View Information Collection Request (ICR) Package
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Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View ICR - OIRA Conclusion
OMB Control No:
0938-1152
ICR Reference No:
201612-0938-021
Status:
Historical Active
Previous ICR Reference No:
201508-0938-001
Agency/Subagency:
HHS/CMS
Agency Tracking No:
CM-CPC
Title:
Collection of Risk Adjustment Data from MA Organizations, Section 1876 Cost HMOS/CMPS, Section 1833 HCPPS, MMPS, and PACE Organizations (CMS-10340)
Type of Information Collection:
Revision of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved with change
Conclusion Date:
04/24/2018
Retrieve Notice of Action (NOA)
Date Received in OIRA:
08/30/2017
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
04/30/2021
36 Months From Approved
04/30/2018
Responses
769,396,692
0
516,493,635
Time Burden (Hours)
19,481
0
34,433
Cost Burden (Dollars)
0
0
0
Abstract:
CMS uses the risk adjustment data to develop individual risk scores for risk adjusted payment under Part C. As required by law, CMS also establishes the risk adjustment methodology and annually publishes the risk adjustment factors for MA organizations and other interested entities in the Advance Notice of Methodological Changes for MA Payment Rates (every February) and the Announcement of Medicare Advantage Payment Rates (every April). Risk adjustment data in particular is used to calibrate the CMS-HCC risk adjustment models using MA patterns of diagnoses, utilization, and expenditures. While establishing a risk adjustment model appropriate for the MA program is the paramount reason for collecting MA risk adjustment, there are other important uses of the data that will improve other key functions undertaken by CMS. Data is used for the calculation of Medicare Disproportionate Share Hospital (DSH) payments. CMS collects inpatient stay information for the Medicare managed care enrollees. In particular, we collect the admission date, discharge date, Health Insurance Claim Number (HICN), and Medicare hospital number/CCN. Further, we also use the data for quality review and improvement activities. For example, MA risk adjustment data may be used in the development and calculation of quality measures for MA organizations. Other uses for the data include geographical acuity studies, utilization trends and detection of abuse as defined in the False Claim Act. Additional uses for the data include verifying the accuracy and validity of the reasonable costs claimed on Cost Reports submitted by section 1876 Cost HMOs/CMPs and section 1833 HCPPs. Finally, as stated in the regulation, we use the data for Medicare coverage purposes. For example, we can use risk adjustment data for the determination of whether day limits have been exhausted and, if not, how many such days are left.
Authorizing Statute(s):
US Code:
42 USC 1395w-23
Name of Law: Risk Adjusted Part D Payment
US Code:
42 USC 1395w-23
Name of Law: Risk Adjusted Part C Payment
US Code:
42 USC 1395w-23
Name of Law: Data Collection
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
81 FR 51916
08/05/2016
30-day Notice:
Federal Register Citation:
Citation Date:
81 FR 87034
12/02/2016
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
6
IC Title
Form No.
Form Name
Connect: Direct Applications for RAPS, Encounter, PDE, and MMP
Electronic Data Interchange (EDI) Agreement
CMS-10340
MAO Electronic Data Interchange (EDI) Agreement
PRS Contract and Contact Verification Form
Risk Adjustment Data Submission
Submitter Application and Instructions
CMS-10340
CSSC Operations Submitter Application (Form and Instruction)
Submitter Authorization Form
CMS-10340
CSSC Operations Submitter Authorization Form
ICR Summary of Burden
Total Approved
Previously Approved
Change Due to New Statute
Change Due to Agency Discretion
Change Due to Adjustment in Estimate
Change Due to Potential Violation of the PRA
Annual Number of Responses
769,396,692
516,493,635
0
0
252,903,057
0
Annual Time Burden (Hours)
19,481
34,433
0
0
-14,952
0
Annual Cost Burden (Dollars)
0
0
0
0
0
0
Burden increases because of Program Change due to Agency Discretion:
No
Burden Increase Due to:
Burden decreases because of Program Change due to Agency Discretion:
No
Burden Reduction Due to:
Short Statement:
The currently approved title for this information collection request is, “Collection of Encounter Data from Medicare Advantage Organizations.” This iteration proposes to revise the title to read, “Collection of Risk Adjustment Data from MA Organizations, Section 1876 Cost HMOS/CMPS, Section 1833 HCPPS, MMPS), and PACE Organizations.” We have revised the CSSC Operations Submitter Application Instruction and CSSC Operations Submitter Authorization Forms (see the attached Crosswalk). Our currently approved burden estimates have not been revised as a result of these changes. While the number of respondents has been adjusted by +8 (from 683 (currently approved) to 691 (proposed), our total time estimate has decreased by -28,136 hours (664 hr -28,800 hr). This net reduction includes -28,800 hours under the Risk Adjustment Data Submission ICR along with +664 hours for the remaining ICRs. Institutional, Professional, and DME companion guides have been added to this package since the system processes all institutional, professional, and DME claims. The burden for these claims is built into the cost of effort for a plan per year that is calculated in section 12 of this Supporting Statement, listed as $840,810. DME claims for risk adjustment data is a smaller portion of Part B claims and therefore the process to create the data in the same format is reduced. We are also requiring that accountable MA management approve their contract jurisdiction before any pharmacy reconciliation reports are submitted to them by completing a PRS Contract and Contact Verification Form. We have clarified the submission timeframes in section 6 of this Supporting Statement based on the release of the reconciliation reports. This information collection effort includes a data collection instrument that is updated annually to validate accountable MA management (i.e. Survey or form).
Annual Cost to Federal Government:
$25,010,000
Does this IC contain surveys, censuses, or employ statistical methods?
No
Does this ICR request any personally identifiable information (see
OMB Circular No. A-130
for an explanation of this term)? Please consult with your agency's privacy program when making this determination.
Yes
Does this ICR include a form that requires a Privacy Act Statement (see
5 U.S.C. §552a(e)(3)
)? Please consult with your agency's privacy program when making this determination.
Yes
Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]?
No
Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]?
No
Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)?
No
Is this ICR related to the Pandemic Response?
Uncollected
Agency Contact:
Mitch Bryman 410 786-5258 Mitch.Bryman@cms.hhs.gov
Common Form ICR:
No
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(a) It is necessary for the proper performance of agency functions;
(b) It avoids unnecessary duplication;
(c) It reduces burden on small entities;
(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;
(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;
(f) It indicates the retention periods for recordkeeping requirements;
(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.
(i) It uses effective and efficient statistical survey methodology (if applicable); and
(j) It makes appropriate use of information technology.
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
Certification Date:
08/30/2017
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