E. Terauda
5 Papers
E. Terauda is an academic researcher. The author has contributed to research in topics: Familial hypercholesterolemia & Medicine. The author has co-authored 1 publications.
Chat about Author
Papers
Management of high-risk acute pulmonary embolism: an emulated target trial analysis.
A. Stadlbauer,Tom Verbelen,Leonhard Binzenhöfer,Tomaž Goslar,Alexander Supady,P. M. Spieth,Marko Noč,Andreas Verstraete,Sabine Hoffmann,Michael Schomaker,Julia Höpler,Marie Kraft,Esther Tautz,Daniel Hoyer,Jörn Tongers,Franz Haertel,Aschraf El-Essawi,Mostafa Salem,Rafael Henrique Rangel,Carsten Hullermann,Marvin Kriz,B. Schrage,Jorge Moisés,M. Sabate,F. Pappalardo,Lisa Crusius,N. Mangner,Christoph Adler,Tobias Tichelbäcker,C. Skurk,Christian Jung,Sebastian Kufner,T. Graf,C. Scherer,Laura E. Villegas Sierra,Hannah Billig,Nicolas Majunke,Walter S. Speidl,Robert Zilberszac,Luis Chiscano-Camón,A. Uribarri,Jordi Riera,Roberto Roncon-Albuquerque,E. Terauda,A. Erglis,Guido Tavazzi,U. Zeymer,Maike Knorr,Juliane Kilo,Sven Möbius-Winkler,Robert H. G. Schwinger,Derk Frank,Oliver Borst,H. Häberle,F. De Roeck,Christiaan J M Vrints,C. Schmid,Georg Nickenig,Christian Hagl,Steffen Massberg,Andreas Schäfer,Dirk Westermann,Sebastian Zimmer,Alain Combes,Daniele Camboni,Holger Thiele,Enzo Lüsebrink +66 more
TL;DR: This study emulates a target trial to evaluate in-hospital mortality in 991 high-risk acute pulmonary embolism patients, comparing four advanced treatment strategies: VA-ECMO, intrahospital thrombolysis, surgical thrombectomy, and percutaneous catheter-directed treatment, with VA-ECMO alone showing highest mortality risk.
2
Number of lipid-lowering medications and attainment of lipid goals in familial hypercholesterolemia patients: Data from the Latvian registry
Georgijs Nesterovics,Vita Saripo,R. Meiere,E. Terauda,G. Skudrina,D. Gilis,Andrejs Erglis,Gustavs Latkovskis +7 more
TL;DR: In this paper , the authors provide contemporary data on the number of used LDL lowering medications, achieved lipid levels and attainment of LDL-C goals in FH patients from the Latvian Registry of FH (LRFH).
Genetic Characteristics of Latvian Patients with Familial Hypercholesterolemia: The First Analysis from Genome-Wide Sequencing
Gustavs Latkovskis,Raimonds Rescenko-Krums,Georgijs Nesterovics,Monta Brīvība,Vita Saripo,D. Gilis,E. Terauda,R. Meiere,G. Skudrina,Andrejs Erglis,Joana Rita Chora,Mafalda Bourbon,Janis Klovins +12 more
TL;DR: Despite the high clinical likelihood of FH, confirmed P/LP variants were detected in only 20.9% of patients in the Latvian cohort when assessed with genome-wide next generation sequencing.
Prehospital thrombolytic treatment of high-risk acute pulmonary embolism
Hugo Lanz,Leonhard Binzenhöfer,Tom Verbelen,A. Stadlbauer,Daniele Camboni,Sebastian Zimmer,Georg Nickenig,H. Thiele,Enzo Lüsebrink,F. Pappalardo,F. De Roeck,Christiaan J M Vrints,A. Uribarri,Jorge Moisés,M. Sabaté,Jeisson Osorio,Luis Chiscano-Camón,Jordi Riera,Carsten Skurk,Hannah Billig,Christoph Adler,T. Tichelbäcker,P. M. Spieth,Lisa Crusius,N. Mangner,Christian Jung,D. Westermann,Esther Tautz,Alexander Supady,Kirsten Krüger,Karl Toischer,Aschraf El-Essawi,Daniel Hoyer,Jörn Tongers,Jochen Dutzmann,Andreas Schäfer,Mostafa Salem,Derk Frank,Marvin Kriz,Benedikt Schrage,Benedikt N Beer,Franz Haertel,Sven Möbius-Winkler,Nicolas Majunke,Tom Adriaenssens,A. Verstraete,Tomaž Goslar,Marko Noč,T. Graf,I. Eitel,Maike Knorr,C. Scherer,Laura Villegas Sierra,Nils Gade,Daniel Roden,Inas Saleh,S. Hoffmann,Michael Schomaker,Julia Höpler,Marie Kraft,Sebastian Kufner,Karsten P Hug,Christian Hagl,Sven Peterss,Nikolaus Kneidinger,Carsten Hullermann,Jan Sackarnd,Alain Combes,Guido Tavazzi,C. Schmid,E. Terauda,A. Erglis,Evija Camane,Santa Strazdina,Liga Vidusa,Oliver Borst,H. Häberle,Walter S. Speidl,Robert Zilberszac,Robert H. G. Schwinger,Silvia Klinger,Antonia Wechsler +81 more
Genetic spectrum in Latvian patients with familial hypercholesterolemia: First data from a whole genome sequencing study
Gustavs Latkovskis,R. Reščenko,Georgijs Nesterovics,M. Briviba,Vita Saripo,D. Gilis,R. Meiere,E. Terauda,G. Skudrina,Andrejs Erglis,Joana Rita Chora,Mafalda Bourbon,Janis Klovins +12 more
TL;DR: This study reports the first whole-genome sequencing data on Latvian patients with familial hypercholesterolemia, detecting 15 pathogenic variants in 34 patients (20.7% diagnostic yield) and highlighting the need for further analysis of polygenic mechanisms and larger sample sizes.