THE CARRIER STATE: METHICILLIN - RESISTANT STAPHYLOCOCCUS AUREUS A HOSPITAL STUDY "SCREENING OF HOSPITAL PERSONNEL" FOR NASAL CARRIAGE OF STAPH AUREUS

Similar documents
STUDY OF IMPETIGO AND THE RESISTANCE PATTERN OF THE ISOLATES TO VARIOUS ANTIBIOTICS

Bacteriuria in Children

Frequency of Nasal Carriage of Staphylococcus Aureus and Its Antimicrobial Resistance Pattern in Patients on Hemodialysis

THE USE OF THE PENICILLINASE-RESISTANT

International Journal of Pharma and Bio Sciences

MRSA The Facts. Staphylococcus aureus MRSA. Staphylococcus aureus, often referred to simply as "staph," What is Staphylococcus aureus?

Staphylococci. What s to be Covered. Clinical Scenario #1

Pathogenic organisms in the sputum of patients

Staphylococcus aureus Epidemic in a Burn Unit

HOSPITAL INFECTION CONTROL

What s to be Covered. Microbiology of staphylococci Epidemiology of S. aureus infections Pathogenesis of S. aureus infections

Risk Factors for Methicillin-Resistant Staphylococcus aureus Colonization in a Geriatric Rehabilitation Hospital

D. A. Leigh and G. Joy. Department of Microbiology, Wycombe General Hospital, High Wycombe, Bucks HP11 2TT, UK

Staphylococci. Gram stain: gram positive cocci arranged in clusters.

Information on Staphylococcal Infections For Day Care Administrators and Care Givers

Clinico-etiological study of pyodermas in a tertiary care hospital

Blood Culture Collection and Interpretation

Staph Infection Fact Sheet

6-8 November EICC, Edinburgh. Registration now open Abstract submission deadline: June 24th

UTI : A NEW APPROACH TO ITS DIAGNOSIS

Microbiology products. Liofilchem Chromatic

MRSA: Implications in Sports Medicine

A new selective blood agar medium for Streptococcus pyogenes and other haemolytic streptococci

Medical/Surgical Asepsis. Presented by: Cynthia Bartlau, RN, PHN, MSN

Laboratory CLSI M100-S18 update. Paul D. Fey, Ph.D. Associate Professor/Associate Director Josh Rowland, M.T. (ASCP) State Training Coordinator

Taking nose, throat and skin swabs. Clinical Skills

Sep Oct Nov Dec Total

Antibiotic resistance of coagulase-negative staphylococci and micrococci

Veerle Compernolle, Gerda Verschraegen, and Geert Claeys* Department of Microbiology, Ghent University Hospital, Ghent, Belgium

Bacterial contamination on Medical Doctors and Medical Students white coats at Kilimanjaro Christian Medical Centre in Moshi Tanzania

Study of etiological factors and sensitivity pattern in CSOM

A SURVEY OF METHICILLIN RESISTANCE

Medical Microbiology

Infection associated with modern surgical procedures

The Impact of Healthcare Associated Infection (HCAI)

MRSA. Meticillin Resistant Staphylococcus aureus. Infection Control Department. Royal Surrey County Hospital. Patient information leaflet

BLOOD CULTURE POLICY FOR PAEDIATRICS

ENG MYCO WELL D- ONE REV. 1.UN 29/09/2016 REF. MS01283 REF. MS01321 (COMPLETE KIT)

Handwashing and antiseptic-containing soaps in hospital

International Journal of Medical Science and Education pissn eissn

CHAPTER 7 Medical/Surgical Asepsis and Infection Control

Outbreak investigation of nosocomial infections

A Norazah, S M Liew, A G M Kamel, Y T Koh, V K E Lim. O r i g i n a l A r t i c l e

Asian Journal of Pharmaceutical Analysis and Medicinal Chemistry Journal home page:

Reducing Blood Culture Contamination in Hospitalized Pediatric Patients

Adenosine Triphosphate Bioluminescence Test of the Nasal Spray Nozzles Attached to an Ear-nose-throat Treatment Unit

