Left ventricular assist device driveline infections in three contemporary devices.
Adult
Aged
Biomarkers
/ blood
C-Reactive Protein
/ analysis
Female
Fibrinogen
/ analysis
Follow-Up Studies
Heart Failure
/ surgery
Heart-Assist Devices
/ adverse effects
Humans
Leukocyte Count
Male
Middle Aged
Patient Readmission
/ statistics & numerical data
Prosthesis-Related Infections
/ blood
Retrospective Studies
Risk Assessment
/ methods
Risk Factors
driveline infection
mechanical circulatory support
readmission
risk factors
ventricular assist device
Journal
Artificial organs
ISSN: 1525-1594
Titre abrégé: Artif Organs
Pays: United States
ID NLM: 7802778
Informations de publication
Date de publication:
May 2021
May 2021
Historique:
revised:
23
09
2020
received:
27
07
2020
accepted:
06
10
2020
pubmed:
15
10
2020
medline:
6
11
2021
entrez:
14
10
2020
Statut:
ppublish
Résumé
Driveline infections (DLI) are common adverse events in left ventricular assist devices (LVADs), leading to severe complications and readmissions. The study aims to characterize risk factors for DLI readmission 2 years postimplant. This single-center study included 183 LVAD patients (43 HeartMate II [HMII], 29 HeartMate 3 [HM3], 111 HVAD) following hospital discharge between 2013 and 2017. Demographics, clinical parameters, and outcomes were retrospectively analyzed and 12.6% of patients were readmitted for DLI, 14.8% experienced DLI but were treated in the outpatient setting, and 72.7% had no DLI. Mean C-reactive protein (CRP), leukocytes and fibrinogen were higher in patients with DLI readmission (P < .02) than in outpatient DLI and patients without DLI, as early as 60 days before readmission. Freedom from DLI readmission was comparable for HMII and HVAD (98% vs. 87%; HR, 4.52; 95% CI, 0.58-35.02; P = .15) but significantly lower for HM3 (72%; HR, 10.82; 95% CI, 1.26-92.68; P = .03). DLI (HR, 1.001; 95% CI, 0.999-1.002; P = .16) or device type had no effect on mortality. DLI readmission remains a serious problem following LVAD implantation, where CRP, leukocytes, and fibrinogen might serve as risk factors already 60 days before. HM3 patients had a higher risk for DLI readmissions compared to HVAD or HMII, possibly because of device-specific driveline differences.
Identifiants
pubmed: 33052592
doi: 10.1111/aor.13843
pmc: PMC8247301
doi:
Substances chimiques
Biomarkers
0
Fibrinogen
9001-32-5
C-Reactive Protein
9007-41-4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
464-472Subventions
Organisme : Austrian Science Fund
ID : FWF-KLI 357
Informations de copyright
© 2020 The Authors. Artificial Organs published by International Center for Artificial Organs and Transplantation and Wiley Periodicals LLC.
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