Anthem Blue Cross Blue Shield of Georgia policy

SHBP Prior Authorization Requirements

SHBP Prior Authorization Requirements is a public Anthem Blue Cross Blue Shield of Georgia policy. It lists 2,569 CPT or HCPCS codes, 2046 of them on the Anthem Blue Cross Blue Shield of Georgia prior authorization list. Not a coverage decision; the payer's own document governs.

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Payer
Anthem Blue Cross Blue Shield of Georgia
Line of business
Commercial
States
GA
Source
www.anthem.com

Codes in this policy

The CPT and HCPCS codes the policy names. A policy can name a code it excludes. Prior authorization status is from the Anthem Blue Cross Blue Shield of Georgia prior authorization list.

CodePrior authorizationDescription on the prior authorization listOther Anthem Blue Cross Blue Shield of Georgia policies
00003Not listedPolicies naming 00003
00004Not listedPolicies naming 00004
00005Not listedPolicies naming 00005
00007Not listedPolicies naming 00007
00008Not listedPolicies naming 00008
00009Not listedPolicies naming 00009
00010Not listedPolicies naming 00010
00011Not listedPolicies naming 00011
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00013Not listedPolicies naming 00013
00022Not listedPolicies naming 00022
00023Not listedPolicies naming 00023
00024Not listedPolicies naming 00024
00025Not listedPolicies naming 00025
00026Not listedPolicies naming 00026
00027Not listedPolicies naming 00027
00028Not listedPolicies naming 00028
00029Not listedPolicies naming 00029
00030Not listedPolicies naming 00030
00031Not listedPolicies naming 00031
00032Not listedPolicies naming 00032
00033Not listedPolicies naming 00033
00035Not listedPolicies naming 00035
00037Not listedPolicies naming 00037
00041Not listedPolicies naming 00041
00046Not listedPolicies naming 00046
00047Not listedPolicies naming 00047
00049Not listedPolicies naming 00049
00052Not listedPolicies naming 00052
00053Not listedPolicies naming 00053
00057Not listedPolicies naming 00057
00059Not listedPolicies naming 00059
00061Not listedPolicies naming 00061
00062Not listedPolicies naming 00062
00070Not listedPolicies naming 00070
00071Not listedPolicies naming 00071
00072Not listedPolicies naming 00072
00089Not listedPolicies naming 00089
00090Not listedPolicies naming 00090
00092Not listedPolicies naming 00092
00095Not listedPolicies naming 00095
00096Not listedPolicies naming 00096
00098Not listedPolicies naming 00098
00103Not listedPolicies naming 00103
00104Not listedPolicies naming 00104
00107Not listedPolicies naming 00107
00111Not listedPolicies naming 00111
00115Not listedPolicies naming 00115
00118Not listedPolicies naming 00118
00120Not listedPolicies naming 00120
00121Not listedPolicies naming 00121
00123Not listedPolicies naming 00123
00129Not listedPolicies naming 00129
00131Not listedPolicies naming 00131
00135Not listedPolicies naming 00135
00140Not listedPolicies naming 00140
00141Not listedPolicies naming 00141
00144Not listedPolicies naming 00144
00145Not listedPolicies naming 00145
00150Not listedPolicies naming 00150
00152Not listedPolicies naming 00152
00153Not listedPolicies naming 00153
00156Not listedPolicies naming 00156
00157Not listedPolicies naming 00157
00158Not listedPolicies naming 00158
00159Not listedPolicies naming 00159
00160Not listedPolicies naming 00160
0016UOn the listOncology (hematolymphoid neoplasia), RNA, BCR/ABL1 major and minor breakpoint fusion transcripts, quantitative PCR amplification, blood or bone marrow, report of fusion not detected or detected with quantitationPolicies naming 0016U
00170On the listAnesthesia for intraoral procedures, including biopsy; not otherwise specifiedPolicies naming 00170
0017UOn the listOncology (hematolymphoid neoplasia), JAK2 mutation, DNA, PCR amplification of exons 12-14 and sequence analysis, blood or bone marrow, report of JAK2 mutation not detected or detectedPolicies naming 0017U
0022UOn the listTargeted genomic sequence analysis panel, non- small cell lung neoplasia, DNA and RNA analysis, 23 genes, interrogation for sequence variants and rearrangements, reported as presence or absence of variants and associated therapy(ies) to considerPolicies naming 0022U
0023UOn the listOncology (acute myelogenous leukemia), DNA, genotyping of internal tandem duplication, p.D835, p.I836, using mononuclear cells, reported as detection or non-detection of FLT3 mutation and indication for or against the use of midostaurinPolicies naming 0023U
0027UOn the listJAK2 (Janus kinase 2) (eg, myeloproliferative disorder) gene analysis, targeted sequence analysis exons 12-15Policies naming 0027U
0036UOn the listExome (ie, somatic mutations), paired formalin- fixed paraffin-embedded tumor tissue and normal specimen, sequence analysesPolicies naming 0036U
0037UOn the listTargeted genomic sequence analysis, solid organ neoplasm, DNA analysis of 324 genes, interrogation for sequence variants, gene copy number amplifications, gene rearrangements, microsatellite instability and tumor mutational burdenPolicies naming 0037U
0040UOn the listBCR/ABL1 (t(9;22)) (eg, chronic myelogenous leukemia) translocation analysis, major breakpoint, quantitativePolicies naming 0040U
0045UOn the listOncology (breast ductal carcinoma in situ), mRNA, gene expression profiling by real-time RT-PCR of 12 genes (7 content and 5 housekeeping), utilizing formalin-fixed paraffin-embedded tissue, algorithm reported as recurrence scorePolicies naming 0045U
