Hakeem A, Shanmugam V. Current trends in the diagnosis and management of post-herniorraphy chronic groin pain. World J Gastrointest Surg 2011; 3(6): 73-81
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World J Gastrointest Surg. Jun 27, 2011; 3(6): 73-81 Published online Jun 27, 2011. doi: 10.4240/wjgs.v3.i6.73
Current trends in the diagnosis and management of post-herniorraphy chronic groin pain
Abdul Hakeem, Venkatesh Shanmugam
Abdul Hakeem, Department of General Surgery, Aintree University Hospital NHS Trust, Longmoor Lane, Liverpool, L9 7AL, United Kingdom
Venkatesh Shanmugam, Department of General and Colorectal Surgery, Nottingham University Hospital NHS Trust, Queens Medical Centre, Nottingham, NG7 2UH, United Kingdom
ORCID number: $[AuthorORCIDs]
Author contributions: Hakeem A did the literature search and wrote the initial draft; Shanmugam V cross-checked the literature search,edited the paper and conceptualised the idea.
Correspondence to: Mr. Abdul Hakeem, MRCS, Department of General Surgery, Aintree University Hospital NHS Trust, Longmoor Lane, Liverpool, L9 7AL, United Kingdom. email@example.com
Telephone: +44-113-8085924 Fax: +44-132-5490293
Received: March 1, 2011 Revised: April 24, 2011 Accepted: May 1, 2011 Published online: June 27, 2011
Inguinodynia (chronic groin pain) is one of the recognised complications of the commonly performed Lichtenstein mesh inguinal hernia repair. This has major impact on quality of life in a significant proportion of patients. The pain is classified as neuropathic and non-neuropathic related to nerve damage and to the mesh, respectively. Correct diagnosis of this problem is relatively difficult. A thorough history and clinical examination are essential, as is a good knowledge of the groin nerve distribution. In spite of the common nature of the problem, the literature evidence is limited. In this paper we discuss the diagnostic tools and treatment options, both non-surgical and surgical. In addition, we discuss the criteria for surgical intervention and its optimal timing.
Mesh inguinal hernia repair is one of the most common operations performed worldwide. Inguinodynia or Chronic Groin Pain following this operation is a potential complication and its incidence can be as high as 62.9%. A quarter of these patients suffer from severe impairment in carrying out their daily routines[2-4]. Courtney et al showed the effect of chronic groin pain on physical and social functioning, thereby limiting the individual’s ability to participate in any paid employment.The rate of chronic groin pain following both open and laparoscopic hernia repair is vastly underreported[6,7]. Hindmarsh et al shown that only 1% of patients with chronic groin pain post-herniorrhaphy were referred for further treatment. The main purpose of this review is to look at the available evidence on diagnostic modalities for this chronic problem and to discuss the varied treatment options practised worldwide.
AETIOLOGY OF CHRONIC GROIN PAIN
The exact aetiology of this complex pain is unknown, although various theories have been proposed. Chronic groin pain has been classified empirically as neuropathic or non-neuropathic in origin. Neuropathic pain is considered to be due to damage to the inguinal nerves and usually develops in the sensory distribution of the injured nerve. Non-neuropathic pain is caused by either mesh-related fibrosis or post-operative fibrosis. The nerves involved are the Ilioinguinal nerve (IIN), the Iliohypogastric nerve (IHN), the genital branch of the Genito-Femoral nerve (GFN) and, rarely, the Lateral Femoral Cutaneous nerve (LFC). These nerves can be damaged either by partial or complete transection, stretching, contusion, crushing, electrical damage or by being caught in the suture used in open repair or the tacks used in laparoscopic repair. Secondary nerve damage can also occur as a result of adjacent inflammatory processes, such as granuloma, or because of excess fibrotic reaction or mesh encasement. Wantz et al showed that handling of the sensory nerves during surgery leads to chronic residual neuralgia.
Heise et al were the first to describe non-neuropathic pain caused by rolling up of the mesh or mesh-related excess fibrosis. Similarly, another pain syndrome, termed “somatic pain”, has been described secondary to damage to the pubic tubercle while anchoring the mesh. A small group of patients have been shown to suffer from diffuse pain around the spermatic cord (funiculodynia), resulting in ejaculatory pain. This has been described as “visceral pain” and is due to venous congestion of the spermatic cord or to mesh encasement of the cord. A combination of neuropathic, non-neuropathic, visceral and somatic pain is common, making clinical or radiological differentiation of the cause extremely difficult.
During laparoscopic repair, the IIN is at risk lateral to the internal ring and the GFN medial to the ring. The IHN is commonly damaged by tacks or staples along its entire length, making it highly vulnerable during laparoscopic mesh fixation[14-16]. Occasional damage to the LFC nerve[17,18] and the femoral nerve have also been shown during laparoscopic repair Although laparoscopic repair has been shown to result in reduced chronic groin pain, exact reasons for this are unclear[20-23].
