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Updated: Apr 20, 2026

Postconditioning with Lactate-enriched Blood for Cardioprotection in ST-segment Elevation Myocardial Infarction
Published on: May 28, 2019
Ischaemic postconditioning reduces infarct size: systematic review and meta-analysis of randomized controlled trials
Caroline Touboul1, Denis Angoulvant2, Nathan Mewton3
1CHRU de Tours, ICCU & Cardiology department, Trousseau Hospital, 37000 Tours, France.
Insights
Cardiac ischaemic postconditioning (IPost) may reduce infarct size (IS) in ST-segment elevation myocardial infarction (STEMI) patients. This meta-analysis suggests IPost reduces IS, but larger trials are needed to confirm clinical benefits.
Area of Science:
- Cardiology
- Interventional Cardiology
- Biomarkers
Background:
- Infarct size (IS) significantly impacts patient outcomes after acute ST-segment elevation myocardial infarction (STEMI).
- Cardiac ischaemic postconditioning (IPost) is an intervention aimed at reducing reperfusion injury, potentially limiting IS.
- IPost has demonstrated feasibility in STEMI patients undergoing primary percutaneous coronary intervention (PPCI).
Purpose of the Study:
- To conduct an updated meta-analysis on the efficacy of IPost in reducing IS.
- To analyze accurate surrogate markers of IS to assess IPost effectiveness.
- To summarize current evidence on IPost for STEMI patients undergoing PPCI.
Main Methods:
- Meta-analysis of randomized controlled trials (RCTs) evaluating IPost in STEMI patients undergoing PPCI.
- Primary outcome: Area Under the Curve of serum creatine kinase release (CK-AUC).
- Secondary outcomes: Other IS surrogate biomarkers, ST-segment resolution, and IS measurements via SPECT and CMR-IS.
Main Results:
- Eleven studies with 1313 patients were included.
- A significant reduction in CK-AUC was observed in the IPost group (SMD -2.84 IU/L, P=0.03).
- Secondary surrogate markers, including CMR-IS, showed non-significant reductions in IS with IPost (SMD -0.36, P=0.16).
Conclusions:
- This meta-analysis indicates that IPost reduces IS, based on surrogate markers.
- Results require cautious interpretation due to limited sample sizes and significant heterogeneity.
- Larger, adequately powered prospective studies are necessary to confirm clinical benefits on cardiac function and patient prognosis.
Background:
Infarct size (IS) is a major determinant of patient outcome after acute ST-segment elevation myocardial infarction (STEMI). Interventions aimed at reducing reperfusion injury, such as cardiac ischaemic postconditioning (IPost), may reduce IS and improve clinical outcomes. IPost has been shown to be feasible in patients with STEMI treated by primary percutaneous coronary intervention (PPCI).
Aims:
To provide an updated summary of the efficacy of IPost, assessed by analysing accurate surrogate markers of IS.
Methods:
We performed a meta-analysis of randomized controlled trials that evaluated the efficacy of IPost in STEMI patients undergoing PPCI. The main outcome was area under the curve of serum creatine kinase release (CK-AUC). Secondary outcomes were other surrogate biomarkers of IS, complete ST-segment resolution, direct measurement of IS by single-photon emission computed tomography and estimation of IS by cardiac magnetic resonance (CMR-IS).
Results:
Eleven studies were retrieved, including 1313 STEMI patients undergoing PPCI with or without IPost. Compared with controls, we observed a significant reduction in CK-AUC (standard mean difference [SMD] -2.84 IU/L, 95% CI -5.43 to -0.25 IU/L; P=0.03). Other surrogate markers, such as CMR-IS (SMD -0.36, 95% CI -0.88 to 0.15; P=0.16), showed a non-significant IS reduction in the IPost group.
Conclusions:
This meta-analysis, dealing with accurate surrogate markers of IS, suggests that IPost reduces IS. However, results should be interpreted cautiously because of limited sample sizes and significant heterogeneity. Whether this translates into improvements in cardiac function and patient prognosis still needs to be demonstrated in larger prospective randomized controlled studies that are powered sufficiently.
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