United States Patent 5601611
Link to this page http://www.wikipatents.com/5601611.html
Inventor(s) Fayram; Timothy A. (Gilroy, CA);
Benedict; George J. (Santa Cruz, CA)
Abstract A cardiac blood flow sensor includes a light source and a photodetector
within a housing. The light source projects a beam through a fiber optic
line having a first end optically connected to the housing and a distal
tip positioned within the patient's heart. Light intermittently reflected
off the moving blood cells is transmitted back through the optic line to
the detector, which generates a varying signal proportional to the
reflected light, and thus proportional to the blood flow rate within the
heart. The flow sensor may be contained in a common housing with a
defibrillator that is implanted in a patient. The sensor may remain
inactive until a potentially unhealthy heart beat rate is detected, upon
which the light source is activated. The defibrillator may be activated
only if the flow sensor has detected a blood flow rate below a
predetermined level.
Title Information
Drawing from US Patent 5601611
Optical blood flow measurement apparatus and method and implantable
defibrillator incorporating same
Publication Date
February 11, 1997
Filing Date
August 5, 1994
Title Information
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Claims
While the invention is described in terms of a preferred embodiment, the
claims are not intended to be so limited:
1. An optical blood flow measurement apparatus comprising:
a housing having a port for transmitting light between the housing interior
and exterior;
a light source within the housing and in optical communication with the
port, such that at least a portion of light emitted by the light source is
transmitted along a first beam path between the light source and the port;
a photodetector having an electrical output, the photodetector being
responsive to the intensity of light impinging on the detector, the
photodetector being positioned within the housing and in optical
communication with the port, such that at least a portion of light
entering the port from outside the housing is transmitted along a second
beam path between the port and the detector to impinge on the detector;
a processor connected to the photodetector's electrical output for
providing a blood flow measurement output; and
a flexible elongated light conduit having a first end optically connected
to the housing port, and a light transmissive distal tip for placement at
a site of flowing blood, such that light from the light source is
transmitted through the conduit, out of the distal tip, and such that at
least a portion of any reflected light is received by the distal tip, and
transmitted to the detector to generate a signal;
whereby light is directed from the light source to the light transmissive
tip and into the blood flow and a portion of the light is reflected back
to the distal tip and a portion of the reflected light is transmitted to
the detector to generate a signal indicative of the blood flow.
2. The apparatus of claim 1 wherein the conduit comprises a fiber optic
line.
3. The apparatus of claim 1 wherein at least a portion of the conduit is
enclosed by a biocompatible sheath.
4. The apparatus of claim 1 including a lens connected to the distal tip of
the conduit.
5. The apparatus of claim 4 wherein the focus lens is a diverging lens.
6. The apparatus of claim 1 including a beam splitter within the housing
and within the first and second beam paths, such that portions of the beam
paths are coextensive with each other between the beam splitter and the
port, and are separate from each other adjacent the respective light
source and photodetector.
7. An optical blood flow measurement apparatus comprising:
a housing having a port for transmitting light between the housing interior
and exterior;
a light source within the housing and in optical communication with the
port, such that at least a portion of light emitted by the light source is
transmitted along a first beam path between the light source and the port;
a photodetector having an electrical output the photodetector being
responsive to the intensity of light impinging on the detector, the
photodetector being positioned within the housing and in optical
communication with the port, such that at least a portion of light
entering the port from outside the housing is transmitted along a second
beam path between the port and the detector to impinge on the detector;
a processor connected to the photodetector's electrical output for
providing a blood flow measurement output, wherein the processor includes
means for calculating a blood flow rate;
a flexible elongated light conduit having a first end optically connected
to the housing port, and a light transmissive distal tip for placement at
a site of flowing blood, such that light from the light source is
transmitted through the conduit, out of the distal tip, and such that at
least a portion of any reflected light is received by the distal tip, and
transmitted to the detector to generate a signal;
whereby light is directed from the light source to the light transmissive
tip and into the blood flow and a portion of the light is reflected back
to the distal tip and a portion of the reflected light is transmitted to
the detector to generate a signal indicative of the blood flow.
