The present invention relates to an apparatus according to claim 1 for collecting or extracting blood escaping or exiting from a wound area. It further relates to a clamping device or pushing device according to claim 31, a depository device according to claim 32 as well as a set according to claim 40.
In dentistry, the use of bone regeneration or replacement, respectively, material as a prosthetic bone material is prevalent. These implantation materials include, e.g., calcified microporous copolymer materials, which are commercially available under the names Bioplant®, HRT®, Synthetic Bone-Alloplast, tricalcium phosphate “Aerosorb” by the company Corasan, “Bio-Oss” by the company Geistlich, and the like.
The above mentioned and further bone regeneration or replacement, respectively, materials are prepared for their use by adding the patient's own blood. The blood used herefor is sucked from the bleeding wound base of the operation site as bone marrow-containing blood and subsequently added to the granular bone regeneration material. The viscous fluid mixture generated herewith can then be delivered manually to the site of action.
Though, apparatuses for delivering the viscous fluid mixture of blood and bone replacement material at the site of action are known from state of the art (see, for example, U.S. Pat. No. 4,366,822); however, so far, no specially prepared apparatus for absorbing the blood from the wound base of the operation site prior to its admixture to the bone replacement material is available a dentist.
One object of the present invention is therefore to propose an apparatus for collecting blood or other fluids escaping from a wound area, in particular for their further use.
The object of the present invention is solved by the feature combination of claim 1
Thus, an apparatus for collecting blood or other fluids escaping from a wound area is proposed, the apparatus comprising a contact device for contacting the bleeding wound area, the contact device comprising a multitude of—in particular blood permeable or blood-admitting—openings or pores (in the following shortly referred to as: pores). The pores serve for absorbing the contacted blood into an interior of the contact device. The interior may comprise or consist of sections of the pores or openings.
The pores may be designed or embodied such that they indeed permit a permeation or penetration of fluid, in particular blood, however, inhibit a permeation or penetration of solid materials such as bone fragments and the like being present in the contacted blood. As a multitude of—e.g., blood permeable—pores are provided, solids or solid objects present in the contacted blood may clog at most some of the pores and thus disable them. With intended use of the apparatus according to the invention, however, a sufficient number of pores that will not clog and therefore serve for the absorption of blood further on will remain in the wound area, e.g., within the patient's oral cavity.
The pores thereby may be embodied such that they evolve a capillary attraction or effect, whereby a suction device or the like is not mandatorily necessary. In addition, an apparatus according to the invention based on capillary attraction may advantageously be operated with, e.g., only one hand. Also, cleaning the suction device and/or discarding disposable articles necessary for operating the suction device, such as tubes and the like, are omitted.
The capillary attraction may additionally be improved by known methods for increasing the surface tension or the wetting capability, respectively, of the material of the apparatus used. An example for such a method is the corona treatment, an electrochemical method for the surface modification of plastic or synthetic materials. The method of plasma-enhanced chemical vapour deposition (PECVD) may also be used herefor.
Preferably, a synthetic material having appropriate biocompatible properties is used as material for the contact device. Such a material may be polyurethane foam. The pores' diameters may be measured such that favourable characteristics are present for absorbing the medium to be absorbed, such as, e.g., blood. The number of cells per inch (ppi) may be set or determined according to the necessary flow properties in or within the material as well as the capillary attraction. For example, a value between 60 and 80 ppi is given. This corresponds to an approximate mean pore diameter between 0.5 and 0.75 mm.
For example, also a polyurethane foam product such as VOCO Pele Tim® by the company VOCO GmbH from Cuxhaven, Germany, e.g., having wedge shape, 6×8 mm, may be used which has already been utilized in the dental field. These foam pellets are advantageously characterized by their hygienic, lint-free application. Additionally, they are sterilizable, if needed.
Advantageous embodiments or developments of the object according to the invention are each subject-matter of the dependent claims.
Thus, in a preferred embodiment, the apparatus according to the invention comprises a suction device for generating a suction acting on the contact device—and via the contact device onto a contacted blood or a different fluid. The advantages associated herewith encompass increasing a suction power or performance and/or absorption capacity of blood present within the wound area. The latter may advantageously shorten the time necessary for collecting the blood. Furthermore, in a case where only small quantities of blood are present, a blood amount sufficient for the respective purpose may be collected more easily.
