US20220062594A1 - Sheath device for inserting a catheter - Google Patents

Abstract

In a sheath device for inserting a catheter into a patient's body, comprising a first sheath having a proximal end and a distal end, wherein when used as intended the distal end of the first sheath is provided for arrangement in the patient's body and the proximal end of the first sheath is provided for arrangement outside the patient's body, and wherein the first sheath comprises a tubular section and a sheath housing, which is disposed at the proximal end of the section and comprises a receiving channel for a catheter, according to the invention the tubular section is detachably held in a clamping element of the sheath housing in a non-positive manner so as to be able to easily shorten the tubular section.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• This application is a continuation of U.S. application Ser. No. 16/696,664, filed Nov. 26, 2019, now allowed, which is a continuation of U.S. application Ser. No. 15/474,592, filed Mar. 30, 2017, now U.S. Pat. No. 10,525,238 B2, which is a continuation of U.S. application Ser. No. 13/261,902, filed May 21, 2014, now U.S. Pat. No. 9,642,984 B2, which is a national phase entry under 35 U.S.C. § 371 of International Application No. PCT/EP2012/076587, filed Dec. 21, 2012, and published as International Publication No. WO 2013/092971 A1, which claims the benefit of U.S. Provisional Application No. 61/579,198, filed Dec. 22, 2011, and claims priority to European Patent Application No. 11075272.2, filed Dec. 22, 2011, the entire disclosures of which are hereby incorporated herein by reference.
TECHNICAL FIELD
• The invention resides in the mechanical field and can advantageously be used in medical engineering. It relates to a sheath device for inserting a catheter into a patient's body, wherein the sheath leads into the patient's body and a proximal end of the sheath protrudes therefrom. The sheath provides a lumen, through which a catheter can be inserted into the patient's body.
BACKGROUND OF THE INVENTION
• Such sheath devices are known in principle. They are used to insert various catheters, for example in the minimally invasive medical field. Such a sheath can, for example, be provided for inserting a blood pump for cardiac support, such a unit comprising a distal pump unit, a hollow catheter and a drive shaft which is guided through the hollow catheter. In miniaturized form, such pumps are often times designed so that they can be radially compressed and inserted, in the compressed state, together with the catheter through a blood vessel of the body. The pump can then be expanded at the site of use, for example in a blood vessel or in a ventricle. In the expanded state, with delivery elements activated, such a pump can then attain the required pumping capacity.
• In addition to such compressible heart pumps, other functional elements are also conceivable, which are introduced into a cavity of a body by means of a sheath according to the invention, such as stents or milling heads for removing plaque from vessels.
• Compared to a direct insertion, inserting such functional elements and catheters by means of a sheath is considerably easier and also associated with fewer medical risks.
• The sheath itself can be inserted, for example into a vascular system, using the known Seldinger Technique. For this purpose, first an opening is introduced in a body vessel by means of a puncturing needle, whereupon a guide wire is pushed in. A dilator is then optionally introduced via the guide wire, and thereupon the sheath itself is pushed in. The guide wire can then be removed, unless it is required for further guide tasks, and other elements can be introduced via the sheath.
• A corresponding method is known from WO 02/43791, for example. According to this document, a heart pump is advanced along a guide wire into the left ventricle of a patient and a pump unit is advanced out of the sheath through the vascular system to the ventricle.
• A corresponding fluid pump, which is provided for high rotational speeds so as to achieve a corresponding pumping capacity, in the form of a blood pump is likewise known from WO 02/43791 A1, but also fromEP 2 047 872.EP 2 047 872 A1 describes a pump which comprises a distal pump unit, to which a proximal shaft hollow catheter adjoins. A drive shaft extending in the shaft catheter is connected to a drive unit for driving the rotor of the pump.
• Using a convenient sheath for inserting a catheter, notably comprising a drive shaft, has the advantage that the catheter, and more particularly a drive shaft, experiences less mechanical stress during insertion. This is advantageous in particular with high mechanical stresses to which a drive shaft is exposed when a blood pump is operated.
• For a convenient use of a corresponding sheath for inserting a catheter, notably comprising a distal pump unit, it is desirable to be able to advance the sheath, together with the hollow catheter, as close as possible to the vicinity of the site of use and then remove the shaft catheter or the pump from the sheath, so as to then be able to retract the sheath at least a certain distance. The unit to be introduced is thus moved the shortest possible distance in the vascular system or corresponding cavities of the patient's body outside a sheath, so that the strain on the vascular walls due to insertion of the foreign object as well as the mechanical stress of the unit to be inserted are substantially reduced.
• On the other hand, such a procedure requires a corresponding excess length of the sheath, which after being advanced and subsequently retracted typically protrudes a certain distance from the patient's body.
BRIEF SUMMARY OF THE INVENTION
• It is the object of the present invention to advantageously design a corresponding sheath device so that it is particularly easy to handle.
• According to the invention, a sheath device for inserting a catheter into a patient's body comprises a first sheath having a proximal end and a distal end, wherein the distal end of the first sheath is disposed inside the patient's body when the sheath is used as intended, while the proximal end protrudes from the patient's body. The first sheath additionally has a tubular section and a sheath housing, which is disposed at the proximal end of the section and comprises a receiving channel for a strand-shaped body, and more particularly for a catheter.
• Because the tubular section is detachably held in a clamping element of the sheath housing in a non-positive manner, the sheath device can first be pushed into the patient's body by a certain distance so as to insert the catheter into the patient's body, the catheter can then be extracted and the sheath device can be pulled a certain distance out of the patient's body. The tubular section can then be released from the clamping particularly easily, and it can be shortened and re-clamped.
