The invention relates to a perfusion circulation system or circuit for extracorporeally preserving vitality of or regenerating organs, limbs or tissue lobes (hereinafter referred to as organs) for use in transplant surgery or the extracorporeal support of the liver or for biochemical or pharmacological examination in extracorporeal organs.
Devices for the perfusion of isolated organs are of prior art.
Hypothermic preservation at temperatures between 0 and 4° C. is practised at a large scale. With different preservation solutions, preservation times of over 24 hours can be achieved. However, organ regeneration is not possible with this standard method. Hypothermic preservation is not a suitable method of preservation of organs from non heart beating donors.
Normothermic liver perfusion devices are used for vital-state maintenance or regeneration of organs from non heart beating donors. Normothermic perfusion is also a method for vital-state maintenance of organs of decerebrate donors.
According to DE 44 07 863 C2, the perfusion device comprises two separate circuits, one perfusate and one dialysate circuit, assigned to which is an oxygenator, and a device for irrigation cleaning. The latter is performed in-between, every time after stopping the two other circuits. Assigned to each circuit is a pump. The working temperature according to the proposal is 21° C. In the animal experiment, the preserved front leg of a pig was lying in the spray jet of the perfusate inside a chamber that had been closed airtight.
According to WO 99/15011 A1, the perfusate is treated, i.e. maintained at temperature, oxygenated and dialyzed, centrally. From the main line, it is distributed by a pump to the number of lines required for perfusing the organ. In the preservation of livers, lines supplying the Vena portae and the Arteria hepatica are provided. Thus, either receives the same perfusate enriched with oxygen, with the volume of flow determined by the flow resistance of the liver vessels. The liver lies in a perfusion chamber. The perfusate leaving the Vena cava flows through the liver and into the chamber and from there in a central collection vessel.
In the early 1980s, Neuhaus, P. developed a close and pressure oscillating liver perfusion (Extrakorporale Leberperfusion: Entwicklung und Erprobung eines neuen Modells-Habilitationsschrift. 1982; Medizinische Hochschule Hannover) in which the liver protected by a plastic cover is placed in a closed organ perfusion chamber that is filled with fluid and to which cyclical pressure fluctuations simulating respiratory excursions are applied from outside. The vascular lumina follow the artificial intraabdominal pressure fluctuations. The result of the perfusion can clearly be improved by this perfusion method, particularly in the lobular periphery. Besides, underperfusion of large areas which due to the size and related weight of a pig's liver with common placement on the underside, is avoided.
Schon, M. R. uses such a fluid-filled, closed perfusion chamber with cyclic pressure fluctuation in a perfusion device for normothermic extracorporeal liver perfusion (Transplantation von Lebern nicht-herzschlagender Spender im Schweineleber-Transplantationsmodell-Habilitationsschrift 1999. Humboldt Universität zu Berlin). Water heated to about 37° C. in an external heat exchanger flows through the organ perfusion chamber. This circuit is needed in addition to the perfusion circuit. As usual, the perfusate is collected after passage through the organ, then it is transferred and maintained at temperature. A part of it is oxygenated and dialyzed. About one half of this partial flow is returned directly to the Arteria hepatica and the other one half is mixed with the remaining perfusate flow by a pump arrangement. The mixed perfusate is fed to the Vena portae via another heat exchanger.
Each partial circuit contains at last one pump, one heat exchanger and at least one reservoir to obtain a physiological dosage and treatment of the perfusate partial flows in the Vena portae, on the one hand, and the Arteria hepatitis, on the other hand. With this arrangement, the author was able to provide experimental evidence that the normothermic preservation is an alternative to cold preservation both in general and also preferentially for the use of livers from non heart beating donors.
This circulation system comes close to the physiological supply of the organ; the required high level of technical equipment, however, seems to be impedimentary to a further approximation to the natural physiology.
The perfusion device described in WO 00/60936 A1 also seems to require a high level of equipment. In addition, the organ (e. g., the liver) regulates itself (autoregulation) during the inflow and outflow of the perfusate, which fails to work optimally in an extracorporeal environment.
It is the object of the invention to come as near as never before to a natural physiological supply of the organ and to maintain this standard reliably. To avoid damage to the isolated organ, it is particularly necessary to exclude or at least reduced damage to the blood by the apparatuses in a sustained way as far as possible and to avoid side effects which are uncontrollable due to the long residence time of the oxygenated perfusate and have a negative affect on the vital-state maintenance of the extracorporeal organ.
According to the invention, this object is attained by the distinguishing features of the main claim. Other useful embodiments of the invention result from the following claims.
The invention is based on the conception to avoid a detrimental effect of apparatuses, foreign surfaces and auxiliary devices. Following another conception of the invention, the residence time of the oxygenated perfusate is kept short. Surprisingly, it was found that a lower level of technological expenditure according to the invention helps reduce damage to the blood and thereby further adapt the vital state maintaining circuit to the natural physiological conditions.
