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Sorted By Test Name - Mayo Medical Laboratories

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FCOCB<br />

90093<br />

COKEM<br />

84140<br />

disorders, and thyroid abnormalities. The inhalation of dust during machining of cobalt alloyed metals can<br />

lead to interstitial lung disease. Improperly handled (60)Co can cause radiation poisoning from exposure<br />

to gamma radiation. Urine cobalt concentrations are likely to be increased above the reference value in<br />

patients with metallic joint prosthesis. Prosthetic devices produced by Zimmer Company and Johnson &<br />

Johnson typically are made of aluminum, vanadium, and titanium. Prosthetic devices produced by Depuy<br />

Company, Dow Corning, Howmedica, LCS, PCA, Osteonics, Richards Company, Tricon, and Whiteside<br />

typically are made of chromium, cobalt, and molybdenum. This list of products is incomplete, and these<br />

products change occasionally; see prosthesis product information for each device for composition details.<br />

Useful For: Detecting cobalt exposure Monitoring metallic prosthetic implant wear<br />

Interpretation: Concentrations > or =2.0 mcg/g creatinine indicate excess exposure. There are no<br />

Occupational Safety and Health Administration (OSHA) blood or urine criteria for occupational exposure<br />

to cobalt. Prosthesis wear is known to result in increased circulating concentration of metal ions. In a<br />

patient with a cobalt-based implant, modest increase (2-4 mcg/g creatinine) in urine cobalt concentration<br />

is likely to be associated with a prosthetic device in good condition. Excessive exposure is indicated when<br />

urine cobalt concentration is >5 mcg/g creatinine, consistent with prosthesis wear. Urine concentrations<br />

>20 mcg/g creatinine in a patient with a cobalt-based implant suggest significant prosthesis wear.<br />

Increased urine trace element concentrations in the absence of corroborating clinical information do not<br />

independently predict prosthesis wear or failure.<br />

Reference Values:<br />

0.0-1.9 mcg/g Creatinine<br />

Reference values apply to all ages.<br />

Clinical References: 1. Keegan GM, Learmonth ID, Case CP: A systematic comparison of the<br />

actual, potential, and theoretical health effects of cobalt and chromium from industry and surgical<br />

implants. Crit Rev Toxicol 2008;38:645-674 2. Lhotka C, Szekes T, Stefan I, et al: Four-year study of<br />

cobalt and chromium blood levels in patients managed with two different metal-on-metal total hip<br />

replacements. J Orthop Res 2003;21:189-195 3. Lison D, De Boeck M, Verougstraete V, Kirsch-Volders<br />

M: Update on the genotoxicity and carcinogenicity of cobalt compounds. Occup Environ Med<br />

2001;58(10):619-625<br />

Cocaine and Benzoylecgonine Screen and GC/MS Confirmation,<br />

Blood-Forensic<br />

Reference Values:<br />

<strong>Test</strong> Performed by: Medtox <strong>Laboratories</strong>, Inc.<br />

402 W. County Road D<br />

St. Paul, MN 55112<br />

Cocaine and Metabolites Confirmation, Meconium<br />

Clinical Information: Cocaine is an alkaloid found in Erythroxylon coca, which grows principally in<br />

the northern South American Andes and to a lesser extent in India, Africa, and Java.(1) Cocaine is a<br />

powerfully addictive stimulant drug. Cocaine abuse has a long history and is rooted into the drug culture<br />

in the United States,(2) and is 1 of the most common illicit drugs of abuse.(3,4) Cocaine is rapidly<br />

metabolized primarily to benzoylecgonine, which is further metabolized to m-hydroxybenzoylecgonine<br />

(m-HOBE).(1,5) Cocaine is frequently used with other drugs, most commonly ethanol, and the<br />

simultaneous use of both drugs can be determined by the presence of the unique metabolite<br />

cocaethylene.(4) Intrauterine drug exposure to cocaine has been associated with placental abruption,<br />

premature labor, small for gestational age status, microcephaly, and congenital anomalies (eg, cardiac and<br />

genitourinary abnormalities, necrotizing enterocolitis, and central nervous system stroke or<br />

hemorrhage).(6) The disposition of drug in meconium, the first fecal material passed by the neonate, is not<br />

well understood. The proposed mechanism is that the fetus excretes drug into bile and amniotic fluid.<br />

Drug accumulates in meconium either by direct deposition from bile or through swallowing of amniotic<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 495

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