TY - JOUR
T1 - Characteristics and Risk Factors of Late-onset Bloodstream Infection beyond 6 Months after Liver Transplantation in Children
AU - Furuichi, Munehiro
AU - Fukuda, Akinari
AU - Sakamoto, Seisuke
AU - Kasahara, Mureo
AU - Miyairi, Isao
N1 - Funding Information:
Accepted for publication June 27, 2017. From the *Division of Infectious Diseases, Department of Medical Subspe-cialties, National Center for Child Health and Development, Tokyo, Japan; †Organ Transplantation Center, National Center for Child Health and Devel-opment, Tokyo, Japan; and ‡Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN. Supported by a grant from the NCCHD 27-6 and 27-1. The authors have no conflicts of interest to disclose. Address for correspondence: Isao Miyairi, MD, Division of Infectious Diseases, Department of Medical Subspecialties, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157–8535 Japan. E-mail: miyairi-i@ncchd.go.jp Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal’s website (www.pidj.com). Copyright 2017 Wolters Kluwer Health, Inc. All rights reserved. ISSN: 0891-3668/18/3703-0263 DOI: 10.1097/INF.0000000000001754
Publisher Copyright:
© 2018 Lippincott Williams and Wilkins. All rights reserved.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Background: Bloodstream infection (BSI) is a major cause of morbidity and mortality after pediatric liver transplantation (LT). However, most studies have focused on BSI occurring within a few months after LT. In this study, we evaluated the characteristics of BSI occurring beyond 6 months after pediatric LT. Methods: We conducted a retrospective cohort study at a pediatric LT center in Japan from November 2005 to March 2016. We evaluated the causative organisms and site of late-onset BSI in children ≤ 18 years of age. The risk factors for developing late-onset BSI and the associations of late-onset BSI with long-Term outcomes were also evaluated. Results: Three hundred forty cases of LT were evaluated. Thirty-eight BSI developed in 29 (9%) LT recipients. There were 42 organisms (nine Gram-positive cocci, 33 Gram-negative rods) isolated from the blood cultures of recipients with late-onset BSI. The most frequent sites of late-onset BSI was intraabdominal infection (18/38; 47%). There were also 14 (39%) episodes with no apparent focus. In multivariate analysis, a prolonged operative time > 12 hours (odds ratio [OR] = 3.55; P = 0.04) and biliary stenosis (OR = 4.60; P = 0.006) were independent risk factors for developing late-onset BSI. Late-onset BSI was associated with increased retransplantation rate (P = 0.04) and mortality (P < 0.001). Conclusion: Late-onset BSI developed in 9% of recipients after pediatric LT. Gram-negative rods accounted for the majority of late-onset BSI as a consequence of abdominal infection, but the focus was often unclear. Prolonged operative time at LT and biliary stenosis were independent risk factors for developing late-onset BSI.
AB - Background: Bloodstream infection (BSI) is a major cause of morbidity and mortality after pediatric liver transplantation (LT). However, most studies have focused on BSI occurring within a few months after LT. In this study, we evaluated the characteristics of BSI occurring beyond 6 months after pediatric LT. Methods: We conducted a retrospective cohort study at a pediatric LT center in Japan from November 2005 to March 2016. We evaluated the causative organisms and site of late-onset BSI in children ≤ 18 years of age. The risk factors for developing late-onset BSI and the associations of late-onset BSI with long-Term outcomes were also evaluated. Results: Three hundred forty cases of LT were evaluated. Thirty-eight BSI developed in 29 (9%) LT recipients. There were 42 organisms (nine Gram-positive cocci, 33 Gram-negative rods) isolated from the blood cultures of recipients with late-onset BSI. The most frequent sites of late-onset BSI was intraabdominal infection (18/38; 47%). There were also 14 (39%) episodes with no apparent focus. In multivariate analysis, a prolonged operative time > 12 hours (odds ratio [OR] = 3.55; P = 0.04) and biliary stenosis (OR = 4.60; P = 0.006) were independent risk factors for developing late-onset BSI. Late-onset BSI was associated with increased retransplantation rate (P = 0.04) and mortality (P < 0.001). Conclusion: Late-onset BSI developed in 9% of recipients after pediatric LT. Gram-negative rods accounted for the majority of late-onset BSI as a consequence of abdominal infection, but the focus was often unclear. Prolonged operative time at LT and biliary stenosis were independent risk factors for developing late-onset BSI.
KW - bacteremia
KW - biliary stenosis
KW - intra-Abdominal infection
KW - mortality
KW - prolonged operative time
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U2 - 10.1097/INF.0000000000001754
DO - 10.1097/INF.0000000000001754
M3 - Article
C2 - 28859015
AN - SCOPUS:85048423358
SN - 0891-3668
VL - 37
SP - 263
EP - 268
JO - Pediatric Infectious Disease Journal
JF - Pediatric Infectious Disease Journal
IS - 3
ER -