Percutaneous kidney postoperative hemostasis administration catheterTechnical Field
The utility model relates to the field of medical instruments, in particular to a percutaneous kidney postoperative hemostasis drug delivery catheter.
Background
Percutaneous nephrolithotripsy lithotripsy (PCNL) is becoming the primary therapeutic modality in the clinic in the treatment of urinary stone diseases. PCNL is a minimally invasive urological technique for establishing a fistulization channel from skin to kidney through waist, also called percutaneous kidney channel, by puncturing, expanding and sheathing, then placing nephroscope into renal pelvis and renal calyx, treating broken stone by utilizing ultrasonic and the like and taking out by a stone taking basket, and is a first line treatment scheme for treating the large-load stones on the upper urinary tract with small wound and high stone clearance rate. However, PCNL is post-operatively symptomatic of sustained hematuria, resulting in prolonged patient hospitalization, heavy post-operative pain and increased medical costs. The current clinical post-PCNL hemostatic treatment mode mainly comprises the following steps: compression hemostasis and drug hemostasis. Among them, hemostasis by compression is the most commonly used method, but excessive mechanical compression may give a more pronounced pain sensation to the patient, causing discomfort to the patient. The hemostatic drug is injected into the percutaneous kidney channel, and can diffuse to the surrounding tissues of the channel through loose soft tissues in the percutaneous kidney channel, thereby achieving the hemostatic effect on venous bleeding, but the injection operation requirement on the hemostatic drug in operation is higher, the aim of uniformly distributing the drug on the wound surface and slowly releasing the drug is not achieved, and the hemostatic effect of the hemostatic drug is reduced. At present, the bleeding situation of the wound surface can not be well solved by only one of compression hemostasis or medicine hemostasis.
Chinese patent application entitled catheter for percutaneous renal channel injection of hemostatic, filed under the name CN205586344U, publication date 2016, 09, 21, which discloses the following: the catheter for percutaneous renal channel injection of hemostatic includes double-cavity catheter and air bag, and its front end is equipped with a group of air holes and several groups of medicine-feeding holes in turn, and the air holes are covered by air bag attached on the outside of double-cavity catheter, and the tail end of double-cavity catheter is equipped with medicine-feeding valve port and air-feeding and air-discharging valve port, and the air-feeding and air-discharging valve ports are communicated with air holes by means of air channel pipeline in the double-cavity catheter, and the medicine-feeding valve port is communicated with medicine-feeding hole by means of medicine pipeline in the double-cavity catheter. The scheme has the advantages that the operation steps of injecting the hemostatic medicine into the channel can be simplified, the hemostatic medicine can be uniformly distributed around the channel, the optimal hemostatic effect is achieved, and meanwhile, the related treatment cost is reduced, but the scheme still has the advantages that the medicine which is changed is easy to flow out of the channel and ooze out of the skin, the requirement on the operation of spraying the medicine in the operation is high, the purposes that the medicine is uniformly distributed on a wound surface and the medicine is slowly released are not achieved, and the hemostatic effect of the medicine is reduced.
How to solve the problems is a technical problem to be solved.
Disclosure of Invention
The utility model aims to provide a percutaneous nephrotomy hemostatic administration catheter which can enable hemostatic drugs to be more uniformly and slowly released and distributed around a channel by improving drug injection and release modes so as to achieve a better hemostatic effect.
In order to achieve the above purpose, the utility model provides a hemostatic administration catheter after percutaneous nephrology operation, comprising a three-way pipe body, wherein the three-way pipe body consists of an administration channel, a filling channel and a drainage channel, a three-way joint is arranged at the tail end of the three-way pipe body, an administration hole and a filling hole are sequentially formed at the front end of the three-way pipe body, the administration hole is wrapped by an administration balloon attached to the outer side of the three-way pipe body, and the filling hole is wrapped by a filling balloon attached to the outer side of the three-way pipe body; the three-way joint is respectively a filling joint, a dosing joint and a drainage joint, wherein the filling joint is communicated with the filling hole through a filling channel, the dosing joint is communicated with the dosing hole through a dosing channel, and the drainage channel is communicated with the drainage joint.
Further, a filling check valve is arranged on the filling joint.
Further, an administration check valve is arranged on the administration connector.
