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BACTEC™ PEDS PLUS™/F Medium



Cat. # Description Qty. Unit
442194 BACTEC™ PEDS PLUS™/F Medium
50 SP
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Intended Use:

BACTEC Peds Plus™/F culture vials (enriched Soybean-Casein Digest broth with CO2) are for aerobic blood cultures. Principal use is with the BACTEC fluorescent series instruments for the qualitative culture and recovery of aerobic microorganisms (mainly bacteria and yeast) from pediatric and other blood specimens which are generally less than 3 mL in volume.


Catalog # Description Quantity Unit
442194 BACTEC™ PEDS PLUS™/F Medium
50 SP

BACTEC™ Peds Plus™/F Culture Vials
Soybean-Casein Digest Broth with Resins

Revision: 01     Revision Date: 06/01/2012    

Intended Use:

BACTEC Peds Plus™/F culture vials (enriched Soybean-Casein Digest broth with CO2) are for aerobic blood cultures. Principal use is with the BACTEC fluorescent series instruments for the qualitative culture and recovery of aerobic microorganisms (mainly bacteria and yeast) from pediatric and other blood specimens which are generally less than 3 mL in volume.



Product Summary:

The sample to be tested is inoculated into the vial which is then inserted into the BACTEC fluorescent series instrument for incubation and periodic reading. Each vial contains a sensor which can detect increases in CO2 produced by the growth of microorganisms. The sensor is monitored by the instrument every ten minutes for an increase in its fluorescence, which is proportional to the amount of CO2 present. A positive reading indicates the presumptive presence of viable microorganisms in the vial. Detection is limited to microorganisms that will grow in a particular type of medium.

Resins have been described for the treatment of blood specimens both prior to and after their inoculation into culture media. Resins have been incorporated into BACTEC culture media to enhance recovery of organisms without a need for special processing.1-3



User Quality Control:

Quality control requirements must be performed in accordance with applicable local, state and/or federal regulations or accreditation requirements and your laboratory's standard Quality Control procedures. It is recommended that the user refer to pertinent CLSI guidance and CLIA regulations for appropriate Quality Control practices.

Do not use culture vials past their expiration date.

Do not use culture vials that exhibit any cracks or defects; discard the vial in the appropriate manner.

Quality Control Certificates are provided with each carton of media. Quality Control Certificates list test organisms, including ATCC™ cultures specified in the CLSI Standard, Quality Control for Commercially Prepared Microbiological Culture Media.8 The range of time-to-detection in hours was ≤ 72 hours for each of the organisms listed on the Quality Control Certificate for this medium:

Organism

Streptococcus pyogenes ATCC 19615
Escherichia coli ATCC 25922
Streptococcus pneumoniae* ATCC 6305
Pseudomonas aeruginosa ATCC 27853
Candida albicans ATCC 18804
Neisseria meningitidis ATCC 13090
Alcaligenes faecalis ATCC 8750
Haemophilus influenzae ATCC 19418
Staphylococcus aureus ATCC 25923

*CLSI Strain

For information on Quality Control for the BACTEC fluorescent series instrument, refer to the appropriate BACTEC fluorescent series instrument User's Manual.



Reagents:

The BACTEC Peds Plus/F culture vials contain the following active ingredients prior to processing:

List of Ingredients
 
  Processed Water  40   mL
  Soybean-Casein Digest Broth  2.75%   w/v
  Yeast Extract  0.25%   w/v
  Animal Tissue Digest   0.10%   w/v
  Sodium Pyruvate  0.10%   w/v
  Dextrose  0.06%   w/v
  Sucrose  0.08%   w/v
  Hemin  0.0005%   w/v
  Menadione  0.00005%   w/v
  Sodium Polyanetholsulfonate (SPS)  0.020%   w/v
  Pyridoxal HCl (Vitamin B6)  0.001%   w/v
  Nonionic Adsorbing Resin  10.0%   w/v
  Cationic Exchange Resin  0.6%   w/v
 
All BACTEC media are dispensed with added CO2.


Warnings and Precautions:

For in vitro Diagnostic Use.

This Product Contains Dry Natural Rubber.

Pathogenic microorganisms, including hepatitis viruses and Human Immunodeficiency Virus, may be present in clinical specimens. "Standard Precautions"4-7 and institutional guidelines should be followed in handling all items contaminated with blood and other body fluids.

Prior to use, each vial should be examined for evidence of damage, contamination or deterioration. Vials displaying evidence of damage or contamination such as leakage, cloudiness, discoloration (darkening), bulging or depressed septum should not be used.

A contaminated vial could contain positive pressure. If a contaminated vial is used for direct draw, contaminated culture media could be refluxed into the patient's vein. Vial contamination may not be readily apparent. When using direct draw procedures, monitor the process closely to avoid refluxing materials into patient.

On rare occasions, the glass bottle neck may be cracked and the neck may break during removal of the flip-off cap or in handling. Also, on rare occasions, a vial may not be sealed sufficiently. In both cases the contents of the vial may leak or spill. If the vial has been inoculated, treat the leak or spill with caution, as pathogenic organisms/agents may be present. Before discarding, sterilize all inoculated vials by autoclaving.

Positive culture vials for subculturing or staining, etc.: Before sampling it is necessary to release gas which often builds up due to microbial metabolism. Sampling should be performed in a biological safety cabinet if possible, and appropriate protective clothing, including gloves and masks, should be worn. See Procedure section for more information on subculturing.

To minimize the potential of leakage during inoculation of specimen into culture vials, use syringes with permanently attached needles or Luer-Lok™ brand tips.



Information shown on this page is a short summary extracted from the Package Insert, available as a PDF under the Related Documents section of this page.