This invention relates to systems and methods for providing emergency treatment for heart conditions and, more particularly, to systems and methods for treating ventricular fibrillation.
In sudden cardiac arrest, the patient is stricken with a life threatening interruption to the normal heart rhythm, typically in the form of ventricular fibrillation (VF) or ventricular tachycardia (VT) that is not accompanied by spontaneous circulation (i.e., shockable VT). In VF, the normal rhythmic ventricular contractions are replaced by rapid, irregular twitching that results in ineffective and severely reduced pumping by the heart. If normal rhythm is not restored within a time frame commonly understood to be approximately 8 to 10 minutes, the patient will die. Conversely, the quicker that circulation can be restored (via CPR and defibrillation) after the onset of VF, the better the chances that the patient will survive the event.
The cessation of blood circulation stops delivery of oxygen to all parts of the body. Cerebral hypoxia, or lack of oxygen supply to the brain, causes victims to lose consciousness and to stop normal breathing. Accordingly, treatment of VF may require ventilation, such as by mouth-to-mouth resuscitation. There is often reluctance among lay rescuers to perform mouth-to-mouth resuscitation. Professional rescuers have overcome this reluctance and have barriers or bag-valve masks obviating the problem. However, lay rescuers do not have these means available and may be therefore be reluctant to provide emergency assistance.
In view of the foregoing, there is a need for instructing rescuers in an emergency situation when ventilation should be performed such that unnecessary mouth-to-mouth ventilation is avoided.
One aspect of the invention provides a method for treating a heart disorder that includes measuring electrical activity of a patient's heart and processing the measured electrical activity to determine a value descriptive of ventricular fibrillation. The method further includes comparing the value to a threshold and producing an output according to the comparison of the value to the threshold, the output instructing a rescuer to perform cardio-pulmonary resuscitation with or without ventilation. Another aspect of the invention provides a defibrillator including a pair of electrodes configured to detect electrical signals from a patient, a user interface configured to provide instructions to a rescuer in accordance with interface control signals, and a controller electrically coupled to the electrodes and user interface. The controller is operable to process electrical signals from the pair of electrodes and determine a value descriptive of ventricular fibrillation. The controller is further operable to compare the value, and in accordance to the comparison of the value to the threshold, generate interface control signals to control the user interface to communicate instructions to a rescuer to perform cardio-pulmonary resuscitation with or without ventilation.
In the drawings:
A pair of electrodes 16 are applied across the chest of the patient 14 by the user 12 in order to acquire an ECG signal from the patient's heart. The defibrillator 10 may be programmed to analyze the ECG signal for signs of arrhythmia such as VF or VT.
An ECG front end circuit 18 is connected to the pair of electrodes 16 that are connected across the chest of the patient 14. The ECG front end circuit 18 operates to amplify, buffer, filter and digitize an electrical ECG signal generated by the patient's heart to produce a stream of digitized ECG samples. The digitized ECG samples are provided to a controller 20 that performs an analysis to detect VF, shockable VT or other shockable rhythm and, in accordance with the present invention, that performs an analysis to determine a treatment regimen which is likely to be successful. If a shockable rhythm is detected in combination with determination of a treatment regimen that indicates immediate defibrillation shock, the controller 20 sends a signal to HV (high voltage) delivery circuit 22 to charge in preparation for delivering a shock and a shock button on a user interface 24 is activated to begin flashing. When the user presses the shock button on the user interface 24 a defibrillation shock is delivered from the HV delivery circuit 22 to the patient 14 through the electrodes 116.
The controller 20 may be coupled to further receive input from a microphone 26 to produce a voice strip. The analog audio signal from the microphone 26 is preferably digitized to produce a stream of digitized audio samples which may be stored, along with ECG and AED event markers, as part of an event summary 28 in a memory 30. The user interface 24 may consist of a display, an audio speaker, and control buttons such as an on-off button and a shock button for providing user control as well as visual and audible prompts. The user interface 24 may serve to display and provide instructions in order to instruct a rescuer how to properly provide treatment. A clock 32 provides real-time clock data to the controller 20 for time-stamping information contained in the event summary 28. The memory 30, implemented either as on-board RAM, a removable memory card, or a combination of different memory technologies, operates to store the event summary 28 digitally as it is compiled over the treatment of the patient 14. The event summary 28 may include the streams of digitized ECG, audio samples, and other event data as previously described.
