A person or animal may have limited or impaired mobility such that typical urination processes are challenging or impossible. For example, a person may experience or have a disability that impairs mobility. A person may have restricted travel conditions such as those experienced by pilots, drivers, and workers in hazardous areas. Additionally, sometimes urine collection is needed for monitoring purposes or clinical testing.
Urinary catheters, such as a Foley catheter, can be used to address some of these circumstances, such as incontinence. Unfortunately, urinary catheters can be uncomfortable, painful, and can lead to complications, such as infections. Further, obtaining samples from urinary catheters, under certain circumstances, may be challenging or difficult under certain circumstances.
In an embodiment, a fluid collection assembly is disclosed. The fluid collection assembly includes a fluid impermeable barrier including a first end region and a second end region longitudinally spaced from the first end. The fluid impermeable barrier includes a sump that forms at least a portion of the first end region. The fluid impermeable barrier defines at least one opening, a chamber in fluid communication with the at least one opening, a fluid reservoir defined by at least a portion of the sump, and a fluid outlet in fluid communication with the fluid reservoir. The fluid collection assembly also includes at least one wicking material disposed in the fluid impermeable barrier. Further, the fluid collection assembly includes a sample port attached to the sump and in fluid communication with the fluid reservoir. The sample port is configured to switch between a closed state that restricts fluid flow through the sample port and an open state that permits fluid flow through the sample port. The sample port is configured to be connected to a fluid collector.
In an embodiment, a fluid collection system is disclosed. The fluid collection system includes a fluid collection assembly and a fluid collector. The fluid collection assembly includes a fluid impermeable barrier including a first end region and a second end region longitudinally spaced from the first end. The fluid impermeable barrier includes a sump that forms at least a portion of the first end region. The fluid impermeable barrier defines at least one opening, a chamber in fluid communication with the at least one opening, a fluid reservoir defined by at least a portion of the sump, and a fluid outlet in fluid communication with the fluid reservoir. The fluid collection assembly also includes at least one wicking material disposed in the fluid impermeable barrier. Further, the fluid collection assembly includes a sample port attached to the sump and in fluid communication with the fluid reservoir. The sample port is configured to switch between a closed state that restricts fluid flow through the sample port and an open state that permits fluid flow through the sample port. The sample port is configured to be connected to a fluid collector.
In an embodiment, a method of using a fluid collection system is disclosed. The method includes attaching the fluid collector to the sample port. The method also includes receiving bodily fluids from an individual through the at least one opening, into the chamber, and to the fluid reservoir. The method further includes removing at least some of the bodily fluids that are present in the fluid reservoir with the fluid collector. Additionally, the method includes detaching the fluid collector from the sample port. Further, the method includes switching the sample port from the open state to the closed state. The method additionally includes removing substantially all of a remainder of the bodily fluids present in the fluid reservoir through the fluid outlet using a suction three.
Features from any of the disclosed embodiments may be used in combination with one another, without limitation, In addition, other features and advantages of the present disclosure will become apparent to those of ordinary skill in the art through consideration of the following detailed description and the accompanying drawings.
The drawings illustrate several embodiments of the present disclosure, wherein identical reference numerals refer to identical or similar elements or features in different views or embodiments shown in the drawings.
Fluid collection assemblies including a sample port, systems including the same, and methods of using the same are disclosed herein. An example fluid collection assembly includes a fluid impermeable barrier including a first end region, a second end region opposite the first end region, and a sump that forms at least a portion of the first end region. The fluid impermeable barrier also defines at least one opening between the first end region and the second end region and a fluid reservoir that is defined by at least a portion of the sump. The fluid collection assembly also includes at least one wicking material disposed in the chamber and a sample port extending from the sump. The sample port is configured to be connected to a fluid collector (e.g., a syringe or a vial). The sample port is in fluid communication with the fluid reservoir such that a sample of the bodily fluids (e.g., urine) received by the fluid collection assembly may be obtained.
During use, the opening of the fluid impermeable barrier is positioned adjacent to the urethral opening of an individual. Bodily fluids (e.g., urine) that are emitted from the urethral opening are received by the wicking material through the opening and flow through the wicking material to the fluid reservoir. The bodily fluids are removed from the fluid reservoir using a suction force.
