INTRODUCTION
Carpal tunnel syndrome is the most common entrapment
syndrome of the upper extremities with an estimated incidence in the general
community of 125/100,000/year. Typically, the dominant hand is affected first.
The clinical hallmark and usual presenting feature of CTS is a pain syndrome
called brachialgia paresthetica nocturna. It arises from compression of the
median nerve in the canal formed by the transverse carpal ligament and carpal
bones. Under pathological circumstances tissue pressure in the carpal tunnel
reaches 30 mmHg, in other words; four times the normal level. Chronic or
recurrent compression of the median nerve causes focal demyelination and
eventually axon degeneration. Temporary ischemia due to compression of the vasa
nervorum accounts for the reversible pain manifesting during the night1.
In most instances, the diagnosis of CTS is reliably
settled by an experienced clinician based on the patient’s history and a
careful neurological examination including Phalen’s maneuver and Tinel’s sign2.
Electro-diagnostic Studies (EDS) are recommended
when median nerve compression causes significant discomfort or sustained
sensorimotor deficits. An electrophysiological work-up is particularly useful
to assess the damage to the median nerve (demyelination versus axon loss)
relevant to therapeutic decisions, to rule out differential diagnoses or
coexistent disease and to confirm the presence of CTS in the event of atypical
complaints, pure motor deficits and prominent neuropathy. Various diagnostic
criteria have been suggested including prolonged motor and sensory latencies of
the median nerve and reduced sensory and motor conduction velocities. The
optimal diagnostic criteria however remain uncertain3.
False negative and false positives can occur even when the most
sensitive methods of EDS are used. Inadequacies of EDS have been partly blamed
on a lack of standardized diagnostic criteria with reports of 16–34% of
clinically defined CTS being missed with EDS, and sensitivities ranging from 49
to 84% considering this, blanket referrals for EDS are an expensive and inefficient
approach to the diagnosis of CTS and may lead to continued diagnostic
uncertainty4.
Magnetic Resonance Imaging provides
anatomical information so; it is probable that the future of imaging will be in
a supplementary role to the already established EDS in cases where anatomical
clarification is required or where the results of EDS are equivocal. With the
increased popularity of endoscopic procedures for CTS, it is becoming
increasingly necessary to establish the underlying anatomy in order to prevent potential
damage to the median nerve in cases where the anatomy is abnormal. Rare
pathological causes of CTS such as ganglion, hemangioma or bony deformity are
more likely to be uncovered with imaging modalities, and their presence may
alter planned surgical intervention4.
Sonography is able to reliably diagnose idiopathic
CTS in a high percentage of patients and rule out secondary CTS due to
abnormalities inside the carpal tunnel such as flexor tendon synovitis, tumors
or ganglia. If no abnormalities are found within the carpal tunnel, sonographic
nerve inspection should be extended proximally upwards to the brachial plexus
to exclude other rare and unusual abnormalities. Recent reports suggest
that sonography should be performed as a first-line investigation after
clinical examinations since the diagnostic value of sonographic findings are
better than physical maneuvers. Other authors have shown that sonography has
similar diagnostic values compared to electrodiagnostic studies. Only one
report found sonography not accurate enough to replace electroneurographic
testing5. In the present study we
aimed at comparing the diagnostic accuracy of various
tests used in the diagnosis of CTS and to determine the properties of the most
accurate one.
PATIENTS AND
METHODS
Fifty two cases of clinically established unilateral
CTS were subjected to three different investigation modalities before surgical
intervention (EDS, MRI and U/S). All patients underwent the open surgical
technique for flexor carpal ligament release. The same surgical technique,
however by different surgeons, was used in all operated cases.
The diagnosis of CTS was made according to American Academy of Neurology criteria, which
include clinical history and symptoms. According to the hand diagram by Katz et
al modified by consensus criteria of the classification of CTS6,
only patients with paresthesia or pain in at least 2 of the first 3 fingers
(classic/probable cases) were included in the study. Physical examination
consisted of evaluating muscular strength and trophism, sensory function, and
provocative clinical tests (Phalen’s and Tinel’s signs).
