Zoll Medical Corporation

Viztec, Inc.

Samsung Electronics Co., Ltd.

Zmd Corporation

Zoll Circulation, Incorporated

Zoll Medical Corpoaration

Other

Zoll Corporation, Inc.

Gary A Freeman

Frederick J Geheb

Annemarie Elizabeth Silver

Ulrich R Herken

Guy Robert Johnson

Thomas E Kaib

Shane S Volpe

Qing Tan

Christopher Luke Kaufman

Weilun Quan

Mark H Totman

Timothy F Stever

Gregory R Frank

Jason T Whiting

James E Brewer

Paolo Giacometti

David Barash

Lisa M Campana

Ziad F Elghazzawi

Steven J Szymkiewicz

Suzanne Crowell

Kent Volosin

Martin E Bures

Daniel M Lisogurski

Jon P Cloutier

Ian B Durrant

Michael Parascandola

Richard A Packer

Rachel H Carlson

Melissa M Dascoli

Donald R Boucher

John C Amann

Jeffrey Resnick

Colin Thomas

David H Freeman

C Shane Reid

Marc Cordaro

Timothy Sean McGough

Gideon Butler

Michael L Lopin

Deborah T Jones

David N Craige, Iii

Phillip Hier Amsler

Frederick K Newey

Christopher L Swenglish

Bruce Edwards

Keith G Lurie

Henry R Halperin

James D Wilson

Anja Metzger

Richard A Rattanni

Norman Alan Paradis

Ward M Hamilton

Jing Pan

Mark Weary

George Reilly

Michael Joseph Riley

Francesco Nicolo

Frederick W Faller

George Beck

Nikhil S Joshi

John Cain

Peter Andrew Lund

Michael R Dupelle

Richard A Helkowski

James Adam Palazzolo

Jeremy Thomas Dabrowiak

Anna Grace Prestezog

Brian Stonecipher

Binwei Weng

Joseph L Helmick

Vladimir Floroff

Naveed Zaidi

Dustin Boutet

Gwenn Ellerby

James G Radzelovage

Byron J Reynolds

James A Patterson, Iii

James R Homuth

Chad Ashmore

Charles E Sawyer, Jr

Gideon D H Butler

Gregory D Mears

Eric A Deines

Gary Ruggiero

Mark Bates

Babs Soller

Steven J Weisner

Wayne F Stanley

Christopher Joseph Desmarais

Kristin A Spang

Allan Scott Baucom

Scott J Robertson

Michael J Gabrin

Mark Baerenrodt

Dan E Goldman

Andrew David Funk

Kristopher M Edgell

John P Pierson

Michael S Erlich

An example of a system for review of clinical data includes a medical device configured to receive patient data signals from patient interface devices coupled to the medical device, and an auxiliary device configured to communicatively couple to the medical device via a communication channel and including an output device, a memory, a communication interface, and a processor configured to establish the communication channel, estimate a transmission age for the patient data, receive the patient data from the medical device via the communication channel, determine a patient data age based on at least one of the transmission age and a playback selection age, select a patient data age threshold based on a patient data context, compare the patient data age to the patient data age threshold to determine a patient data age indication, and provide the patient data and the patient data age indication at the output device.

Handling of age of transmitted data in medical device system

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 system for providing clinical decision support during a clinical encounter with a patient includes a mobile computing device and a remote computing device communicatively coupled to and remotely located from the mobile computing device, the remote computing device configured to receive clinical data during the clinical encounter from a medical device associated with the patient, provide a first interactive display including the clinical data, enable the mobile computing device to access the clinical data, receive user input based on the clinical data from the mobile computing device, and provide the user input and the clinical data at the first interactive display, where the mobile computing device is configured to access the clinical data, provide the clinical data at a second interactive display, prompt a user for the user input based on the clinical data via the second interactive display, and transmit the user input to the remote computing device.

Systems and methods for EMS device communications interface

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

A system for providing role-based data feeds for a plurality of patient caregivers includes a portable central device and a patient data display screen. The central device is configured to obtain the medical data via one or more sensors and/or electrodes configured to couple to the patient and provide the medical data to mobile devices, optionally as multiple role-based data feeds. The central device may include software and hardware configured to feed the medical data to the mobile devices via multiple role-based data feeds. The patient data display screen is configured to display the medical data. Each mobile device may identify an associated type of medical data by displaying a screen enabling a caregiver to select the associated type of medical data based on their role, or may receive a respective role-based data feed from the central device. Each mobile device is configured to display the received medical data.