With conventional catheters (e.g., Foley catheters), sample ports are provided on a tube extending between the urethral opening and a drainage bag. Samples may be obtained from these sample ports by connecting a fluid collector to the port. The fluid collector then removes a sample of the bodily fluids by pulling the bodily fluids flowing in the tube or by kinking the tube followed by collecting the pooled bodily fluids. However, such methods of obtaining samples from the fluid collection assemblies according to any of the embodiments of the present disclosure (e.g., fluid collection assemblies 100, 200, 300a, 300b, 400a, 400b, 400c, 500 and 600 shown in
The samples ports according to any embodiments of the present disclosure remedy at least some of the problems associated with obtaining samples of the bodily fluids using conventional sample ports. For example, the sample ports according to any of the embodiments of the present disclosure extend from the sump of the fluid reservoir instead of located on a portion of the tube. The bodily fluids that are present in the fluid reservoir tend to flow at lower velocities (e.g., are more stationary) that the bodily fluids that flow through the tube. Further, the bodily fluids flow towards the fluid reservoir even in the absence of the suction force since, for example, the fluid reservoir is the gravimetric low point of the fluid collection assembly. As such, the suction force that removes the bodily fluids from the fluid reservoir may be stopped (e.g., the tube is kinked) thereby causing the bodily fluids to pool in the fluid reservoir.
The fluid impermeable barrier 102 defines at least one opening 114, such as a single elongated opening. The opening 114 is located between the first end region 104 and the second end region 106 of the fluid impermeable barrier 102. The opening 114 is configured to be positioned adjacent to a female urethral opening or a buried penis. The fluid impermeable barrier 102 also defines a chamber 116 that is in fluid communication with the opening 114 such that bodily fluids that are discharged by the urethral opening flow through the opening 114 and into the chamber 116. As previously discussed, the bodily fluids that are present in the chamber 116 generally flow towards the fluid reservoir 110. Additionally, the fluid impermeable barrier 102 defines a fluid outlet 118 that allows the bodily fluids to be removed from the fluid reservoir 110. In the illustrated embodiment, the fluid outlet 118 is located on the second end region 106 of the fluid impermeable barrier 102 while the fluid reservoir 110 is located at or near the first end region 104 of the fluid impermeable barrier 102. As such, the fluid collection assembly 100 may include at least one tube 120 positioned in the fluid outlet 118 that extends from the fluid outlet 118 to the fluid reservoir 110 thereby allowing the fluid outlet 118 to be in fluid communication with the fluid reservoir 110. The tube 120 may also extend from the fluid outlet 118 to another component of a fluid collection system, as will be discussed in more detail with regards to
The fluid impermeable barrier 102 may be formed of any suitable material. For example, the fluid impermeable barrier 102 may be formed from silicone, another thermosetting polymer, another suitable fluid impermeable material, or combinations thereof. In an embodiment, as illustrated in
As previously discussed, the fluid impermeable barrier 102 includes a sump 108. The sump 108 may form the first end region 104 of the fluid impermeable barrier 102. The sump 108 includes portions of the fluid impermeable barrier 102 that at least one of defines the fluid reservoir 110 (shown in
At least a portion of the sump 108 may be at least partially transparent (e.g., translucent or transparent). For example, as previously discussed, the sump 108 defines the fluid reservoir 110 of the fluid collection assembly 100. Selecting at least a portion of the sump 108 to be at least partially transparent allows a user (e.g., medical practitioner) to determine when bodily fluids are present in the fluid reservoir 110. As such, the at least partially transparent portions of the sump 108 allows the user to determine when samples of the bodily fluids may be taken. In an embodiment, the at least partially transparent portion of the sump 108 may also include one or more markings (not shown) thereon. The markings formed on the sump 108 may indicate the volume of the bodily fluids that are present in the fluid reservoir 110. In an example, the markings quantitatively (e.g., in milliliters, fluid ounces, etc.) indicate the volume of the bodily fluids that are present in the fluid reservoir 110. In an example, the markings qualitatively indicate the bodily fluids that are present in the fluid reservoir. In such an embodiment, the markings may indicate when a sufficient quantity of fluids are present in the fluid reservoir 110 to obtain a sample. Examples of transparent material that may form at least a portion of the sump 108 include glass, one or more transparent polymers (e.g., polycarbonate, acrylic, polyethylene terephthalate, polyethylene, etc.), or combinations thereof. In an embodiment, at least a portion of the sump 108 may be at least partially opaque to minimize patient embarrassment.
