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Study · Randomized controlled trial · n = 633 · 1995

10 results

Effects of acadesine on the incidence of myocardial infarction and adverse cardiac outcomes after coronary artery bypass graft surgery. Multicenter Study of Perioperative Ischemia (McSPI) Research Group.

The source lists no authors.

Anesthesiology1 Oct 1995Cited by 19 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study10

10 results from studies that gave the peptide. 10 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients, a post hoc analysis with a more specific MI definition found lower MI incidence with high-dose acadesine (P = 0.018, alpha = 0.017, corrected for multiple comparisons).

    In plain wordsIn coronary bypass patients, a post hoc analysis found fewer heart attacks with high-dose acadesine than with placebo.

    Outcome
    DecreasePost hoc myocardial infarction, specific definition
    Study

    n: not reported in source

    Comparator
    Placebo
    Analysis
    Exploratory
    Outcome group
    Cardiovascular events · Cardiovascular
    Studied dose
    0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Measurements

    P value
    0.018 NA
    post hoc myocardial infarction
    Corrected alpha
    0.017 NA
    multiple comparisons

    Source sentences

    Summary
    the incidence of MI was lower (P = 0.018, alpha = 0.017, corrected for multiple comparisons), as were adverse cardiovascular outcomes (P = 0.002) and CVA (P = 0.02) for patients treated with 0.1 mg.kg-1.min-1 acadesine.
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  2. 02HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients, high-dose acadesine reduced adverse cardiovascular outcomes versus placebo in a post hoc analysis.

    In plain wordsIn coronary bypass patients, high-dose acadesine reduced adverse heart and blood vessel outcomes versus placebo in a post hoc analysis.

    Outcome
    DecreasePost hoc adverse cardiovascular outcomes
    Study

    n: not reported in source

    Comparator
    Placebo
    Analysis
    Exploratory
    Outcome group
    Cardiovascular events · Cardiovascular
    Studied dose
    0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Measurements

    P value
    0.002 NA
    post hoc cardiovascular outcomes

    Source sentences

    Summary
    the incidence of MI was lower (P = 0.018, alpha = 0.017, corrected for multiple comparisons), as were adverse cardiovascular outcomes (P = 0.002) and CVA (P = 0.02) for patients treated with 0.1 mg.kg-1.min-1 acadesine.
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  3. 03HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients, high-dose acadesine had lower post hoc stroke incidence versus placebo (P = 0.02).

    In plain wordsIn coronary bypass patients, high-dose acadesine had fewer strokes than placebo in a post hoc analysis (P = 0.02).

    Outcome
    DecreasePost hoc cerebrovascular accident
    Study

    n: not reported in source

    Comparator
    Placebo
    Analysis
    Exploratory
    Outcome group
    Cardiovascular events · Cardiovascular
    Studied dose
    0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Measurements

    P value
    0.02 NA
    post hoc cerebrovascular accident

    Source sentences

    Summary
    the incidence of MI was lower (P = 0.018, alpha = 0.017, corrected for multiple comparisons), as were adverse cardiovascular outcomes (P = 0.002) and CVA (P = 0.02) for patients treated with 0.1 mg.kg-1.min-1 acadesine.
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  4. 04HumanRandomized controlled trialSafety outcome

    In coronary bypass patients, adverse event incidence was similar with acadesine and placebo, except for high-dose uric acid elevation.

    In plain wordsIn coronary bypass patients, adverse event rates were similar with acadesine and placebo, except for higher uric acid at high doses.

    Outcome
    No significant changeAdverse event incidence
    Study

    n = 633

    Comparator
    Placebo
    Outcome group
    Adverse events · Whole body
    Studied dose
    0.05 or 0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Source sentences

    Summary
    There was a similar incidence of adverse events in the acadesine groups and the placebo group, with the exception that serum uric acid transiently increased in the high-dose acadesine group.
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  5. 05HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients, prespecified myocardial infarction incidence did not differ across placebo and both acadesine dose groups.

    In plain wordsIn coronary bypass patients, heart attack rates did not differ across placebo and both acadesine dose groups.

    Outcome
    No significant changePrespecified perioperative myocardial infarction
    Study

    n = 633

    Comparator
    Placebo
    Outcome group
    Cardiovascular events · Cardiovascular
    Studied dose
    0.05 or 0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Measurements

    Perioperative MI incidence
    24%
    three-group comparison, first value listed; group order not stated in the result sentence
    Perioperative MI incidence
    26%
    three-group comparison, second value listed; group order not stated in the result sentence
    Perioperative MI incidence
    21%
    three-group comparison, third value listed; group order not stated in the result sentence
    P value
    0.574 NA
    between the three groups

    Source sentences

    Summary
    The incidence of perioperative MI, using the prespecified MI criterion (EGF Q wave, CK-MB elevation, or autopsy evidence), was not different between groups (24% versus 26% versus 21% [P = 0.574])
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  6. 06HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients, combined cardiovascular outcome incidence did not differ across placebo and both acadesine dose groups.

