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L.2.04.423
Calcium and phosphate are two minerals that are essential for normal bone formation. Throughout childhood, the body uses these minerals to produce bones. If the body does not get enough calcium, or if the body does not absorb enough calcium from the diet, bone production and bone tissues may suffer. Vitamin D is an essential nutrient that plays an important role in calcium homeostasis and bone health. Vitamin D helps the body absorb calcium.
Sunlight and ultraviolet light photoisomerize provitamin D to vitamin D3 (cholecalciferol) in the skin; they are then bound by the vitamin D binding proteins (DBP) and transported via blood to target organs for metabolism and activity. Intestinal absorption is the other major source of vitamin D. As part of the diet, vitamin D is found in fortified milk, fatty fish, cod-liver oil and, to a lesser extent, eggs. In the United States, milk fortified with vitamin D2 (ergocalciferol, a plant steroid) or vitamin D3 (cholecalciferol) is the principal source of dietary vitamin D. In other parts of the world, cereals and bread products are often fortified with vitamin D.
Vitamin D deficiency or resistance is caused by one of four mechanisms:
Impaired availability of vitamin D, secondary to inadequate dietary vitamin D, fat malabsorptive disorders, and/or lack of photoisomerization
Impaired hydroxylation by the liver to produce 25-hydroxyvitamin D
Impaired hydroxylation by the kidneys to produce 1,25-dihydroxyvitamin D
End organ insensitivity to vitamin D metabolites (hereditary vitamin D resistant rickets)
Vitamin D deficiency can lead to osteoporosis in adults. Severe deficiency of vitamin D causes rickets and/or hypocalcemia in infants and children and osteomalacia in adults or adolescents after epiphysial closure; severe vitamin D deficiency may also be associated with hypocalcemia, which may cause tetany or seizures. These disorders occur with the highest frequency among children in malnourished populations and in children with chronic illnesses. Rickets also occurs in children in developed nations if sufficient vitamin D intake is not ensured through the use of supplements and fortified foods, particularly if exposure to sunlight is limited.
The Clinical Guidelines Subcommittee of the Endocrine Society appointed a Task Force to formulate evidence-based recommendations for Vitamin D evaluation, treatment, and prevention. The Task Force recommends screening for vitamin D deficiency in individuals at risk for deficiency using the serum circulating 25-hydroxyvitamin D [25(OH)D] level, measured by a reliable assay, to evaluate vitamin D status in patients who are at risk for vitamin D deficiency. In individuals who are in the high risk groups, it is appropriate to measure serum 25OHD, to supplement with the amount estimated to be needed to reach the target 25OHD level, and then to remeasure three to four months later to verify that the target has been achieved. Although healthy adults initiating vitamin D supplementation (600 to 800 units daily) do not require an initial or follow-up serum 25OHD measurement after starting supplementation, patients being treated specifically for vitamin D deficiency require a repeat 25OHD measurement approximately three to four months after initiating therapy. Ergocal has a ½ life of 21 days, so more frequent testing after initiation of therapy is not indicated.
The Task Force does not recommend population screening for vitamin D deficiency in individuals who are not at risk. Normal risk adults do not need assessment, but all adults who do not have regular effective sun exposure year round should consume at least 600 to 800 international units (units) of daily. In the general population, it is not necessary to perform broad-based screening of serum Vitamin D levels.
Serum measurement of vitamin D [25-hydroxyvitamin D [25(OH)D] is considered medically necessary up to four (4) times per calendar year for the following conditions:
Biliary cirrhosis and other specified disorders of the biliary tract
Blind loop syndrome
Celiac Disease
Dermatomyositis
Hypercalcemia, hypocalcemia or other disorders of calcium metabolism
Hyperparathyroidism or hypoparathyroidism
Hypervitaminosis of vitamin D
Disorders of phosphorus metabolism
Individuals receiving hyperalimentation
Intestinal malabsorption
Liver cirrhosis
Long term use of anticonvulsants, glucocorticoids and other medications known to lower vitamin D levels
Lymphoma
Malnutrition
Myalgia and other myositis not specified
Myopathy related to endocrine diseases
Osteogenesis imperfecta
Osteomalacia
Osteopetrosis
Osteoporosis
Premature osteopenia
Pancreatic steatorrhea
Primary or miliary tuberculosis
Psoriasis
Regional enteritis
Renal, ureteral or urinary calculus (nephrolithiasis)
Rickets
Sarcoidosis
Stage III-V Chronic Kidney Disease and End Stage Renal Disease
Systemic lupus erythematosus
Vitamin D deficiency on replacement therapy; to monitor the efficacy of treatment
Routine serum vitamin D testing is considered not medically necessary when performed for screening purposes in asymptomatic patients (absence of signs, symptoms, or disease).
