- Global Neurosurgical Alliance, Tucson, Arizona, USA
- Karachi Medical and Dental College, Karachi, Pakistan
- College of Medicine, The University of Arizona College of Medicine-Phoenix, USA
- College of Medicine, The University of Arizona College of Medicine-Tucson, USA
- Department of Neurosurgery, University of Arizona, Tucson, Arizona, USA.
Correspondence Address:
Albert Alan, Department of Neurosurgery, University of Arizona, Tucson, Arizona, United States.
DOI:10.25259/SNI_286_2024
Copyright: © 2024 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, transform, 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: Areeba Fareed1,2, Zoha Iftikhar1,2, Ramsha Haider1,2, Safa Irfan Shah1,2, Michelle Ennabe1,3, Albert Alan1,4,5, Martin Weinand4,5. Awake neurosurgery: Advancements in microvascular decompression for trigeminal neuralgia. 28-Jun-2024;15:215
How to cite this URL: Areeba Fareed1,2, Zoha Iftikhar1,2, Ramsha Haider1,2, Safa Irfan Shah1,2, Michelle Ennabe1,3, Albert Alan1,4,5, Martin Weinand4,5. Awake neurosurgery: Advancements in microvascular decompression for trigeminal neuralgia. 28-Jun-2024;15:215. Available from: https://surgicalneurologyint.com/surgicalint-articles/12970/
Abstract
Background: The treatment landscape for trigeminal neuralgia (TN) involves various surgical interventions, among which microvascular decompression (MVD) stands out as highly effective. While MVD offers significant benefits, its success relies on precise surgical techniques and patient selection. In addition, the emergence of awake surgery techniques presents new opportunities to improve outcomes and minimize complications associated with MVD for TN.
Methods: A thorough review of the literature was conducted to explore the effectiveness and challenges of MVD for TN, as well as the impact of awake surgery on its outcomes. PubMed and Medline databases were searched from inception to March 2024 using specific keywords “Awake Neurosurgery,” “Microvascular Decompression,” AND “Trigeminal Neuralgia.” Studies reporting original research on human subjects or preclinical investigations were included in the study.
Results: This review highlighted that MVD emerges as a highly effective treatment for TN, offering long-term pain relief with relatively low rates of recurrence and complications. Awake surgery techniques, including awake craniotomy, have revolutionized the approach to MVD, providing benefits such as reduced postoperative monitoring, shorter hospital stays, and improved neurological outcomes. Furthermore, awake MVD procedures offer opportunities for precise mapping and preservation of critical brain functions, enhancing surgical precision and patient outcomes.
Conclusion: The integration of awake surgery techniques, particularly awake MVD, represents a significant advancement in the treatment of TN. Future research should focus on refining awake surgery techniques and exploring new approaches to optimize outcomes in MVD for TN.
Keywords: Awake craniotomy, Awake surgery, Microvascular decompression, Surgical precision, Trigeminal neuralgia
INTRODUCTION
Trigeminal neuralgia (TN), or tic douloureux, is a neurological disorder that causes sudden and intense pain in the trigeminal nerve distribution. The pain usually lasts a few seconds to a few minutes and is triggered by sensory stimuli or specific facial movements.[
Microvascular decompression (MVD) stands as the pinnacle of surgical intervention for classic TN, earning its reputation as the “gold standard” procedure. MVD involves meticulous exploration using microscopes or endoscopes to identify and alleviate compression on the trigeminal nerve caused by adjacent blood vessels or structures. A crucial aspect of MVD entails placing a cushioning material between the compressing vessel and the trigeminal nerve root to alleviate the pressure and subsequent pain.[
Studies conducted across multiple centers have consistently demonstrated the safety and efficacy of MVD in providing relief to TN patients. Pain relief rates following MVD have been reported to range impressively from 80% to 96%, highlighting its effectiveness in managing TN-associated facial pain.[
The advent of awake surgery presents a notable advancement in the field of MVD. Awake MVD offers several advantages, including real-time patient feedback during the procedure, confirming the effectiveness of decompression, and minimizing risks associated with general anesthesia, particularly in vulnerable patient populations. During awake MVD, patients are typically under local anesthesia with sedation, allowing neurosurgeons to interact with them throughout the procedure. This facilitates immediate feedback on any changes in symptoms, ensuring precise and tailored intervention to address TN-associated pain effectively.[
MATERIALS AND METHODS
A comprehensive review of the literature was carried out on PubMed and Medline databases, focusing on studies exploring the application of terms such as “Awake Neurosurgery,” “Awake craniotomy,” “Conscious sedation,” along with “Microvascular Decompression,” and “Trigeminal Neuralgia.” Only complete manuscripts reporting original studies involving human subjects or preclinical research and published until 2023, were considered for inclusion.
