Development and evaluation of a light emitting diode endoscopic light
source
Neil T. Clancy*
1,2
, Rui Li
1,2
, Kevin Rogers
3,4
, Paul Driscoll
4
, Peter Excel
5
, Ron Yandle
4
, George
Hanna
2
, Nigel Copner
3,4
, Daniel S. Elson
1,2
1
Hamlyn Centre for Robotic Surgery, Imperial College London, UK;
2
Department of Surgery and Cancer, Imperial College London, UK;
3
Faculty of Advanced Technology, University of Glamorgan, UK;
4
Cymtec Ltd. Cardiff, UK;
5
Glyndwr University, Wrexham, UK
ABSTRACT
Light-emitting diode (LED) based endoscopic illumination devices have been shown to have several benefits over arc-
lamp systems. LEDs are energy-efficient, small, durable, and inexpensive, however their use in endoscopy has been
limited by the difficulty in efficiently coupling enough light into the endoscopic light cable. We have demonstrated a
highly homogenised lightpipe LED light source that combines the light from four Luminus LEDs emitting in the red,
green, blue and violet using innovative dichroics that maximise light throughput. The light source spectrally combines
light from highly divergent incoherent sources that have a Lambertian intensity profile to provide illumination matched
to the acceptance numerical aperture of a liquid light guide or fibre bundle. The LED light source was coupled to a
standard laparoscope and performance parameters (power, luminance, colour temperature) compared to a xenon lamp.
Although the total illuminance from the endoscope was lower, adjustment of the LEDs’ relative intensities enabled
contrast enhancement in biological tissue imaging. The LED light engine was also evaluated in a minimally invasive
surgery (MIS) box trainer and in vivo during a porcine MIS procedure where it was used to generate ‘narrowband’
images. Future work using the violet LED could enable photodynamic diagnosis of bladder cancer.
Keywords: Light-emitting diode (LED), laparoscopy, minimally-invasive surgery
1. INTRODUCTION
Minimally-invasive surgery (MIS) has enabled diagnosis and intervention for patients in a manner that minimizes trauma
and reduces recovery time. During these procedures the surgeon does not have a direct line-of-sight to the area under
investigation and is therefore dependent on the quality of the imaging system to relay information on the health of the
tissue as well as its general appearance. Due to the high attenuation of visible light in biological tissue and the relatively
poor light coupling ability of endoscopes, the quality of the light delivery system is of utmost importance.
The current standard light source for most MIS procedures, particularly laparoscopy, is the xenon arc lamp, which
emits over a broad spectrum across the visible range, providing a colour close to daylight. These lamps are high power
but highly inefficient, requiring approximately 300 W of electrical power to deliver just over 1 W of optical power. They
are also expensive, requiring an initial payment of about $8000 and $1500 for replacement bulbs, which have a relatively
short lifetime.
Alternative sources such as laser-phosphor fibres and supercontinuum lasers have been explored but these have
tended to focus on niche areas that require specialized lighting such as narrow lumen work and the single access surgery
regime
1
where high optical power per cross-sectional area is required. A more significant limitation is perhaps the fact
that these devices are currently limited to research models. Commercial devices have focused on providing the surgeon
with more information by enhancing contrast in the tissue. This has been achieved using fluorescence to aid visualization
of tumours
2
, and narrowband imaging (NBI) to increase the visibility of the vasculature
3
. However, separate systems are
required for each of these approaches, leading to increased expenditure. Previous work has indicated that tip-mounted
*n.clancy@imperial.ac.uk; imperial.ac.uk/roboticsurgery
Advanced Biomedical and Clinical Diagnostic Systems X, edited by Tuan Vo-Dinh,
Anita Mahadevan-Jansen, Warren S. Grundfest, Proc. of SPIE Vol. 8214, 82140R · © 2012 SPIE
CCC code: 1605-7422/12/$18 · doi: 10.1117/12.909331
Proc. of SPIE Vol. 8214 82140R-1
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