Further, the filling balloon is a circular balloon.
Further, the administration balloon is a cylindrical balloon.
Further, the capacity of the filling saccule is 1-5ml, and the length is 5-15mm.
Further, the capacity of the filling balloon is 3ml, and the length is 10mm.
Further, the capacity of the administration balloon is 3-8ml, and the length is 15-25mm.
Further, the delivery balloon had a capacity of 5ml and a length of 20mm.
Compared with the prior art, the utility model has the following beneficial effects:
according to the utility model, through the arrangement of the administration balloon and the filling balloon, when in use, medical staff uses the injector to inject hemostatic medicine and filling medium into the administration balloon and the filling balloon through the administration hole and the filling hole respectively, so that the operation steps of injecting hemostatic medicine are simplified, and the continuous operation after percutaneous kidney operation is satisfied; the hemostatic drug can be slowly released to the focus through the administration saccule, so that the drug slow release effect is achieved, the utilization rate of the drug is improved, the administration saccule and the filling saccule can play a role in assisting compression hemostasis at the same time, the hemostatic effect of the hemostatic drug is further improved, and a better hemostatic effect is achieved by combining the two modes of drug hemostasis and compression hemostasis.
In the utility model, as the filling saccule is a round saccule, the filling saccule can play a role of fixing the three-way pipe body and can also assist in hemostasis by compression, thereby further improving the hemostasis effect of the utility model and reducing the hemostatic drug from entering the aggregation system to save the drug; the administration saccule is a cylindrical saccule, so that the medicine can be promoted to enter the peripheral percutaneous kidney channel more uniformly, the function of assisting in hemostasis by compression can be achieved after filling, the postoperative bleeding incidence rate and the hematuria time are reduced, and the recovery period of a patient is accelerated.
The utility model will become more apparent from the following description taken in conjunction with the accompanying drawings which illustrate embodiments of the utility model.
Drawings
FIG. 1 is a schematic view of a first structure according to the present utility model;
fig. 2 is a schematic diagram of a second structure provided by the present utility model.
Reference numerals illustrate: filling the balloon 1; adrug delivery balloon 2; atee body 3 and adrug delivery hole 31; filling thehole 32; a three-way joint 4, afilling check valve 41, adrain joint 42 and anadministration check valve 43; a drainage channel 5; filling the channel 6; adrug administration channel 7; filling the joint 8; the administration connector 9.
Detailed Description
The following description of the embodiments of the present utility model will be made clearly and completely with reference to the accompanying drawings, in which it is apparent that the embodiments described are only some embodiments of the present utility model, but not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the utility model without making any inventive effort, are intended to be within the scope of the utility model.
Referring to fig. 1 to 2, the utility model provides a hemostatic administration catheter after percutaneous nephrology operation, comprising a three-way body 3, wherein the three-way body 3 comprises anadministration channel 7, a filling channel 6 and a drainage channel 5, a three-way joint 4 is arranged at the tail end of the three-way body 3, anadministration hole 31 and afilling hole 32 are sequentially formed at the front end of the three-way body 3, theadministration hole 31 is wrapped by anadministration balloon 2 attached to the outer side of the three-way body 3, and thefilling hole 32 is wrapped by a filling balloon 1 attached to the outer side of the three-way body 3; the three-way joint 4 is respectively a filling joint 8, a dosing joint 9 and adrainage joint 42, wherein the filling joint 8 is communicated with thefilling hole 32 through a filling channel 6, the dosing joint 9 is communicated with thedosing hole 31 through adosing channel 7, and the drainage channel 5 is communicated with thedrainage joint 42.
In the present utility model, the filling joint 8 is provided with afilling check valve 41. When in use, medical staff uses the injector to inject filling medium into the filling joint 8 through the filling one-way valve 41, the filling medium is injected into the filling balloon 1 through the filling channel 6 through thefilling hole 32, the filling medium enables the filling balloon 1 to be in a filling state, and the filling balloon 1 in the filling state plays roles in fixation and hemostasis.
In the present utility model, the administration port 9 is provided with anadministration check valve 43. In use, a medical practitioner uses the syringe to inject hemostatic drug into the administration connector 9 through theadministration check valve 43, into theadministration balloon 2 through theadministration port 31 via theadministration channel 7, and release hemostatic drug into the percutaneous renal channel via theadministration balloon 2.