As previously discussed, the sample port 112 is attached to the sump 108. For example, the sump 108 may define an hole 122 that is adjacent to the fluid reservoir 110. The sample port 112 is attached to the portions of the sump 108 about the hole 122. This allows the sample port 112 to be in fluid communication with the fluid reservoir 110 via the hole 122. Generally, the hole 122 is located at or near the first end region 104 of the fluid impermeable barrier 102 since the first end region 104 is generally at or near the gravimetric low point of the fluid collection assembly 100 during use of the fluid collection assembly 100. As such, even in the absence of a suction force, any bodily fluids that enter the chamber 116 are drawn towards the fluid reservoir 110 and the hole 122.
In an embodiment, as illustrated, the hole 122 is located near (but not at) the first end region 104. Instead, the hole 122 may be located on a back surface 123 of the fluid impermeable barrier 102. The back surface 123 of the fluid impermeable barrier 102 is a surface of the fluid impermeable barrier 102 that is opposite or generally opposite the opening 114 defined by the fluid impermeable barrier 102. Forming the hole 122 on the back surface 123 of the fluid impermeable barrier 102 may facilitate obtaining a sample more effectively than if the hole 122 was formed on another surface of the fluid impermeable barrier 102. For example, during operation, the opening 114 of the fluid impermeable barrier 102 is positioned adjacent to the urethral opening of the individual. As such, any front surface 121 of the fluid impermeable barrier 102 (i.e., any surface of the fluid impermeable barrier 102 that faces the same direction as the opening 114) is likewise positioned adjacent to the urethral opening, mons pubis, or perineal regions of the individual thereby making access to the front surface 121, for the purpose of obtaining a sample, difficult. Further, any side surface 125 of the fluid impermeable barrier 102 (i.e., any surface of the fluid impermeable barrier 202 between the front surface 121 and the back surface 123) is likely to be positioned adjacent or proximate to the thighs of the individual making access to these surface with a fluid collector difficult. Additionally, the first end region 104 of the fluid impermeable barrier 102 may be positioned adjacent to or proximate to a bed when the individual using the fluid collection assembly 100 is lying down thereby making it difficult to access the first end region 104 with a fluid collector. Meanwhile, the back surface 123 of the fluid impermeable barrier 102 may be easily accessible with a fluid collector, especially if the individual using the fluid collection assembly 100 opens their legs slightly. However, it is noted that the hole 122 may be located on any suitable surface of the sump 108, such as at the first end region 104, on the front surface 121 of the sump 108, or on a side surface 125 of the sump 108, without limitation.
The sample port 112 includes an attachment portion 124 that is configured to be attached to the portions of the sump 108 that are around the hole 122. The attachment portion 124 may be attached to the sump 108 using any suitable technique. In an embodiment, the attachment portion 124 is attached to the sump 108 using ultrasonic welding which forms molecular bonds or other strong attachment forces between the attachment portion 124 and the sump 108. However, in some embodiments, the attachment portion 124 may only be attached to the sump 108 using ultrasonic welding when both the attachment portion 124 and the sump 108 are thermoplastic and both the attachment portion 124 and the sump 108 are compatible, which is not always the case. In an embodiment, the attachment portion 124 is configured to be attached to the sump 108 via heat staking. In such an embodiment, the attachment portion 124 is attached to the fluid impermeable barrier 102 via heat staking. In such an embodiment, one of the attachment portion 124 or the portion of the sump 108 that is configured to be attached to the attachment portion 124 includes one or more protrusions while the other of the attachment portion 124 or the portion of the sump 108 that is configured to be attached to the attachment portion 124 defines passageways extending therethrough that are configured to receive respectively ones of the one or more protrusions. After positioning the protrusions through the passageways, pressure and heat are applied to the protrusions which deforms the protrusions into “stakes” that exhibit a general mushroom-like shape. The stakes are then cooled such that the stakes maintain the shape thereof. One benefit of attaching the attachment portion 124 to the sump 108 using heat staking is that the materials that form the attachment portion 124 and the sump 108 do not have to be compatible (unlike ultrasonic welding) and only one of the attachment portion 124 or the sump 108 have to be a thermoplastic material. As such, heat staking may be used to attach the attachment portion 124 to the sump 108 when the attachment portion 124 and the sump 108 include dissimilar materials, though heat staking may also be used when the attachment portion 124 and the sump 108 include similar materials. In an embodiment, the attachment portion 124 may be attached to the sump 108 using other suitable techniques, such as with an adhesive.
In an embodiment, the attachment portion 124 defines a port opening 126 that allows the bodily fluids to flow through the hole 122 and into/through the sample port 112. For example, the attachment portion 124 may exhibit a generally annular shape or other similar shape which may provide a surface to be attached to the sump 108 in a fluid tight manner while also defining the port opening 126.