For this study, only patients with mild CTS were
enrolled; mild cases were defined as those patients who reported only symptoms
without objective motor deficit of thenar eminence muscles and normal objective
sensory function in the median nerve territory of the hand. The mild cases
belonged to stages 1 (nocturnal symptoms and morning symptoms on awakening) and
2 (diurnal symptoms) of a validated historical-objective clinical severity
scale7.
The diagnostic electrophysiological criteria were: For distal motor latency the
cutoff values used in different studies have ranged from 3.8 ms to 4.6 ms;
however an intermediate value (4.2 ms) was considered as a cutoff point in this
study.
The diagnostic MRI criteria were: 1. Swelling of the median nerve,
2. Increased signal intensity on T2-weighted images, and 3. Palmar bowing of
the transverse carpal ligament. The
usefulness of median nerve flattening remains controversial with some papers
suggesting that flattening is a positive indicator of CTS, and others advising
that CTS was more likely in patients who showed no median nerve flattening8.
The diagnostic sonographic criteria were: 1. Enlargement of the median
nerve at the proximal carpal tunnel with an increased cross sectional area over
12 mm2. 2. Changes in median nerve echotexture consistent with edema
(loss of fascicular discrimination with more or less homogeneous hypoechoic
appearance, and indistinct outer margins). 3. Abrupt caliber change (notch
sign) at the proximal margin of the flexor retinaculum. 4. Detection of a large PMA (persistent median
artery) or increased intraneural and perineural vascularity. 5. Dynamic
scanning for detection of additional fluid or accessory muscle bellies. 6.
Palmer bowing and thickening of the flexor retinaculum. A reliable
documentation of this finding, however, will only be achieved with the
application of high frequency sonographic transducers, which allow exact
discrimination of the retinaculum. A cut-off value of > 4 mm between the
most anterior part of the carpal ligament and the base line between the hamatum
and trapezium has been reported to be significant for CTS9.
RESULTS
The study included fifty two patients, twelve (23%) were males while
forty (77%) were females with age range 28-53 years (mean=41.5 years). The
clinical presentations of the studied patients are shown in Table (1) and the
results of different investigation modalities are shown in Table (2).
All patients underwent the standard open surgical technique for carpal
tunnel release following the above investigations, the same surgical technique
have been practiced by different surgeons. All surgeons were blinded to the
results of investigations done, however not for patient’s symptoms or signs.
They all reported positively presence of median nerve compression under the
transverse carpal ligament with its relative thickening to different degrees
during its intraoperative exposure.
All patients were followed up for a period not less than 12 weeks
post-operatively. Thirty seven (71.1%) patients reported complete remission of
previous symptomatology, while the rest fifteen (28.8%) patients showed marked
amelioration of their complaint.
DISCUSSION
Carpal tunnel syndrome is a common entrapment
neuropathy of the median nerve characterized by pain and sensory disturbance
along the distribution of the median nerve and thenar muscle atrophy in the
advanced stages. The diagnosis may be made clinically and with electromyography
(EMG). Ultrasound may also be valuable in the diagnosis of CTS. Several studies
have demonstrated that carpal tunnel ultrasound in combination with clinical
features and EMG was more sensitive and specific than clinical evaluation or
EMG in isolation. Ultrasound has proved to be able to depict normal and
pathologic nerves, including anatomical variants and abnormalities associated
with CTS10.
