Disclosure of Invention
In order to solve the problems in the prior art, the invention provides a combined transplanting source applicator which has the advantages of being capable of being freely combined according to the condition of a patient and meeting the individual treatment of the patient.
In order to achieve the above purpose, the invention adopts the following technical scheme: the combined transplanting source applicator comprises a sleeve, a fixing cap and a plurality of combined blocks, wherein a sealing piece in a ball-segment shape is arranged at one end of the sleeve, the fixing cap is detachably connected to the other end of the sleeve, and a through hole is formed in the fixing cap;
A plurality of limiting plates used for limiting the combined blocks are uniformly distributed on the inner side wall of the sleeve along the circumferential direction of the sleeve, clamping grooves corresponding to the limiting plates are formed in the combined blocks, and the combined blocks are arranged in the sleeve and spliced with the combined blocks to form a cylinder after being limited by the limiting plates; one end of the combined block is attached to the inner side wall of the sealing piece, and the other end of the combined block is attached to the fixing cap;
One end of the combined block, which is in fit connection with the sealing element, is arc-shaped; the surface of the combined block is provided with a notch along the axis direction of the combined block, the center of the combined block is provided with an insertion hole for installing an insertion needle along the axis direction of the combined block, the notch formed after all the combined blocks are spliced is a placement hole for installing an applicator in the cavity, and the diameter of the through hole is larger than the diameter of an internal common tangent circle of all the insertion holes.
One end of the sleeve is in a sphere-like shape, so that the sleeve can be well attached to the tail end of the vagina; set up a plurality of locating parts on the sleeve inside wall for the rotation can not appear after the combined block is installed in the sleeve, be equipped with the fixed cap simultaneously at telescopic other end in order to prevent combined block landing sleeve in the use, be equipped with the through-hole simultaneously on the fixed cap, in order to expose the patchhole with placing the hole, the implantation of convenient insertion needle.
Preferably, an opening for exposing the applicator is formed in the sealing member of the sleeve, and the insertion hole and the placement hole are exposed from the opening.
The opening is provided in the seal of the sleeve to allow the sleeve to be formed in both a distal penetrating type and a distal non-penetrating type, with the physician selecting either the distal penetrating type or the distal non-penetrating type depending on the actual needs of the patient.
Preferably, one end of the combination block in an arc shape comprises a clamping part and a jointing part, the radian of the clamping part is matched with the radian of the inner side wall at the bottom of the sleeve, and the radian of the jointing part is matched with the radian of the outer side wall at the bottom of the sleeve; the combined block is arranged in the sleeve with the opening, and the bayonet part is attached to the inner side wall of the sealing piece of the sleeve and then forms a sphere gap with the attaching part.
The combined block is arc-shaped and one end comprises a clamping part and a fitting part, the clamping part is fitted with the inner side wall of the sleeve sealing piece, then a ball gap is formed between the clamping part and the fitting part, and when the sleeve with the penetrating tail end is adopted, the insertion source applicator extends into the patient to be better fitted with the tail end of the vagina.
Preferably, the clamping groove is located in the middle of the outer side wall of the combined block, and the clamping groove is arranged along the axial direction of the combined block.
The clamping grooves are arranged in the middle of the outer side wall of the combined block or on two sides of the outer side wall of the combined block, and the clamping grooves are arranged along the axial direction of the combined block so as to facilitate positioning of the combined block.
Preferably, the clamping grooves are located on two sides of the outer side wall of the combined block, and the clamping grooves are arranged along the axis direction of the combined block. .
The clamping groove is arranged, the width of the clamping groove is 1/2 of the width of the limiting plate, and the length of the limiting plate is matched with the length of the clamping groove so as to prevent a gap from being formed after the assembly block is assembled.
The beneficial effects of the invention are as follows:
(1) The applicators are freely combined according to the condition of the patient, so that the individual treatment requirement of the patient is met;
(2) The applicator can be reused after disinfection, so that the economic burden of a patient is reduced;
(3) The diameter of the sleeve is determined only according to gynecological examination conditions of a patient, the combined block is determined by image data, a long-time waiting process such as 3D printing is not needed, and the waiting time of the patient is shortened;
(4) The pin holes in the combined block have different angles, so that the inserting difficulty of doctors is reduced;
(5) After the proper sleeve diameter is selected, the vagina is prevented from being stuffed by using the gauze or cotton ball, and the pain of a patient is relieved;
(6) After the sleeve is implanted, the method performs image scanning before the combined block and the insertion needle are inserted, and as the sleeve has a good fixing effect, the organ deformation caused by the implantation of the applicator can be effectively reduced, and the insertion accuracy is improved.
