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Premium member Presentation Transcript ANTIBIOTIC SENSITIVITY TESTING SKILL BASED LEARNING : ANTIBIOTIC SENSITIVITY TESTING SKILL BASED LEARNING Dr.T.V.Rao MD Dr.T.V.Rao MD 1Uses of Antibiotic Sensitivity Testing: Uses of Antibiotic Sensitivity Testing Antibiotic sensitivity test : A laboratory test which determines how effective antibiotic therapy is against a bacterial infections. Antibiotic sensitivity testing will control the use of Antibiotics in clinical practice Testing will assist the clinicians in the choice of drugs for the treatment of infections. Dr.T.V.Rao MD 2What is the goal of Antibiotic Sensitivity testing?: The goal of antimicrobial susceptibility testing is to predict the in vivo success or failure of antibiotic therapy. Tests are performed in vitro , and measure the growth response of an isolated organism to a particular drug or drugs. The tests are performed under standardized conditions so that the results are reproducible. The test results should be used to guide antibiotic choice. The results of antimicrobial susceptibility testing should be combined with clinical information and experience when selecting the most appropriate antibiotic for our patients. Dr.T.V.Rao MD 3 What is the goal of Antibiotic Sensitivity testing ?Components of Antibiotic Sensitivity Testing: Components of Antibiotic Sensitivity Testing 1.The identification of relevant pathogens in exudates and body fluids collected from patients 2. Sensitivity tests done to determine the degree of sensitivity or resistance of pathogens isolated from patient to an appropriate range of antimicrobial drugs 3. Assay of the concentration of an administered drug in the blood or body fluid of patient required to control the schedule of dosage. Dr.T.V.Rao MD 4Why Need Continues for Testing Antibiotic Sensitivity: Why Need Continues for Testing Antibiotic Sensitivity Bacteria have the ability to develop resistance following repeated or subclinical (insufficient) doses, so more advanced antibiotics and synthetic antimicrobials are continually required to overcome them . Antibiotic sensitivity testing is essential part of Medical Care Dr.T.V.Rao MD 5Introduction: Dr.T.V.Rao MD 6 Introduction Susceptibility test, main purposes: As a guide for treatment Sensitivity of a given m.o. to known conc. of drugs Its concentration in body fluids or tissues As an epidemiological tool The emergence of resistant strains of major pathogens (e. g. Shigella, Salmonella typhi ) Continued surveillance of the susceptibility pattern of the prevalent strains (e. g. Staphylococci, Gram-negative bacilli)Introduction: Dr.T.V.Rao MD 7 Methods for antimicrobial susceptibility testing Indirect method cultured plate from pure culture Direct method Pathological specimen e.g. urine, a positive blood culture, or a swab of pus IntroductionWhat Does the Laboratory Need to Know about Antimicrobial Susceptibility Testing (AST) ?: Which organisms to test? What methods to use? What antibiotics to test? How to report results? What Does the Laboratory Need to Know about Antimicrobial Susceptibility Testing (AST) ? Dr.T.V.Rao MD 8Routine Susceptibility Tests: Routine Susceptibility Tests Disk diffusion (Kirby Bauer) Broth micro-dilution MIC NCCLS reference method Etest Dr.T.V.Rao MD 9Preparing for Testing: Dr.T.V.Rao MD 10 Preparing for Testing Inoculum preparation - Number of test organisms can be determined using different methods: Direct count (Microscopic examination) The optical density (OD) at 600 nm (Spectrophotometry) Plate count: making dilution first Turbidity standard (McFarland) routinely performed.Choosing the Appropriate Antibiotic: Dr.T.V.Rao MD 11 Choosing the Appropriate Antibiotic D rugs for routine susceptibility tests : Set 1 : the drugs that are available in most hospitals and for which routine testing should be carried out for every