In yet another preferred embodiment, the apparatus according to the invention comprises a compressing device by means of which pressure may be applied onto the contact device. This way, blood having been absorbed into or within the interior of the contact device may be released more easily from the interior again, for instance by pressing, squeezing, pushing or wringing, e.g., for further use thereof.
Providing a reservoir for a fluid or a blood reservoir at or on the apparatus according to the invention for retaining or storing collected blood after its permeation through the interior of the contact device—and thus through the contact device itself—on the one hand allows for a small design of the interior of the contact device. This further allows for reaching more easily wound areas that are difficult to access or reach by means of the apparatus according to the invention and, by means of the blood reservoir, for storing or retaining blood in a better way and, optionally, using it further on. The blood reservoir may, for instance, be furnished with an anticoagulant coating or substance.
In an again further preferred embodiment of the apparatus according to the invention, the apparatus comprises a connecting device for connecting the apparatus with a customary injection syringe in a fluid communication. According to this embodiment, the apparatus according to the invention may therefore advantageously be connected with material already present in the medical and the dental field, such as injection syringes, in a simple manner. Thereby, the injection syringe may serve for both generating a suction power or performance and for absorbing the blood in the sense of a blood reservoir such as described above comprising the advantages associated therewith.
In an again further preferred embodiment, the apparatus according to the invention comprises a compressing device by means of which pressure is applied by means of a simple pushable or pushing device by a piston. This advantageous embodiment allows for an easy operating of the apparatus with one hand and enables the user to execute other tasks in parallel. Thus, e.g., the wound area from which blood shall be taken by means of the apparatus may be exposed in a better and easier way.
This embodiment further offers the possibility of collecting blood several times from the contact device by applying pressure with a single-handed operation. With this pressure application by the pushable or pushing device, the blood may either flow into an attached reservoir due to gravity, or, with a positioning turned by 180 degrees, be collected in a different container or repository.
In the embodiment comprising the retention or storage in an attached reservoir, there is further proposed an opening in the housing of the reservoir for withdrawing or extracting or draining the blood easily. This offers the advantage that the blood may be further used quickly and easily without having to be conducted through the contact device again. Further an appropriate device for closing this opening is further proposed which may, e.g., be realized by means of a plastic snap connection corresponding to the state of the art.
In an again further preferred embodiment, the apparatus according to the invention comprises a rotary device, the rotary motion of which is transmitted through a thumb or finger by means of a device to or onto a guiding device at or to or onto which the contact device is fixed or attached.
The rotary device may (in the present text, the term “may” is to be understood in the sense of “preferably”) comprise at least one wheel-shaped structure.
The rotary device may convert a rotary motion into a translational motion or a linear motion, in particular a displacement motion.
In a further preferred embodiment, the apparatus according to the invention may comprise a reservoir for a bone regeneration substance. Thus, blood collected by means of the contact device may be prepared for its use within the apparatus.
The present invention may also be used for intaking blood, other fluids or tissue and bone fragments by means of the contact device in order to subsequently discard them. This way, fluids, mostly blood or wound secretions, or impurities or contaminations may be removed during operations by means of the contact device according to the present invention.
The present invention is not limited to its use in dentistry, but can be used in the whole surgical field—e.g., in abdominal surgery. There, substantially larger amounts of blood than in dentistry are common, so that some of the embodiments described above which, e.g., comprise a continuous suction device, offer particular advantages here. Further possible fields of applications are, for instance, orthopaedics or bone surgery, in which the present invention may advantageously be used for, e.g., for the absorption of wound blood from the cancellous bone or spongiosa.
For the above-mentioned and other applications, all embodiments may have a substantially larger scale or measure and may be suited for absorbing a larger amount of blood than is common and necessary in the dental field.
The apparatus according to the invention may further also serve for extracting or taking samples of blood or other fluids. A sample may, e.g., be taken during an operation for a subsequent analysis. Its result may be used for influencing the further course of the operation. Herefor, especially one of the closable embodiments according to the invention is suited.
In an again further preferred embodiment, the apparatus according to the invention comprises a device having a sliding or shifting or pushing mechanism. By means of the pushable or pushing device, the contact device may be transferred into a position, in which structures of the apparatus apply pressure on or onto the contact device such that at least a part of the blood/the fluid retained or stored herein may be discharged from of the contact device.
