Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Dec 1;68(12):1450-1458.
doi: 10.1097/MAT.0000000000001690. Epub 2022 Feb 27.

Driveline Infection in Left Ventricular Assist Device Patients: Effect of Standardized Protocols, Pathogen Type, and Treatment Strategy

Affiliations

Driveline Infection in Left Ventricular Assist Device Patients: Effect of Standardized Protocols, Pathogen Type, and Treatment Strategy

Heidi S Lumish et al. ASAIO J. .

Abstract

Driveline infection (DLI) is common after left ventricular assist device (LVAD). Limited data exist on DLI prevention and management. We investigated the impact of standardized driveline care initiatives, specific pathogens, and chronic antibiotic suppression (CAS) on DLI outcomes. 591 LVAD patients were retrospectively categorized based on driveline care initiatives implemented at our institution (2009-2019). Era (E)1: nonstandardized care; E2: standardized driveline care protocol; E3: addition of marking driveline exit site; E4: addition of "no shower" policy. 87(15%) patients developed DLI at a median (IQR) of 403(520) days. S. aureus and P. aeruginosa were the most common pathogens. 31 (36%) of DLI patients required incision and drainage (I&D) and 5 (5.7%) device exchange. P. aeruginosa significantly increased risk for initial I&D (HR 2.7, 95% CI, 1.1-6.3) and recurrent I&D or death (HR 4.2, 95% CI, 1.4-12.5). Initial I&D was associated with a significant increased risk of death (HR 2.92 (1.33-6.44); P = 0.008) when compared to patients who did not develop DLI. Implementation of standardized driveline care protocol (E2) was associated with increased 2-year freedom from DLI compared to nonstandardized care (HR 0.36, 95% CI, 0.2-0.6, P < 0.01). Additional preventive strategies (E3&E4) showed no further reduction in DLI rates. 57(65%) DLI patients received CAS, 44% of them required escalation to intravenous antibiotics and/or I&D. Presence of P. aeruginosa DLI markedly increased risk for I&D or death. Conditional survival of patients progressing to I&D is diminished. Standardized driveline care protocol was associated with a significant reduction in DLI, while additional preventive strategies require further testing.

PubMed Disclaimer

Conflict of interest statement

Disclosure: P.C.C. is recipient of a research grant from Abbott; he also serves as a consultant for the same company. Y.N. serves as a consultant for Abbott, CryoLife, and Zimmer-Biomet, and as a speaker for Nipro Co. G.T.S. serves as a consultant for Abbott. N.U. serves on advisory boards for Leviticus and Livemetric/Cormetric; he also serves as a consultant for Abbott and Medtronic. The remaining authors have no conflicts of interest to report.

Figures

Figure 1.
Figure 1.
Two-year freedom from driveline infection stratified by era. (Era 1: nonstandardized driveline care protocol; Era 2: standardized driveline care protocol; Era 3: Era 2 and marking of the positioning of driveline exit site; Era 4: Era 3 and “no shower” policy).
Figure 2.
Figure 2.
Distribution of initial pathogen (gram-positive, gram-negative, polymicrobial, culture-negative) stratified by: (A) chronic antibiotic suppression (CAS) use vs. (B) not (No CAS). (C) Antibiotic distribution among patients treated with CAS. CAS, chronic antibiotic suppression: Gram-positive: 21 methicillin-sensitive Staphylococcus aureus, 7 methicillin-resistant Staphylococcus aureus, 2 Diphtheroids, 1 Enterococcus faecalis, 3 coagulase-negative staphylococcus. Gram-negative: 15 Pseudomonas aeruginosa, 6 Serratia marcescens, 4 Klebsiella pneumoniae, 2 Stenotrophomonas maltophilia, 1 Achromobacter xylosoxidans, 1 Acinetobacter baumannii complex, 1 Burkholderia cepacia complex, 1 Enterobacter cloacae, 1 Escherichia coli, 1 Serratia liquefaciens. No CAS: Not on Chronic Antibiotic Suppression: Gram-positive: 7 methicillin-sensitive Staphylococcus aureus, 2 methicillin-resistant Staphylococcus aureus, 1 coagulase-negative staphylococcus, 1 Corynebacterium striatum, 1 Streptococcus viridans. Gram negative: 5 Serratia marcescens, 3 Pseudomonas aeruginosa, 2 Enterobacter cloacae, 2 Enterobacter aerogenes, 2 Stenotrophomonas maltophilia, 1 Acinetobacter baumannii complex, 1 Acinetobacter oitti, 1 Klebsiella pneumoniae
Figure 3.
Figure 3.
(A) Driveline infection prevention strategies implemented over time stratified by Era. (B) Impact of chronic antibiotic suppression on DLI outcomes. (C) Impact of pathogen type on DLI outcomes. (D) Two-year Survival Conditioned Upon Survival to 3 months post-LVAD, stratified by clinical course (no DLI, DLI without I&D, DLI with I&D)

Comment in

References

    1. Teuteberg JJ, Cleveland JC Jr, Cowger J, et al.: The Society of Thoracic Surgeons Intermacs 2019 Annual Report: The Changing Landscape of Devices and Indications. Ann Thorac Surg 109: 649–660, 2020. - PubMed
    1. Quader MA, Wolfe LG, Kasirajan V: Heart transplantation outcomes in patients with continuous-flow left ventricular assist device-related complications. J Heart Lung Transplant 34: 75–81, 2015. - PubMed
    1. Kusne S, Mooney M, Danziger-Isakov L, et al.: An ISHLT consensus document for prevention and management strategies for mechanical circulatory support infection. J Heart Lung Transplant 36: 1137–1153, 2017. - PubMed
    1. Tattevin P, Flécher E, Auffret V, et al.: Risk factors and prognostic impact of left ventricular assist device-associated infections. Am Heart J 214: 69–76, 2019. - PubMed
    1. Pavlovic NV, Randell T, Madeira T, Hsu S, Zinoviev R, Abshire M: Risk of left ventricular assist device driveline infection: A systematic literature review. Heart Lung 48: 90–104, 2019. - PubMed

Publication types

MeSH terms