EP0222870A1

EP0222870A1 - A pacemaker featuring a paraphysiological, circadian operating characteristic

Info

Publication number: EP0222870A1
Application number: EP86903542A
Authority: EP
Inventors: Gino Grassi; Paolo Marconi
Original assignee: Individual
Current assignee: Individual
Priority date: 1985-06-05
Filing date: 1986-05-26
Publication date: 1987-05-27
Also published as: WO1986007270A1; IT8503457A0; IT1202151B

Abstract

Stimulateur cardiaque pourvu d'un dispositif (1) qui fait varier la fréquence émise par un circuit d'horloge (2) exploitant une fonction qui simule autant que possible la variation circadienne naturelle des battements de coeur, prenant ainsi en considération le comportement biorythmique du corps. Ladite fonction peut prendre la forme d'une onde sinusoïdale couvrant une prériode de 24 heures et dont la phase est telle qu'elle présente une amplitude maximum entre 14 et 16 heures et une amplitude minimum entre 2 et 4 heures.Pacemaker provided with a device (1) which varies the frequency emitted by a clock circuit (2) exploiting a function which simulates as much as possible the natural circadian variation of heartbeats, thus taking into account the biorhythmic behavior of the body. Said function can take the form of a sine wave covering a period of 24 hours and the phase of which is such that it has a maximum amplitude between 14 and 16 hours and a minimum amplitude between 2 and 4 hours.

Description

A pacemaker featuring a paraphysiological, circadian operating characteristic^

The invention described relates to a pacemaker in which paraphysiological operation is produced by virtue of the circadian design principle adopted. Extensive observation at experimental and clinical level has by now established the existence of a cir¬ cadian regularity in the heart's natural pacemaking system, traceable to the sinoatrial node. More recently, observation has also confirmed that a circadian rhythm persists in heartbeat even in the event of total atrioventricular stoppage. Circadian rhythm is also manifest in variations of the normal atrioventricular sequence.

Even in transplant situations, the heart of a donor will retain circadian rhythm in its beat notwith¬ standing the absence of sympathetic connections. The regular, natural pacemaking characteristic of the heart can undergo circadian variation resulting from disturbances such as a concentration of hydro- cortisone and catecholamine, electrolytic changes, and above all, direct influence from the nervous system.

Whatever the age bracket into which a given subject may fall, dynamic ECG (Holter) will show a circadian variation in rhythm of the heartbeat, regardless of whether the subject suffers from a heart condition or is 100% fit.

From the trends observed in monitoring heartbeat, it can be deduced, on average, that minimum levels are registered between 02.00 and 06.00 hours, whereas maximum levels occur between 14.00 and 16.00 hours. Dynamic ECG recordings are such that a curve may be plotted to represent heartbeat in the form of a sine wave covering the 24-hour circadian period. It would not appear, from, data furnished by literat¬ ure currently available, that variation in heartbeat bears any relation either to age, in subjects of be¬ tween 16 and 65 years of age, or to sex. Available data would seem to suggest, however, that the female sex registers a generally higher average heartbeat rate than does the male sex.

In the light of the chronobiological modulation thus produced in conjunction with alternating sleep and wakefulness, and with vital bodily functions, the object of the invention described herein is that of embodying a pacemaker that will permit of producing a circadian rhythm in heartbeat exogenously, and of ensuring that the circadian variation produced is commensurate with the overall pattern of endogenous biorhythmic factors normally influencing heartbeat, physical exercise excluded.

