Engineering, 2012, 5, 53-56
doi:10.4236/eng.2012.410B014 Published Online October 2012 (http://www.SciRP.org/journal/eng)
Copyright © 2012 SciRes. ENG
Infra-red Thermal Imaging of the Inner Canthus:
Correlates with the Temperature of the Injured Human B rain
Char maine C hi lds1, Mya Myint Zu 1, Aung Phyo Wai1, Yeo Tseng Tsai1, Shiqian Wu2, Wang Li3
1ALCNS and Department of Surgery, National University of Singapore (NUS), Nati onal Uni versity Hospital (NUH), Sin gapore
2Signal Processing Depar tment, Inst itute for Infocomm Research, Fusionopolis Way, #21 -01 C onnexis, Singapore
3National Metrology Centre (NMC), A*Star, Singapore
Email: nurcc@nus.edu.sg
Received 2012
ABSTRACT
Introduction: Infra-red (IR) thermometr y is a safe and valid meth od to determine in tern al and surface temperat ure in hu man subject s.
Under conditions of brain damage (head injury or stroke) knowledge of changes in the temperature of intracranial tissue is justified
because of the vulnerability of neurons to accelerated damage at temperatures at the upper end of the febrile range. Aim: To deter-
mine the temperatu r e at the inner cant hus (I C ) of the eye as a potential surrogate for brain temperature. Methods: Invasive monitoring
of deep brai n stru ctures, lat eral ventri cle and deep white matter. IR temperat ur e read in gs obtain ed at right and left IC. Results: Strong
correlat io ns were eviden t b etween R and L IC and brai n. Close, as well as poor , agreemen t b etween si tes was sho wn in so me patients
and at some times. For right hemispheric lesions four had a better correlation between TbrV and TRIC when compared to TLIC.
When the correlation between TbrV and TLIC was better compared to TbrV and TRIC, four had a predominant right hemispheric
lesion. Conclusions: Improved techniques for IR thermal imaging accuracy at the bedside has the potential to improve temperature
measure ment agreement . The p red omin ant lesion side may have a b eari ng on maximum ips ilat eral IC temperatu re F ur th er studies are
ongoing in this pilot study population.
Keywords: Brain Temperature; Infra-red Thermometry; Inner Canthus; Th er mal Imaging; Eye
1. Introduction
Temperature changes play a major role in the survival of all
animal speci es [1]. In mammals, body temperature is main-
tained within a relatively ‘tight’ range with normal values of the
order of 36.7oC. Nevertheless, d ifferen ces in t he te mperature o f
the viscera are reported, typically the variation is small only
(<0.5oC) [2]. Whilst a rise in deep body (core) temperature due
to fever is co mmon a fter trauma and critical illn ess it is usually
regarded as an adap tive resp onse with p oten tial survival b enefit
[3] . By contrast, if damage to brain occurs due to ischaemia
(stroke) or trauma (mild to moderate traumatic brain injury,
TBI) the p revailin g view is that even small increases i n temper-
ature will accelerate secon dary damage of vul nerabl e ischaemic
neurons; the consequence being an increased risk of death and
worsened neurological outcome [4].
Knowing when a rise in brain temperature has occurred is
clinically important. It is generally assumed that body tempera-
ture is a reliable ‘surrogate’ for brain temperature but proxy
measures for brain temperature are often unreliable [5]. Direct
monitoring is safe and recommended during neurocritical care
[6] . However, it is customary to revert to body measurement
sites (rectum, tympanum, oral, tympanic) once the patient
leaves the intensive care unit (ICU). Studies from our group
have shown the potential of infra-red (IR) thermometry as a
proxy for brain temperature measurement. In the normal to
febrile temperature range, IR temporal artery measurement is
closer to brain temperature than is IR tympanic membrane
temperature with average differences of 0.3oC only [7]. IR sur-
face temperature measurements at sites other then ear or fore-
head t hus have pot ential as a surrogate for brain temperature.
The aim of the current study was to determine if IR thermal
imaging of the inner canthus of the eye provides a clinically
useful approach to brain temperature estimation in patients with
severe intracereb ral trau ma.
2. Materials and Methods
The stud y was appr oved by th e local resear ch et hi cs committee.