strain S et 2 : the drugs that are tested only : at the special request of the physician or when the causative organism is resistant to the first-choice drugs or when other reasons ( allergy to a drug, or its unavailability ) make further testing justifiedTable 1: Basic sets of drugs for routine susceptibility tests (http://w3.whosea.org/): Dr.T.V.Rao MD 12 Table 1: Basic sets of drugs for routine susceptibility tests ( http :// w3 . whosea . org / ) Set 1 Set 2 Staphylococcus Benzyl penicillin Oxacillin Erythromycin Tetracycline Chloramphenicol Gentamicin Amikacin Co-trimoxazole Clindamycin Intestinal Ampicillin Chloramphenicol Co-trimoxazole Nalidixic acid Tetracycline Norfloxacin Enterobacteriaceae Urinary Sulfonamide Trimethoprim Co-trimoxazole Ampicillin Nitrofurantoin Nalidixic acid Tetracycline Norfloxacin Chloramphenicol Gentamicin Blood and tissues Ampicillin Chloramphenicol Cotrimoxazole Tetracycline Gentamicin Cefuroxime Ceftriaxone Ciprofloxacin Piperacillin Amikacin Pseudomonas aeruginosa Piperacillin Gentamicin Tobramycin AmikacinAntimicrobial Susceptibility Testing: Diffusion method Put a filter disc, or a porous cup/a bottomless cylinder containing measured quantity of drugs on the a solid medium that has been seeded with test bacteria Dilution method vary amount of antimicrobial substances incorporated into liquid or solid media followed by inoculation of test bacteria Dr.T.V.Rao MD 13 Antimicrobial Susceptibility TestingSusceptibility Testing Methods: Susceptibility Testing Methods Inoculate MH plate Place disks on agar plate Incubate plate 18-24 hr, 35 C Measure and record zone of inhibition around each diskDiffusion Method: Dr.T.V.Rao MD 15 Diffusion Method Disc diffusion method : The Kirby-Bauer test Antibiotic-impregnated filter disc* Susceptibility test against more than one antibiotics by measuring size of “ inhibition zone ” 1949: Bondi and colleagues paper disks 1966: Kirby, Bauer, Sherris, and Tuck filter paper disks Demonstrated that the qualitative results of filter disk diffusion assay correlated well with quantitative results from MIC testsDisc Diffusion Method: Dr.T.V.Rao MD 16 Disc Diffusion Method Procedure (Modified Kirby-Bauer method: National Committee f or Clinical Laboratory Standards. NCCLS) Prepare approximately. 10 8 CFU/ml bacterial inoculum in a saline or tryptic soy broth tube (TSB) or Mueller-Hinton broth (5 m l) Pick 3-5 isolated colonies from plate Adjust the turbidity to the same as the McFarland No. 0.5 standard.* S treak the s wab on the surface of the Mueller-Hinton agar (3 times in 3 quadrants) Leave 5-10 min to dry the surface of agarExamining purity of plate Select the Colonies from Pure Isolates : Dr.T.V.Rao MD 17 Examining purity of plate Select the Colonies from Pure Isolates Reflected light Transmitted lightDisk Diffusion Test: Disk Diffusion Test Select colonies Prepare inoculum suspension Prepare inoculum suspension Dr.T.V.Rao MD 18Prepare the Material for Inoculation: Prepare the Material for Inoculation Standardize inoculum Suspension as per Mac farland standard Mix well Dr.T.V.Rao MD 19 Swab the plate with optimal sample: Swab the plate with optimal sample Remove sample Swab plate Dr.T.V.Rao MD 20Select the Disks and Apply: Select the Disks and Apply Select disks Dr.T.V.Rao MD 21Incubate Overnight: Incubate Overnight Dr.T.V.Rao MD 22Disc Diffusion Method: Disc Diffusion Method P lace the appropriate drug-impregnated dis c on the surface of the inoculated agar plate Invert the plates and incubate them at 35 o C , o/n (18-24 h) Measure the diameters of inhibition zone in mm Dr.T.V.Rao MD 23Read the Results with Precision: Read the Results with Precision Transmitted Light Dr.T.V.Rao MD 24Slide 25: Dr.T.V.Rao MD 25 Disc Diffusion Method Measurement of the diameters of inhibition zone Measure from the edge where the growth stats, BUT there are three exceptions With sulfonamides and