Key result
Extended dalteparin reduced death, myocardial infarction, or revascularization compared to placebo in unstable CAD patients with ischaemic episodes on ST-monitoring.
Why the study?
Does extended dalteparin treatment reduce death, myocardial infarction, or revascularization in patients with unstable coronary artery disease identified by multilead ST-monitoring?
RCT (n=629)
placebo-controlled
randomized
Does extended dalteparin treatment reduce death, myocardial infarction, or revascularization in patients with unstable coronary artery disease identified by multilead ST-monitoring?
Continuous multilead ST-monitoring can identify a high-risk subset of patients with unstable coronary artery disease who benefit significantly from extended antithrombotic treatment with dalteparin.
Answers are grounded in this paper and cite their sources.
Extended dalteparin reduces events in ST-monitored unstable CAD with ischaemia; extends evidence for monitoring-guided prolonged antithrombotic therapy.
AIMS: Prolongation of anticoagulant treatment might reduce subsequent cardiac events in patients with unstable coronary artery disease. Multilead ST-segment monitoring identifies patients with a high risk of adverse outcome. The aim was to assess the value of multilead ST-monitoring in prospectively identifying patients who respond to extended anticoagulant treatment with low-molecular weight heparin when treated by a primarily non-invasive strategy. METHODS AND RESULTS: In this substudy of the FRISC II trial, ST-monitoring with a continuous 12-lead ECG or vectorcardiography was performed for 24 h in 629 patients with unstable coronary artery disease randomized to receive either the low-molecular weight heparin dalteparin, or placebo for 3 months after at least 5 days' dalteparin treatment in all patients. Ischaemic episodes were detected in 34% during ST-monitoring. In the group with ischaemic episodes, the extended dalteparin treatment was associated with a lower rate of death, myocardial infarction, or revascularization (35.2% vs 53.4%, relative risk reduction: 34%, P=0.01). In patients without ischaemic episodes, long-term dalteparin treatment had no effect. CONCLUSIONS: In patients with unstable coronary artery disease treated primarily with a non-invasive strategy, ischaemic episodes revealed while on multilead ST-monitoring identifies patients who benefit most from extended treatment with anticoagulants.
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Tomas Jernberg (2002) conducted an RCT in unstable coronary artery disease (n=629). Dalteparin vs. Placebo was evaluated on death, myocardial infarction, or revascularization (relative risk reduction 34%, p=0.01). Extended dalteparin reduced death, myocardial infarction, or revascularization compared to placebo in unstable CAD patients with ischaemic episodes on ST-monitoring.
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