Nasal Carriage of Methicillin- Resistant Staphylococcus aureus and Risk Factors Amongst Inpatients, Outpatients and Hospital Personel
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RESEARCH ARTICLE
P: 14-14
January 2014

Nasal Carriage of Methicillin- Resistant Staphylococcus aureus and Risk Factors Amongst Inpatients, Outpatients and Hospital Personel

Mediterr J Infect Microb Antimicrob 2014;3(3):14-14
1. Ankara Eğitim ve Araştırma Hastanesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Kliniği, Ankara, Türkiye
2. Çukurova Devlet Hastanesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Kliniği, Adana, Türkiye
3. Ankara Ataturk Eğitim ve Araştırma Hastanesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Kliniği, Ankara, Türkiye
4. Gazi Üniversitesi Nanoteknoloji Enstitüsü, Ankara, Türkiye
5. Van Eğitim ve Araştırma Hastanesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Kliniği, Van, Türkiye
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Summary

Introduction: The aim of this study was to determine the ratio of nasal carriage of methicillin-resistant Staphylococcus aureus (MRSA) and the risk factors among 1500 subjects including 689 hospital staff, 609 inpatients, and 202 outpatients in Ankara Training and Research Hospital.

Materials and Methods: Nasal swabs were obtained from hospital staff, inpatients and outpatients, which were then inoculatedinto mannitol-salt agar, oxacillin resistance screening agar base (ORSAB), and chromogenic MRSA agar media, respectively. Methicillin resistance was confirmed with cefoxitin disk by the disk-diffusion test. In statistical analyses, the Chi-square and the Kruskal Wall is tests were used, considering p< 0.05 value statistically significant.

Results: MRSA nasal carriage rate was determined 3.03%, 9.03% and 3.96% in hospital staff, inpatients and outpatients, respectively. The rate of nasal carriage of MRSA amongst doctors, nurses and auxiliary health personnel was 1.36%, 1.735% and 5.06% respectively.

Conclusion: Hospital staff,especially auxiliary health personnel, should be trained on hospital infections, routes of transmission, and protective measures. In addition, in clinics where MRSA infections and colonization is common, hospital staff and inpatients should be screened for MRSA nasal carriage at certain intervals and patients to be admitted to the intensive care and surgical units should undergo screening for MRSA nasal carriage before admission.

INTRODUCTION

Methicillin-resistant Staphylococcus aureus (MRSA) is an important nosocomial pathogen resistant to various antibiotics and disinfectants. It is very important to prevent the spread of MRSA infections. Morbidity and mortality rates of infections caused by MRSA strains and the cost of treatment are high[1,2,3]. It has been reported in many studies carried out in Turkey that the rate of MRSA infection varies between 37-71%[4]. MRSA usually spreads through direct contact with contaminated hands of health care workers; however, nasal carriage among hospital staff and inpatients may be accounted for some nosocomial MRSA infections[5]. Consequently, identification of patients and hospital staff colonized or infected with MRSA, subsequent isolation, and eradication of nasal carriage are necessary for the control of nosocomial MRSA infections[6,7,8]. The aim of this study was to determine the rate of nasal carriage of MRSA amongst hospital staff, inpatients, and outpatients.

Introduction

The aim of this study was to determine the rate of nasal carriage of MRSA amongst hospital staff, inpatients, and outpatients.

Methods

Patients and Samples
In order to determine nasal carriage and risk factors (i.e. antibiotic use in the last six months, hospitalization or history of surgical operation in the previous year, and hospital stay) among hospital staff and patients hospitalized for surgery and/or in internal medicine clinics and intensive care units for more than one week, nasal swabs were taken from a total of one thousand five hundred subjects including 609 patients hospitalized for more than one week, 202 outpatients selected as the control group, and 689 hospital staff members.

