CUTANEOUS CATHETER ANCHORING DEVICE AND METHOD OF STABILIZING A CATHETER SITE

• US 20160101264A1
• Filed: 10/13/2014
• Published: 04/14/2016
• Est. Priority Date: 10/13/2014
• Status: Abandoned Application

• Current Assignee: Benjamin Bertram
• Original Assignee: Benjamin Bertram
• Inventors: Bertram, Benjamin
• Application Number:
  US14/512,640
• Publication Number:
  US 20160101264A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61M 2025/0266 using pads, patches, tapes or the like
• CPC Class Codes: A61M 25/02 Holding devices, e.g. on the body

Abstract

A cutaneous catheter anchoring device and method to prevent occlusion of an indwelling peripheral intravenous catheter and to do so in a way that does not require immobilization of, or significant reduction in the range of motion of, the joint of the particular extremity. The device and method accomplish this by immobilizing multiple areas of the skin'"'"'s surface relative to the indwelling catheter. The device is in close proximity to the indwelling catheter and maintains a smooth, rather than bent or creased, skin surface above the catheter thus preventing creasing or kinking of the catheter itself during times when the patient bends the extremity.

Claims

1. A cutaneous catheter anchoring device (10), comprising,

a body (100) having a first width (110), a second width (120), a circumferential edge (130) defining a perimeter, a top surface (140), a bottom surface (150), and a thickness (160);

wherein the top surface (140) has a surface area of 0.79-7.70 in²;

wherein the thickness (160) is 0.045-0.250″

; and

wherein the perimeter has a total lineal length of straight perimeter sections that is less than 8″

.

2. The device according to claim 1, wherein straight perimeter sections do not intersect and are joined by a curved perimeter section having a radius of curvature of at least twice the thickness (160).

3. The device according to claim 1, wherein at least 50% of the perimeter length is curved.

4. The device according to claim 3, wherein the entire perimeter length is curved.

5. The device according to claim 4, wherein each point along the perimeter has a local radius of curvature and the minimum local radius of curvature is 0.25″

and the maximum local radius of curvature is 6.0″

.

6. The device according to claim 1, wherein the top surface (140) has a surface area of 2.41-5.94 in².

7. The device according to claim 6, wherein the thickness (160) is 0.080-0.125″

and the maximum modulus of elasticity of the body (100) is at least 87,000 lbf/in².

8. The device according to claim 2, wherein the perimeter includes at least two straight perimeter section and all straight perimeter sections have individual lineal lengths of less than 1.5″

.

9. The device according to claim 2, wherein the edge (130) and the bottom surface (150) are joined by a curved edge section having a radius of curvature that is at least 25% of the thickness (160).

10. The device according to claim 8, wherein straight perimeter sections do not intersect and are joined by a curved perimeter section having a radius of curvature of at least 0.25″

.

11. A method for immobilizing an area of skin relative to an indwelling catheter in the vicinity of an insertion site at the antecubital fossa, while allowing flexion of an elbow joint in the vicinity of a catheter insertion site to reduce the risk of occlusion during joint flexion, comprising the steps of:

a) releasably coupling a lateral skin area of at least 0.25 in², located laterally of the insertion site, and a medial skin area of at least 0.25 in², located medially of the insertion site, to a cutaneous catheter anchoring device (10) to reinforce the skin and the catheter insertion site;

b) wherein the cutaneous catheter anchoring device (10) covers a portion of a catheter hub and extends longitudinally beyond a catheter discharge orifice, and wherein the cutaneous catheter anchoring device (10) shifts transversely upon flexion of the elbow joint and maintains the relationship to the coupled lateral skin area and medial skin area thereby shifting the insertion site transversely with the cutaneous catheter anchoring device (10) to prevent kinking of the catheter; and

c) wherein the cutaneous catheter anchoring device (10) includes a body (100) having a first width (110), a second width (120), a circumferential edge (130) defining a perimeter, a top surface (140), a bottom surface (150), and a thickness (160), wherein the top surface (140) has a surface area of 0.79-7.70 in², the thickness (160) is 0.045-0.250″

, and the perimeter has a total lineal length of straight perimeter sections that is less than 8″

.

12. The method of claim 11, further including the step of releasably coupling a distal skin area of at least 0.25 in², located longitudinally beyond the catheter discharge orifice, to the cutaneous catheter anchoring device (10), wherein the distal skin area has a transverse distal skin length of at least 0.125″

.

13. The method of claim 11, wherein the lateral skin area is at least 0.50 in² having a longitudinal lateral skin length of at least 0.50″

, and the medial skin area is at least 0.50 in² having a longitudinal medial skin length of at least 0.50″

.

14. The method of claim 11, wherein the step of releasably coupling the lateral skin area and the medial skin area to the cutaneous catheter anchoring device (10) further includes the step of covering the insertion site with a sterile flexible underlayer (300) attached to the skin, and attaching the body (100) to an exterior of the flexible underlayer (300).

15. The method of claim 11, wherein the maximum modulus of elasticity of the body (100) is at least 87,000 lbf/in².

16. The method of claim 15, wherein the maximum modulus of elasticity of the body (100) is less than 652,000 lbf/in², and the thickness (160) is 0.080-0.125″

.

17. The method of claim 14, wherein the maximum modulus of elasticity of the body (100) is at least ten times greater than the maximum modulus of elasticity of the underlayer (300).

18. The method of claim 11, wherein the shape of the cutaneous catheter anchoring device (10) promotes the transverse shift upon flexion of the elbow joint by having a curved perimeter over at least 50% of the perimeter length.

19. The method of claim 11, wherein the entire perimeter length is curved and each point along the perimeter has a local radius of curvature and the minimum local radius of curvature is 0.25″

and the maximum local radius of curvature is 3.0″

.

20. The method of claim 19, wherein the second width (120) is greater than the first width (110).