Laboratory Procedure Manual

Analyte: Blood Urea Nitrogen (BUN)

Matrix: Serum

Method: Roche Cobas 6000 (c501 module)

Method No.:

Revised:

As performed by: University of Minnesota

Advanced Research and Diagnostic Laboratory (ARDL)
1200 Washington Ave S, Suite 175
Minneapolis, MN 55415

Contact: Anthony Killeen, MD, PhD, Laboratory Director

Jennifer Peters, MT, ASCP, Laboratory Manager

Important Information for Users

The Advanced Research and Diagnostic Laboratory (ARDL) periodically refine these
laboratory methods. It is the responsibility of the user to contact the person listed on the title
page of each write-up before using the analytical method to find out whether any changes
have been made and what revisions, if any, have been incorporated.
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Public Release Data Set Information

This document details the Lab Protocol for testing the items listed in the following table:

Data File Name Variable Name SAS Label

BIOPRO_J LBXSBU Blood Urea Nitrogen (mg/dL)

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1. SUMMARY OF TEST PRINCIPLE AND CLINICAL RELEVANCE

Urea is the final degradation product of protein and amino acid metabolism in the
human body. Proteins are broken down into amino acids, then the amino acids are
deaminated. Ammonia resulting from amino acid deamination is synthesized into urea in
the liver. This urea is then removed by the kidneys, and discharged in the urine. This is
the most important catabolic pathway for eliminating excess nitrogen in the human
body. Urea is typically measured along with creatinine for the differential diagnosis of
pre-renal hyperuremia (cardiac decompensation, water depletion, increased protein
catabolism), renal hyperuremia (glomerulonephritis, chronic nephritis, polycystic kidney,
nephrosclerosis, tubular necrosis), and post renal hyperuremia (obstructions of the
urinary tract.

This method utilizes a coupled enzyme reaction (urease, followed by glutamate

dehydrogenase), with measurement of NADH (converting to NAD+) occurring at 340
nm.

Cobas 6000 Application Code: 427

2. SAFETY PRECAUTIONS

Caution: This product is of human and animal origin. Handle as though capable of
transmitting infectious disease. Wear appropriate PPE when handling equipment,
reagents, and samples.

3. COMPUTERIZATION; DATA SYSTEM MANAGEMENT

ARDL utilizes a highly specialized Laboratory Information System (LIS) (STARLIMS,

Abbott Informatics Corporation; Hollywood, FL, 33021-6755) for all lab functions. Major
instrument platforms are interfaced directly to the LIS, allowing data to be electronically
transferred directly to the main database. The system provides an extensive quality
assurance package and data management tools. Numerous networked computer
workstations are used in the laboratory for data management and transmission, and
also include software for word and spreadsheet creation and manipulation, statistical
analysis, report presentation, and electronic communication. All workstations are user
password protected with job specific security access levels and have idle time out
functionality. All systems are redundantly backed up on a real time basis.

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4. SPECIMEN COLLECTION, STORAGE, AND HANDLING PROCEDURES; CRITERIA

FOR SPECIMEN REJECTION

a. Specimen Type and Requirements: Serum, lithium heparin plasma, K2-EDTA

plasma, and urine are acceptable specimens. Do not use ammonium heparin. The
NHANES Biochem study uses refrigerated serum. This test is analyzed from NHANES
Vial 018.

b. Specimen Volume: Optimum/Minimum volume: 100 μL in a sample cup or 2 mL

microtube (2 μL serum or plasma; 3 uL urine (for onboard 1:50 dilution) for test;
remainder for dead volume).

c. Acceptable Specimens/Unacceptable Specimens: Serum, lithium heparin plasma,

K2-EDTA plasma, and urine are acceptable specimens. Do not use ammonium heparin.
Other anticoagulants are not acceptable.

d. Specimen Stability and Storage: Separated serum or plasma should be removed

from the cells within one hour of collection. Serum or plasma is stable for seven days at
2-8 ºC, one year at -15 to -25 °C, and longer at –70ºC. Urine is stable for seven days at
2-8 °C, one month at -15 to -25 °C, and longer at -70°C. Specimens must be at room
temperature prior to assay. Mix urine specimens well and centrifuge 10 minutes at
2000xg before use.

e. Interferences or limitations: Serum/plasma Icteric index < 60: no interference.

