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DOI: 10.1055/s-0042-1742337
Diagnostic Contradictions in Carpal Tunnel Syndrome[*]
Article in several languages: português | EnglishAbstract
Objective Given the divergence of opinions on the need for complementary tests such as ultrasonography (US) and electroneuromyography (ENMG) for the diagnosis of carpal tunnel syndrome (CTS), we aimed to elucidate which of them presents greater accuracy for the confirmation of the presence or not of this condition.
Methods A total of 175 patients from a hand surgery outpatient clinic were clinically evaluated, and the results of clinical trials (Tinel, Phalen and Durkan), US (normal or altered), and ENMG (normal, mild, moderate and severe) were noted, crossed, and submitted to a statistical analysis to verify the agreement between them.
Results with the sample had a mean age of 53 years, with a prevalence of female patients (159 cases). Of the patients with positive clinical test, 43.7% had normal US and 41.7% had no alterations on the ENMG. Negative results were found on the Tinel in 46.9%, on the Phalen in 47.4%, and on the Durkan in 39.7%. In the crossing between the results of the ENMG and those of the other diagnostic methods, there was little statistical agreement between them.
Conclusion There was no agreement between the results of the clinical examinations, the US and the ENMG in the diagnosis of CTS, and there is no clinical or complementary examination for CTS that accurately determines the therapeutic approach.
Level of Evidence IV, Case Series.
#
Introduction
Carpal tunnel syndrome (CTS) accounts for 90% of all compressive neuropathies,[1] and is characterized by initial symptoms of paresthesia in the fingers innervated by the median nerve and, in advanced conditions, thenar atrophy and atrophy in the musculature innervated by this nerve.[2] The tinel, Phalen and Durkan clinical exams are considered classic tests for the initial evaluation, while ultrasonography (US) and electroneuromyography (ENMG) complement the investigation in dubious cases.[3] [4]
Divergence of opinions between specialists and health services on the real need for complementary tests to confirm this condition, as well as regarding which is the best diagnostic test, sometimes delay treatment, especially for those patients with a tendency towards surgical intervention.[5]
Therefore, we aim to elucidate which examination, clinical or complementary, presents greater accuracy for the diagnosis of CTS, and which is able to support the medical decision in a reliable way in CTS therapy.
#
Casuistry and Methods
An attempt was made to contact by phone 245 patients who attended the hand surgery outpatient clinic due to CTS 6 months before the beginning of the study, and 175 were found and agreed to participate. The research procedures were in accordance with the current ethical standards for research in human beings, and free and informed consent was obtained from all participants.
The inclusion criteria were people of both genders, older than 18 years of age, who presented an ENMG with exclusive diagnostic hypothesis of CTS and at least 1 altered examination (US or ENMG) with a maximum performance interval of 1 month between them. Patients who had other neuropathies described in the ENMG report, those who did not present bilateral wrist US, or which had not been performed at the same time as the ENMG, and patients who had normal US and ENMG were excluded.
The ENMG exam was performed in all patients by the same neurologist using the same electromyograph (Neuropack model, Nihon Kohden Tomioka Corporation, Tomioka, Gunma, Japan), and the results were classified as normal, mild (alteration only in sensory conduction), moderate (altered sensory and motor conduction), and severe (altered sensory and motor conduction, and signs of denervation on needle electromyography).[6] The US scan was evaluated by the same team of radiologists, having as compression criterion the transverse area of the median nerve in the wrist > 10 mm2.
The sample consisted of 175 patients (350 hands), 159 females and 16 males. The mean and standard deviation for age were of 53 ± 9.9 years. Regarding occupational status, 100 (57.2%) patients declared themselves economically active, and 36 (20.6%), in work leave due to CTS. Of those who did not have an occupation, 52 (29.7%) stayed at home and 23 (13.1%) were retired.
The results of the clinical tests (Tinel, Phalen and Durkan) and complementary tests (US and ENMG) were submitted to a statistical analysis with the determination of the Kappa agreement coefficient.[7] [8] The tests were performed with a significance level of 5% (p < 0.05).
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Results
[Table 1] shows the number of hands included with the results of the clinical tests, US and ENMG. Regarding US, 153 (43.7%) hands presented a cross-sectional area of the median nerve ≤ 10 mm2. As for the ENMG, 146 (41.7%) hands had normal results, and, of the altered results, 11.1% were mild, 26.3%, moderate, and 20.9%, severe. When we evaluated the clinical trials alone, negative results were found on the Tinel in 164 (46.9%) hands, on the Phalen in 166 (47.4%) hands, and on the Durkan in 139 (39.7%) hands.
