| 
 Test Name 
 | 
  Calcium urine 
(random) 
 | 
| 
 Test 
Codes 
 | 
 2621 
 | 
| 
 Unit 
 | 
 mg/dL 
 | 
| 
 Station 
 | 
 Chemistry 
 | 
| 
 Synonym 
Name/Abbreviation 
 | 
 Ca, 
urine 
 | 
| 
 CPT 
Code 
 | 
 82340 
 | 
| 
 Performing 
Facility 
 | 
 American 
Medical Labs, Herzliya Pituah 
 | 
| 
 Analyzer 
 | 
 Roche cobas 6000 
 | 
| 
 Test 
Method 
 | 
 Colorimetric 
assay 
 | 
| 
 AML 
preferred tube/ container 
 | 
 Routine 
urinalysis leakproof tube or container, BD urine transport tube, or 
sterile urine cup. 
 | 
| 
   
Sample 
collection 
 | 
  Collect urine in a screw-cup 
plastic container or transfer it to a random urine transport tube. Screw 
the lid on securely. Transport the specimen promptly to the laboratory. 
 
 | 
| 
   
Storage 
Instructions 
 | 
 Refrigerated. 
 
Stability: 
 
48h 
15-25 oC 
4 
days 2-8 oC 
3 
weeks -15to -25 oC 
 | 
| 
 Min. 
Volume 
 | 
 10 mL  
 | 
| 
   
  
  
Comments 
 | 
 Urinary 
calcium reflects in part the relation between GFR and tubular 
reabsorption. A random urine calcium-to-creatinine ratio is used to screen 
for hypercalciuria, as it is found to have a good correlation with 24-hour 
urine calcium excretion. 
Increased urinary excretion of calcium accompanies 
hyperparathyroidism, vitamin D intoxication, diseases that destroy bone 
(such as multiple myeloma), metastasis from prostatic cancer, and 
following calcium supplementation. Urine calcium is increased with 
immobilization, with steroid therapy, with Paget disease, and in primary 
(idiopathic) hypercalciuria. 
 | 
| 
 Turn-Around-Time 
 | 
 One day 
 | 
| 
   
Intended 
Use 
 | 
 Urine 
calcium determinations are used to investigate effects of vitamin D, and 
parathyroid hormone. The results reflect intake, rates of intestinal 
calcium absorption, bone resorption and renal loss. 
 
 | 
| 
   
Limitations 
 | 
 Decreased 
in patients on oral contraceptives. Lacks specificity for 
hyperparathyroidism (HPT) when increased. Five percent of the population 
has hypercalciuria. 
 Measuring range: 0.8-30.1 mg/dL 
 | 
| 
 Patient 
Preparation 
 | 
 No 
patient preparation 
needed 
 | 
| 
   
Reasons 
for Rejection 
 | 
 Quantity 
not sufficient for analysis; improper labeling; improper tubes; specimen 
more than 48 hours old if nonrefrigerated. 
 | 
| 
 Adult 
Reference Ranges 
 | 
 6.8 
– 21.3 mg/dL 
 |