Cumulative 24 hour oral hydromorphone and oxycodone equivalent consumption
IPACK Study in Total Knee Arthroplasty Patients
Brief Summary
This study proposes to compare current multimodal analgesic treatment for TKA with a new multimodal analgesic regimen to demonstrate decreased opioid requirement, time to rehabilitation, and time to reach hospital discharge.
Intervention / Treatment
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Standard of Care (ACB, SA, peri-op pain management) (DRUG)INTERVENTION BEFORE SURGERY Adductor Canal Block will be done using Adductor canal catheter (tube in the thigh) + injection of freezing medication INTERVENTION DURING SURGERY IV propofol for sedation INTERVENTION AFTER SURGERY Injection of salty water through the tube in the thigh x 2
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IPACK and multi-modal analgesic regimen (DRUG)INTERVENTION BEFORE SURGERY 1. Adductor Canal Block will be done using Adductor canal catheter (tube in the thigh) + injection of freezing medication 2. iPACK block ( infiltration between Popliteal Artery and posterior Capsule of the Knee) - injection of freezing medication in the back of the knee INTERVENTION DURING SURGERY 1. IV dexmedetomidine 2. IV ketamine Both for sedation INTERVENTION AFTER SURGERY 1. injection of freezing medication through the tube in the thigh x 2 2. IV dexamethasone 8 mg 1 day after surgery
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Periarticular Local Anesthetic Infiltration (PROCEDURE)INTERVENTION DURING SURGERY
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IV Dexamethasone 8mg at the end of surgery as standard of care (DRUG)INTERVENTION DURING SURGERY
Condition or Disease
- Knee Replacement Arthroplasty
Phase
Study Design
| Study type: | INTERVENTIONAL |
|---|---|
| Status: | Completed |
| Study results: | No Results Available |
| Age: | 18 Years to 85 Years |
| Enrollment: | 78 (ACTUAL) |
| Funded by: | Other |
| Allocation: | Randomized |
| Primary Purpose: | Treatment |
MaskingBlock room and anesthesia staff performing nerve blocks and administering sedation will be informed to which study group patient is allocated. The patient and independent investigator carrying out follow up assessments will remain blinded to the end of the study. If the patient wishes to know the study group assignment, the patient will be informed at the end of their final 6 week follow up. DOUBLE:
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Clinical Trial Dates
| Start date: | Oct 24, 2019 | ACTUAL |
|---|---|---|
| Primary Completion: | Dec 02, 2020 | ACTUAL |
| Completion Date: | Mar 31, 2021 | ACTUAL |
| Study First Posted: | May 17, 2019 | ACTUAL |
| Results First Posted: | Aug 31, 2020 | |
| Last Updated: | Apr 25, 2022 |
Sponsors / Collaborators
Lead Sponsor:
University Health Network, Toronto
Lead sponsor is responsible party
Responsible Party:
N/A
Location
Total knee replacement surgery (TKA) causes severe pain and this procedure is the most common reason patients are prescribed strong opioid drugs in hospital. As a result they are slow to begin rehabilitation after surgery, and are late in hospital discharge. Ontario hospitals are constantly challenged to meet growing demands of TKA and in fact increased demand has overcome the health care system resulting in TKA wait time (Ontario actual: 286 days vs. target: 182 days).1 One strategy to accommodate expanding volume and reduce wait time is to reduce hospital length of stay (LOS) through an enhanced recovery program.2 One essential component is further improvement of postoperative pain treatment to expedite rehabilitation and hospital discharge.
Treatment of severe post TKA pain often requires potent opioids but their excessive and prolonged use has negative consequences e.g., increased perioperative adverse events and longer LOS.3 Approximately 8% of opioid naive TKA patients become chronic opioid users at 6 months and the duration of prescription is the strongest predictor of misuse.4 Knowing that the opioid crisis in Canada is steadily growing and prescription opioids play a significant role in dependence and misuse,5 an effective perioperative opioid minimization analgesic program is mandatory for TKA patients.
