Using MV to classify patient cardiac condition in an implanted device

BACKGROUND OF THE INVENTION

A. Field of Invention

0001This invention pertains to a cardiac implant wherein a metabolic demand parameter, and more particularly, long term variations in this parameter, are used to classify the cardiac condition of the patient into one of five categories, said categories being defined by the New York Heart Association.

B. Background of the Invention

0002In the early days, pacemakers and defibrillators were implanted only for patients with chronic heart disease. Moreover, implanting these devices was thought to be a major, complicated procedure. In recent times, however, the cost of these devices has dropped and the clinicians are performing their implantation so often that the procedure has become routine, rather than a complicated risky procedure. One result of this has been that today a pacemaker or defibrillator device may be frequently <i>used</i> as a precaution even if the patient does exhibit signs of mere cardiac rhythm irregularity which is much less severe than chronic heart disease.

0003Cardiac patients are classified as belonging as one of five classes rated in increasing severity from 0 to 4 based on specific criteria set forth by the New York Heart Association. This classification is normally based on the ability of a patient to do certain types of exercise, and is related to the maximum oxygen consumption of the patient during said exercises. The standard method of obtaining data for classifying a patient therefore is to have the patient perform various exercises at the clinician's office. The clinician monitors various metabolic functions of the patient during these exercises, such as, for example, his oxygen consumption. After the exercise is completed, the physician assigns a classification for the patient, based on standard statistical information for the patient and his sex, weight, age, and so on, with "0" indicating a healthy patient, "1" indicating a mildly impaired patient, and so on. Thus, a patient is placed one of class 0-4. A disadvantage of this old approach is that it can be performed only in a hospital, or a clinician's office, to the inconvenience of the patient.

0004A further problem with present classifying means and method is that the peak oxygen consumption for Class 0 and Class 1 patients is very close and therefore it is difficult to differentiate between these two conditions reliably and accurately.

0005The present invention discloses an apparatus which uses a metabolic parameter monitored by an implanted pacemaker to perform the cardiac classification of the patient. By this means, the classification can be performed and updated automatically without the clinician being present and without the patient being in the clinician's office. Moreover, the classification may be used in the pacemaker itself to alter its programming.

OBJECTIVES AND SUMMARY OF THE INVENTION

0006An objective of the present invention is to provide a pacemaker in which a metabolic demand parameter is used as an indicia of cardiac condition of a patient.

0007A further objective is to provide an implantable pacemaker with an integral cardiac condition classifier used to determine the level or degree of congestive heart failure in a patient.

0008Yet a further objective is to provide a device for classifying the cardiac condition of a patient which is more convenient than the prior art use of oxygen consumption.

0009Other objectives and advantages of embodiments of the invention shall become apparent from the following description. As mentioned above, the condition of patients with congestive heart failure or cardiac impairment, is related to and is normally classified by their oxygen consumption during peak exercise levels. However, this same parameter, i.e., oxygen consumption is also related to certain metabolic demand parameters indicative of the hemodynamic demand during the exercise. One such parameter particularly suited for the present application is the minute volume. Typically, minute volume is obtained by measuring the transthoracic impedance measured across the pulmonary cavity during at least one complete breathing cycle.

0010More particularly, two values of interest are the peak MV, that is, the minute volume during peak exercise, and the rest MV, i.e., the value of MV during rest periods. Embodiment of the present invention may take advantage of the fact that the ratio of these two values can be used as an accurate indicia of the patient's condition.

0011In addition to MV, other physiological parameters may also be used to determine the classification of the patient. These parameters may include the QT interval or cardiac contractibility.

0012In accordance with the present invention,there is provided a pacemaker as defined in claim 1.

0013Briefly, a rate responsive pacemaker constructed in accordance with an embodiment of the present invention includes an intrinsic sensor for sensing intrinsic events, a pace generator for generating pacing pulses on demand and a controller for generating commands for the pace generator. The pacemaker further includes a physiological demand sensor for sensing the metabolic demand of the patient. This demand is converted into a corresponding metabolic indicated pacing parameter, such as a pacing rate or pacing interval. This parameter and the sensed event are used by the controller to generate the pacing commands.