8. An implantable defibrillator including an optical blood flow measurement
apparatus, said measurement apparatus comprising:
a housing having a port for transmitting light between the housing interior
and exterior;
a light source within the housing and in optical communication with the
port, such that at least a portion of light emitted by the light source is
transmitted along a first beam path between the light source and the port;
a photodetector having an electrical output, the photodetector being
responsive to the intensity of light impinging on the detector, the
photodetector being positioned within the housing and in optical
communication with the port, such that at least a portion of light
entering the port from outside the housing is transmitted along a second
beam path between the port and the detector to impinge on the detector;
a processor connected to the photodetector's electrical output for
providing a blood flow measurement output;
a flexible elongated light conduit having a first end optically connected
to the housing port, and a light transmissive distal tip for placement at
a site of flowing blood, such that light from the light source is
transmitted through the conduit, out of the distal tip, and such that at
least a portion of any reflected light is received by the distal tip, and
transmitted to the detector to generate a signal;
whereby light is directed from the light source to the light transmissive
tip and into the blood flow and a portion of the light is reflected back
to the distal tip and a portion of the reflected light is transmitted to
the detector to generate a signal indicative to the blood flow; and
whereby at least a first portion of the defibrillator is contained within
the housing and operably connected to the processor, said processor
including means to detect a blood flow rate from said reflected light, the
defibrillator further including means for detecting a cardiac arrhythmia
and means for delivering a therapy in response thereto, the means for
detecting a cardiac arrhythmia being responsive to the detected blood flow
rate signal from the processor, such that operation of the means for
delivering is dependent on the detected blood flow rate.
9. The defibrillator of claim 8 wherein said means for detecting a cardiac
arrhythmia includes a heart rate sensor coupled to said processor to
provide an indication of said arrhythmia based on a sensed heart rate.
10. A method of measuring blood flow in the blood stream of a patient, the
method comprising the steps:
generating light;
transmitting the light through a flexible conduit having a distal tip
immersed in the patient's blood stream;
projecting the light from the conduit onto blood cells within the blood
stream;
receiving at the distal tip of the conduit reflected light from the cells;
transmitting the reflected light through the conduit to a photodetector;
generating an electrical signal in response to the reflected light
intensity;
analyzing the electrical signal to determine the blood flow rate whereby
the blood flow rate provides an indication of the hemodynamic performance
of the patient's heart.
11. A method of measuring blood flow in the blood stream of a patient, the
method comprising the steps:
generating light;
transmitting the light through a flexible conduit having a distal tip
immersed in the patient's blood stream;
projecting the light from the conduit onto blood cells within the blood
stream and diverging the light within the blood stream such that the light
may reflect off blood cells;
receiving at the distal tip of the conduit reflected light from the cells;
transmitting the reflected light through the conduit to a photodetector;
generating an electrical signal in response to the reflected light
intensity;
analyzing the electrical signal to determine the blood flow rate whereby
the blood flow rate provides an indication of the hemodynamic performance
of the patient's heart.
12. The method of claim 10 and further including the step of inserting the
distal tip into a chamber of the patient's heart and wherein the step of
projecting the light includes projecting the light within the patient's
heart.
Claims
Description
FIELD OF THE INVENTION
This invention relates to apparatus and method for measurement of fluid
flow, and more particularly to measurement of blood flow.
BACKGROUND AND SUMMARY OF THE INVENTION
The human heart may suffer from two classes of rhythmic disorders or
arrhythmias: Bradycardia and tachyarrhythmia. Bradycardia occurs when the
heart beats too slowly, and may be treated by a common pacemaker
delivering low voltage (about 1 V) pacing pulses. Of concern here is
tachyarrhythmia, which involves an abnormally high heart rate between
about 100 to 200 beats per minute, but without hemodynamic or blood flow
efficiency. Of particular concern is a ventricular tachycardia, in which
the ventricles have not completely filled before they contract, thus
diminishing the volume of blood pumped. The pumping inefficiency is
generally proportional to the heart rate. A severe form of tachyarrythmia
is fibrillation, which occurs at heart rates of 180 to 300 beats per
minute, and involves erratic, disorganized beating that pumps virtually no
blood.
Implantable cardioverters/defibrillators (ICD) or pulse generators are used
for antitachycardia pacing to correct rapid heart rates by delivering a
rapid sequence of pacing pulses of 1 to 10 volts to break the arrhythmia.
ICD devices treat severe tachycardia with cardioversion, by delivering a
shock of 100 to 750 volts synchronously with the peak of the heart's
R-wave signal as detected by an electrocardiogram (ECG). Heart
fibrillation receives similar therapy, but the erratic ECG signal may not
provide a clear R-wave peak for synchronization.