Laboratory Study
Nasal swabs were inoculated into mannitol-salt agar (Oxoid, UK), oxacillin resistance screening agar (ORSAB, Oxoid, UK), and chromogenic MRSA agar media (Chromagar MRSA, Dr. A. Rambach, Paris, France). Culture plates were kept in the incubator at 37ºC and evaluated for growth at the 24th, 48th and 72nd hours. Catalase and coagulase test-positive colonies appearing yellow in the mannitol salt agar medium and staining as gram positive cocciin Gram staining were identified as S. aureus while colonies appearing yellow in mannitol agar, blue in ORSAB and/or pink or lilac in chromogenic MRSA agar medium were evaluated for methicillin resistance. Catalase and coagulase testpositive colonies which grew in mannitol agar and appeared yellow but did not grow in ORSAB and/or chromogenic MRSA agar medium and were stained gram-positive cocci in Gram staining were evaluated as methicillin-sensitive S. aureus (MSSA). Single colony passage was performed from the proper colonies. The confirmation of methicillin-resistance in S. aureus strains was made according to the Clinical and Laboratory Standards Institute (CLSI) criteria by the disk diffusion method using cefoxitin disk in Mueller-Hinton agar medium[9]. In addition, the sensitivity of isolated MRSA strains to various antibiotics was investigated with the Kirby-Bauer disk diffusion method with regard to CLSI recommendations[9]. In the quality control of media and antibiotic disks, ATCC 43300 (MRSA) and ATCC 25923 (MSSA) standard strains were used.Statistical analyses were carried out in the Depart-ment of Biostatistics in the Medical School of Ankara University.

Statistical Analysis
Chi-square and Kruskal Wall is tests were used in the statistical evaluation and A p value of < 0.05 was considered statistically significant.

Results

There was no significant difference between hospital personnel and inpatients in terms of antibiotic resistance, except for erythromycin and ciprofloxacin. Resistance to erythromycin and ciprofloxacin was higher in strains isolated from inpatients than those isolated from healthcare personnel (p< 0.05).

Discussion

In a study by Lucet et al., all patients in fourteen intensive care units were screened for nasal cultures[10]. Patients were inquired for previous hospitalization, surgical operation, antibiotic use, chronic diseases, and immunosuppression. A total of two thousand three hundred and forty-eight patients were screened and MRSA carriage was in 6.9% (162 cases). In multivariate analysis, the risk factors for MRSA carriage were age over 60 years, long period of hospitalization of patients referred from other hospitals, previous history of hospitalization, surgical operation, and open skin lesions. Porter et al. investigated the prevalence of MRSA and MSSA nasal carriage during hospitalization in the surgical intensive care[13]. They reported MSSA nasal carriage in 22.3% of the patients (126/565) admitted to the ICU and 3% (n= 16) MRSA nasal carriage. Mortality rate was higher in MRSA carriers than that of in MSSA carriers and noncarriers. Friedmann et al. reported that fifteen out of 167 patients were nasal carriers of MRSA upon admission to the hospital[14]. Eveillard et al. have demonstrated MRSA nasal carriage in sixty (6.2%) out of 965 healthcare workers[15]. MRSA prevalence was higher in those working in clinical services than in those working in non-clinical service departments (9.25% and 2.15%, respectively).

Baykam et al. screened nine hundred patients for MRSA upon hospital admission, and 11 MRSA strains (1.2%) were detected[12]. All MRSA strains were positive for the mecA and Panton-Valentine leucocidin gene. Eight of the 11 MRSA-positive patients (72%) had a history of hospitalization within the previous 12 months.

In the present study, the rate of MRSA nasal carriage was 3.04%, 9.03% and 3.96% in hospital staff, inpatients and outpatients, respectively. It was significantly higher in inpatients (p< 0.001). Among the hospital personnel, carriage rate was 1.36% among physicians, 1.73% among nurses and 5.06% among auxiliary healthcare personnel. The rate in auxiliary healthcare personnel was significantly higher than the rates among physicians and nurses (p< 0.05). Carriage rate was higher in surgical clinics for both healthcare personnel and inpatients (p< 0.05). Of the MRSA-carrier inpatients, 63.6% had admitted in surgical clinics and 36.4% in internal medicine clinics. S. aureus nasal carriage and MRSA nasal carriage rates in inpatients and outpatients in various studies are shown in Table 4. Risk factors for MRSA infection and colonization include recent admission to the hospital, surgical intervention, intravenous drug use, underlying disease, close contact with hospital personnel, antibiotic use in the last six months, institutionalization and the presence of hospital personnel among family members[5, 8, 11, 16]. In our study, hospital personnel, inpatients and outpatients were evaluated for risk factors for MRSA nasal carriage. In inpatients and outpatients, the rate of antibiotic use was higher than that of the hospital personnel (p< 0.05). Among inpatients, the rate of admission to hospital and surgical operation was higher than those of hospital personnel and outpatients (p< 0.05). Moreover, the rate of underlying diseases was also higher among inpatients (diabetes, chronic renal failure, hypertension etc.) (p< 0.05). The limitation to this study was that the presence of the mecA gene was not detected by polymerase chain reaction method regarded as the gold standard for the detection of methicillin resistance. Askarian et al. have reported the prevalence of nasal carriage of MSSA to be 25.7% and MRSA to be 5.3% in 600 healthcare workers in Iran[17]. In this study, it was reported that the highest MRSA carriage rates were in the surgical wards and the emergency department. It was also reported that the occupation of nursing was an independent risk factor for nasal MRSA carriage. In Turkey, the rate of nasal MRSA carriage has been reported between 4-16% in various studies[18, 19]. Cesur and Cokca have reported the rate of MRSA nasal carriage to be 6% among hospital personnel and 2.6% among outpatients[5]. In this study, MRSA nasal carriage rate was 6.12% among physicians, 6.57% among nurses, and 5.17% among auxiliary health personnel. Erdenizmenli et al. have investigated the rate of MSSA and MRSA nasal carriage in five hundred outpatients and 102 healthcare workers[20]. They reported the rate of MSSA nasal carriage to be 9.4% among outpatients; whereas, no MRSA carriage could be detected. In healthcare workers, they have reported the rate of MSSA nasal carriage to be 8.8% and the rate of MRSA nasal carriage to be 0.98% (only in one person). In the present study, the MRSA nasal carriage rate was significantly higher among auxiliary healthcare staff than those among physicians and nurses. This difference may be due to the fact that auxiliary healthcare staff is not adequately informed about hospital infections.