BRIEF HISTORY OF MVD
In 1934, Dr. Walter E. Dandy discovered that compression on the trigeminal nerve root was caused by a superior cerebellar artery (SCA) loop in 30.7% of cases and by a branch of the petrosal vein in 14% of cases.[
In 1959, Dr. W. James Gardner and his colleagues adopted this approach and conducted a study on the decompression of the sensory root of the trigeminal nerve. They accomplished this by selectively sectioning the posterior lateral part of the nerve. The study found that this approach resulted in significant improvement in pain relief for patients suffering from TN.[
During his observations, Jannetta noticed the SCA pulsating and crushing the trigeminal nerve root, which he believed was the cause of the tic. He also proposed that treating vascular cross-compression could have therapeutic benefits. Jannetta explained his neurovascular compression (NVC) theory and suggested that decompressing the nerve in a non-traumatic way could potentially cure the disease without causing facial weakness.[
A few months later, Jannetta and Rand performed the first MVD for TN, which was successful and provided permanent pain relief to the patient.[
SUPERIOR LONG-TERM EFFICACY OF MVD COMPARED TO OTHER TREATMENTS
MVD is significantly more effective than other forms of treatment for TN in the long run. When performed by experienced surgeons, MVD not only swiftly alleviates pain but also exhibits relatively low rates of recurrence and complications. As the leading surgical option for treating TN, MVD is associated with better long-term success rates and reduced chances of recurrence despite offering only partial relief.[
The method of managing MVD involves a surgical procedure designed to locate and relieve the pressure that the surrounding vascular structures are exerting on the trigeminal nerve. A tiny craniotomy allows the neurosurgeon to access the root entry zone (REZ) of the trigeminal nerve, where vascular compression frequently takes place. Using microsurgical techniques, the offending vessels are carefully dissected and padded with a Teflon felt or other suitable material to prevent further compression.[
The outcomes of MVD are remarkable, with many patients experiencing significant and sustained pain relief following the procedure. However, complications associated with MVD are also a point of concern and require careful consideration before opting for this treatment. The surgical procedure can be complex, requiring precision and expertise to navigate the delicate structures in the posterior fossa. Potential complications, although relatively low, include cerebrospinal fluid leakage, hearing loss, facial weakness, and infection. In addition, variability in outcomes poses a significant hurdle, with some patients experiencing suboptimal pain relief or recurrence of symptoms over time.[
HOW AWAKE SURGERY CHANGES THE LANDSCAPE OF MVD
The advent of awake surgery heralds numerous benefits, with the foremost being the optimization of tumor resection while preserving neurological function. Awake craniotomy offers a range of advantages, including a reduced necessity for postoperative monitoring in the Intensive Care Unit (ICU), leading to shorter or even eliminated ICU stays.[
In addition, postoperative discomfort, such as pain, nausea, and vomiting, is diminished in awake craniotomy compared to procedures conducted under general anesthesia.[
Moreover, comparative studies between awake and asleep surgeries demonstrate a higher quantity of total resections achievable through awake craniotomy, contributing to an increased extent of resection (EOR).[
In an investigation, Gubian and Rosahl’s meta-analysis unveiled promising success rates for both MVD at 86.9% and radiosurgery at 71.1%.[
The landscape of surgery undergoes a significant shift with the integration of awake procedures, as demonstrated by a recent study on TN. Abdulrauf et al. introduce a groundbreaking approach by demonstrating the feasibility of conducting awake MVD for TN. They suggest that within the framework of awake surgery, individuals who undergo MVD and experience persistent symptoms may benefit from additional insights gained during the awake phase.[
