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Presents Overview Part 1 MultiChrome

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Page 1: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Presents

Overview Part 1 MultiChrome

Page 2: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

MultiChrome TM

TM

Veterinary Microbiology Culture System

MultiChrome GP(+)Exp 3/10

Lot #123 MultiChrome GP(-)

Procedures and Techniques For Performing In-house Cultures using Kacey MultiChrome™ Bi-pates.

Gram Positive Gram Negative

Page 3: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Sensi-Rings™ Quick Reference Card

Kacey Diagnostics Quick Reference For Culture & Sensitivity StudyINNOCULATION OF CULTURE BI-PLATE

1) Remove the plate from refrigerator & pre-heat in the incubator @37 degrees for 15-20 minutes prior to inoculating the Kacey MultiChrome bi-plate.

2) Using a sterile inoculating loop ( 20uL) for liquids and a Kacey Sterile Swab for solids ,inoculate the sample onto both sides of the Kacey Multichrome Bi-plate, by utilizing a zigzag streaking motion.

3) Replace clear lid and place Kacey MultiChrome Bi-plate in the incubator upside down (inverted position) and incubate at 37°C +/- 2 degree C for no less then 24 hours . The plate should be examined after 24 hours, but no later than 48 hours after incubation.

INOCULATION OF MULLER HINTON (MH) PLATE

1) Using the Kacey Swab or loop containing the now diluted WST & Turbidity adjusted dilution streak the 1st time the entire periphery of the Mueller Hinton plate making a 360° circle.

2) Streak a 2nd time again the Muller Hinton Plate with a fresh sample of the WST dilution usingbroad strokes starting at theto 3 o’clockposition.

3) Streak a 3rd time again the Muller Hinton plate with a fresh sample of the WST dilution using wide broad strokes starting at the 11 to 5 o’clock position 4) Remove “Sensi-Ring” from the foil pouch with tweezers at the inner tab & place the “Sensi-Ring” facing down onto the MH plate tapping down in non-disk areas, label the specimen to be incubated.5) Place the MH Inoculated plate into an incubator upside down, set timer & incubate for 24 hours. Remove & read inhibition zones with Kacey Clear Acetate Reader.

1 2 3TRANSFER TO MULLER HINTON PLATE USING KACEY “WST” TUBES 1) Taking a Kacey Sterile Swab or Loop carefully dab into the three (3) different places containing the bacteria on the MultiChrome Bi-plate.

2) Immediately place the sterile Kacey Swab or Loop containing the bacteria into the Kacey Working Solution tube (WST which contains 1.0 ml of sterile 0.085%solution). Mix the Kacey Swab or Loop with a gentle twirling motion while in the WST tube for approximately 3-5 seconds.

3) Compare sample to the Kacey Turbidity Standard (white cap) KTS. Sample should match in turbidity, if not add more WST sol (green top) or more sample to match KTS tube. (see enclosed Turbidity Card).

Quick reference only. Refer to detailed instruction manual for additional information.

GN

GP

24 HrsWSTDilution

Rotate Swab 3-5 sec

24 Hrs

GN

GP

12

3

New Kacey Sterile Swab Compare to KTS tube(white top) & match turbidity by adding more WST(grn top) solution or more sample

KTS White Tube

Sample

Page 4: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

BACTERIA AS A PATHOGEN

In veterinary medicine we routinely see them affecting nine areas:

Outer Ear InfectionsUrinary Tract InfectionsConjunctival infectionsGenital infectionsWound/abscessSkin InfectionsUpper Respiratory InfectionsMastitisSepticemia

Page 5: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

MultiChrome™ Supplies For Each Test

MultiChrome GP(+)Exp 3/10

Lot #123 MultiChrome GP(-)

• 1 MultiChrome™ bi-plate• A sterile “Rayon”* swab included or sterile loop included with MultiChrome™ kit.• Incubator: We recommend the Kacey Mini-Incubator with its individual timers for up to six cultures.

*Always use Rayon swabs as chemicals in cotton can alter results.

Page 6: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Kacey Mini Incubator Up Close

• Small foot print (8”w x 13”hx12”d)

· Precise Digital temperature control

· Numbered trays fit both round & rectangle plates

· Six individual timers

· Audible/Visible alerts

· Energy efficient, UL listed · Made in the USA

·1year warranty

Just Load… Press Timer...and Walk Away!