There was no significant difference between hospital personnel and inpatients in terms of antibiotic resistance, except for erythromycin and ciprofloxacin. Resistance to erythromycin and ciprofloxacin was higher in strains isolated from inpatients than those isolated from healthcare personnel. In a study by Cesur and Cokca, no statistically significant difference was reported between the rates of resistance in MRSA strains isolated from hospital personnel and outpatients[5].

As a result, in order to prevent MRSA nasal carriage and development of infection, infection control measures should be developed and strictly implemented. Antibiotic use is an important risk factor for MRSA colonization. Training hospital personnel, especially auxiliary healthcare personnel, is very important. Low education level among auxiliary healthcare personnel and the lack of information about hospital infections may account for the high rate of nasal carriage in this group. We recommend that the hospital personnel should be trained on hospital infections, their routes of contamination, and preventive measures for the prevention and control of hospital infections. On the other hand, hospital personnel and inpatients admitted in clinics where hospital infections and colonization are common should be screened at certain intervals for MRSA carriage, and patients should be screened for MRSA nasal carriage before admission to intensive care and surgical units.

ACKNOWLEDGMENT
This study was supported by The Scientific and Technological Research Council of Turkey (TUBITAK), project number: SBAG-188.

References

1Barakate MS, Yang YX, Foo SH, Vickery AM, Sharp CA, Fowler LD, et al. An epidemiological survey of methicillinresistant Staphylococcus aureus in a tertiary referral hospital. J Hosp Infect 2000;44:19-26.
2Lowy DF. Staphylococcus aureus. N Engl J Med 1998;339:520-32.
3Waldvogel FA. Staphylococcus aureus (including toxic shock syndrome). In: Mandell GL, Bennett JE, Dolin R (eds). Principles and Practice of Infectious Diseases. Philadelphia: Lippincot Williams and Willkins, 2000;1:2069-2.
4Arman D. Türkiye'de hastane infeksiyonu kontrolüne yönelik çalışmalar. Hastane İnfeksiyonları Dergisi 1997;1:144-52.
5Cesur S, Çokca F. Nasal carriage of methicillin resistant Staphylococcus aureus among hospital staff and outpatients. Infect Control Hosp Epidemiol 2004;25:169-71.
6Reboli AC, John JF, Platt CG, Cantey JR. Methicillinresistant Staphylococcus aureus outbreak at a Veterians Affairs Medical Center: importance of carriage of the organism by hospital personnel. Infect Control Hosp Epidemiol 1990;11:291-6.
7Hardy K, Price C, Szczepura A, Gossain S, Davies R, Stallard N, et al. Reduction in the rate of methicillin-resistant Staphylo-coccus aureus acquisition in surgical wards by rapid screening for colonization: a prospective, crossover study. Clin Microbiol Infect 2010;16:333-9.
8Kluytmans J, van Belkum A, Verbrugh H. Nasal carriage of Staphylococcus aureus: epidemiology, underlying mechanisms, and associated risks. Clin Microbiol Rev 1997;10:505-20.
9CLSI, Antimicrobial Susceptibility Testing/Clinical Laboratory Standards. CLSI Document M2-A8 Disk difüzyon. Gür D (editör). Ankara, 2005:45-51.
10Lucet JC, Chevret S, Durand-Zaleski I, Chastang C, Régnier B. Multicenter Study Group. Prevalence and risk factors for carriage of methicillin- resistant Staphylococcus aureus at admission to the intensive care unit: results of multicenter study. Arch Intern Med 2003;163:181-8.
