The present invention relates to a dual lumen fiber optic medical infusion line. In particular, a dual lumen fiber optic medical infusion line, wherein a first lumen is configured to receive a fiber optic cable or line and the second lumen is configured to allow transmission of medical fluids and a method of manufacture thereof.
The present disclosure relates generally to systems, apparatuses, and methods for improving the administration of medical infusion utilizing advanced sensor assemblies and leveraging computational intelligence to improve patient care and reduce practitioner cognitive load. Medical infusion serves to administer medications, fluids, nutrients, solutions, and other materials intravenously to a patient. Patients are often administered medical infusion using intravenous infusion tubing or lines (‘IVT’). Such intravenous infusion tubing generally consists of flexible, polymer tubing connected at one end to a fluid source and at another end to a needle or port assembly that provides access to a blood vessel of a patient. It is not uncommon for many infusion tubes, each connected to a different source of fluid (medical infusion pump), to be used simultaneously to deliver several medications at once to a single patient. It is also not uncommon for the needles or port assemblies to be located adjacent to one another, such as multiple adjacent needles, providing access into the brachial vein running through the arm of the patient.
Distinguishing between multiple infusion tubes is a difficult task, and medication delivery error as a result of improperly distinguishing one infusion tube from another is a serious problem in current infusion systems. The confusion of one infusion tube from another is one of the leading causes of preventable medication error. It is potentially life-threatening and is a serious and ongoing concern and cost to medical facilities. Distinguishing between multiple infusion lines is a difficult task that is placed in an atmosphere of high stress and rapid timing. The medical industry refers to the atmosphere as placing a high cognitive load on practitioners. This high cognitive load can lead to medication delivery error as a result of improperly distinguishing one medical infusion line from another. Arguably, the confusion of one medical infusion line from another is one of the leading causes of preventable medication error.
As a result of the difficulties in distinguishing between multiple medical infusion lines and their associated fluid sources and outputs, as well as the potentially life-threatening possibilities that can occur if incompatible medications are injected through the same medical infusion line, there is a need for accurate identification of medical infusion lines. Thus, the problem solved is addressed with material science, computational engineering, and new systems and methods for manufacturing and installing illuminating medical infusion lines. These systems and methods improve upon current practices by including electronic illuminators with side scattering fiber optics to facilitate illumination, detection, and verification of medical infusion lines. Further, the systems and methods herein are engineered to equip and rapidly deploy lifesaving medical infusion identification.
Aspects of systems and methods for manufacturing, preparing, and installing illuminated medical infusion lines are disclosed. In one aspect a dual lumen fiber optic medical infusion line is disclosed. The dual lumen fiber optic medical infusion line is comprised of a first elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a first lumen extending throughout the entire length of the first elongate body, the first elongate body is a hollow structure defined by a first sidewall extending circumferentially about the first elongate body having an exterior surface and an interior surface. The dual lumen fiber optic medical infusion line is further comprised of a second elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a second lumen extending throughout the entire length of the second elongate body, the second elongate body is a hollow structure defined by a second sidewall extending circumferentially about the second elongate body having an exterior surface and an interior surface, the exterior surface of the second elongate body is engaged to the exterior surface of the first elongate body. The fiber optic cable having a proximal end and a distal end disposed within the first lumen of the first elongate body. Further, the fiber distal end cap engaged to the distal end of the fiber optic cable.
Implementations may include one or more of the following features. In one aspect, a dual lumen fiber optic medical infusion line is disclosed. The dual lumen fiber optic medical infusion line comprising a first elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a first lumen extending throughout the entire length of the first elongate body, the first elongate body is a hollow structure defined by a first sidewall extending circumferentially about the first elongate body having an exterior surface and an interior surface. The dual lumen fiber optic medical infusion line further comprising a second elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a second lumen extending throughout the entire length of the second elongate body, the second elongate body is a hollow structure defined by a second sidewall extending circumferentially about the second elongate body having an exterior surface and an interior surface; the exterior surface of the second elongate body is engaged to the exterior surface of the first elongate body. Further, a fiber optic cable having a proximal end and a distal end, the fiber optic cable is disposed within the first lumen of the first elongate body. Wherein the proximal end extends outward from the proximal end of the first elongate body and the distal end extends outward from the distal end of the first elongate body, the proximal end of the fiber optic cable and the distal end of the fiber optic cable are not circumferentially surrounded by the first sidewall. A distal end cap engaged to the distal end of the fiber optic cable. A fiber funnel cap engaged to the proximal end of the fiber optic cable.
