The present invention is generally directed to skin-lancing devices and is more specifically directed to a skin lancing device having an improved endcap for more effective lancing and more efficient vacuum formation.
Lancing devices are used for obtaining capillary blood from body sites. A typical user of a lancing device is a person in a program of self-blood-glucose-monitoring for treatment of diabetes. Such a user presses an endcap of the lancing device at a selected puncture site, activates the lancing device to puncture the skin at the site, and draws capillary blood for testing. To minimize any discomfort caused by the puncture, the lancing device typically controls the depth of the puncture, quickly withdraws the lancet from the skin once a puncture has been made, and prevents the lancet from rebounding and reentering the puncture or causing a second puncture.
Once a puncture has been made, the lancing device remains on the site and a vacuum is created to draw skin partially into an end cap of the device. As this occurs, a small amount of blood forms on the skin at the puncture site. The vacuum is then released and the lancing device is removed from the skin. The drop of blood on the surface of the skin at the puncture site is then applied to a test sensor.
Some lancing devices include a gasket connected to the lancet that reciprocates in the lancing device as the lancet moves through a lancing stroke. The gasket is in airtight contact with the inside of the lancing device such that as the gasket slides within the lancing device, air is displaced and a vacuum is created.
It is desirable that lancing devices be as comfortable as possible to use. Further, it is desirable for a lancing device to have accurate placement and puncture depth for the lance, so that an appropriate amount of blood collects with only one lancing operation, decreasing or eliminating the possibility that a second lancing operation will be necessary. Additionally, it is desirable for a lancing device to create and maintain sufficient vacuum for a drop of blood of a predictable volume to collect. The present invention is directed to an improved lancing device endcap.
An endcap according to one embodiment of the present invention is provided with a contoured skin-contact surface to facilitate the drawing of skin into the endcap
The contour of an endcap according to the present invention preferably includes a narrowing skin-receiving area that causes skin to bulge within the skin-receiving area, preparing the skin for puncturing by a lance to a desired puncture depth.
Increased contact between skin and a lancing device endcap according to some embodiments of the present invention increases the effectiveness and duration of vacuum formation within a vacuum cavity.
Additional features of the present invention will be more fully understood upon reference to the figures.
a-3d are time elapse images of use of a lancing device having an endcap according to one embodiment of the present invention.
While the invention is susceptible to various modifications and alternative forms, specific embodiments are shown by way of example in the drawings and will be described in detail herein. However, it should be understood that the invention is not intended to be limited to the particular forms disclosed. Rather, the invention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Referring now to
As the plunger 12 is depressed farther, a lance 20, such as a sterile needle lance, quickly extends out of the open end 14 of the lancing device 10 and is then quickly retracted within the endcap 18. Following the lancing operation, a vacuum is formed within a vacuum cavity 22 by the movement of the diaphragm within the lancing device 10. The vacuum cavity 22 is bounded by the inner surfaces of the endcap 18 and by the surface 23 of skin against which the endcap 18 is placed. Further details of operation of lancing devices according to some embodiments of the present invention will be understood with reference to U.S. Pat. No. 6,152,942 which is incorporated by reference herein in its entirety. According to an alternative embodiment, a puncturing process starts when sufficient pressure has been exerted between the endcap and the skin surface 23 to initiate the puncture.
The endcap 18 of the present invention is provided with features that improve the performance of the lancing device 10.
The second portion 28 of the endcap 18 is narrower than the first portion 26 of the endcap 18. A skin-contact surface 30 slopes inwardly from an outer wall 32 along a blunt skin-contact edge 34. The skin-contact surface 30 is widest at the skin-contact edge 34 and gradually narrows from the open end 14 of the lancing device to an inner wall 36. According to one embodiment of the present invention, the skin-contact surface 30 follows a parabolic contour from the skin-contact edge 34 to a linear inner wall 36. Other contours, such as circular contours, may be used to form the skin-contact surface 30. In the embodiment shown in
As shown in
The operation of an endcap 18 according to the present invention will be more completely understood with reference to
Turning to
In
Endcaps according to the present invention are capable of maintaining a vacuum pressure of −10 mm Hg for six seconds or longer. Further, the control of puncture depth limits the amount of pain and injury associated with the puncture while providing an adequate blood sample. Reduced pain and injury promotes increased testing and the improved feedback results in better control of blood sugar.
Endcaps according to the present invention may be made of a variety of materials. It is preferable for endcaps according to the present invention to be transparent, enabling a user to view the collection of a blood sample 42 and to withdraw the endcap from the skin surface when a sufficient volume of blood has been collected. It is preferred for endcaps according to the present invention to be disposable and easily attached to and removed from a lancing device.
While the present invention has been described with reference to one or more particular embodiments, those skilled in the art will recognize that many changes may be made thereto without departing from the spirit and scope of the present invention. Each of these embodiments and obvious variations thereof is contemplated as falling within the spirit and scope of the claimed invention, which is set forth in the following claims.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US05/11340 | 4/1/2005 | WO | 9/11/2006 |
Number | Date | Country | |
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60558243 | Apr 2004 | US |