Skip to main content
  • Research article
  • Open access
  • Published:

Dermatome Mapping Test in the analysis of anatomo-clinical correlations after inguinal hernia repair

Abstract

Background

Nerve identification is recommended in inguinal hernia repair to reduce or avoid postoperative pain. The aim of this prospective observational study was to identify nerve prevalence and find a correlation between neuroanatomy and chronic neuropathic postoperative inguinal pain (CPIP) after 6 months.

Material

A total of 115 patients, who underwent inguinal hernia mesh repair (Lichtenstein tension-free mesh repair) between July 2018 and January 2019, were included in this prospective observational study. The mean age and BMI respectively resulted 64 years and 25.8 with minimal inverse distribution of BMI with respect to age. Most of the hernias were direct (59.1%) and of medium dimension (47.8%). Furthermore, these patients were undergoing Dermatome Mapping Test in preoperatively and postoperatively 6 months evaluation.

Results

Identification rates of the iliohypogastric (IH), ilioinguinal (II) and genitofemoral (GF) nerves were 72.2%, 82.6% and 48.7% respectively. In the analysis of nerve prevalence according to BMI, the IH was statistically significant higher in patients with BMI < 25 than BMI ≥ 25 P (< 0.05). After inguinal hernia mesh repair, 8 patients (6.9%) had chronic postoperative neuropathic inguinal pain after 6 months. The CPIP prevailed at II/GF dermatome. The relation between the identification/neurectomy of the II nerve and chronic postoperative inguinal pain after 6 months was not significant (P = 0.542).

Conclusion

The anatomy of inguinal nerve is very heterogeneous and for this reason an accurate knowledge of these variations is needed during the open mesh repair of inguinal hernias. The new results of our analysis is the statistically significant higher IH nerve prevalence in patients with BMI < 25; probably the identification of inguinal nerve is more complex in obese patients. In the chronic postoperative inguinal pain, the II nerve may have a predominant role in determining postoperative long-term symptoms. Dermatome Mapping Test in an easy and safe method for preoperative and postoperative 6 months evaluation of groin pain. The most important evidence of our analysis is that the prevalence of chronic pain is higher when the nerves were not identified.

Peer Review reports

Background

Neuroanatomy of inguinal canal is characterized by great variability [1]. Nerve identification may be difficult because their course or structure may be barely evident [2, 3]. Since inguinal nerves have a relatively superficial course, groin surgery requires particular caution in order to prevent iatrogenic nerve injuries [4, 5]. Failure of local anesthetic procedures and chronic postoperative inguinal pain (CPIP), also known as inguinodynia, are the most common and significant postoperative complications [6]. CPIP is defined as pain persisting beyond the third month after surgical intervention [7] and can affect up to 12% of patients operated on for inguinal hernia. Up to 6% of patients have moderate-severe CPIP which negatively affects their quality of life as it may impact daily activities or, in the worst cases, it may render the patient an invalid [6, 7]. Since inguinal hernias are a quite common and in many countries the Lichtenstein repair is the most frequently used procedure, in particular for primary unilateral groin hernias. CPIP should not be underestimated in planning surgery and patients should always be informed of the eventuality of this post-operative complication [8]. The Lichtenstein tension-free hernioplasty is currently one of the most popular techniques for open repair of inguinal hernias. Local anesthesia is safe and generally preferable for Lichtenstein procedure. Lichtenstein tension-free mesh repair, is based on the following steps:

  • Cutaneous incision about 1 cm above and parallel to the inguinal ligament, beginning from the pubic tubercle and extending 5–6 cm laterally.

  • Opening of the subcutaneous fat.

  • Opening of the Scarpa fascia until the external oblique aponeurosis with accurate visualization of the external inguinal ring and of the lower border of the inguinal ligament.

  • Opening of the deep fascia of the thigh to check the femoral canal for a femoral hernia.

  • Division of the external oblique aponeurosis from the external ring laterally, preserving the ilioinguinal nerve.

  • Mobilization of the superior (protecting the iliohypogastric nerve) and inferior flaps of the external oblique aponeurosis.

  • Mobilization of the spermatic cord, along with the cremaster, including the ilioinguinal nerve, the genitofemoral nerve, and the spermatic vessels.

  • Opening of the coverings of the spermatic cord and identification and isolation of the hernia sac.

