Comparing a Modified Mini-incision Approach Versus the Conventional Approach for Carpal Tunnel Release

All selected cases with primary CTS will be submitted to:

I) Preoperative evaluation:

A- Careful history taking: Brief history based on the characteristics of pain, sensory disturbances including numbness, tingling, and/or weakness involving the median nerve distribution. Patients were additionally inquired about their functional status, normal activities, ability to work, family history of diabetes and the use of medications.

B- The visual analogue scale (VAS) (0= no pain to 10= worst possible pain), will be used to assess the severity of diabetic neuropathic pain.

C- Neurosensory examination mainly included percussion over a distribution of the affected peripheral nerve (Tinel sign) and two-point discrimination (2-PD) using the Disk-Criminator.

D- Nerve conduction velocity (NCV).

II) Surgical Technique:

All patients are positioned on the operating table in supine position and anesthetized with local anaesthesia.

A) For the conventional approach: a palmar longitudinal incision began at the axis of the ring finger, passed between the thenar and hypothenar eminences, and continued proximally to the proximal flexor crease of the wrist. After exposing the underlying transverse carpal ligament, its ulnar side was cut longitudinally. The median nerve was identified and protected, and then the wound was closed in routine manner.

B) For the new mini-incision approach: a special metal guide with a groove at the center is used. The incision is started above the proximal flexor crease of the wrist and is advanced proximally for 1.5-2.0 cm. After opening the superficial fascia, blunt dissection with a mosquito clamp is performed till the median nerve appears and the guide is inserted into the carpal tunnel, then a scissor is inserted along the groove in the guide and the transverse carpal ligament is cut proximally and distally.

III) Postoperative follow up:

The follow-up was conducted mainly on an outpatient basis comparing the postoperative outcome in both groups as regard improvement of symptoms, postoperative complications, scar effect and recurrence of symptoms. Patients will be followed up at 2 weeks, 1 month, 3 months, and 6 months post decompression.

Inclusion criteria

• Patients with primary CTS attending Mansoura university hospitals with EMG-and NCS-proved median neuropathy at the wrist.
• Failed conservative treatment.
• Absence of any other hand pathology.
• Positive Tinel sign presented at the site of nerve entrapment (the carpal tunnel at the wrist for the median nerve).
• Signed informed consent.

Exclusion criteria

• Presence of proximal radiculopathy.
• Previous history of cervical spondylosis.
• Inflammatory joint disease and gout.
• Presence of combined nerve compression.
• Having a previous hand or upper extremity surgery.
• Patients with incomplete follow-up data were also excluded from this study.
• Psychiatric disease or any other condition that is at risk of being influenced by the study or that might have affected completion of the study.
• Patient refusal