Lifeline Scientific, Inc Update on Retrospective Kidney Transplant Study
24 February 2014 - 6:01PM
RNS Non-Regulatory
TIDMLSI
Lifeline Scientific, Inc
24 February 2014
24 February 2014
Lifeline Scientific, Inc.
("Lifeline" or the "Company")
Retrospective Study of all Kidney Transplants in the US Between
2000 and 2011 supports Lifeline Scientific
Lifeline Scientific (AIM: LSI: LSIC:), the transplantation
technology company that manufactures the LifePort Kidney
Transporter (LifePort), welcomes the publication of the 15 January
edition of Transplantation (1) . In the study, 94,709 renal
transplants in the USA between 2000 and 2011 were analysed with
respect to delayed graft function ('DGF'), after pulsatile
perfusion (PP), and also DGF after cold static storage at varying
cold ischemic times ('CIT') with different donor groups. DGF is
known to adversely impact near and long term graft performance and
survival rates. (2.3.4)
When stratified by donor type and CIT, the adjusted odds of DGF
were lower for all cold ischemic times in standard criteria donors
('SCD') transplants. The adjusted odds of DGF were lower with
perfusion when CIT was greater than 6 hours in expanded criteria
donors ('ECD') transplants. When CIT was between 6 and 24 hours in
donors after circulatory death ('DCD') transplants, CIT was
independently associated with a greater risk of DGF irrespective of
storage method, but this effect was substantially modified by using
machine perfusion.
The conclusion of the paper was that perfusion is associated
with a reduced risk of DGF irrespective of donor type and CIT.
Although PP modifies the impact of CIT on the risk of DGF, it does
not eliminate its association with DGF, suggesting the optimal
strategy to reduce DGF is to minimize CIT and utilize PP in all
deceased donor transplants.
David Kravitz, CEO of Lifeline commented: "This retrospective
study of close to 95,000 patients adds to the already significant
body of evidence in the medical literature that machine perfusion
leads to improved patient outcomes by reducing delayed graft
function across all types of deceased donor kidneys. This study
also supports findings published in the New England Journal of
Medicine in 2009 from the landmark European Machine Perfusion Trial
(MPT), the first ever prospective, randomized, statistically
powered, multi-centre study that compared machine perfusion to cold
static storage. Both studies clearly demonstrate the utility of
active preservation. As clinician awareness of this evidence grows,
machine perfusion is gaining momentum as a clinical standard of
care. This was our dream when developing LifePort, which has now
become the market leading machine preservation system worldwide.
Clinicians have found that organ viability is better maintained
with LifePort, thereby helping to improve post transplant outcomes
and make more organs available to satisfy the increasing demand for
transplantable kidneys. "
References:
1. Gill J et al, Transplantation. 2014 97(1)
2. Jochmans I et al. Ann Surg 2010; 252(5): 756-764.
3. Daly PJA et al. BJU Int 2005; 96(4): 498-501.
4. Koning OHJ et al. Transplantation 1997; 63(11):
1620-1628.
For further information:
Lifeline Scientific, Inc. www.lifeline-scientific.com
David Kravitz, CEO Tel: +1 847 294 0300
Lisa Kieres, CFO Tel: +1 847 294 0300
Panmure Gordon (UK) Limited Tel: +44 (0)20 7886 2500
Freddy Crossley/Fred Walsh
(Corporate Finance)
Adam Pollock (Corporate
Broking)
Walbrook Tel: +44 (0)20 7933 8780
or lifeline@walbrookpr.com
Paul McManus Mob: +44 (0)7980 541 893
Mike Wort Mob: +44 (0)7900 608 002
About Lifeline Scientific Inc.
Lifeline Scientific, Inc. is a Chicago-based global medical
technology company with regional offices in Brussels and Sao Paulo.
The Company's focus is the development of innovative products and
services that improve transplant outcomes and lower the overall
costs of transplantation. Its lead product is the market-leading
and clinically validated LifePort Kidney Transporter. Devices for
preservation of the liver, pancreas, heart and lung are in late
stage pre-clinical development. Also visit:
www.organ-recovery.com.
About LifePort Kidney Transporter
Created with the challenges of organ recovery and transport in
mind, LifePort Kidney Transporter is a proprietary medical device
designed to provide improved kidney preservation, evaluation and
transport prior to transplantation. LifePort is the world's leading
machine preservation device for kidneys. Employed by surgeons in
over 160 transplant programmes in 27 countries worldwide, LifePorts
have successfully preserved over 47,000 kidneys indicated for
clinical transplant. The product provides a sealed, sterile,
protected environment where a solution is gently pumped through the
kidney at cold temperatures to minimise damage while the organ is
outside the body. LifePort is lightweight and portable, allowing
organs to be perfused from the time of donor recovery until
recipient transplantation. It is designed to travel unaccompanied
by land or air, safely transporting the kidneys across town or
between countries. While the kidney is being perfused, LifePort
records data on temperature, flow rate, vascular resistance and
pressure every 10 seconds, providing surgeons with additional data
prior to transplant. LifePort is the only system with clinical
outcomes data produced from an independent, prospective,
randomised, statistically powered, multi-centre clinical trial.
Study results have been widely published in scientific journals,
including the New England Journal of Medicine. Data indicates that
patients receiving LifePort preserved kidneys experienced
significant reduction in the incidence and duration of delayed
graft function and increased graft survival at 1-year and 3-years
post-transplant. LifePort has also been recognised for design and
engineering distinctions. It has received prominent awards for
design excellence from the medical device industry, has been
selected for exhibition at the Smithsonian Cooper-Hewitt National
Design Museum and is part of the permanent Collection of The Museum
of Modern Art (MoMA) in New York City.
Lifeline Scientific, Inc. Stock
As a US Company on the Aim exchange, Lifeline Scientific, Inc.
(AIM: LSI, LSIC) trades under two lines of stock. While affiliates
of the Company are required to hold restricted (RegS) shares, all
others may hold restricted or unrestricted. Unrestricted shares may
be electronically traded through the CREST system. Both lines of
stock have identical rights, preferences and privileges.
Non-affiliates may transfer restricted shares to the unrestricted
line after purchase through the Company's registrar. Total shares
outstanding for the Company at this time are 19,446,959.
This information is provided by RNS
The company news service from the London Stock Exchange
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