0046UOn the listFLT3 (fms-related tyrosine kinase 3) (eg, acute myeloid leukemia) internal tandem duplication (ITD) variants, quantitativePolicies naming 0046U
0048UOn the listOncology (solid organ neoplasia), DNA, targeted sequencing of protein-coding exons of 468 cancer- associated genes, including interrogation for somatic mutations and microsatellite instability, matched with normal specimens, utilizing formalin- fixed paraffin-embedded tumor tissue, report of clinically significant mutation(s)Policies naming 0048U
0049UOn the listNPM1 (nucleophosmin) (eg, acute myeloid leukemia) gene analysis, quantitativePolicies naming 0049U
0050UOn the listTargeted genomic sequence analysis panel, acute myelogenous leukemia, DNA analysis, 194 genes, interrogation for sequence variants, copy number variants or rearrangementsPolicies naming 0050U
00530Not listedPolicies naming 00530
00534Not listedPolicies naming 00534
00580On the listAnesthesia for heart transplant or heart/lung transplantPolicies naming 00580
0071TOn the listFocused ultrasound ablation of uterine leiomyomata, including MR guidance; total leiomyomata volume less than 200 cc of tissuePolicies naming 0071T
0072TOn the listFocused ultrasound ablation of uterine leiomyomata, including MR guidance; total leiomyomata volume greater or equal to 200 cc of tissuePolicies naming 0072T
0075TNot listedPolicies naming 0075T
0076TNot listedPolicies naming 0076T
00796On the listAnesthesia, Intraperitoneal Proc, Upper Abdomen, W/Laparoscopy; Liver Transplant, RecipientPolicies naming 00796
00797Not listedPolicies naming 00797
00802Not listedPolicies naming 00802
0094UOn the listGenome (eg, unexplained constitutional or heritable disorder or syndrome), rapid sequence analysisPolicies naming 0094U
0095TOn the listRemoval of total disc arthroplasty (artificial disc), anterior approach, each additional interspace, cervicalPolicies naming 0095T
0098TOn the listRevision including replacement of total disc arthroplasty (artificial disc), anterior approach, each additional interspace, cervicalPolicies naming 0098T
0101UOn the listHereditary colon cancer disorders (eg, Lynch syndrome, PTEN hamartoma syndrome, Cowden syndrome, familial adenomatosis polyposis), genomic sequence analysis panel utilizing a combination of NGS, Sanger, MLPA, and array CGH, with mRNA analytics to resolve variants of unknown significance when indicated (15 genes [sequencing and deletion/duplication], EPCAM and GREM1 [deletion/duplication only])Policies naming 0101U
0102UOn the listHereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer, hereditary endometrial cancer), genomic sequence analysis panel utilizing a combination of NGS, Sanger, MLPA, and array CGH, with mRNA analytics to resolve variants of unknown significance when indicated (17 genes [sequencing and deletion/duplication])(cid:9)Policies naming 0102U
0103UOn the listHereditary ovarian cancer (eg, hereditary ovarian cancer, hereditary endometrial cancer), genomic sequence analysis panel utilizing a combination of NGS, Sanger, MLPA, and array CGH, with mRNA analytics to resolve variants of unknown significance when indicated (24 genes [sequencing and deletion/duplication], EPCAM [deletion/duplication only])Policies naming 0103U
0111UOn the listOncology (colon cancer), targeted KRAS (codons 12, 13, and 61) and NRAS (codons 12, 13, and 61) gene analysis utilizing formalin-fixed paraffin- embedded tissuePolicies naming 0111U
0129UOn the listHereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer, hereditary endometrial cancer), genomic sequence analysis and deletion/duplication analysis panel (ATM, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, and TP53)Policies naming 0129U
0153UOn the listOncology (breast), mRNA, gene expression profiling by next-generation sequencing of 101 genes, utilizing formalin-fixed paraffin-embedded tissue, algorithm reported as a triple negative breast cancer clinical subtype(s) with information on immune cell involvementPolicies naming 0153U
0154UOn the listOncology (urothelial cancer), RNA, analysis by real- time RT-PCR of the FGFR3 (fibroblast growth factor receptor 3) gene analysis (ie, p.R248C [c.742C>T], p.S249C [c.746C>G], p.G370C [c.1108G>T], p.Y373C [c.1118A>G], FGFR3- TACC3v1, and FGFR3-TACC3v3) utilizing formalin- fixed paraffin-embedded urothelial cancer tumor tissue, reported as FGFR gene alteration statusPolicies naming 0154U
0155UOn the listOncology (breast cancer), DNA, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha) (eg, breast cancer) gene analysis (ie, p.C420R, p.E542K, p.E545A, p.E545D [g.1635G>T only], p.E545G, p.E545K, p.Q546E, p.Q546R, p.H1047L, p.H1047R, p.H1047Y), utilizing formalin-fixed paraffin-embedded breast tumor tissue, reported as PIK3CA gene mutation statusPolicies naming 0155U
0163TNot listedPolicies naming 0163T
0164TNot listedPolicies naming 0164T
0165TNot listedPolicies naming 0165T
0170UOn the listNeurology (autism spectrum disorder [ASD]), RNA, next-generation sequencing, saliva, algorithmic analysis, and results reported as predictive probability of ASD diagnosisPolicies naming 0170U
0177UOn the listOncology (breast cancer), DNA, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) gene analysis of 11 gene variants utilizing plasma, reported as PIK3CA gene mutation statusPolicies naming 0177U
0179UOn the listOncology (non-small cell lung cancer), cell-free DNA, targeted sequence analysis of 23 genes (single nucleotide variations, insertions and deletions, fusions without prior knowledge of partner/breakpoint, copy number variations), with report of significant mutation(s)Policies naming 0179U
