Patent Application
20100280841
This disclosure relates generally to medical systems and, more particularly, to medical systems that can be used to communicate with implanted medical devices, amongst other things.
Embodiments of the invention are related to medical systems and methods that can be used to communicate with and collect information from implanted medical devices, amongst other things.
In one embodiment, a system for automatically adjudicating arrhythmia episode information includes an episode database having episode data regarding a plurality of different arrhythmia episodes generated from at least one data-generating device and an adjudication processor configured to receive as input episode data regarding one of the different arrhythmia episodes and output characterization data characterizing the input episode data, wherein the characterization data includes an arrhythmia classification. The arrhythmia classification is selected from a group comprising at least monomorphic ventricular tachycardia (MVT). The system further includes an episode processor configured to process the characterization data and episode data, provide at least one report on the characterization data related to a plurality of the different arrhythmia episodes, and provide at least one programming recommendation or at least one alert.
In another embodiment, a system for automatically adjudicating arrhythmia episode information includes at least one cardiac rhythm management device that is implanted in a patient and an episode database having episode data regarding a plurality of different arrhythmia episodes generated from the at least one cardiac rhythm management devices that is implanted in a patient. The system further includes an adjudication processor configured to receive as input episode data regarding one of the different arrhythmia episodes and output characterization data characterizing the input episode data, wherein the characterization data includes an arrhythmia classification. The arrhythmia classification is selected from a group comprising at least polymorphic ventricular tachycardia/ventricular fibrillation (PVT/VF), monomorphic ventricular tachycardia (MVT) and atrial fibrillation (AF). The episode data input includes at least a portion of an intracardiac electrogram. The system further includes an adjudication database for storing the characterization data output by the adjudication processor and an episode processor configured to process characterization data and episode data, provide at least one programming recommendation for the data-generating device, and provide a report for a particular patient on the number of arrhythmia episodes classified as PVT/VF and on the number of episodes classified as MVT.
In yet another embodiment, a method for automatically adjudicating arrhythmia episode information includes the steps of providing an episode database having episode data regarding a plurality of different arrhythmia episodes generated from at least one data-generating device, processing the episode data for one of the different arrhythmia episodes, and outputting characterization data characterizing the episode data. The characterization data includes an arrhythmia classification, wherein arrhythmia classification is selected from a group comprising at least monomorphic ventricular tachycardia (MVT). The method further includes processing the characterization data, providing at least one report on the characterization data, and providing at least one programming recommendation or at least one alert to the data-generating device.
This summary is an overview of some of the teachings of the present application and is not intended to be an exclusive or exhaustive treatment of the present subject matter. Further details are found in the detailed description and appended claims. Other aspects will be apparent to persons skilled in the art upon reading and understanding the following detailed description and viewing the drawings that form a part thereof, each of which is not to be taken in a limiting sense. The scope of the present invention is defined by the appended claims and their legal equivalents.
The invention may be more completely understood in connection with the following drawings, in which:
While the invention is susceptible to various modifications and alternative forms, specifics thereof have been shown by way of example and drawings, and will be described in detail. It should be understood, however, that the invention is not limited to the particular embodiments described. On the contrary, the intention is to cover modifications, equivalents, and alternatives falling within the spirit and scope of the invention.
This disclosure relates generally to medical data-generating devices and, more particularly, to systems that collect information from medical devices. In particular, this disclosure relates to systems and methods for analyzing and utilizing the information collected. In some embodiments, the data-generating devices are implanted. In some embodiments, the information gathered includes an intracardiac electrogram. In some embodiments, the data-generating devices are devices that monitor cardiac rhythms. Such devices may be a part of a cardiac rhythm management system (CRM systems) that includes an implantable cardiac rhythm management device (CRM device), an external interface device and a patient management computer system.
Some implantable medical devices can be used to provide pacing therapy to patients who have cardiac rhythm problems. For example, an implanted cardiac rhythm management (CRM) device can be used to provide pacing therapy to a patient with sinus node dysfunction, where the heart fails to properly initiate depolarization waves, or an atrio-ventricular conduction disturbance, where the conduction of depolarization waves through the heart tissue is impaired.
Many types of CRM devices communicate with devices located outside of the body, which can receive information from the implanted device including sensor information and information about events, such as when the implanted device has provided therapy. In some cases, the external interface device can also transmit operational parameters to an implanted CRM device, that is, program the device.
These external interface devices can be provided to a patient, often in a patient's home, and can collect information from the implanted device, and provide that information to a computer system designed to monitor the patient's status. An exemplary remote patient management system is the LATITUDE® patient management system, available from Boston Scientific Corporation, Natick, Mass. Aspects of exemplary remote patient management and monitoring systems are described in U.S. Pat. No. 6,978,182, the content of which is herein incorporated by reference in its entirety.
