Abstract
ObjectivesDue to severe limitations of dental pulp sensitivity tests, the direct recording of pulsed blood flow, using photoplethysmography (PPG), has been proposed. In vivo evaluation is methodologically difficult and in vitro models have hitherto been adversely influenced by shortcomings in emulating the in vivo situation. Consequently, the aim of this study was to test an improved data ...
Abstract
ObjectivesDue to severe limitations of dental pulp sensitivity tests, the direct recording of pulsed blood flow, using photoplethysmography (PPG), has been proposed. In vivo evaluation is methodologically difficult and in vitro models have hitherto been adversely influenced by shortcomings in emulating the in vivo situation. Consequently, the aim of this study was to test an improved data acquisition system and to use this configuration for recording pulsed blood in a new model.Materials and methodsWe introduced a PPG signal detection system by recording signals under different blood flow conditions at two wavelengths (625 and 940nm). Pulsed blood flow signals were measured using an in vitro model, containing a molar with a glass pulp and a resin socket, which closely resembled in vivo conditions with regard to volumetric blood flow, pulp anatomy, and surrounding tissue.ResultsThe detection system showed improved signal strength without stronger blanketing of noise. On the tooth surface, it was possible to detect signals emanating from pulsed blood flow from the glass pulp and from surrounding tissue at 625nm. At 940nm, pulp derived signals were recorded, without interference signals from surrounding tissue.ConclusionThe PPG-based method has the potential to detect pulsed blood flow in small volumes in the pulp and (at 625nm) also in adjacent tissues.Clinical relevanceThe results show the need for clear differentiation of the spatial origins of blood flow signals of any vitality test method to be applied to teeth.
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