Head and neck
Published: 2019-10-22

Recurrent Bell’s palsy: outcomes and correlation with clinical comorbidities

Department of Sense Organs, University Sapienza of Rome, Italy
Department of Sense Organs, University Sapienza of Rome, Italy
Department of Sense Organs, University Sapienza of Rome, Italy
Department of Sense Organs, University Sapienza of Rome, Italy
Department of Neurosciences, S. Camillo- Forlanini Hospital, Rome, Italy
Department of Sense Organs, University Sapienza of Rome, Italy
Department of Oral and Maxillo-Facial Surgery, University Sapienza of Rome, Italy
Department of Sense Organs, University Sapienza of Rome, Italy
Department of Sense Organs, University Sapienza of Rome, Italy
Department of Oral and Maxillo-Facial Surgery, University Sapienza of Rome, Italy
Recurrent Alternating Bell’s palsy Facial paralysis Outcomes


Recurrent Bell’s palsy (RBP) has been reported to range from 2.6 to 15.2% of primary Bell’s palsy (BP) and has been associated with systemic comorbidities such as diabetes and hypertension. A retrospective analysis of patients affected by BP and RBP were performed to define the signs and symptoms associated with recurrence and the outcomes. Clinical and subjective characteristics of 341 patients affected by facial palsy were analysed. Facial function was assessed via House-Brackmann and Sunnybrook grading system. Characteristics of the palsy and systemic comorbidities (diabetes, hypertension, herpetic infections, autoimmunity disorders, audio-vestibular symptoms) were analysed in BP and RBP patients applying Fisher exact and the Mann-Whitney U tests, while time to recovery was explored with univariate and multivariate analysis. Twenty-four patients presented two or more episodes of facial palsy, representing a recurrence rate of 7%. Associated symptoms (e.g. retroauricular pain, taste disorder, dry eye etc.) were similar between BP and RBP patients. RBP occurred at older age than primary episode (p = 0.03). Recurrence was a risk factor for delayed recovery (p = 0.02), although final facial function was similar between the two groups. In conclusion, no significant differences were found between primary BP patients and RBP patients in terms of symptoms, palsy severity and presence of comorbidities. Delayed facial nerve function recovery in RBP did not affect the final outcome. Treatment of facial nerve recurrences must be the same of the primary episode, although the presence of prodromal symptoms may alert the patient and early corticosteroid treatment may be commenced even before the onset of paresis.


The sudden onset of facial palsy is most commonly due to stroke or Bell’s palsy (BP). BP is the most frequent form of peripheral palsy of the facial nerve and represents about 60% of all aetiologies, with a diversely reported annual incidence between 8 and 52.8 new cases per 100,000 individuals 1-3. It is believed that reactivation of Herpes viruses in the endonevrium of the geniculate ganglion can play a role in the onset of peripheral idiopathic facial nerve palsy 4-6, but the aetiology is not yet completely defined. Medical treatment is based on high-dose of corticosteroids and antiviral agents, even if there is limited evidence of the efficacy of the latter 7 8.

Recurrent Bell’s palsy (RBP), either ipsilateral or contralateral to the side affected in the primary episode, is a relatively rare disease. The incidence of recurrent facial palsy has been reported to range from 2.6 to 15.2 % of patients who already had a primary episode 9-17. It was first reported to occur by Devriese and Peltz 10, who first identified alternating or recurrent palsies as those recurrences that affect the contralateral or ipsilateral facial nerve.

The data regarding prognosis of RBP, when compared to primary BP, are conflicting, partly because classification of degree of palsy is not uniform across studies. It is, therefore, not clear whether the pathogenetic mechanisms underlying RBP are the same as BP, and consequently if the therapeutic approaches should be different.

In the present study, subjects presenting with recurrent facial palsy were selected from all patients presenting with unilateral idiopatic facial palsy visited in a tertiary referral centre; the clinical characteristics and prognosis of patients with primary and recurrent BP were compared to define the signs and symptoms associated with recurrence and prognosis of outcomes.

Materials and methods


This study was designed as a retrospective cohort study on subjects treated at Policlinico Umberto I University Hospital of Rome, between May 2010 and March 2018. The protocol was approved by the ethics committee of the University (authorisation number # 29-05-08/1432) and written informed consent was administered to each patient before commencing any study-related procedure. In order to obtain a homogeneous cohort of subjects, the eligibility criteria were: age 14 to 89 years; unilateral Bell’s Palsy diagnosed by clinical ENT and neurological assessment; treatment within 48 hours after the onset of the initial symptoms of BP; standardised oral pharmacological treatment with prednisone 1 mg/kg for 10 days plus valacyclovir 500 mg TID for 6 days. Exclusions criteria included: pregnancy; palsy due to metabolic, neurological, infective, neoplastic, toxic or iatrogenic disease; traumatic injury to the facial nerve, VZV infection (Ramsay-Hunt syndrome), Melkersson-Rosenthal syndrome.

