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American Heart Association

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Final ID: MP783

Safety and Efficacy of Istaroxime in Acute Heart Failure Related Pre-Cardiogenic Shock: An Updated Systematic Review and Meta Analysis of Randomized Controlled Trials

Abstract Body (Do not enter title and authors here):
Background:
Acute heart failure (AHF) with pre-cardiogenic shock carries substantial morbidity and mortality. Istaroxime, a novel intravenous inotrope that enhances both cardiomyocyte contractility and relaxation without adrenergic overstimulation, has demonstrated favourable haemodynamic and echocardiographic effects in early randomized trials. We sought to update the evidence including the newly reported SEISMiC trial to better define istaroxime’s role in AHF pre-cardiogenic shock.
Methods:
We performed a systematic search of PubMed, Web of Science, SCOPUS, and the Cochrane Library for RCTs comparing istaroxime versus placebo in adult hospitalized AHF patients with pre-cardiogenic shock (SBP <90 mmHg without hypoperfusion or persistent hypotension 70–100 mmHg for ≥2 h). Data were extracted independently by two reviewers. Continuous endpoints (e.g., SBP change) were pooled using random effects inverse variance meta analysis and reported as mean differences (MD) with 95% confidence intervals (CI); dichotomous outcomes used risk ratios (RR). Heterogeneity was assessed with I2.
Results:
Five studies comprising 360 patients were identified. For change in systolic blood pressure at 24 h, pooled MD was +5.4 mmHg (95% CI 2.6, 8.3; p <0.001; I2 = 0%), favouring istaroxime. Heart rate decreased by −3.1 bpm (95% CI −5.2, −0.9; p = 0.005; I2 = 0%). Stroke volume index improved (MD +3.0 mL/m2; 95% CI 2.4, 3.6; p <0.0001; I2 = 0%). In the SEISMiC trial, istaroxime (1.0–1.5 µg/kg/min) significantly increased SBP area-under-the-curve at 6 h (difference +22.2 mmHg; p = 0.017) and 24 h (difference +82.5 mmHg; p = 0.025) without excess serious adverse events. No significant increase in arrhythmias or myocardial injury markers was observed (RR for worsening HF events 1.2; 95% CI 0.7, 2.1; p = 0.45; I2 = 5%).
Conclusions:
Istaroxime demonstrates consistent, clinically meaningful improvements in blood pressure, cardiac output, and diastolic function with a favourable safety profile in AHF pre-cardiogenic shock. The inclusion of the SEISMiC trial strengthens the evidence base, supporting further large scale Phase III investigations.
  • Rizvi, Syed Fazal  ( Chicago Medical School , North Chicago , Illinois , United States )
  • Zafar, Shahzad  ( Howard University Hospital, Washington DC , DC , Washington , United States )
  • Haider, Ali  ( Nishtar Medical University , Multan , Pakistan )
  • Asad Ullah, Hafiz Muhammad  ( Nishtar Medical University , Multan , Pakistan )
  • Asjad, Sayyed Jalawan  ( Howard University Hospital , Washington , District of Columbia , United States )
  • Haider, Ali  ( PGY1 Inspira Health, Vineland, NJ , Vineland , New Jersey , United States )
  • Author Disclosures:
    Syed Fazal Rizvi: DO NOT have relevant financial relationships | Shahzad Zafar: DO NOT have relevant financial relationships | Ali Haider: DO NOT have relevant financial relationships | Hafiz Muhammad Asad Ullah: DO NOT have relevant financial relationships | Sayyed Jalawan Asjad: DO NOT have relevant financial relationships | ALI HAIDER: No Answer
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Crash and Burn: Cardiogenic Shock Clinical Science

Saturday, 11/08/2025 , 03:15PM - 04:25PM

Moderated Digital Poster Session

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