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Published on: April 25, 2014
Inflammatory Indices in Patients with Myocardial Infarction Complicated by Cardiogenic Shock, and Their
Irina Kologrivova1, Maria Kercheva1,2, Oleg Panteleev1,2
1Cardiology Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, 111A Kievskaya, Tomsk 634012, Russia.
Insights
Systemic inflammation markers, particularly the systemic inflammation response index (SIRI), help predict survival in myocardial infarction with cardiogenic shock (MI-CS) patients. Declining inflammation at advanced stages may signal immune suppression.
Area of Science:
- Cardiology
- Immunology
- Critical Care Medicine
Background:
- Myocardial infarction complicated by cardiogenic shock (MI-CS) has high mortality.
- Systemic inflammation is crucial in MI-CS, but its role across disease stages is unclear.
Purpose of the Study:
- To assess systemic inflammation indices (NLR, PLR, SII, SIRI, AISI) in MI-CS patients.
- To correlate these indices with Society for Cardiovascular Angiography and Interventions (SCAI) stages and survival.
Main Methods:
- Retrospective study of 132 MI-CS patients (SCAI stages A-E).
- Analysis of demographic, clinical, laboratory, and outcome data.
- Calculation of inflammatory indices from complete blood counts.
Main Results:
- PLR, SII, and AISI peaked at SCAI stage C, declining at stage E.
- SIRI was a key prognostic marker for stage C, linked to infarct size and heart rate.
- Elevated SIRI (≥ 3.34) correlated with significantly lower two-year survival (p=0.006).
Conclusions:
- Inflammation indices, especially SIRI, offer prognostic value in MI-CS.
- SIRI reflects disease severity and immune response heterogeneity.
- Declining inflammation at advanced stages may indicate immune suppression, necessitating personalized treatments.
Abstract:
Background: Myocardial infarction complicated by cardiogenic shock (MI-CS) remains a critical condition with high mortality rates, despite advances in treatment. Systemic inflammation plays a significant role in MI-CS progression; however, its dynamics across different stages of the Society for Cardiovascular Angiography and Interventions (SCAI) classification remain poorly understood. This study aimed to evaluate indices of systemic inflammation-neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), systemic inflammation response index (SIRI), and aggregate index of systemic inflammation (AISI)-in MI-CS patients, correlating them with SCAI stages and survival outcomes. Methods: A single-center retrospective study included 132 patients with MI-CS, categorized into SCAI stages A-E. All patients were assessed for demographic, clinical, and laboratory data, procedural and treatment characteristics, MI timing, and outcomes. Complete blood count test data were used to calculate inflammatory indices and evaluate types of immune reactions. Results: PLR, SII, and AISI peaked at SCAI stage C and declined significantly at stage E, suggesting suppressed inflammation in advanced shock. SIRI emerged as a key prognostic marker for stage C patients, with elevated levels associated with larger infarct size, higher heart rate, and predominant innate immune activation. Patients with SIRI ≥ 3.34 had significantly lower two-year survival (log-rank test, p = 0.006). Conclusions: Inflammation indices, particularly SIRI, provide valuable prognostic insights in MI-CS, reflecting disease severity and heterogeneity of immune response. The decline in inflammatory indices at SCAI stage E may indicate immune suppression in extreme MI-CS, underscoring the need for personalized therapeutic strategies.
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