0200TOn the listPercutaneous sacral augmentation (sacroplasty), unilateral injection(s), including the use of a balloon or mechanical device, when used, 1 or more needlesPolicies naming 0200T
0201TOn the listPercutaneous sacral augmentation (sacroplasty), bilateral injections, including the use of a balloon or mechanical device, when used, 2 or more needlesPolicies naming 0201T
0202TOn the listPosterior vertebral joint(s) arthroplasty (eg, facet joint[s] replacement), including facetectomy, laminectomy, foraminotomy, and vertebral column fixation, injection of bone cement, when performed, including fluoroscopy, single level, lumbar spinePolicies naming 0202T
0205UOn the listOphthalmology (age-related macular degeneration), analysis of 3 gene variants (2 CFH gene, 1 ARMS2 gene), using PCR and MALDI- TOF, buccal swab, reported as positive or negative for neovascular age-related macular-degeneration risk associated with zinc supplementsPolicies naming 0205U
0207UNot listedPolicies naming 0207U
0209UOn the listCytogenomic constitutional (genome-wide) analysis, interrogation of genomic regions for copy number, structural changes and areas of homozygosity for chromosomal abnormalitiesPolicies naming 0209U
0211UOn the listOncology (pan-tumor), DNA and RNA by next- generation sequencing, utilizing formalin-fixed paraffin-embedded tissue, interpretative report for single nucleotide variants, copy number alterations, tumor mutational burden, and microsatellite instability, with therapy associationPolicies naming 0211U
0212UOn the listRare diseases (constitutional/heritable disorders), whole genome and mitochondrial DNA sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, probandPolicies naming 0212U
0213TOn the listInjection(s), diagnostic or therapeutic agent, paravertebral facet (zygapophyseal) joint (or nerves innervating that joint) with ultrasound guidance, cervical or thoracic; single levelPolicies naming 0213T
0213UOn the listRare diseases (constitutional/heritable disorders), whole genome and mitochondrial DNA sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, each comparator genome (eg, parent, sibling)Policies naming 0213U
0214TOn the listnjection(s), diagnostic or therapeutic agent, paravertebral facet (zygapophyseal) joint (or nerves innervating that joint) with ultrasound guidance, cervical or thoracic; second levelPolicies naming 0214T
0214UOn the listRare diseases (constitutional/heritable disorders), whole exome and mitochondrial DNA sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, probandPolicies naming 0214U
0215TOn the listInjection(s), diagnostic or therapeutic agent, paravertebral facet (zygapophyseal) joint (or nerves innervating that joint) with ultrasound guidance, cervical or thoracic; third and any additional level(s)Policies naming 0215T
0215UOn the listRare diseases (constitutional/heritable disorders), whole exome and mitochondrial DNA sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, each comparator exome (eg, parent, sibling)Policies naming 0215U
0216TOn the listInjection(s), diagnostic or therapeutic agent, paravertebral facet (zygapophyseal) joint (or nerves innervating that joint) with ultrasound guidance, lumbar or sacral; single level(cid:9)Policies naming 0216T
0216UOn the listNeurology (inherited ataxias), genomic DNA sequence analysis of 12 common genes including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variantsPolicies naming 0216U
0217TOn the listInjection(s), diagnostic or therapeutic agent, paravertebral facet (zygapophyseal) joint (or nerves innervating that joint) with ultrasound guidance, lumbar or sacral; second levelPolicies naming 0217T
0217UOn the listNeurology (inherited ataxias), genomic DNA sequence analysis of 51 genes including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variantsPolicies naming 0217U
0218TNot listedPolicies naming 0218T
0218UOn the listNeurology (muscular dystrophy), DMD gene sequence analysis, including small sequence changes, deletions, duplications, and variants in non-uniquely mappable regions, blood or saliva, identification and characterization of genetic variantsPolicies naming 0218U
0228TNot listedPolicies naming 0228T
0229TNot listedPolicies naming 0229T
0229UOn the listBCAT1 (Branched chain amino acid transaminase 1) or IKZF1 (IKAROS family zinc finger 1) (eg, colorectal cancer) promoter methylation analysisPolicies naming 0229U
0230TNot listedPolicies naming 0230T
0230UOn the listAR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X chromosome inactivation), full sequence analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (STR) expansions, mobile element insertions, and variants in non-uniquely mappable regionsPolicies naming 0230U
0231TNot listedPolicies naming 0231T
0231UOn the listCACNA1A (calcium voltage-gated channel subunit alpha 1A) (eg, spinocerebellar ataxia), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (STR) gene expansions, mobile element insertions, and variants in non- uniquely mappable regionsPolicies naming 0231U
0232UOn the listCSTB (cystatin B) (eg, progressive myoclonic epilepsy type 1A, Unverricht-Lundborg disease), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (STR) expansions, mobile element insertions, and variants in non-uniquely mappable regionsPolicies naming 0232U
0233UOn the listFXN (frataxin) (eg, Friedreich ataxia), gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, short tandem repeat (STR) expansions, mobile element insertions, and variants in non-uniquely mappable regionsPolicies naming 0233U
