bupivacaine liposome
bupivacaine liposome (injection)
(byoo-pi-vi-kane lye-poe-some) bupivacaineliposomeinjection,Exparel
(trade name)Classification
Therapeutic: anesthetics topical localPharmacologic: amides
Indications
Action
Therapeutic effects
Pharmacokinetics
Time/action profile (blood levels)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
infiltration | unknown | 0.5–2 hr | 96 hr† |
Contraindications/Precautions
Adverse Reactions/Side Effects
Central nervous system
- central nervous system toxicity (life-threatening)
- dizziness
- drowsiness
- headache
- insomnia
Cardiovascular
- peripheral edema
- prolonged AV conduction
- tachycardia
Gastrointestinal
- constipation (most frequent)
- nausea (most frequent)
- vomiting (most frequent)
Dermatologic
- pruritus
Hematologic
- anemia
Musculoskeletal
- back pain
- muscle spasm
Miscellaneous
- hypersensitivity reactions including anaphylactoid-like reactions and laryngeal edema (life-threatening)
- fever
- procedural pain
Interactions
Drug-Drug interaction
Should not be administered concurrently with local lidocaine, wait at least 20 minutes before infiltration with bupivacaine liposome.Should not be admixed with other local anesthetics.Should not be used within 96 hr of other formulations of bupivacaine ; overall exposure and risk of toxicity/adverse reactions will be ↑.Route/Dosage
Availability
Nursing implications
Nursing assessment
- Assess infiltrated area for pain following administration and periodically during therapy.
- Monitor cardiovascular and respiratory status (vital signs, level of consciousness) constantly following infiltration. Notify health care professional immediately if signs of cardiac toxicity (atrioventricular block, ventricular arrhythmias, cardiac arrest) occur.
- Monitor for central nervous system toxicity. Notify health care professional promptly if they occur. Early signs of central nervous system toxicity include (restlessness, anxiety, incoherent speech, lightheadedness, numbness and tingling of the mouth and lips, metallic taste, tinnitus, dizziness, blurred vision, tremors, twitching, depression or drowsiness.
- Monitor for signs and symptoms of allergic reactions (urticaria, pruritus, erythema, angioneurotic edema, laryngeal edema, tachycardia, sneezing, nausea, vomiting, syncope, excessive sweating, elevated temperature, severe hypotension). Have resuscitative equipment available.
Potential Nursing Diagnoses
Acute pain (Indications)Implementation
- Do not confuse with propofol. In a syringe suspension is milky white and may be mistaken for other medications. Label syringe to ensure dose is not administered IV.
- Infiltration: May be administered undiluted or diluted with preservative–free 0.9% NaCl up to 0.89 mg/mL. Invert vial multiple times to re-suspend particles immediately prior to withdrawal from vial. Injected with a 25 gauge or larger bore needle slowly into soft tissues of surgical site with frequent aspiration to check for blood and minimize risk of intravascular injection. Use diluted suspension within 4 hrs of preparation in a syringe. Vials are for single dose; discard unused portions. May be stored in refrigerator for up to 1 month prior to opening. Do not use if solution is discolored or has been frozen; freeze indicator turns from green to white if exposed to freezing temperatures.
- Do not administer in an area with povidone iodine until dry. If administered with other non-bupivacaine local anesthetics, administer other agents first and wait at least 20 min before infiltrating with bupivacaine liposome. Do not administer other forms of bupivacaine within 96 hr of bupivacaine liposome.
Patient/Family Teaching
- Inform patient that infiltration may cause temporary loss of sensation or motor activity in infiltrated area.
- Instruct patient to notify health care professional of pregnancy is known or suspected or if breast feeding.
Evaluation/Desired Outcomes
- Prolongation of postoperative analgesia.