Clonal expansion of Staphylococcus epidermidis strains causing Hickman catheter-related infections in a hemato-oncologic department. 1998

J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
Department of Medical Microbiology & Infectious Diseases, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands. nouwen@bacl.azr.nl

The detailed analysis of 411 strains of coagulase-negative staphylococci (CoNS) obtained from 40 neutropenic hemato-oncologic patients (61 Hickman catheter episodes) on intensive chemotherapy is described. By random amplification of polymorphic DNA (RAPD) analysis, a total of 88 different genotypes were detected: 51 in air samples and 30 in skin cultures prior to insertion, 12 in blood cultures after insertion, and only 5 involved in catheter-related infections (CRI). Two RAPD genotypes of Staphylococcus epidermidis predominated, and their prevalence increased during patient hospitalization. At insertion, these clones constituted 11 of 86 (13%) CoNS isolated from air samples and 33 of 75 (44%) CoNS isolated from skin cultures. After insertion, their combined prevalence increased to 33 of 62 (53%) in catheters not associated with CRI and 139 of 188 (74%) in catheters associated with CRI (P = 0.0041). These two predominant S. epidermidis clones gave rise to a very high incidence of CRI (6.0 per 1,000 catheter days) and a very high catheter removal rate for CRI, 70%, despite prompt treatment with vancomycin. A likely source of S. epidermidis strains involved in CRI appeared to be the skin flora in 75% of cases. The validity of these observations was confirmed by pulsed-field gel electrophoresis (PFGE) of SmaI DNA macrorestriction fragments of blood culture CoNS isolates. Again, two predominant CoNS genotypes were found (combined prevalence, 60%). RAPD and PFGE yielded concordant results in 75% of cases. Retrospectively, the same two predominant CoNS clones were also found among blood culture CoNS isolates from the same hematology department in the period 1991 to 1993 (combined prevalence, 42%) but not in the period 1978 to 1982. These observations underscore the pathogenic potential of clonal CoNS types that have successfully and persistently colonized patients in this hemato-oncology department.

UI MeSH Term Description Entries
D009181 Mycoses Diseases caused by FUNGI. Fungus Diseases,Fungal Diseases,Fungal Infections,Fungus Infections,Disease, Fungal,Disease, Fungus,Diseases, Fungal,Diseases, Fungus,Fungal Disease,Fungal Infection,Fungus Disease,Fungus Infection,Infection, Fungal,Infection, Fungus,Infections, Fungal,Infections, Fungus
D009503 Neutropenia A decrease in the number of NEUTROPHILS found in the blood. Neutropenias
D002405 Catheterization, Central Venous Placement of an intravenous CATHETER in the subclavian, jugular, or other central vein. Central Venous Catheterization,Venous Catheterization, Central,Catheterization, Central,Central Catheterization,Catheterizations, Central,Catheterizations, Central Venous,Central Catheterizations,Central Venous Catheterizations,Venous Catheterizations, Central
D002408 Catheters, Indwelling Catheters designed to be left within an organ or passage for an extended period of time. Implantable Catheters,In-Dwelling Catheters,Catheter, In-Dwelling,Catheter, Indwelling,Catheters, In-Dwelling,In Dwelling Catheters,In-Dwelling Catheter,Indwelling Catheter,Indwelling Catheters
D002939 Ciprofloxacin A broad-spectrum antimicrobial carboxyfluoroquinoline. Bay-09867,Ciprinol,Cipro,Ciprofloxacin Hydrochloride,Ciprofloxacin Hydrochloride Anhydrous,Ciprofloxacin Monohydrochloride Monohydrate,Anhydrous, Ciprofloxacin Hydrochloride,Bay 09867,Bay09867,Hydrochloride Anhydrous, Ciprofloxacin,Hydrochloride, Ciprofloxacin,Monohydrate, Ciprofloxacin Monohydrochloride,Monohydrochloride Monohydrate, Ciprofloxacin
D005838 Genotype The genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS. Genogroup,Genogroups,Genotypes
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000391 Air Microbiology The presence of bacteria, viruses, and fungi in the air. This term is not restricted to pathogenic organisms. Microbiology, Air
D001431 Bacteriological Techniques Techniques used in studying bacteria. Bacteriologic Technic,Bacteriologic Technics,Bacteriologic Techniques,Bacteriological Technique,Technic, Bacteriological,Technics, Bacteriological,Technique, Bacteriological,Techniques, Bacteriological,Bacteriologic Technique,Bacteriological Technic,Bacteriological Technics,Technic, Bacteriologic,Technics, Bacteriologic,Technique, Bacteriologic,Techniques, Bacteriologic
D012867 Skin The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS.

Related Publications

J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
July 1991, The American journal of medicine,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
July 2001, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
January 1984, Infection,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
November 1983, Lancet (London, England),
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
August 1998, International journal of antimicrobial agents,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
July 2007, Pathologie-biologie,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
September 2018, Klinicka mikrobiologie a infekcni lekarstvi,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
January 1999, The Mount Sinai journal of medicine, New York,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
October 1975, Journal of clinical microbiology,
J L Nouwen, and A van Belkum, and S de Marie, and J Sluijs, and J J Wielenga, and J A Kluytmans, and H A Verbrugh
January 1989, JPEN. Journal of parenteral and enteral nutrition,
Copied contents to your clipboard!