Lidocaine-Bupivacaine Spinal Proves Safe and Effective in Outpatient Total Joint Arthroplasty.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 40939942.
- Also identified by DOI 10.1016/j.arth.2025.09.006.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
The utilization of spinal anesthetics has been integral to the implementation of rapid recovery protocols, which allow for same-day discharge following total joint arthroplasty (TJA). The purpose of this investigation was to determine the safety and efficacy of a single-dose spinal containing a mixture of lidocaine and bupivacaine in the setting of outpatient TJA. A prospective observational study was analyzing patients undergoing elective, outpatient, primary total hip arthroplasty (THA), total knee arthroplasty (TKA), and unicompartmental knee arthroplasty (UKA) receiving a single-shot spinal consisting of a mixture of two mL of 2% isobaric lidocaine and 0.7 mL of 0.5% bupivacaine along with titrated propofol sedation. The incidence of complications, including transient neurological symptoms (TNS), as well as the length of motor blockade, time to ambulation, and time to discharge, were recorded. The final cohort included 208 patients, of whom 47 underwent THA, 145 underwent TKA, and 16 underwent UKA. There were 6.1% of patients who experienced nausea, of which less than half experienced vomiting (2.9%), 1.6% of patients experienced urinary retention, and 0.0% of patients experienced TNS. The ability to perform plantarflexion and dorsiflexion of the ankle was consistently regained first (198.3 minutes), followed by the ability to begin ambulating (235.0 minutes), then by sensation to the dorsum of the foot (310.0 minutes), and lastly, criteria for discharge (359.0 minutes). The ability to ambulate was regained first by patients undergoing UKA (226.2 minutes), followed by TKA (235.6 minutes) and then THA (321.0 minutes). Visual analog pain scores (VAS) upon arrival to the post-anesthesia care unit (PACU) averaged 3.0 across all groups. A spinal anesthetic containing a mixture of lidocaine and bupivacaine proved safe and effective, with a mean duration of action of 198 minutes, without compromising rapid recovery protocols or same-day discharge.