Nasal Carriage of Staphylococcus aureus among Pediatric Health Care Workers in a Pediatric Intensive Care Unit

Similar documents
AUTHORS: Elaine H. Kho, M.D.*, Jonathan Lim, M.D.*

Staphylococcus aureus nasal carriage in diabetic patients in a tertiary care hospital

Int.J.Curr.Microbiol.App.Sci (2018) 7(1):

Volume-7, Issue-2, April-June-2016 Coden IJABFP-CAS-USA Received: 5 th Mar 2016 Revised: 11 th April 2016 Accepted: 13 th April 2016 Research article

Methicillin-Resistant Staphylococcus aureus

Nasal carriage of methicillin resistant Staphylococcus aureus amonghealthcareworkers at a tertiary care hospital in Western Nepal

JMSCR Vol. 03 Issue 06 Page June 2015

NASAL COLONIZATION WITH STAPHYLOCOCCUS AUREUS IN BASRA MEDICAL AND DENTISTRY STUDENTS

Detection and Quantitation of the Etiologic Agents of Ventilator Associated Pneumonia in Endotracheal Tube Aspirates From Patients in Iran

Antimicrobial Resistance and Molecular Epidemiology of Staphylococcus aureus in Ghana

MRSA CROSS INFECTION RISK: IS YOUR PRACTICE CLEAN ENOUGH?

Prevalence & Risk Factors For MRSA. For Vets

Does Screening for MRSA Colonization Have A Role In Healthcare-Associated Infection Prevention Programs?

Int.J.Curr.Microbiol.App.Sci (2016) 5(12):

EDUCATIONAL COMMENTARY - Methicillin-Resistant Staphylococcus aureus: An Update

Nature and Science, 5(3), 2007, Olowe, Eniola, Olowe, Olayemi. Antimicrobial Susceptibility and Betalactamase detection of MRSA in Osogbo.

SURVIVABILITY OF HIGH RISK, MULTIRESISTANT BACTERIA ON COTTON TREATED WITH COMMERCIALLY AVAILABLE ANTIMICROBIAL AGENTS

Ophthalmology Research: An International Journal 2(6): , 2014, Article no. OR SCIENCEDOMAIN international

MRSA Outbreak in Firefighters

Concise Antibiogram Toolkit Background

Antimicrobial Resistance

Antimicrobial Resistance Acquisition of Foreign DNA

Consequences of Antimicrobial Resistant Bacteria. Antimicrobial Resistance. Molecular Genetics of Antimicrobial Resistance. Topics to be Covered

MID 23. Antimicrobial Resistance. Consequences of Antimicrobial Resistant Bacteria. Molecular Genetics of Antimicrobial Resistance

CHAPTER 1 INTRODUCTION

GUIDE TO INFECTION CONTROL IN THE HOSPITAL

J of Evolution of Med and Dent Sci/ eissn , pissn / Vol. 4/ Issue 27/ Apr 02, 2015 Page 4644

Active Bacterial Core Surveillance Site and Epidemiologic Classification, United States, 2005a. Copyright restrictions may apply.

Animal Antibiotic Use and Public Health

FM - Male, 38YO. MRSA nasal swab (+) Due to positive MRSA nasal swab test, patient will be continued on Vancomycin 1500mg IV q12 for MRSA treatment...

Staphylococcus Aureus

A Study on Bacterial Flora on the Finger printing Surface of the Biometric Devices at a Tertiary Care Hospital

Safe Patient Care Keeping our Residents Safe Use Standard Precautions for ALL Residents at ALL times

BACTERIOLOGICALL STUDY OF MICROORGANISMS ON MOBILES AND STETHOSCOPES USED BY HEALTH CARE WORKERS IN EMERGENCY AND ICU S

Study of Nasal Carriage of Staphylococcus aureus with Special Reference to Methicillin Resistance among Nursing Staff

BMR Microbiology. Research Article

Q1. (a) Clostridium difficile is a bacterium that is present in the gut of up to 3% of healthy adults and 66% of healthy infants.

