1Department of Imaging and Pathology, Faculty of Medicine, Catholic University of Leuven, 3000 Leuven, Belgium.
2Department of Oral and Maxillofacial Surgery, St. John’s Hospital, 3600 Genk, Belgium.
3Faculty of Medicine, Morphology Research Group, Hasselt University, 3590 Diepenbeek, Belgium.
Correspondence Address: Prof. Constantinus Politis, Department of Imaging and Pathology, Faculty of Medicine, Catholic University of Leuven, 3000 Leuven, Belgium. E-mail: email@example.com
This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License (http://creativecommons.org/licenses/by-nc-sa/3.0/), 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.
Neuropathic pain is characterized by spontaneous and provoked pain and other signs reflecting neural damage. Aberrant regeneration following peripheral nerve lesions leaves neurons unusually sensitive and prone to spontaneous pathological activity, abnormal excitability and heightened sensitivity to stimuli. This review covers the current understanding of neuropathic pain after bilateral sagittal split osteotomy (BSSO) of the lower jaw. The reported incidence of neuropathic pain after mandibular osteotomies is less than 1%, while the incidence in patients with iatrogenic inferior alveolar nerve (IAN) injuries during BSSO can be as high as 45%. The factors which modulate the healing process toward neuropathic pain during or after nerve damage have not yet been elucidated. Patients at highest risk for developing post-BSSO neuropathic pain are older than 45 years and have undergone procedures involving IAN compression, partial severance, or complete discontinuity of the lingual nerve with a proximal stump neuroma, patients with nerve injury repair delayed longer than 12 months and patients with chronic illnesses that compromise healing or increase risk for peripheral neuropathy. Although neuropathic pain tends to be long-lasting, some patients can recover completely. Preventive measures include risk assessment prior to surgery, prevention of nerve damage during surgery, and early repair of nerve injury.
Bilateral sagittal split osteotomy, incidence, management, neuropathic pain, risk factor
Neuropathic pain is a complex, chronic pain state caused by a lesion of the somatosensory nervous system. It usually results from tissue injury and excludes pain from a condition preceding surgery. Neuropathic pain can arise from damage to the nerve pathways at any point from the terminals of the peripheral nociceptors to the cortical neurons in the brain. In this type of pain, nerve fibers may be damaged, dysfunctional, or injured, resulting in a change in nerve function at both the site of injury and adjacent tissue. These damaged nerve fibers in turn send incorrect signals to other pain centers.
Neuropathic pain is characterized by spontaneous and provoked pain mostly of a burning character, by positive symptoms such as paresthesias and dysesthesias, and by negative signs (sensory deficits) reflecting neural damage. Sensory disturbances in the area of surgery show a strikingly strong association with persistent postsurgical pain, suggesting nerve damage as a contributing factor in a significant portion of cases.[2,3] Many investigations have confirmed the relevance of surgery as the initiating event for the development of persistent pain, even after a minor operation, such as tooth extraction.
Bilateral sagittal split osteotomy (BSSO) is a common procedure used to treat mandibular deformity. Because mandibular osteotomies are performed in close proximity to the neurovascular bundle in the mandibular canal, there is a high risk of injury to the inferior alveolar nerve (IAN).[4-6] IAN injury during surgery largely results from manipulation of the nerve, its vascular supply, or structures surrounding the nerve during surgery.[7-9] The placement of semi-rigid fixation plates and screws may also cause nerve damage either directly or via compression of the nerve between bony segments after screw fixation.
Inferior alveolar nerve-related neuropathic pain following iatrogenic damage to the nerve is a disabling condition that severely affects the quality of daily life.[10-12] This review covers the current knowledge regarding neuropathic pain after BSSO and its incidence, pathophysiology, risk factors, management, and steps for prevention.
