872 IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, VOL. 60, NO. 3, MARCH 2013
Multiscale Entropy Study of Medical Laser
Speckle Contrast Images
Anne Humeau-Heurtier*, Guillaume Mah´ e, Sylvain Durand, and Pierre Abraham
Abstract—Laser speckle contrast imaging (LSCI) is a noninva-
sive full-field optical imaging technique that gives a 2-D microcir-
culatory blood flow map of tissue. Due to novelty of commercial
laser speckle contrast imagers, image processing of LSCI data is
new. By opposition, the numerous signal processing works of laser
Doppler flowmetry (LDF) data—that give a 1-D view of microvas-
cular blood flow—have led to interesting physiological information.
Recently, analysis of multiscale entropy (MSE) of LDF signals has
been proposed. A nonmonotonic evolution of MSE with two dis-
tinctive scales—probably dominated by the cardiac activity—has
been reported. We herein analyze MSE of LSCI data. We compare
LSCI results with the ones of LDF signals obtained during the
same experiment. We show that when time evolution of LSCI sin-
gle pixels is studied, MSE presents a monotonic decreasing pattern,
similar to the one of Gaussian white noises. By opposition, when
the mean of LSCI pixel values is computed in a region of interest
(ROI) and followed with time, MSE pattern becomes close to the
one of LDF data, for ROI large enough. LSCI is gaining increased
interest for blood flow monitoring. The physiological implications
of our results require future study.
Index Terms—Blood flow, laser speckle imaging, medical image
processing, multiscale entropy (MSE), optical imaging, perfusion.
I. INTRODUCTION
T
HE monitoring of microvascular blood flow has become
a major interest in clinical routines and clinical research
(see, e.g., [1]). Laser speckle contrast imaging (LSCI) is a re-
cent noninvasive real-time imaging technique that has gained
increased attention for a full-field imaging of microcirculatory
blood flow [1]–[7]. LSCI exploits the random speckle pattern
generated when tissue is illuminated by a coherent laser light.
A camera is used to obtain a quick snapshot image of the time-
integrated speckle pattern [8], [9]. The speckle size is deter-
mined by the aperture size of the imaging device. With flow, the
speckle pattern is decorrelated (blurred). The level of blurring
is quantified by the speckle contrast value. A low level of blood
Manuscript received February 28, 2012; revised July 2, 2012 and May 30,
2012; accepted July 9, 2012. Date of publication August 1, 2012; date of current
version March 7, 2013. Asterisk indicates corresponding author.
∗
A. Humeau-Heurtier is with the Laboratoire d’Ing´ enierie des Syst` emes
Automatis´ es, LUNAM Universit´ e, Universit´ e d’Angers, 49000 Angers, France
(e-mail: anne.humeau@univ-angers.fr).
G. Mah´ e and P. Abraham are with the Laboratoire de Physiologie
et d’Explorations Vasculaires, LUNAM Universit´ e, Universit´ e d’Angers,
49033 Angers cedex 01, France (e-mail: gumahe@chu-angers.fr; piabraham@
chu-angers.fr).
S. Durand is with the LUNAM Universit´ e, Universit´ e du Maine, 72085 Le
Mans cedex 9, France (e-mail: sylvain.durand@univ-lemans.fr).
Color versions of one or more of the figures in this paper are available online
at http://ieeexplore.ieee.org.
Digital Object Identifier 10.1109/TBME.2012.2208642
Fig. 1. Laser speckle contrast image (perfusion image) of a zone on the
forearm of a healthy subject.
flow leads to a high contrast; a high level of blood flow leads
to a low contrast. The speckle contrast in the speckle pattern is
used to create a perfusion map [1] (see an example in Fig. 1).
The speckle contrast K is defined as the ratio of the standard
deviation to the mean intensity I , as [10]
K =
σ
s
I
(1)
where σ
s
refers to the spatial standard deviation of the speckle
intensity. The speckle contrast depends on the exposure time T
of the camera as [9]
K
2
=
σ
2
s
(T )
I
2
=
1
T I
2
T
0
C
t
(τ )dτ. (2)
C
t
(τ ) is the autocovariance of the intensity fluctuations in a
single speckle
C
t
(τ )= [I (t) −I
t
][I (t + τ ) −I
t
]
t
(3)
where ...
t
means a time-averaged quantity. However, it has
also been shown that the second moment is properly calculated
as [8]
K
2
=
σ
2
s
(T )
I
2
=
1
T
2
I
2
T
0
T
0
C
t
(τ − τ
)dτ dτ
=
2
T I
2
T
0
1 −
τ
T
C
t
(τ )dτ. (4)
Speckle contrast is computed from the mean and standard
deviation of the speckle intensity which are generally deter-
mined from a square region of N
pixels
, i.e., N
1
2
pixels
× N
1
2
pixels
.
For large values of N
pixels
, the speckle contrast is estimated
more accurately (the statistics are better) but the spatial resolu-
tion is worse. For small values of N
pixels
, the large variation in
the speckle contrast estimation reduces sensitivity to vascular
variations. Rapid hardware devices for real-time laser speckle
imaging have been proposed [11]. Cheng et al. [12] developed
a technique where the contrast is calculated based on one pixel
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