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JBJS welcomes reader comments on published articles. Letters to the Editor are reviewed by JBJS editors but are not peer-reviewed. To submit your letter, please follow the "submit a response" link that appears in the content box at the upper right of the full text of the article.
Letters to the Editor to:
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- Scientific Articles:
Brent Graham
- The Value Added by Electrodiagnostic Testing in the Diagnosis of Carpal Tunnel Syndrome
J Bone Joint Surg Am 2008; 90: 2587-2593
[Abstract]
[Full text]
[PDF]
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Electronic letters published:
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Dr. Graham responds to Mr. Kamath and Mr. Stothard
- Brent Graham, MD
(24 March 2009)
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Value of A History Based Questionaire In The Diagnosis of Carpal Tunnel Syndrome
- Vijay Kamath, Prof. John Stothard
(24 March 2009)
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Autonomic Dysfunction in Carpal Tunnel Syndrome
- Venkat R. Mekala, Quamar Bismil, MSK Bismil
(5 February 2009)
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Dr. Graham responds to Dr. Ring
- Brent A. Graham, MD, MSc, FRCSC
(22 December 2008)
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Is carpal tunnel still a syndrome?
- David Ring, MD
(4 December 2008)
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Dr. Graham responds to Mr. Kamath and Mr. Stothard |
24 March 2009 |
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Brent Graham, MD Toronto Western Hospital
Send letter to journal:
Re: Dr. Graham responds to Mr. Kamath and Mr. Stothard
Brent.Graham{at}uhn.on.ca Brent Graham, MD
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Clearly the issue of establishing the right gold standard for carpal
tunnel syndrome is a difficult one. The key consideration is that of
consensus. Whatever criterion is chosen as the gold standard for the
diagnosis – expert clinical evaluation, electrodiagnostic tests or
response to treatment – there must be a consensus that this is an
acceptable standard or that criterion will lack usefulness. It is clear
that many, possible a majority, of diagnosticians do not believe that
electrodiagnostic testing should be the gold standard. As the study
showed in most instances, this test doesn’t add materially to the
diagnostic process. Unfortunately, the response to treatment, while it is
appealing as a logical correlate to diagnosis is flawed for a number of
reasons. To begin with, not all those who have a diagnosis are
necessarily treated so an evaluation of the value response to treatment
isn’t really possible in many instances. In addition, it is clear that
some patients who do not have carpal tunnel syndrome get better when they
are treated for something else and conversely many instances when patients
who do have carpal tunnel syndrome do not seem to improve after treatment.
The causes for this can be many: inadequate release, delayed improvement
due to wallerian degeneration secondary to prolonged or extreme
compression, and the various effects on workers’ compensation on the
apparent outcome of treatment. Because of these considerations, we have
chosen the consensus of a panel of experts as the most reliable standard
for the diagnosis in carpal tunnel syndrome, though admittedly perfect
consensus on this idea may not exist. Nonetheless, excellent consensus
was obtained among the disparate group of medical and surgical experts who
contributed to the original scale.
In our original communication describing the diagnostic scale, the
weightings were described and based on the logistic regression model that
was developed from the data. Figure 3 in the JBJS paper shows a point
system for clinical use that is based on the regression coefficients in
the model.
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Value of A History Based Questionaire In The Diagnosis of Carpal Tunnel Syndrome |
24 March 2009 |
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Vijay Kamath, Post CCT Fellow James Cook University Hospital, Middlesborough, United Kingdom, Prof. John Stothard
Send letter to journal:
Re: Value of A History Based Questionaire In The Diagnosis of Carpal Tunnel Syndrome
vijaykamath{at}doctors.org.uk Vijay Kamath, et al.
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To the Editor:
The studies by Graham (1,2) use techniques that
are well established in developing consensus management for common
conditions. We were especially interested to learn that for carpal tunnel syndrome,
the clinical history and examination can produce the same diagnostic
conclusions as nerve conduction studies.
We looked at this problem some years ago
using a rather simpler statistical model and came to the same
conclusion (3).The difficulty we had noted with many previous research
publications(especially those studying the sensitivity and specificity of individual tests or combination of tests e.g. Phalens
and Tinel test) was that Nerve Conduction Studies were used as the so called
gold Standard.
To compare these tests with nerve conduction studies, we needed a new standard;
the standard we adopted was improvement of symptoms after Carpal
tunnel surgery. We found that history taking was much more revealing
diagnostically than were the results of individual tests. This is because a Phalens test is
sensitive but not specific as it is present in a fair number of people
without carpal tunnel syndrome, and a Tinel test is only present in 30 to
40 percent of people with known carpal tunnel syndrome (but is specific as
it is not present in people without).
We constructed a questionnaire based
on the patient's history that could be
administered by primary care physicians (3).
The methodology used by Dr. Graham (1) gives a full list of unweighted
clinical diagnostic criteria that include only two history items, numbness
and tingling in the median nerve distribution, and nocturnal numbness. In our history based questionnaire (3), we weighted these items heavily but we feel that these two questions alone are not sufficient to capture the whole relevant history.
