Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/28568
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dc.contributor.authorMARTENS, Pieter-
dc.contributor.authorVercammen, Jan-
dc.contributor.authorCeyssens, Wendy-
dc.contributor.authorJacobs, Linda-
dc.contributor.authorLuwel, Evert-
dc.contributor.authorVan Aerde, Herwig-
dc.contributor.authorPotargent, Peter-
dc.contributor.authorRenaers, Monique-
dc.contributor.authorDUPONT, Matthias-
dc.contributor.authorMULLENS, Wilfried-
dc.date.accessioned2019-07-01T11:17:41Z-
dc.date.available2019-07-01T11:17:41Z-
dc.date.issued2018-
dc.identifier.citationESC HEART FAILURE, 5(4), p. 562-569-
dc.identifier.issn2055-5822-
dc.identifier.urihttp://hdl.handle.net/1942/28568-
dc.description.abstractAimsIn patients with palliative end-stage heart failure, interventions that could provide symptomatic relief and prevent hospital admissions are important. Ambulatory continuous intravenous inotropes have been advocated by guidelines for such a purpose. We sought to determine the effect of intravenous dobutamine on symptomatic status, hospital stay, mortality, and cost expenditure. Methods and resultsAll consecutive end-stage heart failure patients not amenable for advanced therapies and discharged with continuous intravenous home dobutamine from a single tertiary centre between April 2011 and January 2017 were retrospectively analysed. Dobutamine (fixed dose) was infused through a single-lumen central venous catheter with a small pump that was refilled by a nurse on a daily basis. Symptomatic status was longitudinally assessed as the change in New York Heart Association class and patient global assessment scale. Antecedent and incident heart failure hospitalizations were determined in a paired fashion, and cost impact was assessed. A total of 21 patients (age 779years) were followed up for 869 +/- 647days. At first follow-up (6 +/- 1weeks) after the initiation of dobutamine, patients had a significant improvement in New York Heart Association class (-1.29 +/- 0.64; P<0.001), global assessment scale (<0.001), and N-terminal pro-brain natriuretic peptide (6247 vs. 2543pg/mL; P=0.033). Incident heart failure hospitalizations assessed at 3, 6, and 12months were significantly reduced (P<0.001 for all) in comparison with antecedent heart failure hospitalizations over the same time period. Cost expenditure was significantly lower at 3 (P<0.001), 6 (P=0.005), and 12months (P=0.001) after initiation of dobutamine. Mortality rate at 1year was 48% with 9/12 (75%) patients dying at home, most often from progressive pump failure. ConclusionsContinuous intravenous home dobutamine in patients with palliative end-stage heart failure is feasible and associated with improved symptomatic status, heart failure hospitalizations, and health-care-related costs. Nevertheless, results should be interpreted in the context of the small and retrospective design. Larger studies are necessary to evaluate the effect of dobutamine in palliative end-stage heart failure.-
dc.description.sponsorshipResearch Foundation - Flanders (FWO) [1127917N]; foundation Limburg Sterk Merk (LSM); Ziekenhuis Oost-Limburg; Jessa Hospital; Hasselt University-
dc.language.isoen-
dc.publisherWILEY PERIODICALS, INC-
dc.rights2018 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology.ESC HEART FAILUREESC Heart Failure2018;5: 562–569Published online 17 January 2018 in Wiley Online Library (wileyonlinelibrary.com)DOI:10.1002/ehf2.12248This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any me-dium, provided the original work is properly cited and is not used for commercial purposes-
dc.subject.otherEnd-stage heart failure; Dobutamine; Mortality and morbidity; Cost-
dc.subject.otherEnd‐stage heart failure; Dobutamine; Mortality and morbidity; Cost-
dc.titleEffects of intravenous home dobutamine in palliative end-stage heart failure on quality of life, heart failure hospitalization, and cost expenditure-
dc.typeJournal Contribution-
dc.identifier.epage569-
dc.identifier.issue4-
dc.identifier.spage562-
dc.identifier.volume5-
local.format.pages8-
local.bibliographicCitation.jcatA1-
dc.description.notes[Martens, Pieter; Vercammen, Jan; Ceyssens, Wendy; Jacobs, Linda; 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. [Van Aerde, Herwig; Potargent, Peter] Primary Care Phys Reg Genk, Genk, Belgium. [Renaers, Monique] Wit Geel Kruis, Clin Care Pathway Home Dobutamine, Limburg, Germany. [Mullens, Wilfried] Hasselt Univ, Fac Med & Life Sci, Biomed Res Inst, Diepenbeek, Belgium.-
local.publisher.placeSAN FRANCISCO-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1002/ehf2.12248-
dc.identifier.isi000440649400003-
item.fulltextWith Fulltext-
item.fullcitationMARTENS, Pieter; Vercammen, Jan; Ceyssens, Wendy; Jacobs, Linda; Luwel, Evert; Van Aerde, Herwig; Potargent, Peter; Renaers, Monique; DUPONT, Matthias & MULLENS, Wilfried (2018) Effects of intravenous home dobutamine in palliative end-stage heart failure on quality of life, heart failure hospitalization, and cost expenditure. In: ESC HEART FAILURE, 5(4), p. 562-569.-
item.contributorMARTENS, Pieter-
item.contributorVercammen, Jan-
item.contributorCeyssens, Wendy-
item.contributorJacobs, Linda-
item.contributorLuwel, Evert-
item.contributorVan Aerde, Herwig-
item.contributorPotargent, Peter-
item.contributorRenaers, Monique-
item.contributorDUPONT, Matthias-
item.contributorMULLENS, Wilfried-
item.validationecoom 2019-
item.accessRightsOpen Access-
crisitem.journal.issn2055-5822-
crisitem.journal.eissn2055-5822-
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