Patent Grant
8321011
Defibrillators and defibrillator-external pacemakers are employed to restore and maintain a heart's normal rhythm in either an emergency situation such as cardiac arrest, or voluntarily to normalize a person's rhythm in non-life threatening situations (e.g., atrial fibrillation).
Use of a defibrillator requires specific certification resulting from such programs as the American Heart Association's Advanced Life or Base Life Support courses. Further institutional or organizational training or competency evaluation may also be required. These requirements generally remain true for both manual and semi-automatic (AED) defibrillators. In order to maximize familiarity with this lifesaving equipment, institutions and organizations generally require periodic recertification and or demonstration of competency. In part, these training requirements are an attempt to maximize an operator's chance of successfully using a defibrillator.
Use of a defibrillator, particularly in emergency situations, places a great deal of stress on its operator. As such, even trained users still make mistakes when trying to operate a defibrillator. At least one study has demonstrated that upwards of 50 percent of defibrillator failures can be attributed to operator errors. Failure to use the defibrillator correctly can cause delays and compromise therapy. Bone, Defibrillator Failures: Causes and Problems and Recommendations for Improvement, JAMA, Vol. 264, No. 8 (1990).
Another factor contributing to operator errors is that many institutions and organizations possess different models of defibrillators that employ different operating interfaces, terminology, etc. The difference in operating systems can cause delays and mistakes, both of which may compromise therapy.
Operators are generally required to perform daily test and maintenance on a defibrillator. Such activities may require operation from a DC (battery) source that leads one to disconnect the defibrillator from AC power, source. It is not beyond reason that an operator, after completing a daily test might leave the defibrillator in the powered on condition, and not connect to the AC power source. Such conditions would drain the battery and render the defibrillator therapeutically useless. Another such example might be the disconnecting of therapeutic electrodes for daily test purposes. If not reconnected, delays might result that compromise therapy.
The current state of the art employs visual prompts or nonspecific tones to communicate user errors, and/or communicate corrective actions to defibrillator operators.
In an attempt to overcome these shortcomings, some defibrillators have incorporated a variety of high and low pitched tones as alert alarms to draw attention to the device. Initially successful, their shortcoming has become a lack of specificity. Over the years there has been proliferation of tonal alarms on a variety of medical equipment likely to be present in an emergency resuscitation. Further, the growing trend toward incorporating more vital sign parameters into pre-hospital defibrillators also raises the number of warning tones rescuers must decipher.
In recent years voice prompts have been employed to simplify the therapeutic use of defibrillators. That is they guide users, some minimally trained, through the setup and use of a defibrillator for delivery of a potentially lifesaving electrical shock (e.g., attaching electrodes, prompting need for CPR, and shock delivery). Most recently, defibrillators have begun to expand the range of the voice prompting to include the ABCs (airway, breathing, chest compressions) of resuscitation, and to provide feedback on the quality and rate of chest compressions. Olson U.S. Pat. No. 5,792,190 and Edward U.S. Application No. 2003/0216785 describe the use of voice prompts as part of an AED interface; they generally describe the role of voice prompts as instructions for a series of operations performed by the operator for the treatment of a patient, including the deployment and use of an AED. Nova U.S. Pat. Nos. 6,334,070 and 6,697,671 and Snyder U.S. Pat. No. 6,356,785 expand the use of therapeutic voice prompts to include BLS and ALS treatment protocols; operational faults are communicated to the operator by visual indicators (e.g., LED) or non-specific tonal sounds. Stendahl U.S. Pat. No. 5,955,956 describes the use of an audible alarm system in an AED in response to processor detected faults that are found during a periodic self-test. Borgenicht U.S. Pat. No. 6,405,082 describes the use of tonal and verbal prompts to confirm the therapeutic modes of a defibrillator, i.e., to alert the operator that the defibrillation mode has been selected, or that one is charging for synchronized cardioversion.
