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Summary

There is currently no standard of care or best practice for managing post-operative pain for patients undergoing hip arthroscopy. Perioperative pain with these procedures can be substantial. It has been shown that up to 90% of patients in the Post-anesthesia care unit (PACU) following hip arthroscopy report pain scores of 7/10. Poor pain management following hip fracture surgery directly results in increased time spent in high cost health care areas and delayed time to ambulation. Continuous regional anesthesia following hip arthroplasty has been shown to reduce narcotic consumption and related side-effects (reduction of post-operative pain, delirium, and length of stay). The purpose of this research is to evaluate the effectiveness of a fascia iliaca nerve block in reducing post-operative pain within the first 24 hours following hip arthroscopy. Additionally, the pharmacokinetics of the drug ropivacaine will be studied via laboratory analysis of blood samples. Ultimately, the objective of this research is to develop a standard of care or best practice for the management of post-operative pain following hip arthroscopy. This study will include the entire age range of patients who are seen for hip arthroscopy at Boston Children's Hospital, for which there is a 35 year age limit. Both sexes will be included in the study. The study design will be real catheter versus a sham catheter(control). All subjects will receive general anesthesia. The catheters (real or sham) will be administered after the induction of general anesthesia and before the beginning of the surgery until 24 hours after recorded PACU admittance time. The anesthesia team placing the block will not be blinded. The orthopaedic surgeon (Dr. Yen) and all evaluators will be blinded to the absence or presence of a real catheter. In the case of a sham catheter, the anesthesia team will rig a pump to look like it is dispensing local anesthesia. To determine the pharmacokinetics of ropivicaine during standard fascia iliaca block, following induction of general anesthesia, a large bore IV catheter will be inserted for the purpose of blood draws (all patients).