Antimicrobial Resistance

Annual Surveillance Summary: Methicillin- Resistant Staphylococcus aureus (MRSA) Infections in the Military Health System (MHS), 2016

Geoffrey Coombs 1, Graeme Nimmo 2, Julie Pearson 1, Samantha Cramer 1 and Keryn Christiansen 1

Group b strep and macrodantin

Methicillin-resistant Staphylococcus aureus (MRSA) on Belgian pig farms

Source: Portland State University Population Research Center (

GENERAL NOTES: 2016 site of infection type of organism location of the patient

Aerobic bacterial infections in a burns unit of Sassoon General Hospital, Pune

Annual Surveillance Summary: Methicillinresistant Staphylococcus aureus (MRSA) Infections in the Military Health System (MHS), 2017

Int.J.Curr.Microbiol.App.Sci (2017) 6(3):

SUPPLEMENT ARTICLE. S114 CID 2001:32 (Suppl 2) Diekema et al.

Antimicrobial Susceptibility Patterns of Salmonella Typhi From Kigali,

Lab Exercise: Antibiotics- Evaluation using Kirby Bauer method.

Summary of the latest data on antibiotic resistance in the European Union

Authors Kiran Chawla, Chiranjay Mukhopadhayay, Bimala Gurung, Priya Bhate, Indira Bairy,

Int.J.Curr.Microbiol.App.Sci (2018) 7(8):

Detection of inducible clindamycin resistance among clinical isolates of Staphylococcus aureus in a tertiary care hospital

Int.J.Curr.Microbiol.App.Sci (2015) 4(9):

GeNei TM. Antibiotic Sensitivity. Teaching Kit Manual KT Revision No.: Bangalore Genei, 2007 Bangalore Genei, 2007

Understanding the Hospital Antibiogram

Methicillin resistant Staphylococcus aureus : a multicentre study

Preventing Multi-Drug Resistant Organism (MDRO) Infections. For National Patient Safety Goal

Methicillin-Resistant Staphylococcus aureus (MRSA) Infections Activity C: ELC Prevention Collaboratives

North West Neonatal Operational Delivery Network Working together to provide the highest standard of care for babies and families

Today s Agenda: 9/30/14

MRSA Control : Belgian policy

Bacterial Pathogens in Urinary Tract Infection and Antibiotic Susceptibility Pattern from a Teaching Hospital, Bengaluru, India

Burn Infection & Laboratory Diagnosis

January 2014 Vol. 34 No. 1

An Approach to Appropriate Antibiotic Prescribing in Outpatient and LTC Settings?

Antimicrobial Susceptibility Patterns

Annual Report: Table 1. Antimicrobial Susceptibility Results for 2,488 Isolates of S. pneumoniae Collected Nationally, 2005 MIC (µg/ml)

Antimicrobial Stewardship Strategy: Antibiograms

Staphylococcal Nasal Carriage of Health Care Workers

HOSPITAL-ACQUIRED INFECTION/MRSA EYERUSALEM KIFLE AND GIFT IMUETINYAN OMOBOGBE PNURSS15

Prophylactic antibiotic timing and dosage. Dr. Sanjeev Singh AIMS, Kochi

Saxena Sonal*, Singh Trishla* and Dutta Renu* (Received for publication January 2012)

Inducible clindamycin resistance among Staphylococcus aureus isolates

Success for a MRSA Reduction Program: Role of Surveillance and Testing

Approval Signature: Original signed by Dr. Michel Tetreault Date of Approval: July Review Date: July 2017

Taking Action to Prevent and Manage Multidrug-resistant Organisms and C. difficile in the Nursing Home: Part 1 Reviewing the organisms

Multidrug-Resistant Organisms: How Do We Define them? How do We Stop Them?

