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
112142	POST-HOSPITALIZATION OUTCOMES STUDIES		Migrated

ICR Details

OMB Control No: 0935-0074	ICR Reference No: 199408-0935-001
Status: Historical Active	Previous ICR Reference No: 199404-0935-002
Agency/Subagency: HHS/AHRQ	Agency Tracking No:
Title: POST-HOSPITALIZATION OUTCOMES STUDIES
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: 09/01/1994
	Date Received in OIRA: 08/22/1994
Terms of Clearance: Approved for use through 9/96 with the understanding that this effort is preliminary in nature and its methodology (in particular, reliance on a potentially unrepresentative subset of Medicare fiscal interme- diaries for case selection) may not be an appropriate sampling approac for future outcomes evaluations. As discussed in its response to OMB concerns dated 8/11/94, AHCPR notes the wide variation between fiscal intermediaries for discharge disposition and limitations in Medicare discharge data. In addition, AHCPR notes existing limitations in the use of ICD-9 administrative data, particularly for comorbidities and complications. Although AHCPR will validate these data using medical records, persistent discrepencies in these data could confound the study's results. OMB expects that: 1) AHCPR thoroughly will caveat dissemination of these data with explanations of its limitations; and 2) methodologies presented in future outcomes studies will reflect AHCPR's enhanced understanding from this study of data limitations and variances between hospitals in discharge practices.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/1996	09/30/1996	10/31/1994
Responses	2,690	0	2,690
Time Burden (Hours)	2,206	0	2,206
Cost Burden (Dollars)	0	0	0

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Abstract: THE POST-HOSPITALIZATION OUTCOMES STUDIES WILL PROVIDE INFORMATION ABO 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) INDICATO

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

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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: 08/22/1994

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