Hemolytic index <1000: no interference. Lipemic index < 1000: no interference.

Drugs: No interference was found at therapeutic concentrations using common drug

panels.

In very rare cases, gammopathy, in particular type IgM (Waldenström's

macroglobulinemia), may cause unreliable results.

Urine: Drugs: No interference was found at therapeutic concentrations using common

drug panels.

f. Specimen Handling and Transport: Mix specimens well, allow clot to fully form (if
serum), and centrifuge 10 minutes at 2000 x g before use. Aliquot a minimum of 0.1 mL.

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Store sample in refrigerator until shipment. Ship at refrigerated temperature.

Specimens must be at room temperature prior to assay.

5. PROCEDURES FOR MICROSCOPIC EXAMINATIONS; CRITERIA FOR REJECTION

OF INADEQUATELY PREPARED SLIDES

“Not applicable for this procedure.”

6. EQUIPMENT AND INSTRUMENTATION, MATERIALS, REAGENT PREPARATION,

CALIBRATORS (STANDARDS), AND CONTROLS

a. Reagents and Supplies

• Roche Cat. No. 04460715190, UREAL reagent kit (500 tests):

b. Reagent Preparation

• R1 reagent. NaCl 9 %

• R2 reagent. TRIS buffer: 220 mmol/L, pH 8.6; 2-oxoglutarate: 73 mmol/L; NADH: 2.5
mmol/L; ADP: 6.5 mmol/L; urease (jack bean): ≥ 300 μkat/L; GLDH (bovine liver): ≥
80 μkat/L; preservative; nonreactive stabilizers

• Storage and stability. Keep reagents stored at 2-8°C until use. The reagents are
stable for 8 weeks refrigerated on the analyzer.

c. Equipment/Instrumentation-

• Roche Cobas 6000 Chemistry Analyzer (Roche Diagnostics Corporation,

Indianapolis, IN 46250)

• The Millipore Elix Gulfstream Clinical 35 System is designed to meet CLSI Clinical
Laboratory Reagent Water (CLRW) standards. Water purification is achieved by
reverse osmosis, electrodeionization, bactericidal 254 nm UV lamp and 0.22 μm
filtration.

d. Specimens are run in singleton

e. Quality Control

• Normal pooled serum control (CQ). Stable at -80°C for up to 4 years, at refrigerated
temperature for up to 1 day and at room temperature for up to 4 hours.

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• Roche Precipath U Plus Control (catalog #12149443160). Roche Diagnostics 9115

Hague Road Indianapolis, IN 46250-0457). Stable until expiration date on package
when unopened and stored at 2-8°C. To prepare, open bottle 1 and pipette in
exactly 3.0 mL of diluent (bottle 2). Dissolve by gentle swirling for 30 minutes.
Prepared control is stable for 12 hours at room temperature, 5 days at 2-8°C, and
one month at -20°C (when frozen once).

7. CALIBRATION AND CALIBRATION VERIFICATION PROCEDURES

Roche Calibrator for Automated Systems (C.F.A.S.), catalog #10759350190. The

calibrator is stable until the expiration date on the bottle when stored at 4ºC. The
lyophilized calibrator is prepared with 3.0 mL of deionized water. Pipette the water into
the bottle, and then dissolve by gentle swirling within 30 minutes. Avoid formation of
foam while mixing. The prepared calibrator is stable for eight hours at room
temperature, two days at 4ºC, and one month at –20ºC (frozen once).

Traceability: This method has been standardized against SRM 909b.

Calibration frequency: A two-point calibration (H2O + C.F.A.S.) must be performed

when there is a reagent lot number change, and after the reagent has been on the
analyzer for 4 weeks. The Cobas 6000 will not allow testing to proceed until a
successful calibration has been completed. Monitor control values to determine stability
of the current calibration.