0014In addition, the pacemaker also includes an analyzer for analyzing the physiological demand. More particularly, this demand is monitored for a period of weeks and months to determine the levels of the physiological demand corresponding to various levels of physical activity. The variation in these levels is indicative of the classification of the degree of congestive heart failure in the patient. More specifically, the maximum and rest minute volume levels are determined and the ratio of these levels is used to generate a minute volume indicia. A preselected chart is then used to convert this indicia into a standard classification of the patient's congestive heart failure, said classification ranging from 0 for substantially no cardiac deficiency to a maximum of IV.

0015This ratio can also be used to limit the MAX rate allowed for the patient. Very low ratio indicates low MAX rate.

0016Once this classification is derived, it may be stored in a memory for downloading into a programmer in the future. In addition, the classification may be used by the controller to optimize the pacing regime for the pacemaker. In this manner, the pacemaker is automatically adapted to the level of CHF of the patient

BRIEF DESCRIPTION OF THE DRAWINGS

0017<ul id="ul0001" list-style="none" compact="compact"><li>Figure 1 shows a block diagram of a pacemaker constructed in accordance with an embodiment of this invention;</li><li>Figure 2 shows details of a classifier circuit for the pacemaker of Figure 1;</li><li>Figure 2a shows typical heart rates at rest for patients of class 0-IV;</li><li>Figure 2b shows typical heart rates at peak exercise for patients at class 0-IV;</li><li>Figure 2c shows incremental increase in heart rate from rest to peak exercise for patients of class 0-IV;</li><li>Figure 3 shows graphically typical maximum oxygen consumption values of patients with different degrees of CHF;</li><li>Figure 4 shows graphically typical peak minute volume values of patients with various degrees of CHF;</li><li>Figure 5 shows graphically typical average minute volume values of patients with various degrees of CHF; and</li><li>Figure 6 shows graphically expected values for the minute volume indicia generated by the circuit of Figure 2 for patients with various degrees of CHF.</li></ul>

DETAILED DESCRIPTION OF THE INVENTION

0018Referring first to Figure 1, a pacemaker 10 constructed in accordance with an embodiment of the present invention includes a cardiac sensor 12 for sensing intrinsic cardiac events and generating in response to cardiac sense signals. The pacemaker 10 further includes an impedance detector 14 for measuring the transthoracic impedance of the patient during at least one breathing cycle.

0019The impedance measured by detector 14 is converted into a minute volume by MV converter 16. It should be understood that other parameters may be used as well, such as the QT interval. The minute volume MV is used as metabolic demand parameter. This MV parameter is fed to a mapping circuit 18 which uses an RRF (rate response function) to generate in response to said MV parameter a metabolic indicated pacing parameter (MIP). This parameter MIP is fed to a state machine 20. The state machine 20 uses a preprogrammed set of rules to generate pacing commands on demand in response to the MIP parameter from mapping circuit 18 and the sensed signals from cardiac sensor 12. These commands are provided to a pacing generator 22 which in response generates pacing pulses. (For the sake of simplicity a single chamber operation is described, it being understood that normally pacemaker 10 operates in a dual chamber mode such as DDD or DDDR). A typical set of rules for the state machine for a DDDR mode is described in U.S. Patent No. 5,441,523.

0020Importantly, the pacemaker 10 further includes a metabolic parameter analyzer 24 which analyzes the MV parameter to generate an MV indicia (MVI). This indicia is provided to a classifier 26 which generates a patient classification PC corresponding to the MVI.

0021As shown in more detail in Figure 2, the metabolic parameter analyzer 24 includes a comparator 30, a timer 32 and an accumulator 34. The analyzer further includes another accumulator 36 and an averager 38. The operation of the analyzer 24 is now described.

0022Figures 2a-2c show that, as the severity of CHF increases, the difference between the intrinsic heart rate from rest and peak exercise level decreases drastically.

0023The New York Heart Association defines CHF in terms of peak or maximum oxygen consumption during exercise, as shown in Figure 3. As can be seen from this Figure, oxygen consumption falls drastically from Class 0 (no heart problem) to Class IV (severe CHF). Importantly, a similar graph for the maximum minute volume shown in Figure 4 shows a very similar trend from Class 0 to Class IV. This comparison thus supports the validity of the basic premise of the invention, that is, that the heart condition of a patient may be determined from a physiological demand parameter such as the MV parameter. A further observation to be made, is that, as discussed above, and shown in Figures 2a, 2b, and 5, heart rate and the MV parameter at rest actually increases from patients with no cardiac problems (Class 0) to patients in Class IV. As a result, the ratio of the MV max to MV rest decreases drastically from about 10 for Class 0 to about 2 for Class IV. This phenomenon is exploited by the presented invention as follows.