The sample port 112 includes a valve 128. As used herein, the valve 128 includes any suitable mechanism that is configured to switch between a closed state that restricts fluid flow therethrough and an open state that permits fluid flow therethrough. In an embodiment, the valve 128 may be a split septum fitting that includes a deformable flexible material defining an gap 130 (e.g., slit, pin hole, etc.). The valve 128 may be configured such that the gap 130 is sufficiently small that fluid cannot flow therethrough (e.g., the gap 130 is defined by a hydrophobic material) when the valve 128 is in a relaxed state (i.e., closed state). However, pressing against the valve 128 with, for example, a fluid collector causes the flexible material of the valve 128 to deform and increase the size of the gap 130 such that fluid may flow through the gap 130. Removing the pressure applied to the valve 128 may cause the gap 130 to decrease in size such that the gap 130 again exhibits a size sufficiently small that fluid cannot flow therethrough. In an embodiment, the valve 128 includes a plastic layer (e.g., a plastic membrane) extending across an opening thereof (e.g., the port opening 126). The plastic layer may not initially define a gap. However, a syringe may easily penetrate the plastic layer to form a gap. However, the gap may exhibit a size, after removal of the syringe, that is sufficiently small that fluid cannot flow therethrough (e.g., the plastic layer is formed of a hydrophobic material). In an embodiment, the valve 128 may include a mechanical valve that switches between the open and closed states thereof responsive to actuation of an actuator. For example, the valve 128 may include a butterfly valve, a ball valve, or any other suitable mechanical valve.
In an embodiment, the valve 128 is spaced from the attachment portion 124. In such an embodiment, the sample port 112 may include at least one wall 132 extending from the attachment portion 124 to the valve 128. The wall 132 may define a passageway 134 extending from the port opening 126 to the valve 128. The wall 132 may facilitate attachment of a fluid collector to the sample port 112. In an example, the wall 132 may include one or more threads 136 formed therein. The threads 136 may secure the fluid collector to the sample port 112 while taking a sample. The threads 136 may also allow the connection device to be connected to the sample port 112 by twisting (e.g., without applying a pressure to the sump 108) which may prevent contraction of the sump 108. In an example, the wall 132 allows the fluid collector to be attached to the sample port 112 using a luer lock mechanism.
The fluid collection assembly 100 includes at least one wicking material 138 disposed in the chamber 116. In the illustrated embodiment, referring to
The fluid permeable support 140 can be positioned relative to the permeable membrane 142 such that the fluid permeable support 140 maintains the permeable membrane 142 in a particular shape. In an embodiment, the fluid permeable support 140 can be configured to maintain the permeable membrane 142 against or near the urethral opening of the individual. For example, the fluid permeable support 140 can include a portion having a curved shape in contact with the permeable membrane 142 such that the permeable membrane 142 is also curved, thus creating a comfortable and secure interface for engagement with the urethral opening and/or the area of the body near the urethral opening.
In an embodiment, the fluid permeable support 140 can be made of a rigid plastic. In an embodiment, the fluid permeable support 140 can have any suitable shape and be formed of any suitable material. For example, the fluid permeable support 140 can be flexible. Additionally, the fluid permeable support 140 can be formed of aluminum, a composite of plastic and aluminum, some other metal and/or a composite. In an embodiment, the fluid permeable support 140 can be formed of a natural material, such as, for example, plant fibers (e.g., Greener Clean manufactured by 3M®). The natural material can include openings that allow fluid to flow through the natural material. In an embodiment, the fluid permeable support 140 can be cylindrical and can define a lumen. In an embodiment, the fluid permeable support 140 can be formed of perforated coated paper, such as tubular waxed paper. In an embodiment, the fluid permeable support 140 may be formed from spun plastic, such as non-woven permeable nylon and/or polyester webbing.
The fluid permeable membrane 142 can be formed of a material that is permeable to the bodily fluids and has wicking properties. The fluid permeable membrane 142 can have a high absorptive rate and a high permeation rate such that the bodily fluids can be rapidly absorbed by the fluid permeable membrane 142 and/or transported through the fluid permeable membrane 142. In an embodiment, the fluid permeable membrane 142 can be a ribbed knit fabric. In an embodiment, the fluid permeable membrane 142 can include and/or have the moisture-wicking characteristic of gauze, felt, terrycloth, thick tissue paper, and/or a paper towel. In an embodiment, the fluid permeable membrane 142 can be soft and/or minimally abrasive such that the fluid permeable membrane 142 does not irritate the skin of the user. The fluid permeable membrane 142 can be configured to wick bodily fluids away from the urethral opening and/or the skin of the individual such that the dampness of the skin of the individual is lessened and infections are prevented. Additionally, the wicking properties of the fluid permeable membrane 142 can help prevent bodily fluids from leaking or flowing beyond the assembly onto, for example, a bed. In an embodiment, the fluid permeable membrane 142 can be formed of fine denier polyester fibers coated with a thermoplastic water-based binder system.