In an again further preferred embodiment, the apparatus according to the invention comprises a housing having an opening which is embodied, e.g., longitudinally. Through the opening, the piston that is later on arranged slidably or shiftably in or within the housing, and comprising an accommodation device for the contact device and a section for initiating a displacement or shifting or sliding motion or a pushing or pushable device, respectively, may be inserted in or mounted with, respectively, the housing.
For this purpose, the apparatus according to the invention may be designed or embodied substantially in two pieces (housing and piston), not considering the contact device for once in this case. This two-piece embodiment offers the advantage that the parts may each be easily produced, e.g., by using an injection-moulding process. Furthermore, the assembly can be easily accomplished due to the small amount of parts. The assembly of both parts may moreover preferably be carried out by hand or manually, i.e., without using any tools. This provides for the advantage that the parts may be produced, sterilized and packed separately and be assembled at the end user's site. This allows for treating the several or different parts differently (e.g., sterilizing them or designing them germ-reduced or germ-free in different ways). It is known to the person skilled in the art, that during a sterilization process of synthetic materials or plastics, for instance, polyethylene, which is often used in medical products, deformations of material may occur. Such deformations may lead to fitting problems between piston and housing and disadvantageously complicate or even inhibit any displacement or shifting or sliding motion. Thus, with parts having already been assembled before sterilization, it may come to—using as an example the present invention—that a displacing or moving or shifting of the piston within the housing is no longer guaranteed. Through the possibility of the two-piece embodiment, however, it is advantageously possible to prepare the parts of the apparatus according to the invention separately and thereby, e.g., already sterilize them and have them assembled by the user, e.g., only when required. As only two parts are involved, this is possible on-site in a quick and easy manner, without any special effort, preferably also without any tools.
In an again further preferred embodiment, the two parts (piston and housing) of the previous embodiment may comprise appropriate limiting devices such that their disassembly is aggravated or preferably inhibited without being destructed once having been put together or assembled.
Suitable limiting devices may, for example, be designed or embodied by—in particular elastic—plastic barbed hooks that allow for an assembly of the two parts, while, however, inhibiting or notably aggravating their disassembly by the user. The construction principles of such plastic barbed hooks, e.g., in the form of snap lock or catch, are known to the skilled person.
The limiting devices may, for instance, during mounting, the piston into the housing, lock or snap or snap in, or during displacing or moving or shifting the piston in or within the housing for the first time after mounting, depending on the constructional embodiment.
When or if the snapping function is actuated after displacing or moving or shifting the piston for the first time, after the mounting a confining of the displacement path of the piston may be effected thereby and a renewed positioning of the piston into the starting position and the disassembly may be inhibited or aggravated, respectively.
Providing limiting devices in the proposed embodiment may advantageously prevent the user from disassembling the parts after having used the apparatus, possibly cleaning the parts and processing or preparing them for further use. This way, the known risks in connection with the handling of blood known to the skilled person are prevented.
In an again further preferred embodiment, the housing may be produced from a transparent plastic or synthetic material in order to enable an, e.g., optical control of the retraction of the piston.
In a further preferred embodiment, the apparatus according to the invention has the shape of tweezers or is in at least one section designed or embodied having the shape of tweezers. It comprises at least two arms having at least one jaw each for gripping, in particular clamping, the contact device, as well as at least one clamping or pushing or pushable, respectively, device by means of which an action or effect may be exerted on sections of the apparatus for fixing the arms in a position relative to each other.
The present invention furthermore proposes a depository device for depositing or accommodating the apparatus according to the invention. This device serves for storing the contact device in moments in which it is not required during the treatment of the patient, whereby it should be further usable nevertheless. Therefor, the depository device may encompass a socket or a pedestal comprising at least one opening provided or intended and arranged for supporting the apparatus according to the invention in the interior of the opening. Alternatively, the depository device comprises at least one bolt or spike or pin on or onto which the apparatus may be put or slipped.
Hereby, in a preferred embodiment, preferably a clamping effect may be exerted onto the contact device by means of sidewalls or other sections in order to further securing the contact device against an unintended falling out of the depository device.
Furthermore, the depository device may be designed or embodied in its geometry for accommodating the contact device. Both elements therefore may have been provided to match each other upon producing them.