Normally, the spacing between successive R-wave peaks is used to determine
the heart rate. Extremely high or irregular heart rates clearly require
therapy. Moderately elevated heart rates may be of ambiguous origin,
either from healthy exercise, or from the disorders discussed above. To
distinguish between these causes, treatment techniques have included
measurement of blood pressure, oxygen saturation, Doppler ultrasound
parameters, and ECG morphology. These techniques have limited accuracy and
practicality, particularly outside of a clinical setting.
The present invention avoids the limitations of existing techniques and
devices by providing a cardiac blood flow sensor that measures blood flow
within the heart. The apparatus includes a light source and a
photodetector within an implanted housing. The light source projects a
beam through a flexible elongated light conduit having a first end
optically connected to the housing and a distal tip positioned within the
patient's heart. Light reflected off the moving blood cells is transmitted
back through the conduit to the detector, which generates a varying signal
proportional to the reflected light, and proportional to the blood flow
rate within the heart. The flow rate may then be used to determine whether
a tachycardia is physiologic or pathologic in origin.
The flow sensor may be contained in a common housing with a defibrillator
that is implanted in a patient. The sensor may remain inactive until a
potentially unhealthy heart beat rate is detected, upon which the light
source is activated. The defibrillator may be activated only if the flow
sensor has detected a blood flow rate below a predetermined level.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is an anterior view of a patient implanted with a preferred
embodiment of the invention.
FIG. 2 is a schematic view of the embodiment of FIG. 1.
FIG. 3 is an enlarged view of the embodiment of FIG. 1.
DETAILED DESCRIPTION OF A PREFERRED EMBODIMENT
FIG. 1 shows an Implantable Cardioverter/Defibrillator (ICD) and flow
sensor unit 10, including a single housing 12 and a flexible fiber optic
line 14. The optic line serves as a light conduit extending from the
housing, and terminates at a distal tip 16. The entire unit 10 is
implanted in a patient 20, with the housing 12 located in the patient's
pectoral or abdominal region. The optic line 14 extends from the housing
to an incision 21 in the patient's subclavian vein 22. The optic line 14
passes through the incision, and extends downwardly through the vein into
the heart 24, with the distal tip 16 positioned within the right ventricle
26. The line may be secured to a wall of the right ventricle with the
distal tip extending away from the wall. This configuration provides a
viewing angle which is more likely perpendicular to the direction of blood
flow 25, and may thereby improve the efficiency of the system. A
sensing/pacing lead 27 extends from the housing 12 into the ventricle 26,
and is secured to the apex of the right ventricle using tines or a screw
tip. Surgical implantation may be achieved by encasing the line 14 in a
semi-rigid hollow catheter, which may be inserted transvenously. The
catheter is removed after the line is positioned.
FIG. 2 shows the ICD and flow sensor unit 10. A laser 28 emits a beam of
polarized light along a first beam path 30, through a collimating lens 32
that generates a beam of parallel rays. The beam then passes through a
polarization sensitive beam splitter 38, which transmits the polarized and
collimated laser beam. The transmitted beam encounters a concentrating
lens 40. A first end 39 of the optic line 14 is positioned at the focal
point of the lens 40, so that the parallel rays of the beam are focused
into the core of the optic line 14. The beam is then transmitted through
the line toward the line's distal tip 16.
FIG. 3 shows the optical details of the distal tip 16 of the optic line 14.
The optic line 14 includes a sheath 41 formed of silicone or other
biocompatible material to permit long term use in the blood stream. A
divergent lens 42 is positioned over the terminus 44 of the line 14 so
that light transmitted through the line is intercepted by the lens 42. The
lens preferably has a negatively curved surface that diverges the
generally parallel rays emitted by the optic line. Alternatively, the lens
may have a positive curvature that focuses the generally parallel rays
emitted by the optic line to a focal point.
