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    PFAS-Sentinels.org

        ^{A division of Consortium for Universal Health System Metrics -}     

CUHSM.ORG is committed to helping our nation achieve better and affordable care, and improving the overall health of Americans. 

Providers need CMS compliant report systems that are cost effective to stay competitive in the ever changing regulatory environment.

CUHSM.ORG  provides QPP report solutions that efficiently acquire clinical data and compile submissions for secure delivery to CMS.  

Specifically, CUHSM.ORG analyzes QCDR implementation issues and administers solutions
     for the following action items:
 

Benefit #1

Our process minimizes impact on your workflow 

Problem: Your current registry uses PQRS processes that require your organization to dedicate internal resources to CMS quality Reporting.

 

Solution: Our procedure reduces the impact of QPP reporting by using QCDR processes to take action items off your plate.  We combine efficient EHR Data Mining with thorough clinical data validation to improve Quality Reporting logistics, making the best use of clinicians who review QPP submissions.  No longer does your organization need to dedicate internal resources to calculate the numerator.

Benefit #2
Expedite compliance with multiple Quality Report mandates

Problem: Multiple quality submissions are mandated by multiple requestors including:

CMS, CDC, The Joint Commission (TJC), Medicaid, Immunization registries and multiple State health agencies.   

This list is not exhaustive, and, as time goes on, will encompass more 3rd party payers that implement quality programs that contain healthcare costs. 

 

Your EHR Vendor struggles to compile multiple quality submissions that fulfill all of the mandated requirements and are accurate and on time.  Multiple sources of regulation add to this workload with an onslaught of asynchronous updates.  Your organization balks at the cost, time and resources required for the upgrades required for onslaught of multiple QRDA mandates.
 

Solution: QRDA Pro Shield 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. 

Benefit #3
Merges Hospital and Ambulatory quality processes

Problem: Most 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 efficient tools that are ONC certified for both Eligible Hospitals (EH), Critical Access Hospitals (CAH) and Eligible Providers (EP).

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 process.
 

Benefit #4
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 submission generation process.

Benefit: Validated CMS submissions save time and staff resources. 
CUHSM thoroughly analyzes the data integrity and audit trails within QRDA submissions to optimize all elements and stages of CMS submission review.

Missed appointments, non-adherence to regimens, and lack of engagement in preventive care all deter positive outcomes. 

The CUHSM Patient Adherence System^TM  reduces these interruptions to the healing process.   By using suitable CUHSM Patient Adherence Measures (PAM), Patient Adherence can be quantified in order to improve followup targeted communications and adjust appropriate risk factors that correlate with specific patient interactions.    More info...

Benefit #6
 Embedded audit trails facilitate automated review

We leverage proven audit trail technologies from the Financial Industry to manage the review process of complex QRDA documents that are sourced by multiple EP electronic record systems. 

CUHSM.ORG provides a portfolio of quality report submission services to achieve these goals:

        - Analyze, design and administer staged procedures inherent in CMS reporting processes

        - Identify, localize and coordinate data acquisition issues

        - Collaborative seminars and roundtables to facilitate implementation solutions

Your choice of our integrated CMS submission process
     saves your organization time, effort and resources

CUHSM.ORG  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...

QCDR roundtable progress at ONC 2014 Meeting Details here

PFAS-Sentinels QCDR Measures approved by CMS - Non QPP Program - Patient Adherence Measures
• 2014 • 2015 • 2016 • 2017 • 2018 • 2019 • 2017_07_Non_Compliance_letter • 2017_QCDRbenchmarks •

For more information, contact us via email at clientservices@PFAS-Sentinels.org

Phone:  (888) 979-2499 x2

Universal Health System Metric Tools referenced on this site:
CMS Submission Toolkit, CST-CMS Submission Template, PQRS Audit Tool, PQRS Validator, GPRO Aggregator,
    QCDR-HISP, QRDASolutions, and NwHIN Sleuth are trademarks of CMS Gateways, LLC
All other products mentioned are registered trademarks or trademarks of their respective companies.

QCDR-HISP = Qualified Clinical Data Registry - Health Information Service Provider

Questions or problems regarding technical problems for this web site should be directed to webmaster@PFAS-Sentinels.org
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Last modified: Thursday September 08, 2022.