In an embodiment, the at least one of the fluid permeable support 140 or the fluid permeable membrane 142 may be omitted from the fluid collection assembly 100 such that the wicking material 138 only includes a single material. In an embodiment, the wicking material 138 may include three or more materials, such as the fluid permeable support 140, the fluid permeable membrane 142, and at least one additional material. Regardless, one or more components of the wicking material 138 may include permeable material designed to wick or pass fluid therethrough. The permeable properties referred to herein may be wicking, capillary action, diffusion, or other similar properties or processes, and are referred to herein as “permeable” and/or “wicking.” Such “wicking” may not include absorption of one or more components of the bodily fluids (e.g., urine) into the one or more components of the wicking material 138. Put another way, substantially no absorption of one or more components of the bodily fluids into the one or more components of the wicking material 138 may take place after the wicking material 138 is exposed to the bodily fluids. While no absorption is desired, the term “substantially no absorption” may allow for nominal amounts of absorption of one or more components of the bodily fluids into the wicking material 138 (e.g., absorbency), such as less than about 10 wt % of the dry weight of the wicking material 138, less than about 7 wt %, less than about 5 wt %, less than about 3 wt %, less than about 2 wt %, less than about 1 wt %, or less than about 0.5 wt % of the dry weight of the wicking material 138. In an embodiment, the fluid collection assembly 100 may include one or more absorbent or adsorbent materials instead of or in addition to the wicking material 138.
Additional examples of fluid collection assemblies are disclosed in U.S. Pat. No. 10,226,376 filed on Jun. 1, 2017, the disclosure of which is incorporated herein, in its entirety, by this reference.
As will be discussed in more detail with regards to
The fluid collection assembly 100 may form part of a fluid collection system that includes at least one fluid collector. For example,
Referring to
The fluid collector 144a may also include a fluid reservoir 150a that is in fluid communication with the collector port 148a. For example, the fluid reservoir 150a may receive any bodily fluids that are received by the collector port 148a. The fluid collector 144a may also include a plunger 152 connected to the fluid reservoir 150a. The plunger 152 may be configured to selectively pull bodily fluids through the collector port 148a and into the fluid reservoir 150a and/or push the bodily fluids from the fluid reservoir 150a and through the collector port 148a responsive to manipulation of the plunger 152 by an user of the fluid collector 144a.
Referring to
It is noted that the fluid collection systems disclosed herein may be used with fluid collectors other than the fluid collectors illustrated in
Referring to
The sample port 212 includes an attachment portion 224. As previously discussed, the attachment portion 224 may be attached to any portion of the sump 208. In the illustrated embodiment, the attachment portion 224 is attached to the first end region 204 of the fluid impermeable barrier 202, though it is noted that the attachment portion 224 may be attached to another portion of the sump 208 (e.g., front surface 221, a back surface 223, or a side surface 225). The sample port 212 also include a valve 228 and, optionally, at least one rigid wall 232.
As previously discussed, certain regions of the sump 208 may be difficult to access with a fluid collector when the fluid collection assembly 200 is positioned adjacent to the urethral opening of the individual. For example, the first end region 204 may be difficult to access when the individual is lying down or sitting because the front surface 221 of the fluid impermeable barrier 202 is adjacent or proximate to the urethral opening, the side surface 225 of the fluid impermeable barrier 202 may be adjacent to the thighs of the individual, and the back surface 223 may be difficult to access if the individual's legs are closed. It is noted that the legs of the individual may need to remain closed (thereby preventing access to the back surface 223) to keep the fluid collection assembly 200 adjacent to the urethral opening and to prevent leaks of the bodily fluids. To resolve these issues, in the illustrated embodiment, the sample port 212 includes a tube 260 extending from the attachment portion 224 to the valve 228 (e.g., to the wall 232). The tube 260 defines a passageway (not shown, obscured) that allows the attachment portion 224 to be in fluid communication with the valve 228 such that the valve 228 may remove bodily fluids from the fluid reservoir (not shown, obscured). Generally, the tube 260 is flexible thereby allowing the valve 228 to be moved to a location that is easily accessible.