Detailed Description
Embodiments of the present invention will be described in detail below with reference to the accompanying drawings.
Example 1:
As shown in fig. 1,2,3, 4, 8 and 9, a combined transplanting source applicator comprises a sleeve 1, a fixing cap 2 and a plurality of combined blocks 3, wherein a sealing piece 13 in a spherical segment shape is arranged at one end of the sleeve 1, the fixing cap 2 is detachably connected to the other end of the sleeve 1, and a through hole 4 is arranged on the fixing cap 2;
A plurality of limiting plates 5 used for limiting the combined block 3 are uniformly distributed on the inner side wall of the sleeve 1 along the circumferential direction of the sleeve, clamping grooves 6 corresponding to the limiting plates 5 are formed in the combined block 3, and the combined block 3 is arranged in the sleeve 1 and is combined and spliced with the sleeve 1 into a cylinder after being limited by the limiting plates 5; one end of the combined block 3 is attached to the inner side wall of the sealing piece 13, and the other end is attached to the fixing cap 2;
One end of the combined block 3, which is in fit connection with the sealing element 13, is arc-shaped; the surface of the combined block 3 is provided with a notch 10 along the axis direction, the center of the combined block 3 is provided with an insertion hole 7 for installing an insertion needle along the axis direction, the notch 10 formed after all the combined blocks 3 are spliced is a placement hole 8 for installing an intra-cavity applicator, and the diameter of the through hole 4 is larger than the diameter of an internal common tangent circle of all the insertion holes 7.
The sealing element 13 of the sleeve 1 is in a sphere-like shape, so that the sleeve 1 can be well attached to the tail end of the vagina; set up a plurality of locating parts on sleeve 1 inside wall for the rotation can not appear after the assembly piece 3 is installed in sleeve 1, be equipped with fixed cap 2 simultaneously at sleeve 1's the other end in order to prevent assembly piece 3 landing out sleeve 1 in the use, be equipped with through-hole 4 simultaneously on fixed cap 2, in order to expose insertion hole 7 and placement hole 8, the implantation of convenient insertion planting needle.
Example 2:
As shown in fig. 5 to 7, in this embodiment, on the basis of embodiment 1, an opening 9 through which the applicator is exposed is provided in the sealing member 13 of the sleeve 1, and the insertion hole 7 and the placement hole 8 are exposed from the opening.
The provision of the opening 9 in the seal 13 of the sleeve 1 is intended to allow the sleeve 1 to be formed in both an end-penetrating type and an end-non-penetrating type, the physician selecting either the end-penetrating type or the end-non-penetrating type depending on the actual needs of the patient.
Example 3:
1-9, in this embodiment, on the basis of embodiment 1, one end of the combination block 3 in an arc shape includes a bayonet part 11 and a fitting part 12, where the radian of the bayonet part 11 matches the radian of the inner side wall of the bottom of the sleeve 1, and the radian of the fitting part 12 matches the radian of the outer side wall of the bottom of the sleeve 1; the combined block 3 is installed in the sleeve 1 provided with an opening, and the bayonet part 11 is attached to the inner side wall of the sealing member 13 of the sleeve 1 and then forms a sphere gap with the attaching part.
The arc-shaped end of the combined block 3 comprises a clamping part 11 and a fitting part 12, the clamping part 11 is fitted with the inner side wall of the bottom of the sleeve 1, and then forms a ball gap with the fitting part 12, so that the end of the insertion source applicator extending into the patient body is better fitted with the tail end of the vagina when the tail end penetrating type sleeve 1 is adopted.
Example 4:
As shown in fig. 1,3, 6, 8 and 9, in this embodiment, on the basis of embodiment 1, the clamping groove 6 is located in the middle of the outer side wall of the combined block 3, and the clamping groove 6 is disposed along the axial direction of the combined block 3.
The clamping grooves 6 are positioned in the middle of the outer side wall of the combined block 3 or on two sides of the outer side wall of the combined block 3, and the clamping grooves 6 are all arranged along the axial direction of the combined block 3 so as to facilitate positioning of the combined block 3.
Example 5:
As shown in fig. 1 to 3, in this embodiment, on the basis of embodiment 1, the clamping grooves 6 are located on both sides of the outer side wall of the combined block 3, and the clamping grooves 6 are disposed along the axial direction of the combined block 3.
The clamping groove 6 is arranged, the width of the clamping groove 6 is 1/2 of the width of the limiting plate 5, and the length of the limiting plate 5 is matched with the length of the clamping groove 6 so as to prevent gaps from being formed after the combined block 3 is assembled, and the later dose irradiation precision is affected.
