Sociedad Americana de Hirudoterapia

Prognostic value of early sustained ventricular arrhythmias in ST-segment elevation myocardial infarction treated by primary percutaneous coronary intervention: A substudy of VALIDATE-SWEDEHEART trial

Research article published in Heart Rhythm O2 (2022)

Última actualización: June 18, 2026Revisado por: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportEnsayos clínicosSeguridad y control de infeccionesDemidova MM et al. · Heart Rhythm O2, 2022

Abstract

BACKGROUND: Prognostic assessment of ventricular tachycardia (VT) or ventricular fibrillation (VF) in ST-segment elevation myocardial infarction (STEMI) is based mainly on distinguishing between early (<48 hours) and late arrhythmias, and does not take into account its time distribution with regard to reperfusion, or type of arrhythmia. OBJECTIVE: We analyzed the prognostic value of early ventricular arrhythmias (VAs) in STEMI with regard to their type and timing. METHODS: The prespecified analysis of the multicenter prospective Bivalirudin versus Heparin in ST-Segment and Non-ST-Segment Elevation Myocardial Infarctionin Patients on Modern Antiplatelet Therapy in the Swedish Web System for Enhancement and Development of Evidence-based Care in Heart Disease evaluated according to Recommended Therapies Registry Trial included 2886 STEMI patients undergoing primary percutaneous coronary intervention (PCI). VA episodes were characterized regarding their type and timing. Survival status at 180 days was assessed through the population registry. RESULTS: Nonmonomorphic VT or VF was observed in 97 (3.4%) and monomorphic VT in 16 (0.5%) patients. Only 3 (2.7%) early VA episodes occurred after 24 hours from symptom onset. VA was associated with higher risk of death (hazard ratio 3.59; 95% confidence interval [CI] 2.01-6.42) after adjustment for age, sex, and STEMI localization. VA after PCI was associated with an increased mortality compared with VA before PCI (hazard ratio 6.68; 95% CI 2.90-15.41). Early VA was associated with in-hospital mortality (odds ratio 7.39; 95% CI 3.68-14.83) but not with long-term prognosis in patients discharged alive. The type of VA was not associated with mortality. CONCLUSION: VA after PCI was associated with an increased mortality compared with VA before PCI. Long-term prognosis did not differ between patients with monomorphic VT and nonmonomorphic VT or VF, but events were few. VA incidence during 24 to 48 hours of STEMI is negligibly low, thus precluding assessment of its prognostic importance.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal Article

Resumen

VALIDATE-SWEDEHEART substudy of 2886 STEMI patients; ventricular arrhythmia after PCI was associated with 6.68-fold higher mortality vs VA before PCI.

Por qué esto importa para la hirudoterapia

This prespecified substudy of the VALIDATE-SWEDEHEART trial analyzed the prognostic value of early ventricular arrhythmias in 2,886 ST-segment-elevation myocardial infarction patients undergoing primary PCI, finding that VA after PCI was associated with significantly higher mortality than VA before PCI (HR 6.68), while early VA was associated with in-hospital but not long-term mortality in patients discharged alive. The parent trial compared bivalirudin versus heparin, which is the only tangential link to the hirudin/leech-derived anticoagulant family. For ASH, relevance is minimal: this is a cardiac arrhythmia prognostication study with no leech-related intervention, outcome, or hypothesis. CAVEAT: This study involves no leeches, leech therapy, or leech secretome; the bivalirudin connection is incidental to the arrhythmia-focused analysis, and findings have no direct application to hirudotherapy.

Citación

Prognostic value of early sustained ventricular arrhythmias in ST-segment elevation myocardial infarction treated by primary percutaneous coronary intervention: A substudy of VALIDATE-SWEDEHEART trial.

Demidova MM et al. · Heart Rhythm O2, 2022

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: June 18, 2026

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