Field of the Invention
The present invention relates to a catheter's system that can be used for infusion of fluids (drugs, water and nutrients) to the body, with concurrent aspiration of biological material (blood, pus, pathological tissue, toxic substances) from the body, in human and, or, animal tissue, without any blockage problems.
Description of Related Art
There are many kinds of catheters which are used for fluid infusion and aspiration in a clinical or preclinical setting. Traditionally, the catheter's tip that is inserted in biological material, is called “distal” and the tip that stays outside is called “proximal”.
Most of existing catheters have a single lumen and through this lumen the user can alternatively infuse or aspirate liquids.
For example, in a clinical setting, the common intravenous catheter either aspirates blood samples—usually immediately after it's insertion to the vein—or infuses solutions of drugs and, or, nutrients—usually for many hours or days following insertion.
These catheters can infuse or aspirate large quantities of liquids, but they cannot do it concurrently in order to have a constant exchange of drugs and nutrients with the extra-cellular fluid or pathological liquid accumulations of the tissue.
The concurrent fluid exchange is desirable both for monitoring and therapeutic reasons.
There are few catheters with multiple lumina, which can concurrently infuse and aspirate liquids.
For example, the microdialysis catheter after its introduction to a human or animal tissue is continuously perfused with liquid solutions from a pump connected to its proximal tip. The catheter consists of two concentric lumina, or tubes, that are covered at their distal tip by a membrane. Usually the central tube is the efferent and the peripheral tube is the afferent part of the catheter. Part of the perfused liquid is infused to the tissue through the catheter's membrane at its distal end, and extra-cellular fluid is aspirated through the same membrane and the efferent lumen.
Microdialysis catheters and similar catheters, however, were designed for tissue monitoring, and the above described concurrent infusion and aspiration takes place at a few microliter/minute rate flow range and through very small membrane pores.
For therapeutic applications we need much greater liquid exchange rate and membranes or cages with big pores so that it is possible to evacuate low viscosity liquids like pus that block all existing catheters.
A common problem of all kinds of existing catheters for biological fluids is their blockage, due to corking of biological material into their lumen's tip or its covering.
For example, the end therapy catheter system claims to possess the desired liquid exchange rate and blockage free operation through a moving part.
It consists of two concentrical tubes, one infusing and one aspirating, connected properly to infusion and aspiration devices at their proximal tip, and having a filter or membrane or grid or mesh cage covering their distal tip, which contains a hydrodynamically moving device for concurrent infusion and aspiration. The infusing tube is appropriately connected to a moving device that irrigates the surrounding the catheter space, while simultaneously propels with its movement the aspiration through the other tube.
The following documents are considered the most relevant state of the art as mentioned above:
According to the present invention, provided is a fluid exchange catheter system, including infusion and aspiration devices connected to a catheter having two or more lumina. The system further includes a mechanism for creating programmable changes of pressure in infusing and aspirating lumen of the catheter. Accordingly, infused fluids mix with biological fluids, and the mechanism allows this fluid mixture to evacuate without catheter blockage.
As illustrated in schematic form in
The pressure differences in the system are created by any pattern of positive pressures of the infusing pump and the accordingly synchronized pattern of negative pressures of the aspirating pump (pressures always refer to the pressure at the catheter's tip surrounding tissue).
The system allows a fully and safely controllable infusion-aspiration rate and unobstructed fluid exchange.
For example, in one of the many possible system's versions regarding construction and operational mode, a peristaltic pump (E) is programmed to infuse the liquid with a +200 mmHg pressure for 5 sec followed by 10 sec of stop, while the aspirating tube is blocked (N), and a peristaltic pump (A) is programmed to aspirate with a −100 mmHg pressure during the next 15 sec, while the infusing tube is blocked (N), in a 30 sec cycle of operation.
Lots of patterns of pressure changes can be applied depending on the underlying pathology or the research protocol. Both these (infusion and aspiration) pressures at the ends of the system, can be monitored to be kept synchronized into a predetermined range and phase difference and can be protected by alarms and automatic stops (N), whenever there is any system's dysfunction detection, by flow and, or, pressure detector devices (N) placed appropriately in the system for safety (against over-infusion, over-aspiration etc).
Alternatively the infusion and aspiration devices of the system can be fluid containers (E, A), simply using the hydrostatic pressure forces created by their position relative to the catheter's tip, as moving forces for the infused fluid to enter and the aspirated fluid to leave the tissue at the catheter's insertion site.
For this version of the fluid exchange catheter's system, we could simply include only one automatic button (N) programmed to compress the aspirating (and infusing) tube for 5 sec, followed by 5 sec of free flow of the aspirated (and infused) fluid or programmed for any other pattern of time intervals for free and blocked flow.
Any mode of synchronized changes of pressure at any point of the fluid exchange catheter's system, is transferred directly at the infusing and aspirating tip of the catheter through the liquid column of infused or aspirated fluids.
The fluid exchange catheter has a bifurcation part of any configuration, in order to split the two opposite flows in two different lumina.
