Shock Index as a predictor for In-hospital mortality in patients with non-ST-segment elevation myocardial infarction

Akihiro Kobayashi1, Naoki Misumida1, Daniel Luger1

  • 1Department of Internal Medicine, Mount Sinai Beth Israel, New York, USA.

Insights

Elevated shock index (SI), a heart rate to systolic blood pressure ratio, predicts higher in-hospital mortality in patients with non-ST-segment elevation myocardial infarction (NSTEMI). This finding aids in risk stratification for NSTEMI patients.

Area of Science:

  • Cardiology
  • Critical Care Medicine
  • Clinical Risk Stratification

Background:

  • Shock index (SI) is a known predictor of mortality in ST-segment elevation myocardial infarction.
  • The prognostic utility of SI in non-ST-segment elevation myocardial infarction (NSTEMI) remains less understood.

Purpose of the Study:

  • To investigate the prognostic value of the shock index in patients diagnosed with NSTEMI.
  • To determine if an elevated SI is associated with adverse outcomes such as cardiogenic shock and in-hospital mortality in NSTEMI patients.

Main Methods:

  • Retrospective analysis of 481 NSTEMI patients undergoing coronary angiography.
  • Calculation of SI (heart rate/systolic blood pressure) upon presentation.
  • Comparison of baseline characteristics, angiographic data, cardiogenic shock rates, and in-hospital mortality between patients with SI >= 0.7 and SI < 0.7.

Main Results:

  • 103 patients (21.4%) had an SI >= 0.7.
  • Patients with SI >= 0.7 exhibited a lower left ventricular ejection fraction and a significantly higher total incidence of cardiogenic shock (7.8% vs. 2.1%, p=0.001).
  • In-hospital mortality was significantly higher in the SI >= 0.7 group (4.9% vs. 0.5%, p=0.006).

Conclusions:

  • An elevated shock index (SI >= 0.7) is associated with increased cardiogenic shock and higher in-hospital mortality in patients with NSTEMI.
  • SI serves as a valuable, readily available tool for risk stratification in NSTEMI patients.
  • Further research may explore therapeutic implications based on SI values in NSTEMI.
Abstract

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