- CMS revenue
- Customer base
- Quality Rating
Reduce your financial exposure
Problem: In 2017,
CMS has changed the game:
PQRS is gone. GPRO is gone.
Qualified Registry XML submissions are gone.
And your practice needs a proven solution to comply with the new
CMS MACRA report processes. See ACO solution
Proven Solution: Since
2015, CUHSM clients have used our
proven MACRA compliant submission process.
Proof: Participating ACO
providers have achieved positive financial results with our
proven MACRA compliant services and toolkit.
CUHSM was the sole QCDR to
successfully generate QRDA submissions for multiple ACO
providers for the CMS 2015 PY.
Benefit: Your income is protected
with CUHSM's tested MACRA processes .
Minimize MACRA related interruptions
Problem: A poorly
planned transition to MACRA processes will require expensive EHR
upgrades, IT support and cause workflow interruptions. Many
Qualified Registries have been unsuccessful in shoehorning legacy
PQRS processes into MACRA support roles.
Solution: Our MACRA QRDA Submission
process uses proven techniques that minimize workflow interruptions.
Muliple discrete programs that review over 6,400+ parameters to expedite data validation and scrubbing processes
where errors are identified at all stages of the QRDA
Benefit: Validated CMS submissions save time and staff resources.
analyzes the data integrity and audit
trails within QRDA submissions to optimize all elements and stages
of CMS submission review.
Expedite compliance with multiple reporting mandates
Problem: 2017 mandates
require a new quality report format:QRDA:
CMS, CDC, The Joint Commission (TJC), CDC and State agencies burden your staff and vendors to submit accurate
organization balks at the cost, time and resources required for the
upgrades required for onslaught of multiple QRDA mandatess.
Solution: QRDA Pro
leverages your current technology and workflow to achieve MACRA, QPP, IPPS/IQR,
and TJC compliance.
Benefit #1: CUHSM
shields your IT systems
from QRDA regulatory updates, minimizing costly changes to
your existing technology.
Benefit #2: No longer must you
switch EHR vendors to generate validated QRDA submissions.
Merged your processes for
Hospital and Ambulatory quality submissions
organizations duplicate effort by having two independent departments for ambulatory and
hospital reporting due to unique specifications.
Solution: Our unified QRDA/eCQM report process uses
that are ONC certified for both Eligible Hospitals (EH), Critical
Access Hospitals (CAH) and Eligible
This enables you to
merge reporting resources required for QPP, IQR, The Joint
Commission (TJC) and other QRDA
quality report mandates (Medicaid, CDC).
Benefit: Duplicate efforts are eliminated,
conserving yYour resources by a merged report
Improved Patient Adherence
appointments, non-adherence to regimens, and lack of engagement in
preventive care all deter positive outcomes.
Using suitable Patient Adherence Measures (PAM), patient adherence can be quantified in
order to initiate followup targeted communications and adjust
appropriate risk factors that correlate with patient interactions.
is committed to helping our nation achieve
better and affordable care, and improving the overall health of
by providing efficient solutions that deliver accurate PQRS submissions to
"Providers require CMS
Compliant Report systems that are cost effective
to stay competitive in the ever changing regulatory environment"
to take advantage of our integrated CMS submission process saves your
organization time, effort and resources.
has engineered and implemented the following QRDA and QCDR solutions:
delivers turnkey and custom solutions
to corporate and registry clients that
that are cost effective
to stay competitive in the ever changing regulatory environment.
provides a portfolio
of quality report submission services
to achieve these goals:
design and administer staged procedures inherent in CMS reporting
localize and coordinate EHR vendor sensitive issues
Collaborative seminars and roundtables to facilitate implementation
Common Point Access Methods with thorough data validation and
to fulfill CMS requirements for Qualified Clinical Data Registry (QCDR),
compiles and validates CMS submissions with our Submission Generation
by using our efficient Data-Mining processes for
patient experience databases and
provides a secure, reliable QCDR Cloud
to fully leverage your existing
registry IT to enable
your organization to orchestrate a tiered, efficient QCDR
submission process. More...
progress at ONC 2014 Meeting