Carpal tunnel syndrome

Changed by Joshua Yap, 26 Mar 2024
Disclosures - updated 16 Jul 2023: Nothing to disclose

Updates to Article Attributes

Body was changed:

Carpal tunnel syndrome results from compression of the median nerve(tunnel syndrome) within the carpal tunnel. It is a cause of significant disability and is one of three common median nerve entrapment syndromes, the other two being anterior interosseous nerve syndrome and and pronator teres syndrome.

Epidemiology

The prevalence of carpal tunnel syndrome is estimated to be 2.7-5.83-6% of the general adult population, with a lifetime incidence of 10-15%, depending on occupational risk 4.

Carpal tunnel syndrome usually occurs between ages 36 and 60 and is more common in women, with a female-to-male ratio of (F:M = 2-5:1).

Associations

Clinical presentation

Carpal tunnel syndrome is primarily defined by pain and sensory symptoms:

  • brachialgia paraesthetica nocturna, or nocturnal ascending pain emanating from the wrist, is typical

  • sensory symptoms affect the first three digits and, depending on innervation patterns, the radial aspect of the fourth digit

  • positive Tinel test: paraesthesias elicited by tapping the median nerve at the wrist

  • positive Phalen test: paraesthesias caused by wrist flexion over 30-60°

Hand weakness, as a rule, is a late and often functionally irrelevant symptom 5.

The dominant hand is affected more frequently, and bilateral involvement has been reported to occur in ~30% (range 8-50%) of cases.

The clinical presentation can harbour some pitfalls. Sensory and pain symptoms of the pronator teres syndrome (PTS) and carpal tunnel syndrome can overlap; one can distinguish the two by examining for numbness of the forearm, which does not occur in carpal tunnel syndrome and ask about nocturnal exacerbation, which is atypical in PTS. Provocation Provocation tests as detailed above can help further.

Pathology

There is a wide spectrum of causative pathologies, converging on two mechanisms of disease, both of which lead to entrapment 5:

A useful mnemonic to remember these causes is MEDIAN TRAP.

Associations

Radiographic features

Ultrasound and MRI are the two imaging modalities that best lend themselves to investigating entrapment syndromes. Next to directly visualising direct causes and anatomical variants (e.g. a Gantzer muscle), recognising pathological muscle signal patterns on MRI can point to the affected nerve.

Ultrasound

In imaging median nerve syndromes, ultrasound is useful in examining carpal tunnel syndrome, potentially revealing, in fully developed cases, a triad of:

  • palmar bowing of the flexor retinaculum (>2 mm beyond a line connecting the pisiform and the scaphoid)

  • distal flattening of the nerve

  • enlargement of the nerve proximal to the flexor retinaculum

Enlargement of the nerve seems to be the most sensitive and specific criterion, but what cut-off value for pathological size remains debated; the normal cross-sectional area (CSA) is given at 9-11 mm2 (0.09-0.11 cm2), but the range of CSAs deemed pathological is wide. According to one study, a 2 mm2 difference in nerve CSA between the level of the pronator quadratus and the carpal tunnel has a 99% sensitivity and 100% specificity for carpal tunnel syndrome 9.

Intraneural hyper-vascularisation is another feature with high diagnostic accuracy, although may be absent in chronic cases 16,17.

Some of the other proposed findings include ref:

If a bifid median nerve is present, measuring measuring the combined cross-sectional area can be performed with an increase in cross-sectional area of ≥4 mm2 between between the median nerve at the proximal-third pronator quadratus level and in the carpal tunnel providing >90% sensitivity/specificity for carpal tunnel syndrome 15.

MRI

MRI has good-to-excellent sensitivity (84-100%) and specificity (85-94%) for diagnosing carpal tunnel syndrome when using cross-sectional area >15 mm2 as a cut-off 12,13. MRI is especially well-suited for detecting masses, arthritic changes, and normal variants (e.g. bifid median nerve)5.

In carpal tunnel syndrome, MRI can demonstrate 4:

  • palmar bowing of the flexor retinaculum

  • nerve thickening at the carpal tunnel inlet (level of the pisiform)

  • nerve flattening at the carpal tunnel outlet (level of the hook of hamate)

  • increased cross-sectional area

    • ultrasound values do not correlate with MRI values 11

    • >15 mm2 at at the carpal tunnel inlet or outlet can be used as a diagnostic criterion or cut-off 12,13

    • >19 mm2 has been proposed as a marker for severe carpal tunnel syndrome 13

  • oedema or loss of fat within the carpal tunnel

  • neural oedema +/- contrast enhancement

Treatment and prognosis

It is initially often treated conservatively with splinting and non-steroidal anti-inflammatory drugs (NSAIDS). Corticosteroid injections into the carpal tunnel can alleviate symptoms temporarily for about 4 weeks.

Surgical release of the flexor retinaculum is indicated in cases of pronounced nocturnal pain, permanent dysaesthesias and prolonged distal motor latency on electroneurography (> 6;6 ms).

