Next Article in Journal
Optimal Upfront Treatment in Surgically Resectable Pancreatic Cancer Candidates: A High-Volume Center Retrospective Analysis
Previous Article in Journal
Pharmacodynamics and Outcomes of a De-Escalation Strategy with Half-Dose Prasugrel or Ticagrelor in East Asians Patients with Acute Coronary Syndrome: Results from HOPE-TAILOR Trial
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Electrodiagnostic Studies in the Surgical Treatment of Carpal Tunnel Syndrome—A Systematic Review

1
Medical Centre for Postgraduate Education, Department of Plastic Surgery, Professor W. Orlowski Memorial Hospital, 231st Czerniakowska Street, 00-416 Warsaw, Poland
2
Department of Anatomy, Jagiellonian University Medical College, 12th Kopernika Street, 31-034 Krakow, Poland
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2021, 10(12), 2691; https://doi.org/10.3390/jcm10122691
Submission received: 8 May 2021 / Revised: 13 June 2021 / Accepted: 17 June 2021 / Published: 18 June 2021
(This article belongs to the Section Orthopedics)

Abstract

:
The aim of our paper was to provide comprehensive data on the role of electrodiagnostic (EDX) studies in the surgical treatment of carpal tunnel syndrome (CTS). An extensive search was conducted through the major electronic database to identify eligible articles. Data extracted included grade of CTS based on neurophysiological testing, preoperative data of EDX studies, time of complete or partial resolution after surgery, postoperative Boston carpal tunnel questionnaire (CTQ) scores, age, sex, intraoperative and postoperative data of EDX studies, time to complete or partial resolution of symptoms, and number of patients without postsurgical improvement. Our main findings revealed that that electrodiagnostic testing is still a powerful tool for diagnosis of CTS. Moreover, it can also detect other pathologies. EDX testing provides a quantitative measure of the physiological function of the median nerve, which may be used to guide surgical treatment. Thirdly, when the outcome of surgery is unsatisfactory, NCS can assist in determining the reason for failure.

1. Introduction

Carpal tunnel syndrome (CTS), first described in 1863 by Sir James Paget, is the most common focal entrapment mononeuropathy [1]. It is defined as a compression of the median nerve at the wrist associated with decreased function of the nerve at this level [2,3]. There are several risk factors of CTS including genetic heredity, diabetes mellitus, thyroid disease, obesity, rheumatoid arthritis, and pregnancy [4,5,6]. However, most cases of carpal tunnel syndrome are idiopathic [7]. CTS often affects persons of working age and may lead to absences from work and a marked decline in performance. Regardless of the risk factors, the prevalence of the disease in the general population is about 15% [8]. CTS constitutes the most expensive upper extremity musculoskeletal disorder in the United States, with costs exceeding $2 billion annually [9].
Primary diagnosis of CTS is based on characteristic clinical symptoms such as paresthesia (mainly numbness and tingling), pain at the wrist and hand and in severe cases weakness or atrophy of hand muscles. There are also some provocative tests for CTS, among which Phalen’s wrist flexion test, Tinel’s median nerve percussion test and Durkan’s carpal compression test are most commonly used in the clinical setting. In terms of investigations, electrodiagnostic (EDX) studies constitute a useful objective measure in CTS diagnosis [10]. EDX studies include nerve conduction studies (NCSs) and electromyography (EMG). NCSs confirm CTS by detecting impaired median nerve conduction across the carpal tunnel, with normal conduction elsewhere. EMG assesses pathologic changes in the muscles innervated by the median nerve, typically the abductor pollicis brevis muscle [11]. In cases with longstanding and severe compression, there will be evidence of denervation on EMG sampling of the abductor pollicis brevis muscle.
Treatment options for CTS include wrist splinting, therapeutic ultrasound, local corticosteroid injections, and carpal tunnel release surgery [12]. Analysis of the costs of CTS treatment, including indirect non-healthcare costs such as loss of productivity caused by absence from work, led to the conclusion that established CTS is best treated with surgery [12]. Surgery has also been shown to be superior to non-operative treatment for patients with symptoms of CTS without changes due to denervation [13].

EDX Testing Technique

The results of electrodiagnostic studies have been found to be highly sensitive and specific for the diagnosis of CTS. EDX testing is performed by using generally accepted standardized techniques according to the American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) summary statement [11]. In patients suspected of CTS, the following EDX studies are recommended: median sensory or mixed nerve conduction study, median motor conduction study, needle examination of APB, ulnar or/and radial motor and sensory NCSs (in order to exclude a peripheral neuropathy), and needle electromyography of the limb muscles innervated by the C5toT1 roots (in order to exclude a cervical radiculopathy, brachial plexopathy, and a proximal median neuropathy) be performed as part of the examination of patients suspected of CTS [14]. In cases of severe CTS in which the median sensory potentials and the compound muscle action potential (CMAP) from abductor pollicis brevis (APB) muscle are absent, a lumbrical-interosseous distal motor latency (DML) comparison is performed [15]. The severity of CTS is usually classified according to results obtained from the NCS which reflects the degree of demyelination and axonal loss in the median nerve [16].
Prolonged motor and sensory latencies of the median nerve and reduced sensory and motor conduction velocities in properly performed NCSs are accepted as diagnostic criteria for CTS. Many factors may influence the amplitude and latency of an individual nerve, giving a false-positive or false-negative result. Such factors include age, sex, finger diameter, concurrent systemic disease, obesity, and temperature. Applying a NCS as a relative comparison of two nerve segments, i.e., the median nerve and another nerve segment that does not travel through the carpal tunnel, could be useful. This technique is the most sensitive and accurate, with a sensitivity of 80–92% and specificity of 80–99% [10]. The electrophysiological classification of the severity of CTS has been defined by the American Association of Electrodiagnostic Medicine (AAEM) [17].

