PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
June 1, 1992Circulation209 citationsOpen Access

A randomized trial of late reperfusion therapy for acute myocardial infarction. Thrombolysis and Angioplasty in Myocardial Infarction-6 Study Group.

View Full Paper
ETEric J. TopolRCRobert M. CaliffMVMichel Vandormael

Key Result

Tissue-type plasminogen activator significantly improved infarct vessel patency compared to placebo (65% vs 27%, p<0.0001) in patients presenting 6 to 24 hours after acute myocardial infarction.

Study Design

Type

RCT (n=197)

Blinding

Double-blind

Randomization

randomly assigned

Structured PICO

Does tissue-type plasminogen activator improve infarct vessel patency in patients with acute myocardial infarction presenting 6 to 24 hours after symptom onset?

P
Population
197 patients with acute myocardial infarction presenting with 6 to 24 hours of symptoms and ECG ST elevation, followed for up to 6 months.
I
Intervention
Tissue-type plasminogen activator (100 mg over 2 hours)
C
Comparator
Placebo
O
Outcome
Infarct vessel patency assessed by coronary angiography within 24 hourssurrogate

Late reperfusion with tissue-type plasminogen activator improves infarct vessel patency and prevents cavity dilatation but does not improve late systolic function in patients presenting 6-24 hours after acute myocardial infarction.

Main Result

Absolute Event Rate: 65% vs 27%

p-value: p=<0.0001

Limitations

  • Requires data from large-scale trials designed to assess mortality reduction to determine overall potential benefit.
  • Requires data from large-scale trials designed to assess mortality reduction

Abstract

BACKGROUND: Experimental and observational clinical studies of acute coronary occlusion have suggested that late reperfusion prevents infarct expansion and facilitates myocardial healing. The purpose of this trial was to assess whether infarct vessel patency could be achieved in late-entry patients and what benefit, if any, can be demonstrated. METHODS AND RESULTS: In a double-blind fashion, 197 patients with 6 to 24 hours of symptoms and ECG ST elevation were randomly assigned to tissue-type plasminogen activator (100 mg over 2 hours) or placebo. Coronary angiography within 24 hours was used to determine infarct vessel patency status. Patients with infarct-related occluded arteries were then eligible for a second randomization to either angioplasty (34 patients) or no angioplasty (37 patients). Ventricular function and cavity size were reassessed at 1 month by gated blood pool scintigraphy and at 6 months by repeat cardiac catheterization. The primary end point, infarct vessel patency, was 65% for plasminogen activator patients compared with 27% in the placebo group (p less than 0.0001). There were no differences between these groups in ejection fraction or infarct zone regional wall motion at 1 or 6 months. At 6 months, infarct vessel patency was 59% in both groups. In the placebo group, there was a significant increase in end-diastolic volume from acute phase of 127 ml to 159 ml at 6-month follow-up (p = 0.006) but no increase in cavity size for the plasminogen activator group patients. Coronary angioplasty was associated with an initial 81% recanalization success and improved ventricular function at 1 month, but by late follow-up no advantage could be demonstrated for this procedure, and there was a 38% spontaneous recanalization rate in the patients assigned to no angioplasty. CONCLUSIONS: The study demonstrates that it is possible to achieve infarct vessel recanalization in the majority of late-entry patients with either thrombolytic therapy or angioplasty. Thrombolytic intervention had a favorable effect on prevention of cavity dilatation and left ventricular remodeling, but there are no late benefits on systolic function after thrombolysis or coronary angioplasty. The conclusions concerning overall potential benefit of applying late reperfusion therapy will require data from large-scale trials designed to assess mortality reduction.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Topol et al. (1992) conducted an RCT in acute myocardial infarction (n=197). tissue-type plasminogen activator vs. placebo was evaluated on infarct vessel patency (p=<0.0001). Tissue-type plasminogen activator significantly improved infarct vessel patency compared to placebo (65% vs 27%, p<0.0001) in patients presenting 6 to 24 hours after acute myocardial infarction.

synapsesocial.com/papers/6a0895a01e0fcf4a43e8d9aahttps://doi.org/10.1161/01.cir.85.6.2090
Ask AI
Helpful
Bookmark
Share
View Full Paper