Single Shot vs Continuous Interscalene Block for Rotator Cuff Repair
| Status: | Completed |
|---|---|
| Conditions: | Chronic Pain, Orthopedic |
| Therapuetic Areas: | Musculoskeletal, Orthopedics / Podiatry |
| Healthy: | No |
| Age Range: | 18 - 90 |
| Updated: | 3/1/2014 |
| Start Date: | August 2010 |
| End Date: | October 2013 |
| Contact: | TARIQ MALIK, MD |
| Email: | tmalik@dacc.uchicago.edu |
| Phone: | 773 834 3643 |
Comparison of Pain Relief After Single Shot Interscalene Block With Continuous Interscalene Block for Arthroscopic Rotator Cuff Shoulder Surgery: A Randomized Study
1. Rotator cuff have painful post surgery recovery.
2. Single shot interscalene with oral analgesics may or may not be enough
3. Continuous nerve block may be too much for the surgery
4. The idea is to compare two techniques to see if the two techniques can improve patient
pain control and satisfaction.
2. Single shot interscalene with oral analgesics may or may not be enough
3. Continuous nerve block may be too much for the surgery
4. The idea is to compare two techniques to see if the two techniques can improve patient
pain control and satisfaction.
After consent patients will be randomized to one of the two groups: Control Group or the
Experimental Group. Patients will be blinded to the group assignment.
In the Control Group the patient will be given single shot interscalene block using
ultrasound technique following established guidelines. The procedure will be done after
starting intravenous access and placing standard anesthesia monitors (EKG, Blood Pressure
Cuff and Pulse-Ox) on the patient. Following accepted aseptic guidelines the nerves will be
visualized at the base of the neck using ultrasound machine. Once proper nerve roots or
trunks visualized 3 mg/kg of 0.5 % bupivacaine will be injected in small blouses.
In the Experimental Group, after placement of monitors, the nerves will be visualized using
ultrasound machine. There after a catheter will be placed. They subjects will be dosed
using 0.5% bupivacaine 3 mg/kg for the surgery via the catheter.
The extent of block before the surgery will be evaluated at 30 minutes post injection.
Surgery will be done with sedation. Conversion of anesthetic technique to general anesthesia
will be considered failure of the technique to provide adequate surgical anesthesia.
At the end of the case the patient will be taken to recovery and will be evaluated for pain.
If patient is having pain of 3 or more then they will be treated as follows.
In single shot group will be offered to be blocked again or treated with oral narcotics.
In the catheter group patient will be dosed with 10 ml 1% lidocaine. If it fails to provide
any relief then the catheter will be pulled back and another 10 ml1% lidocaine will be
given. If still not effective then it will be replaced. Refusal of patient to replace the
catheter will result in patient dropping out of the study.
Working catheter will be left in place for at least 48 hrs. Patients will be allowed to take
oral pain medicines as prescribed by their surgeons. The patient will be sent home with pain
pump to continuously give them 0.125% bupivacaine at 5 ml per hr with an option to get extra
dose of 5 ml q hr if needed. The pain control will be monitored by phone daily till catheter
comes out.
Experimental Group. Patients will be blinded to the group assignment.
In the Control Group the patient will be given single shot interscalene block using
ultrasound technique following established guidelines. The procedure will be done after
starting intravenous access and placing standard anesthesia monitors (EKG, Blood Pressure
Cuff and Pulse-Ox) on the patient. Following accepted aseptic guidelines the nerves will be
visualized at the base of the neck using ultrasound machine. Once proper nerve roots or
trunks visualized 3 mg/kg of 0.5 % bupivacaine will be injected in small blouses.
In the Experimental Group, after placement of monitors, the nerves will be visualized using
ultrasound machine. There after a catheter will be placed. They subjects will be dosed
using 0.5% bupivacaine 3 mg/kg for the surgery via the catheter.
The extent of block before the surgery will be evaluated at 30 minutes post injection.
Surgery will be done with sedation. Conversion of anesthetic technique to general anesthesia
will be considered failure of the technique to provide adequate surgical anesthesia.
At the end of the case the patient will be taken to recovery and will be evaluated for pain.
If patient is having pain of 3 or more then they will be treated as follows.
In single shot group will be offered to be blocked again or treated with oral narcotics.
In the catheter group patient will be dosed with 10 ml 1% lidocaine. If it fails to provide
any relief then the catheter will be pulled back and another 10 ml1% lidocaine will be
given. If still not effective then it will be replaced. Refusal of patient to replace the
catheter will result in patient dropping out of the study.
Working catheter will be left in place for at least 48 hrs. Patients will be allowed to take
oral pain medicines as prescribed by their surgeons. The patient will be sent home with pain
pump to continuously give them 0.125% bupivacaine at 5 ml per hr with an option to get extra
dose of 5 ml q hr if needed. The pain control will be monitored by phone daily till catheter
comes out.
Inclusion Criteria:
- adult
- rotator cuff surgery
- agreeing to regional block for pain control
Exclusion Criteria:
- pregnancy
- neuropathy
- any allergies to local anesthetics
- any contraindication to nerve blocks
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