- Department of Neurosurgery, San Filippo Neri Hospital/ASL Roma 1, Rome, Italy,
- Department of Neurosurgery, Federal Center of Neurosurgery, Tyumen Oblast, Russian Federation,
- Department of Neurosurgery, The State Education Institution of Higher Professional Training, The First Sechenov Moscow State Medical University under Ministry of Health, Russian Federation.
Correspondence Address:
Luciano Mastronardi
Department of Neurosurgery, Federal Center of Neurosurgery, Tyumen Oblast, Russian Federation,
Department of Neurosurgery, The State Education Institution of Higher Professional Training, The First Sechenov Moscow State Medical University under Ministry of Health, Russian Federation.
DOI:10.25259/SNI_702_2020
Copyright: © 2020 Surgical Neurology International This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.How to cite this article: Luciano Mastronardi1,3, Franco Caputi1, Guglielmo Cacciotti1, Carlo Giacobbo Scavo1, Raffaelino Roperto1, Albert Sufianov2,3. Microvascular decompression for typical trigeminal neuralgia: Personal experience with intraoperative neuromonitoring with level-specific-CE-Chirp® brainstem auditory evoked potentials in preventing possible hearing loss. 11-Nov-2020;11:388
How to cite this URL: Luciano Mastronardi1,3, Franco Caputi1, Guglielmo Cacciotti1, Carlo Giacobbo Scavo1, Raffaelino Roperto1, Albert Sufianov2,3. Microvascular decompression for typical trigeminal neuralgia: Personal experience with intraoperative neuromonitoring with level-specific-CE-Chirp® brainstem auditory evoked potentials in preventing possible hearing loss. 11-Nov-2020;11:388. Available from: https://surgicalneurologyint.com/surgicalint-articles/10385/
Abstract
Background: Permanent hearing loss after posterior fossa microvascular decompression (MVD) for typical trigeminal neuralgia (TTN) is one of the possible complications of this procedure. Intraoperative brainstem auditory evoked potentials (BAEPs) are used for monitoring the function of cochlear nerve during cerebellopontine angle (CPA) microsurgery. Level-specific (LS)-CE-Chirp® BAEPs are the most recent evolution of classical click BAEP, performed both in clinical studies and during intraoperative neuromonitoring (IONM) of acoustic pathways during several neurosurgical procedures.
Methods: Since February 2016, we routinely use LS-CE-Chirp® BAEPs for monitoring the function of cochlear nerve during CPA surgery, including MVD for trigeminal neuralgia. From September 2011 to December 2018, 71 MVDs for TTN were performed in our department, 47 without IONM of acoustic pathways (Group A), and, from February 2016, 24 with LS-CE-Chirp BAEP (Group B).
Results: Two patients of Group A developed a permanent ipsilateral anacusia after MVD. In Group B, we did not observe any permanent acoustic deficit after surgery. In one case of Group B, during arachnoid dissection, intraoperative LS-CE-Chirp BAEP showed a temporary lag of V wave, resolved in 5 min after application of intracisternal diluted papaverine (0.3% solution without excipients).
Conclusion: MVD is widely considered a definitive surgical procedure in the management of TTN. Even though posterior fossa MVD is a safe procedure, serious complications might occur. In particular, the use of IONM of acoustic pathways during MVD for TTN might contribute to prevention of postoperative hearing loss.
Keywords: Brainstem auditory evoked potentials, Hearing preservation, Level-specific-CE-Chirp stimuli, Microvascular decompression, Retrosigmoid approach, typical trigeminal neuralgia
INTRODUCTION
Typical trigeminal neuralgia (TTN) is characterized by severe temporary facial pain in the distribution of the trigeminal nerve that is unilateral, paroxysmal, provokable, and without sensory loss.[
Microvascular decompression (MVD) is the most effective treatment for patients with TTN. The success rate ranges from 80% to 90% and postoperative mortality is 0.1% (0.02–0.2).[
Using of intraoperative neuromonitoring (IONM) with brainstem auditory evoked potentials (BAEP) and avoiding of impairment of the acoustic nerve might contribute to the prevention of the postoperative hearing impairment.[
In particular, LS-CE-Chirp® BAEPs seem to be the fastest noninvasive monitoring technique of cochlear nerve in cerebellopontine angle (CPA) and skull base surgery.[
We report our preliminary experience with IONM of acoustic pathways with BAEP evoked with LS-CE-Chirp for minimizing hearing loss associated with MVD for TTN, comparing the results with those a previous series operated on without any cochlear nerve monitoring.
MATERIALS AND METHODS
From September 2011 to December 2018, 71 patients with TTN were operated on with MVD by retrosigmoid (RS) approach. The patients were divided into two groups: forty-seven patients operated on without IONM of acoustic pathways (Group A) and 24 patients intraoperatively monitored with LS-CE-Chirp BAEP (Group B).