A retrospective analysis of urine culture results issued by the microbiology department, Teaching Hospital, Karapitiya

Antibiotic usage in nosocomial infections in hospitals. Dr. Birgit Ross Hospital Hygiene University Hospital Essen

Other Enterobacteriaceae

Microbiology : antimicrobial drugs. Sheet 11. Ali abualhija

Pathogens and Antibiotic Sensitivities in Post- Phacoemulsification Endophthalmitis, Kaiser Permanente, California,

Risk Factors for Persistent MRSA Colonization in Children with Multiple Intensive Care Unit Admissions

Preventing Surgical Site Infections. Edward L. Goodman, MD September 16, 2013

Staphylococcus aureus nasal carriers and the prevalence of methicillin resistant Staphylococcus aureus among medical students

The importance of infection control in the era of multi drug resistance

BELIEFS AND PRACTICES OF PARENTS ON THE USE OF ANTIBIOTICS FOR THEIR CHILDREN WITH UPPER RESPIRATORY TRACT INFECTION

Healthcare-associated Infections Annual Report March 2015

Bacterial Resistance of Respiratory Pathogens. John C. Rotschafer, Pharm.D. University of Minnesota

PREVALENCE AND ANTIMICROBIAL SUSCEPTIBILITY PATTERN OF METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS: A MULTICENTRE STUDY

GUIDE TO INFECTION CONTROL IN THE HOSPITAL. Antibiotic Resistance

Research Article Staphylococcus aureus: Screening for Nasal Carriers in a Community Setting with Special Reference to MRSA

Antibiotic-resistant Staphylococcus aureus in dermatology and burn wards

Importance of handwashing prior to wound dressings in prevention of nosocomial infection in surgical wards

FREQUENCY OF METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS (MRSA) COLONIZATION AMONGST HOSPITAL STAFF IN TEACHING HOSPITALS OF PESHAWAR

The Hospital Environment as a Source of Resistant Gram Negatives

Inducible clindamycin resistance and nasal carriage rates of Staphylococcus aureus among healthcare workers and community members.

Comparison of Antibiotic Resistance and Sensitivity with Reference to Ages of Elders

Transcription:

PIDSP Journal 212 Vol 13 No.1 Copyright 212 44 Nasal Carriage of Staphylococcus aureus among Pediatric Health Care Workers in a Pediatric Intensive Care Unit AUTHORS: Pablito M. Planta Jr., MD*, Armi Grace G. Laiño, MD*, Ma. Noreen B. Alqueza, MD* Ma. Liza M. Gonzales, MD* *Philippine General Hospital CORRESPONDENCE: Dr. Pablito M. Planta, Jr., MD Email: jojoplantamd@yahoo.com KEYWORDS Staphylococcus, Staphylococcus aureus, MRSA, nasal carriage ABSTRACT Background/Objective: An outbreak of nosocomial infections through nasal carriage of organisms by health care workers may also occur. The health care workers (who are in close contact with the patients are possible sources of hospital-acquired infections. Staphylococci are a leading cause of bacteremia, surgical wound infections and nosocomial infection in many areas around the globe. The objective of this study was to determine the nasal carriage rate of Staphylococcus aureus among health care workers in a pediatric intensive care unit. Methods: Twenty six healthcare workers in a pediatric intensive care unit of a tertiary hospital were included. Cultures from the anterior nares were obtained using a sterile cotton tip swab, which was moistened with sterile normal saline solution. Samples were then analyzed using standard microbiological methods. The susceptibilities of the isolates to antibiotics were then determined by the Kirby Bauer disk diffusion method. Nasal carriage rate of Staphylococcus aureus was determined. Results: The mean age of the subjects was 35 years (range 22-56) old. There were 2 nurses (76.9%), 4 (15.4%) nurse assistants, and 2(7.7%) utility workers; 3 (11. 5%) were males and 23 (88.5%) were females. Two subjects (7.7%) grew Staphylococcus aureus. Both reported 1% sensitivity to all tested antibiotics except for Penicillin G which showed 1% resistance. Twenty four of the subjects (92.3%) grew Staphylococcus epidermidis, 5 (2.83%) were methicillin resistant. All showed 1% sensitivity to Gatifloxacin, Levofloxacin, Oxacillin, and Vancomycin. There was high resistance (62.5%) to Penicillin G. Conclusion: The nasal carriage rate (7.7%) of Staphylococcus aureus in this study is lower compared to earlier reports. The results of this study showed higher nasal carriage of Staphylococcus epidermidis (92.3%).

