Published: 2019-10-22

Observational study on risk factors determining residual dizziness after successful benign paroxysmal positional vertigo treatment: the role of subclinical BPPV

UOC Otorinolaringoiatria, AOU Policlinico P. Giaccone, Palermo, Italy, Istituto Euro-Mediterraneo di Scienza e Tecnologia - IEMEST, Palermo, Italy
Department of Science for Health Promotion and Mother and Child Care G. D’Alessandro; University of Palermo, Italy
Clinical Epidemiology and Cancer Registry Operative Unit, University Hospital Policlinico “Paolo Giaccone”, Palermo, Italy
Dipartimento Biomedicina e Neuroscienze Cliniche, Università degli Studi di Palermo, Italy
Residual dizziness Benign paroxysmal positional vertigo Subjective BPPV Dizziness Nystagmus


After successful treatment for benign paroxysmal positional vertigo, many patients may complain of residual dizziness. Possible explanations may be the persistence of otolith into canal insufficient to provoke noticeable nystagmus, utricular dysfunction and undiagnosed coexisting vestibular disorder. We conducted a prospective observational case-control study, focusing on the role of risk factors in determining residual dizziness after BPPV treatment. In the present study, 148 patients were recruited and residual dizziness was documented in the 57.5% of the cohort. Among patients with residual dizziness 36 had subclinical BPPV and after retreatment, although nystagmus was not clinically evident, there was resolution of dizziness. We conclude that residual otoliths may play a role in determining post-maneuver residual dizziness that is often linked to subclinical BPPV; this conclusion is also supported by the high prevalence of BPPV recurrence in patients with residual dizziness, as confirmed by our analysis. The main cause appears to be linked with dispersed otolith in semicircular canals.


Benign paroxysmal positional vertigo (BPPV) accounts for about 20% of vestibular complaints 1. Being a mechanical disorder of the semicircular canals, management consists of “mechanical” repositioning of the otoconial debris, also called otolith or canalith, detached from vestibular sensorineural epithelia. Posterior semicircular canal (PSC) is the most involved by BPPV with approximately 90% of cases, while horizontal semicircular canal (HSC) is the next most common 2; superior semicircular canal (SSC) involvement is rare. The canalithiasis consists of dispersed fragments of otoliths into semicircular canals, which are able to cause vertigo when, by gravity, move into canals. The repositioning maneuvers to treat canalithiasis are well established and used widespread, with some variations recently reported in literature 3.

In clinical practice, among patients admitted to emergency for vertigo, 8-9% are diagnosed with BPPV 4. The treatment of BPPV is often simple and immediate, giving the patient a prompt resolution of the symptoms. Some patients with resistant BPPV require several maneuvers to reach adequate results, while other patients, after initial resolution of symptoms, show delayed positional nystagmus due to canal reentry of otoliths 5.

Furthermore, patients without noticeable nystagmus during diagnostic assessment for BPPV, although experiencing vertigo and autonomic symptoms while the diagnostic test are performed, are diagnosed as subjective (subclinical) BPPV, since dispersed otolith are unable to give a clinical manifestation of nystagmus, and is manageable in the same manner of traditional BPPV 6.

Despite successful BPPV treatments, many patients complain of residual dizziness (RD) that is described variously by patients and can be classified as non-vestibular dizziness, based on the characteristics of the disequilibrium and absence of nausea and vomiting 7.

We conducted a prospective case-control study on BPPV treated by canalith repositioning maneuvers, focusing on the role of residual debris in determining subclinical BPPV as a cause of RD.

