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Test Code LAB2978 Discordant Heparin Panel

Clinical System Name

Discordant Heparin Panel

Description

Panel includes: PTT and Heparin PTT, Corrected

 

PTTs for patients on heparin that do not agree with heparin levels measured by the anti-Xa heparin activity assay are termed discordant. The most common cause of discordant PTTs is a prolonged baseline PTT that alters the response of the PTT to heparin producing falsely high heparin PTTs compared to the anti-Xa heparin activity. Reasons for a prolonged baseline PTT include factor deficiency and deficiency in contact activation, including contact factor deficiencies and phospholipid neutralization by lupus inhibitors. In most cases the heparin activity result is a better indication of the anticoagulant effect of unfractionated heparin therapy as it is sensitive to only heparin and antithrombin levels in plasma. The heparin activity result, however, can be falsely lowered by increased levels of bilirubin and/or hemoglobin. With high levels of hemolysis and/or icterus the anti-Xa heparin activity assay can fail due to saturation of the spectrophotometer, leaving the PTT as the only option for UFH monitoring in these patients.

 

To adjust for the effect of prolonged baseline PTTs, a baseline-corrected PTT is calculated. The baseline PTT on heparin is determined using automated heparin neutralization with protamine but is not reported.

 

The Discordant Heparin Panel reports two results

1) Patients original PTT on heparin = PTT

2) Baseline-corrected PTT on heparin = Heparin PTT, Corrected

 

If the baseline PTT is normal, the original PTT and Heparin PTT, Corrected are close to the same value indicating concordance. If the original PTT and Heparin PTT, Corrected are substantially different it indicates PTT discordance and the Heparin PTT, Corrected should be used for heparin monitoring with a PTT heparin therapeutic range of 66 to 108 sec.

Note: Heparin PTT, Corrected - calculation unavailable for PTT>200 seconds.

Sample Requirements

Specimen: Whole Blood

Container(s): Lt Blue/Citrate

Required Vol: (1) 1.8 mL or (1) 2.7 mL 

Minimum Vol: N

 

Note:  This is enough for a UNF Heparin and Discordant Heparin Panel to be run on the same sample. 

 

Preferred method of collection is venipuncture with vacuum fill. Test results are affected by incorrect blood volume. Use of a Vascular Access Device for the collection of coag testing is not recommended. Please review the Coagulation Lab Collection Job Aid for detailed instructions.

Processing Instructions: Main Campus

Deliver whole blood to Coag bench. Coag Technologist will process.

 

Reject due to: clotted, insufficient quantity (underfill), or improper collection (overfill).

Spin: Y

Aliquot: Y

Storage location: Core 14 Freezer ( -70 C).

 

Specimen should be centrifuged within one hour of collection. Transfer upper 3/4 layer of plasma to plastic tube affixed with large Epic aliquot label. Do not pool. Assay immediately. 
 

Processing Instructions: Offsite & Regional Clinics

Reject due to: clotted, insufficient quantity (underfill), or improper collection (overfill).

Spin: Y

Aliquot: Y

Storage location:  -70 C (preferred) or -20 C. 

 

Specimen should be centrifuged within one hour of collection. Double spin, transfer upper 3/4 layer of plasma to plastic tube affixed with large sample label. Freeze one aliquot of plasma at -70 C (preferred) or -20 C. Preferred plasma volume: 1.0 mL, minimum plasma volume: 0.6 mL. Do not pool. 

 

Non-Children's Hospital Offsite collection: Ship completely frozen on dry ice.

 

Children's Hospital Regional Clinic collection: Ship completely frozen in frozen Nalgene Labtop cooler with ice pack inside an insulated soft cooler.

Stability

Specimen Type Temperature Time
Citrated platelet-poor plasma Room temp ≤4 h
  Refrigerated N
  Frozen   -20 C or -70 C ≤3 m

 

Performing Laboratory

Seattle Children's Laboratory

Department

Department:  Coagulation

 

Phone Number: 206 987-2617 (Client Services)

Synonyms

LAB2978

Heparin PTT, Corrected

Availability

STAT Performed TAT
Y

Daily

1 h

 

Methodology

Method:  Electromagnetic mechanical clot detection assay by STA-R MAX

Analytical Volume: 100 uL plasma

Limitations: Method is affected by insufficient quantity (underfill), improper collection (overfill), improper processing, and improper storage. High hematocrit greater than or equal to 56% requires a citrate adjusted tube.

Reference Range

Age Baseline APTT
Newborn - 3 Months 25 - 40 sec
3 Months and Older 25 - 35 sec

There are no established reference ranges for premature newborns.

CPT Codes

85730

Critical Values

≥ 150 seconds.

 

Heparin PTT, Corrected, Therapeutic Range

66 – 108 sec