No single accurate value appears to be available for the overall prevalence of neuropathic pain. The development of chronic pain after surgery is fairly common, with estimates ranging from 10% to 50% after many common operations. The pain may be severe in 2-10% of these patients and is usually considered to be neuropathic.[14,15]
Information about neuropathic pain following orthognathic surgery is sparse.[16,17] Borstlap et al. prospectively followed 222 patients after BSSO surgery and reported no incidence of neuropathic pain. The reported incidence of neuropathic pain in the literature after mandibular osteotomies is less than 1% while the reported incidence in patients with iatrogenic IAN injuries during BSSO can be as high as 45%. Marchiori et al. reported seven cases of neuropathic pain among 1671 patients after BSSO, for an incidence of 0.42%, while Politis et al. reported 6 cases of neuropathic pain from 900 BSSOs with an incidence of 0.67%.
Other reports[16,21] describe an incidence as high as 5% of neuropathic pain among patients who sustained peripheral trigeminal nerve injuries after sagittal split ramus osteotomy. Teerijoki-Oksa et al. prospectively followed 19 patients after BSSO surgery and found a 5% overall occurrence of neuropathic pain at 1-year follow-up, which is similar to the overall estimated incidence of neuropathic pain after traumatic and iatrogenic nerve injuries. Jääskeläinen et al., on the other hand, found a 45% incidence of neuropathic pain in 58 patients with iatrogenic sensory deficits of the IAN and lingual nerve (LN).
Microsurgical repair of a damaged IAN after orthognathic surgery does not alleviate neuropathic pain if the latter was present before the repair. Furthermore, it does not cause neuropathic pain if the pain was not present beforehand.
The IAN is at significant risk in all stages of surgery [Table 1], and nerve manipulation during BSSO is a known risk factor for nerve injury. This nerve can be damaged at the following points: the spyx during the placement of a retractor posterior to or above the lingual, the ascending ramus during a horizontal osteotomy cut, the bone cut at the lower border of the mandible, the connecting bone cut between the lower border and the buccal osteotomy of the mandibular body, with chiseling during the sagittal split, between bone fragments after the bony movement, during placement of the osteosynthesis material and during insertion of an osteosynthesis screw.
Location, cause, and type of nerve damage during BSSO
|Location||Cause||Type of lesion|
|Osteotomy area||Chisels, compression bony surfaces, freeing nerve, screws, piezo, drill, saw||Compression, crushing, transection|
|Lower border||Partial or total transection||Drill, saw, piezo|
Grades of nerve injury are categorized into neuropraxia, axonotmesis, or neurotmesis, depending on the extent of the damage. In clinical settings, various combinations of nerve damage can coexist, giving rise to a variety of sensory dysfunctions. After a peripheral nerve lesion, aberrant regeneration may occur. In some patients, neurons become unusually sensitive and develop a spontaneous pathological activity, abnormal excitability, and heightened sensitivity to chemical, thermal, and mechanical stimuli. Persistent pain or neuropathic pain such as allodynia, and pain and discomfort with occlusion[27,28] can occur.
The main features of neuropathic pain include constant pain, which can be superficial or deep, sharp or aching, lancinating pain (i.e. sudden and sharp, severe bursts of pain), and allodynia (i.e. pain experienced after normally nonpainful stimuli, like light touch). The discomfort is usually of a chronic nature and may be described by the patient as a burning sensation, a sharp, stabbing, or shooting pain, or "like an electric shock".
The complaints often seem to be out of proportion to the pain that would be expected to accompany the original injury.[3,19] Neuropathic pain resulting from axonal nerve injury is often associated with crushing or stretching nerve injuries rather than total nerve transaction. Other characteristics of neuropathic pain include a lack of response to anti-inflammatory pain killers (nonsteroidal anti-inflammatories, paracetamol), improved symptoms in the mornings, minimal sleep disturbance, and worsening during the day or with stress, fatigue, and illness.
The proximity of the mandibular canal to the lower border of the mandible is an important factor in self-reported hypoesthesia of the lower lip. The exposure and dissection of the IAN from the mandibular canal during surgery has been shown to significantly increase the risk of neurosensory disturbance, while patients with a laceration of the IAN have higher chance of developing neuropathic pain.
