The primary objective of this study is to assess the feasibility and impact of implementing
the ESC 0-1 hour high sensitive troponin pathway in clinical practice and with specific
reference to the 0-3 hour pathway currently in use.
The principal outcome measure will be the safety of the 0-1 hour protocol (which is less
established and has limited data on safety when implemented in clinical practice)
- the investigators propose to compare 2 'gold standard' NICE recommended/ESC
guideline-backed pathways; the accelerated 0-1 hour troponin clinical pathway versus the
conventional 0-3-hour pathway, in a randomised multicentre controlled study.
- The primary outcome is to compare percentage safe (with the emphasis and sample
size calculation on safety) discharge by 4 hours from presentation by means of the
0-3 hours versus the 0-1-hour (with the 0 hour in both pathways incorporating
discharge using the limit of detection).
- the investigators propose to use high sensitivity troponin T (hs cTnT) (ROCHE,
Elecsys assay as this is currently in routine clinical use at the site) for this
purpose and also perform comparative analyses using a high sensitivity troponin I
(hs cTnI) assay (ABBOTT, Architect).
- Redundant blood sample will also be used to evaluate point of care testing (POCT), with
additional blood sample taken for POC. These samples will be undertaken as part of
routine clinical care and will not require additional venepuncture (and will only be
analysed if consent is gained for tissue use in research) population. A co-primary
endpoint will be single sample rule-out by point of care troponin (POCT) (with a value
of <4ng/l in those with chest pain onset >3 hours from presentation) as assessed in the
recent APACE study of triage true POC.11 A comparison of this rule-out in terms of
effectiveness (percentage discharge) and safety (sensitivity) will be made with ROCHE
lod (<5ng/l)12 and the optimised rule-out of Abbott architect (HSTNI<5ng/l)13
2.2 Secondary objectives
- The relative performance of the Abbott Architect high sensitivity troponin I (hs TnI) ,
Quidel's TriageTrue and Siemens Attellica troponin I assay will also be assessed in
terms of the primary and secondary endpoints by reference to high sensitivity troponin T
(hs cTnT) with cut-points for Abbott hs-cTn I from the BACC study used for the 0-1-hour
- The performance of the novel machine learning algorithm, the Myocardial Ischemic Injury
Index (MI3, Abbott) will also be assessed retrospectively with regard to safety and
efficacy. This sub study using fully anonymized data will be performed in association
with coinvestigators from Abbott Diagnostics (appendix 1).
- To understand if low levels of Growth Differentiation Factor (GDF-15), could expand safe
discharge beyond the LOD. This will be tested for retrospectively in stored plasma
- To assess if point of care troponin samples at time points at 1 to 3 hours (additional
samples) mirror gold standard high sensitive troponin analysis with respect to diagnosis
of acute or chronic myocardial injury and/or type 1 or type 2 myocardial infarction.
- Hypothesis That an accelerated 0-1-hour troponin protocol, when implemented into clinical
practice as a pragmatic RCT, will effect safe discharge with greater numbers discharged, by 4
hours from presentation, compared to the use of the more conventional 0-3 hour troponin
Means to test hypothesis: A two-arm parallel group, two-centre randomised controlled trial of
0-1-hour high sensitivity troponin T (hs cTnT) compared to a 0-3-hour pathway as rules for
rapid discharge of suspected ACS. (both incorporating single presentation sample limit of
detection (LOD) high sensitive troponin as a rule for discharge, or cut-off selected by
The power of the study is on safety rather than percent discharge achieved by 4 hours as this
is the primary focus for clinicians and health care institutions. (By virtue of the earlier
sampling the 0-1 hour troponin sampling is likely to allow greater discharges by 4 hours and
the sample size for safety easily accommodates this aspect).
4. Outcomes: 4.1 Primary endpoint
- the investigators will compare safe discharge by each strategy (ie the ESC 0-1 hour
pathway versus 0-3 pathway) and the proportion actually discharged by each pathway at 4
hours. The exact definition of safety will be percentage (of cohort randomised to each
pathway) safely discharged by 4 hours of presentation to accident and emergency (Safety will
be judged by type 1 myocardial infarction, cardiovascular death by 4 weeks with sensitivity
>98% - the study will be powered on safety to establish whether 0-1-hour performance is
equivalent to 0-3-hour sampling by means of a non-inferiority analysis- see statistics).
(Type 1 myocardial infarction is due to acute coronary atherothrombotic myocardial injury
with either plaque rupture or erosion and, often, associated thrombosis. A separate analysis
will also be undertaken with inclusion of type 2 MI as well as type 1 MI as an endpoint
4.2 Co-primary endpoint: There will be a comparison of the real time performance of point of
care troponin (POCT) assay to that of a sample sent for analysis in the laboratory (the
current gold standard of central laboratory analysis using HS cTn).The primary interest will
be in presentation sample POC rule-out (triage true (quidel) POC <4ng/l with CP onset >3
hours compared to LOD or optimised rule-out of ROCHE (elecsys) assay, siemens attelica and
Abbott architect. There will be a similar comparison made with siemens VTLI troponin I POC
assay using FDA approved cut-points for MI rule-out
4.3 Secondary Endpoints:
- Type 1 myocardial infarction (adjudicated with the use of Abbott hs cTnI) and
cardiovascular death* at 4 weeks (target for safety negative predictive value (NPV)
>99.5% and sensitivity >98%). (co-primary endpoint). This analysis will be repeated
incorporating both type 1 and 2 MI definition. (prespecified secondary analysis)
- All cause death, type 1 myocardial infarction and urgent or emergency revascularisation.
This analysis will be repeated incorporating both type 1 and 2 MI definition.
(prespecified secondary analysis)
- Proportion with rule-out or rule-in MI in the 0-1 hour and 0-3 hour
- Prediction of MI with myocardial ischemic injury index (MI3) algorithm9
- HEART ≤3 and a modified HEART score for rule-out MI at 30 days15
- Proportion with repeat presentations to accident and emergency within 30 days
- Proportion undergoing coronary angiography and coronary revascularisation in 0-1 versus
0-3 hour pathway
- Performance of point of care troponin samples at time points at 1 to 3 hours (additional
samples to 0 hour) with respect to diagnosis of acute or chronic myocardial injury
and/or type 1 myocardial infarction
- Rule out of MI with GDF-15 (Growth Differentiation Factor 15)
- Cardiovascular deaths include deaths that result from an myocardial infarctions
(MI), sudden cardiac death, death due to heart failure (HF), death due to stroke,
death due to cardiovascular procedures, death due to cardiovascular haemorrhage,
and death due to other cardiovascular causes and deaths that do not have a clear
non- cardiovascular cause.