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Pain Levels Did Not Differ Following Uncomplicated Third Molar Extractions Utilizing Liposomal Bupivacaine Versus Standard Bupivacaine.
James, Jeffrey; Benton, Bryan; Faigen, Alexander; Bloomquist, Ryan; Farmaha, Jaspreet; Hollingsworth, Chris.
Affiliation
  • James J; Associate Professor, Program Director and Interim Chairmen Department of Oral and Maxillofacial Surgery, Dental College of Georgia, Augusta University, Augusta, GA. Electronic address: jejames@augusta.edu.
  • Benton B; Private Practice, Savannah, GA.
  • Faigen A; Resident, Oral and Maxillofacial Surgery, Dental College of Georgia Augusta University, Augusta, GA.
  • Bloomquist R; Medical Student, University of South Carolina School of Medicine, Columbia, SC.
  • Farmaha J; Research Coordinator, Dental College of Georgia, Augusta University, Augusta, GA.
  • Hollingsworth C; Dental Student, Dental College of Georgia, Augusta University, Augusta, GA.
J Oral Maxillofac Surg ; 81(2): 206-212, 2023 02.
Article in En | MEDLINE | ID: mdl-36243034
ABSTRACT

PURPOSE:

Operations in the oral cavity are often characterized by an acute period of postoperative pain historically mitigated via opioids and other analgesics. The purpose of the study was to determine if liposomal bupivacaine infiltration (LBI) following uncomplicated extraction of bilateral, mandibular third molars will significantly reduce postoperative pain when compared to standard bupivacaine. MATERIALS AND

METHODS:

The study was designed as a parallel-arm randomized clinical trial. The sample size was calculated for the primary outcome variable postoperative pain levels measured at 48-hours. Using a power analysis, a sample size of n = 13 for each group was required. Patients meeting the inclusion/exclusion criteria requiring exodontia from November 4, 2018, to June 16, 2022, were recruited out of the oral and maxillofacial surgery clinic. The patients were randomized and divided into 2 groups. Group A was administered 0.50% bupivacaine (with 1200,000 epinephrine) via infiltration while group B underwent LBI. The primary outcome of interest was postoperative pain levels followed by the secondary outcomes of postoperative narcotic analgesic use, return to oral function, and satisfaction. Patient demographics and characteristics were analyzed as potential covariates utilizing the Fisher exact test and t test for continuous outcomes, respectively.

RESULTS:

Thirty patients were recruited for the study. The average age of patients receiving the third molar operation was 24.1 ± 5.8 years. Of the 30, 62.5% were female, and 37.5% were male. Seventy-five percent of the patients were Caucasian, 20.8% were African American, and 4.2% were Asian. Forty-eight-hour postoperative interviews revealed mean pain levels of 2.5 ± 2.8 in the control group and 2.9 ± 2.3 in the LBI group (P = .730) as measured on a visual analog scale. The 48-hour postoperative interview identified a mean of 1.9 ± 2.1 narcotic pills used in the control group and 2.5 ± 5.0 pills used in the LBI group (P = .693).

CONCLUSIONS:

Mandibular LBIs following bilateral mandibular third molar extractions showed no statistically significant advantage over the standard bupivacaine at either time point analyzed. Furthermore, no statistically significant difference was found regarding narcotic use between the 2 groups.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bupivacaine / Anesthetics, Local Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: J Oral Maxillofac Surg Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bupivacaine / Anesthetics, Local Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: J Oral Maxillofac Surg Year: 2023 Document type: Article