COMPLEX SYMPTOMS OF CHRONIC GROIN PAIN
The complex symptoms of post-herniorrhaphy chronic pain vary depending on the involvement of the nerve or nerves, amount of mesh-related fibrosis and damage to spermatic cord structures. The neuropathic symptoms include pain (neuralgia), burning sensation (paraesthesia), reduced sensation (hypoaesthesia) and increased sensation (hyperaesthesia). The pain may radiate to the hemi-scrotum, upper leg or back.
Neuropathic pain is usually characterised by the presence of a trigger point, its episodic nature and by being aggravated by walking or sitting. It is variously described as a stabbing, burning, shooting or pricking sensation. In contrast, non-neuropathic pain is a constant dull-ache over the entire groin area with no specific trigger point and is usually aggravated by strenuous exercise.Patients commonly describe it as a gnawing, tender, pulling or pounding sensation.
A small group of patients also report numbness over the groin or thigh, with the most common point of maximal tenderness at the pubic tubercle. These patients have inflammation of the pubic tubercle either due to stitches made on the pubic bone during open repair or application of tacks in laparoscopic repair. Another range of symptoms are related to sexual dysfunction due to vas engulfment and inflammatory reaction caused by the mesh. Patients describe ejaculatory pain in the region of superficial ring or testicular or labial pain due to GFN irritation. Other complaints included diminished quality of life, mood swings and depression[26,27].
DIAGNOSIS OF CHRONIC GROIN PAIN
The diagnosis of chronic groin pain begins with a comprehensive patient history and good knowledge of the anatomy of inguinal nerves. The history should include the commonly encountered risk factors for chronic groin pain which include age below median, female gender, postoperative complications, recurrent hernia repair, open repair techniques, history of preoperative pain and an interval of less than 3 years from surgery.
Due to the infrequent presentation of chronic groin pain, there is no clear consensus on the diagnosis of this iatrogenic problem. Neuropathic pain is usually distributed along the sensory innervations of the affected nerve(s) and can be reproduced by tapping the skin medial to the antero-superior iliac spine or over an area of local tenderness (Tinel’s test). The clinical differentiation of ilioinguinal, iliohypogastric and genitofemoral neuralgia is difficult, frequently resulting in misdiagnosis and inappropriate treatment[29,30]. This is because of the overlapping sensory innervations of these three nerves, peripheral communication between their nerve twigs and, most importantly, their common roots of origin. Along with these anatomical factors, fibrosis caused by the procedure and the mesh causes a degree of non-neuropathic pain in most cases, thereby making it difficult to delineate the neuropathic cause clinically.
Deysine et al and Starling et al used IIN block and recommended IIN neurectomy if the block relieved pain. If pain persisted after IIN block, L1-L2 plexus block was carried out and, if this relived pain, GFN neurectomy was then performed. If pain was partially relieved by both blocks, groin exploration of both nerves was then carried out. There is no consensus on how these nerve blocks should be performed and how the results should be interpreted. Bower et al showed that after an unspecified nerve block, 13 out of 15 patients had pain relief and went on to have their IIN, IHN and/or LFC nerve excised. Again, there were no clear criteria for putting the patient through neurectomy.
Heise et al suggested that nerve block neither predicts nor changes outcome. They suggested that if hernia is done without mesh, then nerve blocks are needed to identify nerve involvement. However, if a mesh is present, the sensitivity of the test is poor due to lack of spread of anaesthetic agent because of mesh-related fibrosis. Though peripheral nerve blocks or paravertebral blocks have been tried, they lack the ability to differentiate the involved nerve and are only helpful temporarily as a means of relieving pain.
CT or MRI scans are helpful in identifying non-neuropathic causes of chronic groin pain by identifying mesh-related pathologies, recurrent hernias and occasionally neuromas[35,36]. A few studies have use MR Neurography to differentiate the involved nerves by studying the water content of the inguinal nerves. Kim et al carried out electromyograms on all patients, specifically looking for denervation of the pyramidalis muscle which is supplied by the IIN nerve. They showed that 91% of IIN neurectomies and 90% of combined neurectomies were successful, although there no mention of the rate of pain recurrence.
TREATMENT OPTIONS FOR CHRONIC GROIN PAIN
The treatment of chronic groin pain can be a difficult ordeal for both the patient and the clinician. Many algorithms have been put forward for management of chronic groin pain[2,39], but none of them has been proved in randomised trials. Pain related to neuropraxia (intact axon and myelin sheath), is usually temporary and may resolve itself in around 6 mo post-herniorraphy. As time progresses, chronic groin pain disappears without treatment in 30% of the patients, remains mild in 45% and in 25% of them it persists as severe pain affecting their everyday life.
