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Updated: May 12, 2025

Use of a Percutaneous Ventricular Assist Device/Left Atrium to Femoral Artery Bypass System for Cardiogenic Shock
Published on: August 16, 2021
Cardiogenic shock in systemic sclerosis: a retrospective study of acute ventricular dysfunction
Aitor Uribarri1,2,3, Alfredo Guillen-Del Castillo4,5, Yassin Belahnech6,7,8
1Department of Cardiology, Hospital Universitari Vall d'Hebron, Barcelona, Spain. auribarrig@gmail.com.
Insights
Systemic sclerosis patients experiencing cardiogenic shock and acute ventricular dysfunction have a high mortality rate. Myocarditis is a likely cause, indicating a need for better cardiac care in systemic sclerosis.
Area of Science:
- Cardiology
- Rheumatology
- Pathology
Background:
- Cardiac involvement is a leading cause of death in systemic sclerosis (SSc).
- Acute ventricular dysfunction and cardiogenic shock in SSc patients have unclear underlying causes.
- This study investigates the characteristics and outcomes of SSc patients with acute ventricular dysfunction and cardiogenic shock.
Purpose of the Study:
- To elucidate the clinical, imaging, and pathological features of acute ventricular dysfunction in systemic sclerosis (SSc) patients presenting with cardiogenic shock.
- To assess the in-hospital and six-month outcomes of this patient cohort.
- To identify potential drivers of cardiac dysfunction in SSc.
Main Methods:
- Observational study of 10 SSc patients with cardiogenic shock and acute ventricular dysfunction (2010-2023).
- Analysis of clinical, laboratory, imaging (including cardiac MRI), and pathological data.
- Six-month outcome assessment.
Main Results:
- The cohort was predominantly female (90%) with diffuse cutaneous SSc (70%) and significant hemodynamic instability.
- All patients had pericardial effusion, and cardiac MRI revealed late gadolinium enhancement, prolonged T2 relaxation times, and reduced left ventricular ejection fraction (LVEF).
- Myocarditis with inflammatory cell infiltration was confirmed pathologically; in-hospital mortality was 60%, with limited LVEF recovery at six months in survivors.
Conclusions:
- Acute ventricular dysfunction and cardiogenic shock in SSc are associated with high mortality and poor recovery.
- The phenotype is linked to diffuse cutaneous SSc and musculoskeletal involvement, with myocarditis as a probable underlying mechanism.
- There is an urgent need for enhanced cardiac-focused management strategies for SSc patients.
Abstract:
Cardiac involvement in systemic sclerosis (SSc) is a major cause of morbidity and mortality, with ventricular dysfunction and cardiogenic shock being among the most severe complications. The underlying causes of acute ventricular dysfunction in these patients remain unclear. This observational study included 10 SSc patients admitted with cardiogenic shock and acute ventricular dysfunction between 2010 and 2023, excluding those with prior heart disease. Clinical, laboratory, imaging, and pathological data were analyzed, with outcomes assessed at six months. The cohort was 90% female, with a mean age of 58.8 ± 3.8 years. Most had diffuse cutaneous SSc (70%) and musculoskeletal involvement (50%), with an average disease duration of 4.8 ± 5.2 years. All patients presented with severe hemodynamic instability, with a mean systolic blood pressure of 78.4 ± 6.7 mmHg and elevated troponin levels (2077 ± 3379 ng/L). Pericardial effusion was observed in all, and 30% required pericardiocentesis. CMR showed presence of late gadolinium enhancement and prolonged T2 relaxation time and reduced ventricular function (LVEF 31 ± 8%). Biopsies revealed myocarditis with T lymphocyte and macrophage infiltration. In-hospital mortality was 60%. Among survivors, partial ventricular recovery was seen at six months, with an average LVEF improvement of 10 ± 10%. SSc patients with cardiogenic shock and acute ventricular dysfunction face high mortality and limited recovery. The phenotype is associated with diffuse cutaneous SSc and musculoskeletal involvement, likely driven by myocarditis, highlighting the need for improved cardiac-focused treatments in SSc.
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