Variable and result |
n (%) |
---|---|
(N = 350) |
|
Ultrasound |
|
Normal |
153 (43.7) |
Altered |
197 (56.3) |
Electroneuromyography |
|
Normal |
146 (41.7) |
Mild |
39 (11.1) |
Moderate |
92 (26.3) |
Severe |
73 (20.9) |
Tinel |
|
Negative |
164 (46.9) |
Positive |
186 (53.1) |
Phalen |
|
Negative |
166 (47.4) |
Positive |
184 (52.6) |
Durkan |
|
Negative |
139 (39.7) |
Positive |
211 (60.3) |
[Table 2] shows the crossing of the US with the isolated clinical tests, as well as the discrepancy of in their results. We observed negative US and positive Tinel in 84 (24.0%) hands, and positive US and negative Tinel in 95 (27.1%) hands, with a Kappa of −0.031. For the US and Phalen, we found negative US and positive Phalen in 76 (21.7%) hands, and positive US and negative Phalen in 89 (25.4%) hands, with a Kappa of 0.051. For the US and Durkan, we observed negative US and positive Durkan in 90 (25.7%) patients, and positive US and negative Durkan in 76 (21.7%) patients, with a Kappa of 0.026.
Variable and result |
Ultrasound – n (%) |
Total – n (%) |
Kappa |
|
---|---|---|---|---|
Negative |
Positive |
95% confidence interval |
||
Tinel – n (%) |
−0.031 |
|||
Negative |
69 (19.7) |
95 (27.1) |
164 (46.9) |
(−0.135–0.073) |
Positive |
84 (24.0) |
102 (29.1) |
186 (53.1) |
|
Phalen – n (%) |
0.051 |
|||
Negative |
77 (22.0) |
89 (25.4) |
166 (47.4) |
(−0.053–0.155) |
Positive |
76 (21.7) |
108 (30.9) |
184 (52.6) |
|
Durkan – n (%) |
0.026 |
|||
Negative |
63 (18.0) |
76 (21.7) |
139 (39.7) |
(−0.078–0.130) |
Positive |
90 (25.7) |
121 (34.6) |
211 (60.3) |
|
Total – n (%) |
153 (43.7) |
197 (56.3) |
350 (100) |
In [Table 3], when we evaluated the crossing of the ENMG with the other diagnostic methods, we observed little agreement between the ENMG and US, as well as between the ENMG and the clinical tests.
Variable and result |
Electroneuromyography – n (%) |
Total – n (%) |
Kappa |
Sens. |
Spec. |
|
---|---|---|---|---|---|---|
Negative |
Positive |
95%CI |
95%CI |
95%CI |
||
Ultrasound – n (%) |
0.212 |
65.2 |
56.2 |
|||
Negative |
82 (23.4) |
71 (20.3) |
153 (43.7) |
(0.108–0.316) |
(58.2–71.7) |
(47.7–64.4) |
Positive |
64 (18.3) |
133 (38.0) |
197 (56.3) |
|||
Tinel – n (%) |
−0.062 |
50.5 |
43.2 |
|||
Negative |
63 (18.0) |
101 (28.9) |
164 (46.9) |
(−0.166–0.042) |
(43.4–57.5) |
(35.0–51.6) |
Positive |
83 (23.7) |
103 (29.4) |
186 (53.1) |
|||
Phalen – n (%) |
−0.049 |
50.5 |
44.5 |
|||
Negative |
65 (18.6) |
101 (28.9) |
166 (47.4) |
(−0.153–0.055) |
(43.4–57.5) |
(36.3–53.0) |
Positive |
81 (23.1) |
103 (29.4) |
184 (52.6) |
|||
Durkan – n (%) |
−0.035 |
58.8 |
37.7 |
|||
Negative |
55 (15.7) |
84 (24.0) |
139 (39.7) |
(−0.139–0.069) |
(51.7–65.6) |
(29.8–46.1) |
Positive |
91 (26.0) |
120 (34.3) |
211 (60.3) |
|||
Total – n (%) |
146 (41.7) |
204 (58.3) |
350 (100) |
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Discussion
Patients with a clinical diagnosis of CTS and complementary tests incompatible with each other have been constantly observed by hand surgeons, as well as by professionals in the fields of occupational medicine and medico-legal examinations, with a greater number of lawsuits due to this condition. One of the difficulties to better characterize patients with CTS resides in the definition of which is the most appropriate diagnostic method to verify this condition.