In general, the invention features a medical caregiving device (e.g.; a defibrillator) that incorporates corrective voice prompts that navigate users around operator errors. The voice prompts may, for example, address errors of readiness (e.g., failing to connect the defibrillator to an AC power source, failing to pre-connect electrodes, etc.), errors of omission (i.e., forgetting to do something, such as attempting to deliver a shock before the defibrillator is charged), and errors of commission (i.e., doing the wrong thing, such as attempting to shock VF when in the synchronization mode). The voice prompts may address errors in the delivery of therapy (e.g., attempting to shock VF when in the synchronization mode) or they may address errors other than in the delivery of therapy (e.g., failing to connect to an AC power source).
In general the invention features a medical device of the type used for assisting a user in delivering therapy to a patient, the device comprising a user interface including a speaker configured to deliver voice prompts to a user to assist the user in operating the device; at least one sensor or circuit element configured to detect an error made by the user in operating the device; a memory in which a plurality of different voice prompts are stored; a processor configured to determine which of the different voice prompts should be selected for delivery based on the detected error; and circuitry configured to work with the memory and the user interface and speaker to deliver the selected voice prompt.
In preferred implementations, one or more of the following features may be incorporated. The device may include a defibrillator. The selected voice prompts may address errors in the delivery of therapy, or they may address errors other than errors in the delivery of therapy. The voice prompts may include a prompt to correct the user's error in failing to select the defibrillation mode. The voice prompts may include a prompt to correct the user's error in selecting synchronized delivery of electrical stimulation during a cardiac arrest situation. The voice prompts may include a prompt to correct the user's error in failing to charge the defibrillator's battery. The voice prompts may include a prompt to correct the operator's failure to connect the device to AC power. The voice prompts may include a prompt to correct operator errors associated with the storage, management, deletion, transmission, or correction of information. The voice prompts may include a prompt to correct operator errors associated with the use of removable forms of media. The voice prompts may include a prompt to correct operator errors associated with the use of wired or wireless transmission of data. The voice prompts may include a prompt to correct operator errors associated with recording, displaying, storing, or printing of electrocardiographic (ECG) data. The voice prompts may include a prompt to correct operator errors related to analysis of electrocardiographic (ECG) data. The voice prompts may include a prompt to correct operator errors associated with vital signs monitoring. The vital signs monitoring may comprise one or more of the following: heart rate, temperature, blood pressure (non-invasive and invasive), pulse oximetry, end tidal CO2, respiration, blood gases, CO, or blood chemistries. The voice prompts may include a prompt relating to errors in calibration, sensor replacement, environmental issues (i.e. high ambient lighting), or cable placement. The voice prompts may include a prompt to correct operator errors associated with transcutaneous pacing. The voice prompts may include a prompt relating to increasing or decreasing pacing rate.
Providing voice prompts rather than audible tones or visual information on a display provides a much more effective means of informing the user of an error, and of informing him of how to correct that error. The voice prompts get the attention of the user, and they are more effective at getting the user to take appropriate action.
Other features and advantages of the invention will be found in the detailed description, drawings, and claims.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
There are a great many possible implementations of the invention, too many to describe herein. Some possible implementations that are presently preferred are described below. It cannot be emphasized too strongly, however, that these are descriptions of implementations of the invention, and not descriptions of the invention, which is not limited to the detailed implementations described in this section but is described in broader terms in the claims.
Other examples of errors that could be corrected by voice prompts include: (1) the operator's failure to insert a memory card into the device; (2) the operator's failure to make an online connection prior to attempting to send data; (3)
Preferably, a voice prompt does more than alert the user of an error; it goes on to instruct the user as to the corrective action that needs to be taken.
Many other implementations of the invention other than those described above are within the invention, which is defined by the following claims. For example, the invention can be applied to external defibrillators of the type used within the hospital as well as outside the hospital.
This application is a continuation of U.S. application Ser. No. 10/952,451, filed on Sep. 28, 2004 now U.S. Pat. No. 7,729,757, which application is a continuation in part of U.S. application Ser. No. 10/841,367, filed on May 7, 2004 now U.S. Pat. No. 7,706,878, and entitled, “Automated Caregiving Device with Prompting Based on Caregiver Progress” (both incorporated herein by reference).
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| Number | Date | Country |
|---|---|---|
| 03024521 | Mar 2003 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20100234910 A1 | Sep 2010 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10952451 | Sep 2004 | US |
| Child | 12787689 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10841367 | May 2004 | US |
| Child | 10952451 | US |