co-trimoxazole , ignore slight growth within the zone Certain Proteus spp . may swarm into the area of inhibition When beta-lactamase producing Streptococci are tested, zone of inhibition are produced with a heaped-up, clearly defined edge, regardless of the size of the inhibition zone, they should be reported as resistantLook at the Charts for establishing the zones of Sensitivity: Dr.T.V.Rao MD 26 Look at the Charts for establishing the zones of Sensitivity The zone sizes are looked up on a standardized chart to give a result of sensitive, resistant, or intermediate . Many charts have a corresponding column that also gives the MIC (minimal inhibitory concentration) for that drug.Slide 27: Dr.T.V.Rao MD 27 Disc Diffusion Method Reporting the Results Interpretation of results By comparing with the diameters with “ standard tables ” Susceptible Intermediate susceptible Low toxic antibiotics: Moderate susceptible High toxic antibiotics: buffer zone btw resistant and susceptible ResistantFactors Affecting Size of Zone of Inhibition : Dr.T.V.Rao MD 28 Factors Affecting Size of Zone of Inhibition Inoculum density Timing of disc application Temperature of incubation Incubation time Larger zones with light inoculum and vice versa If after application of disc, the plate is kept for longer time at room temperature, small zones may form Larger zones are seen with temperatures < 35 o C Ideal 16-18 hours; less time does not give reliable resultsSlide 29: Dr.T.V.Rao MD 29 Factors Affecting Size of Zone of Inhibition Size of the plate Depth of the agar medium (4 mm) Proper spacing of the discs (2.5 cm) Smaller plates accommodate less number of discs Thin media yield excessively large inhibition zones and vice versa Avoids overlapping of zonesSlide 30: Dr.T.V.Rao MD 30 Factors Affecting Size of Zone of Inhibition Potency of antibiotic discs Composition of medium Acidic pH of medium Alkaline pH of medium Reading of zones Deterioration in contents leads to reduced size Affects rate of growth, diffusion of antibiotics and activity of antibiotics Tetracycline, novobiocin, methicillin zones are larger Aminoglycosides, erythromycin zones are larger Subjective errors in determining the clear edgeQuality Assurance in Antibiotic Susceptibility Testing : Dr.T.V.Rao MD 31 Quality Assurance in Antibiotic Susceptibility Test ing Visit - WHO-Regional Office for South East Asia website Medium: Mueller-Hinton agar plates Enterococcus faecalis (ATCC 29212 or 33l86) and a disc of co-trimoxazole 20 mm in diameter of the inhibition zone Procedure: Modified Kirby-Bauer method recommended by National Committee on Clinical Laboratory Services (NCCLS) Susceptibility test with quality control strainsQuality Assurance in Antibiotic Susceptibility Testing with Control strains: Dr.T.V.Rao MD 32 Quality Assurance in Antibiotic Susceptibility Test ing with Control strains Susceptibility test with quality control strains for every new batch of Mueller-Hinton agar Staphylococcus aureus (ATCC 25923) Escherichia coli (ATCC 25922) Pseudomonas aeruginosa (ATCC 2785 )Slide 33: Dr.T.V.Rao MD 33 Quality Assurance in Antibiotic Susceptibility Test Salient features of quality control Use antibiotic discs of 6 mm diameter Use correct content of antimicrobial agent per disc Store supply of antimicrobial discs at -20 o C Use Mueller-Hinton medium for antibiotic sensitivity determination Use appropriate control cultures Use standard methodology for the testNeed for Modified Methods: Modified Methods in Disc diffusion for Antibiotic sensitivity testing to be used for detections of following bacterial isolates 1 MRSA 2 ESBL 3 Enterobacteriaceae and Gram negative bacteria and Carbapenems resistant using Modified Hodge test Dr.T.V.Rao MD 34 Need for Modified MethodsDilution Method: 35 Dilution Method Minimum Inhibition Concent ration (MIC) The lowest concentration of antimicrobial agent that inhibits