Abstract: This disclosure relates to systems and methods for performing ossicular reconstructions. An exemplary ossicular reconstruction system may include one or more adjustable prosthetic devices and micro-measuring devices. The adjustable prosthetic devices may be adjusted in terms of length, angulation, or both.

Abstract: This disclosure relates to systems and methods for performing nerve monitoring. An exemplary nerve monitoring system may include one or more stimulating devices for stimulating target nerves and one or more recording devices for recording responses from muscles associated with the target nerves. The methods can be employed for simultaneously monitoring the recurrent laryngeal nerve, the superior laryngeal nerve, and the vagus nerve during a surgical procedure.

Abstract: This disclosure relates to systems and methods for performing ossicular reconstructions. An exemplary ossicular reconstruction system may include one or more adjustable prosthetic devices and micro-measuring devices. The adjustable prosthetic devices may be adjusted in terms of length, angulation, or both.

Abstract: A passive ossicular prosthesis has a sound-conducting prosthesis body with a first coupling element for mechanical connection to the incus, malleus, or an actuator end piece of an active hearing aid at one end. The bight is made of a strip-shaped metallic material, partially open toward the outside via a gap-type opening and is intraoperatively crimped in the middle ear for permanent attachment. There is a second coupling element at the other end of the prosthesis body for connection to a further component of the ossicular chain or directly to the inner ear. The bight includes elongated perforations with longitudinal axes extending, in the implanted state, along a curved trajectory at a right angle or slant relative to an axis parallel to the longitudinal axis (a) of the enclosed object to reduce spring action and stiffness and markedly reduce the force to be applied for the crimping.

Abstract: A passive ossicular prosthesis has a sound-conducting prosthesis body with a first coupling element for mechanical connection to the incus, malleus, or an actuator end piece of an active hearing aid at one end. The bight is made of a strip-shaped metallic material, partially open toward the outside via a gap-type opening and is intraoperatively crimped in the middle ear for permanent attachment. There is a second coupling element at the other end of the prosthesis body for connection to a further component of the ossicular chain or directly to the inner ear. The bight includes elongated perforations with longitudinal axes extending, in the implanted state, along a curved trajectory at a right angle or slant relative to an axis parallel to the longitudinal axis (a) of the enclosed object to reduce spring action and stiffness and markedly reduce the force to be applied for the crimping.

Abstract: A nerve monitoring device, including a cannula, a sensor for monitoring a nerve, and an optional support element, can be inserted into an anatomic space. The cannula, sensor and/or support element can automatically conform to and match the geometry of the anatomic space, which can enhance desired contact between the sensor and anatomic features, such as muscles, nerves or tissue in the space in an atraumatic manner. The sensor, cannula and/or support element can include one or more strips or other elements that convert from a retracted mode to an expanded mode in which the strips or elements expand, enlarge or otherwise move to match the geometry of the space and place the sensors in precise monitoring proximity relative to the target muscles, nerves or tissues. An exemplary application of the device is in the field of laryngeal monitoring, however, the device is well suited for other applications.

Abstract: A nerve monitoring device, including a cannula, a sensor for monitoring a nerve, and an optional support element, can be inserted into an anatomic space. The cannula, sensor and/or support element can automatically conform to and match the geometry of the anatomic space, which can enhance desired contact between the sensor and anatomic features, such as muscles, nerves or tissue in the space in an atraumatic manner. The sensor, cannula and/or support element can include one or more strips or other elements that convert from a retracted mode to an expanded mode in which the strips or elements expand, enlarge or otherwise move to match the geometry of the space and place the sensors in precise monitoring proximity relative to the target muscles, nerves or tissues. An exemplary application of the device is in the field of laryngeal monitoring, however, the device is well suited for other applications.

Abstract: A nerve monitoring device is provided that includes a cannula and a sensor for monitoring a nerve. The device can be inserted into an internal body space at a desired depth of insertion and at a desired rotational orientation to monitor the activity of the nerve and/or an associated muscle(s). At least one of the cannula, the sensor and a sensor support element can be configured to enhance desired contact between the sensor and anatomic features, such as muscles, nerves or tissue, within the body space in an atraumatic manner. At least one of the sensor, cannula and support element can be reconfigurable from a first configuration to a different second configuration, where the second configuration conforms to the anatomical geometry of at least a portion of the body space so that the sensor satisfactorily contacts the target muscle(s) and/or nerve to monitor the same.

Abstract: The present invention provides a nerve monitoring device. The device includes a cannula, a sensor for monitoring the nerve and an alignment device. The cannula can be any surgical cannula, and is preferably an endotracheal tube. The sensor can be an electrode or other sensor that is capable of sensing nerve activity. The alignment device is a device that ensures that after insertion of the nerve sensor into a patient, the sensors are aligned to properly monitor the target nerve or muscle. The internal alignment device may communicate externally to surgeon by using electromagnetic energy as either a transmittor or a receiver. The mismatch of triangular laryngeal anatomy to circular cannula anatomy can be compensated for by a) altering the geometry (external shape) of the cannula and b) using soft, felt-like expandable electrodes. Rotational error can be compensated for by using a multi-electrode array wherein the optimized recording montage can be simply selected on the external recording device.