View Information Collection Request (ICR) Package
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View Information Collection (IC) List
View Supporting Statement and Other Documents
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:
0938-1109
ICR Reference No:
201312-0938-017
Status:
Historical Active
Previous ICR Reference No:
200912-0938-005
Agency/Subagency:
HHS/CMS
Agency Tracking No:
21225
Title:
Hospital Outpatient Quality Data Program (HOPQDRP) (CMS-10250)
Type of Information Collection:
Revision of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
02/06/2014
Retrieve Notice of Action (NOA)
Date Received in OIRA:
12/23/2013
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
02/28/2017
36 Months From Approved
02/28/2014
Responses
5,071,000
0
1,821,340
Time Burden (Hours)
2,906,749
0
1,802,186
Cost Burden (Dollars)
0
0
0
Abstract:
This information is used by CMS to direct its contractor, including Quality Improvement Organizations (QIOs), to focus on particular areas of improvement, and to develop quality improvement initiatives. The information is made available to hospitals for their use in internal quality improvement initiatives. Most importantly, this information is available to Medicare beneficiaries, as well as to the general public, to provide hospital information to assist them in making decisions about their health care.
Authorizing Statute(s):
PL:
Pub.L. 111 - 148 3014
Name of Law: Affordable Care Act
PL:
Pub.L. 109 - 432 109(a)
Name of Law: Quality reporting for hospital outpatient services and ambulatory surgical center services
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:
78 FR 43533
07/19/2013
30-day Notice:
Federal Register Citation:
Citation Date:
78 FR 74825
12/10/2013
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
9
IC Title
Form No.
Form Name
Hospital Outpatient Quality Data Program (HOPQDRP) - Abstracting Burden (CY 2009 and CY2010)
Hospital Outpatient Quality Data Program (HOPQDRP) - CY 2011 Data Validation
Hospital Outpatient Quality Data Program (HOPQDRP) - Notice of Participation (2010)
CMS-10250
CMS-10250.Notice of Participation
Hospital Outpatient Quality Data Program (HOPQDRP) - Notice of Participation (2011)
CMS-10250
CMS Notice of Participation
Hospital Outpatient Quality Data Program (HOPQDRP) CY 2011 Data Abstraction
Hospital Outpatient Quality Data Program - Data Abstraction (CY 2014)
Hospital Outpatient Quality Data Program - Data Abstraction (CY 2015)
Hospital Outpatient Quality Data Program - Data Abstration (CY 2016)
Hospital Outpatient Quality Data Program - Data Validation (CY 2014)
Hospital Outpatient Quality Data Program - Data Validation (CY 2015)
Hospital Outpatient Quality Data Program - Data Validation (CY 2016)
Hospital Outpatient Quality Data Program - Notice of Participation (CY 2014)
CMS-10250, CMS-10250, CMS-10250, CMS-10250
Notice of Participation
,
Request for Reconsideration Part 1
,
Request for Reconsideration Part 2
,
Extroadinary Circumstances
Hospital Outpatient Quality Data Program - Notice of Participation (CY 2015)
CMS-10250
Notice of Participation
Hospital Outpatient Quality Program - Notice of Participation (CY 2016)
CMS-10250
Notice of Participation
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
5,071,000
1,821,340
0
3,249,660
0
0
Annual Time Burden (Hours)
2,906,749
1,802,186
0
1,104,563
0
0
Annual Cost Burden (Dollars)
0
0
0
0
0
0
Burden increases because of Program Change due to Agency Discretion:
Yes
Burden Increase Due to:
Miscellaneous Actions
Burden decreases because of Program Change due to Agency Discretion:
Yes
Burden Reduction Due to:
Miscellaneous Actions
Short Statement:
The program has increased the number of measures included in its data collection requirements. However, the newly proposed measures have data submission via a web-based tool, either directly to CMS or via the NHSN. These increases are in adherence to section 3013 of ACA which requires CMS to identify gaps where no quality measures exist and existing quality measures that need improvement, updating, or expansion.
Annual Cost to Federal Government:
$11,500,000
Does this IC contain surveys, censuses, or employ statistical methods?
Yes
Part B of Supporting Statement
Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002?
No
Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]?
Yes
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:
Denise King 410 786-1013 Denise.King@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:
12/23/2013
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