bacterial growth/ multiplication Minimum Bactericidal Concentration (MBC) or Minimum Lethal Concentration (MLC) The lowest concentration of antimicrobial agent that allows less than 0.1% of the original inoculum to surviveAntimicrobial susceptibility testing using micro-broth dilutions: Antimicrobial susceptibility testing using micro-broth dilutions • • • • • • • • • • • • • 96 well microtiter plate ug/ml 64 32 16 8 4 2Broth Dilution Method: 37 Broth Dilution Method Procedure Making dilutions (2-fold) of antibiotic in broth Mueller-Hinton, Tryptic Soy Broth Inoculation of bacterial inoculum, incubation, overnight Controls: no inoculum, no antibiotic Turbidity visualization MIC Sub culturing of non-turbid tubes , overnight Growth (bacterial count) MBCCreating Dilutions: Dr.T.V.Rao MD 38 Creating DilutionsBroth Dilution Method : 39 Broth Dilution Method Day 1 Add 1 ml of test bacteria ( 1*10 6 CFU/ml ) to tubes containing 1 ml broth and concentration of antibiotic (mg/l) Controls: C1 = No antibiotic, check viability on agar plates immediately C2 = No test bacteria Bacterial conc.= 5*10 5 CFU/ml Incubate 35 o C, o/n 128 64 32 16 8 4 2 C1 C2 64 32 16 8 4 2 1 C1 C2Slide 40: 40 Broth Dilution Method Day 2 Record visual turbidity Subculture non-turbid tubes to agar plates (use 0.01 ml standard loop) MIC = 16 mg/l 64 32 16 8 4 2 1 C1 C2 0.01 ml (spread plate), Incubate 35 o C, o/n 64 32 16 Day 3 Determine CFU on plates: At 16 mg/ = 700 CFU/ml > 0.1% of 5*10 5 CFU/ml MBC = 32 mg/lBroth Dilution Method: 41 Broth Dilution Method 100% of original bacterial conc. = 5*10 5 CFU/ml 0.1% = [(5*10 5) *0.1]/100 CFU/ml = 500 CFU/ml The bacteria count should be less than 5 CFU on agar plate subcultured with 0.01 ml 500*0.01 = 5 CFUBroth Dilution Method are Technically Difficult : Dr.T.V.Rao MD 42 Broth Dilution Method are Technically Difficult Disadvantages : Only one antibiotic & one organism can be tested each time Time-consuming Solutions?? Agar dilution method Disc diffusion method Micro broth dilution methodMicro broth Dilution Method: 43 Micro broth Dilution Method Micro dilution plates: “Micro dilution/ Micro broth dilutions” 96 wells / plate: simultaneously performed with many tests organisms/ specimens, less reagent required Manually prepared Commercially prepared Frozen or Dried/ lyophilized Consistent performance but high cost May suffer from degradation of antibiotic during shipping and storageAgar Dilution Method: 44 Agar Dilution Method Procedure Making dilutions of antimicrobial agent in melted media and pouring plates One concentration of antibiotic/ plate Possible for several different strains/plate 64 uGu/ml 32 ug/ml 16 ug/mlAgar Dilution Method: 45 Agar Dilution Method Procedure Inoculation of bacterial inoculum (McFarland No. 0.5) Using a replicating inoculator device called “ A Steers-Foltz replicator” Delivers 0.001 ml of bacterial inoculum Incubation Spot of growth MIC 32 ug/mlMinimal inhibitory concentration : Dr.T.V.Rao MD 46 Minimal inhibitory concentration The lowest concentration of antimicrobial agent that inhibits the growth of a bacterium Interpret: Susceptible Intermediate ResistantClinical Conditions when MICs are Useful : Clinical Conditions when MICs are Useful Endocarditis Meningitis Septicemia Osteomyelitis Immunosuppressed patients (HIV, cancer, etc.) Prosthetic devices Patients not responding despite “S” Reports Dr.T.V.Rao MD 47Inoculum Preparation MIC Testing (NCCLS Reference Method): Dr.T.V.Rao MD 48 Inoculum Preparation MIC Testing ( NCCLS Reference Method) Standardize inoculum suspension Final inoculum concentration 3 – 5 x 10 5 CFU/ml (3 – 5 x 10 4 CFU/well)Select Micro titration plate and prepare optimal inoculum: Dr.T.V.Rao MD 49 Select Micro titration plate and prepare optimal inoculum Micro dilution MIC tray Prepare inoculum suspensionDilute & mix inoculum suspension : Dr.T.V.Rao MD 50 Dilute & mix inoculum