New HIPAA Standards Clear Regulatory Hurdle, Approach Flaming Commentary Hoops
Tired of the ambiguities and outdated constraints of the electronic claim, remittance advice, eligibility and other X12 transactions? Help is on the way. Or at least it's coming into view.
The enabling regulation to adopt a new version of those standards has cleared the Department of Health and Human Services and has been passed on to Office of Management and Budget for final review. OMB has 30 days [OOPS! Meant to verify this before posting. In truth the rule of thumb is 90 days for the review; insiders say it is on a fast track, though. -Ed.] to approve it (with or without revisions negotiated with HHS) or reject it.
I was fortunate to have the opportunity to participate in some of the X12 workgroups that built the new standards, and am certain that the new standards will improve efficiency and reduce the number of customizations and workarounds. We won't be able to say goodbye to those nasty Companion Guides, but at least they will be thinner.
Besides reducing ambiguity in hundreds of passages -- saying when NOT to send data as well as when to send it, for example -- the updates incorporate a number of issues currently vexing implementers:
- Unambiguous instructions for consistent implementation of National Provider Identifier submissions across all transactions and all payers.
- Intrinsic support for the Present on Admission data, rather than the K3 stopgap introduced last year.
- Support for the ICD-10 codeset, not available in the current 4010A1 standards.
- Better, clearer remittance advice instructions and standards, including mandatory utilization of the Remark Codes segment.
The standards were developed over a period of months and published back in 2004 and 2005. First the draft guides were released for public comment, then the workgroups responded to each of comments and finalized the implementation guides (now referred to as "Technical Report 3's" or TR3's) and submitted them for approval via X12's consensus process.
It has taken three years for HHS to put together the regulatory language to adopt them.
And once that draft regulation is released will come another comment period.
Um, what was that?
X12 is anxious about this. Tagging a regulatory comment period on to the standards development comment period brings a lot of new participants out of the woodwork. While techically this may improve the end result, it also stands to send the standards folks back to their own review/comment/edit process, further delaying implementation.
Last time this happened, it was under the deadline for adoption of the original HIPAA standards -- the finished 4010 guides got hurriedly updated with the A1 Addendas, and the industry has had to work out of two sets of books ever since. (I recommend purchasing the Combined Guides for those who have difficulty reading out of two volumes at once. They're not "official" but they will keep you from making a lot of errors or at least getting a lot of headaches. Go to www.wpc-edi.com and check out the HIPAA link.)
I haven't been able to participate in X12 for awhile, but I know they are all over this. I hope that some of their collaboration with the regulators produces both better standards and better adoption processes. We soon shall see.








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