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Sorted By Test Name - Mayo Medical Laboratories

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EPOR<br />

61679<br />

FESC<br />

91458<br />

FFES<br />

no erythropoietic response to EPO therapy, but high-normal or high EPO levels, may have additional,<br />

unrecognized cause(s) for their anemia. If no contributing factors can be identified after adequate further<br />

study, the possibility that the patient may have developed EPO-antibodies should be considered. This can<br />

be a serious clinical situation that can result in red cell aplasia, and should prompt expeditious referral to<br />

hematologists or immunologists skilled in diagnosing and treating this disorder.<br />

Reference Values:<br />

2.6-18.5 mIU/mL<br />

Clinical References: 1. Tefferi A: Diagnosing polycythemia vera: a paradigm shift. <strong>Mayo</strong> Clin Proc<br />

1999;74:159-162 2. Hoagland HC: Myelodysplastic (preleukemia) syndromes: the bone marrow factory<br />

failure problem. <strong>Mayo</strong> Clin Proc 1995;70:673-677 3. Casadeval N: Pure red cell aplasia and<br />

anti-erythropoietin antibodies in patients treated with epoetin. Nephrol Dial Transplant 2003;18 (Suppl.<br />

8):viii37-viii41 4. Fisher JW: Minireview: Erythropoietin: Physiology and Pharmacology Update. Exp<br />

Biol Med 2003;228:1-14 5. Strippoli GFM, Manno C, Schena FP, Craig JC: Haemoglobin and<br />

haematocrit targets for the anaemia of chronic kidney disease. The Cochrane Library, 2005, Volume 2<br />

Erythropoietin Receptor (EPOR) Gene, Exon 8 Sequencing<br />

Clinical Information: Only orderable as part of a profile. For further information see HEMP/61337<br />

Hereditary Erythrocytosis Mutations.<br />

Useful For: Only orderable as part of a profile. For further information see HEMP/61337 Hereditary<br />

Erythrocytosis Mutations.<br />

Interpretation: Only orderable as part of a profile. For further information see HEMP/61337<br />

Hereditary Erythrocytosis Mutations.<br />

Reference Values:<br />

Only orderable as part of a profile. For further information see HEMP/61337 Hereditary Erythrocytosis<br />

Mutations.<br />

Clinical References:<br />

Escitalopram, Serum/Plasma<br />

Reference Values:<br />

Reporting limit determined each analysis<br />

Synonym(s): Celexa/Lexapro<br />

Steady-state peak plasma levels from patients on regimen of<br />

10 or 30 mg/day of Escitalopram:<br />

21 and 64 ng/mL, respectively, and occur at approximately<br />

4 hours post dose.<br />

This test is not Chiral specific. Patients who have taken Racemic<br />

Citalopram (Celexa), as opposed to Escitalopram (Lexapro), within<br />

the past 3 days may have falsely elevated values.<br />

<strong>Test</strong> Performed <strong>By</strong>: NMS Labs<br />

3701 Welsh Road<br />

Willow Grove, PA 19090-0437<br />

Estradiol Free, Serum (includes Estradiol and SHBG)<br />

91215<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 684

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