Further implementations may include one or more of the following features. In one aspect, a method of manufacturing a dual lumen fiber optic medical infusion line is disclosed. The method includes providing a fiber optic cable. Next, extruding a dual lumen fiber optic medical infusion line from a polymeric material, the dual lumen fiber optic medical infusion line comprising: (a) a first elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a first lumen extending throughout the entire length of the first elongate body, the first elongate body is a hollow structure defined by a first sidewall extending circumferentially about the first elongate body having an exterior surface and an interior surface; (b) a second elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a second lumen extending throughout the entire length of the second elongate body, the second elongate body is a hollow structure defined by a second sidewall extending circumferentially about the second elongate body having an exterior surface and an interior surface; the exterior surface of the second elongate body is engaged to the exterior surface of the first elongate body. Then, preparing a distal end cap and preparing a fiber funnel cap. Then feeding a fiber optic cable through the first elongate body and attaching the distal end cap to the distal end of the fiber optic cable. Lastly, attaching the fiber funnel cap to the proximal end of the fiber optic cable.
Many aspects of the present disclosure will be better understood with reference to the following drawings. The components in the drawings are not necessarily to scale, with emphasis instead being placed upon clearly illustrating the principles of the disclosure. Moreover, in the drawings, like reference numerals designate corresponding parts throughout the several views. It should be recognized that these implementations and embodiments are merely illustrative of the principles of the present disclosure. Therefore, in the drawings:
The presently disclosed subject matter now will be described more fully hereinafter with reference to the accompanying drawings, in which some, but not all embodiments of the presently disclosed subject matter are shown. Like numbers refer to like elements throughout. The presently disclosed subject matter may be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will satisfy applicable legal requirements. Indeed, many modifications and other embodiments of the presently disclosed subject matter set forth herein will come to mind to one skilled in the art to which the presently disclosed subject matter pertains having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is to be understood that the presently disclosed subject matter is not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims.
Throughout this specification and the claims, the terms “fiber optic cable,” “fiber optic line,” and “fiber optic” are used to mean a side scattering or side emitting or side glow fiber optic cable, wherein light or illumination is purposefully emitted as it traverses the length of the cable or line.
Throughout this specification and the claims, the terms “comprise,” “comprises,” and “comprising” are used in a non-exclusive sense, except where the context requires otherwise. Likewise, the term “includes” and its grammatical variants are intended to be non-limiting, such that recitation of items in a list is not to the exclusion of other like items that can be substituted or added to the listed items.
Medical infusion typically serves to administer medications, fluids, nutrients, solutions, and other materials intravenously to a patient. Patients are often administered medical infusion using intravenous infusion lines. Such intravenous infusion lines generally consist of flexible, plastic tubing connected at one end to a fluid source and at another end to a needle or port that provides access to a blood vessel of a patient. It is not uncommon for many infusion lines, each connected to a different source of fluid (medical infusion pump), to be used simultaneously to deliver several medications at once to a single patient. It is also not uncommon for the needles or ports to be located adjacent one another, such as multiple adjacent needles providing access into the brachial vein running through the arm of the patient.
Distinguishing between multiple infusion lines is a difficult task that is placed in an atmosphere of high stress and rapid timing. The medical industry refers to the atmosphere as placing a high cognitive load on practitioners. This high cognitive load can lead to medication delivery error as a result of improperly distinguishing one medical infusion line from another. Arguably, the confusion of one medical infusion line from another is one of the leading causes of preventable medication error. As a result of the difficulties in distinguishing between multiple medical infusion lines and their associated fluid sources and outputs, as well as the potentially life-threatening possibilities that can occur if incompatible medications are injected through the same medical infusion line, there is a need for accurate identification of medical infusion lines.
Similarly, the disclosure herein may also be applied to many other environments where a cognitive load, or otherwise environment restrictions, may place a burden on traditional techniques. For example, tracing of lines within the Information Technology (IT') field may enable rapid detection and identification. In other aspects, the disclosed embodiments may be useful for the energy sector, where illumination needs may be utilized to send signals through long distances and to have a system that may rapidly deploy and integrate with little additional cost. Therefore, there is a need to improve electronic illuminators with a more advanced sensor system, and provide on board intelligence that allows multi-functional use and adaptability.
