2.2 The importance of proper labelling and form completion
The importance of proper specimen labelling and completion of the submission form cannot be overemphasised.
In a diagnostic investigation, all the specimens submitted on the same day from a single or multiple animals from the same farm that appear to have a clinically related condition, are of a similar age or belong to the same group, should be submitted using a single form, and the laboratory should consider them as a single case number. This will enable a holistic interpretation of the results.
Poorly completed submission forms, in particular when accompanying multiple specimens, may lead to misunderstandings with undesired consequences for correctly interpreting diagnostic results. In addition:
- Regulatory testing or testing for notifiable bacteria may require the use of official forms. Failure to submit them may elicit government sanctions.
- Incomplete submission forms may exclude the submissions from any applicable public subsidy.
- Most laboratories offer pre-defined testing panels for different syndromes. The lack of details such as animal’s age or clinical findings may result in unnecessary testing. For example, testing for entero-toxigenic Escherichia coli in calves older than 10 days of age is unnecessary as only younger calves are affected.
- Poorly completed submission forms often prevents the recovery of the information from the laboratory database for passive surveillance purposes.
Activity 4: Receiving and processing specimens in your workplace
Use the question prompts below to think about the clinical specimens arriving in your laboratory and how they are processed.
- Are multiple, related specimens taken on the same day from animals considered as a single case?
- How frequently are inadequate forms submitted, and what is the procedure if this happens?
- Is there anything that can be improved in your system?
Discussion
Guidance on the correct procedures to follow should be given in the appropriate
You may want to have a discussion with your laboratory manager if you notice omissions or errors in the SOP or have improvements to suggest.
2.1.2 Solid specimens