Because the distal tip 16 of the optic line 14 is immersed in blood, the
light transmitted through the diverging lens is intermittently reflected
off the suspended blood cells 50 passing closely in front of the lens. As
a blood cell moves past the diverging lens 42, the amount of reflected
light will momentarily increase substantially. With the vast number of
cells normally passing by the focal point 48 and generating intermittent
reflections, the reflected beam will have a rapidly varying optical signal
corresponding to the volume of blood flow. Normal blood flow is estimated
to result in a frequency of about 500 kHz, with tachyarrythmia resulting a
lower frequency. An absolute blood flow rate is not necessary for a
determination of whether to apply therapy; only a determination that the
flow rate has undergone a significant relative drop is needed. The
frequency threshold for therapy may be set at a level well below the
normal frequency as determined for a patient of particular
characteristics.
A portion of the reflected light is received by the diverging lens 42, and
is transmitted back up the optic line 14 to the housing 12. The light
reflected off the hemispherical blood cells will lose its polarization.
Returning to FIG. 2, the intermittent reflected light re-enters the housing
12, and is collimated by lens 40 so that it follows a reflected beam path
54. The reflected beam encounters the beam splitter 38, which reflects 50
percent of the reflected beam perpendicularly from the beam splitter.
After leaving the beam splitter, the reflected beam passes through a
filter 56 that selectively transmits the wavelength emitted by the laser,
reducing optical crosstalk from any stray light of other frequencies. In
an alternative embodiment, the filter 56 is omitted. The reflected beam
then passes through a lens 58, which focuses the light onto a fast silicon
photodetector 60, which generates a varying electrical signal
corresponding to the intensity of the intermittent incident light.
The photodetector has an electrical output line 62 that carries the varying
signal. A processor 66 is connected to line 62, and processes the varying
signal from the photodetector to estimate the blood flow within the
ventricle, or to determine if there has been a significant drop in the
frequency of the reflected light. The processor is electrically connected
to conventional ICD circuitry 70, which provides cardiac therapy by
selectably applying a voltage to the connected electrode sensing/pacing
lead 27, or to a defibrillation lead electrode(not shown). The lead 27 is
capable of sensing the heart rate and providing Brady pacing or
antitachycardia pacing. An additional return electrode (not shown)
providing a "ground" for the high voltage shocks may be placed in the
superior vena cava, or may use the housing of a pectorally implanted
device. The therapy provided by the defibrillator is not necessarily a
defibrillation shock, but is frequently antitachycardia pacing or a
cardioversion shock. The defibrillator includes a heart rate sensor (not
shown) that permits activation of the flow sensor light source 28 only
when the heart rate exceeds a rate that may be problematic. The device may
be programmed to provide therapy only if the flow sensor processor 66
indicates a blood flow below the preselected rate.
The processor 66 or ICD circuitry 70 may also be programmed to apply
therapy in response to the satisfaction of more complex conditions. A
complex function of the heart rate, measured flow rate, characteristics of
the patient, and other interacting variables may be used to determine when
therapy is indicated.
In the preferred embodiment, the light source may be provided by a solid
state laser diode emitting polarized light at a 830 nm or 615 nm
wavelength. Alternatives such as light emitting diodes, or other
conventional sources may be used. While coherent light is useful for
analyzing the motion of extended objects by detecting the reflected
pattern variations, and may be usefully employed herein, the illustrated
embodiment may use incoherent light to detect microscopic objects that
intermittently interrupt the beam. The use of the term light is not
intended to limit the invention to visible wavelengths; a wider range of
wavelengths may be used. The distal tip lens 42 is preferably formed of or
coated with a material formulated to prevent an accumulation of platelets
from obscuring the lens. One suitable coating is Parylene C.TM., from
Specialty Coating Systems of Indianapolis, Ind. A coating thickness of 2
um and coefficient of friction of 0.05 to 0.10 is preferred. The optic
line is preferably a single mode 5 to 10 micron type having a diffuse tip,
although other types may be employed.
In the secondary embodiment employing a converging lens at the distal tip,
a large, non-single mode core fiber optic line having a functional
diameter of 0.5-1.0 mm may be used. The light source may be an LED or a
laser diode, with a focusing lens being required in conjunction with an
LED to concentrate the light onto the fiber. For proper focusing at the
distal tip, an air gap should be provided between the end of the optic
line and the lens. The focused spot size formed will be on the order of
the diameter of the optic line, with a depth of focus approximately twice
the optic line diameter. Thus, the spot will encompass numerous blood
cells at any one time. Therefore, a lower signal-to-noise ratio is
expected with a converging lens than with the preferred diverging lens.
* * * * *
Description