• This makes it particularly easy to cut the sheath device to the suitable size after use, so that it does not protrude from the patient's body any further than necessary.
• According to an advantageous embodiment of the invention, the tubular section can be displaced into the sheath housing when the clamping element is released. The tubular section can thus be accommodated in the sheath housing, removed within the sheath housing or removed through a proximal opening of the sheath housing.
• It seems to be particularly useful for the tubular section to lead into the sheath housing in direct extension of the receiving channel for the catheter. This design makes the insertion of a catheter into the tubular section particularly simple, in that the catheter is first inserted into the sheath housing, guided in the receiving channel thereof and thus directed without effort to the mouth of the tubular section. It can thus be assured that the insertion of the catheter into the proximal end of the sheath device is simplified and can be reliably carried out.
• This design also allows the proximal end of the tubular section of the sheath to be easily pushed into the receiving channel inside the sheath housing, so as to either be accommodated there or be removed.
• According to a further advantageous embodiment of the invention, the clamping element comprises an elastically deformable clamping ring, which surrounds the tubular section and can be pressed by a manipulating element such that the ring radially clamps the tubular section. Such a damping element has a particularly simple mechanical design, is reliable, saves space and is easy to operate. It effects a non-positive fixation of the tubular section, which can also easily be released again.
• To this end, the clamping ring may be radially deformable by axial pressure action. The ring can be designed as an elastomeric ring for this purpose, or as a slotted ring which is made of a plastic material or a metal.
• As an elastomeric ring, the clamping ring can be pressed flat, for example by means of a pressure piece, wherein the ring expands radially inward and outward, whereby the inside diameter of the ring is decreased. If the clamping ring is a slotted plastic or metal ring, it can be compressed radially inward, for example under the action of a wedge-shaped body on the radial outside of the ring. For this purpose, for example a ring having a wedge-shaped cross-section can be used, which is moved axially relative to the tubular element. The clamping ring can also have a conical cross-section. In a preferred embodiment, it is a clamping ring which also assures a fluid-tight connection between the sheath housing and the tubular element, as can be implemented in form of the aforementioned elastomeric ring, for example. However, the sealing action can also be implemented by anadditional sealing element73, for example when using a slotted plastic or metal ring.
• The clamping element may comprise a screw element, for example for axially pressing a clamping ring. The screw element can then be used, for example, to press a pressure piece against the clamping ring in the axial direction.
• So as to facilitate the severability of portions of the tubular section so as to shorten the same, the tubular section can advantageously have at least one predetermined breaking point at least at the proximal end, the predetermined breaking point being used to sever a longitudinal section of the tubular section. In some regions, the tubular section can comprise peripheral indents or perforations or other weakened regions of the material in the circumferential direction, for example, which can optionally also be predetermined by a molecular structure.
• The tubular section can likewise have one or more predetermined breaking points or tear lines extending the axial direction, which are known in so-called peel-away introducer sheaths, in the case of such tear lines, a sheath can be opened starting at one end by pulling two or more casing parts apart and can be pulled off. For this purpose, a tubular section can also comprise handling elements at the proximal end, such as loops or tabs.
• According to the invention, the sheath device can also comprise a cutting element, by means of which a part of the tubular section can be severed, or perforated, notched or scored for the purpose of easier severing. For example, one or more blades can be inserted in the sheath housing so that the tubular section is automatically notched when it is pushed through the sheath housing. Such notching can, for example, take place in the longitudinal direction of the tubular section. It is also possible to provide a blade which, during a rotation of the sheath housing relative to the tubular section, creates a cut or a weakened region of the tubular section in the circumferential direction.
• Such blades can be produced from very hard material, such as a ceramic material, for example, so that even tubular sections which are reinforced, notably reinforced by a metal woven fabric, can be cut. It is also possible to provide substantially needle-shaped blades, which can cut both during a movement of the tubular section in the axial direction and during a rotation in the circumferential direction.
• According to a particularly advantageous embodiment of the invention, the cutting element comprises at least one blade, which is movably guided, notably in the sheath housing, and is notably movably guided radially toward the catheter. Such a blade may be actuated by means of a handle70 which is located on the outside of the sheath housing, so that a cut for severing a portion of the tubular section can be made using a simple manual movement when pushing the tubular section out of the patient's body and displacing it relative to the sheath housing.
• In addition to a sheath device of the type described above, the invention also relates to a catheter system comprising a catheter and such a sheath device, wherein according to the invention the sheath housing advantageously may comprise a further clamping element on the proximal side of the clamping element, wherein the further clamping element is provided so as to radially clamp the catheter or so as to radially clamp a second sheath surrounding the catheter and/or a functional element which is connected to the catheter.
• The corresponding further clamping element can, in principle, likewise comprise a clamping ring and can, for example, have the same design as the first clamping element so as to fix the tubular section. However, the further clamping element can also have a different design than the first clamping element and in general be designed in accordance with one of the afore-described variants of a clamping element.