Chronic groin pain has been shown to be aggravated by walking, stooping or hyper-extension of the hip and relieved by recumbent position and flexion of the hip and thigh. Hence, some clinicians have advised lifestyle changes, advocating sedentary lifestyle or sedentary occupations to negate the neuropathic pain caused by movement. This leads to poor quality of life and loss of productivity and is not now recommended because of the availability of better medical and surgical modalities.
Many clinicians use pharmacologic agents to manage chronic groin pain. These include non-steroidal anti-inflammatory drugs (NSAIDs), opioids, muscle relaxants, antiepileptics and antidepressants. However, these drugs may not prove helpful in relieving all types of chronic groin pain. The anti-depressants and antiepileptics are helpful in neuropathic pain whereas opioids or NSAIDs are usually minimally effective or ineffective for neuropathies. In most studies, NSAIDs were used as the first line analgesic treatment. Kim et al used gabapentin or oral steroids as second line agents following the failure of NSAIDs. The steroids work by reducing the inflammation and oedema surrounding entrapped nerves. The efficacy of these treatment regimens has not been proven and majority of patients suffer recurrence with worse pain due to development of resistance to analgesics.
Physical and psychological therapies
Physical therapies including massage, physiotherapy and acupuncture have been tried. Keller et al used thermotherapy to temporarily negate the painful stimulus. Ferzli et al tried Capsaicin cream applied topically as a counter-irritant to desensitize painful stimulus. These physical techniques may reduce pain temporarily but few, if any, can prevent the recurrence of pain.
Nerve blocks reversibly interfere with neuronal transmission, leading to temporary pain relief. This can, therefore, be both diagnostic and therapeutic. The ideal nerve block would specifically anaesthetise the nerve proximal to the injury but this is technically challenging. Various chemical agents used for blockade are shorter- or longer- acting local anaesthetics, steroids and glycerol as well as neurolytic solutions such as alcohol or phenol. Commonly, these agents prevent neuronal transmission through nerve fibres either by blocking membrane ion channels or by denaturation of axon proteins. They can also be used with non-pharmacologic techniques like cryoanalgesia and transcutaneous electrical nerve stimulation, depending upon the response to the anaesthetic agents. All these therapeutic modalities have their own risks, therefore a positive diagnostic block should guide the further use of therapeutic blocks.
There is little published information on the success rate of nerve block as this depends on the experience of the surgeon or the anaesthetist performing the procedure. There is no consensus on approach or the type of anaesthetic agent to be used for therapeutic inguinal nerve blockade. Previously, blind injection of local anaesthetics was practiced, based on knowledge of the anatomy of the nerves. Recently Ultrasound guided blocks have been shown to be highly accurate and selective for blockade of either the IIN or the IHN, thereby increasing success rates. In a case reported by Hartrick, GFN block was attempted through a trans-psoas approach using the L3-L4 vertebral space as a guide. This anecdotal evidence cannot be generalised to the population and more extensive controlled trials are needed.
Alcohol or phenol injection has been tried for reducing chronic inflammation caused by mesh or post-operative fibrosis. Neuro-destructive procedures, such as cryo-ablation which destroy the nerve fibres by coagulation at very low temperatures (-40°C), have been shown to give some temporary pain relief. Following cryo treatment pain recurred due to axonal regeneration. Radiofrequency pulses, working by thermo-coagulating nerves at very high temperatures, have been shown to cause temporary pain relief in ilioinguinal neuralgia. Again, definite evidence for their effectiveness is lacking.
The surgical treatment of chronic groin pain was first described by Stulz et al in 1982. They performed IIN neurectomy on 5 patients with chronic groin pain following inguinal hernia repair, achieving a 100% success rate. However, surgical explorations and neurectomy carried out by other groups during this period were quite unsuccessful. Hameroff et al performed IIN neurectomy on 2 patients with 100% recurrent pain after few months. Harms et al reported similar problems, also in two patients. The first patient had 2 unsuccessful explorations, followed by successful GFN block and 3rd exploration leading to GFN neurectomy. Second patient had IIN neurectomy on 1st exploration and, due to recurrence of pain further, exploration and GFN neurectomy. Since then a number of studies have shown success rates ranging from 70%-100%[11,12,24,27,29,30,32-34,38,41,48-59] (Table 1).
Table 1 Studies showing neurectomy performed by open, laparoscopic or a combination of both open and laparoscopic approach.
