Major Funding Boost for Top Clinical Research Institute
For Immediate Release Thursday June 14th
New
Zealand’s leading clnical research organisation has been
rewarded with a major funding extension, in recognition of
its on-going excellence and achievements in the field of
medical research.
The Medical Research Institute of New Zealand (MRINZ) has been granted more than $1.7 million in funding for the next three years, as result of a recent Health Research Council of New Zealand (HRC) review of its Independent Research Organisations. It follows on from the $6.8 million, four year HRC funding grant awarded to MRINZ back in 2014.
Professor Richard Beasley, Director of the MRINZ, welcomes the HRC’s Independent Research Organisation (IRO) funding decision. He says it recognizes and rewards the unique capability and national importance of their Wellington-based Institute.
“This funding has been crucial to the development of the MRINZ as New Zealand’s leading clinical research organization with the capability to undertake pivotal multinational, randomized, controlled trials across a range of fields of medicine”.
Professor Beasley says the on-going funding commitment provides the certainty and stability necessary to increase both the depth and breadth of the MRINZ’s research programmes, and will allow for an increase in the number of specialist staff and associated infrastructure support.
“Progress in some
areas of MRINZ research has already changed clinical
practice, improving outcomes for patients in New Zealand and
internationally” he says. “This funding extension will
enable us to further expand existing research programmes and
develop new ones based on national and international
networks”.
The HRC review was part of a seven year
funding agreement with four New Zealand IRO’s, all of
which operate outside of the Crown Research Institute and
university sector. A total of $27 million was granted from
2014-2017; $17 million has now been allocated for the second
(2018-2020) funding period.
Top MRINZ Research Highlights for each of the 11 main programmes for 2014-17, the period of the HRC IRO funding include:
1. Asthma:
The Lancet commission on asthma, a major
treatise which challenges the current management of asthma,
and proposes a paradigm shift in the thinking about asthma
[Pavord et al, Lancet 2017]. Together with the updated NZ
Asthma Guidelines [Beasley et al, NZMJ 2016], it has the
potential to change practice in
NZ.
2. Cardiothoracic Surgery:
The RCT showing that in cardiac surgery a more restrictive
transfusion strategy is non-inferior to a more liberal
strategy [Mazer et al. NEJM 2017]. When the results of this
study are translated into practice, it will result in a
significant decrease in blood transfusions in these
patients.
3. Complementary
Medicine: The RCT which showed that medical
grade Kanuka honey is effective in the treatment of the skin
condition rosacea [Braithwaite et al, BMJOpen 2015]. This
has led to a NZ biotechnology company (HoneyLab) marketing
kanuka honey for rosacea in NZ and
internationally.
4. COPD: The RCT which
showed that a high flow nasal cannulae device has a
favourable physiological safety profile when administered to
patients with COPD [McKinstry et al, Respirology 2017].
This has provided important evidence to support the use of
the Fisher & Paykel Healthcare high flow nasal therapy
device globally.
5. Emerging
Therapeutics: The demonstration that
angiotensin II is effective in the treatment of vasodilatory
shock in intensive care [Khanna et al, NEJM 2017]. This
therapeutic agent is the first new pharmacological agent
shown to be effective in the treatment of shock in the last
50 years, and should be available for use in NZ within the
next few years.
6. Infectious
Disease: The largest trial of septic patients
ever undertaken will have a major impact on clinical
practice [Venkatesh et al. NEJM 2018]. The key message is
that steroids for septic shock do not alter day 90 mortality
but speed up resolution of shock, reduce ICU length of stay,
decrease time until weaning of life support, and reduce
transfusion
requirements.
7. Influenza:
The randomised placebo controlled trial which
showed that paracetamol has no beneficial effect in the
treatment of influenza infection [Jefferies et al,
Respirology 2016]. Together with the related study in
critically ill patients [Young et al, NEJM 2015], this study
has challenged current practice of routinely administering
paracetamol to patients with
fever.
8. Intensive Care: The
demonstration that saline has a similar safety profile as
the more expensive buffered IV fluid in critically ill
patients in ICU [Young et al, JAMA 2016]. These findings
provide reassurance about the safety of IV saline which is
administered to around 1 million patients in the world every
day.
9. Oxygen: The TSANZ adult
oxygen guidelines which provided practical evidence based
recommendation for the use of acute oxygen therapy [Beasley
et al, Respirology 2016]. Many recommendations made in
these guidelines are based on research undertaken at the
MRINZ.
10. Pleural disease: The
demonstration that insertion of an indwelling pleural
catheter has a favourable efficacy/safety profile compared
with conventional pleurodesis for malignant pleural
effusions [Thomas et al, JAMA 2017]. These findings have
led to a change in practice with indwelling pleural catheter
insertion now being the preferred method to treat pleural
effusions secondary to lung cancer.
11. Venous
thromboembolism: Identifying the VTE risk
associated with prolonged seated immobility at work
[Braithwaite et al, JRSM Open 2016]. This has led to the
assessment of different novel devices to reduce the risk of
VTE in situations in which prolonged seated immobility
cannot be
avoided.
ENDS