MultiChrome GP(+)Exp 3/10

Lot #123 MultiChrome GP(-)

Patent Pending

Page 7: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Pre-heat incubator.

• Pre heat incubator (98.6 F or 37 C default) which will take approximately 30 minutes. The Kacey Mini Incubator will automatically default to this temperature when plugged in.

98.6 F or 37C

Page 8: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Pre-heat MultiChrome™ plate.• Remove a plate from the refrigerator and thaw MultiChrome™ plate for approx 9-10 min. Place plate upside down to avoid condensation landing on media.

• The Kacey Mini Incubator has a “Red” pre-heat timer button which allows you set a 10 minute warning.

MultiChrome GN(-)MultiChrome GP(+)

Exp 3/10 Lot #123

Page 9: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Obtain sample and inoculateMultiChrome™ plate.

• Using a sterile loop or rayon swab obtain a sample from the affected area.

• Streak both the Gram (+) and (-) chambers of the plate in a zigzag fashion.

MultiChrome GN(-)MultiChrome GP(+)

Exp 3/10 Lot #123

Page 10: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Incubate sample.

• Cover MultiChrome™ plate with lid and turn upside down.• Place in incubator and incubate for 24 hours. On the Kacey Mini Incubator press one of six pre-set 24 hours timers and walk away.

MultiChrome GN(-)MultiChrome GP(+)

Exp 3/10 Lot #123

24 hours

Page 11: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Read sample.

• At 24 hours remove from incubator and read.

• Note whether the colony is a Gram (+) or (-) as you reference the following color chart. Also, keep in mind the types of bacteria most associated with different affected areas of the body (see the next slide).

24 hours

Page 12: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Commonly found bacteria

• Based on results, a further course of action can now be with taken to determine the most efficacious antibiotic(s) using the Sensi-Ring™ sensitivity system.

• The following is a list of commonly found Aerobic Bacteria in small animal practice:

Gram Positive: Staphylococci, Streptococci, Enterococci

Gram Negative: E coli, Proteus, Klebsiella, Pseudomonas

Ear: Staphylococci, Pseudomonas, Proteus, E. coli, Enterococci, Streptococci

UTI: Staphylococci, Proteus, E. coli, Klebsiella, Enterococci, occasionally Pseudomonas

Skin & Wound: Staphylococci, Streptococci, Pseudomonas, Enterococci, Proteus

Page 13: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Color reference chart

Gram NegativeGram Positive

Strep (+)

Mixed Staph/Strep (+)

• This is a partial list of the various bacteria seen on MultiChrome™. Some bacteria may look slightly different than shown, but the colors and Gram (+), (-) designation remain constant. This library will continue to grow for use a reference guide.

Page 14: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Bacterial pathogen probability charts for Canine and Feline:These reference charts suggest the highest and lowest percentage for infectionof various parts of the body by common pathogenic bacteria. Once identified proceed with accepted veterinary antibiotic protocols for treatment of pathogens.

Species: CaninePercentage

Probability            

Bacteria UTI Ear Bone Skin Genital Wound Blood URIStaph Intermedius 10-15% 25-30% 40-50% 60-70% 15-25% 25-35% 25-35% 30-35%E. Coli >50% 10-20% 10-20% 20-30% 30-35% 20-30% 35-45% 15-20%Enterococcus faecalis <10% NGS 10-20% NGS NGS NGS NGS NGSProteus mirabilis 15% 20-25% 10-20% <10% NGS 10-20% NGS NGSObligate anerobes NGS NGS NGS NGS NGS 25-35% 10-20% NGSPseudomonas NGS 15-25% NGS <10% <10% 10-20% 10-20% <10%Klebsiella 10-15% NGS NGS NGS NGS NGS 20-35% <10%Pasturella NGS NGS NGS NGS 10-25% NGS NGS 15-20%

                 

NGS= Not Generally Seen              

Species: Feline Percent   Probability        

Bacteria Conjunctival Genital UTI Wound URI SkinPasturella 10-20% 15-25% 10-15% 30-40% >50% >50%E. Coli NGS 30-35% 40-45% 10-20% 15-20% 20-30%Proteus mirabilis NGS NGS 10-15% <10% <10% <10%Pseudomonas NGS <10% <10% NGS <10% NGSObligate anerobes NGS 10-25% NGS 25-35% NGS NGSKlebsiella NGS NGS NGS NGS NGS NGSChlamydia psittoci 50-75% NGS NGS NGS NGS NGSB-hemolytic strep 15-25% NGS NGS NGS NGS NGS

             

NGS= Not Generally Seen           Probability reference charts taken from “Target: The Antimicrobial Reference Guide to Effective Treatment” , second edition, revised. Author: Dr. David Aucoin, DVM, Diplomate of the American College of Veterinary Clinical Pharmacology. Data on file, Kacey® Asheville, N.C. 28801.

