|Publication number||US20070060808 A1|
|Application number||US 11/225,295|
|Publication date||15 Mar 2007|
|Filing date||12 Sep 2005|
|Priority date||12 Sep 2005|
|Also published as||US8260391, US8971979, US20100280344, US20120277560, WO2007033177A2, WO2007033177A3|
|Publication number||11225295, 225295, US 2007/0060808 A1, US 2007/060808 A1, US 20070060808 A1, US 20070060808A1, US 2007060808 A1, US 2007060808A1, US-A1-20070060808, US-A1-2007060808, US2007/0060808A1, US2007/060808A1, US20070060808 A1, US20070060808A1, US2007060808 A1, US2007060808A1|
|Original Assignee||Carine Hoarau|
|Export Citation||BiBTeX, EndNote, RefMan|
|Referenced by (10), Classifications (11), Legal Events (1)|
|External Links: USPTO, USPTO Assignment, Espacenet|
1. Field of the Invention
The present invention relates generally to medical devices and, more particularly, to sensors used for sensing physiological parameters of a patient.
2. Description of the Related Art
This section is intended to introduce the reader to various aspects of art that may be related to various aspects of the present invention, which are described and/or claimed below. This discussion is believed to be helpful in providing the reader with background information to facilitate a better understanding of the various aspects of the present invention. Accordingly, it should be understood that these statements are to be read in this light, and not as admissions of prior art
In the field of medicine, doctors often desire to monitor certain physiological characteristics of their patients. Accordingly, a wide variety of devices have been developed for monitoring many such physiological characteristics. Such devices provide doctors and other healthcare personnel with the information they need to provide the best possible healthcare for their patients. As a result, such monitoring devices have become an indispensable part of modern medicine.
One technique for monitoring certain physiological characteristics of a patient is commonly referred to as pulse oximetry, and the devices built based upon pulse oximetry techniques are commonly referred to as pulse oximeters. Pulse oximetry may be used to measure various blood flow characteristics, such as the blood-oxygen saturation of hemoglobin in arterial blood, the volume of individual blood pulsations supplying the tissue, and/or the rate of blood pulsations corresponding to each heartbeat of a patient. In fact, the “pulse” in pulse oximetry refers to the time varying amount of arterial blood in the tissue during each cardiac cycle.
Pulse oximeters typically utilize a non-invasive sensor that transmits light through a patient's tissue and that photoelectrically detects the absorption and/or scattering of the transmitted light in such tissue. One or more of the above physiological characteristics may then be calculated based upon the amount of light absorbed or scattered. More specifically, the light passed through the tissue is typically selected to be of one or more wavelengths that may be absorbed or scattered by the blood in an amount correlative to the amount of the blood constituent present in the blood. The amount of light absorbed and/or scattered may then be used to estimate the amount of blood constituent in the tissue using various algorithms.
Pulse oximetry readings depend on pulsation of blood through the tissue. Thus, any event that interferes with the ability of the sensor to detect that pulsation can cause variability in these measurements. Motion artifacts occur when a patient's movements cause interference in the signal detected by the sensor. Motion artifacts can also occur in response to outside forces acting on the sensor. For example, a patient may be jostled by healthcare workers in emergency room settings. The type of force acting on a sensor will determine the nature of the motion artifact.
Generally, sensors are vulnerable to motion artifacts when the optical distance, or path length, between a sensor's emitter and detector varies due to an undesired mechanical change in the conformation of the sensor while in use. The mechanical deformation of the sensor may be in the form of a compression of the sensor, causing a decrease in path length. Alternately, a sensor may flex or move in a manner that increases the distance between an emitter and detector, resulting in an increase in path length. In any case, variability in the optical path length due to motion can cause motion artifacts and obscure the desired pulse oximetry signal.
Certain aspects commensurate in scope with the originally claimed invention are set forth below. It should be understood that these aspects are presented merely to provide the reader with a brief summary of certain forms that the invention might take and that these aspects are not intended to limit the scope of the invention. Indeed, the invention may encompass a variety of aspects that may not be set forth below.
There is provided a sensor that includes a sensor body, and an emitter and a detector disposed on the sensor body. The sensor also includes a motion damping structure associated with the sensor body, whereby the motion damping structure is adapted to damp a force experienced by the sensor body.
There is also provided a pulse oximetry system that includes: a pulse oximetry monitor; and a pulse oximetry sensor adapted to be operatively coupled to the monitor. The sensor includes a sensor body, and an emitter and a detector disposed on the sensor body. The sensor also includes a motion damping structure associated with the sensor body, whereby the motion damping structure is adapted to damp a force experienced by the sensor body.
There is also provided a method of operating a sensor that includes damping a mechanical force affecting a sensor such that an effective force experienced by at least one of a emitter or a detector is less than the mechanical force.
