This invention pertains in general to the field of radiation protection devices for protection against ionizing radiation, particular for use in medical interventions. More particularly, the invention relates to a radiation protection shielding system comprising at least one radiation protection drape sized to at least partially cover the patient from a proximity of a radiated area of the patient to the feet of the patient. The radiation protection drape may comprise at least a first section and a second section. The first section may be partitioned from the second section from a first edge of the radiation protection drape towards a second edge of the radiation protection drape.
In interventional procedures with radiologic guidance using radiation systems, such as X-ray radiation systems, the clinical staff, such as the endovascular clinician, is continuously exposed to ionizing radiation. The vast majority of the ionizing radiation the clinical staff is exposed to is scattered radiation from the patient and operating table.
The clinical staff protects themselves from radiation mainly in two ways, here called the conventional systems; 1) radiation shielding devices (exemplified in roof or floor mounted protective shields, radiation protection shields mounted under the operating table; and 2) personal radiation shielding garments (such as lead or no-lead aprons, thyroid protection and lead eyeglasses). Alternative radiation protection systems may be radiation protection patches that are applied on the patient as to create zones with lower scatter radiation in the clinical environment. Another example is a system that dresses the operator with a floor or roof mounted radiation protection garment, thus, to maximize radiation protection without the operator needing to carry the weight of a personal radiation shielding garment. Still another example is to reduce radiation by a system of protective panels around the interventional area. However, there is no optimal radiation protection solution as conventional as well as the alternative radiation protective systems reveal flaws in protection to the staff. In the conventional radiation garment systems, typically only 75% of the body of the staff is protected, leaving arms, legs and head exposed to high doses of radiation. In the example with the system that dresses the operator with a floor or roof mounted radiation protection garment (e.g. Zero-Gravity, by TIDI Products, USA), the system only allows one person in the operating room to be protected, the other staff will remain dependent on conventional radiation protection equipment.
The conventional protection system used today is accepted as the standard and is mandatory in all interventional procedures with radiologic guidance using radiation systems, such as endovascular procedures, to reduce the radiation dose to the clinical staff. Every member of the staff has a dosimeter at their left breast pocket under their lead aprons for monitoring of personal radiation exposure. For example, in endovascular operation rooms with modern dose optimized x-ray systems equipped with a protection system, such as described above, the yearly cumulative doses measured under the lead aprons on catheterization laboratory staff are in the range of 2-4% of the yearly allowed dose of 20 mSv. Although occupational radiation dose limits are being monitored and seldom reached, chronic exposure to low dose radiation have been shown to have harmful biological effects that may become apparent years later, such as cancer and cataract. Further, as the dose is measured on the torso, under the radiation protection garment and any accumulated dose on arms, legs and head is not considered in the annual dose limit.
The personal lead or no-lead protection aprons weigh approximately 4-8 kg, pending on size and protection level. The weight of the lead aprons put significant strain on the clinician that needs to carry these when working inside the operating room. Orthopedic injuries and disorders to the back, neck, shoulders, hips and knees as well as chronic fatigue are common for workers in the interventional operating environment as a consequence of carrying heavy personal lead protection.
Hence, an effective radiation protection system to protect against radiation exposure to the staff in interventional procedures with radiologic guidance and at the same time to reduce the risk of orthopedic injury and disorders among the staff would be advantageous.
U.S. Pat. No. 4,670,658 discloses a multi-ply sheet having a center ply support matrix in which the radio opaque compound barium sulfate is distributed as a powder and is supported by the matrix. The barium sulfate is present in an amount sufficient to block scatter radiation produced by the medical radiology procedures. The multi-ply sheet is a single sheet that is disposable and designed with cost in mind. The radiation protective material suggested is barium sulphate, which is known as a cost efficient material but has at the same time a relatively low protective performance to radiation shielding. Conformity over the patient and operating table is critical to avoid leaks of radiation and properly reduce the radiation exposure to the clinical staff and although the suggested solutions in U.S. Pat. No. 4,670,658 may reduce radiation exposure, there is an evident risk that the inherent constitution of the solution may jeopardize the radiation barrier since the barium sulfate powder makes the multi-ply sheet stiff and brittle.
Accordingly, embodiments of the present invention preferably seek to mitigate, alleviate or eliminate one or more deficiencies, disadvantages or issues in the art, such as the above-identified, singly or in any combination by providing embodiments of a radiation protection system according to embodiments of the invention.
