Nasal carriers are more likely to acquire exogenous Staphylococcus aureus strains than non-carriers

被引:19
作者
Ghasemzadeh-Moghaddam, H. [1 ,2 ]
Neela, V. [1 ]
van Wamel, W. [3 ]
Hamat, R. A. [1 ]
Shamsudin, M. nor [1 ,4 ]
Hussin, N. Suhaila Che [5 ]
Aziz, M. N. [5 ]
Haspani, M. S. Mohammad [6 ]
Johar, A. [7 ]
Thevarajah, S. [7 ]
Vos, M.
van Belkum, A. [3 ,8 ]
机构
[1] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Med Microbiol & Parasitol, Serdang 43400, Selangor, Malaysia
[2] North Khorasan Univ Med Sci, Fac Med, Bojnurd, Iran
[3] Erasmus MC, Dept Med Microbiol & Infect Dis, Rotterdam, Netherlands
[4] Univ Putra Malaysia, Inst Biosci, Marine Sci Lab, Serdang 43400, Selangor, Malaysia
[5] Hosp Kuala Lumpur, Pathol Labs, Kuala Lumpur, Malaysia
[6] Hosp Kuala Lumpur, Dept Neurosurg, Kuala Lumpur, Malaysia
[7] Hosp Kuala Lumpur, Dept Dermatol, Kuala Lumpur, Malaysia
[8] BioMerieux, R&D Microbiol, La Balme Les Grottes, France
关键词
Colonization; colonization interference; MRSA; nasal carriage; Staphylococcus aureus; SURGICAL-SITE INFECTIONS; BLOOD-STREAM INFECTIONS; METHICILLIN-RESISTANT; MRSA INFECTION; CARRIAGE; MORTALITY; MUPIROCIN; IMPACT; RISK; EPIDEMIOLOGY;
D O I
10.1016/j.cmi.2015.07.006
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We performed a prospective observational study in a clinical setting to test the hypothesis that prior colonization by a Staphylococcus aureus strain would protect, by colonization interference or other processes, against de novo colonization and, hence, possible endo-infections by newly acquired S. aureus strains. Three hundred and six patients hospitalized for >7 days were enrolled. For every patient, four nasal swabs (days 1, 3, 5, and 7) were taken, and patients were identified as carriers when a positive nasal culture for S. aureus was obtained on day 1 of hospitalization. For all patients who acquired methicillin-resistant S. aureus (MRSA) or methicillin-susceptible S. aureus via colonization and/or infection during hospitalization, strains were collected. We note that our study may suffer from false-negative cultures, local problems with infection control and hospital hygiene, or staphylococcal carriage at alternative anatomical sites. Among all patients, 22% were prior carriers of S. aureus, including 1.9% whom carried MRSA upon admission. The overall nasal staphylococcal carriage rate among dermatology patients was significantly higher than that among neurosurgery patients (n = 25 (55.5%) vs. n = 42 (16.1%), p 0.005). This conclusion held when the carriage definition included individuals who were nasal culture positive on day 1 and day 3 of hospitalization (p 0.0001). All MRSA carriers were dermatology patients. There was significantly less S. aureus acquisition among non-carriers than among carriers during hospitalization (p 0.005). The mean number of days spent in the hospital before experiencing MRSA acquisition in nasal carriers was 5.1, which was significantly lower than the score among non-carriers (22 days, p 0.012). In conclusion, we found that nasal carriage of S. aureus predisposes to rather than protects against staphylococcal acquisition in the nose, thereby refuting our null hypothesis. Clinical Microbiology and Infection (C) 2015 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:998.e1 / 998.e7
页数:7
相关论文
共 36 条
[21]   Species-specific and ubiquitous-DNA-based assays for rapid identification of Staphylococcus aureus [J].
Martineau, F ;
Picard, FJ ;
Roy, PH ;
Ouellete, M ;
Bergeron, MG .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) :618-623
[22]   Is methicillin-resistant Staphylococcus aureus replacing methicillin-susceptible S. aureus? [J].
Mostofsky, Elizabeth ;
Lipsitch, Marc ;
Regev-Yochay, Gili .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2011, 66 (10) :2199-2214
[23]   Longitudinal genetic analyses of Staphylococcus aureus nasal carriage dynamics in a diverse population [J].
Muthukrishnan, Gowrishankar ;
Lamers, Ryan P. ;
Ellis, Austin ;
Paramanandam, Vanathy ;
Persaud, Alana B. ;
Tafur, Sergio ;
Parkinson, Christopher L. ;
Cole, Alexander M. .
BMC INFECTIOUS DISEASES, 2013, 13
[24]   Human factor in Staphylococcus aureus nasal carriage [J].
Nouwen, J ;
Boelens, H ;
van Belkum, A ;
Verbrugh, H .
INFECTION AND IMMUNITY, 2004, 72 (11) :6685-6688
[25]   EFFICACY EVALUATION OF A 4-PERCENT CHLORHEXIDINE GLUCONATE AS A FULL-BODY SHOWER WASH [J].
PAULSON, DS .
AMERICAN JOURNAL OF INFECTION CONTROL, 1993, 21 (04) :205-209
[26]   TREATMENT OF STAPHYLOCOCCUS-AUREUS NASAL CARRIERS IN CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS WITH MUPIROCIN - LONG-TERM RESULTS [J].
PEREZFONTAN, M ;
GARCIAFALCON, T ;
ROSALES, M ;
RODRIGUEZCARMONA, A ;
ADEVA, M ;
RODRIGUEZLOZANO, I ;
MONCALIAN, J .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 22 (05) :708-712
[27]   NOSOCOMIAL BLOOD-STREAM INFECTIONS - SECULAR TRENDS IN RATES, MORTALITY, AND CONTRIBUTION TO TOTAL HOSPITAL DEATHS [J].
PITTET, D ;
WENZEL, RP .
ARCHIVES OF INTERNAL MEDICINE, 1995, 155 (11) :1177-1184
[28]   MAJOR TRENDS IN THE MICROBIAL ETIOLOGY OF NOSOCOMIAL INFECTION [J].
SCHABERG, DR ;
CULVER, DH ;
GAYNES, RP .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 :S72-S75
[29]   MUPIROCIN TREATMENT OF NASAL STAPHYLOCOCCAL COLONIZATION [J].
SCULLY, BE ;
BRIONES, F ;
GU, JW ;
NEU, HC .
ARCHIVES OF INTERNAL MEDICINE, 1992, 152 (02) :353-356
[30]   Evaluation of protein A gene polymorphic region DNA sequencing for typing of Staphylococcus aureus strains [J].
Shopsin, B ;
Gomez, M ;
Montgomery, SO ;
Smith, DH ;
Waddington, M ;
Dodge, DE ;
Bost, DA ;
Riehman, M ;
Naidich, S ;
Kreiswirth, BN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (11) :3556-3563