Impact of discontinuing routine fluoroquinolone prophylaxis in neutropenic allogeneic haematopoietic stem cell transplant recipients: an observational study

被引:3
作者
Stern, Anat [1 ,2 ]
Henig, Israel [3 ]
Cohen, Maya [2 ]
Gur, Ivan [4 ]
Henig, Oryan [5 ,6 ]
Zuckerman, Tsila [2 ,3 ]
Paul, Mical [1 ,2 ]
机构
[1] Rambam Hlth Care Campus, Infect Dis Inst, Haifa, Israel
[2] Technion Israel Inst Technol, Bruce Rappaport Sch Med, Haifa, Israel
[3] Rambam Hlth Care Campus, Dept Hematol, Haifa, Israel
[4] Rambam Hlth Care Campus, Internal Med Dept, Haifa, Israel
[5] Tel Aviv Univ, Fac Med, Tel Aviv, Israel
[6] Tel Aviv Sourasky Med Ctr, Infect Prevent & Control Unit, Tel Aviv, Israel
关键词
VIRIDANS STREPTOCOCCI; CANCER-PATIENTS; SOLID TUMORS; LEVOFLOXACIN; INFECTIONS; BACTEREMIA; GUIDELINES; RESISTANCE; EPIDEMIOLOGY; SOCIETY;
D O I
10.1093/jac/dkae360
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Uncertainty exists as to the role of fluoroquinolone (FQ) prophylaxis for patients undergoing allogeneic haematopoietic stem cell transplantation (HSCT) in the era of rising antibiotic resistance. Objectives: We aimed to evaluate rates of bloodstream infections (BSI), resistance patterns and outcomes of patients after discontinuing routine FQ prophylaxis administration. Methods: All adult recipients of first HSCT from 2017 to 2020 were retrospectively included and classified according to time of HSCT as FQ group (HSCT January 2017-December 2018) or no FQ group (January 2019-December 2020). The primary outcome was Gram-negative (GN) BSI from day -7 to 30 days post-HSCT. The independent association between the study period and BSI was assessed using survival analysis, and adjusting for confounders. Results: We included 254 patients, 130 (51%) and 124 (49%) in the FQ and no FQ groups, respectively. Compared to the FQ group, no FQ had significantly more GN BSI (21% versus 33%, P = 0.027) and the median time to first GN BSI was significantly shorter [4 (IQR 1-8) days versus 6 (1-10) days, P = 0.009]. Following adjustment, FQ prophylaxis remained associated with lower hazard for GN BSI (hazard ratio 0.57, 95% CI 0.34-0.93). Eighty-two GN BSI episodes had FQ susceptibility testing. More GN BSI episodes were FQ resistant in the FQ group (68.9% versus 41.6%, P = 0.021). No significant difference was found for 30-day mortality, time to first febrile neutropenia and time to first broad-spectrum antibiotics between the groups (P was not significant). Conclusions: FQ prophylaxis is associated with fewer GN BSI in the early post-HSCT period even in high FQ resistance settings, with FQ resistance rates reaching >60% following prophylaxis.
引用
收藏
页码:3289 / 3296
页数:8
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