The contact device may in a further preferred embodiment be secured in the depository device by geometrical, physical embodiments of the depository device alone. Herefor, indentations, stops, ledges, protrusions and the like may be provided.
The depository device according to the invention may, instead of a socket or pedestal, comprise fixing or attaching devices for a detachable connection, which may ensure a spacing of the apparatus deposited in the depository device or the contact device, respectively, from a possibly unclean or unsterile depository area. Those fixing or attaching devices may, among others, include clamping devices, bolts or spikes or pins already mentioned above etc.
The depository device according to the invention may be designed or embodied for being secured against unintendedly overturning or toppling over. This includes reducing the risk of overturning or toppling over yet.
In the following, the present invention is exemplarily illustrated by means of the appended drawing, in which same reference numerals denote same or identical or similar components. In the partly greatly simplified figures, it applies:
a shows the sixth embodiment of
b shows a seventh embodiment of
The contact device 17 comprises a multitude of pores 19 through which blood may enter into an interior of the contact device 17 that is not further specified or illustrated in
Should individual pores 19 of the contact device 17 be clogged by, e.g., sucking in bone fragments during use of the apparatus 1 according to the invention when absorbing blood, the blood may still be absorbed through the contact device 17 into the section 13 serving as blood reservoir, in which negative pressure is present. The apparatus 1 according to the invention may thus also be used for collecting blood from a contaminated—or generally comprising solids or solid objects—wound base.
In the section 13 of the
It is obvious that the section 21 as well as its side walls 23 may comprise each suitable form or shape for optimized squeezing blood out of the sponge-like contact device 17. Thus, they may be designed or embodied funnel-shaped, tapered, triangular and the like. Also wavy or undulating profiles as well as sharp edges may be provided. As indicated in
It is pointed out that, e.g., the reservoir effect of the section 13 of
The sponge-like design of the contact device 17 of the second embodiment of
The housing may, in particular in the second embodiment of
Due to the simple and integrated arrangement of the pushable or pushing device 27 in or within the housing 29, it may be possible to perform the whole handling with one hand.
Furthermore, due to the simple constructional design, it is possible to produce the whole apparatus 1, except for the contact device 17, in a cost-effective plastic or resin injection-moulding process. This is of particularly advantage when using the apparatus 1 in connection with blood and bone regeneration material, due to reasons known to the skilled person. Also a subsequent, known sterilization process is easily feasible.
In
Furthermore, also a suction device not specified and not shown here may be attached to the tubing. The suction resulting therefrom may enhance the capillary effect of the contact device 17 for being filled with blood and/or suck off the blood out of the reservoir 13. Thus, a continuous emptying of the reservoir 13 independent from the location and position of the apparatus 1 is possible.
In
The pushing device 27 may thereby extend from an interior of the apparatus 1 to an exterior.
The pushing device 27 may preferably be shiftable through an opening of a periphery of the jacket or jacket limiting surface of the apparatus 1.
It may preferably not be shiftable or movable through a front surface of the apparatus.
In
Subsequently, the elastically widened material of the edge or border or rim of the partial opening 41 ideally completely returns into the original position or the initial state. The use of tools is advantageously not required herefor.
The contact device 17 may, however, also initially be brought or put to a smaller or narrower diameter or measure by twisting or skewing or warping the partial opening 41 without widening the borders or rims thereof, and then, in this form or shape, be introduced through the partial opening 41 or an arbitrarily designed slot into an interior of the piston 7, where it then may unfold again into a form or shape having a larger diameter by means of unfolding and thereby jam or clamp in or within the interior of the piston 7. The use of tools is again advantageously not required herefor.
Due to the mechanical clamping, no further fixing aids such as adhesives or additional mechanical connections or linkages such as clips or cramps, respectively, rivets or studs, respectively, hooks and the like are necessary. Thus, a step of adhering or combining or connecting, respectively, by means of tools is advantageously dispensable. Furthermore, components of the adhesive may not enter, e.g., an oral cavity. Additionally, injuries caused by sharp-edged or hard additional mechanical connections or linkages may not occur, as such linkages are not required for the proposed clamping. With the proposed clamping, an endangerment of the patient may therefore advantageously be ruled out.
Apart from the saw tooth profile 43, all other geometries—also having barbed hooks and the like—or appropriate profiles for the purpose of mechanical clamping are also possible. These may also protrude into an interior of the piston 7 and thereby contribute to a further increase or enhancement of the degree of fixation or the fixation effect.
