The present invention in general relates to medical devices and in particular to a device and method to serially irrigate fluid followed by evacuation of the fluid in the uterus, with extension of the fluid into the Fallopian tubes, for the purpose of collecting cells from the Fallopian tubes.
Ovarian cancer is a cancer that begins in an ovary, and is the result of the development of abnormal cells that have the ability to invade or spread to other parts of the body. In 2012, ovarian cancer occurred in 239,000 women and resulted in 152,000 deaths worldwide, which made ovarian cancer the seventh most common cancer and the eighth most common cause of death from cancer in women. Ovarian cancer is disproportionately deadly because this type of cancer lacks any clear early detection or screening test, meaning that most cases of ovarian cancer are not diagnosed until they have reached advanced stages. Thus, ovarian cancer screening is of high clinical interest because the disease is not typically detectable at its early stages, when it is the most curable.
Occasionally, ovarian tumor cells may migrate into the uterus. Thus, it would be useful to have a device that may irrigate a portion of the Fallopian tubes on both sides, and collect the irrigation fluid for cell analysis in the search for an ovarian malignancy. Furthermore, ovarian cancer cells may proceed in a retrograde direction from the ovary into the Fallopian tube. It is also thought that some ovarian cancers have their origins in the Fallopian tube. Therefore, the ability to flush fluid into the Fallopian tube and to collect this fluid is desirable from a diagnostic standpoint.
Introduction of fluid into the uterus is commonly performed for a hysterosalpingogram (HSG), a diagnostic radiologic procedure involving introduction of contrast material under pressure into the uterus, to cause the contrast to flow into the Fallopian tubes for visualization of the uterus and Fallopian tubes. However, retrieval of injected fluid is extremely difficult or impossible to perform. The uterus is a muscular organ with a tiny intraluminal volume (approximately 3-5 cc) with a collapsible structure, and the Fallopian tube has a small diameter (approximately 1 mm at its proximal portion). At the junction of the uterus and the Fallopian tube is the uterotubal junction, where the lumen is 0.3 to 0.5 mm in diameter. Thus, irrigation requires significant pressure to cause injected fluid to track from the uterus into the tube, and attempts to retrieve the injected fluid are generally unsuccessful. When a vacuum is drawn on an intrauterine catheter, the uterus collapses around the catheter and prevents withdrawal of injected fluid.
Infusion catheters are used for hysterosalpingography. During hysterosalpingography, infusion catheters are advanced into the uterus, while an enlarged portion of the catheter seals against the cervical os to allow fluid pressure to be developed in the uterus. The cervical sealing portion of the catheter may be a balloon, a solid dilated structure on the catheter body, or a foam stopper. Infusion catheters are designed to inject fluid, and fluid retrieval is not contemplated or performed with these catheters. Thus, there exists a need for a device and method to serially irrigate fluid, followed by evacuation of the fluid in the uterus, with extension of the fluid into the Fallopian tubes, for the purpose of collecting cells from the Fallopian tubes for examination and analysis, while also avoiding the pain and discomfort experienced by patients during the diagnostic procedure.
An uterotubal irrigation system is provided that includes a cannula with an external sheath that has a larger inner diameter than an external diameter of an irrigation tube positioned within the sheath so as to form an evacuation channel between the external sheath and the irrigation tube along a length of the cannula, and where a distal end of the sheath is connected to a second distal end of the irrigation tube; a syringe in fluid communication via an irrigation port with the irrigation tube and a fluid reservoir, the said syringe having a primary vacuum port connected to a primary vacuum line connected to a vacuum source; an evacuation port connecting the cannula to the syringe; a second vacuum line that is smaller then the primary vacuum line in fluid communication with the evacuation channel and a collection tube, the collection tube for storing a fluid evacuated from a patient's uterus following injection of the fluid that has been previously stored in the fluid reservoir; and two or more slits formed in a distal end of the sheath, the two or more slits expanding outward with the retraction of the irrigation tube to form an evacuation basket to support uterine walls of the patient's uterus under an applied vacuum during fluid evacuation from the uterus. The syringe further includes a plunger having a plunger seal, where the plunger is biased with a spring so that the plunger seal is positioned to block the primary vacuum port into the syringe, and a vacuum produced by the vacuum source is pulled through the second vacuum line to evacuate the injected fluid via the evacuation basket and the evacuation channel.