Study procedures

Two routinely scale systems were used to assess the facial palsy severity in the clinical practice: the House-Brackmann facial grading (HB) scale 18 and the Sunnybrook facial (SB) grading system 19. The HB scale measures the global degree of paresis/paralysis, ranging from grade I (normal function) to VI (complete paralysis). It was chosen for its simplicity of assessment, most frequent use and robustness. Nevertheless, this scale lacks accuracy on synkinesis and regional asymmetry; therefore, the SB scale system, with a score ranging from 0 to 100, was added as it provides regional scores at rest and motion also in addition to accurate information on synkinesis.

Each patient was evaluated at his/her first visit and 10 days - 1, 3, 6 months post onset. Patients were interviewed to gather information on diabetes, hypertension, previous herpetic infections, systemic infections, autoimmunity disorders, audio-vestibular symptoms and family history of facial palsy. For the palsy itself, information about the presence and side of recurrence and time lapse between episodes, and all associated symptoms, were collected.

Patients who at first examination had HB ≥ IV or who had no improvements to HB II-III grade after 10 days underwent the following: brain MRI with gadolinium, audiometric and impendence tests, and electrophysiological tests (electromyography, electroneurography and blink reflex). Furthermore, patients with HB grade > IV, who did not show improvement at the second clinical assessment and were negative for secondary palsy, were referred to physical rehabilitation 20.

Statistical analysis

Data are presented as proportion and mean ± standard deviation or median (interval), as appropriate. Differences between patients with BP and RBP were tested by Fisher’s exact test and Mann-Whitney U test for categorical and continuous variables, respectively. Time to recovery was explored with univariate (Log-Rank test) time-to-event analyses. To further verify if the time to recovery was truly different in patients with BP and RBP, we ran a Cox proportional hazards regression model in a stepwise fashion to obtain hazard ratios (HRs) and corresponding 95% confidence intervals (CIs). The main time variable was defined as the period (days) elapsed from palsy onset and the last available visit or outcome reached (i.e. recovery to a HB equal or less than grade II). Demographic and clinical variables were included Aa covariates of interest: sex, age, HB and SB grades (entered as multilevel variable), first BP or RBP episode, familial history and presence or absence and type of comorbidity (hypertension, diabetes, audio-vestibular symptoms, autoimmunity, herpetic infections). Two-tailed p-values < 0.05 were considered as significant, without correction for multiple comparisons considering the exploratory nature of the present study. Data were analysed using the Statistical Package for Social Sciences, version 16.0 (IBM SPSS Inc., Chicago, Ill., USA).


A total of 341 patients (198 men, 143 women, mean age 50.2 ± 17.9 years, range: 14 to 89) attended the Emergency Department due to BP from May 2010 to March 2018.

Of these 341 patients, 30 were lost to follow-up and 22 had incomplete data collection, and we thus analysed the data of 289 patients. The mean HB grade was 3.7 ± 1.07, the Sunnybrook score was 40.7 ± 20.8. Twenty-four patients (7.0%) had a RBP. All patients with RBP were included in the analysis with exception of one patient at his third episode of facial palsy with clinical characteristics of Melkersson-Rosenthal syndrome (oedema of the lips, lingua plicata and relapsing facial palsy). Table I shows the characteristics of patients according to either a first BP episode (n = 265) or RBP (n = 24). Patients with RBP were older than the other patients (p = 0.03). The two groups did not differ in terms of sex, BP severity (HB and SB), or presence of comorbidities.

Eleven patients presented the palsy on their right side, and 13 on their left side. In RBP subjects, the median time from the previous episode was 6 years (interval: 2-33); the paresis involved the ipsilateral and contralateral side in 12 and 7 cases, respectively, while the remaining 5 cases were not able to report the previously affected side. The time elapsed from the previous BP episode and the previously affected side (ipsilateral or contralateral) did not influence the outcome. Interestingly, we found that patients with recurrent BP in the contralateral side were more likely to have hypertension (6 of 7) than those presenting a further ipsilateral BP episode (1 of 12) (p = 0.02) in the absence of other significant differences. Nevertheless, we do not think that this finding has a clinical correlation.