Page 15: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Treatment.

• Many organisms can be easily identified and treated after the use of the MultiChrome™ system without further testing. However, for organisms that have proven resistant to typical antibiotic regimens it may be necessary to conduct a Sensitivity test.

• Kacey Diagnostics has made “Sensitivity” testing easy, accurate and cost effective as the MultiChrome™ by introducing the Sensi-Ring system in the next section.

Page 16: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Sensi-Rings™ Quick Reference Card

Kacey Diagnostics Quick Reference For Culture & Sensitivity StudyINNOCULATION OF CULTURE BI-PLATE

1) Remove the plate from refrigerator & pre-heat in the incubator @37 degrees for 15-20 minutes prior to inoculating the Kacey MultiChrome bi-plate.

2) Using a sterile inoculating loop ( 20uL) for liquids and a Kacey Sterile Swab for solids ,inoculate the sample onto both sides of the Kacey Multichrome Bi-plate, by utilizing a zigzag streaking motion.

3) Replace clear lid and place Kacey MultiChrome Bi-plate in the incubator upside down (inverted position) and incubate at 37°C +/- 2 degree C for no less then 24 hours . The plate should be examined after 24 hours, but no later than 48 hours after incubation.

INOCULATION OF MULLER HINTON (MH) PLATE

1) Using the Kacey Swab or loop containing the now diluted WST & Turbidity adjusted dilution streak the 1st time the entire periphery of the Mueller Hinton plate making a 360° circle.

2) Streak a 2nd time again the Muller Hinton Plate with a fresh sample of the WST dilution usingbroad strokes starting at theto 3 o’clockposition.

3) Streak a 3rd time again the Muller Hinton plate with a fresh sample of the WST dilution using wide broad strokes starting at the 11 to 5 o’clock position 4) Remove “Sensi-Ring” from the foil pouch with tweezers at the inner tab & place the “Sensi-Ring” facing down onto the MH plate tapping down in non-disk areas, label the specimen to be incubated.5) Place the MH Inoculated plate into an incubator upside down, set timer & incubate for 24 hours. Remove & read inhibition zones with Kacey Clear Acetate Reader.

1 2 3TRANSFER TO MULLER HINTON PLATE USING KACEY “WST” TUBES 1) Taking a Kacey Sterile Swab or Loop carefully dab into the three (3) different places containing the bacteria on the MultiChrome Bi-plate.

2) Immediately place the sterile Kacey Swab or Loop containing the bacteria into the Kacey Working Solution tube (WST which contains 1.0 ml of sterile 0.085%solution). Mix the Kacey Swab or Loop with a gentle twirling motion while in the WST tube for approximately 3-5 seconds.

3) Compare sample to the Kacey Turbidity Standard (white cap) KTS. Sample should match in turbidity, if not add more WST sol (green top) or more sample to match KTS tube. (see enclosed Turbidity Card).

Quick reference only. Refer to detailed instruction manual for additional information.

GN

GP

24 HrsWSTDilution

Rotate Swab 3-5 sec

24 Hrs

GN

GP

12

3

New Kacey Sterile Swab Compare to KTS tube(white top) & match turbidity by adding more WST(grn top) solution or more sample

KTS White Tube

Sample

Page 17: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Step 1: Obtaining live cultured bacteria from a Kacey MultiChrome™ bi-plate.

• Using the yellow loop, take 3 or 4 passes through the bacterial growth on the MultiChrome™.

For bacterial colonies in both chambers see next slide.

Page 18: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Sensi-Ring™ Supplies For Each Test

For added convenience we also offer a Culture & Sensitivity Starter Kitenough for four complete tests with all the supplies you need. Product #20241

• Kacey Mueller Hinton Plate• Loop• Rayon Swab• Red Top Turbidity Tube• Appropriate Sensi-Ring™• Kacey Micro Incubator

Page 19: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Procedure For MultiChrome bi-plates with bacteria on both the Gram Positive and

Negative side.• In this case, you will prepare two Kacey Maxi Mueller Hinton plates as indicated. One for the (+) and one for the (-).