In one aspect, the LED is configured to the electronic illuminator and is controlled through a printed circuit board (‘PCB’). In the example of
The electronic illuminator, in one aspect, comprises a housing, along with a rigid-flex PCB or RF-PCB or PCB, and a power source. The housing may be comprised of a polymeric material and have various metal or other heat transferring locations, effectively forming external heat sinks within the housing that connects to an internal heat sink. Further, in other aspects, the housing may be comprised of metal or a blend of polymeric material and a metal, thus forming a protective enclosure for the various assemblies and subsystems. In one aspect the housing allows the electronic illuminator to be water tight or dust proof, and in other aspects it may be rated for waterproofing for a certain period of time at specific atmospheric pressure. Rubber gaskets may align the surfaces of the housing, as well as rubber material for grip, such as textured rubber where a user may come into contact with the electronic illuminators housing. The rubber gaskets assist in water proofing, vibration, dust proofing, and may further attribute to ingress protection, allowing some examples to achieve ratings such as IP65, IP66, and IP67.
Returning to the RF-PCB, in one example it may be configured with an ambient light sensor that is operatively configured within the housing of the electronic illuminator. The ambient light sensor may be any number of makes or models, for example, it may be a sensor manufactured by Lite-On™, such as the LTR-329ALS-01. In one aspect, the flexible region of the RF-PCB allows for adjusting and aligning the ambient light sensor to offset from the LED, therefore allowing for detection of whether or not the LED is powered, along with the LED's relative intensity, and detection of environmental lux. These features incorporated with the onboard microcontroller allow for automatic light intensity configuration through the power drivers on the RF-PCB. In another aspect the ambient light sensor converts light intensity to a digital signal, such as lux, thought an analog to digital converter on the sensor, and transmits the lux value to a microcontroller. In another aspect the conversion is processed on a microcontroller on the RF-PCB, and further used to determine behavior of an electronic illuminator. Even further embodiments, the processing may occur on a microprocessor, wherein the microprocessor may be standalone, or it may be incorporated onto the microcontroller unit.
In one aspect, a sensory system for an electronic illuminator to detect the presence and color of a fiber funnel cap is disclosed. A sensory system comprises various components, assemblies, and configurations disclosed herein. In one example a sensory system is configured to a light source, such as a light emitting diode (‘LED’). An LED is typically comprised of a silicon lens, a ceramic substrate, a thermal pad, a bond layer, an LED chip or microprocessor, a phosphorous layer, and a cathode. The entire construction is typically within a few millimeter package. Typically, several LED chips are packaged together to provide enough luminous flux to serve the purpose of illuminating.
In another aspect, an electronic illuminator is configured with a fiber detection assembly. Wherein the fiber detection assembly is a hall effect sensor or hall sensor. The assembly may be comprised of a plurality of magnets and a steel bar to create a tuned magnetic field, so as to resemble a key or signature that allows detection of fiber insertion into the electronic illuminator. The key or signature may be unique to a fiber line, to a color, or may be coded for other intelligence. The fiber detection assembly further having a three dimensional magnetic flux density based on at least one or more magnets configured to the electronic illuminator, typically near the translucent cap or electronic illuminator cap.
In additional aspects, a cap color detection assembly is incorporated onto the RF-PCB of an electronic illuminator. Wherein the cap color detection assembly detects the color of the cap, or a funnel cap, or other design enabled to configure into or on an electronic illuminator to direct light along the fiber optic cable. The cap color detection assembly, in one aspect, may be comprised of an R/G/B sensor, a light emitting component and an integrated circuit or microprocessor. In further aspects, the cap color detection assembly may be positioned towards the light emitting diode, so as to receive the light radiation directly. Additionally, a cap color detection assembly may comprise a color code band detection, wherein the cap comprises a multiple band color code and the cap color detection assembly is capable of scanning the multiple band code and returning instructions, such as the color the band is coded for or additionally, whether the code also instructs things such as sound, illuminance patterns, or other system alerts.
In additional aspects, an ambient light sensor, a fiber detection assembly, and a cap color detection assembly are operatively configured to the RF-PCB, also referred to generally as a PCB, in the electronic illuminator. The three subsystems work in coordination, and may rely on one another, for example, the ambient light sensor may work in coordination with the fiber detection assembly to determine if a fiber optic cable is present, or if it has illumination running through it. Such procedures may be used to detect a failure in the fitting of the fiber optic line, or may also detect unauthentic, or not genuine configurations.
Referring now to additional aspects of the electronic illuminator. In one aspect the housing may be further comprised of a heat sink. The heat sink may be metal based or based from other transferable materials that allow the dissipation of heat energy from the LED, the power drivers, the microcontroller, and the various microprocessors onboard an example system. Furthermore, the heat sink may be aligned with the power source, such as a battery. The battery may comprise any number of chemistries that are available to provide durational power support for the electronic illuminator.
