The present disclosure relates generally to various examination and diagnostic tools for examination of female human patients. In particular, examination of a female's cervix and/or uterus. For example, legacy uterus sounds are probe type instruments that are used to measure the length and direction of, and/or to dilate, the cervix and/or uterus of the female patient. As another example, legacy probes are to measure depth from body fluid markings on the probes or using additional non-sterile instruments to mark depth.
Known instruments and probes are not entirely satisfactory for the range of applications in which they are employed. Such uterine examinations, also referred to as uterine sounding, may require the use of multiple different sounds and probes. Use of multiple different sounds and/or probes may result in longer examination periods, discomfort to the female patients, and/or may even cause tissue damage. Accordingly, there is a need in the art to provide an improved apparatus and method to conduct examination of the cervix and/or uterus of a female patient
Thus, there exists a need for widgets that improve upon and advance the design of known widgets. Examples of new and useful widgets relevant to the needs existing in the field are discussed below.
The present disclosure is directed to a uterine thermochromic probe comprising a probe handle, a probe head, and a probe body comprising a thermochromic material, wherein the probe body couples the probe handle to the probe head. In some examples, the probe body tapers from a wide end at the probe handle to a narrow end at the probe head. In some further examples, the uterine thermochromic probe is formed from a continuous piece of thermochromic material.
The disclosed uterine thermochromic probes will become better understood through review of the following detailed description in conjunction with the figures. The detailed description and figures provide merely examples of the various inventions described herein. Those skilled in the art will understand that the disclosed examples may be varied, modified, and altered without departing from the scope of the inventions described herein. Many variations are contemplated for different applications and design considerations; however, for the sake of brevity, each and every contemplated variation is not individually described in the following detailed description.
Throughout the following detailed description, examples of various uterine thermochromic probes are provided. Related features in the examples may be identical, similar, or dissimilar in different examples. For the sake of brevity, related features will not be redundantly explained in each example. Instead, the use of related feature names will cue the reader that the feature with a related feature name may be similar to the related feature in an example explained previously. Features specific to a given example will be described in that particular example. The reader should understand that a given feature need not be the same or similar to the specific portrayal of a related feature in any given figure or example.
The following definitions apply herein, unless otherwise indicated.
“Substantially” means to be more-or-less conforming to the particular dimension, range, shape, concept, or other aspect modified by the term, such that a feature or component need not conform exactly. For example, a “substantially cylindrical” object means that the object resembles a cylinder, but may have one or more deviations from a true cylinder.
“Comprising,” “including,” and “having” (and conjugations thereof) are used interchangeably to mean including but not necessarily limited to, and are open-ended terms not intended to exclude additional elements or method steps not expressly recited.
Terms such as “first”, “second”, and “third” are used to distinguish or identify various members of a group, or the like, and are not intended to denote a serial, chronological, or numerical limitation.
“Coupled” means connected, either permanently or releasably, whether directly or indirectly through intervening components.
“Communicatively coupled” means that an electronic device exchanges information with another electronic device, either wirelessly or with a wire-based connector, whether directly or indirectly through a communication network.
“Controllably coupled” means that an electronic device controls operation of another electronic device.
Apparatus and Method for a Uterine Thermochromic Probe
With reference to the figures, uterine thermochromic probes will now be described. The uterine thermochromic probes discussed herein function to provide information from an examination of a female's cervix and/or uterus. For example, the tactile sensations felt by the medical practitioner while using the uterine thermochromic probes allows the medical practitioner to sense various anatomical characteristics of the examined cervix and/or uterus. The uterine thermochromic probes color changes in response to the patient's body temperature, allowing the medical practitioner to more accurately measure a location of interest within the uterus of the female patient. The medical practitioner may visually see the location of the color transition on the uterine thermochromic probes after examination, and then visually determined a length and direction of the patient's cervix and/or uterus by inspecting measurement indicators on the uterine thermochromic probes. The uterine thermochromic probes may also be used to dilate patient's cervix and/or uterus.
The reader will appreciate from the figures and description below that the presently disclosed uterine thermochromic probes address many of the shortcomings of conventional uterine instruments and probes. For example, the uterine thermochromic probes provide information that only multiple conventional instruments and/or probes. Utilizing a single probe reduces examination periods, discomfort to the female patients, and/or may reduce tissue damage.
Uterine Thermochromic Probe
With reference to
The various embodiments of the uterine thermochromic probe 100 employ a thermochromic material that changes color when the temperature of the thermochromic material reaches or exceeds a threshold temperature. In a preferred embodiment, the threshold temperature is greater than the ambient air temperature typically encountered in an examination room (or a temperature that might be encountered while the uterine thermochromic probe 100 is in transport to the examination room). Preferably, the threshold temperature is less that the normal body temperature of the female patient who is undergoing an examination. In an example embodiment, the threshold temperature of the thermochromic material is approximately thirty-one degrees (31°) Celsius (87.8° Fahrenheit). Any suitable thermochromic material may be used in the various embodiments. Further, any suitable threshold temperature, or threshold temperature range, may be defined by the selected thermochromic material in the various embodiments. In an example embodiment, the threshold temperature range is thirty degrees (30°) to forty degrees (40°) Celsius.