Manual calibration should be performed if:

• A reagent lot change has not occurred in the past 6 months

• After major service or repairs

• As needed for troubleshooting

If calibration fails perform the following corrective action steps in sequence:

• Check reagent and calibrator for appropriate lot numbers, expiration dates,
preparation and storage conditions.

• Repeat calibration with new calibrator.

• Repeat calibration with new reagent and new calibrator

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• If successful calibration is not achieved, discontinue testing and notify the

supervisor.

8. OPERATING PROCEDURE INSTRUCTIONS; CALCULATIONS; INTERPRETATION

OF RESULTS

a. Instrument Operation: The Roche/Hitachi Cobas 6000 analyzer series is a fully

automated, random-access, software controlled system for immunoassay and
photometric analyses intended for qualitative and quantitative in vitro determinations
using a wide variety of tests. The Cobas 6000 analyzer series is optimized for
workloads using a combination of photometric and ion-selective electrode (ISE)
determinations (c501 module), and electrochemiluminescence (ECL) signal in the
immunoassay analysis module (e601 module). The ISE system is used in the
quantitation of sodium, potassium and chloride. The photometric system can
measure colorimetric or immunoturbidimetric reactions utilizing end point or kinetic
(rate) absorbance measurements. Test ordering end execution on the Cobas 6000
and data entry in the STARLIMS host computer system may be done manually or
these tasks may be executed via a barcode-based bi-directional interface. The
Cobas 6000 can utilize both of these two systems simultaneously.

b. Professional Judgement: Check results for error flags and take appropriate
corrective action. Investigate alert values and delta checks.

c. Result Entry

STARLIMS test code: BUN, UUN

Manual entry.

• Results are reported to the whole number, as in x mg/dL.

• Report low serum results as <2 mg/dL.

• Check results for error flags and take appropriate corrective action.

• Investigate alert values and delta checks.

9. REPORTABLE RANGE OF RESULTS

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Out of Range results: Certain tests have pre-programmed limits that trigger an
automatic re-analysis by the COBAS. These limits may be low-end values or high-end
values (but within technical range). If the duplicate value is in agreement with the initial
value, then the initial value is reported.

Results are reported to the whole number (as x) in mg/dL. Report low results as <2
mg/dL.

a. Reportable Range of Test Results: Reportable Range 2-336 mg/dL

Intra-assay %CV (10 within-day replicates at a concentration of 18.6 mg/dL) 1.3%

Intra-assay %CV (10 within-day replicates at a concentration of 57.19 mg/dL) 1.3%

Inter-assay %CV (between day replicates at a concentration of 15.3 mg/dL) 2.0%

Inter-assay %CV (between day replicates at a concentration of 54.0 mg/dL) 2.0%

Dilutions: The confirmed analytical measurement range of the assay is 2 -112 mg/dL for
serum and 13-5447 mg/dL for urine. Serum samples exceeding the high limit are
automatically diluted (1:3) by the instrument. Results from serum samples diluted using
the rerun function are automatically multiplied by 3.

Reference Range: Serum, adult (18-60 yrs.) 6-23 mg/dL

Critical Results: None

10. QUALITY CONTROL (QC) PROCEDURE

•Normal pooled serum control (CQ). Stable at -80°C for up to 4 years, at

refrigerated temperature for up to 1 day and at room temperature for up to 4
hours.

•Roche Precipath U Plus Control (catalog #12149443160). Roche Diagnostics

9115 Hague Road Indianapolis, IN 46250-0457). Stable until expiration date on
package when unopened and stored at 2-8°C. To prepare, open bottle 1 and
pipette in exactly 3.0 mL of diluent (bottle 2). Dissolve by gentle swirling for 30
minutes. Prepared control is stable for 12 hours at room temperature, 5 days at
2-8°C, and one month at -20°C (when frozen once).

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•Both levels of quality control are analyzed at the start of the day and results are
verified for acceptability prior to testing specimens. Quality control is also
analyzed at the end of the shift, with change in reagent, after major maintenance,
or as needed for troubleshooting.