The existence of remote patient management systems such as the LATITUDE® patient management system has provided a large amount of data about patients with implanted medical devices. For example, these systems store information about patient characteristics, patient sensor readings including electrocardiogram (EGM), device settings and delivery of therapy by the device. The sensor readings can include information associated with arrhythmia episodes experienced by the patient.
In one embodiment, a system uses this storehouse of patient-related data to analyze the device performance, understand a particular patient, understand a patient population group or improve therapy provided by the device. Such a system may operate outside of the device itself, such as on a server that is not at the same location as any of the data-gathering devices. As a result, a large amount of computer processing resources and memory can be devoted to utilizing the patient-related data.
“Arrhythmia episode” is defined to mean activity of a patient's body within a time period of particular interest. The time period can be a time when there is abnormal activity, for example, abnormal cardiac activity. “Episode data” is defined to include sensor readings from a medical data-generating device before, during and after the episode, and can also include device settings, actions that were taken by the device and other information. According to the system described herein, an episode database stores episode data about episodes that have occurred.
One or more data-generating devices generate episode data about arrhythmia episodes. The episode database may have episode data about a plurality of arrhythmia episodes generated by one device, or generated by multiple devices. In one embodiment, the episode database is external to any of the data-generating devices. However, in another embodiment, the episode database is located within one of the data generating devices. The episode data can include demographic information about the patient, an electrogram from during the arrhythmia episode, an indication of any therapy that was administered during the episode (such as shock or anti-tachycardia pacing), an indication of the patient's response to any therapy, and information about the patient's condition.
The episode data may also include information from the patient's electronic medical record, device settings at the time of the episode, counter information such as the patient's atrial arrhythmia burden, the patient's drug therapy history, and the patient's ablation history. The patient's ablation history may indicate complete heart block, for example. There are many other examples of possible episode data, which will be further described herein.
The episode data or part of the episode data for a particular episode can be analyzed using an adjudication algorithm to determine an arrhythmia classification and other types of characterization data about the arrhythmia episode. The characterization data can be stored in an adjudication database. In some embodiments, the characterization data is sent to the data-generating device to be stored. Once an arrhythmia classification has been generated for a particular episode or a group of episodes, then it is possible to provide patients and clinicians with many different types of reports related to the episode data. It is also possible for the system to analyze the characterization data to provide programming recommendations for the data-generating device where certain conditions are present. It is also possible to query the adjudication database for many different types of information that may be useful to clinicians, researchers or regulators. Also, the system may be configured to issue alerts for situations that merit attention, where the particular conditions that define those situations are present. One such alert is a patient disposition recommendation, such as an instruction for the patient to go to an emergency room to seek immediate medical help or an instruction for a patient to schedule a clinic visit in the near future.
One example of an arrhythmia episode data-generating device is an implantable cardiac rhythm management arrhythmia episode data-generating device. Specific implantable cardiac rhythm management devices include a pacemaker, a cardioverter-defibrillator, a cardiac resynchronization device, a heart rhythm monitoring device, or the like. However, it is also possible to generate episode data from external devices, including external pacemakers, external cardioverter-defibrillators, and external resynchronization devices. Additional examples of external devices that monitor cardiac activity include ambulatory electrocardiography devices or Holter monitors, which continuously monitor electrical activity of the heart for 24 hours or more. A data-generating device is one that is capable of providing information about an arrhythmia episode experienced by a particular patient.
An adjudication processor is capable of extracting certain features from the episode data which are very helpful in properly classifying the arrhythmia episode. The features may be based on domain knowledge used by physicians to classify the episode data. For example, the electrogram can be used to determine if the arrhythmia episode originates from the atrium or ventricle of the heart through analyzing the timing of the atrial and ventricle activities. The determination can alternatively or in addition be based on the morphology information from the electrograms from different atrial and ventricular channels.
In one embodiment, the adjudication processor is operatively connected to the episode database and is configured to receive as input episode data regarding one of the different arrhythmia episodes. The adjudication processor uses an automated method or algorithm to generate characterization data about the arrhythmia episode. More than one algorithm can be used. For example, different algorithms can be used for different applications. Examples of classification algorithms that can be used for the adjudication algorithm include decision tree algorithms, Naïve Bayes algorithms, support vector machine algorithms, and other pattern recognition algorithms.
