Background: Prognostic stratification of acute myocarditis (AM) presenting with normal left ventricular ejection fraction (LVEF) relies mostly on late gadolinium enhancement (LGE) characterization. Left ventricular peak global longitudinal strain (LV-GLS) measured by feature tracking analysis might improve prognostication of AM presenting with normal LVEF. Methods: Data of patients undergoing cardiac magnetic resonance (CMR) for clinically suspected AM in seven European Centres (2013–2020) were retrospectively analysed. Patients with AM confirmed by CMR and LVEF ≥50% were included. LGE was visually characterized: localized versus. non-localized, subepicardial versus midwall. LV-GLS was measured by dedicated software. The primary outcome was the first occurrence of an adverse cardiovascular event (ACE) including cardiac death, life-threatening arrhythmias, development of heart failure or of LVEF <50%. Results: Of 389 screened patients, 256 (66%) fulfilled inclusion criteria: median age 36 years, 71% males, median LVEF 60%, median LV-GLS -17.3%. CMR was performed at 4 days from hospitalization. At 27 months, 24 (9%) patients experienced ≥1 ACE (71% developed LVEF <50%). Compared to the others, they had lower median LV-GLS values (−13.9% vs. −17.5%, p =.001). At Kaplan–Meier analysis, impaired LV-GLS (both considered as > −20% or quartiles), non-localized and midwall LGE were associated with ACEs. Patients with LV-GLS ≤−20% did not experience ACEs. LV-GLS remained associated with ACEs after adjustment for non-localized and midwall LGE. Conclusion: In AM presenting with LVEF ≥50%, LV-GLS provides independent prognostic value over LGE characterization, improving risk stratification and representing a rationale for further studies of therapy in this cohort.

Global longitudinal strain by CMR improves prognostic stratification in acute myocarditis presenting with normal LVEF

Andreis A.;
2022-01-01

Abstract

Background: Prognostic stratification of acute myocarditis (AM) presenting with normal left ventricular ejection fraction (LVEF) relies mostly on late gadolinium enhancement (LGE) characterization. Left ventricular peak global longitudinal strain (LV-GLS) measured by feature tracking analysis might improve prognostication of AM presenting with normal LVEF. Methods: Data of patients undergoing cardiac magnetic resonance (CMR) for clinically suspected AM in seven European Centres (2013–2020) were retrospectively analysed. Patients with AM confirmed by CMR and LVEF ≥50% were included. LGE was visually characterized: localized versus. non-localized, subepicardial versus midwall. LV-GLS was measured by dedicated software. The primary outcome was the first occurrence of an adverse cardiovascular event (ACE) including cardiac death, life-threatening arrhythmias, development of heart failure or of LVEF <50%. Results: Of 389 screened patients, 256 (66%) fulfilled inclusion criteria: median age 36 years, 71% males, median LVEF 60%, median LV-GLS -17.3%. CMR was performed at 4 days from hospitalization. At 27 months, 24 (9%) patients experienced ≥1 ACE (71% developed LVEF <50%). Compared to the others, they had lower median LV-GLS values (−13.9% vs. −17.5%, p =.001). At Kaplan–Meier analysis, impaired LV-GLS (both considered as > −20% or quartiles), non-localized and midwall LGE were associated with ACEs. Patients with LV-GLS ≤−20% did not experience ACEs. LV-GLS remained associated with ACEs after adjustment for non-localized and midwall LGE. Conclusion: In AM presenting with LVEF ≥50%, LV-GLS provides independent prognostic value over LGE characterization, improving risk stratification and representing a rationale for further studies of therapy in this cohort.
2022
e13815
1
acute myocarditis; cardiac magnetic resonance; global longitudinal strain; normal left ventricular ejection fraction; prognostic stratification
Porcari A.; Merlo M.; Baggio C.; Gagno G.; Cittar M.; Barbati G.; Paldino A.; Castrichini M.; Vitrella G.; Pagnan L.; Cannata A.; Andreis A.; Cecere A.; Cipriani A.; Raafs A.; Bromage D.I.; Rosmini S.; Scott P.; Sado D.; Di Bella G.; Nucifora G.; Marra M.P.; Heymans S.; Imazio M.; Sinagra G.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1893995
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