PIDSP Journal 212 Vol 13 No.1 Copyright 212 INTRODUCTION The nosocomial infection rate in the Philippine General Hospital remains high; this becomes a significant hazard to patients. The health care workers (physicians, medical students, nurses, nurse assistants, utility workers, etc.), who are in close contact with the patients are possible sources of such hospital-acquired infection, with many of the pathogenic organisms transmitted by hand carriage: This is the rationale behind the recommendation for everyone to practice proper hand washing before and after examining patients. It has been established that strict compliance to hand washing reduces hospital-acquired infections. However, an outbreak of nosocomial infections through nasal carriage of organisms by health care workers is also a possibility. Staphylococci are the leading cause of bacteremia, surgical wound infections, and infections of bioprosthetic materials in the United States; they are the second leading cause of nosocomial infections overall. Staphylococcus aureus is the most important human pathogen in the genus. Despite the availability of potent antimicrobial agents, improved public health conditions, and hospital-infection control measures, it has remained a major human pathogen. 1 Carriage of Staphylococcus aureus plays a key role in the epidemiology and pathogenesis of infection because of both the diversity and the severity of the infections caused by this organism. It is also a major risk factor for the development of both community-acquired and nosocomial infections. 2, 6 In U.S. hospitalsin the National Nosocomial Infections Surveillance System, Staphylococcus aureus accounted for 13% of isolates recovered from patients with nosocomial infections from 1979 to 1995; the percentage has increased in recent years. Multidrug-resistant strains of Staphylococci had been reported with increasing frequency worldwide, including isolates that were resistant to methicillin, lincosamides, macrolides, aminoglycosides, fluoroquinolones, or combinations of these antibiotics. The severe consequences of infection with Staphylococcus aureus heightened the importance of prevention. 3 Several studies have documented that these infections were commonly caused by the patient's own commensal flora. The original reservoir(s) from which patients acquire these isolates remained unclear. While some infected patients were colonized with Staphylococcus aureus at the time of hospitalization, others likely became colonized, often with more highly antibiotic-resistant isolates, during their hospital stay. 1 Hospital personnel were among those implicated as possible sources of the potentially antibiotic-resistant pathogens. Transmission of the pathogens to patients was then likely to occur during routine patient care. Despite the possible importance of this sequence of events, the questions of whether health care workers are more likely to be colonized with Staphylococcus aureus and if these organisms reflect those found in the hospital setting, have received limited attention in the local setting, thus this study. This study determined the nasal carriage rate of Staphylococcus aureus among pediatric healthcare workers in the Philippine General Hospital Pediatric Intensive Care Unit. MATERIALS AND METHODS Study Population Pediatric health care workers (physicians, nurses, nurse assistants, utility workers, etc.) at the Philippine General Hospital Pediatric Intensive Care Unit were included in the study. Healthcare workers who were on antibiotics, on intranasal corticosteroids, and those with current upper respiratory tract infections were excluded. Cultures from the anterior nares were obtained from all the subjects after an 8-hour duty using a sterile cotton tip swab moistened with sterile normal saline solution (.9%). The nares was chosen for sampling because it was the native colonization site for staphylococci and usually represented colonization rather 45