One example of characterization data is an arrhythmia classification. The characterization data is stored in an adjudication database. In one example, the options for the arrhythmia classification include monomorphic ventricular tachycardia (MVT), polymorphic ventricular tachycardia/ventricular fibrillation (PVT/VF), supraventricular tachycardia (SVT), atrial-ventricular (AV) nodal re-entrant tachycardia (AVNRT), atrial fibrillation (AF), atrial flutter (AFL), atrial tachy (AT), sinus tachy (ST), dual tachy (DT), pacemaker-mediated tachycardia (PMT), one-to-one AV ratio with constant ventricular morphology, oversensing, noise and indeterminate. It is also possible for the system to provide more or fewer arrhythmia classifications than those listed. In one embodiment, the arrhythmia classification options include at least MVT. In one embodiment, the arrhythmia classification options include at least polymorphic ventricular tachycardia/ventricular fibrillation (PVT/VF), monomorphic ventricular tachycardia (MVT) and atrial fibrillation (AF). In various embodiments, there are three or more, four or more, five or more and six or more options for the arrhythmia classification.
In one embodiment, another aspect of the characterization data is an annotation of which part of the episode data was the basis for the arrhythmia episode classification. For example, the system may specify in the characterization data that a portion of the electrogram was the basis for the arrhythmia classification determination, or that multiple portions of, or the entire electrogram was the basis for the arrhythmia classification. For example, the user could note that the atrial, ventricle, shock or a combination of the parts of the electrogram was the basis for the arrhythmia classification. The characterization data can also include a likelihood, or confidence index, associated with each arrhythmia classification. In another embodiment, the annotation may include a justification for the characterization. For example, the episode may be characterized as MVT because a ventricular rate is higher than an atrial rate and only one morphology of the arrhythmia is observed. The characterization data may also include an annotation of a module of a decision process that leads to the arrhythmia episode classification.
Another possible aspect of the characterization data is a classification of the arrhythmia episode as being hemodynamically stable or hemodynamically unstable. A hemodynamically unstable arrhythmia typically cannot be tolerated by patients and needs to be treated immediately. Some SVT or AF arrhythmia episodes may be hemodynamically unstable. For a hemodynamically stable arrhythmia, the therapy may be withheld to allow the arrhythmia episode to resolve on its own. The classification of whether an arrhythmia episode is hemodynamically stable or hemodynamically unstable can be obtained from additional physiological sensors, such as a pressure sensor, and can be applied to most types of arrhythmias. The following published U.S. patent applications discuss examples of implementations of hemodynamic stability detection from implantable sensors for tachyarrhythmia classifications, and are hereby incorporated herein in their entireties: U.S. Published Patent Application Nos. 2007/0142866, 2008/0051843 and 2008/0281367.
An episode processor is provided in one embodiment of the system to perform processing of the adjudication database such as in order to provide reports, patient alerts including patient disposition recommendations, or programming recommendations. A user interface device may also be provided in order to provide these to a user.
In one embodiment, a system is configured to process a single episode at a time from a data-generating device. In one embodiment, such a system is located in the data-generating device, while in another embodiment the system is separate from the data-generating device and merely receives episode data from the data-generating device.
The episode database 402 may contain only a single episode, or the episode database may be a library of arrhythmia episodes from one data-generating device. The episode database may also be a library of arrhythmia episodes from multiple data-generating devices.
The system may be configured to toll an arrhythmia counter for individual patients at step 324 as the characterization data is output to provide a record of the number of different types of arrhythmia episodes that a particular patient has experienced. For example, the episode processor is configured in one embodiment to track and provide a report for a particular patient on the number of arrhythmia episodes classified as polymorphic ventricular tachycardia/ventricular fibrillation (PVT/VF), on the number of arrhythmia episodes classified as supraventricular tachycardia (SVT), and on the number of arrhythmia episodes classified as MVT. The episode processor may further be configured to track and provide a report for a particular patient on the number of arrhythmia episodes classified as one or more of the following: polymorphic ventricular tachycardia/ventricular fibrillation (PVT/VF), supraventricular tachycardia (SVT), AV nodal re-entrant tachycardia (AVNRT), atrial fibrillation (AF), atrial flutter (AFL), atrial tachy, sinus tachy (ST), dual tachy (DT), pacemaker-mediated tachycardia (PMT), one-to-one, oversensing, noise, indeterminate, hemodynamically stable and hemodynamically unstable. The system may also provide counters for any instances when inappropriate therapy was delivered during atrial fibrillation or during SVT.
The system may also categorize the morphology of episodes within a specific arrhythmia classification, such as SVT or MVT. The system may also categorize the response of the patient to therapy. The system may also be configured to provide historical trending for individual patients to show the change in the types, timing and morphology of arrhythmia episodes that a particular patient has experienced over time. The system may receive a query at step 326 and provide a report on the characterization data at step 328. There are many other types of reports that can be provided. The system may be automatically queried to produce the report each time an episode is processed. The system may also generate a report for a pre-set number of queries on a regular basis, such as daily, weekly, or monthly.
