The invention relates to a method of determining blood pressure and an apparatus for determining blood pressure. The invention is particularly directed to determining blood pressure at the superficial temporal artery.
The following discussion of the background to the invention is intended to facilitate an understanding of the present invention. However, it should be appreciated that the discussion is not an acknowledgment or admission that any of the material referred to was published, known or part of the common general knowledge in any jurisdiction as at the priority date of the application.
Blood pressure is commonly measured at arteries positioned in a patient's arm. Such measurements may be taken by invasive means or non-invasive means. Blood pressure measurements in the arteries of the brain are generally measured using invasive methods to determine the pressure at the Internal Carotid artery (CA), and Middle cerebral artery (MCA). This traditional invasive measurement provides early predicators of stroke and the chance of stroke reoccurrence, however due to the invasive nature of such measurements they are not routine tests. There are risks that blood will form a clot around the tip of the catheter, blocking the artery and making it necessary to operate to reopen the vessel. There is a remote risk of the catheter puncturing the artery causing internal bleeding. It is also possible that the catheter tip will separate material from the inner lining of the artery, causing a block downstream in the blood vessel.
Transcranial cardio Doppler TCCD is another method that provides assessment of blood flow velocities in the major cranial vessels using ultrasound techniques. However, the measurements obtained are of the blood movement through the artery. The Doppler must be correctly positioned to ensure there is movement in the direction of the ultrasound beam. Ambiguity in the Doppler signal known as aliasing can occur. This requires adjustments in the pulse repetition by a skilled operator and the pulse repetition frequency may be further constrained by the range of sample volume. Similarly there is a large amount of adjustment as to the frequency used, such adjustment requires a great amount of skill and experience. The choice of frequency is a compromise between better sensitivity to flow (higher frequencies) and better penetration (lower frequencies). The capability of ultrasound to penetrate bone to permit sampling of flow dynamics in the large intracranial vessels is inversely proportional to skull thickness. Thickening of the bone in stroke-age patients, however, may obviate detection.
Accordingly, it is an object of the present invention to determine the blood pressure of a patient at arteries within brain while ameliorating the problems of current devices and techniques.
Throughout this document, unless otherwise indicated to the contrary, the terms “comprising”, “consisting of”, and the like, are to be construed as non-exhaustive, or in other words, as meaning “including, but not limited to”.
An apparatus and method enables a reading of blood pressure of the brain at the superficial temporal artery to give an indication of blood related diseases. The apparatus is non-invasive. Preferably a reading of blood pressure of the brain is measured as a continuous beat to beat rate on both the left superficial temporal artery and the right superficial temporal artery simultaneously during the same heart beat. Where the waveform measured from the left temporal artery differs from the wave form measured from the right temporal artery this may be an indication of an impending stroke or an indication that a stroke has recently happened. Further the indices of the wave forms may be used as a clinical indication of other blood related diseases
The invention will now be described, by way of example only, with reference to the accompanying drawings, in which:
In accordance with a first embodiment of the invention referring to
Components of the sensor 12 according to the preferred embodiment are similar to those discussed in patent application WO/2002/030277 which is incorporated herewith by reference. The sensor 12 according to the preferred embodiment includes a transducer, which produces a voltage output according to pressure changes acting on its diaphragm. A plunger 16 is affixed next to the diaphragm of the transducer. The plunger 16 and sensor 12 of the current system is build to a smaller scale that that disclosed in WO/2002/030277 to negotiate the constraints of the proximity of the superficial temporal artery to the pinna of the ear. It is important that the plunger 16 is able to be positioned such that applanation pressure can be exerted on the superficial temporal artery to allow measurement of a waveform.
The plunger 16 is a specially designed hemispherical component made of a rigid material. In the preferred embodiment the plunger 16 is made of a molded polymer plastic which is biocompatible. The hemispherical surface of the plunger 16 is adapted to push onto the superficial temporal artery of a subject and partially occludes the superficial temporal artery. The base of the plunger 16 housed within the sensor covers the surface of the diaphragm and is in direct contact with the diaphragm.