•The analytical measurement range (AMR) must be validated every 6 months or

after major maintenance or service procedures. The laboratory enrolls in the
College of American Pathologist (CAP) linearity program. BUN is included in the
LN2 kit that is shipped twice per year. Follow kit instructions for preparation.
Analyze samples in duplicate. Results are due within two to four weeks of receipt
of kit. Results are submitted online to the CAP website by the lead or supervisor.
The linearity report is available online at the CAP website shortly after the due
date. Confirm reported values are within acceptability limits. Place instrument
printouts, worksheets and CAP results in the CAP three ring binder.

•New Lot Verification: Each new reagent lot must be verified for acceptability
before being placed into use. Calibration, quality control, and comparison of at
least 5 patient samples on the old and new lots must be performed and found to
be within acceptable limits before a new lot can be placed into use.

• Quarterly Technical Progress Report:

Progress reports for each quarter of the calendar year are submitted to
NHANES. The report includes 1) a summary of the status of all specimens
including date of arrival, deviations from protocol, handling, storage, and
manipulation of vials and all laboratory procedures used, 2) a description of any
major problems such as missing data, out of range values or inconsistent data
and what was done to overcome them, internal and external quality control for
runs containing NHANES specimens, instrument calibration and repairs, reagent
lots and dates of use.

11. REMEDIAL ACTION IF CALIBRATION OR QC SYSTEMS FAIL TO MEET

ACCEPTABLE CRITERIA

• If QC values are outside of specified ranges, do the following, in order, until QC

is acceptable:

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1. Repeat the analysis using fresh QC material.

2. Perform a calibration.

3. Check for system problems.

4. Contact Roche Technical Support for assistance and possible service dispatch.
Phone: 1-800-428-2336; account number: 55042919

12. LIMITATIONS OF METHOD; INTERFERING SUBSTANCES AND CONDITIONS

a. Limit of Detection (standard 1 + 3 SD): 2 mg/dL

Analytical Measurement Range: 2-112 mg/dL

b. Serum/plasma Icteric index < 60: no interference.Hemolytic index <1000: no

interference. Lipemic index < 1000: no interference. Drugs: No interference was
found at therapeutic concentrations using common drug panels. In very rare cases,
gammopathy, in particular type IgM (Waldenström's macroglobulinemia), may cause
unreliable results. Urine: Drugs: No interference was found at therapeutic
concentrations using common drug panels.

13. REFERENCE RANGES (NORMAL VALUES)

Serum, adult (18-60 yrs.) 6-23 mg/dL

14. CRITICAL CALL RESULTS ("PANIC VALUES")

Not applicable.

15. SPECIMEN STORAGE AND HANDLING DURING TESTING

Specimens are stored at refrigerated temperature between sample receipt and analysis
on the instrument. Specimens must be at room temperature prior to assay. Specimens
are returned to refrigerated or frozen temperature post analysis depending on the study
specific requirements.

16. ALTERNATE METHODS FOR PERFORMING TEST OR STORING SPECIMENS IF

TEST SYSTEM FAILS

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Should the testing system become inoperable, discontinue testing and notify the
supervisor. While instrument trouble-shooting or repair occurs; keep specimens at
refrigerated or frozen temperature depending on study specific requirements.

17. TEST RESULT REPORTING SYSTEM; PROTOCOL FOR REPORTING CRITICAL

CALLS (IF APPLICABLE)

All data is reported electronically via an eFile that is uploaded to the WESTAT secure
website within 21 days of receipt of specimens.