Genioplasty and age at the time of surgery are significant predictors of hypoesthesia after BSSO, a 1-year increase in age may increase the odds of hypoesthesia of the lower lip by 5%, and the odds of hypoesthesia for patients with concurrent genioplasty are 4.5-fold greater than the odds for patients without concurrent genioplasty. Other factors include smoking and gender (women are at higher risk for hypoesthesia).[27,29]
Patients most likely to develop neuropathic pain after BSSO are older than fourty-five years and have undergone a procedure involving compression or partial severance of the IAN or complete discontinuity of the LN with a proximal stump neuroma. Others at risk include those with nerve injury repair delayed past twelve months, patients with chronic illnesses that compromise healing or enhance the risk for developing peripheral neuropathy (e.g. diabetes mellitus) and patients with preexisting chronic pain from any cause (e.g. lower back pain, postthoracotomy syndrome). Furthermore, potentially at risk are patients with certain psychological features such as depression, anger issues, posttraumatic stress disorder, and victims of abuse who have lost the ability to trust.[19,26,30,31] Patients undergoing orthognathic surgery are usually young and healthy, which may explain the low incidence of neuropathic pain after BSSO surgery.
Chronic neuropathic pain represents a heterogeneous group of diseases in which pain is caused by nerve damage owing to various etiologies. Before pain is perceived in the central nervous system, different descending mechanisms must modulate the initial nociceptive stimulus. The imbalance between the amount of stimuli and the efficacy of modulation mechanisms is processed as the sensation of pain. High-magnitude or repetitive nociceptive impulses cause peripheral and central neuronal changes, leading to the maintenance and exacerbation of the pain sensation. These alterations are often irreversible and responsible for patient reports of long-term pain, even after many unsuccessful treatments. Most of the current ideas regarding the pathophysiology of neuropathic pain originated from experimental work in animal models. The underlying mechanisms are described below.
Pain sensations are normally elicited by activity in unmyelinated (C-) and thinly myelinated (Aδ-) primary afferent neurons. These nociceptors are usually silent in the absence of stimulation and respond best to potentially noxious stimuli. Neurons become abnormally sensitive after damage to peripheral nerves and develop pathological spontaneous activity. These pathological changes result from molecular and cellular changes at the level of the primary afferent nociceptor that are triggered by the nerve lesion. They are expressed as increased spontaneous firing, lowered activation threshold, and expanded receptive fields.
Hyperactivity of the peripheral nociceptor results in secondary changes in the dorsal horn of the spinal cord with an associated increase in general excitability of multi-receptive spinal cord neurons. This hyper-excitability is manifested by increased neuronal activity in response to noxious stimuli, expansion of neuronal receptive fields, and spread of spinal hyper-excitability to other segments. Central sensitization is initiated and maintained by activity in pathologically sensitized C-fibers. Importantly, the activation of both descending facilitatory and inhibitory supraspinal pain control systems requires intense noxious stimulation, resulting in activation of these brainstem centers to finally activate the descending arm of thespino-bulbo-spinal circuit. An imbalance between facilitatory and inhibitory systems, with higher activity in the former and lower in the latter, contributes to central neuronal sensitization and to the development and maintenance of pain.
Some patients experience a profound cutaneous deafferentation of the painful area without significant allodynia. In BSSO and orofacial neuropathic pain, the simultaneous occurrence of an exposed nerve or partial axonal IAN injury together with disruption of the bony environment of the IAN is a risk factor. The formation of a neuroma from a severed nerve ending has been associated with neuropathic pain, which is attributed to altered sensory processing in either the trigeminal ganglion or the central trigeminal nerve center. Politis et al. found no visible nerve damage on panoramic radiographs or magnetic resonance imaging (MRI) or computerized tomography (CT) scans in their case series of neuropathic pain after BSSO surgery, except in one patient in whom neuropathic pain started after loss of fixation and pathological movement of the bone segments due to pseudarthrosis. In this patient, the neuropathic pain disappeared after bone grafting and stabilization of the segments with adequate fixation.
