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减少ICU中抗生素抵抗病原体发生率的策略
Strategies to Reduce the Incidence of Antibiotic-Resistant
Pathogens in the ICU
Henry Masur, MD
Introduction
At the 32nd Critical Care Congress, strategies to reduce
the frequency of antibiotic-resistant pathogens received
considerable attention. Marin H. Kollef, MD,[1] of Washington
University School of Medicine in Manchester, Missouri,
stressed that in every intensive care unit (ICU), the
incidence of resistance should be closely monitored,
just as ICUs monitor the frequency of self-extubations
and deep vein thrombosis. Collecting and reviewing data
that indicate what the pathogens are in a unit, and
what their antimicrobial susceptibility is, must be
the foundation for an ICU's program to reduce the incidence
of infectious complications, and to minimize antibiotic
resistance.
Antibiotic
Rotation in the ICU
Antibiotic
Use in Sepsis
Focusing
Drug Antibiotic Delivery on Infected Tissue
Limiting
Antibiotic Use in the ICU
Once-Daily
Dosing of Aminoglycosides
New
Agents on the Horizon
References
1. Kollef MH. Infection: antibiotics. Rotation of empiric
antibiotics in the ICU. Program and abstracts of the
32nd Critical Care Congress; January 28-February 2,
2003; San Antonio, Texas.
2. Rahal JJ, Urban C, Horn D, et al. Class restriction
of cephalosporin use to control total cephalosporin
resistance in nosocomial Klebsiella. JAMA. 1998;280:1233-1237.
3. Kollef MH. Hospital-acquired pneumonia and de-escalation
of antimicrobial treatment. Crit Care Med. 2001;29:1473-1475.
4. Kollef MH. Is there a role for antibiotic cycling
in the intensive care unit? Crit Care Med. 2001;29(4
suppl):N135-N142.
5. Landman D, Chockalingam M, Quale JM. Reduction in
the incidence of methicillin-resistant Staphylococcus
aureus and ceftazidime-resistant Klebsiella pneumoniae
following changes in a hospital antibiotic formulary.
Clin Infect Dis. 1999;28:1062-1066.
6. Gruson D, Hilbert G, Vargas F, et al. Rotation and
restricted use of antibiotics in a medical intensive
care unit. Impact on the incidence of ventilator-associated
pneumonia caused by antibiotic-resistant gram-negative
bacteria. Am J Respir Crit Care Med. 2000;162(3 Pt 1):837-843.
7. Cohen J. Infection: antibiotics. Antibiotic choice
in sepsis: Does it really matter? Program and abstracts
of the 32nd Critical Care Congress; January 28-February
2, 2003; San Antonio, Texas.
8. Kreger BE, Craven DE, McCabe WR. Gram-negative bacteremia.
IV. Re-evaluation of clinical features and treatment
in 612 patients. Am J Med. 1980;68:344-355.
9. Warren HS. Infection: antibiotics. Can aminoglycosides
be targeted to infected tissue by using chemoattractant
peptides? Program and abstracts of the 32nd Critical
Care Congress; January 28-February 2, 2003; San Antonio,
Texas.
10. Marshall J. Infection: antibiotics. Minimizing antibiotic
use in the ICU. Program and abstracts of the 32nd Critical
Care Congress; January 28-February 2, 2003; San Antonio,
Texas.
11. Singh N, Rogers P, Atwood CW, Wagener MM, Yu VL.
Short-course empiric antibiotic therapy for patients
with pulmonary infiltrates in the intensive care unit.
A proposed solution for indiscriminate antibiotic prescription.
Am J Respir Crit Care Med. 2000;162(2 Pt 1):505-511.
12. Fagon JY, Chastre J, Wolff M, et al. Invasive and
noninvasive strategies for management of suspected ventilator-associated
pneumonia. A randomized trial. Ann Intern Med. 2000;132:621-630.
13. Timm E. Infection: antibiotics. Once daily aminoglycoside
dosing in ICU patients. Program and abstracts of the
32nd Critical Care Congress; January 28-February 2,
2003; San Antonio, Texas.
14. O'Grady N. Infection: antibiotics. New agents in
late-stage development. Program and abstracts of the
32nd Critical Care Congress; January 28-February 2,
2003; San Antonio, Texas.
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