Zoll Medical Corporation

Annemarie Elizabeth Silver

Gary A Freeman

Ulrich R Herken

Frederick J Geheb

Guy Robert Johnson

Paolo Giacometti

Lisa M Campana

Christopher Luke Kaufman

Qing Tan

Martin E Bures

Timothy F Stever

Melissa M Dascoli

Michael Joseph Riley

Gideon Butler

Richard A Packer

Vladimir Floroff

George Beck

John Cain

Jon P Cloutier

Steven J Weisner

Babs Soller

Gwenn Ellerby

Wayne F Stanley

Peter J Scott

Sean M Frick

Gary L Hochstettler

Shin-Luen Chai

Ian B Durrant

Frederick W Faller

John C Amann

Christopher Joseph Desmarais

Scott J Robertson

Justin R Carroll

Mohamed Abdelaziz

Fred Geheb

Jochen H Hoelscher

Jill Elaine Maxwell

Catherine A Hodge

Matthew R Vawter

Michael Buonadonna

Gary L Hochstetler

Tracy N Ashmore

Patricia A Daggett

Frederik Geheb

A system for documenting emergency medical events related to treatment of a patient is provided. The system includes a medical device configured to obtain physiological information from the patient and generate a first plurality of log entries that mark events that occur during treatment of the patient. The system also includes a mobile device configured to receive input for generating a second plurality of log entries that mark events that occur during treatment, establish a communicative connection with the medical device to access the first plurality of time-stamped log entries, and present, during the treatment of the patient, a single consolidated event log that includes the first plurality of log entries and the second plurality of log entries.

Systems and methods for documenting emergency care

A medical system includes a manual patient ventilation unit defining an airflow path arranged so that when the unit is applied to a patient the airflow path is in fluid communication with the patient's airway. The patient ventilation unit includes a ventilation bag configured to enable manual ventilation of the patient by a rescuer, an airflow sensor in the airflow path positioned to sense the presence of ventilation airflow and measure a gas flow rate in the airflow path, and a pressure sensor in the airflow path positioned to sense gas pressure in the airflow path. The system also includes a processor arranged to receive data generated by the airflow sensor and the pressure sensor and determine one or more ventilation quality parameters based at least in part on a gas flow volume calculated based on the sensed gas flow rate and gas pressures.

Ventilator system reporting

Example defibrillator electrode assemblies compression assemblies are described that may be dimensioned and configured for use on a patient despite physical constraints that limit the area or locations on a patient onto which an electrode assembly may be placed. A cardio pulmonary resuscitation (CPR) assembly is also described that protects a patient with a transthoracic incision from further injury during application of CPR compressions proximate to the incision.

Configurable electrodes and sensors

Systems and methods related to the field of cardiac resuscitation, and in particular to devices for assisting rescuers in performing cardio-pulmonary resuscitation (CPR).

Defibrillator charging

Embodiments of the present disclosure relate generally to the use of spectral sensors during a cardiac arrest event. More specifically, the present disclosure relates to the use of spectral sensors for measuring changes in pH and muscle oxygen saturation to estimate subject down time and evaluating the effectiveness of the clinical treatment administered during a cardiac arrest event. Given the narrow window of time in which emergency treatment must be administered, as well as the lack of information concerning the subject's condition, there is a need for a fast and accurate method of estimating the onset of the cardiac arrest emergency and evaluating the effectiveness of the emergency treatment being administered.

Using PH and SMO2 from a spectral sensor as an indication of subject down time

Devices and methods for CPR chest compression with active decompression.

Chest compression devices for augmented CPR

A medical system for assisting with an intubation procedure for a patient. The system comprising airflow sensors configured to obtain data indicative of airflow in the patient's airway and physiological sensors configured to obtain information regarding airflow in the patient's lungs. The system further including a monitoring device communicatively coupled to the airflow sensors and the physiological sensors. The patient monitoring device comprising at least one processor coupled to memory and configured to: provide a user interface on a display and assist the rescuer in determining proper placement of an endotracheal tube, receive the data indicative of the airflow in the patient's airway, receive the physiological information regarding the airflow in the patient's lungs, and determine whether the tube is properly placed based on the received physiological information, and present an output of the determination of whether the ET tube was properly placed.

Systems and methods for assisting patient airway management

A defibrillation device system includes sensors configured to receive patient data signals and including an ultrasound sensor, a defibrillator coupled to at least one of the sensors and including a screen configured to provide a first user interface, and a processor configured to provide a data display at the first user interface that includes a visual representation of the patient data. The system includes a mobile computing device configured to communicatively couple with the defibrillator at a time of the defibrillator's use and including a screen configured to provide a second user interface, and a processor configured to provide a data display at the second user interface. The second data display includes ultrasound data and a second visual representation of patient data included in the first visual representation, provides playback controls, and modifies the second data display based on user input received via the playback controls.

