et al[15]	80	HB III – 1	HB I – 1	Prednisone (1 mg/kg/d, orally or intravenously for 5 days; then, tapered to zero over the following 10 days); Acyclovir (250 mg/8h for 7 days intravenously or 800 mg 5 times/d orally, for 7 days)	1 year	65 (81.25%)
		HB IV – 21	HB I – 17 HB II – 2 HB III – 2
		HB V – 38	HB I – 20 HB II – 12 HB III – 5 HB IV – 1
		HB VI – 20	HB I – 4 HB II – 9 HB III – 7
Total	882	–	–	–	–	621 (70.4%)

Abbreviation: AT, after treatment; BT, before treatment; HB, graduation on the House-Brackmann facial palsy scale.

Out of the 882 patients described in these studies, 829 (93.99%) had facial palsy grades III to VI on the HB scale. Following treatment, 621 out of the 882 (70.4%) achieved a score of I–II on the HB scale (“good prognosis”).

Regarding the HB graduation before treatment, 53 (6%) were HB II, 150 (17%) HB III, 289 (32.7%) HB IV and 390 (44.2%) HB V or VI. After treatment, 621 (70.4%) achieved HB I or II and 261 (29.6%) achieved HB III, IV, or V. All of the patients were treated with steroids[1] [2] [3] [4] [5] [6] [7] [8] [11] [12] [13] [14] [15] [16] [17]; however, Furuta et al[7] only administered them to patients with facial palsy grades IV–VI at the initial examination. Antiviral agents were used in all patients, in exception of the 47 patients described in Kinishi et al's study.[14] These authors conducted a clinical trial in which 91 patients were treated with steroids (methylprednisolone, 500 mg on day 1, 250 mg on days 2 and 3, and 100 mg/d for 3 days thereafter), aciclovir (4000 mg/d for 7 days), dextran (500 mL/d for 7 days), vitamins B6 and B12 and peripheral vasodilators; another 43 patients received the same treatment but without the antiviral. Among the patients that received acyclovir, 85 (93.4%) achieved a good prognosis for facial palsy (HB I or II), compared with only 32 (68%) of the group that did not receive the antiviral agent (p < 0.05). Some authors treated patients with other drugs or therapies, such as dextran (500 mL for 7 days),[6] [14] peripheral vasodilators,[6] adenosine triphosphate (ATP),[14] and vitamins B6 and B12.[14]

The rate of complete recovery regarding the type of steroid associated with acyclovir varied among the studies.[1] [4] [7] [11] [14] [15] [16] [17] Regarding the patients treated with prednisone, 290 out of the 419 patients (69.2%) achieved a good prognosis; among the 192 patients treated with prednisolone, 118 (61.4%) achieved facial palsy HBI or II, versus 29 out of the 38 (76.3%) that received hydrocortisone, and 118 of the 145 (81.3%) patients treated with methylprednisolone. These results are presented in [Table 2].

Table 2 Number of patients that achieved a good prognosis of the facial palsy, according to the different classes of steroids associated to acyclovir

	No. of patients that achieved good prognosis with Prednisone	No. of patients that achieved good prognosis with Prednisolone	No. of patients that achieved good prognosis with Hydrocortisone	No. of patients that achieved good prognosis with Methylprednisolone
Ryu et al[16]	–	91/155	–	–
Zainine et al[4]	–	–	10/15	–
Shim et al[17]	225/339	–	–	–
Boemo et al[1]	–	–	–	33/54
Furuta et al[7]	–	27/37	–	–
Uri et al[11]	–	–	19/23	–
Kinishi et al[14]	–	–	–	85/91
Murakami et al[15]	65/80	–	–	–
Total	290/419 (69.2%)	118/192 (61.4%)	29/38 (76.3%)	118/145 (81.3%)

Some studies[6] [16] compared the facial nerve recovery rate in patients with and without metabolic diseases. Patients with diabetes mellitus achieved worse recovery rates than patients without systemic diseases (p < 0.05). Patients older than 60 years with RHS had a delayed recovery of the facial nerve when compared with younger patients (p < 0.05),[6] [14] probably due to a less efficient cellular immune system, rather than a reduction in humoral immunity.[8] Nonetheless, the Uri et al[11] study did not evidence differences in the prognosis of facial palsy according to age and gender.

Regarding the prognostic factors, the association between facial palsy and cochleovestibular impairment has worse prognosis than isolated facial nerve palsy (p = 0.029).[11] Shim et al,[15] in a case-control study, observed that the recovery of the facial paralysis was worse when associated with impairment of other cranial nerves, regardless of the initial grade on the HB scale (p < 0.05).[15]

Discussion

Ramsay Hunt syndrome is responsible for 12% of cases of facial paralysis, with a worse prognosis than Bell's palsy.[11] Other pathologic changes include damage of the Corti organ and Scarpa ganglion, leading to hearing loss and vertigo.[4]

Although previous studies have reported a 10% recovery rate of patients with complete facial palsy even with correct treatment,[11] in our study, 51.4% of patients with facial palsy graded as HB V to VI treated with steroids plus antiviral agents achieved HB I or II.

Treatment of RHS involves high doses of steroids and virostatic agents, especially acyclovir. The drugs, dosages, and period of treatment used by each author are described in [Table 1]. Even though the antiviral agents might theoretically cause several damaging effects, the number of the adverse effects on the selected studies was not significant.[3]

Some authors treated patients with other drugs or therapies, such as dextran (500 mL for 7 days),[6] [14] peripheral vasodilators,[6] adenosine triphosphate (ATP),[14] and vitamins B6 and B12.[14] However, many studies did not report the dosage, time of treatment, or period between the initial symptoms of facial palsy and treatment. Thus, it was difficult to define a treatment protocol and to compare the success of the treatments.

