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Validation of methods for prediction of clinical output levels of active middle ear implants from measurements in human cadaveric ears.


ABSTRACT: Today, the standard method to predict output levels of active middle ear implants (AMEIs) before clinical data are available is stapes vibration measurement in human cadaveric ears, according to ASTM standard F2504-05. Although this procedure is well established, the validity of the predicted output levels has never been demonstrated clinically. Furthermore, this procedure requires a mobile and visually accessible stapes and an AMEI stimulating the ossicular chain. Thus, an alternative method is needed to quantify the output level of AMEIs in all other stimulation modes, e.g. reverse stimulation of the round window. Intracochlear pressure difference (ICPD) is a good candidate for such a method as it correlates with evoked potentials in animals and it is measurable in cadaveric ears. To validate this method we correlated AMEI output levels calculated from ICPD and from stapes vibration in cadaveric ears with outputs levels determined from clinical data. Output levels calculated from ICPD were similar to output levels calculated from stapes vibration and almost identical to clinical data. Our results demonstrate that both ICPD and stapes vibration can be used as a measure to predict AMEI clinical output levels in cadaveric ears and that ICPD as reference provided even more accurate results.

SUBMITTER: Grossohmichen M 

PROVIDER: S-EPMC5696479 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

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Validation of methods for prediction of clinical output levels of active middle ear implants from measurements in human cadaveric ears.

Grossöhmichen Martin M   Waldmann Bernd B   Salcher Rolf R   Prenzler Nils N   Lenarz Thomas T   Maier Hannes H  

Scientific reports 20171120 1


Today, the standard method to predict output levels of active middle ear implants (AMEIs) before clinical data are available is stapes vibration measurement in human cadaveric ears, according to ASTM standard F2504-05. Although this procedure is well established, the validity of the predicted output levels has never been demonstrated clinically. Furthermore, this procedure requires a mobile and visually accessible stapes and an AMEI stimulating the ossicular chain. Thus, an alternative method is  ...[more]

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