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Reporting the Correct Modifier for 340B Drugs

Published on 

Tuesday, April 17, 2018

 | Billing 

The Outpatient Prospective Payment System (OPPS) final rule is released each year around the first of November, and that only gives hospitals two months (during an already busy and short-staffed holiday season I might add) to implement the new requirements for the coming year. Sometimes this means beginning to make changes before final guidance and addenda are available – a good way to get a jump on necessary revisions. The caution for this approach is to be sure to check any additional guidance and revised addenda prior to implementation and make the necessary adjustments.

For example, the 2018 OPPS final rule required the reporting of modifiers for drugs purchased through the 340B drug discount program. Modifier JG is reported with separately payable drugs with a status indicator of “K” by most hospitals purchasing drugs through the 340B program. The JG modifier causes Medicare payment to be made at average sale price (ASP) minus 22.5%, instead of the ASP +6% that is paid for separately payable drugs not purchased through the 340B program and a few other exceptions. Modifier TB is reported on the applicable drugs by certain excepted types of providers (rural sole-community hospitals, children’s hospitals and cancer hospitals) and for pass-through drugs which have a status indicator of “G.” If your hospital proactively added the applicable modifiers to your chargemaster, did you remember to verify that the status indicator for each drug did not change for 2018?

In claim review, MMP has observed some drugs, whose status indicator changed from “G” in 2017 to “K” in 2018, being reported with the incorrect modifier. Status indicator “G” pass-through drugs purchased through the 340B program are reported with a TB modifier, but once their SI changes to “K” they are to be reported with a JG modifier resulting in a reduced drug payment. Below is a table of those drugs that had a status indicator of “G” for 2017 that changed to “K” for 2018.

HCPCS CodeOct-17
SI
Jan-18
SI
ChangeFull Description (2018)
J0596GKG to KInjection, C1 esterase inhibitor (recombinant), Ruconest, 10 units
J0695GKG to KInjection, ceftolozane 50 mg and tazobactam 25 mg
J0875GKG to KInjection, dalbavancin, 5 mg
J1833GKG to KInjection, isavuconazonium, 1 mg
J2407GKG to KInjection, oritavancin, 10 mg
J2502GKG to KInjection, pasireotide long acting, 1 mg
J2547GKG to KInjection, peramivir, 1 mg
J2860GKG to KInjection, siltuximab, 10 mg
J3090GKG to KInjection, tedizolid phosphate, 1 mg
J7313GKG to KInjection, fluocinolone acetonide, intravitreal implant, 0.01 mg
J8655GKG to KNetupitant 300 mg and palonosetron 0.5 mg
J9032GKG to KInjection, belinostat, 10 mg
J9039GKG to KInjection, blinatumomab, 1 microgram
J9271GKG to KInjection, pembrolizumab, 1 mg
J9299GKG to KInjection, nivolumab, 1 mg

Hospitals may want to verify again that the modifiers they are reporting for drugs purchased through the 340B program are correct and appropriate based on the drug’s OPPS status indicator. When billing Medicare, it is a good idea to check and double-check as things can change in an instant.

Article Author: Debbie Rubio, BS MT (ASCP)
Debbie Rubio, BS MT (ASCP), was the Manager of Regulatory Affairs and Compliance at Medical Management Plus, Inc. Debbie has over twenty-seven years of experience in healthcare including nine years as the Clinical Compliance Coordinator at a large multi-facility health system. In her current position, Debbie monitors, interprets and communicates current and upcoming regulatory and compliance issues as they relate to specific entities concerning Medicare and other payers.

This material was compiled to share information.  MMP, Inc. is not offering legal advice. Every reasonable effort has been taken to ensure the information is accurate and useful.