dc.contributor.author
Hadzibegovic, Sara
dc.contributor.author
Lena, Alessia
dc.contributor.author
Churchill, Timothy W.
dc.contributor.author
Ho, Jennifer E.
dc.contributor.author
Potthoff, Sophia
dc.contributor.author
Denecke, Corinna
dc.contributor.author
Rösnick, Lukas
dc.contributor.author
Heim, Katrin Moira
dc.contributor.author
Kleinschmidt, Malte
dc.contributor.author
Sander, Leif Erik
dc.contributor.author
Witzenrath, Martin
dc.contributor.author
Suttorp, Norbert
dc.contributor.author
Krannich, Alexander
dc.contributor.author
Porthun, Jan
dc.contributor.author
Friede, Tim
dc.contributor.author
Butler, Javed
dc.contributor.author
Wilkenshoff, Ursula
dc.contributor.author
Pieske, Burkert
dc.contributor.author
Landmesser, Ulf
dc.contributor.author
Anker, Stefan D.
dc.contributor.author
Lewis, Gregory D.
dc.contributor.author
Tschöpe, Carsten
dc.contributor.author
Anker, Markus S.
dc.date.accessioned
2022-12-09T15:49:47Z
dc.date.available
2022-12-09T15:49:47Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/37242
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-36954
dc.description.abstract
Aims: Viral-induced cardiac inflammation can induce heart failure with preserved ejection fraction (HFpEF)-like syndromes. COVID-19 can lead to myocardial damage and vascular injury. We hypothesised that COVID-19 patients frequently develop a HFpEF-like syndrome, and designed this study to explore this.
Methods and results: Cardiac function was assessed in 64 consecutive, hospitalized, and clinically stable COVID-19 patients from April-November 2020 with left ventricular ejection fraction (LVEF) ≥50% (age 56 ± 19 years, females: 31%, severe COVID-19 disease: 69%). To investigate likelihood of HFpEF presence, we used the HFA-PEFF score. A low (0-1 points), intermediate (2-4 points), and high (5-6 points) HFA-PEFF score was observed in 42%, 33%, and 25% of patients, respectively. In comparison, 64 subjects of similar age, sex, and comorbidity status without COVID-19 showed these scores in 30%, 66%, and 4%, respectively (between groups: P = 0.0002). High HFA-PEFF scores were more frequent in COVID-19 patients than controls (25% vs. 4%, P = 0.001). In COVID-19 patients, the HFA-PEFF score significantly correlated with age, estimated glomerular filtration rate, high-sensitivity troponin T (hsTnT), haemoglobin, QTc interval, LVEF, mitral E/A ratio, and H2 FPEF score (all P < 0.05). In multivariate, ordinal regression analyses, higher age and hsTnT were significant predictors of increased HFA-PEFF scores. Patients with myocardial injury (hsTnT ≥14 ng/L: 31%) vs. patients without myocardial injury, showed higher HFA-PEFF scores [median 5 (interquartile range 3-6) vs. 1 (0-3), P < 0.001] and more often showed left ventricular diastolic dysfunction (75% vs. 27%, P < 0.001).
Conclusion: Hospitalized COVID-19 patients frequently show high likelihood of presence of HFpEF that is associated with cardiac structural and functional alterations, and myocardial injury. Detailed cardiac assessments including echocardiographic determination of left ventricular diastolic function and biomarkers should become routine in the care of hospitalized COVID-19 patients.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
High-sensitivity troponin T
en
dc.subject
Diastolic dysfunction
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Heart failure with preserved ejection fraction according to the HFA-PEFF score in COVID-19 patients: clinical correlates and echocardiographic findings
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1002/ejhf.2210
dcterms.bibliographicCitation.journaltitle
European Journal of Heart Failure
dcterms.bibliographicCitation.number
11
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.pagestart
1891
dcterms.bibliographicCitation.pageend
1902
dcterms.bibliographicCitation.volume
23
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
33932255
dcterms.isPartOf.issn
1388-9842
dcterms.isPartOf.eissn
1879-0844