Cargando…

1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital

BACKGROUND: Recurrent central line-associated bloodstream infections (CLABSI) in children present a unique challenge to infection prevention efforts but guidelines for management are lacking. METHODS: We reviewed CLABSI data at Texas Children’s Hospital (TCH) from fiscal years (FY) 2017-2019. A char...

Descripción completa

Detalles Bibliográficos
Autores principales: Foster, Catherine, Marquez, Lucila, Koy, Tjin, Campbell, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777030/
http://dx.doi.org/10.1093/ofid/ofaa439.1557
_version_ 1783630811610742784
author Foster, Catherine
Marquez, Lucila
Koy, Tjin
Campbell, Judith
author_facet Foster, Catherine
Marquez, Lucila
Koy, Tjin
Campbell, Judith
author_sort Foster, Catherine
collection PubMed
description BACKGROUND: Recurrent central line-associated bloodstream infections (CLABSI) in children present a unique challenge to infection prevention efforts but guidelines for management are lacking. METHODS: We reviewed CLABSI data at Texas Children’s Hospital (TCH) from fiscal years (FY) 2017-2019. A chart review to characterize clinical features, risk factors, and outcomes of patients with recurrent CLABSIs in FY2019 was performed. Descriptive statistics and Fisher’s exact test were used. RESULTS: Recurrent CLABSIs increased from FY 2017-2019 [20% (26/126) to 33% (44/131)] (P=0.03). In FY2019, 15 patients accounted for 44 CLABSIs (Figure 1). Underlying conditions included aplastic anemia (4), hemophagocytic lymphohistiocytosis (3), malignancy (4), genetic disease (2), congenital heart disease (1) and biliary atresia (1). Two-thirds of the CLABSIs occurred in the setting of severe neutropenia (ANC < 100 cells/mm(3)) though only 16 (36%) were classified as mucosal barrier injury. The median time between line insertion and date of infection was 41 days (range 1-105). Line type included central venous catheters (25, 57%), peripherally inserted central catheters (17, 39%) and implantable ports (2, 5%). Most lines (80%) had double lumens. The most common organisms included: Gram-negative bacilli (15), coagulase negative staphylococci (14), viridans group streptococci (6) Candida spp. (5), Enterococcus faecalis (3) and Staphylococcus aureus (3). Four CLABSIs were polymicrobial. Patients with >2 CLABSIs were more likely to have subsequent infections with the same organism as compared to patients with only 2 CLABSIs (P=0.01). Lines were removed promptly (19, 43%), had delayed removal (removal >72 hours from infection date) (10, 23%) or remained in place (15, 34%). Lines were removed for all episodes of fungemia (5/44) and for most Gram-negative infections (10/12). Six of 7 Escherichia coli CLABSIs were breakthrough fluoroquinolone-resistant infections in patients on levofloxacin. Single Episode and Recurrent CLABSIs at Texas Children’s Hospital for Fiscal Year 2019 [Image: see text] CONCLUSION: Recurrent CLABSI accounted for a third of CLABSIs in FY2019. Line mismanagement was not a key contributor to recurrent CLABSI. Breakthrough CLABSIs in patients on levofloxacin prophylaxis need further investigation. For patients with CLABSIs due to Staphylococci decolonization may be considered. DISCLOSURES: All Authors: No reported disclosures
format Online
Article
Text
id pubmed-7777030
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77770302021-01-07 1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital Foster, Catherine Marquez, Lucila Koy, Tjin Campbell, Judith Open Forum Infect Dis Poster Abstracts BACKGROUND: Recurrent central line-associated bloodstream infections (CLABSI) in children present a unique challenge to infection prevention efforts but guidelines for management are lacking. METHODS: We reviewed CLABSI data at Texas Children’s Hospital (TCH) from fiscal years (FY) 2017-2019. A chart review to characterize clinical features, risk factors, and outcomes of patients with recurrent CLABSIs in FY2019 was performed. Descriptive statistics and Fisher’s exact test were used. RESULTS: Recurrent CLABSIs increased from FY 2017-2019 [20% (26/126) to 33% (44/131)] (P=0.03). In FY2019, 15 patients accounted for 44 CLABSIs (Figure 1). Underlying conditions included aplastic anemia (4), hemophagocytic lymphohistiocytosis (3), malignancy (4), genetic disease (2), congenital heart disease (1) and biliary atresia (1). Two-thirds of the CLABSIs occurred in the setting of severe neutropenia (ANC < 100 cells/mm(3)) though only 16 (36%) were classified as mucosal barrier injury. The median time between line insertion and date of infection was 41 days (range 1-105). Line type included central venous catheters (25, 57%), peripherally inserted central catheters (17, 39%) and implantable ports (2, 5%). Most lines (80%) had double lumens. The most common organisms included: Gram-negative bacilli (15), coagulase negative staphylococci (14), viridans group streptococci (6) Candida spp. (5), Enterococcus faecalis (3) and Staphylococcus aureus (3). Four CLABSIs were polymicrobial. Patients with >2 CLABSIs were more likely to have subsequent infections with the same organism as compared to patients with only 2 CLABSIs (P=0.01). Lines were removed promptly (19, 43%), had delayed removal (removal >72 hours from infection date) (10, 23%) or remained in place (15, 34%). Lines were removed for all episodes of fungemia (5/44) and for most Gram-negative infections (10/12). Six of 7 Escherichia coli CLABSIs were breakthrough fluoroquinolone-resistant infections in patients on levofloxacin. Single Episode and Recurrent CLABSIs at Texas Children’s Hospital for Fiscal Year 2019 [Image: see text] CONCLUSION: Recurrent CLABSI accounted for a third of CLABSIs in FY2019. Line mismanagement was not a key contributor to recurrent CLABSI. Breakthrough CLABSIs in patients on levofloxacin prophylaxis need further investigation. For patients with CLABSIs due to Staphylococci decolonization may be considered. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7777030/ http://dx.doi.org/10.1093/ofid/ofaa439.1557 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
Foster, Catherine
Marquez, Lucila
Koy, Tjin
Campbell, Judith
1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital
title 1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital
title_full 1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital
title_fullStr 1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital
title_full_unstemmed 1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital
title_short 1375. Characterization of Recurrent Central Line-associated Bloodstream Infections at Texas Children’s Hospital
title_sort 1375. characterization of recurrent central line-associated bloodstream infections at texas children’s hospital
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777030/
http://dx.doi.org/10.1093/ofid/ofaa439.1557
work_keys_str_mv AT fostercatherine 1375characterizationofrecurrentcentrallineassociatedbloodstreaminfectionsattexaschildrenshospital
AT marquezlucila 1375characterizationofrecurrentcentrallineassociatedbloodstreaminfectionsattexaschildrenshospital
AT koytjin 1375characterizationofrecurrentcentrallineassociatedbloodstreaminfectionsattexaschildrenshospital
AT campbelljudith 1375characterizationofrecurrentcentrallineassociatedbloodstreaminfectionsattexaschildrenshospital