The carpal tunnelis bound by
1. the carpal bones arching dorsally;
2. the hook of the hamate and the pisiform medially;
3. the scaphoid tubercle and trapezial ridge laterally.
4. The palmar aspect, or “roof,” of the carpal tunnel is formed by the flexor retinaculum,
.
7.
The palmar aspect,or “roof,” of the carpal tunnel is formed by the flexor retinaculum
flexor retinaculum consisting of
• deep forearm fascia proximally,
• transverse carpal ligament over the wrist, and
• aponeurosis between the thenar and hypothenar muscles distally.
10.
• most palmarstructure in the carpal tunnel is the median nerve.
• Lying dorsal (deep) to the median nerve in the carpal tunnel are the nine long finger and
thumb flexor tendons.
11.
Carpal tunnel syndrome
•affect 1% to 10% of the population.
• in 30 to 60 years old
• women = 3men.
more likely to develop carpal tunnel syndrome,
• Older,
• overweight,
• physically inactive individuals
carpal tunnel risk factors in industrial workers
• female sex,
• obesity,
• cigarette smoking,
• vibrations with job tasks.
12.
pathophysiology:
• Elevation ofcarpal tunnel pressures of more than 20 to 30 mm Hg impedes epineurial
blood flow, and nerve function is impaired.
• Reduction in cross-sectional area along the length of the carpal tunnel
14.
Carpal tunnel syndromeis primarily a clinical diagnosis,
• tingling and numbness
• in median nerve distribution
• Pain,
• deep,
• aching, or throbbing,
• diffusely in the hand
• may radiate up the forearm.
• Thenar muscle atrophy
• in late-stage nerve compression.
16.
DIAGNOSIS
Clinical: symptoms
in themedian nerve distribution
1. numbness,
2. pain,
3. paresthesia
• Paresthesia is the most frequent symptom,
• often awakening patients with burning and numbness of the hand
• is relieved by exercise.
17.
DIAGNOSIS
Clinical: signs
Tinel sign
•in most patients
• percussing the median nerve at the wrist.
Atrophy of the median-innervated thenar muscles
• in half of patients
.
18.
DIAGNOSIS
Explain
TEST Percussion Test(Tinel Test)
HOW PERFORMED Lightly tap along median nerve
from proximal to distal
CONDITION TESTED Site of nerve lesion
POSITIVE RESULT “Electric” tingling response in
fingers
INTERPRETATION OF POSITIVE
RESULT
Probable CTS if Positive at the
wrist (Sensitivity 0,60,
specificity 0,67)
DIAGNOSIS
Clinical: signs
Durkan testOR carpal compression
test
direct compression is applied to the
median nerve for 30 seconds with the
thumbs
Explain
TEST Carpal Tunnel compression Test
(Dukan)
HOW PERFORMED Direct compression of median
nerve at carpal tunnel
CONDITION TESTED Paresthesia in response to
compression
POSITIVE RESULT Parasthesia within 30 s
INTERPRETATION OF POSITIVE
RESULT
Probable CTS (Sensitivity 0,87,
specificity 0,90)
21.
Explain
TEST Static two– point
discrimination
HOW PERFORMED Determine minimal
separation of two distinct
points when applied to
palmar fingertip
CONDITION TESTED Innervation density of slow-
adapting fibers
POSITIVE RESULT Failure to determine
separation of at least 5 mm
INTERPRETATION OF
POSITIVE RESULT
Advanced nerve
dysfunction
Explain
TEST Moving two – point
discrimination
HOW PERFORMED As above, with movement of
the points
CONDITION TESTED Innervation density of fast -
adapting fibers
POSITIVE RESULT Failure to determine
separation of at least 4 mm
INTERPRETATION OF
POSITIVE RESULT
Advanced nerve dysfunction
22.
Explain
TEST Semmes –Weinstein
monofilaments
HOW PERFORMED Monofilaments of increasing
diameter touched to palmar
side of digiti until patient can
determine which digiti is
taouched
CONDITION TESTED Threshold of slowly adapting
fibers
POSITIVE RESULT Value > 2.83
INTERPRETATION OF POSITIVE
RESULT
Median nerve impairment
(sensitivity 0,83)
Sensibility testing
Semmes-Weinstein monofilament pressure
testing was the most accurate in determining
early nerve compression. combination with
wrist flexion test 82% sensitivity and 86%
specificity.
