Morbidity following transcrestal and lateral sinus floor elevation: A randomized trial

Aim To comparatively evaluate the morbidity following maxillary sinus floor elevation according to either transcrestal (tSFE) or lateral (lSFE) approach with concomitant implant placement. Materials & Methods Patients with ≥1 edentulous maxillary posterior site with residual bone height (RBH) of...

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Published inJournal of clinical periodontology Vol. 45; no. 9; pp. 1128 - 1139
Main Authors Farina, Roberto, Franceschetti, Giovanni, Travaglini, Domenico, Consolo, Ugo, Minenna, Luigi, Schincaglia, Gian Pietro, Riccardi, Orio, Bandieri, Alberto, Maietti, Elisa, Trombelli, Leonardo
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.09.2018
John Wiley and Sons Inc
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Summary:Aim To comparatively evaluate the morbidity following maxillary sinus floor elevation according to either transcrestal (tSFE) or lateral (lSFE) approach with concomitant implant placement. Materials & Methods Patients with ≥1 edentulous maxillary posterior site with residual bone height (RBH) of 3–6 mm were enrolled. tSFE was performed in association with a xenograft and a collagen matrix. For lSFE, the sinus was grafted with the xenograft, and the antrostomy was covered with a membrane. Implants were inserted concomitantly. The postoperative course was assessed through questionnaires. Pain level (VASpain) was recorded using a 100‐mm visual analogue scale. Results Twenty‐nine and 28 patients were included in tSFE and lSFE group, respectively. On the day of surgery, VASpain was significantly higher for tSFE compared to lSFE, and similar from day 1 to 14. tSFE was characterized by significantly lower incidence of swelling, bruising and nasal discharge/bleeding. Significantly less severe limitation in swallowing, continuing daily activities, eating, speaking, opening the mouth and going to school/work was found for tSFE only at specific postsurgery intervals. Conclusions lSFE was associated with lower pain on the day of surgery, and tSFE revealed lower postoperative morbidity as well as more tolerable postoperative course.
Bibliography:Funding information
The study was supported by a research grant by Regione Emilia‐Romagna Programma di Ricerca Regione‐Università Area 1 “Ricerca Innovativa” Bando Giovani Ricercatori “Alessandro Liberati”’ 2013; project PRUA1GR‐2013‐00000168, and by a research grant of the Osteology Foundation, Lucerne, Switzerland (project #13‐063).
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ClinicalTrials.gov ID: NCT02415946
ISSN:0303-6979
1600-051X
DOI:10.1111/jcpe.12985