This study is a prospective, double-blind, randomized comparison study of different anesthesia methods in rhytidoplasty surgery. The study is designed to determine whether post-operative side-effect profiles in patients undergoing elective cosmetic facelift surgery can be decreased through the use of propofol/ketamine anesthesia with bispectral monitoring (PKA-BIS) rather than general anesthesia, without increasing intra-operative time, side-effect profiles, or patient recall. Approximately 30 subjects undergoing facelift surgery performed by the principal investigator will participate.
PKA-BIS arm receives the following medications: clonidine 0.1-0.2mg glycopyrrolate 0.2mg propofol infusion titrated to BIS of 60-75 ketamine 50mg + additional ketamine not to exceed 200mg aggregate dosage throughout the case local anesthetic (lidocaine/marcaine mix) General Anesthesia arm receives the following medications: Pre-operatively: Pepcid 20mg Scopolamine 1.5mg transdermal patch Versed 2mg Zofran 8mg Reglan 10mg Glycopyrrolate - dose determined by anesthesiologist During the case, medication choices and dosing were dependent on the anesthesiologist - all general anesthesia cases received inhalational anesthetic (type of anesthetic also varied based on anesthesiologist's choice)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
TRIPLE
Enrollment
30
Mercy Facial Plastic Surgery Center
Springfield, Missouri, United States
Pain (QOR-40/VAS)
Quality of recovery score (QOR-40) in PACU and POD#1, VAS POD#1 and POD#7
Time frame: 1 week
Nausea/vomiting (QOR-40)
Quality of recovery score (QOR-40) in PACU and POD#1
Time frame: 24 hours
Time to awakening
staff recorded
Time frame: 4 hours
Time to discharge
staff recorded
Time frame: 4 hours
Overall feeling of well-being (QOR-40/VAS)
Quality of recovery score (QOR-40) in PACU and POD#1, VAS POD#1 and POD#7
Time frame: 1 week
Cost (reported as a mean)
comparison between two groups (reported as a mean)
Time frame: 1 day
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