18. TRANSFER OR REFERRAL OF SPECIMENS; PROCEDURES FOR SPECIMEN

ACCOUNTABILITY AND TRACKING

Specimen Receipt:

Shipments for NHANES generally will arrive on Tuesdays and/or Wednesdays. These
shipments are recorded on the Log of Quality Assurance located in a binder labeled
NHANES Shipping Log in the receiving area. The specimen barcode numbers in the
boxes are checked against the manifests. The receipt date is written on top of the
boxes. The frozen samples (vial 11-Iron/UIBC & vial 13-CRP) are placed in the
designated -70°C freezer and the refrigerated samples (vial 18-Biochem panel) are
placed in the designated 2-8°C refrigerator until analysis. The manifests are filed in a
binder labeled NHANES Shipping Manifests located in the receiving area. All labels are
removed from the shipping box and the provided airbill is attached for return shipment.

Quality Assurance Log:

A Quality Assurance Specimen Receipt and Specimen Return Log is maintained by

laboratory staff. The following parameters are tracked: NHANES shipper I.D., NHANES
Container I.D., Vial #, Date Received, Specimen Receipt Conditions, Number of
Specimens Received, 2.5% QC Repeats, Total Number of Specimens, 21 Day Due
Date, Analysis Date, Date Results Sent, Number of Days For Result Return, Thaw Date
(if applicable), Return To Freezer Date, Number of Days at Refrigerated Temperature, 1
Year Discard or Return Date, NHANES Quarterly Report Date

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Specimen Ordering/Labeling:

Electronic files for all NHANES specimens are sent via email from Westat, Inc to the
NHANES contact person shortly before they are to be received. These files include the
Sample ID, Analyte Type, Slot No, Sample Collection Date, Sample Comment, Age
Grouping, Astro ID, Receipt Date, Analysis Date, Run Number, Tech ID, Analyte Result,
Result Comment, Adjusted Result, QC Repeat, LOD, Change Reason, and Change
Reason Other. The first seven columns are protected and cannot be altered. The files
are saved on the laboratory’s common S drive in the NHANES Biochem folder. After
analysis, the contact person returns the completed files via their website to Westat, Inc.

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The NHANES spreadsheets are used to set up pending batches for batch accession
upload in the Laboratory Information system (STARLIMs). New labels are generated out
of the Laboratory Information System (STARLIMs). The new bar-coded labels are
attached to a carrier tube. The Cobas analyzer reads the bar-coded label for the sample
ID and test information.

Specimen Storage:

The temperatures for all freezers and refrigerators are monitored 24 hours a day/ 7 days
a week. If the temperature for any unit falls outside the allowable range, action is taken
to resolve the problem. If the temperature cannot be corrected, the contents are moved
to a different unit.

Specimen Handling/Specimen Return:

Prior to analysis, the specimens are stored in the designated 2-8°C refrigerator. On the
day of analysis, the specimens are selected and thawed by the technician operating the
COBAS. After analysis and the QC repeats have been run, the specimens are refrozen.
After 1 year, the specimen vials that have at least 0.2ml of sample remaining will be
shipped to SriSai Biopharmaceuticals in Frederick, MD. These specimens will be
shipped on dry ice via Federal Express.

19. SUMMARY STATISTICS AND QC GRAPHS

See following page.

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Summary Statistics and QC Chart for Blood Urea Nitrogen (mg/dL)

Start End Standard Coefficient of

Lot N Date Date Mean Deviation Variation
186345 84 18JAN17 30MAY18 53.6 0.9 1.7
Q 122 18JAN17 22JAN19 15.3 0.5 3.0
203060 38 04JUN18 22JAN19 53.8 0.9 1.6

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REFERENCES

1. Cobas 6000 Analyzer Operator’s Manual. Roche Diagnostics Inc., 9115 Hague Road
Indianapolis, IN 46250-0457. Version 5.0.

2. Roche Calibrator for Automated Systems (C.F.A.S.) package insert. Version 2011-
08, V6. Roche Diagnostics Inc., 9115 Hague Road Indianapolis, IN 46250-0457.

3. Roche Precipath U Plus package insert, Version 2011-04, V4. Roche Diagnostics
Inc., 9115 Hague Road Indianapolis, IN 46250-0457.

4. Roche UREAL reagent package insert. Version 2010-06, V5. Roche Diagnostics
Inc., 9115 Hague Road Indianapolis, IN 46250-0457.

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