Materials and methods

All consecutive patients admitted for BPPV to our ENT divisions in the period 2012-2014 were included in the study, according to the approval of the institutional review board. Recent vertigo other than BPPV, head trauma and lifetime history of previous episodes of vertigo other than BPPV were considered as exclusion criteria. Residual dizziness was expressed as sensation of unsteadiness or lightheadedness without rotational vertigo 8. Data of included patients were prospectively collected in an electronic database. The following variables were recorded: age (< 40; 40-65; > 65), gender (male/female), side (left/right), tinnitus (yes/not), hearing loss (yes/not), previous BPPV episodes (yes/not), affected semicircular canal (PSC, LSC, SSC), recurrence (yes/not), liberatory nystagmus (yes/not), number of maneuvers done, success of maneuvers (yes/not) and residual dizziness (yes/not). All patients underwent otolaryngologic examination, pure tone audiometry, evaluation of nystagmus with infrared video-Frenzel lens, diagnostic test for positional nystagmus with Dix-Hallpike manoeuvre for PSC, supine roll-test for HSC, head-hanging manoeuvre for SSC, video Head Impulse Test (vHIT) done with Interacoustics Eyseecam® and Vestibular Evoked Myogenic Potentials (VEMPs) with Hedera Biomedics Socrates®. Ocular and Cervical VEMPs were done by Air-conducted stimulus examining both ears separately by tone burst 130 dB at 500 Hz. Normative values considered in all patients for VEMPs were: latency values, inter-amplitude and inter-latency asymmetry between range 0-45%, and absent or not reproducible wave; for vHIT symmetric gain and absence of overt and/or covert saccades was considered as normal, the gain value was not considered because several issue about to assess normative 9. The PSC diagnostic test was considered positive when nystagmus was appropriate with head position as torsional type with up-beating component. The HSC was considered positive when during supine head roll-test a direction changing horizontal nystagmus was detected, and for SSC when during head-hanging test a down-beating nystagmus with latency, crescendo and transience was observed with or without torsional component 10. The treatment included the same manoeuvre in all patients related to canal involved to avoid bias due to type of manoeuvre: Gans manoeuvre for PSC BPPV 3, Gufoni and Yacovino manoeuvre respectively for HSC and SSC involvement 2 11. The success of treatment was defined as disappearance of both symptoms and nystagmus at diagnostic tests performed 45 minutes after treatment. The clinical features of BPPV were recorded: side involved, canal involved, number of manoeuvres done to treat the BPPV, presence of liberatory nystagmus, canal re-entry or canal switch 5 and recurrence of BPPV after successful treatment. Follow-up was done with clinical control at one and two weeks after treatment and with control visits at 6 months and 12 months even if symptoms were absent. The presence of dizziness even without nystagmus at clinical control was recorded, and the vertigo elicited during the diagnostic manoeuvre for BPPV without clinical evidence of nystagmus was considered as subclinical (subjective) BPPV 6. The recurrence was defined as further BPPV episodes with noticeable nystagmus at otoneurologic examination in the follow-up period. All patients with persistence of untreatable dizziness underwent to imaging to exclude pathologies of the central nervous system. Distributions of continuous variables in different groups were analysed by T-student test parametric method. For categorical variables, comparisons were performed using Chi-square test with Yates correction and Fisher’s exact Test. Univariate and multivariate logistic regression analysis were performed. Odds ratios and 95% confidence intervals were calculated. Statistical significance was set at p < 0.05. Data were analysed using the R statistical software package, version 2.2.0. Informed consent was obtained from all participants.


During the study period, 165 patients were treated for BPPV at our institutions, but 17 patients were lost during follow-up. We conducted our analysis on 148 patients, 92 (62.2%) females and 56 (37.8%) males, average age 53 (s.d. = 13.9) and median age 53, who were recruited according to the inclusion criteria. 63.5% of cases were in the 40-64 age category. No spontaneous nystagmus was recorded. Residual dizziness was documented in 57.5% of the sample. Most of the cases (76.4%) had PSC involvement at clinical examination. Tinnitus was present in 23 subjects (15.5%). The audiometric test revealed a sensorineural hearing loss (SNHL) in 65 patients: 22 mild SNHL and 43 severe SNHL. Imaging performed in 25 patients with persistence of dizziness after retreatment excluded a central nervous system pathology. VEMPs were presents in all subjects complaining of residual dizziness or recurrent BPPV; the mean P1/N1 latency for c-VEMPs was 15.9/23.6 msec (SD 1.9/2.4); no latency or amplitude asymmetry was recorded with interaural difference under 30% (SD 5%). vHIT was also normal (absence of covert and/or overt saccades) in all patients with no asymmetric gain value recorded.

At least one episode of recurrence was documented during follow-up in 18 patients (12.2%), which statistically differed between the comparison group by age, canal re-entry and absence of liberatory nystagmus during the first session of treatment (Table I). In 65 patients, more than one manoeuvre was needed to obtain BPPV resolution.

The logistic regression model documented significant risk excess for recurrence of BPVV associated with age (OR = 1.063; C.I. = 1.014-1.12), while a significant high reduction associated with success of therapeutic manoeuvre (OR = 0.028; C.I. = 0.001-0.33).

In Table II, comparison between patients complaining residual dizziness (57.4%) and the ones without residual dizziness (42.6%) is shown. Female gender (p = 0.00), advanced age (p = 0.00), previous episodes of BPPV (p = 0.01), more than one manoeuvre for treatment (p = 0.00) and recurrence of BPPV (p = 0.00) explained the statistical difference between the two groups.

