To minimise disruption to laboratory workflow, the Integrated Laboratory does not routinely encourage the use of add-on tests. In addition, the accuracy of some test results may be affected by specimen storage conditions and the time elapsed between sample collection and receipt of the add-on request.
Where feasible, the laboratory will accommodate add-on requests provided all of the following criteria are met.
Criteria for Acceptance
An add-on test request may be accepted only if all of the following criteria are met:
The patient is an inpatient.
Only one add-on request is permitted per specimen.
The original laboratory request has already been registered in the Laboratory Information System (LIS).
The Total Laboratory Automation (TLA) system is operating normally (i.e. not during downtime).
The add-on request is within the specified acceptance time limit (refer below).
The requested test is not included in the list of tests unsuitable for add-on requests (refer below).
The specimen remains suitable for analysis (e.g. adequate volume, not haemolysed, not otherwise compromised).
The request is not urgent. Add-on tests are processed with routine priority only. If an urgent result is required, a new specimen should be collected and submitted as an urgent request.
The requested test is not within the established Minimum Retesting Interval (MRI). If repeat testing is clinically justified, the add-on request must be discussed with the Integrated Laboratory Medical Officer/Chemical Pathologist (office hours) or the On-Call Pathologist (after hours).
A valid add-on request form is received.
Time Limit for Add-on Requests
All requests for additional testing shall be submitted as soon as possible after the original request. Taking into account specimen stability and the need to maintain efficient laboratory operations, the following time limits shall apply:
Tests Unsuitable for Add-on Requests
The following tests cannot be requested as add-on tests:
1. Labile / Unstable Analytes (rapidly change after collection)
Ammonia
Lactate
Blood Gas
2. Tests Requiring Special Handling
Therapeutic Drug Monitoring (TDM)
3. Tests Requiring Separate Specimen Tube or Specific Collection Requirements
Glucose
Procalcitonin (PCT)
Parathyroid Hormone (PTH)
HbA1c
Urine based tests
Note: This list is not exhaustive. The laboratory reserves the right to decline any add-on request where specimen suitability or analytical requirements cannot be met.
Procedure for Requesting an Add-on Test
Contact the Integrated Laboratory (Ext. 8241/8242) to request an add-on test.
For most add-on requests, the request may be made directly to the Medical Laboratory Technologist (MLT).
However, consultation with a Chemical Pathologist is required for:
Non-routine tests
Tests not included in the approved add-on test list
Critical or exceptional cases where the add-on request does not meet the established acceptance criteria
Provide the following information:
Original Request Laboratory ID
Patient identification
Test(s) requested
Laboratory personnel will perform a preliminary assessment of the request.
If the request is considered suitable, complete a new laboratory request form. The standard mandatory patient and request information must be completed. In addition, the following information specific to the add-on request must be included:
Clearly indicate "ADD-ON REQUEST" and “Original specimen Laboratory ID” on the form
Additional test(s) requested
Details of communication with laboratory staff (name of laboratory personnel, date and time).
Name, signature and official stamp of the requesting clinician.
Submit the completed request form to the laboratory immediately.
Processing of Add-on Requests
Accepted add-on requests will be processed with the same priority as routine inpatient specimens.
Submission of an add-on request does not guarantee that testing will be performed. The laboratory reserves the right to reject an add-on request if the specimen is no longer suitable for analysis, including but not limited to insufficient specimen volume, specimen deterioration, or failure to meet analytical requirements.
If the add-on request cannot be processed, a comment stating the reason will be added to the patient report.