Treprostinil
Treatment Appears to Improve Health of Pulmonary Arterial
Hypertension Patients: Presented at CHEST
Patients can handle safely be treated for up to 1 year
with subcutaneous treprostinil (Remodulin) for pulmonary
arterial hypertension (PAH), researchers reported here
at CHEST 2006, the annual meeting of the American College
of Chest Physicians.
"There is limited information on the long-term
use of treprostinil for treatment of pulmonary arterial
hypertension," said Francisco Soto, MD, assistant
professor of pulmonary/critical care medicine, Medical
College of Wisconsin, Milwaukee, Wisconsin.
In his oral presentation on October 24th, Dr. Soto
reviewed the changes in patients' distance on the 6-minute
walk test, finding significant improvement at both 6
months and 1 year of treatment.
At baseline, 32 evaluable patients were able to walk
an average of 226 m, but increased that distance to
277 m after 6 months of treprostinil therapy (P = .001).
After 12 months, the 23 evaluable patients had increased
their distance on the 6-minute walk test from a baseline
of 243 m to 329 m (P = .0009).
In the 1-year follow-up of 31 patients on treprostinil
who, at the start of the study, had an average World
Health Organization Class of 3.12, the average was reduced
to 1.83 (P = .001), Dr. Soto said. After 1 year, among
20 patients evaluated for cardiac index, the difference
from an average of 2.92 to 3.44 reached statistical
significance (P = .02), he said.
Most patients who discontinued use of the drug complained
of pain at the site of injection, but in 41 patients
who began using the drug in 2002 at his institution,
7 patients stopped their treatment -- and 2 of these
patients stopped because of pain at the site of injection.
Three other patients died, 1 was incarcerated and 1
received a transplant.
"Subcutaneous administration of treprostinil is
an excellent alternative for severe pulmonary arterial
hypertension," Dr. Soto concluded. "It has
a safe profile, good tolerance and clinical and hemodynamic
benefits."
Dr. Soto said the retrospective study was initiated
by the investigators, who did not receive any funds
from pharmaceutical or other industry sources.
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