Lupus Anticoagulant (LAC)
Introduction Lupus-like
Anticoagulant (LAC) has been linked to a variety of clinical findings,
including arterial and venous thromboembolic events, thrombocytopenia and
recurrent pregnancy loss. LAC is an antiphospholipid antibody directed
against negatively charged phospholipids that is identified functionally
by prolongation of in vitro phospholipid-dependent coagulation tests such
as Activated Partial Thromboplastin Time (APTT), Prothrombin Time (PT) or
dilute Russell's Viper Venom Time (dRVVT). IL TestTM LAC Screen and IL
TestTM LAC Confirm are dRVVT reagents used in the detection of LAC because
they are more specific tests for the evaluation of LAC that APTT or PT.
The prevalence of LAC in patients with a history of recurrent pregnancy
loss varies between 1 to 5% depending on the population studies. Among
pregnancies in which no treatment is given, 86% are complicated by
embryonic or fetal loss.

Indications for
Testing All individuals with a history of arterial or venous
thrombosis, lupus erythematosus or the presence of elevated
antiphospholipid antibodies as well as all women experiencing two or more
pregnancy losses should be screened for the presence of a circulating LAC.
If the results of the screening test are elevated, the presence of LAC
should be confirmed through the performance of the dRVVT.

Detection
Method Lupus-like Anticoagulant (LAC) is detected using dRVVT.
dRVVT in the presence of calcium directly activated Factor X in the test
sample. IL TestTM LAC Screen and IL TestTM LAC Confirm are unaffected by
contact factor abnormalities and factor VII deficiency or inhibitors.
Heparin interference is neutralized using polybrene. As a result, IL
TestTM LAC Screen and IL TestTM LAC Confirm are more specific tests for
the evaluation of LAC than APTT or PT.

Interpretation of Test
Results The final result is expressed by a ratio of IL TestTM
LAC Screen / IL TestTM LAC Confirm:
| Normal range |
0.8 to 1.2 |
| LAC weakly present |
1.2 to 1.5 |
| LAC moderately present |
1.5 to 2.0 |
| LAC strongly present |
> 2.0 |

Specimen Collection and Shipping
Requirements
- Collect plasma from a one (1) blue top tube.
- Spin, separate, freeze and ship in prepaid FedEx mailers overnight,
next day morning.

Turn around Time Processing
of specimens begins immediately upon receipt at our facilities. Results
are routinely available within 7 to 10 days and are initially faxed, then
mailed to the requesting physician.

Cost
Included in our fees
are specimen collection and shipping materials, all courier and shipping
charges, telephone and written reports, and consultation with physicians.
Please call 1-877-737-7652 for pricing information.

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References Coulam CB, Kaider
BD, Kaider AS, Janowicz RG. Roussev RG. Antiphospholipid antibodies
associated with implantation failure after IVF/ET. J Assist Reprod Genet
1997; 14:603-8.
Coulam CB. The role of antiphospholipid antibodies in reproduction:
questions answered and raised at the 18th annual meeting of the American
Society of Reproductive Immunology. Am J Reprod Immunol 1999; 41:1-4.
Kaider AS, Kaider BD, Janowicz PB, Roussev RG. Immunodiagnostic
evaluation in women with reproductive failure. Am J Reprod Immunol 1999;
42: 335-346.
Sher G, Zouves C, Feinman M, Maassarani G, Matzner W, Chong P, Ching
W.A rational basis for the use of combined heparin/aspirin and IVIG
immunotherapy in the treatment of recurrent IVF failure associated with
antiphospholipid antibodies. Am J Reprod Immunol 39:391-94.
Sher G, Matzner W, Feinman M, Maassarani G, Zouves C, Chong P, Ching W.
The selective use of heparin/aspirin therapy, alone or in combination with
intravenous immunoglobulin G, in the management of antiphospholipid
antibody-positive women undergoing in vitro fertilization. Am J Reprod
Immunol. 1998; 40:74-82.

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