Key result
A clinical pathway using a single low hs-cTnI level for early discharge in potential ACS patients showed no significant difference in 12-month all-cause death (0.62% vs 0.97%, p=0.35) or MI.
Why the study?
A single hs-cTnI early discharge pathway reduced ED length of stay without increasing 30-day adverse events, but 1-year outcomes remained to be reported.
Does an early discharge pathway based on a single low hs-cTnI level safely increase direct ED discharges without increasing death or MI at 1 year in patients with potential ACS?
Cohort (n=2,255)
Does an early discharge pathway based on a single low hs-cTnI level safely increase direct ED discharges without increasing death or MI at 1 year in patients with potential ACS?
Absolute Event Rate: 0.62% vs 0.97%
p-value: p=0.35
An early discharge pathway based on a single low hs-cTnI level safely increases direct ED discharges and reduces length of stay without increasing 1-year mortality or MI in potential ACS patients.
Supports 1-year safety of hs-cTnI early-discharge pathway; extends 30-day data but leaves open need for randomized confirmation.
BACKGROUND: A pathway incorporating an option for early discharge based on a single low level of high-sensitivity cardiac troponin I (hs-cTnI) at presentation increases the proportion of patients presenting with a potential acute coronary syndrome (ACS) that can be discharged directly from the emergency department (ED), reducing length of stay without any increase in adverse events at 30 days. Here, we report the 1-year outcomes of patients managed using this pathway. METHODS: We recruited two cohorts of patients with a potential ACS, without high-risk features. The 'standard' cohort was managed according to the Australian national guidelines and the Single Troponin Accelerated Triage ('STAT') cohort was managed using the study pathway. 12-month outcomes were assessed using linked administrative data. RESULTS: Between May 2018 and October 2019, we recruited 2255 patients (1131 standard vs 1124 STAT), mean age 55 years, 53% male. 709 (63%) patients managed using the STAT pathway were discharged directly from ED, compared with 403 (38%) patients using the standard pathway, with a 47 min reduction in median hospital length of stay. At 12 months, there were no significant differences in unadjusted all-cause death (STAT 0.62% vs standard 0.97%, p=0.35) or myocardial infarction (MI) (STAT 0.62% vs standard 1.24%, p=0.13). CONCLUSIONS: A clinical pathway which incorporates early discharge based on a single low serum hs-cTnI is associated with an increased proportion of patients with a potential ACS discharged directly from the ED and reduced length of stay, without an increase in death or MI at 1 year.
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Barnes et al. (2025) conducted a cohort in potential acute coronary syndromes (n=2,255). Single Troponin Accelerated Triage (STAT) pathway vs. Standard pathway (Australian national guidelines) was evaluated on all-cause death (p=0.35). A clinical pathway using a single low hs-cTnI level for early discharge in potential ACS patients showed no significant difference in 12-month all-cause death (0.62% vs 0.97%, p=0.35) or MI.
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