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Test ID: MMLNS
Antimicrobial Susceptibility, Nocardia species

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Useful For Suggests clinical disorders or settings where the test may be helpful

Determining the resistance of species of Nocardia and other aerobic actinomycetes to antimicrobial agents

Additional Tests Lists test(s) that are always performed, at an additional charge, with the initial test(s)

Test IDReporting NameAvailable SeparatelyAlways Performed
SSNSSusceptibility Nocardia speciesNo, (Bill Only)Yes

Testing Algorithm Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.

When this test is ordered, Susceptibility Nocardia species will be performed and charged.

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

Method Name A short description of the method used to perform the test

Minimum Inhibitory Concentration (MIC)
Antimicrobials for Nocardia species are: ceftriaxone, tobramycin, ciproflazacin, minocycline, imipenem, amikacin, clarithromycin, trimethoprim/sulfamethoxazole, linezolid, augmentin, and moxifloxacin.

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Susceptibility, Nocardia species

Aliases Lists additional common names for a test, as an aid in searching

Amikacin
Amikacin Sulfate (Amikin)
Amikin (Amikacin Sulfate)
Amoxicillin and Clavulanate Potassium (Augmentin)
Augmentin (Amoxicillin and Clavulanate Potassium)
Ciprofloxacin
Clarithromycin
Imipenim
Linezolid (Zyvox)
MIC (Minimum Inhibitory Concentration)
Minimum Inhibitory Concentration (MIC)
Minocycline
Moxifloxacin
Nocardia Susceptibilities
Sulfamethoxazole
Susceptibility Testing
Tobramycin
Zyvox (Linezolid)
Cefepime
Ceftriaxone
Trimethoprim/sulfamethoxazole

Specimen Type Describes the specimen type needed for testing

Varies

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

Specimen Type: Organism

Container/Tube:

Preferred: Middlebrook 7H10 agar slant without antimicrobials

Acceptable: Sabouraud's dextrose agar slant or similar media without antimicrobials (eg, 7H11 agar slant, LJ, MGIT [7H9] broth media)

Specimen Volume: Isolate

Collection Instructions:

1. Organism must be in pure culture, actively growing.

2. Place specimen in a large infectious container (Supply T146) and label as an etiologic agent.

Additional Information:

1. Specimen source is required.

2. See Antimicrobial Susceptibility Tests and Infectious Specimen Shipping Guidelines in Special Instructions.

Forms: If not ordering electronically, submit a Microbiology Request Form (Supply T244) with the specimen.

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis

NA

Lipemia

NA

Icterus

NA

Other

Agar plate

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
VariesAmbient (preferred)
 Refrigerated 

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Nocardia asteroides, the most commonly recognized aerobic actinomycete, causes significant disease in immunocompromised patients. Clinical presentations can include pneumonia, skin abscess, bacteremia, brain abscess, eye infection, and joint infection. Other species associated with human disease include Nocardia brasiliensis, Nocardia otitidiscaviarum, Nocardia farcinica, Nocardia nova, and Nocardia transvalensis.

 

Treatment usually consists of trimethoprim-sulfamethoxazole, sometimes in combination with other antimicrobials, such as amikacin. However, some patients develop drug allergy, others develop resistant isolates due to noncompliance, and some antimicrobials penetrate the central nervous system better than others. Therefore, the selection of appropriate agents becomes extremely important to patient outcome.

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

The following are interpretive values for susceptibility testing of Nocardia species using a broth microdilution method. 

           

Antimicrobial Agent

Concentration Range mcg/mL

Interpretations

S

I

R

Trimethoprim/ Sulfamethoxazole(3)

0.25/4.75-8/152

< or =2/38

-

> or =4/76

Linezolid(2)

1-32

< or =8

-

-

Ciprofloxacin

0.12-4

< or =1

2

> or =4

Imipenem

2-64

< or =4

8

> or =16

Moxifloxacin(1,3)

0.25-8

-

-

-

Cefepime(3)

1-32

< or =8

16

> or =32

Augmentin(3)

2/1-64/32

< or =8/4

16/8

  > or =32/16

Amikacin

1-64

< or =8

-

 > or =16

Ceftriaxone(3)

4-64

< or =8

16-32

> or =64

Doxycycline

0.12-16

< or =1

2-4

  > or =8

Minocycline(3)

1-8

< or =1

2-4

  > or =8

Tobramycin

1-16

< or =4

8

  > or =16

Clarithromycin

0.06-16

< or =2

4

  > or =8

Interpretation Provides information to assist in interpretation of the test results

Interpretive values for susceptibility testing of Nocardia species using a broth microdilution method. (Values expressed in mcg/mL):

 

Antimicrobial Agent

Interpretations

S

I

R

Trimethoprim/ Sulfamethoxazole(3)

< or = 2/38

-

> or =4/76

Linezolid(2)

< or =8

-

-

Ciprofloxacin

< or =1

2

> or =4

Imipenem

< or =4

8

> or =16

Moxifloxacin(1,3)

-

-

-

Cefepime(3)

< or =8

16

> or =32

Augmentin(3)

< or =8/4

16/8

> or =32/16

Amikacin

< or =8

-

> or =16

Ceftriaxone(3)

< or =8

16-32

> or =64

Doxycycline

< or =1

2-4

> or =8

Minocycline(3)

< or =1

2-4

> or =8

Tobramycin

< or =4

8

> or =16

Clarithromycin

< or =2

4

> or =8

 

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

No significant cautionary statements

Clinical Reference Provides recommendations for further in-depth reading of a clinical nature

1. Corti ME, Villafane-Fioti MF: Nocardiosis: a review. Int J Infect Dis 2003;7:243-250

2. Saubolle MA, Sussland D: Nocardiosis: review of clinical and laboratory experience. J Clin Microbiol 2003;41:4497-4501

3. Brown-Elliott BA, Brown JM, Conville PS, Wallace RJ Jr: Clinical and laboratory features of the Nocardia species based on current molecular taxonomy. Clin Microbiol Rev 2006;19:259-282

Method Description Describes how the test is performed and provides a method-specific reference

A standardized inoculum made from a pure culture of aerobic actinomycete is prepared and inoculated into wells of a microtiter plate containing different concentrations of 13 antimicrobial agents. These include trimethoprim/ sulfamethoxazole, linezolid, ciprofloxacin, imipenem, moxifloxacin, cefepime, augmentin, amikacin, ceftriaxone, doxycycline, minocycline, tobramycin, and clarithromycin.

 

Growth at specified breakpoints is indicative of resistance.(Wallace RJ Jr, Steele LC: Susceptibility testing of Nocardia species for the clinical laboratory. Diagn Microbiol Infect Dis 1988;9:155-66; Clinical Laboratory Standards Institute: Susceptibility Testing of Mycobacteria, Nocardiae, and Other Aerobic Actinomycetes. CLSI document M24-A, CLSI, Wayne, PA, 2003)

Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

One or two times per week; NA

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

12 days

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

28 days

Performing Laboratory Location The location of the laboratory that performs the test

Rochester

Test Classification Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

87186

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
MMLNSSusceptibility, Nocardia speciesIn Process