veNTIlATIoN - Green Cross Publishing
veNTIlATIoN - Green Cross Publishing
veNTIlATIoN - Green Cross Publishing
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product news<br />
52<br />
Micardis (telmisartan) approved by the<br />
EC to reduce the risk of cardiovascular<br />
morbidity in high risk patients<br />
Micardis is now indicated by the European Commission for<br />
the reduction of CV morbidity in patients with manifest<br />
atherothrombotic CV disease or type 2 diabetes with<br />
documented target organ damage.<br />
• Micardis (telmisartan) is the ONLy treatment in its<br />
class with this indication, demonstrating proven<br />
cardiovascular (CV) protection in patients at high<br />
CV risk<br />
• This new indication is based on a review of clinical<br />
trials, including results from the ONTARGET trial<br />
• Patients at-risk of heart attack and stroke can now<br />
benefit from this new indication.<br />
Ingelheim, Germany, 27 November 2009: Boehringer<br />
Ingelheim announced today that the European<br />
Commission has approved Micardis (telmisartan) for the<br />
reduction of cardiovascular morbidity in patients with:<br />
I. manifest atherothrombotic cardiovascular disease<br />
(history of coronary heart disease, stroke, or<br />
peripheral arterial disease) or,<br />
II. type 2 diabetes mellitus with documented target<br />
organ damage.<br />
Micardis is the first treatment in its class to be approved<br />
for this indication.<br />
Professor Giuseppe Mancia, Professor of Medicine and<br />
Chairman of the Department of Clinical Medicine of the<br />
University of Milan, Bicocca, Italy said, “This new indication<br />
of telmisartan is a significant development for physicians<br />
and their at-risk patients. Prevention of CV events is vital<br />
as these are the primary causes of pathological death<br />
in Europe, due to lack of proper control of treatable risk<br />
factors and disease. The approval of telmisartan offers<br />
patients a well-tolerated treatment option which also<br />
provides CV protection.”<br />
The European Commission approval is based upon a<br />
review of clinical trial results, including the ONTARGET<br />
trial involving 25,620 patients and confirmed Micardis<br />
as the only treatment option in its class with proven<br />
cardiovascular protective effects in patients with high CV<br />
risk. The results also demonstrated that Micardis is better<br />
tolerated than the previous gold standard ramipril and is<br />
associated with higher treatment adherence.<br />
Approximately 10,000 people in Ireland die each year<br />
from cardiovascular disease making it the leading cause of<br />
death in Ireland, accounting for 36% of all deaths.<br />
Micardis is one of the most studied antihypertensives<br />
in clinical trials and is widely used with over five million<br />
patient years since its approval. Its safety profile is similar<br />
to that of placebo.<br />
Cubitan, new evidence demonstrates<br />
faster healing of pressure ulcers in<br />
nourished patients<br />
Nutricia Advanced Medical Nutrition has<br />
announced seminal research on Cubitan,<br />
the only oral nutritional supplement<br />
(ONS) specifically indicated for the dietary<br />
management of wounds, which could<br />
change the way healthcare professionals<br />
treat patients with pressure ulcers. Results<br />
from a randomised controlled trial (CUBE<br />
trial) reveal that Cubitan promotes faster<br />
healing of pressure ulcers in nourished<br />
patients compared to standard wound<br />
care treatment. Cubitan also results in<br />
significantly fewer dressings and less<br />
nursing time spent on wound care which suggests potential<br />
cost savings with its usage.<br />
Professor Jos Schols, the lead investigator from Maastricht<br />
University, The Netherlands, comments that, “It is an<br />
important trial for us as previous studies on ONS in pressure<br />
ulcer healing have focused on malnourished patients, which<br />
meant it was difficult to establish whether the benefits seen<br />
were a result of correcting malnutrition. As the CUBE trial<br />
focused on non-malnourished patients we know that the<br />
benefits seen are a result of Cubitan affecting the wound<br />
itself and not due to correcting deficiencies. Not only are<br />
these results interesting from a clinical point of view, but<br />
the data on wound dressings indicates there may be an<br />
economic benefit of using Cubitan – something we are keen<br />
to investigate further”.<br />
This new research was announced just weeks after further<br />
data from Italy demonstrated more effective wound healing<br />
with Cubitan over a standard enteral nutritional formula.<br />
Cubitan is the only nutritional intervention specially<br />
indicated for the dietary management of wounds and it<br />
should be used in both the prevention and treatment of<br />
wounds. At €2.07 Cubitan is the same price as all other high<br />
protein oral nutritional supplements but it contains the<br />
highest amount of wound specific nutrients; zinc, vitamin C,<br />
vitamin E and arginine.<br />
Clonfolic 0.4mg 28 pack<br />
Clonmel Healthcare wish to inform you that from 1 st February<br />
2010 Clonfolic 0.4mg 28 pack will no longer be available as a<br />
GMS reimbursable Product. Clonfolic 0.4mg 28 pack will still be<br />
available as an OTC product only.<br />
Please rest assured that the 98 pack size of Clonfolic 0.4mg<br />
remains GMS reimbursable.<br />
If you have any queries please contact 01-620 4000.<br />
www.yourmedicines.ie<br />