  • Inversion (preferred), division, resection, or ligation of the sac, as indicated.

  • Placement and fixation of mesh to the edges of the defect or weakness in the posterior wall of the inguinal canal to make a new artificial internal ring.

  • Mandatory resection of any nerves that are injured or of doubtful integrity.

  • Gentle pulling of the testes back down to their normal scrotal position.

  • Closure of spermatic cord layers, the external oblique aponeurosis, subcutaneous tissue, and the skin.

  • The operative site is cleaned and a sterile dressing applied. Local infiltration of bupivacaine or ropivacaine may be useful.

The European Hernia Society recommends that in cases where an open approach is indicated (as in case of recurrence after a laparoscopic procedure), the Lichtenstein technique be utilized as the preferred method [6]. Mesh attachment with the use of adhesive glue may be faster and less likely to cause post-op pain if compared to attachment via suture material. Guidelines recommend intraoperative inguinal nerve identification in order to limit or prevent postoperative pain [6] and to reduce the risk of iatrogenic injury, such as entrapment between prosthetic material and tissue [9]. Recently, a systematic review and meta-analysis of worldwide literature, which analyzed identification rates of the three inguinal nerves, found great heterogeneity among studies in particular in Europe [10]. Inguinal nerve identification is performed routinely by few surgeons, despite several studies concluding that this procedure is safe and does not affect operative time [11,12,13,14].

Based on these premises, the first aim of this prospective observational study was to identify inguinal nerves during surgery, searching for significant correlations between identification rates during hernia repair and CPIP. The research was undertaken according to the Italian Privacy Laws concerning collection, storage, and analysis of private data. A formal Institutional Research Ethics Board (Perugia University, S. Maria of Misericordia Perugia Hospital and S. Maria Terni Hospital) approval was not required because of the non-interventional, retrospective, and anonymous study design; however, a signed consent for the treatment and the analysis of data for scientific purpose was obtained from all patients or relatives either at admission or as soon as they could give it. The protocol of the study was accepted from Scientific Committee of SICADS (SocietàItaliana di ChirurgiaAmbulatoriale e Day Sugery) and published in the CUDS’ (Club Unità Day Surgery) (web site https://www.clubdaysurgery.it/).

Methods

Inclusion and exclusion criteria

Patients included consecutive male patients, aged 18 years and older, undergoing elective open Lichtenstein repair for unilateral primary inguinal hernia. Exclusion criteria: complicated hernias (incarcerated, strangulated, or recurrent); chronic use of analgesics, antidepressants, anxiolytics, anticonvulsants, abuse of alcohol and drugs; fibromyalgia, herpes zoster.

Outcomes

Primary outcomes: intraoperative identification of the inguinal nerves.

Secondary outcomes: chronic postoperative inguinal pain after 6 months.

Interventions

All the interventions were performed according to the Lichtenstein technique with a light macroporous mesh in polipropilene. Modification to the original technique consisted in prophylactic inguinal neurectomy (IIN) and mesh fixation with fibrin glue.

Characteristics of patients

Before surgery, demographics and anamnesis/comorbidities, which could influence sensitivity for local pain, were collected in an excel table. Furthermore, patients signed an informed consent for the procedure. In addition, they were asked to describe local symptoms and the investigator performed a physical examination. Preoperative pain was localized according to the dermatomal distribution of the three inguinal nerves (Dermatome Pain Mapping Test) (Fig. 1). Pain severity was scored according to the seven criteria of the Inguinal Pain Questionnaire (IPQ) [15]. Intraoperatively, hernia characteristics were recorded according to the EHS (European Hernia Society) classification [6, 16]. Surgeons searched for the iliohypogastric (IH), ilioinguinal (II) and genitofemoral (GF) nerves according to the Lichtenstein procedure. Nerves were isolated; their major diameter was measured in millimeters during the mesh hernia repair. Only the II nerve was cut with scissors and their proximal stumps were tied in order to prevent any hindrance caused by mesh or scar tissues and to reduce the risk of neuroma formation. In our study, the course of the nerves was not recorded.

