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Myocardial Perfusion Imaging After Severe COVID-19 Infection Demonstrates Regional Ischemia Rather Than Global Blood Flow Reduction.
Thornton, George D; Shetye, Abhishek; Knight, Dan S; Knott, Kris; Artico, Jessica; Kurdi, Hibba; Yousef, Souhad; Antonakaki, Dimitra; Razvi, Yousuf; Chacko, Liza; Brown, James; Patel, Rishi; Vimalesvaran, Kavitha; Seraphim, Andreas; Davies, Rhodri; Xue, Hui; Kotecha, Tushar; Bell, Robert; Manisty, Charlotte; Cole, Graham D; Moon, James C; Kellman, Peter; Fontana, Marianna; Treibel, Thomas A.
  • Thornton GD; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Shetye A; Institute of Cardiovascular Science, University College, London, United Kingdom.
  • Knight DS; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Knott K; Institute of Cardiovascular Science, University College, London, United Kingdom.
  • Artico J; Institute of Cardiovascular Science, University College, London, United Kingdom.
  • Kurdi H; Royal Free London NHS Foundation Trust, London, United Kingdom.
  • Yousef S; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Antonakaki D; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Razvi Y; Institute of Cardiovascular Science, University College, London, United Kingdom.
  • Chacko L; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Brown J; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Patel R; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Vimalesvaran K; Royal Free London NHS Foundation Trust, London, United Kingdom.
  • Seraphim A; Division of Medicine, National Amyloidosis Center, University College, London, United Kingdom.
  • Davies R; Royal Free London NHS Foundation Trust, London, United Kingdom.
  • Xue H; Division of Medicine, National Amyloidosis Center, University College, London, United Kingdom.
  • Kotecha T; Royal Free London NHS Foundation Trust, London, United Kingdom.
  • Bell R; Division of Medicine, National Amyloidosis Center, University College, London, United Kingdom.
  • Manisty C; Royal Free London NHS Foundation Trust, London, United Kingdom.
  • Cole GD; Division of Medicine, National Amyloidosis Center, University College, London, United Kingdom.
  • Moon JC; Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Kellman P; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Fontana M; Barts Heart Center, Barts Health NHS Trust, London, United Kingdom.
  • Treibel TA; Institute of Cardiovascular Science, University College, London, United Kingdom.
Front Cardiovasc Med ; 8: 764599, 2021.
Article in English | MEDLINE | ID: covidwho-1598692
ABSTRACT

Background:

Acute myocardial damage is common in severe COVID-19. Post-mortem studies have implicated microvascular thrombosis, with cardiovascular magnetic resonance (CMR) demonstrating a high prevalence of myocardial infarction and myocarditis-like scar. The microcirculatory sequelae are incompletely characterized. Perfusion CMR can quantify the stress myocardial blood flow (MBF) and identify its association with infarction and myocarditis.

Objectives:

To determine the impact of the severe hospitalized COVID-19 on global and regional myocardial perfusion in recovered patients.

Methods:

A case-control study of previously hospitalized, troponin-positive COVID-19 patients was undertaken. The results were compared with a propensity-matched, pre-COVID chest pain cohort (referred for clinical CMR; angiography subsequently demonstrating unobstructed coronary arteries) and 27 healthy volunteers (HV). The analysis used visual assessment for the regional perfusion defects and AI-based segmentation to derive the global and regional stress and rest MBF.

Results:

Ninety recovered post-COVID patients {median age 64 [interquartile range (IQR) 54-71] years, 83% male, 44% requiring the intensive care unit (ICU)} underwent adenosine-stress perfusion CMR at a median of 61 (IQR 29-146) days post-discharge. The mean left ventricular ejection fraction (LVEF) was 67 ± 10%; 10 (11%) with impaired LVEF. Fifty patients (56%) had late gadolinium enhancement (LGE); 15 (17%) had infarct-pattern, 31 (34%) had non-ischemic, and 4 (4.4%) had mixed pattern LGE. Thirty-two patients (36%) had adenosine-induced regional perfusion defects, 26 out of 32 with at least one segment without prior infarction. The global stress MBF in post-COVID patients was similar to the age-, sex- and co-morbidities of the matched controls (2.53 ± 0.77 vs. 2.52 ± 0.79 ml/g/min, p = 0.10), though lower than HV (3.00 ± 0.76 ml/g/min, p< 0.01).

Conclusions:

After severe hospitalized COVID-19 infection, patients who attended clinical ischemia testing had little evidence of significant microvascular disease at 2 months post-discharge. The high prevalence of regional inducible ischemia and/or infarction (nearly 40%) may suggest that occult coronary disease is an important putative mechanism for troponin elevation in this cohort. This should be considered hypothesis-generating for future studies which combine ischemia and anatomical assessment.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Language: English Journal: Front Cardiovasc Med Year: 2021 Document Type: Article Affiliation country: Fcvm.2021.764599

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Language: English Journal: Front Cardiovasc Med Year: 2021 Document Type: Article Affiliation country: Fcvm.2021.764599