There is consensus among several authors that CTS presents frequently in females, reaching a rate of 97.7%,[9] similar to that of the present study, in which 90.9% of the cases occurred in women. We found a mean age of 53 years, which can be explained by factors in this age group, such as axon loss and vascular abnormality, that increase the susceptibility of the peripheral nerve to the effects of compression.[9]
In an analysis of the complementary tests, we understand that CTS diagnosis only by US is reckless, since the literature is vast in demonstrating conflicting values of normality of the median nerve (ranging from 10 mm2 to 14 mm2).[10] [11] [12] [13] The finding of 43.7% of patients with a clinical diagnosis of CTS and normal ultrasound result, almost twice the rate found by Mondelli et al.,[14] further reinforces our questions regarding the usefulness of US in isolation for the accurate diagnosis of CTS.
As for the electroneuromyographic study, the finding of patients with clinical symptoms of CTS and normal ENMG result is not uncommon. According to the studies by Padua et al. [15] and Bagatur and Zorer,[16] more than half of the patients with CTS diagnosed by ENMG are asymptomatic, which was also consistent with the present study. Nevertheless, we found altered ENMG results in 58.3% of the hands, with the moderate degree being the most prevalent.
Regarding the reliability of the clinical tests, the study by De Krom et al.[17] prresent low predictive value for the diagnosis of CTS, as occurred in the present study, which makes us consider the Tinel, Phalen and Durkan tests deficient when used isolatedly for the definition of who really carries the condition. However, the Durkan test was the one that obtained the highest sensitivity and specificity in relation to the others, which makes us recommend the inclusion of this test in the outpatient routine in patients with suspicion of STC.
The present study revealed little agreement between the ENMG and US, as well as between the ENMG and the clinical tests, with very low Kappa values. Furthermore, we found that the clinical tests had no statistical association with CTS severity, which demystifies the excessive rate of requests for complementary tests without correlation with the complaint and with the detailed examination of the patient.
#
Conclusion
The present study demonstrated that the accurate diagnosis of CTS is still controversial, since to date there is no highly-sensitive and specific tool capable of defining the condition, with no agreement regarding the clinical examination, the US scan and the ENMG in the diagnosis of CTS. We conclude that there is no clinical or complementary examination for CTS that accurately determines the therapeutic approach.
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* Work performed at the Hand Surgery and Microsurgery Service of Santa Casa of São Paulo, São Paulo, SP, Brazil.
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Referências
- 1 Eren Y, Yavasoglu NG, Comoglu SS. The relationship between QDASH scale and clinical, electrophysiological findings in carpal tunnel syndrome. Adv Clin Exp Med 2018; 27 (01) 71-75
- 2 Keith MW, Masear V, Chung K. et al. Diagnosis of carpal tunnel syndrome. J Am Acad Orthop Surg 2009; 17 (06) 389-396
- 3 Hansen PA, Micklesen P, Robinson LR. Clinical utility of the flick maneuver in diagnosing carpal tunnel syndrome. Am J Phys Med Rehabil 2004; 83 (05) 363-367
- 4 Amirfeyz R, Clark D, Parsons B. et al. Clinical tests for carpal tunnel syndrome in contemporary practice. Arch Orthop Trauma Surg 2011; 131 (04) 471-474
- 5 Bickel KD. Carpal tunnel syndrome. J Hand Surg Am 2010; 35 (01) 147-152
- 6 Stevens JC. American Association of Electrodiagnostic Medicine. AAEM minimonograph #26: the electrodiagnosis of carpal tunnel syndrome. Muscle Nerve 1997; 20 (12) 1477-1486
- 7 Fleiss JL. The design and analysis of clinical experiments. New York: Wiley; 1986
- 8 Kirkwood BR, Sterne JAC. Essential medical statistics. 2nd ed.. Massachusetts, USA: Blackwell Science; 2006
- 9 Nordstrom DL, DeStefano F, Vierkant RA, Layde PM. Incidence of diagnosed carpal tunnel syndrome in a general population. Epidemiology 1998; 9 (03) 342-345
- 10 Kwon BC, Jung KI, Baek GH. Comparison of sonography and electrodiagnostic testing in the diagnosis of carpal tunnel syndrome. J Hand Surg Am 2008; 33 (01) 65-71
