Acute Pain, Anesthesia, Conduction, Arthroplasty, Replacement, Knee
Conditions
Brief summary
This study will prospectively investigate the efficacy of Adductor canal block with periarticular infiltration Vs Adductor canal block, Periarticluar infiltration and Sensory posterior articular nerve of the knee block in patients undergoing total knee arthroplasty. The study will aid in answering question whether SPANK block is an effective adjunct in preventing posterior knee pain without causing motor blockade.
Detailed description
Total knee arthroplasty (TKA)is a common orthopedic surgical procedure. Optimal pain control is necessary for early recovery and discharge. TKA is considered one of the more painful surgical procedures, peripheral nerve blocks and multimodal analgesia are incorporated into clinical practice to provide patient comfort, decrease postoperative opioid requirement, facilitate early ambulation and enhance patient satisfaction.Adductor canal nerve block (ACB) and intraoperative periarticular infiltration (PAI) are routine clinical practice followed at our institute for postoperative pain control. Although ACB provided analgesia to peripatellar and anterior intra-articular aspect of knee joint, it does not relieve posterior knee pain which can be moderate to severe in intensity. Many techniques have been employed for posterior knee pain including sciatic nerve block and infiltration between popliteal artery and posterior capsule of the knee joint (IPACK) with limited success. Sciatic nerve block is considered gold standard but is rarely used due to associated motor weakness, which may delay ambulation and decrease participation in physical therapy postoperatively . In recent times IPACK block has gained popularity but there are concerns about local anesthetic injection close to surgical field and total dose of local anesthetic exceeding the recommended amount if combined with periarticular infiltration as is the practice at our institute. SPANK block was described in 2015 by Kardash et al for posterior knee pain while sparing motor function. The block is performed at the level of femoral shaft above the femoral epicondyle, on the medial side of the leg, with needle positioned just superficial to posteromedial femoral periosteum and 15 ml of local anesthetic is injected, decreasing concerns for local anesthetic toxicity, and invasiveness close to surgical field as compared to IPACK block which requires 30 ml of local anesthetic. Efficacy of SPANK block has been demonstrated as rescue analgesic for posterior knee pain after TKA, and a trial is underway to evaluate efficacy of ACB an SPANK block versus ACB alone \[5\].There is no literature evaluating benefit of SPANK block when added to ACB and PAI which is a standard practice. If SPANK block proves to be effective in controlling posterior knee pain, with motor sparing effect it can help reduce postoperative opioid requirement, help achieve same day discharge and prove to be another small step towards fighting opioid epidemic. Hence, we propose this study to evaluate added benefit of SPANK block to ACB and PAI with regards to postoperative pain control.
Interventions
PROCEDUREadductor canal block
The block is performed in supine position under ultrasound guidance using 22 G Touhy needle advanced in plane and 15 cc of 0.5% Ropivacaine ( local anesthetic) with dexmedetomidine 20-30 mcg depending on the age of the patient is injected at midthigh level lateral to the femoral artery in adductor canal to provide sensory blockade to the anterior aspect of the knee.
PROCEDURESPANK
SPANK: The block is performed in supine position, using 22 G Touhy needle, under ultrasound guidance, needle is advanced in plane to posteromedial shaft of femur taking care to avoid popliteal artery, and 0.5% ropivacaine 15 cc, dexmedetomidine 20-30mcg and dexamethasone 4 mg is injected into inner thigh above the knee provide sensory block to posterior aspect of the knee.
DRUGRopivacaine
ropivacaine 0.5% will be use in the block
Sponsors
Bruce Ben-David
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
At the office of acute pain management, one member of the research team will be responsible for providing the anesthesiologist in charge of performing the block with a sealed envelope. Each envelope will be labeled with a number corresponding to a matching number labeled on each patient binder. This envelope will contain the information regarding the block type based on randomization to be administered to the patient. Once the anesthesiologist knows which block he is going to administer, he will reseal the envelope and return it to the research team member. This process will allow only the anesthesiologist performing the block to have knowledge of the block type he or she is administering, keeping research team members blinded. The envelopes and binders will be kept by the principal investigator in a safe place and only reopened to be analyzed at the end of the study.
Intervention model description
The study will be conducted as prospective, randomized, single blinded, parallel trial at the University of Pittsburgh Medical Center (UPMC) Shadyside Hospital.
Eligibility
Sex/Gender
ALL
Age
19 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
Patients between the ages of 19 and 90 years old. BMI 18-45 ASA class I-II-III
Exclusion criteria
Simultaneous bilateral TKA. History of substance abuse. BMI \>45. Patients that did not received Intrathecal anesthesia. Infection at the site of injection (either for spinal or PNB). Pregnancy. Non english speaking or inability to participate in the study. Patients with coagulopathy or With INR \>1,5 the day of the surgery. Pharmacologic coagulopathy: patients on xarelto, plavix, or any kind of Blood Thinners. Chronic steroid use: patients with consumption of steroid for more than 3 months. Chronic pain: pain for more than 3 months. Chronic opiate use : consumption of opioids for more than 3 months.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain score using Numerical rating Scale (NRS) with ambulation at 24 hours after total knee arthroplasty | At 24 hours after surgery | Patient will describe the pain experienced after surgery on a scale from 1-10 being 10 the worst pain ever experienced, this will be registered in the format designed for this purpose and at the end of the study will be analyzed |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time to first opioid Consumption | During the first 24 after surgery | The amount of time measured from the end of the surgery when the patient leaves the operating room to the time when they receive their first dose of any opioid medication. |
| Opioid consumption | During the first 24 after surgery | will be measured using morphine equivalents during first 24 hours after knee surgery, starting when the patient leaves the operating room |
| Extent of motor blockade in various lower extremity muscle groups | During the first 24 after surgery | This outcome will be reported by physical therapy on medical records |
| Pain scores at rest and with movement at 6, 12 and 24 hours after the surgery measured using Numerical Rating Scale (NRS). | It will be measured at 6 hours, 12 hours, 24 hours after surgery | Patient will describe the pain experienced after surgery in rest and in movement at 6,12,24 hours on a scale from 1-10 being 10 the worst pain ever experienced. |
| Patient satisfaction with the pain management strategy provided after first 24 hours. | During the first 24 after surgery | patient satisfaction survey will be answered by the patient at 24 hours after surgery. This questionnaire will have a score of satisfaction from1-5, being 5 the maximum satisfaction experienced by the patient. |
| Local anesthetic toxicity reported in the medical records if is present. | During the first 24 after surgery | Local Anesthetic Toxicity is defined by symptoms such as metallic taste, tinnitus, drowsiness, after administering a dose of local anesthetics.This will be reported in the medical record and by the physician on call.t We will measure the number of participants that present these kind of symptoms if any. |
| Nausea and vomiting | During the first 24 after surgery | The presence or absence of nausea and vomiting, and the number of episodes during the first 24 hours after surgery.The outcome assessor will ask directly to the patient about this symptoms.we will measure the number of patients that report these symptoms. |
| Time that the patient takes to walk 100 feet after surgery | During the first 24 after surgery | This outcome will be reported by physical therapy on medical records |
Countries
United States
Outcome results
None listed