Conditions

Hip Surgery Corrective, Anesthesia; Functional

Recruitment Status

Withdrawn

Detailed Description

This study will be a randomized, double-blinded, placebo controlled study. All patients who are scheduled to undergo a hip arthroscopy with Dr. Yen who meet the inclusion/exclusion criteria will be approached and informed consent and assent when indicated would be obtained.Attending surgeon, anesthesia care team, PACU nursing staff, inpatient ward nursing staff and evaluators will be blinded to study group. Regional Anesthesia team and pharmacy staff will be not blinded to assignment of patient group but will have no additional contact with patient after provision of sham or actual perineural catheter. the study design will be real catheter versus a sham catheter, or control. All subjects will receive general anesthesia. The catheters (real or sham) will be administered after the induction of general anesthesia and before the beginning of the surgery until 24 hours after recorded PACU admittance time. The anesthesia team placing the block will not be blinded. The orthopaedic surgeon (Dr. Yen) and all evaluators will be blinded to the absence or presence of a real catheter. In the case of a sham catheter, the anesthesia team will rig a pump to look like it is dispensing local anesthesia. General Anesthesia a) Induction (IV): i. propofol: 2-4 mg/kg [9] ii. fentanyl: 2 mcg/kg administered iii. decadron: 4 mg as an antiemetic b) Airway: i. Airway management will be chosen by the anesthesiologist in charge of the case. c) Maintenance of anesthesia i. Sevoflurane 1.1 minimum alveolar concentration (MAC) ii. If heart rate or blood pressure increase > 20% above baseline (tachycardia as determined the morning of surgery in the holding area), anesthesiologist will administer1 microgram/kg fentanyl as bolus. May repeat as often as every 10 minutes. Maximum 8 doses. iii. With patient movement, anesthesiologist will administer propofol 1 mg/kg intravenous push. May repeat every 5 minutes as necessary. d) Emergence i. Discontinue isoflurane ii. Zofran 4 mg IV iii. Ketorolac 0.5 mg/kg IV; max dose 30 mg. Perineural Catheter: Actual and sham will be hooked to infusion pump and receptacle Pharmacy will label the infusion pumps, and will cover these labels in such a way that the cover can be immediately at any point if needed. Regional anesthesia team will double check the correct direction of the stopcock of the tubing set. a) Drug Group: i. Fascia Iliaca Catheter placement Administrator: Regional Anesthesiologist Minimum of three years anesthesia training Cannot be blinded, but will not contact/communicate with patient after surgery Appropriate laterality identified Site prepared using aseptic technique Localization of target site beneath fascia iliaca plane using portable ultrasound Aseptic preparation of probe with sterile sheath 38mm linear probe (BK Medical, USA) 15 MHz frequency Needle: 18g x 10mm echogenic enhanced needle 20G catheter inserted 3 cm beyond needle tip ii. Local anesthetic bolus Ropivacaine 0.5 ml/kg total in divided doses a. Aspirate every 5 ml Administered via needle iii. Dressing: 1. Liquid adhesive to skin 2. Sorbaview dressing (2x2) applied directly over catheter on skin 3. Catheter coiled once on top sorbaview and clear plastic dressing applied over sorbaview 4. 3x3 gauze taped over dressing to cover insertion site 5. Catheter labeled: "Fascia Iliaca Catheter" b) Control Group i. Fascia Iliaca Catheter placement 1. Administrator: Regional Anesthesiologist Minimum of three years anesthesia training Cannot be blinded, but will not contact/communicate with patient after surgery 2. Appropriate laterality of surgery identified 3. Site prepared using aseptic technique 4. Localization of target site beneath fascia iliaca plane using portable ultrasound a. Aseptic preparation of probe with sterile sheath b. 38mm linear probe (BK Medical, USA) c. 15 MHz frequency 5. 20 g catheter tip laid at appropriate insertion site ii. Dressing: 1. Liquid adhesive to skin 2. Sorbaview dressing (2x2) applied directly over catheter on skin 3. Catheter coiled once on top sorbaview and clear plastic dressing applied over sorbaview 4. 3x3 gauze taped over dressing to hide insertion site 5. Catheter labeled: "Fascia Iliaca Catheter" Infusion a) Pharmacy to prepare and label all infusion syringes b) Actual content (ropivacaine 0.1%) to be covered but immediately available in case of need to know. Violation of blinding to be obvious when tubing set removed. A non-blinded member of the study team will remove the set. i. Drug Group: Ropivacaine 0.1% ii. Control: Ropivacaine 0.1% to plastic bag c) Device: bodyguard infusion pump d) Rate: 0.3 ml/kg/hr; max 15 to start within the first hour after the block is placed. e) Infusion bag to be changed out as needed by nursing staff per usual routine (depends on volume of bag, weight of patient) Surgical Procedure Hip arthroscopy performed i. Pre-operative: Patient padded, per usual method Range Of Motion check by Yen and/or surgical staff Patient placed in traction device Xrays taken (AP pelvis, Dunn, frog leg, false profile). Must get view of lesion. Leg prepped/draped in normal fashion At conclusion of surgical procedure, patients in both groups to receive standard local anesthetic infiltration i. 20 cc total 10 ml 0.2% ropivacaine intra-articular into hip joint 5 ml 0.2% ropivacaine to each trochlear site (x2) Post-operative Methods All patients will remain in the hospital for a minimum of 24 hours following surgery per Dr. Yen's normal hip arthroscopy standard of care. A blinded observer will record pain scores at 30 minutes, 1 hour, 2 hours, 4 hours, 6 hours, and 24 hours postoperatively. Pain scores will be measures at rest by an 11-point numeric rating scale (NRS) ranging from 0-10, where 0 is no pain and 10 is worst pain imaginable. All patients should complete the study and have measurements at each time point. Patient demographics including age and gender as well as surgical characteristics including length of surgery, estimated blood loss, and surgery type will be recorded. Blinded observers will also record the time until patients require additional morphine, the amount of morphine consumed at each time it was requested, and whether the patient reported nausea or experienced vomiting within the first 24 hours post-operatively. PACU a) Time 0 = PACU arrival time b) Pain scores: i. Obtained by trained, blinded nurse observers ii. Recorded per policy with minimum evaluation every 15 minutes iii. Recorded using 11 point numeric rating scale (NRS) 1. 0 = no pain; 10 = severe pain c) PCA (patient controlled analgesia) available and initiated upon arrival to PACU i. Opioid: morphine ii. Bolus dose: 0.025 mg/kg; lockout 10 minutes iii. Hourly limit: 0.15 mg/kg/hr iv. Nurse rescue bolus: 0.05 mg/kg; lockout 60 minutes 1. To be administered for NRS > 7 v. continuous hourly infusion = 0 Inpatient Wards Nurses will evaluate pain per usual practice. Documented minimum every 4 hours. i. pain scores >7, nurse will administer: nurse rescue bolus via PCA ii. No dermatome test to prevent the introduction of bias by inadvertently un-blinding subjects. Pharmacokinetic Methods To determine the pharmacokinetics of ropivicaine during standard fascia iliaca block [10-13]. Following induction of general anesthesia, a large bore IV catheter will be inserted for the purpose of blood draws (all patients) Blood Sampling (all patients) Volume 2ml Time = zero defined as immediately following bolus of ropivicaine or sham equivalent First hour: collected at 5, 10, 15, 30, 35, and 60 minutes. Analysis: Internal lab Blood samples will be centrifuged to separate the plasma and stored at -20 degrees C until assay. Plasma ropivacaine levels analyzed by gas chromatography

Eligibility Criteria

Inclusion Criteria:

Patient age at surgery is 12-35.
Able to provide informed consent and/or assent.
Diagnosis is Femoro-acetabular impingement (FAI) and/or labral tear.
Surgery will involve and be limited to hip arthroscopy and osteoplasty of the acetabular rim or femoral head/neck junction.
Surgery will be performed by Dr. Yi-Meng Yen.
Admission status: 24 hour admission to hospital.
No contraindication to study procedures

Exclusion Criteria:

Hip revision surgery
Underlying neurologic disorder affecting pain perception.
Underlying neurocognitive disorder or developmental delay affecting ability to convey feelings of pain to medical staff.
Underlying opioid use or addiction.
Significant concomitant hip pathology.
Active infection over catheter site.
History of chronic pain (not localized to the hip) requiring consistent opioid consumption for greater than or equal to 6 months within year prior to surgery.
Allergy to local anesthetics
Allergy to fentanyl
Allergy to midazolam
Allergy to morphine
American Society of Anesthesia class 3 or higher.

Intervention

Intervention Type

Intervention Name

Procedure

Drug group Fascia iliaca nerve block

Procedure

Control group sham nerve block

Phase

Phase 3

Gender

All

Min Age

12 Years

Max Age

35 Years

Download Date

January 28, 2022

Principal Investigator

Karen Boretsky

Primary Contact Information

For more information on this trial, visit clinicaltrials.gov.

Contact

For more information and to contact the study team: