Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/29861
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dc.contributor.authorMARTENS, Pieter-
dc.contributor.authorNUYENS, Dieter-
dc.contributor.authorRivero-Ayerza, Maximo-
dc.contributor.authorVan Herendael, Hugo-
dc.contributor.authorVercammen, Jan-
dc.contributor.authorCeyssens, Wendy-
dc.contributor.authorLuwel, Evert-
dc.contributor.authorDUPONT, Matthias-
dc.contributor.authorMULLENS, Wilfried-
dc.date.accessioned2019-10-28T12:38:04Z-
dc.date.available2019-10-28T12:38:04Z-
dc.date.issued2019-
dc.identifier.citationCLINICAL RESEARCH IN CARDIOLOGY, 108(10), p. 1074-1082-
dc.identifier.issn1861-0684-
dc.identifier.urihttp://hdl.handle.net/1942/29861-
dc.description.abstractBackground Sacubitril/valsartan reduced the occurrence of sudden cardiac death in the PARADIGM-HF trial. However, limited information is available about the mechanism. Methods Heart failure (HF)-patients receiving sacubitril/valsartan for a class-I indication equipped with an implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy (CRT) with remote tele-monitoring were retrospectively analyzed. Device-registered arrhythmic-events were determined [ventricular tachycardia/fibrillation (VT/VF), appropriate therapy, non-sustained VT (NsVT; > 4beats and < 30 s), hourly premature ventricular contraction (PVC)-burden], following sacubitril/valsartan initiation (incident-analysis) and over an equal time period before initiation (antecedent-analysis). Reverse remodeling to sacubitril/valsartan was defined as an improvement of left ventricular ejection fraction of >= 5% between baseline and follow-up. Results A-total of 151 HF-patients with reduced LVEF (29 +/- 9%) were included. Patients were switched from ACE-I or ARB to equal doses of sacubitril/valsartan (expressed as %-target-dose; before = 58 +/- 30% vs. after = 56 +/- 27%). The mean follow-up of both the incident and antecedent analysis was 364 days. Following the initiation, VT/VF-burden dropped (individual patients with VT/VF pre_n = 19 vs. post_n = 10, total-episodes of VT/VF pre_n = 51 vs. post_n = 14, both p < 0.001), resulting in reduced occurrence of appropriate therapy (pre_n = 16 vs. post_n = 6; p < 0.001). NsVT-burden per patient also dropped (mean episodes pre_n = 7.7 +/- 11.8 vs. post_n = 3.7 +/- 5.4; p < 0.001). There was no impact on atrial-fibrillation burden. PVC-burden dropped significantly which was associated with an improvement in BiV-pacing in patients with < 90% BiV-pacing at baseline. A higher degree of reverse remodeling was associated with a lower burden of NsVT and PVCs (both p < 0.05). Conclusion Initiation of sacubitril/valsartan is associated with a lower degree of VT/VF, resulting in less ICD-interventions. This beneficial effect on ventricular arrhythmias might be related to cardiac reverse remodeling.-
dc.description.sponsorshipPieter Martens is supported by a doctoral fellowship by the Research Foundation-Flanders (FWO, Grant number: 1127917N). Pieter Martens and Wilfried Mullens are researchers for the Limburg Clinical Research Program (LCRP) UHasselt-ZOL-Jessa, supported by the foundation Limburg Sterk Merk (LSM), Hasselt University, Ziekenhuis Oost-Limburg and Jessa Hospital.-
dc.language.isoen-
dc.publisherSPRINGER HEIDELBERG-
dc.rightsSpringer-Verlag GmbH Germany, part of Springer Nature 2019-
dc.subject.otherSacubitril/valsartan; Pharmacology; Heart failure; Ventricular arrhythmias; Reverse remodeling-
dc.subject.otherSacubitril; valsartan; Pharmacology; Heart failure; Ventricular arrhythmias; Reverse remodeling-
dc.titleSacubitril/valsartan reduces ventricular arrhythmias in parallel with left ventricular reverse remodeling in heart failure with reduced ejection fraction-
dc.typeJournal Contribution-
dc.identifier.epage1082-
dc.identifier.issue10-
dc.identifier.spage1074-
dc.identifier.volume108-
local.format.pages9-
local.bibliographicCitation.jcatA1-
dc.description.notes[Martens, Pieter; Nuyens, Dieter; Rivero-Ayerza, Maximo; Van Herendael, Hugo; Vercammen, Jan; Ceyssens, Wendy; Luwel, Evert; Dupont, Matthias; Mullens, Wilfried] Ziekenhuis Oost Limburg, Dept Cardiol, Schiepse Bos 6, B-3600 Genk, Belgium. [Martens, Pieter] Hasselt Univ, Doctoral Sch Med & Life Sci, Diepenbeek, Belgium. [Mullens, Wilfried] Hasselt Univ, Fac Med & Life Sci, Biomed Res Inst, Diepenbeek, Belgium.-
local.publisher.placeHEIDELBERG-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1007/s00392-019-01440-y-
dc.identifier.isi000487041600002-
item.accessRightsRestricted Access-
item.fulltextWith Fulltext-
item.validationecoom 2020-
item.contributorMARTENS, Pieter-
item.contributorNUYENS, Dieter-
item.contributorRivero-Ayerza, Maximo-
item.contributorVan Herendael, Hugo-
item.contributorVercammen, Jan-
item.contributorCeyssens, Wendy-
item.contributorLuwel, Evert-
item.contributorDUPONT, Matthias-
item.contributorMULLENS, Wilfried-
item.fullcitationMARTENS, Pieter; NUYENS, Dieter; Rivero-Ayerza, Maximo; Van Herendael, Hugo; Vercammen, Jan; Ceyssens, Wendy; Luwel, Evert; DUPONT, Matthias & MULLENS, Wilfried (2019) Sacubitril/valsartan reduces ventricular arrhythmias in parallel with left ventricular reverse remodeling in heart failure with reduced ejection fraction. In: CLINICAL RESEARCH IN CARDIOLOGY, 108(10), p. 1074-1082.-
crisitem.journal.issn1861-0684-
crisitem.journal.eissn1861-0692-
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