Complications

Differential diagnosis

Possible differential diagnoses of carpal tunnel syndrome include:

  • -<p><strong>Carpal tunnel syndrome</strong> results from compression of the <a href="/articles/median-nerve-2">median nerve</a> (<a href="/articles/tunnel-syndrome">tunnel syndrome</a>) within the <a href="/articles/carpal-tunnel">carpal tunnel</a>. It is a cause of significant disability and is one of three common <a href="/articles/median-nerve-entrapment-syndromes">median nerve entrapment syndromes</a>, the other two being <a href="/articles/anterior-interosseous-nerve-syndrome-1">anterior interosseous nerve syndrome</a> and <a href="/articles/pronator-teres-syndrome-2">pronator teres syndrome</a>. </p><h4>Epidemiology</h4><p>The prevalence of carpal tunnel syndrome is estimated to be 2.7-5.8% of the general adult population, with a lifetime incidence of 10-15%, depending on occupational risk <sup>4</sup>.</p><p>Carpal tunnel syndrome usually occurs between ages 36 and 60 and is more common in women, with a female-to-male ratio of 2-5:1.</p><h4>Clinical presentation</h4><p>Carpal tunnel syndrome is primarily defined by pain and sensory symptoms: </p><ul>
  • +<p><strong>Carpal tunnel syndrome</strong> results from compression of the <a href="/articles/median-nerve-2">median nerve</a>&nbsp;(<a href="/articles/tunnel-syndrome">tunnel syndrome</a>) within the <a href="/articles/carpal-tunnel">carpal tunnel</a>. It is a cause of significant disability and is one of three common <a href="/articles/median-nerve-entrapment-syndromes">median nerve entrapment syndromes</a>, the other two being <a href="/articles/anterior-interosseous-nerve-syndrome-1">anterior interosseous nerve syndrome</a>&nbsp;and <a href="/articles/pronator-teres-syndrome-2">pronator teres syndrome</a>.&nbsp;</p><h4>Epidemiology</h4><p>The prevalence of carpal tunnel syndrome is estimated to be 3-6% of the general adult population, with a lifetime incidence of 10-15%, depending on occupational risk <sup>4</sup>.</p><p>Carpal tunnel syndrome usually occurs between ages 36 and 60 and is more common in women (F:M = 2-5:1).</p><h5>Associations</h5><ul><li><p><a href="/articles/persistent-median-artery-of-the-forearm">persistent median artery of the forearm</a></p></li></ul><h4>Clinical presentation</h4><p>Carpal tunnel syndrome is primarily defined by pain and sensory symptoms:&nbsp;</p><ul>
  • -</ul><p>Hand weakness, as a rule, is a late and often functionally irrelevant symptom <sup>5</sup>.</p><p>The dominant hand is affected more frequently, and bilateral involvement has been reported to occur in ~30% (range 8-50%) of cases.</p><p>The clinical presentation can harbour some pitfalls. Sensory and pain symptoms of the <a href="/articles/pronator-teres-syndrome-2">pronator teres syndrome</a> (PTS) and carpal tunnel syndrome can overlap; one can distinguish the two by examining for numbness of the forearm, which does not occur in carpal tunnel syndrome and ask about nocturnal exacerbation, which is atypical in PTS. Provocation tests as detailed above can help further.</p><h4>Pathology</h4><p>There is a wide spectrum of causative pathologies, converging on two mechanisms of disease, both of which lead to entrapment <sup>5</sup>:</p><ul>
  • +</ul><p>Hand weakness, as a rule, is a late and often functionally irrelevant symptom <sup>5</sup>.</p><p>The dominant hand is affected more frequently, and bilateral involvement has been reported to occur in ~30% (range 8-50%) of cases.</p><p>The clinical presentation can harbour some pitfalls. Sensory and pain symptoms of the <a href="/articles/pronator-teres-syndrome-2">pronator teres syndrome</a> (PTS) and carpal tunnel syndrome can overlap; one can distinguish the two by examining for numbness of the forearm, which does not occur in carpal tunnel syndrome and ask about nocturnal exacerbation, which is atypical in PTS.&nbsp;Provocation tests as detailed above can help further.</p><h4>Pathology</h4><p>There is a wide spectrum of causative pathologies, converging on two mechanisms of disease, both of which lead to entrapment <sup>5</sup>:</p><ul>
  • -</ul><p>A useful mnemonic to remember these causes is <a href="/articles/carpal-tunnel-syndrome-causes-mnemonic-2">MEDIAN TRAP</a>.</p><h5>Associations</h5><ul><li><p><a href="/articles/persistent-median-artery-of-the-forearm">persistent median artery of the forearm</a></p></li></ul><h4>Radiographic features</h4><p>Ultrasound and MRI are the two imaging modalities that best lend themselves to investigating entrapment syndromes. Next to directly visualising direct causes and anatomical variants (e.g. a <a href="/articles/gantzer-muscle">Gantzer muscle</a>), recognising pathological muscle signal patterns on MRI can point to the affected nerve.</p><h5>Ultrasound</h5><p>In imaging median nerve syndromes, ultrasound is useful in examining carpal tunnel syndrome, potentially revealing, in fully developed cases, a triad of:</p><ul>