According to a first aspect of the invention, a radiation protection shielding system comprises at least one radiation protection drape sized to at least partially cover the patient from a proximity of a radiated area of the patient to the feet of the patient. The radiation protection drape comprises at least a first section and a second section. The first section may be partitioned from the second section from a first edge of the radiation protection drape towards a second edge of the radiation protection drape.
The first section may be partitioned from the second section from the first edge to the second edge of the radiation protection drape and being separable from the second section. Alternatively or additionally, the first section is partitioned from the second section from the first edge partly to the second edge. The first section may be partly separated from the second section.
The first section may have a varying radiation protection level across the first section.
The second section may comprise a first portion and a second portion. The first portion and the second portion may be separated along an edge of each of the first portion and the second portion. Furthermore, each of the first portion and the second portion may comprise a fastener to temporarily fasten and unfasten the first portion to/from the second portion.
The radiation protection drape and/or garment may comprise one or several radiation attenuating layers positioned in between two protecting layers of non-radiation attenuating material attached to each other in a perimeter, hence separating the metals in the attenuating material from the outside of the radiation protection drape and/or garment.
The radiation protection drape may comprise at least one fenestration for a femoralis area of the patient. The fenestration may be located along an edge of the first section and an edge of the second section, along which the first section and the second section are partitioned.
The second edge of the radiation protection drape may be located at the fenestration. The first section and the second section may be partitioned from the first edge to the second edge of the radiation protection drape.
The radiation protection drape may comprise a third section separated from the first section and the second section. The third section may be sized to partially cover the fenestrated area of the radiation protection drape.
The radiation protection drape may comprise at least one fastening device located at where the first section is partitioned from the second section. The fastening device may, e.g., comprise hooks and loops, and/or magnets.
The radiation protection drape may be sized to extend over the rim of an operating table when positioned over a patient lying on the operating table. Furthermore, the radiation protection drape may be sized to extend over the rim of the operating table and at least partially towards to the floor on at least one side of the operating table, most preferably at least 10 cm over the rim of the operating table. Hence, the radiation protection drape may cover the side of the patient when lying on the operating table.
The radiation protection shielding system may further comprise at least one floor or ceiling mounted radiation shielding screen to be positioned between clinical staff and a radiated area at an upper body portion of the patient.
The radiation protection shielding system may further comprise at least one floor or table mounted radiation protection drape section configured to cover at least a part of an area under the table, such as being sized to cover least one long side and/or one foot-end side of the operating table.
The radiation protection drape may have a radiation protection level corresponding to 0.25 to 1 mm lead equivalency, most preferably 0.35-0.7 mm lead equivalency.
The radiation protection shielding system may comprise a radiation protection garment. The radiation protection garment may comprise at least one panel sized to extend over at least the front side of a torso of a wearer. The panel may have a radiation protection level of 0.05 to 0.35 mm lead equivalency. Hence, the radiation protection drape may have a higher radiation protective level than the panel of the radiation protection panel. Furthermore, when made of the same material, the panel of the radiation protection garment may be lighter per surface area than the radiation protection drape. The staff may be protected from all or substantially all of the radiation scatter from the patient by the radiation protection drape, and from any residual radiation scatter by the radiation protection garment. Since the residual radiation scatter will be low, the radiation protection garment can be made lighter. Thus the embodiments of the invention improves working environment for the staff in the operating room, while at the same time reduce the risk for work related orthopedic injuries and disorders to the back, neck, shoulders, hips and knees as well as chronic fatigue as a consequence of carrying heavy personal lead protection. These benefits are provided while at the same time improving the radiation protection for the staff.
Other embodiments of the invention comprise a radiation protection drape having slits and/or openings in proximetry to the left and/or right radialis area of the patient. Such slit or opening allows for the patients arm to extend through the radiation barrier, thus to provide easy access to the radialis entry point, with little additional radiation exposure to the clinical staff.
In yet another embodiment of the invention, the radiation protection drape to be positioned on the patient comprises one attenuating compound whereas a radiation protection garment to be used by a clinical practitioner comprises another attenuating compound.
The radiation protection drape to be positioned on the patient may have a attenuating compound comprising primarily of Antimony. The radiation protection garment to be used by the clinical practitioner may comprise an attenuating compound primarily consisting of Bismuth and/or Wolfram. With different attenuating compounds in the radiation protection drape and the radiation protection garment, the protection can be made more efficient. Each attenuating compound can be selected to shield against radiation with a specific wavelength and sequenced in this order thus to more efficiently reduce radiation. Therefore, the radiation protection per surface area is more efficient, and the drape and garment can be made lighter with the benefits described herein.
