Implant-supported mandibular overdentures in very old adults: a randomized controlled trial

F Müller, E Duvernay, A Loup, L Vazquez, F R Herrmann, M Schimmel, F Müller, E Duvernay, A Loup, L Vazquez, F R Herrmann, M Schimmel

Abstract

The purpose of this study was (1) to investigate denture satisfaction following the conversion of existing mandibular complete dentures to implant overdentures (IOD) in very old edentulous patients who depend on help for activities of daily living and (2) to evaluate secondary end points, such as functional, structural, nutritional, and patient-centered aspects. For this randomized clinical trial, 2 interforaminal short implants were placed in the intervention group (n = 16, 85.0 ± 6.19 yrs) to retain mandibular IODs; the control group (n = 18, 84.1 ± 5.55 yrs) received conventional relines. During the first year, no implant was lost; however, 2 patients died. IODs proved more stable, and participants in the intervention group demonstrated significantly higher denture satisfaction as well as an increased oral health-related quality of life compared to the control group. Maximum voluntary bite force improved significantly with IODs, yet the chewing efficiency was not different between groups. Masseter muscle thickness increased with IODs, mainly on the preferred chewing side. Body mass index decreased in both groups, but the decline tended to be smaller in the intervention group; blood markers and the Mini Nutritional Assessment did not confirm this tendency. These results indicate that edentulous patients who depend on help for activities of daily living may benefit from IODs even late in life.

Trial registration: ClinicalTrials.gov NCT01928004.

Keywords: dental implants; dental prostheses; geriatric dentistry; mastication; nutritional status; patient satisfaction.

Conflict of interest statement

The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article.

Figures

Figure.
Figure.
CONSORT flow diagram. Time points of assessment were baseline, intervention (implant loading/reline), and 3 and 12 months after the intervention (3M and 12M, respectively).

Source: PubMed

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