As known, VF changes with time from its onset. In particular, as time passes from the onset of VF, heart muscle fluctuations become less vigorous. Physiological experiments also support a premise that ventilation may not be necessary early in VF, primarily because of remnant oxygen in the blood. In the early stages of VF, it may be therefore be better for a rescuer to focus on performing chest compressions without ventilation in order to circulate remnant oxygen in the blood before it has been depleted. As a result, the rescuer can be relieved of the burden (and reluctance) to provide ventilation at this time and concentrate on performing chest compressions.
According to embodiments of the present invention, characteristics of VF are measured to assess how long VF has been occurring in order to determine whether ventilation should be performed with chest compressions during administration of CPR and instruct a rescuer accordingly.
One example method for characterizing VF based on an ECG is described in International Publication Number WO 2006/136974, entitled “Defibrillator With Automatic Shock First/CPR First Algorithm” [hereinafter the '974 publication] which is incorporated herein by reference. As described in the '974 publication, a return of spontaneous circulation (ROSC) score can be calculated from ECG data collected by a defibrillator, such as defibrillator 10 (
As discussed in the '974 publication, a ROSC score can be calculated in several ways. For one example, the ROSC score can be calculated as the mean magnitude of the bandwidth limited first derivative (or first difference, which is a discrete-time analog) of the ECG over a period of a few seconds. Another example is to calculate a ROSC score from the median magnitude of the first derivative of the ECG. The '974 publication provides a more detailed description of the calculation of a ROSC score.
In an embodiment of the present invention, a ROSC score is used to determine whether ventilation should be performed with chest compressions during administration of CPR and instructs a rescuer accordingly. The thresholds for the values of the ROSC used to determine when to administer a shock first or perform CPR first in the '974 publication may also be used in the present invention for evaluating when to include ventilation when administering CPR. In an alternative embodiment, a different threshold may also be used. In other embodiments, characteristics of the ECG such as amplitude, frequency content, frequency content in a specific frequency band, or any combination of these characteristics, may be used to characterize a patient's VF, and consequently, provide a basis for determining whether ventilation should be performed with chest compressions during administration of CPR and instruct a rescuer accordingly.
At step 40 the VF characteristic is compared to a ventilation threshold. If the VF characteristic is not below the threshold, suggesting that VF recently began and remnant oxygen present in the blood can be circulated, the defibrillator 10 instructs a rescuer to perform chest compressions without ventilation during administration of CPR, if necessary, at step 42. Such instructions allow the rescuer to focus on providing chest compressions, which has the benefits of addressing any reluctance by the rescuer to perform CPR because of ventilating the patient, as well as limiting interruptions during chest compressions. In contrast, if the VF characteristic is below the threshold, suggesting that VF has been ongoing and remnant oxygen has been depleted, the defibrillator 10 instructs the rescuer to perform chest compressions with ventilation during administration of CPR, if necessary, at step 46.
However, if no shockable rhythm is identified at 58 or no shock is advised at 62, then the same or another VF characteristic referred to as f2 is compared with a ventilation threshold at 70. If this VF characteristic is above the applicable ventilation threshold, indicating that some residual oxygen remains in the blood stream, then a prompt is produced advising that CPR be performed without the inclusion of ventilation, e.g., only chest compressions. However if the comparison of the VF characteristic with the ventilation threshold shows that the characteristic is below the ventilation threshold, then CPR with ventilation is advised to introduce oxygen into the blood stream through ventilation such as mouth-to-mouth resuscitation, and to force the oxygenated blood through the body with chest compressions. Preferably the CPR is performed with the aid of a compression puck attached to the defibrillator by which the defibrillator prompts can assist the delivery of CPR if needed, as described in U.S. Pat. No. 6,306,107 (Myklebust et al. The Myklebust et al. system receives a signal in response to each chest compression and is therefore capable of monitoring when the CPR chest compressions begin and end. At the end of CPR the protocol of
During the process 34 of
From the foregoing it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IB08/51282 | 4/4/2008 | WO | 00 | 10/5/2009 |
Number | Date | Country | |
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60911097 | Apr 2007 | US |