MEASUREMENT OF HUMAN SKIN COMPRESSION DYNAMICALLY USING AN
AUTOMATED PHOTOGRAMMETRIC TECHNIQUE
Gary Robertson
ShapeQuest Inc. Ottawa, Canada
gary@ shapecapture.com
Commission V, WG V/3
KEY WORDS:
Automatic target reading, stereo matching, dot target projection, synchronized digital cameras, digital image matching, real time
measurement, dynamic measurement, human skin, human tissue compression, peripheral vascular disease.
ABSTRACT:
This paper describes the procedure used to measure human tissue compression and distortion at a dynamic rate. This is part of an
ongoing research program on skin tissue and is set up to monitor capillary occlusion especially over areas of boney prominences.
The monitoring of the skin surfaces allows us to measure the swelling as to the shape of the object applying the pressure.
Eventually the tissue recovers, and normal capillary flow is restored, the pattern of least pressure recovers first and the most
pressure recovering last. This whole response is affected by multiple factors, including illness, peripheral vascular disease, and
heart disease to name a few. This research is also applied to monitor the lapse rate of human skin indention. To meet the demand
for near real time measurement of this magnitude requires special hardware configurations and software integration and solutions
in hardware as to provide near real time throughput. The system utilizes multiple synchronized digital cameras with a precision
pattern projector. The projection system projects a fine mesh of dots on the skin surface and auto point measurement and stereo
matching are also utilized to measure the surface at near real time rates.
1. INTRODUCTION
1.1 Background:
The following describes the historical research we have
undertaken over the years regarding skin imprint analysis
manly in regard to forensic applications. It also describes the
expanded areas where this research is applied.
Initially, the work led to procedures used to locate and measure
imprint or impact marks on skin. This forensic analysis
covered imprints found on suspects and murder victims. The
key to impact or imprint mark analysis is the ability to locate
the mark that in most cases might not be visible to the human
eye. Several detailed analyses were made including. image
acquisition techniques utilizing laser or ALS (Alternate Light
Source) with the digital images. In addition, we implemented a
procedure using target or pattern generation and automated
target reading of the imprint to generate a 3D model and x.y.z.
coordinate data. Also, in this study is digital image matching
and measurement of the object that made the mark. One of the
major areas of this study was using pigskin in a comparison for
developing a database for ante mortem and post-mortem
marks. This research developed the procedures used to
precisely (positional accuracy in the micron range) model the
same imprints on pig and human skin and how close the actual
relationship is.
The second phase of the research involved more analysis of
ante, and post mortem skin imprints including lab controlled
studies of imprints at the instant of death with sub micron
accuracy. At this point, we discovered that the lapse rate of
skin or its dispersion rate back to normality stops at the
moment of death. We also worked on the characteristics at
time of death including the analysis of the frozen state of skin
utilizing pigs.
We now have a system to measure human tissue compression
and distortion at a dynamic rate. This is part of our ongoing
research program on skin tissue and is set up to monitor
capillary occlusion especially over areas of boney prominences.
The monitoring of the skin surfaces allows us to measure the
swelling as to the shape of the object applying the pressure.
This research follows earlier testing to calculate the elasticity
and coefficients of human and pig skin, in addition to the
property analysis of ante-mortem and post mortem imprint
marks on human and pig skin. This precise modelling of skin
has opened a new area of research since the ante mortem
marks can be used to determine time of death calculations from
the time the imprint was made.
1.2 Current:
We are now looking at various responses that would affect the
lapse rate of skin including drugs, illness, peripheral vascular
disease, heart disease and also the characteristics of frozen
skin. The testing of these various conditions gives us a
comparison of skin lapse rates from normal, that is skin
imprints from individuals with no medical condition or
situations where the use of drugs would affect the lapse rate of
skin. For the first part of the testing we looked at conditions
that would relate directly to circulation. In this case we studied
individuals with conditions of CREST and Raynaud's.
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