Referring to methods herein, in one aspect a method for detecting the presence of a fiber in an electronic illuminator is disclosed. In one aspect, the method comprises provisioning an electronic illuminator with an ambient light sensor and a fiber detection assembly. Wherein the ambient light sensor is configured to receive light from outside of the electronic illuminator, thus its configuration on the back side of the RF-PCB allows for diffused exterior light to be acquired through a translucent ring on the exterior housing of the electronic illuminator. Next, the ambient light sensor or microcontroller unit acquires the light intensity and coverts it to a digital signal (lux). Next, the MCU determines the lux based on the digital signal. Then the hall effect sensor on the fiber detection assembly acquires a magnetic flux density. The MCU then determines a tesla value based on the magnetic flux density. Through the hall effect sensor and the ambient light sensor, the presence of a fiber optic cable may be detected with a digital signal and tesla value, or may be detected independently by either assembly or sensor. Further, when acquiring a magnetic flux density through the hall effect sensor on the fiber detection assembly, the strength of the magnetic flux may be represented based on output voltage. Lastly, the example aspect discloses alerting, by the electronic illuminator, that a fiber optic cable is present. Further, the electronic illuminator may use the subsystem for authenticating that the fiber optic cable is authentic for use with the electronic illuminator based on tesla value alone or in combination with cap color detection assembly.
Referring now to
Continuing, in the example, a RF-PCB 104 is disclosed, wherein the flex portion is folded unto itself, forming a location for the R/G/B sensor of a cap color detection system. The folds allow for blocking of the ambient light sensor from the onboard LED of the electronic illuminator, wherein the ambient light sensor acquires environmental lux from the clear housing, also referred to as a translucent ring 102, at the proximal end of the electronic illuminator 100. In other aspects the translucent ring 102 may be opaque or may have a window in it that allows for environmental light. In further embodiments the light from the side emitting fiber optic line may be used to determine environmental lux. Additionally, the magnets supplied for the hall effect sensor forming the fiber detection assembly are embedded within the translucent ring 102, or positioned near the translucent ring 102, to form a magnetic field.
A battery 106 is disclosed along with an internal heat sink 112, wherein the battery powers the electronic illuminator's various assemblies and the internal heat sink 112 works to dissipate heat to the external heat sink on the housing. An LED assembly 110 is positioned to connect with the fiber funnel cap to project light through the side emitting fiber optic line 108. An end cap 114 to the electronic illuminator holds the batteries in place and may further house a communications module or assembly as well as an antenna. With regard to the battery 106, the electronic illuminator, in one aspect, may work in coordination with the ambient light sensor and the cap color detection assembly or the fiber detection assembly to regulate usage of power and to form a swarm of sensors for intelligent power management. In one aspect, the ambient light sensor detects lux in the environment and controls LED power output from the power driver to conserve energy. Further, the cap color detection assembly may detect the fiber funnel cap is not engaged and thus automatically turn the system off. Similarly, the fiber detection assembly may detect an absence of a fiber and a fiber funnel cap, therefore turning the power off until the fiber funnel cap is attached.
Referring now to
Various examples disclosed herein contain reference to the electronic illuminator, and are identified in
In another aspect of the example of
The LED assembly 228 on the RF-PCB 210 is configured with a lens 220, wherein the lens 220 is situated to receive the fiber for illumination. The fiber side, in one aspect, is equipped with a fiber funnel cap, that configures to the translucent ring 214 and is held in place by a locking mechanism or through magnetic force and use of magnets, such as a magnet assembly 216, or other configurations of magnets. The R/G/B sensor 226, comprising the cap color detection assembly, is disclosed facing inwards toward the receiving orifice of the fiber funnel cap. Additionally, the magnet assembly 216, in coordination with the steel bar 218 provides a magnetic flux key or signature that may be utilized for fiber detection, as well as authentication and security. Wherein the electronic illuminator may be configured to authorize use of a signature or flux key.
Referring now to
The various components, assemblies, sensors, and subsystems may be in communication utilizing an inter-integrated circuit (‘I2C’) interface for intra-board communication. Additional communications protocols such as wireless, Bluetooth™, and other radio standards may be additional chipsets configured with the onboard MCU.
Turning now to
Referring now to
In the example of
Turning now to
Illuminance is analogous to the radiometric unit watt per square meter, but with the power at each wavelength weighted according to the luminosity function, a standardized model of human visual brightness perception. Illuminance is a measure of how much luminous flux is spread over a given area. One can think of luminous flux (measured in lumens) as a measure of the total “amount” of visible light present, and the illuminance as a measure of the intensity of illumination on a surface. A given amount of light will illuminate a surface more dimly if it is spread over a larger area, so illuminance is inversely proportional to area when the luminous flux is held constant.
