Key result
Direct PTCA tended to result in lower end-systolic volumes compared to intravenous rt-PA in successfully reperfused AMI patients (43 vs 59 cc, P=0.09), suggesting a more marked effect on remodeling.
Why the study?
Does direct PTCA improve left ventricular remodeling compared to intravenous rt-PA in patients with acute myocardial infarction?
RCT (n=26)
Randomized
Yes
Does direct PTCA improve left ventricular remodeling compared to intravenous rt-PA in patients with acute myocardial infarction?
Direct PTCA may be more effective than systemic rt-PA in counteracting left ventricular remodeling in patients with large acute myocardial infarctions.
Answers are grounded in this paper and cite their sources.
May support direct PTCA over rt-PA to limit post-AMI remodeling; extends reperfusion comparisons but needs confirmation.
The purpose of this study was to compare the effect of direct percutaneous transluminal coronary angioplasty (PTCA) and intravenous recombinant tissue plasminogen activator (rt‐PA) on left ventricular remodeling in patients with acute myocardial infarction (AMI). To address this issue, patients with AMI randomly assigned to direct PTCA or intravenous rt‐PA as part of a large multicenter study (Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries [GUSTO] IIb Angioplasty Substudy) were evaluated with two‐dimensional echocardiography at predischarge. An echocardiographic infarct size index and the end‐diastolic and end‐systolic left ventricular volumes were computed. Patients with an infarct size index equal to or higher than the mean value were considered to have a large infarction. Of 26 enrolled patients, 13 were assigned to PTCA (9 successfully reperfused: i.e., TIMI‐3 flow after PTCA) and 13 to rt‐PA (10 successfully reperfused: i.e., ST resolution after rt‐PA). In patients considered successfully reperfused, end‐systolic volumes tended to be lower in PTCA patients than in rt‐PA patients (43 ± 17 cc vs 59 ± 21 cc, P = 0.09), although there were no differences in infarct size index (7.3 ± 2.8 vs 7.0 ± 2.8) and ejection fraction (52%± 10% vs 46%± 12%). End‐systolic volume depended on infarct size index in the overall patient population (r = 0.60, P = 0.007) and in rt‐PA patients (r = 0.80, P =0.005), while no correlation was found in PTCA patients. Considering patients with large AMIs, end‐systolic volumes were higher in the four patients treated with rt‐PA than in the four patients treated with direct PTCA (P < 0.01). Considering all the 26 enrolled patients, these differences were also present, but they did not reach statistical significance. In conclusion, our results suggest that, in patients with large AMIs, adequate reperfusion obtained by direct PTCA has a more marked effect in counteracting ventricular remodeling than that obtained by systemic rt‐PA. This beneficial effect of direct PTCA, independent of any reduction in regional wall‐motion abnormalities, should be taken into account when comparing the clinical value of direct PTCA with that of systemic thrornbolysis in the treatment of AMI.
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Golia et al. (1999) conducted an RCT in Acute myocardial infarction (AMI) (n=26). Direct percutaneous transluminal coronary angioplasty (PTCA) vs. Intravenous recombinant tissue plasminogen activator (rt-PA) was evaluated on End-systolic volume in successfully reperfused patients (p=0.09). Direct PTCA tended to result in lower end-systolic volumes compared to intravenous rt-PA in successfully reperfused AMI patients (43 vs 59 cc, P=0.09), suggesting a more marked effect on remodeling.
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