In another embodiment of the invention, the radiation protection garment comprises one or several textile radiation protection panels integrated in a set of pants and shirt thus to construct a scrub suit, such panels essentially covering the front and/or the back of the wearer. The embodiments of the invention provide numerous benefits for clinical staff and patient. For example, the invention provides for enhanced protection for the clinical staff including protection for the head, arms and legs without the need for a heavy radiation protection garment. Any additional protection garment, such as a lower protection garment in order to protect from residual or stray scatter radiation, can have reduced protective level and therefore be made lighter. The removal of weight from the clinical staff will benefit in stamina and avoiding work related injuries and disorders, such as described above. It will further also improve the movability and range of the operator and staff. The inherent weight of the patient drape has been commented as calming and caressing to the patient in the same functionality as having a weight blanket. Furthermore, the benefits described above are available while the safety of the patient is not compromised due to any inaccessibility to body parts of the patient in emergency situations. Further benefits and/or advantages of embodiments of the invention are described in the detailed description of the invention.
It should be emphasized that the term “comprises/comprising” when used in this specification is taken to specify the presence of stated features, integers, steps or components but does not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof.
These and other aspects, features and advantages of which embodiments of the invention are capable of will be apparent and elucidated from the following description of embodiments of the present invention, reference being made to the accompanying drawings, in which
Specific embodiments of the invention will now be described with reference to the accompanying drawings. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. The terminology used in the detailed description of the embodiments illustrated in the accompanying drawings is not intended to be limiting of the invention.
The following description focuses on embodiments of the present invention applicable as a radiation protection system for medical procedures wherein radiologic guidance using radiation systems, such as X-ray radiation systems, continuously exposes the endovascular staff to ionizing radiation. However, it will be appreciated that the invention is not limited to this application but may be applied to many other procedures, such as other areas where a radiation protection system may be used to protect the staff from scatter radiation.
The radiation protection drape 2 may be sized to at least partially cover the patient from a proximity of a radiated area of the patient to the feet of the patient. In some embodiments, the radiation protection drape 2 may be sized to cover the feet of the patient. The radiation protection drape 2 may be sized to cover the patient from the torso, as is illustrated in
In some embodiments such as is illustrated in
In some embodiments, the first section 3 is partitioned from the second section 4 from the first edge 5 partly to the second edge 6. Thus the first section 3 may be only partly separated from the second section 4. Still the second section 4 may be folded along the separation for quick and easy access to the portion of the patient covered by the second section 4. At the same time, the risk of the second section 4 falling on the floor and being contaminated when folded to uncover the patient is reduced. This also enhances the patient safety.
In some embodiments, the first section 3 has a varying radiation protection level across the first section. For example, a section closer to the torso has a higher radiation protective level than a section towards the feet. In some embodiments, a higher radiation protective level is in the range of 0.35-0.7 mm lead equivalence, and a lower radiation protection is in the range of 0.25-0.5 mm lead equivalence. The radiation protection level may vary in steps or continuously from a first end of the first section 3 to an opposing end of the first section 4.
In some embodiments, such as is illustrated in
In some embodiments, each of the first portion 4a and the second portion 4b may comprise at least one fastener device 8a, 8b, 8c to temporarily fasten and unfasten the first portion 4a to/from second portion 4b. The fastener device 8a, 8b, 8c, may comprise a hook and loop system or magnets attached to each of the first portion 4a and the second portion 4b. Hence, accidental separation of the first portion 4a and the second portion 4b is provided. Thus accidental exposure to radiation scatter is avoided.
The first portion 4a and the second portion 4b may be sized to be overlapping in an area where they are separated. The overlap may be in the range of 1-10 cm. Such overlap provides for prevention of scatter radiation at the separation between the first portion 4a and the second portion 4b.
In some embodiments, the first portion 4a and the second portion 4b of the second section 4 are partially permanently attached to the first section 3 at the lower end each of each of the first portion 4a and the second portion 4b. Again, this prevents accidental separation of the first portion 4a and the second portion 4b when in the folded position and that any of the first portion 4a and the second portion 4b falls on the fall and becomes contaminated during an interventional procedure.