Patients included in this study had socially useful hearing. In particular, selection criteria were pure tone audiogram better than 50 dB loss and speech discrimination score better than 50% (50/50 criterion; AAO-HNS Class A-B).[
LS-CE-Chirp BAEPs are currently used by neuro-otological unit of our hospital and approved from Internal Ethics Committee for neurosurgical intraoperative monitoring too. For this reason, we did not request the approval for this retrospective observational study.
According to the International Headache Society,[ Paroxysmal attacks lasting from few second to maximum 2 min Distribution of severe intensity pain along one or more trigeminal divisions Quality of pain: sudden, burning or stabbing, intense, sharp, and superficial Precipitation from trigger points or by definite daily activities No symptoms between the attacks Absence of neurological deficits Exclusion of other possible causes of facial pain Positive response to carbamazepine.
Magnetic resonance imaging was performed in all cases for searching possible neurovascular conflict with the root entry zone (REZ) of trigeminal nerve. Patients who had previous MVD or who were classified as American Society of Anesthesiologists (ASA) Grade III or higher were excluded from the study.
The operative outcomes are subjectively considered to be: (a) excellent (complete relief), if patients became pain free; (b) good (partial relief), if patients tolerated the pain well with medications or referred mild pain not requiring medications; and (c) poor, if patients had minimal or no relief from TTN or presented neurological deficits (even if not severe).
Surgical procedure
Patients were operated on in lateral position, under general anesthesia. The RS craniectomy was approximately 3 squared-cm, with exposition of sigmoid and transverse sinuses. Dura mater was opened and CSF was slowly released from arachnoid upper part of CPA cistern, to obtain cerebellar decompression. Using microneurosurgical technique and instruments, the arachnoid surrounding the trigeminal nerve was opened sharply. The entire cisternal part of the nerve was exposed from the REZ. Conflicting vessels were gently dissected and moved away from the nerve; among them, small pieces of Teflon were inserted to prevent relapse of the compression. Small pieces of fibrillary surgical and gel foam were placed around and fibrin glue was applied for fixing the vessel in the new position. The superior petrosal vein (SPV) and its main branches were protected and spared. The dura was closed accurately and the bone reapplied with miniplates and miniscrews.
IONM of cochlear nerve in Group B
Since February 2016, we routinely use LS-CE-Chirp® BAEP (Nicolet Viking III, Viasys HealthCare, Madison USA/ Hochberg, Germany) for monitoring the function of cochlear nerve during CPA surgery, including MVD for TTN. BAEPs evoked with LS-CE-Chirp® (Interacoustics Eclipse-EP15 ABR system) provide enhanced neural synchronicity and faster detection of larger amplitude wave V.[
Each patient received a BAEP audiometry immediately before surgery. BAEPs were evoked with LS-CE-Chirp® stimuli by means subdermal needles or surface electrodes placed at the vertex (Cz) and on each earlobe (A1 and A2).
Sound pressure ranged between 60 dB and 100 dB HL. Contralateral ear was masked with noise at 50 dB HL. During arachnoidal dissection around 5th, 7th, and 8th nerves and vessels, on surgeon’s request, one or more series of 400–1200 acoustic stimuli were performed.
RESULTS
General data
The mean age of the entire cohort was 59.8 ± 5.4 years (range, 40–84 years). There were 22 men and 49 women. There were not relevant differences in the mean age and sex distribution between Groups A and B. All patients were in ASA Grade I or II.
The second and third branches of trigeminal nerve were affected most frequently in both cohorts. The superior cerebellar artery (SCA), alone or in association with other vessels, was the dominant conflicting vessel in 62 cases (87.3%), without relevant differences between Groups A and B. Other vessels involved alone or coinvolved were anterior-inferior cerebellar artery (AICA) in eight cases, the vertebral artery in three, and the petrosal vein in one patient.
Outcome: Pain control
At a mean follow-up 28.5 ± 5.3 months (range, 10 months–7 years), 63 patients (88.7%) had good pain outcome without necessity of any medication for pain. A total of 7 patients (9.9%) experienced recurrence of pain during the follow-up. An 84-year-old woman died 6 months after surgery for basal ganglia spontaneous cerebral hemorrhage.
Complications
Surgical mortality was zero in both cohorts. Headaches, nausea, and vomiting were minor and transient complications after surgery equally distributed in both groups, successfully treated with symptomatic medical therapy. One patient had CSF leak repaired with conservative treatment and one had small cerebellar hematoma gradually reabsorbed.