- 11 Moran L, Perez M, Esteban A, Bellon J, Arranz B, del Cerro M. Sonographic measurement of cross-sectional area of the median nerve in the diagnosis of carpal tunnel syndrome: correlation with nerve conduction studies. J Clin Ultrasound 2009; 37 (03) 125-131
- 12 Akcar N, Özkan S, Mehmetoglu O, Calisir C, Adapinar B. Value of power Doppler and gray-scale US in the diagnosis of carpal tunnel syndrome: contribution of cross-sectional area just before the tunnel inlet as compared with the cross-sectional area at the tunnel. Korean J Radiol 2010; 11 (06) 632-639
- 13 Chammas M, Boretto J, Burmann LM, Ramos RM, Dos Santos Neto FC, Silva JB. Carpal tunnel syndrome - Part I (anatomy, physiology, etiology and diagnosis). Rev Bras Ortop 2014; 49 (05) 429-436
- 14 Mondelli M, Filippou G, Gallo A, Frediani B. Diagnostic utility of ultrasonography versus nerve conduction studies in mild carpal tunnel syndrome. Arthritis Rheum 2008; 59 (03) 357-366
- 15 Padua L, Coraci D, Erra C. et al. Carpal tunnel syndrome: clinical features, diagnosis, and management. Lancet Neurol 2016; 15 (12) 1273-1284
- 16 Bagatur AE, Zorer G. The carpal tunnel syndrome is a bilateral disorder. J Bone Joint Surg Br 2001; 83 (05) 655-658
- 17 de Krom MC, Knipschild PG, Kester AD, Spaans F. Efficacy of provocative tests for diagnosis of carpal tunnel syndrome. Lancet 1990; 335 (8686): 393-395
Endereço para correspondência
Publication History
Received: 21 July 2021
Accepted: 14 October 2021
Article published online:
04 February 2022
© 2022. Sociedade Brasileira de Ortopedia e Traumatologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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Referências
- 1 Eren Y, Yavasoglu NG, Comoglu SS. The relationship between QDASH scale and clinical, electrophysiological findings in carpal tunnel syndrome. Adv Clin Exp Med 2018; 27 (01) 71-75
- 2 Keith MW, Masear V, Chung K. et al. Diagnosis of carpal tunnel syndrome. J Am Acad Orthop Surg 2009; 17 (06) 389-396
- 3 Hansen PA, Micklesen P, Robinson LR. Clinical utility of the flick maneuver in diagnosing carpal tunnel syndrome. Am J Phys Med Rehabil 2004; 83 (05) 363-367
- 4 Amirfeyz R, Clark D, Parsons B. et al. Clinical tests for carpal tunnel syndrome in contemporary practice. Arch Orthop Trauma Surg 2011; 131 (04) 471-474
- 5 Bickel KD. Carpal tunnel syndrome. J Hand Surg Am 2010; 35 (01) 147-152
- 6 Stevens JC. American Association of Electrodiagnostic Medicine. AAEM minimonograph #26: the electrodiagnosis of carpal tunnel syndrome. Muscle Nerve 1997; 20 (12) 1477-1486
- 7 Fleiss JL. The design and analysis of clinical experiments. New York: Wiley; 1986
- 8 Kirkwood BR, Sterne JAC. Essential medical statistics. 2nd ed.. Massachusetts, USA: Blackwell Science; 2006
- 9 Nordstrom DL, DeStefano F, Vierkant RA, Layde PM. Incidence of diagnosed carpal tunnel syndrome in a general population. Epidemiology 1998; 9 (03) 342-345
- 10 Kwon BC, Jung KI, Baek GH. Comparison of sonography and electrodiagnostic testing in the diagnosis of carpal tunnel syndrome. J Hand Surg Am 2008; 33 (01) 65-71
- 11 Moran L, Perez M, Esteban A, Bellon J, Arranz B, del Cerro M. Sonographic measurement of cross-sectional area of the median nerve in the diagnosis of carpal tunnel syndrome: correlation with nerve conduction studies. J Clin Ultrasound 2009; 37 (03) 125-131
- 12 Akcar N, Özkan S, Mehmetoglu O, Calisir C, Adapinar B. Value of power Doppler and gray-scale US in the diagnosis of carpal tunnel syndrome: contribution of cross-sectional area just before the tunnel inlet as compared with the cross-sectional area at the tunnel. Korean J Radiol 2010; 11 (06) 632-639
- 13 Chammas M, Boretto J, Burmann LM, Ramos RM, Dos Santos Neto FC, Silva JB. Carpal tunnel syndrome - Part I (anatomy, physiology, etiology and diagnosis). Rev Bras Ortop 2014; 49 (05) 429-436
- 14 Mondelli M, Filippou G, Gallo A, Frediani B. Diagnostic utility of ultrasonography versus nerve conduction studies in mild carpal tunnel syndrome. Arthritis Rheum 2008; 59 (03) 357-366
- 15 Padua L, Coraci D, Erra C. et al. Carpal tunnel syndrome: clinical features, diagnosis, and management. Lancet Neurol 2016; 15 (12) 1273-1284
- 16 Bagatur AE, Zorer G. The carpal tunnel syndrome is a bilateral disorder. J Bone Joint Surg Br 2001; 83 (05) 655-658
- 17 de Krom MC, Knipschild PG, Kester AD, Spaans F. Efficacy of provocative tests for diagnosis of carpal tunnel syndrome. Lancet 1990; 335 (8686): 393-395