摘要:
In an embodiment, a medical device can be used with a power adapter system. In addition, it can receive a data set from the power adapter system, and examine the data set to determine whether the data set confirms or not an authentication of the power adapter for use with the medical device. If the authentication is not confirmed, the external medical device can operate differently than otherwise. For example, power can be drawn from the power adapter system only if an inside battery is not charged.
摘要:
A method for operating an external medical device such as a defibrillator includes obtaining a data set from a battery pack and examining the data set to determine whether the battery pack is authenticated for use in the external medical device. If the examination does not confirm the authentications the method includes causing the device to follow a non-authenticated battery pack protocol. The non-authenticated battery pack protocol may include drawing power from the non-authenticated battery pack only if it is the only available source of power for the external medical device. It may include limiting functionality of the external medical device. It may include modifying the battery status information display for the non-authenticated battery pack. A power system for an external medical device may include a power source external to the medical device and including a memory which stores data indicative of an authorized status of the power source and a processor in the medical device configured to analyze the data and to control a function of the medical device based at least in part on the authorization status.
摘要:
In an embodiment, a medical device can be used with a power adapter system. In addition, it can receive a data set from the power adapter system, and examine the data set to determine whether the data set confirms or not an authentication of the power adapter for use with the medical device. If the authentication is not confirmed, the external medical device can operate differently than otherwise. For example, power can be drawn more slowly from the power adapter system.
摘要:
In an embodiment, a medical device can be used with a power adapter system. In addition, it can receive a data set from the power adapter system, and examine the data set to determine whether the data set confirms or not an authentication of the power adapter for use with the medical device. If the authentication is not confirmed, the external medical device can operate differently than otherwise. For example, power can be drawn from the power adapter system only if an inside battery is not charged.
摘要:
In an embodiment, a medical device can be used with a power adapter system. In addition, it can receive a data set from the power adapter system, and examine the data set to determine whether the data set confirms or not an authentication of the power adapter for use with the medical device. If the authentication is not confirmed, the external medical device can operate differently than otherwise. For example, power can be drawn more slowly from the power adapter system.
摘要:
A method for operating an external medical device such as a defibrillator includes obtaining a data set from a battery pack and examining the data set to determine whether the battery pack is authenticated for use in the external medical device. If the examination does not confirm the authentication, the method includes causing the device to follow a non-authenticated battery pack protocol. The non-authenticated battery pack protocol may include drawing power from the non-authenticated battery pack only if it is the only available source of power for the external medical device. It may include limiting functionality of the external medical device. It may include modifying the battery status information display for the non-authenticated battery pack. A power system for an external medical device may include a power source external to the medical device and including a memory which stores data indicative of an authorized status of the power source and a processor in the medical device configured to analyze the data and to control a function of the medical device based at least in part on the authorization status.
摘要:
Techniques for determining whether one or more leads are not adequately connected to a patient, e.g., for ECG monitoring, are described. The techniques involve injection of an integrated signal (which includes a test signal) into one lead, and monitoring the driven lead and the response at the other leads, including the common mode and the difference between the other leads. These “lead-off” detection techniques may be provided by an external defibrillator that provides three-wire ECG monitoring. Techniques for determining a type of a cable coupled to a defibrillator are also described. The cable-type identification may allow a defibrillator to, for example, operate in either a three-wire ECG monitoring mode or a therapy mode, based on whether a three-wire ECG cable or a defibrillation cable is coupled to the defibrillator.
摘要:
Techniques for determining whether one or more leads are not adequately connected to a patient, e.g., for ECG monitoring, are described. The techniques involve injection of an integrated signal (which includes a test signal) into one lead, and monitoring the driven lead and the response at the other leads, including the common mode and the difference between the other leads. These “lead-off” detection techniques may be provided by an external defibrillator that provides three-wire ECG monitoring. Techniques for determining a type of a cable coupled to a defibrillator are also described. The cable-type identification may allow a defibrillator to, for example, operate in either a three-wire ECG monitoring mode or a therapy mode, based on whether a three-wire ECG cable or a defibrillation cable is coupled to the defibrillator.
摘要:
Time after time studies find that often, even when administered by trained professionals, cardiopulmonary resuscitation (CPR) compression rates and depth are inadequate. Too week, shallow or too forceful compressions may contribute to suboptimal patient outcome. Several parameters are crucial for optimal and properly-administered CPR. Crucial parameters include proper hand positioning on the patient's chest, depth of compression of 4-5 cm, and compression rate of 100 compressions per minute. The crucial parameters are often affected by patient parameters, and relative to the patient, rescuer parameters, such as patient thoracic volume; weight; age; gender; and rescuer's, relative to the patient's, parameters, such as weight, height; physical form, etc. Proposed is an automated CPR feedback device with user programmable settings for assisting with real-time feedback and subsequently correcting rescuers patient customized CPR technique.
摘要:
Time after time studies find that often, even when administered by trained professionals, cardiopulmonary resuscitation (CPR) compression rates and depth are inadequate. Too week, shallow or too forceful compressions may contribute to suboptimal patient outcome. Several parameters are crucial for optimal and properly-administered CPR. Crucial parameters include proper hand positioning on the patient's chest, depth of compression of 4-5 cm, and compression rate of 100 compressions per minute. The crucial parameters are often affected by patient parameters, and relative to the patient, rescuer parameters, such as patient thoracic volume; weight; age; gender; and rescuer's, relative to the patient's, parameters, such as weight, height; physical form, etc. Proposed is an automated CPR feedback device with user programmable settings for assisting with real-time feedback and subsequently correcting rescuers patient customized CPR technique.