2. Aims

The aim of this systematic review is to
(1)
provide comprehensive data on the role of electrodiagnostic (EDX) studies in the surgical treatment of carpal tunnel syndrome.
(2)
review pre- and postoperative data on patients with CTS evaluated via EDX testing.
(3)
analyze in detail patients baseline and preoperative clinical data with respect to electrophysiological condition.
Recent findings have revealed an absence of linear association between neurophysiological severity of the CTS and postoperative outcome, and thus there is a need to thoroughly explore pre- and postoperative clinical data to evaluate if EDX is still a powerful tool for diagnosing and developing treatment plans for carpal tunnel release [18,19,20,21,22].

3. Methods

3.1. Literature Search

A comprehensive database search was performed between May and August 2020 in PubMed using a combination of search terms: “carpal tunnel syndrome” AND “electrodiagnostic studies” OR “carpal tunnel syndrome” AND “nerve conduction studies”. Relevant publications were included for initial assessment. Duplications were eliminated and additional eligible articles from other sources (references of reviewed full-texts and from relative journals) were included. This study was performed in compliance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) (Supplement) [23].

3.2. Eligibility Criteria

After initial an assessment of articles by title/abstract, all found full texts of included studies met the following inclusion criteria: (1) provided preoperative data (EDX results with comparison of clinical examination and/or CTQs (carpal tunnel questionnaires) scores of patients with carpal tunnel syndrome who underwent surgery) and (2) provided their postsurgical outcomes (with or without postoperative EDX results). Exclusion criteria were (1) patients diagnosed without EDX testing, (2) non-surgical treatment of CTS, (3) publications presenting only preoperative data, or (4) publications focused only on the diagnostic value of EDX testing. Letters to the editors, case reports, and conference abstracts were also excluded from the systematic review. Each publication was independently assessed by three authors (A.P., P.P., A.M.). Disagreements during the screening process were discussed and led to a consensus among the authors.

3.3. Data Extraction

Data from final eligible articles were extracted and recorded by one of the searchers (A.M.) and collected data was independently checked and verified by two other authors (A.P., P.P.). Collected information included: grade of the CTS based on neurophysiological testing, preoperative data of EDX studies, time of complete or partial resolution after surgery, postoperative CTQs scores, age, sex, postoperative and intraoperative data of NCSs, time to complete or partial resolution of symptoms, and number of patients without postsurgical improvement.

3.4. Quality Assessment

The quality of 32 included studies was evaluated using the Newcastle–Ottawa scale (NOS) [24]. NOS comprises 9 items (‘stars’; each star for the most important factor) grouped into 3 sections: Selection (0–4 stars), Comparability (0–2 stars), Outcome (0–3 stars) for the assessment of cohort studies. Score 9 indicates the best quality of the publication, scores ≤5 indicate low quality. NOS scores of each included study are presented in Table 1.

4. Results

A total of 2397 publications were identified by initial literature search. After additional records (n = 7) and removing duplications (n = 324), 2080 studies were included for initial assessment by title and/or abstract. Among those, 1956 publications were excluded after title/abstract screening, while 103 full texts were assessed for eligibility. Forty-five studies presenting irrelevant data and seventeen publications with reported incomplete data were excluded. Reviews and letters to the editor were also not included in the systematic review. A total of 32 of the initial 2080 publications identified were included in this study. A flow chart presenting the processing of articles through the study following the PRISMA protocol is presented in Figure 1 [23].
A total of 24 studies presented detailed pre- and postoperative data and extracted data of these publications were presented in Table S1 (supplement available online). The summary of Table 2 and graphic presentation of the prognostic value of EDX according to confirmed significant correlation between preoperative EDX and recovery after surgery (Figure 2) are included below:
According to our results, the majority of publications did not confirm the prognostic value of EDX (only 2 of 28 articles). Padua et al. [25,26] revealed a strong correlation between neurophysiological severity of CTS and recovery, while 8 of 28 publications suggest a weak prognostic value of the EDX.

Bias Assessment

NOS scores of included publications are presented in Table 1. Mean NOS score (±SD) was 6.56 ± 1.34.

