Inpatient rehabilitation facilities (IRFs) continue to face audits for multiple agencies, and additional documentation requests (ADRs) have become routine rather than the exception. In our last article, we encouraged IRFs to stay focused through 2017 on establishing processes to monitor compliance with the documentation requirements to support IRF claims. The question seems to be not “who’s auditing now?” but “who isn’t?”
In this article, we will look at some of the Medicare Administrative Contractors’ (MACs’) activities over recent months and provided some updates based on their reported activities from their own websites. While not all the MACs have posted issues and/or results of recent reviews, several MACs are actively reviewing IRFs, and we’ve summarized that information below.
WPS Government Health Administrators
WPS completed prepayment reviews for CMGs 0701-0704 and/or 0801-0806, regardless of tier level, during the period of Oct. 1, 2016 through Dec. 31, 2016. Of the 288 claims reviewed, 97 of them were denied in full related to the following documentation issues:
- Documentation did not support that upon admission to the IRF, the patient required intensive rehabilitation therapy services that are uniquely provided in IRFs;
- Documentation did not support that the patient’s medical management and rehabilitation needs demanded an inpatient stay and close physician involvement; and
- Documentation was insufficient to support that the service(s) billed met Medicare technical requirements and medical necessity guidelines.
Current prepayment reviews continued for CMGS A0801-A0804 and A2001-A2004 in Alabama, Georgia, and Tennessee, as well as D0801-D0804 in the state of Alabama.
These issues have been ongoing for Cahaba, and there doesn’t appear to be an end date. Orthopedic and debility cases are frequently denied for several reasons.
On Jan. 9, 2017, CGS posted an informational article on Comprehensive Error Rate Testing (CERT) errors and common denial reasons noted in CGS’s CERT reviews. Five common reasons for denial by CERT were listed as:
- Patient not able to participate in the regimen;
- Documentation shows patient did not participate in the regimen;
- Documentation shows patient did not receive the required amount of therapy minutes;
- The preponderance of therapy minutes delivered should have been individual, but there were high levels of group and/or concurrent therapy; and
- The rehabilitation physician did not see the patient on a regular basis.
Noridian has been completing focused reviews in California and Nevada since September 2014, and we have previously reported findings from those reviews. The most recent review period was from Oct. 1, 2016 through Dec. 31, 2016. Of 346 claims reviewed, 247 of them were denied for the following reasons:
- Documentation did not support that the minimum intensity requirements were consistently met for the provision of therapy services (reason for the largest majority of claims denials); and
- Documentation requirements were not consistently met for the post-admission physician evaluation, preadmission screening, individualized overall plan of care, interdisciplinary team conference, and medical necessity of the IRF.
In Oregon, 55 of 179 claims reviewed from May 2, 2016 through Nov. 8, 2016 were denied – an overall error rate of 31 percent. Not surprisingly, the reasons for denial were identical to those in California and Nevada.
In Washington, 255 claims were reviewed from Feb. 27, 2016 through Oct. 25, 2016, with 55 claims being denied in full for an error rate of 22 percent. Again, the denial reasons matched those in Noridian’s other samples.
Novitas continues to have active edits for prepayment review for the following CMGs: A0701, A0702, A0703, A0704, A0801, A0802, A0803, A0804, A0805, and A0806 – all of them orthopedic, and these include hip fractures, which are important to IRFs in meeting CMS-13 compliance.
Other communications from Novitas list the common documentation errors for claims reviewed:
- Missing documentation to support that the rehabilitation physician has specialized training or experience in inpatient rehabilitation;
- The beneficiary did not receive the required amount of therapies, or a significant portion of the therapies were provided in group or concurrent settings;
- Time requirements for preadmission screening and post-admission evaluations were not met; and
- The interdisciplinary team meeting notes were missing.
On Dec. 5, 2016, Palmetto posted notifications of prepayment review on all fracture of the lower extremity CMG codes, 0701-0704 for all tier levels (A thru D).
In Palmetto’s web-based IRF training on Feb. 15, 2017, it outlined the common reasons for denial on recent CERT reviews, mainly due to documentation issues:
- Missing required documentation;
- One or more of the following documents were missing: preadmission screening, post-admission physician evaluation, interdisciplinary team meeting notes, plan of care developed by rehabilitation physician;
- Signatures were:
- Missing, incomplete, or illegible, including the lack of professional credentials and/or inconsistent e-signature entry;
- Missing or unsigned admission order to the IRF; and
- Timeliness of completion for the preadmission assessment and post-admission physician evaluation.
And Don’t Forget the OIG
The 2017 U.S. Department of Health and Human Services (HHS) Office of Inspector General (OIG) Work Plan continues prior reviews of whether IRFs billed claims in compliance with Medicare documentation and coverage requirements, and it adds a new focus on doing case reviews of IRF patients who might not be suited for intensive therapy.
And Supplemental Medical Review Contractor (SMRC) Reviews
StrategicHealthSolutions, the current SMRC, is conducting post-payment medical review of IRF services. Prior reviews by the SMRC have resulted in error rates as high as 90 percent being recorded, although StrategicHealthSolutions reports improvements in performance in more recent audits.
What Are the Trends?
While the focus of the reviews continues to be on the detailed documentation requirements to support medical necessity that were updated in January 2010, we see two things trending in the process:
- Technical Denials
There are many denials that occur because IRFs fail to meet specific timing or detail requirements for the payment of services. And while there has been some improvement in this area, these errors and subsequent denials continue to plague the industry.
- Completion of the post-admission physician evaluation more than 24 Hours after admission;
- Failure to meet the intensity-of-therapy requirements – three hours of therapy a minimum of five days per week, or in well-documented exceptions, at least 15 hours per week; and
- Attendance at the weekly team meeting of the required attendees.
- A Higher Scrutiny of Therapy Services
In recent audits, we have seen denials specifically related to therapy services, including:
- Patients denied because the preadmission assessment did not demonstrate that “at the time of admission” the patient could reasonably be expected to participate in intensive therapy;
- Denials based on lack of specificity of therapy intensity, frequency, and duration in the individualized plan of care;
- Lack of documentation to support that the patient received the requisite levels of therapy service; and
- Denials when the preponderance of therapy minutes was not 1:1 but the patient had a high percentage of group and/or concurrent care.
The Bottom Line
IRFs should be well-prepared for the bigger focus on therapy requirements as the auditing process continues to evolve, and they should incorporate practices into each phase of the IRF care delivery and documentation process to ensure compliance.
Our next article will focus on therapy compliance and provide some tips and tools for IRFs in monitoring this area.