The illuminance provided by a light source on a surface perpendicular to the direction to the source is a measure of the strength of that source as perceived from that location. Like all photometric units, the lux has a corresponding “radiometric” unit. The difference between any photometric unit and its corresponding radiometric unit is that radiometric units are based on physical power, with all wavelengths being weighted equally, while photometric units take into account the fact that the human eye's image-forming visual system is more sensitive to some wavelengths than others, and accordingly every wavelength is given a different weight. The weighting factor is known as the luminosity function.
The lux is one lumen per square meter (1 m/m2), and the corresponding radiometric unit, which measures irradiance, is the watt per square meter (W/m2). There is no single conversion factor between lux and W/m2. There exists a different conversion factor for every wavelength, and it is not possible to make a conversion unless one knows the spectral composition of the light. The peak of the luminosity function is at 555 nm (green); the eye's image-forming visual system is more sensitive to light of this wavelength than any other. For monochromatic light of this wavelength, the amount of illuminance for a given amount of irradiance is maximum: 683.002 lux per 1 W/m2; the irradiance needed to make 1 lux at this wavelength is about 1.464 mW/m2. Other wavelengths of visible light produce fewer lux per watt-per-meter-squared. The luminosity function falls to zero for wavelengths outside the visible spectrum.
For a light source with mixed wavelengths, the number of lumens per watt can be calculated by means of the luminosity function. In order to appear reasonably “white”, a light source cannot consist solely of the green light to which the eye's image-forming visual photoreceptors are most sensitive, but must include a generous mixture of red and blue wavelengths, to which they are much less sensitive.
This means that white (or whitish) light sources produce far fewer lumens per watt than the theoretical maximum of 683.002 lm/W. The ratio between the actual number of lumens per watt and the theoretical maximum is expressed as a percentage known as the luminous efficiency. For example, a typical incandescent light bulb has a luminous efficiency of only about 2%. In reality, individual eyes vary slightly in their luminosity functions. However, photometric units are precisely defined and precisely measurable. They are based on an agreed-upon standard luminosity function based on measurements of the spectral characteristics of image-forming visual photoreception in many individual human eyes.
In the example of
In other aspects, there exists a translucent ring at the proximal location of the illuminator to detect the ambient light difference from that of the LED's of the electronic illuminator. In one aspect, the ambient light sensor is placed on a flexible region of a RF-PCB in a location that is shaded from luminance of the fiber source. If the ambient light sensor detects ambient light with no fiber attached it can switch the microcontroller into low power mode. The ambient light sensor, in other aspects, assists with power control and sleep wake. In other aspects, the ambient light sensor detects errors within the LED or within the electronic illuminator. The ambient light sensor, in additional embodiments is equipped to detect occlusion of the signal of the electronic illuminator and to alert or otherwise inform users of an issue with the electronic illumination system.
Referring now to
Continuing, in
Referring now to
Examples of Benefits and Features for an R/G/B Sensor are disclosed in the table below:
In one aspect, an R/G/B sensor, as part of the cap color detection assembly is configured to read a multiple band code, wherein the bands may be coded or preprogrammed within the MCU to illuminate at a specific spectrum, such as to produce a specific color of light. The multiple band code may be transcribed as rings on a fiber side cap or along the fiber line, that when engaged with the electronic illuminator allows reading of the multiple band code and transmission from the cap color detection assembly to an MCU for signaling or communicating to the LED power drivers.
Referring now to
In one aspect, a cap color assembly utilizes an R/G/B sensor to identify the cap color, wherein once acquired, communicates with an MCU which in turn instructed LED power drivers to illuminate for the specific color. In other aspects, a cap color detection assembly may be coded to specific instructions, such as to illuminate with a pattern, or to indicate expected luminosity outside of the ambient light sensor, to play an audio signal, or other cognitive aspect such as identifying with medical fluid treatment. In one aspect, a red cap or red band pattern may be programmed for blood products, or blood infusion. Whereas a green cap or green band pattern may be programmed for nutrients, and blue for saline, these are but a few possibilities with the systems and methods disclosed herein.
Referring now to
Referring now to
In additional aspects a watermark, or color array, for a series of color bands may be used for security and authentication. In one aspect a series of banded color codes is placed and read by the cap color detection assembly within the electronic illuminator. If the color code is a match the electronic illuminator functions, if the color code is not a match the electronic illuminator provides notification. Notification can consist of a signal or transmission, or other notification that the fiber is either not genuine, or is inserted incorrectly, or there is a failure within the system. Additionally, in another aspect, the color bands or watermark may also provide input to the electronic illuminator regarding the LED transmission color to illuminate the fiber line with.