Written informed consent was obtained from the patient’s
spouse or relative before measu rements were taken.
Patients: Adults aged >21 years with severe traumatic brain
injury (TBI) admitted for neurocritical care were eligible for
inclusion in the study. All patients were intubated and sedated
and mechan icall y ventilat ed and were admitted to the I CU after
neurosurgery or as direct admissions to ICU for neuromonitor-
ing. The patients were treated in accordance with local Neuro-
critical care guidelines and studied for a maximum of 5 days
from arrival to ICU.
2.1. Monitoring
Invasive brain monitoring: Temperature monitoring was ob-
tained at two brain sites; within brain tissue (Tbrt) and within
the lateral ventricle (Tbr V). Thermal images of facial skin tem-
perature were also o btained.
2.2. Materials
Tbrt was measured using a multiparameter (temperature, pres-
C. CHILDS ET AL.
Copyright © 2012 SciRes. ENG
54
sure, oxygen sensor) tissue probe (Neurovent-PTO; Raumedic,
Munchberg, Germany). The sensor tip was positioned approx-
imately 3-4 cm in deep white matter of the frontal lobe. TbrV
was measured using a second integrated probe (pressure and
temperature sensor; Neurovent-Temp-IFD-S -C; Raumedic,
Munchberg, Germany) with sensor tip positioned within the
lateral ven tricle.
Non-cont act IR thermal imagin g: Ther mal images of the face
were obtained using a FLIR Systems Thermographic Camera
(Model TMT365). The FLIR camera was calibrated to fever
screening standards of the National Metrology Centre (NMC),
A*STAR, Singapore.
2.3. Methods
Camera emiss ivity was set to 0.98. At each imaging session, the
IR camera was po sit io ned and the focus adjusted to ensure clar-
ity and accuracy of the image an d temperature values. The tar-
get region of interest ( ROI) was temperatu re of right inn er can-
thus (TRIC) and left inner canthus (TLIC). A series of three con-
secutive IR images were captu red at each measure ment in terval
with patients lying supine. All IR images were taken at the
same ‘tilt angle’ from a standing position at the bedside. To
obviat e the effect o f patient to camera distan ce on the t empera-
ture reading, manual adjustment was made to approximate 1
meter. A FLIR Quick Report 1.2 was used to document tem-
peratu re (oC) readings fro m the images . The maximu m temper-
ature reading of each ROI (Figure 1) was used in data analysis.
2.4. Data Analysis
Data analysis consists of three parts: 1) probability of distribu-
tion of FLIR temperature measurements. As random error oc-
curs in measurement, the random measurements follow a spe-
cific distribution; generally as a normal distribution; 2) correla-
tion analysis, i.e., to determine whether the readings of
TRIC/TLIC fro m FLIR images are correlated with br ain tempera-
ture (Tbrt, and TbrV); 3) curve fitting between TRIC/TLIC and
Tbrt/Tbr V in order to predict the brain temperature by the mea-
surement TRI C/TLIC.
L
Figur e 1. R OI of Inner c anthus of patient with severe TBI. L =left
side face. Grey colour indicates region of highest temperature val-
ues.
3. Results
Twelve patients (8 male) aged 21-78 (median 50) years with
severe TBI were studi ed 7-60 (median 16) hours after injury in
below thermoneutral ambient conditions, typically of approx
18oC . Clinical care and nursing procedures in the ICU pre-
vented o btaini ng a consis tent numbers o f FLIR i mages for each
patient. FLIR images were taken on 8-55 (median 30) occasions.
Every effort was made to obtain ‘simultaneous’ readings of
TbrV and TRIC/TLIC and Tbrt and TRIC/TLIC. No significant
effect of ti me was ob served for FLIR te mperatu re r eadi ngs with
respect to brain temperature. IC temperatures followed a nor-
mal distribution (Figure 2).
In 6 of 12 patients the correlation between TRIC and TLIC was
better with respect to ventricular temperature (TbrV) and in 5
patients correlations for TRIC and TLIC were better for brain
tissue temperature (Tbrt). In one patient only, the correlations
between Tbr V and TRIC and TbrV and TLIC were comparable.