The shown piston 7, in the representation of
As a material for the piston 7, exemplarily polyurethane or polyester, preferably in medical grade specification, may be used.
In
In its lower or bottom representation,
The piston 7 further comprises a pushing device 45, by means of which the piston 7 may be shifted or moved, e.g., by means of the thumb in or within a housing described later on.
In its front end (at the left border of the representation of
The housing 51 shown partially and in a top view in the upper portion of
The slot 53 preferably connects an interior of the apparatus 1 with an exterior.
The slot 53 comprises two widenings or broadenings or enlargings 55 and 57.
As can be seen by means of the dashed lines between the upper and the lower representation of
The enlargings 55 and 57 and the broader or wider sections 47 and 49 are to be understood as a device based on the lock-and-key principle. According to the invention, any other device than the device shown in the drawing may be used, by means of which a lock-and-key principle may be realized. In particular, the invention is not restricted to exactly two enlargings and two wider sections. A different number of enlargings and/or wider sections is also conceivable.
The device based on the lock-and-key principle preferably prevents the piston's 7 falling out of or unauthorized removal from the housing 51 in a radial direction or in a transverse or cross direction of the housing 51.
Already during insertion of the piston 7 into the housing 51, or upon displacing or shifting the piston 7 within the slot 53 of the housing 51 for the first time, and by means of fixing or attaching devices not shown in
For the housing of the apparatus 1, exemplarily a medical-grade styrene (or styrol)-butadiene is used.
The clamping or pushable or pushing, respectively, device 63 is designed such that it may fix the arms 58, 59 of the apparatus 1 according to the invention in at least one position relative to each other. Thus, the distance between the jaws 60, 61 is ensured or kept.
Furthermore, the clamping or pushable or pushing, respectively, device 63 according to the invention may be designed in order to adjust or set the distance between the arms 58, 59 in such a variable manner that the apparatus 1 is thus adapted or adjusted or fit to the different sizes of the contact device 17.
The clamping or pushable or pushing, respectively, device 63 may be an element which is independent from the apparatus 1, or it may be permanently—but preferably displaceably or shiftably—connected with the apparatus 1. It may, e.g., be a section thereof.
The clamping or pushable or pushing, respectively, device 63 may be designed such that it may be displaced or shifted forwards and backwards in the longitudinal direction of the apparatus 1.
The upper representation of
The lower representation of
One or more jaws 60, 61 may comprise barbed hooks or other devices for increasing or enhancing an adhesion of the jaws 60, 61 at or on the contact device 17, for hooking in or into the contact device 17, or for a differently designed frictional and/or form closure connection of at least one of the jaws 60, 61 with the contact device 17.
The clamping or pushable or pushing, respectively, device 63 may also be placed in a second position (not shown) over or above the contact device 17. In the second position, the contact device 17 or a section hereof is compressed, and the blood—or fluid in general—present therein may be squeezed or pushed out thereof.
Furthermore, the clamping or pushable or pushing, respectively, device 63 may be designed for being turned around or about the longitudinal axis of the apparatus 1. Thereby, the contact device 17 may be wrung or wrung out. Suitable guiding structures (not shown) for achieving a rotary motion may be provided in a section of the clamping or pushable or pushing, respectively, device 63 and/or at or on the apparatus 1.
a shows a front view of the jaws 60, 61 of the apparatus 1 according to the invention of
b shows the jaws 60, 61 in a front view of a further embodiment, wherein the jaws 60, 61 of the apparatus 1 according to the invention are each arch-shaped or C-shaped in a cross-section thereof. Preferably, they may each form a semicircle. Together, their inner circumferences may preferably form a full circle. Thus, sections of the contact device having a round or circular cross-section may advantageously be accommodated with substantially the same pressure distributed across the circumference or periphery of the section. The clamping or pushable or pushing, respectively, device 63 may again be circular in a cross-section, as is exemplarily shown in
Number | Date | Country | Kind |
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10 2008 028 525.0 | Jun 2008 | DE | national |
10 2009 005 058.2 | Jan 2009 | DE | national |
10 2009 014 503.6 | Mar 2009 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP09/04334 | 6/16/2009 | WO | 00 | 2/23/2011 |