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

A system for managing and distributing patient reports regarding medical devices to end users includes at least one processor configured to perform instructions to receive, from at least one therapeutic medical device, first physiological information relating to at least one therapeutic medical device patient and receive, from at least one monitoring medical device, second physiological information relating to at least one monitoring medical device patient. The at least one processor is also configured to perform instructions to process the first physiological information and the second physiological information, generate a plurality of patient reports from the processed first physiological information and from the processed second physiological information, receive a selection from an end user via an end user terminal, and provide at least one patient report of the plurality of patient reports to the end user terminal based on the received selection.

Mobile monitoring and patient management system

Disclosed is a wearable cardiac therapeutic system including a plurality of therapy electrodes disposed in a garment and a fluid pressure source including a barrel configured to house the conductive gel and an actuation mechanism. A therapy controller is configured to detect an arrhythmic event in a patient based on sensed electrical activity of the patient's heart, initiate an activation signal indicating that the conductive gel is to be released on to the body of the patient, and cause the delivery of one or more electrical therapeutic shocks to the heart of the patient. Gel activator circuitry is configured to receive the activation signal from the therapy controller, and cause the fluid pressure source to expel the conductive gel onto the body of the patient proximate the one or more of the therapy electrodes and prior to the delivery of the one or more electrical shocks to the patient.

Systems and methods for conductive gel deployment

In one aspect, a portable medical treatment and guidance apparatus for interactively assisting a user in treating a patient is provided. The apparatus can include: a housing having at least one compartment; a plurality of medical supplies housed within the at least one compartment; a user interface configured to provide an interactive query flow for assisting the user in providing medical treatment; at least one sensor adapted to detect removal of at least one medical item of the plurality of medical supplies; and at least one processor and memory mechanically coupled to the housing and communicatively coupled to the user interface, the at least one sensor, and communications circuitry.

Inventory management of portable medical treatment and guidance apparatuses

In at least one example, a medical device is provided. The medical device includes at least one therapy electrode, at least one electrocardiogram (ECG) electrode, at least one acoustic sensor, and at least one processor coupled with the at least one acoustic sensor, the at least one ECG electrode, and the at least one therapy electrode. The at least one processor can receive at least one acoustic signal from the at least one acoustic sensor, receive at least one electrode signal from the ECG electrode, detect at least one unverified cardiopulmonary anomaly using the at least one electrode signal, and verify the at least one unverified cardiopulmonary anomaly with reference to data descriptive of the at least one acoustic signal.

Medical device with acoustic sensor

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

A system for assisting a rescuer in performing cardio-pulmonary resuscitation (CPR) on a patient includes: a proximity sensor configured to be positioned at a location corresponding to a location of a rescuer's hand when delivering compressions to a patient's chest, the proximity sensor configured to produce a signal indicative of the rescuer's hands being released from the patient's chest; a medical device operatively coupled with the proximity sensor and configured to provide resuscitative treatment to the patient; and a controller communicatively coupled with the medical device and the proximity sensor. The controller is configured to: determine, based upon the signal from the proximity sensor, if the rescuer's hands have been released from the patient's chest, and trigger an action by the medical device in response to a determination that the rescuer's hands have been released from the patient's chest.

System for assisting rescuers in performing cardio-pulmonary resuscitation (CPR) on a patient

Among other things, in one aspect, we describe a system for assisting with cardiopulmonary resuscitation (CPR). The system includes at least one sensor; and one or more processors configured for calculating a chest compliance relationship based on data received from the at least one sensor, and determining a neutral position of chest compression based at least in part on a feature of the chest compliance relationship. The system can take the form of an active compression-decompression device.

Chest compliance directed chest compressions

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

According to at least one aspect, a wearable cardiac device is provided. The wearable cardiac device includes a garment worn about a torso of a patient, at least one sensing electrode to monitor cardiac activity of the patient, and a controller including a plurality of separate and distinct modules distributed about and/or integrated into the garment. The plurality of separate and distinct modules includes, for example, an operations module coupled to the at least one sensing electrode and configured to detect at least one cardiac condition of the patient and/or a communications module coupled to the operations module to communicate with an external device. In some examples, the wearable cardiac device may be configured as a treatment device and include an energy storage module coupled to at least one therapy electrode and configured to store energy for at least one therapeutic shock to be applied to the patient.

Garments for wearable medical devices

Growing community of inventors

Waltham, MA, United States of America

Gary A Freeman