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. 2017 May 12;34(9):586–592. doi: 10.1136/emermed-2016-206148

Table 3.

Incidence of the primary and secondary efficacy outcomes stratified by trial group

Outcome Total
n=131
Intervention
n=66
Control
n=65
OR (95% CI),p value
Early discharge within 4 hour without prevalent AMI or incident
MACE at 30 days, n (% (95% CI))
22 (17%) 17 (26%) 5 (8%) Unadjusted
Adjusted*
4.16 (1.43 to 12.09), p0.009
5.45 (1.73 to 17.11), p=0.004
Prevalent AMI, n (%) 9 (7) 3 (5) 6 (9) 0.47 (0.11 to 1.96), p=0.30
Incident MACE at 30 days†, n (%) 6 (5) 3 (5) 3 (5) 0.98 (0.19 to 5.06), p=0.985
Incident MACE at 90 days†, n (%) 9 (7) 5 (8) 4 (6) 1.36 (0.35 to 5.34), p=0.656
Incident MACE at 180 days†, n (%) 11 (8) 6 (9) 5 (8) 1.30 (0.37 to4.56), p=0.678
Hospital length of stay (median, IQR) 1 (0–1) 1 (0–1) 1 (0–1) p=0.54‡
Patient satisfaction (mean score, SD) 3.8 (1.0) 3.8 (1.0) 3.8 (1.1) p=0.80‡
Re-attendance at an ED, n (%) 18 (23) 10 (23) 8 (23) p=0.97
Any further investigation for heart disease within 30 days, n (%) 27 (21) 15 (23) 12 (18) p=0.55
Myocardial perfusion imaging (thallium scan) within 30 days, n (%) 8 (28) 3 (19) 5 (38) p=0.24
Stress ECG within 30 days, n (%) 1 (4) 1 (7) 0 (0) p=0.34
Coronary angiography within 30 days, n (%) 9 (32) 4 (27) 5 (38) p=0.51

*Adjusted for trial centre, age, gender, cardiovascular risk factors and history of prior coronary artery disease. This is the prespecified primary analysis.

†Incident death, AMI or coronary revascularisation (not including prevalent AMI). NB, no patients who were discharged early developed a MACE.

Mann-Whitney U test.

MACE, major adverse cardiac event.