None
The coverage guidelines outlined in the Medical Policy Manual should not be used in lieu of the Member's specific benefit plan language.
Medically Necessary is defined as those services, treatments, procedures, equipment, drugs, devices, items or supplies furnished by a covered Provider that are required to identify or treat a Member's illness, injury or Mental Health Disorders, and which Company determines are covered under this Benefit Plan based on the criteria as follows in A through D:
A. consistent with the symptoms or diagnosis and treatment of the Member's condition, illness, or injury; and
B. appropriate with regard to standards of good medical practice; and
C. not solely for the convenience of the Member, his or her Provider; and
D. the most appropriate supply or level of care which can safely be provided to Member. When applied to the care of an Inpatient, it further means that services for the Member's medical symptoms or conditions require that the services cannot be safely provided to the Member as an Outpatient.
For the definition of medical necessity, “standards of good medical practice” means standards that are based on credible scientific evidence published in peer-reviewed medical literature generally recognized by the relevant medical community, and physician specialty society recommendations, and the views of medical practitioners practicing in relevant clinical areas and any other relevant factors. BCBSMS makes no payment for services, treatments, procedures, equipment, drugs, devices, items or supplies which are not documented to be Medically Necessary. The fact that a Physician or other Provider has prescribed, ordered, recommended, or approved a service or supply does not in itself, make it Medically Necessary.
10/01/2013: New policy added.
08/14/2015: Medical policy revised to add ICD-10 codes.
06/07/2016: Policy number L.2.04.423 added. Policy Guidelines updated to add medically necessary definition.
09/08/2016: Code Reference section updated to make correction: ICD-10 diagnosis code E70.00 should be E70.0.
09/30/2016: Code Reference section updated to add new ICD-10 diagnosis code K90.41.
10/18/2016: Code Reference section updated to make correction: ICD-10 diagnosis code K90.41 should be K90.49.
09/29/2017: Code Reference section updated to add new ICD-10 diagnosis codes C96.20, C96.21, C96.22, C96.29, M33.03, M33.13, and M33.93, effective 10/01/2017. Removed deleted ICD-10 diagnosis code K90.4. Revised code descriptions for ICD-10 diagnosis codes M33.00 - M33.09 and M33.10 - M33.19.
03/27/2018: Code Reference section updated to add new CPT code 0038U as investigational, effective 04/01/2018.
05/31/2018: Deleted outdated reference in Sources section.
09/25/2018: Code Reference section updated to add new ICD-10 diagnosis codes E72.89, M79.10, M79.18, effective 10/01/2018.
02/14/2019: Code Reference section updated to remove deleted ICD-10 diagnosis code C96.2.
09/24/2020: Code Reference section updated to add new ICD-10 diagnosis code E70.89, effective 10/01/2020. Removed deleted ICD-10 diagnosis codes E72.8 and M79.1.
02/21/2023: Policy reviewed. Policy statements unchanged. Policy Guidelines updated to change "Nervous/Mental Conditions" to "Mental Health Disorders" and "Medically Necessary" to "medical necessity." Code Reference section updated to remove deleted ICD-10 diagnosis code N18.3. Added ICD-10 diagnosis codes N18.30 - N18.32.
09/29/2023: Code Reference section updated to add new ICD-10 diagnosis codes E20.810, E20.811, E20.812, E20.818, E20.819, E20.89, K90.821, K90.822, K90.829, and K90.83, effective 10/01/2023.
04/10/2024: Policy reviewed; no changes.
08/16/2024: Code Reference section updated to add ICD-10 diagnosis codes Q98.0 - Q98.4.
10/01/2024: Code Reference section updated to add new ICD-10 diagnosis codes C86.00, C86.01, C86.10, C86.20, C86.21, C86.30, C86.31, C86.40, C86.41, C86.50, C86.51, C86.60, and C88.40.
03/27/2025: Policy reviewed; no changes.
Endocrine Physician Advisory Committee
Premera Blue Cross Vitamin D Testing Medical Policy
Novitas Solutions LCD L30273 - Vitamin D Assay Testing
Should Family Physicians Screen for Vitamin D Deficiency? No: Screening Is Unnecessary, and Routine Supplementation Makes More Sense, COLIN KOPES-KERR, MD, Touro University College of Osteopathic Medicine, Vallejo, California, Am Fam Physician. 2013 Apr 15;87(8):online.
Should Family Physicians Screen for Vitamin D Deficiency? Yes: Targeted Screening in At-Risk Populations Is Prudent, LEIGH M. ECK, MD, University of Kansas Medical Center, Kansas City, Kansas, Am Fam Physician. 2013 Apr 15; 87(8):online.
http://www.nlm.nih.gov/medlineplus/ency/article/002405.htm - Vitamin D
UptoDate® – Vitamin d insufficiency and deficiency in children and adolescents
UptoDate® – Treatment of vitamin D deficiency in adults
UptoDate® – Overview of vitamin D
This may not be a comprehensive list of procedure codes applicable to this policy.