Compression or crush lesions cannot be routinely visualized after orthognathic surgery by either CT or MRI secondary to artifacts from orthodontic appliances. Pathologic elongation of the nerve in BSSO surgery is certainly possible when the mandible has been surgically widened after a BSSO advancement with a midline split. Here too, cone beam CT, CT, and MRI cannot be used to directly visualize the nerve damage.
The diagnosis of neuropathic pain should be made only when the history and signs are indicative of neuropathy in conjunction with a neuro-anatomically correlated pain distribution and sensory abnormalities within the area of pain. There should be partial or complete sensory loss in all or part of the painful area, and confirmation of a lesion or disease by quantitative sensory testing, surgical evidence, imaging, clinical neurophysiology, and/or biopsy.
Neuropathic pain should also be differentiated from other similar orofacial pain. The differential diagnosis of neuropathic pain includes inflammatory pain, traumatic trigeminal neuropathy, persistent idiopathic facial pain (atypical facial pain), atypical odontalgia, complex regional pain syndrome, and trigeminal neuralgia.
Neuropathic pain tends to be long-lasting, although some patients recover completely, and others may find relief with pharmacotherapy and learn to cope with their symptoms. Neuropathic pain is treated mainly with anti-depressants and anti-epileptics, whereas simple analgesics are not efficacious. Management of pain should be tailored to the individual patient on the basis of pain type(s), the causative disease(s), and psychosocial aspects.
The assessment of neuropathic pain needs to include the measurement of multiple aspects of the quality of life. Mood, physical and social functioning, and pain-coping strategies such as catastrophizing and social support are all important domains. As with other chronically painful conditions, cognitive-behavioral interventions may improve the quality of life in neuropathic pain conditions. Reassurance and counseling of patients with neuropathic pain will go a long way toward alleviating their condition.
Neuropathic pain treatment remains unsatisfactory despite a substantial increase in the number of trials. The use of low-dose anti-depressants (amitriptyline, nortriptyline is effective for symptomatic relief. Carbamazepine, phenytoin, and valproic acid are effective in ameliorating diabetic neuropathy-related pain. Other anti-epileptic agents, including lamotrigine, oxcarbazepine, and topiramate, show some benefit for the treatment of neuropathic pain, although some studies have found them to be ineffective.[37,38]
Topical 5% lidocaine patches offer a new therapeutic alternative for patients suffering from neuropathic pain. These patches have been shown to be useful in a subgroup of patients.
In BSSO patients, an accurate preoperative patient history, as well as early identification of the patient with severe or prolonged pain with the aim of initiating pain treatment as early as possible, is the key to success.[29,34] Kuhlefelt et al. suggest that patients with IAN damage after BSSO be put on neuropathic pain medication immediately postoperatively before pain is well established. Psychological support and the volunteer of information by the surgeon are also important at this time.
Early repair of nerve injury has been deemed to be the most critical factor in the surgical management and prevention of neuropathic pain. For example, once the neuropathic pain has set in, late surgical trigeminal nerve repair will not improve the patient's symptoms. When an iatrogenic nerve injury is suspected, regular follow-up is advised. If there is no improvement during 10-12 weeks of follow-up or there are complaints of dysesthesia, surgical exploration, localization, and immediate repair or repair within days is advised. Repair should be carried out with a tension-free approximation.
Patient profiling should be done and identification of risk factors for developing neuropathic pain made in all patients scheduled for orthognathic surgery. Proper localization of the IAN before BSSO is also an essential preventive step. The advent of cone beam CT has made IAN canal assessment in three-dimensions possible.
Furthermore, the development and modification of surgical techniques to reduce nerve injury during BSSO, such as safe surgical access to the mandibular nerve at the infratemporal fossa, and a modified technique to control the lower mandibular border cut, have been critical in reducing the incidence of damage to the IAN. Also useful is assessment of the IAN during BSSO, as by continuous monitoring of the status of the mandibular nerve through observation of changes in the sensory action potentials of the nerve during surgery.
