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Introduction

The Schilling test is used to determine the cause of a vitamin B12 deficiency, which can result from lack of intrinsic or extrinsic factors or malabsorption in the ileum. Absorption of this vitamin requires that it be bound to intrinsic factor, a glycoprotein secreted by the gastric mucosa. Pernicious anemia, the most common and severest form of vitamin B12 deficiency, involves a deficiency of intrinsic factor, which reduces absorption of the vitamin in the ileum. Intestinal malabsorption syndrome, pancreatic disorders, and medications can also cause this vitamin deficiency.

The test involves the oral administration of a capsule of vitamin B12 labeled with the radioactive substance cobalt as cyanocobalamin Co 57 to determine gastrointestinal absorption of the vitamin. An injection of a nonradioactive vitamin B12 can be given in addition to the oral dose to enhance saturation of binding sites, intestinal absorption, and renal excretion of the radionuclide. A 24-hour urine specimen is then collected. Test results are expressed as the percentage of radionuclide excreted in the urine in relation to the amount administered. If less than 5 to 15 percent of the radionuclide is excreted, a two-stage test is indicated. For the second phase, an oral dose of intrinsic factor is given in addition to the labeled and unlabeled doses of the vitamin. If subsequent excretion of vitamin B12 reaches normal levels, pernicious anemia is confirmed; if not, malabsorption syndrome is present.79

Reference Values

Normally, 15-40% of a 0.5-mg dose and 5-40% of a 1.0-mg dose of radioactive vitamin B12 excreted
Less than 7% of the smaller dose and 0-3% of the larger dose excreted in impaired absorption states

Interfering Factors

Indications

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Care Before Procedure

Nursing Alert


Nursing Care Before the Procedure

Client preparation is the same as for any nuclear laboratory study (see section under "Total Blood Volume Study").

Procedure

One-Stage Test. The client voids and the urine is discarded. If a radionuclide study has been performed recently, a sample of the urine to be discarded can be sent to the laboratory for radioactivity residual. A 0.5- to 1.0-mg capsule of labeled vitamin B12 is administered orally. This dose is followed by an IM dose of 1000 mg of unlabeled B12 1 to 2 hours later (depending on laboratory preference). Foods and fluids can be resumed after the IM injection. All urine is collected for 24 hours in a container without a preservative (48 to 72 hours in those with renal disease) and sent to the laboratory for analysis (see Appendix II). When absorption is normal, vitamin B12 in excess of body needs is excreted by the kidneys. If absorption is impaired, the vitamin either does not appear in the urine or is found in only limited amounts. The unabsorbed B12 is excreted in the feces.

Two-Stage Test. The client voids and the urine is discarded. If the test is performed on the day after a one-stage test, a specimen from the first morning voiding should be checked by the laboratory for persistent radioactivity. A 0.5- to 1.0-mg capsule of labeled vitamin B12 is administered orally. The client can then eat breakfast, after which a 60-mg dose of intrinsic factor is administered orally. In 1 to 2 hours, an IM dose of 1000 mg of unlabeled vitamin B12 is administered ("flushing dose"). This dose competes with the absorbed radioactive material for binding sites and allows excretion of the radioactive B12 in the urine. All urine is collected for 24 hours in a container as in the one-stage test. Findings are based on the amount of B12 excreted in the urine over a specific period.

Care After Procedure

Nursing Care After the Procedure

Care and assessment after the test are the same as for any nuclear laboratory test (see section under "Total Blood Volume Study").