bone marrow transplantation;
bacterial infection;
antibiotics;
D O I:
10.1038/sj.bmt.1703413
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
Adequate infection prophylaxis and empirical antibiotic therapy are of critical importance after hematopoietic stem cell transplantation (HSCT). We examined the evolution of bacterial susceptibility to antibiotics in 492 patients (198 allografts and 294 autografts) transplanted between 1982 and 1999 and evaluated whether ciprofloxacin prophylaxis and an empirical antibiotic regimen (glycopeptide + third-generation cephalosporin) were still valid. We collected all susceptibility tests performed during the initial hospitalization on blood cultures as well as routine surveillance cultures and analyzed susceptibility to ciprofloxacin and to major antibiotics used in our unit. Gram-positive cocci rapidly became resistant to ciprofloxacin (susceptibility around 70% in 1990 to less than 20% in 1998) but sensitivity to glycopeptides remained unaltered. There was a rapid decline in the number of patients colonized with Gram-negative bacilli in the early years of ciprofloxacin prophylaxis. However, susceptibility to ciprofloxacin fell sharply from around 90% in 1990 to around 30% in 1999. In parallel, susceptibility to ceftazidime also decreased to less than 80% in recent years. Piperacillin (+/-tazobactam) did not show any variation over time and its efficacy remained too low (about 60%). Imipenem as well as recently introduced cefepim and meropenem showed stable and excellent profiles (>90% susceptibility). In conclusion: (1) quinolone prophylaxis has now lost most of its value; (2) the choice of a third-generation cephalosporin for empirical antibiotic therapy may no longer be the best because of the emergence of Gram-negative strains resistant to beta-lactamases, such as Enterobacter sp. More appropriate regimens of empirical antibiotic therapy in HSCT recipients may be based on the use of a carbapenem or fourth-generation cephalosporin.
机构:
Karolinska Inst, Dept Med Huddinge, Div Hematol, S-14186 Stockholm, Sweden
Karolinska Univ Hosp, Dept Hematol, S-14186 Stockholm, SwedenKarolinska Inst, Dept Med Huddinge, Div Hematol, S-14186 Stockholm, Sweden
Ljungman, Per
Hakki, Morgan
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机构:
Oregon Hlth & Sci Univ, Div Infect Dis, Portland, OR 97201 USAKarolinska Inst, Dept Med Huddinge, Div Hematol, S-14186 Stockholm, Sweden
机构:
Univ Sao Paulo, Hosp Clin, Grp Infect Immunocompromised Patients, Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Grp Infect Immunocompromised Patients, Sao Paulo, Brazil
Ramos, Jessica Fernandes
Batista, Marjorie Vieira
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机构:
Univ Sao Paulo, Hosp Clin, Grp Infect Immunocompromised Patients, Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Grp Infect Immunocompromised Patients, Sao Paulo, Brazil
Batista, Marjorie Vieira
Costa, Silvia Figueiredo
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机构:
Univ Sao Paulo, Hosp Clin, Grp Infect Immunocompromised Patients, Sao Paulo, Brazil
Univ Sao Paulo, Sch Med, Dept Infect Dis, Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Grp Infect Immunocompromised Patients, Sao Paulo, Brazil
机构:
Karolinska Inst, Dept Med Huddinge, Div Hematol, S-14186 Stockholm, Sweden
Karolinska Univ Hosp, Dept Hematol, S-14186 Huddinge, SwedenKarolinska Inst, Dept Med Huddinge, Div Hematol, S-14186 Stockholm, Sweden
Ljungman, Per
Hakki, Morgan
论文数: 0引用数: 0
h-index: 0
机构:
Oregon Hlth & Sci Univ, Div Infect Dis, Portland, OR 97201 USAKarolinska Inst, Dept Med Huddinge, Div Hematol, S-14186 Stockholm, Sweden