Journal of Antimicrobial Chemotherapy 2009 63(Supplement 1):i41-i43; doi:10.1093/jac/dkp082
© The Author 2009. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Summary and comments
Janos Sinkó1,
Bart Jan Kullberg2,
John E. Edwards3,4 and
Elias Anaissie5,6,*
1 Department of Bone Marrow Transplantation, Szent László Hospital, Budapest, Hungary
2 University Medical Centre St Radboud, Nijmegan University Centre for Infections, Nijmegan, The Netherlands
3 David Geffen School of Medicine at UCLA, Los Angeles, CA, USA
4 Los Angeles Biomedical Research Institute at Harbor—UCLA Medical Center, Torrance, CA, USA
5 Myeloma Institute for Research and Therapy, 4301 West Markham MS 776, Little Rock, AR 2205, USA
6 UAMS, Little Rock, AR 72205, USA
* Corresponding author. Tel: +1-501-686-8250; Fax: +1-501-686-6442; E-mail: anaissieeliasj@uams.edu
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Monotherapy
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Empirical monotherapy of febrile neutropenic patients represents
a lifetime's achievement for the few brave pioneers. Unravelling
the inverse correlation between the number of circulating granulocytes
and incidence of infection drew attention to a specific patient
population, namely those with fever and neutropenia. At that
time, the outlook for those with Gram-negative bacteraemia was
dismal, so recognition of those at risk made immediate antimicrobial
treatment possible before microbiological results became available.
Initially, the goals of empirical therapy could only be achieved
by using combinations of antimicrobials; typically one or more
β-lactams plus an aminoglycoside. The development of safe
β-lactam antibiotics with a broader spectrum of activity
and more potent anti-
Pseudomonas activity led some to consider
the possibility of
. . . [Full Text of this Article]
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Moulds
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Prophylaxis
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Empirical therapy
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Pre-emptive therapy
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Future developments
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Mucositis
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Transparency declarations
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