학술논문

Comparison of preemptive etoricoxib and dexamethasone in third molar surgery – a randomized controlled clinical trial of patient-reported and clinical outcomes.
Document Type
Article
Source
Clinical Oral Investigations. Sep2023, Vol. 27 Issue 9, p5263-5273. 11p. 1 Diagram, 4 Charts, 2 Graphs.
Subject
*THIRD molars
*PREMEDICATION
*CLINICAL trials
*RANDOMIZED controlled trials
*DENTAL extraction
*DEXAMETHASONE
*TREATMENT effectiveness
Language
ISSN
1432-6981
Abstract
Objectives: To compare preemptive single-dose etoricoxib and dexamethasone on postoperative patient satisfaction (pPS) and clinical parameters following the impacted mandibular third molar (IMTM) extraction. Materials and Methods: A parallel-group, triple-blinded, controlled clinical study included a total of 90 patients (n = 30), randomized to receive: etoricoxib 90 mg, dexamethasone 4 mg, or no premedication (control group) 1 h before surgery. Paracetamol 500 mg was prescribed as rescue medication (RM). Check-ups were scheduled at 24 h, 48 h, and day 7 post-surgery. At each time point, pPS was assessed using the 5-point Likert scale. RM parameters, swelling, trismus, and the occurrence of adverse events were also recorded, and patients were instructed to rate the perceived pain on Visual Analogue Scale. Results: In all the follow-up periods, data indicated significantly higher pPS scores in the preemptive medication groups when compared to the control group (p < 0.05). Both regimens delayed the first RM intake when compared to controls. In the etoricoxib group, a significantly lower total RM consumption was observed (p < 0.05). Dexamethasone significantly decreased swelling at each check-up and increased mouth opening at day 7 after the surgery (p < 0.05). Conclusions: Preemptive etoricoxib and dexamethasone elevate pPS after IMTM surgery. Etoricoxib improves RM parameters, while dexamethasone ameliorates the patient's postoperative functional ability. Clinical Relevance: Preemptive etoricoxib and dexamethasone use may decrease patients' discomfort following the impacted mandibular third molar extraction. Trial registration: ClinicalTrials.gov Identifier: NCT05791721. Date of Registration: 28/03/2023 (retrospectively registered). [ABSTRACT FROM AUTHOR]