Severe nerve injuries often result from drilling too deep past the bone into the nerve, or from placing the osteosynthesis screw on the nerve during fixation. The use of intraoperative CT during BSSO allows for the intraoperative evaluation of osteosynthesis screw penetration and depth. Intraoperative CT also allows for immediate assessment of treatment and provides the option to modify treatment if necessary. These preventive measures will help reduce the incidence of neuropathic pain and improve the quality of life of BSSO patients.
Because neuropathic pain after BSSO involves an injured peripheral nerve which sends incorrect signals to neurons located in Meckel’s cave, a temporary inhibition of such signals might be beneficial. Affordable long-acting liposomal local anesthetics, navigation guided procedures targeted at the exit of the mandibular nerve in the oval foramen, and miniaturized intra-oral neurostimulators applied proximal to the site of the nerve damage are possible treatment options that are currently under investigation.
Neuropathic pain after BSSO surgery is rare in spite of the frequent hypoesthesia that accompanies this surgical procedure. Contributing factors include patient factors (age, gender, patient profile), nerve-related factors (elongation, crushing, compression, transection), and local factors around the nerve (ischemia, bone infection). Once neuropathic pain has been established for more than three months, microsurgical nerve repair is unlikely to be successful in relieving the pain.
Agbaje Jimoh Olubanwo is a postdoctoral researcher of the fund for Scientific Research (FWO-Vlaanderen).
There are no conflicts of interest.
1. Haroutiunian S, Nikolajsen L, Finnerup NB, Jensen TS. The neuropathic component in persistent postsurgical pain: a systematic literature review. Pain 2013;154:95-102.DOIPubMed
2. Macrae WA. Chronic pain after surgery. Br J Anaesth 2001;87:88-98.DOIPubMed
3. Dobrogowski J, Przeklasa-Muszynska A, Wordliczek J. Persistent post-operative pain. Folia Med Cracov 2008;49:27-37.PubMed
4. Al-Bishri A, Rosenquist J, Sunzel B. On neurosensory disturbance after sagittal split osteotomy. J Oral Maxillofac Surg 2004;62:1472-6.DOIPubMed
5. Boutault F, Diallo R, Marecaux C, Modiga O, Paoli JR, Lauwers F. Neurosensory disorders and functional impairment after bilateral sagittal split osteotomy: role of the anatomical situation of the alveolar pedicle in 76 patients. Rev Stomatol Chir Maxillofac 2007;108:175-82.DOIPubMed
6. D'Agostino A, Trevisiol L, Gugole F, Bondi V, Nocini PF. Complications of orthognathic surgery: the inferior alveolar nerve. J Craniofac Surg 2010;21:1189-95.DOIPubMed
7. Wijbenga JG, Verlinden CR, Jansma J, Becking AG, Stegenga B. Long-lasting neurosensory disturbance following advancement of the retrognathic mandible: distraction osteogenesis versus bilateral sagittal split osteotomy. Int J Oral Maxillofac Surg 2009;38:719-25.DOIPubMed
8. Yoshioka I, Tanaka T, Khanal A, Habu M, Kito S, Kodama M, Oda M, Wakasugi-Sato N, Matsumoto-Takeda S, Fukai Y, Tokitsu T, Tomikawa M, Seta Y, Tominaga K, Morimoto Y. Relationship between inferior alveolar nerve canal position at mandibular second molar in patients with prognathism and possible occurrence of neurosensory disturbance after sagittal split ramus osteotomy. J Oral Maxillofac Surg 2010;68:3022-7.DOIPubMed
9. Yamauchi K, Takahashi T, Kaneuji T, Nogami S, Yamamoto N, Miyamoto I, Yamashita Y. Risk factors for neurosensory disturbance after bilateral sagittal split osteotomy based on position of mandibular canal and morphology of mandibular angle. J Oral Maxillofac Surg 2012;70:401-6.DOIPubMed