Referring now to
Referring now to
Similarly, referring to
Referring now to
In one aspect, the Hall sensor 1402 on the electronic illuminator detects the presence of the fiber line through a series of magnets placed on the front cap of the electronic illuminator. In one embodiment the electronic illuminator creates a 3D magnetic flux density that is capable of sensing to +/−160 mT. In other embodiments a range exists over +/−160 mT. The Hall sensor is equipped with a programmable flux resolution to 65 uT. Therefore, enabling position detection and X-Y angular and fiber orientation and measurements. The 3d magnetic flux is also known as a magnetic flux key or signature, and such signature can be used for authentication and verification of the illuminating infusion line or the fiber line. Further, in other aspects, the Hall sensor 1402 controls the power supply and sleep wake functionality. The hall sensor 1402 is further equipped to provide energy saving aspects by controlling functionality of on/off, sleep/wake, rest state of a microcontroller. In other aspects, the Hall sensor 1402 enables device security through detection of a flux key or signature.
In the example of
Continuing with
Referring now to
Continuing, the protective end cap 1504, with a polished surface, is also made of a resilient material such as a hard plastic or metal that allows for protection of the fiber optic line 1502 so it does not fray or come into contact with patients. Additionally, the protective end cap is smooth and made to be non-abrasive and easy to clean, with no openings or otherwise which allows for prevention of bacterial growth and reusability.
Further, the protective end cap 1504 may be equipped with a one line antennae that is utilized for communicating over radio frequency, thus adding an additional layer of communication to the fiber optic line. The one line antennae acts as a passive wireless antenna and may be used for determining fiber optic line length or for verification and authentication.
Referring now to
Continuing, the fiber funnel cap 1602 may come in a variety of colors and the color is detected by the cap color detection assembly, wherein the MCU may power an LED driver to the specific cap color. Further, the fiber funnel cap 1602 may be equipped with bands, such as a multiple band code, or a SKU, or QR code, that allows for the R/G/B sensor of the cap color detection assembly to read the bands or code and transmit to the MCU a signal for the color to illuminate by the LED power driver. Therefore, the fiber optic cable, including the fiber funnel cap may be “programmed” from manufacture to illuminate a specific LED driver within the electronic illuminator. The system therefore reduces cognitive load on practitioners as the fiber funnel caps are coded with the matching color, reducing overhead and allowing design to provide function.
Referring now to
Referring to
The dual lumen fiber optic medical infusion line 1800 includes a second elongate body 1812 that is substantially cylindrical and extends from a proximal end to a distal end. The second elongate body 1812 is a hollow structure that contains a second lumen 1814 defined by a second sidewall 1816 extending circumferentially about the second elongate body 1812. The second lumen 1814 is configured as a fluid transmission channel and extends the length of the second elongate body 1812 from the proximal end to the distal end. The second sidewall 1816 has a substantially constant thickness throughout the length of the second elongate body 1812 with an interior surface 1818 and an exterior surface 1820. The interior surface 1818 and the exterior surface 1820 preferably have a circular inner and circular outer cross section.
The first elongate body 1802 and the second elongate body 1812 are engaged to each other. The exterior surface of the first sidewall 1806 of the first elongate body 1802 is engaged to the second sidewall 1816 of the second elongate body 1812 in a manner that the first elongate body 1802 and the second elongate body 1812 are parallel each other and preferably engaged to each other the entire length of the first elongate body 1802 and the second elongate body 1812.
A separator zone 1822 is disposed between the first elongate body 1802 and the second elongate body 1812 and preferably extends the entire length of the dual lumen fiber optic medical infusion line 1800. The dual lumen fiber optic medical infusion line 1800 may be created through an extrusion process, wherein the second elongate body 1812 is engaged to the first elongate body 1802. Since the second elongate body 1812 and the first elongate body 1802 are generally cylindrical and have a circular cross section, the point of engagement on the exterior surface 1820 of the second elongate body 1812 the exterior surface of the first elongate body 1802 is minimal and does not occupy a large portion of surface area of the exterior surfaces (1810, 1820), as shown in
The first elongate body 1802 and the second elongate body 1812 have a circular cross section and each sidewall (1806, 1816) contains a point of tangency, which is a portion on each sidewall (1806, 1816) where the tangent is perpendicular to the radius of the circular cross-sectional portions of each sidewall (1806, 1816). During the manufacturing process, the degree of bonding between the second elongate body 1812 and the first elongate body 1802 can be selected to provide desirable separation properties within the separation zone 1822. The preferred separation properties allow a user to manually separate the second elongate body 1812 and the first elongate body 1802 along the separation zone. This separation allows the dual lumen fiber optic medical infusion line 1800 to be placed adjacent other medical accessories, such as an IV line accessory requirements (filters, lures, single way valves, and the like).