The usual presenting feature of CTS is a pain
syndrome known as brachialgia paresthetica nocturna. Patients,
usually women in their fourth and fifth decade, are awakened from sleep in the
early morning hours with pain radiating from the wrist proximally into the
forearm and arm, and report numbness and tingling in the hand, stiffness of the
fingers, and characteristic swelling sensations. All complaints rapidly resolve
after repeated hand movements such as shaking. In the early stage no gross
abnormalities can be observed within the nerve. Sensory disturbance usually
appears before motoric deficiency since sensory fibers are more pressure
sensitive than motoric fibers. According to Nora et al., 2005 paresthesia is
the most characteristic feature followed by pain and cramps11. In
the current study, similar results was found where forty patients (77%) were
females with mean age = 41.5 years. The most common presenting
feature is paresthesia or pain in at least 2 of the first 3 fingers and it was
found in all patients (100%).
Historically, clinical provocative tests such as
Phalen’s and Tinel’s have been used to aid in the diagnosis of CTS. A wide
range of sensitivities and specificities have been reported in the literature12. Phalen’s test is said to be positive when
flexion at the wrist for 60 sec leads to pain or paresthesia in the
distribution of the median nerve. These tests have quoted sensitivities of
10–90% and specificities of 33–100%. A detailed systematic review of over 3,000
cases reported a sensitivity of 68% and specificity of 73% for Phalen’s test
and concluded that it was a useful test, but false negatives should be expected.
Tinel’s test is said to be positive when tapping over the volar surface of the
wrist causes paresthesia in the fingers innervated by the median nerve. Tinel’s
is generally thought to be less sensitive than Phalen’s; however, specificities
have been recorded as high as 100%13. In the present study the
results of provocative clinical tests were: Phalen’s sign positive in
(86.5%) of patients, while Tinel’s sign was positive in (82.6%).
Since American
Academy of Neurology
(ANN) previously stated the diagnosis of CTS is mostly clinical with the
morphofunctional test aimed in confirming the diagnosis, No consensus exists
regarding the type and number of nerve conduction tests needed to establish the
neurophysiological diagnosis. Moreover, there is no consensus on the definition
of abnormality. In addition to median nerve motor and wrist-digit sensory
latency measurements, numerous new tests have been successively introduced to
improve the sensitivity of nerve conduction tests. Performing multiple nerve
conduction tests on an individual would increase the likelihood of obtaining a
false positive result. Measurements of wrist-palm sensory conduction or
median-ulnar comparison have been considered superior to distal motor and
digit-wrist sensory latency measurements, particularly in detecting patients
with mild CTS14.
The EDS diagnostic uncertainty associated with
clinical signs may lead to clinicians non-selectively referring patients for
nerve conduction studies with the belief that it represents a diagnostic gold
standard. However, EDS have their own diagnostic hurdles. False negative and
false positives can occur even when the most sensitive methods of EDS are used3.
Graham15 looked at the value added by EDS in diagnosing patients
with clinically defined CTS. They reported that for the majority of patients,
EDS did not change the probability of diagnosing the condition. This was an
interesting discovery and supports and emphasis on clinical history and
examination in identifying patients with CTS.
Kamath and Stothard16 carried out a
prospective study involving 107 patients to assess whether a similar structured
health questionnaire would be able to diagnose CTS with similar sensitivities
and specificities to EDS. They used symptom relief after surgery as the
diagnostic gold standard and reported equivalent sensitivities and positive
predictive values (PPV) between their questionnaire (sensitivity, 85%; PPV,
90%) and EDS (sensitivity, 92%; PPV, 92%). They concluded that such a questionnaire
could be used to fast track those patients who scored highly for surgery,
bypassing usual outpatient referrals and EDS. This goes against the
recommendations of the American
Academy of Orthopedic
Surgeons, who recommend EDS for all patients being considered for surgery17.
In the present study the electro diagnostic studies (EDS) performed for twenty
patients with clinical criteria of CTS, only seventeen patients (85%) were
positive and the remaining three patients were false negative.