First patient had 2 unsuccessful exploration, followed by successful GFN block and 3rd exploration with GFN neurectomy. Second patient had IIN neurectomy on 1st exploration and due to recurrence of pain further exploration and GFN neurectomy
History and clinical examination alone was done for pre-operative assessment. Mesh removal alone did not relieve pain in any patients. IIN was commonly excised. Majority of patients had excellent pain relief, no differentiation could be done to identify those with hernia repair
Diagnostic nerve blocks were attempted in all patients. 8 out of 30 patients responded to conservative treatment and the rest were subjected to IIN neurectomy alone. No follow-up data was available and complications were not mentioned
All patients had failed medical treatment. No clear information on diagnosis of nerve entrapment, One patient had previous unsuccessful GFN resection and another patient had previous failed IIN resection
3/33, 10% had recurrent pain, but no clear mention about hernia patients
NM for hernia patients
33 patients were operated for CGP, but only 16 had previous hernia repair. Diagnostic nerve blocks done on all patients. Of all 33 patients operated, 91% of IIN neurectomies and 90% of combined IIN + IHN neurectomies were successful
Diagnosis of neuropathy was done using clinical findings and positive Tinel’s sign. All patients had failed conservative treatment with systemic analgesics, injection of local anaesthetics and steroids, and physiotherapy. Radical neurectomy done in all cases. GFN not excised in any case
All patients had previous open hernia repair and 2 failed percutaneous nerve blocks to treat CGP. TAPP repair done initially, followed by groin exploration, mesh removal and nerve transection. Too short follow-up
Percutaneous nerve block was unsuccessful in all patients. Initially transabdominal diagnostic laparoscopy was performed irrespective of the route of initial surgery. Mesh was placed in the opposite location to the first mesh (laparoscopic if the first was open and vice-versa). Too short follow-up
Removal of the foreign body (mesh) alone has not been shown to relieve chronic groin pain. It is thought that it is due to chronic inflammation around the nerves from the mesh-induced reaction and the consequent degenerative nerve damage. Traditionally, surgical treatment of chronic groin pain includes groin exploration, mesh removal and neurectomy. Open chemical neurolysis has been tried, but does not resolve the problem of neuromas and secondary scarification. Freeing the nerve alone (physical neurolysis) has been tried but with high failure rates[27,53]. Similarly simple division of the nerves without resection is not recommended. The entire length of the nerves should be excised, in order to involve all the neural connections between the nerves. Neurectomy with or without mesh excision is usually the preferred surgical treatment but there are no current consensus on which surgical approach should be chosen and which nerve should be excised. Heise et al found that 62% of patients who had mesh removal plus neurectomy achieved excellent results in comparison with the mesh-removal-alone group where the success rate was 50%. They concluded that concurrent neurectomy affords better results than mesh removal alone. Recently radio-frequency ablation of inguinal nerves have used with the aim for ablating the painful impulses transmitted by injured nerves. Rozen et al found that after radio-frequency ablation at T12, L1, L2 root level 4 out of 5 patients showed complete resolution of pain 4 to 9 mo later. Again, there is a lack of systematic evidence to support these findings.
The IIN can be identified lateral to the internal ring and then traced towards the external ring and resected as distally as possible. The IHN can be identified by the separation of the external oblique aponeurosis from the underlying internal oblique muscle as proximally as possible. With the IHN, dissection should include the intramuscular section, in order to look for nerve entrapped by sutures, mesh plugs or tacks. The GFN is usually identified through a retro-peritoneal (flank) approach. In a very rare case of LFC nerve involvement, decompression was performed by releasing the inguinal ligament on the anterior superior iliac spine and the lateral fibres of internal oblique aponeurosis.
Amid adopted an anterior approach, where the nerve could be identified within the lateral crus of the internal ring, within the internal ring or between the spermatic cord and the inguinal ligament. He showed that complete resection might not be possible with this approach, but that even partial resection is sufficient if the other 2 nerves are resected completely. He devised a single stage procedure, where simultaneous IIN, IHN and GFN neurectomies were performed under local anaesthetic with proximal end implantation of these nerves. Amid also devised a technique of implantating the cut end of the IIN and IHN within the fibres of the internal oblique, reducing the risk of adherence with aponeurotic structures and thereby reducing the chance of recurrent pain. For GFN, the nerve was cut under tension in order to retract the nerve into the internal ring. In a retrospective review of 225 patients who underwent surgery for neuropathic and non-neuropathic pain, 11% had traumatic neuroma, 32% had nerve entrapment by suture, staple or mesh and 57% had perineural fibrosis. They showed complete improvement in 85% of their patients, while 15% of them had transient insignificant pain with no functional impairment. Four of the 225 patients showed no benefit from this triple neurectomy. Krähenbühl et al performed laparoscopic triple neurectomies using a retro-peritoneal approach and showed complete cure in three patients. Ducic et al adopted an open inguinal approach to identify the GFN postero-lateral to the cord, traced the nerve from there all the way to the pre-peritoneum and resected under tension. They showed 100% pain relief in 4 patients treated with GFN neurectomy.