The test we developed has been cited in 15 publications including an
information leaflet for primary care physicians developed by the Arthritis and Rheumatism Council (4).
If we look at the diagnostic criteria in appendix 2 of the original
article by Dr. Graham et al. (2), we see that the formula is:
p(CTS)/1-p(CTS)=eb+b1X1+b2X2+b3X3+b4X4=b5x5+b6X6
where b0=-2.4;variable present=1, absent=0;b1=1.44;x1= thenar
atrophy;b2=1.44;x2=Phalens test;b3=1.30;x3=loss of 2-point discrimination;
b4=1.16;x4 =Tinel’s sign;b5=1.16;x5=nocturnal
numbness;b6=1.03;x6=numbness, median nerve distribution
The application of this formula is probably too complex for general
screening. We wonder if Dr. Graham has any comments as to how it could be
made more “user friendly”.
The authors did not receive any outside funding or grants in support of their research for or preparation of this work. Neither they nor a member of their immediate families received payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or direct, any benefits to any research fund, foundation, division, center, clinical practice, or other charitable or nonprofit organization with which the authors, or a member of their immediate families, are affiliated or associated.
References
1. Graham B. The value added by electrodiagnostic testing in the
diagnosis of carpal tunnel syndrome. J Bone Joint Surg Am. 2008;90:2587-93.
2. Graham B, Regehr G, Naglie G, Wright JG. Development and validation
of diagnostic criteria for carpal tunnel syndrome. J Hand Surg [Am]. 2006;31:919-24.
3. Kamath V, Stothard J. A clinical questionnaire for the diagnosis of
carpal tunnel syndrome [erratum in J Hand Surg [Br]. 2004; 29(1):95-6]. J
Hand Surg [Br]. 2003;28(5):455-9.
4. Barnardo J. Carpal Tunnel Syndrome: 2004: No 3ARC Booklet, Reports
on the Rheumatic Diseases Series 5. |
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Autonomic Dysfunction in Carpal Tunnel Syndrome |
5 February 2009 |
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Venkat R. Mekala, Senior House Officer Trauma and Orthopaedics Mayday University Hospital, Croydon, Quamar Bismil, MSK Bismil
Send letter to journal:
Re: Autonomic Dysfunction in Carpal Tunnel Syndrome
mvr_reddy2000{at}yahoo.com Venkat R. Mekala, et al.
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To the Editor:
We read the article by Dr Graham (1) with great interest. The article
reinforces the widely-held concept that Carpal Tunnel Syndrome (CTS) is a
clinical diagnosis and that electrodiagnostic studies seldom add to
clincal decision making.
With this in mind, readers of The Journal should be aware that all
three components of the peripheral nerve are potentially affected by
compression neuropathy and that autonomic dysfuction in CTS is often
overlooked.
A recent prospective study confirmed that the autonomic deficit is
CTS is real and quantifiable and can be used as an adjunct to diagnosis (2).
The authors did not receive any outside funding or grants in support of their research for or preparation of this work. Neither they nor a member of their immediate families received payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or direct, any benefits to any research fund, foundation, division, center, clinical practice, or other charitable or nonprofit organization with which the authors, or a member of their immediate families, are affiliated or associated.
References
1. Brent Graham
The Value Added by Electrodiagnostic Testing in the Diagnosis of Carpal Tunnel Syndrome
J Bone Joint Surg Am 2008; 90: 2587-2593.
2. Kumar A, Bismil Q, Morgan B, Ashbrooke A, Davies S, Solan M. The
"biro test" for autonomic dysfunction in carpal tunnel syndrome. J Hand
Surg Eur Vol. 2008 Jun;33(3):355-7. |
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Dr. Graham responds to Dr. Ring |
22 December 2008 |
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Brent A. Graham, MD, MSc, FRCSC, Hand Surgeon, Director University of Toronto/University Health Network Hand Program, Toronto Western Hospital
Send letter to journal:
Re: Dr. Graham responds to Dr. Ring
Brent.Graham{at}uhn.on.ca Brent A. Graham, MD, MSc, FRCSC
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Dr. Ring brings up a few important points that are worth considering.
As diagnosticians our task is to evaluate the presenting complaint of the
patients and make an analysis of its most likely cause. Frequently the
complaint of pain will predominate in a patient with a condition like
nerve compression. Nonetheless it is well accepted that the cardinal
symptom in these cases is a sensory disturbance. This dysesthesia can
certainly be considered painful but the first objective of the clinician
is to understand what it is that the patients are experiencing, regardless
of their description. There is no diagnostic value in taking the
complaint of pain at face value if it is clear that what they actually
mean is painful dysesthesia. The sensory disturbance is a marker for
considering a neurologic basis for the symptoms. If there is pain that is
not associated with a sensory disturbance then an alternative diagnosis
should be sought. This principle is reflected in the composition of the
CTS-6, which as Dr Ring points out, has a strong focus on nerve
dysfunction. The development of this instrument was methodologically
rigorous and it’s content essentially summarizes the practices of expert
clinicians from a wide spectrum of both medical and surgical specialties
[1]. It has to be concluded that this is the approach with the greatest
diagnostic utility.