The tube 260 may exhibit any suitable length. For example, the tube 260 may exhibit a length that is greater than about 2.5 cm, greater than about 5 cm, greater than about 7.5 cm, greater than about 10 cm, greater than about 12.5 cm, greater than about 15 cm, greater than about 20 cm, greater than about 25 cm, greater than about 30 cm, greater than about 40 cm, greater than about 50 cm, greater than about 60 cm, greater than about 70 cm, greater than about 80 cm, greater than about 90 cm, greater than about 1 m, greater than about 1.5 m, greater than about 2 m, or in ranges of about 2.5 cm to about 7.5 cm, about 5 cm to about 10 cm, about 7.5 cm to about 12.5 cm, about 10 cm to about 15 cm, about 12.5 cm to about 20 cm, about 15 cm to about 25 cm, about 20 cm to about 30 cm, about 25 cm to about 40 cm, about 30 cm to about 50 cm, about 40 cm to about 60, about 50 cm to about 70 cm, about 60 cm to about 80 cm, about 70 cm to about 90 cm, about 80 cm to about 1 m, about 90 cm to about 1,5 m, or about 1 m to about 2 m. The length of the tube 260 may be selected based on a number of factors. In an example, the length of the tube 260 may be selected on the size of the individual wherein larger individuals (e.g., more obese, tall, or otherwise larger individuals) may require the tube 260 to exhibit a longer length than when the individual is smaller. In an example, the length of the tube 260 may be selected based on which region of the sump 208 the sample port 212 is attached. In an example, the tube 260 may need to exhibit a longer length when the sample port 212 is attached to the first end region 204 than when the sample port 212 is attached to the back surface 223 since the first end region 204 may be spaced further from an easily accessible location than the back surface 223. In an example, the length of the tube 260 may be selected based on the size of the fluid reservoir since increasing the length of the tube 260 increases the amount of bodily fluids the tube 260 may store therein. As such, the tube 260 may exhibit an increased length when used with a small fluid reservoir than when the tube 260 is used with a large fluid reservoir.
The fluid reservoir of the fluid collection assemblies disclosed herein are configured to hold bodily fluids therein until the bodily fluids are removed using a suction force from a tube. Generally, the suction three from the tube removes the bodily fluids quickly from the fluid reservoir. However, kinking the tube or otherwise stopping the suction force may cause the bodily fluids to pool in the fluid reservoir. Thus, in some embodiments, the fluid reservoir disclosed herein may need to exhibit a volume that is greater than similar conventional fluid collection assemblies to prevent overfilling the fluid reservoir since overfilling the fluid reservoir may cause the bodily fluids to leak from the chamber. For example, the fluid reservoirs of the fluid collection assemblies disclosed herein may exhibit a volume that is greater than 15 milliliters (“mL”), greater than about 30 mL, greater than about 50 mL, greater than about 75 mL, greater than about 100 mL, greater than about 150 mL, greater than about 200 mL, greater than about 250 mL, greater than about 300 mL, greater than about 400 mL, greater than about 500 mL, greater than about 600 mL, greater than about 700 mL, greater than about 800 mL, or in ranges of about 15 mL to about 50 mL, about 30 mL to about 75 mL, about 50 mL to about 100 mL, about 75 mL to about 150 mL, about 100 mL to about 200 mL, about 150 mL to about 250 mL, about 200 mL to about 300 mL, about 250 mL to about 400 mL, about 300 mL to about 500 mL, about 400 mL to about 600 mL, about 500 mL to about 700 mL, or about 600 mL to about 800 mL.
The volume of the fluid reservoir may depend on a number of factors. In an example, the volume of the fluid reservoir may depend on whether the individual using the fluid collection assembly can control urination. For instance, an individual who has no control over urination may urinate more often than an individual who has control over urination. As such, the volume of a fluid reservoir may be smaller (e.g., less than 400 mL, less than 300 mL, or less than 200 mL) for an individual who has no control over urination than the volume of a fluid reservoir for an individual who has control over urination. It is noted that an individual who has control over urination may still use a fluid collection assembly with a volumetrically small fluid reservoir when the individual is given direction to urinate frequently. In an example, the volume of the fluid reservoir may depend on whether the suction force is expected to be stopped to obtain a sample since not stopping the suction force allows the fluid reservoir to exhibit a relatively small volume. In an example, the volume of the fluid reservoir may be selected based on the expected size of the bladder of the individual. For instance, a child or a smaller individual may use a fluid collection assembly having a relatively small fluid reservoir compared to larger individuals. In an example, as previously discussed, the size of the fluid reservoir may depend on whether the sample port includes a tube and the relative length of the tube.
