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53 Cards in this Set

  • Front
  • Back
Radiculopathy of which 2 nerve roots is most likely to be mistaken clinically for CTS?
(255) C6-7
Your patient has a strong clinical picture for CTS, normal EMG, normal routine median and ulnar NCS but positive comparison tests between nerves. Is it common or rare for patients to present like this, with strong clinical picture for CTS but abnormalities only on the most sensitive comparison NCS tests?
(255) Common
3. Is it common or rare for patients to have little or no clinical findings of CTS and have definite findings of median neuropathy on NCS/EMG?
(255) Common
Name 3 thumb muscles supplied by the median nerve after it passes through the carpal tunnel.
(257) APB, OP, superficial head of FPB
Is CTS usually unilateral or bilateral?
(257) Bilateral
Is median mononeuropathy on NCS/EMG usually unilateral or bilateral?
(257) Bilateral
Does CTS usually effect both hands equally?
(257,259 ) No. Dominant hand is usually more affected. If nondominant hand is more affected, look for identifiable specific cause such as mass lesion.
How proximal may CTS pain may radiate?
(257) CTS pain may involve hand, wrist, forearm, arm and rarely shoulder. The neck is not affected.
If asked directly, most patients with CTS will admit that which digit is spared paresthesias?
(257) Little finger
In CTS, are nocturnal paresthesias common or rare?
(257) Common
In CTS, are sensory or motor fibers affected first?
(257) Sensory
In CTS, is functional impairment from reduced strength common or rare?
(257) Rare
Will most CTS patients have positive Tinel’s at the wrist?
(257)Yes
Is Tinel’s at the wrist qualitatively specific for CTS?
No
Which test, Phalen’s or Tinel’s, is better for CTS?
(258) Phalen’s is more sensitive and specific.
How long might you have to wait to get a positive Phalen’s in CTS? (258)
2 minutes
Why should Phalen’s be done with straight elbows?
To avoid compressing the ulnar nerve at the cubital tunnel.
19. Your patient has unmistakable NCS/EMG findings of median neuropathy but has no symptoms. Do they have CTS? Do they need treatment?
(258-9) No and no.
20. Your patient has paresthesias in the hand but no pain. Do these symptoms prejudice you in favor of or against a diagnosis of CTS?
(258 Table 17-2); (261). Paresthesias and no pain are inconsistent with CTS (258 Table 17-2); always question the diagnosis of CTS in the absence of pain (261).
Name 2 endocrine disorders associated with CTS.
(259) DM, hypothyroidism
Name 2 conditions which are more common in women which are associated with CTS.
(259) Pregnancy, RA.
Name a disease which is associated with CTS which could be thought to result in build up of proteins in the carpal tunnel.
(259) Amyloidosis
Suspect radiculopathy instead of CTS if there is pain in which location?
(259) Neck
25. Suspect radiculopathy instead of CTS if symptoms are made worse by motion around which body part?
(259) Neck
26. Pain from CTS may radiate into the forearm, upper arm and even shoulder. Can CTS paresthesias radiate in this distribution?
(259) No; sensory abnormality in thenar eminence or proximally suggests alternative causes.
If NCS show low median motor amplitudes, name 3 common classes of causes other than CTS.
(261) Cervical radiculopathy, polyneuropathy, median neuropathy at elbow.
What is more common in CTS: demyelination or axonal loss?
(261-2) Demyelination.
29. Your patient with clinical evidence of CTS has normal values for all median motor and sensory studies of the affected limb. What type of NCS that doesn’t involve the contralateral limb should be done next?
(262) Comparison studies to ulnar and radial nerves.
30. Even with optimal technique, is NCS a qualitatively sensitive means of detecting median neuropathy at the wrist?
(262, 267) Yes. With inclusion of comparison studies to ulnar and radial nerves, ‘diagnostic yield’ is 95%. Page 267: 97% sensitivity.
There are many comparison tests between median and ulnar or radial nerves. Typically the difference in distal latencies is considered significant if it is greater than what value?
(262) 0.4ms to 0.5ms are cut-offs for the more common tests.
32. If you overstimulate and cause depolarization of an adjacent nerve, can you reliably tell this from the shape of the wave form?
(262) Not always; wave form may appear normal but you may nonetheless be getting bad data.
Where do you stimulate in the palm for the median nerve palmar mixed nerve study?
(264) Eight centimeters from the recording electrodes on a line connecting the median nerve at the wrist to the webspace between the index and middle fingers.
Where do you stimulate in the palm for the ulnar nerve palmar mixed nerve study?
