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22220 Aluminum, Serum (AL)

Aluminum, Serum (AL)
Test Code: ALUM
Synonyms/Keywords
​Ref Lab Code: 8372, Al (Aluminum), Serum
Useful For
​Preferred monitoring for aluminum toxicity in patients undergoing dialysis
 
Preferred test for routine aluminum screening 
 
Monitoring metallic prosthetic implant wear
Specimen Requirements
Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​Serum Royal Blue Top tube (RBTT)​ 1.2 mL​ 0.3 mL​
Collection Processing Instructions

​See Metals Analysis-Collection and Transport in Special Instructions for complete instructions.
Trace Metals Analysis - Specimen Collection and Transport

Additional Information: High concentrations of gadolinium and iodine are known to interfere with most metals tests. If either gadolinium- or iodine-containing contrast media has been administered, a specimen should not be collected for 96 hours.
Specimen Stability Information
Specimen Type Temperature Time
Serum​ Refrigerated (preferred)​ 7 days​
Ambient ​ 7 days​
Frozen ​ 7 days​
Rejection Criteria
Gross icterus
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
Mayo Medical Laboratories
Wednesday, Friday​
1 day​
Dynamic Reaction Cell-Inductively Coupled Plasma-Mass Spectrometry (DRC-ICP-MS) ​
Reference Lab
Reference Range Information
0-6 ng/mL (all ages)
<60 ng/mL (dialysis patients-all ages)
Interpretation
​Patients in renal failure not receiving dialysis therapy invariably have serum aluminum levels above the 60 ng/mL range.
 
McCarthy(1) and Hernandez(2) describe a biochemical profile that is characteristic of aluminum overload disease in dialysis patients:
-Patients in renal failure with no signs or symptoms of osteomalacia or encephalopathy usually had serum aluminum <20 ng/mL and parathyroid hormone (PTH) concentrations >150 pg/mL, which is typical of secondary hyperparathyroidism.
-Patients with signs and symptoms of osteomalacia or encephalopathy had serum aluminum >60 ng/mL and PTH concentrations <50 pg/mL (PTH above the reference range, but low for secondary hyperparathyroidism).
-Patients who had serum aluminum >60 ng/mL and <100 ng/mL were identified as candidates for later onset of aluminum overload disease that required aggressive efforts to reduce their daily aluminum exposure. This was done by switching them from aluminum-containing phosphate binders to calcium-containing phosphate binders, by ensuring that their dialysis water had <10 ng/mL of aluminum and ensuring the albumin used during postdialysis therapy was aluminum-free.
 
Prosthesis wear is known to result in increased circulating concentration of metal ions.(3) Modest increase (6-10 ng/mL) in serum aluminum concentration is likely to be associated with a prosthetic device in good condition. Serum concentrations >10 ng/mL in a patient with an aluminum-based implant not undergoing dialysis suggest significant prosthesis wear. Increased serum trace element concentrations in the absence of corroborating clinical information do not independently predict prosthesis wear or failure.
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
​82108
Synonyms/Keywords
​Ref Lab Code: 8372, Al (Aluminum), Serum
Ordering Applications
Ordering Application Description
​Centricity ​Aluminum, Serum (AL)
​Cerner ​Aluminum Level (8373)
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​Serum Royal Blue Top tube (RBTT)​ 1.2 mL​ 0.3 mL​
Collection Processing

​See Metals Analysis-Collection and Transport in Special Instructions for complete instructions.
Trace Metals Analysis - Specimen Collection and Transport

Additional Information: High concentrations of gadolinium and iodine are known to interfere with most metals tests. If either gadolinium- or iodine-containing contrast media has been administered, a specimen should not be collected for 96 hours.
Specimen Stability Information
Specimen Type Temperature Time
Serum​ Refrigerated (preferred)​ 7 days​
Ambient ​ 7 days​
Frozen ​ 7 days​
Rejection Criteria
Gross icterus
Useful For
​Preferred monitoring for aluminum toxicity in patients undergoing dialysis
 
Preferred test for routine aluminum screening 
 
Monitoring metallic prosthetic implant wear
Reference Range Information
0-6 ng/mL (all ages)
<60 ng/mL (dialysis patients-all ages)
Interpretation
​Patients in renal failure not receiving dialysis therapy invariably have serum aluminum levels above the 60 ng/mL range.
 
McCarthy(1) and Hernandez(2) describe a biochemical profile that is characteristic of aluminum overload disease in dialysis patients:
-Patients in renal failure with no signs or symptoms of osteomalacia or encephalopathy usually had serum aluminum <20 ng/mL and parathyroid hormone (PTH) concentrations >150 pg/mL, which is typical of secondary hyperparathyroidism.
-Patients with signs and symptoms of osteomalacia or encephalopathy had serum aluminum >60 ng/mL and PTH concentrations <50 pg/mL (PTH above the reference range, but low for secondary hyperparathyroidism).
-Patients who had serum aluminum >60 ng/mL and <100 ng/mL were identified as candidates for later onset of aluminum overload disease that required aggressive efforts to reduce their daily aluminum exposure. This was done by switching them from aluminum-containing phosphate binders to calcium-containing phosphate binders, by ensuring that their dialysis water had <10 ng/mL of aluminum and ensuring the albumin used during postdialysis therapy was aluminum-free.
 
Prosthesis wear is known to result in increased circulating concentration of metal ions.(3) Modest increase (6-10 ng/mL) in serum aluminum concentration is likely to be associated with a prosthetic device in good condition. Serum concentrations >10 ng/mL in a patient with an aluminum-based implant not undergoing dialysis suggest significant prosthesis wear. Increased serum trace element concentrations in the absence of corroborating clinical information do not independently predict prosthesis wear or failure.
For more information visit:
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
Mayo Medical Laboratories
Wednesday, Friday​
1 day​
Dynamic Reaction Cell-Inductively Coupled Plasma-Mass Spectrometry (DRC-ICP-MS) ​
Reference Lab
For billing questions, see Contacts
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
​82108
For most current information refer to the Marshfield Laboratory online reference manual.