The dual lumen fiber optic medical infusion line 1800 can be made from one or a combination of different materials. These materials may include PVC, Silicon, PMMA, polyamide (nylon), polyurethane, polyethylene (HDPE, LDPE, or LLDPE), polypropylene, PTFE (Teflon), synthetic or natural rubbers, plastic compositions, such as linear, branched, and cross-linked polymers, isomers, or polymer blends, polymeric material, stainless steel or other metal material and combinations thereof. The dual lumen fiber optic medical infusion line 1800 may be made from processes known to those skilled in the art, but the preferred process is extrusion. An extrusion process is typically used to create objects of a fixed or semi-fixed cross sectional profile. A material is typically pushed through a die of the desired cross section. Extrusion provides the ability to create very complex cross sections. Extrusion often forms parts with good cross sections.
The first elongate body 1802 of the dual lumen fiber optic medical infusion line 1800 is configured to receive a fiber optic cable 1824. The first lumen 1804 of the first elongate body 1802 receives and houses the fiber optic cable 1824. The fiber optic cable 1824 may be a side scattering or side emitting fiber optic cable as described herein. The fiber optic cable 1824 has a diameter less than the diameter of the sidewall 1806, allowing the fiber optic cable 1824 to be inserted and housed within the first lumen 1804 of the first elongate body 1802, as shown in
The second lumen 1814 is configured to allow transmission of fluid through the second elongate body 1812. The second lumen 1814 is a fluid transmission channel, conduit, or hollow passage through the second elongate body 1812 that allows the transmission of fluids, such as a liquid medicament, through the dual lumen fiber optic medical infusion line 1800. The second elongate body 1812 may be directly attached to current medical infusion platforms and components, including filters, infusion pumps, manifolds, a vial, an IV bag and other infusion components that will occur to those skilled in the art.
In further aspects, the first elongate body 1802 may be separated from the second elongate body, wherein the second elongate body, may contain a filter, wherein the first elongate body may run alongside said filter, and reconnect on the other side. In such aspects the first elongate body 1802 is capable of bypassing line impediments and configuring with a variety of inline medical infusion assemblies. Thus, the disclosure herein may be retrofitted to medical assemblies and incorporated across platforms.
A distal end cap 1504, as described herein and shown in
An example process for manufacturing a dual lumen fiber optic medical infusion line 1800 is illustrated in
Certain implementations of systems and methods consistent with the present disclosure are provided as follows:
Implementation 1. A dual lumen fiber optic medical infusion line, comprising: a first elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a first lumen extending throughout an entire length of the first elongate body, the first elongate body is a hollow structure defined by a first sidewall extending circumferentially about the first elongate body having an exterior surface and an interior surface; a second elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a second lumen extending throughout an entire length of the second elongate body, the second elongate body is a hollow structure defined by a second sidewall extending circumferentially about the second elongate body having an exterior surface and an interior surface, the exterior surface of the second elongate body is engaged to the exterior surface of the first elongate body; a fiber optic cable having a proximal end and a distal end disposed within the first lumen of the first elongate body; and a distal end cap engaged to the distal end of the fiber optic cable.
Implementation 2. The dual lumen fiber optic medical infusion line of implementation 1, further comprising a fiber funnel cap engaged to the proximal end of the fiber optic cable.
Implementation 3. The dual lumen fiber optic medical infusion line of implementation 2, wherein the fiber funnel cap is engaged to an electronic illuminator.
Implementation 4. The dual lumen fiber optic medical infusion line of implementation 1, wherein the fiber optic cable is a side emitting fiber optic cable.
Implementation 5. The dual lumen fiber optic medical infusion line of implementation 1, further comprising a separator zone between the second elongate body and the first elongate body for enabling the second elongate body to be separated from the first elongate body.
Implementation 6. The dual lumen fiber optic medical infusion line of implementation 1, wherein the first elongate body is composed of a transparent material, allowing light emitted by the fiber optic cable to be visible through the first elongate body.
Implementation 7. The dual lumen fiber optic medical infusion line of implementation 1, wherein the second elongate body is configured to allow transmission of a fluid through the second elongate body.
Implementation 8. The dual lumen fiber optic medical infusion line of implementation 1, wherein the distal end cap comprises an antenna.