Based on analysis of the characterization data at step 323, the system can also be configured to issue an alert at step 330 if a condition exists that merits attention. For example, an alert can be issued if ventricular anti-tachycardia therapy was delivered to a patient during an arrhythmia episode classified as SVT, AF or atrial flutter (AFL). An alert can be issued if a shock was delivered without any anti-tachycardia pacing (ATP) being attempted before the shock during an arrhythmia episode classified as MVT. If an episode is classified as oversensing, an alert may be issued. Another scenario where an alert is desirable is where a ventricular tachycardia that required treatment, such as a hemodynamic unstable SVT, was not detected by a cardiac rhythm management device, and so no treatment was provided during that episode. Yet another scenario where an alert is desirable is where a shock was delivered to a hemodynamically stable arrhythmia.
Another type of alert that may be issued is a patient disposition recommendation, which is a communication directed to the patient or a caregiver to take a specific action, which can be delivered through a patient management system. For example, if multiple arrhythmias are observed in a very short duration of time, the recommendation may be, “Seek immediate medical help.” If the arrhythmia is similar to arrhythmia episodes observed before, and the device behaved properly, the recommendation may be, “Device functioning properly. Nurse, please call to check on patient.” If the arrhythmia is different from what were observed before, or programming changes are needed, the recommendation may be, “Schedule a clinic visit.” The particular patient disposition recommendations and when the recommendations are provided may be selected by a caregiver such as a physician.
The system can also be configured to provide programming recommendations at step 332 based on the analysis of the episode data and the characterization data. The system may recommend changes to the detection parameters of the data-generating device, such as adjustment of the parameters related to tachycardia detection, including the number of tachy zones, the rate cutoff, the initial detection durations, sustained rate duration (SRD), and other parameters. For example, if MVT is observed in the VF zone, then the system may recommend that the VF zone threshold be increased.
Other tachycardia detection parameters that may be suggested to be modified include morphology-based discrimination features and turning on or off specific or all detection enhancements. Other possible recommendations for detection parameters include reprogramming adjustable threshold values, for example, the atrial fibrillation rate and a stability threshold.
The system may also recommend programming changes that govern how therapy is delivered. For example, tachycardia therapy parameters may be changed to benefit the patient. For example, if MVT is observed and anti-tachycardia pacing (ATP) is turned off, the system may recommend turning on the anti-tachycardia pacing. In another example, use of ATP may be recommended where the arrhythmia classification is MVT, where MVT was previously treated with shock, and where ATP had not previously been tried for a patient. In yet another example, if ATP is not effective to assist the patient during a particular arrhythmia episode, the system may recommend switching the therapy settings to a different setting. The system may also recommend changing brady/sensing parameters, such as sensitivity and refractory parameters when oversensing/undersensing is detected.
Another programming recommendation that can be made is to change the parameters for storage of data in the data generating device. For example, if an arrhythmia classification is indeterminate, the system may recommend that a five-minute data interval be retained before each episode for future episodes. In another example, if the arrhythmia classification is one-to-one AV ratio with constant ventricular morphology, the system may recommend a detection parameter enhancement to look for gradual onset of tachycardia, which would indicate sinus tachycardia. If the detection enhancement revealed sudden atrial onset, then atrial tachycardia would be indicated.
Alerts, reports and programming recommendations can be graphically displayed for a patient, patient caregiver or other user of the system. This display can be provided via external interface devices or other user interface devices associated with the system, as further described herein. In one embodiment, the programming recommendations are presented to a patient caregiver for approval and implementation. In another embodiment, the programming recommendations or certain programming recommendations are automatically implemented in a data-generating device, and the patient caregiver is notified of the changes.
In one embodiment, a user of an automated adjudication system is given an opportunity to review the arrhythmia classification and other characterization data determined by the adjudication processor for a particular arrhythmia episode and overwrite that information.
Many different user interfaces may be used to permit overwriting of the data by displaying information for the user and accepting input from the user. A user interface device connected to a patient monitoring system can be used to overwrite the data.
Particular arrhythmia episodes where an overwrite operation is carried out represent situations for which it may be possible for the arrhythmia adjudication algorithm to be fine-tuned and improved. For example, the adjudication algorithm can be fine-tuned for an individual patient on the basis of the overwritten results. An individualized algorithm may be developed for a particular patient. An adjudication algorithm may also be catered to a particular set of patient characteristics. In addition, an adjudication algorithm applied broadly can also be improved and fine-tuned on the basis of overwritten results. Over time, an adaptive adjudication algorithm can be developed based on user input. The system prompts the user to consider revising the adjudication algorithm at step 362. The modified algorithm may be applied to the previous episodes from the patient or other patients to re-characterize the previous episodes.
Where an episode database contains arrhythmia episode data from many different patients, it is possible to perform many different types of analysis using that data to analyze device performance, improve device operation, analyze different patient groups, analyze different arrhythmia types or analyze arrhythmias from a particular clinic.