Fig. 1
figure 1

Dermatomes Mapping Test

Follow-up

Follow-up was set at the sixth postoperative month. Data on local symptoms were collected through a physical examination and by IPQ administration, which was completed in presence of the investigator in order to help with an explanation of the questions [15]. In the presence of pain, regardless of its severity, patients were asked to complete the "Douleur Neuropathique en 4 questionnaire” (DN4) to identify neuropathic pain [17]. A clinical examination was performed preoperatively and postoperatively according to the principles of the dermatome-mapping test (Figs. 2, 3, 4 and 5) [18].

Fig. 2
figure 2

Dermatomes Mapping Test. O = Hypoesthesia or numbness

Fig. 3
figure 3

Dermatomes Mapping Test. O = hypoesthesia or numbness

Fig. 4
figure 4

Dermatomes Mapping Test. O = hypoesthesia or numbness. X = pain

Fig. 5
figure 5

Dermatomes Mapping Test. O = hypoesthesia or numbness. X = pain

Statistical analysis

Primary outcomes: Nerve identification rates, separated according to the hernia dimension above-mentioned dichotomous variables, were analyzed with the Chi Square test, setting the confidence interval (CI) to 95% (P < 0.05). The Levene test for the homogeneity of the variance (CI 95%) and Student’s T Test were used to verify the equality of the above-mentioned methods.

Secondary outcomes: Preoperative pain and postoperative (6 months) symptoms were analyzed separately. Sample means of preoperative pain (IPQ scores) were calculated for each nerve separately in the presence (identification) and absence of the nerves, respectively. The Levene test (CI 95%) and Student’s-T Test were used. Correlations between hernia dimension, IPQ score and nerve dimension were tested by Pearson's test.

Results

A total of 115 patients, who underwent inguinal hernia mesh repair between July 2018 and January 2019, were included in this prospective observational study. The mean age and BMI respectively resulted 64 years and 25.8 with minimal inverse distribution of BMI with respect to age. Most of the hernias were direct (59.1%) and of medium dimension (47.8%) (Table 1).

Table 1 Characteristics of patients and hernia

Many of the patients were in the age range of between 75 and 84 years (27%), while the 72% of the total were between 55 and 84 years old. Twelve patients (10.4%) were lost to follow-up.

Identification of the inguinal nerves

The II was the most frequently identified nerve (95 patients, 82.6%). The prevalence of the IH nerve (83 patients, 72%) and GF (56 patients, 48.7%) was lower (Table 2). In the analysis of nerve prevalence according to BMI the IH was statistically significant higher in patients with BMI < 25 than BMI ≥ 25 P (< 0.05).

Table 2 Nerve prevalence according to BMI

No correlation was found between age and nerve detection. Prevalence according to inguinal hernia dimension resulted significantly different for the II nerve in favor of the smallest (≤ 3 cm) (Table 3).

Table 3 Nerve prevalence according to inguinal hernia dimension

Preoperative groin pain

Over half the patients (n.78/115, 67.8%) had preoperative groin pain. Prevalence of pain during activity and rest, which impaired activities, was 65.4% and 35% respectively. This was prevalent in II/GF dermatome (41/78, 52.6%), IH (11/78, 14%) and IH + II/GF dermatomal distribution (11.5%) (Table 4).

Table 4 Localization and type of groin preoperative pain

Out of three patients with diffuse pain only one had pain influencing activities (IPQ > 3). Pain at rest was prevalent in II/GF dermatome (44%) followed by IH + II/GF localization (15%). Pain during activity resulted more prevalent in II/GF dermatome (57%). Pain with IPQ ≤ 3 prevailed in II/GF region (54%) while IPQ > 3 was less prevalent in this region (48%) in favor of IH + II/GF dermatomes (14%) (Table 5).

Table 5 Localization and type of postoperative pain at 6 months

Chronic postoperative inguinal pain after 6 months

Fifteen patients (13%) had chronic postoperative inguinal pain after 6 months. The CPIP prevailed at II/GF dermatome (66%). In eight patients’ pain was probably of neuropathic origin (DN4 > 3) (53%). Five of these patients presented preoperative pain in the same region and had pain with IPQ > 3. In the other patients pain was probably of nociceptive origin (DN4 ≤ 3) (Table 5, Fig. 6).

Fig. 6
figure 6

Localization and type of postoperative pain at 6 months

Analysis of 6-month follow-up outcomes with respect to nerve identification and neurectomy

The identification of the IH nerve was performed in 72.2% and the relation between the identification of the IH nerve and chronic postoperative inguinal pain after 6 months was not significant (P = 0.562). When the IH nerve was missing, prevalence of pain was lower (6% vs 12%) and prevalence of hypoesthesia was similar (12–13%). Both the mentioned symptoms prevailed in absence of the IH nerve (6% vs 1%).

