Lymph Node Fine Needle Aspirate
Test Name | Lymph Node Fine Needle Aspirate |
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Alternate Name(s) | (Information Unavailable) |
Laboratory Module | Cytology |
Ordering Mnemonic | All specimens must be accompanied by a completed manual or Meditech generated cyto-pathology non-gynecological requisition. All mandatory fields must be satisfied in order to complete the request. In the case of computer downtime use the standard cytopathology non-gynecological requisition. |
Specimen Type | An excised FNA of the lymph node |
Collection Container | Collect in cytology fixative |
Container Information | |
Collection Information |
I.1.All specimens must be accompanied by a completed manual or Meditech generated cyto-pathology non-gynecological requisition. All mandatory fields must be satisfied in order to complete the request. In the case of computer downtime use the standard cytopathology non-gynecological requisition. (ii) hospital unique number (iii) date of birth (iv) Ontario Health Insurance Number with version code. (b) Submitting area identifiers: Hospital site (BGH or The Willett) and the submitting department (Emergency, Ambulatory Care etc.). (c) Submitting physician's name. (d) Date of specimen collection (e) Pre- and post-operative presumptive diagnosis. (f) A brief clinical history, relevant pathological and radiological findings. (g) Specimen information (i) specimen type/source (ii) specimen site I.2. If received, the specimen container must be labeled. Addressograph labels are preferred, otherwise the following information must be provided, clearly written in ink: (a) Patient identifiers - (i) patient's full name (ii) hospital unique number (iii) and at least one other unique additional identifier (ie. date of birth, OHIN). (b) Date of specimen collection. (c) Specimen type and site, as it is written on the Cytology Requisition form. This information must be recorded on the side of the specimen container and not the lid. If a specimen is known or suspected to contain unique or extreme biohazard (e.g. CJD) the container shall be so marked. I.3.Place labeled slides with the patients name and specimen type, in a cardboard slide holder and drying and attach an addressograph label on the outside of the holder. I.4. Place specimen containers in a biohazard bag (if applicable). The requisition should be placed in the outer pouch of the biohazard bag. Taking the FNA and preparing smears 1. Fine needle aspirate is taken from the patient and physician expels part of the needle contents onto the labeled slide (with pencil, NO pen).
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Test Schedule | Monday to Friday prior to 1:00pm |
Routine Turnaround Time | 1 week |
Stat Turnaround Time | 2 days |
Reference Interval | (Information Unavailable) |
Critical Values | (Information Unavailable) |
Lab Process Notes | (Information Unavailable) |
Storage and Transport | Specimens should be stored at room temperature in the cytology box |
Test Referred To | BGH, On site |