• The invention further relates to a method for inserting a catheter comprising a functional element disposed at the end thereof into a patient's body, wherein the catheter is inserted into the sheath housing and the tubular section and thereupon is inserted in the tubular section into the patient's, the tubular section is then pulled a certain distance out of the patient's body in the proximal direction, and the clamping elements is released and the tubular section is moved into the sheath housing.
• After being moved into the sheath housing and/or pushed through the sheath housing, the tubular section can be shortened. Before or after shortening, the tubular section can again be clamped by means of the clamping element.
• The shortening is advantageously carried out by tearing open the tubular section in the longitudinal direction, notably starting from the proximal end of the tubular section, and by then tearing it off.
BRIEF DESCRIPTION OF THE DRAWINGS
• The invention will be shown in drawings and described hereafter based on an exemplary embodiment.
• FIG. 1 is a schematic overview of a vascular system comprising an inserted first sheath;
• FIG. 2 is a detailed view of a section ofFIG. 1;
• FIG. 3 shows an embodiment of the invention comprising a first sheath and a second sheath;
• FIG. 4 shows an embodiment of a pump;
• FIG. 5 shows a second sheath comprising a pump extracted therefrom;
• FIGS. 6, 7 show the pulling of a pump into a second sheath;
• FIGS. 8, 9 show the transfer of a pump from a second sheath into a first sheath;
• FIG. 10 is a longitudinal section through a sheath housing comprising a tubular section;
• FIG. 11 is a longitudinal section through a portion of a sheath housing comprising a cutting element;
• FIG. 12 is a longitudinal section through a sheath housing comprising a clamping element for the tubular section and a further clamping element; and
• FIG. 13 is a longitudinal section through an alternative clamping ring comprising a conical pressure piece.
DETAILED DESCRIPTION OF THE DRAWINGS
• FIG. 1 shows a schematic humanvascular system1. One of thefemoral arteries2 is located in the groin region and is connected to theaortic arch3 via an aorta and then leads into theventricle4. Anintroducer sheath10 is first inserted into thefemoral artery2, for example using the Seldinger Technique. The femoral artery, or any blood vessel, is punctured for this purpose, for example using a steel cannula having a cutting tip. Aguide wire12 is pushed through the steel cannula, which is inserted into the puncture site, and inserted into theleft ventricle4 retrogradely via theaortic arch3. After the puncturing cannula is removed, thefirst sheath10, which is designed as an introducer sheath and comprises atubular section11 and optionally a dilator, which is not shown here, is threaded on the guide wire and inserted into the vascular system through the punctured site, wherein the sheath is inserted a short distance into the lumen of the vascular system or even to the site of use of an element to be inserted. Thereafter, a fluid pump is inserted into the vascular system through theintroducer sheath10.
• Thetubular section11 of thefirst sheath10 is inserted into the artery such that the proximal end of thefirst sheath10 is located outside the femoral artery and can thus be used for inserting a pump, for example. It is thus possible to thread the pump on theguide wire12 so as to guide the pump into the left ventricle by means of the guide wire.
• It is also possible to guide thetubular section11 of thefirst sheath10 through the guide wire into the left ventricle and to then remove theguide wire12 from the first sheath. A pump unit that may be present is then guided through the first sheath volume into the vicinity of or into theleft ventricle4.
• In the present example, the method is only illustrated based on the insertion of a pump into the left ventricle so as support a cardiac function. However, it is easy to see for a person skilled in the art that the pump, or another functional element, can also be disposed and introduced in other regions of the endogenous vascular system.
• FIG. 2 shows the region ofFIG. 1 in which thefirst sheath10 is guided from outside through the endogenous tissue into the lumen LG of thefemoral artery2. The first sheath comprises atubular section11, which is connected to asheath housing13 at the proximal end. Thetubular section11 defines a lumen L₁, which has an inside diameter d₁₁. This inside diameter widens toward the proximal end of thetubular section11 in a trumpet-like shape in theregion14.
• Thesheath housing13 contains a haemostatic valve, which is known from the prior art. This valve prevents fluid present in the lumen LG from exiting to the outside through the lumen L₁.
• In the illustration ofFIG. 3, thefirst sheath10 ofFIG. 2 is coupled to asecond sheath20. Only atubular section21, which defines a lumen L₂having an inside diameter d₂₁, is shown of thesecond sheath20. The outside diameter of the distal end of thesecond sheath20 is such that it can be inserted into thesheath housing13. However, the inside diameter d₂₁is larger than the inside diameter d₁₁.
• A pump, which is not shown and present in the lumen L₂, can now be transferred into the first sheath lumen L₁from the second sheath lumen L₂by pressing. The pump is then transported through the first sheath lumen L₁to the site in the vascular system where the pump is intended to effect the action thereof The pump can either be guided on a guide wire for this purpose, or it can be introduced without guide wire through the first sheath lumen. The first sheath can be advanced distally to the site of use of the pump before the pump is pushed out, so as to protect the pump and the vascular walls as well as the shaft catheter.
• A possible embodiment of apump30 will be described in more detail based onFIG. 4. Thepump30 comprises adistal pump unit31 and ashaft catheter32, which adjoins the proximal end of thedistal pump unit31. At the proximal end, which is not shown, theshaft catheter32 comprises a coupling for coupling theshaft catheter32 to a drive element. The drive element can be disposed outside the patient's body and causes a flexible shaft extending in theshaft catheter32 to rotate, which in turn drives thedistal pump unit31.
• The distal pump unit comprises apump housing33, which is produced from intersecting nitinol struts. Portions of the nitinol housing are provided with acoating34, which extends distally and proximally of arotor35 disposed in thehousing33. The rotor is connected to theshaft36 extending through theshaft catheter32 and thus caused to rotate. The housing and the rotor can be compressed, which is to say the pump is a self-decompressible pump. The pump deploys after the distal pump unit is pushed out at the distal end of a sheath. So as to compress the pump in preparation for the implantation, the distal pump unit is pulled into the distal end of a sheath lumen of a second sheath. The inside diameter of the sheath lumen is at least greater than the outside diameter of the shaft catheter.