A process of using the uterotubal irrigation system is provided that includes inserting a cannula into the patient's uterus; expanding the evacuation basket by retracing the irrigation tube; injecting a fluid into the patients uterus; evacuating the fluid from the patient's uterus and retrieving and collecting the fluid in the collection tube; and wherein the injecting and evacuating are controlled with the depression of the syringe plunger to modulate the degree of vacuum. During the process of using the uterotubal irrigation system, the injecting and evacuating are staggered to serially and repetitively inject and retrieve multiple fluid aliquots to provide a sufficient fluid volume and number of sample cells for evaluation. In a specific embodiment the process is a hysterosalpingogram (HSG) procedure.
An uterotubal irrigation system is provided that includes a catheter with two opposing outlet openings on a distal tip of the catheter that injects an irrigation fluid in two opposing jets that splay out laterally toward the openings of a patient's Fallopian tubes when the catheter is inserted in the uterus of the patient, where the two opposing outlets are angled toward the openings to the patient's Fallopian tubes, an occlusion balloon or a plug that is situated on a wall of the catheter at a distance between 1.5 to 2.5 centimeters proximal to the distal tip of the catheter that is inflated to seal the patient's cervical os prior to insertion of the catheter distal tip into the patient's uterus; and a collection inlet proximal to the distal catheter tip for collecting the injected irrigation fluid.
A process of using the uterotubal irrigation catheter system is provided that includes inflating the occlusion balloon; inserting the catheter into a patient's uterus; injecting a fluid into the uterus; and evacuating the fluid from the patient's uterus and retrieving and collecting the fluid at the collection port. The process of injecting and evacuating are staggered to serially and repetitively inject and retrieve multiple fluid aliquots to provide a sufficient fluid volume and number of sample cells for evaluation. In a specific embodiment the process is a hysterosalpingogram (HSG) procedure.
The present invention has utility as an uterotubal irrigation system and process for implanting hysterosalpingogram (HSG) procedures. Embodiments of the inventive uterotubal irrigation system serially irrigate fluid followed by evacuation of the fluid in the uterus, with extension of the fluid into the Fallopian tubes, for the purpose of collecting cells from the Fallopian tubes. Due to the tiny volume of the uterus, a single injection of several cc's of fluid followed by evacuation will yield a minimal amount of fluid for analysis. It is thus necessary to repetitively inject and retrieve multiple fluid aliquots to provide sufficient fluid volume and sample cells for evaluation. It is also important to stagger the steps of fluid injection and fluid retrieval, otherwise a concomitant injection and evacuation will prevent fluid from ever entering the Fallopian tube.
It is to be understood that in instances where a range of values are provided that the range is intended to encompass not only the end point values of the range but also intermediate values of the range as explicitly being included within the range and varying by the last significant figure of the range. By way of example, a recited range from 1 to 4 is intended to include 1-2, 1-3, 2-4, 3-4, and 1-4.
Embodiments of the uterotubal irrigation system provide a partially flexible cannula that is introduced through the cervical os into the uterine cavity. The inventive cannula has an enlarged external plug of approximately 2 cm that is proximal to the distal tip of the cannula, to occlude the os and permit infusion of fluid into the uterus. The inventive cannula has an internal tube for irrigation, and an external sheath with multiple slits near the distal end of the cannula. The distal tip of the external sheath is attached to the distal end of the irrigation tube. In specific embodiments, the inner diameter of the external sheath is approximately 0.5 mm greater than the outer diameter of the irrigation tube. The irrigation tube passes through a sliding seal on the proximal end of the external sheath. An irrigation port on the proximal end of the irrigation tube permits fluid infusion, while an evacuation port on the proximal end of the external sheath allows evacuation of fluid via the space between the outer diameter of the irrigation tube and the inner diameter of the external sheath. When the irrigation tube is retracted relative to the external sheath, a series of slits on the sheath at the distal tip of the cannula expand outward to form a basket to maintain the uterine cavity and prevent the uterine cavity from collapse due to a vacuum draw during evacuation of fluid for cell analysis.
Embodiments of the inventive uterotubal irrigation system provide serial fluid injection followed by fluid evacuation. The injection and evacuation modes of embodiments of the inventive system are controlled with the depression of a syringe plunger to modulate the degree of vacuum exhibited in the evacuation mode of the irrigation cannula. The system utilizes a port in the side of the syringe body, where upon full retraction of the syringe plunger against a stop set at a predetermined volume (e.g., 5 cc), the plunger seal covers and seals the port. Parallel vacuum lines are present in the system, where one vacuum line is a small diameter (approximately 0.5 mm) line that connects to the evacuation port on the external sheath of the irrigation cannula, and the other vacuum line is a large diameter (approximately 5-10 mm along the majority of its length) line that extends to the vacuum source. A collection tube is positioned in-line between the evacuation port on the irrigation cannula and the large diameter pressure line. When the spring loaded syringe plunger is completely retracted, during refilling of the syringe from a fluid source, the plunger seal closes off the vacuum port into the syringe from the large vacuum line, and a vacuum is pulled through the small diameter line to evacuate fluid via the expanded basket on the irrigation cannula. When the syringe plunger is depressed to inject fluid, the port on the side of the syringe connected to the large diameter vacuum line is opened. During plunger depression, the majority of vacuum flow is derived from the large diameter line, with its low fluid resistance, and a minimal vacuum is experienced in the small diameter line to drain the fluid as the fluid is being injected by the syringe. The flow rate and negative pressure provided by the vacuum source is also maintained at a moderate level to render the system functional. A one-way valve is present at the fluid irrigation source, so that fluid may only be introduced into the syringe and out of the irrigation cannula upon syringe depression and retraction.