Analysis of the characterization data at step 376 can provide many different types of reports, including the reports previously described. Queries may be performed on types of arrhythmias at step 378. One possible query specifies the arrhythmia type as determined by the adjudication algorithm in prior adjudications. The system may provide a report on the percentages of episodes from a particular patient, such as the percentage of episodes classified as VF, AF, noise, MVT and other. Another possible query is the percentages of arrhythmia types in the entire library.
Queries may also be performed for patients or for episodes experienced by patients in specific populations groups or with specific characteristics at step 380. For example, the system may be queried for patients with specified characteristics, such as a history of AF episodes or an increase of X % in the AF burden within the last Y months. The system may also report on the episodes in a particular patient segment, such as gender group, age group, race group, a group with specific medical history factors, a group of patients at a particular clinic, a group of patients within a particular geographic region, or within a particular country.
It is also possible to query the system to obtain reports on device performance and therapy delivery at step 382. Examples of therapy that can be provided by a CRM device include ventricular anti-tachycardia therapy such as ventricular anti-tachycardia pacing, cardioversion and shock. A report on therapy delivery can be broken down into categories such as non-treated and/or non-sustained episodes, anti-tachycardia pacing (ATP) only, and shock therapy.
A query may combine one or more of patient, episode and therapy characteristics. Each of the queries discussed herein and many more can be used to generate a report at step 384.
Further examples of episode data will now be described. In one embodiment, the episode data can include a statement of the device type or device types which generated the data, such as a Holter monitor, pacemaker, single chamber implantable cardioverter defibrillator (ICD), dual chamber ICD, cardiac resynchronization therapy defibrillator (CRT-D) or other devices. Some devices generate an arrhythmia classification, such as non-sustained ventricular tachy arrhythmia (VT), sustained ventricular tachy arrhythmia, atrial fibrillation (AF) and supraventricular tachycardia (SVT). This device-generated arrhythmia classification may also be part of the episode data.
It is also possible that the episode data includes caregiver annotations related to the particular arrhythmia episode. Caregiver annotations may include an assigned arrhythmia classification and many other types of information related to the particular episode.
The episode data can also include electrocardiogram (EGM) recorded before, during and after the duration of the episode. The EGM may be generated by an implanted device. The EGM is an intracardiac EGM in one embodiment.
In one embodiment, the episode data includes both a first and second EGM. The first EGM may be an intracardiac EGM from an implanted device, while the second EGM is a surface EGM from an external device. In one embodiment, both a first and second EGM within the episode data are an intracardiac EGM.
The episode data may also include sensor readings from the patient including physiologic sensors such as a subcutaneous electrogram sensor, pressure sensor, an accelerometer, a temperature sensor and an impedance sensor. Other types of sensor readings that can be included in episode data include readings from a sleep sensor, functional capacity indicator, autonomic tone indicator, sleep quality indicator, cough indicator, anxiety indicator, and cardiovascular wellness indicator for calculating a quality of life indicator quantifying a patient's overall health and well-being. Additional sensor readings that can be included are from a thermometer, a sphygmomanometer or other external devices.
In one embodiment, the episode data also includes pace and sense markers on the EGM, which can indicate when along the course of the EGM the patient's heart rate can be classified in certain ways, such as ventricular tachy arrhythmia (VT), atrial fibrillation (AF) and supraventricular tachycardia (SVT).
In one embodiment, the episode data also includes device diagnostics which are measurements recorded by the device, and which can include average atrial heart rate, average ventricular heart rate and many other measurements.
The episode data can also include the devices response to the arrhythmia, such as anti-tachycardia pacing (ATP) therapy or shock therapy, and more specific descriptions of the therapy. The response information can be shown on the EGM strip and/or textually. In certain embodiments, the episode data can further include information on how the patient responded to the therapy, and information on subsequent therapy that was delivered.
In addition, the episode data can also include the device settings that were present during the episode. Examples of device settings include therapy settings such as what type of pacing or shock therapy will be applied when the device concludes that certain cardiac arrhythmias are occurring. For example, ATP therapy involves delivering a series of timed pacing pulses where it is possible to define the number of bursts delivered, the number of pacing pulses within each burst, and many other criteria. ATP therapy can fall into several different schemes, and each device has its own terminology describing the ATP therapy schemes. For some devices available from Boston Scientific Corporation, some of the ATP therapy schemes are named a burst scheme, a ramp scheme, and scan scheme or a ramp/scan scheme. The specifics of these ATP therapy scheme names, and when they will be delivered to the patient, are examples of device settings that may be a part of the episode data.
Another type of device setting is shock therapy parameters, which govern the shock energy, timing of shock delivery, shock vector configuration, as well as many other qualities of shock therapy.