  • +</ul><p>A useful mnemonic to remember these causes is <a href="/articles/carpal-tunnel-syndrome-causes-mnemonic-2">MEDIAN TRAP</a>.</p><h4>Radiographic features</h4><p>Ultrasound and MRI are the two imaging modalities that best lend themselves to investigating entrapment syndromes. Next to directly visualising direct causes and anatomical variants (e.g. a <a href="/articles/gantzer-muscle">Gantzer muscle</a>), recognising pathological muscle signal patterns on MRI can point to the affected nerve.</p><h5>Ultrasound</h5><p>In imaging median nerve syndromes, ultrasound is useful in examining carpal tunnel syndrome, potentially revealing, in fully developed cases, a triad of:</p><ul>
  • -<li><p><a href="/articles/median-nerve-flattening-ratio" title="Median nerve flattening ratio">flattening ratio</a> of over x 3</p></li>
  • +<li><p><a href="/articles/median-nerve-flattening-ratio" title="Median nerve flattening ratio">flattening ratio</a> of over 3 times</p></li>
  • -</ul><p>If a bifid median nerve is present, measuring the combined cross-sectional area can be performed with an increase in cross-sectional area of ≥4 mm<sup>2</sup> between the median nerve at the proximal-third pronator quadratus level and in the carpal tunnel providing &gt;90% sensitivity/specificity for carpal tunnel syndrome <sup>15</sup>.</p><h5>MRI</h5><p>MRI has good-to-excellent sensitivity (84-100%) and specificity (85-94%) for diagnosing carpal tunnel syndrome when using cross-sectional area &gt;15 mm<sup>2</sup> as a cut-off <sup>12,13</sup>. MRI is especially well-suited for detecting masses, arthritic changes, and normal variants (e.g. <a href="/articles/bifid-median-nerve">bifid median nerve</a>) <sup>5</sup>.</p><p>In carpal tunnel syndrome, MRI can demonstrate <sup>4</sup>:</p><ul>
  • +</ul><p>If a bifid median nerve is present,&nbsp;measuring the combined cross-sectional area can be performed with an increase in cross-sectional area of ≥4 mm<sup>2</sup>&nbsp;between the median nerve at the proximal-third pronator quadratus level and in the carpal tunnel providing &gt;90% sensitivity/specificity for carpal tunnel syndrome <sup>15</sup>.</p><h5>MRI</h5><p>MRI has good-to-excellent sensitivity (84-100%) and specificity (85-94%) for diagnosing carpal tunnel syndrome when using cross-sectional area &gt;15 mm<sup>2</sup> as a cut-off <sup>12,13</sup>. MRI is especially well-suited for detecting masses, arthritic changes, and normal variants (e.g. <a href="/articles/bifid-median-nerve">bifid median nerve</a>)&nbsp;<sup>5</sup>.</p><p>In carpal tunnel syndrome, MRI can demonstrate <sup>4</sup>:</p><ul>
  • -<li><p>&gt;15 mm<sup>2</sup> at the carpal tunnel inlet or outlet can be used as a diagnostic criterion or cut-off <sup>12,13</sup></p></li>
  • +<li><p>&gt;15 mm<sup>2</sup>&nbsp;at the carpal tunnel inlet or outlet can be used as a diagnostic criterion or cut-off <sup>12,13</sup></p></li>
  • -</ul><h4>Treatment and prognosis</h4><p>It is initially often treated conservatively with splinting and <a href="/articles/non-steroidal-anti-inflammatory-drugs">non-steroidal anti-inflammatory drugs (NSAIDS)</a>. Corticosteroid injections into the carpal tunnel can alleviate symptoms temporarily for about 4 weeks. </p><p>Surgical release of the flexor retinaculum is indicated in cases of pronounced nocturnal pain, permanent dysaesthesias and prolonged distal motor latency on electroneurography (&gt; 6 ms). </p><h5>Complications</h5><ul>
  • +</ul><h4>Treatment and prognosis</h4><p>It is initially often treated conservatively with splinting and <a href="/articles/non-steroidal-anti-inflammatory-drugs">non-steroidal anti-inflammatory drugs (NSAIDS)</a>. Corticosteroid injections into the carpal tunnel can alleviate symptoms temporarily for about 4 weeks.</p><p>Surgical release of the flexor retinaculum is indicated in cases of pronounced nocturnal pain, permanent dysaesthesias and prolonged distal motor latency on electroneurography (&gt;6 ms).</p><h5>Complications</h5><ul>
Images Changes:

Image 1 Diagram ( update )

Caption was changed:
Figure 1: carpal tunnel diagram

Image 5 MRI (T1 C+ fat sat) ( update )

Caption was changed:
Kiloh-Nevin syndrome

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