There is a layer of gel between the diaphragm and the plunger 16 to filter out interference and sharp changes due to unnatural movement. It also dampens the noise ratio. The plunger depth is specially designed such that on most normal heads, it could occlude not more than half the diameter of the superficial temporal artery 102 when the head band 14 is comfortably worn. This will enable full and faithful transmission of the arterial pulsation to be picked up, including the expansion of the arterial walls, the turbulence of the flow and the vibration transmitted along the artery wall from the heart.
As the plunger 16 and the diaphragm are the only moving units at each pulsation, the arterial pressure is accurately picked up as a waveform as each heart beat reaches the superficial temporal artery. For a change in pressure between 0 mmHg-300 mmHg, the displacement of the diaphragm against the pressure variation forms a linear relationship. The range of voltage change in the sensor for such an equation is between 0.5V to 4V, after amplification of the signal. The hemispherical plunger 16 allows for faithful transmission of a continuous beat to bead measurement of the wave form of each heart beat.
Referring to
Preferably, the linking piece 22 is cylindrical with fine threads 24 that can be screwed into an aperture 26 within one end of the head band 14. The aperture contains tracts to facilitate fine movement of the linking piece 22 into and out of the aperture 26.
Each pressure sensor 12 also is connected to a data and control cable 28. As shown in
In this manner, the overall visual impact of the apparatus 10 is similar to that of a pair of conventional headphones. The pressure sensors 12 may have padding for the comfort of the wearer
The apparatus 10 will now be described with reference to its intended use.
Referring to
The internal location of the superficial temporal artery is depicted in
Following appropriate positioning of the apparatus 10, each sensor 12a, 12b sends its blood pressure measurement signals to a processing station 104 via their respective cables 28a, 28b.
On receipt of the various signals, the processing station 104 separates the measurement data according to the sensor 12 that produced the data.
In the final adjustment the output for both the left superficial temporal artery 102a and the right superficial temporal artery 102b in ADC units is zeroed or leveled. This is achieved by adjusting the fine tuning of the plunger against the superficial temporal artery 102 by turning the linking piece 22 into and out of the aperture 26 at the end of the head band 14. It is important that the applanation pressure on the artery is equalized between both the left superficial temporal artery and the right superficial temporal artery to ensure that any variations between the waveforms measured on both sides is not due to a variation in the applanation pressure. Once the device is secured in position the measurement is quite constant and can be taken over a long time with the wearer being in almost any position.
The main aortic artery branches into the left and right common carotid artery A these arteries branch further into two internal carotid arteries C and two external carotid arteries B. The left common carotid artery A branches into the left internal carotid artery C and the left external carotid artery B. Similarly the right common carotid artery A branches into the right internal carotid artery C and the right external carotid artery B. Due to this branching any narrowing or blockages of the arteries will affect blood flow which will be reflected in the waveform measured at the superficial temporal artery. Medical procedures are often limited to arteries in one side of the brain. Similarly problems related to narrowing of the arteries, blockages or other complications may be in one branch eg: in the left internal carotid artery. Measuring and comparing both sides of the main cranial arteries can be used to assess the adequacy of cerebral circulation and blood pressure in the arteries from both sides of the brain.
For example in neonates with extracorporeal membrane oxygenation there is sometimes a need for right common carotid reconstruction that would benefit from monitoring blood pressure in both right and left side arteries. Similarly in high risk stroke cases differences between the blood pressure in the right and the left side arteries using the apparatus 10 provides a non invasive method of detecting obstructive lesions of the arteries or aneurisms that generally only occur in arteries on one rather than both sides of the brain. Such monitoring can be beneficial in people who have never had a stroke or in monitoring post stroke patients. As the measurement is non-invasive which is less risky than invasive methods, the apparatus 10 can be used to monitor a much larger group.
Blood pressure monitoring with the apparatus 10 can be conducted over a long time frame while the person carries out their normal daily activities and recorded so that the data can be passed to a medical practitioner for further analysis.
It should be appreciated by the person skilled in the art that the above invention is not limited to the embodiment described. In particular, the following modifications and improvements may be made without departing from the scope of the present invention:
Number | Date | Country | Kind |
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200808179-6 | Nov 2008 | SG | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/SG2009/000395 | 10/27/2009 | WO | 00 | 5/4/2011 |