0234UOn the listMECP2 (methyl CpG binding protein 2) (eg, Rett syndrome), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non-uniquely mappable regionsPolicies naming 0234U
0235UOn the listPTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome), full gene analysis, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non-uniquely mappable regionsPolicies naming 0235U
0236UOn the listSMN1 (survival of motor neuron 1, telomeric) and SMN2 (survival of motor neuron 2, centromeric) (eg, spinal muscular atrophy) full gene analysis, including small sequence changes in exonic and intronic regions, duplications, deletions, and mobile element insertionsPolicies naming 0236U
0237UOn the listCardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia), genomic sequence analysis panel including ANK2, CASQ2, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, RYR2, and SCN5A, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non-uniquely mappable regionsPolicies naming 0237U
0238UOn the listOncology (Lynch syndrome), genomic DNA sequence analysis of MLH1, MSH2, MSH6, PMS2, and EPCAM, including small sequence changes in exonic and intronic regions, deletions, duplications, mobile element insertions, and variants in non- uniquely mappable regionsPolicies naming 0238U
0239UOn the listTargeted genomic sequence analysis panel, solid organ neoplasm, cell-free DNA, analysis of 311 or more genes, interrogation for sequence variants, including substitutions, insertions, deletions, select rearrangements, and copy number variationsPolicies naming 0239U
0242UOn the listTargeted genomic sequence analysis panel, solid organ neoplasm, cell-free circulating DNA analysis of 55-74 genes, interrogation for sequence variants, gene copy number amplifications, and gene rearrangementsPolicies naming 0242U
0244UOn the listOncology (solid organ), DNA, comprehensive genomic profiling, 257 genes, interrogation for single-nucleotide variants, insertions/deletions, copy number alterations, gene rearrangements, tumor-mutational burden and microsatellite instability, utilizing formalin-fixed paraffin-embedded tumor tissuePolicies naming 0244U
0250UOn the listOncology (solid organ neoplasm), targeted genomic sequence DNA analysis of 505 genes, interrogation for somatic alterations (SNVs [single nucleotide variant], small insertions and deletions, one amplification, and four translocations), microsatellite instability and tumor-mutation burdenPolicies naming 0250U
0253TOn the listInsertion of anterior segment aqueous drainage device, without extraocular reservoir; internal approach, into the suprachoroidal spacePolicies naming 0253T
0260UOn the listRare diseases (constitutional/heritable disorders), identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mappingPolicies naming 0260U
0263TOn the listIntramuscular autologous bone marrow cell therapy, with preparation of harvested cells, multiple injections, one leg, including ultrasound guidance, if performed; complete proPolicies naming 0263T
0264TOn the listIntramuscular autologous bone marrow cell therapy, with preparation of harvested cells, multiple injections, one leg, including ultrasound guidance, if performed; complete proPolicies naming 0264T
0264UOn the listRare diseases (constitutional/heritable disorders), identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mappingPolicies naming 0264U
0265TOn the listIntramuscular autologous bone marrow cell therapy, with preparation of harvested cells, multiple injections, one leg, including ultrasound guidance, if performed; unilateral oPolicies naming 0265T
0265UOn the listRare constitutional and other heritable disorders, whole genome and mitochondrial DNA sequence analysis, blood, frozen and formalin-fixed paraffin- embedded (FFPE) tissue, saliva, buccal swabs or cell lines, identification of single nucleotide and copy number variantsPolicies naming 0265U
0266UOn the listUnexplained constitutional or other heritable disorders or syndromes, tissue-specific gene expression by whole-transcriptome and next- generation sequencing, blood, formalin-fixed paraffin-embedded (FFPE) tissue or fresh frozen tissue, reported as presence or absence of splicing or expression changesPolicies naming 0266U
0267UOn the listRare constitutional and other heritable disorders, identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping and whole genome sequencingPolicies naming 0267U
0268UOn the listHematology (atypical hemolytic uremic syndrome [aHUS]), genomic sequence analysis of 15 genes, blood, buccal swab, or amniotic fluidPolicies naming 0268U
0269UOn the listHematology (autosomal dominant congenital thrombocytopenia), genomic sequence analysis of 22 genes, blood, buccal swab, or amniotic fluidPolicies naming 0269U
0270UOn the listHematology (congenital coagulation disorders), genomic sequence analysis of 20 genes, blood, buccal swab, or amniotic fluidPolicies naming 0270U
0272UOn the listHematology (genetic bleeding disorders), genomic sequence analysis of 60 genes and duplication/deletion of PLAU, blood, buccal swab, or amniotic fluid, comprehensivePolicies naming 0272U
0273UOn the listHematology (genetic hyperfibrinolysis, delayed bleeding), analysis of 9 genes (F13A1, F13B, FGA, FGB, FGG, SERPINA1, SERPINE1, SERPINF2 by next-generation sequencing, and PLAU by array comparative genomic hybridization), blood, buccal swab, or amniotic fluidPolicies naming 0273U