Other types of device setting include detection settings that set forth the heart rate, rate of onset, and other criteria by which the device will classify the episode as certain arrhythmia types. Another type of device setting is frequently referred to as detection enhancements. These settings can be used to ensure that it is appropriate to delivery therapy to the patient by checking for the presence or absence of certain criteria. If the criteria are present, the detection enhancement settings may cause the device to delay or inhibit therapy delivery, bypass therapy inhibition, or bypass a sequence of ATP therapy in favor of shock therapy. Examples of specific detection enhancement criteria include the following, where the name for the programming feature for some devices available from Boston Scientific Corporation is included in parenthesis: certain therapy inhibitor conditions can be bypassed if the ventricular rate is greater than the atrial rate (V Rate>A Rate), ventricular therapy can be inhibited if the atrial rhythm is too fast (AFib Rate Threshold), ventricular therapy can be inhibited if the ventricular rhythm is unstable (Stability), and ventricular therapy can be inhibited if the patient's heart rate increases gradually (Onset). These parameters and whether they are turned on or off can be displayed along with other device settings in one embodiment.
Another aspect of the episode data is physiologic data collected by sensors such as a pressure sensor, an accelerometer, a temperature sensor or an impedance sensor. The episode data may also include physiologic data from many other types of sensors.
Further detailed embodiments of the hardware of the system will now be described with respect to the attached FIGS.
One embodiment of a data-generating device is a CRM device, as will now be described with reference to
The implantable medical device 114 can be in communication with an external interface system 116. In some embodiments, communication between the implantable medical device 114 and the external interface system 116 can be via inductive communication through a wand 110 held on the outside of the patient 112 near the implantable medical device 114. However, in other embodiments, communication can be carried out via radiofrequency transmission, acoustically, or the like.
The implantable medical device 114 can include one or more implantable sensors in order to gather data regarding the patient 112. For example, the implantable medical device 114 can include an activity level sensor, a respiration sensor, a blood pressure sensor, an impedance sensor, or other sensors.
The implantable medical device 114 can be configured to store data over a period of time, and periodically communicate with the external interface system 116 in order to transmit some or all of the stored data.
The external interface system 116 can be for example, a programmer, a programmer/recorder/monitor device, a computer, a patient management system, a personal digital assistant (PDA), or the like. As used herein, the term programmer refers to a device that programs implanted devices, records data from implanted devices, and allows monitoring of the implanted device. Exemplary programmer/recorder/monitor devices include the Model 3120 Programmer, available from Boston Scientific Corporation, Natick, Mass. The external interface system 116 can include a user input device, such as a keyboard 120 and/or a mouse 128. The external interface system 116 can include a video output channel and video output device, such as a video display 118 for displaying video output. The displayed video output can include a user interface screen. In addition, the video display 118 can also be equipped with a touch screen, making it into a user input device as well.
The external interface device 116 can display real-time data and/or stored data graphically, such as in charts or graphs, and textually through the user interface screen. In addition, the external interface device 116 can present textual information to a user along with several response options. The external interface device 116 can also input and store a user's response to a question, and can store a user's text response in some embodiments.
In one embodiment, the external interface device 116, which can also be referred to as a user interface, is in communication with a patient management computer system 132. The communication link between the user interface 116 and the patient management computer system 132 may be via phone lines, the Internet 130, or any other data connection. The user interface 116 can also be used when it is not in communication with a device, but is only in communication with the patient management computer system 132.
In one embodiment, the external interface device 116 is capable of changing the operational parameters of the implantable medical device 114, and is therefore referred to as a programmer. Typically, programmers are used to interface with CRM devices in a clinic or hospital setting. In this context, the user of the external interface device is a physician or trained technician.
Each component of the patient management system 200 can communicate using the communication system 210. Some components may also communicate directly with one another. The various components of the example patient management system 200 illustrated herein are described below.
Data-generating devices 202, 204, and 206 can be implantable devices or external devices that may provide one or more of the following functions with respect to a patient: (1) sensing, (2) data analysis, and (3) therapy. For example, in one embodiment, devices 202, 204, and 206 are either implanted or external devices used to measure a variety of physiological, subjective, and environmental conditions of a patient using electrical, mechanical, and/or chemical means. The devices 202, 204, and 206 can be configured to automatically gather data or can require manual intervention by the patient or another person. The devices 202, 204, and 206 can be configured to store data related to the physiological and/or subjective measurements and/or transmit the data to the communication system 210 using a variety of methods, described in detail below. Although three devices 202, 204, and 206 are illustrated in the example embodiment shown, many more devices can be coupled to the patient management system. In one embodiment, each of the devices 202, 204 and 206 is serving a different patient. In one embodiment, two or more devices are serving a single patient.
The devices 202, 204, and 206 can be configured to analyze the measured data and act upon the analyzed data. For example, the devices 202, 204, and 206 can be configured to modify therapy or provide an alarm based on the analysis of the data.