(264) Eight centimeters from the recording electrodes on a line connecting the ulnar nerve at the wrist to the webspace between the fourth and fifth digits.
35. Name an ulnar-median nerve comparative study that would be useful in assessing for CTS a patient who had diabetic polyneuropathy with an absence of both ulnar and median SNAPs in the hand.
. (265) Median Second Lumbrical-vs-Ulnar Interossei distal motor latency comparison measures CMAPs so may be possible in such a patient.
36. Where is the recording electrode (G1) placed for the Median Second Lumbrical-vs-Ulnar Interossei distal motor latency comparison test?
(265) Just lateral to the midpoint of the third metacarpal.
37. The amplitude of the APB CMAP when stimulating at the palm divided by the amplitude when stimulating just proximal to the wrist should not be greater than what number in normals?
(267) Amplitude ratio greater than 1.2 is abnormal and suggests conduction block with demyelination.
38. Name 2 possible sources of error that could change the amplitude ratio for the aforementioned comparison.
(267) Stimulations might not be supramaximal (many causes including poor stimulus site and inadequate stimulus), and an adjacent nerve may be inadvertently activated
39. If the amplitude of the APB CMAP when stimulating at the palm divided by the amplitude when stimulating just proximal to the wrist is 3, would this be better explained by a purely focal demyelinating or a purely axonal loss lesion?
(267) This would be consistent with conduction block from a focal demyelination.
40. What is the technical difficulty which makes difficult the radial vs median thumb SNAP comparison?
(268) The median nerve travels to the thumb at an angle, making it difficult to measure the true distance.
41. In normal people, is conduction velocity of median SNAP faster in the wrist to palm segment or the palm to finger segment?
(269) In normals, the wrist to palm segment is faster because the nerve fibers are larger and warmer proximally.
42. What differential of median sensory conduction velocity between palm to finger and wrist to palm segments is consistent with CTS?
(269) If the palm to finger segment is > 10m/s faster than the wrist to palm segment, this is consistent with CTS.
Which is the key muscle to EMG to assess for CTS?
(271) APB
Your needle study of APB is normal. Does this rule out CTS?
(271) no
Radiculopathy of which 2 dermatomes is most likely to mimic the paresthesias of CTS?
(271) C6, C7
Name 2 muscles supplied by the median nerve and innervated by C6-7
(271) pronator teres, flexor carpi radialis
47. Your exhaustive NCS to r/o CTS is normal. EMG of APB, PT and triceps is normal. H&P doesn’t suggest other neurogenic causes of symptoms. According to the algorithm on p271, how many further muscles need you test to complete your study?
(271) none.
If you highly suspect entrapment of the median nerve at the PT, what findings would you expect to find with needle study of the PT?
(273) The PT is spared in entrapment of the median nerve at the PT. In general, the muscles for which the entrapment syndromes are named (piriformis, supinator, PT) are spared in entrapment syndromes, as innervation occurs proximal to the nerve piercing the muscle.
Distal latency greater than what percentage of upper limit of normal is evidence of demyelination?
(274) If distal latency is greater than 130% of the upper limit of normal, axonal loss with drop out of the fastest fibers is not sufficient to explain this slowing; demyelination must be part of the pathology.
Conduction velocity less than what percentage of the lower limit of normal is evidence of demyelination?
(274) If the conduction velocity is less than 75% of the lower limit of normal, axonal loss with drop out of the fastest fibers is not sufficient to explain this slowing; demyelination must be part of the pathology.
51. Is it common or rare for patients with severe CTS to have diminished conduction velocity in the forearm?
(274) It is common for patients with severe CTS to have diminished conduction velocity in the forearm. This may be due to axonal loss and drop out of the fastest fibers or from conduction block at the wrist affecting the fastest fibers most. It does not imply additional lesions.
52. Name a non-endocrine disease which predisposes you to CTS, radiculopathy, distal symmetric sensorimotor polyneuropathy, and vasculitic neuropathy resulting in mononeuritis multiplex.
(277) Rheumatoid arthritis.
Is it common or rare for a patient to have clinical CTS with all NCS and EMG tests normal?
(278) This is rare. In these patients there is no demyelination or axonal loss, but transient ischemia from intermittent compression.
54. The role of EMG/NCS in CTS includes confirming diagnosis and looking for possible coexisting conditions. How does the study help determine treatment?
(274, 278) EMG/NCS helps determine treatment by assessing severity. Case 1 showed a patient with chronic axonal loss and reinervation; this patient would need surgical referral.