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An experimental
immunosuppressant drug, everolimus, appears to be significantly
more effective than the current therapy, Imuran, in reducing the
severity and incidence of serious complications in heart transplant
patients, according to a report in the New England Journal of
Medicine.
Researchers
said that everolimus appears to prevent or significantly reduce
a condition called chronic rejection syndrome, in which muscle
cells in the blood vessel walls proliferate, narrowing the vessels
and squeezing the supply of blood to the new heart.
The condition
occurs in at least half of all heart transplant patients, and
often results in death or rejection of the new organ.
In a study
led by Dr. Howard J. Eisen of Temple University School of Medicine,
researchers at 52 centers in the United States, South America,
Canada and Europe gave 634 patients either Imuran (azathioprine),
1.5 milligrams a day of everolimus, or double that dose.
Thirty percent
of those patients on the higher dose of the experimental drug
developed thickened blood vessels compared to 53 percent of those
on Imuran. And the average thickening was much smaller among patients
on everolimus.
After one
year, 53 percent of the patients on Imuran had died, needed a
second new heart, or had episodes of rejection that impaired blood
flow or needed extra treatment. That
compared with only 32 percent on the higher dose of everolimus.
Researchers
also reported that everolimus significantly reduced the incidence
of cytomegalovirus (CMV) infection, a major problem after transplantation.
"The
impressive ability of everolimus to decrease the incidence and
severity of cardiac allograft vasculopathy could offer transplant
patients a powerful tool to improve long-term survival -- one
of the major challenges in transplantation," said Eisen.
Other
Sources: New England Journal of Medicine
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