5. Discussion

Carpal tunnel syndrome is often but not invariably caused by a demonstrable median neuropathy at the wrist (MNW). Thus, there are patients with CTS with normal EDX and asymptomatic patients with MNW as detected by EDX. Hence, NCSs provide a reliable measure to document MNW, not CTS, i.e., to demonstrate the underlying lesion responsible for the symptoms and signs of CTS. They support the diagnosis of CTS, but cannot make it by themselves. Thus, the defined abnormalities of nerve conduction need not be symptomatic. Patients with abnormal NCSs but no symptoms probably should not be labeled as having CTS but rather as MMW cases [27]. A study by De Kleermaeker et al. demonstrates that most patients with clinically defined CTS and normal EDX results will benefit from carpal tunnel release [28].
While nerve conduction abnormalities commonly improve following successful decompression surgery, they often do not normalize [28,29]. It can therefore be difficult to attribute a nerve conduction abnormality to recurrence of nerve compression in a patient who had previously undergone decompression surgery, particularly if preoperative studies were not performed. This is one of a number of reasons why NCSs should be undertaken in all patients with suspected carpal tunnel syndrome prior to surgery. It is worth mentioning that during the past few years, ultrasonographic (US) confirmation of CTS diagnosis has proven to be an easily applicable, patient-friendly, low-cost test. However, US cannot replace EDX for confirmation of clinical diagnosis of CTS. An abnormal US test result has a high positive predictive value for abnormal EDX results in clinically defined CTS [30].
Electrodiagnostic studies have an important role in predicting the outcome of surgical decompression, disclosing other pathologies, particularly in atypical cases, and providing a useful baseline if patients do not improve after surgery. Clinical recovery was associated with preoperative EDX according to Padua et al., 1996, 1997; Padua’s electrophysiological scale was associated with postoperative functional status according to Malladi et al., 2009. Despite these findings, most publications reveal only weak or no association with clinical recovery. The slowing of SNCV may be the only manifestation of early CTS [26]. DML is a routine neurophysiological parameter in the diagnosis of CTS and can be easily obtained, but it has a low diagnostic sensitivity and a low prognostic value in no-operated hands with CTS [31]. However, it appears to be a useful preoperative indicator of the neurophysiological results that can be expected after surgical decompression of the median nerve. Data of Padua et al. suggest that when DML is still within normal limits at the time of surgery, there is an excellent possibility that full nerve function will be restored, and neurophysiological normalization usually parallels the disappearance of CTS symptoms. When the DML is 4 to 6 ms, the possibility of neurophysiological normalization appears to be around 50% at 6 months. Prolongation of DML over 6 ms is not associated with neurophysiological normalization. In patients with DML ranging from 4 to 6 ms and more, a dramatic reduction of CTS sensory symptoms is observed, with disappearance of nocturnal symptoms; nonetheless, in some cases sensory and/or motor deficits can still be present after surgery [28]. Some authors revealed predictive value of DML [32], but still there is lack of strong association according to other authors.
Finestone et al. and Rivlin et al. observed that outcomes after carpal tunnel release (CTR) were not affected by preoperative EDX grade. As all EDX grades benefit from surgical treatment, EDX evaluation may not be necessary to define treatment in patients with uncomplicated carpal tunnel syndrome [33,34].
The American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) practice parameter for EDX in CTS and the Normative Data Task Force (NDTF) outlines EDX studies and reference values considered standard of care in patients with clinical suspicion of CTS. These studies are valid and reproducible in confirming median neuropathy at the wrist with a high degree of sensitivity (>85%) and specificity (95%). EDX confirms the diagnosis of median neuropathy at the wrist, evaluates its severity, determines its pathophysiology, (axon loss versus demyelination) and excludes cervical radiculopathy and coincidental ulnar nerve disease or polyneuropathy. Patients undergoing CTR without resolution of symptoms were identified as having an alternative diagnosis upon EDX (polyneuropathy, radiculopathy, motor neuron disease, spondylotic myelopathy, syringomyelia, and multiple sclerosis). This is confirmed also by Basiri et al., who conclude that EDX studies are often necessary for exclusion of other possible causes of symptomatology, such as cervical radiculopathy, brachial plexopathy, and a proximal median neuropathy [35].
During the past few years, ultrasonographic (US) confirmation of CTS diagnosis has been the subject of many studies for several reasons. It is executed by comparing cross-sectional area measurements of the median nerve obtained at the level of the carpal tunnel with those obtained at the level of the pronator quadratus muscle. According to Claes et al. US cannot replace EDX for confirmation of clinical diagnosis of CTS [30]. However, an abnormal US test result has a high positive predictive value for abnormal EDX result in clinically defined CTS. US might reveal relevant anatomic information preoperatively that rarely has a direct influence on treatment management of patients with CTS. US testing, taking morphometric data into account, does not have the same diagnostic value as EDX does in confirming CTS.
