G
Gerard C.M. Linssen
Researcher at University Medical Center Groningen
Publications - 81
Citations - 3040
Gerard C.M. Linssen is an academic researcher from University Medical Center Groningen. The author has contributed to research in topics: Stent & Population. The author has an hindex of 23, co-authored 81 publications receiving 2326 citations.
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Journal ArticleDOI
The Na^+/H^+ exchange inhibitor eniporide as an adjunct to early reperfusion therapy for acute myocardial infarction : Results of the evaluation of the safety and cardioprotective effects of eniporide in acute myocardial infarction (ESCAMI) trial
Uwe Zeymer,Harry Suryapranata,Jean Pierre Monassier,Grzegorz Opolski,John Davies,Gundars Rasmanis,Gerard C.M. Linssen,Ulrich Tebbe,Rolf Schröder,Rolf Tiemann,Thomas Machnig,Karl-Ludwig Neuhaus +11 more
TL;DR: Administration of the NHE-1 inhibitor eniporide, before reperfusion therapy in patients with acute ST elevation MI, did not limit infarct size or improve clinical outcome, but there was a significant reduction of the incidence of heart failure in patients reperfused late (>4 h).
Journal ArticleDOI
Sacubitril/Valsartan Across the Spectrum of Ejection Fraction in Heart Failure
Scott D. Solomon,Muthiah Vaduganathan,Brian Claggett,Milton Packer,Milton Packer,Michael R. Zile,Michael R. Zile,Karl Swedberg,Karl Swedberg,Jean L. Rouleau,Marc A. Pfeffer,Akshay S. Desai,Lars Lund,Lars Køber,Inder S. Anand,Nancy K. Sweitzer,Gerard C.M. Linssen,Béla Merkely,Juan Luis Arango,Dragos Vinereanu,Chen Huan Chen,Michele Senni,Antonio S. Sibulo,Sergey Boytsov,Victor Shi,Adel R. Rizkala,Martin Lefkowitz,John J.V. McMurray +27 more
TL;DR: The therapeutic effects of sacubitril/valsartan, compared with a renin-angiotensin-aldosterone–system inhibitor alone, vary by LVEF with treatment benefits, particularly for heart failure hospitalization, that appear to extend to patients with heart failure and mildly reduced ejection fraction.
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A randomized controlled trial in second-generation zotarolimus-eluting Resolute stents versus everolimus-eluting Xience V stents in real-world patients: the TWENTE trial
Clemens von Birgelen,Mounir W.Z. Basalus,Kenneth Tandjung,K. Gert van Houwelingen,Martin G. Stoel,J. (Hans) W. Louwerenburg,Gerard C.M. Linssen,Salah A.M. Saïd,Miep A.W.J. Kleijne,Hanim Sen,Marije M. Löwik,Job van der Palen,Job van der Palen,Patrick M.J. Verhorst,Frits H.A.F. de Man +14 more
TL;DR: Resolute ZES were noninferior to Xience V EES in treating "real-world" patients with a vast majority of complex lesions and "off-label" indications for drug-eluting stents, which were implanted with liberal use of post-dilation.
Journal ArticleDOI
Very thin strut biodegradable polymer everolimus-eluting and sirolimus-eluting stents versus durable polymer zotarolimus-eluting stents in allcomers with coronary artery disease (BIO-RESORT): a three-arm, randomised, non-inferiority trial
Clemens von Birgelen,Clemens von Birgelen,Marlies M. Kok,Liefke C. van der Heijden,Peter W. Danse,Carl E. Schotborgh,Martijn Scholte,R. Melvyn Tjon Joe Gin,Samer Somi,K.G. van Houwelingen,Martin G. Stoel,Frits H.A.F. de Man,J. (Hans) W. Louwerenburg,Marc Hartmann,Paolo Zocca,Gerard C.M. Linssen,Job van der Palen,Job van der Palen,Carine J.M. Doggen,Marije M. Löwik +19 more
TL;DR: This large-scale, investigator-initiated, multicentre, assessor and patient blinded, three-arm, randomised, BIO-RESORT non-inferiority trial investigated in allcomers the safety and efficacy of three stents eluting either everolimus, sirolimus, or zotarlimus, of which the biodegradable polymer everolitus-eluting stent was never before assessed.
Journal ArticleDOI
Third-generation zotarolimus-eluting and everolimus-eluting stents in all-comer patients requiring a percutaneous coronary intervention (DUTCH PEERS): a randomised, single-blind, multicentre, non-inferiority trial
Clemens von Birgelen,Clemens von Birgelen,Hanim Sen,Ming Kai Lam,Peter W. Danse,Gillian A.J. Jessurun,Raymond W.M. Hautvast,Gert van Houwelingen,Alexander R. Schramm,R. Melvyn Tjon Joe Gin,J. (Hans) W. Louwerenburg,Frits H.A.F. de Man,Martin G. Stoel,Marije M. Löwik,Gerard C.M. Linssen,Salah A.M. Saïd,Mark B. Nienhuis,Patrick M.J. Verhorst,Mounir W.Z. Basalus,Catharina Jacoba Maria Doggen,Kenneth Tandjung +20 more
TL;DR: Ease of stent delivery was shown by very low numbers of patients requiring treatment other than their assigned study treatment, and non-inferior to the everolimus-eluting stent, and 12-month follow-up results were available for 1810 patients.