Resected tissue from neurectomy should be sent for histology to confirm the removal of the involved nerve. Most importantly, there should be an informed decision about post-neurectomy numbness in the area of corresponding nerve innervation.
Criteria for surgical treatment
Surgical treatment is required if refractory pain persists after treatment with oral analgesics and/or local nerve(s) blockades. Nerve block must have resulted in a complete or substantial decrease in pain before neurectomy can be recommended. There are no defined limits on how often nerve blocks can be carried out and the practice has varied among surgeons worldwide. Deysine et al employed IIN block and if it was effective on first use, IIN neurectomy was then considered. No information is given on the success rate of nerve blockade from this study or the reasons for selecting successful IIN block alone as an indication for surgical treatment. Kim et al also relied on nerve blocks alone as an indication for neurectomy. They concluded that the nerve blocks were sensitive enough if carried out by an experienced anaesthetist. Bower et al showed temporary pain relief in 13 of their 17 patients following unspecified nerve block. These patients went on to have IIN, IHN or LFC neurectomy depending on operative findings. Failure or recurrence of pain following at least two attempted nerve blocks is the criterion for choosing surgery followed in most units worldwide.
Loos et al showed that previous pain treatment is a predictor of poor operative treatment result. Kehlet et al studied factors for persistent post-surgical pain and found that a few patients suffer from central nervous system sensitisation, making them refractory to any form of treatment and poor candidates for surgical exploration. Nerve blocks and TENS are effective treatments for such patients and surgery should be avoided. Currently there is no consensus on the type of assessment tool for patients needing neurectomy and, as a result, there is no definitive protocol available for selecting patients for surgical exploration.
Timing of surgical intervention
Differences in the assessment of chronic groin pain, and variations in diagnostic practice and in the length of trial period with nerve blocks, have meant that the timing of surgical intervention has been widely varied. The timing of surgical intervention should ideally be at least 6 mo after herniorraphy to give adequate time for any neuropraxia to settle and time to try medical management.
A combined open and laparoscopic approach has been proposed by two groups[41,57]. Keller et al used a protocol where after removal of mesh from the previous hernia repair, further mesh was placed in the opposite location to the first mesh (laparoscopic, if previously open repair and vice versa). Twenty of 21 patients reported significant resolution of symptoms at 6 wk follow-up. Results showed that an initial laparoscopic approach aids examination of the inguinal areas to rule out a recurrent hernia or any other inguinal pathology. At the same time if a previous laparoscopic repair was performed, the mesh was excised and triple neurectomy plus re-do repair carried out using an open approach. Conversely, if an open repair was done previously, the inguinal areas were checked initially using laparoscopy and a TAPP repair performed, followed by mesh removal plus triple neurectomy through the previous open incision. These authors also found that one patient with testicular pain and a previous plug-and-patch repair, had the vas engulfed by mesh. Removal of the plug with the vas cured his symptoms, thereby avoiding an unnecessary neurectomy which would have been performed if open approach alone was applied.
Rosen et al took a similar approach in patients with previous open inguinal hernia repair, using initial laparoscopic evaluation and TAPP repair, followed by open exploration, removal of mesh and then IIN and IHN neurectomy. They believed that removal of GFN was not needed, as none of their patients had any ejaculatory or other sexual symptoms. In one patient with chronic orchalgia following previous plug and patch repair, the initial diagnostic laparoscopy showed plug mesh engulfing the vas deferens, and the resection of both led to permanent relief of pain. The other 11 patients showed significant improvement in their pain following neurectomy. To date, there are no randomised studies comparing the open and laparoscopic approaches for neurectomy. The majority of the available results are from individual case series and are, therefore, biased by individual surgeon’s laparoscopic abilities and the small number of patients reported.
Which nerve should be excised?
A review of surgical treatment for chronic groin pain carried out by Aasvang et al showed that the details of surgical treatments used were not evidence based and varied between different published studies. There was no clear explanation in most studies of why only one or two nerve were resected, rather than all three. Neurectomy should ideally resect the entire length of the nerve as far proximally as possible, to leave a smoothly cut end. There is still no consensus on whether only the affected or the entrapped nerve should be removed, or whether three nerves should be removed on the basis that remaining nerve branches may still transfer pain stimuli. Resection of the three nerves, IIN, IHN and GFN, has been shown to permanently relive chronic groin pain at the expense of inguinal numbness.