According to the invention, this objective is attained in that in a perfusion device for the extracorporeal preservation of organs with a perfusion circuit and a dialysate circuit the dialysate passes through the organ perfusion chamber. During this process, the organ is protected by a plastic cover. The dialysate circulates through the dialyzer. Although, in doing so, the concentration of contaminant in the dialysate can increase, it remains within controllable limits. Due to the size of the organ perfusion chamber, the temperature remains relatively constant. Its temperature can be maintained by a controllable, large-area temperature arrangement of relatively low output. The temperature which is simply adjusted in this manner can also be used for maintaining the temperature of the perfusate. For this, in one preferred embodiment of the invention, the dialysate is connected to at least one heat exchanger as a source of heat and cold, respectively.
Furthermore, the invention is based on the conception to provide, in the perfusion circuit, at least one control valve for setting the ratio of the part flows through, and to the at least one inlet of, the organ to be preserved.
The mixing of the perfusate is performed reliably in one of the two reservoirs. The circuit is controlled digitally by a process computer. The simple design and the clearness of the vital-state maintaining circuit according to the invention makes manual control, particularly in emergency operation, possible in advantageous manner, which can also be performed reliably.
With the arrangement according to the invention, at least one more pump and circuit, respectively, is saved in comparison with the prior art.
For biochemical and pharmacological examinations, in particular, devices according to the invention are coupled and connected in parallel. Thereby, essential technical apparatuses, namely pumps, valves and reservoirs, and the medical apparatuses, namely the dialyzer and/or the oxygenator, are used jointly by the coupled individual components. With this coupled arrangement, an equivalent test arrangement is attained.
The following examples of embodiments show how according to the invention an independent dosing of different perfusates to more than one organ inlet can be attained.
With reference to the accompanying drawings, one example of the embodiment of the invention will now be described in detail.
Herein,
In all figures, organ perfusion chamber 1 is sectioned at the level of organ 3 and depicted as top view.
Reference will now be made to
An isolated organ 3 that is to be preserved lies—protected by protective cover 4—in a box-shaped organ perfusion chamber 1. A controllable temperature device 2 is executed as heating mat and is disposed at the bottom of organ perfusion chamber 1. Organ perfusion chamber 1 is completely filled with dialysate 6 and serves as dialysate reservoir. Following is a dialysate circuit with dialyzer Dia, driven by pump P3, for cleaning the perfusate. Flowing through dialyzer Dia, the perfusate is not only cleaned as intended, its temperature is also maintained. In the example of the embodiment, organ 3 is a liver. It has the two inlets Vena portae V.p. and Arteria hepatica A.h. and the outlet Vena cava V.c., through which the perfusate enters and leaves, respectively, as described below. Further secondary outlets, for example, for the bile, are not shown. As described by Neuhaus, organ perfusion chamber 1 is subjected to cyclical pressure fluctuations to simulate an intraabdominal breathing excursion.
The perfusate leaving the Vena cava V.c. is collected in reservoir R1 and pumped by pump P1. One part flows in a second reservoir R2 through valve V2. The other part passes through dialyzer Dia and an oxygenator Ox. The dialyzed, oxygenated and temperature-maintained partial flow of the perfusate is directly available at the inlet of Arteria hepatica A.h., for one, and at another control valve V1, for another. The perfusate partial flows passing valves V1 and V2 mix in a reservoir R2.
The mixed perfusate is pumped in Vena portae V.p. by pump P2. With the two pumps P1 and P2, control valves V1 and V2 and reservoir R2, an independent dosing of the partial flows through the vessels of the organ, liver vessels in this case, is attained.
By way of example, riser 5 has been placed vertically on perfusion chamber 1 as level indication means. In
Several measuring probes pick up characteristics and parameters of the circuit, for example, filling level, pressure, temperature and enable the processing of these signals for an indicating device or a digital process control.
Reference will now be made to
In this version, reservoir R2 and pump P2 have been omitted in comparison with the previous example of an embodiment. The mixing of the perfusate for Vena portae V.p. occurs through a Y-connector, the supply lines to the organ.
With reference to
In contrast to the two first embodiments, oxygenator Ox and dialyzer Dia are disposed in separate branches. As before, the temperature of the perfusate is maintained in the dialyzer branch. To maintain the temperature of the perfusate also on passage through oxygenator Ox, heat exchanger WT is provided. Heat exchanger WT is connected to the dialysate circuit. In another form of this embodiment, valve V2 can be dispensed with without loss of the physiological supply of extracorporeal organ 3.
A fourth embodiment with reference to
Number | Date | Country | Kind |
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10340487.2 | Sep 2003 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/DE04/01945 | 9/2/2004 | WO | 5/19/2006 |