Comparison of Efficacy and Safety of Treatment with Ofloxacin-Piperacillin and Amikacin-Piperacillin in Immunodepressed Febrile Neutropenic Patients

Drugs ◽  
1993 ◽  
Vol 45 (Supplement 3) ◽  
pp. 305-306
Author(s):  
J.L. Harousseau ◽  
J.P. Lamagnere ◽  
M. Boasson ◽  
D. Guyotat ◽  
P. Moreau ◽  
...  
2006 ◽  
Vol 42 (5) ◽  
pp. 597-607 ◽  
Author(s):  
B. Jaksic ◽  
G. Martinelli ◽  
J. P. Oteyza ◽  
C. S. Hartman ◽  
L. B. Leonard ◽  
...  

1997 ◽  
Vol 41 (8) ◽  
pp. 1704-1708 ◽  
Author(s):  
D Yamamura ◽  
R Gucalp ◽  
P Carlisle ◽  
M Cimino ◽  
J Roberts ◽  
...  

An open-label randomized trial comparing the efficacy and safety of cefepime versus piperacillin plus gentamicin (P+G) given intravenously for the treatment of febrile episodes in neutropenic patients with underlying malignancy was conducted at two oncology centers. Over a 30-month period 111 patients were enrolled and 99 patients were found to be suitable for evaluation. At the 72-h time of evaluation, cefepime monotherapy and P+G combination therapy produced comparable clinical response rates (78% for both). P+G and cefepime produced comparable response rates in microbiologically documented (78 versus 71%), clinically documented (100 versus 100%), and possible (75 versus 79%) infections. The P+G and cefepime treatments achieved comparable microbiological eradication of gram-negative (100 versus 71%) (P = 0.09) and gram-positive (44 versus 70%) (P = 0.37) organisms. There were no statistically significant differences in the rates of superinfection between the groups; however, more superinfections of fungal origin were noted in the P+G group. Cefepime was demonstrated to be an effective and safe treatment for febrile episodes in neutropenic patients with malignancies, and its lack of nephrotoxicity compared to P+G was noteworthy. Cefepime appears to be a candidate for monotherapy in febrile neutropenic cancer patients.


Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4661-4661
Author(s):  
Joon Seong Park ◽  
Dong Hwan Kim ◽  
Chul Won Choi ◽  
Seong Hyun Jeong ◽  
Jin-Hyuk Choi ◽  
...  

Abstract Abstract 4661 Introduction Invasive or possible fungal infection is often fatal and its incidence is increasing in febrile neutropenic patients with hematological malignancies. Thus, empirical antifungal agent should be carefully selected for those patients. Patients and Methods The study was conducted as a prospective multicenter trial to document the efficacy and safety of micafungin (Mycamine®), a class of echinocandin, as an empirical antifungal agent in febrile neutropenic patients. Micafungin was administrated for sustained fever (>38.4°C) on day 3 - 5 after initiation of empirical antibiotic therapy. The overall success rate according to the composite score (no breakthrough fungal infection, survival for seven days beyond the end of therapy, did not discontinue therapy prematurely, had resolution of fever during the period of neutropenia, and successfully treated a documented base-line fungal infection) and side effects were evaluated. Results A total of 47 patients with AML, ALL, MDS or lymphomas were enrolled. The overall success rate was 61.7% (29/47). Three patients (6.4 %) experienced grade 3/4 elevated aspartate aminotransferase and ten patients (21 %) showed grade 3/4 hyperbilirubinemia and nine of which resolved, and four patients died of septic shock. Patients with young age (< 50 yr) and ALL rather than AML showed a better response to micafungin. Less profoundly neutropenic (≥50 /mm3) patients revealed a better response, as did the patients who recovered from fever or neutropenia. Conclusions Micafungin has been reported to have an excellent efficacy (61.7 %) and safety profile when used as an empirical antifungal agent to treat febrile neutropenic patients with hematological disorders. Disclosures: No relevant conflicts of interest to declare.


2010 ◽  
Vol 16 (2) ◽  
pp. 113-117 ◽  
Author(s):  
Masaki Fujita ◽  
Hiroshi Ouchi ◽  
Tsukasa Ohshima ◽  
Yuichi Inoue ◽  
Ichiro Inoshima ◽  
...  

