S
Sverre E. Kjeldsen
Researcher at University of Oslo
Publications - 771
Citations - 95426
Sverre E. Kjeldsen is an academic researcher from University of Oslo. The author has contributed to research in topics: Blood pressure & Left ventricular hypertrophy. The author has an hindex of 94, co-authored 735 publications receiving 89059 citations. Previous affiliations of Sverre E. Kjeldsen include University of Michigan & Cornell University.
Papers
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Hypertension management during the COVID-19 pandemic: what can we learn for the future?
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888-1 N-terminal pro brain natriuretic peptide predicts cardiovascular events in patients with hypertension and left ventricular hypertrophy: A LIFE study
Michael H. Olsen,Kristian Wachtell,Christian Hall,Hans Ibsen,Jens Rokkedal,Sverre E. Kjeldsen,Richard B. Devereux,Björn Dahlöf,Per Hildebrandt +8 more
TL;DR: Nt-proBNP, more than Nt- ProANP, strongly predicts cardiovascular events in patients with hypertension and LV hypertrophy, especially in patients without diabetes or clinically overt cardiovascular disease.
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Hyper-responsiveness to low-dose epinephrine infusion in mild essential hypertension.
TL;DR: The hypertensive patients showed a hyper-responsiveness to amounts of epinephrine which corresponds well to the plasma concentration achieved during psychological and physical activity.
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Relationship of diastolic function to new or persistent electrocardiographic left ventricular hypertrophy
TL;DR: In hypertensive patients undergoing antihypertensive therapy, persistence or development of Cornell product ECG LVH at year-3 follow-up is modestly associated with LV diastolic dysfunction, suggesting that diastolics dysfunction may be a mechanism via which changing ECGLVH influences HF risk.
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Renal Denervation After Symplicity HTN-3 - Back to Basics. Review of the Evidence.
Alexandre Persu,Fadl Elmula M. Fadl Elmula,Yu Jin,Ingrid Os,Sverre E. Kjeldsen,Jan A. Staessen +5 more
TL;DR: The overall blood pressure lowering effect of RDN seems rather limited and the characteristics of true responders remain largely unknown, Accordingly, RDN is not ready for clinical practice.