The relation between the identification/neurectomy of the II nerve and chronic postoperative inguinal pain after 6 months was not significant (P = 0.542). Narrative analysis is in accordance with the literature since the II resulted the most identified nerve (82.6% in our series vs 84.3% in the literature) and the association of this nerve with pain has been extensively studied. Indeed, prevalence of chronic pain resulted noticeably higher when the II nerve was missing (20% vs 8%): about double the overall incidence of the whole series. Prevalence of the hypoesthesia was slightly higher after neurectomy (13% vs 10%). Both the above-mentioned symptoms were prevalent in the absence of the nerve (5% vs 2%). Most of the patients who resulted negative at follow-up underwent II neurectomy.

Overall postoperative hypoesthesia

Hypoesthesia was detected in 17 patients (14.8%). No cases of severe hypoesthesia compromising quality of life occurred. This complication was prevalent in II/GF dermatomal distribution (10 pts).

Discussion

Inguinal nerves have a superficial course and they are exposed to risk of iatrogenic injuries [19]; nerve identification is recommended both to prevent injuries and to perform a more effective local anesthesia [6].

Recently, a systematic review and meta-analysis of worldwide literature reported the identification rates of the inguinal nerves both during open inguinal hernia repair and during cadaveric dissections [10]. Overall prevalence of IH, II, GF nerves resulted 74.2%, 84.3% e 48.2%, respectively. From this review, it is clear that nerve identification during hernia repair is more difficult than in cadaver studies, and greatly depends on the preparedness, expertise and skills of the surgeon [20, 21]. Some studies have tried to find a correlation between BMI (weight) age and cross-sectional area of nerves of the upper and lower limbs [22,23,24]. In our experience (II 82.6%, IH 72% and GF 48.7%) was in line with the precedent literature. The news of our analysis is the statistically significant higher IH nerve prevalence in patients with BMI < 25. In the literature, it is reported how preoperative pain is related to postoperative pain [25, 26]. Chronic postoperative pain can be influenced by concomitant pain in other regions and by the general physical preoperative state [27]. Inadequate or failure in controlling perioperative acute pain can cause postoperative pain [25, 28]. Furthermore, central sensibilization and neuronal plasticity following intense and prolonged inflammation may predispose to hyperalgesia, thus favoring the passage from acute to chronic pain [8].

In the present study, pain was classified by dermatomal localization through the Dermatome Inguinal Mapping Test and its severity that took into consideration both intensity and impact on activities as well as quality of life with the Inguinal Pain Questionnaire (IPQ) [15]. We aimed to discriminate neuropathic from nociceptive postoperative pain. Nociceptive pain derives from tissue damage or inflammation, which stimulates the nociceptors. It can be subsequent to prosthesis malpositioning, dislocation, “meshoma”, excessive inflammatory response to foreign material or because of periostitis in case of sutures placed over the pubic tubercle. It is usually continuous and present at rest [19]. Neuropathic pain, otherwise, is subsequent to direct or secondary damage of nervous structures. Paresthesia, allodynia, hyperesthesia, hypoesthesia accompanies this type of pain [9]. Neuropathic pain is usually exacerbated by physical activity. Unfortunately, in the literature, a clear differentiation of these two types of pain is difficult to establish since it depends on the diagnostic methodology employed and on the patient’s characteristics [29]. Distension of the peritoneum weakened conjoint tendon and aponeurotic traumas can be possible causes of preoperative pain [30]. Most authors focus on preoperative pain in relation to the II nerve. A recent prospective study supported the hypothesis that preoperative pain can be due to compression neuropathy on the II nerve, with its enlargement in correspondence of the external inguinal ring [31]. The same authors did not find any significant relation between preoperative pain and the type of hernia, or the course of the IH and II nerves [31].