In the present utility model, the inflatable balloon 1 is a circular balloon. The capacity of the filling saccule 1 can be set to be 1-5ml, the length is 5-15mm, and the specific length is 3ml and the length is 10mm; the filled saccule 1 can play a role in fixing the three-way pipe body 3, can be used for closing a passage between a percutaneous kidney channel and a collection system, reduces hemostatic drugs from entering the collection system, and can assist in hemostasis by compression under the filled saccule 1.
In the present utility model, theadministration balloon 2 is a cylindrical balloon. The capacity of theadministration balloon 2 can be set to 3-8ml, the length is 15-25mm, and the specific length is 5ml and the length is 20mm; theadministration saccule 2 can be made of elastic dialytic materials, after hemostatic drugs are injected into the administration saccule 2 through theadministration holes 31, the administration saccule 2 fills to play a role in assisting compression hemostasis, and the hemostatic drugs are slowly released into the percutaneous kidney channel through the saccule membrane with dialysis function, so that the drug slow release effect is achieved, the utilization rate of the drugs is improved, meanwhile, theadministration saccule 2 is a cylindrical saccule, so that the drugs can be more uniformly distributed around the compression part, and the drugs can be more uniformly promoted to enter the surrounding percutaneous kidney channel.
When the embodiment is specifically used, firstly, medical staff uses a cystoscope sheath to slowly extend the front end of the three-way pipe body 3 into the renal calyx, wherein the length of the three-way pipe body 3 can be 245-265mm, specifically 255mm, and the distance between the front end of the three-way pipe body 3 and the filling saccule 1 can be 0-10mm, specifically 5mm; then, filling medium is injected into the filling joint 8 through thefilling check valve 41 by using the injector, the filling medium is injected into the filling balloon 1 through thefilling hole 32 through the filling channel 6, the filling medium enables the filling balloon 1 to be in a filling state to play a role in assisting compression hemostasis, the three-way pipe body 3 can be fixed in the percutaneous kidney channel, and meanwhile, a passage between the percutaneous kidney channel and the collecting system is closed, so that hemostatic medicines are reduced from entering the collecting system; next, a hemostatic drug is injected into the administration connector 9 through theadministration check valve 43 by using the syringe, and the hemostatic drug is injected into theadministration balloon 2 through theadministration hole 31 through theadministration channel 7, wherein the interval between the filling balloon 1 and theadministration balloon 2 can be set to be 0-6mm, specifically 3mm, and theadministration balloon 2 can be made of an elastic dialyzing material; after the hemostatic drug is injected into theadministration balloon 2 through theadministration hole 31, theadministration balloon 2 fills to play a role in assisting compression hemostasis, and the hemostatic drug is slowly released into the percutaneous kidney channel through the capsule membrane with dialysis function, so that the drug slow release effect is achieved, the utilization rate of the drug is improved, meanwhile, theadministration balloon 2 is a cylindrical balloon, the drug can be more uniformly distributed around the compression part, and the drug can be more uniformly promoted to enter the percutaneous kidney channel around; the filled saccule 1 and the administration saccule 2 compress the wall of the renal calyx after filling, thereby preventing blood from entering the renal calyx to coagulate into blood clots, and reducing the bleeding condition of the wound surface of a patient; finally, the front end of the drainage channel 5 is an open micro-end communicated with thedrainage joint 42, so as to ensure larger drainage flow, and waste generated in operation and incompletely utilized medicines can be drained to the outside of the patient through the drainage channel 5 and thedrainage joint 42.
The preferred embodiments of the present utility model have been described above. It is to be understood that the utility model is not limited to the specific embodiments described above, wherein devices and structures not described in detail are to be understood as being implemented in a manner common in the art; any person skilled in the art can make many possible variations and modifications to the technical solution of the present utility model or modifications to equivalent embodiments without departing from the scope of the technical solution of the present utility model, using the methods and technical contents disclosed above, without affecting the essential content of the present utility model. Therefore, any simple modification, equivalent variation and modification of the above embodiments according to the technical substance of the present utility model still fall within the scope of the technical solution of the present utility model.