Comparison of microbial adherence to antiseptic and antibiotic central venous catheters using a novel agar subcutaneous infection model

被引:18
作者
Gaonkar, TA [1 ]
Modak, SM [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Surg, New York, NY 10032 USA
关键词
colonization; antimicrobials; silver sulfadiazine; chlorhexidine;
D O I
10.1093/jac/dkg361
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
An agar subcutaneous infection model (agar model), which simulates the rat subcutaneous infection model (rat model), was developed to assess the ability of antimicrobial catheters to resist microbial colonization. The catheters were implanted in the agar and rat models and the insertion sites were infected immediately or on day 7, 14 or 21 post-implantation. The catheters implanted in the agar model were transferred to fresh media one day before infection on day 7, 14 or 21. The efficacy of chlorhexidine and silver sulfadiazine impregnated (CS) catheters, CS catheters with higher levels of chlorhexidine (CS+ catheters), minocycline-rifampicin (MR) catheters and silver catheters against Staphylococcus aureus and rifampicin-resistant Staphylococcus epidermidis RIF-r2 was compared in the agar and rat models. No significant difference in the adherence or the drug release was found between the in vitro and in vivo models. In both models, CS+ and MR catheters were effective against S. aureus even when infected on day 14, whereas CS catheters were colonized when challenged on day 7. CS+ catheters were effective against S. epidermidis RIF-r2, whereas MR catheters showed adherence when infected on day 7. CS+ catheters prevented colonization of all the organisms including, Enterobacter aerogenes, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Candida albicans in the agar model, whereas MR catheters were effective only against S. aureus and S. epidermidis strains. Silver catheters were ineffective against all the organisms. The agar model may be used to predict the in vivo efficacy of antimicrobial catheters against various pathogens.
引用
收藏
页码:389 / 396
页数:8
相关论文
共 32 条
[1]  
Bach A, 1995, ZBL BAKT-INT J MED M, V283, P208
[2]   In vitro zones of inhibition of coated vascular catheters predict efficacy in preventing catheter infection with Staphylococcus aureus in vivo [J].
Bassetti, S ;
Hu, J ;
D'Agostino, RB ;
Sherertz, RJ .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2000, 19 (08) :612-617
[3]   Prolonged antimicrobial activity of a catheter containing chlorhexidine-silver sulfadiazine extends protection against catheter infections in vivo [J].
Bassetti, S ;
Hu, J ;
D'Agostino, RB ;
Sherertz, RJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (05) :1535-1538
[4]  
BJORNSON HS, 1982, SURGERY, V92, P720
[5]   POSSIBLE ROLE OF CAPILLARY ACTION IN PATHOGENESIS OF EXPERIMENTAL CATHETER-ASSOCIATED DERMAL TUNNEL INFECTIONS [J].
COOPER, GL ;
SCHILLER, AL ;
HOPKINS, CC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (01) :8-12
[6]   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
[7]   THE USE OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS TO PREVENT ADHERENCE OF STAPHYLOCOCCUS-EPIDERMIDIS TO MEDICAL POLYMERS [J].
FARBER, BF ;
WOLFF, AG .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (04) :861-865
[8]   COMPARISON OF 4-PERCENT CHLORHEXIDINE GLUCONATE IN A DETERGENT BASE (HIBICLENS) AND POVIDONE-IODINE (BETADINE) FOR THE SKIN PREPARATION OF HEMODIALYSIS-PATIENTS AND PERSONNEL [J].
GOLDBLUM, SE ;
ULRICH, JA ;
GOLDMAN, RS ;
REED, WP ;
AVASTHI, PS .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1983, 2 (05) :548-552
[9]   DECREASED BACTERIAL ADHERENCE AND BIOFILM FORMATION ON CHLORHEXIDINE AND SILVER SULFADIAZINE-IMPREGNATED CENTRAL VENOUS CATHETERS IMPLANTED IN SWINE [J].
GREENFELD, JI ;
SAMPATH, L ;
POPILSKIS, SJ ;
BRUNNERT, SR ;
STYLIANOS, S ;
MODAK, S .
CRITICAL CARE MEDICINE, 1995, 23 (05) :894-900
[10]  
HAMPTON AA, 1988, SURG CLIN N AM, V68, P57