MRSA Positive. An information guide

Prevalence of Methicillin Resistant Staphylococcus aureus on computer mice on the campus of Southern Adventist University

Lab 4. Blood Culture (Media) MIC AMAL-NORA-ALJAWHARA 1

Ecology of Nasal Staphylococci

Rifampin Resistance. Charlottesville, Virginia i0w organisms in Trypticase soy broth (BBL Microbiology

Chapter 11 PREVENTING INFECTION. Elsevier items and derived items 2010 by Mosby, Inc. an affiliate of Elsevier Inc. All rights reserved

Renal Unit. Catheter Related Bacteraemia Guidelines

Cost-Benefit Analysis in Healthcare Creating investment incentives to drive adoption of a technical innovation

Chapter 7 8/23/2016. Asepsis and Infection Control. Asepsis. Asepsis (Cont.) Microorganisms. Infection control and prevention

Panel discussion-aidc 2017 Rapport with the microbiology lab-how it helps your patient

Haemodialysis central venous catheter-related sepsis management guideline Version 3. NAME M. Letheren Chair Clinical Effectiveness Advisory Group

PEGCO Inc. 532 N. RIDGEWOOD AVE DAYTONA BEACH, FL Phone: (386) Fax (386)

Bloodborne Pathogens

This program will outline infection prevention measures known to help reduce the risk of patients getting a healthcare associated infection (HAI).

Healthcare-Associated Infections Across the Spectrum of Care

II- Streptococci. Practical 3. Objective: Required materials: Classification of Streptococci: Streptococci can be classified according to:

THE SENSITIVITY OF STAPHYLOCOCCI AND OTHER WOUND BACTERIA TO ERYTHROMYCIN, OLEANDOMYCIN, AND SPIRAMYCIN

Enteric Illness. Shigellosis

Chapter 12. Preventing Infection. Elsevier items and derived items 2014, 2010 by Mosby, an imprint of Elsevier Inc. All rights reserved.

(multidrug-resistant Pseudomonas aeruginosa; MDRP)

A.F. GENITAL SYSTEM. ITEMS NECESSARY BUT NOT INCLUDED IN THE KIT A.F. GENITAL SYSTEM Reagent (ref ) Mycoplasma Transport Broth (ref.

Discussion points CLSI M100 S19 Update. #1 format of tables has changed. #2 non susceptible category

NHS GG&C Public Health Protection Unit (PHPU)/ Infection Control Policy. For investigation and management of PVL SA

Routine endotracheal cultures for the prediction of sepsis in ventilated babies

Chapter 13. Preventing Infection. Copyright 2019 by Elsevier, Inc. All rights reserved.

ENGLISH FOR PROFESSIONAL PURPOSES UNIT 3 HOW TO DEAL WITH CLOSTRIDIUM DIFFICILE

Labquality External Quality Assesment Programmes General Bacteriology 1 1/2010

Abstract. J Pak Med Assoc

Urine bench. John Ferguson Sept 2013

2/11/ Six elements of infection: (portal of exit)

MRSA. and You. A Guide for You and Your Family. (Methicillin Resistant Staphylococcus aureus) CH-IPC 001

Topical antimicrobial agents in wound care. Professor Val Edwards-Jones Manchester Metropolitan University UK

RAPID REDUCTION OF STAPHYLOCOCCUS AUREUS POPULATIONS ON STAINLESS STEEL SURFACES BY ZEOLITE CERAMIC COATINGS CONTAINING SILVER AND ZINC IONS

Evaluation of methicillin-resistant Staphylococcus aureus (MRSA) colonization in pigs and people that work with pigs in Ontario Veterinary College

Methicillin-Resistant Staphylococcus aureus (MRSA) S urveillance Report 2008 Background Methods

320 MBIO Microbial Diagnosis. Aljawharah F. Alabbad Noorah A. Alkubaisi 2017

Staphylococcal Food Poisoning

were interviewed with regard to the possible risk factors of prior colonization with MR coagulase-negative staphylococci

SUPPLEMENTAL TESTING. Tan Thean Yen

Aerobic bacteria isolated from diabetic septic wounds

Self-Instructional Packet (SIP)

Incidence per 100,000

Management of Catheter Related Bloodstream Infection (CRBSI), including Antibiotic Lock Therapy.