Ilioinguinal neurectomy alone has also been shown to be an effective treatment for relieving chronic groin pain in several studies[29,32,38]. Starling et al performed IIN neurectomy alone in 17 patients and showed complete pain relief in 15 of them. Kim et al showed similar results, with 19 of their 21 patients showing considerable pain relief following isolated IIN neurectomy. In a retrospective review of 19 patients, Keller et al showed that triple neurectomy was performed in 7, dual neurectomy in 9 and at least one nerve was excised in 18 patients. Of 19 patients only one had recurrent pain a year after neurectomy.
Loos et al followed a tailored neurectomy approach where, depending on intra-operative findings of nerve involvement or mesh pathology, the nerve was excised with or without mesh. According to these authors, this protocol avoids the removal of all three nerves, as proposed by Amid, avoiding the consequent chronic numbness. In a retrospective review of 68 patients who underwent tailored neurectomy, 12 patients (17.6%) needed further operation because of persistent pain. This study showed a complete pain relief in 52%, partial pain relief in 24% and pain unchanged in 24% at 1.5 years median follow-up.
Vuilleumier et al in a prospective cohort study of neuropathic groin pain patients, defined a radical neurectomy where the inguinal canal was explored through an anterior approach and mesh, IIN and IHN were removed radically by sharp dissection, ends of the nerves being tied with prolene sutures. They showed that median pain score (VAS) decreased significantly post-operatively, with 41 (95%) reporting complete relief and 2 (5%) having partial relief from pain. There had been a median of 6 mo work incapacity in theses patients but all of them returned to work 6 wk post-operatively. Vuilleumier et al suggested that as GFN is a small nerve and neurectomy of GFN can cause damage to spermatic blood vessels, the procedure should not recommended. Overall, there is no consensus on which nerve should be excised for the treatment of chronic groin pain.
Dealing with neurectomized nerve ends
The transacted nerve can be ligated, cauterised or buried within the muscle fibres. Keller et al did not ligate the cut nerve ends until bleeding occurred, because of the risk of neuroma formation at the tied end. Majority of surgeons usually tie the nerve end with absorbable suture and tuck it under the internal oblique muscle.
Currently there are no long-term results available from large studies on the safety of surgical mesh removal with or without neurectomy.
Pubic periosteal reaction or osteitis
If there is pubic periosteal reaction or osteitis, then possible causative agents such as suture materials, staples or rolled up meshes should be removed. Steroid injection can be useful when used intra-operatively or post-operatively if pain persists.
Chronic groin pain is not uncommon. It is particularly common in patients with pre-operative pain due to hernia and in patients who are of younger age. Diagnosing chronic groin pain is difficult and needs a high level of patient co-operation. Pain severity is subjective and will remain difficult to evaluate until better scoring systems are developed. In most studies pain is measured subjectively prior to initiation of medical or surgical treatment. Occasionally, objective assessment tools like VAS are used or there is correlation with pre-operative pain scores before treatment is given. There is currently a lack of consensus on the appropriate transition from medical to surgical management of these patients.
The role of surgery in patients with chronic groin pain is controversial and due to various surgical methodologies adopted by surgeons worldwide, data are highly confusing and difficult to interpret. Moreover, the current treatment regimens for chronic groin pain have limited success and their long-term benefits and quality of life effects are still uncertain. A randomised clinical trial comparing nerve blocks vs surgical neurectomy is currently being undertaken to obtain a definitive answer to this difficult problem.
Peer reviewers: Hayrullah Derici, MD, Associate Professor, Department of General Surgery, Balikesir University Medical Faculty, Balikesir 10145, Turkey; Marty Zdichavsky, MD, Department of General, Visceral and Transplant Surgery, University Hospital Tübingen, Hoppe-Seyler-Str. 3, 72076 Tübingen, Germany
S- Editor Wang JL L- Editor Hughes D E- Editor Zheng XM
Poobalan AS, Bruce J, King PM, Chambers WA, Krukowski ZH, Smith WC. Chronic pain and quality of life following open inguinal hernia repair.Br J Surg. 2001;88:1122-1126.
Bay-Nielsen M, Perkins FM, Kehlet H. Pain and functional impairment 1 year after inguinal herniorrhaphy: a nationwide questionnaire study.Ann Surg. 2001;233:1-7.
Staal E, Nienhuijs SW, Keemers-Gels ME, Rosman C, Strobbe LJ. The impact of pain on daily activities following open mesh inguinal hernia repair.Hernia. 2008;12:153-157.
Kalliomäki ML, Sandblom G, Gunnarsson U, Gordh T. Persistent pain after groin hernia surgery: a qualitative analysis of pain and its consequences for quality of life.Acta Anaesthesiol Scand. 2009;53:236-246.
Courtney CA, Duffy K, Serpell MG, O'Dwyer PJ. Outcome of patients with severe chronic pain following repair of groin hernia.Br J Surg. 2002;89:1310-1314.
