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Impact of a change in antibacterial prophylaxis on bacteremia and hospitalization rates following outpatient autologous peripheral blood stem cell transplantation for multiple myeloma
Author(s) -
Kim J.H.,
Goulston C.,
Zangari M.,
Tricot G.,
Boyer M.W.,
Hanson K.E.
Publication year - 2014
Publication title -
transplant infectious disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.69
H-Index - 67
eISSN - 1399-3062
pISSN - 1398-2273
DOI - 10.1111/tid.12225
Subject(s) - medicine , bacteremia , levofloxacin , ertapenem , multiple myeloma , transplantation , sepsis , melphalan , surgery , antibiotics , meropenem , antibiotic resistance , microbiology and biotechnology , biology
Background Levofloxacin is routinely used for the prevention of invasive bacterial infections during autologous peripheral blood stem cell transplantation ( APBSCT ). However, increasing rates of bacterial sepsis were noted at our institution among multiple myeloma ( MM ) patients undergoing outpatient APBSCT with melphalan‐based chemotherapy and levofloxacin prophylaxis. We assessed the impact of a change in antibacterial prophylaxis from oral levofloxacin (Period 1) to sequential oral levofloxacin followed by ertapenem (Period 2). Methods Electronic medical records were reviewed to identify MM patients who underwent APBSCT in the outpatient clinic between October 2007 and April 2012. Results Over a 4.5‐year period, 165 outpatient APBSCT s were eligible for the analysis. Fewer overall bacteremias occurred during Period 2 as compared with Period 1 (0.5 cases per 100 person‐days vs. 2.4 cases per 100 person‐days, P < 0.001). In addition, fewer patients were hospitalized for neutropenic fever while receiving sequential prophylaxis (45.7% vs. 75.7% of outpatient APBSCT recipients during Periods 2 and 1, respectively; P < 0.001). In K aplan– M eier analysis, receipt of sequential prophylaxis (Period 2) was significantly associated with overall bacteremia‐free survival within 30 days after the APBSCT ( P < 0.001). No significant differences were seen in the number of patients developing C lostridium difficile infection or ertapenem‐resistant gram‐negative bacteremia between study periods. Conclusion In conclusion, sequential prophylaxis may effectively prevent episodes of bacteremia and hospitalizations in neutropenic MM outpatient APBSCT recipients. Prospective studies that involve larger numbers of MM patients with extended periods of follow‐up are ultimately required to define the safety and efficacy of sequential antibacterial prophylaxis.