10. Colella G, Cannavale R, Vicidomini A, Lanza A. Neurosensory disturbance of the inferior alveolar nerve after bilateral sagittal split osteotomy: a systematic review. J Oral Maxillofac Surg 2007;65:1707-15.DOIPubMed
11. Lee EG, Ryan FS, Shute J, Cunningham SJ. The impact of altered sensation affecting the lower lip after orthognathic treatment. J Oral Maxillofac Surg 2011;69:e431-45.DOIPubMed
12. Renton T, Yilmaz Z, Gaballah K. Evaluation of trigeminal nerve injuries in relation to third molar surgery in a prospective patient cohort. Recommendations for prevention. Int J Oral Maxillofac Surg 2012;41:1509-18.DOIPubMed
13. Macrae WA. Chronic post-surgical pain: 10 years on. Br J Anaesth 2008;101:77-86.DOIPubMed
14. Johansen A, Romundstad L, Nielsen CS, Schirmer H, Stubhaug A. Persistent postsurgical pain in a general population: prevalence and predictors in the Tromso study. Pain 2012;153:1390-6.DOIPubMed
15. Schug SA. Persistent post-surgical pain: a view from the other side of the fence. Pain 2012;153:1344-5.DOIPubMed
16. Bagheri SC, Meyer RA, Khan HA, Wallace J, Steed MB. Microsurgical repair of the peripheral trigeminal nerve after mandibular sagittal split ramus osteotomy. J Oral Maxillofac Surg 2010;68:2770-82.DOIPubMed
17. Tay AB, Zuniga JR. Clinical characteristics of trigeminal nerve injury referrals to a university centre. Int J Oral Maxillofac Surg 2007;36:922-7.DOIPubMed
18. Borstlap WA, Stoelinga PJ, Hoppenreijs TJ, van't Hof MA. Stabilisation of sagittal split advancement osteotomies with miniplates: a prospective, multicentre study with two-year follow-up. Part I. Clinical parameters. Int J Oral Maxillofac Surg 2004;33:433-41.DOIPubMed
19. Marchiori EC, Barber JS, Williams WB, Bui PQ, O'Ryan FS. Neuropathic pain following sagittal split ramus osteotomy of the mandible: prevalence, risk factors, and clinical course. J Oral Maxillofac Surg 2013;71:2115-22.DOIPubMed
20. Politis C, Lambrichts I, Agbaje JO. Neuropathic pain after orthognathic surgery. Oral Surg Oral Med Oral Pathol Oral Radiol 2014;117:e102-7.DOIPubMed
21. Jaaskelainen SK, Teerijoki-Oksa T, Forssell H. Neurophysiologic and quantitative sensory testing in the diagnosis of trigeminal neuropathy and neuropathic pain. Pain 2005;117:349-57.DOIPubMed
22. Teerijoki-Oksa T, Jaaskelainen SK, Soukka T, Virtanen A, Forssell H. Subjective sensory symptoms associated with axonal and demyelinating nerve injuries after mandibular sagittal split osteotomy. J Oral Maxillofac Surg 2011;69:e208-13.DOIPubMed
23. Kehlet H, Jensen TS, Woolf CJ. Persistent postsurgical pain: risk factors and prevention. Lancet 2006;367:1618-25.DOI
24. Westermark A, Bystedt H, von Konow L. Inferior alveolar nerve function after sagittal split osteotomy of the mandible: correlation with degree of intraoperative nerve encounter and other variables in 496 operations. Br J Oral Maxillofac Surg 1998;36:429-33.DOI
25. Seddon HJ. A classification of nerve injuries. Br Med J 1942;2:237-9.DOIPubMedPMC
26. Costigan M, Scholz J, Woolf CJ. Neuropathic pain: a maladaptive response of the nervous system to damage. Annu Rev Neurosci 2009;32:1-32.DOIPubMedPMC
27. Politis C, Sun Y, Lambrichts I, Agbaje JO. Self-reported hypoesthesia of the lower lip after sagittal split osteotomy. Int J Oral Maxillofac Surg 2013;42:823-9.DOIPubMed
28. Agbaje JO, Salem AS, Lambrichts I, Jacobs R, Politis C. Systematic review of the incidence of inferior alveolar nerve injury in bilateral sagittal split osteotomy and the assessment of neurosensory disturbances. Int J Oral Maxillofac Surg 2014;10:440-8.