In the majority of cases, a careful history and physical examination are sufficient to make a clinical diagnosis of CTS and make initial treatment decisions [27,36,37]. However, many patients present with multiple problems and/or their presentation is atypical. An EDX examination can confirm the clinical impression of CTS, which is reassuring for both the patient and physician. Other patients may have coexisting or confounding diagnoses that EDX testing and consultation can help sort out. Additionally, it is important to add that EDX studies with high sensitivity and lower specificity (e.g., ring-finger method) are suspected to lead to more false-positive diagnoses, and there is a requirement to establish cut-off values for these methods [27,35,38]. Performing, interpreting, and reporting high-quality and evidence-based EDX testing can potentially lead to improved outcomes in many patients. Some authors presented prognostic value of individual EDX methods, e.g., second lumbrical-interossei nerve test (2L-IN) [39] which could also be a better alternative EDX method in analysis nerve conduction in patients with severe thenar atrophy (which is suspected to alter NCS results) [35,40,41].
While both traditionalists and contemporary thinkers agree that a diagnosis can be made based on clinical symptoms, traditionalists argue that EDX, also known as nerve conduction studies, is the gold standard for confirming a CTS diagnosis [42,43]. They further claim that other provocative tests like Tinel’s and Phalen’s are not reliable and that ultrasound cannot be used to make a diagnosis of CTS [44]. Another study revealed lower NPV of ultrasound studies in comparison with NCSs in patients with very low suspicion of the CTS [45]. The diagnostic validity of commonly used clinical tests is debated. Studies have shown the Phalen test to have a sensitivity ranging from 10% to 88% and specificity ranging from 47% to 100% [45], but some authors have revealed that there is a correlation between positive Phalen’s and Tinel’s signs and preoperative EMG results, but in the same study there was no confirmed significant correlation between these provocative tests and nerve conduction velocity [45,46]. Additionally, CTS can have an atypical presentation with symptoms that differ from those previously mentioned. Due to these factors, EDX testing is commonly utilized to confirm a diagnosis. More recently, the American Academy of Orthopedic Surgeons’ Clinical Practice Guidelines have indicated that EDX may be helpful but not required to establish the diagnosis of CTS [47].
There are data suggesting that EDX testing can provide some information regarding prognosis after surgery. Preoperative electrodiagnostic testing is useful in predicting symptom recovery after carpal tunnel surgery and the severity on preoperative nerve conduction studies predicts the rate of postoperative symptom resolution [48]. Electrodiagnostic studies should be obtained before surgery to confirm the diagnosis and estimate prognosis because patients with more severe CTS are less likely to experience complete recovery after surgery [26,32,34,45,46,49,50,51,52].
The observations of Bland et al. imply that NCS findings are shown to be of prognostic value for surgical carpal tunnel decompression [53]. Patients with absent sensory and motor responses, most of whom probably have degeneration of many median nerve fibers rather than conduction block, had the worst outcomes [18,25,26,34,39,50,52,53]. Patients with moderate neurophysiologic abnormalities had the best outcomes. Some authors have analyzed which factors have a significant impact on the outcomes of patients with CTS who are treated surgically. According to the results of a multivariate analysis, there is no association between preoperative NCS results (median to ulnar latency > 0.5 ms) and improvement after surgery. It also revealed that only sex and age are statistically significant preoperative factors [19]. Some findings reveal that younger patients more often report recurrence of symptoms, but their NCS results showed better nerve condition in comparison with older patients [20]. There are other data suggesting an absence of association between preoperative NCS results and outcome [21,36,53,54]. Additionally, there are numerous publications that confirm that there is a correlation between preoperative NCS results and postsurgical outcome, wherein patients with mild and moderate CTS achieved improvement and complete relief earlier than patients with severe CTS [18,25,26,32,34,39,46,52,53,55,56,57]. Immediate improvement (intraoperative increase of conduction velocity) after decompression is related to reversible metabolic damage in nerve fibers, and this phenomenon is observed in some cases of mild CTS [58]. Those with normal NCS had outcomes almost as poor as those at the opposite end of the severity scale, possibly because some of the neurophysiologically negative cases were mistaken clinical diagnoses.
Perhaps more surprising, then, is the fact that patients with mild CTS—especially those in whom sophisticated, newer neurophysiologic techniques are required to show any abnormality—had poorer outcomes than did those with nerve conduction results of middle severity [32,34,53,59,60].
Change of job was more often observed in patients without improvement of symptoms [59] and better results were noticed in groups of patients with light activity in comparison with patients performing types of work with higher number of repetitions and which require higher loads [22,59,61].
EDX study has a considerable associated cost [62], the procedure itself is uncomfortable for patients, and there is literature suggesting that it is not routinely required for the diagnosis of CTS [63]. The prevalence of surgeons who perform CTR without preoperative neurophysiological test varies depending on surgical specialty [63,64]. Furthermore, some authors suggest that clinical severity of the CTS based on score of carpal tunnel questionnaire score might be sufficient to predict NCS results [64] or postsurgical outcomes [65], and there are also data arguing against clinical prediction of NCS results [66]. Gomes et al. distinguished independent factors that predicted neurophysiological diagnosis of CTS, including BMI ≥ 30, nocturnal worsening of symptoms, and awakening or positive provocative tests, but the authors noted that basing diagnosis on the clinical picture alone is still insufficient to diagnose CTS correctly [67,68].
Some surgeons specializing in plastic surgery, orthopedics, or neurosurgery, who perform the procedure of carpal tunnel release, see no value in NCS as part of their routine management of CTS patients, while neurophysiologists believe that their tests do add clinical value and should be carried out in every patient with suspected CTS before surgery [25,32,69].

