TY - JOUR
T1 - Optimal timing of invasive angiography in stable non-ST-elevation myocardial infarction
T2 - The Leipzig Immediate versus early and late PercutaneouS coronary Intervention triAl in NSTEMI (LIPSIA-NSTEMI Trial)
AU - Thiele, Holger
AU - Rach, Justus
AU - Klein, Norbert
AU - Pfeiffer, Dietrich
AU - Hartmann, Andreas
AU - Hambrecht, Rainer
AU - Sick, Peter
AU - Eitel, Ingo
AU - Desch, Steffen
AU - Schuler, Gerhard
N1 - Funding Information:
The study was supported in part by free tirofiban medication from MSD SHARP & DOHME GmbH, Germany, and Iroko Pharmaceuticals, LLC, PA, USA.
PY - 2012/8
Y1 - 2012/8
N2 - AimsThe optimal timing of intervention in non-ST-elevation myocardial infarction (NSTEMI) remains uncertain. The aim of this multicentre trial was to assess whether an immediate invasive approach is superior to an early invasive or a selective invasive approach with respect to reduction of large infarction. Methods and resultsPatients with NSTEMI were randomized to either an immediate (<2 h after randomization; n = 201), an early (1048 h after randomization; n = 200), or a selective invasive approach with high invasive percentage (n = 201). The primary outcome was the peak creatine kinase (CK)-myocardial band (MB) activity during index hospitalization; key secondary clinical endpoints were the composite of (i) death and non-fatal infarction; (ii) death, non-fatal infarction, and refractory ischaemia; (iii) death, non-fatal infarction, refractory ischaemia, and rehospitalization for unstable angina within 6 months.The median time from randomization to angiography was 1.1 h in the immediate vs. 18.6 h in the early and 67.2 h in the selective invasive group (P< 0.001). There was no significant difference in the peak CK-MB activity between groups. The key secondary clinical endpoints were similar between groups at 6-month follow-up: death and infarction: 21.0 vs. 16.0 vs. 14.5; P = 0.17; death, infarction, refractory ischaemia: 20.9 vs. 21.5 vs. 22.0; P = 0.98; death, infarction, refractory ischaemia, rehospitalization: 26.0 vs. 26.5 vs. 24.5; P = 0.91, respectively. ConclusionsIn NSTEMI patients, an immediate invasive approach does not offer an advantage over an early or a selective invasive approach with respect to large myocardial infarctions as defined by peak CK-MB levels, which is supported by similar clinical outcomes.
AB - AimsThe optimal timing of intervention in non-ST-elevation myocardial infarction (NSTEMI) remains uncertain. The aim of this multicentre trial was to assess whether an immediate invasive approach is superior to an early invasive or a selective invasive approach with respect to reduction of large infarction. Methods and resultsPatients with NSTEMI were randomized to either an immediate (<2 h after randomization; n = 201), an early (1048 h after randomization; n = 200), or a selective invasive approach with high invasive percentage (n = 201). The primary outcome was the peak creatine kinase (CK)-myocardial band (MB) activity during index hospitalization; key secondary clinical endpoints were the composite of (i) death and non-fatal infarction; (ii) death, non-fatal infarction, and refractory ischaemia; (iii) death, non-fatal infarction, refractory ischaemia, and rehospitalization for unstable angina within 6 months.The median time from randomization to angiography was 1.1 h in the immediate vs. 18.6 h in the early and 67.2 h in the selective invasive group (P< 0.001). There was no significant difference in the peak CK-MB activity between groups. The key secondary clinical endpoints were similar between groups at 6-month follow-up: death and infarction: 21.0 vs. 16.0 vs. 14.5; P = 0.17; death, infarction, refractory ischaemia: 20.9 vs. 21.5 vs. 22.0; P = 0.98; death, infarction, refractory ischaemia, rehospitalization: 26.0 vs. 26.5 vs. 24.5; P = 0.91, respectively. ConclusionsIn NSTEMI patients, an immediate invasive approach does not offer an advantage over an early or a selective invasive approach with respect to large myocardial infarctions as defined by peak CK-MB levels, which is supported by similar clinical outcomes.
UR - http://www.scopus.com/inward/record.url?scp=84863633765&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehr418
DO - 10.1093/eurheartj/ehr418
M3 - Journal articles
C2 - 22108830
AN - SCOPUS:84863633765
SN - 0195-668X
VL - 33
SP - 2035
EP - 2043
JO - European Heart Journal
JF - European Heart Journal
IS - 16
ER -