Recommendation ID
NICE recommends the collection of further outcome data through clinical audit in centres adopting 'early rule-out protocols' with high-sensitivity troponin testing. The data collected through audit should be sufficient to allow analysis of the optimal timing of samples taken after presentation to an emergency department and the optimal high-sensitivity troponin test cut-offs for both ruling out and ruling in NSTEMI.
Any explanatory notes
(if applicable)

Source guidance details

Comes from guidance
Myocardial infarction (acute): Early rule out using high-sensitivity troponin tests (Elecsys Troponin T high-sensitive, ARCHITECT STAT High Sensitive Troponin-I and AccuTnI+3 assays)
Date issued
October 2014

Other details

Is this a recommendation for the use of a technology only in the context of research? No  
Is it a recommendation that suggests collection of data or the establishment of a register?   yes  
Last Reviewed 27/11/2014