J. E. DEGENER, A. C. W. SMIT, M. F. MICHEL H. A. VALKENBURG* AND L. MULLER*

Preventing & Controlling the Spread of Infection

GUIDE TO INFECTION CONTROL IN THE HOSPITAL. Carbapenem-resistant Enterobacteriaceae

Infection Control and Asepsis. Copyright 2010, 2006 by Saunders, an imprint of Elsevier Inc. All rights reserved.

Impact of hospital infections on our

THE INCIDENCE of infections caused by

PIDSP Journal 2011 Vol 12 No.1 Copyright 2011

Bacteriological Profile of Post Traumatic Osteomyelitis in a Tertiary Care Centre

MRSA. (Methicillin-resistant Staphylococcus aureus) Patient & Family Guide.

Central Venous Access Devices and Infection

The Clinical Significance of Blood Cultures. Presented BY; Cindy Winfrey, MSN, RN, CIC, DON- LTC TM, VA- BC TM

Transcription:

THE CARRIER STATE: METHICILLIN - RESISTANT STAPHYLOCOCCUS AUREUS A HOSPITAL STUDY "SCREENING OF HOSPITAL PERSONNEL" FOR NASAL CARRIAGE OF STAPH AUREUS Abstract Pages with reference to book, From 35 To 38 Bushra Ashiq ( Department of Microbiology, Jinnah Postgraduate Medical Centre, Karachi. ) Methicillin resistant Staph Aureus (MRSA) were studied in a 300 bedded Central Government Hospitat Rawalpindi, in which 291 staff members were screened by nasal swabbing. Of 1 25 cases carrying staph aureus 5 (1.78%) were methicillin resistant. They were treated with Bacitracin ointment to be applied to interior nares four times a day for one week. Hexachiorophane baths daily, chlorhexidine shampoo once daily for a week, and were taken off duty from wards for one day (JPMA 39: 35, 1989). INTRODUCTION In the twenty years since the introduction of antibiotics, hospital acquired infections due to staph aureus became a curse. Often the organism was resistant to penicillin and other antibiotics. Methicillm was introduced in 1959 and outbreaks due to MRSA in mid-1960 s were rather uncommon 1. This may be because of control of infection procedures, restraint in the use of antibiotics, availability of B4actamase stable penicillins and possibly a natural reduction in the virulence and transmissibility of staph aureus. In early 1970 s, there was internationally a general decline in the incidence of MRSA and there have been only two detailed reports of Hospital outbreaks from USA 1,2. Problems with methicillin resistant staph aureus emerged again in late half of 1970 s. These MRSA, usually resistant to flumerous antibiotics including Gentamicin and Chloramphenicol, may be sensitive to Rifampicin and Fusidic acid and always sensitive to Vancomycin. Despite the early reports of Shanson et a1 3 and the occasional isolates of MRSA in U.K. in later half of 1970 s the U.K. strain rarely gave rise to cross infection following standard patient isolation procedures. The extensive studies of Lid well and his colleagues demonstrated staff nasal carriage as a significant source of staphylococci for new nasal acquisition by patients and the contribution of staff nasal organism was even greater when the strain was tetracycline resistant 4,5. Nasal carrier of staph aureus can disperse significant number of organism into the environment 6. To control the possible transmission of MRSA from staff to patient a screening programme was carried out in 1979 to find out the incidence of nasal carriage of these organisms among staff of a Central Government Hospital. MATERIAL AND METHODS Members of the staff (doctors, nurses, ward boys, operation theatre staff, House Keeping) of 300 bedded Central Government Hospital, Rawalpindi were screened. Nasal Swabbing This method was selected due to limited time, facilities, financial support and, being easily sampled site, may be named as an indirect means of detecting staff who carry MRSA at other sites of the body 3 and chances by the transmission by nasal shedders, who are more dangerous than throat carriers, is