Among patients readmitted for residual dizziness following clinical vestibular examination, 36 were diagnosed with a subclinical BPPV, while only 2 patients had subclinical BPPV at follow-up in the group without RD (p = 0.00). No recurrence was detected in patients with subclinical BPPV who underwent retreatment of the same canal.


Residual dizziness is a frequent complaint of patients after treatment for BPPV, even if therapeutic success was achieved, which might be present in two-thirds of cases. Four theories have been hypothesised to explain the RD: 1) remaining otoconial debris due to incomplete repositioning that can produce soft positional vertigo, because the remaining debris are insufficient to deflect the cupula to a degree able to provoke overt nystagmus 12 13; 2) BPPV is not only a disorder of the semicircular canals, but also of otolith organs that sense orientation in the space, and otolith dysfunction might account for transient mild dizziness 14 15; 3) another vestibular lesion that is difficult to identify from history alone might coexist with BPPV, and the prevalence of less-specific dizziness was significantly higher in BPPV patients with additional peripheral or central vestibular dysfunction 16; 4) delayed recovery might be due to the longer time needed for central adaptation after particle repositioning.

The English literature also reports that patients with residual dizziness have higher anxiety scores than patients with no residual dizziness 8. Anxiety has been demonstrated to play a role in dizziness, and anxiety and dizziness are comorbid in a larger percentage of patients than would be expected from chance alone 17 18.

The vestibular system participates in autonomic regulation adjusting cardiovascular control during body movement and change in posture 19 20. Patients with BPPV occasionally experience postural light-headedness when righting from a sitting position, despite successful repositioning procedures 21; it is similar to orthostatic dizziness reported by patients with orthostatic hypotension 22.

One-third of patients with BPPV have some abnormality of autonomic system response as shown by orthostatic hypotension tilting test or blood pressure response during Valsalva manoeuvre; the rate of autonomic dysfunction is higher in patient with residual dizziness than in those without 23.

Residual dizziness was found to be related to duration of vertigo before repositioning manoeuvre. A longer duration of BPPV was associated with the presence of residual dizziness after the particle repositioning maneuver 7. In our observation, patients with more than one episode of BPPV in their history had a significantly increased risk to develop a RD, which is increased if the patient is more than 65 years of age. Our dataset showed that the elderly population has a generically high risk of BPPV recurrence, effectively confirming our previous results, where we described some risk factors (hypertension, diabetes, osteoporosis) that influence the high rate of recidivism in patients over 65 years 24. The increased prevalence in the elderly population is considered to be caused by changes in otoconia morphology, possibly related to vascular damage in the inner ear 25, although signs of inner ear aging such as tinnitus and hearing loss have showed no relationship with RD in our patients. Elderly patients affected by BPPV also complain of dizziness and unsteadiness instead of typical positional vertigo; this may be due to unconscious avoidance of positions provoking vertigo rather than decreased perception of vestibular stimuli related to otolith organ damage 26. Furthermore, in the elderly we found a reduced success rate of repositioning manoeuvres that may be linked to that chronic vascular damage of the inner ear and modification of otoconia. This reduced success rate of treatment was parallel to a significantly increased rate of RD in those patients, which leads to the consideration that some dispersed otolith into semicircular canals may play the main role in RD.

The responsibility of dispersed fragments of otolith could also be hypothesised by our observation that patients who underwent more than one repositioning manoeuvre in the same session had an increased risk to have RD in the post-manoeuvre period, as shown by logistic regression where the success of the manoeuvre reduced the recurrence rate.

In a previous report, we described the linkage of canal re-entry BPPV risk with number of manoeuvres, thinking that the otolith may be dispersed into canals 5. Although patients do not complain a true positional vertigo after treatment, they may have dizziness due to otolith fragment, the mass of which is not enough to elicit a true positional vertigo. Effectively, we noted a high percentage of subclinical BPPV in patients with RD, which after retreatment, even if nystagmus was not clinically evident, had resolution of dizziness 27 28. However, the RD may be linked not only with dispersed otolith (main cause of subclinical BPPV), but also with age, BPPV recurrence and absence of liberatory nystagmus that could predict the chance of RD as shown in our analysis. In our opinion, following the reported dataset, residual otoliths play a main role in determining post-manoeuvre RD that is often linked to subclinical BPPV; this conclusion is also supported by the high prevalence of BPPV recurrence in patients with RD, as confirmed in our analysis.