There are several models of pacemaker commercially available, in effect, that are not synchronized with spontaneous physiological atrial activity, such act¬ ivity being either non-existent, or unreliable. At all events, conventional pacemakers are designed to generate a minimum number of beats per minute, beneath which the rate must not drop. Minimum bpm is fixed in VVI types, and is program- mable at preset levels in externally controlled VVIM types. In DVI , VDD and DDD types, the disappearance or significant weakening of the atrial signal is compensated by emission of a fixed, preset bpm by the pulse generator; in this instance, however, bpm neither follows nor takes account of bioryhthm. The same disadvantage occurs with those types of pace¬ maker which vary heartbeat according to biological or metabolic parameters such as pH value, temperat¬ ure and breathing; heartbeat is varied only when the individual expends physical or mental effort, whilst minimum bpm remains a fixed quantity that does not adapt to chronobiological requirements. Recent work in the field shows that a fixed minimum (conventionally 60...70bpm) can constitute a hazard to the individual, especially during the night when reduced biological activity would dictate a lower heartbeat rate^'; this is particularly the case in patients suffering from disease of the sinoatrial node . The invention as described and claimed herein over¬ comes the drawbacks aforementioned, setting forth a pacemaker which not only is sensitive to triggered physiological change, such as would be produced by physical effort, but also responds to biorhythmic variation in the state of the individual. One of the advantages obtained with a pacemaker ac¬ cording to the invention consists in the fact that it can be embodied simply by connection of a sine wave pulse ^'generator to the input of the clock of a conventional pacemaker; the signal produced by such a device, covering a 24 hour period and variable in amplitude, will thus be integrated with that of the cloc.k generator. The invention will now be described in detail by way of example, with the aid of the accompanying sheets of graphs and diagrams, in which: fig 1 shows the natural curve traced by chronobio- logically induced circadian variation in heartbeat; fig 2 shows the stimulus curve, produced by a pace- maker according to the invention, relating solely to chronobiologically induced circadian variation in heartbeat ; fig 3 is the block diagram illustrating a pacemaker according to the invention; fig 4 is a detailed block diagram of the block de¬ noted 1 in fig 3; fig 5 is the block diagram of a programmable pace¬ maker according to the invention. The pacemaker disclosed is suitable for all current methods of producing cardiac stimulus, and is defin¬ able as paraphysiological, inasmuch as it takes ac¬ count of circadian rhythm in an individual's heart¬ beat. According to the invention, embodiment of a circuit that will reproduce the periodic, circadian type of variation encountered in heartbeat, is made possible by virtue of the fact that such variation can be considered as a sine wave (fig 1).

Fig 3 is a basic block diagram of the pacemaker as described herein, which implements one of the simpl¬ est of cardiac stimulus methods, namely VVI and AAI , that is, ventricular or auricular 'on demand' . The pacemaker stimulates the ventricle (or the auricle) , and is inhibited whenever the muscular depolarizat¬ ion signal, amplified by the block denoted 5, rises above the preset bpm dictated by a clock generator 2 and divider 3.

In a circadian pacemaker according to the invention, use is made of a VC0 (voltage controlled oscillator) the clock frequency of which can be varied by appli¬ cation of a voltage. In pacemakers of sophisticated design, therefore, the input stage of the clock 2 may be in receipt of a signal representing variation in biological or metabolic parameters (pH value, or breathing &c.) from the block denoted 11. The sine wave signal, with its period of 24 hours, will thus vary the beats per minute between preset maximum and minimum levels, which are dictated by the sine wave generated by block 1 and the clock frequency emitted by block 2. Phase of the sine wave is adjusted such as to respond to the normal chronological conditions illustrated in the graph of fig 1.

An example of the method of producing a signal with periodic time of 24 hours is given in fig 4, which illustrates a digital generator. The circuit of fig 4 utilizes digital filter techno¬ logy, and produces a frequency F that is- tied to the clock frequency 6 by the formula: (F = Rn F ), where F is the clock frequency 6 and n is the number of divider stages 7 utilized in the counter 18.

The network of resistances denoted R , R , ... R

1 2 n-1 is calculated utilizing the formula:

where k = 1, 2, ... n-1 Data given by way of example relates to a counter 18 (see fig 4) incorporating ten divider stages; clock frequency would be F = 20 F with F = l/86400Hz. The clock frequency may be produced by a quartz type generator giving a period of 4.12msec, and utilizing a 20-stage binary divider.

Resistances R would be geared to R , and calculated n 1 as follows:

R = 1 . 9R ; R „ = 2 . 618R : R „ = 3 . 07R ; R _^ = 3 . 23R : 2 1 3 1 4 1 5 1 R 4„; R7-, = R3„; R8₀ = R2-.; R_Λ9 = R„1 The curve of the resulting sine wave will not appear continuous, but as a series of steps (fig 2) corres¬ ponding to the number of divider stages incorporated into the system; thus, the greater the value of n, the smaller the steps will become. The curve illustrated reflects the example described above, where for each 24h/2n interval one produces a variation in bpm of (F - F . )/n, plus or minus max mm according to phase. With a periodic amplitude variation range of 20bpm and using ten stages, a variation of 2 beats every 72 minutes will be produced.