29. Kuhlefelt M, Laine P, Suominen AL, Lindqvist C, Thoren H. Nerve manipulation during bilateral sagittal split osteotomy increases neurosensory disturbance and decreases patient satisfaction. J Oral Maxillofac Surg 2014;72:2052.e1-5.DOIPubMed
30. Boogaard S, Heymans MW, Patijn J, de Vet HC, Faber CG, Peters ML, Loer SA, Zuurmond WW, Perez R. Predictors for persistent neuropathic pain: a Delphi survey. Pain Physician 2011;14:559-68.PubMed
31. Haythornthwaite JA, Benrud-Larson LM. Psychological assessment and treatment of patients with neuropathic pain. Curr Pain Headache Rep 2001;5:124-9.DOIPubMed
32. Granovsky Y. Conditioned pain modulation: a predictor for development and treatment of neuropathic pain. Curr Pain Headache Rep 2013;17:361.DOIPubMed
33. Fields HL, Rowbotham M, Baron R. Postherpetic neuralgia: irritable nociceptors and deafferentation. Neurobiol Dis 1998;5:209-27.DOIPubMed
34. Mensink G, Zweers A, Wolterbeek R, Dicker GG, Groot RH, van Merkesteyn RJ. Neurosensory disturbances one year after bilateral sagittal split osteotomy of the mandibula performed with separators: a multi-centre prospective study. J Craniomaxillofac Surg 2012;40:763-7.DOIPubMed
35. Al-Sabbagh M, Okeson JP, Khalaf MW, Bhavsar I. Persistent pain and neurosensory disturbance after dental implant surgery: pathophysiology, etiology, and diagnosis. Dent Clin North Am 2015;59:131-42.DOIPubMed
36. Attal N, Cruccu G, Haanpaa M, Hansson P, Jensen TS, Nurmikko T, Sampaio C, Sindrup S, Wiffen P, Force ET. EFNS guidelines on pharmacological treatment of neuropathic pain. Eur J Neurol 2006;13:1153-69.DOIPubMed
37. Zin CS, Nissen LM, Smith MT, O'Callaghan JP, Moore BJ. An update on the pharmacological management of post-herpetic neuralgia and painful diabetic neuropathy. CNS Drugs 2008;22:417-42.DOIPubMed
38. Jensen TS, Finnerup NB. Management of neuropathic pain. Curr Opin Support Palliat Care 2007;1:126-31.DOIPubMed
39. Clere F, Delorme-Morin C, George B, Navez M, Rioult B, Tiberghien-Chatelain F, Ganry H. 5% lidocaine medicated plaster in elderly patients with postherpetic neuralgia: results of a compassionate use programme in France. Drugs Aging 2011;28:693-702.DOIPubMed
40. Agbaje JO, Sun Y, Lambrichts I, Vrielinck L, Schepers S, Politis C. Safe surgical access to the mandibular nerve at the infratemporal fossae. J Craniofac Surg 2014;25:1454-7.DOIPubMed
41. Politis C, Lambrichts I, Sun Y, Vrielinck L, Schepers S, Agbaje JO. Attachment rate of the inferior alveolar nerve to buccal plate during bilateral sagittal split osteotomy influences self-reported sensory impairment. J Craniofac Surg 2014;25:2121-6.DOI
Shahani Noor et al., Neuroimmunology and Neuroinflammation, 2019
Jong Sook Yi et al., Plastic and Aesthetic Research, 2019
Faiez N. Hattab et al., Stomatological Disease and Science, 2019
Ángela Rojas et al., Hepatoma Research, 2018
Gennadi V. Glinsky et al., Journal of Cancer Metastasis and Treatment, 2017
Xiao-Lin Chen et al., Neuroimmunology and Neuroinflammation, 2017
Paola Razzore et al., Journal of Cancer Metastasis and Treatment, 2016
Ghazaleh Tabatabai et al., Journal of Cancer Metastasis and Treatment, 2016
Forhad Hossain Chowdhury et al., Neuroimmunology and Neuroinflammation, 2015
Atef Ben Nsir et al., Neuroimmunology and Neuroinflammation, 2015