PIDSP Journal 212 Vol 13 No.1 Copyright 212 than transient skin coverage. 13 The swabs were inoculated using blood agar plates and incubated for 24 to 48 hours. Samples were then analyzed using standard microbiological methods. The susceptibilities of the isolates to 11 antibiotics (cefazolin, chloramphenicol, ciprofloxacin, erythromycin, gatifloxacin, levofloxacin, oxacillin, penicillin, tetracycline, trimethoprim-sulfamethoxazole, and vancomycin) were determined by the Kirby Bauer disk diffusion method according to the National Committee for Clinical Laboratory Standards guidelines. The results of the cultures were collected and tabulated according to the frequency of positive cultures in each category, and the sensitivity and resistance of Staphylococcus aureus and Staphylococcus epidermidis to the most frequently used antibiotics in clinical practice. Statistical Analysis Sample size estimate for a single proportion was computed at 26 with 95% confidence level. Analysis and data interpretation was done by the investigator. Frequencies were obtained and percentages were calculated by study variables. RESULTS A total of 26 subjects from among the 35 rotating in the pediatric intensive care unit were included in this study. Three did not give their consent while 6 were on leave. The mean age of the subjects was 35 years (range 22-56) with years in service ranging from 1 month to 25 years. Subjects included 2 nurses (76.9%), 4 (15.4%) nurse assistants, and 2 utility workers (7.7%). According to sex distribution pattern, 3 (11.5%) were males and 23 (88.5%) were females. Table 1. Demographic data of pediatric health care workers in the PGH-PICU Category Male Female Total Nurses Nurse Assistants Utility Worker 1 (5) 2 (1) 19 (95) 4 (1) 2 (76.9) 4 (15.4) 2 (7.7) Total 3 (11.5) 23 (88.5) 26 (1) Staphylococcus aureus carriers Of the 26 subjects, two (7.7%) grew Staphylococcus aureus. Table 2 contains details on the nasal carriage rates of Staphylococcus aureus among subjects in the different categories. Staphylococcus aureus was isolated in 2 (1%) nurses out of the 2 that were included in the study. The nurse assistants and utility workers were clear of nasal carriage. Table 2. Nasal carriage of Staphylococcus aureus among pediatric healthcare workers in the PGH-PICU Category Subject No. with % Nurses Nurse Assistants Utility Worker 2 S. aureus 2 4 2 Total 26 2 7.7% This study also showed the growth of Staphylococcus epidermidis in 24 of the subjects, which accounted for 92.3%; There were 18 (9%), 4 (1%) and 2 (1%) from the nurses, nurse assistants and utility workers, respectively. The resistance pattern is showed in Table 5. Table 3. Nasal carriage of Staphylococcus epidermidis and MRSE among health care workers in PGH-PICU Category Subject No. with S. epidermidis 1 No. with MRSE 46

PIDSP Journal 212 Vol 13 No.1 Copyright 212 Nurses Nurse Assistants Utility Workers 2 4 2 18 (9) 4 (1) 2 (1) 4 (22.2) 1 (25) Total 26 24 (92.3) 5 (2.8) Antimicrobial susceptibility studies of Staphylococcus aureus isolates by the Kirby- Bauer disc diffusion methods showed 1% sensitivity to all tested antibiotics, except for penicillin G, which showed 1% resistance. With regards to the antimicrobial sensitivity and resistance profile of Staphylococcus epidermidis isolates, 1% of the isolates were sensitive to gatifloxacin, levofloxacin, oxacillin, and vancomycin. Ciprofloxacin showed 87.5% sensitivity and 12.5% resistance. Both Chloramphenicol and tetracycline showed 83.33% sensitivity and 16.6% resistance, while both trimethoprim sulfamethoxazole and cefazolin showed 75% sensitivity and 25% resistance. Erythromycin has 66.66% sensitivity and 33.33% resistance. An important finding in Table 5 showed a high resistance (62.5%) of Staphylococcus epidermidis to penicillin G, but with low sensitivity (37.5%). Table 4. Antibiotic sensitivity and resistance pattern of Staphylococcus aureus (N=2) Antibiotic Sensitive Resistant Cefazolin Chloramphenicol Ciprofloxacin Erythromycin Gatifloxacin Levofloxacin Oxacillin Penicillin G Tetracycline Cotrimoxazole Vancomycin 2 (1) 2 (1) 2 (1) 2 (1) 2 (1) 2 (1) 2 (1) 2 (1) 2 (1) 2 (1) 2(1) DISCUSSION It has often been suggested that certain strains of Staphylococcus aureus have a special ability to colonize hospital staff 14 : They colonize the anterior nares and moist body areas of humans. The anterior nares have been shown to be the main reservoir of Staphylococcus aureus in adults and children. Nasal carriage of Staphylococcus aureus has been demonstrated to be a significant risk factor for nosocomial and community-acquired infections in a variety of populations. 15 There is paucity of information on the nasal carriage of Staphylococcus aureus among pediatric health care workers in the pediatric intensive care unit and its importance in Staphylococcus aureus spread. In this study, the nasal carriage rate of Staphylococcus aureus among health care workers in the pediatric intensive care unit and its susceptibility and resistance profile were studied. Table 5. Antibiotic sensitivity and resistance pattern of Staphylococcus epidermidis (N=24) Antibiotic Cefazolin Chloramphenicol Ciprofloxacin Erythromycin Gatifloxacin Levofloxacin Oxacillin Penicillin G Tetracycline Cotrimoxazole Vancomycin Sensitive 18 (75) 2 (83) 21 (88) 16 (67) 2 (1) 2 (1) 2 (1) 9 (38) 2 (83) 18 (75) 2 (1) Resistant 6 (25) 4 (17) 3 (12) 8 (33) 15 (62) 4 (17) 6 (25) The organism may be transmitted from the nose to the skin, where colonization seemed to be more transient. Person-to-person transmission was the usual mode of spread occurring via the hands, nasal discharges, and rarely by aerosol. 16 Mucin appeared to be the critical surface that was colonized in a process involving interactions between staphylococcal 47