A recent prospective study comparing the diagnostic
utility of ultrasound versus EDS found equivalent sensitivities between the two
techniques18. Sensitivities for EDS and ultrasound were 67.1% and
64.7%, respectively; however, if both EDS and ultrasound were considered
together, the sensitivity increased to 76.5%. This suggests a role for
ultrasound as a diagnostic adjunct to the established EDS. The study also
highlights the diagnostic shortfalls of these investigations with 23.5% of
patients with clinically diagnosed CTS remaining undetected (4).
On looking to the present study, 19 (86.3%) of 22
patients examined by ultrasonography were confirmed to be CTS according to the
previous criteria. This result is comparable to the results yielded on electro
diagnostic studies (EDS) performed in the same study (i.e. 85% were positive
when tested for EDS) and this means equivalent sensitivities between the two
techniques.
A prospective cohort study by Jarvik et al.19,
attempted to further delineate the role of MRI in the diagnosis of CTS. They
reviewed 105 patients and followed the patients for 1 year specifically looking
at the ability of MRI to identify those patients likely to benefit from surgery
and to compare its diagnostic usefulness to that of EDS. They demonstrated that
both MRI and EDS were able to predict those patients who would benefit from
surgical intervention; however, neither technique correlated well with
patient’s perceived severity of symptoms. They did show some evidence to
suggest that there is a patient preference for MRI over EDS with 76% of their
patients reporting EDS to be unpleasant compared to 21% finding MRI unpleasant.
Imaging provides anatomical information whilst EDS gives information on
impairment of nerve fiber function and is able to rule out polyneuropathy and
nerve conduction problems elsewhere in the body. With this in mind it is
probable that the future of imaging will be in a supplementary role to the
already established EDS in cases where anatomical clarification is required or
where the results of EDS are equivocal4.
In the current series MRI was able to predict
those patients who would benefit from surgical intervention; where all patients
(100%) subjected to MRI examination were positive for CTS diagnostic criteria,
confirming the clinical status. However, there is a patient preference for MRI
over EDS, while others declare that the cost of MRI is unaffordable, hence EDS
is the alternative. From our point of view neither EDS nor MRI would be better
for the patient anyway; this is because of the high cost, technically
demanding, and patient exposure to unpleasant complicated tools (invasive
electrodes in EDS, noisy and time consuming in MRI).
It has been found that ultrasonography (especially
the high frequency US)
is highly valuable in assessing patients with clinical suspension of CTS, this
may be related to many causes that include: wide availability, reasonable cost,
time saving, well accepted to patients, no contraindications to its usage, and
high accuracy rate. All these advantages make it superior to other contemporary
investigation tools20.
Conclusion
In conclusion, In mild cases of CTS, the sensitivity
of the electrodiagnostic tests and US is very near, US is not an alternative
diagnostic tool to electrodiagnostic tests and vice versa, but they are
complementary; US provides anatomic information of the nerve and its
surrounding structures while the electrodiagnostic tests provides information
on the level of the lesion and the function of the nerve fibers. However, NCV
and classic needle electromyography are indispensable to resolve clinical
uncertainties and to rule out similar events such as cervical radiculopathy,
brachial plexopathy and polyneuropathy. Finally, the diagnosis of CTS is
essentially by clinical evaluation of the patient, however an added
investigation is recommended to support the diagnosis. The dispute is what
investigation tool that provides accurate and rapid diagnosis with the least
cost. It was found that ultrasound is superior to other modalities in this respect.
[Disclosure:
Authors report no conflict of interest]
REFERENCES
1. Szabo RM, Chidgey LK. Stress
carpal tunnel pressures in patients with carpal tunnel syndrome and normal
patients. J Hand Surg.1989; 14:624–7.
2. Kuschner SH, Ebramzadeh E,
Johnson D, Brien WW, Sherman R.
Tinel’s sign and Phalen’s test in carpal tunnel syndrome. Orthopedics. 1992;
15:1297–302.
