Leveling drape for endovascular procedures
12544174 ยท 2026-02-10
Inventors
Cpc classification
A61B2046/201
HUMAN NECESSITIES
A61B2046/236
HUMAN NECESSITIES
A61B46/23
HUMAN NECESSITIES
International classification
A61B46/23
HUMAN NECESSITIES
Abstract
A sterile surgical drape includes left and right inflatable supports leveling the upper surface of the drape to better corral instruments during angiographic procedures. An optional center inflatable support helps center the drape and provides a continuation of this work surface. Multiple sealable openings can be provided at common groin and wrist locations.
Claims
1. A surgical drape comprising: a sterile sheet sized to cover an area of a patient when lying in a horizontal position on a table, the sheet having left and right edges extending laterally beyond a left and right side of the patient; and a first and second inflatable chamber attached under the left and right edges and sized to elevate the left and right edges above the table when inflated; and further including a third inflatable chamber positioned between the first and second inflatable chambers and sized to be positioned between legs of the patient.
2. The sterile drape of claim 1 wherein the left and right edges extend beyond the first and second inflatable chambers to provide a downwardly extending drape section when positioned on the patient on a radiographic table.
3. The sterile drape of claim 2 wherein the downwardly extending drape section provides an upwardly open pouch.
4. The sterile drape of claim 3 wherein an opening of the pouch is releasably sealable.
5. The sterile drape of claim 1 wherein the sterile sheet provides at least two openings positioned at at least one of a patient groin area and patient wrist area, the openings having releasable covers.
6. The sterile drape of claim 5 wherein the releasable covers are adhesively attached sheets.
7. The sterile drape of claim 1 wherein the first and second inflatable chamber have an inflated height of at least 4 inches between a lower surface adapted to contact the table when inflated and an upper surface defining a height of the left or right edges, respectively.
8. The sterile drape of claim 1 wherein the first and second inflatable chambers hold the sterile sheet to enforce an upwardly concave surface when positioned flanking legs of an average sized patient and inflated.
9. The sterile drape of claim 1 wherein the sterile sheet is sized to cover a superior portion of the patient above a groin region and an inferior portion of the patient below the groin region and the first and second inflatable chambers are limited to the inferior portion.
10. The sterile drape of claim 1 wherein the first, second, and third inflatable chambers include an interconnecting pressure equalization channel.
11. The sterile drape of claim 1 wherein each of the first, second, and third inflatable chambers provides separate inflation valves.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
(8) Referring now to
(9) In one nonlimiting example, all or a center of the drape material 11 may be laminated from four layers including a first layer being a high-density polyethylene film having a thickness of approximately five mils with small apertures to allow fluids to flow to an absorbent layer underneath while blocking lint from the absorbent layer from reaching the patient. This layer may be blue in color to absorb light from the overhead lamps and reduces glare for the doctor and comport with traditional trade coloring. This layer may be high-density polyethylene, 4.8 mils. thick, and weighs 13.6 grams per square meter. The second layer is an absorbent nonwoven white, unembossed air laid fabric composed of bleached virgin wood pulp fibers and bonded with a latex binder made by fiberizing cellulose (wood) pulp in a series of hammemills. The fiberized pulp is then blown onto a wire screen running through an air laid machine. Each side of the web may be sprayed with a binder to hold the fibers in sheet form. This layer may be approximately 70 mils. thick and is intended to absorb liquid. The third layer is a polyethylene film whose main function is to act as a barrier for fluid leakage to the patient and is 2 mils. thick. The final layer may be a print-bonded polyester laminated to the bottom side of the drape and acts as a comfort layer between the patient and the polyethylene film. The layers may be laminated together by a water-based adhesive.
(10) In one embodiment, the surgical drape 10 is sized to cover a wrist region 16 and groin region 18 of the patient and may, for example, extend from the patient's shoulders to the patient's in for a patient of average size. In one nonlimiting example, the surgical drape 10 may have an inferior-superior length 20 of 130 inches (or greater than 77 inches) and a lateral width 22 of 90 inches (or greater than 30 inches). Importantly, the drape is sized to have a lateral width 22 greater than the width of the patient table 14 (for example, greater than 26 inches) so as to have a skirt portion 24 that will drape down below the patient table 14 during use, for example, by a distance greater than 6 inches.