The fluid collection assemblies may exhibit a variety of different structures that allow the fluid reservoirs to exhibit the volumes disclosed herein. For example,
The fluid impermeable barrier 302a includes a sump 308a defining a fluid reservoir 310a. The sump 308a defines a bulge 362 which increases the volume of the fluid reservoir 310a. For example, the bulge 362 may cause the fluid reservoir 310a defined to exhibit a maximum reservoir width WR that is measured perpendicular to the longitudinal axis 364a of the fluid impermeable barrier 302a. It is noted that the maximum reservoir width WR does not extend into the hole 322 defined by the fluid impermeable barrier 302a or a passageway 334 defined by the sample port 312. The maximum reservoir width WR is greater than a maximum chamber width WC of the chamber 316a, wherein the maximum chamber width WC is measured at a location that is spaced from the fluid reservoir 310a. The greater width of the maximum reservoir width WR relative to the maximum chamber width WC increases the volume of the fluid reservoir 310a than if the fluid impermeable barrier 302a did not include the bulge 362.
In an embodiment, the maximum reservoir width WR may be greater than the maximum chamber width WC by at least a factor of about 1.25, at least a factor of about 1.5, at least a factor of about 1.75, at least a factor of about 2, at least a factor of about 2.5, at least a factor of about 3, at least a factor of about 3.5, at least a factor of about 4, or at least a factor of about 5. In an embodiment, the maximum reservoir width WR may be about 3 cm to about 4 cm, about 3.5 cm to about 4.5 cm, about 4 cm to about 5, about 4.5 cm to about 6 cm, about 5 cm to about 7 cm, about 6 cm to about 8 cm, about 7 cm to about 9 cm, about 8 cm to about 10, about 9 cm to about 11 cm, or greater than 10 cm and the maximum chamber width WC may be about 1 cm to about 3 cm, about 2 cm to about 4 cm, or about 3 cm to about 5 cm. The maximum reservoir width WR and the ratio of the maximum reservoir width WR to the maximum chamber width WC may be selected based on the desired volume of the fluid reservoir 310a.
Instead of increasing the width of the fluid reservoir, in an embodiment, the fluid reservoir may exhibit an elongated length. For example,
The fluid reservoir 310b (e.g., a substantially unoccupied fluid reservoir 310b) may exhibit a maximum length L. The maximum length L may be measured from the at least one wicking material 338b to the first end region 304 of the fluid impermeable barrier 302b. For example, the maximum L of the fluid reservoir 310b may be measured parallel to a longitudinal axis 364b of the of the fluid impermeable barrier 302b. Increasing the maximum length L of the fluid reservoir 310b increases the volume of the fluid reservoir 310b thereby increasing the quantity of bodily fluids that may be stored in the fluid reservoir 310b.
The maximum length L of the fluid reservoir 310b may be greater than the length of fluid reservoirs of conventional fluid collection assemblies. In an embodiment, the maximum length L may be greater than about 3 cm, greater than about 4 cm, greater than about 5 cm, greater than about 6 cm, greater than about 7 cm, greater than about 8 cm, greater than about 9 cm, greater than about 10 cm, greater than about 12.5 cm, greater than about 15 cm, or in ranges of about 3 cm to about 5 cm, about 4 cm to about 6 cm, about 5 cm to about 7 cm, about 6 cm to about 8 cm, about 7 cm to about 9 cm, about 8 cm to about 10 cm, about 9 cm to about 12.5 cm, or about 10 cm to about 15 cm. The maximum length L of the fluid reservoir 310b may be selected based on the desired volume of the fluid reservoir 310b.
As previously discussed, the fluid impermeable barriers disclosed herein may be at least partially formed from silicone or another easily deformable material. Such fluid impermeable barriers allow the fluid collection assemblies disclosed herein to be fitted to an individual. For example, the curvature and topography of the region about the urethral opening may be different for different individuals. The easily deformable fluid impermeable barrier allows the fluid collection assembly to easy conform to the curvature and topography of each individual, However, the easily deformable material of the fluid impermeable barrier may inadvertently deform when a fluid collector is connected to the sample port. When bodily fluids are present in the fluid reservoir, inadvertently deforming the fluid impermeable barrier may decrease the volume of the fluid reservoir and cause the bodily fluids to leak from the chamber.