There is also provided a method of manufacturing a sensor that includes providing a sensor body on which an emitter and a detector are disposed. The method also includes providing a motion damping structure disposed on the sensor body.
Advantages of the invention may become apparent upon reading the following detailed description and upon reference to the drawings in which:
One or more specific embodiments of the present invention will be described below. In an effort to provide a concise description of these embodiments, not all features of an actual implementation are described in the specification. It should be appreciated that in the development of any such actual implementation, as in any engineering or design project, numerous implementation-specific decisions must be made to achieve the developers' specific goals, such as compliance with system-related and business-related constraints, which may vary from one implementation to another. Moreover, it should be appreciated that such a development effort might be complex and time consuming, but would nevertheless be a routine undertaking of design, fabrication, and manufacture for those of ordinary skill having the benefit of this disclosure.
In accordance with the present technique, sensors for pulse oximetry or other applications utilizing spectrophotometry are provided that reduce motion artifacts by damping the effects of patient movement or outside forces. For example, sensors are provided that have various motion damping mechanisms adapted to reduce the effect of motion or outside forces on a pulse oximetry measurement.
Motion artifacts in pulse oximetry are often generated by the movement of the pulse oximetry sensor relative to the optically probed tissue, which is typically caused by patient movement. Because pulse oximetry is often used in settings where it is difficult to prevent patient motion, it is desirable to provide a mechanism for reducing the effects of motion on the pulse oximetry measurement. For example, a squeezing motion by a patient may mechanically deform a sensor, causing the sensor's emitter and detector to change position relative to one another, resulting in a motion artifact. The squeezing motion may be damped by converting the mechanical energy of patient movement into thermal energy by damping the force with an impact-absorbing fluid or solid, thus dissipating the force and reducing mechanical deformation of the sensor. The force of squeezing may be damped such that the effective force experienced by the sensor's emitter and/or detector is reduced, and the relative change in the position of the emitter relative to the detector is also reduced. Similarly, outsides forces, such as the mechanical force of an object pressing against a sensor, can be damped by absorbing the force such that the effective force experienced by the sensor components is reduced.
Mechanical forces, including those caused by translational and/or kinetic energy of an object, may be impeded by opposing forces. Specifically, as a force acts on a pulse oximetry sensor, it is opposed by the inertia of the sensor as well as the opposing force of a damper. The amplitude of the mechanical energy of movement is attenuated through energy lost to inertia and damping. For example, energy may be lost to viscous damping with a fluid, or by yielding or plastic straining of a damping material. Additionally, some energy will be converted to thermal energy through frictional forces.
Sensors are disclosed herein having a motion damping mechanism to reduce the effect of motion or outside forces on the measurements of physiological parameters, such as pulse oximetry measurements.
In other embodiments (not shown), the sensor 10A may have multiple dashpots 14 disposed on the sensor body 16 on the surface 24 that does not contact the sensor site of the patient's tissue during normal use. It may be advantageous to provide motion damping mechanisms on multiple sides of the sensor 10A, as it is difficult to predict the types of motion that the sensor 10A may experience. For example, dashpots 14 may be distributed on the sensor body 16 in locations directly opposing each other across the digit 12. Further, it should be understood that a dashpot 14 according to the present technique may be adapted to damp forces applied at various angles. The piston 18 may be adapted move through the fluid 22 at an angle that corresponds to the angle with which the force was applied.
In certain embodiments, a fluid may used to damp mechanical energy by other techniques. For reasons related to total sensor weight, it may be desirable to employ a lightweight motion damping device in conjunction with disposable sensors. For example,
In another embodiment, as shown in
It is also contemplated that a fluid may damp mechanical energy to reduce its direct action on an emitter 52 or a detector 54.
In another embodiment,
The fluid (e.g. fluid 22, fluid 34, fluid 46, fluid 60, or fluid 68) described in the above embodiments may be any suitable fluid with the appropriate rheological properties for damping mechanical energy, such as a viscoelastic fluid or gel. In certain embodiments, the fluid may be air or other gases and gas mixtures. In other embodiments, the fluid may be an oil or liquid, such as mineral oil. Other examples of suitable fluids include, but are not limited to, polyethylene glycol, liquid silicone, magnetorheological fluids, and polyurethane polymer gels. It is contemplated that the fluid may be a mixture of liquid and gas. In certain embodiments, it may be desirable employ a gas or gas mixture for reasons related to cost, manufacturing convenience, and total sensor weight. In situations where a sensor may be exposed to more extreme outside forces, it may be desirable to employ a viscoelastic oil, as oils generally provide more efficient damping than gases.
