Intercontinental study on pre-engraftment and post-engraftment Gram-negative rods bacteremia in hematopoietic stem cell transplantation patients: Risk factors and association with mortality
•Center` fluoroquinolone prophylaxis allo-HSCT policy does not influence pre-engraftment Gram-negative rods bacteremia (GNRB) rate.•Low post-engraftment GNRB rate in allo-HSCT patients in JACIE/FACT-accredited centers.•High pre-engraftment GNRB rate in auto-HSCT patients with autoimmune diseases.•Lo...
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Published in | The Journal of infection Vol. 81; no. 6; pp. 882 - 894 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.12.2020
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Subjects | |
Online Access | Get full text |
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Summary: | •Center` fluoroquinolone prophylaxis allo-HSCT policy does not influence pre-engraftment Gram-negative rods bacteremia (GNRB) rate.•Low post-engraftment GNRB rate in allo-HSCT patients in JACIE/FACT-accredited centers.•High pre-engraftment GNRB rate in auto-HSCT patients with autoimmune diseases.•Low pre-engraftment GNRB rate in auto-HSCT centers with active infection control team.•MDR GNRB associated with increased post-HSCT mortality.
We present here data on Gram-negative rods bacteremia (GNRB) rates, risk factors and associated mortality.
Data on GNRB episodes were prospectively collected in 65 allo-/67 auto-HSCT centers in 24 countries (Europe, Asia, Australia). In patients with and without GNRB, we compared: demography, underlying disease, HSCT-related data, center` fluoroquinolone prophylaxis (FQP) policy and accreditation status, and involvement of infection control team (ICT).
The GNRB cumulative incidence among 2818 allo-HSCT was: pre-engraftment (pre-eng-allo-HSCT), 8.4 (95% CI 7–9%), post-engraftment (post-eng-allo-HSCT), 5.8% (95%CI: 5–7%); among 3152 auto-HSCT, pre-eng-auto-HSCT, 6.6% (95%CI: 6–7%), post-eng-auto-HSCT, 0.7% (95%CI: 0.4–1.1%). GNRB, especially MDR, was associated with increased mortality.
Multivariate analysis revealed the following GNRB risk factors:
(a) pre-eng-allo-HSCT: south-eastern Europe center location, underlying diseases not at complete remission, and cord blood source;
(b) post-eng-allo-HSCT: center location not in northwestern Europe; underlying non-malignant disease, not providing FQP and never accredited.
(c) pre-eng-auto-HSCT: older age, autoimmune and malignant (vs. plasma cell) disease, and ICT absence.
Benefit of FQP should be explored in prospective studies. Increased GNRB risk in auto-HSCT patients transplanted for autoimmune diseases is worrying. Infection control and being accredited are possibly protective against bacteremia. GNRB are associated with increased mortality. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0163-4453 1532-2742 1532-2742 |
DOI: | 10.1016/j.jinf.2020.11.002 |