Trimethoprim In Vitro Antibacterial Activity is Not Increased by Adding Sulfamethoxazole for Pediatric Escherichia coli Urinary Tract Infection

被引:6
作者
Nguyen, Hiep T. [1 ]
Hurwitz, Richard S. [3 ]
DeFoor, W. Robert [5 ]
Minevich, Eugene [5 ]
McAdam, Alexander J. [2 ]
Mortensen, Joel E. [6 ]
Novak-Weekley, Susan M. [4 ]
Minnillo, Brian J.
Elder, Jack S. [7 ]
机构
[1] Childrens Hosp Boston, Dept Urol, Boston, MA 02115 USA
[2] Childrens Hosp Boston, Dept Lab Med, Boston, MA 02115 USA
[3] Kaiser Permanente Med Ctr So Calif, Dept Urol, Los Angeles, CA USA
[4] So Calif Permanente Med Grp Reg Reference Labs, Dept Microbiol, N Hollywood, CA USA
[5] Cincinnati Childrens Hosp Med Ctr, Div Pediat Urol, Cincinnati, OH USA
[6] Cincinnati Childrens Hosp Med Ctr, Dept Pathol & Lab Med, Cincinnati, OH USA
[7] Childrens Hosp Michigan, Vattikuti Urol Inst, Henry Ford Hlth Syst, Dept Urol, Detroit, MI 48201 USA
关键词
urinary tract; urinary tract infections; Escherichia coli infections; trimethoprim-sulfamethoxazole combination; drug hypersensitivity; TOXIC EPIDERMAL NECROLYSIS; PHARMACOKINETICS; COTRIMOXAZOLE; SULFONAMIDES; COMBINATIONS; CHILDREN;
D O I
10.1016/j.juro.2010.03.084
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: The combination of trimethoprim/sulfamethoxazole is often used to treat uncomplicated urinary tract infections in children. The rationale for combining trimethoprim and sulfamethoxazole is that they may act synergistically to increase antibacterial activity. However, approximately 3% of patients show allergic reactions to sulfamethoxazole, of which some are serious (liver failure and Stevens-Johnson syndrome). We determined whether adding sulfamethoxazole is necessary to increase in vitro antibacterial activity for pediatric urinary tract infection compared to that of trimethoprim alone. Materials and Methods: We prospectively identified 1,298 children with urinary tract infection (greater than 100,000 cfu/ml Escherichia coli) from a total of 4 American regions. In vitro susceptibility of bacterial isolates to sulfamethoxazole, trimethoprim and trimethoprim/sulfamethoxazole was determined using disk diffusion. Ampicillin susceptibility was tested at 2 sites. At 1 site all uropathogens from consecutive urinary isolates were evaluated. Results: E. coli susceptibility to trimethoprim was 70%, comparable to the 70% of trimethoprim/sulfamethoxazole (p = 0.9) and higher than the 56.9% of sulfamethoxazole (p < 0.05). This susceptibility pattern was without regional differences. At 2 sites susceptibility to trimethoprim was significantly higher than to ampicillin. At 1 site the susceptibility of other uropathogens to trimethoprim and trimethoprim/sulfamethoxazole was similar to that of E. coli. Conclusions: In children with urinary tract infection in vitro susceptibility to trimethoprim was comparable to that to trimethoprim/sulfamethoxazole and significantly higher than to sulfamethoxazole. This finding was similar at all sites. Adding sulfamethoxazole appears unnecessary and may represent a risk to patients. Trimethoprim can be used as an alternative to trimethoprim/sulfamethoxazole based on in vitro antibacterial susceptibility. Routine trimethoprim/sulfamethoxazole use for urinary tract infection should be carefully reevaluated.
引用
收藏
页码:305 / 310
页数:6
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