The code(s) listed below are ONLY medically necessary if the procedure is performed according to the "Policy" section of this document.
Code Number | Description | ||
CPT-4 | |||
82306 | Vitamin D; 25 hydroxy, includes fraction(s), if performed | ||
HCPCS | |||
ICD-9 Procedure | ICD-10 Procedure | ||
ICD-9 Diagnosis | ICD-10 Diagnosis | ||
010.0 – 018.96 | Tuberculous infection, code range | A15.0 - A19.9 | Tuberculous (code range) |
135 | Sarcoidosis | D86.0 - D86.9 | Sarcoidosis code range |
200.00 – 202.98 | Lymphomas | C81.00 - C81.99 | Hodgkin lymphoma |
C82.00 - C82.99 | Follicular lymphoma | ||
C83.00 - C83.99 | Non-follicular lymphoma | ||
C84.00 - C84.Z9 | Mature T/NK-cell lymphomas | ||
C85.10 - C85.99 | Other specified and unspecified types of non-Hodgkin lymphoma (code range) | ||
C86.00 - C86.60 | Other specified types of T/NK-cell lymphoma (code range) (C86.00, C86.01, C86.10, C86.20, C86.21, C86.30, C86.31, C86.40, C86.41, C86.50, C86.51, C86.60 New 10/01/2024) | ||
C88.40 | Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue [MALT-lymphoma] not having achieved remission (New 10/01/2024) | ||
C91.40 - C91.42 | Hairy cell leukemia (code range) | ||
C96.0 | Multifocal and multisystemic (disseminated) Langerhans-cell histiocytosis | ||
C96.20, C96.21, C96.22, C96.29 | Malignant mast cell tumor | ||
C96.4 | Sarcoma of dendritic cells (accessory cells) | ||
C96.9 | Unifocal Langerhans-cell histiocytosis | ||
C96.A | Histiocytic sarcoma | ||
C96.Z | Other specified malignant neoplasms of lymphoid, hematopoietic and related tissue | ||
252.00 – 252.08 | Hyperparathyroidism | E21.0 | Primary hyperparathyroidism |
E21.1 | Secondary hyperparathyroidism, not elsewhere classified | ||
E21.2 | Other hyperparathyroidism | ||
E21.3 | Hyperparathyroidism, unspecified | ||
252.1 | Hypoparathyroidism | E20.0 - E20.9 | Hypoparathyroidism |
E89.2 | Postprocedural hypoparathyroidism | ||
263.0 – 263.9 | Other and unspecified protein-calorie malnutrition | E44.0 - E44.1 | Protein-calorie malnutrition of moderate and mild degree |
E45 | Retarded development following protein-calorie malnutrition | ||
E46 | Unspecified protein-calorie malnutrition | ||
268.0 | Rickets, active | E55.0 | Rickets, active |
268.1 | Rickets, late effect | E64.3 | Sequelae of rickets |
268.2 | Osteomalacia, unspecified | M83.0 - M83.9 | Adult osteomalacia |
268.9 | Unspecified vitamin D deficiency | E55.9 | Vitamin D deficiency, unspecified |
270.0 – 270.9 | Disorders of amino-acid transport and metabolism | E70.0 - E70.9 | Disorders of aromatic amino-acid metabolism |
E71.0 | Maple-syrup-urine disease | ||
E71.110 - E71.128 | Other disorders of branched-chain amino-acid metabolism | ||
E71.2 | Disorder of branched-chain amino-acid metabolism, unspecified | ||
E72.00 - E72.09 | Disorders of amino-acid transport | ||
E72.10 - E71.19 | Disorders of sulfur-bearing amino-acid metabolism | ||
E72.20 - E72.29 | Disorders of urea cycle metabolism | ||
E72.3 | Disorders of lysine and hydroxylysine metabolism | ||
E72.4 | Disorders of ornithine metabolism | ||
E72.50, E72.51, E72.59, E72.8 | Disorders of glycine metabolism | ||
E72.89 | Other specified disorders of amino-acid metabolism | ||
E72.9 | Disorder of amino-acid metabolism, unspecified | ||
275.3 | Disorders of phosphorus metabolism | E83.30 - E83.39 | Disorders of phosphorus metabolism and phosphatases |
275.41 | Hypocalcemia | E83.51 | Hypocalcemia |
275.42 | Hypercalcemia | E83.52 | Hypercalcemia |
275.49 | Other disorders of calcium metabolism | E83.59 | Other disorders of calcium metabolism |
278.4 | Hypervitaminosis D | E67.3 | Hypervitaminosis D |
278.8 | Other hyperalimentation | E67.8 | Other specified hyperalimentation |
