Objectives: The purpose of this clinical trial was to evaluate the influence of in-office dental bleaching on the pulp oxygen saturation (SpOp) reading. . SpOp was measured using a pulse oximeter in 112 upper and lower anterior teeth (canines and incisors) of patients submitted to bleaching. Whitegold Office 35% (WGO) (upper and lower left hemiarch) and Whiteness HP Auto Mixx 35% (WHP) (upper and lower right hemiarch) bleaching agents were used. SpO measurements (teeth and index finger) were taken before and after each of the three application sessions of the agents. In the 4 session, in which no bleaching gel was used, only SpO was measured. Before and after the bleaching sessions, a colorimetric device performed the teeth color reading. The waiting time between sessions was 7 days. Data were analyzed by the Friedman, Kruskal-Wallis, and Mann-Whitney tests ( = 0.05). Color change (Δ) data were correlated (Spearman's Rho test) with the SpOp levels.
Results: Neither of the two bleaching agents showed significant differences between the readings when evaluated individually (WGO, =0.780, and WHP, =0.494). When taken together, the results showed significant difference between the readings performed, with higher median values after bleaching sessions: before (97.3) and after (98.6) 1 session; before (98.3) and after (98.3) 2 session; before (98.3) and after (99.0) 3 session; and after 1 week (98.3). The dental groups formed by maxillary lateral incisors (=0.012) and mandibular incisors ( < 0.001) showed a significant difference. Spearman's Rho test showed a nonsignificant and weak correlation between Δ and SpOp in most comparisons.
Conclusions: The in-office dental bleaching influenced the SpOp reading, regardless of the dental group evaluated or the bleaching agent used. . This study provides information about the influence of in-office tooth whitening on the pulp SpOp levels. The observation of pulp vitality during and after the use of bleaching agents is important for the follow-up of patients undergoing tooth whitening. The use of a pulse oximeter may be a viable and painless alternative to perform this monitoring. The clinical trial was registered with the Brazilian Registry of Clinical Trials (ReBEC; registration number: https://clinicaltrials.gov/ct2/show/RBR-68xbth).
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072050 | PMC |
http://dx.doi.org/10.1155/2022/1598145 | DOI Listing |
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