    In plain wordsIn coronary bypass patients, combined heart and blood vessel outcome rates did not differ across placebo and both acadesine dose groups.

    Outcome
    No significant changeAll cardiovascular outcomes
    Study

    n = 633

    Comparator
    Placebo
    Outcome group
    Cardiovascular events · Cardiovascular
    Studied dose
    0.05 or 0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Measurements

    All cardiovascular outcomes incidence
    30%
    three-group comparison, first value listed; group order not stated in the result sentence
    All cardiovascular outcomes incidence
    30%
    three-group comparison, second value listed; group order not stated in the result sentence
    All cardiovascular outcomes incidence
    22%
    three-group comparison, third value listed; group order not stated in the result sentence
    P value
    0.151 NA
    between the three groups

    Source sentences

    Summary
    The incidence of perioperative MI, using the prespecified MI criterion (EGF Q wave, CK-MB elevation, or autopsy evidence), was not different between groups (24% versus 26% versus 21% [P = 0.574]), nor was the incidence of all cardiovascular outcomes (30% versus 30% versus 22% [P = 0.151]).
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  7. 07HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients, acadesine did not change myocardial infarction incidence assessed by Holter or transesophageal echocardiography versus placebo.

    In plain wordsIn coronary bypass patients, acadesine did not change heart attack incidence measured by Holter or transesophageal echocardiography compared with placebo.

    Outcome
    No significant changeMyocardial infarction incidence by Holter or echocardiography
    Study

    n = 633

    Comparator
    Placebo
    Outcome group
    Cardiovascular events · Cardiovascular
    Studied dose
    0.05 or 0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Source sentences

    Summary
    No differences were found in the incidence or characteristics of MI (Holter or transesophageal echocardiography).
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  8. 08HumanRandomized controlled trialSafety outcome

    In coronary bypass patients, high-dose acadesine transiently increased serum uric acid versus placebo.

    In plain wordsIn coronary bypass patients, high-dose acadesine temporarily increased blood uric acid compared with placebo.

    Outcome
    IncreaseSerum uric acid
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Adverse events · Whole body
    Studied dose
    0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Source sentences

    Summary
    There was a similar incidence of adverse events in the acadesine groups and the placebo group, with the exception that serum uric acid transiently increased in the high-dose acadesine group.
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  9. 09HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients with Q-wave infarction, high-dose acadesine lowered peak median CK-MB versus placebo.

    In plain wordsIn coronary bypass patients with Q-wave heart attacks, high-dose acadesine lowered the peak heart injury marker compared with placebo.

    Outcome
    DecreasePeak median CK-MB in Q-wave infarction
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Measurements

    P value
    0.042 NA
    peak median CK-MB

    Source sentences

    Summary
    In patients with Q-wave infarction, the high-dose acadesine group had a lower peak median CK-MB (P = 0.042) and area under the CK-MB curve (P = 0.021).
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)
  10. 10HumanRandomized controlled trialEfficacy outcome

    In coronary bypass patients with Q-wave infarction, high-dose acadesine lowered CK-MB area under the curve versus placebo.

    In plain wordsIn coronary bypass patients with Q-wave heart attacks, high-dose acadesine reduced cumulative heart injury marker levels compared with placebo.

    Outcome
    DecreaseCK-MB area under curve in Q-wave infarction
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    0.1 mg.kg-1.min-1 plus 5 micrograms/ml cardioplegia · Intravenous infusion and cardioplegic solution · 7 hAs given in this study (human).

    Measurements

    P value
    0.021 NA
    CK-MB area under curve

    Source sentences

    Summary
    In patients with Q-wave infarction, the high-dose acadesine group had a lower peak median CK-MB (P = 0.042) and area under the CK-MB curve (P = 0.021).
    1 context sentence
    Summary · context
    633 patients undergoing CABG surgery were randomized in a double-blind fashion to receive either placebo (n = 212), low-dose acadesine (0.05 mg.kg-1.min-1, n = 214), or high-dose acadesine (0.1 mg.kg-1.min-1, n = 207)

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Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    21 Oct 2026, 15:58 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 12:50 UTC

    First added · source update from Europe PMC

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