Hint and Tips to Improve the Quality of your Cytology Submissions

Labelling and Identification of sample sites

  • if more than one site, ensure that all slides are clearly labelled to denote which site. It is often useful to use a number key and explain the key on the submission form (ie 1- chest x 2 slides, 2 – thigh x 2 slides).
  • Include the location, size, duration & patient information on the submission form.
  • Please provide a recent history pertinent to the cytology. Providing the pathologist with a concise and relevant patient history will provide you with a more accurate and diagnostically useful report.
Example of a poorly spread aspirate .

Smear Preparation

  • A push smear is the most commonly used method for fluid aspirates. The same method used when preparing a blood smear.
  • Stop smear BEFORE end of slide, otherwise important cells disappear over the edge.
  • Don’t use the droplet technique.
  • Thicker material can bespread evenly with a second overlaying slide. Gently pull the slides apart to smoothly spread the material.
  • Impression smears and swabs often only represent the surface process therefore a fine needle aspirate (FNA) is the sample if choice.
  • if you have a swab, gently ROLL material, don’t smear.
Example of spread material.

Submission of slides

  • NEVER submit only 1 slide. 2-4 slides is generally a good submission size.
  • Leave all slides unstained slide in-house to ensure that a diagnostic sample has been taken before submission to the external lab is always recommended.
  • Ensure all slides are completely dry before placing in the slide mailer and store at room temperature (Storage of slides in refrigerator causes condensation and lysis).
  • Send all slides in to the lab (including the stained slide)
  • Package the slides in a separate bag to any formalin fixed histology samples that are being submitted at the same time. (Formalin fume can cause a fixation artefact on the cytology slides making them non-diagnostic).

Fluid samples that require cytological evaluation and culture should be submitted in an EDTA tube (cytology) & a plain tube (for culture). If only a small volume of fluid is available submit just the plain tube.

Plain tubes suitable are Microcentrifuge/Eppendorf or universal tubes. Plain blood tubes are unsuitable.

Fluid Submission

Body Cavity Effusions

  • Always submit fluid with pre-prepared slides as direct smears are often not helpful.
  • Refrigerate the fluid sample if there is a delay in sending to a laboratory.
  • Please submit a succinct relevant history.

Mass Fluids/Synovial Fluids & Washes

  • Always submit fluid with pre-prepared slides & provide a succinct relevant history.

Prostatic Wash

  • Have a low diagnostic accuracy. Neoplastic cells are often not recovered in specimens obtained by prostatic massage and wash. Prostatic massage may produce septicaemia in dogs with acute bacterial prostatitis or a prostatic abscess.
  • An open direct FNA is best with a biopsy for histopathology if possible. 

CSF & Urine

  • Submit in a EDTA tube (and a plain tube if culture is also required).
  • Please submit a succinct relevant history.

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