Risk factors for candidemia in neonatal intensive care unit patients

被引:379
作者
Saiman, L
Ludington, E
Pfaller, M
Rangel-Frausto, S
Wiblin, RT
Dawson, J
Blumberg, HM
Patterson, JE
Rinaldi, M
Edwards, JE
Wenzel, RP
Jarvis, W
机构
[1] Columbia Univ, Dept Pediat, New York, NY 10032 USA
[2] Univ Iowa, Coll Med, Dept Biostat, Iowa City, IA USA
[3] Univ Iowa, Coll Med, Dept Med, Iowa City, IA 52242 USA
[4] Emory Univ, Sch Med, Dept Med, Atlanta, GA USA
[5] Grady Mem Hosp, Atlanta, GA 30335 USA
[6] Ctr Dis Control & Prevent, Hosp Infect Program, Atlanta, GA USA
[7] Univ Texas, Hlth Sci Ctr, Dept Med, San Antonio, TX 78284 USA
[8] Univ Calif Los Angeles, Sch Med, Dept Med, Los Angeles, CA 90024 USA
[9] Virginia Commonwealth Univ, Med Coll Virginia, Dept Med, Richmond, VA 23298 USA
关键词
Candida; neonates; premature infants; fungal colonization; risk factors;
D O I
10.1097/00006454-200004000-00011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Candida species are important nosocomial pathogens in neonatal intensive care unit (NICU) patients, Methods, A prospective cohort study was per formed in six geographically diverse NICUs from 1993 to 1995 to determine the incidence of and risk factors for candidemia, including the role of gastrointestinal (GI) tract colonization. Study procedures included rectal swabs to detect fungal colonization and active surveillance to identify risk factors for candidemia, Candida strains obtained from the GI tract and blood were analyzed by pulsed field gel electrophoresis to determine whether colonizing strains caused candidemia. Results. In all, 2847 infants were enrolled and 35 (1.2%) developed candidemia (12.3 cases per 1000 patient discharges or 0.63 case per 1000 catheter days) including 23 of 421 (5.5%) babies less than or equal to 1000 g, After adjusting for birth weight and abdominal surgery, forward multivariate logistic regression analysis demonstrated significant risk factors, including gestational age <32 weeks, 5-min Apgar <5; shock, disseminated intravascular coagulopathy, prior use of intralipid, parenteral nutrition, central venous catheters, H2 blockers, intubation or length of stay >7 days before candidemia (P < 0.05), Catheters, steroids and GI tract colonization were not independent risk factors, but GI tract colonization preceded candidemia in 15 of 35 (43%) case patients. Conclusions. Candida spp. are an important cause of late onset sepsis in NICU patients. The incidence of candidemia might be decreased by the judicious use of treatments identified as risk factors and avoiding H2 blockers.
引用
收藏
页码:319 / 324
页数:6
相关论文
共 32 条
[1]  
BALEY JE, 1984, PEDIATRICS, V73, P144
[2]  
BALEY JE, 1986, PEDIATRICS, V78, P225
[3]  
BECKSAGUE CM, 1993, J INFECT DIS, V167, P1247, DOI 10.1093/infdis/167.5.1247
[4]  
BECKSAGUE CM, 1994, PEDIATR INFECT DIS J, V13, P1110, DOI 10.1097/00006454-199412000-00008
[5]   DECREASED ADHERENCE, CHEMOTAXIS AND PHAGOCYTIC ACTIVITIES OF NEUTROPHILS FROM PRETERM NEONATES [J].
BEKTAS, S ;
GOETZE, B ;
SPEER, CP .
ACTA PAEDIATRICA SCANDINAVICA, 1990, 79 (11) :1031-1038
[6]   USE OF DNA-FINGERPRINTING AND BIOTYPING METHODS TO STUDY A CANDIDA-ALBICANS OUTBREAK IN A NEONATAL INTENSIVE-CARE UNIT [J].
BETREMIEUX, P ;
CHEVRIER, S ;
QUINDOS, G ;
SULLIVAN, D ;
POLONELLI, L ;
GUIGUEN, C .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1994, 13 (10) :899-905
[7]  
BOTAS CM, 1995, PEDIATRICS, V95, P883
[8]   The role of the gastrointestinal tract in hematogenous candidiasis: From the laboratory to the bedside [J].
Cole, GT ;
Halawa, AA ;
Anaissie, EJ .
CLINICAL INFECTIOUS DISEASES, 1996, 22 :S73-S88
[9]   NOSOCOMIAL PNEUMONIA IN INTUBATED PATIENTS GIVEN SUCRALFATE AS COMPARED WITH ANTACIDS OR HISTAMINE TYPE-2 BLOCKERS - THE ROLE OF GASTRIC COLONIZATION [J].
DRIKS, MR ;
CRAVEN, DE ;
CELLI, BR ;
MANNING, M ;
BURKE, RA ;
GARVIN, GM ;
KUNCHES, LM ;
FARBER, HW ;
WEDEL, SA ;
MCCABE, WR .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (22) :1376-1382
[10]   INCIDENCE OF CANDIDA-PARAPSILOSIS COLONIZATION IN AN INTENSIVE-CARE NURSERY POPULATION AND ITS ASSOCIATION WITH INVASIVE FUNGAL DISEASE [J].
ELMOHANDES, AE ;
JOHNSONROBBINS, L ;
KEISER, JF ;
SIMMENS, SJ ;
AURE, MV .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1994, 13 (06) :520-524