POST-HOSPITALIZATION OUTCOMES STUDIES

Forms and Documents

Document	Type	Status	Availability

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Collection	Type	Status	Form
112141	POST-HOSPITALIZATION OUTCOMES STUDIES		Migrated

ICR Details

OMB Control No: 0935-0074	ICR Reference No: 199404-0935-002
Status: Historical Active	Previous ICR Reference No: 199203-0935-001
Agency/Subagency: HHS/AHRQ	Agency Tracking No:
Title: POST-HOSPITALIZATION OUTCOMES STUDIES
Type of Information Collection: Reinstatement with change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 07/01/1994
	Date Received in OIRA: 04/04/1994
Terms of Clearance: OMB provides a limited approval of this effort through 10/94 under the following conditions: 1) no later than 7/94 AHCPR briefs OMB on it new approach of using claims files and FIs to sample hospitals and patients. OMB requests that prior to the briefing, AHCPR prepares a Table of Hospital Characteristics for all 13 FIs (as it did in Appendi J, Table I). This table should be expanded to included any available data demonstrating variances in length of stay and discharge practices for subacute care. In addition, AHCPR should be prepared to present such data for all remaining FIs; 2) AHCPR should be prepared to discuss the validity of the ICD-9-CM codes on claims and how they rela to information in the medical record. AHCPR may wish to discuss the results of a study it has conducted on hospital coding practices; and 3) though the pilot's nonresponse was low, AHCPR should discuss its plans to evaluate nonresponse bias. OMB waives publication of the Federal Register notice for the next submission, and will complete its review within 30 days to allow AHCPR to field this effort before the end of the fiscal year.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	10/31/1994	10/31/1994
Responses	2,690	0	0
Time Burden (Hours)	2,206	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: THE POST-HOSPITALIZATION OUTCOMES STUDIES WILL PROVIDE INFORMATION ABOUT THE EXPERIENCE OF MEDICARE BENEFICIARIES FOLLOWING HOSPITALIZATION FOR ELECTIVE TOTAL HIP REPLACEMENT AND CHOLECYSTECTOMY THIS INFORMATION LINKED TO MEDICARE DATA CAN DEVELOP KNOWLEDGE ABOUT: 1) THE NATURAL HISTORY OF DISEASE, 2) THE EFFECTIVENESS OF TREATMENT, AND 3) INDICATORS OF PATIENTS WHO ARE HIGH RISK FOR

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
POST-HOSPITALIZATION OUTCOMES STUDIES

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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	2,690	0	0	2,690	0	0
Annual Time Burden (Hours)	2,206	0	0	2,206	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:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? No

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]? Uncollected

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)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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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: 04/04/1994

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