Abstract: The kits and methods of the present invention relate to the diagnosis of cardiovascular disorders. In one aspect, the invention discloses a method and a kit for determining whether a subject has a fragile plaque disorder. In one aspect, the invention discloses a method and a kit for determining whether the subject has an occlusive disorder. In one aspect, the invention discloses a method and a kit for determining whether the subject has a restenosis disorder. Other methods of the present invention relate to the selection of therapeutics for a patient with a cardiovascular disease.

Abstract: A housing retains a lancet body which encloses a needle whose tip is covered by a cap. The cap has a head provided with flanges. These flanges locate within notches at the end of the housing on only two sides of the housing. The location of the flanges within the notches holds the lancet within the body, before use, so as to compress a spring positioned between a head and a slotted portion of the housing. When the device is to be used, the head of the cap is rotated through 90° so as to detach the cap from the rest of the lancet body and release the flanges from the notches. This allows the lancet body to be actuated by a sprung-loaded trigger-release mechanism, when required, so that the tip of the needle projects momentarily through the opening at the end of the housing and then bounces back.

Abstract: When a trigger of an injection device is released, a main spring (4) expands, driving a member (7) forwards. This compresses a weak spring (11), but a spring (5) is stiff enough to remain expanded. A syringe (2) is thus thrust forwards via a collar (9), so that a needle (3) projects from a barrel (1). The spring (4) continues to expand after the syringe has reached its forward position, with the spring (11) fully compressed, so that the stem (8) of the member (7) acts on a piston (14) within the syringe (2), to expel the dose while the spring (5) is caused to be compressed. The spring (5) ensures that the syringe is retained in its forward position during this phase.

Abstract: A lancet has a generally tubular body (1). A hollow insert (4) with a closed end plugs one end of the body (1), and it has a co-axial projection (5) forming a sharp tip proud of that end of the body. The body (1) and insert (4) are simultaneously formed by twin shot moulding, the body being of polyethylene and the insert being of a liquid crystal polymer which will create a sharp tip of adequate strength.