An inventive embodiment of the uterotubal irrigation system is provided as a catheter for cell sampling that has two outlet openings on the catheter distal tip that inject irrigation fluid in two opposing jet streams that splay out laterally toward the os or openings of both Fallopian tubes. The two separate opposing outlets on the distal tip of the catheter are angled toward the openings to the Fallopian tubes, where the irrigation channels within the catheter bend outward toward the outlet openings. In operation an occlusion balloon or a plug that is situated at a distance between 1.5 to 2.5 centimeters proximal to the tip of the catheter is inflated to seal the cervical os prior to insertion of the catheter tip into the uterus. In a specific embodiment, the occlusion balloon or a plug is situated at a distance of 2.0 centimeters proximal to the tip of the catheter. The occlusion balloon seals the cervical os during the irrigation and fluid collection process. The injected irrigation fluid proceeds a distance into both Fallopian tubes, and the fluid then circulates back into the uterine cavity, where the fluid exits via a collection port in the catheter. In an inventive embodiment, the collection inlet is approximately 1 cm proximal to the distal catheter tip. The retrieved irrigation fluid undergoes cytologic examination to detect the presence of malignant cells.
Embodiments of the catheter based uterotubal irrigation system provide serial fluid injection followed by fluid evacuation. An inventive fluid injection device is provided that may be used in conjunction with the inventive cell collection irrigation catheter to limit the amount of pressure used for injection. The use of embodiments of the inventive fluid injection device may be used to avoid the pain and discomfort experienced by the patient during the diagnostic procedure. Embodiments of the pressure limiting fluid injection device have a syringe plunger that is composed of a compression spring connected to the distal sealing plunger face. A threaded plunger advances to compress the compression spring. The threaded plunger contains a groove along its length that is keyed by a pin that extends through the syringe body into the groove. A drive disc is rotatably fixed on the proximal end of the syringe body, and the drive disc contains internal threads that mate with the threaded plunger. When the drive disc is rotated, the threaded plunger moves forward to compress the fluid inside the syringe. The maximal pressure that may be developed by the syringe is determined by a clutch disc that lies coaxially outside the drive disc. At a predetermined amount of torque, the clutch disc slips relative to the drive disc. The torque setting may be set by adjusting the friction that exists between the clutch disc and the drive disc. In a specific embodiment, one or more clutch adjustment screws extending through the clutch disc may be tightened down on the drive disc, so that the torque exerted on the threaded plunger will be limited to a given level. This in turn limits the degree of compression exerted by the spring, thus limiting the injection pressure. The pressure limiting injection device incorporates the compression spring for energy storage, such that continuous rotation of the clutch disc is unnecessary for fluid injection. Rather, the clutch disc is rotated to bring the syringe to the desired injection pressure level, and then rotated at intervals as necessary to re-pressurize the system. In a specific embodiment the full retraction of the syringe plunger provides a predetermined volume of irrigation fluid (e.g., 5 cc).
Referring now to the figures, FIG.1 is a picture of an uterotubal irrigation system 10 according to an embodiment of the invention. A syringe 19 with a user controlled plunger 16 is outwardly biased by spring 18, and a plunger seal 22 rests against a plunger stop 20 positioned so that the plunger seal 22 blocks the primary vacuum port 14 on the side of the syringe 19 to the primary vacuum line 46 (see
In operation as shown in
Embodiments of the pressure limiting fluid injection device 100 of
The foregoing description is illustrative of particular embodiments of the invention, but is not meant to be a limitation upon the practice thereof. The following claims, including all equivalents thereof, are intended to define the scope of the invention.
This application claims priority benefit of U.S. Provisional Application Ser. No. 61/968,226 filed Mar. 20, 2014; the contents of which are hereby incorporated by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2015/021858 | 3/20/2015 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 61968226 | Mar 2014 | US |