Assessing the relationship between the use of nonsteroidal antiinflammatory drugs and necrotizing fasciitis caused by group A streptococcus

被引:115
作者
Aronoff, DM
Bloch, KC
机构
[1] Univ Michigan Hlth Syst, Div Infect Dis, Dept Med, Ann Arbor, MI 48109 USA
[2] Vanderbilt Univ, Sch Med, Div Infect Dis, Dept Med, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Prevent Med, Nashville, TN 37212 USA
关键词
D O I
10.1097/00005792-200307000-00001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Group A streptococcal (GAS) necrotizing fasciitis is a rapidly progressive soft tissue infection. Elderly and chronically ill individuals are at greatest risk, particularly when skin breakdown is present. Reports suggest that nonsteroidal antimflammatory drugs (NSAIDs) increase the risk of developing GAS necrotizing fasciitis, impede its timely recognition and management, and accelerate the course of infection. We present a literature review conducted to examine these hypotheses and present a case of GAS necrotizing fasciitis associated with rofecoxib use. Initial symptoms of fasciitis may be nondescript, mimicking more benign conditions such as cellulitis, arthritis, or musculoskeletal pain. Case reports and retrospective studies suggest that the application of NSAIDs to relieve these nonspecific symptoms can delay diagnosis and treatment of GAS necrotizing fasciitis. However, prospective studies do not support a risk of developing GAS necrotizing fasciitis as a result of NSAID therapy, or a worsening of established streptococcal infection. To avoid the application of NSAIDs in lieu of aggressive medical and surgical management of streptococcal fasciitis, clinicians must understand the early symptoms of GAS necrotizing fasciitis that precede visible soft tissue necrosis. A rational approach to patients presenting with localized soft tissue pain will enhance detection and therapy of this rapidly progressive, life-threatening disease.
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页码:225 / 235
页数:11
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共 63 条
[1]   Antipyretics: Mechanisms of action and clinical use in fever suppression [J].
Aronoff, DM ;
Neilson, EG .
AMERICAN JOURNAL OF MEDICINE, 2001, 111 (04) :304-315
[2]   Molecular analysis of the role of the group A streptococcal cysteine protease, hyaluronic acid capsule, and M protein in a murine model of human invasive soft-tissue infection [J].
Ashbaugh, CD ;
Warren, HB ;
Carey, VJ ;
Wessels, MR .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (03) :550-560
[3]  
Barnham M, 1997, ADV EXP MED BIOL, V418, P145
[5]   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
[6]  
Basma H, 1999, INFECT IMMUN, V67, P1871
[7]   The initial outpatient-physician encounter in group a streptococcal necrotizing fasciitis [J].
Bisno, AL ;
Cockerill, FR ;
Bermudez, CT .
CLINICAL INFECTIOUS DISEASES, 2000, 31 (02) :607-608
[8]   Current concepts - Streptococcal infections of skin and soft tissues [J].
Bisno, AL ;
Stevens, DL .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (04) :240-245
[9]   Fever: pathological or physiological, injurious or beneficial? [J].
Blatteis, CM .
JOURNAL OF THERMAL BIOLOGY, 2003, 28 (01) :1-13
[10]   Effect of paracetamol on parasite clearance time in Plasmodium falciparum malaria [J].
Brandts, CH ;
Ndjave, M ;
Graninger, W ;
Kremsner, PG .
LANCET, 1997, 350 (9079) :704-709