23.
Explain
TEST Hand Diagram
HOWPERFORMED Patient marks site of pain or
altered sensation on outlined
hand diagram
CONDITION TESTED Patient’s perception of
symtoms
POSITIVE RESULT Markings on palmar side of
radial digits, without marking in
palm
INTERPRETATION OF POSITIVE
RESULT
Probable CTS ( Sensitivity 0,96,
specificity 0,73, negative
predictive value 0,91
24.
DIAGNOSIS
Clinical: signs
mean pressurewithin the carpal tunnel
NORMAL:
• 25 mm Hg with the wrist in neutral position,
• 31 mm Hg with the wrist in flexion,
• 30 mm Hg with the wrist in extension.
in CTS
• 32 mm Hg. with wrist in neutral position,
• 99 mm Hg with 90 degrees of wrist flexion
• 110 mm Hg with the wrist at 90 degrees of extension.
25.
DIAGNOSIS
Clinical: signs
highest sensitivity
•Durkan nerve compression,
• hand diagram score,
• night pain,
• Semmes-Weinstein testing after a Phalen test had the.
The most specific tests
• hand diagram
• Tinel sign.
26.
DIAGNOSIS
Clinical: signs
a patientwith
1. abnormal hand diagram,
2. positive Durkan test,
3. abnormal Semmes-Weinstein sensibility testing,
4. night pain
had a very high probability of having carpal tunnel syndrome.
if all four tests were normal, the probability of CTS was very low.
27.
DIAGNOSIS
Clinical: signs
IN provocativetests,
• wrist flexion, the most sensitive test
• nerve percussion, the most specific and the least sensitive.
• Durkan test more specific (90%) and more sensitive (87%) than either the Tinel or Phalen test
28.
DIAGNOSIS
electrodiagnostic studies
Abnormal:
• Adistal motor latency of more than 4.5 milliseconds (ms)
• a sensory latency of more than 3.5 ms
• positive sharp waves,
• fibrillations at rest,
• decreased motor recruitment,
• complex repetitive discharges indicative of nerve damage.
29.
DIAGNOSIS
Nerve conduction studiesare
• 90% sensitive
• 60% specific
• are reliable confirmatory tests.
• occasionally normal, in patients with classic clinical signs and symptoms
• may be abnormal in asymptomatic patients.
30.
DIAGNOSIS
LIMITS: to determinetreatment.
• no significant data for prediction of functional recovery or reemployment after carpal
tunnel release,
• Nor does it increase the diagnostic value of the four commonly used tests
• abnormal hand diagram,
• abnormal Semmes-Weinstein testing,
• positive Durkan compression,
• night pain
• false-negative rates of 10%,
Postoperative electrodiagnostic testing may help assess recurrent symptoms
31.
DIAGNOSIS
MRI
• not routinelyused for diagnosis.
major advantage
• high soft-tissue contrast,
• detailed images of bones and soft tissues.
Ultrasound
• sensitivity over 97% when the median nerve diameter is greater than 10 mm2 at the
level of the pisiform
32.
the diagnosis ofcarpal tunnel syndrome should be based on
clinical acumen and physical examination in the
vast majority of patients
ancillary tests should be reserved for patients
without clear presentations.
TREATMENT
response to injectionfaster in
• men
• older than 40
• not to inject directly into the nerve.
• Injection as a diagnostic tool in patients without osteophytes or tumors in the canal.
• Injection also helps to eliminate the possibility of other syndromes, especially cervical disc
or TOS.
35.
TREATMENT
factors in determiningthe failure /success of nonoperative treatment:
1. age older than 50 years,
2. duration longer than 10 months,
3. constant paresthesia,
4. stenosing flexor tenosynovitis,
5. a positive Phalen test result in less than 30 seconds.