0274TOn the listPercutaneous laminotomy/laminectomy (interlaminar approach) for decompression of neural elements, (with or without ligamentous resection, discectomy, facetectomy and/or foraminotomy), any method, under indirect image guidance (eg, fluoroscopic, CT), single or multiple levels, unilateral or bilateral; cervical or thoracicPolicies naming 0274T
0274UOn the listHematology (genetic platelet disorders), genomic sequence analysis of 62 genes and duplication/deletion of PLAU, blood, buccal swab, or amniotic fluidPolicies naming 0274U
0275TNot listedPolicies naming 0275T
0276UOn the listHematology (inherited thrombocytopenia), genomic sequence analysis of 42 genes, blood, buccal swab, or amniotic fluidPolicies naming 0276U
0277UOn the listHematology (genetic platelet function disorder), genomic sequence analysis of 40 genes and duplication/deletion of PLAU, blood, buccal swab, or amniotic fluidPolicies naming 0277U
0278UOn the listHematology (genetic thrombosis), genomic sequence analysis of 14 genes, blood, buccal swab, or amniotic fluidPolicies naming 0278U
0297UOn the listOncology (pan tumor), whole genome sequencing of paired malignant and normal DNA specimens, fresh or formalin-fixed paraffin-embedded (FFPE) tissue, blood or bone marrow, compPolicies naming 0297U
0298UOn the listOncology (pan tumor), whole transcriptome sequencing of paired malignant and normal RNA specimens, fresh or formalin-fixed paraffin- embedded (FFPE) tissue, blood or bone marroPolicies naming 0298U
0299UOn the listOncology (pan tumor), whole genome optical genome mapping of paired malignant and normal DNA specimens, fresh frozen tissue, blood, or bone marrow, comparative structural variPolicies naming 0299U
0300UOn the listOncology (pan tumor), whole genome sequencing and optical genome mapping of paired malignant and normal DNA specimens, fresh tissue, blood, or bone marrow, comparative sequencPolicies naming 0300U
0306UOn the listOncology (minimal residual disease [MRD]), next- generation targeted sequencing analysis, cell-free DNA, initial (baseline) assessment to determine a patient-specific panel for future comparisons to evaluate for MRDPolicies naming 0306U
0307UOn the listOncology (minimal residual disease [MRD]), next- generation targeted sequencing analysis of a patient-specific panel, cell-free DNA, subsequent assessment with comparison to previously analyzed patient specimens to evaluate for MRDPolicies naming 0307U
0312TNot listedPolicies naming 0312T
0313TNot listedPolicies naming 0313T
0314TNot listedPolicies naming 0314T
0315TNot listedPolicies naming 0315T
0316TNot listedPolicies naming 0316T
0317TNot listedPolicies naming 0317T
0318UOn the listPediatrics (congenital epigenetic disorders), whole genome methylation analysis by microarray for 50 or more genes, bloodPolicies naming 0318U
0326UOn the listTargeted genomic sequence analysis panel, solid organ neoplasm, cell-free circulating DNA analysis of 83 or more genes, interrogation for sequence variants, gene copy number amplifications, gene rearrangements, microsatellite instability and tumor mutational burdenPolicies naming 0326U
0329UOn the listOncology (neoplasia), exome and transcriptome sequence analysis for sequence variants, gene copy number amplifications and deletions, gene rearrangements, microsatellite instability and tumor mutational burden utilizing DNA and RNA from tumor with DNA from normal blood or saliva for subtraction, report of clinically significant mutation(s) with therapy associationsPolicies naming 0329U
0331UOn the listOncology (hematolymphoid neoplasia), optical genome mapping for copy number alterations and gene rearrangements utilizing DNA from blood or bone marrow, report of clinically sPolicies naming 0331U
0332UOn the listOncology (pan-tumor), genetic profiling of 8 DNA- regulatory (epigenetic) markers by quantitative polymerase chain reaction (qPCR), whole blood, reported as a high or low probability of responding to immune checkpoint-inhibitor therapyPolicies naming 0332U
0333UOn the listOncology (liver), surveillance for hepatocellular carcinoma (HCC) in high-risk patients, analysis of methylation patterns on circulating cell-free DNA (cfDNA) plus measurement of serum of AFP/AFP- L3 and oncoprotein des-gamma-carboxy- prothrombin (DCP), algorithm reported as normal or abnormal resultPolicies naming 0333U
0334UOn the listOncology (solid organ), targeted genomic sequence analysis, formalin-fixed paraffin- embedded (FFPE) tumor tissue, DNA analysis, 84 or more genes, interrogation for sequence vaPolicies naming 0334U
0335TOn the listInsertion of sinus tarsi implantPolicies naming 0335T
0335UOn the listRare diseases (constitutional/heritable disorders), whole genome sequence analysis, including small sequence changes, copy number variants, deletions, duplications, mobile element insertions, uniparental disomy (UPD), inversions, aneuploidy, mitochondrial genome sequence analysis with heteroplasmy and large deletions, short tandem repeat (STR) gene expansions, fetal sample, identification and categorization of genetic variantsPolicies naming 0335U
0336UOn the listRare diseases (constitutional/heritable disorders), whole genome sequence analysis, including small sequence changes, copy number variants, deletions, duplications, mobile element insertions, uniparental disomy (UPD), inversions, aneuploidy, mitochondrial genome sequence analysis with heteroplasmy and large deletions, short tandem repeat (STR) gene expansions, blood or saliva, identification and categorization of genetic variants, each comparator genome (eg, parent)Policies naming 0336U
0342TOn the listTherapeutic apheresis with selective HDL delipidation and plasma reinfusionPolicies naming 0342T