6. Conclusions

EDX study is not only a diagnostic test for CTS but can also detect other pathologies. Secondly, EDX study provides a quantitative measure of the physiological function of the median nerve, which may be used to guide surgical treatment and for prognosis. Thirdly, when the outcome of surgery is unsatisfactory, EDX testing can assist in determining the reason for failure.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/jcm10122691/s1. Table S1 Pre- and postoperative clinical and electrophysiological evaluation of patients with CTS.

Funding

The authors received no financial support for the research, authorship, and/or publication of this article.

Acknowledgments

We would like to thank Bartłomiej Noszczyk, the Head of the Department of Plastic Surgery, Medical Centre for Postgraduate Education, W. Orlowski Memorial Hospital for his help and support at every stage of this work.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wang, L. Guiding treatment for carpal tunnel syndrome. Phys. Med. Rehabil. Clin. N. Am. 2018, 29, 751–760. [Google Scholar] [CrossRef]
  2. Day, C.S. Fractures of the Metacarpals and Phalanges. In Green’s Operative Hand Surgery, 7th ed.; Elsevier: Philadelphia, PA, USA, 1993; Chapter 7. [Google Scholar]
  3. Keith, M.W.; Masear, V.; Chung, K.C.; Maupin, K.; Andary, M.; Amadio, P.C.; McGowan, R. American Academy of Orthopaedic Surgeons Clinical Practice Guideline on diagnosis of carpal tunnel syndrome. J. Bone Jt. Surg. Am. 2009, 91, 2478–2479. [Google Scholar] [CrossRef]
  4. Karpitskaya, Y.; Novak, C.B.; Mackinnon, S.E. Prevalence of smoking, obesity, diabetes mellitus, and thyroid disease in patients with carpal tunnel syndrome. Ann. Plast Surg. 2002, 48, 269–273. [Google Scholar] [CrossRef]
  5. Palumbo, C.F.; Szabo, R.M.; Olmsted, S.L. The effects of hypothyroidism and thyroid replacement on the development of carpal tunnel syndrome. J. Hand Surg. Am. 2000, 25, 734–739. [Google Scholar] [CrossRef]
  6. Stolp-Smith, K.A.; Pascoe, M.K.; Ogburn, P.L., Jr. Carpal tunnel syndrome in pregnancy: Frequency, severity, and prognosis. Arch. Phys. Med. Rehabil. 1998, 79, 1285–1287. [Google Scholar] [CrossRef]
  7. Ashworth, N. Carpal tunnel. BMJ 2014, 349, g6437. [Google Scholar]
  8. Atroshi, I.; Gummesson, C.; Johnsson, R.; Ornstein, E.; Ranstam, J.; Rosén, I. Prevalence of carpal tunnel syndrome in a general population. JAMA 1999, 282, 153–158. [Google Scholar] [CrossRef]
  9. Dale, A.M.; Harris-Adamson, C.; Rempel, D.; Gerr, F.; Hegmann, K.; Silverstein, B.; Burt, S.; Garg, A.; Kapellusch, J.; Merlino, L.; et al. Prevalence and incidence of carpal tunnel syndrome in US working populations: Pooled analysis of six prospective studies. Scand. J. Work Environ. Health 2013, 39, 495–505. [Google Scholar] [CrossRef] [PubMed]
  10. Werner, R.A.; Andary, M. Carpal tunnel syndrome: Pathophysiology and clinical neurophysiology. Clin. Neurophysiol. 2002, 113, 1373–1381. [Google Scholar] [CrossRef]
  11. Jablecki, C.K.; Andary, M.T.; Floeter, M.K.; Miller, R.G.; Quartly, C.A.; Vennix, M.J.; Wilson, J.R. Practice parameter: Electrodiagnostic studies in carpal tunnel syndrome. Neurology 2002, 58, 1589–1592. [Google Scholar] [CrossRef] [Green Version]
  12. O’Connor, D.; Marshall, S.; Massy-Westropp, N.; Pitt, V. Non-surgical treatment (other than steroid injection) for carpal tunnel syndrome. Cochrane Database Syst. Rev. 2003, CD003219. [Google Scholar] [CrossRef] [PubMed]
  13. Korthals-de Bos, I.B.; Gerritsen, A.A.; Van Tulder, M.W.; Rutten-van Mölken, M.P.; Adèr, H.J.; De Vet, H.C.; Bouter, L.M. Surgery is more cost-effective than splinting for carpal tunnel syndrome in the Netherlands: Results of an economic evaluation alongside a randomized controlled trial. BMC Musculoskelet Disord. 2006, 7, 86. [Google Scholar] [CrossRef] [Green Version]
  14. Guidelines in electrodiagnostic medicine. American Association of Electrodiagnostic Medicine. Muscle Nerve 1992, 15, 229–253. [CrossRef] [PubMed]
  15. Preston, D.C.; Logigian, E.L. Lumbrical and interossei recording in carpal tunnel syndrome. Muscle Nerve 1992, 15, 1253–1257. [Google Scholar] [CrossRef]
  16. Beck, J.D.; Wingert, N.C.; Rutter, M.R.; Irgit, K.S.; Tang, X.; Klena, J.C. Clinical outcomes of endoscopic carpal tunnel release in patients 65 and over. J. Hand Surg. Am. 2013, 38, 1524–1529. [Google Scholar] [CrossRef] [PubMed]
  17. Ibrahim, I.; Khan, W.S.; Goddard, N.; Smitham, P. Carpal tunnel syndrome: A review of the recent literature. Open Orthop J. 2012, 6, 69–76. [Google Scholar] [CrossRef] [Green Version]
  18. Iida, J.; Hirabayashi, H.; Nakase, H.; Sakaki, T. Carpal tunnel syndrome: Electrophysiological grading and surgical results by minimum incision open carpal tunnel release. Neurol. Med. Chir. 2008, 48, 554–559. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Watchmaker, J.D.; Watchmaker, G.P. Independent Variables Affecting Outcome of Carpal Tunnel Release Surgery. Hand 2017, 13, 1558944717703739. [Google Scholar] [CrossRef]