3. Lew HL, Date ES, Pan SS, Wu P, Ware PF, Kingery WS. Sensitivity,
specificity, and variability of nerve conduction velocity measurements in
carpal tunnel syndrome. Arch Phys Med Rehabil. 2005; 86:12–6.
4. Mathew S. Prime, Palmer J, Wasim S. Khan, Nicholas J. Goddard.
Is there Light at the End of the Tunnel? Controversies in the Diagnosis and
Management of Carpal Tunnel Syndrome. HAND. 2010; 5:354–60.
5. Kwon BC, Jung KI, Baek GH.
Comparison of sonography and electrodiagnostic testing in the diagnosis of
carpal tunnel syndrome. J Hand Surg. 2008; 33:65–71.
6. Katz JN, Stirrat CR, Larson
MG, Fossel AH, Eaton HM, Liang MH. A self-administered hand symptom diagram for
the diagnosis and epidemiologic study of carpal tunnel syndrome. J Rheumatol. 1990; 17:1495–8.
7. Giannini F, Cioni R,
Mondelli M, Padua
R, Gregori B, D’Amico P, et al. A new clinical scale of carpal tunnel syndrome:
validation of the measurement and clinical-neurophysiological assessment. Clin
Neurophysiol. 2002; 113:71–7.
8. Radack DM, Schweitzer ME,
Taras J. Carpal tunnel syndrome: are the MR findings a result of population selection bias? Am J
Roentgenol. 1997; 169:1649–53.
9. Buchberger W, Judmaier W,
Birbamer G, Lener M, Schmidauer C. Carpal tunnel syndrome: diagnosis with high-resolution sonography. AJR
Am J Roentgenol. 1992; 159:793–8.
10. Beekman R, Visser LH.
High-resolution sonography of the peripheral nervous system-a review of the literature. Eur J Neurol.
2004; 11: 305–14.
11. Nora DB, Becker J, Ehlers JA,
Gomes I. What symptoms are truly caused by median nerve compression in carpal tunnel syndrome?
Clin Neurophysiol. 2005; 116:275–83.
12. Katz J, Simmons B. Carpal
tunnel syndrome. N Eng J Med. 2002; 346:1807–12.
13. Aroori S, Spence R. Carpal
tunnel syndrome. Ulster
Med J. 2008; 77:6–17.
14. Jackson DA, Clifford JC. Electrodiagnosis of
mild carpal tunnel syndrome. Arch Phys Med Rehabil. 1989; 70:199–204.
15. Graham B. The value added by
electro-diagnostic testing in the diagnosis of carpal tunnel syndrome. J Bone Surg Am. 2008;
90:2587–93.
16. Kamath V, Stothard J. A
clinical questionnaire for the diagnosis of carpal tunnel syndrome. J Hand Surg
Br. 2003; 28:455–9.
17. Keith MW, Masear V, Chung KC,
Maupin K, Andary M, Amadio PC, et al. American Academy of Orthopaedic Surgeons Clinical Practice
Guideline on diagnosis of carpal tunnel syndrome. J Bone Joint Surg AM. 2009;
91:2478–9.
18. Mondelli M, Filippou G, Gallo
A, Frediani, B. Diagnostic
utility of ultrasonography versus nerve conduction studies in mild carpal
tunnel syndrome. Arthritis Rheum. 2008; 59:357–66.
19. Jarvik JG, Comstock BA,
Heagerty PJ, Haynor DR, Fulton-Kehoe D, Kliot M, et al. Magnetic resonance
imaging compared with electrodiagnostic studies in patients with suspected
carpal tunnel syndrome: predicting outcomes, function and surgical benefit at 1
year. J Neurosurg. 2008; 108:541–50.
20. Karadaf YS, Karadaf O,
Ciçekli E, Oztürk S, Kiraz S, OzbakÂr S, et al. Severity of carpal tunnel
syndrome assessed with high frequency ultrasonography. Rheumatol Int. 2010;
30(6):761-5.