For comparison purposes, “good prognosis” (adequate response to treatment) was considered when the HB grade increased to I or II after treatment. The percentage of patients with a good prognosis varied from 61.1% to 100% in the different studies.[1] [2] [4] [6] [11] [16] [17] In our data, 621 out of the 882 patients (70.4%) achieved HB I or II.[1] [2] [4] [6] [7] [8] [11] [12] [13] [14] [15] [16] [17]

Regarding the different treatment regimens proposed, 68% of the patients with III to VI on the HB scale achieved a good prognosis when treated with steroids without the antiviral agent,[14] versus 70.5% of patients treated with steroids plus antiviral agents.[1] [2] [4] [6] [7] [8] [11] [12] [13] [14] [15] [16] [17] More specifically, 51.4% of the patients with facial palsy grade V and VI completely recovered the facial motor function (HB I or II)[1] [2] [3] [7] [8] [11] [12] [13] [15] [16] [17] when treated with steroids plus antiviral agents.

Kinishi et al[14] compared the evolution of patients with facial palsy due to RHS treated with corticosteroids with or without antiviral agents. They demonstrated better evolution of patients treated with methylprednisolone and acyclovir (93.4% versus 68% of the patients who did not receive acyclovir) (p < 0.01). De Ru et al[3] demonstrated an odds-ratio (OR) for a complete recovery of the facial palsy of 5.5 (95% confidence interval [95% CI] = 1.6–18.8) with antiviral agents, 2.9 (95% CI = 1.6–5.4) with steroids in monotherapy, and 8.4 (95% CI = 3.7–18.9) when both treatments were combined, when compared with no treatment at all. The OR of the combined therapy versus only steroids was 2.8 (95% CI = 1.3–5.8). Although the studies used different kinds of steroids, dosages, and periods of treatment, the treatment proposed by Kinishi et al[14] (methylprednisolone at 500 mg on day 1, 250 mg on days 2 and 3, and 100 mg for 4 days thereafter, associated with oral acyclovir, 400 mg 5x/d for 7 days) achieved the higher rate of recovery. Nonetheless, the comparison between the results achieved by the different types of steroids did not achieve statistical significance (p > 0.05). A study of the molecular mechanisms of corticosteroids conducted by Tsai[18] showed that methylprednisolone has a higher affinity to glucocorticoid receptors, and a higher anti-inflammatory action when compared with the prednisone, prednisolone, or hydrocortisone; these facts might explain the best results achieved by the authors that used methylprednisolone comparing to other steroids.

Coulson et al[5] showed that the group of patients treated with oral prednisone 1 mg/kg for 14 days, followed by a declining dose of 10 mg/d down to 0 mg, associated with acyclovir 200 mg 5x/d for 21 days 5 days after the onset of the paralysis achieved greater improvement of symptoms than patients treated earlier (p = 0.005). A possible explanation for this is that the anti-inflammatory action of the steroids should be present at the moment that the inflammation is most intense to achieve the best efficacy.[5] Nonetheless, a study conducted by De Ru[3] demonstrated that best results are achieved when the treatment is initiated on the early onset of the disease. Murakami et al[15] also showed significant differences in the improvement of facial nerve function depending on the time elapsed between the onset of the symptoms and the start of treatment – the best results are achieved when treatment is introduced before the fifth day of the first symptoms. The same authors indicated that intravenous and oral drugs are equally efficient in terms of the recovery of the function of the facial nerve. They also reported that most of the patients with RHS did not require hospitalization.[15]

Furuta et al[7] observed that patients with VZV in the oropharynx or with a viral load above 10,000 copies per 50 μL in the saliva had a worse recovery of the facial nerve function than patients with the isolated cutaneous form of the zoster infection (p = 0.0019). Thus, the level of VZV DNA in the saliva reflects the kinetics of the viral reactivation in the facial nerve. Other parameters related to worse prognosis were lagophthalmus and dry eye (p < 0.05), which indicates the involvement of the large superficial petrosal nerve.[5]

None of the selected studies refer to surgical management of the facial palsy in Ramsay Hunt syndrome. Bodénez et al,[19] however, proposed a flowchart regarding to the surgical approach – if the patient maintains complete facial palsy (HB V or VI) after the clinical treatment, the electromyography shows axonal loss higher than 95% and a time elapsed since the beginning of the facial palsy of 15 days, a surgical approach may be indicated.

Final Comments

Overall, patients with Ramsay Hunt syndrome achieved a high rate of complete recovery of the facial nerve function (70.4%) after the different proposed treatments. The combination of steroids and acyclovir reached better recovery rates than steroids in monotherapy. Dosage and period of treatment greatly varied among studies.

Clinical data such as age, associated metabolic diseases, impairment of the cochleovestibular, or other cranial nerves, oropharynx lesions, dry eye, and lagophthalmus must be assessed at the initial physical examination, since they suggest worse prognosis of the facial palsy secondary to Ramsay Hunt syndrome.

• References

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Address for correspondence

Rafael da Costa Monsanto, MD

Centro de Estudos - Departamento de Otorrinolaringologia do Banco de Olhos de Sorocaba (BOS)

Praça Nabek Shiroma, 210, Jardim Emília, Sorocaba/SP, Zip code 18031-060

Brazil   

Email: [e-mail]