Considering the symptoms associated at onset of paresis among patients affected by RBP, 10 presented retroauricular pain, 4 dysgeusia, 4 dry eye, 4 hyperlacrymation and 3 patients had dry mouth; these symptoms were present alone or in combination. All the patients except one were at their second palsy; 15 palsies were ipsilateral and 8 contralateral. The patient affected by Melkersson-Rosenthal syndrome already presented 1 palsy on his left side and 3 on the right side. Five patients reported a family history of BP. Three patients, already treated in our clinic for BP, came to our observation with prodromal symptoms (retroauricular pain, dry eye, dysgeusia) before the onset of paresis that occurred within the next following days 21.

A total of 224 patients (78%) recovered from BP after a mean time of 63.4 days (interval: 2 to 357), while the remaining 65 (22%) did not completely recover after 6 months of follow-up.

Figure 1 shows the Kaplan-Meier curve displaying time to recovery from BP according to study group (first BP episode versus recurrent BP). Patients with first BP episode recovered faster than those with RBP (p = 0.04 by the Log-Rank test). No difference in terms of final facial function was found between the two groups.

Findings from the Cox regression model are shown in Table II. As expected, higher HB grades were associated with delayed recovery (HR: 1.00 for grade III, 0.61 for grade IV, 0.42 for grade V or VI; p < 0.001). Also, RBP was a risk factor for delayed recovery (HR: 0.52; p = 0.02). The remaining clinical variables, including sex, age and comorbidities, did not contribute to fit the model.


Recurrence of peripheral facial palsy is well known and has been reported by several studies; physicians and rehabilitation therapists should inform patients presenting with a primary episode that recurrence may occur even after several years. In the present study, 24 of 289 patients (7%) developed a second episode of facial palsy, a percentage that is in accordance with data present in the literature 9-17. Although RBP has been associated with systemic comorbidities such as diabetes and hypertension 9 10 22-25, our results did not show such a correlation. Findings in the literature are often discordant as far as correlation of comorbidities with severity of outcomes, mainly due to composition and homogeneity of study groups, follow-up times and differences in classification of severity of palsy.

Many studies have addressed the incidence of recurrence with respect to the side, ipsilateral or contralateral. Ralli et al. 14 found an increased incidence in the contralateral side compared to the ipsilateral side, while Navarrete et al. 22 found a major incidence on the right side, regardless if ipsilateral or contralateral. Almost all studies agree in judging ipsilateral RBP as being worst in terms of long-term prognosis. Nevertheless, no clear follow-up timing has been established, and clinical evaluation of degree of palsy and systematic statistical approaches have been used. In their study, Ralli et al. 14 evaluated 35 patients with recurrent unilateral BP. The incidence of recurrence was higher in younger patients, with a poorer prognosis for palsies occurring on the same side of the primary episode. Similarly, Navarrete et al. 22 found worse recovery in patients where recurrence occurred ipsilaterally to the primary episode. On the contrary, Cirpaciu and coauthors 13 did not find differences in the recurrence rate between RBP presenting in the ipsilateral or contralateral side respect to the primary BP. The authors reported a prevalence of incidence in young females (68% of the cases), in subjects with age between 21 and 30 years and with a family history of multiple episodes of RBP. In our study, a family history of BP was present in 5 patients (20%) suggesting a genetic predisposition for this pathology. Indeed, some studies found an association of certain human leukocyte antigens (HLAs) with the palsy, although these findings were not confirmed by other studies 26 27.

The association between recurrent facial palsy and diabetes mellitus has been reported with an incidence between 5.6% and 28.6% 10 11 15 23 25. However, other authors have found no difference in diabetes incidence between primary and recurrent BP 9.

The study of Chung et al. 9 analysed the differences between primary and recurrent BP as far as the role of degree of palsy, side and comorbidities over palsy prognosis. The authors have studied a large population (1,257 subjects) affected by BP correlating the degree of palsy, assessed via House-Brackmann classification, electrophysiologic tests and MRI. In their study, the incidence of RBP was 5.7%. The study group was homogeneous as far as treatment with steroids and antivirals, and outcomes were evaluated after a minimum of 6 months follow-up. The rate of recovery for BP was significantly higher (88.4%) than RBP (72.2%). Interestingly, while diabetes did not seem to influence incidence of RBP, recurrence was significantly higher in subjects who were pregnant or affected by hypertension, although these factors were no longer signicant after logistic regression analysis.

Some studies have shown that the peak of incidence was in a younger age 10 13 14 23 and described women as most susceptible to recurrence (68%) 13. In the present study, a higher incidence was found in elderly patients, which is probably was due to a time factor that increased the probability to develop a second episode of paresis. Moreover, in our study, synkinesis did not seem to have higher prevalence in RBP. One possible reason is that synkinesis was found to have a prevalence at a younger age 28, due to functional and structural changes related to aging that reduce recovery of the peripheral nervous system after injury.

