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MDCG<br />

86880<br />

MORP<br />

83132<br />

SPSM<br />

9184<br />

Monospecific Direct Coombs IgG, Blood<br />

Clinical Information: IgG antibody may be present on patient or donor (transfused) RBCs and may<br />

cause hemolysis. The antibodies may be directed against self-antigens (autoimmune hemolysis), maternal<br />

antigens (hemolytic disease of the newborn), donor antigens (eg, alloimmune transfusion reaction), or<br />

drugs. The presence of in vivo coating of RBC with IgG can be demonstrated by the direct antiglobulin<br />

(Coombs) test.<br />

Useful For: Detecting antibodies bound to RBC Investigation of hemolytic anemia<br />

Interpretation: The presence or absence of IgG is used in conjunction with other testing and clinical<br />

data to aid in the characterization of Hemolysis as immune-mediated. Possible causes include<br />

autoimmune hemolytic anemia, drug-induced hemolysis, hemolytic disease of the newborn, and<br />

alloimmune reactions to recently transfused RBC.<br />

Reference Values:<br />

Negative<br />

If positive, reaction is graded (positive 1+ to 4+).<br />

Morphine, Unconjugated, Serum<br />

Clinical Information: Morphine interacts primarily with mu-opioid receptor to mediate its effects,<br />

but also shows some affinity for kappa-opioid receptor.(1) Its major metabolites are glucuronide<br />

conjugates including: inactive morphine-3-glucuronide (M3G, approximately 60%), active<br />

morphine-6-glucuronide (M6G, approximately 10%), and a small amount of<br />

morphine-3,6-diglucuronide.(2, 3) The enzyme UDP-glucuronosyltransferase-2B7 (UGT2B7) is primarily<br />

responsible for morphine glucuronidation.(2)<br />

Useful For: Monitoring morphine therapy Routine drug monitoring is not indicated in all patients.<br />

Compliance monitoring is indicated in patients who are being treated for acute pain requiring excessive<br />

dose. Assessing toxicity<br />

Interpretation: The minimal effective peak serum concentration of unconjugated morphine for<br />

analgesia is 20 ng/mL. Peak therapeutic serum concentrations of 70 ng/mL to 450 ng/mL occur 30<br />

minutes after intravenous dose, 1 hour after intramuscular or subcutaneous dose, or 2 hours after oral<br />

dose. Patients continuously administered morphine develop tolerance; they can tolerate serum<br />

concentrations up to 1,500 ng/mL. Death may be associated with serum total morphine >700 ng/mL in the<br />

nontolerant subject.(4)<br />

Reference Values:<br />

Therapeutic: 70-450 ng/mL<br />

Tolerant patients: 700 ng/mL<br />

Clinical References: 1. Gutstein HB, Akil H: Opioid analgesics. In Goodman & Gilman's The<br />

Pharmacological Basis of Therapeutics, 11th edition. Edited by LL Brunton, JS Lazo, KL Parker. New<br />

York, McGraw-Hill Book Company, 2006, pp 547-590; available from URL:<br />

http://www.accessmedicine.com/content.aspx?aID=940653 2. Coffman BL, Rios GR, King CD, et al:<br />

Human UGT2B7 catalyzes morphine glucuronidation. Drug Metab Dispos 1997;25:1-4 3. Wittwer E,<br />

Kern SE: Role of morphine's metabolites in analgesia: concepts and controversies. AAPS J 2006 May<br />

26;8(2):E348-352 4. Baselt RC: Morphine. In Dispositition of Toxic Drugs and Chemical in Man. 8th<br />

edition. Edited by RC Baselt, Foster City, CA, Biomedical Publications, 2008, pp 1057-1061<br />

Morphology Evaluation (Special Smear)<br />

Clinical Information: Under normal conditions, the morphology and proportion of each blood cell<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 1232

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