Nienhuijs S, Staal E, Strobbe L, Rosman C, Groenewoud H, Bleichrodt R. Chronic pain after mesh repair of inguinal hernia: a systematic review.Am J Surg. 2007;194:394-400.
Beldi G, Haupt N, Ipaktchi R, Wagner M, Candinas D. Postoperative hypoesthesia and pain: qualitative assessment after open and laparoscopic inguinal hernia repair.Surg Endosc. 2008;22:129-133.
Hindmarsh AC, Cheong E, Lewis MP, Rhodes M. Attendance at a pain clinic with severe chronic pain after open and laparoscopic inguinal hernia repairs.Br J Surg. 2003;90:1152-1154.
Wantz GE. Testicular atrophy and chronic residual neuralgia as risks of inguinal hernioplasty.Surg Clin North Am. 1993;73:571-581.
Heise CP, Starling JR. Mesh inguinodynia: a new clinical syndrome after inguinal herniorrhaphy?J Am Coll Surg. 1998;187:514-518.
Delikoukos S, Fafoulakis F, Christodoulidis G, Theodoropoulos T, Hatzitheofilou C. Re-operation due to severe late-onset persisting groin pain following anterior inguinal hernia repair with mesh.Hernia. 2008;12:593-595.
O'Dwyer PJ, Alani A, McConnachie A. Groin hernia repair: postherniorrhaphy pain.World J Surg. 2005;29:1062-1065.
Davis CJ, Arregui ME. Laparoscopic repair for groin hernias.Surg Clin North Am. 2003;83:1141-1161.
Amid PK. Commentary on: Pokorny H, Klingler A, Schmid T, Fortelny R, Hollinsky C, Kawji R, Steiner E, Pernthaler H, Függer R, Scheyer M (2008) Recurrence and complications after laparoscopic versus open inguinal hernia repair: results of a prospective randomized multicenter trial.Hernia. 2008;12:441.
Broin EO, Horner C, Mealy K, Kerin MJ, Gillen P, O'Brien M, Tanner WA. Meralgia paraesthetica following laparoscopic inguinal hernia repair. An anatomical analysis.Surg Endosc. 1995;9:76-78.
Keating JP, Morgan A. Femoral nerve palsy following laparoscopic inguinal herniorrhaphy.J Laparoendosc Surg. 1993;3:557-559.
Grant AM, Scott NW, O'Dwyer PJ. Five-year follow-up of a randomized trial to assess pain and numbness after laparoscopic or open repair of groin hernia.Br J Surg. 2004;91:1570-1574.
Heikkinen T, Bringman S, Ohtonen P, Kunelius P, Haukipuro K, Hulkko A. Five-year outcome of laparoscopic and Lichtenstein hernioplasties.Surg Endosc. 2004;18:518-522.
Kumar S, Wilson RG, Nixon SJ, Macintyre IM. Chronic pain after laparoscopic and open mesh repair of groin hernia.Br J Surg. 2002;89:1476-1479.
Myers E, Browne KM, Kavanagh DO, Hurley M. Laparoscopic (TEP) versus Lichtenstein inguinal hernia repair: a comparison of quality-of-life outcomes.World J Surg. 2010;34:3059-3064.
Vuilleumier H, Hübner M, Demartines N. Neuropathy after herniorrhaphy: indication for surgical treatment and outcome.World J Surg. 2009;33:841-845.
Aasvang EK, Møhl B, Kehlet H. Ejaculatory pain: a specific postherniotomy pain syndrome?Anesthesiology. 2007;107:298-304.
Hair A, Paterson C, Wright D, Baxter JN, O'Dwyer PJ. What effect does the duration of an inguinal hernia have on patient symptoms?J Am Coll Surg. 2001;193:125-129.
Ducic I, West J, Maxted W. Management of chronic postoperative groin pain.Ann Plast Surg. 2008;60:294-298.
Kalliomäki ML, Meyerson J, Gunnarsson U, Gordh T, Sandblom G. Long-term pain after inguinal hernia repair in a population-based cohort; risk factors and interference with daily activities.Eur J Pain. 2008;12:214-225.
Starling JR, Harms BA. Diagnosis and treatment of genitofemoral and ilioinguinal neuralgia.World J Surg. 1989;13:586-591.
Harms BA, DeHaas DR, Starling JR. Diagnosis and management of genitofemoral neuralgia.Arch Surg. 1984;119:339-341.
Rab M, Ebmer And J, Dellon AL. Anatomic variability of the ilioinguinal and genitofemoral nerve: implications for the treatment of groin pain.Plast Reconstr Surg. 2001;108:1618-1623.
Deysine M, Deysine GR, Reed WP. Groin pain in the absence of hernia: a new syndrome.Hernia. 2002;6:64-67.