PIDSP Journal 212 Vol 13 No.1 Copyright 212 protein and mucin carbohydrate. The role of interference by other commensal bacteria, secretory IgA, or specific staphylococcal adhesions was unknown. 3 As in previous investigations done, this study revealed a reservoir of asymptomatic Staphylococcus aureus colonized healthcare workers. The result of the surveillance cultures done in this investigation showed that 7.7 % of the pediatric intensive care unit personnel were carriers of Staphylococcus aureus. In previous studies done, the colonization rate of Staphylococcus aureus carriage may range from 14% 45%. The result could mean that the nasal carriage rate of Staphylococcus aureus was lower compared to earlier reports. Though it was low, pediatric intensive care unit personnel found to be Staphylococcus aureus carriers in their anterior nares were possible causes of its spread. From the results, it can be seen that aside from Staphylococcus aureus, most of the isolates showed growth of Staphylococcus epidermidis. Staphylococcus epidermidis, often previously dismissed as culture contaminants, were now assuming greater importance as true pathogens. 1 In recent years, Staphylococcus epidermidis, one of the staphylococcal species most frequently isolated from the microflora of humans, has emerged as a major pathogen in nosocomial infections; Of the S. epidermidis strains circulating in the hospital environment, as many as 7% can be resistant to methicillin. The establishment of methicillin-resistant S. epidermidis (MRSE as resident flora in the hospital environment was worrisome since these strains, which were predominantly involved in nosocomial infections can accumulate resistance-determinants to practically all classes of antimicrobials. These strains were also potentially transferable to S. aureus and other microorganisms. 17 Today, with the global issue of multidrugresistant bacteria, there is every reason to consider the possibility of MRSE as a true pathogen and not just a mere contaminant. The existence of nasal carriers of, MRSE, their identification, and the significance of their presence in the PICU, have not been investigated well before. The nasal carriage rate of MRSE in this study (2.83%) corresponds to the study done by Tammelin A, et al, on dispersal of MRSE by staff in an operating suite for thoracic and cardiovascular surgery. Said study showed nasal carriage rate of 28 % in women and 33% in men 23. It was not clear whether MRSE should be regarded as part of the normal resident flora of human skin, in the same way as methicillin-sensitive S. epidermidis, or as a transient skin contaminant. This probably depends on which population is studied: hospital staff spending several hours a day in an environment where the selection of resistant bacterial strains is favored or healthy individuals without hospital contacts. One interesting finding to note was the high sensitivity rate (1%) of Staphylococcus aureus to Oxacillin despite worldwide reports of its high resistance rate to this drug, especially in the hospital setting. Navarro-Almario et. al., in 1987, did a review of the antibiotic susceptibility pattern of Staphylococcus aureus isolates at the Philippine General Hospital. Out of the 213 isolates shown to be oxacillinresistant by disc diffusion method, only 3 (2.3%) were confirmed to be truly resistant by MIC. 1 The study by Ontengco et. al. on Methicillin-resistant Staphylococcus aureus isolates from Filipino patients (1999-23), which showed high resistance (87.1-96.1%) to Penicillin and Staphylococcus aureus strains remained highly susceptible to erythromycin, levofloxacin, ciprofloxacin, tetracycline, vancomycin, and cotrimoxazole. 21 Oxacillin resistance in this study was 18%. Unfortunately, the latest Antimicrobial resistance surveillance in the Philippines shows an increasing trend of MRSA, with 21 data showing Oxacillin resistance at 54%. Thus it would be important to revisit the nasal carriage of health workers in the present decade to see if it reflects the present MRSA resistance in the Philippines 48