0343UOn the listOncology (prostate), exosome-based analysis of 442 small noncoding RNAs (sncRNAs) by quantitative reverse transcription polymerase chain reaction (RT-qPCR), urine, reported as molecular evidence of no-, low-, intermediate- or high-risk of prostate cancerPolicies naming 0343U
0345TOn the listTranscatheter mitral valve repair percutaneous approach via the coronary sinusPolicies naming 0345T
0346UNot listedPolicies naming 0346U
0355TNot listedPolicies naming 0355T
0356UOn the listOncology (oropharyngeal or anal), evaluation of 17 DNA biomarkers using droplet digital PCR (ddPCR), cell-free DNA, algorithm reported as a prognostic risk score for cancer recurrencePolicies naming 0356U
0358UOn the listNeurology (mild cognitive impairment), analysis of β- amyloid 1-42 and 1-40, chemiluminescence enzyme immunoassay, cerebral spinal fluid, reported as positive, likely positive, or negativePolicies naming 0358U
0361UNot listedPolicies naming 0361U
0368UOn the listOncology (colorectal cancer), evaluation for mutations of APC, BRAF, CTNNB1, KRAS, NRAS, PIK3CA, SMAD4, and TP53, and methylation markers (MYO1G, KCNQ5, C9ORF50, FLI1, CLIP4, ZNF132 and TWIST1), multiplex quantitative polymerase chain reaction (qPCR), circulating cell-free DNA (cfDNA), plasma, report of risk score for advanced adenoma or colorectal cancerPolicies naming 0368U
0379UOn the listTargeted genomic sequence analysis panel, solid organ neoplasm, DNA (523 genes) and RNA (55 genes) by next-generation sequencing, interrogation for sequence variants, gene copy number amplifications, gene rearrangements, microsatellite instability, and tumor mutational burdenPolicies naming 0379U
0388UOn the listOncology (non-small cell lung cancer), next- generation sequencing with identification of single nucleotide variants, copy number variants, insertions and deletions, and structural variants in 37 cancer-related genes, plasma, with report for alteration detectionPolicies naming 0388U
0391UOn the listOncology (solid tumor), DNA and RNA by next- generation sequencing, utilizing formalin-fixed paraffin-embedded (FFPE) tissue, 437 genes, interpretive report for single nucleotide variants, splice-site variants, insertions/deletions, copy number alterations, gene fusions, tumor mutational burden, and microsatellite instability, with algorithm quantifying immunotherapy response scorePolicies naming 0391U
0397UNot listedPolicies naming 0397U
0398TNot listedPolicies naming 0398T
0400UOn the listObstetrics (expanded carrier screening), 145 genes by next-generation sequencing, fragment analysis and multiplex ligation-dependent probe amplification, DNA, reported as carrier positive or negativePolicies naming 0400U
0401UOn the listCardiology (coronary heart disease [CHD]), 9 genes (12 variants), targeted variant genotyping, blood, saliva, or buccal swab, algorithm reported as a genetic risk score for a coronary eventPolicies naming 0401U
0402TOn the listCollagen cross-linking of cornea, including removal of the corneal epithelium, when performed, and intraoperative pachymetry, when performedPolicies naming 0402T
0408TOn the listInsertion or replacement of permanent cardiac contractility modulation system, including contractility evaluation when performed, and programming of sensing and therapeutic parameters; pulse generator with transvenous electrodesPolicies naming 0408T
0409TOn the listInsertion or replacement of permanent cardiac contractility modulation system, including contractility evaluation when performed, and programming of sensing and therapeutic parameters; pulse generator onlyPolicies naming 0409T
0410TOn the listInsertion or replacement of permanent cardiac contractility modulation system, including contractility evaluation when performed, and programming of sensing and therapeutic parameters; atrial electrode onlyPolicies naming 0410T
0411TOn the listInsertion or replacement of permanent cardiac contractility modulation system, including contractility evaluation when performed, and programming of sensing and therapeutic parameters; ventricular electrode onlyPolicies naming 0411T
0412TOn the listRemoval of permanent cardiac contractility modulation system; pulse generator onlyPolicies naming 0412T
0413TOn the listRemoval of permanent cardiac contractility modulation system; transvenous electrode (atrial or ventricular)Policies naming 0413T
0414TOn the listRemoval and replacement of permanent cardiac contractility modulation system pulse generator onlyPolicies naming 0414T
0415TOn the listRepositioning of previously implanted cardiac contractility modulation transvenous electrode, (atrial or ventricular lead)Policies naming 0415T
0416TOn the listRelocation of skin pocket for implanted cardiac contractility modulation pulse generatorPolicies naming 0416T
0417TOn the listProgramming device evaluation (in person) with iterative adjustment of the implantable device to test the function of the device and select optimal permanent programmed values with analysis, including review and report, implantable cardiac contractility modulation systemPolicies naming 0417T
0418TOn the listInterrogation device evaluation (in person) with analysis, review and report, includes connection, recording and disconnection per patient encounter, implantable cardiac contractility modulation systemPolicies naming 0418T
0421TNot listedPolicies naming 0421T
0424TNot listedPolicies naming 0424T
0425TNot listedPolicies naming 0425T
0426TNot listedPolicies naming 0426T
