De-Escalation and Discontinuation of Empirical Antibiotic Treatment in a Cohort of Allogeneic Hematopoietic Stem Cell Transplantation Recipients during the Pre-Engraftment Period

被引:33
|
作者
Gustinetti, Giulia [1 ]
Raiola, Anna Maria [2 ,3 ]
Varaldo, Riccardo [2 ,3 ]
Galaverna, Federica [2 ,3 ]
Gualandi, Francesca [2 ,3 ]
Del Bono, Valerio [1 ]
Bacigalupo, Andrea [4 ]
Angelucci, Emanuele [2 ,3 ]
Viscoli, Claudio [1 ]
Mikulska, Malgorzata [1 ]
机构
[1] Univ Genoa, Osped Policlin San Martino, Dept Hlth Sci DISSAL, Div Infect Dis,IRCCS Oncol, Genoa, Italy
[2] Osped Policlin San Martino, IRCCS Oncol, Div Hematol, Genoa, Italy
[3] Osped Policlin San Martino, IRCCS Oncol, Hematopoiet Stem Cell Transplantat Unit, Genoa, Italy
[4] Univ Cattolica Sacro Cuore, Fdn Policlin Univ Gemelli, Ist Ematol, Rome, Italy
关键词
De-escalation; Discontinuation; Neutropenia; Hematopoietic stem cell transplantation; Bloodstream infections; Fluoroquinolone prophylaxis; BLOOD-STREAM INFECTIONS; NEUTROPENIC PATIENTS; SEVERE SEPSIS; HEMATOLOGIC MALIGNANCIES; ANTIMICROBIAL TREATMENT; FEBRILE NEUTROPENIA; LEUKEMIA PATIENTS; UNKNOWN ORIGIN; THERAPY; RESISTANCE;
D O I
10.1016/j.bbmt.2018.03.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To investigate rates and outcomes of antibiotic de-escalation during pre-engraftment neutropenia in allogeneic hematopoietic stem cell transplantation (HSCT) recipients. 110 consecutive HSCTs performed between January 2013 and March 2014 were analyzed. De-escalation was defined as narrowing the spectrum of antibiotic treatment either within (early) or after 96 hours (late) from starting antibiotics. Discontinuation, considered a form of de-escalation, was defined as stopping antibiotics before engraftment. De-escalation failure was defined as restarting/escalating antibiotics within 96 hours after de-escalation. Predictors of deescalation were analyzed. Among 102 patients who started antibiotics and were included, 68 (67%) received monotherapy (mainly piperacillin-tazobactam, n = 58), whereas 34 (33%) received combination therapy (mainly meropenem plus glycopeptide, n = 24). Median duration of neutropenia was 17 days. Bloodstream infections (BSIs) were diagnosed in 28 patients (20%). Early de-escalation rate was 25.5% (n = 26) and mostly consisted of reducing the spectrum of beta-lactams (n = 11, 42%). In comparison with theoretical scenario of continuing therapy until engraftment, the median savings in terms of antibiotic days were 10 for meropenem, 8 for piperacillin-tazobactam, and 7 for vancomycin. Failure rate of early de-escalation was 15% (4/26). Late deescalation rate was 30.4% (n = 31) and failure rate 19% (6/31). The rate of de-escalation any time before engraftment was 55.9% (n = 57), including discontinuation in 33 patients (32%). Death at day 60 after HSCT occurred in 3 patients who never underwent de-escalation. Acute myeloid disease and BSIs were independent predictors of early de-escalation. De-escalation, including discontinuation, is feasible and safe in pre-engraftment neutropenia after allogeneic HSCT. (C) 2018 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1721 / 1726
页数:6
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