Liposomal Bupivacaine Versus Standard Analgesia in TJA
Status: | Completed |
---|---|
Conditions: | Arthritis, Arthritis, Osteoarthritis (OA) |
Therapuetic Areas: | Rheumatology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | July 2014 |
End Date: | October 2015 |
Efficacy of Liposomal Bupivacaine Versus Standard Analgesia in Pain Management of Total Joint Arthroplasty
The purpose of this study is to determine whether liposomal bupivacaine is effective in the
management of pain following total joint arthroplasty, as compared to standard of care
analgesia.
management of pain following total joint arthroplasty, as compared to standard of care
analgesia.
Liposomal bupivacaine (Exparel®) is a local anesthetic made up of liposomal encapsulated
bupivacaine. It is designed to be injected at the time of surgery into the local soft
tissues. Because of its unique liposomal delivery system, Liposomal bupivacaine (Exparel®)
has been shown to provide up to 96 hours of pain relief following surgeries. This makes it
an attractive option in total joint arthroplasty patients. Combined with the proven efficacy
of regional anesthesia, intraoperative liposomal bupivacaine (Exparel®) may provide extended
pain relief following total joint arthroplasty. This has the potential to avoid the need for
opioid medications. With better pain control, medication side effects can be avoided and
patient's length of stay in the hospital can be shortened.
bupivacaine. It is designed to be injected at the time of surgery into the local soft
tissues. Because of its unique liposomal delivery system, Liposomal bupivacaine (Exparel®)
has been shown to provide up to 96 hours of pain relief following surgeries. This makes it
an attractive option in total joint arthroplasty patients. Combined with the proven efficacy
of regional anesthesia, intraoperative liposomal bupivacaine (Exparel®) may provide extended
pain relief following total joint arthroplasty. This has the potential to avoid the need for
opioid medications. With better pain control, medication side effects can be avoided and
patient's length of stay in the hospital can be shortened.
Inclusion Criteria:
1. Clinical diagnosis of osteoarthritis
2. Elected to undergo primary TKA, THA, or TSA
Exclusion Criteria:
1. Age < 18 years
2. Pregnant or breastfeeding
3. Non-English speaking
4. Unable to give informed consent
5. Previous open hip, knee or shoulder surgery
6. Pre-determined patients discharging to ECF
7. Patients with allergies to bupivacaine
8. Patients currently taking opioid pain medication
9. Patients with contraindication to nerve blocks
10. Patients undergoing simultaneous bilateral joint replacement, as this would require
>1 dose of liposomal bupivacaine (Exparel®) per patient for each surgical site
11. Patients with severe hepatic disease
12. Patients with chronic heart disease as defined as a decreased ejection fraction
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