0427TNot listedPolicies naming 0427T
0428TNot listedPolicies naming 0428T
0429TNot listedPolicies naming 0429T
0430TNot listedPolicies naming 0430T
0431TNot listedPolicies naming 0431T
0432TNot listedPolicies naming 0432T
0433TNot listedPolicies naming 0433T
0434TNot listedPolicies naming 0434T
0435TNot listedPolicies naming 0435T
0436TNot listedPolicies naming 0436T
0449TOn the listInsertion of aqueous drainage device, without extraocular reservoir, internal approach, into the subconjunctival space; initial devicePolicies naming 0449T
0450TNot listedPolicies naming 0450T
0468TNot listedPolicies naming 0468T
0474TOn the listInsertion of anterior segment aqueous drainage device, with creation of intraocular reservoir, internal approach, into the supraciliary spacePolicies naming 0474T
0483TOn the listTranscatheter mitral valve implantation/replacement (TMVI) with prosthetic valve; percutaneous approach, including transseptal puncture, when performedPolicies naming 0483T
0484TOn the listTranscatheter mitral valve implantation/replacement (TMVI) with prosthetic valve; transthoracic exposure (eg, thoracotomy, transapical)Policies naming 0484T
0494TOn the listSurgical preparation and cannulation of marginal (extended) cadaver donor lung(s) to ex vivo organ perfusion system, including decannulation, separation from the perfusion system, and cold preservation of the allograft prior to implantation, when performedPolicies naming 0494T
0495TOn the listInitiation and monitoring marginal (extended) cadaver donor lung(s) organ perfusion system by physician or qualified health care professional, including physiological and laboratory assessment (eg, pulmonary artery flow, pulmonary artery pressure, left atrial pressure, pulmonary vascular resistance, mean/peak and plateau airway pressure, dynamic compliance and perfusate gas analysis), including bronchoscopy and X ray when performed; first two hours in sterile fieldPolicies naming 0495T
0496TNot listedPolicies naming 0496T
0501TNot listedPolicies naming 0501T
0502TNot listedPolicies naming 0502T
0503TNot listedPolicies naming 0503T
0504TNot listedPolicies naming 0504T
0505TOn the listEndovenous femoral-popliteal arterial revascularization, with transcatheter placement of intravascular stent graft(s) and closure by any method, including percutaneous or open vascular access, ultrasound guidance for vascular access when performed, all catheterization(s) and intraprocedural roadmapping and imaging guidance necessary to complete the intervention, all associated radiological supervision and interpretation, when performed, with crossing of the occlusive lesion in an extraluminal fashionPolicies naming 0505T
0510TOn the listRemoval of sinus tarsi implantPolicies naming 0510T
0511TOn the listRemoval and reinsertion of sinus tarsi implantPolicies naming 0511T
0515TOn the listInsertion of wireless cardiac stimulator for left ventricular pacing, including device interrogation and programming, and imaging supervision and interpretation, when performed; complete system (includes electrode and generator [transmitter and battery])Policies naming 0515T
0516TOn the listInsertion of wireless cardiac stimulator for left ventricular pacing, including device interrogation and programming, and imaging supervision and interpretation, when performed; electrode onlyPolicies naming 0516T
0517TOn the listInsertion of wireless cardiac stimulator for left ventricular pacing, including device interrogation and programming, and imaging supervision and interpretation, when performed; pulse generator component(s) (battery and/or transmitter) onlyPolicies naming 0517T
0518TNot listedPolicies naming 0518T
0519TOn the listRemoval and replacement of pulse generator for wireless cardiac stimulator for left ventricular pacing, including device interrogation and programming; both components (battery and transmitter)Policies naming 0519T
0520TOn the listRemoval and replacement of pulse generator for wireless cardiac stimulator for left ventricular pacing, including device interrogation and programming; battery component onlyPolicies naming 0520T
0521TNot listedPolicies naming 0521T
0522TNot listedPolicies naming 0522T
0524TOn the listEndovenous catheter directed chemical ablation with balloon isolation of incompetent extremity vein, open or percutaneous, including all vascular access, catheter manipulation, diagnostic imaging, imaging guidance and monitoringPolicies naming 0524T
0525TOn the listInsertion or replacement of intracardiac ischemia monitoring system, including testing of the lead and monitor, initial system programming, and imaging supervision and interpretation; complete system (electrode and implantable monitor)Policies naming 0525T
0526TOn the listInsertion or replacement of intracardiac ischemia monitoring system, including testing of the lead and monitor, initial system programming, and imaging supervision and interpretation; electrode onlyPolicies naming 0526T
0527TOn the listInsertion or replacement of intracardiac ischemia monitoring system, including testing of the lead and monitor, initial system programming, and imaging supervision and interpretation; implantable monitor onlyPolicies naming 0527T
0528TOn the listProgramming device evaluation (in person) of intracardiac ischemia monitoring system with iterative adjustment of programmed values, with analysis, review, and reportPolicies naming 0528T
0529TOn the listInterrogation device evaluation (in person) of intracardiac ischemia monitoring system with analysis, review, and reportPolicies naming 0529T