EMS decision support interface, event history, and related tools

Embodiments of the present invention include a system having at least one sensor configured to monitor a muscle oxygen saturation (SmO2) level of a patient who is undergoing cardiac arrest and to generate a signal representing SmO2 level; a user interface device; a processor communicably coupled to the user interface device, the processor configured to cause the user interface device to present an array of two or more possible nodes of a clinical decision support tree, wherein at least one of the nodes indicates cardiopulmonary resuscitation (CPR) treatment of the patient with no ventilation, and wherein at least another of the nodes indicates CPR treatment of the patient with active ventilation; determine which of the two or more possible nodes should be emphasized based on the SmO2 level; and update the array of the two or more possible nodes based on the determination.

Use of muscle oxygen saturation and PH in clinical decision support

A system for providing a visual summary of a condition of a patient when traumatic brain injury (TBI) is suspected or diagnosed includes at least one patient condition sensor configured to sense data representative of a patient condition parameter of interest for a TBI patient; at least one airflow sensor configured to sense data representative of ventilations provided to the patient; at least one visual display for providing the visual summary to a user; and at least one controller. The at least one controller is configured to cause the visual display to provide the visual summary. The visual summary can include at least one visual representation of at least one patient condition parameter for each time interval of a plurality of time intervals, at least one visual representation of ventilation information, and a visual indication of when at least one patient condition parameter is outside of a target range.

Rescue performance metrics for CPR and traumatic brain injury

A patient-coupled resuscitation device for use with a plurality of medical devices is provided. The resuscitation device includes a portion configured to provide treatment, a connector configured to connect the resuscitation device to one of a first medical device and a second medical device, and a housing including a memory and associated circuitry. The memory and associated circuitry is configured to store a device identifier to identify the resuscitation device; receive medical treatment information from the first medical device, the medical treatment information including at least one of: patient physiological data, patient characteristic data, and rescuer performance data; receive timing information of the medical treatment information from the first medical device; record the medical treatment information and the timing information; and transfer, upon detecting a connection to the second medical device, the medical treatment information and the timing information to the second medical device.

Accessory-based storage for use with a medical device

An external defibrillator system includes one or more compression sensors; one or more physiological sensors; and at least one processor. The at least one processor is configured to: receive and process chest compression signals and physiological signals from the sensors, determine values for chest compression depth and/or chest compression rate based on the received chest compression signals, determine a trend of at least one physiological parameter over a period comprising multiple chest compressions based on the received physiological signals, adjust a target chest compression depth and/or target chest compression rate based on the determined trend of the at least one physiological parameter, compare the determined values for chest compression depth and/or chest compression rate to the adjusted target compression depth and/or the adjusted target compression rate, and provide feedback about the quality of chest compressions performed on the patient.

Defibrillator display including CPR depth information

A feedback device for an acute care provider includes: at least one motion sensor; a haptic output component for providing feedback having a varying haptic pattern to the acute care provider regarding performance of a resuscitation activity; and a controller. The controller can be configured to receive and process a signal representative of performance of the resuscitation activity from the at least one motion sensor, compare the acute care provider's performance of the resuscitation activity to a target performance of the resuscitation activity, and cause the haptic output component to provide haptic feedback to the acute care provider by changing the haptic pattern based, at least in part, on the signal from the at least one motion sensor and the comparison of the acute care provider's performance to the target performance of the resuscitation activity. The device can be adapted to be wrist-worn by the acute care provider.

Wrist-worn device for coordinating patient care

A flow sensor system for ventilation treatment comprises a flow conduit configured to allow gas flow between a first region and a second region, the flow conduit defining a lumen for the gas flow; a flow restrictor disposed within the lumen of the flow conduit between the first region and the second region; a first absolute pressure sensor disposed adjacent to the first region of the flow conduit and configured to measure a pressure of the gas flow at the first region of the flow conduit; and a second absolute pressure sensor disposed adjacent to the second region of the flow conduit and configured to measure pressure of the gas flow at the second region of the flow conduit.

Flow sensor for ventilation

Methods and devices are described, such as for chest compression depth measurement for CPR performed on infants and for allowing active decompression of a patient's chest during a release phase of a chest compression cycle. An anterior segment of a resilient wrap-around structure may be positioned on the patient's sternum, including a first motion sensor. A posterior segment of the resilient wrap-around structure may be positioned on the patient's back, including a second motion sensor. Chest compressions may be provided such that the first motion sensor moves in fixed relation with the patient's sternum and the second sensor moves in fixed relation with the patient's back. Active decompression may be allowed for, including the resilient wrap-around structure exerting an expansive force on the patient's chest wall during a release phase of a chest compression cycle and hastening expansion of the patient's chest during the release phase.

CPR chest compression monitor with reference sensor

Growing community of inventors

Bedford, MA, United States of America

Annemarie Elizabeth Silver