eCQM Requirements for The Joint Commission ORYX® Initiative for Quality Improvement
We’ve said it before, and we will say it again; 2017 is an historic time for electronic quality reporting. Have we beat that into your head enough?
For the first time, all major regulatory programs require eCQM submission as a part of successful completion of the program. The following video will provide you with a brief overview of the 2017 eCQM reporting requirements for one specific program, The Joint Commission’s ORYX® initiative for quality improvement.
If you don’t feel like watching a short video explanation (because you’re definitely not a millennial) then feel free to continue reading to get the written recap of The Joint Commission’s eCQM reporting requirements.
1. Hospitals must submit four of the available 13 eCQMs
This is the first time that eCQMs are required as a part of The Joint Commission program. Also note, this differs from CMS’ requirement for the Inpatient Quality Reporting (IQR) program, which requires four eCQMs from an available list of 15 eCQMs.
Additional Options: You may elect to report additional measures relevant to services provided and patient populations served by the hospital.
2. You must submit for one quarter of 2017
The Joint Commission is asking you to dive right into the eCQM world this year. You must you report on four eCQMs and you must report one quarter’s worth of data. We suggest you begin submitting your measures as soon as the submission window opens (October 1, 2017), however, you do have until March 15th of 2018 to get your data submitted to The Joint Commission.
Note: Your data must be submitted no later than 8 p.m. CT on the submission deadline.
3. Reporting options
You have two reporting options in 2017. You may either choose to:
a. Use an acceptable ORYX® vendor, like Medisolv, to submit your eCQM data or
b. Complete a direct submission through The Joint Commission portal.
The easier option is to use an acceptable ORYX® vendor to submit your eCQMs, but if you choose to direct submit there are a few guidelines you must follow.
a. The data file that you submit must use EHR technology that’s certified to the 2014 or 2015 edition of CEHRT.
b. The EHR technology must be listed on the ONC Certified Health IT Product List.
c. All files submitted to The Joint Commission must be in the QRDA 1 file format.
Keep in mind that if you choose direct submission, then the submission portal will only open for testing in Quarter four of 2017 with the ability to actually submit in early 2018.
Medisolv is a quality reporting solution that helps hospitals and clinicians monitor and submit their eCQMs to various regulatory programs such as The Joint Commission and CMS.
So, if you’re looking for someone to help you with implementation, validation and submission of eCQMs, then send us a note. We’d love to have a chat and see if we are good fit for your needs.
Ultimate Regulatory Requirements Package
CMS and The Joint Commission have been saying for a while that they are aligning the two programs to make it easier for hospitals to report their eCQM and chart-abstracted measure data to both organizations. So why is it so hard to find the information that you need for both programs in a consistent manner?
We understand. That’s why Medisolv put together our Ultimate Quality Reporting Package. We scoured through multiple CMS and Joint Commission documents to standardize and simplify the requirements for you.This bundle includes:
CMS IQR Program
The Joint Commission ORYX®
PLUS: An Acronym Reference Guide