Radiation device with shield portion

Surgery – Radioactive substance applied to body for therapy – Radioactive substance placed within body

Reexamination Certificate

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Reexamination Certificate

active

06238332

ABSTRACT:

BACKGROUND OF THE INVENTION AND RELATED ART STATEMENT
The invention relates to a radiation device for radiation therapy, and more particularly, a rapid exchange radiation device which is used in a percutaneous transluminal coronary angioplasty (PTCA) procedure and/or in a stent implantation into a patient's body lumen.
The PTCA procedure has been a standard procedure for re-vascularization of coronary artery. For example, in the PTCA procedure, a catheter having a balloon at the distal end is introduced into the coronary artery to enlarge a stenosis, i.e. constriction in the coronary artery. However, re-stenosis and re-closure of the lesion after the PTCA procedure is a problem thereafter. Namely, in 35 to 40 percent of the angioplasty cases, re-stenosis occurs within 6 months after the PTCA procedure.
In the treatment of the stenosis in the artery, there has been used another device called “stent”, i.e. generally tubular shaped device which functions to support a desired part of the artery, such as a lesion enlarged by a balloon catheter, from the inside thereof. The stent prevents occurrence of re-stenosis, and lowers the rate of re-stenosis to 13 to 19%. Furthermore, according to the recent study, radiation therapy combined with a stent implantation has shown better results, and lowers the rate of occurrence of re-stenosis to 1 to 9%. Therefore, it is better to use radiation therapy combined with the stent implantation in the PTCA procedure for preventing re-stenosis.
Radiation therapy as stated above can be used in the standard PTCA procedure alone as well as in the PTCA procedure combined with the stent implantation. In either case, the lesion is exposed to the pre-calculated dosage of radiation. It is believed that the exposure to radiation would partially destroy DNA of target cells damaged by the PTCA procedure or stent procedure, so that the excessive proliferation of the cells damaged by the PTCA procedure or stent procedure can be minimized.
There are several methods of applying radiation to the target cells or lesion. In the first method, a guide wire generally used in the PTCA procedure is provided with a radioactive core imbedded at the tip thereof, and radiation is applied by the radioactive core in the guide wire. In the second method, radioactive pellets or cells are mechanically located to the lesion site, and radiation is applied by the radioactive pellets or cells. After desired exposure of radiation to the lesion, the radioactive pellets or cells are removed from the lesion by the mechanical system. In the third method, radioactive fluid is injected into a PTCA balloon catheter which is frequently used in the PTCA procedure, so as to apply radiation to the target lesion.
In the above described methods, however, there are following disadvantages. Firstly, since the radioactive pellets or the device having the radioactive source, such as the guide wire having the radioactive source at the tip thereof, are placed directly inside a patient's body lumen, such as an artery, the radioactive pellets or the device with the radioactive source are not used again.
Also, in the method using the guide wire with the radioactive source at the tip thereof, in order to apply radiation therapy, the guide wire preliminary inserted inside the patient's lumen for another treatment in the PTCA procedure has to be withdrawn first, and the guide wire having the radioactive core has to be introduced inside the patient's body lumen again to locate the tip of the guide wire at the lesion. Thus, exchange of the guide wire in the meandering body lumen is cumbersome and may cause damage to the artery or blood vessel.
Furthermore, after enough dosage of radiation is applied to the lesion, the radiation catheter is required to be withdrawn as quickly as possible so as not to cause excessive radiation. Also, it is required that the radiation device should be handled quickly because of its affect to other people. Thus, it has been sought that the radiation therapy can be made easily and quickly.
Accordingly, an object of the invention is to provide a radiation device, which can provide radiation only to a required portion in a body lumen at a required time.
Another object of the invention is to provide a radiation device as stated above, wherein a radiation source can be placed inside the body lumen smoothly and rapidly, and can be removed quickly from the required portion after enough dosage of radiation.
A further object of the invention is to provide a radiation device as stated above, wherein the radiation source once used inside the patient's body lumen can be reused.
A still further object of the invention is to provide a radiation device as stated above, wherein the radiation source can be introduced into the required portion by a guide wire used in the general PTCA procedure.
Further objects and advantages of the invention will be apparent from the following description of the invention.
SUMMARY OF THE INVENTION
A radiation device of the invention is designed to be disposed in a body lumen. The radiation device is formed of a sheath to be disposed in the body lumen, and an elongated radiation member. The sheath includes a guide wire passageway to allow a guide wire to pass therethrough, and a sheath passageway extending throughout a substantial portion thereof. The elongated radiation member is inserted into the sheath passageway.
The radiation member includes an outer member having a shield portion at a front part thereof, and an inner member slidably situated in the outer member and having a radiation portion at a front part thereof. The inner member is arranged in the outer member such that when radiation is not required, the radiation portion is located inside the shield portion, and when radiation is required, the radiation portion is disposed outside the shield portion. Since the radiation member is inserted into the sheath passageway, the radiation member is not contaminated at all by the use. It is possible to use the radiation member to different patients.
When the radiation device of the invention is used, firstly, the guide wire is introduced inside the body lumen to be located at the lesion, and the sheath is introduced into the lesion by sliding along the guide wire. Then, the radiation member including the inner and outer members is slid into the sheath passageway. At this time, the radiation portion of the inner member is located inside the shield portion of the outer member.
When the radiation therapy is made, the radiation portion is disposed outside the shield portion by moving the inner or outer member to thereby apply radiation to the lesion. After the adequate exposure of radiation to the lesion, the inner or outer member is moved to locate the radiation portion inside the shield portion, and then, the radiation member including the inner and outer members is quickly and easily withdrawn from the sheath. Therefore, the radiation member can be reused for another patient or another procedure, and overdosing of radiation can be prevented.


REFERENCES:
patent: 5213561 (1993-05-01), Weinstein et al.
patent: 5383853 (1995-01-01), Jung et al.
patent: 5938582 (1999-08-01), Ciamacco, Jr. et al.

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