In practice, the medical practitioner may have many uterine thermochromic probes 100 of different lengths and sizes to facilitate examination of different ages and/or sizes of female patients. Further, a plurality of different uterine thermochromic probes 100 may be used to measure different parts of the cervix and/or uterus of a particular female patient. Each uterine thermochromic probe 100, when withdrawn, accurately indicates the depth of the uterine thermochromic probe 100 into a particular part of the cervix and/or uterus of the female patient. After noting the insertion lengths based on visual inspection of the location of the color change and the measurement indicators 108, the uterine thermochromic probe 100 may be discarded into a suitable container.
In some embodiments, as shown in
In another example, a larger uterine thermochromic probe 100 comprises the following dimensions. The first section 118 increases in diameter from four (4) millimeters (mm) at the first diameter 110 to seven (7) millimeters (mm) at the second diameter 112. The second section 120 continues to increase in diameter from seven (7) millimeters (mm) at the second diameter 112 to nine (9) millimeters (mm) at the third diameter 114. The third section 122 continues to increase in diameter from nine (9) millimeters (mm) at the third diameter 114 to ten (10) millimeters (mm) at the fourth diameter 116.
In some examples, the uterine thermochromic probe may be sterilized and saved for re-use if the thermochromic material of the probe body 104 changes back to its original color. Alternatively, embodiments that employ a cover or strip of thermochromic material that is removably secured to the probe body 104 can be reused by removing the used thermochromic material, performing a sterilization of the uterine thermochromic probe 100, and then securing new thermochromic material to the uterine thermochromic probe 100.
Probe Handle 102
As can be seen in
The medical practitioner conducting the examination will experience tactile sensations in the probe handle 102, which are communicated from the probe body 104 and/or the probe head 106 back to the probe handle 102. The tactile sensations felt by the medical practitioner allow the medical practitioner to sense various anatomical characteristics of the examined cervix and/or uterus of the patient.
Probe Body 104
In the example shown in
The melting point of the solvent defines the threshold temperature at which the thermochromic material changes color. In response to the thermochromic material reaching or exceeding the threshold temperature, the solvent causes the color developer to change the color of the thermochromic material. Any suitable color may be used for the former color and the color developer so long as the difference between the colors are significantly different so as to enable the medical practitioner to visually identify the location of the transition between the former color and the color developer.
In other embodiments, other parts of, or all of, the uterine thermochromic probe 100 are made of the thermochromic material. In some embodiments, the probe body 104 is covered in a layer or coating of the thermochromic material. In some embodiments, a cover or strip of thermochromic material may be removably secured to the probe body 104 to facilitate later reuse of the uterine thermochromic probe 100.
Preferably, the probe body 104 is made of a semi-rigid, yet flexible, material. The flexible probe body 104 facilitates movement and passage of the probe head 106 of the uterine thermochromic probe 100 into and through the cervix and/or uterus of the female patient during an examination. The medical practitioner conducting the examination will experience tactile sensations in the probe handle 102, which are communicated from the probe body 104 and/or the probe head 106 back to the probe handle 102. The tactile sensations felt by the medical practitioner allows the medical practitioner to sense various anatomical characteristics of the examined cervix and/or uterus.
Probe Head 106
In the example shown in
The shape of the probe head 106 and the flexibility of the probe body 104 are designed to minimize the possibility of wall perforation and tissue damage in the cervix and uterus of the female patient, and to facilitate the tactile sensation experienced by the medical practitioner during an examination. Because the probe body 104 changes color in response to the patient's body temperature, the medical practitioner can more accurately measure a location of interest within the uterus of the female patient. The medical practitioner may visually see the location of the color transition on the probe body 104 after removal of the uterine thermochromic probe 100 from the uterus, and then visually determined the length by inspecting the measurement indicators 108 on the probe body 104 (See
Plurality of Measurement Indicators 108
In the example shown in
Color Change
The disclosure above encompasses multiple distinct inventions with independent utility. While each of these inventions has been disclosed in a particular form, the specific embodiments disclosed and illustrated above are not to be considered in a limiting sense as numerous variations are possible. The subject matter of the inventions includes all novel and non-obvious combinations and subcombinations of the various elements, features, functions and/or properties disclosed above and inherent to those skilled in the art pertaining to such inventions. Where the disclosure or subsequently filed claims recite “a” element, “a first” element, or any such equivalent term, the disclosure or claims should be understood to incorporate one or more such elements, neither requiring nor excluding two or more such elements.
Applicant(s) reserves the right to submit claims directed to combinations and subcombinations of the disclosed inventions that are believed to be novel and non-obvious. Inventions embodied in other combinations and subcombinations of features, functions, elements and/or properties may be claimed through amendment of those claims or presentation of new claims in the present application or in a related application. Such amended or new claims, whether they are directed to the same invention or a different invention and whether they are different, broader, narrower or equal in scope to the original claims, are to be considered within the subject matter of the inventions described herein.
This application claims priority to copending U.S. Application, Ser. No. 63/071,577, filed on Aug. 28, 2020, which is hereby incorporated by reference for all purposes.
Number | Date | Country | |
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63071577 | Aug 2020 | US |