Multispot monitoring for use in optical coherence tomography
Optical coherence tomography (herein “OCT”) based analyte monitoring systems are disclosed. In one aspect, techniques are disclosed that can identify fluid flow in vivo (e.g., blood flow), which can act as a metric for gauging the extent of blood perfusion in tissue. For instance, if OCT is to be used to estimate the level of an analyte (e.g., glucose) in tissue, a measure of the extent of blood flow can potentially indicate the presence of an analyte correlating region, which would be suitable for analyte level estimation with OCT. Another aspect is related to systems and methods for scanning multiple regions. An optical beam is moved across the surface of the tissue in two distinct manners. The first can be a coarse scan, moving the beam to provide distinct scanning positions on the skin. The second can be a fine scan where the beam is applied for more detailed analysis.
1. A system for determining an analyte level in tissue, the system comprising:
an optical coherence tomography system configured to be aligned to a tissue region of a subject through an optical coupler, wherein the tissue region includes at least a first tissue site and a second tissue site;
a scanner in communication with the optical coherence tomography system and configured to:
scan a beam over the first tissue site using the optical coupler to collect a first set of optical coherence tomography measurements; and
scan the beam over the second tissue site using the optical coupler to collect a second set of optical coherence tomography measurements; and
a processor configured to:
determine, based on the first set of optical coherence tomography measurements, that the first tissue site is an analyte correlating region, wherein an analyte correlating region comprises a tissue site that is valid for measuring an analyte level;
determine, based on the second set of optical coherence tomography measurements, that the second tissue site is not an analyte correlating region and not valid for measuring an analyte level;
cause the scanner to monitor the first tissue site and process optical coherence tomography measurements associated with the first tissue site to measure the analyte level; and
cause the scanner to not monitor and not processing optical coherence tomography measurements associated with the second tissue site.
2. The system of claim 1 , wherein the first and second tissue sites comprise spatially distinct two-dimensional regions of a skin surface of the subject.
3. The system of claim 1 , wherein the scanner is further configured to:
scan the beam over at least one additional tissue site using the optical coupler to collect optical coherence tomography measurements corresponding with each additional tissue site.
4. The system of claim 1 , wherein determining that the first tissue site is valid for measuring an analyte level comprises:
determining a tissue hydration level of the first tissue site.
5. The system of claim 1 , wherein the processor is further configured to:
aggregate a plurality of measures of the analyte level to provide an aggregated measure of the analyte level.
6. The system of claim 5 , wherein the processor is further configured to:
calibrate the optical coherence tomography system using the aggregated measure of the analyte level in the tissue.
7. The system of claim 1 , wherein the tissue region comprises a spatial area of skin of the subject.
8. The system of claim 1 , wherein the analyte level comprises a blood glucose level.
9. The system of claim 1 , wherein at least one of scanning the beam over the first tissue site or scanning the beam over the second tissue site comprises scanning a plurality of tissue depths.
10. The system of claim 1 , wherein areas associated with the first tissue site and the at least second tissue site do not overlap.