  20. Aghda, A.K.; Asheghan, M.; Amanollahi, A. Comparisons of electrophysiological and clinical findings between young and elderly patients with Carpal Tunnel Syndrome. Rev. Neurol. 2020, 176, 387–392. [Google Scholar] [CrossRef]
  21. Braun, R.M.; Jackson, W.J. Electrical studies as a prognostic factor in the surgical treatment of carpal tunnel syndrome. J. Hand Surg. Am. 1994, 19, 893–900. [Google Scholar] [CrossRef]
  22. Glowacki, K.A.; Breen, C.J.; Sachar, K.; Weiss, A.P. Electrodiagnostic testing and carpal tunnel release outcome. J. Hand Surg. Am. 1996, 21, 117–121. [Google Scholar] [CrossRef]
  23. Moher, D.; Liberati, A.; Tetzlaff, J.; Altman, D.G.; The PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA Statement. PLoS Med. 2009, 6, e1000097. [Google Scholar] [CrossRef] [Green Version]
  24. Wellsss, G.; Shea, B.; O’Connell, D.; Peterson, J.; Welch, V.; Losos, M. The Newcastle-Ottawa scale for assessing the quality of nonrandomised studies in meta-analyses. Available online: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp (accessed on 1 August 2020).
  25. Padua, L.; Lomonaco, M.; Aulisa, L.; Tamburrelli, F.; Valente, E.M.; Padua, R.; Gregori, B.; Tonali, P. Surgical prognosis in carpal tunnel syndrome: Usefulness of a preoperative neurophysiological assessment. Acta Neurol. Scand. 1996, 94, 343–346. [Google Scholar] [CrossRef] [PubMed]
  26. Padua, L.; Lo Monaco, M.; Padua, R.; Tamburrelli, F.; Gregori, B.; Tonali, P. Carpal tunnel syndrome: Neurophysiological results of surgery based on preoperative electrodiagnostic testing. J. Hand Surg. Br. 1997, 22, 599–601. [Google Scholar] [CrossRef]
  27. Werner, R.A.; Andary, M. Electrodiagnostic evaluation of carpal tunnel syndrome. Muscle Nerve 2011, 44, 597–607. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. De Kleermaeker, F.G.C.M.; Meulstee, J.; Claes, F.; Kasius, K.M.; Verhagen, W.I.M. Treatment outcome in patients with clinically defined carpal tunnel syndrome but normal electrodiagnostic test results: A randomized controlled trial. J. Neurol. 2017, 264, 2394–2400. [Google Scholar] [CrossRef]
  29. Sonoo, M.; Menkes, D.L.; Bland, J.D.P.; Burke, D. Nerve conduction studies and EMG in carpal tunnel syndrome: Do they add value? Clin. Neurophysiol. Pract. 2018, 3, 78–88. [Google Scholar] [CrossRef] [PubMed]
  30. Claes, F.; Kasius, K.M.; Meulstee, J.; Verhagen, W.I. Comparing a new ultrasound approach with electrodiagnostic studies to confirm clinically defined carpal tunnel syndrome: A prospective, blinded study. Am. J. Phys. Med. Rehabil. 2013, 92, 1005–1011. [Google Scholar] [CrossRef] [PubMed]
  31. Mühlau, G.; Both, R.; Kunath, H. Carpal tunnel syndrome--course and prognosis. J. Neurol. 1984, 231, 83–86. [Google Scholar] [CrossRef]
  32. Fowler, J.R.; Cipolli, W.; Hanson, T. A Comparison of Three Diagnostic Tests for Carpal Tunnel Syndrome Using Latent Class Analysis. J. Bone Jt. Surg. Am. 2015, 97, 1958–1961. [Google Scholar] [CrossRef] [PubMed]
  33. Finestone, H.M.; Woodbury, G.M.; Collavini, T.; Marchuk, Y.; Maryniak, O. Severe carpal tunnel syndrome: Clinical and electrodiagnostic outcome of surgical and conservative treatment. Muscle Nerve 1996, 19, 237–239. [Google Scholar] [CrossRef]
  34. Rivlin, M.; Kachooei, A.R.; Wang, M.L.; Ilyas, A.M. Electrodiagnostic Grade and Carpal Tunnel Release Outcomes: A Prospective Analysis. J. Hand Surg. Am. 2018, 43, 425–431. [Google Scholar] [CrossRef] [PubMed]
  35. Basiri, K.; Katirji, B. Practical approach to electrodiagnosis of the carpal tunnel syndrome: A review. Adv. Biomed Res. 2015, 4, 50. [Google Scholar] [CrossRef]
  36. Finsen, V.; Russwurm, H. Neurophysiology not required before surgery for typical carpal tunnel syndrome. J. Hand Surg. Br. 2001, 26, 61–64. [Google Scholar] [CrossRef] [PubMed]
  37. Kortlever, J.T.P.; Becker, S.J.E.; Zhao, M.; Ring, D. Borderline Nerve Conduction Velocities for Median Neuropathy at the Carpal Tunnel. J. Hand Surg. Am. 2020, 45, 379–388. [Google Scholar] [CrossRef]
  38. Miyaji, Y.; Kobayashi, M.; Oishi, C.; Mizoi, Y.; Tanaka, F.; Sonoo, M. A new method to define cutoff values in nerve conduction studies for carpal tunnel syndrome considering the presence of false-positive cases. Neurol. Sci. 2020, 41, 669–677. [Google Scholar] [CrossRef] [PubMed]
  39. Inukai, T.; Uchida, K.; Kubota, C.; Takamura, T.; Nakajima, H.; Baba, H. Second lumbrical-interossei nerve test predicts clinical severity and surgical outcome of carpal tunnel syndrome. J. Clin. Neurosci. 2013, 20, 1224–1227. [Google Scholar] [CrossRef]
  40. Inukai, T.; Uchida, K.; Kubota, C.; Takamura, T.; Nakajima, H.; Baba, H. Additional method for diagnosis of carpal tunnel syndrome: Value of the second lumbrical-interossei test (2L-INT). Hand Surg. 2013, 18, 49–52. [Google Scholar] [CrossRef]
