Analysis of the Effectiveness of Lornoxicam and Flurbiprofen on Management of Pain and Sequelae Following Third Molar Surgery: A Randomized, Controlled, Clinical Trial
Abstract:The aim of this study was to analyze the effectiveness of Lornoxicam and Flurbiprofen in reducing perioperative sequelae after impacted mandibular third molar surgery. Ninety-one patients who needed surgical extraction of an impacted mandibular third molar were selected for the study. All subjects were randomly allocated to receive one of the following treatments twice a day for 5 days after surgery: placebo (n = 29), Flurbiprofen (n = 31), or Lornoxicam (n = 31). The primary outcome was postoperative pain, ev… Show more
“…After that, it is common to observe the decrease of the expected postoperative complications resulting in a significant improvement of the quality of life 13 . Accordingly, many clinicians [13][14][15][16] have emphasized the necessity for better control of pain, swelling, and trismus in patients who undergo third molar surgery. The use of local or systemic corticosteroids and nonsteroidal anti-inflammatory drugs is often recommended.…”
Aim: It was to evaluate the use of topical ozone gel on post-operative sequelae following impacted lower third molar surgery. Subjects and Methods: the current study included 30 patients divided randomly into equal three groups. Clinical examination included assessment of maximal mouth opening and cheek dimensions preoperatively. Panoramic x-ray was used for evaluation of the location and configuration of impacted lower third molar, surrounding bone, mandibular canal and adjacent tooth. The maximal mouth opening and check dimensions were remeasured postoperatively at days 2, 5 and 7. All readings were recorded and analyzed statistically. Results: Results showed statistical significance regarding pain while there was no statistical significance regarding mouth opening and swelling. Conclusion: Topical ozone gel is useful for the reduction of postoperative pain after lower third molar surgery.
“…After that, it is common to observe the decrease of the expected postoperative complications resulting in a significant improvement of the quality of life 13 . Accordingly, many clinicians [13][14][15][16] have emphasized the necessity for better control of pain, swelling, and trismus in patients who undergo third molar surgery. The use of local or systemic corticosteroids and nonsteroidal anti-inflammatory drugs is often recommended.…”
Aim: It was to evaluate the use of topical ozone gel on post-operative sequelae following impacted lower third molar surgery. Subjects and Methods: the current study included 30 patients divided randomly into equal three groups. Clinical examination included assessment of maximal mouth opening and cheek dimensions preoperatively. Panoramic x-ray was used for evaluation of the location and configuration of impacted lower third molar, surrounding bone, mandibular canal and adjacent tooth. The maximal mouth opening and check dimensions were remeasured postoperatively at days 2, 5 and 7. All readings were recorded and analyzed statistically. Results: Results showed statistical significance regarding pain while there was no statistical significance regarding mouth opening and swelling. Conclusion: Topical ozone gel is useful for the reduction of postoperative pain after lower third molar surgery.
“…Isola et al, used Lornoxicam, Flurbiprofen and placebo for pain control after impacted third molar surgery, in their study. They reported that the peak pain level in the flurbiprofen group was 12 hours 18 .…”
Section: Discussionmentioning
confidence: 99%
“…Isola et al, evaluated the efficacy of Lornoxicam, Flurbiprofen and Placebo on pain and edema after impacted third molar surgery and found that flurbiprofen was less effective than lornoxicam in the first 24 hours on pain, however, reported that all medicine group was equally effective on edema 18 . In our study, systemic and topical flurbiprofen form was used for postoperative pain and edema control after the third molar surgery.…”
ARAŞTIRMA / RESEARCH Efficiency of topical and systemic flurbiprofen on pain and edema after impacted third molar surgery and comparison of gastrointestinal adverse effects Topikal ve sistemik flurbiprofenin gömülü üçüncü molar cerrahisi sonrası ağrı ve ödem üzerine etkilerinin ve gastrointestinal yan etkilerinin karşılaştırılması Abstract Öz
“…As an explanation of the results of the present study, it should be highlighted that the dysfunctional damage at the endothelium level found in patients with periodontitis and with CVD can be determined by a specific inflammatory and immune pathway in which MPO modulates a response towards pathogenic bacteria of the oral biofilm which are exacerbated during the active phases of periodontal damage. It has also been shown that MPO, during periodontal disease, mediates the immune response at the endothelial level through specific heat shock proteins which has been shown to be useful for stimulating the production of cross-reactive T cells [47][48][49][50][51][52]. In this regard, this process which sees MPO as a key modulator [53][54][55][56][57][58], has also been shown to influence the host defense mechanism that determines a subsequent activation of endothelial cell production [55,[58][59][60][61][62][63] which leads to an increased risk of future tissue damage effects due to periodontal pathogens bacteria in several oral diseases [43,[64][65][66][67][68].…”
In this trial, we evaluated the influence on plasma and salivary myeloperoxidase (MPO) levels of periodontal health, coronary heart disease (CHD), periodontitis, or both periodontitis and CHD. Clinical and periodontal parameters were collected from periodontitis patients (n = 31), CHD patients (n = 31), patients with both periodontitis and CHD (n = 31), and from healthy patients (n = 31) together with saliva and plasma samples. The median concentrations of salivary and plasma MPO were statistically higher in the CHD patients [plasma: 26.2 (18.2–34.4) ng/mg; saliva 83.2 (77.4–101.5) ng/mL, p < 0.01] and in the periodontitis plus CHD patients [plasma: 27.8 (22.5–35.7) ng/mg; saliva 85.6 (76.5–106.7) ng/mL, p < 0.001] with respect to periodontitis and control patients. Through a univariate regression analysis, c-reactive protein (CRP) and CHD (both p < 0.001) and periodontitis (p = 0.024) were statistically correlated with MPO in plasma. The multivariate regression analysis demonstrated that only CRP was statistically the predictor of MPO in plasma (p < 0.001). The multivariate regression analysis in saliva demonstrated that, regarding MPO levels the only predictors were CRP (p < 0.001) and total cholesterol (p = 0.035). The present study evidenced that subjects with CHD and periodontitis plus CHD had higher plasma and salivary levels of MPO compared to subjects with periodontitis and healthy controls.
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