0530TOn the listRemoval of intracardiac ischemia monitoring system, including all imaging supervision and interpretation; complete system (electrode and implantable monitor)Policies naming 0530T
0531TOn the listRemoval of intracardiac ischemia monitoring system, including all imaging supervision and interpretation; electrode onlyPolicies naming 0531T
0532TOn the listRemoval of intracardiac ischemia monitoring system, including all imaging supervision and interpretation; implantable monitor onlyPolicies naming 0532T
0537TNot listedPolicies naming 0537T
0538TNot listedPolicies naming 0538T
0539TNot listedPolicies naming 0539T
0540TNot listedPolicies naming 0540T
0544TOn the listTranscatheter mitral valve annulus reconstruction, with implantation of adjustable annulus reconstruction device, percutaneous approach including transseptal puncturePolicies naming 0544T
0545TOn the listTranscatheter tricuspid valve annulus reconstruction with implantation of adjustable annulus reconstruction device, percutaneous approachPolicies naming 0545T
0569TOn the listTranscatheter tricuspid valve repair, percutaneous approach; initial prosthesisPolicies naming 0569T
0570TNot listedPolicies naming 0570T
0581TOn the listAblation, malignant breast tumor(s), percutaneous, cryotherapy, including imaging guidance when performed, unilateralPolicies naming 0581T
0584TOn the listIslet cell transplant, includes portal vein catheterization and infusion, including all imaging, including guidance, and radiological supervision and interpretation, when performed; percutaneousPolicies naming 0584T
0585TOn the listIslet cell transplant, includes portal vein catheterization and infusion, including all imaging, including guidance, and radiological supervision and interpretation, when performed; laparoscopicPolicies naming 0585T
0586TOn the listIslet cell transplant, includes portal vein catheterization and infusion, including all imaging, including guidance, and radiological supervision and interpretation, when performed; openPolicies naming 0586T
0587TNot listedPolicies naming 0587T
0588TNot listedPolicies naming 0588T
0589TNot listedPolicies naming 0589T
0590TNot listedPolicies naming 0590T
0596TOn the listTemporary female intraurethral valve-pump (ie, voiding prosthesis); initial insertion, including urethral measurementPolicies naming 0596T
0597TOn the listTemporary female intraurethral valve-pump (ie, voiding prosthesis); replacementPolicies naming 0597T
0616TNot listedPolicies naming 0616T
0617TNot listedPolicies naming 0617T
0618TNot listedPolicies naming 0618T
0620TOn the listEndovascular venous arterialization, tibial or peroneal vein, with transcatheter placement of intravascular stent graft(s) and closure by any method, including percutaneous or open vascular access, ultrasound guidance for vascular access when performed, all catheterization(s) and intraprocedural roadmapping and imaging guidance necessary to complete the intervention, all associated radiological supervision and interpretation, when performedPolicies naming 0620T
0627TOn the listPercutaneous injection of allogeneic cellular and/or tissue-based product, intervertebral disc, unilateral or bilateral injection, with fluoroscopic guidance, lumbar; first level [VAST, Via Disc]Policies naming 0627T
0628TNot listedPolicies naming 0628T
0629TOn the listPercutaneous injection of allogeneic cellular and/or tissue-based product, intervertebral disc, unilateral or bilateral injection, with CT guidance, lumbar; first level [VAST, Via Disc]Policies naming 0629T
0630TNot listedPolicies naming 0630T
0655TOn the listTransperineal focal laser ablation of malignant prostate tissue, including transrectal imaging guidance, with MR-fused images or other enhanced ultrasound imagingPolicies naming 0655T
0672TOn the listEndovaginal cryogen-cooled, monopolar radiofrequency remodeling of the tissues surrounding the female bladder neck and proximal urethra for urinary incontinencePolicies naming 0672T
0686TOn the listHistotripsy (ie, non-thermal ablation via acoustic energy delivery) of malignant hepatocellular tissue, including image guidancePolicies naming 0686T
0745TOn the listCardiac focal ablation utilizing radiation therapy for arrhythmia; noninvasive arrhythmia localization and mapping of arrhythmia site (nidus), derived from anatomical image data (eg, CT, MRI, or myocardial perfusion scan) and electrical data (eg, 12-lead ECG data), and identification of areas of avoidancePolicies naming 0745T
0746TOn the listCardiac focal ablation utilizing radiation therapy for arrhythmia; conversion of arrhythmia localization and mapping of arrhythmia site (nidus) into a multidimensional radiation treatment planPolicies naming 0746T
0747TOn the listCardiac focal ablation utilizing radiation therapy for arrhythmia; delivery of radiation therapy, arrhythmiaPolicies naming 0747T
1108GNot listedPolicies naming 1108G
1118ANot listedPolicies naming 1118A
11920On the listTattooing, intradermal introduction of insoluble opaque pigments to correct color defects of skin, including micropigmentation; 6.0 sq cm or lessPolicies naming 11920
11921On the listTattooing, intradermal introduction of insoluble opaque pigments to correct color defects of skin, including micropigmentation; 6.1 to 20.0 sq cmPolicies naming 11921
11922Not listedPolicies naming 11922

And 2,269 more in the original policy.

All Anthem Blue Cross Blue Shield of Georgia policies · Anthem Blue Cross Blue Shield of Georgia prior authorization CPT list

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