CardioSource WorldNews | Page 24
CLINICAL
NEWS
American College of Cardiology Extended Learning
The final diagnosis was centrally adjudicated. The
primary endpoint was time from first medical contact to discharge from ED or admission to hospital.
After ambulance arrival, the first troponin was
available in 38 minutes in POC-troponin and 139
minutes in UC patients. In the study group, troponin was > 0.01 ng/ml in 17.4% and > 0.03 ng/ml
in 9.8%. Patients spent a median of 9.0 hours from
ing by ambulance were randomized to usual care
(UC; n = 296) or POC-troponin (n = 305), with a
conventional sensitivity troponin assay approved for
POC use by Health Canada.4 ST-elevation myocardial
infarction (MI) patients or those with noncardiovascular symptoms were excluded. Pre-hospital highsensitivity troponin was analyzed on a POC device
and made available to the paramedic and ED staff.
first medical contact to final disposition, and 165
(27.4%) were admitted to the hospital. Despite the
gain of 101 minutes in time to first troponin, the
primary endpoint was just a little shorter in patients
randomized to POC-troponin (median 8.8 hours [6.2
to 10.8]) compared with UC (median 9.1 hours [6.7
to 11.2]; p = 0.05). That suggests there is still some
optimization to be gained with this approach. Plus, it
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Please see Full Prescribing Information and Medication Guide, including Boxed Warning.
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$AVINGS CARD
RxBIN#
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PCN#
PRX2000
ID#
XXXXXXXXXXXX
GROUP#
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This offer is invalid for cash-paying patients and those whose prescription claims are reimbursed, in
whole or in part, by any governmental program. See back of card for additional details and restrictions.
Please see Full Prescribing Information and Medication Guide, including Boxed Warning.
If you fill your prescription through mail order, please call 1-866-923-1953 for reimbursement information.
*This offer is invalid for cashpaying patients and those
whose prescription claims
are eligible to be reimbursed,
in whole or in part, by any
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SELECTED SAFETY: SIGNIFICANT BLEEDING RISK
Bleeding, including life-threatening and fatal bleeding, is the most commonly reported adverse reaction.
Please see Brief Summary of Prescribing Information, including Boxed Warning regarding
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Effient and the Effient logo are registered trademarks of Eli Lilly and Company.
©Daiichi Sankyo, Inc. and Lilly USA, LLC 03/2016. All Rights Reserved.
PGHCPISI03Oct2011 PP-PG-US-0893.
®
12 months
ACTIVATION EXPIRATION DATE
12/31/2016