Chronic neuropathic pain is defined as a pain, which lasts beyond the third postoperative month [32]. A systematic review evaluated the prevalence of neuropathic pain in the context of chronic postoperative pain [33]. Neuropathic pain is characterized by a descriptive and a sensorial component. Evaluation of pain considering only these parameters is not adequate since sensitivity alterations may be subsequent to nociceptive stimuli too [33]. For this reason, it is better to consider the neuropathic connotation of pain as probable instead of certain. Probability is higher depending on the strength of the methods employed [34]. Descriptive and sensitivity testing should be completed by specific questionnaires such as the DN4 and a thorough physical examination [17, 33, 34].

The same review reported that the prevalence of chronic (probable) neuropathic postoperative pain was about 31% [33]. In our series, the incidence of probable neuropathic postoperative pain (DN4 = 4) was 33%. This pain was prevalent in II/GF dermatomes. In the majority of patients had CPIP in region of GF nerve, which had the lowest identification rate. The reason for that may be the accidental cut of the nerve intraoperatively. Therefore, the change of strategy into endoscopic procedures in treating many obese patients may be useful to avoid this injury. Indeed, in males the identification of the genital branch of GF nerve is very difficult for its location near cremasteric muscle fibers along the posteromedial spermatic cord and cremasteric vein [35].

Conclusion

The identification of inguinal nerves is very heterogeneous (II 82.6%, IH 72% and GF 48.7%), for this reason an accurate knowledge of these variations is needed during the open mesh repair of inguinal hernias. The new results of our analysis is the statistically significant higher IH nerve prevalence in patients with BMI < 25; probably the identification of inguinal nerve is more complex in obese patients. In the chronic postoperative inguinal pain, the II nerve may have a predominant role in determining postoperative long-term symptoms, in effect this pain prevailed pain at II/GF dermatome and in 1/3 of cases there is a neuropathic groin pain. Furthermore, Dermatome Mapping Test in an easy and safe method for preoperatively and postoperatively 6 months evaluation of groin pain. The most important evidence of our analysis is that the prevalence of chronic pain is higher when the nerves were not identified.

Availability of data and materials

The datasets used during the current study are available from the First Author Roberto Cirocchi (mail: roberto.cirocchi@unipg.it) on reasonable request.

Abbreviations

BMI:

Body mass index

CPIP:

Chronic postoperative inguinal pain

CUDS:

Club Unità Day Surgery

DN4:

DouleurNeuropathiqueen 4 questionnaire

EHS:

European Hernia Society

GF:

Genitofemoral nerve

IH:

Iliohypogastric nerve

II:

Ilioinguinal nerve

IIN:

Ileo-inguinal neurectomy

IPQ:

Inguinal Pain Questionnaire

SICADS:

Società Italiana di Chirurgia Ambulatoriale e Day Sugery

References

  1. Frassanito L, Zanfini BA, Pitoni S, et al. Ultrasound guided genitofemoral nerve block for inguinal hernia repair in the male adult: a randomized controlled pilot study. Minerva Anestesiol. 2018;84:189–95.

    PubMed  Google Scholar 

  2. Lange JF, Wijsmuller AR, van Geldere D, Simons MP, Swart R, Oomen J. Feasibility study of three-nerve-recognizing. Lichtenstein procedure for inguinal hernia. Br J Surg. 2009;96(10):1210–4.

    Article  CAS  Google Scholar 

  3. Pandhare SR, Gaikwad AP. Anatomical study of ilioinguinal nerve and its clinical correlation. Int J Curr Res Rev. 2013;5(9):69–75.

    Google Scholar 

  4. Emeksiz S, Ozden H. Effects of variable courses of Inguinal nerves on pain in patients undergoing Lichtenstein repair for inguinal hernia: preliminary results. Act Chir Belg. 2013;3:196–202.

    Article  Google Scholar 

  5. Graham DS, MacQueen IT, Chen DC. Inguinal neuroanatomy: implications for prevention of chronic postinguinal hernia pain. Int J Abdom Wall Hernia Surg. 2018;1:1–8.

    Google Scholar 

  6. HerniaSurge Group. International guidelines for groin hernia management. Hernia. 2018;22(1):1–165.

    Article  Google Scholar 

  7. Itani KMF, Fitzgibbons R. Approach to Groin Hernias. JAMA Surg. 2019;154(6):551–2.

    Article  Google Scholar 

  8. Bjurstrom MF, Nicol AL, Amid PK, Chen DC. Pain control following inguinal herniorrhaphy: current perspectives. J Pain Res. 2014;7:277–90.