According to a study, it was observed that, except for Teflon granuloma, all other issues primarily arise due to the absence of intraoperative neurophysiological indicators that could promptly alert surgeons to suboptimal decompression during the surgery itself, thereby mitigating recurrences and the need for further interventions.[
FUTURE DIRECTIONS AND CHALLENGES OF AWAKE MVD FOR TN
The developments and challenges in awake craniotomy techniques may also apply to awake surgery for MVD in treating TN.[
New treatments such as targeted ultrasound provide fresh approaches to managing TN and have shown encouraging early outcomes in preclinical research. Targeted ultrasound relieves pain without requiring invasive surgery using precisely focused ultrasound waves to ablate the target tissue.[
Moreover, given the continuous progress in surgical methods and technology, it is clear that further investigation and refinement of endoscope-assisted procedures may be necessary in the future directions of MVD for TN. This means that there is a need to investigate further and refine the use of endoscopes alongside traditional operating microscopes in MVD procedures.[
Challenges persist in MVD for TN as not all patients experience successful outcomes, with varied rates of pain relief and symptom recurrence. Factors influencing recurrence include pain location, gender, and vascular compression. However, other factors such as age, onset side, disease duration, and recurrence show partial relevance and lack statistical significance.[
CONCLUSION
The integration of awake surgery techniques, particularly awake MVD, represents a significant advancement in the treatment of TN. By optimizing surgical precision and patient safety, awake surgery techniques have the potential to enhance the success rates of MVD and improve patient outcomes. Despite these advancements, challenges remain in the field of MVD for TN. Variability in patient responses and the need for further refinement of surgical methods pose ongoing challenges. In addition, the identification of optimal anesthetic approaches for awake MVD and the integration of newer technologies, such as targeted ultrasound, require further investigation.
Future research should focus on refining awake surgery techniques and exploring new approaches to optimize outcomes in MVD for TN. Multidisciplinary collaboration and continued advancements in surgical methods and technology are essential for addressing the complexities of TN management and improving patient care.
Ethical approval
The Institutional Review Board approval is not required.
Declaration of patient consent
Patient’s consent was not required as there are no patients in this study.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.
Disclaimer
The views and opinions expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Journal or its management. The information contained in this article should not be considered to be medical advice; patients should consult their own physicians for advice as to their specific medical needs.
References
1. Abdeen K, Kato Y, Kiya N, Yoshida K, Kanno T. Neuroendoscopy in microvascular decompression for trigeminal neuralgia and hemifacial spasm: Technical note. Neurol Res. 2000. 22: 522-6
2. Abdulrauf SI, Urquiaga JF, Patel R, Albers JA, Sampat VB, Baumer M. Awake Microvascular decompression for trigeminal neuralgia: Concept and initial results [published correction appears in World Neurosurg 2019;131:80]. World Neurosurg. 2018. 113: e309-13
3. Allam AE, Khalil AA, Eltawab BA, Wu WT, Chang KV. Ultrasound-guided intervention for treatment of trigeminal neuralgia: An updated review of anatomy and techniques. Pain Res Manag. 2018. 2018: 5480728
4. Bendtsen L, Zakrzewska JM, Abbott J, Braschinsky M, Di Stefano G, Donnet A. European Academy of neurology guideline on trigeminal neuralgia. Eur J Neurol. 2019. 26: 831-49