In the specific embodiments for treating cervical cancer patients:
1) The preparation of the patient before the implantation, such as intestinal tract treatment, placement of a urethral catheterization package, instrument disinfection and the like.
2) And selecting whether to use the intrauterine cavity for treatment, if so, implanting the intrauterine cavity, and if not, skipping the step, and executing the step 3).
3) The appropriate size of the sleeve 1 is selected according to the vaginal condition of the patient, the tip-penetrating sleeve 1 is implanted, and the sleeve 1 and the uterine cavity tube (if used) are secured with a fixing bracket.
4) And scanning the image of the patient, and determining and recording the needle inserting angle and the needle inserting depth of the inserting needle in a certain direction according to the image of the patient.
5) The combination block 3 to be used in a certain direction is determined according to the diameter of the sleeve 1 and the recorded needle inserting angle.
6) The combination block 3 in a certain determined direction is inserted into the corresponding direction in the sleeve 1, the fixing cap 2 is screwed, and the combination block 3 is prevented from sliding.
7) Marking points are made at the connecting ends of the inserting needles according to the length of the sleeve 1 and the recorded inserting needle depth, and the marking point positions = inserting needle length- (the length of an inserting hole in the combined block 3 plus the inserting needle depth).
8) And implanting the inserting needle to the mark point position. The number of the inserting needle can be selected in the step, and the number of the inserting needle is guaranteed to be consistent with the number of the reconstructed applicator in the planning and design process.
9) And performing image scanning after the insertion needle is implanted, determining the target area and the position of the organs at risk, and properly adjusting if the angle and the depth of the insertion needle are unsatisfactory.
10 And (3) drawing a target area and organs at risk according to the image after the implantation of the implantation needle, giving a prescription, and designing a treatment plan and irradiating.
11 And (3) taking out the insertion needle and the combined insertion source applicator after treatment is finished, removing the fixing cap 2, taking out the combined block 3, and cleaning and sterilizing. The patient is subjected to the next treatment.
Treatment of vaginal off-center tumors:
1) Preparation of the patient before treatment, such as intestinal tract treatment, placement of a urinary catheter, disinfection of the apparatus, etc.
2) The size of the sleeve 1 and the matched combined block 3 are selected according to the vagina condition of a patient, the combined block 3 is inserted into the non-penetrating sleeve 1 at the tail end, the fixing cap 2 is screwed down to prevent the combined block 3 from sliding,
3) The sleeve 1 is fixed by a fixing bracket by an implantation combined implantation source applicator.
4) And scanning the image of the patient, and delineating the target area and the organs at risk according to the image after the combined implantation source is inserted.
5) Given a prescription, a treatment plan is designed. In this process, it is determined whether or not a certain direction combination block 3 is implanted with the insertion needle according to the target area and the position of the organs at risk.
6) The top of the pin is inserted to the bottom of the directional combination block 3, namely the end of the non-penetrating sleeve 1, and the point of the pin reconstructed in the step 5) is also shown.
7) And (5) treating.
8) And taking out the transplanting needle and the combined transplanting source applicator after treatment is finished, removing the fixing cap 2, taking out the combined block 3, and cleaning and sterilizing. The patient is subjected to the next treatment.
Treatment for rectal cancer:
1) Preparation of the patient before treatment, such as intestinal tract treatment, placement of a urinary catheter, disinfection of the apparatus, etc.
2) The size of the sleeve 1 and the matched combined block 3 are selected according to the rectum condition of a patient, the combined block 3 is inserted into the non-penetrating sleeve 1 at the tail end, the fixing cap 2 is screwed down to prevent the combined block 3 from sliding,
3) The sleeve 1 is fixed by a fixing bracket by an implantation combined implantation source applicator.
4) And scanning the image of the patient, and delineating the target area and the organs at risk according to the image after the combined implantation source is inserted.
5) Given a prescription, a treatment plan is designed. In this process, it is determined whether or not a certain direction combination block 3 is implanted with the insertion needle according to the target area and the position of the organs at risk.
6) The top of the pin is inserted to the bottom of the directional combination block 3, namely the end of the non-penetrating sleeve 1, and the point of the pin reconstructed in the step 5) is also shown.
7) And (5) treating.
8) And taking out the transplanting needle and the combined transplanting source applicator after treatment is finished, removing the fixing cap 2, taking out the combined block 3, and cleaning and sterilizing. The patient is subjected to the next treatment.
The fixing device mentioned in the present invention is an existing fixing device for radiotherapy.
The foregoing examples merely illustrate specific embodiments of the invention, which are described in greater detail and are not to be construed as limiting the scope of the invention. It should be noted that it will be apparent to those skilled in the art that several variations and modifications can be made without departing from the spirit of the invention, which are all within the scope of the invention.