2002 ◽  
Vol 36 (10) ◽  
pp. 1525-1531 ◽  
Author(s):  
Dawn I Warkentin ◽  
Joel B Epstein ◽  
Lara M Campbell ◽  
Judy G Yip ◽  
Victoria C Cox ◽  
...  

BACKGROUND: It is common practice to administer acyclovir as prophylaxis to patients with hematologic malignancies during neutropenia; however, effective therapy requires frequent dosing, which is difficult in this setting. Valacyclovir has greater oral bioavailability and requires less frequent dosing. OBJECTIVE: To evaluate the efficacy and safety of valacyclovir compared with acyclovir. METHODS: Patients who had been treated with chemotherapy or stem-cell transplantation were randomized to receive acyclovir 400 mg orally 3 × daily (n = 51), valacyclovir 500 mg orally twice daily (n = 48), or valacyclovir 250 mg orally twice daily (n = 52) during neutropenia. RESULTS: Clinical success, defined as the absence of an active herpes simplex virus (HSV) lesion or asymptomatic viral shedding, was similar between the 3 groups (acyclovir 96%, valacyclovir 500 mg 95%, valacyclovir 250 mg 100%). The overall rates of adverse events were similar in the 3 groups. CONCLUSIONS: Prophylactic treatment with valacyclovir is an effective and safe alternative to acyclovir for the prevention of HSV reactivation in patients with hematologic malignancies.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 3729-3729
Author(s):  
Seong Hyun Jeong ◽  
Dae Young Kim ◽  
Jun Ho Jang ◽  
Yeung-Chul Mun ◽  
Sung-Hyun Kim ◽  
...  

Abstract Background: Micafungin, one of the powerful ecchinocandins, needs to be clarified its efficacy and safety of empirical therapy on febrile neutropenic patients compared with other anti-fungal drugs such as azole compounds. Methods: A randomized, multi-center, prospective study (age-, sex-, diagnosis-, risk-controlled) was conducted for a comparison of efficacy and safety between micafungin and intravenous itraconazole as an empirical therapy on febrile neutropenic patients with acute leukemia. Anti-fungal drugs (study drug, micafungin; control drug, itraconazole) were administrated for sustained high fever following appropriate empirical antibiotic therapy (°Ã 3 days of combination antibiotics). The overall success rate [if the patient meets all of the following criteria: (1) no breakthrough fungal infection; (2) survived for 7 days past the end of the therapy; (3) no premature discontinuation; (4) disappearance of fever during neutropenia; (5) successfully treated base-line fungal infection] and side effects were evaluated. And duration of fever and neutropenic fever were estimated and compared between two groups. Results: A total of 134 patients with acute leukemia were enrolled in the study (86 patients with AML, 41 patients with ALL, 7 patients with secondary leukemia). The overall success rate of micafungin and itraconazole was 63.6% and 53.2%, respectively (p = NS) (Figure 2). However, duration of fever and duration of neutropenic fever were significantly shorter in micafungin group (p = 0.0007, p = 0.0118, respectively) and survival benefit was marginal (OS, median months, 10.93 vs. 4.77, p = NS) (Figure 1). Grade III-IV adverse events including hyperbilirubinemia (2 vs. 7), elevation of transaminase level (2 vs. 4), electrolytes imbalance (1 vs. 2), atrial fibrillation (1 vs. 0), and anaphylaxis (1 vs. 0) occurred at 7 and 13 patients in micafungin (10.4%) and itraconazole (18.8%) group, respectively. All adverse events were manageable however, 4 patients died of progression of infection in each group. Conclusion: This randomized, controlled, prospective study documented that micafungin, when compared with itraconazole, showed significantly superior effect on shortening the duration of fever and neutropenic fever, resulting in marginal survival benefit on acute leukemia patients who are suffering from life-threatening neutropenic period under anti-leukemic therapy. Disclosures No relevant conflicts of interest to declare.


2010 ◽  
Vol 124 (2) ◽  
pp. 92-97 ◽  
Author(s):  
Joon Seong Park ◽  
Dong Hwan Kim ◽  
Chul Won Choi ◽  
Seong Hyun Jeong ◽  
Jin-Hyuk Choi ◽  
...  

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