I would concur with Dr. Ring that were electrodiagnostic testing
taken as the reference standard then a clinical evaluation would not add
much to the diagnostic process. However I would submit that a careful and
simple clinical evaluation using the CTS-6 criteria is certainly easier,
less costly, timelier and less uncomfortable for patients so I would not
agree with Dr. Ring that “an objective, neurophysiologic reference
standard” is required. The reliable conduct of a clinical assessment
encompassed by the CTS-6 should be well within the scope of any primary
care physician and even, as the study showed, an appropriately trained
allied health worker. As for the patient with “moderate to severe nerve
dysfunction”, the data in the paper shows that the changes in the
probability of carpal tunnel syndrome resulting from electrodiagnostic
testing are particularly small in these patients.
Finally, with respect to the extent of symptoms that bring a patient
to the physician, it seems unlikely that any kind of generalization is
possible. It is true however that whatever kind of treatment is
recommended it must be based on a diagnosis that is reliably established,
preferably with the least expense and discomfort. For most cases of
carpal tunnel syndrome it appears that this should not require the use of
electrodiagnostic testing.
Reference
1. Graham, B., et al., Development and validation of diagnostic
criteria for carpal tunnel syndrome. J Hand Surg [Am], 2006. 31(6): p. 919
-24. |
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Is carpal tunnel still a syndrome? |
4 December 2008 |
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David Ring, MD, Orthopaedic Hand and Upper Extremity Surgeon Massachusetts General Hospital
Send letter to journal:
Re: Is carpal tunnel still a syndrome?
dring{at}partners.org David Ring, MD
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To the Editor:
In his recent article(1), Dr. Graham found that electrophysiological testing did not appreciably alter the odds of having carpal tunnel syndrome that were based on clinical criteria alone. It should be acknowledged that his criteria (the CTS-6) focus on nerve dysfunction (numbness, atrophy, weakness, and abnormal provocative tests) whereas other diagnostic/severity criteria (e.g. those of Levine and colleagues (2)) give strong weight to pain complaints. I think it is correct of Dr. Graham to conclude that electrodiagnostic testing does not add much when symptoms and signs characteristic of median nerve dysfunction at the carpal tunnel are present, but there are more practical and meaningful ways to interpret his data and analysis.
Consider the converse of his conclusion, which while not specifically evaluated is very likely to be true: in the presence of abnormal electrophysiological testing of the median nerve at the carpal tunnel, clinical criteria do not appreciably affect the odds of carpal tunnel syndrome at the wrist. The differences between the lax and stringent criteria for diagnosing carpal tunnel syndrome on the basis of electrophysiological testing are probably not clinically relevant because these thresholds represent--at worst--very mild median nerve dysfunction at the carpal tunnel. Such mild median nerve dysfunction does not seem to bring most of us to the doctor and, if we do go, a night splint is usually satisfactory initial treatment. As such, we should be most interested in the moderate to severe median nerve dysfunction that would satisfy any electrophysiological threshold. This line of thinking supports an objective, neurophysiological reference standard for this diagnosis.
Either way you argue it, Dr. Graham’s work adds to the growing evidence that carpal tunnel syndrome is no longer a syndrome (a collection of symptoms and signs). Just as consumption became tuberculosis, it seems appropriate to diagnose and treat the discrete, objective, verifiable disease of median nerve dysfunction at the carpal tunnel rather than carpal tunnel syndrome.
For me, the key to interpreting Dr. Graham’s data or any data about carpal tunnel syndrome is to remember that the popular conception of carpal tunnel syndrome (and therefore that of most health providers) remains wrist and hand pain associated with typing. As science clarifies that carpal tunnel syndrome is best conceived of as objective, verifiable median nerve dysfunction at the carpal tunnel, nonspecific activity-related arm pains will no longer be misplaced in this diagnosis and our understanding and management of both median nerve dysfunction at the carpal tunnel and non-specific activity related arm pain will improve.
The author did not receive any outside funding or grants in support of his research for or preparation of this work. Neither he nor a member of his immediate family received payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or direct, any benefits to any research fund, foundation, division, center, clinical practice, or other charitable or nonprofit organization with which the author, or a member of his immediate family, is affiliated or associated.
References
1. Brent Graham
The Value Added by Electrodiagnostic Testing in the Diagnosis of Carpal Tunnel Syndrome
J Bone Joint Surg Am 2008; 90: 2587-2593
2. Levine DW, Simmons BP, Koris MJ, Daltroy LH, Hohl GG, Fossel AH, Katz JN. A self-administered questionnaire for the assessment of severity of symptoms and functional status in carpal tunnel syndrome. J Bone Joint Surg Am. 1993 Nov;75(11):1585-92. |
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