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Steven
Warren, Chairman - Technical Director of Medilux Healthcare Limited,
coordinates a series of training programmes here in the UK at both
The Royal Society of Medicine and Berkely Square. Half day, Evening
as well as One or two day training programmes on a variety of topics
are offered on a regular basis throughout the year.
In
this section of the Internet site you can access certificated one
day courses, training seminars and a whole host of related training
resources to support the ongoing development of your clinical practice
in line with future professional standards and developments.
To
contact Mr. Warren please e-mail
s.warren@mediluxhealth.net
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CURRENT
COURSES 2009/2010
Episcan® Ultrasound Tissue Scanning
Certificated ONE & TWO DAY course on applications
of the Episcan® Dermal Ultrasound Scanner. Duration
10 am to 5 pm - One whole day seminar.
LOCATION: Royal Society of Medicine, Wimpole Street, London.
Course
Medical Professionals One Day Training - Ultrasound Scanning
Duration
10am to 5pm - One whole day for certification. LOCATION:
Royal Society of Medicine, Wimpole Street, London.
The
basis of ultrasound versus other imaging modalities.
EPSICAN® system - overview and detailed operation
EPSICAN® imaging in various medical disciplines
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EPISCAN®
AND TISSUE SCANNING
Books
Principles of Wound Care by Mick Miller and Mary
Dyson, Macmillian Magazine Ltd, 1996 ISBN 0-9527697-0-0
Chronic
Wound Care - A problem based learning approach. By Moya J. Morison;
Liza E. Ovington & Kay Wilkie ISBN 0-7234-3235-X
Papers
ULTRASOUND
ABSTRACTS
[1]
Harland, C.C.,, Bamber, J.C., Gusterson, B.A. and Mortimer,
P.S. (1993) High Frequency, high resolution B-scan ultrasound
in the assessment of skin tumours. British Journal of Dermatology,
128, 525-532.
SUMMARY:
Sixteen skin tumours and one BCG vaccination granuloma were examined
by 20-MHz B-scan ultrasound. Images were compared with closely
matched histological sections of excised lesions. The correlation
between histology and ultrasound was excellent for maximum tumour
depth measurements (r = 0.96, P <0.0001), but less good for
maximum width (r = 0.84, P <0.0001), because of the elastic
contraction of tissue at excision. Architectural detail of lesions
on histological sections corresponded well with that on ultrasound
images. There was a good correlation for heterogeneity (collagen
distribution vs. echo pattern (r =0.86, P<0.0001), and between
collagen content and echogenicity of lesions (r = 0.69, P <0.003).
Strong correlations were also obtained for echogenicity vs. spacing
of collagen bundles (r = 0.65, P <0.0005), echogenicity vs.
collagen bundle size (r = 0.58, P <0.02), and echogenicity
vs. cellularity (r = -0.68, P <0.003). Results for dermatolfibroma
were atypical, due to paradoxical low internal echogenicity and
increased echo absorption. B-scanning is a reliable non-invasive
method for assessing tumour dimensions, and has potential for
the study of tumour characteristics for diagnostic purposes.
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[2]
Application of high-frequency ultrasound to the objective assessment
of healing. WOUNDS: Proceedings of the 2nd Conference on Advances
in Wound Management. Macmillan Press, London, pp.26-29.
Whiston, R.J., Young, S.R., Lunch, J.A., Harding, K.G. and Dyson,
M. (1992)
SUMMARY: A collaborative programme of research has been set up
between the Wound Healing Research Unit at the University of Wales
College of Medicine and the Tissue Repair Research Unit at UMDS,
Guy's Hospital, to establish a rapid, sensitive, repeatable and
quantitative non-invasive method of imaging tissue both in and
adjacent to wound sites. In this pilot study patients were scanned
using high frequency diagnostic ultrasound (Supra Scanner, Supra
Medical Corp). B-mode ultrasound images yielded detailed echo
profiles of the scanned tissues. Using computerised image analysis
techniques it is possible to interpret more fully these echo images
and to establish mathematically the difference between intact,
uninjured tissue and the tissue occupying the wound site. This
information was used to measure quantitatively the changes which
occur within the wound tissue with time. It may also be used to
compare the effectiveness of therapeutic measures in improving
the outcome of the healing process. The results of this pilot
study suggest that this method of wound assessment will have considerable
clinical value.
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[3]
Young, S.R., Lynch, J.A., Liepins, P.J. and Dyson, M. (1992)
Ultrasound imaging: a non-invasive method of wound assessment.
Proceedings of the 2nd Conference on Advances in Wound Management.
Macmillan Press, London, pp. 29-31.
SUMMARY: Wound repair rate and quality can be studied using a
number of techniques. However, the techniques which tend to yield
the most informative quantitative data, e.g. histology, tend to
be the most traumatic to the patient, involving the biopsy of
delicate healing sites. There are some non-invasive methods currently
in use, e.g. wound area measurements taken from either tracings
or photographs, and there have also been attempts to correlate
wound colour with the healing status. The value of these methods
is limited since they only yield information about the surface
characteristics of the wound.