  41. Kasius, K.M.; Claes, F.; Verhagen, W.I.M.; Meulstee, J. Motor Nerve Conduction Tests in Carpal Tunnel Syndrome. Front. Neurol. 2019, 10, 149. [Google Scholar] [CrossRef]
  42. Urits, I.; Gress, K.; Charipova, K.; Orhurhu, V.; Kaye, A.D.; Viswanath, O. Recent Advances in the Understanding and Management of Carpal Tunnel Syndrome: A Comprehensive Review. Curr. Pain Headache Rep. 2019, 23, 70. [Google Scholar] [CrossRef]
  43. Sears, E.D.; Lu, Y.-T.; Wood, S.M.; Nasser, J.S.; Hayward, R.A.; Chung, K.C.; Kerr, E.A. Diagnostic Testing Requested Before Surgical Evaluation for Carpal Tunnel Syndrome. J. Hand Surg. Am. 2017, 42, 623–629. [Google Scholar] [CrossRef] [PubMed]
  44. Sucher, B.M.; Schreiber, A.L. Carpal tunnel syndrome diagnosis. Phys. Med. Rehabil. Clin. N. Am. 2014, 25, 229–247. [Google Scholar] [CrossRef] [PubMed]
  45. Colombo, J.; Shah, S. Utilization of Electrodiagnostic Testing for Carpal Tunnel Syndrome by General Practitioners Prior to Hand Surgery Consultation. Hand 2019, 14, 56–58. [Google Scholar] [CrossRef] [PubMed]
  46. Ezquerra-Herrando, L.; Gómez-Vallejo, J.; Corella-Abenia, E.; Albareda-Albareda, J. Factores pronósticos en la cirugía del síndrome del túnel carpiano [Prognosis factors in carpal tunnel syndrome surgery]. Acta Ortop. Mex. 2014, 28, 160–163. [Google Scholar] [PubMed]
  47. American Academy of Orthopaedic Surgeons. Management of Carpal Tunnel Syndrome Evidence-Based Clinical Practice Guideline. Available online: www.aaos.org/ctsguideline (accessed on 12 October 2017).
  48. Fowler, J.R.; Munsch, M.; Huang, Y.; Hagberg, W.C.; Imbriglia, J.E. Pre-operative electrodiagnostic testing predicts time to resolution of symptoms after carpal tunnel release. J. Hand Surg. Eur. Vol. 2016, 41, 137–142. [Google Scholar] [CrossRef]
  49. Bland, J.D. A neurophysiological grading scale for carpal tunnel syndrome. Muscle Nerve. 2000, 23, 1280–1283. [Google Scholar] [CrossRef]
  50. Mondelli, M.; Reale, F.; Padua, R.; Aprile, I.; Padua, L. Clinical and neurophysiological outcome of surgery in extreme carpal tunnel syndrome. Clin. Neurophysiol. 2001, 112, 1237–1242. [Google Scholar] [CrossRef]
  51. Claes, F.; Kasius, K.M.; Meulstee, J.; Grotenhuis, J.A.; Verhagen, W.I. Treatment outcome in carpal tunnel syndrome: Does distribution of sensory symptoms matter? J. Neurol. Sci. 2014, 344, 143–148. [Google Scholar] [CrossRef]
  52. Kronlage, S.C.; Menendez, M.E. The benefit of carpal tunnel release in patients with electrophysiologically moderate and severe disease. J. Hand Surg. Am. 2015, 40, 438–444. [Google Scholar] [CrossRef]
  53. Bland, J.D. Do nerve conduction studies predict the outcome of carpal tunnel decompression? Muscle Nerve 2001, 24, 935–940. [Google Scholar] [CrossRef]
  54. Jordan, R.; Carter, T.; Cummins, C. A systematic review of the utility of electrodiagnostic testing in carpal tunnel syndrome. Br. J. Gen. Pract. 2002, 52, 670–673. [Google Scholar]
  55. Schrijver, H.M.; Gerritsen, A.A.M.; Strijers, R.L.M.; Uitdehaag, B.M.J.; Scholten, R.J.P.M.; De Vet, H.C.W.; Bouter, L.M. Correlating nerve conduction studies and clinical outcome measures on carpal tunnel syndrome: Lessons from a randomized controlled trial. J. Clin. Neurophysiol. 2005, 22, 216–221. [Google Scholar] [PubMed]
  56. Nathan, P.A.; Keniston, R.C.; Meadows, K.D. Electrical studies as a prognostic factor in the surgical treatment of carpal tunnel syndrome. J. Hand Surg. Am. 1996, 21, 526–527. [Google Scholar] [CrossRef]
  57. Magnussen, M.J.; Morren, J. Electrodiagnostic Testing in the Diagnosis and Management of Carpal Tunnel Syndrome. Orthopedics 2017, 40, 263. [Google Scholar] [CrossRef] [Green Version]
  58. Luchetti, R.; Schoenhuber, R.; Alfarano, M.; Montagna, G.; Pederzini, L.; Soragni, O. Neurophysiological assessment of the early phases of carpal tunnel syndrome with the inching technique before and during operation. J. Hand Surg. Br. 1991, 16, 415–419. [Google Scholar] [CrossRef]
  59. Higgs, P.E.; Edwards, D.F.; Martin, D.S.; Weeks, P.M. Relation of preoperative nerve-conduction values to outcome in workers with surgically treated carpal tunnel syndrome. J. Hand Surg. Am. 1997, 22, 216–221. [Google Scholar] [CrossRef]
  60. Rotman, M.B.; Enkvetchakul, B.V.; Megerian, J.T.; Gozani, S.N. Time course and predictors of median nerve conduction after carpal tunnel release. J. Hand Surg. Am. 2004, 29, 367–372. [Google Scholar] [CrossRef]
  61. Padua, L.; Aprile, I.; Monaco, M.L.; Padua, R.; Pasqualetti, P.; Nazzaro, M.; Tonali, P. Italian multicentre study of carpal tunnel syndrome: Clinical-neurophysiological picture and diagnostic pathway in 461 patients and differences between the populations enrolled in the northern, central and southern centres. Italian CTS Study Group. Ital. J. Neurol. Sci. 1999, 20, 309–313. [Google Scholar] [CrossRef] [PubMed]