Hearing outcome
Two patients of Group A developed a permanent ipsilateral anacusia after MVD (AAO-HNS Class D).[
No one of the patients of Group B had a postoperative permanent reduction of hearing or anacusia. In a 62-year old man, intraoperative BAEP showed a lag of V wave of 1 ms during arachnoid dissection, likely due to vasospasm of internal auditory artery (IAA) probably caused by arachnoid tractions. Intracisternal injection of pure papaverine without excipients (60 mg/2 ml), diluted in 20 cc of 0.9% saline solution, was used as a direct treatment of vasospasm.[
DISCUSSION
According to Love and Coakham (2001), the segmental demyelination of trigeminal sensory nerve at the entry point in the brainstem is the cause of idiopathic TTN; the demyelination is usually related to chronic compression of the nerve root where it comes out from the pons.[
The first line of treatment is medical therapy, usually carbamazepine or other similar antiepileptic drugs. In addition, ablative procedures are as glycerol injections, radiosurgery, and radiofrequency rhizotomy.[
In their large systematic review on 6847 MVDs performed for TTN, Xia et al. (2014) reported a success rate of 83.5%, a surgical mortality of 0.1%, and some possible complications as facial numbness (9.1%), facial palsy (2.9%), CSF leak (1.6%), and incisional infection (1.3%). In particular, hearing deficits may occur in 1.9% (0.2–3.9%).[
IONM is very useful for reducing the incidence of SNHL after MVD. In a retrospective study evaluating the length of cerebellar retraction and the changes of intraoperative BAEP during MVD, Lee et al.[
By means transcranial Doppler ultrasonography assistance, Qi et al. (2015)[
The treatment and prevention of vasospasm could minimize the possible vascular injuries of acoustic nerve. After inducing mechanically vasospasm of IAA in animal model, Morawski et al. demonstrated how topical diluted papaverine (PPV) influenced successfully the distortion of otoacoustic emissions.[
Among several existing monitoring methods, intraoperative BAEP is useful and reliable for the preservation of hearing function in patients undergoing MVD, as suggested by many authors. The American Clinical Neurophysiology Society and American Society of Neurophysiological Monitoring recommend to alert the surgeon when significant changes in BAEP occur, especially when wave V latency increases ≥ 1.0 ms and/or amplitude decreases ≥50%.[
Level-specific (LS) CE-Chirp® BAEPs are the most recent evolution of classical click BAEP, performed both in clinical studies and IONM of acoustic pathways during several neurosurgical procedures.[
LS-CE-Chirp® BAEPs are currently in our department used since 2016, for IONM of cochlear nerve during CPA surgery, including MVD for TTN. On comparing 47 MVDs for TTN without IONM of acoustic pathways (Group A) and 24 with LS-CE-Chirp BAEP (Group B), we observed that two patients of Group A experienced a postoperative permanent ipsilateral anacusia, whereas in Group B, no one of the patients had a permanent acoustic impairment after MVD. In one case, during arachnoid dissection, intraoperative IONM showed a transient elongation of V wave, resolved 5 min after the application of intracisternal diluted PPV (0.3% solution without excipients).[
CONCLUSION
MVD represents the definitive microsurgical procedure for curing TTN. Even though it is widely considered a safe procedure, SNHL and other complications might occur. The use of IONM of cochlear nerve might contribute to prevent postoperative hearing deficits.
Ethical approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee (name of institute/committee) and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Declaration of patient consent
Patient’s consent not required as patients identity is not disclosed or compromised.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References
1. Bartindale M, Kircher M, Adams W, Balasubramanian N, Liles J. Hearing loss following posterior fossa microvascular decompression: A systematic review. Otolaryngol Head Neck Surg. 2018. 158: 62-75
2. Bennett L, Patel NK, Fuller G. Trigeminal neuralgia and its management. BMJ. 2007. 334: 201-5
3. Chadwick GM, Asher AL, van der Veer CA, Pollard RJ. Adverse effects of topical papaverine on auditory nerve function. Acta Neurochir (Wien). 2008. 150: 901-9
4. Chen GQ, Wang XS, Wang L, Zheng JP. Arterial compression of nerve is the primary cause of trigeminal neuralgia. Neurol Sci. 2014. 35: 61-6
5. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Headache classification committee of the international headache society. Cephalalgia. 1988. 8: 1-96