In some embodiments, a closure indicator is positioned at an overlap between the first section 3 and the second section 4, and/or between the first portion 4a and the second portion 4b. The closure indicator is configured to detect if the sections 3, 4 and/or the portions 4a, 4b are completely closed. Such a detection system may be provided by an electrical system with conductors that create a closed circuit when the sections 3, 4 and/or the positions 4a, 4b are completely closed. The electrical system may alternatively or additionally be wireless, such as a conductive system, for example including the magnets described herein. A closure indicator may also be provided for a table mounted radiation protection drape section 15 (described below), that detects that the drape is completely attached to the operating table. The closure indicator for the table mounted radiation protection drape section 15 may be provided separately from the closure indicator of any of the sections 3, 4 and/or the portions 4a, 4b. Alternatively, a common closure indicator is provided for the table mounted radiation protection drape section 15 and one or more of the sections 3, 4 and/or the portions 4a, 4b. The closure indicator can be provided together with any of the embodiments described herein. The closure indicator further enhances the safety of embodiments of the invention to ensure that no stray scatter passes the radiation barrier at a non-completely closed section of the radiation shielding protection system.
In some embodiments, such as is illustrated in
The radiation protection drape 2 may comprise at least one fenestration 10 for a femoralis area. The fenestration 10 may be located along an edge of the first section 3 and/or an edge of the second section 4, along which the first section 3 and the second section 4 are partitioned. In the embodiments of the
As is illustrated in
Any of the first section 3 and the second section 4 may be positioned under a sterile barrier. Hence, the radiation protection drape may be for multiple-use. This provides for having enhanced radiation protection properties of the radiation protection drape 2. Radiation protection drapes made for single uses less efficient radiation protective material for costs reasons, whereas multiple use drapes can be made of more efficient radiation protective materials. However, over time the multiple use drapes are more cost efficient. Hence, embodiments of the invention are cost efficient while at the same time providing enhanced safety.
As is illustrated in
In some embodiments, such as is illustrated in
As is illustrated in
As is illustrated in
As is illustrated in
The radiation protection drape 2 and any section of the radiation protection system may have a radiation protection level corresponding to 0.1 to 1 mm lead equivalency, most preferably 0.35-0.7 mm lead equivalency.
As illustrated in
The radiation protection drape 2 and/or garment 17 of the embodiments of the invention may be made of the material disclosed in WO2014163574 by the same applicant as the present invention and which is incorporated herein in its entirety for all purposed. For example, the radiation protection drape 2 and/or garment 17 of the embodiments may comprise one or several layers of the material, as is disclosed in WO2014163574, such as to provide a varying radiation protection, as discussed above.
In
The table in
The table in
The table in
Using embodiments of the invention as visualized by Examples 1 and 2 reduces the exposure of the first operator with a factor 7, based on mean values, as compared to a conventional radiation protection set-up as displayed in Example 3. In individual positions over the body of the first operator, such as on the left chest side of the first operator (position C-D) in the lower body (position 5-9), the reduction may be greater.
The lead equivalency as described herein may be measured according to the standard IEC 61331-1:2014.
Measuring radiation exposure illustrates the benefits of radiation protection for the health care worker using embodiments of the invention. The presented data in Table 1 below have been collected from cardiology interventions within the specialty of Percutaneous coronary intervention, PCI. Dosimeters have been placed on the first operator, who was positioned next to the operating table in the area around the radialis position and towards the leg of the patient. In
The X-ray equipment used during the measurements was Philips Multi Diagnost Eleva FD (Koninklijke Philips Electronics N.V.) The operating table was at zero-degree angle and an under-table X-ray tube position was used with normal rotation angles for cardiovascular interventions. The tube voltage was at approximately 90 kV. In all measurements, RaySafes (Unfors RaySafe AB, Billdal, Sweden) i3 Real-time dosimetry System was used to indicate the amount of scattered radiation exposed to the first operator. The dosimeters were placed at four different dosimeter positions, which were all on the outside of the radiation protection apron of the first operator abdomen. In table 1, the four different dosimeter positions (DP) on the first operator are indicated as DP1, DP2, DP3, and DP4. DP1 was positioned at the right side of the chest, DP2 was at the left side of the chest, DP3 was on the left side of the hip, and PD4 was placed center belly. During the interventions, a ceiling mounted lead screen 114 from Mavig (Mavig Stahlgruberring 5, Munich, Germany) of 0.5 mm Lead equivalence was used. A radiation protection drape section 115 formed a table skirt on the side of the operating table from the foot end to the shoulder level of the patient. The table skirt was from Kenex (Kenex, Greenway, Harlow Business park, Harlow, England) of 0.5 mm Lead equivalence was placed on the side of the operating table together with table skirt extension mounted in a hinge from the operating table (partially illustrated in
The first section was partitioned from the second section from the first edge to the second edge of the radiation protection drape and being separable from the second section. However, this is not necessary in all embodiments of the invention.
The first section was partitioned from the second section from the first edge partly to the second edge, and the first section was partly separated from the second section. However, this is not necessary in all embodiments of the invention.
The first section had a varying radiation protection level across the first section. However, this is not necessary in all embodiments of the invention.