The predominant lesion side may have a bearing on maxi-
mum ipsilateral IC temperature. For right hemispheric lesions
(n=5) four had a better co rrelation bet ween TbrV and TRIC when
compared to TLIC. Wh en the correlation between Tbr V and TLIC
was better compared to Tbr V with TRIC four of five had a pre-
dominant right hemispheric lesion. Patients had better out-
comes when higher IC values were ‘right sided’ and worse
out comes when IC valu es were ‘l eft sided’.
Whilst the correlations between TbrV and RIC and TbrV and
LIC were strong (for example in patient 5; 0.8208 and 0.7638
respectively) neither IC temperature provided a consistently
reliable measure for brain temperature. Figure 3 shows the
agreement between brain and R and L IC temperatures with
small and large di fferences between the sites .
For patient 3, correlations between TbrV and RIC and TbrV
and LIC were strongly positive (0.9585 and 0.9542 respective-
ly). Differences between the sites were <1.0oC for more than
half of the meas urement interval s (Figure 4).
4. Discussion
The medial canthus has a key functional role in providing a
32 33 34 35 36 37 38
0. 005
0. 01
0. 05
0. 1
0. 25
0. 5
0. 75
0. 9
0. 95
0. 99
0. 995
Data
P robabil i t y
P robabil i ty plot for Normal di stri buti on
RIC
Figure 2. Probability plot shows Normal Distribution of TRIC (oC).
C. CHILDS ET AL.
Copyright © 2012 SciRes. E NG
55
Figure 3. Bland-Altman plot showing temperature differences be-
tween ventricular brain temperature (TbrV) and comparators for
patient 5. (Comparator: TRIC = Right Inner Canthus Temperature
(+); TLIC= Left Inner Canthus Temperature (o).)
Figure 4. Bland-Altman plot showing temperature differences be-
tween ventricular brain temperature (TbrV) and comparators for
patient 3. (Co mparator: TRIC = Right Inner Canthus Temperature
(+); TLIC= Left Inner Canthus Temperature (o).)
fix ed -point fulcrum for the function of the eyelid. Anatomically,
the IC has been exploited during mass fever scanning (pan-
demic infections such as SARS) due to the proximity of the
arterial supply at the skin surface. Within this small IC region
lie branches of ophthalmic, dorsal nasal, supratrochlear and
superior palpebral arteries and angular artery [8]. As the angu-
lar artery (giving off three branches) lies directly beneath the
skin of the inner canthus and originates from the ophthalmic
artery (supratrochlear branch), the dense supply of vessels and
thus blood perfusion makes this site a potentially useful spot for
estimation of core temperature [9]. In this study we have also
obtained pilot data to assess the potential of the IC as a bio-
marker for anatomic al lesio n side and TBI outcome.
In previous studies, differences between body (tympanic) and
IC temperature deviated significantly, both sites were criticized
for their poor reliability in estimation of core temperature. In-
troducing the oesophageal site to improve the reliability of the
‘core’ measurement did not reduce the variability of the mea-
surement s bet ween sit es. In th e cu rren t stud y, brai n t emperatu re
obviated any possibility that the ‘gold standard’ was influenced
by ambient conditions, the thermistor tip being deep within
white matter or ventricle. Whilst the IC consistently reflected
the temporal changes in brain temperature during normothermia
and during fever, suggesting a potential for the technique in
clinical practice, the differences between brain and IC temper-
ature were inconsistent; at times within 0.4o or 0.5oC of brain
but at other times too large (e.g.1.0oC to 1.5oC) to be clini-
cally useful. Further studies are required to determine whether
improvements in measurement technique would yield a better
accurac y of the IR measurements to esti mate b r ain temperature.
By undertaking the current pilot study we have discovered a
novel potential for IR thermal imaging; a ‘putative’ role of the
highest recorded IC temperature as a biomarker to predict ‘si-
dedness’ of the predominant TBI lesion. Here differences in
temperature might be due to inflammation and higher arterial
perfusion associated with the region of the lesion. Whilst this
finding remains to be investigated further, it may be of potential
clinical value in patients where CT imaging is not available.
Studi es are now ongoing in this area.
5. Acknowledgements
Our thanks go to our neurosurgical colleagues and the doctors
and nurses of the intensive care unit, NUH for their continued
support of our research. This work was supported via a grant
support (CC) from the National University of Singapore.
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