6. . American academy of otolaryngology-head and neck surgery foundation, INC. Otolaryngol Head Neck Surg. 1995. 113: 179-80
7. di Scipio E, Mastronardi L. CE-Chirp® ABR in cerebellopontine angle surgery neuromonitoring: Technical assessment in four cases. Neurosurg Rev. 2015. 38: 381-4
8. Hou SM, Seaber AV, Urbaniak JR. Relief of blood-induced arterial vasospasm by pharmacologic solutions. J Reconstr Microsurg. 1987. 3: 147-51
9. Kabatas S, Albayrak SB, Cansever T, Hepgul KT. Microvascular decompression as a surgical management for trigeminal neuralgia: A critical review of the literature. Neurol India. 2009. 57: 134-8
10. Lee MH, Lee HS, Jee TK, Jo KI, Kong DS, Lee JA. Cerebellar retraction and hearing loss after microvascular decompression for hemifacial spasm. Acta Neurochir (Wien). 2015. 157: 337-43
11. Lemos L, Alegria C, Oliveira J, Machado A, Oliveira P, Almeida A. Pharmacological versus microvascular decompression approaches for the treatment of trigeminal neuralgia: Clinical outcomes and direct costs. J Pain Res. 2011. 4: 233-44
12. Love S, Coakham HB. Trigeminal neuralgia: Pathology and pathogenesis. Brain. 2001. 124: 2347-60
13. Lunsford LD, Apfelbaum RI. Choice of surgical therapeutic modalities for treatment of trigeminal neuralgia: Microvascular decompression, percutaneous retrogasserian thermal, or glycerol rhizotomy. Clin Neurosurg. 1985. 32: 319-33
14. Mastronardi L Caputi F, Rinaldi A, Cacciotti G, Roperto R, Scavo CG. Typical trigeminal neuralgia: Comparison of results between patients older and younger than 65 years operated on with microvascular decompression by retrosigmoid approach. J Neurol Surg A Cent Eur Neurosurg. 2020. 81: 28-32
15. Mastronardi L, di scipio E, Cacciotti G, Roperto R, Scavo CG. Hearing preservation after removal of small vestibular schwannomas by retrosigmoid approach: Comparison of two different ABR neuromonitoring techniques. Acta Neurochir (Wien). 2019. 161: 69-78
16. Mastronardi L, di scipio E, Cacciotti G, Roperto R. Vestibular schwannoma and hearing preservation: Usefulness of level specific CE-Chirp ABR monitoring. A retrospective study on 25 cases with preoperative socially useful hearing. Clin Neurol Neurosurg. 2018. 165: 108-15
17. Morawski K, Telischi FF, Merchant F, Namyslowski G, Lisowska G, Lonsbury-Martin BL. Preventing internal auditory artery vasospasm using topical papaverine: An animal study. Otol Neurotol. 2003. 24: 918-26
18. Park K, Hong SH, Hong SD, Cho YS, Chung WH, Ryu NG. Patterns of hearing loss after microvascular decompression for hemifacial spasm. J Neurol Neurosurg Psychiatry. 2009. 80: 1165-7
19. Qi J, Jia W, Zhang L, Zhang J, Wu Z. Risk factors for postoperative cerebral vasospasm after surgical resection of acoustic neuroma. World Neurosurg. 2015. 84: 1686-90
20. Scavo CG, Roperto R, Cacciotti G, Corrivetti F, Mastronardi L. Prophylactic effect of topical diluted papaverine in preventing hearing loss during microvascular decompression for typical trigeminal neuralgia: Case report and technical note. Interdiscip Neurosurg. 2019. 15: 11-4
21. Takeda M, Tsuboi Y, Kitagawa J, Nakagawa K, Iwata K, Matsumoto S. Potassium channels as a potential therapeutic target for trigeminal neuropathic and inflammatory pain. Mol Pain. 2011. 7: 5
22. Thirumala PD, Carnovale G, Loke Y, Habeych ME, Crammond DJ, Balzer JR. Brainstem auditory evoked potentials’ diagnostic accuracy for hearing loss: Systematic review and meta-analysis. J Neurol Surg B Skull Base. 2017. 78: 43-51
23. Tomasello F, Esposito F, Abbritti RV, Angileri FF, Conti A, Cardali SM. Microvascular decompression for trigeminal neuralgia: Technical refinement for complication avoidance. World Neurosurg. 2016. 94: 26-31
24. Vargas CR, Iorio ML, Lee BT. A systematic review of topical vasodilators for the treatment of intraoperative vasospasm in reconstructive microsurgery. Plast Reconstr Surg. 2015. 136: 411-22
25. Xia L, Zhong J, Zhu J, Wang YN, Dou NN, Liu MX. Effectiveness and safety of microvascular decompression surgery for treatment of trigeminal neuralgia: A systematic review. J Craniofac Surg. 2014. 25: 1413-7
26. Ying T, Thirumala P, Gardner P, Habeych M, Crammond D, Balzer J. The incidence of early postoperative conductive hearing loss after microvascular decompression of hemifacial spasm. J Neurol Surg B Skull Base. 2015. 76: 411-5
27. Zhou X, Alambyan V, Ostergard T, Pace J, Kohen M, Manjila S. Prolonged intracisternal papaverine toxicity: Index case description and proposed mechanism of action. World Neurosurg. 2018. 109: 251-7