In vitro and in vivo efficacy of catheters impregnated with antiseptics or antibiotics: Evaluation of the risk of bacterial resistance to the antimicrobials in the catheters

被引:81
作者
Sampath, LA [1 ]
Tambe, SM [1 ]
Modak, SM [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Surg, New York, NY 10032 USA
关键词
D O I
10.1086/501836
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
OBJECTIVE: To compare the efficacy of a new antiseptic catheter containing silver sulfadiazine and chlorhexidine on the external surface and chlorhexidine in the lumens to an antibiotic catheter impregnated with minocycline and rifampin on its external and luminal surfaces. DESIGN: Experimental trial. METHODS: Antimicrobial spectrum of catheters was determined by zones of inhibition. Resistance to luminal colonization was tested in vitro by locking catheter lumens with Staphylococcus epidermidis or Staphylococcus aureus culture after 7 days of perfusion. In vitro development of resistance to the antiseptic or antibiotic combination used in catheters was investigated. In vivo efficacy was tested (rat subcutaneous model) by challenge with sensitive or antibiotic-resistant bacteria. RESULTS: Antiseptic and antibiotic catheters exhibited broad-spectrum action. However, antibiotic catheters were not effective against Candida species and Pseudomonas aeruginosa. Both catheters prevented luminal colonization. Compared to controls, both test catheter,., resisted colonization when challenged with S aureus 7 and 14 days' postimplant (P < .05). Repeated in vitro exposure of S epidermidis culture to the antibiotic and antiseptic combinations led to small increases in the minimum inhibitory concentration (15 times and 2 times, respectively). Unlike the antibiotic catheter, the in vitro and in vivo activity of the antiseptic catheter was unaffected by the resistance profile of the test organism. Antiseptic catheters were more effective than antibiotic catheters in preventing colonization by rifampin-resistant S epidermidis in vivo (P < .05). CONCLUSIONS: Antiseptic and antibiotic catheters exhibit similar efficacy; however, when challenged with a rifampin-resistant strain, the antibiotic catheter appeared to be more susceptible to colonization than the antiseptic device.
引用
收藏
页码:640 / 646
页数:7
相关论文
共 34 条
[1]   High-level mupirocin resistance among Spanish methicillin-resistant Staphylococcus aureus [J].
Alarcón, T ;
Sanz, JC ;
Blanco, F ;
Domingo, D ;
López-Brea, M .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1998, 17 (12) :877-879
[2]  
Bach A, 1995, ZBL BAKT-INT J MED M, V283, P208
[3]   In vitro susceptibility of Staphylococcus aureus isolated from blood to currently used antistaphylococcal drugs [J].
Baiocchi, P ;
Galie, M ;
Santini, C ;
Carfagna, P ;
Cassone, M ;
Tarasi, D ;
Venditti, M .
JOURNAL OF CHEMOTHERAPY, 1998, 10 (01) :25-28
[4]  
Ciresi DL, 1996, AM SURGEON, V62, P641
[5]   A comparison of two antimicrobial-impregnated central venous catheters [J].
Darouiche, RO ;
Raad, II ;
Heard, SO ;
Thornby, JI ;
Wenker, OC ;
Gabrielli, A ;
Berg, J ;
Khardori, N ;
Hanna, H ;
Hachem, R ;
Harris, RL ;
Mayhall, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (01) :1-8
[6]  
ELLIOTT TSJ, 1993, J ANTIMICROB CHEMOTH, V32, P905
[7]   SENSITIVITY AND RESISTANCE OF ESCHERICHIA-COLI AND STAPHYLOCOCCUS-AUREUS TO CHLORHEXIDINE [J].
FITZGERALD, KA ;
DAVIES, A ;
RUSSELL, AD .
LETTERS IN APPLIED MICROBIOLOGY, 1992, 14 (02) :33-36
[8]   In vitro and in vivo effects of rifampin on Staphylococcus epidermidis graft infections [J].
Garrison, JR ;
Henke, PK ;
Smith, KR ;
Brittian, KR ;
Lam, TM ;
Peyton, JC ;
Bergamini, TM .
ASAIO JOURNAL, 1997, 43 (01) :8-12
[9]   Acquisition of methicillin resistance and progression of multiantibiotic resistance in methicillin-resistant Staphylococcus aureus [J].
Ito, T ;
Hiramatsu, K .
YONSEI MEDICAL JOURNAL, 1998, 39 (06) :526-533
[10]   INVITRO EFFICACY OF A CENTRAL VENOUS CATHETER (HYDROCATH) LOADED WITH TEICOPLANIN TO PREVENT BACTERIAL-COLONIZATION [J].
JANSEN, B ;
JANSEN, S ;
PETERS, G ;
PULVERER, G .
JOURNAL OF HOSPITAL INFECTION, 1992, 22 (02) :93-107