Risk factors for vancomycin-resistant enterococcus bacteremia and its influence on survival after allogeneic hematopoietic cell transplantation

被引:0
作者
M Tavadze
L Rybicki
S Mossad
R Avery
M Yurch
B Pohlman
H Duong
R Dean
B Hill
S Andresen
R Hanna
N Majhail
E Copelan
B Bolwell
M Kalaycio
R Sobecks
机构
[1] Internal Medicine,Department of Infectious Diseases
[2] Cleveland Clinic,Division of Infectious Diseases (Transplant/Oncology)
[3] Quantitative Health Sciences,Department of Pediatric Hematology and Oncology
[4] Cleveland Clinic Lerner Research Institute,undefined
[5] Medicine Institute,undefined
[6] Cleveland Clinic,undefined
[7] John Hopkins,undefined
[8] Hematologic Oncology and Blood Disorders,undefined
[9] Cleveland Clinic Taussig Cancer Institute,undefined
[10] Cleveland Clinic,undefined
[11] Levine Cancer Institute,undefined
[12] Carolinas Healthcare System,undefined
来源
Bone Marrow Transplantation | 2014年 / 49卷
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摘要
Vancomycin-resistant enterococcus (VRE) is a well-known infectious complication among immunocompromised patients. We performed a retrospective analysis to identify risk factors for the development of VRE bacteremia (VRE-B) within 15 months after allogeneic hematopoietic cell transplantation (alloHCT) and to determine its prognostic importance for other post-transplant outcomes. Eight hundred consecutive adult patients who underwent alloHCT for hematologic diseases from 1997 to 2011 were included. Seventy-six (10%) developed VRE-B at a median of 46 days post transplant. Year of transplant, higher HCT comorbidity score, a diagnosis of ALL, unrelated donor and umbilical cord blood donor were all significant risk factors on multivariable analysis for the development of VRE-B. Sixty-seven (88%) died within a median of 1.1 months after VRE-B, but only four (6%) of these deaths were attributable to VRE. VRE-B was significantly associated with worse OS (hazard ratio 4.28, 95% confidence interval 3.23–5.66, P<0.001) in multivariable analysis. We conclude that the incidence of VRE-B after alloHCT has increased over time and is highly associated with mortality, although not usually attributable to VRE infection. Rather than being the cause, this may be a marker for a complicated post-transplant course. Strategies to further enhance immune reconstitution post transplant and strict adherence to infection prevention measures are warranted.
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页码:1310 / 1316
页数:6
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