• The rotor may be displaceable relative to the pump housing in the axial direction, notably by means of an axial displacement of the drive shaft. However, the rotor may also be fixed in the axial direction relative to the pump housing.
• The pump optionally comprises anoutflow hose37, which defines a flow duct for the pumped fluid located proximally of therotor35. Discharge openings, which are not shown in detail, are located at the proximal end of theoutflow hose37.
• The pump can, of course, also be switched from pumping operation to suction operation, so that the pump no longer conducts fluid from the distal end to the proximal end, but vice versa.
• A detailed description of a further suitable pump can be found indocument EP 2 047 872 A1, for example.
• The function of the system shall now be described based onFIGS. 5 to 9.
• FIG. 5 shows apump30′, which substantially corresponds to thepump30 ofFIG. 4. To simplify matters, details of the pump are not shown. Only the bellied housing and the “pigtail” located distal of the bellied housing are shown, the pigtail preventing the heart pump from being suctioned against the cardiac wall. Theshaft catheter32′ runs proximal of thedistal pump unit31′. Asecond sheath20′ is provided, which encloses aregion38′ of theshaft catheter32′ and comprises a lumen L₂, the inside diameter d₂₁of which is smaller than the diameter of thedistal pump unit31′ when it is deployed.
• Thepump30′ shown inFIG. 5 is a compressible pump, which is to say thedistal pump unit31′, which comprises the pump housing and the rotor located therein, among other things, is designed such that it can be compressed, which is to say that the diameter thereof can be decreased. After a quality inspector or a physician, for example, has confirmed the correct function of thepump30′, such as by observing the rotational movement of the rotor unit located in thedistal pump unit31′ during a test run, thedistal pump unit31′ is pulled into the lumen L₂of thesecond sheath20′ by pulling theshaft catheter32′ in the proximal direction. By pulling the pump into thesecond sheath20′, bending or damage of the shaft catheter or of the shaft extending therein is prevented. Thepump30′ shown inFIG. 5 and thesecond sheath20′ enclosing theregion38′ of theshaft catheter32′ form asystem200 which allows the function of thepump30′ to be tested in due time before surgery and the pump to be compressed by pulling thedistal pump unit31′ into the distal end of thesecond sheath20′, and thus prevent damage to the shaft.
• Although the system can be implemented both with actively decompressible pumps and with self-decompressible pumps, it is particularly suitable for self-decompressible pumps, which is to say pumps in which the distal pump unit automatically restores the original size outside the sheath.
• FIG. 6 shows an intermediate step when pulling thedistal pump unit30′ into the lumen of thesecond sheath20′. It is apparent that thedistal pump unit30′ can be compressed and reduced to a smaller diameter, so that thedistal pump unit30′ can be accommodated in the lumen of thesecond sheath20′.
• FIG. 6 further shows acoupling39′ adjoining theshaft catheter32′, the coupling allowing the shaft extending in the shaft catheter to be coupled to a drive unit. Because thecoupling39′ often times has a larger outside diameter than the inside diameter of the lumen L₂, thesecond sheath20′ is usually added from the proximal end of theshaft catheter32′ in the distal direction before thecoupling39′ is mounted, so that the pump is shipped as asystem200, which is to say the pump comprising thesecond sheath20′ located proximal of thedistal pump unit31′ and thesub-assembled coupling39′.FIG. 6 also shows a slightly trumpet-shaped expansion of the distal end of thesecond sheath20′. The trumpet-shaped expansion24′ makes it easier for thedistal pump unit31′ to be pulled into the lumen L₂of thesecond sheath20′.
• InFIG. 7 finally thedistal pump unit31′ is located entirely in the lumen L₂of thesecond sheath20″. Thesecond sheath20″ comprises twosub-assembled grip units22″, which allow better holding or removal of thesecond sheath20″ when pulling thedistal pump unit31′ into the lumen L₂, or subsequent tearing. If a “pigtail” is present, the same is advantageously likewise pulled into the lumen L₂, so that thedistal pump unit31′, together with the components of the pump located distal of thedistal pump unit31′, are present in the lumen L₂.
• It is apparent fromFIG. 8 how thesystem200 comprising thepump30′ andsecond sheath20″ is combined in an operative connection with thefirst sheath10 to form asystem100. First, the distal end of thesecond sheath20″ is inserted into the sheath housing of thefirst sheath10. As soon as the distal tip of thesecond sheath20″ is seated against the mouth of the tubular section of thefirst sheath10, the pump is transferred from thesecond sheath20′ into thefirst sheath10′ by pushing the pump in the distal direction, the pushing taking place by pushing of theshaft catheter32′. The diameter of thedistal pump unit31′ is thus reduced further to the inside diameter d₁₁of the lumen L₁.
• FIG. 9 shows the subsequent step, in which thedistal pump unit31′ is located entirely in the lumen L₁of thefirst sheath10. The fact that thedistal pump unit31′ is located entirely in the lumen L₁of thefirst sheath10 can be indicated, for example, by using a colored marking50 which is applied to the outside of theshaft catheter32.
• Thesecond sheath20″, which is designed as a “peel-away” sheath, is then removed from theshaft catheter32′ by tearing open the peel-away sheath from the proximal end to the distal end and pulling it off theshaft catheter32′. The directed tearing open from the proximal end to the distal end can be supported by notches A, however it is primarily based on the orientation of the molecule chains of the plastic material that is used from the proximal direction in the distal direction.
• After the peel-away sheath has been removed, thepump30′ is guided further inside the lumen L₁of thefirst sheath10 to the desired location.
• The first sheath can optionally be advanced to the immediate vicinity of the site of use before or after the pump has been inserted using the distal sheath mouth. The first sheath has the required length to do so.
• A reinforcement of thesecond sheath20″ is not required, in particular when pulling thedistal pump unit31′ into the distal end of the second sheath lumen L₂, because the risk of the shaft kinking during a pulling motion is significantly reduced.
• When the pump is transferred from the second sheath to the first sheath, as shown based onFIGS. 7 to 9, the second sheath may comprise a reinforcing structure in form of an introduced wire, or thetubular section21″ of thesheath20″ is not produced from a flexible plastic material, but from a non-deformable plastic material or metal.