  62. Zhang, D.; Earp, B.E.; Blazar, P. Utility of ‘baseline’ electrodiagnostic studies for carpal tunnel release. J. Hand Surg. Eur. Vol. 2019, 44, 273–277. [Google Scholar] [CrossRef]
  63. Claes, F.; Verhagen, W.I.; Meulstee, J. Current practice in the use of nerve conduction studies in carpal tunnel syndrome by surgeons in the netherlands. J. Hand Surg. Eur. Vol. 2007, 32, 663–667. [Google Scholar] [CrossRef]
  64. Sangram, B.S.; Mayne, A.I.W.; Jariwala, A.C. Can we accurately predict nerve conduction study outcome using a carpal tunnel syndrome questionnaire? Surgeon 2019, 17, 156–159. [Google Scholar] [CrossRef] [PubMed]
  65. Jansen, M.C.; Evers, S.; Slijper, H.P.; de Haas, K.P.; Smit, X.; Hovius, S.E.; Selles, R.W. Predicting Clinical Outcome After Surgical Treatment in Patients With Carpal Tunnel Syndrome. J. Hand Surg. Am. 2018, 43, 1098–1106. [Google Scholar] [CrossRef] [PubMed]
  66. Lo, J.K.; Finestone, H.M.; Gilbert, K. Prospective evaluation of the clinical prediction of electrodiagnostic results in carpal tunnel syndrome. PM & R 2009, 1, 612–619. [Google Scholar] [CrossRef] [PubMed]
  67. Gomes, I.; Becker, J.; Ehlers, J.A.; Nora, D.B. Prediction of the neurophysiological diagnosis of carpal tunnel syndrome from the demographic and clinical data. Clin. Neurophysiol. 2006, 117, 964–971. [Google Scholar] [CrossRef]
  68. Fowler, J.R. Nerve Conduction Studies for Carpal Tunnel Syndrome: Gold Standard or Unnecessary Evil? Orthopedics 2017, 40, 141–142. [Google Scholar] [CrossRef] [Green Version]
  69. Martić, V. Concordance of clinical and neurophysiologic diagnoses of carpal tunnel syndrome. Vojnosanit Pregl. 2015, 72, 247–250. [Google Scholar] [CrossRef]
Figure 1. Flow-chart of systematic review.
Figure 1. Flow-chart of systematic review.
Jcm 10 02691 g001
Figure 2. Percentage pie chart presenting prognostic value of EDX.
Figure 2. Percentage pie chart presenting prognostic value of EDX.
Jcm 10 02691 g002
Table 1. NOS score of included studies.
Table 1. NOS score of included studies.
AuthorSelectionComparabilityOutcome
Schlagenhauff & Glasauer 1971323
Grudberg et al., 1983312
Luchetti et al., 1991312
Seror 1992423
Braun et al., 1994211
Lang et al., 1995213
Padua 1996323
Glowacki et al., 1996323
Concannon et al., 1997312
Higgs et al., 1997313
Padua et al., 1997323
Choi et al., 1998323
Nakamura et al., 1999212
Dudley Porras et al., 2000211
Mondelli et al., 2001212
Finsen et al., 2001212
Bland et al., 2001211
Uchiyama et al., 2002313
Kouyoumdjian et al., 2002313
Borisch et al., 2003323
Rotman et al., 2004312
Schrijver et al., 2005322
Tay et al., 2006213
Ginanneschi et al., 2008213
Malladi et al., 2009313
Inukai et al., 2012313
Tahririan et al., 2012313
Beck et al., 2013323
Fowler et al., 2015313
Kronlage et al., 2015323
De Kleermaeker et al., 2017212
Rivlin et al., 2018322
Mean ± SD2.72 ± 0.521.34 ± 0.482.50 ± 0.67
Table 2. Pre- and postoperative clinical and electrophysiological evaluation of patients with CTS.
Table 2. Pre- and postoperative clinical and electrophysiological evaluation of patients with CTS.
AuthorNumber of EDX TestsNumber of Tests with Significant Prognostic ValueGrading
(No = 0, Yes = 1)
Prognostic Value
(Strong = 2, Weak = 1, Not Confirmed = 0)
Schlagenhauff & Glasauer 19711000
Grudberg 19831000
Seror 19922000
Braun 19942010
Lange 19952000
Padua 19963212
Głowacki 19962000
Concannon 19971010
Padua 19973312
Choi 19982010
Nakamura 19994010
Dudley Porras 20004211
Mondelli 20015111
Finsen 20011010
Bland 20014011
Kouyoumdjian 20023010
Borisch 20032000
Schrijver 20053000
Tay 20062010
Malladi 20092111
Inukai 20125111
Tahririan 20123010
Beck 20131010
Fowler 20151111
Kronlage 20152111
DeKleemaeker 20174000
Rivlin 20181111
Rivlin 20181111
strong—significant confirmed prognostic value in all groups of patients
weak—confirmed significant prognostic value in some groups
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Osiak, K.; Mazurek, A.; Pękala, P.; Koziej, M.; Walocha, J.A.; Pasternak, A. Electrodiagnostic Studies in the Surgical Treatment of Carpal Tunnel Syndrome—A Systematic Review. J. Clin. Med. 2021, 10, 2691. https://doi.org/10.3390/jcm10122691

AMA Style

Osiak K, Mazurek A, Pękala P, Koziej M, Walocha JA, Pasternak A. Electrodiagnostic Studies in the Surgical Treatment of Carpal Tunnel Syndrome—A Systematic Review. Journal of Clinical Medicine. 2021; 10(12):2691. https://doi.org/10.3390/jcm10122691

Chicago/Turabian Style

Osiak, Katarzyna, Agata Mazurek, Przemysław Pękala, Mateusz Koziej, Jerzy A. Walocha, and Artur Pasternak. 2021. "Electrodiagnostic Studies in the Surgical Treatment of Carpal Tunnel Syndrome—A Systematic Review" Journal of Clinical Medicine 10, no. 12: 2691. https://doi.org/10.3390/jcm10122691

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop