| Literature DB >> 29326845 |
Kwame Owusu-Edusei1, Carla A Winston1, Suzanne M Marks1, Adam J Langer1, Roque Miramontes1.
Abstract
OBJECTIVE: To evaluate TB test usage and associated direct medical expenditures from 2013 private insurance claims data in the United States (US).Entities:
Year: 2017 PMID: 29326845 PMCID: PMC5672639 DOI: 10.1155/2017/3816432
Source DB: PubMed Journal: Tuberc Res Treat ISSN: 2090-150X
Current procedural terminology (CPT) codes and their description for the TB-specific and the nonspecific TB tests.
| CPT code | Description (source: American Medical Association online CPT search [ |
|---|---|
|
| |
| 86480 | Tuberculosis test, cell mediated immunity antigen response measurement; gamma interferon (QuantiFERON-TB Gold In-Tube [QFT-GIT])† |
| 86481 | Tuberculosis test, cell mediated immunity antigen response measurement; enumeration of gamma interferon-producing T-cells in cell suspension (T-SPOT.TB [T-Spot])† |
| 86580 | Skin test; tuberculosis, intradermal |
| 87555 | Infectious agent detection by nucleic acid (DNA or RNA); |
| 87556 | Infectious agent detection by nucleic acid (DNA or RNA); |
| 87557 | Infectious agent detection by nucleic acid (DNA or RNA); |
|
| |
|
| |
| 71020 | Radiologic examination, chest, 2 views, frontal and lateral |
| 71260 | Computed tomography, thorax; with contrast material(s) |
| 87116 | Culture, tubercle, or other acid-fast bacilli (e.g., TB, AFB, and mycobacteria) any source, with isolation and presumptive identification of isolates |
| 87118 | Culture, mycobacterial, definitive identification, each isolate |
| 87143 | Culture, typing; gas liquid chromatography (GLC) or high pressure liquid chromatography (HPLC) method |
| 87149 | Culture, typing; identification by nucleic acid (DNA or RNA) probe, direct probe technique, per culture or isolate, each organism probed |
| 87150 | Culture, typing; identification by nucleic acid (DNA or RNA) probe, amplified probe technique, per culture or isolate, each organism probed |
| 87153 | Culture, typing; identification by nucleic acid sequencing method, each isolate (e.g., sequencing of the 16S rRNA gene) |
| 87158 | Culture, typing; other methods |
| 87188 | Susceptibility studies, antimicrobial agent; macrobroth dilution method, each agent |
| 87190 | Susceptibility studies, antimicrobial agent; mycobacteria, proportion method, each agent |
| 87206 | Smear, primary source with interpretation; fluorescent and/or acid fast stain for bacteria, fungi, parasites, viruses, or cell types |
| 87550 | Infectious agent detection by nucleic acid (DNA or RNA); mycobacteria species, direct probe technique |
| 87551 | Infectious agent detection by nucleic acid (DNA or RNA); mycobacteria species, amplified probe technique |
| 87552 | Infectious agent detection by nucleic acid (DNA or RNA); mycobacteria species, quantification |
| 87798 | Infectious agent detection by nucleic acid (DNA or RNA), not otherwise specified; amplified probe technique, each organism |
| 87799 | Infectious agent detection by nucleic acid (DNA or RNA), not otherwise specified; quantification, each organism |
†The brand names for the respective IGRA testing method CPT codes (i.e., QuantiFERON-TB Gold In-Tube [QFT-GIT] for 86480 and T-SPOT.TB [T-Spot] for 86481) were used because they were the only IGRA tests approved by the Food and Drug Administration (FDA) as of 2013 [7].
Figure 1Estimated claims rates (number/100,000 enrollees) for the TB-specific tests. TB, tuberculosis; NAAP, nucleic acid amplification probe; NADP, nucleic acid direct probe; NAQ, nucleic acid quantification. The brand names for the respective IGRA testing method CPT codes (i.e., QuantiFERON-TB Gold In-Tube [QFT-GIT] for 86480 and T-SPOT.TB [T-Spot] for 86481) were used because they were the only IGRA tests approved by the Food and Drug Administration (FDA) as of 2013 [7].
