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Published on: February 12, 2011
Characterisation of Post-Sepsis Cardiomyopathy Using Cardiovascular Magnetic Resonance
Samuel Malomo1, Thomas Oswald1, Edward Stephenson1
1Sussex Cardiac Centre, Royal Sussex County Hospital, Brighton BN2 5BE, UK.
Insights
Post-sepsis cardiomyopathy often involves left ventricular (LV) enlargement and dysfunction, with evidence of myocardial fibrosis but not significant edema weeks after sepsis recovery. This understanding is crucial for developing new treatments for this condition.
Area of Science:
- Cardiology
- Intensive Care Medicine
- Medical Imaging
Background:
- Post-sepsis cardiomyopathy (PSC) is linked to poor cardiovascular outcomes but is poorly understood, hindering therapeutic development.
- Characterizing PSC is essential for advancing treatment strategies and improving patient prognosis.
- Cardiovascular magnetic resonance (CMR) imaging offers a detailed method for assessing cardiac structure and function in PSC.
Purpose of the Study:
- To characterize the cardiac manifestations of post-sepsis cardiomyopathy (PSC) using cardiovascular magnetic resonance (CMR) imaging.
- To investigate the presence of myocardial fibrosis and edema in patients recovering from sepsis.
- To provide insights into the pathophysiology of PSC for future therapeutic interventions.
Main Methods:
- A cohort of 22 patients with acute sepsis and suspected cardiac injury underwent CMR (cines, T1/T2-mapping, LGE) 47 days (IQR: 22-122) post-admission.
- Age- and gender-matched healthy controls (n=16) were included for comparison.
- CMR parameters assessed included left ventricular (LV) volumes, ejection fraction, and myocardial tissue characterization (native T1/T2, LGE).
Main Results:
- 59% of post-sepsis patients exhibited left ventricular (LV) dilatation with significantly elevated LV volumes compared to controls.
- 50% of patients had LV systolic dysfunction (ejection fraction < 50%), with most showing non-ischaemic late gadolinium enhancement (LGE).
- Elevated septal native T1 values indicated myocardial fibrosis, while similar T2 values suggested minimal myocardial edema weeks post-sepsis.
Conclusions:
- Post-sepsis cardiomyopathy is characterized by LV dilatation, systolic dysfunction, and non-ischaemic myocardial fibrosis.
- Significant myocardial edema is not a prominent feature several weeks after sepsis recovery.
- Further multi-center studies are required to validate these findings and develop targeted therapies for PSC.
Abstract:
Background: Post-sepsis cardiomyopathy is associated with an increased risk of adverse cardiovascular outcomes. It remains poorly understood, which limits therapeutic development. This study characterised post-sepsis cardiomyopathy using cardiovascular magnetic resonance (CMR) imaging. Methods: Patients admitted with acute sepsis and suspected cardiac injury or heart failure who subsequently (47 days [IQR: 22-122]) underwent CMR at a UK tertiary cardiac centre were included. Age- and gender-matched controls (n = 16) were also included. Subjects underwent CMR at 1.5 Tesla with cines, native T1- and T2-mapping, and late gadolinium enhancement (LGE) imaging. Results: Of the 22 post-sepsis patients (age 50 ± 13 years; 64% males), 13 patients (59%) had left ventricular (LV) dilatation. Patients had significantly elevated left ventricular (LV) end-diastolic and end-systolic volume indices compared to controls (p = 0.011 and p = 0.013, respectively). Eleven patients (50%) had LV systolic dysfunction (ejection fraction < 50%), most of whom (8/11) had non-ischaemic patterns of LGE (n = 7 mid-wall; n = 1 mid-wall/patchy). In the eleven patients with preserved LV systolic function (ejection fraction ≥ 50%), three patients (27%) had significant LGE (n = 1 mid-wall; n = 1 subepicardial/mid-wall; n = 1 patchy). Compared to controls, patients had elevated septal native myocardial T1 values (p < 0.001) but similar septal native myocardial T2 values (p = 0.090), suggesting the presence of myocardial fibrosis without significant oedema. Conclusions: Post-sepsis cardiomyopathy is characterised by LV dilatation, systolic dysfunction, and myocardial fibrosis in a non-ischaemic distribution. Significant myocardial oedema is not prominent several weeks post-recovery. Further work is needed to test these findings on a multi-centre basis and to develop novel therapies for post-sepsis cardiomyopathy.
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