Capture of biologic and biosimilar dispensings in a consortium of U.S.-based claims databases: Utilization of national drug codes and Healthcare Common Procedure Coding System modifiers in medical claims
- PMID: 31802568
- DOI: 10.1002/pds.4934
Capture of biologic and biosimilar dispensings in a consortium of U.S.-based claims databases: Utilization of national drug codes and Healthcare Common Procedure Coding System modifiers in medical claims
Abstract
Purpose: To assess the capture of biologics (originator and biosimilar) in the Biologics and Biosimilars Collective Intelligence Consortium (BBCIC) Distributed Research Network (DRN), with a focus on medical claim National Drug Code (NDC), a new data field, and Healthcare Common Procedure Coding System (HCPCS) modifier.
Methods: We conducted a repeated cross-sectional study among patients with medical and pharmacy benefits enrolled in insurance plans participating in the BBCIC DRN between 1 January 2013 and 30 September 2017. We calculated the proportion of medical claims with ≥1 NDC and identified select biologics using four different approaches: (a) specific HCPCS alone, (b) specific HCPCS and NDC, (c) non-specific HCPCS with NDC, and (d) HCPCS with modifiers (applicable to biosimilars). Numbers of dispensings were calculated for each biologic by approach and select patient and claim characteristics.
Results: More than 1.5 million eligible participants contributed approximately 4 million person-years of data, including 1.2 billion medical claims. The proportion of medical claims with ≥1 NDC increased from 1.2% in 2013 to 3.0% in 2017. Medical claim NDCs identified 39% and 28% of vedolizumab dispensed in 2014 and 2015 and 30% of Epogen/Procrit dispensed overall. Out of 26,381 filgrastim biosimilar dispensings identified, 51% had a HCPCS modifier and 12% had a medical claim NDC for Zarxio. HCPCS modifiers and medical claim NDCs were present for 38% and 3% of all infliximab biosimilars dispensed (total n = 1,244).
Conclusions: Medical claim NDC and HCPCS modifier improves identification of select biologics without product-specific HCPCS code, thereby facilitating product-specific biologic research.
Keywords: Medical Claim National Drug Code; biologics; biosimilars; healthcare common procedure coding system modifiers; pharmacoepidemiology.
© 2019 John Wiley & Sons, Ltd.
References
REFERENCES
-
- Strom BL, Kimmel SE, Hennessy S. Pharmacoepidemiology. 5th ed. Hoboken, NJ: Wiley-Blackwell; 2012.
-
- Centers for Medicare & Medicaid Services. Medicare Part B drug average sales price: Part B Biosimilar biological product payment and required modifiers. 2018. https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Part-B-Drugs/McrPa.... Accessed October 23, 2018.
-
- National Drug Code Requirement: UnitedHealthcare Commercial and UnitedHealthcare Medicare Advantage Professional and Hospital Outpatient Claims. https://www.uhcprovider.com/content/dam/provider/docs/public/claims/NDC-.... Accessed March 30, 2019.
-
- ATFoBCI S, Baldziki M, Brown J, et al. Utilizing data consortia to monitor safety and effectiveness of biosimilars and their innovator products. J Manag Care Spec Pharm. 2015;21(1):23-34.
-
- Mendelsohn AB, Barr CE, Brown JS, et al. Development and management of a distributed research network for evaluating real-would outcomes for originator biologics and biosimilars. J Manag Care Pharm. 2018;24(10-a suppl):S101-S102.