Clonal spread of staphylococci among patients with peritonitis associated with continuous ambulatory peritoneal dialysis

被引:28
作者
Monsen, T [1 ]
Olofsson, C
Rönnmark, M
Wiström, J
机构
[1] Univ Umea Hosp, Dept Clin Bacteriol, S-90185 Umea, Sweden
[2] Univ Umea Hosp, Dept Infect Dis, S-90185 Umea, Sweden
关键词
viral infection; peritonitis; dialysate; epidemiology; PFGE; coagulase-negative staphylococci;
D O I
10.1046/j.1523-1755.2000.00882.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Peritonitis is the most important complication of continuous ambulatory peritoneal dialysis (CAPD). Coagulase-negative staphylococci (CNS) are the most common causes of peritonitis, only limited information is available regarding the distribution and epidemiology of different CNS species associated with CAPD peritonitis. Methods. CNS isolated from dialysis effluent from CAPD patients with peritonitis was identified by species and further analyzed with pulsed-field gel electrophoresis (PFGE). Results. A total of 216 microorganisms (206 bacteria and 10 Candida species) were isolated from 196 consecutive culture-positive CAPD samples obtained from 75 patients. One hundred and twenty-one (56%) isolates represented staphylococci. The four most frequently isolated staphylococcal species were Staphylococcus epidermidis (70 isolates), Staphylococcus aureus (31 isolates), Staphylococcus hemolyticus (10 isolates), and Staphylococcus hominis (4 isolates). PFGE analysis revealed the clonal spread among patients of three different clones of S. epidermidis and one clone of S. aureus among the investigated patients. Indistinguishable isolates of either S. epidermidis, S. hominis, or S. aureus were also isolated in repeated samples from several patients. Conclusion. PFGE is a useful method for the epidemiological evaluation of staphylococci-associated CAPD infections and should replace older and less accurate methods, such as antibiotic sensitivity patterns. We recommend that CNS isolates from patients with CAPD-associated peritonitis should be saved for future investigations and typing, which would aid in the management of this patient category.
引用
收藏
页码:613 / 618
页数:6
相关论文
共 19 条
[1]   MULTIPLEX POLYMERASE CHAIN-REACTION FOR DETECTION OF GENES FOR STAPHYLOCOCCUS-AUREUS THERMONUCLEASE AND METHICILLIN RESISTANCE AND CORRELATION WITH OXACILLIN RESISTANCE [J].
BRAKSTAD, OG ;
MAELAND, JA ;
TVETEN, Y .
APMIS, 1993, 101 (09) :681-688
[2]   RECURRENT CAPD PERITONITIS CAUSED BY COAGULASE-NEGATIVE STAPHYLOCOCCI - REINFECTION OR RELAPSE DETERMINED BY CLINICAL-CRITERIA AND TYPING METHODS [J].
BROWN, AL ;
STEPHENSON, JR ;
BAKER, LRI ;
TABAQCHALI, S .
JOURNAL OF HOSPITAL INFECTION, 1991, 18 (02) :109-122
[3]   Outcomes of single organism peritonitis in peritoneal dialysis: Gram negatives versus gram positives in the Network 9 Peritonitis Study [J].
Bunke, CM ;
Brier, ME ;
Golper, TA .
KIDNEY INTERNATIONAL, 1997, 52 (02) :524-529
[4]   TYPING OF COAGULASE-NEGATIVE STAPHYLOCOCCI FROM PERITONITIS IN CAPD PATIENTS BY THE PHP-CS SYSTEM AND REA [J].
JUNG, K ;
BRAUNER, A ;
KUHN, I ;
RANSJO, U ;
HYLANDER, B ;
FLOCK, JI ;
MOLLBY, R .
APMIS, 1995, 103 (09) :679-685
[5]   SIMPLIFIED SCHEME FOR ROUTINE IDENTIFICATION OF HUMAN STAPHYLOCOCCUS SPECIES [J].
KLOOS, WE ;
SCHLEIFER, KH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1975, 1 (01) :82-88
[6]   UPDATE ON CLINICAL-SIGNIFICANCE OF COAGULASE-NEGATIVE STAPHYLOCOCCI [J].
KLOOS, WE ;
BANNERMAN, TL .
CLINICAL MICROBIOLOGY REVIEWS, 1994, 7 (01) :117-140
[7]   LABORATORY DIAGNOSIS OF PERITONITIS IN PATIENTS ON CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS [J].
LUDLAM, HA ;
PRICE, TNC ;
BERRY, AJ ;
PHILLIPS, I .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (09) :1757-1762
[8]   Molecular epidemiology of Staphylococcus epidermidis isolates in a hematological unit during a 4-month survey [J].
Lyytikainen, O ;
Valtonen, V ;
Sivonen, A ;
Ryhanen, R ;
VuopioVarkila, J .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1995, 27 (06) :575-580
[9]   An inexpensive and reliable method for routine identification of staphylococcal species [J].
Monsen, T ;
Rönnmark, M ;
Olofsson, C ;
Wiström, J .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1998, 17 (05) :327-335
[10]  
Monsen T, 1999, SCAND J INFECT DIS, V31, P399, DOI 10.1080/00365549950163860