11Scudeller L, Leoncini O, Boni S, Navarra A, Rezzani A, Verdirosi S, et al. MRSA carriage: the relationship between community and healthcare setting. A study in an Italian hospital. J Hosp Infect 2000;46:222-9.
12Baykam N, Esener H, Ergonul O, Kosker PZ, Cirkin T, Celikbas A, et al. Methicillin-resistant Staphylococcus aureus on hospital admission in Turkey. Am J Infect Control 2009;37247-9.
13Porter R, Subramini K, Thomas AN, Chadwick P. Nasal carriage of Staphylococcus aureus on admission to intensive care: incidence and prognostic significance. Intensive Care Med 2003;29:655-8.
14Friedmann R, Raveh D, Zartzer E, Rudensky B, Broide E, Attias D, et al. Prospective evaluation of colonization with extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae among patients at hospital admission and of subsequent colonization with ESBL-producing Enterobacteriaceae among patients during hospitalization. Infect Control Hosp Epidemiol 2009;30:534-42.
15Eveillard M, Martin Y, Hidri N, Boussougant Y, Joly- Guillou ML. Carriage of methicillin-resistant Staphylococcus aureus among hospital employees: prevalence, duration, and transmission to households. Infect Control Hosp Epidemiol 2004;25:114-20.
16Boyce JM. Methicillin resistant Staphylococcus aureus in hospitals and long-term care facilities: microbiology, epidemiology and preventive measureus. Infect Control Hosp Epidemiol 1992;13:725-37.
17Askarian M, Zeinal Zadeh A, Japoni A, Alborzi A, Memish ZA. Prevalence of nasal carriage of methicillin-resistant Staphylococcus aureus and its antibiotic susceptibility pattern in healthcare workers at Namazi Hospital, Shiraz, Iran. Int J Infect Dis 2009;13:e241-7.
18Çaylan R, Aydın K, Koksal İ, Kostakoğlu U. Hastanemizde nozokomiyal stafilokoklarda metisilin direncinin saptanması ve personelde MRSA taşıyıcılığı. Mikrobiyol Bul 1999;33:163-9.
19Kaleli İ, Özen N, Yalçın AN, Akşit F. Hastane personelinde burunda S. aureus taşıyıcılığının saptanması. İnfeksiyon Dergisi (Turkish Journal of Infection) 1997;11:243-5.
20Erdenizmenli M, Yapar N, Senger SS, Özdemir S, Yüce A. Investigation of colonization with methicillin-resistant and methicillin-susceptible Staphylococcus aureus in an outpatient population in Turkey. Jpn J Infect Dis 2004;57:172-5.
21AkouaKoffi C, Dje K, Toure R, Guessennd N, Acho B, Faye Kette H, et al. Nasal carriage of methicillin-resistant Staphylococcus aureus among health care personnel in Abidijan. Dakar Med 2004;49:70-4.
22Nawas T, Fakhoury J. Nasal carriage of methicillin resistant Staphylococcus aureus by hospital staff in North Jordon. J Hosp Infect 1991;17:223-9.
23Hidron AI, Kourbatova EV, Halvosa JS, Terrell BJ, McDougal LK, Tenover FC, et al. Risk factors for colonisation with methicillin-resistant Staphylococcus aureus (MRSA) in patients admitted to an urban hospital: emergence of community-associated MRSA nasal carriage. Clin Infect Dis 2005;41:159-66.
24Troillet N, Carmeli Y, Samore MH, Dakos J, Eichelberger K, DeGirolami PC, et al. Carriage of methicillin- resistant Staphylococcus aureus at hospital admission. Infect Control Hosp Epidemiol 1998;19:181-5.
25Kenner J, O'Connor T, Piantanida N, Fishbain J, Eberly B, Viscount H, et al. Rates of carriage of methicillin-resistant and methicillin-susceptible Staphylococus aureus in an outpatient population. Infect Control Hosp Epidemiol 2003;24:439-44.
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