Implementation 9. A dual lumen fiber optic medical infusion line, comprising: a first elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a first lumen extending throughout an entire length of the first elongate body, the first elongate body is a hollow structure defined by a first sidewall extending circumferentially about the first elongate body having an exterior surface and an interior surface; a second elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a second lumen extending throughout an entire length of the second elongate body, the second elongate body is a hollow structure defined by a second sidewall extending circumferentially about the second elongate body having an exterior surface and an interior surface; the exterior surface of the second elongate body is engaged to the exterior surface of the first elongate body; a fiber optic cable having a proximal end and a distal end, the fiber optic cable is disposed within the first lumen of the first elongate body; wherein the proximal end extends outward from the proximal end of the first elongate body and the distal end extends outward from the distal end of the first elongate body, the proximal end of the fiber optic cable and the distal end of the fiber optic cable are not circumferentially surrounded by the first sidewall; a distal end cap engaged to the distal end of the fiber optic cable; and a fiber funnel cap engaged to the proximal end of the fiber optic cable.
Implementation 10. The dual lumen fiber optic medical infusion line of implementation 9, wherein the distal end cap comprises an antenna.
Implementation 11. The dual lumen fiber optic medical infusion line of implementation 9, wherein the distal end cap has a polished surface that is highly reflective of light.
Implementation 12. The dual lumen fiber optic medical infusion line of implementation 9, wherein the distal end cap is composed of a resilient material for protecting the fiber optic cable.
Implementation 13. The dual lumen fiber optic medical infusion line of implementation 9, wherein the first elongate body is composed of a transparent material, allowing light emitted by the fiber optic cable to be visible through the first elongate body.
Implementation 14. The dual lumen fiber optic medical infusion line of implementation 9, further comprising a separator zone between the second elongate body and the first elongate body for enabling the second elongate body to be separated from the first elongate body.
Implementation 15. The dual lumen fiber optic medical infusion line of implementation 9, wherein the fiber funnel cap is engaged to an electronic illuminator.
Implementation 16. A method of manufacturing a dual lumen fiber optic medical infusion line, comprising: providing a fiber optic cable; extruding a dual lumen fiber optic medical infusion line from a polymeric material, the dual lumen fiber optic medical infusion line comprising: (a) a first elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a first lumen extending throughout an entire length of the first elongate body, the first elongate body is a hollow structure defined by a first sidewall extending circumferentially about the first elongate body having an exterior surface and an interior surface; (b) a second elongate body that is substantially cylindrical and extends from a proximal end to a distal end and includes a second lumen extending throughout an entire length of the second elongate body, the second elongate body is a hollow structure defined by a second sidewall extending circumferentially about the second elongate body having an exterior surface and an interior surface; the exterior surface of the second elongate body is engaged to the exterior surface of the first elongate body; preparing a distal end cap; preparing a fiber funnel cap; feeding a fiber optic cable through the first elongate body; attaching the distal end cap to the distal end of the fiber optic cable; and attaching the fiber funnel cap to the proximal end of the fiber optic cable.
Implementation 17. The method of manufacturing a dual lumen fiber optic medical infusion line of implementation 16, wherein the fiber optic cable is jacketed.
Implementation 18. The method of manufacturing a dual lumen fiber optic medical infusion line of implementation 16, wherein the second elongate body is configured to allow transmission of a fluid through the second lumen of the second elongate body.
Implementation 19. The method of manufacturing a dual lumen fiber optic medical infusion line of implementation 16, wherein the distal end cap comprises an antenna.
Implementation 20. The method of manufacturing a dual lumen fiber optic medical infusion line of implementation 16, providing an electronic illuminator and attaching the electronic illuminator to the fiber funnel cap.
It should be emphasized that the above-described embodiments of the present disclosure are merely possible examples of implementations set forth for a clear understanding of the principles of the disclosure. Many variations and modifications may be made to the above-described embodiment(s) without departing substantially from the spirit and principles of the disclosure. All such modifications and variations are intended to be included herein within the scope of this disclosure and protected by the following claims.
This application is related and claims priority to U.S. Provisional Patent Application No. 63/138,961 entitled “Electronic Illuminator” filed on Jan. 19, 2021. This application is also related to and co-filed with utility applications “Assemblies and Subsystems for Electronic Illuminators”, “Systems and Methods for Controlling Microorganism Load with an Electronic Illuminator”, “Medical Infusion Line Electronic Illuminator”, “Systems and Methods for Authenticating Medical Infusion Lines with an Electronic Illuminator.” The entire disclosure of said applications are incorporated herein by reference.
Number | Date | Country | |
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63138961 | Jan 2021 | US |