I work for a DME and respiratory therapy provider and I'm taking a closer
look at the Home Oxygen reporting requirements on the 837P transaction.  We
currently provide detailed Oxygen Certificate of Medical Necessity (CMN)
information to the Medicare DMERC carriers.  Reading the IG it looks like
Home Oxygen information is divided between the following segments:
CR5 - Home Oxygen Therapy Information (page 423) (Required on all initial,
renewal and revision home oxygen therapy claims.
CRC - DMERC Condition Indicator (page 432) (Required on all oxygen therapy
and DME claims that require a CMN)
DTP - Date - Last Certification Date (page 442) (Required if it's necessary
to include supporting documentation for DMERC claims and on CMNs)
DTP - Date - Oxygen Saturation/Arterial Blood Gas Test (page 449) (Required
on initial oxygen therapy service lines involving CMNs.)
MEA - Test Result (page 464) (Required on service lines which bill/report
Concentration, Hemoglobin, Hematocrit, Epoetin Starting Dosage, Creatin and
Oxygen)
REF - Oxygen Flow Rate (page 480) (Required on oxygen therapy CMN claims
where service line reports oxygen flow rate.
PER - Ordering Provider Contact Info (page 538) (Required when service
involve an oxygen therapy CMN)

The situational usage for most of these is related to the CMN, however the
CR5 and MEA situational usage seems to be related to all oxygen claims, ie
not just CMN and therefore not just Medicare/DMERC.

The information on CR5 and MEA includes detailed clinical results which we
don't collect except for Medicare patients.  To my knowledge, we don't have
payors looking for this information either.

Questions:
1) Are the different Situational Usage definitions for these various
segments an oversight by those writing the IG or was it intentional?
2)   Are there any payors out there who will be looking for this
information?

Any help you can provide would be greatly appreciated!

Thanks.

Zena Jacobi
Systems Analyst Specialist
Apria Healthcare
Phone: 949-639-2477
Fax: 949-639-6667




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