The second section comprised a first portion and a second portion, where the first portion and the second portion were separated along an edge of each of the first portion and the second portion, and comprised a fastener to temporarily fasten and unfasten the first portion to/from second portion. However, this is not necessary in all embodiments of the invention.
The radiation protection drape comprised one fenestration for a femoralis area of the patient, wherein the fenestration was located along the partition of the first section and the second section. However, this is not necessary in all embodiments of the invention.
The second edge was located at the fenestration, the first section and the second section were partitioned from the first edge to the second edge. However, this is not necessary in all embodiments of the invention.
The radiation protection drape comprised a third section separated from the first section and the second section and was sized to partially cover the fenestrated area of the radiation protection drape. However, this is not necessary in all embodiments of the invention.
The radiation protection shielding system comprised a fastening device, in the form of magnets located at where the first portion was partitioned from the second portion. However, this is not necessary in all embodiments of the invention.
The radiation protection drape was sized to extend over the rim of the long side of the operating table facing the first operator, when positioned over the patient lying on the operating table, and towards to the floor on the side of the operating table, about 10 cm over the rim of the operating table, such as to cover the side of the patient when laying on the operating table. However, this is not necessary in all embodiments of the invention.
The ceiling mounted radiation shielding screen 114 was positioned between clinical staff and the radiated area at an upper body portion of the patient. However, this is not necessary in all embodiments of the invention.
The radiation protection shielding system comprised a table mounted radiation protection drape section that was configured to cover at least a part of the area under the table.
In combination with the radiation protection drape, a radiation protection garment in the form of an apron was used by the first operator. However, this is not necessary in all embodiments of the invention.
On the patient, the radiation protection drape with a first section 103 and a second section 104 had a 0.5 mm Lead equivalence and was mounted as illustrated in
In Table 1, the radiation exposure to the dosimeters, placed on the first operator in the intervention field when the embodiments of the Invention as described in example 4, is presented. The values in Table 1 are in micro Sievert, and the average exposure is the average registered exposure towards the First operator. The average reduction efficacy denotes the quotient between the average exposure to the first operator and the emitted dose, represented by a dosimeter placed under the head of the patient. This value may vary pending on the type of intervention and the time of image guiding needed during the intervention. As can be seen in Table 1, the radiation exposure registered under the head of the patient was highest for Patient 4, which is an indication that image guiding with radiation was used more than for Patients 1 to Patient 3. For Patient 2, the radiation exposure was the lowest.
It can be concluded that the embodiment in Example 4 reduces the radiation exposure towards the first operator effectively, with a 99% to 100% reduction of radiation. With the registered level of radiation emitted to the first operator, the need for body worn radiation protection is reduced and a radiation protection apparel of lower protection level can be carried, or no body worn radiation protection apparel is needed. Hence, embodiments of the invention, as illustrated with example 4, provide numerous benefits for clinical staff and patient as described above in the sections “Summary of the Invention” and “Description of Embodiments”.
As will be apparent, the features and attributes of the specific embodiments disclosed above may be combined in different ways to form additional embodiments, all of which fall within the scope of the present disclosure.
Conditional language used herein, such as, among others, “can,” “could,” “might,” “may,” “e.g.,” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain embodiments include, while other embodiments do not include, certain features, elements and/or states. Thus, such conditional language is not generally intended to imply that features, elements and/or states are in any way required for one or more embodiments or that one or more embodiments necessarily include logic for deciding, with or without author input or prompting, whether these features, elements and/or states are included or are to be performed in any particular embodiment.
Any process descriptions, elements, or blocks in the flow diagrams described herein and/or depicted in the attached figures should be understood as potentially representing modules or segments. Alternate implementations are included within the scope of the embodiments described herein in which elements or functions may be deleted, executed out of order from that shown or discussed, including substantially concurrently or in reverse order, depending on the functionality involved, as would be understood by those skilled in the art.
It should be emphasized that many variations and modifications may be made to the above-described embodiments, the elements of which are to be understood as being among other acceptable examples. All such modifications and variations are intended to be included herein within the scope of this disclosure and protected by the following claims.
The present invention has been described above with reference to specific embodiments. However, other embodiments than the above described are equally possible within the scope of the invention. Different method steps than those described above may be provided within the scope of the invention. The different features and steps of the invention may be combined in other combinations than those described. The scope of the invention is only limited by the appended patent claims.
Number | Date | Country | Kind |
---|---|---|---|
2250265-2 | Feb 2022 | SE | national |
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/SE2023/050165 | 2/24/2023 | WO |