Patent Application
20200077929
Pulse oximeters have conventionally been used to measure the oxygen saturation of arterial blood continuously. To use the pulse oximeters, a probe is attached to the tip of a subject's finger or earlobe and both red and the probe applies infrared light having different wavelengths to the living body from the probe at given time intervals, and the oximeter calculates the oxygen saturation from the ratio between the RED and IR of light absorbance. In a typical case, the red light has a reference wavelength of 660 nm and the infrared light has a wavelength of 900 nm; two light-emitting diodes of these wavelengths and one photodiode for light reception may be contained in the probe.
Although fetal heart monitors can be used as a surrogate means to attempt to measure fetal blood oxygen saturation levels, this method is indirect, and thus does not give a fully complete understanding of the fetal status. As a result of this lack of full understanding, emergency medical decisions, such as when to start an emergency caesarean section (C-section) must be made with incomplete knowledge. As a practical matter, doctors sometimes err on the side of caution, which may result in unnecessary C-sections, and the attendant high medical expenses and maternal post-childbirth complications.
Previous attempts to provide this missing fetal blood oxygen saturation levels include the OxiFirst system, produced by Mallinckrodt/Nellcor, now part of Tyco Healthcare. This system, which obtained FDA approval in 2000, works by directly placing the tip of a pulse oximeter sensor up the maternal birth canal, through the cervix, into the uterus and onto the cheek or temple of the fetus. This method is described in U.S. Pat. Nos. 5,813,980; 5,109,849, 4,938,218 which are incorporated by reference as if fully set forth herein. Unfortunately, due to the high invasiveness and bother of the procedure, the method met with limited medical acceptance in the field, and the manufacturer eventually decided to stop selling the device.
U.S. Pat. No. 5,135,006, which is incorporated by reference as if fully set forth herein, shows a method and apparatus for monitoring the fetus in a birth canal during labor. This fetal monitor probe monitors heartbeat and does not directly measure the blood oxygenation.
U.S. Pat. No. 10,415,163, which is incorporated by reference as if fully set forth herein, is based on similar pulse oximetry principal for non-invasive monitoring of fetal blood oxygenation by directing light at the abdomen of a pregnant woman, and detecting light scattered and reflected by fetal and maternal tissues back to the surface of the mother's abdomen. It may not be as accurate because of the distance between the probe and the fetus during delivery.
U.S. Pat. No. 7,469,158, which is incorporated by reference as if fully set forth herein, is also based on similar pulse oximetry principal for non-invasive monitoring of fetal blood oxygenation but requires it to be screwed in the scalp. It presents a more invasive technology than is desirable.
U.S. Pat. No. 8,417,307, which is incorporated by reference as if fully set forth herein, relates to a transmissive type blood oximeter for measuring the oxygenation, but it cannot be used in case of fetal measurements.
Thus, there exists a need for a less invasive, accurate, pulse oximeter with a probe that can accurately and safely measure arterial oxygen saturation of a fetus.
During childbirth process, trauma to an infant can readily arise, ultimately resulting in fetal hypoxia, academia, and brain damage. Such unfavorable conditions can be prevented by measuring the fetus' blood-oxygen level and heart rate. Without a fetal pulse oximeters, blood oxygen level cannot be monitored non-invasively reliably, which reduces the chance for birth complications to be recognized in time. A noninvasive system to implement such goals and maximize the potential welfare of the fetus may include devices to measure oxygen saturation of hemoglobin (SpO2) that have been available for at least 50 years. Such a device may be an oxy probe that uses a trans-reflective method of SpO2 measurement where oxygen saturation data can be transmitted through wire, fiber optics, and or using a radio frequency link, fetal monitor data can be analyzed, compared to existing data base, and or transmitted via radio waves or internet.
The underling principal of operation is based on the red and infrared light absorption characteristics of oxygenated and deoxygenated hemoglobin. Oxygenated hemoglobin absorbs more infrared light and allows more red light to pass through. Deoxygenated (or reduced oxygen) hemoglobin absorbs more red light and allows more infrared light to pass through. Red light is in the 640-720 nm wavelength light band. Infrared light is in the 840-920 nm wavelength light band. The embodiment includes a cylindrical housing 100 having two different light sources 130a, 130b, collectively 130 (if a single source), that emit emitted light 127 and a detector or sensor 125 with an opaque partition 110 between sources and detector such a way that the detector 125 will see the reflected light 129 as shown in
In an alternate embodiment, the probe for measuring hemoglobin oxygenation may require two wavelength emitters, Red (640-720 nm) and IR (840-920). Thus, further emitters may be used in this instance using the same probe configuration in which two other wavelengths can be added. An optional feature for detecting proximity to a fetus may be integrated into the probe.
