Test ID RPDE Rapidly Progressive Dementia Evaluation, Spinal Fluid
Ordering Guidance
In individuals with a high clinical suspicion of Alzheimer disease, order ADEVL / Alzheimer Disease Evaluation, Spinal Fluid.
This test can only be performed on specimens collected and transported in polypropylene tubes. If this test is ordered and a polystyrene tube is received, it will be canceled and automatically reordered by the laboratory as CJDE / Creutzfeldt-Jakob Disease Evaluation, Spinal Fluid.
For cases where there is high suspicion of human prion disease supported by clinical or paraclinical magnetic resonance imaging features, order CJDE / Creutzfeldt-Jakob Disease Evaluation, Spinal Fluid.
Early in the disease course, or in atypical cases, the disease progression may be slower and include significant clinical overlap (dementia, rigidity, myoclonus) with other potential causes of rapidly progressive dementia, including Alzheimer disease. In the latter case, it would be more appropriate to order this test.
Specimen Required
Supplies: CJD/RPD Evaluation Kit (T966)
Container/Tube:
Preferred: 2 Sarstedt CSF False Bottom Tubes 63.614.625 (2.5 mL)
Acceptable: Sarstedt 72.703.600 (1.5 mL) or Sarstedt 72.694.600 (2 mL)
Specimen Volume: 2 tubes; each containing 1.5 to 2.5 mL
Collection Instructions:
1. Perform lumbar puncture and discard the first 1 to 2 mL of cerebrospinal fluid (CSF).
2. Collect two tubes of CSF directly into an acceptable collection tube until the tube is at least 50% full.
3. Send CSF specimen in original collection tube. Do not aliquot.
Note: Polystyrene collection tubes are not acceptable. Exposure of CSF to polystyrene tubes may result in falsely low Abeta42 concentrations.
The Alzheimer's Association consensus protocol for handling of CSF for clinical measurements of Abeta42 and tau recommends using the drip method for CSF collection and directly collecting into a low-bind polypropylene tube. Although some clinicians prefer the syringe pull method due to speed of collection, the drip method reduces the risk of Abeta42 binding to the plastic of any syringe used.
4. Collection instructions can also be found on Spinal Fluid Specimen Collection Instructions for Creutzfeldt-Jakob Disease and Rapidly Progressive Dementia Evaluations (T974).
Useful For
Evaluation of individuals presenting with rapidly progressive dementia of uncertain disease etiology and a differential diagnosis of Creutzfeldt-Jakob disease and rapidly progressive Alzheimer disease
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
RPDEI | RPD Eval Interp, CSF | No | Yes |
RTQPC | RT-QuIC Prion, CSF | No | Yes |
TTPTQ | t-Tau/p-Tau | No | Yes |
ADRTQ | Alzheimer's Disease Evaluation, CSF | No | Yes |
Special Instructions
Method Name
RPDEI: Medical Interpretation
RTQPC: Real-Time Quaking-Induced Conversion (RT-QuIC)
TTPTQ: Calculation
ADRTQ: Electrochemiluminescent Immunoassay (ECLIA)
Reporting Name
Rapid Progress Dementia Eval, CSFSpecimen Type
CSFSpecimen Minimum Volume
See Specimen Required
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
CSF | Frozen (preferred) | 28 days | BlueTop SARSTEDT |
Refrigerated | 14 days | BlueTop SARSTEDT | |
Ambient | 12 hours | BlueTop SARSTEDT |
Reference Values
RT-QuIC PRION, CSF:
Negative
t-TAU/p-TAU:
≤18
p-TAU/ABETA 42:
≤0.028
BETA-AMYLOID (1-42) (Abeta42):
>834 pg/mL
TOTAL TAU:
≤238 pg/mL (Alzheimer disease)
≤393 pg/mL (Creutzfeldt-Jakob disease)
PHOSPHORYLATED TAU 181:
≤21.6 pg/mL
Day(s) Performed
Monday through Friday, Sunday
Report Available
3 to 8 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
84999
83520 x 3
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
RPDE | Rapid Progress Dementia Eval, CSF | 104134-2 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
PTABQ | p-Tau/Abeta42 | 41027-4 |
620307 | RT-QuIC Prion, CSF | 101662-5 |
TTPTQ | t-Tau/p-Tau | 101752-4 |
620377 | RPD Eval Interp, CSF | 69048-7 |
ADINQ | AD Interpretation | 69048-7 |
AB42Q | Abeta42 | 33203-1 |
TTAUQ | Total-Tau | 30160-6 |
PTAUQ | Phospho-Tau(181P) | 72260-3 |
NY State Approved
YesForms
If not ordering electronically, complete, print, and send a Neurology Specialty Testing Client Test Request (T732) with the specimen.