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Date of preparation April 2014 │BRI001081 ACC.14 Annual Scientific Sessions of the American College of Cardiology Washington DC 29-31 March 2014
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Acc2014 10

Nov 12, 2014

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Acc2014 10
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Page 1: Acc2014 10

Date of preparation April 2014 │BRI001081

ACC.14Annual Scientific Sessions of the American College of Cardiology

Washington DC

29-31 March 2014

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Disclaimer

• AstraZeneca abides by the Medicines Australia Code of Conduct (Edition 17) and AstraZeneca Global Policies, and as such will not engage in the promotion of unregistered products or unapproved indications.

• These highlights have been suggested by a group of cardiologists who attended ACC.14, compiled by an external medical writer and sponsored by AstraZeneca. 

• Statements of fact and opinions expressed are those of the speakers individually and, unless expressly stated to the contrary, are not the opinion or position of AstraZeneca. AstraZeneca does not endorse or approve, and assumes no responsibility for, the content, accuracy, or completeness of the information presented.  Presentations are intended for educational purposes only and do not replace independent professional judgement.

• Please refer to the appropriate approved Product Information before prescribing any agents mentioned in these highlights.

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Undetectable hs-cTnT allows safe discharge of chest pain patients

Commentary:

Associate Professor Chris ZeitzQueen Elizabeth Hospital, Adelaide

Late-breaking trial

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39 of 8907 patients with hs-cTnT had MI within 30 days

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• In Australia, chest pain assessment and management consumes significant health care resources.

• Patients clinically assessed as high-risk ACS should be managed as such regardless of troponin level(s).

• Patients clinically assessed as not being high-risk ACS are considered for early discharge unless repeat ECGs and biomarkers change.

• This study shows that the decision to discharge non-high-risk patients can safely be made at a much earlier time point than is currently practised.

• Nevertheless, additional strategies that can identify the very few low-risk patients that will still have adverse events should be considered

Commentary: Associate Professor Chris Zeitz