Potentially multidrug-resistant non-fermentative Gram-negative pathogens causing nosocomial pneumonia

被引:44
作者
Ferrara, AM [1 ]
机构
[1] Univ Pavia, IRCCS, Policlin San Matteo, Dept Haematol Pneumol Cardiovasc & Surg Sci, I-27100 Pavia, Italy
关键词
Pseudomonas aeruginosa; Acinetobacter baumannii; Stenotrophomonas maltophilia; nosocomial pneumonia; antimicrobial resistance;
D O I
10.1016/j.ijantimicag.2005.11.005
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Owing to its high morbidity and mortality, nosocomial pneumonia represents a particularly serious illness and one of the most frequent complications in ventilated patients admitted to the Intensive Care Unit. Gram-negative microorganisms, such as Pseudomonas aeruginosa, Acinetobacter baumannii and Stenotrophomonas maltophilia, are the most relevant pathogens responsible for particularly difficult-to-treat nosocomial pneumonia. The intrinsic resistance of these bacteria to many antimicrobial agents and, in addition, the variety of their increasingly recognised acquired resistance mechanisms make their management in the hospital setting problematic. Antimicrobials that retain the best activity against P. aeruginosa include carbapenems, piperacillin, cefepime, ceftazidime, ciprofloxacin and certain aminoglycosides, whilst carbapenems and sulphamethoxazole/trimethoprim remain the most active agents against A. baumannii and S. maltophilia, respectively. However, the growing emergence among these microorganisms of multidrug-resistant (MDR) isolates and the severity of associated infections call for potential alternative drugs. Sulbactam alone or in combination with ampicillin may represent an acceptable option for MDR A. baumannii as well as colistin, which also covers MDR P. aeruginosa. Newer fluoroquinolones and some tetracyclines may be alternative drugs both for MDR S. maltophilia and A. baumannii. However, large-scale controlled clinical trials are needed to confirm these promising therapeutic options. (c) 2005 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:183 / 195
页数:13
相关论文
共 128 条
[1]   Activities of ciprofloxacin and moxifloxacin against Stenotrophomonas maltophilia and emergence of resistant mutants in an in vitro pharmacokinetic-pharmacodynamic model [J].
Ba, BB ;
Feghali, H ;
Arpin, C ;
Saux, MC ;
Quentin, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (03) :946-953
[2]   The treatment of respiratory pseudomonas infection in cystic fibrosis - What drug and which way? [J].
Banerjee, D ;
Stableforth, D .
DRUGS, 2000, 60 (05) :1053-1064
[3]   Use of aerosolized colistin sodium in cystic fibrosis patients awaiting lung transplantation [J].
Bauldoff, GS ;
Nunley, DR ;
Manzetti, JD ;
Dauber, JH ;
Keenan, RJ .
TRANSPLANTATION, 1997, 64 (05) :748-752
[4]   The increasing role of Acinetobacter species as nosocomial pathogens [J].
Eugénie Bergogne-Bérézin .
Current Infectious Disease Reports, 2001, 3 (5) :440-444
[5]   Acinetobacter spp, as nosocomial pathogens: Microbiological, clinical, and epidemiological features [J].
BergogneBerezin, E ;
Towner, KJ .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (02) :148-+
[6]  
Beringer P, 2001, Curr Opin Pulm Med, V7, P434, DOI 10.1097/00063198-200111000-00013
[7]   LOW MAGNESIUM AND PHOSPHOLIPID CONTENT OF CELL WALLS OF PSEUDOMONAS-AERUGINOSA RESISTANT TO POLYMYXIN [J].
BROWN, MRW ;
WATKINS, WM .
NATURE, 1970, 227 (5265) :1360-&
[8]   DOUBLE-BLIND-STUDY OF ENDOTRACHEAL TOBRAMYCIN IN THE TREATMENT OF GRAM-NEGATIVE BACTERIAL PNEUMONIA [J].
BROWN, RB ;
KRUSE, JA ;
COUNTS, GW ;
RUSSELL, JA ;
CHRISTOU, NV ;
SANDS, ML .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (02) :269-272
[9]  
Campbell GD, 1996, AM J RESP CRIT CARE, V153, P1711
[10]   Multi-resistant Gram-negative bacilli:: from epidemics to endemics [J].
Cantón, R ;
Coque, TM ;
Baquero, F .
CURRENT OPINION IN INFECTIOUS DISEASES, 2003, 16 (04) :315-325