Figure 2Estimated claims rates (number/100,000 enrollees) for the nonspecific TB tests. TB, tuberculosis; NAAP, nucleic acid amplification probe; NADP, nucleic acid direct probe; NAQ, nucleic acid quantification; NA, nucleic acid; NOS, not otherwise specified; GLC, gas liquid chromatography; HPLC, high pressure liquid chromatography.
Summary regression results. Dependent variable: log of the medical expenditures of test for 86580 (TST) and 86480 (QFT-GIT). N = 628,595.
| Independent variables | Coefficient ( | Transformed coefficient (%) [95% CI]‡ |
|---|---|---|
| Age of patient | 0.0048 [0.0045 to 0.0051] | 0.48 [0.45 to 0.51] |
| Age-squared variable | −0.0000558 [−0.0000603 to −0.0000513] | −0.0056 [−0.0060 to −0.0051] |
| Quantity of services | 0.16263 [0.1577 to 0.1676] | 16.26 [15.77 to 16.76] |
| Gender | ||
| Male | Referent | Referent |
| Female | −0.0032 [−0.0059 to −0.0006] | −0.32 [−0.59 to −0.06] |
| Data supplier | ||
| Employer | Referent | Referent |
| Health plan | −0.0059 [−0.0091 to −0.0026] | −0.59 [−0.91 to −0.26] |
| Drug coverage? | ||
| No | Referent | Referent |
| Yes | −0.005 [−0.0086 to −0.0014] | −0.5 [−0.86 to −0.14] |
| Region | ||
| South | Referent | Referent |
| Northeast | 0.1147 [0.1111 to 0.1183] | 12.15 [11.75 to 12.56] |
| North Central | 0.2134 [0.2092 to 0.2176] | 23.79 [23.27 to 24.31] |
| West | 0.2795 [0.2757 to 0.2833] | 32.25 [31.75 to 32.75] |
| Unknown | 0.1743 [0.1653 to 0.1833] | 19.04 [17.97 to 20.12] |
| Health plan type | ||
| Comprehensive | Referent | Referent |
| Exclusive provider organization (EPO) | −0.0692 [−0.083 to −0.0553] | −6.69 [−7.96 to −5.38] |
| Health maintenance organization (HMO) | −0.007 [−0.0195 to 0.0056] | −0.7 [−1.93 to 0.56] |
| Point of service (POS) | −0.0478 [−0.0609 to −0.0348] | −4.67 [−5.91 to −3.42] |
| Preferred provider organization (PPO) | −0.0306 [−0.0428 to −0.0183] | −3.01 [−4.19 to −1.81] |
| POS with capitation | −0.1314 [−0.1502 to −0.1127] | −12.31 [−13.95 to −10.66] |
| Consumer driven health plan (CDHP) | −0.0795 [−0.0928 to −0.0662] | −7.64 [−8.86 to −6.41] |
| High deductible health plan (HDHP) | −0.0996 [−0.1129 to −0.0863] | −9.48 [−10.68 to −8.27] |
| Expenditures (difference) | ||
| 86580 (TST) | Referent | Referent |
| 86480 (QFT-GIT) | 2.0627 [2.0587 to 2.0666] | 686.72 [683.58 to 689.79] |
Significance levels: p < 0.01; p < 0.05. †The t-values associated with the coefficients were derived from bootstrap-generated standard errors with 50 replications. ‡Because the dependent variables in the regression analyses were the natural log of dependent variable (medical expenditures), the coefficients were transformed as coefficient (β)∗100 and interpreted as the relative change (in percentage) per unit change in the independent variable (IV) for the continuous IVs and as (e − 1)∗100 and interpreted as the relative difference (in percentage) in the estimated medical expenditures when compared with the referent (or omitted) category [13]. The brand names for the respective IGRA testing method CPT codes (i.e., QuantiFERON-TB Gold In-Tube [QFT-GIT] for 86480 and T-SPOT.TB [T-Spot] for 86481) were used because they were the only IGRA tests approved by the Food and Drug Administration (FDA) as of 2013 [7].