In an embodiment, the leakage caused by connecting the fluid collector to the sample port may be mitigated by connecting the fluid collector to the sample port before bodily fluids are present in the fluid reservoir (e.g., before stopping the suction force). in an embodiment, the inadvertent deformation may be mitigated by using threads to connect the fluid collector to the sample port since the force required to tread the fluid collector onto the sample port, if performed properly, may only deform the fluid impermeable barrier an insignificant amount. In an embodiment, the attachment portion of the sample port may exhibit a large diameter (e.g., may extend radially outwardly from the walls of the sample port) that mitigates any deformation by spreading any force caused by connecting the fluid collector to the sample port over a larger area of the fluid impermeable barrier.
In an embodiment, the inadvertent deformation of the fluid impermeable barrier may be mitigated by increasing the rigidity of the sump relative to the rest of the fluid impermeable barrier. For example,
Referring to
Referring to
The support structure 470b is configured to support the sump 408b thereby increasing the rigidity of the sump 408b. In an embodiment, the support structure 470b is formed from a material exhibiting an elasticity (i.e., Young's modulus) that is greater than the sump 408b. For example, the support structure 470b may include epoxy, polyacetal, polyester, metal, or any other suitable material. In an embodiment, the support structure 470b is formed from a material exhibiting an elasticity that is equal to or less than the sump 408b since even such support structures increase the rigidity of the sump 408. In an embodiment, the support structure 470b is a solid plate (e.g., bent or molded plate). in an embodiment, the support structure 470b is a mesh since the mesh may be lighter than the solid plate which make the fluid collection assembly 400b easier to use without significantly decreasing the rigidity of the support structure 470b.
Disposing the support structure 470b in the fluid reservoir 410b may prevent the support structure 470b from coining in contact with an individual using the fluid collection assembly 400b which may make the fluid collection assembly 400b more comfortable to use. However, the presence of the support structure 470b in the fluid reservoir 410b may at least one of decrease the volume of the fluid reservoir 410b, compress the at least one wicking material 438, or require the at least one wicking material 438 to exhibit a non-cylindrical shape. As such, referring to
The embodiments disclosed above are for fluid collection assemblies that are configured to receive bodily fluids from a female urethral opening or a buried penis. However, the principles and concepts disclosed herein may be used with fluid collection assemblies that are configured to have the openings thereof receive a urethral opening (e.g., male urethral opening) such that the urethral opening is disposed in the chamber. For example,
As previously discussed, the opening 514 is configured to receive the urethral opening. As such, the wicking material 538 does not extend across the opening 514. Instead, the wicking material 538 may exhibit a shape that corresponds to the shape of the fluid impermeable barrier 502 such that a portion of the chamber 516 is substantially unoccupied and the substantially unoccupied portion of the chamber 516 may receive the urethral opening. Further, the sample port 512 is attached to the sump 508. As such, the sample port 512 may be the same or substantially similar to any of the sample ports disclosed herein.
Additional examples of fluid collection assemblies that include an opening that is configured to receive a urethral opening that may include the features and principles disclosed herein are disclosed in U.S. patent application Ser. No. 16/433,773 filed on Jun. 6, 2019, the disclosure of which is incorporated herein, in its entirety, by this reference.
While various aspects and embodiments have been disclosed herein, other aspects and embodiments are contemplated. The various aspects and embodiments disclosed herein are for purposes of illustration and are not intended to be limiting.
Terms of degree (e.g., “about,” “substantially,” “generally,” etc.) indicate structurally or functionally insignificant variations. In an example, when the term of degree is included with a term indicating quantity, the term of degree is interpreted to mean ±10%, ±5%, +2% or 0% of the term indicating quantity. In an example, when the term of degree is used to modify a shape, the term of degree indicates that the shape being modified by the term of degree has the appearance of the disclosed shape. For instance, the term of degree may be used to indicate that the shape may have rounded corners instead of sharp corners, curved edges instead of straight edges, one or more protrusions extending therefrom, is oblong, is the same as the disclosed shape, etc.
This application claims priority to U.S. Provisional Patent Application No. 62/926,767 filed on Oct. 28, 2019, the disclosure of which is incorporated herein, in its entirety, by this references.
Filing Document | Filing Date | Country | Kind |
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PCT/US2020/057562 | 10/27/2020 | WO |
Number | Date | Country | |
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62926767 | Oct 2019 | US |