03.12.2012 Views

veNTIlATIoN - Green Cross Publishing

veNTIlATIoN - Green Cross Publishing

veNTIlATIoN - Green Cross Publishing

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

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 />

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!