Complexity of coronary artery disease in infarct-related cardiogenic shock and multivessel disease: a substudy of the DanGer Shock trial.

EuroInterventionOct 5, 2026 (epub)
Clinical ResearchCardiologyOpen access

Jasmine M Marquard, Rasmus P Beske, Christian Hassager et al.

✦ AI-curated · Sources linked

In 30 seconds

This study, a secondary analysis of the DanGer Shock trial, evaluated the prognostic significance of baseline and residual SYNTAX scores in 256 patients with multivessel disease and infarct-related cardiogenic shock. It found that a high baseline SYNTAX score was linked to increased odds of 180-day all-cause mortality (adjusted OR 3.12).

Key findings

  • A high baseline SYNTAX score was associated with higher odds of 180-day all-cause mortality (adjusted OR 3.12).
  • The residual SYNTAX score independently predicted 180-day all-cause mortality.
  • In patients with isolated LM lesions, mAFP use was linked to lower odds of 180-day mortality (adjusted OR 0.17).

Why it matters

Understanding the relationship between SYNTAX scores and mortality can help clinicians assess risk in patients with multivessel disease and cardiogenic shock, potentially guiding treatment decisions.

Source

Published in EuroIntervention. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Cardiology

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.