• To each MH plate you will add the appropriate Sensi-Ring disk Example: place a Gram (+) in the MH plate with Gram (+) and

Gram (-) in the MH plate with Gram (-). Then incubate each.

Page 20: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Mixing with Saline (WST) to dilute

• Insert the yellow loop into the saline and twirl to make a cloudy solution. This is an important step to avoid overgrowth of a bacterial colony.

Page 21: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Comparing Sample to Standard

• Compare your red top tube against the Standard (white top tube) which comes which every kit. They should match closely in turbidity. You can place the barcode card behind them to compare. If sample is too opaque, add more WST solution from dropper enclosed.

SampleStandard

White Tube

Kacey C&S Turbidity Card

Directions On Back

Place Behind Tubes

Page 22: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Sensi-Rings™ Quick Reference Card

Kacey Diagnostics Quick Reference For Culture & Sensitivity StudyINNOCULATION OF CULTURE BI-PLATE

1) Remove the plate from refrigerator & pre-heat in the incubator @37 degrees for 15-20 minutes prior to inoculating the Kacey MultiChrome bi-plate.

2) Using a sterile inoculating loop ( 20uL) for liquids and a Kacey Sterile Swab for solids ,inoculate the sample onto both sides of the Kacey Multichrome Bi-plate, by utilizing a zigzag streaking motion.

3) Replace clear lid and place Kacey MultiChrome Bi-plate in the incubator upside down (inverted position) and incubate at 37°C +/- 2 degree C for no less then 24 hours . The plate should be examined after 24 hours, but no later than 48 hours after incubation.

INOCULATION OF MULLER HINTON (MH) PLATE

1) Using the Kacey Swab or loop containing the now diluted WST & Turbidity adjusted dilution streak the 1st time the entire periphery of the Mueller Hinton plate making a 360° circle.

2) Streak a 2nd time again the Muller Hinton Plate with a fresh sample of the WST dilution usingbroad strokes starting at theto 3 o’clockposition.

3) Streak a 3rd time again the Muller Hinton plate with a fresh sample of the WST dilution using wide broad strokes starting at the 11 to 5 o’clock position 4) Remove “Sensi-Ring” from the foil pouch with tweezers at the inner tab & place the “Sensi-Ring” facing down onto the MH plate tapping down in non-disk areas, label the specimen to be incubated.5) Place the MH Inoculated plate into an incubator upside down, set timer & incubate for 24 hours. Remove & read inhibition zones with Kacey Clear Acetate Reader.

1 2 3TRANSFER TO MULLER HINTON PLATE USING KACEY “WST” TUBES 1) Taking a Kacey Sterile Swab or Loop carefully dab into the three (3) different places containing the bacteria on the MultiChrome Bi-plate.

2) Immediately place the sterile Kacey Swab or Loop containing the bacteria into the Kacey Working Solution tube (WST which contains 1.0 ml of sterile 0.085%solution). Mix the Kacey Swab or Loop with a gentle twirling motion while in the WST tube for approximately 3-5 seconds.

3) Compare sample to the Kacey Turbidity Standard (white cap) KTS. Sample should match in turbidity, if not add more WST sol (green top) or more sample to match KTS tube. (see enclosed Turbidity Card).

Quick reference only. Refer to detailed instruction manual for additional information.

GN

GP

24 HrsWSTDilution

Rotate Swab 3-5 sec

24 Hrs

GN

GP

12

3

New Kacey Sterile Swab Compare to KTS tube(white top) & match turbidity by adding more WST(grn top) solution or more sample

KTS White Tube

Sample

Page 23: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Why use Kacey Sensi-Ring™?

In house rapid identification (24 hours) of bacterial antibiotic sensitivity using 8 of the most common veterinary antibiotic choices per ring.

Cost Effective: Less than 1/3 the cost of a commercial laboratory like Antech and Idexx.

Specific Sensi-Ring for both Gram Positive and Gram Negative

System specific Sensi-Ring:- Urinary Tract Infection

- Ear Infection- Skin and Wound Infection

Page 24: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Removing the diluted sample with enclosed Rayon* Swab

• Take a sample using the applicator tip of the swab.

* Do not use cotton swabs even if sterile. Cotton will release a chemical that will alter the results.