RD may be a long lasting complaint in patients treated for BPPV. The pathophysiology may be related with several diseases and comorbidities. Our study focused on dispersed otolith into semicircular canals as a risk factor for RD. The high prevalence of subclinical BPPV among patients readmitted for RD is one of the possible explanations. Advanced age and recurrence of BPPV may be predictive of post-treatment RD. However, more than half of patients with RD remain without an explanation of the likely cause, and warranting further studies.

Figures and tables

No recurrence Recurrence P-value
N 130 (%)87.8% N 18 (%)12.2%
Gender Male 48(85.7%) 8(14.3%) 0.7
Female 82(89.1%) 10(10.9%)
Age Average 52.7S.d. (13,94) 67.3s.d. (13,79) 0.006
Previous BPPV None 60(93.7%) 4(6.3%) 0.1
> 1 70(83.3%) 14(16.7%)
Number of CRM 1 76(91.6%) 7(8.4%) 0.2
> 1 54(83.1%) 11(16.9%)
Canal reentry No 126(89.4%) 15(10.6%) 0.04
Yes 4(57.1%) 3(42.9%)
Liberatory Ny No 1(25%) 3(75%) 0.006
Yes 129(89.6%) 15(10.4%)
Table I.Comparison between patients with and without recurrence. Age, canal reentry and presence of liberatory nystagmus were significant predictor of recurrence.
Residual dizzinessYes Residual dizzinessNo P-value
85 (%)57.4% 63 (%)42.6%
Gender Male 24(42.9%) 32(57.1%) 0.005
Female 61(66.3%) 31(33.7%)
Age Average 57S.d. (14,41) 47s.d. (10,78) 0.000001
Previous BPPV None 29(45.3%) 35(54.7%) 0.01
More than one 56(66.7%) 28(33.3%)
Numbers of manoeuvres One 34(41%) 49(59%) 0.000004
More than one 51(78.5%) 14(21.5%)
Liberatory Ny No 26(68.4%) 12(52.6%) 0,1
Yes 59(28.2%) 51(71.8%)
Canal reentry No 80(56.7%) 61(43.7%) 0.7
Yes 5(71.4%) 2(28.6%)
Success of manoeuvres No 4(100%) 0(0%) 0.1
Yes 81(56.3%) 63(43.7%)
Recurrence No 68(52.3%) 62(47.7%) 0.0005
Yes 17(94.4%) 1(5.6%)
Table II.Comparison between patients with and without persistence of dizzy symptoms after treatment; numbers of manoeuvres and recurrence were predictive of persistent dizziness.


