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Arrangements for the detection of the presence and/or concentration of an analyte in a sample of bodily fluid include diffuse transmission, diffuse reflection and edge or waveguide illumination arrangements. A vertical flow assay arrangement and/or technique is also disclosed, and includes a detecti

Arrangements for the detection of the presence and/or concentration of an analyte in a sample of bodily fluid include diffuse transmission, diffuse reflection and edge or waveguide illumination arrangements. A vertical flow assay arrangement and/or technique is also disclosed, and includes a detection component that can be in the form of an array of optical detection elements. A number of assay pad constructions are described which may include at least one or more of the following components: a prefilter component, a reflective component, a membrane component, a reagent component, a mesh component, and a component to prevent lateral spreading.

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1. An arrangement constructed and arranged to detect the presence or concentration of an analyte present in bodily fluid, the arrangement comprising: a channel member configured to receive a sample of the bodily fluid from a conduit;an assay pad in fluid communication with the channel member, the as

1. An arrangement constructed and arranged to detect the presence or concentration of an analyte present in bodily fluid, the arrangement comprising: a channel member configured to receive a sample of the bodily fluid from a conduit;an assay pad in fluid communication with the channel member, the assay pad containing a reagent;a plurality of detectors, each detector constructed and arranged to produce a signal indicative of a reaction between the analyte and the reagent; andelectronics constructed and arranged to monitor and interpret the signals produced by the plurality of detectors to provide the following outputs:(i) an estimate of the volume of the sample received by the channel member based at least in part on the number of detectors that produce a signal indicating a reaction between the analyte and the reagent; and (ii) information about the kinetics of the reaction between the analyte and the reagent based at least in part on the time between signals. 2. The arrangement of claim 1, wherein the electronics further comprise at least one corrective algorithm. 3. The arrangement of claim 1, wherein the electronics generate an overall reading based on the signals produced by the individual detectors. 4. The arrangement of claim 1, wherein the conduit comprises a skin penetration member. 5. The arrangement of claim 4, wherein the skin penetration member comprises a microneedle. 6. The arrangement of claim 1, further comprising at least one light source adapted to provide light incident upon the assay pad. 7. The arrangement of claim 1, wherein the plurality of detectors comprises an array of detectors. 8. The arrangement of claim 7, wherein the array of detectors comprises a linear array. 9. The arrangement of claim 7, wherein the array of detectors comprises an array of CMOS detectors. 10. A method useful in detecting the presence or concentration of an analyte present in bodily fluid, the method comprising: receiving a sample of the bodily fluid in a channel member; bringing the sample into contact with an assay pad, the assay pad containing a reagent;producing a plurality of signals from a plurality of detectors upon a reaction between the analyte and the reagent; andmonitoring and interpreting the at least one signal to provide the following outputs: (i) an estimate of the volume of the sample received by the channel member based at least in part on the number of detectors that produce a signal indicating a reaction between the analyte and the reagent; and(ii) information about the kinetics of the reaction between the analyte and the reagent based at least in part on the time between signals. 11. The method of claim 10, further comprising applying at least one corrective algorithm to the plurality of signals. 12. The method of claim 10, further comprising generating an overall reading based on the signals produced by the plurality of detectors. 13. The method of claim 10, further comprising providing a skin penetration member. 14. The method of claim 13, wherein the skin penetration member comprises a microneedle. 15. The method of claim 10, further comprising providing light incident upon the assay pad. 16. The method of claim 10, further comprising producing the a plurality of signals with an array of detectors. 17. The method of claim 16, wherein the array of detectors comprises a linear array. 18. The method of claim 16, wherein the array of detectors comprises an array of CMOS detectors.