5. Berger I, Nayak N, Schuster J, Lee J, Stein S, Malhotra NR. Microvascular decompression versus stereotactic radiosurgery for trigeminal neuralgia: A decision analysis. Cureus. 2017. 9: e1000
6. Bina RW, Palsma RS, Weinand ME, Kasoff WS. Peripheral nerve stimulation for refractory trigeminal pain: Recent single-institution case series with long-term follow-up and review of the literature. Neuromodulation. 2020. 23: 796-804
7. Bohman LE, Pierce J, Stephen JH, Sandhu S, Lee JY. Fully endoscopic microvascular decompression for trigeminal neuralgia: Technique review and early outcomes. Neurosurg Focus. 2014. 37: E18
8. Brown T, Shah AH, Bregy A, Shah NH, Thambuswamy M, Barbarite E. Awake craniotomy for brain tumor resection: The rule rather than the exception?. J Neurosurg Anesthesiol. 2013. 25: 240-7
9. Charalampaki P, Kafadar AM, Grunert P, Ayyad A, Perneczky A. Vascular decompression of trigeminal and facial nerves in the posterior fossa under endoscope-assisted keyhole conditions. Skull Base. 2008. 18: 117-28
10. Cruccu G, Finnerup NB, Jensen TS, Scholz J, Sindou M, Svensson P. Trigeminal neuralgia: New classification and diagnostic grading for practice and research. Neurology. 2016. 87: 220-8
11. Dandy WE. Concerning the case of trigeminal neuralgia. Am J Surg. 1934. 24: 447-55
12. De Toledo IP, Conti Réus J, Fernandes M, Porporatti AL, Peres MA, Takaschima A. Prevalence of trigeminal neuralgia: A systematic review. J Am Dent Assoc. 2016. 147: 570-6.e2
13. Eseonu CI, Rincon-Torroella J, ReFaey K, Lee YM, Nangiana J, Vivas-Buitrago T. Awake craniotomy vs craniotomy under general anesthesia for perirolandic Gliomas: Evaluating perioperative complications and extent of resection. Neurosurgery. 2017. 81: 481-9
14. Gamaleldin OA, Donia MM, Elsebaie NA, Abdelkhalek Abdelrazek A, Rayan T, Khalifa MH. Role of fused three-dimensional time-of-flight magnetic resonance angiography and 3-dimensional T2-weighted imaging sequences in neurovascular compression. World Neurosurg. 2020. 133: e180-6
15. Gardner WJ, Miklos MV. Response of trigeminal neuralgia to “decompression” of sensory root; discussion of cause of trigeminal neuralgia. JAMA. 1959. 170: 1773-6
16. Gentilini A, Schaniel C, Morari M, Bieniok C, Wymann R, Schnider T. A new paradigm for the closed-loop intraoperative administration of analgesics in humans. IEEE Trans Biomed Eng. 2002. 49: 289-99
17. Ghazanwy M, Chakrabarti R, Tewari A, Sinha A. Awake craniotomy: A qualitative review and future challenges. Saudi J Anaesth. 2014. 8: 529-39
18. Groshev A, Padalia D, Patel S, Garcia-Getting R, Sahebjam S, Forsyth PA. Clinical outcomes from maximum-safe resection of primary and metastatic brain tumors using awake craniotomy. Clin Neurol Neurosurg. 2017. 157: 25-30
19. Gubian A, Rosahl SK. Meta-analysis on safety and efficacy of microsurgical and radiosurgical treatment of trigeminal neuralgia. World Neurosurg. 2017. 103: 757-67
20. Hao YB, Zhang WJ, Chen MJ, Chai Y, Zhang WH, Wei WB. Sensitivity of magnetic resonance tomographic angiography for detecting the degree of neurovascular compression in trigeminal neuralgia. Neurol Sci. 2020. 41: 2947-51
21. Hervey-Jumper SL, Berger MS. Technical nuances of awake brain tumor surgery and the role of maximum safe resection. J Neurosurg Sci. 2015. 59: 351-60
22. Hervey-Jumper SL, Li J, Lau D, Molinaro AM, Perry DW, Meng L. Awake craniotomy to maximize glioma resection: Methods and technical nuances over a 27-year period. J Neurosurg. 2015. 123: 325-39
23. Holste K, Chan AY, Rolston JD, Englot DJ. Pain outcomes following microvascular decompression for drug-resistant trigeminal neuralgia: A systematic review and meta-analysis. Neurosurgery. 2020. 86: 182-90
24. Jannetta PJ, Rand RW. Transtentorial retrogasserian rhizotomy in trigeminal neuralgia by microneurosurgical technique. Bull Los Angeles Neurol Soc. 1966. 31: 93-9
25. Jannetta PJ, Skinner DB, Ebert PA, editors. Microsurgical exploration and decompression of the facial nerve in hemifacial spasm. Current Topics in Surgical Research. New York: Academic Press; 1970. 2: 217-20
