Medical testing device with calibrated indicia

• US 5,099,857 A
• Filed: 11/29/1989
• Issued: 03/31/1992
• Est. Priority Date: 05/29/1987
• Status: Expired due to Fees

• Current Assignee: Northern Sydney Area Health Service, Royal North Shore Hospital and Area Health Service
• Original Assignee: Northern Sydney Area Health Service
• Inventors: Baldo, Brian A., Tovey, Euan R.
• Primary Examiner(s): Yasko, John D.
• Assistant Examiner(s): Gutowski, Anthony
• Application Number:
  US07/449,825
• Time in Patent Office: 853 Days
• Field of Search: 604/46, 604/47, 604/51, 128/743, 206/364, 206/367, 206/439
• US Class Current: 600/556
• CPC Class Codes: A61B 17/205 Vaccinating by means of needles or other puncturing devices
• CPC Class Codes: A61B 5/411 Detecting or monitoring allergy or intolerance reactions to an allergenic agent or substance
• CPC Class Codes: A61B 5/441 Skin evaluation, e.g. for skin disorder diagnosis

Abstract

A disposable medical testing device (17) adapted to be held against the skin of a patient, which enables the performance of skin testing for the diagnosis of both immediate hypersensitivity and delayed hypersensitivity immune reactions. The device is comprised of a hollow body with a sealed chamber in which is mounted a movable needle (3) capable of penetrating a patient'"'"'s skin to a predetermined depth and a test reagent container (2). The device (17) is manipulable by a user to reduce the volume of the chamber and moving the needle thus releasing the reagent and causing penetration of the skin. The released reagent is delivered to the skin penetration site, and any resulting skin reaction is observed and recorded. Embodiments of the invention marked with a calibrated scale on a releasable transparent layer and details of patient and test date which allow multiple antigen tests to be performed are also disclosed. A method of testing for immune response using the device (17) is also disclosed.

Claims

1. A medical testing device adapted to be held against the skin of a patient to perform a test, said device comprising:

a hollow body having wall means defining a sealed chamber containing a test reagent therein,

a releasably attachable transparent layer releasably connected to the body and including calibrated indicia to enable a test result to be measured, said transparent layer forming a skin engaging surface of the device and, in use, being located against the patient'"'"'s skin,

a needle connected to said hollow body and being located within the body, said needle having at least one point extending toward said transparent layer and being moveable to extend beyond said body to penetrate the patient'"'"'s skin to a predetermined depth,

said device being adapted to be depressible by a user to cause the needle to penetrate said wall means of said chamber and release said reagent therefrom, said point extending beyond said transparent layer into the patient'"'"'s skin to said predetermined depth to cause said reagent to flow thereto.

2. The device according to claim 1, further comprising a bottom cover removably affixed to said transparent layer.

3. The device according to claim 1, wherein said needle has a plurality of points facing, in use, said transparent layer, to enhance flow of the reagent to the skin.

4. The device according to claim 1, wherein said needle is fluted to enhance flow of the reagent to the skin.

5. The device according to claim 1, wherein said needle is grooved to enhance flow of the reagent to the skin.

6. The device according to claim 1, wherein the cross section of the needle is enlarged to prevent penetration of the skin beyond the predetermined depth.

7. The device according to claim 1, wherein the test reagent is an antigen.

8. The device according to claim 1, wherein the test reagent further contains a stabilizer.

9. The device according to claim 1, wherein the test reagent further contains a preservative.

10. The device according to claim 1, wherein the test reagent further contains a buffer.

11. The device according to claim 1, wherein the test reagent is contained within a capsule or reservoir disposed within the hollow body.

12. The device according to claim 11, wherein the needle is provided with at least one further point facing in a direction opposite said point facing said transparent layer and the capsule is located adjacent the further point or points.

13. The device according to claim 1, wherein the test reagent is contained within a porous matrix.

14. The device according to claim 1, wherein the test reagent contains an additive to form a paste.

15. The device according to claim 1, wherein the test reagent contains an additive to form a gel.

16. The device according to claim 1, wherein the transparent layer has a surface capable of being written on so that the result of the test can be recorded thereon.

17. The device according to claim 1, wherein the body of the device is provided with a structure deformable to reduce the volume of said chamber.

18. The device according to claim 11, wherein a collapsible layer is provided within said body and surrounding said capsule or reservoir which permits the volume of the chamber to be reduced on application of pressure to the device.

19. A medical testing device comprising at least one of a strip or sheet containing a plurality of testing devices, each device comprising:

a hollow body having wall means defining a sealed chamber containing a test reagent therein,

a releasably attachable transparent layer releasably connected to the body and including calibrated indicia to enable a test result to be measured, said transparent layer forming a skin engaging surface of the device and, in use, being located against the patient'"'"'s skin,

a needle connected to said hollow body and being located within the body, said needle having at least one point extending toward said transparent layer and being moveable to extend beyond said body to penetrate the patient'"'"'s skin to a predetermined depth,

said device being adapted to be depressible by a user to cause the needle to penetrate said wall means of said chamber and release said reagent therefrom, said point extending beyond said transparent layer into the patient'"'"'s skin to said predetermined depth to cause said reagent to flow thereto, each of said devices containing a different test reagent in its associated sealed chamber.

20. A medical testing device adapted to be held against the skin of a patient to perform a test, said device comprising:

a hollow body containing a test reagent therein,

a releasably attachable transparent layer releasably connected to the body and including calibrated indicia to enable the test result to be measured, said transparent layer forming a skin engaging surface of the device and which, in use, is located against the skin of the patient,

a needle located within the hollow body and coated by said test reagent, said needle having at least one point facing said transparent layer and being moveable to extend beyond said body to penetrate the patient'"'"'s skin to a predetermined depth,

and wherein said device is adapted to be depressible by a user to cause said point to extend beyond said transparent layer and penetrate into the patient'"'"'s skin to a predetermined depth and to cause said reagent to flow thereto.

21. A method of testing for an immune response with a medical testing device including a hollow body having wall means defining a sealed chamber containing a test reagent therein, a releasably attachable transparent layer connected to the body and including calibrated indicia to enable a test result to be measured, a needle connected to the body and being located within the device, said needle having a least one point facing the transparent layer of the device, comprising the steps of:

(a) attaching the device to the patient'"'"'s skin by affixing the releasably attachable transparent layer against the skin;

(b) manipulating said needle so that it penetrates the sealed chamber and extends beyond the body and transparent layer to penetrate the patient'"'"'s skin, said needle by penetrating the wall means of the chamber causing reagent to be released therefrom through the transparent layer and into the patient'"'"'s skin; and

(c) removing the hollow body by separating it from the releasably attachable transparent layer, said transparent layer remaining against the patient'"'"'s skin.