• none of these factors 2/3 cure
• one factor 59.6% cure
• two factors 17%
• three factors, 7%
• five factors 0%
36.
TREATMENT
intermediate and advanced(chronic) syndromes early carpal tunnel release.
• Extensive neurolysis no significant effect.
• Internal neurolysis
does not improve the motor or sensory outcome of carpal tunnel release.
• epineurotomy no clinical benefit to carpal tunnel release.
37.
TREATMENT
Treatment of acutecarpal tunnel syndrome should be individualized
acute increase in carpal tunnel pressure (e.g., after a Colles fracture),
change in wrist position without release
not improved surgery usually is indicated.
TREATMENT
signs and symptomspersistent and progressive,
carpal tunnel release
• results are good
• benefits to last
• Maximal improvement in the first 6 months
• After 6 months, there is no significant improvement but thenar atrophy
may disappear,
• not achieve complete relief in
• older than 70 years or
• advanced nerve compression.
40.
TREATMENT
release in idiopathicCTS with intermittent symptoms
•uniformly successful;
• release in diabetic and nondiabetic patients was
• follow-up period of 6 months.
• similarly beneficial
• for long-term (10 years),
• diabetes had worse outcomes
41.
TREATMENT
metabolic syndrome
• adelay in the recovery process.
• more severe grade of carpal tunnel syndrome
• delayed functional recovery at up to 6 months’ follow-up,
42.
TREATMENT
moderate disease (prolongedsensory and motor latencies)
• complete resolution of pain and paresthesias at 3 months after surgery,
severe disease (prolonged sensory or motor latencies plus either absent sensory or mixed
nerve action potential or low amplitude or absent compound motor action potential),
• incomplete symptom reduction at 1 year after carpal tunnel release
43.
TREATMENT
surgical technique surgeon’sexpertise.
minimally invasive techniques
• earlier return to work
• less postoperative discomfort,
• outcomes are similar at 6 months.
44.
TREATMENT
In a RCTstudy:
endoscopic release
• earlier return to work
• improved strength during the early postoperative period.
• Results at 6 months or later were similar to open except
• greater risk of nerve injury
• lower risk of scar tenderness
endoscopic release may appeal to patients who require an early return to work and activities,
45.
TREATMENT
SURGICAL RELEASE
Limited approaches,
1.“double incision” of Wilson
2. “minimal incision” of Bromley
offer rapid recovery as ascribed to the endoscopic techniques.
“carpal tunnel tome” through a small palmar incision minimize the soft-tissue trauma and
provides adequate exposure
Regardless of the technique selected, all structures to be incised should be seen and
identified and safety of the median nerve verified before carpal tunnel release
46.
TREATMENT
SURGICAL RELEASE
Limited approachesfor open carpal tunnel release
“double incision” of Wilson
Transverse incision
proximal to anterior wrist
crease between FCU and
FCR
Distal incision between
proximal palmar crease
and 1 cm distal to
hamate hook in line with
radial border of ring
TREATMENT
SURGICAL RELEASE
Mini-palm openrelease technique
A. longitudinal incision begins just distal to
the distal wrist flexion crease and slightly
ulnar to the midline of the wrist and extends
distally approximately 2.0 to 3.0 cm in line
with the third web space
49.
TREATMENT
SURGICAL RELEASE
Mini-palm openrelease technique
B. Exposure of transverse carpal
ligament (TCL) with parallel palmar
fascia fibers and hypothenar fat
retraction.
50.
TREATMENT
SURGICAL RELEASE
Mini-palm openrelease technique
C, After division of TCL, distal 2.0
cm of antebrachial fascia is divided
with a Metzenbaum, The TCL division
should be such that 3 to 4 mm of it is
left attached to the hamate hook to
avoid flexor tendon ulnar subluxation
51.
TREATMENT
SURGICAL RELEASE
Mini-palm openrelease technique
D. In this patient, median nerve
is adherent to divided radial TCL
leaf and was subsequently
externally neurolyzed.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
• palmar incisions should be well ulnar to it to avoid the median nerve
palmar cutaneous branch.