more if all other possibilities are eliminated by proper hospital asepsis technique. Right and left si4es of anterior nares were sampled by rubbing upto 1½ cm by sterile cotton wool swabs moistened with sterile normal saline. All swabs were inoculated within one hour of collection on relevant culture media. Specimens were processed mainly to detect carriage of staph aureus only. They were inoculated on blood agar and Mannitol salt agar and incubated at 37 C overnight, aerobically. Any staphylococcus aureus isolated was confirmed by slide and tube coagulase test, Dnase and phosphatase tests. Plates were further incubated for 24 hours and any further isolation of staph aureus looked for, other pathogenic organisms isolated were kiebsiella pneumoniae, Pseudomona aeroginosa, and Candida albicans. Sensitivity was done by stoke disc diffusion method7. Disc used for antimicrobial sensitivity testing were (ug/ml) Penicillin 2 units, Erythromycin 5 ug, Tetracycline 25 ug, Gentamicin 10 ug, Fusidic acid 10 ug, Sulphonamide 100 ug, Cotrimoxazole 25 ug, Clindamycin 2 ug, Methicillin 10 ug. Sensitivity to Vancomycin and for some strains to Gentamicin could not be done due to non-availability of Sensitivity Discs. Media used for antimicrobial susceptibility testing was Iso-sensitest agar (Oxide ltd.) RESULTS Two hundred and ninety one nasal swab were processed; 11 contaminated specimens excluded from the study and 281 specimens Total cases positive Ibr slap/i aureus carriage were 125 (44.5%) and total cases carrying pathogenic organisms including staph aureus were 130 (46%). No pathogens were found in 151 specimens and so they were defined as culture negative. Methicillin rdsistant staph aureus carrier staff were 5 in number. Organisms isolated in addition to staphylococcus included Kiebsiella pneumoniae in 4 cases of which one staff was carrying methicillin sensitive staph aureus (MSSA) as well, one had candida albicans, two had pseudomonas of whom one case had both pseudomonas pyocynae and staph aureus. He had deflected nasal septum which helps carriage of pseudomona spp. All these cases were suffering from symptomatic infections. These organisms were sensitive to most of the antibiotics in use and were given treatment for their symptoms. Follow up cultures could not be done.

Table I shows the antibiotic sensitivity pattern of staph aureus to commonly used antibiotics. Most of the resistance of staph aureus was noted.to penicillin (69%) and tetracycline (41%). Fusidic acid sensitivity could be done for only 51 isolates (98% sensitive), gentamicin sensitivity was available to 20 isolates and none of them was resistant.

Table-II shows the details of nasal carriage of Methicilin sensitive staph aureus (MASSA) and MRSA in Hospital personnel. MRSA was carried by one physician, one nurse, two ward boys and one house keeping staff. All the 5 MRSA strains were resistant to penicillin, 4 were resistant to tetracycline and one moderate-resistant (carried by house keeping staff), three were resistant to Suiphonamide and Septran, two to Lincomycin. Three were fully sensitive to Erythromycin and two moderate-resistant, all sensitive to Fusidic acid. Gentamicin sensitivity could not be made available to these isolates because of non-availability of discs. DISCUSSION In the present study Methicillin sensitive staph was 42.7% of considered population and 43% of total population. Prevalence of MRSA was 1.78% of total population. All MRSA were resistant to penicillin, and 4 to tetracycline. These were also multi-drug resistant and all resistant to more than one or two antimicrobials. In the light of studies by Lidwell et al 4,5 it was assumed that these isolates may act as important sources for transmission of infection. In study by Klimek 8 of Hospital personnel in an outbreak, out of 202 staff members, 5 personnel (2.45%) carried MRSA and total staph carriage was 20.30%. In study of Craven et al 9 overall carrier rate of staph aureus sensitive and resistant to oxacillin was 17% while our carrier rate was much higher, 44.50%. In a survey no carrier of oxacillin resistant staph aureus was found in early 1979 in Hospital personnel but in late 1979 the MRSA rate was 3.3% 9 while our rate was 1.78% which is much lower may be because of multiple factors relating to population studied. In practice, staff nasal carriage during outbreak had either a low prevalence, or was absent. 508 employees, screened at the University of Virginia Medical Centre, who had direct contact with patients and who were colonised or infected with an outbreak strain, revealed that only 2 (0.4%) who carried MRSA 10. Scrutiny of studies by authors mentioned suggests a further reason to support the