Summary results showing the unadjusted and adjusted average medical expenditures for all the tests (2013 United States dollars).
| Test | Unadjusted average medical expenditures | Adjusted average medical expenditures† | CMS | Relative difference from CMS |
|---|---|---|---|---|
|
| ||||
| 86481 (T-SPOT.TB [T-Spot]) | 140.77 [104.52] | 105.81 [103.72–107.94] | 102.99 | 2.7% |
| 87556 (NAAP; | 123.34 [141.54] | 74.45 [68.53–80.87] | 48.24 | 54.3% |
| 87557 (NAQ; | 77.53 [25.84] | 73.1 [68.09–78.47] | 58.88 | 24.1% |
| 86480 (QuantiFERON-TB Gold In-Tube [QFT-GIT]) | 86.96 [88.08] | 69.14 [68.83–69.46] | 85.20 | −18.8% |
| 87555 (NADP; | 73.77 [75.4] | 45.78 [37.51–55.88] | 27.57 | 66.1% |
| 86580 (tuberculin skin test [TST]) | 10.52 [26.59] | 8.68 [8.67–8.69] | 8.64 | 0.4% |
|
| ||||
|
| ||||
| 71260 (chest computerized tomography) | 454.23 [573.78] | 251.11 [250.33–251.89] | 266.40 | −5.7% |
| 87153 (culture, typing; NA sequencing, each isolate) | 193.31 [149.87] | 145.08 [135.66–155.15] | 158.57 | −8.5% |
| 87150 (culture, typing; NAAP, each org. probed) | 275.85 [396.52] | 135.04 [130.26–140] | 48.24 | 179.9% |
| 87552 (NAQ; mycobacteria species) | 127.85 [88.91] | 92.66 [52.48–163.61] | 58.88 | 57.4% |
| 87799 (NAQ, NOS; each organism) | 122.78 [307.61] | 78.86 [78.36–79.36] | 58.88 | 33.9% |
| 87550 (NADP; mycobacteria species) | 84.55 [85.42] | 60.42 [45.03–81.07] | 27.57 | 119.1% |
| 87798 (NAAP, NOS; each organism) | 78.58 [138.91] | 47.54 [47.44–47.63] | 48.24 | −1.4% |
| 87551 (NAAP; mycobacteria species) | 84.12 [221.03] | 45.89 [41.94–50.21] | 48.28 | −5.0% |
| 87188 (susceptibility studies; macrobroth dilution) | 125.81 [207.41] | 39.65 [35.72–44.01] | 9.12 | 334.7% |
| 71020 (chest radiograph; 2 views) | 63.39 [101.58] | 38.16 [38.13–38.2] | 30.96 | 23.3% |
| 87143 (culture, typing; GLC/HPLC) | 60.96 [61.75] | 37.08 [32.77–41.96] | 17.22 | 115.3% |
| 87116 (culture, tubercle/other acid-fast bacilli) | 57.36 [91.95] | 31.32 [30.94–31.71] | 14.85 | 110.9% |
| 87190 (susceptibility studies; mycobacteria) | 51.69 [70.78] | 24.8 [18.56–33.13] | 7.77 | 219.1% |
| 87118 (culture, mycobacterial, each isolate) | 37.62 [50.52] | 20.35 [19.38–21.37] | 15.04 | 35.3% |
| 87149 (culture, typing; NADP, each org. probed) | 25.35 [75.55] | 18.51 [18.44–18.57] | 27.57 | −32.9% |
| 87206 (smear microscopy) | 25 [52.12] | 12.69 [12.58–12.8] | 7.39 | 72.4% |
| 87158 (culture, typing; other methods) | 14.53 [28.34] | 9.08 [8.7–9.48] | 7.19 | 26.3% |
†Arranged in decreasing order of magnitude. Significance levels: p < 0.01, p < 0.05 higher than the next estimate. CMS, Centers for Medicare and Medicaid Services; SD, standard deviation; TB, tuberculosis; NAAP, nucleic acid amplification probe; NADP, nucleic acid direct probe; NAQ, nucleic acid quantification; NA, nucleic acid; NOS, not otherwise specified; GLC, gas liquid chromatography; HPLC, high pressure liquid chromatography. The brand names for the respective IGRA testing method CPT codes (i.e., QuantiFERON-TB Gold In-Tube [QFT-GIT] for 86480 and T-SPOT.TB [T-Spot] for 86481) were used because they were the only IGRA tests approved by the Food and Drug Administration (FDA) as of 2013 [7].