In one embodiment, devices 202, 204, and 206 provide therapy. Therapy can be provided automatically or in response to an external communication. Devices 202, 204, and 206 are programmable in that the characteristics of their sensing, therapy (e.g., duration and interval), or communication can be altered by communication between the devices 202, 204, and 206 and other components of the patient management system 200. Devices 202, 204, and 206 can also perform self-checks or be interrogated by the communication system 210 to verify that the devices are functioning properly. Examples of different embodiments of the devices 202, 204, and 206 are provided herein.
Devices implanted within the body have the ability to sense and communicate as well as to provide therapy. Implantable devices can provide direct measurement of characteristics of the body, including, without limitation, electrical cardiac activity (e.g., a pacemaker, cardiac resynchronization management device, defibrillator, etc.), physical motion, temperature, heart rate, activity, blood pressure, breathing patterns, ejection fractions, blood viscosity, blood chemistry, blood glucose levels, and other patient-specific clinical physiological parameters, while minimizing the need for patient compliance. Derived measurements can also be determined from the implantable device sensors (e.g., a sleep sensor, functional capacity indicator, autonomic tone indicator, sleep quality indicator, cough indicator, anxiety indicator, and cardiovascular wellness indicator for calculating a quality of life indicator quantifying a patient's overall health and well-being).
Devices 202, 204, and 206 can also be external devices, or devices that are not implanted in the human body, that are used to measure physiological data (e.g., a thermometer, sphygmomanometer, or external devices used to measure blood characteristics, body weight, physical strength, mental acuity, diet, heart characteristics, and relative geographic position).
The patient management system 200 may also include one or more remote peripheral devices 209 (e.g., cellular telephones, pagers, PDA devices, facsimiles, remote computers, printers, video and/or audio devices) that use wired or wireless technologies to communicate with the communication system 210 and/or the host 212.
The example database module 214 includes a patient database 400, an episode database 402, an adjudication database 404, a population database 406, and a medical database 408, all of which are described further below. The patient database 400 includes patient specific data, including data acquired by the devices 202, 204, and 206, as well as a patient's medical records and historical information. The population database 406 includes non-patient specific data, such as data relating to other patients and population trends. The example medical database 408 includes clinical data relating to the treatment of diseases, such as historical trend data for multiple patients in the form of a record of progression of their disease(s) along with markers of key events.
The episode database 402 has episode data regarding a plurality of different arrhythmia episodes generated from those of devices 202, 204, and 206 that provide arrhythmia episode data. The adjudication database 404 includes adjudication conclusions associated with the episode data such as arrhythmia episodes. The adjudication database 404 and the episode database 402 can actually be a single database with shared data that is used as either episode data or adjudication data depending on the particular data set being presented to the user.
Information can also be provided from an external source, such as external database 600. For example, the external database 600 includes external medical records maintained by a third party, such as drug prescription records maintained by a pharmacy, providing information regarding the type of drugs that have been prescribed for a patient or, in another example, authorization data from patient groups that have authorized users to view arrhythmia episode data.
The example analysis module 216 includes a patient analysis module 500, device analysis module 502, population analysis module 504, and a learning module 506. Patient analysis module 500 may utilize information collected by the patient management system 200, as well as information for other relevant sources, to analyze data related to a patient and provide timely and predictive assessments of the patient's well-being. Device analysis module 502 analyzes data from the devices 202, 204, and 206 and external interface devices 208 to predict and determine device issues or failures. Population analysis module 504 uses the data collected in the database module 214 to manage the health of a population. Learning module 506 analyzes the data provided from the various information sources, including the data collected by the patient system 200 and external information sources, and may be implemented via a neural network (or equivalent) system to perform, for example, probabilistic calculations. In one embodiment, the learning module uses artificial intelligence to improve its ability to adjudicate arrhythmias using physician-selected diagnoses.
The analysis module 216 further includes an adjudication processor 510, and episode processor 512 and an overwrite processor 514. In one embodiment, the adjudication processor is operatively connected to at least the episode database 402 and is configured to receive as input episode data regarding one of the different arrhythmia episodes. The adjudication processor uses an automated method or algorithm to generate characterization data about the arrhythmia episode. The characterization data, including an arrhythmia classification for each arrhythmia episode that is analyzed, is stored in the adjudication database 404.
The episode processor 512 performs processing of the adjudication database such as in order to provide reports, patient alerts, or programming recommendations. The overwrite processor 514 can analyze data provided from the episode database 402, the adjudication database 404, and other portions of the patient management system 200 to determine what particular portion of episode data for one of the arrhythmia episodes from the episode database should be displayed to a user. Overwrite processor 514 can, through the delivery module 218 described below, provide the means for graphically displaying a portion of data selected from arrhythmia episode data related to an arrhythmia episode of a patient, such as data generated by a data-generating device and stored in the episode database.