26. Kanpolat Y, Savas A, Bekar A, Berk C. Percutaneous controlled radiofrequency trigeminal rhizotomy for the treatment of idiopathic trigeminal neuralgia: 25-year experience with 1,600 patients. Neurosurgery. 2001. 48: 524-32 discussion 532-4
27. Kaufmann AM, Price AV. A history of the Jannetta procedure. J Neurosurg. 2019. 132: 639-46
28. Lee HS, Cho KR, Park K, Jeon C. Management of cerebrospinal fluid leakage after microvascular decompression surgery: Clinical strategy. Life (Basel). 2023. 13: 1771
29. Maarbjerg S, Gozalov A, Olesen J, Bendtsen L. Trigeminal neuralgia--a prospective systematic study of clinical characteristics in 158 patients. Headache. 2014. 54: 1574-82
30. Manninen PH, Tan TK. Postoperative nausea and vomiting after craniotomy for tumor surgery: A comparison between awake craniotomy and general anesthesia. J Clin Anesth. 2002. 14: 279-83
31. Martinoni EP, Pfister CA, Stadler KS, Schumacher PM, Leibundgut D, Bouillon T. Model-based control of mechanical ventilation: Design and clinical validation. Br J Anaesth. 2004. 92: 800-7
32. Pallud J, Dezamis E. Functional and oncological outcomes following awake surgical resection using intraoperative corticosubcortical functional mapping for supratentorial gliomas located in eloquent areas. Neurochirurgie. 2017. 63: 208-18
33. Park CK, Park BJ. Surgical treatment for trigeminal neuralgia. J Korean Neurosurg Soc. 2022. 65: 615-21
34. Patchana T, Lopez JA, Majeed G, Ho A, Alarcon T, Plantak N. The awake craniotomy: A patient’s experience and a literature review. Cureus. 2022. 14: e26441
35. Peker S, Sirin A. Primary trigeminal neuralgia and the role of pars oralis of the spinal trigeminal nucleus. Med Hypotheses. 2017. 100: 15-8
36. Rana MH, Khan AA, Khalid I, Ishfaq M, Javali MA, Baig FA. Therapeutic approach for trigeminal neuralgia: A systematic review. Biomedicines. 2023. 11: 2606
37. Rand RW, Kurze TL. Facial nerve preservation by posterior fossa transmeatal microdissection in total removal of acoustic tumors. J Neurol Neurosurg Psychiatry. 1965. 28: 311-6
38. Rand RW. Gardner neurovascular decompression of the trigeminal and facial nerves for tic douloureux and hemifacial spasm. Surg Neurol. 1981. 16: 329-32
39. Rand RW. The Gardner neurovascular decompression operation for trigeminal neuralgia. Acta neurochir. 1981. 58: 161-6
40. Ratha V, Roopesh Kumar VR, Subramaniam S, Kumar S, Sankaran V, Suresh Bapu KR. Awake microvascular decompression with fat-Teflon sandwich technique: Clinical implications of a novel approach for cranial nerve neuralgias. J Clin Neurosci. 2019. 64: 77-82
41. Sade B, Lee JH. Microvascular decompression for trigeminal neuralgia. Neurosurg Clin N Am. 2014. 25: 743-9
42. Sandell T, Eide PK. Effect of microvascular decompression in trigeminal neuralgia patients with or without constant pain. Neurosurgery. 2008. 63: 93-9 discussion 99-100
43. Singh D, Dutta G, Jagetia A, Singh H, Srivastava AK, Tandon M. Microvascular decompression for trigeminal neuralgia: Experience of a tertiary care center in India and a brief review of literature. Neurol India. 2021. 69: S206-12
44. Spina A, Mortini P, Alemanno F, Houdayer E, Iannaccone S. Trigeminal neuralgia: Toward a multimodal approach. World Neurosurg. 2017. 103: 220-30
45. Taarnhøj P. Decompression of the trigeminal root. J Neurosurg. 1954. 11: 299-305
46. Wang DD, Raygor KP, Cage TA, Ward MM, Westcott S, Barbaro NM. Prospective comparison of long-term pain relief rates after first-time microvascular decompression and stereotactic radiosurgery for trigeminal neuralgia. J Neurosurg. 2018. 128: 68-77
47. 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
48. Zakrzewska JM, Linskey ME. Trigeminal neuralgia. BMJ. 2014. 348: g474
49. Zheng JH, Sun K, Zhang HT, Xie YJ, Wang-Yang LX, Chen HY. A study on the recurrence rate of trigeminal neuralgia after MVD and the related factors. J Neurol Surg B Skull Base. 2020. 81: 572-8