The distal end of the outer lumen-tube holds an exchange surface that can be a filter or membrane or grid or mesh cage or nothing—just the open tip of the aspirating lumen.
Fluid, which can vary from distilled water to nutrient solutions with drugs, that is supplied through the infusion device (E) to the inner lumen-tube (1), reaches the distal end of the catheter (O), where substance exchange occurs between the infused fluid and substances contained in the surrounding tissue's extracellular fluid. The fluid mixture returns to an aspiration device or collection tank (A). Arrows represent pressure gradients.
In order to remove organic substances that are built up on the exchange surface, and consequently block the catheter, a fluid jet, receiving its supply from the inner lumen's hole(s), is dispersed against the liquid exchange surface's inner wall periodically, unblocking thus the membrane or mesh or grid or filter covering. When just the open tip of the aspirating lumen is the exchange surface, the jet from the infusing lumen unblocks the aspirating lumen.
The construction material of the catheter's system should be in conformity to the norms and regulations existing for clinical and laboratory catheters, including biocompatibility issues etc.
Number | Date | Country | Kind |
---|---|---|---|
20050100452 | Sep 2005 | GR | national |
This application is a continuation of U.S. patent application Ser. No. 13/769,524, filed on Feb. 18, 2013, which is a divisional of U.S. patent application Ser. No. 12/065,019, filed on Feb. 27, 2008, which issued as U.S. Pat. No. 8,398,581, which is the United States national stage of International Application No. PCT/GR2006/000043, filed on Aug. 25, 2006, which claims priority to Greek Patent Application No. 20050100452, filed on Sep. 2, 2005, the contents of each of which are expressly incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
2560915 | Bamberger | Jul 1951 | A |
3189031 | Andersen | Jun 1965 | A |
3669116 | Heyer | Jun 1972 | A |
3812855 | Banko | May 1974 | A |
3955574 | Rubinstein | May 1976 | A |
3965901 | Penny et al. | Jun 1976 | A |
4228802 | Trott | Oct 1980 | A |
4536179 | Anderson et al. | Aug 1985 | A |
4694832 | Ungerstedt | Sep 1987 | A |
4752289 | Balding et al. | Jun 1988 | A |
4755175 | Nilsson | Jul 1988 | A |
4902276 | Zakko | Feb 1990 | A |
5030210 | Alchas | Jul 1991 | A |
5213571 | Fujio et al. | May 1993 | A |
5312400 | Bales | May 1994 | A |
5378230 | Mahurkar | Jan 1995 | A |
5441481 | Mishra et al. | Aug 1995 | A |
5562612 | Fox | Oct 1996 | A |
5925016 | Chornenky et al. | Jul 1999 | A |
5957882 | Nita et al. | Sep 1999 | A |
6379326 | Cimino | Apr 2002 | B1 |
6669679 | Savage et al. | Dec 2003 | B1 |
7540879 | Loaldi | Jun 2009 | B2 |
7780638 | Deniega et al. | Aug 2010 | B1 |
8257306 | Grathwohl | Sep 2012 | B2 |
8398581 | Panotopoulos | Mar 2013 | B2 |
8684967 | Engel et al. | Apr 2014 | B2 |
8882707 | Tsoukalis | Nov 2014 | B2 |
9623177 | Panotopoulos | Apr 2017 | B2 |
20010041860 | Barbut | Nov 2001 | A1 |
20020165492 | Davey et al. | Nov 2002 | A1 |
20030187494 | Loaldi | Oct 2003 | A1 |
20040030281 | Goble et al. | Feb 2004 | A1 |
20040059363 | Alvarez et al. | Mar 2004 | A1 |
20050240146 | Nash et al. | Oct 2005 | A1 |
20060173244 | Boulais et al. | Aug 2006 | A1 |
20060184098 | Bamitz et al. | Aug 2006 | A1 |
20060247553 | Diermann et al. | Nov 2006 | A1 |
20070197959 | Panotopoulos | Aug 2007 | A1 |
20080103516 | Wulfman et al. | May 2008 | A1 |
20090054827 | Eide | Feb 2009 | A1 |
20100204634 | Baxter et al. | Aug 2010 | A1 |
20110106004 | Eubanks et al. | May 2011 | A1 |
20110218492 | McDaniel et al. | Sep 2011 | A1 |
20120289895 | Tsoukalis | Nov 2012 | A1 |
20130035628 | Garrison et al. | Feb 2013 | A1 |
20140046244 | Ray et al. | Feb 2014 | A1 |
20140228869 | Bonnette et al. | Aug 2014 | A1 |
20150282821 | Look | Oct 2015 | A1 |
Number | Date | Country |
---|---|---|
0251512 | Jan 1988 | EP |
1451418 | Oct 1976 | GB |
03089031 | Oct 2003 | WO |
2005023354 | Mar 2005 | WO |
2011011493 | Jan 2011 | WO |
Number | Date | Country | |
---|---|---|---|
20170216502 A1 | Aug 2017 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 12065019 | US | |
Child | 13769524 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 13769524 | Feb 2013 | US |
Child | 15489006 | US |