Antimicrobial use and outcomes in patients with multidrug-resistant and pansusceptible Salmonella Newport infections, 2002-2003

被引:25
作者
Devasia, RA
Varma, JK
Whichard, J
Gettner, S
Cronquist, AB
Hurd, S
Segler, S
Smith, K
Hoefer, D
Shiferaw, B
Angulo, FJ
Jones, TF
机构
[1] Tennessee Dept Hlth, Nashville, TN USA
[2] Ctr Dis Control & Prevent, EPO, Epidem Intelligence Serv, Atlanta, GA USA
[3] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, Foodborne & Diarrheal Dis Branch, Div Bacterial & Mycot Dis, Atlanta, GA USA
[4] Calif Emerging Infect Program, Oakland, CA USA
[5] Colorado Dept Publ Hlth & Environm, Denver, CO USA
[6] Connecticut Emerging Infect Program, New Haven, CT USA
[7] Georgia Emerging Infect Program, Atlanta, GA USA
[8] Minnesota Dept Hlth, Minneapolis, MN USA
[9] New York State Dept Hlth, Albany, NY USA
[10] Oregon Dept Human Serv, Portland, OR USA
关键词
D O I
10.1089/mdr.2005.11.371
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Multidrug-resistaut Salmonella Newport with decreased susceptibility to ceftriaxone (MDR-AmpC) is becoming increasingly common in its food animal reservoirs and in humans. Few data exist on rates of antimicrobial use or differences in clinical outcomes in persons infected with MDR-AmpC or other Salmonella strains. We conducted a case-comparison analysis of data from a multistate population-based case-control study to identify antimicrobial treatment choices and differences in clinical outcomes in those infected with MDR-AmpC compared to pansusceptible S. Newport. Of isolates from 215 laboratory-confirmed S. Newport cases, 54 (25%) were MDR-AmpC, 146 (68%) were pansusceptible, and 15 (7%) had other resistance patterns; 146 (68%) patients with S. Newport were treated with antimicrobial agents and 66 (33%) were hospitalized. Over two-thirds of cases at low-risk for serious complications received antimicrobial therapy, most commonly with fluoroquinolones, to which this strain was susceptible. There were no significant differences in symptoms, hospitalization, duration of illness, or other outcomes between the persons infected with MDR-AmpC and pansusceptible S. Newport. Although currently prevalent MDR-AmpC S. Newport strains remains susceptible to the antimicrobial most commonly prescribed for it, continued efforts to reduce unnecessary use of antimicrobial agents in food animals and humans are critical to prevent further development of resistance to quinolones and cephalosporins, which is likely to lead to substantial adverse outcomes.
引用
收藏
页码:371 / 377
页数:7
相关论文
共 41 条
[1]   Surveillance for sporadic foodborne disease in the 21st century: The FoodNet perspective [J].
Allos, BM ;
Moore, MR ;
Griffin, PM ;
Tauxe, RV .
CLINICAL INFECTIOUS DISEASES, 2004, 38 :S115-S120
[2]   Public health consequences of use of antimicrobial agents in food animals in the United States [J].
Anderson, AD ;
Nelson, JM ;
Rossiter, S ;
Angulo, FJ .
MICROBIAL DRUG RESISTANCE, 2003, 9 (04) :373-379
[3]   BACTERIAL ENTERIC INFECTIONS IN PERSONS INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS [J].
ANGULO, FJ ;
SWERDLOW, DL .
CLINICAL INFECTIOUS DISEASES, 1995, 21 :S84-S93
[4]   Origins and consequences of antimicrobial-resistant nontyphoidal Salmonella:: Implications for the use of fluoroquinolones in food animals [J].
Angulo, FJ ;
Johnson, KR ;
Tauxe, RV ;
Cohen, ML .
MICROBIAL DRUG RESISTANCE, 2000, 6 (01) :77-83
[5]  
[Anonymous], 2002, M100S12 NCCLS
[6]   EFFECT OF ANTIBIOTIC THERAPY IN ACUTE SALMONELLOSIS ON FECAL EXCRETION OF SALMONELLAE [J].
ASERKOFF, B ;
BENNETT, JV .
NEW ENGLAND JOURNAL OF MEDICINE, 1969, 281 (12) :636-&
[7]  
Bager F, 2001, VET RES, V32, P285, DOI 10.1051/vetres:2001125
[8]   Use of antibiotic susceptibility patterns and pulsed-field gel electrophoresis to compare historic and contemporary isolates of multi-drug-resistant Salmonella enterica subsp enterica serovar Newport [J].
Berge, ACB ;
Adaska, JM ;
Sischo, WM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (01) :318-323
[9]   Characterization of plasmids carrying CMY-2 from expanded-spectrum cephalosporin-resistant Salmonella strains isolated in the United States between 1996 and 1998 [J].
Carattoli, A ;
Tosini, F ;
Giles, WP ;
Rupp, ME ;
Hinrichs, SH ;
Angulo, FJ ;
Barrett, TJ ;
Fey, PD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (05) :1269-1272
[10]  
*CDCP, 2004, NAT ANT RES MON SYST