• Another option for stabilizing the pump and the second sheath is that of holding thesecond sheath20″ by way of a supportingelement40 in form of a stable outer sleeve when advancing thepump30′ in the distal direction, which is to say in particular when transferring thepump30′ from the second sheath into the first sheath.
• Hereafter, another possible variant of a method for inserting a pump into a left ventricle shall be described. As a preparatory measure, the pump is first filled with a sterile physiological salt solution and is thus completely freed from air. Then, the peel-away sheath located proximal of the distal pump unit is advanced to a potentially present outflow hose. The diameter of the peel-away sheath is10 Fr, for example. After the peel-away sheath has been advanced to the outflow hose, the peel-away hose is surrounded by a sleeve-shaped element so as to hold the second sheath. The distal pump unit is then pulled into the peel-away sheath, optionally by performing a slight rotational movement, by performing a pulling motion in the proximal direction on the shaft catheter. The pump is advanced into the second sheath so far that a potentially present pigtail is likewise secured in the peel-away sheath. These steps make it possible to examine the functional capability of the pump even before surgery and to insert the pump only then into a sheath, without having to act under time pressure. For example, it is only then that the vascular system is punctured so as to insert the first sheath. However, so as to save time, it is thus also possible for an assistant to prepare the pump, while the user already carries out the puncturing.
• After a 9 Fr introducer sheath, for example, has been introduced into the left ventricle, a potentially present dilator is pulled out of the introducer sheath and removed therefrom.
• The pump, which is held in the peel-away sheath and which initially is, for example, enveloped by the sleeve so as to hold the second sheath, is then pushed into the sheath housing until the tip of the peel-away sheath strikes against a mechanical stop. The pump is then transferred from the peel-away sheath into the tubular section by pushing the shaft catheter. As soon as the distal pump unit has been completely transferred into the introducer sheath, as can be verified based on an optical marking on the catheter shaft, for example, the peel-away sheath can be torn open and pulled off the shaft catheter. The pump is then advanced inside the first sheath into the left ventricle. The first sheath is subsequently pulled back out of the left ventricle, to the point where the descending aorta begins.
• The positioning of the distal pump unit in the left ventricle can be controlled by way of radioscopy, for example. For this purpose, an X-ray visible marking is located on the pump housing or in the vicinity thereof, for example on the catheter, or the pump housing itself is visible to X-rays. The discharge region of the pump, which is to say the discharge openings of an outflow hose, should likewise be located in the region of the ascending aorta. This can also be checked using an X-ray visible marking. A potentially present pigtail catheter tip should make contact with the tip of the left ventricle.
• So as to remove the pump from the ventricle, the pump is retracted into the introducer sheath by means of a pulling force that is applied to the shaft catheter and is removed from the arterial vascular system in the compressed state. If the first sheath has already been shortened, the pump can also first be retracted a certain distance into the shaft catheter so as to compress the pump. For this purpose, the shaft catheter may comprise a pull-in funnel into which the pump can be pulled by pulling on the drive shaft. The first sheath and further remaining components are then removed from the vascular system.
• The invention provides a particular advantage when a long sheath is used during the implantation and explanation of the pump. The long sheath is not only used, as is customary in the prior art, to insert the pump into an endogenous lumen, but also to guide the pump through the sheath lumen into the vicinity of the site of action. To this end it is advantageous in the medical field if the sheath has a length between 40 and 120 cm. The length is determined by the later site of action of the pump and the patient's physique.
• If the pump is pulled out of the endogenous lumen together with the long sheath, bleeding of the femoral artery is stopped by means of a pressure dressing. As an alternative, the pump can be pulled out of the sheath lumen of the long sheath. A further guide wire can then be placed through the lumen of the sheath, and an element for closing the puncture can be guided via this guide wire after the sheath has been removed. This allows improved stemming of the bleeding to be achieved.
• FIGS. 10 to 13 show in particular an embodiment of the first sheath according to the invention, comprising one or more clamping elements for fixing atubular section41 in asheath housing43.
• FIG. 10 shows a longitudinal section of asheath housing43, which substantially has the shape of a cylindrical sleeve which is closed at least at thedistal end44 facing the patient's body by apressure screw45. Thesheath housing43 has acontinuous receiving channel46 for atubular section41 of the first sheath. In the illustration ofFIG. 10, coming from the patient's body, thetubular section41 is shown continuously up to the flushingspace47 of the receivingchannel46, and then in dotted form in the proximal direction. This indicates that thetubular section41 can be axially displaced relative to thesheath housing43 inside the receivingchannel46 or, in other words, thesheath housing43 can be displaced on thetubular section41.
• So as to insert a functional element, for example a pump, into the first sheath, thetubular section41 is usually pulled out of thesheath housing43 in the distal direction so far, or it is positioned during production of the first sheath, so that it ends approximately at the level of thefirst stop piece48. A second sheath comprising a retracted pump, as described above, can be advanced up to this point, so as to then move the pump from the second sheath into the first sheath.
• The first clamping element comprises elements such as thefirst pressure screw45, afirst clamping ring50 made of an elastomeric material, and thefirst stop piece48.
• The pressure screw is screwed to the sheath housing by means of an external thread in an overlapping region with thedistal end44 of thesheath housing43. Manually rotating thepressure screw45 thus brings about a movement of the pressure screw in the axial direction, which results in axial compression or expansion of the clampingring50. During an axial compression, the clampingring50 tends to give way radially inward and outward so as to maintain the volume thereof and thus clamps thetubular section41, because it experiences resistance at the proximal side by thefirst stop piece48.