No difference was found between BP and RBP concerning SB score and HB grade as far as palsy severity, although in the Kaplan-Meier analysis primary BP showed a significant faster recovery.

As far as RBP characteristics are concerned, time elapsed from the previous palsy episode did not differ between ipsilateral and contralateral presentation. Concerning symptoms associated with paresis, their distribution was not significantly different between the two groups. Nevertheless, the previous experience of a primary BP episode led 3 of our patients to attend our facial palsy centre before onset of the paresis when only retroauricular pain and taste disorder were present, which allowed us to begin corticosteroid treatment in the very early stage of the paresis.

In the present study, no significant difference was found between the incidence of RBP in ipsilateral or contralateral recurrence, although there was a mild prevalence for the ipsilateral side.

Recurrence and higher HB grades were risk factors for delayed recovery, confirming the findings of Chung and al. 9. Patients with primary BP recovered faster than patients with RBP (p = 0.05). Nevertheless, despite the delayed recovery in RBP, no difference was found in final facial function. Other studies found different recovery rates between the two groups 9 10 15, possibly because of the presence of other confounding factors such as incidence of comorbidities and differences in therapeutic approaches.


In conclusion, no significant difference in terms of symptoms, palsy severity and presence of comorbidities was found between primary BP patients and RBP patients. Final facial nerve function, even if delayed in recurrences, was similar in the two groups. The management of a recurrent facial palsy must be the same as the primary episode; nevertheless, the presence of prodromal symptoms may alert the patient to go to emergency department, allowing the beginning of corticosteroid treatment in the very early stage of the paresis.

Figures and tables

Fig. 1.Kaplan-Meier curve showing the time to Bell’s Palsy recovery in patients with a first episode (BP) (n = 265; grey line) and in those with recurrence (RBP) (n = 24; black line).

First BP episode Recurrent BP P-value
N 265 24 -
Gender (female:male) 113:152 10:14 1.00
Age, years 49.4 ± 18.1 57.2 ± 14.0 0.03
HB score 3.95 ± 0.65 3.83 ± 0.92 0.68
SB score 40.7 ± 21 40.4 ± 20.2 0.60
Presence of comorbidity 186 19 0.48
Hypertension 83 11 0.17
Diabetes 28 5 0.17
Autoimmunity disease 18 0 0.38
Infectious disease 5 2 0.11
Audio-vestibular abnormal 37 4 0.76
Herpes virus infection 108 12 0.39
Familial history of BP 27 (10%) 5 (20%) 0.16
Follow-up, days 60 ± 58 70 ± 59 0.34
Table I.Main characteristics of study sample (n = 289) according to the presence of a first BP episode or a recurrent BP.
N HR 95% CIs p
HB gradeIIIIVV or VI 1178587 1.000.610.42 -0.42-0.880.29-0.60 -0.01< 0.001
First BP episodeRecurrent BP 26524 1.000.52 -0.29-0.91 -0.02
Table II.Cox regression model (stepwise fashion) showing variables predictive for BP recovery.