Current multimodal analgesic treatment for TKA consists of oral non opioid drugs e.g., acetaminophen and non steroidal anti-inflammatory agents (NSAIDs) and surgeon performed peri-articular local anesthesia infiltration, however this is only partially effective.6 The regional analgesic effect is often short lived (\< 8 hours). Failure to sustain effective analgesia necessitates continued heavy reliance on opioids.
Several new treatments have been recently described for post TKA pain. They are: IV dexamethasone (steroid),7 dexmedetomidine (alpha 2 agonist)8, ketamine (NMDA antagonist)9 and 2 novel nerve block procedures- adductor canal block10 and iPACK block (infiltration between popliteal artery and posterior capsule of the knee).11 While each individual intervention has demonstrable analgesic benefit, the impact of incorporating all new treatments into the current analgesic regimen remains unknown.
The investigators believe that the new multimodal analgesic regimen proposed in this study will significantly decrease opioid requirement, time to rehabilitation, and time to reach hospital discharge criteria. It may also decrease the duration of opioid prescription for pain relief after hospital discharge. Although investigator's preliminary experience with this new regimen in 10 patients is promising, robust evidence showing its sustained opioid sparing analgesic effect is lacking.
Treatment of severe post TKA pain often requires potent opioids but their excessive and prolonged use has negative consequences e.g., increased perioperative adverse events and longer LOS.3 Approximately 8% of opioid naive TKA patients become chronic opioid users at 6 months and the duration of prescription is the strongest predictor of misuse.4 Knowing that the opioid crisis in Canada is steadily growing and prescription opioids play a significant role in dependence and misuse,5 an effective perioperative opioid minimization analgesic program is mandatory for TKA patients.
Current multimodal analgesic treatment for TKA consists of oral non opioid drugs e.g., acetaminophen and non steroidal anti-inflammatory agents (NSAIDs) and surgeon performed peri-articular local anesthesia infiltration, however this is only partially effective.6 The regional analgesic effect is often short lived (\< 8 hours). Failure to sustain effective analgesia necessitates continued heavy reliance on opioids.
Several new treatments have been recently described for post TKA pain. They are: IV dexamethasone (steroid),7 dexmedetomidine (alpha 2 agonist)8, ketamine (NMDA antagonist)9 and 2 novel nerve block procedures- adductor canal block10 and iPACK block (infiltration between popliteal artery and posterior capsule of the knee).11 While each individual intervention has demonstrable analgesic benefit, the impact of incorporating all new treatments into the current analgesic regimen remains unknown.
The investigators believe that the new multimodal analgesic regimen proposed in this study will significantly decrease opioid requirement, time to rehabilitation, and time to reach hospital discharge criteria. It may also decrease the duration of opioid prescription for pain relief after hospital discharge. Although investigator's preliminary experience with this new regimen in 10 patients is promising, robust evidence showing its sustained opioid sparing analgesic effect is lacking.
Participant Groups
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Standard of care: Adductor Canal Block(ACB), Spinal Anesthesia (SA) and Peri-op Pain management
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iPACK and multi-modal analgesic regimen
Eligibility Criteria
| Sex: | All |
|---|---|
| Minimum Age: | 18 |
| Maximum Age: | 85 |
| Age Groups: | Adult / Older Adult |
| Healthy Volunteers: | Yes |
Inclusion criteria:
* English-speaking;
* Age 18 - 85;
* BMI ≤ 38;
* Undergoing unilateral primary total knee arthroplasty surgery.