Starling JR, Harms BA, Schroeder ME, Eichman PL. Diagnosis and treatment of genitofemoral and ilioinguinal entrapment neuralgia.Surgery. 1987;102:581-586.
Bower S, Moore BB, Weiss SM. Neuralgia after inguinal hernia repair.Am Surg. 1996;62:664-667.
Amid PK, Hiatt JR. New understanding of the causes and surgical treatment of postherniorrhaphy inguinodynia and orchalgia.J Am Coll Surg. 2007;205:381-385.
Amid PK. Radiologic images of meshoma: a new phenomenon causing chronic pain after prosthetic repair of abdominal wall hernias.Arch Surg. 2004;139:1297-1298.
Filler A. Magnetic resonance neurography and diffusion tensor imaging: origins, history, and clinical impact of the first 50,000 cases with an assessment of efficacy and utility in a prospective 5000-patient study group.Neurosurgery. 2009;65:A29-A43.
Kim DH, Murovic JA, Tiel RL, Kline DG. Surgical management of 33 ilioinguinal and iliohypogastric neuralgias at Louisiana State University Health Sciences Center.Neurosurgery. 2005;56:1013-120; discussion 1013-120;.
Lichtenstein IL, Shulman AG, Amid PK, Montllor MM. Cause and prevention of postherniorrhaphy neuralgia: a proposed protocol for treatment.Am J Surg. 1988;155:786-790.
Sen H, Sizlan A, Yanarateş O, Senol MG, Inangil G, Sücüllü I, Ozkan S, Dağli G. The effects of gabapentin on acute and chronic pain after inguinal herniorrhaphy.Eur J Anaesthesiol. 2009;26:772-776.
Keller JE, Stefanidis D, Dolce CJ, Iannitti DA, Kercher KW, Heniford BT. Combined open and laparoscopic approach to chronic pain after inguinal hernia repair.Am Surg. 2008;74:695-700; discussion 700-1.
Ferzli GS, Edwards ED, Khoury GE. Chronic pain after inguinal herniorrhaphy.J Am Coll Surg. 2007;205:333-341.
Eichenberger U, Greher M, Kirchmair L, Curatolo M, Moriggl B. Ultrasound-guided blocks of the ilioinguinal and iliohypogastric nerve: accuracy of a selective new technique confirmed by anatomical dissection.Br J Anaesth. 2006;97:238-243.
Murovic JA, Kim DH, Tiel RL, Kline DG. Surgical management of 10 genitofemoral neuralgias at the Louisiana State University Health Sciences Center.Neurosurgery. 2005;56:298-303; discussion 298-303.
Nahabedian MY, Dellon AL. Outcome of the operative management of nerve injuries in the ilioinguinal region.J Am Coll Surg. 1997;184:265-268.
Loos MJ, Scheltinga MR, Roumen RM. Tailored neurectomy for treatment of postherniorrhaphy inguinal neuralgia.Surgery. 2010;147:275-281.
Lee CH, Dellon AL. Surgical management of groin pain of neural origin.J Am Coll Surg. 2000;191:137-142.
Amid PK. Causes, prevention, and surgical treatment of postherniorrhaphy neuropathic inguinodynia: triple neurectomy with proximal end implantation.Hernia. 2004;8:343-349.
Ducic I, Dellon AL. Testicular pain after inguinal hernia repair: an approach to resection of the genital branch of genitofemoral nerve.J Am Coll Surg. 2004;198:181-184.
Rosen MJ, Novitsky YW, Cobb WS, Kercher KW, Heniford BT. Combined open and laparoscopic approach to chronic pain following open inguinal hernia repair.Hernia. 2006;10:20-24.
Zacest AC, Magill ST, Anderson VC, Burchiel KJ. Long-term outcome following ilioinguinal neurectomy for chronic pain.J Neurosurg. 2010;112:784-789.
Wong J, Anvari M. Treatment of inguinodynia after laparoscopic herniorrhaphy: a combined laparoscopic and fluoroscopic approach to the removal of helical tackers.Surg Laparosc Endosc Percutan Tech. 2001;11:148-151.
Rozen D, Parvez U. Pulsed radiofrequency of lumbar nerve roots for treatment of chronic inguinal herniorraphy pain.Pain Physician. 2006;9:153-156.
Amid PK. A 1-stage surgical treatment for postherniorrhaphy neuropathic pain: triple neurectomy and proximal end implantation without mobilization of the cord.Arch Surg. 2002;137:100-104.
Aasvang E, Kehlet H. Surgical management of chronic pain after inguinal hernia repair.Br J Surg. 2005;92:795-801.
Loos MJ, Verhagen T, Scheltinga MR, Roumen RM. A randomised controlled trial of injection therapy versus neurectomy for post-herniorrhaphy inguinal neuralgia: rationale and study design.Hernia. 2010;14:593-597.