• Thetubular section41 is thus axially fixed relative to thesheath housing43. This fixation can easily be released by loosening thepressure screw45, so that thetubular section41 is then easy to axially displace in thesheath housing43. To this end, when it is relaxed, the clamping ring can have an inside diameter that equal to or larger than the diameter of the first sheath.
• So if thetubular section41 is first pushed as far as possible into the patient's body to allow insertion of the pump, protected by the sheath, to the site of use, for example a ventricle, thetubular section41 is pulled out after the pump has been removed and the sheath as a whole protrudes relatively little from the patient's body. The clampingelement48,45,50 can then be released and thesheath housing43 can be pushed closer to the patient's body on thetubular section41. Thetubular section41 then extends completely through thesheath housing43 and optionally protrudes from the same in the proximal direction. Using means which will be described in more detail hereafter, thetubular section41 can then be severed in some regions so as to remove the excess length.
• A so-called combined haemostatic valve, which is composed of adome valve51 and avalve plate52, is provided inside thesheath housing43 to provide better sealing action. The valve plate closes thesheath housing43 if at this point neither thetubular section41 nor a shaft catheter extends through the receivingchannel46, while thedome valve51 is optimized so as to provide tight sealing around a strand-shaped body, for example the tubular section or a catheter.
• Afurther pressure screw54 is provided at theproximal end53 of thesheath housing43, the pressure screw basically functioning in the same manner as thefirst pressure screw45 and effecting the compression of asecond clamping ring56 relative to a secondmechanical stop57 via apressure piece55. A special feature that should be mentioned here is that the distal end of thesecond clamping ring56 has a conical shape, which favors a deformation radially inward when exerting an axial pressure by way of thepressure screw54. Thesecond stop57 has a conical design in the opposite direction. However, it is also possible at this point to use anon-conical clamping ring56, and instead one which has a rectangular or round cross-section.
• It is then possible to additionally dispose one or more further valves in the flushing space between the clampingelement48,45,50 and the flushinginlet58, whereby it is assured that a fluid-tight connection exists between thetubular section41 and thesheath housing43, even if the clampingelement48,45,50 is released.
• FIG. 10 schematically indicates aflushing element58, which allows the flushingspace47 to be flushed with a liquid that prevents microbes from penetrating into the patient's body through the first sheath. This flushing is particularly effective if thetubular section41 ends in the flushingspace47 or on the distal side thereof, so that the flushing liquid can reach both the outside and the inside of thetubular section41.
• FIG. 11 shows, by way of example, the arrangement and operating principle of a cutting element according to the invention.
• If no precut predetermined breaking points, or no predetermined breaking points that are predefined in another manner, for example by a predetermined molecule structure or regional weakening of the wall thickness of thetubular section21, are provided, these can be introduced in a suitable manner when using the first sheath by way of a cutting element. In the region of the flushingspace47 of thesheath housing43 inFIG. 11, a cutting element comprising blades59,60 is provided, which cuts the tubular section in the circumferential section, for example during a rotation of the sheath housing relative to the tubular section. It is also possible to introduce cuts in the axial direction.
• For this purpose, the blades59,60 can also be disposed such that they cut in the longitudinal direction during a movement of thetubular section41 in the axial direction, as indicated by thearrow61. It is possible to provide blades both for cutting in the circumferential direction and for cutting in the longitudinal direction.
• FIG. 11 also shows that the blades59,60 can be moved radially toward thetubular section41 by actuation from outside thesheath housing43. There, a guide72 extending in the radial direction for one or more blade holders70, a corresponding seal75 and a suspension74 can be provided, so that microbes are prevented from penetrating via this displacement element for the blades and the blades, when not actuated, radially have a distance from thetubular section41. After use of the first sheath, it is then possible to manually apply pressure to the blades and the portion of thetubular section41 that is not required can be cut off. A stop71, prevents the cutting depth from exceeding a critical dimension and causing damage to a catheter which may be present inside the sheath.
• The blades shown can also form a cutting element for a second sheath.
• FIG. 12 shows an advantageous use of the second clamping element on the proximal side of thesheath housing43 after thetubular section41 has been shortened, and ashaft catheter66 leads out of the proximal end of thetubular section41 and then on to a coupling element, which is not shown, for a drivable shaft of a pump and out of thesheath housing43. The shaft catheter is sealed in theaforementioned dome seal51, and the clamping element, together with the elements of thesecond pressure screw54 and of thesecond clamping ring56, which is axially compressed by thepressure piece55 relative to thesecond stop57, gives way radially inward far enough for theshaft catheter66, which has a substantially smaller outside diameter than thetubular section41 or a second sheath, to be clamped and in particular to be additionally sealed. Both thetubular section41 and theshaft catheter66 protruding therefrom can thus be fixed in thesheath housing43.
• The second clamping element is likewise suitable for fixing the second sheath with thesecond clamping ring56, when inserting a second sheath into thesheath housing43, such that the second sheath is sufficiently fixed relative to thesheath housing43, and notably relative to thetubular section41, so as to allow theshaft catheter66 to be pushed through.
• The first and second clamping rings50,56 can be produced from an elastomer, for example a rubber or a silicone elastomer, and can thus be fully elastic, but be deformable without being able to compress the volume. At this point, using an elastic foamed material in which some of the volume can be compressed is also conceivable.
• FIG. 13 is a schematic view of another type of aclamping ring62, which can be produced from a plastic material or a metal, for example, and in particular can be slotted and thus be radially compressible. The slotted clampingring62 has a conical outside contour, against which the conical contour of apressure piece63 pushes so as to radially compress the clamping ring as soon as an axial pressure force is exerted on thepressure piece63 in the direction of thearrow65, for example by a pressure screw shown above. The slotted clampingring62 is axially fixed by thestop piece64.