Exclusion criteria:
* inability to give informed consent
* patient refusal
* pregnancy, patients who are breastfeeding
* contraindication to nerve blocks or multimodal analgesia
* contraindication or hypersensitivity to any of the study drugs (celecoxib, acetaminophen, morphine, ropivacaine, bupivacaine, ketamine, dexmedetomidine, dexamethasone, ketorolac, epinephrine, sulfonamides)
* chronic pain disorders (\> 50 mg oral morphine equivalence per day at time of recruitment)
* medical or recreational use of marijuana and substance abuse (e.g., alcoholism),
* complications after surgery that result in discharge to a location other than home
* severe cardiovascular diseases e.g., heart failure, significant dysrhythmias; uncontrolled low blood pressure e.g., systolic blood pressure ≤ 100 mm Hg while on antihypertensive medication(s)
* respiratory diseases e.g., severe asthma, urticaria, or allergic-type reactions after taking acetylsalicylic acid (ASA) or other NSAIDs; severe acute or chronic respiratory disease and obstructive airway
* severe or active liver disease
* severe inflammatory bowel disease
* severe renal impairment (creatinine clearance \<30 mL/min)
* uncontrolled diabetes (type 1 or 2)
* active bleeding condition (e.g., postoperative or gastro-intestinal bleeding)
* severe psychiatric disorders and intake of monoamine oxidase inhibitors
* neurologic disorders (e.g., operative extremity neuropathy, delirium tremens, uncontrolled convulsive disorders, increased cerebrospinal or intracranial pressure)
* English-speaking;
* Age 18 - 85;
* BMI ≤ 38;
* Undergoing unilateral primary total knee arthroplasty surgery.
Exclusion criteria:
* inability to give informed consent
* patient refusal
* pregnancy, patients who are breastfeeding
* contraindication to nerve blocks or multimodal analgesia
* contraindication or hypersensitivity to any of the study drugs (celecoxib, acetaminophen, morphine, ropivacaine, bupivacaine, ketamine, dexmedetomidine, dexamethasone, ketorolac, epinephrine, sulfonamides)
* chronic pain disorders (\> 50 mg oral morphine equivalence per day at time of recruitment)
* medical or recreational use of marijuana and substance abuse (e.g., alcoholism),
* complications after surgery that result in discharge to a location other than home
* severe cardiovascular diseases e.g., heart failure, significant dysrhythmias; uncontrolled low blood pressure e.g., systolic blood pressure ≤ 100 mm Hg while on antihypertensive medication(s)
* respiratory diseases e.g., severe asthma, urticaria, or allergic-type reactions after taking acetylsalicylic acid (ASA) or other NSAIDs; severe acute or chronic respiratory disease and obstructive airway
* severe or active liver disease
* severe inflammatory bowel disease
* severe renal impairment (creatinine clearance \<30 mL/min)
* uncontrolled diabetes (type 1 or 2)
* active bleeding condition (e.g., postoperative or gastro-intestinal bleeding)
* severe psychiatric disorders and intake of monoamine oxidase inhibitors
* neurologic disorders (e.g., operative extremity neuropathy, delirium tremens, uncontrolled convulsive disorders, increased cerebrospinal or intracranial pressure)
Primary Outcomes
Secondary Outcomes
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0, 12, 18, 24, 36 and 48 hours after surgery and also pain scores during physical therapy daily
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Analgesic consumption at 12, 18, 36 and 48 hours and 1, 2 and 6 weeks after surgery
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Treatment effect will be estimated using a linear regression model, with baseline QoR score as a covariate.
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The post TKA milestones are: knee flexion ≥ 90 degrees, get in and out of bed by self, safe transfer to bathroom with or without assistance, walk with an assistive device on a level surface for a short distance and being able to climb up and down 2 or 3 stairs. steps or flights of stairs?
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The 4 criteria are: 1) adequate analgesia (numerical rating scale \<4/10); 2) independence from IV opioids ≥ 12 hours; 3) ability to independently stand and sit down (evaluated with the Timed Up and Go test and 4) unassisted ambulation ≥ 30 mins (evaluated with the 6-min walk test)
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muscle weakness, systemic toxicity
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nausea, vomiting, dizziness, sedation
More Details
| NCT Number: | NCT03954379 |
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| Other IDs: | 18-5920 |
| Study URL: | https://clinicaltrials.gov/study/NCT03954379 |
Last updated: Sep 29, 2023