|
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z # |
Alpha Defensin, Synovial Fluid, LFA
Test Code12188
CPT Codes
83518
Preferred Specimen
0.6 mL synovial fluid collected in a plain red-top tube
Patient Preparation
This test should only be used for patients with a total joint prosthesis.
Minimum Volume
0.10 mL
Instructions
Specimen source and type of joint are required. If not obtained from a prosthetic joint, testing will be canceled.
Ask-at-Order-Entry questions must be answered. "Not Given" or "NG" answers are not acceptable. Freshly collected synovial fluid only.
Note: Synovial fluid obtained after repeated aspirations within a short time period might lead to false-negative results due to the lack of buildup of alpha defensin.
The use of synovial fluid diluted with saline, blood, contrast agent, or any substances injected into the joint may lead to false-negative results.
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Room temperature: Unacceptable
Refrigerated: 7 days
Frozen: Unacceptable
Refrigerated: 7 days
Frozen: Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Gross hemolysis
Methodology
Lateral Flow Assay (LFA)
Setup Schedule
Set up: Sun-Fri; Report available: 1-2 days
Reference Range
Negative
Clinical Significance
Detection of alpha defensins 1-3, human host response proteins, in synovial fluid of adults with a total joint replacement who are being evaluated for revision surgery.
This test is not intended to be used to determine timing for reimplantation in 2-stage procedures.
This test is not intended to be used to determine timing for reimplantation in 2-stage procedures.