• A first concept of the invention relates to a sheath device for inserting a catheter into a lumen, in particular of a patient's body, comprising a first sheath (10,11,13,21,21″,21″,41,43) having a proximal end and a distal end, which is located in particular on the patient body side, wherein the first sheath comprises a sheath housing (13,43) having a receiving channel, which hereafter is referred to as the first receiving channel, and a further receiving channel for receiving a tubular section, which extends distally from the sheath housing and which in particular runs coaxially relative to the first receiving channel and in which the tubular section can be axially displaced and fixed.
• The first and the further receiving channels are located in particular coaxially relative to each other and axially behind each other, and the tubular section can also extend through both receiving channels.
• A second concept of the invention relates to a sheath device according to the first concept, wherein the diameter of the first receiving channel differs from the diameter of the further receiving channel. The diameter of the first receiving channel can be smaller or larger than the diameter of the further receiving channel. However, it is also conceivable for the diameter of the first receiving channel to substantially correspond to the diameter of the further receiving channel.
• According to a third concept of the invention, a clamping element (54,54′,55,56,56′,57,57′) for fixing a strand-shaped body in the first receiving channel and/or for fixing a tubular section (11,21,21′,21″,41) in the further receiving channel by way of clamping can be provided in the first receiving channel (46) and/or in the further receiving channel according to the first concept or the second concept of the invention.
• At least one of the clamping elements (54,54′,55,56,56′,57,57′) can, for example, be designed such that it selectively allows clamping of a strand-shaped body having a first diameter or of a strand-shaped body having a second diameter, wherein the first diameter is different from the second diameter.
• For this purpose, for example, a clamping mechanism comprising a clamping screw can be provided, which has several preferred clamping positions. These can, for example, be implemented by various positions of the clamping screw.
• According to a fourth concept of the invention, which relates to a sheath device according to the first, second or third concept, additionally a radial expansion of the first or further receiving channel containing a flushing element can be provided in the sheath housing (13,43) in the region of the first receiving channel and/or the further receiving channel.
• The flushing element can, for example, comprise one or more radial fluid connections for supplying and removing a fluid.
• In the region of the radial expansion, for example at one of the axial ends thereof, additionally a valve can be provided for closing off the radial expansion in a fluid-tight manner.
• The valve may comprise a valve plate and/or a dome valve.
• A fifth concept of the invention relates to a sheath device according to the first or any one of the subsequent concepts (2 to 4) of the invention, wherein a cutting device comprising at least one blade is provided, which has at least one possible position, in which it radially protrudes into the first receiving channel or into the further receiving channel or into the expanded region, and more particularly into the flushing space.
• For example, at least one blade that cuts in the circumferential direction of a receiving channel or a blade that cuts in the axial direction may be provided for this purpose. The respective blade(s) can each be displaceable in the radial direction with respect to the receiving channel or the expanded region between at least one cutting position and a non-cutting position, in particular a position that does not protrude into a receiving channel. The displacement can take place against the counterforce of a spring76, which cooperates with the knife or a knife holder.
• In addition, a fluid-tight guide channel can be provided for each of the knives.
• A sixth concept of the invention relates to a sheath device according to the first or any one of the subsequent concepts (2 to 5) of the invention, comprising a tubular section that is located in the further receiving channel.
• A seventh concept of the invention relates to a catheter device comprising a sheath device according to any one of the preceding concepts and comprising a catheter, which extends through the receiving channel on the inside and together with a second sleeve-shaped sheath, wherein the second sheath is fixed in the first receiving channel, in particular in a clamping element (54,54′,55,56,56′,57,57′) of the first receiving channel.
• An eighth concept of the invention relates to a method for inserting a catheter (32,66) into a patient's body by means of a sheath device according to any one of the preceding concepts of the invention and by means of a second sheath (20,20′,20″,20″), wherein first the second sheath, together with the catheter, is inserted into the first sheath (10,11,13,21,21′,21″,41′,43), and more particularly up to the end of the tubular section and abutting the same, the second sheath is then fixed by means of a clamping element (54,54′,55,56,56′,57,57′), and thereafter the catheter is transferred from the second sheath into the first sheath.
• A ninth concept of the invention relates to a method according to the ninth concept, wherein the second sheath (20,20′,20″,20′″) is removed, in particular by tearing it open or off, after the catheter has been inserted into the first sheath.
• A tenth concept of the invention relates to a method according to the eighth or ninth concept, wherein the catheter is fixed in a clamping element (54,54′,55,56,56′,57,57′) after the second sheath (20,20′,20″,20′″) has been removed.
• An eleventh concept of the invention relates to a method for inserting a catheter into a patient's body by means of a sheath device according to any one of the preceding concepts of the invention, wherein a tubular section (11,21,21′,21″,41) is introduced into the sheath housing (13,43) and likewise is introduced into a lumen of a patient's body, wherein then a functional element is introduced into the lumen of the patient's body through the sheath device, wherein then the tubular section is pulled at least a certain distance out of the lumen of the patient's body, wherein the sheath housing is displaced in the distal direction relative to the tubular section, and wherein then the tubular section is fixed on the sheath housing by means of a clamping element and/or is cut off inside the sheath housing.