Work has begun at the Tissue Repair Research Unit at UMDS to test
the effectiveness of a diagnostic ultrasound machine, the Supra
Scanner (Supra Medical Corp), as a means of obtaining quantitative
data about the nature of tissue at and adjacent to the wound site.
The machine gives very high resolution images (approximately 65
microns) of this tissue up to a depth of 37mm. The images can
be obtained in both A and B scan modes which together provide
detailed information about the echogenicity of the scanned tissue.
Examination of the echo profiles from a pilot study using computerised
image analysis indicates that this method of wound assessment
is sensitive, reproducible and quantitative, and should prove
to be useful in evaluating the effectiveness of various therapeutic
modalities.
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[4]
International Journal of Aesthetic and Restorative Surgery
Volume 4, Number 2, 1996, Pages 1-5
High Frequency Diagnostic Ultrasound: A non-invasive, Quantitative
Aid for Testing the Efficacy of Moisturizers
STEVE R. YOUNG, PhD, A. Erian, MD and M.Dyson
ABSTRACT: The effect of moisturizing the skin was examined ultrasonically
in 60 volunteers with a mean age of 53 years. The volunteers used
either a twice daily application of a moisturizer or a twice daily
massage to the side of their face in the region superficial to
the zygomatic arch. The skin was assessed ultrasonically by using
a 20 MHz B scan device. Assessments were conducted pre-treatment
and on days 1, 3, 7, 14 and 21 after the start of treatment. In
addition to epidermal and dermal thickness measurements, changes
in dermal echogenicity were assessed by using fractal analysis
on the ultrasound scans. The results showed that the mean epidermal
and dermal thickness did not change in response to massage only.
However, the moisturized skin showed a mean increase in epidermal
thickness of 26%. The mean dermal thickness did not change. The
fractal nature of the ultrasound scans did not change during the
test period, indicating that the dermal component of the skin
remained stable and had not changed structurally. The benefits
of using high frequency ultrasound to assess the efficacy of moisturizing
products has been demonstrated in this study. By using this technique
it was possible to noninvasively assess the skin before, during,
and after treatment and to target specifically where in the skin
the treatments have had their effect.
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[5]
British Journal of Dermatology 1998: 138: 815-820
Dermal oedema assessed by high frequency ultrasound in venous
leg ulcers
H.Hu, T.T.Phan, G.w.Cherry and T.J. Ryan
SUMMARY: Oedema is considered a key pathogenic factor in the development
of venous leg ulcers. The purpose of this study was to determine
the localization of oedema in legs with ulcers. Twelve patients
with 13 venous leg ulcers (one bilateral), with a duration of
7-18 months, were examined by high-frequency B-mode ultrasound
scanner. This was performed at three sites in the leg (low, middle
and upper sites of the lower leg). In the same group of patients,
the legs without ulcers were used as controls. The echogenicity
and the thickness of the whole dermis were quantified by digital
image analysis: the echogenicities of the upper (papillary) and
lower portions of the dermis were measured. In the upper site
no significant difference was found between the legs with ulcers
and controls. In the middle and low sites of legs with ulcers,
the dermal echogenicities were 34% and 64% (P<0.01) less than
those in controls, and the dermal thicknesses were 0.4 mm and
0.8 mm (P<0.01) thicker than those in controls, respectively.
This indicated intradermal oedema existing in the lower part (gaiter
area) of the legs with ulcers. The ratios of low echogenic pixels
in the upper and lower portions of the dermis, in the middle and
low sites of legs with ulcers, were 0.5 and 0.9 (P <0.05 and
P < 0.1) respectively higher than those in controls, suggesting
the papillary dermis as a preferential site of oedema formation.
The present study demonstrates that in the low sites of legs with
ulcers, a marked increase in oedema was seen in the papillary
dermis. This may add to the understanding of the origin of leg
ulcer in the gaiter area of the leg.
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(c)
Medilux Healthcare Limited. 2003 - 2009. All rights reserved
VAT No 887 9818 33 Comp Reg 5925249 Webmaster
- Steven Warren s.warren@mediluxhealth.net.
Medilux
Healthcare Limited is a specialised marketing company. We promote devices
on the basis of the Manufacturers' representations as to quality and efficacy
and where possible we provide additional information as to the conditions
which may benefit from their use but we do not guarantee that they will
be suitable or effective for all purchasers. We do not examine or diagnose
patients or recommend treatments and where we promote medical services
this is on an information-only basis. Patients contract directly with
these providers and all clinical decisions are made by them alone.
.
All rights reserved. Any
unauthorised copying, duplication, or distribution in whole or in part,
by any means, including electronic copying, is a violation of this copyright.
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