The SpO2 monitoring PROBE (called oxy probe herein) may include, as labeled:
100. Probe body or housing
105. Soft clear probe Tip
110. Probe optical divider
115. Probe wire
120. Integrated circuit IC or PC Board
125. Sensor/detector Chip
127. Emitted light.
129. Reflected or received light.
130
a, 130b. Light sources
130. LED Chips
135. Probe Connector
140. Emitter Cavity
145. Sensor Cavity
200. Fetus
As shown in
The oxy probe may be housed in a housing 100, with dimensions of approximately 0.5 inch in diameter and 2.2-inch-long. A top 0.5 inch of the probe may include the sensor 125, emitters 130 and optical insert 110. These are nominal dimensions and can vary based on requirements, but are chosen to minimize invasiveness to the pregnant woman. The optical divider 110 may be opaque and divide the tip 105 of the probe 100 in two compartments, maintaining the optical isolation between the emitter cavity 140 and sensor 145 cavity (compartments) such that the only way for light to pass between the compartments is through reflection off another surface. The tip of the probe 100 may have a clear, soft, flexible elastomeric material lens 105 that extends into the cavities 140, 145 in such a way as to act as a seal to prevent any fluids from entering the cavities 140, 145 (
This oxy probe 100 may accommodate additional sensors for monitoring other conditions of a patient, including an arterial hemoglobin oxygen saturation sensor. Most common pulse oximeters used in the hospitals are of transmittance type, whereas the emitters 130s. 130b are placed on one side and the light goes through the tissue to the sensor 125 on the opposite side of the tissue. Alternatively, the emitter 130 and sensor 125 components used in both cases may be similar, with the difference that in the reflective probe, the light reflected by the tissue is compared to light going through the tissue.
This oxy probe 100 may be used on any location on the body and it does not have to be pressed against the tissue, for example, close (<1.0 mm) contact with the surface renders accurate data. For monitoring a fetus 200, the oxy probe 100 may be applied through a dilated cervix. The oxy probe 100 may monitor the condition of a fetus 200 during the peripartum process, measuring fetal heart rate, arterial hemoglobin oxygen saturation, electrical activity of the heart, or a combination thereof, by touching the scalp of the fetus 200 (as shown in
The optical divider 110 may be made of an opaque material that prevents transmission of light reaching the sensor 125 compartment directly from the light source 130. The housing 100 of the probe may be made of a light reflecting color such as white.
The probe tip 105, as mentioned above, may be made of optically clear soft silicon or similar materials. This clear tip 105 enables the emitted light 127 from the light source 130 to reach fetal tissue with minimal loss and allows the light to reflect back as reflected light 129 to the sensor 125 efficiently. The tip 105 being soft, also seals the probe tip such that no fluids can reach the emitter 130 and sensor 125. The sealed probe 100 can function properly to obtain accurate readings even on wet surfaces as well as when completely immersed in a fluid.
The light source 130 can include two or more light emitting diodes (LED) configured to emit light at a selected wavelength. When including more emitters, additional emitters may include a third light emitter that emits an emitted light of 550 nm to 620 nm to enable detection of other tissue bio parameters.
The detector 135 may include one or more silicon photodiodes that produce current linearly proportional to the intensity of light striking it. The detector 135 can detect the absorption and/or scattering of the light from the tissue as well as the frequency of the light emitted from the light source 130.
Unlike conventional pulse oximeters, the devices described herein need not be in direct contact with the patient's skin in order to obtain an accurate, consistent reading also due to their being highly directional and having very high gain. As mentioned above, the oxy probe can be positioned 1 mm or less away from the skin surface and still obtain accurate oxygen saturation and heart beat readings. The probe need not be mechanically coupled to the body to obtain an accurate reading. Because the device need not be in direct contact with the skin and there is no need for mechanical coupling to a patient, the problems that can result including pressure point injuries, pressure necrosis, exsanguinations, discomfort, compression marks, erroneous measurements, infections and other issues caused by direct contact with a device can be avoided.
While the invention has been described with reference to the embodiments above, a person of ordinary skill in the art would understand that various changes or modifications may be made thereto without departing from the scope of the claims.
| Number | Date | Country | |
|---|---|---|---|
| 62718754 | Aug 2018 | US |