Claims (21)

1.-14. (canceled)

15. A sheath device for inserting a catheter in a patient's body, comprising:

a first sheath having a proximal end and a distal end, wherein the distal end of the first sheath is configured to be inserted in a patient's body and the proximal end of the first sheath is configured to remain outside the patient's body, and wherein the first sheath comprises:

a sheath housing, wherein the sheath housing comprises a first clamping element, a second clamping element on a proximal side of the first clamping element, and a receiving channel for a catheter; and

a tubular section located within the sheath housing, wherein the tubular section is detachably held in the first clamping element.

16. The sheath device ofclaim 15, wherein the tubular section can be displaced into the sheath housing when the first clamping element is released.

17. The sheath device ofclaim 15, wherein the tubular section is configured to move in a longitudinal direction relative to the sheath housing.

18. The sheath device ofclaim 15, wherein the first clamping element comprises an elastically deformable first clamping ring and the second clamping element comprises an elastically deformable second clamping ring.

19. The sheath device ofclaim 18, wherein the first clamping ring and the second clamping ring are produced from an elastomer or from a slotted ring made of a plastic material or a metal.

20. The sheath device ofclaim 18, wherein the first clamping element comprises a first screw element for axially pressing the first clamping ring and the second clamping element comprises a second screw element for axially pressing the second clamping ring.

21. The sheath device ofclaim 18, wherein the first clamping ring can be radially deformed by an axial pressure action.

22. The sheath device ofclaim 18, wherein the first clamping ring surrounds the tubular section and can be pressed by a first screw element such that the first clamping ring radially clamps the tubular section.

23. The sheath device ofclaim 15, wherein the first clamping element comprises a first hemostatic valve.

24. The sheath device ofclaim 23, wherein the first hemostatic valve is configured to seal around the tubular section.

25. The sheath device ofclaim 15, wherein the second clamping element comprises a second hemostatic valve.

26. The sheath device ofclaim 15, wherein the catheter is detachably held in the second clamping element.

27. The sheath device ofclaim 15, further comprising a second sheath surrounding the catheter.

28. The sheath device ofclaim 27, wherein the tubular section is configured to allow passage of the catheter from the second sheath into the tubular section.

29. The sheath device ofclaim 27, wherein the second sheath is detachably held in the second clamping element.

30. The sheath device ofclaim 29, wherein the second sheath is detachably held in the second clamping element by a second clamping ring of the second clamping element.

31. The sheath device ofclaim 18, wherein the second clamping ring can be radially deformed by an axial pressure action.

32. The sheath device ofclaim 18, wherein the second clamping ring has a conical shape.

33. The sheath device ofclaim 32, wherein the second clamping element further comprises a second stop, wherein the second stop has a conical shape that is shaped in a direction opposite to the conical shape of the second clamping ring.

34. The sheath device ofclaim 33, wherein the second clamping ring is axially fixed inside the sheath housing by the second stop.

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