PIDSP Journal 212 Vol 13 No.1 Copyright 212 CONCLUSION This study suggests that Staphylococcus aureus nasal colonization is present among pediatric healthcare workers in the Philippine General Hospital and that the nasal carriage rate (7.7%) is low compared to previous studies done locally and internationally. If the pediatric intensive care personnel are identified as vectors of transmission, their isolates are likely to reflect the antibiotic susceptibility profile prevalent in the area. An important finding is the high antibiotic sensitivity to Oxacillin. However, a high resistance rate (1%) to Penicillin G was noted. The Staphylococcus aureus remained highly susceptible (1%) to Cefazolin, Chloramphenicol, Ciprofloxacin, Erythromycin, Gatifloxacin, Levofloxacin, Tetracycline, Cotrimoxazole, and Vancomycin. The results also showed that nasal carriage of Staphylococcus epidermidis is even higher compared to Staphylococcus aureus and has high resistance (62.5%) to Penicillin G. RECOMMENDATION This study however involved only a single area, so an intradepartmental surveillance is recommended to determine the true nasal carriage rate of Staphylococcus aureus among pediatric health care workers of the Philippine General Hospital. It is necessary to have a reliable system of surveillance not just for patients but for personnel as well. LIMITATIONS OF THE STUDY This study was conducted among pediatric healthcare workers at the Pediatric Intensive Care Unit of the Philippine General Hospital and did not include other pediatric healthcare workers in the different areas of the Department of Pediatrics. Data gathering was done during the month of October 25. All other personnel at the PICU during the time of the study who were on leave were excluded. RECOMMENDATIONS It is recommended that antibiotic resistance surveillance be continually monitored for trends in resistance. Likewise, the clinical outcomes of the UTI after completion of treatment should also be studied. REFERENCES 1. Atilano, MA., Pena A., Chua, J., Coronel R., Prevalence of Methicillin - Resistant Staphylococcus aureus and Methicillin-resistant Coagulase Negative Staphylococcus in a Tertiary Hospital, PJMID, 21; 3:(4) 2. Cespedes, C., Miller, M, Quagliarello, B., Vavagiakis, P., Klein, R., Lowy, F., Differences between Staphylococcus aureus isolates from Medical and Nonmedical Hospital Personnel, J Clin Microbiol. 22; 4(7): 2594-2597. 3. von Eiff, C., Becker, K., Machka, K., Stammer, H., Peters, G., Nasal Carriage as a source of Staphylococcus aureus Bacteremia, 21; 344: 11-16. 4. Saxena, S., Singh, K., Talwar, V., Methicillin-resistant Staphylococcus aureus Prevalence in Community in the East Delhi Area. Jpn J Infect Dis, 23; 56: 54-56. 5. Algaithy, AA, Bilal NE, Gedebou M, Weily AH, Nasal carriage and antibiotic resistance of Staphylococcus aureus isolates from hospital and nonhospital personnel in Abha, Saudi Arabia, Trans R Soc Trop Med Hyg. 2; 94 (5): 54-6. Yazgi, H., Ertek, M., Ozbek, A., Kadanali A., Nasal carriage of Staphylococcus aureus in hospital personnel and the normal population and antibiotic resistance of the isolates, Mikrobiyol Bul. 23; 37 (2-3): 137-42. 7. Dimitrov T, Udo EE, Grover S. Point surveillance of Staphylococcus aureus among medical staff in Infectious Disease Hospital, Kuwait, Med Princ Pract. 23; 12 (3): 139-44. 8. Bischoff, WE, Wallis ML, Tucker KB, Reboussin BA, Sherertz RJ, Staphylococcus aureus nasal carriage in a student community :prevalence, clonal relationships, and risk factors, Infect Control Hosp Epidemiol 24; 25 (6): 485-91. 9. Cesur, S., Cocka, F., Nasal carriage of methicillinresistant Staphylococcus aureus among hospital staff and outpatients, Infect control Hosp Epidemiol. 24; 25 (2): 169-71. 1. Scarnato F, Mallaret MR, Croize J, Kouabenan DR, Dubois M, Maitre A, DeGaudemaris R. Incidence and prevalence of methicillin-resistant Staphylococcus aureus nasal carriage among healthcare workers in geriatric departments: relevance to preventive measures, Infect Control Hosp Epidemiol. 23; 24 (6): 456-8. 11. Akoua Koffi C, Dje K, Toure R, Guessand N, Acho B, Faye Kette H, Loukou YG, Dosso M. Nasal carriage of methicillin-resistant Staphylococcus aureus among health care personnel in Abidjan, Dakar Med. 24; 49 (1): 7-4. 49