Page 25: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Inoculate diluted bacteria onto Kacey Maxi* Mueller Hinton plate

• Using the diluted bacteria solution on the soaked swab, evenly distribute the sample onto a warmed Kacey Maxi Muller Hinton plate (37 degrees 15-20 min).

• Streak the plate as shown below. 11-5, 1-7, 9-3 o’clock

*Kacey Maxi Mueller Hinton plates are “true” 100mm plates. Most commercially sold Muller Hinton plates are 88mm and will not work with this system.

Page 26: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Apply the Sensi-Ring™

• Pick the appropriate Sensi-Ring™ ie. Gram Positive, Gram Negative, UTI or Skin/wound depending on samples origin.

• Grasp the tab on the inside of the ring and lower onto the agar upside down with lettering facing agar, centering the ring with tweezers.

Page 27: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Tamp down Sensi-Ring™

• Make sure that all of the disks touch the agar plate to allow antibiotic diffusion.

Page 28: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Incubate Upside Down

• Place Kacey Maxi Mueller Hinton plate now inoculated upside down to prevent any contamination. • Place into a preheated Kacey incubator at 37 degrees for 24 hours.

24 hours

Page 29: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Remove and read after 24 hours

• Carefully remove plate from incubator keeping it upside down so that Sensi-Ring letters can be seen.

Page 30: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Use the Kacey Zone Reader Card

• Place Kacey Maxi Mueller Hinton Plate upside down with antibiotic letters facing up.• Place Zone Reader over the plate and align the notch of the Reader to the notch of the Sensi-Ring.• Concentric circles should now encircle all of the disks.• Read the Inhibition Zone in mm for each disk.

Notch

Page 31: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Log Test Results

• Using the Patient Lab Report form supplied log inhibition zones for each antibiotic disk.

Page 32: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Treat with appropriate antibiotic

• Based on results, a course of action can now be taken with the most efficacious antibiotic(s).

• The following is a list of commonly found Aerobic Bacteria in small animal practice:

Gram Positive: Staphylococci, Streptococci, Enterococci

Gram Negative: E coli, Proteus, Klebsiella, Pseudomonas

Ear: Staphylococci, Pseudomonas, Proteus, E. coli, Enterococci, Streptococci

UTI: Staphylococci, Proteus, E. coli, Klebsiella, Enterococci, occasionally Pseudomonas

Skin & Wound: Staphylococci, Streptococci, Pseudomonas, Enterococci, Proteus

Page 33: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

MRSA & MRSP

Can be detected with Sensi-Ring™ Skin and Wound

Page 34: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Sensi-Rings™ case samples

Case study: 2 year old canine which cultured on the MultiChrome™ both a large colony of Gram Positive Staph in pink and a smaller Strep colony in blue. The colonies when tested for sensitivity using the Sensi-Ring™ indicated sensitivity to a variety of antibiotics not previously used.

Staph

Strep

Page 35: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

UTI and Ear samples

Page 36: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Sensi-Rings™ Ability to identify different strains of bacteria.

• Sensi-Rings™ used to identify antibiotic sensitivity on different strains of cultured Staphylococci.

Page 37: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

Disposal of plate & clean up

• Once read, plates should be sprayed with a bactericidal agent, covered with its lid taped shut, placed in a plastic bag and disposed of in your bio-hazard bin.

• If you have a Kacey Sanitizer unit (coming soon) follow its instructions. Place lid back on the plate, tape it shut, bag it and dispose of it in your bio-hazard bin.

• Dispose of all used supplies in your bio-hazard bin.

• Spray your counters down and wash your hands in an aseptic manor. Remember, these are live cultures.

Page 38: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

• Identify your top performing clinic/hospital for use as reference

• Purchase of one of the following components per month

• Sign official agreement

• Agreement can be cancelled by either party with a 30 day notice in writing of the cancellation

Incubator Promotion

Page 39: Presents Overview Part 1 MultiChrome. MultiChrome TM Veterinary Microbiology Culture System MultiChrome GP(+) Exp 3/10 Lot #123 MultiChrome GP(-) Procedures

1854 A Hendersonville RdAsheville, NC 28803Ph: 1(828)685-3569Fax: 1(828)685-3571www.kaceyinc.org

“Kacey Products Providing Better Animal Care”

Kacey Diagnostics © 2014 All Rights ReservedRev 10.20.14

“MultiChrome”, “Sensi-Rings” are trademarks of Kacey® Inc.