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Switching Fluoroquinolones in Patients with Neutropenia May Increase
Infection Risks: Presented at ICAAC
By Paula Moyer
WASHINGTON, DC -- December 19, 2005 -- Researchers have found that
moxifloxacin (Avelox) could contribute to an increased rate of
Clostridium difficile colitis when compared to levofloxacin (Levaquin)
in patients with hematologic cancers who have prolonged neutropenia.
The investigators recommend that physicians exercise caution when
considering a switch from one fluoroquinolone agent to another in
patients with neutropenia who are on antibiotic prophylaxis.
Principal investigator Stefan Reuter, MD, Assistant Professor of
Internal Medicine, University Hospital, Ulm, Germany, presented the
findings here on December 17th at the 45th annual Interscience
Conference on Antimicrobial Agents and Chemotherapy (ICAAC).
Dr. Reuter and co-investigators had noticed a problem in patients who
were switched from levofloxacin to moxifloxacin (Avelox). "Both the
number of Gram-negative bacteremias and the number of infections of
Clostridium difficile with associated diarrhea were higher under
moxifloxacin-prophylaxis as compared to
levofloxacin," he said.
"These findings may indicate that fluoroquinolones are not
interchangeable in the neutropenia setting," he added.
However, he stressed that the findings were based on patients from one
center, and that further research would be necessary before concluding
definitively that such a switch is detrimental.
The investigators conducted the study because they had assumed
moxifloxacin -- the broadest of the antibacterial agents -- might make
it an ideal prophylactic agent to use in treating patients with
neutropenia.
They conducted a prospective observational study in which moxifloxacin
was used as a prophylactic agent for 1 year for the treatment of 156
patients with hematologic cancers who had prolonged neutropenia. The
investigators assessed the rates of Gram-negative or -positive
bacteremia, rates of C. difficile-positive tests, and deaths from
infection during the study period. They compared these rates to those
of a historical control group
of 235 patients who had been treated with levofloxacin prior to the
study period. They then compared these findings to those of 30
patients in whom levofloxacin was re-introduced in a
post-observational study period of 19 weeks.
The study included all patients
undergoing chemotherapy for hematological malignancies with an
expected duration of neutropenia of at least 5 days. The investigators
followed patients prospectively from the first day of neutropenia
until 2 days after their neutrophil levels returned to normal.
The investigators compared 283 neutropenic episodes with moxifloxacin
prophylaxis to 451 episodes with levofloxacin prophylaxis.
Gram-negative bacteremia was detected in 10.6% of patients on
moxifloxacin and 5.5% of the historical control group on levofloxacin.
In the post-observational period the investigators documented one
episode of Gram-negative bacteremia during 25 neutropenic episodes
(4%). The investigators are still following these patients, Dr. Reuter
said. The rates of C. difficile infection were 31.1% in the patients
treated with moxifloxacin, 6.3% in the historical controls, and 13.6%
in the patients treated with levofloxacin in the post-observational
study.
Rates of Gram-positive bacteremia were 16% for the moxifloxacin group,
19% for the historical controls, and 31.4% for those treated with
levofloxacin after the observational study.
Death rates related to infection were 6.4% in the moxifloxacin group,
4.3% in the historical controls, and 6.7% in the post-observation
period group.
"We don't know if the switch back to levofloxacin caused the drops in
Gram-negative bacteremia and C. difficile," Dr. Reuter said. "Because
the hospital instituted more diligent infection control measures at
the same time, it is difficult to discern which caused the decrease in
infection."
[Presentation title: Moxifloxacin-Prophylaxis during Neutropenia in
Patients with Hemato-Oncological Malignancies. Abstract K-1540]
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