(11) Referring still to
(12) Positioned inferiorly to the left and right wrist openings 30 so as to be free from interference with the patient's hands are a left and right inflatable chamber 34a and 34b extending in a generally inferior-superior direction to flank and be outside of the patient's right and left leg (as depicted) during use. Positioned slightly below the groin openings 32 and centered between the left and right inflatable chambers 34 is a central inflatable chamber 36 that may fit between the patient's legs 46 when the surgical drape 10 is properly positioned and also extend parallel to the patient's superior-inferior axis. These inflatable chambers 34 and 36 may be constructed of a flexible polymer material that is airtight and may be adhered or welded to the drape material 11 or may be formed in part from the drape material 11 for its constituent layers. Generally, each of the inflatable chambers 34 and 36 may provide a generally superior-inferiorly extending tube leading to flexible end panels 50, the latter enforcing the desired cross-sectional shape of the chambers 34 and 36. Internal gusseting may also be provided to control the cross-sectional shape as desired.
(13) Patch pockets 40a and 40b may be attached to outer surfaces of the skirt portions 24 to open upwardly when the skirt portions 24 are draped downwardly over the edges of the table 14. The patch pockets 40 may extend in an inferior-superior direction by more than 20 inches to regions above and below the groin region 18 and wrist regions 16 and may have a height of at least 6 inches. Generally, the patch pockets 40 will be fluid resistant to retain liquids and materials inserted therein. In some embodiments, the patch pockets 40 may include a drain valve at their lowest extent (not shown) to enable them to be connected to suction tubing to remove blood and or fluid accumulated during the procedure that could pull laterally on the surgical drapes 10.
(14) Referring now to
(15) For this purpose, a lower edge of the inflatable chambers 34 may contact an upper surface of the left and right edges of the table 14 to the left and right of the patient's legs 46 providing positive support of the work surface 44. Alternatively, inflatable chambers 34 may provide a buttress against the outer surfaces of the patient's legs 46 supporting the work surface 48 in cantilever. In the former case the height of the inflatable chamber 34 may be at least four inches and preferably greater than five inches between an upper surface of the table 14 and the work surface 44.
(16) The inflatable chambers 34a and 34b will generally have an increasing height as one moves from a medial to a lateral position thus providing an angular lower surface that offers a self-centering of the surgical drape 10. Similarly, the central inflatable chamber 36 may be downwardly convex to be self-centered between the patient's legs and to provide appropriate spacing between the patient's legs 46. The central inflatable chamber 36 may be sized to descend to contact the table 14 or (as depicted) may operate in a truss fashion to provide a support of the drape material 11 between the patient's legs supported by the patient's legs.
(17) Referring now to
(18) The upper openings of the patch pockets 40 may provide for adhesive or hook and loop closure fasteners 59 to allow them to be releasably secured in a closed position during or after use.
(19) Referring now to
(20) Referring now to
(21) Referring now to
(22) Certain terminology is used herein for purposes of reference only, and thus is not intended to be limiting. For example, terms such as upper, lower, above, and below refer to directions in the drawings to which reference is made. Terms such as front, back, rear, bottom and side, describe the orientation of portions of the component within a consistent but arbitrary frame of reference which is made clear by reference to the text and the associated drawings describing the component under discussion. Such terminology may include the words specifically mentioned above, derivatives thereof, and words of similar import. Similarly, the terms first, second and other such numerical terms referring to structures do not imply a sequence or order unless clearly indicated by the context.
(23) When introducing elements or features of the present disclosure and the exemplary embodiments, the articles a, an, the and said are intended to mean that there are one or more of such elements or features. The terms comprising, including and having are intended to be inclusive and mean that there may be additional elements or features other than those specifically noted. It is further to be understood that the method steps, processes, and operations described herein are not to be construed as necessarily requiring their performance in the particular order discussed or illustrated, unless specifically identified as an order of performance. It is also to be understood that additional or alternative steps may be employed.
(24) It is specifically intended that the present invention not be limited to the embodiments and illustrations contained herein and the claims should be understood to include modified forms of those embodiments including portions of the embodiments and combinations of elements of different embodiments as come within the scope of the following claims. All of the publications described herein, including patents and non-patent publications, are hereby incorporated herein by reference in their entireties.
(25) To aid the Patent Office and any readers of any patent issued on this application in interpreting the claims appended hereto, applicants wish to note that they do not intend any of the appended claims or claim elements to invoke 35 U.S.C. 112(f) unless the words means for or step for are explicitly used in the particular claim.