screening of staff for nasal carriage, namely as an indirect mean of detecting staff who carry MRSA at other sites, e.g., colonised 3,9 None of staff personnel carrying MRSA had any evidence of clinical infection at other sites. We were not able to under take more extensive screening study by taking specimen from other carriage sites of body. The Hospital personnel carrying MRSA in our study were given Bacitracin ointment four times a day for both anterior nares for one week, hexac hiorophane bath and chlorhexid me gluconate shampoo daily for a week and removed from duty from wards for 24 hours. Follow up cultures could not be done. The practice of hand washing for all patient contacts before and after touching patient was strictly enforced and use of disposable gloves and rigorous notouch dressing technique recommended. This study emphasizes the importance of identifying and possibly avoiding the introduction of a hospital staff member, carrier of MRSA into the hitherto unaffected hospital, for reducing the reservoir by the use of antiseptics for colonised sites, skin and superficial sites. This screening study helped us to identify the MRSA carrier staff who could transmit them to patients attended by them and might have caused clinical infection and sepsis. AC ENOWLEDGEMENTS I am thankful to Dr. Syed Mohsin Ali, then Medical Superintendent, Central Government Hospital, Rawalpindi for providing me full cooperation for collection of specimens from Central Government Hospital, Rawalpindi and Major General Syed Azhar Ahmad (then Brigadier) Commanding Officer A.F.I.P. for providing laboratory facilities. REFERENCES 1. Barrett, F.F., McGehee, R.F. Jr. and Finland, M. Methicillin-resistant Staphylococcus aureus at Bostan city hospital; bacteriologic and epidemiological observations. N. Engl. J. Med., 1968; 279 ; 441. 2. 0 Toole, R.D., Drew, W.L., Dahlgren, BJ. and Beaty, A.N. An outbreak of methicillin resistant Staphylococcus aureus infections. Observations in hospital and nursing home. JAMA., 1970; 213: 3. Shanson, D.C., Kensit, J.A. and Duke, R. Outbreak of hospital infection with a strain of Staphylococcus aureus resistant to gentamicin and methicillin. Lancet,1976;1 :1347. 4. Lidwell, O.M., Polakoff, S., Jevons, M.P., Parker, M.T., Shooter, R.A., French, V.I. and Dnkerley, D.R. Staphylococcus infection in thoracis surgery experience in a sub-divided ward. J. Hyg (Lond.), 1966; 64321. 5. Lidwell, O.M., Davies, J., Payne, LW. Newman, P. and Villiarns, R.E.O. Nasal acquisition of Staphylococcus aureus in partly divided ward. 3. Hyg (Lond.), 1971; 69:113. 6. White, A. Relation between quantitative nasal cultures and dissemination of staphylococci. 3. Lab. Clin. Med., 1961; 58: 273. 7. Stokes, E.J. and Waterworth, P.M. Antibiotic sensitivity tests by diffusion methods. Association of Clinical Pathologists, Broad Sheet No. 55, 1972. 8. luimek, JJ., Marsik, FJ., Bartlett, R.C., Weir, B., Shea, P. and Quintilani, R. Clinical, epidemiological and bacteriologic observations of an outbreak of methicillin-resistant staphylococcus aureus at a large community hospital. Am. J. Med., 1976; 61:340. 9. Craven, D.E., Reed, C., Kollisch, M., DeMaria, A., Lichtenberg, D., Shen, K. and McCabe, W.R. A large outbreak of infections caused by a strain of staphylococcus aureus resistant to o xacillin and aminoglycoside. Am. J. Med., 1981;71:53. 10. Thompson, R.L., Cabezudo, 1. and Wenzel, R.P. Epidemiology of nosocomial infection caused by methicillin resistant Staphylococcus aureus. Ann. Intern. Med., 1982;97: 309.