  1. 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.
  2. Franzke P, Bitsch A, Walther M. Weather, weather changes and the risk of Bell’s palsy: a multicenter case-crossover study. Neuroepidemiology. 2018; 51:207-15. DOI
  3. Holland NJ, Bernstein JM. Bell’s palsy. BMJ Clin Evid. 2014;2014.
  4. Esaki S, Yamano K, Katsumi S. Facial nerve palsy after reactivation of herpes simplex virus type 1 in diabetic mice. Laryngoscope. 2015; 125:E143-8. DOI
  5. Stjernquist-Desatnik A, Skoog E, Aurelius E.. Detection of herpes simplex and varicella-zoster viruses in patients with Bell’s palsy by the polymerase chain reaction technique. Ann Otol Rhinol Laryngol. 2006; 115:306-11. DOI
  6. Turriziani O, Falasca F, Maida P. Early collection of saliva specimens from Bell’s palsy patients: quantitative analysis of HHV-6, HSV-1, and VZV. J Med Virol. 2014; 86:1752-8. DOI
  7. Sullivan FM, Swan IR, Donnan PT. Early treatment with prednisolone or acyclovir in Bell’s palsy. N Eng J Med. 2007; 357:1598-607. DOI
  8. Gagyor I, Madhok VB, Daly F. Antiviral treatment for Bell’s palsy (idiopathic facial paralysis). Cochrane Database Syst Rev. 2015; 11:CD001869. DOI
  9. Chung DH, Park DC, Byun JY. Prognosis of patients with recurrent facial palsy. Eur Arch Otorhinolaryngol. 2012; 269:61-6. DOI
  10. Pitts DB, Adour KK, Hilsinger RL. Recurrent Bell’s palsy: analysis of 140 patients. Laryngoscope. 1998; 98:535-40. DOI
  11. Devriese PP, Pelz PG. Recurrent and alternating Bell’s palsy. Ann Otol Rhinol Laryngol. 1969; 78:1091-4. DOI
  12. Boddie HG. Recurrent Bell’s palsy. J Laryngol Otol. 1972; 86:1117-20.
  13. Cirpaciu D, Goanta CM, Cirpaciu MD. Recurrences of Bell’s palsy. J Med Life. 2014; 7:68-77.
  14. Ralli G, Magliulo G.. Bell’s palsy and it’s recurrences. Arch Otolaryngol. 1988; 244:387-90. DOI
  15. Hallmo P, Elverland HH, Mair IW. Recurrent facial palsy. Arch Otorhinolaryngol. 1983; 237:97-102. DOI
  16. Yanagihara N, Mori H, Kozawa T. Bell’s palsy: nonrecurrent v recurrent and unilateral v bilateral. Arch Otolaryngol. 1984; 110:374-7. DOI
  17. Takahashi A, Sahashi K, Nakao N. Recurrent Bell’s palsy: analysis of 21 cases. Facial Nerve Research Japan. 1981; 1:85-8.
  18. House JW, Brackmann DE. Facial nerve grading system. Otolaryngol Head Neck Surg. 1985; 93:146-7. DOI
  19. Ross BG, Fradet G, Nedzelski JM. Development of a sensitive clinical facial grading system. Otolaryngol Head Neck Surg. 1996; 114:380-6.
  20. Nicastri M, Mancini P, De Seta D. Efficacy of early physical therapy in severe Bell’s palsy: a randomized controlled trial. Neurorehabil Neural Repair. 2013; 27:542-51. DOI
  21. De Seta D, Mancini P, Minni A. Bell’s palsy: symptoms preceding and accompanying the facial paresis. ScientificWorldJournal. 2014; 2014:801971. DOI
  22. Navarrete ML, Céspedes R, Mesa M. Recurrent Bell’s facial palsy: our experience. Acta Otorrinolaringol Esp. 2001; 52:682-6.
  23. van Amstel AD, Devriese PP. Clinical experiences with recurrences of Bell’s palsy. Arch Otorhinolaryngol. 1988; 245:302-6. DOI
  24. Scola Yurrita B, Ramírez Calvo C, Scola Pliego E. Parálisis facial recidivante idiopática. Acta Otorrinolaringol Esp. 2004; 55:343-5.
  25. Mamoli B, Neumann H, Ehrmann L.. Recurrent Bell’s palsy: etiology, frequency, prognosis. J Neurol. 1977; 216:119-25. DOI
  26. Shibahara T, Okamura H, Yanagihara N.. Human leukocyte antigens in Bell’s palsy. Ann Otol Rhinol Laryngol Suppl. 1988; 137:11-3.
  27. Döner F, Kutluhan S.. Familial idiopathic facial palsy. Eur Arch Otorhinolaryngol. 2000; 257:117-9. DOI
  28. Mancini P, De Seta D, Prosperini L. Prognostic factors of Bell’s palsy: multivariate analysis of electrophysiological findings. Laryngoscope. 2014; 124:2598-605. DOI


P. Mancini

Department of Sense Organs, University Sapienza of Rome, Italy

V. Bottaro

Department of Sense Organs, University Sapienza of Rome, Italy

F. Capitani

Department of Sense Organs, University Sapienza of Rome, Italy

G. De Soccio

Department of Sense Organs, University Sapienza of Rome, Italy

L. Prosperini

Department of Neurosciences, S. Camillo- Forlanini Hospital, Rome, Italy

P. Restaino

Department of Sense Organs, University Sapienza of Rome, Italy

M. De Vincentiis

Department of Oral and Maxillo-Facial Surgery, University Sapienza of Rome, Italy

A. Greco

Department of Sense Organs, University Sapienza of Rome, Italy

G.A. Bertoli

Department of Sense Organs, University Sapienza of Rome, Italy

D. De Seta

Department of Oral and Maxillo-Facial Surgery, University Sapienza of Rome, Italy


© Società Italiana di Otorinolaringoiatria e Chirurgia Cervico Facciale , 2019

  • Abstract viewed - 3082 times
  • PDF downloaded - 1050 times