In certain embodiments, impact-absorbing solids and/or foams with viscoelastic properties may be appropriate for mechanical damping of motion to reduce motion artifacts in a pulse oximetry sensor. For example, a clip-style sensor 10F is illustrated in
A sensor, illustrated generically as a sensor 10, may be used in conjunction with a pulse oximetry monitor 76, as illustrated in
The sensor 10 includes an emitter 86 and a detector 88 that may be of any suitable type. For example, the emitter 86 may be one or more light emitting diodes adapted to transmit one or more wavelengths of light in the red to infrared range, and the detector 88 may be a photodetector selected to receive light in the range or ranges emitted from the emitter 86. For pulse oximetry applications using either transmission or reflectance type sensors the oxygen saturation of the patient's arterial blood may be determined using two or more wavelengths of light, most commonly red and near infrared wavelengths. Similarly, in other applications, a tissue water fraction (or other body fluid related metric) or a concentration of one or more biochemical components in an aqueous environment may be measured using two or more wavelengths of light, most commonly near infrared wavelengths between about 1,000 nm to about 2,500 nm. It should be understood that, as used herein, the term “light” may refer to one or more of infrared, visible, ultraviolet, or even X-ray electromagnetic radiation, and may also include any wavelength within the infrared, visible, ultraviolet, or X-ray spectra.
The emitter 86 and the detector 88 may be disposed on a sensor body 90, which may be made of any suitable material, such as plastic, foam, woven material, or paper. Alternatively, the emitter 86 and the detector 88 may be remotely located and optically coupled to the sensor 10 using optical fibers. In the depicted embodiments, the sensor 10 is coupled to a cable 78 that is responsible for transmitting electrical and/or optical signals to and from the emitter 86 and detector 88 of the sensor 10. The cable 78 may be permanently coupled to the sensor 10, or it may be removably coupled to the sensor 10—the latter alternative being more useful and cost efficient in situations where the sensor 10 is disposable.
The sensor 10 may be a “transmission type” sensor. Transmission type sensors include an emitter 86 and detector 88 that are typically placed on opposing sides of the sensor site. If the sensor site is a fingertip, for example, the sensor 10 is positioned over the patient's fingertip such that the emitter 86 and detector 88 lie on either side of the patient's nail bed. In other words, the sensor 10 is positioned so that the emitter 86 is located on the patient's fingernail and the detector 88 is located 180° opposite the emitter 86 on the patient's finger pad. During operation, the emitter 86 shines one or more wavelengths of light through the patient's fingertip and the light received by the detector 88 is processed to determine various physiological characteristics of the patient. In each of the embodiments discussed herein, it should be understood that the locations of the emitter 86 and the detector 88 may be exchanged. For example, the detector 88 may be located at the top of the finger and the emitter 86 may be located underneath the finger. In either arrangement, the sensor 10 will perform in substantially the same manner.
Reflectance type sensors generally operate under the same general principles as transmittance type sensors. However, reflectance type sensors include an emitter 86 and detector 88 that are typically placed on the same side of the sensor site. For example, a reflectance type sensor may be placed on a patient's fingertip or forehead such that the emitter 86 and detector 88 lie side-by-side. Reflectance type sensors detect light photons that are scattered back to the detector 88.
While the invention may be susceptible to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and have been described in detail herein. However, it should be understood that the invention is not intended to be limited to the particular forms disclosed. Indeed, the present techniques may not only be applied to measurements of blood oxygen saturation, but these techniques may also be utilized for the measurement and/or analysis of other blood constituents. For example, using the same, different, or additional wavelengths, the present techniques may be utilized for the measurement and/or analysis of carboxyhemoglobin, met-hemoglobin, total hemoglobin, intravascular dyes, and/or water content. Rather, the invention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the following appended claims.
|Citing Patent||Filing date||Publication date||Applicant||Title|
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|US7881762||30 Sep 2005||1 Feb 2011||Nellcor Puritan Bennett Llc||Clip-style medical sensor and technique for using the same|
|US7894869||9 Mar 2007||22 Feb 2011||Nellcor Puritan Bennett Llc||Multiple configuration medical sensor and technique for using the same|
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|WO2010073913A1 *||10 Dec 2009||1 Jul 2010||Konica Minolta Sensing, Inc.||Probe for measuring living body information|
|Cooperative Classification||A61B5/7207, A61B5/6826, A61B5/14552, A61B5/6838, Y10T29/49826|
|European Classification||A61B5/1455N2, A61B5/68B2J1, A61B5/68B3L, A61B5/72B2|
|12 Sep 2005||AS||Assignment|
Owner name: NELLCOR PURITAN BENNETT INCORPORATED, CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:HOARAU, CARINE;REEL/FRAME:016980/0699
Effective date: 20050902