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dc.contributor.authorLlerena-Velastegui J.
dc.contributor.authorSantafe-Abril G.
dc.contributor.authorVillacis-Lopez C.
dc.contributor.authorHurtado-Alzate C.
dc.contributor.authorPlacencia-Silva M.
dc.contributor.authorSantander-Aldean M.
dc.contributor.authorTrujillo-Delgado M.
dc.contributor.authorFreire-Oña X.
dc.date.accessioned2024-11-12T13:43:11Z
dc.date.available2024-11-12T13:43:11Z
dc.date.issued2024
dc.identifier.issn1462806
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85177870744&doi=10.1016%2fj.cpcardiol.2023.102118&partnerID=40&md5=f66088e61e00ffa3a87120c3a687431f
dc.identifier.urihttp://hdl.handle.net/10818/62792
dc.description.abstractLeft ventricular assist devices (LVADs) have marked a milestone in the evolution of treatment for patients with end-stage heart failure. Their popularity and use are steadily rising. This systematic review and meta-analysis aimed to evaluate the effectiveness of LVADs in improving the survival rate of patients with end-stage heart failure and to identify the complications or adverse events associated with LVAD use. Articles for this systematic review and meta-analysis were sourced from PubMed, Google Scholar, and the Cochrane Library databases. Only studies that met the predefined PICOS eligibility criteria were analyzed. LVADs significantly improved the 6, 12, 18, and 24-month survival rates in patients with end-stage heart failure compared to no LVAD or other therapies: OR 1.87 (95%CI [1.27-2.76]), OR 2.29 (95%CI [1.61-3.26]), OR 2.07 (95%CI [0.61-6.61]), and OR 1.73 (95%CI [0.88-3.41]) for 6, 12, 18, and 24 months, respectively. The incidence of adverse events was significantly higher in the LVAD group than in the non-LVAD treatments: bleeding OR 12.53 (95%CI [2.60-60.41]), infections OR 4.15 (95%CI [1.19-14.45]), stroke OR 2.58 (95%CI [1.38-4.82]), and arrhythmia OR 2.81 (95%CI [1.64-4.80]). Overall, complications were higher in the LVAD group compared to those without LVAD treatment. Hospital readmissions due to adverse events were significantly more frequent in the LVAD group, OR 2.98 (95%CI [1.38-6.43]). Despite the elevated risk of adverse events associated with LVADs, these devices have demonstrated a notable enhancement in the survival outcomes for patients with end-stage heart failure. © 2023 Elsevier Inc.en
dc.formatapplication/pdfes_CO
dc.language.isoenges_CO
dc.publisherCurrent Problems in Cardiologyes_CO
dc.relation.ispartofseriesCurrent Problems in Cardiology Vol. 49 N° 1
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceUniversidad de La Sabanaes_CO
dc.sourceIntellectum Repositorio Universidad de La Sabanaes_CO
dc.titleEfficacy and Complication Profiles of Left Ventricular Assist Devices in Adult Heart Failure Management: A Systematic Review and Meta-Analysisen
dc.typejournal articlees_CO
dc.type.hasVersionpublishedVersiones_CO
dc.rights.accessRightsopenAccesses_CO
dc.identifier.doi10.1016/j.cpcardiol.2023.102118


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