Evaluation of Anterior Quadratus Lumborum Block for Postoperative Analgesia in Hip Arthroscopy
- Conditions
- Hip Disease
- Interventions
- Device: Ultrasound
- Registration Number
- NCT03432650
- Lead Sponsor
- Hospital for Special Surgery, New York
- Brief Summary
Hip arthroscopy is performed frequently and the postoperative course often involves moderate to severe pain. There remains no definitive perioperative pain regimen that has been proven to be effective and safe for this ambulatory procedure. Some institutions perform peripheral nerve blocks either preoperatively or postoperatively as a rescue block. All of these PNBs lead to quadriceps weakness which may impede earlier mobilization and physical therapy. While some case reports exist, there have not been any studies evaluating the QLB for hip arthroscopy patients. As previously mentioned, the technique is easy to perform, well-tolerated by patients, and avoids side effects such as hypotension, urinary retention, or the quadriceps weakness associated with lumbar plexus blockade.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 96
- Patients scheduled for hip arthroscopy
- Ability to follow study protocol
- English Speaking
- Hepatic or renal insufficiency
- Younger than 18 years old and older than 80
- Allergy or intolerance to one of the study medications
- Chronic gabapentin/pregabalin use (regular use for longer than 3 months)
- Chronic opioid use (daily opioids use for longer than 3 months)
- Patients contraindicated to undergo a spinal anesthetic
- Non English Speakers
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description QLB Block + Standard of Care Ultrasound Patients will receive either a spinal (4cc Mepivacaine) or combined spinal epidural anesthetic (dose up 50 5 cc 2% lidocaine) with IV sedation. Intraoperative anti-emetics will consist of IV ondansetron and IV dexamethasone. Intra-operative analgesics will be IV fentanyl, IV acetaminophen, IV ketorolac, and IV ketamine. No Block will be given. Patients will receive a single shot anterior QLB (30cc 0.5% Bupivacaine with 2mg preservative free dexamethasone). QLB Block + Standard of Care Bupivacaine + dexamethasone Patients will receive either a spinal (4cc Mepivacaine) or combined spinal epidural anesthetic (dose up 50 5 cc 2% lidocaine) with IV sedation. Intraoperative anti-emetics will consist of IV ondansetron and IV dexamethasone. Intra-operative analgesics will be IV fentanyl, IV acetaminophen, IV ketorolac, and IV ketamine. No Block will be given. Patients will receive a single shot anterior QLB (30cc 0.5% Bupivacaine with 2mg preservative free dexamethasone).
- Primary Outcome Measures
Name Time Method Numerical Pain Rating System (NRS) Pain Scores 24 hours after Post Anesthesia Care Unite (PACU) arrival Pain scores at rest and with movement will be through 24 hours after surgery. Score scale is from 0-10. 0 means no pain, 10 means worst pain. A lower score is a better outcome.
- Secondary Outcome Measures
Name Time Method Number of Patients With Presence of IAFE (Intraabdominal Fluid Extravasation) Following Surgery Immediately post-op in OR Incidence of Hypotension Up to Post Op Day 1 Opioid Use After Surgery to Post Operative Day 1 Amount of opioids taken after surgery
Antiemetic Use Up to Post Op Day 1 Patient Satisfaction With Post Op Pain Control Up to Post Op Day 1 Scale of 0-10; 0 being extremely dissatisfied and 10 being extremely satisfied
Change in Quadriceps Motor Strength on Surgical Side Up to Post Op Day 1 Change in Quadriceps Motor Strength from Pre-Op Baseline Quadriceps Strength
Number of Participants With Hospital Admission Up to Post Op Day 1 Urinary Retention Up to Post Op Day 1 Incidence of Urinary Retention in recovery
Number of Patients With Nausea/Vomiting Up to Post Op Day 1 Patient Score on Quality of Recovery-40 (QoR40) Inventory. Up to Post Op Day 1 Validated QoR40 survey score. Survey questions are added up to provide a final score. Higher score is reflective of a better outcome. Minimum score is 40, maximum score is 200.
Trial Locations
- Locations (1)
Hospital of Special Surgery
🇺🇸New York, New York, United States