  1. De Stefano A, Dispenza F, Citraro L. Are postural restrictions necessary for management of posterior canal benign paroxysmal positional vertigo?. Ann Otol Rhinol Laryngol. 2011; 120:460-4. DOI
  2. Riggio F, Dispenza F, Gallina S. Management of benign paroxysmal positional vertigo of lateral semicircular canal by Gufoni’s manoeuvre. Am J Otolaryngol. 2009; 30:106-11. DOI
  3. Dispenza F, Kulamarva G, De Stefano A.. Comparison of repositioning maneuvers for benign paroxysmal positional vertigo of posterior semicircular canal: advantages of hybrid maneuver. Am J Otolaryngol. 2012; 33:528-32. DOI
  4. Von Brevern M, Radtke A, Lezius F. Epidemiology of benign paroxysmal positional vertigo: a population based study. J Neurol Neurosurg Psychiatry. 2007; 78:710-5. DOI
  5. Dispenza F, De Stefano A, Costantino C. Canal switch and re-entry phenomenon in benign paroxysmal positional vertigo: difference between immediate and delayed occurrence. Acta Otolaryngol Ital. 2015; 35:116-20.
  6. Balatsouras DG, Korres SG. Subjective benign paroxysmal positional vertigo. Otolaryngol Head Neck Surg. 2012; 146:98-103. DOI
  7. Seok JI, Lee HM, Yoo JH. Residual dizziness after successful repositioning treatment in patients with benign paroxysmal positional vertigo. J Clin Neurol. 2008; 4:107-10. DOI
  8. Teggi R, Giordano L, Bondi S. Residual dizziness after successful repositioning maneuvers for idiopathic benign paroxysmal positional vertigo in the elderly. Eur Arch Otolaryngol. 2011; 268:507-11. DOI
  9. Janky KL, Patterson JN, Shepard NT. Effects of device on video head impulse test (vHIT) gain. J Am Acad Audiol. 2017; 28:778-85. DOI
  10. Herdman SJ. Advances in the treatment of vestibular disorders. Phys Ther. 1997; 77:602-18. DOI
  11. Yacovino DA, Hain TC, Gualtieri F.. New therapeutic maneuver for anterior canal benign paroxysmal positional vertigo. J Neurol. 2009; 256:1851-5. DOI
  12. Di Girolamo S, Paludetti G, Briglia G. Postural control in benign paroxysmal positional vertigo before and after recovery. Acta Otolaryngol. 1998; 118:289-93. DOI
  13. Di Girolamo S, Ottaviani F, Scarano E. Postural control in horizontal benign paroxysmal positional vertigo. Eur Arch Otolaryngol. 2000; 257:372-5. DOI
  14. Von Brevern M, Schmidt T, Schonfeld U. Utricular dysfunction in patients with benign paroxysmal positional vertigo. Otol Neurotol. 2006; 27:92-6.
  15. Gall RM, Ireland DJ, Robertson DD. Subjective visual vertical in patients with benign paroxysmal positional vertigo. J Otolaryngol. 1999; 28:162-5.
  16. Pollak L, Davies RA, Luxon LL. Effectiveness of the particle repositioning maneuver in benign paroxysmal positional vertigo with and without additional vestibular pathology. Otol Neurotol. 2002; 23:79-83.
  17. Furman JM, Jacob RG. Psychiatric dizziness. Neurology. 1997; 48:1161-6. DOI
  18. Jacob RG, Furman JM. Psychiatric consequences of vestibular dysfunction. Curr Opin Neurol. 2001; 14:41-6.
  19. Pezzoli M, Garzano M, Pecorari GC. Benign paroxysmal positional vertigo and orthostatic hypotension. Clin Auton Res. 2010; 20:27-31. DOI
  20. Yates BJ, Miller AD. Properties of sympathetic reflexes elicited by natural vestibular stimulation: implication for cardiovascular control. J Neurophysiol. 1994; 71:2087-92. DOI
  21. Magliulo G, Bertin S, Ruggieri M. Benign paroxysmal positional vertigo and post-treatment quality of life. Eur Arch Otolaryngol. 2005; 262:627-30. DOI
  22. Kim HA, Lee H, Park KJ. Autonomic dysfunction in patients with orthostatic dizziness: validation of orthostatic grading scale and comparison of Valsalva maneuver and head-up tilt testing results. J Neuro Sci. 2013; 325:61-6. DOI
  23. Kim HA, Lee H.. Autonomic dysfunction as a possible cause of residual dizziness after successful treatment in benign paroxysmal positional vertigo. Clin Neurophysiol. 2014; 125:608-14. DOI
  24. De Stefano A, Dispenza F, Suarez H. A multicenter observational study on the role of comorbidities in the recurrent episodes of benign paroxysmal positional vertigo. Auris Nasus Larynx. 2014; 41:31-6. DOI
  25. Yang YS, Hwang CH, Shin JY. Age-related changes on the morphology of otoconia. Laryngoscope. 2006; 116:996-1001. DOI
  26. Oghalai JS, Manolidis S, Barth JL. Unrecognized benign paroxysmal positional vertigo in elderly patients. Otolaryngol Head Neck Surg. 2000; 122:630-4. DOI
  27. Albera A, Boldreghini M, Canale A. Vertigo returning to the sitting position after the Semont manoeuvre. Is it a prognostic symptom?. Acta Otorhinolaryngol Ital. 2018; 38:145-50. DOI
  28. Casani AP, Cerchiai N, Navari E.. Paroxysmal positional vertigo despite complete vestibular impairment: the role of instrumental assessment. Acta Otorhinolaryngol Ital. 2018; 38:563-8. DOI


F. Dispenza

UOC Otorinolaringoiatria, AOU Policlinico P. Giaccone, Palermo, Italy, Istituto Euro-Mediterraneo di Scienza e Tecnologia - IEMEST, Palermo, Italy

W. Mazzucco

Department of Science for Health Promotion and Mother and Child Care G. D’Alessandro; University of Palermo, Italy

S. Mazzola

Clinical Epidemiology and Cancer Registry Operative Unit, University Hospital Policlinico “Paolo Giaccone”, Palermo, Italy

F. Martines

Dipartimento Biomedicina e Neuroscienze Cliniche, Università degli Studi di Palermo, Italy


© Società Italiana di Otorinolaringoiatria e Chirurgia Cervico Facciale , 2019

  • Abstract viewed - 4875 times
  • PDF downloaded - 1627 times