suspensionPour inoculum into reservoir and inoculate MIC tray: Dr.T.V.Rao MD 51 Pour inoculum into reservoir and inoculate MIC trayIncubate overnight Do not forget to check the purity of Inoculum: Dr.T.V.Rao MD 52 Incubate overnight Do not forget to check the purity of Inoculum Inoculate purity plate Optimal Use of Purity Plates: Optimal Use of Purity Plates Sub final test suspension to non-selective medium (after inoculating MIC test) Streak for isolation (avoid several specimens per plate - may not reveal contaminants if no isolated colonies) Examine before reading MIC (usually at 16-20 h) Re-incubate if Antibiograms questionableSlide 54: - + 64 32 16 8 4 2 1 >64 0.5 Read MICs >64The gradient technique, Etest®: Dr.T.V.Rao MD 55 The gradient technique, Etest® Etest is a well established AST method in microbiology laboratories around the world. The Etest technique comprises a predefined gradient of antibiotic concentrations on a plastic strip, and can be used to determine the Minimum Inhibitory Concentration (MIC) of antibiotics, antifungal agents and antimycobacterial agents.E test – MIC Reports are helpful in Critical management decisions: Dr.T.V.Rao MD 56 E test – MIC Reports are helpful in Critical management decisions Quantitative MIC data is a prerequisite for the management of critical infections , including sepsis, especially among critical care patients. Etest is particularly valuable in such situations, when on-scale MICs are needed for treatment decisions.Antimicrobial Gradient Testing E-test®: Antimicrobial Gradient Testing E-test® Read plates after recommended Incubation Read MIC where elipse intersects scaleMIC of the Bacteria can be read Directly: Dr.T.V.Rao MD 58 MIC of the Bacteria can be read DirectlySlide 59: MIC on a strip abbiodisk.comSerum Susceptibility Tests: 5-Jan-06 Chiang Mai University 60 Serum Susceptibility Tests To determine drug concentration in the patient’s serum = MIC*SIT The Serum Inhibitory Titer ( SIT ) The highest dilution of patient’s serum that inhibit bacteria To determine the ability of drug in the patient’s serum to kill bacteria The Serum Bactericidal Level ( SBL ) The lowest dilution of patient’s serum that kills bacteria Technically DemandingAntibiotic Sensitivity testing can be done with automation: Antibiotic Sensitivity testing can be done with automation Dr.T.V.Rao MD 61VITEK 2 Automates Reporting of Resistance: Dr.T.V.Rao MD 62 VITEK 2 Automates Reporting of Resistance Integrated in the VITEK 2 system is the Advanced Expert System (AES™) , a software which validates and interprets susceptibility test results, and detects antibiotic resistance mechanisms. The AES Expert System is the most developed software system in this field, and is capable of identifying even emerging and low-level resistance.What is the Role of Microbiology Departments: Each laboratory should have a staff member with the time, interest, and expertise to provide leadership in antibiotic testing and resistance. This person would read relevant publications, network with other laboratories, and evaluate potentially useful tests to detect new forms of resistance before new CLSI-recommended tests become available ” - Ken Thomson, Emerging Infect. Dis., 2001 Dr.T.V.Rao MD 63 What is the Role of Microbiology DepartmentsReferences: 1Usanee Anukool (Ph.D .) Clinical Microbiology,AMS , Chiang Mai University 2 National Committee For Clinical Laboratory Standards. 1998. NCCLS document M100 - S8 . Performance Standards for Antimicrobial Susceptibility Testing. 8th edition, NCCLS, Waynae, Pa. Dr.T.V.Rao MD 64 ReferencesFor Articles of Interest on Antibiotics follow me on: Dr.T.V.Rao MD 65 For Articles of Interest on Antibiotics follow me onSlide 66: Created by Dr.T.V.Rao MD for ‘e’ learning resources for Microbiologists in Developing World Email email@example.com Dr.T.V.Rao MD 66 You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.