359.5 | Myopathy in endocrine diseases classified elsewhere | G73.7 | Myopathy in diseases classified elsewhere |
555.0 - 555.9 | Regional enteritis | K50.00 - K50.919 | Crohn's disease (regional enteritis) (code range) |
556.0 - 556.9 | Ulcerative colitis | K51.00 - K51.919 | Ulcerative colitis |
571.2 | Alcoholic cirrhosis of liver | K70.2 | Alcoholic fibrosis and sclerosis of liver |
K70.30, K70.31 | Alcoholic cirrhosis of liver (code range) | ||
571.5 | Cirrhosis of liver without mention of alcohol | K74.60, K74.69 | Other and unspecified cirrhosis of liver |
571.6 | Biliary cirrhosis | K74.3 | Primary biliary cirrhosis |
K74.4 | Secondary biliary cirrhosis | ||
K74.5 | Biliary cirrhosis, unspecified | ||
576.8 | Other specified disorders of biliary tract | K83.5 | Biliary cyst |
K83.8 | Other specified diseases of biliary tract | ||
K87 | Disorders of gallbladder, biliary tract and pancreas in diseases classified elsewhere | ||
579.0 - 579.9 | Celiac disease | K90.0 | Celiac disease |
K90.1 | Tropical sprue | ||
K90.2 | Blind loop syndrome, not elsewhere classified | ||
K90.3 | Pancreatic steatorrhea | ||
K90.821, K90.822, K90.829 | Short bowel syndrome | ||
K90.83 | Intestinal failure | ||
K90.89 | Other intestinal malabsorption | ||
K90.9 | Intestinal malabsorption, unspecified | ||
| K90.49 | Malabsorption due to intolerance, not elsewhere classified | |
585.3 | Chronic kidney disease, Stage III (moderate) | N18.30 - N18.32 | Chronic kidney disease, stage 3 (moderate) |
585.4 | Chronic kidney disease, Stage IV (severe) | N18.4 | Chronic kidney disease, stage 4 (severe) |
585.5 | Chronic kidney disease, Stage V | N18.5 | Chronic kidney disease, stage 5 |
585.6 | End stage renal disease | N18.6 | End stage renal disease |
588.0 | Renal osteodystrophy | N25.0 | Renal osteodystrophy |
592.0 – 592.9 | Calculus of kidney and ureter | N20.0 - N20.9 | Calculus of kidney and ureter |
594.0 – 594.9 | Calculus of lower urinary tract | N21.0 - N21.9 | Calculus of lower urinary tract |
696.1 | Other psoriasis | L40.0 - L40.9 | Psoriasis (code range) |
710.0 | Systemic lupus erythematosus | M32.0 - M32.9 | Systemic lupus erythematosus (SLE) |
710.3 | Dermatomyositis | M33.00 - M33.09 | Juvenile dermatomyositis |
M33.10- M33.19 | Other dermatomyositis | ||
M33.90 - M33.99 | Dermatopolymyositis, unspecified | ||
729.1 | Myalgia and myositis, unspecified | M60.80 - M60.9 | Other myositis (code range) |
M79.10 | Myalgia, unspecified site | ||
M79.18 | Myalgia, other site | ||
M79.7 | Fibromyalgia | ||
733.00 - 733.09 | Osteoporosis | M81.0 - M81.8 | Osteoporosis without current pathological fracture |
733.90 | Disorder of bone and cartilage, unspecified | M85.9 | Disorder of bone density and structure, unspecified |
M89.9 | Disorder of bone, unspecified | ||
M94.9 | Disorder of cartilage, unspecified | ||
756.51 | Osteogenesis imperfecta | Q78.0 | Osteogenesis imperfecta |
756.52 | Osteopetrosis | Q78.2 | Osteopetrosis |
Q98.0 - Q98.4 | Klinefelter's syndrome (code range) | ||
775.4 | Hypocalcemia and hypomagnesemia of newborn | P71.0 - P71.9 | Transitory neonatal disorders of calcium and magnesium metabolism |
V58.65 | Long-term (current) use of steroids | Z79.51 - Z79.52 | Long term (current) use of steroids |
V58.69 | Long-term (current) use of other medications | Z79.899 | Other long term (current) drug therapy |
Investigational Codes
Code Number | Description |
CPT-4 | |
0038U | Vitamin D, 25 hydroxy D2 and D3, by LC-MS/MS, serum microsample, quantitative |
HCPCS | |
ICD-10 Procedure | |
ICD-10 Diagnosis |
CPT copyright American Medical Association. All rights reserved. CPT is a registered trademark of the American Medical Association.