Overwrite processor 514 also requests from a user any changes in the characterization data determined by the adjudication processor, and can articulate the request for user input characterizing an arrhythmia episode. The request may be a direct question to a user, a series of choices provided to the user, or simply a blank space on the user interface configured to accommodate the user input. The overwrite processor 514 may also store the overwrite history for individual users.
One or more portions of the analysis module 216, such as the adjudication processor 510 and episode processor 512, may be located remotely from other parts of the patient management system 200.
Delivery module 218 coordinates the delivery of reports, patient alerts or programming recommendations based on the analysis performed by the host 212. For example, based on the data collected from the devices and analyzed by the host 212, the delivery module 218 can deliver information to the caregiver, user, or to the patient using, for example, a display provided on the external interface device 208. A user interface device 516 that is independent of a data-generating device may also be used to deliver information. The external interface device 208 and user interface device 516 are also configured, according to multiple embodiments, to display a report, alert, or programming recommendation, receive overwrite information from a user, and receive other data from the user. Displayed data, as described above, can be determined by the episode processor 512, overwrite processor 514 and delivery module 218.
External interface devices 208 to display information, such as programmer/recorder/monitors, can include components common to many computing devices. User interface devices 516 to display and received information from users can also include components common to many computing devices. Referring now to
In one embodiment, the external interface device includes a central processing unit (CPU) 805 or processor, which may include a conventional microprocessor, random access memory (RAM) 810 for temporary storage of information, and read only memory (ROM) 815 for permanent storage of information. A memory controller 820 is provided for controlling system RAM 810. A bus controller 825 is provided for controlling data bus 830, and an interrupt controller 835 is used for receiving and processing various interrupt signals from the other system components.
Mass storage can be provided by diskette drive 841, which is connected to bus 830 by controller 840, CD-ROM drive 846, which is connected to bus 830 by controller 845, and hard disk drive 851, which is connected to bus 830 by controller 850. User input to the programmer system may be provided by a number of devices. For example, a keyboard and mouse can connected to bus 830 by keyboard and mouse controller 855. DMA controller 860 is provided for performing direct memory access to system RAM 810. A visual display is generated by a video controller 865 or video output, which controls video display 870. The external system can also include a telemetry interface 890 or telemetry circuit which allows the external system to interface and exchange data with an implantable medical device. It will be appreciated that some embodiments may lack various elements illustrated in
Referring now to
The implantable device can include a microprocessor 948 (or processor) that communicates with a memory 946 via a bidirectional data bus. The memory 946 typically comprises ROM or RAM for program storage and RAM for data storage. The implantable device can be configured to execute various operations such as processing of signals and execution of methods as described herein. A telemetry interface 964 is also provided for communicating with an external unit, such as a programmer device or a patient management system.
The implantable device can include ventricular sensing and pacing channels comprising sensing amplifier 952, output circuit 954, and a ventricular channel interface 950 which communicates bidirectionally with a port of microprocessor 948. The ventricular sensing and pacing channel can be in communication with stimulation lead 930 and electrode 934. The implantable device can include atrial sensing and pacing channels comprising sensing amplifier 958, output circuit 960, and an atrial channel interface 956 which communicates bidirectionally with a port of microprocessor 948. The atrial sensing and pacing channel can be in communication with stimulation lead 928 and electrode 932. For each channel, the same lead and electrode can be used for both sensing and pacing. The channel interfaces 950 and 956 can include analog-to-digital converters for digitizing sensing signal inputs from the sensing amplifiers and registers which can be written to by the microprocessor in order to output pacing pulses, change the pacing pulse amplitude, and adjust the gain and threshold values for the sensing amplifiers.
It should be noted that, as used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the content clearly dictates otherwise. It should also be noted that the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
It should also be noted that, as used in this specification and the appended claims, the phrase “configured” describes a system, apparatus, or other structure that is constructed or configured to perform a particular task or adopt a particular configuration. The phrase “configured” can be used interchangeably with other similar phrases such as “arranged”, “arranged and configured”, “constructed and arranged”, “constructed”, “manufactured and arranged”, and the like.
One of ordinary skill in the art will understand that the modules, circuitry, and methods shown and described herein with regard to various embodiments of the invention can be implemented using software, hardware, and combinations of software and hardware. As such, the illustrated and/or described modules and circuitry are intended to encompass software implementations, hardware implementations, and software and hardware implementations.
All publications and patent applications in this specification are indicative of the level of ordinary skill in the art to which this invention pertains. All publications and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated by reference.
This application is intended to cover adaptations or variations of the present subject matter. It is to be understood that the above description is intended to be illustrative, and not restrictive. The scope of the present subject matter should be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.
This application claims the benefit of U.S. Provisional Application No. 61/175,232, filed May 4, 2009, the content of which is herein incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61175232 | May 2009 | US |