The option exists of employing an active integrating amplifier 10 to smooth out the steps and obtain more gradual variation. However, adopting a counter 18 in which 'n' is much higher, say, 30 stages, the steps would become so shallow that an individual would re¬ main unaware of the variation in heartbeat between one step and the next.

Still referring to fig 4, the block denoted 9 ampli¬ fies and adjusts the sine wave of fig 2 in order to vary amplitude commensurately with the physiological characteristics of the individual.

It will be noted that the circuit in question can be integrated without difficulty adopting CMOS techno¬ logy, by virtue of its digital operation. Whilst the sine wave illustrated in fig 2 provides a sufficiently accurate approximation of the circadian rhythm in heartbeat, the effective curve can be ap¬ proached yet further by varying the value of the re¬ sistances R , which may be achieved by calculation, n where a mathematical equation representing the curve is made available, or by experimenting with the re¬ sistance settings on a trial-and-error basis. The device thus embodied permits of engineering cir¬ cadian rhythm exogenously adopting paraphysiological criteria simulative of natural bio-rhythm, and may be fitted to any type of pacemaker to the end of en¬ suring that an acceptable bpm is generated. Fig 5 illustrates a development of fig 3,^* in which one has the standard programming options fo'r cardiac stimulus parameters as already featured in program¬ mable pacemakers: mean bpm is varied by the block denoted 14, and pulse width by the block denoted 15; amplitude of the signal fed into the circuit 20 pro¬ ducing the output pulses is varied by the block de¬ noted 16; a block denoted 17 alters the sensitivity threshold. In addition, one has integration of the parameters which take account of circadian rhythm by incorporation of a device as in fig 4, signifying programming facilities governing start of the sine wave phase, via block 12, mean bpm (F - F )/2, max min via block 14, and the maximum permissible variation

(F - F . ) , via block 13. max min

The implanted pacemaker can be programmed utilizing any of the methods currently employed; moreover, the identification code can remain the same as those al¬ ready in use. Bpm can be programmed by way of the pacemaker's VC0 , and maximum permissible variation between F and max

F set by adjusting amplitude of the sine wave signal applied to the VC0 trigger.

Phase can be adjusted at the moment of implanting a pacemaker according to the invention, for instance, by accelerating the clock frequency 6 (fig 4) until coincident with the value dictated by the sine wave at that particular instant.

Claims

1) A pacemaker, characterized in that it comprises a device (1) designed to vary the clock frequecy of the pacemaking signal according to a function simul¬ ative of the natural circadian rhythm in heartbeat.

2) A pacemaker, comprising a clock pulse generator and characterized in that it comprises a device (1) de¬ signed to supply a signal to the input of the clock circuit (2) that is variable according to a function simulative of the natural circadian rhythm in heart¬ beat.

3) A pacemaker as in claim 2, wherein the clock circuit (2) is a voltage controlled oscillator, and a volt¬ age signal supplied by the device (1) is integrated with the signal produced by the clock circuit (2).

4) A pacemaker as in claim 3, wherein the output signal produced by the device (1) varies by distinct steps.

5) A pacemaker as in claim 4, wherein the device (1) is embodied as a digital pulse generator comprising a clock circuit (6), a signal divider (18) the stages (7) of which correspond in number to the steps that separate any two consecutive peaks of the output signal, and an amplifier (9) designed to permit of varying amplitude of the output signal generated by the device (1) . 6) A pacemaker as in claim 5, wherein the device (1) further comprises an integrating amplifier (10) the purpose of which is to attenuate the discontinuous effect of stepped variation in the output signal pro¬ duced by the device (1), thereby investing it with sinusoidal waveform.

7) A programmable pacemaker as in claim 3, wherein the output signal produced by the device (1) is program¬ mable at the outset in respect both of the mean bpm generated and of its permissible variation.