    PubMed  PubMed Central  Google Scholar 

  9. Mattoo S, Paul V, Kachroo SL, et al. Outcome of elective prophylactic ilioinguinal neurectomy in prevention of chronic groin pain after open inguinal hernia repair. J Evol Med Dent Sci. 2016;5(35):1992–7.

    Article  Google Scholar 

  10. Cirocchi R, Henry BM, Mercurio I, et al. Is it possible to identify the inguinal nerves during hernioplasty? A systematic review of the literature and meta-analysis of cadaveric and surgical studies. Hernia. 2019;23(3):569–81.

    Article  CAS  Google Scholar 

  11. Alfieri S, Amid PK, Campanelli G, et al. International guidelines for prevention and management of postoperative chronic pain following inguinal hernia surgery. Hernia. 2011;15:239–49.

    Article  CAS  Google Scholar 

  12. Barazanchi AWH, Fagan PVB, Smith BB, Hill AG. Routine neurectomy of inguinal nerves during open onlay mesh hernia repair. Ann Surg. 2016;264:64–72.

    Article  Google Scholar 

  13. Amid PK, Shulman AG, Lichtenstein IL. Open “tensionfree” repair of inguinal hernias: the Lichtenstein technique. Eur J Surg. 1996;162:447–53.

    CAS  PubMed  Google Scholar 

  14. Sun P, Cheng X, Deng S, Hu Q, Sun Y, Zheng Q. Mesh fixation with glue versus suture for chronic pain and recurrence in Lichtenstein inguinal hernioplasty. Cochrane Database Syst Rev. 2017;2:CD010814.

    PubMed  Google Scholar 

  15. Fränneby U, Gunnarsson U, Andersson M, Heuman R, Nordin P, Nyrén O, Sandblom G. Validation of an Inguinal Pain Questionnaire for assessment of chronic pain after groin hernia repair. Br J Surg. 2008;95(4):488–93.

    Article  Google Scholar 

  16. Miserez M, Alexandre JH, Campanelli G, et al. The European hernia society groin hernia classification: simple and easy to remember. Hernia. 2007;11(2):113–6.

    Article  CAS  Google Scholar 

  17. Bouhassira D, Attal N, Alchaar H, et al. Comparison of pain syndromes associated with nervous or somatic lesions and development of a new neuropathic pain diagnostic questionnaire (DN4). Pain. 2005;114(1–2):29–36.

    Article  Google Scholar 

  18. Álvarez R. Dermatome mapping: preoperative and postoperative assessment. In: Jacob B, Chen D, Ramshaw B, Towfigh S, editors. The SAGES manual of groin pain. London: Springer; 2016. p. 2016.

    Google Scholar 

  19. Gawlas IA, Peacock WJ. Groin pain: a neurologic and musculoskeletal anatomic review. In: Jacob B, Chen D, Ramshaw B, Towfigh S, editors. The SAGES manual of groin Pain. London: Springer; 2016. p. 2016.

    Google Scholar 

  20. Lorenz R, Stechemesser B, Reinpold W, et al. Development of a standardized curriculum concept for continuing training in hernia surgery: German Hernia School. Hernia. 2017;21(2):153–62.

    Article  CAS  Google Scholar 

  21. Wang Y, Wu T, Terry MJ, et al. Improved perioperative analgesia with ultrasound-guided ilioinguinal/iliohypogastric nerve or transversus abdominis plane block for open inguinal surgery: a systematic review and meta-analysis of randomized controlled trials. J Phys Ther Sci. 2016;28:1055–60.

    Article  Google Scholar 

  22. Lothet EH, Bishop TJ, Walker FO, Cartwright MS. Ultrasound-derived nerve cross-sectional area in extremes of height and weight. J Neuroimaging. 2019;29(3):406–9.

    Article  Google Scholar 

  23. Pan TJ, White RJ, Zhang C, Imbriglia J, Hagberg WC, Fowler JR. Does BMI, age, gender, or diabetes affect cross-sectional area of the median nerve in asymptomatic patients? Level 4 evidence. J Hand Surg. 2015;40(9):e40.

    Article  Google Scholar 

  24. Cartwright MS, Mayans DR, Gillson NA, Griffin LP, Walker FO. Nerve cross-sectional area in extremes of age. Muscle Nerve. 2013;47(6):890–3.

