Carpal tunnel syndrome (CTS) is the most common compressive neuropathy in the upper extremity. While carpal tunnel release (CTR), both open (OCTR) and endoscopic (ECTR), is safe and effective, there are questions regarding the use of postoperative dressings after surgery. It is not currently known if dressing choices influence post-operative pain, function or patient satisfaction after ECTR. A less cumbersome dressing (bandaid) may allow patients to perform daily tasks with more ease after surgery. The purpose of this investigation is to compare postoperative pain scores and patient satisfaction after ECTR for patients treated with conventional post-operative bulky soft tissue dressings versus those treated with a bandaid after surgery. The hypothesis is that patients using a bandaid after surgery will have an easier time with functional tasks after surgery and that pain scores will not significantly differ between the two groups. Furthermore, this study aims to determine if there are differences in patient satisfaction, functional outcomes, complications, and unscheduled healthcare contact between these two groups. This will be a randomized, controlled investigation.
Carpal tunnel syndrome (CTS) is the most common compressive neuropathy in the upper extremity. While carpal tunnel release (CTR), both open (OCTR) and endoscopic (ECTR), is safe and effective, there are questions regarding the use of postoperative dressings after surgery. With recent attention to the opioid epidemic, there have been increasing efforts to reduce narcotic usage postoperatively while still controlling expected postoperative pain. Recent authors have found that many patients, particularly older patients, do not require any opioid analgesia after CTR with 47% of men and 36% of women consuming no narcotics after CTR (CHAPMAN). Furthermore, while splints have historically been used after surgery, their need has recently been questioned (LOGLI). It is not currently known if dressing choices influence post-operative pain, function or patient satisfaction after ECTR. A less cumbersome dressing (bandaid) may allow patients to perform daily tasks with more ease after surgery. The purpose of this investigation is to compare postoperative pain scores and patient satisfaction after ECTR for patients treated with conventional post-operative bulky soft tissue dressings versus those treated with a bandaid after surgery. The hypothesis is that patients using a bandaid after surgery will have an easier time with functional tasks after surgery and that pain scores will not significantly differ between the two groups. Furthermore, this study aims to determine if there are differences in patient satisfaction, functional outcomes, complications, and unscheduled healthcare contact between these two groups. This will be a randomized, controlled investigation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Bandaid dressing
Conventional bulky soft tissue dressing
Visual Analog Scale Pain Score
best 0-10 worst; continuous scale to measure current pain level
Time frame: 0-12 months
Boston Carpal Tunnel Questionnaire
ranges from 1 to 5, with a higher score indicating greater disability; -specific measure of self-reported symptom severity and functional status
Time frame: 0-12 months
PROMIS Pain Interference
best 0-100 worst; measures the effects of a patient's pain on their daily activities and lifestyle
Time frame: 0-12 months
PROMIS Self-Efficacy Manage Symptoms
best 0-100 worst; measures a patient's ability to cope with their symptoms related to the procedure
Time frame: 0-12 months
PROMIS Upper Extremity
worst 0-100 best; measures physical function of upper extremities
Time frame: 0-12 months
QuickDASH
best 0-100 worst; functional outcome score for disabilities of the arm, shoulder, and hand
Time frame: 0-12 months
number of participants with unscheduled healthcare contact
unscheduled healthcare contact includes patient calls/messages, emergency room visits, or scheduled clinic visits
Time frame: 0-12 months
morphine equivalents
morphine equivalents consumed for post-operative pain control
Time frame: 0-12 months
number of participants with complications
complications after surgery including infection and delayed healing
Time frame: 0-12 months
Satisfaction with overall outcome
11 point Likert scale; worst 0-10 best
Time frame: 0-12 months
Satisfaction postoperative pain control
11 point Likert scale; worst 0-10 best
Time frame: 0-12 months
Satisfaction with the dressing
11 point Likert scale; worst 0-10 best
Time frame: 0-12 months
Grip Strength Measurement
Using Jamar Hand Dynamometer, in kilograms ranging from worst 0-90 best
Time frame: 0-12 months
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