pathology এর চিত্র ফলাফলCollection of stool
1.      Stools samples should be collected in clean leak-proof containers without disinfectant or detergent residue and with tight-fitting, leak-proof lids.
2.      Unpreserved stool should be refrigerated, if possible, and processed within a maximum of 2 hours after collection.
3.      Specimens that cannot be cultured within 2 hours of collection should be placed in transport medium and refrigerated immediately.
Caution: Specimens should not be collected from bedpans, because the bed pans may contain residual disinfectant or other contaminants.
Transport media for fecal specimens
Media appropriate for the transport of fecal specimens that are suspected to contain Shigella, Vibrio cholerae, or Salmonella (including serotype Typhi) specimens are:
1.      Cary-Blair transport medium
High pH (8.4)
Medium of choice for transport and preservation of V. cholera
Cary-Blair transport medium can be used to transport many bacterial enteric pathogens, including Shigella, Salmonella, and Vibrio cholerae
2.      Amies’and Staurt’s transport media
Acceptable for Shigella and Salmonella (including ser. Typhi), but they are inferior to Cary-Blair for transport of V. cholerae.
3.      Alkaline peptone water
This medium may be used to transport V. cholerae, but this medium is inferior to Cary-Blair and should be used only when Cary-Blair medium is not available. Alkaline peptone water should not be used if subculture will be delayed more than 6 hours from the time of collection, because other organisms will overgrow vibrios after 6 hours.
4.      Buffered glycerol saline (BGS)
It’s a liquid medium which can be used for Shigella but this transport medium is unsuitable for transport of V. cholerae.
Rejection of fecal Specimens
Stool specimens are unacceptable if any of the following conditions apply;
1.      The information in the label does not match the information in the requisition
2.      The specimen has not been transported in the proper medium (information about media already provided in the blog post above)
3.      The quantity of specimen is insufficient for testing

Related Posts:

  • Cultivation of Anaerobic Bacteria Cultivation of Anaerobic Bacteria Main Principle: reduce the O2 content of culture medium and remove any oxygen already present inside the system or in the medium . Oxygen is ubiquitous in the air so special methods are n… Read More
  • Preservation of Pure Cultures of Bacteria Refrigeration Pure cultures can be successfully stored at 0-4°C either in refrigerators or in cold-rooms. This method is applied for short duration (2-3 weeks for bacteria and 3-4 months for fungi) because the metabolic … Read More
  • Indole Test Indole test is used to determine the ability of an organism to split amino acid tryptophan to form the compound indole. Tryptophan is hydrolysed by tryptophanase to produce three possible end products – one of which is in… Read More
  • Streak Plate Technique For organisms that grow well on agar plate, streak plate is the method of choice for obtaining pure culture. The key principles of this method is that, by streaking, a dilution gradient (number of cells decrease as they… Read More
  • Direct ELISA Procedure and Mechanism Enzyme-linked immunosorbent assay (ELISA) is extremely sensitive test that is used to detect specific antibodies or antigens. The direct ELISA is a test for the detection of antigen. In this procedure, a known antibody… Read More

0 Comments:

Powered by Blogger.

Visitors

213148
Print Friendly Version of this pagePrint Get a PDF version of this webpagePDF


 download University Notes apps for android

Popular Posts

Flag Counter