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:
200912-0938-005
Status:
Historical Active
Previous ICR Reference No:
Agency/Subagency:
HHS/CMS
Agency Tracking No:
Title:
Information Collection Requirements for the Hospital Outpatient Quality Data Program (HOPQDRP) (CMS-10250)
Type of Information Collection:
Existing collection in use without an OMB Control Number
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved with change
Conclusion Date:
10/01/2010
Retrieve Notice of Action (NOA)
Date Received in OIRA:
12/11/2009
Terms of Clearance:
Since the HOPQDRP reporting requirements tend to change annually with each annual outpatient prospective payment system (PPS) rule, this ICR is approved for one year. Because this ICR is associated with rulemaking, CMS agrees to coordinate the publication of the 60 & 30 day Federal Register Notices with the issuance of the proposed and final outpatient PPS. In order to comment meaningfully on the burden and utility of these reporting requirements, the public needs access to all technical specifications on how each performance measure will be calculated (e.g. the denominators and numerators). Therefore, all such technical specifications need to be submitted with the ICR in order for the ICR package to be considered complete. These technical specifications must also match up with the year in question (i.e. the 2008 specifications should not be submitted for the 2009 measures). Incomplete submissions will be returned to the agency as "improper submissions." Finally, CMS agrees to include this ICR in the next ICB as a "bootleg" collection.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
10/31/2013
36 Months From Approved
Responses
1,821,340
0
0
Time Burden (Hours)
1,802,186
0
0
Cost Burden (Dollars)
0
0
0
Abstract:
CMS will use the information collected to direct its contractor, including Quality Improvement Organizations (QIOs), to focus on particular areas of improvement, and to develop quality improvement initiatives. The information will be made available to hospitals for their use in internal quality improvement initiatives. Most importantly, this information is available to beneficiaries, as well as to the public in general, to provide hospital information to assist them in making decisions about their health care. CMS conducts focus groups or market testing prior to public reporting hospital quality data on the Hospital Compare website.
Authorizing Statute(s):
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:
PL: Pub.L. 109 - 432 109(a) Name of Law: Quality reporting for hospital outpatient services and ambulatory surgical center services
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
0938-AP41
Final or interim final rulemaking
74 FR 60316
11/20/2009
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
74 FR 35232
07/20/2009
30-day Notice:
Federal Register Citation:
Citation Date:
74 FR 60316
11/20/2009
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
5
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
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
1,821,340
0
24,800
1,796,540
0
0
Annual Time Burden (Hours)
1,802,186
0
916,026
886,160
0
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:
This is a new information collection request.
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]?
No
Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]?
Uncollected
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:
William Parham 4107864669
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:
12/11/2009