PIDSP Journal 212 Vol 13 No.1 Copyright 212 12. Pujol M, Pena C, Pallares R, et al. Nosocomial Staphylococcus aureus bacteremia among nasal carriers of methicillin-resistant and methicillinsusceptible strains. Am J Med 1996; 1:59-516. 13. Patrick CH, John JF, Levkoff AH, Atkins LM. Relatedness of strains of methicillin-resistant coagulase negative Staphylococcus colonizing hospital personnel and producing bacteremias in a neonatal intensive care unit. The Pediatric Infectious Disease Journal, 1992; 11(11): 935-94. 14. Cookson, B., Peters, B., Webster M., Phillips I., Rahman, M., Noble W., Staff Carriage of Epidemic Methicillin-Resistant Staphylococcus aureus, Journal of Clinical Microbiology, 1989; 27(7), 1471-1476. 15. Nakamura M, Rohling K, Shashaty M, Lu H, Tang Y, Edwards K. Prevalence of methicillin-resistant Staphylococcus aureus nasal carriage in the community pediatric population. Pediatric Infectious Disease Journal, 22; (21) 917-21. 16. American Academy of Pediatrics. Staphylococcal Infections. Red Book: Report of the Committee on Infectious Diseases. 23 rd edition. Elk Grove Village, Illinois: American Academy of Pediatrics; 1994: 423-43. 17. Miragaia M, Couto I, Pereira S, Kristinsson K, Westh H, Jarlov J, Carriço J et. al., Molecular Characterization of Methicillin-Resistant Staphylococcus epidermidis clones: Evidence of Geographic Dissemination. J Clin Microbiol. 22; 4(2): 43 438. 18. Carlos, C. The 21 Antimicrobial Resistance Surveillance Data Progress Report January-December 21 Available at http://www.ritm.gov.ph/arsp/21 ARSP Progress Report Summary.pdf 19. We M, Pineda C, Torres T, Cordero C, Saniel, M, Velmonte M. Nosocomial Acquisition of Oxacillin- Resistant Staphylococcus aureus (ORSA) at the Philippine General Hospital. Unpublished 2. Erdenizmenli M, Yapar N, Senger S, Ozdemir S, Yuce A. Investigation of Colonization with Methicillin- Resistant and Methicillin- Susceptible Staphylococcus aureus in an Outpatient Population in Turkey. Jpn J Infect Dis, 23; 56: 54-56. 21. Ontengco D, Baltazar L, Santiago R, Matias R, Isaac C, Tuazon A. Methicillin-resistant Staphylococcus aureus Isolates from Filipino Patients (1999-23). Phil J Microbiol Infect Dis 24; 33(3):15-11 22. Tejero A, Gutierrez MA, Aiquel MJ, Brandago M., Gonzales C, Broussain MT, Nasal carriage of staphylococcus aureus among personnel working in a teaching hospital, Enferm Infec Microbiol Clin. 1991; 9 (6): 351-3. 23. Tammelin, A., Domicel, P.,Hambræus, A., Ståhle, Dispersal of methicillin - resistant Staphylococcus epidermidis by staff in an operating suite for thoracic and cardiovascular surgery: relation to skin carriage and clothing. Journal of Hospital Infection, 2; 44: 119 126. 5