Effects of Selective and Nonselective Nonsteroidal Anti-inflammatory Drugs on Antibiotic Efficacy of Experimental Group A Streptococcal Myonecrosis

被引:44
作者
Hamilton, Stephanie M. [1 ]
Bayer, Clifford R. [1 ]
Stevens, Dennis L. [1 ,2 ]
Bryant, Amy E. [1 ,2 ]
机构
[1] US Dept Vet Affairs, Off Res & Dev, Boise, ID USA
[2] Univ Washington Sch Med, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
Streptococcus pyogenes; myonecrosis; NSAIDs; SOFT-TISSUE INFECTIONS; TOXIC-SHOCK-SYNDROME; NECROTIZING FASCIITIS; PRIMARY VARICELLA; MICE; PENICILLIN; PYOGENES; SUSCEPTIBILITY; INHIBITION; EXPRESSION;
D O I
10.1093/infdis/jit594
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Epidemiologic evidence suggests that nonsteroidal anti-inflammatory drugs (NSAIDs) contribute to more severe group A streptococcal (GAS) infections, yet a beneficial role for NSAIDs has been demonstrated in other experimental bacterial infections. Methods. Nonselective (ketorolac tromethamine, ibuprofen, indomethacin), COX-1-selective (SC-560), or COX-2-selective (SC-236) NSAIDs +/- antibiotics (penicillin, clindamycin) were given to mice challenged intramuscularly with M-type 3 GAS and disease course was followed for 14 days. Results. All nonselective NSAIDs significantly accelerated mortality and reduced antibiotic efficacy; COX-selective NSAIDs had no significant effects. Conclusions. Use of nonselective NSAIDs, either alone or as adjuncts to antibiotic therapy, for GAS soft tissue infection may contribute to worse outcomes.
引用
收藏
页码:1429 / 1435
页数:7
相关论文
共 29 条
[1]   An unbiased systems genetics approach to mapping genetic loci modulating susceptibility to severe streptococcal sepsis [J].
Abdeltawab, Nourtan F. ;
Aziz, Ramy K. ;
Kansal, Rita ;
Rowe, Sarah L. ;
Su, Yin ;
Gardner, Lidia ;
Brannen, Charity ;
Nooh, Mohammed M. ;
Attia, Ramy R. ;
Abdelsamed, Hossam A. ;
Taylor, William L. ;
Lu, Lu ;
Williams, Robert W. ;
Kotb, Malak .
PLOS PATHOGENS, 2008, 4 (04)
[2]   Assessing the relationship between the use of nonsteroidal antiinflammatory drugs and necrotizing fasciitis caused by group A streptococcus [J].
Aronoff, DM ;
Bloch, KC .
MEDICINE, 2003, 82 (04) :225-235
[3]   Susceptibility to severe streptococcal sepsis: use of a large set of isogenic mouse lines to study genetic and environmental factors [J].
Aziz, R. K. ;
Kansal, R. ;
Abdeltawab, N. F. ;
Rowe, S. L. ;
Su, Y. ;
Carrigan, D. ;
Nooh, M. M. ;
Attia, R. R. ;
Brannen, C. ;
Gardner, L. A. ;
Lu, L. ;
Williams, R. W. ;
Kotb, M. .
GENES AND IMMUNITY, 2007, 8 (05) :404-415
[4]   Streptococcal toxic shock syndrome: a description of 14 cases from North Yorkshire, UK [J].
Barnham, MRD ;
Weightman, NC ;
Anderson, AW ;
Tanna, A .
CLINICAL MICROBIOLOGY AND INFECTION, 2002, 8 (03) :174-181
[5]  
BISNO AL, 2005, PRINCIPLES PRACTICE, P2362
[6]   The COX-2 pathway is essential during early stages of skeletal muscle regeneration [J].
Bondesen, BA ;
Mills, ST ;
Kegley, KM ;
Pavlath, GK .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (02) :C475-C483
[7]  
BROOKS PM, 1991, NEW ENGL J MED, V324, P1716
[8]   Altered IL-4 mRNA stability correlates with Th1 and Th2 bias and susceptibility to hypersensitivity pneumonitis in two inbred strains of mice [J].
Butler, NS ;
Monick, MM ;
Yarovinsky, TO ;
Powers, LS ;
Hunninghake, GW .
JOURNAL OF IMMUNOLOGY, 2002, 169 (07) :3700-3709
[9]   Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease [J].
Dial, S ;
Delaney, JAC ;
Barkun, AN ;
Suissa, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 294 (23) :2989-2995
[10]   Inducible Cyclooxygenase Released Prostaglandin E2 Modulates the Severity of Infection Caused by Streptococcus pyogenes [J].
Goldmann, Oliver ;
Hertzen, Erika ;
Hecht, Alexander ;
Schmidt, Heike ;
Lehne, Sabine ;
Norrby-Teglund, Anna ;
Medina, Eva .
JOURNAL OF IMMUNOLOGY, 2010, 185 (04) :2372-2381