• A curved incision ulnar and parallel to the thenar crease is not
advisable because the palmar cutaneous branch of the median
nerve proximally may be more at risk of injury.
• We prefer to use the incision described for the mini-palm
technique :
• longitudinal incision begins just distal to the distal wrist flexion
crease and slightly ulnar to the midline of the wrist (center dot
reference point) and extends distally approximately 2.0 to 3.0 cm in
line with the third web space
54.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
continued proximally if necessary.
Angle the incision toward the ulnar side of the wrist to
avoid:
1. crossing the flexor creases at a right angle,
2. Cutting the palmar cutaneous sensory
branch, lies in the interval between the PL
and the FCR
55.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
When severed:
• We do not attempt to repair
• Section it more proximally to be covered by the middle finger sublimis muscle.
• causes a painful neuroma
• later require excision from the scar
56.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
Maintain longitudinal orientation so that the incision is generally to the
• ulnar side of the long finger axis
• radial border of the ring fourth ray.
57.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
Carefully divide TCL and avoid damage to the median nerve and its recurrent branch
Incidence of extraligamentous, subligamentous, and transligamentous course of thenar
branch.
58.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
Fibers of the transverse carpal ligament can extend
distally farther than expected
59.
TREATMENT
EXTENDED OPEN CARPALTUNNEL
RELEAS
A successful carpal tunnel release usually
requires division of all THREE components
60.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
Be aware of potential anomalies:
• connections between the FPL and the index flexor digitorum profundus
• flexor digitorum superficialis;
• palmaris longus,
• hypothenar,
• lumbrical muscle bellies;
• median and ulnar nerve branches and interconnections
61.
TREATMENT
EXTENDED OPEN CARPALTUNNEL
RELEAS
Avoid injury to the superficial palmar arterial arch,
which is 5 to 8 mm distal to the distal margin of
the transverse carpal ligament.
62.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
Inspect the flexor tenosynovium. Tenosynovectomy may occasionally be indicated, especially
in patients with rheumatoid arthritis
63.
TREATMENT
EXTENDED OPEN CARPALTUNNEL RELEAS
POSTOPERATIVE CARE.
• light compression dressing
• volar splint for 14 to 21 days.
• hand is actively used as soon as possible
• dependent position is avoided.
• dressing removed 2 or 3 days after the surgery, and then gentle washing and showering
of the hand is permitted.
• sutures are removed after 10 to 14 days.
64.
UNRELIEVED OR RECURRENTCTS
• The recurrence rate after primary carpal tunnel release is approximately 2%
• Unrelieved symptoms may lead to a repeat operation in 12% of patients
65.
UNRELIEVED OR RECURRENTCTS
CAUSES:
• incomplete release of the transverse carpal ligamen
• re-formation of the flexor retinaculum
• scarring in the carpal tunnel
• median or palmar cutaneous neuroma
• palmar cutaneous nerve entrapment
• recurrent granulomatous or inflammatory tenosynovitis
• hypertrophic scar in the skin
66.
UNRELIEVED OR RECURRENTCTS
Worse results in Patients with
• normal preoperative electrodiagnosticstudies
• patients who had filed for compensation
• and patients with ulnar nerve symptoms
#11 lexor Retinaculum and the Carpal Tunnel
NOTE: (1) The flexor retinaculum anteriorly and the carpal bones posteriorly form a restricted space called the carpal tunnel at the anterior
wrist region. Through the space pass the superficial and deep flexor digitorum tendons, the median nerve, and the tendon of the flexor pollicis
longus muscle.
(2) If a pathological process occurs within the space, such as fibrosis due to trauma or an inflammatory process that results in scar formation, the
space could diminish in size and undue pressure could be put on the median nerve. This could result in a wasting of the thenar muscles, and
this condition is called a carpal tunnel syndrome.
(3) In addition to the median nerve, the carpal tunnel has coursing through it the tendons of the superficial and deep flexor digitorum muscles,
along with the tendon of the flexor pollicis longus muscle. The ulnar nerve and ulnar artery and the radial artery are NOT structures within the
space.
(Contributed by Dr. Gene L. Colborn, Medical College of Georgia.)