    Article  Google Scholar 

  25. Wright R, Born DE, D’Souza N, Hurd L, Gill R, Wright D. Why do inguinal hernia patients have pain? Histology points to compression neuropathy. Am J Surg. 2017;213(5):975–82.

    Article  Google Scholar 

  26. Reinpold WMJ, Nehls J, Eggert A. Nerve management and chronic pain after open inguinal hernia repair. Ann Surg. 2011;254(1):163–8.

    Article  Google Scholar 

  27. Johansen A, Romundstad L, Nielsen CS, Schirmer H, Stubhaug A. Persistent postsurgical pain in a general population: prevalence and predictors in the Tromsø study. Pain. 2012;153:1390–6.

    Article  Google Scholar 

  28. Aasvang EK, Gmaehle E, Hansen JB, et al. Predictive risk factors for persistent post herniotomy pain. Anesthesiology. 2010;112(4):957–69.

    Article  Google Scholar 

  29. Lange JF, Kaufmann R, Wijsmuller AR, et al. An international consensus algorithm for management of chronic postoperative inguinal pain. Hernia. 2015;19(1):33–43.

    Article  CAS  Google Scholar 

  30. Charalambous MP, Charalambous CP. Incidence of chronic groin pain following open mesh inguinal hernia repair, and effect of elective division of the ilioinguinal nerve: meta-analysis of randomized controlled trials. Hernia. 2018;22(3):401–9.

    Article  CAS  Google Scholar 

  31. Wright R, Salisbury T, Landes J. Groin anatomy, preoperative pain, and compression neuropathy in primary inguinal hernia: what really matters. Am J Surg. 2019;217(5):873–7.

    Article  Google Scholar 

  32. Hakeem A, Shanmugam V. Inguinodynia following Lichtenstein tension-free hernia repair: a review. World J Gastroenterol. 2011;17(14):1791–6.

    Article  Google Scholar 

  33. Haroutiunian S, Nikolajsen L, Finnerup NB, Jensen TS. The neuropathic component in persistent postsurgical pain: a systematic literature review. Pain. 2013;154(1):95–102.

    Article  Google Scholar 

  34. Treede RD, Jensen TS, Campbell JN, et al. Neuropathic pain: redefinition and a grading system for clinical and research purposes. Neurology. 2008;70:1630–5.

    Article  CAS  Google Scholar 

  35. Cesmebasi A, Yadav A, Gielecki J, Tubbs RS, Loukas M. Genitofemoral neuralgia: a review. Clin Anat. 2015;28(1):128–35.

    Article  Google Scholar 

Download references

Acknowledgements

Kyriacos Andreas Kyriacou for the English language revision. Prof. Paolo Negro for the revision of the manuscript.

Funding

No funding was obtained for this study.

Author information

Authors and Affiliations

Authors

Contributions

Protocol draft: RCi, CN, CB, AS, DM, VD, MF, PP, FS; Acquisition of data: RCi, GR, CN, AD, RCo, GT; Data analysis: NV; Data interpretation: RC, CR, GZ; Review of drafts: IM, GR, PB, ML, PF. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Isabella Mercurio.

Ethics declarations

Ethics approval and consent to participate

The research was undertaken according to the Italian Privacy Laws concerning collection, storage, and analysis of private data. A formal Institutional Research Ethics Board (Perugia University, S. Maria of Misericordia Perugia Hospital and S.Maria Terni Hospital) approval was not required because of the non-interventional, retrospective, and anonymous study design; however, a signed consent for the treatment and the analysis of data for scientific purpose was obtained from all patients or relatives either at admission or as soon as they could give it. The protocol of the study was accepted from Scientific Committee of SICADS (SocietàItaliana di ChirurgiaAmbulatoriale e Day Surgery) and published in the CUDS’ (Club Unità Day Surgery) (web site https://www.clubdaysurgery.it/). All methods were carried out in accordance with SICADS guidelines. Informed consent obtained from study participants during recovery was written, verbal during follow up.

Consent for publication

Not applicable.

Competing interests

All authors declare no financial and non-financial competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Cirocchi, R., Mercurio, I., Nazzaro, C. et al. Dermatome Mapping Test in the analysis of anatomo-clinical correlations after inguinal hernia repair. BMC Surg 20, 319 (2020). https://doi.org/10.1186/s12893-020-00988-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12893-020-00988-1

Keywords