0024Referring to Figure 2, the value of MV is sampled at regular intervals and stored in accumulator 36. This accumulator 36 accumulates the value of MV over a predetermined time period, such as, for example, a month. The value thus stored is averaged by an averager 38. Since everyone is most of the time at rest, the output of the average 38 is the MVavr value for the patient at rest. MVav (which is identical to the MV at rest) is shown in Figure 5 for patients of various heart conditions.

0025The value MVav and the sampled MV is also fed to comparator 30. Comparator 30 is used to detect a rise in the instantaneous value of MV The output of comparator 30 is fed to a 30 sec. timer 32 used to insure that a particular high MV episode lasts long enough to be considered a true rise and not just a transient phenomenon. If the timer finds that the MV stays high long enough, the high MV is fed to accumulator 34. This accumulator has the same time constant as the accumulator 36. Its output corresponds to the maximum MV (MVmax) for the patient, as charted in Figure 4.

0026The two values, MVav and MVmax are fed to a divider 40 which divides, for example, MVmax by MVav. It is expected that the resultant ratio r may normally range from 1 to 12 or more. Another comparator 42 is used to insure that the ratio r does not exceed a preset threshold value, such as 15. If r is excessive, then it may be due to some anomaly and is ignored. However, if it is lower than 15, then an indicia MVI is generated which is equal to r. In other words:<maths id="math0001" num=""><math display="block"><mrow><mtext>For r≤15,MVI=r;</mtext></mrow></math><img file="EP0804939B1_D0001.tif" /></maths><maths id="math0002" num=""><math display="block"><mrow><mtext>For r>15,MVI=0.</mtext></mrow></math><img file="EP0804939B1_D0002.tif" /></maths>

0027Returning to Figure 1, the indicia MVI is fed to a classifier 26. The classifier 26 may be, for example, a look-up table. The classifier then uses the MVI indicia to assign to classification for the patient One set of definitions for this purpose is illustrated in Figure 6. According to this Figure, the classification of a patient PC is defined as follows: <tables id="tabl0001" num="0001"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row rowsep="1"><entry namest="col1" nameend="col1" align="center"><b>MVI</b></entry><entry namest="col2" nameend="col2" align="center"><b>CLASSIFICATION (PC)</b></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="center">>10</entry><entry namest="col2" nameend="col2" align="center">0</entry></row><row><entry namest="col1" nameend="col1" align="center">6-10</entry><entry namest="col2" nameend="col2" align="center">I</entry></row><row><entry namest="col1" nameend="col1" align="center">4-6</entry><entry namest="col2" nameend="col2" align="center">II</entry></row><row><entry namest="col1" nameend="col1" align="center">3-4</entry><entry namest="col2" nameend="col2" align="center">III</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="center"><3</entry><entry namest="col2" nameend="col2" align="center">IV</entry></row></tbody></tgroup></table></tables>

0028This classification PC is stored in a memory 28 for data logging, and later, downloading to a programmer. Optionally, this patient classification may also be provided to the state machine which in response may device to change its pacing rates. For example, one of the parameters used to derive an optimal pacing regime is the peak allowable pacing rate. Traditionally, an age-predicted heart rate is used for this maximum level using the formula:<maths id="math0003" num=""><math display="block"><mrow><mtext>Pacing rate (max) = 220-age (beats/minute).</mtext></mrow></math><img file="EP0804939B1_D0003.tif" /></maths>

0029In the present invention. this formula is modified as:<maths id="math0004" num=""><math display="block"><mrow><mtext>Pacing rate (max) = 220-age- K (beats/minute)</mtext></mrow></math><img file="EP0804939B1_D0004.tif" /></maths>    where K = 6 (10-MVI).

0030In the above description, the physiological characteristic used to determine the indicia was minute volume. Other physiological parameters may also be used, such as QT interval or cardiac contractility, and so on.

0031Although the invention has been described with reference to several particular embodiments, it is to be understood that these embodiments are merely illustrative of the application of the principles of the invention. Accordingly, the embodiments described in particular should be considered exemplary, not limiting, with respect to the following claims.