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Start Preamble
AGENCY:
Agency for Healthcare Research and Quality, HHS.
ACTION:
Notice.
SUMMARY:
This notice announces the intention of the Agency for Healthcare Research and Quality (AHRQ) to request that the Office of Management and Budget (OMB) approve the proposed information collection project: “Improving Quality through Health IT: Testing the Feasibility and Assessing the Impact of Using Existing Health IT Infrastructure for Better Care Delivery.” In accordance with the Paperwork Reduction Act of 1995, 44 U.S.C. 3506(c)(2)(A), AHRQ invites the public to comment on this proposed information collection.
DATES:
Comments on this notice must be received by April 15, 2008.
ADDRESSES:
Written comments should be submitted to: Doris Lefkowitz, Reports Clearance Officer, AHRQ, by e-mail at doris.lefkowitz@ahrq.hhs.gov.
Copies of the proposed collection plans, data collection instruments, and specific details on the estimated burden can be obtained from the AHRQ Reports Clearance Officer.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports Clearance Officer, (301) 427-1477, or by e-mail at doris.lefkowitz@ahrq.hhs.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
Proposed Project
Improving Quality Through Health IT: Testing the Feasibility and Assessing the Impact of Using Existing Health IT Infrastructure for Better Care Delivery
AHRQ proposes to assess how the use of health information technology (IT) can improve care delivery and outcomes in community health centers. AHRQ is specifically interested in improving the quality of care provided in a community clinic setting through better management of laboratory information. The study will measure the impact of health IT tools on two problems: duplicate laboratory tests and the failure to follow up on laboratory test results of HIV patients and women screened for cervical cancer. In addition, AHRQ will measure the impact of health IT on compliance with evidence-based guidelines for laboratory tests. The study will also investigate whether disparities between vulnerable populations and the general population exist in both laboratory screening rates and rates of abnormal laboratory test results without follow up. To assess the extent of these problems and the impact of health IT, AHRQ will evaluate both quantitative and qualitative components. The qualitative component will use interviews with key informants in two community health centers to gather data on laboratory information processes, laboratory information communication problems and use of health IT tools.
Method of Collection
Quantitative data will be collected directly from the clinical data warehouse used by the participating community health centers to routinely collect laboratory data. The collection will be accomplished using database reports. Qualitative data will be collected through key informant interviews conducted in each of the two participating community health centers. Key informants will include physicians, nurses, medical assistants, IT personnel, and administrators. The total number of interviews to be conducted at both sites is forty-one.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours. A total of forty-one in-person interviews will be conducted with administration and clinical personnel: eighteen interviews from administrative personnel and twenty-three interviews from clinical personnel. The question set is the same for both clinical and administrative personnel. The estimated time per response is 1.5 hours for a total of 61.5 burden hours.
Exhibit 2 shows the estimated annualized burden for the respondents' time to provide the requested data. The hourly rate of $32.13 is a weighted average of the administrative personnel hourly wage of $19.68 and the clinical personnel hourly wage of $41.88. The total cost burden is $1,976.Start Printed Page 8875
Exhibit 1.—Estimated Annualized Burden Hours
Data collection Number of respondents Number of responses per respondent Hours per response Total burden hours In-person interviews 41 1 1.5 61.5 Total 43 na na 61.5 Exhibit 2.—Estimated Annualized Cost Burden
Data collection Number of respondents Total burden hours Average hourly wage rate* Total cost burden In-person interviews 41 61.5 $32.13 $1,976 Total 41 na na 1,976 * Based upon the actual site personnel wages. Clinical personnel averages are weighted by the number of physicians, nurses and medical assistants in the sample. Administrative personnel averages are weighted by the number of administrators, lab, IT and other support personnel. Total average is weighted by relative number of administrative and clinical personnel being interviewed. Estimated Annual Costs to the Federal Government
The total cost to the Federal Government for this project is $393,457 over a two-year period. The average annual cost is $196,728. the following is a breakdown of average annual costs:
Direct Costs: Personnel $108,320 Consultancies 24,400 Data support 5,000 Travel 2,575 Supplies 100 IRB review 125 Indirect Costs: Indirect costs 40% 56,208 Request for Comments
In accordance with the above-cited Paperwork Reduction Act legislation, comments on AHRQ's information collection are requested with regard to any of the following: (a) Whether the proposed collection of information necessary for the proper performance of AHRQ's health care research and health care information dissemination functions, including whether the information will have practical utility; (b) the accuracy of AHRQ's estimate of burden (including hours and costs) of the proposed collection(s) of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information upon the respondents, including the use of automated collection techniques or other forms of information technology.
Comments submitted in response to this notice will be summarized and included in the Agency's subsequent request for OMB approval of the proposed information collection.
All comments will become a matter of public record.
Start SignatureDated: February 6, 2008.
Carolyn M. Clancy,
Director.
[FR Doc. 08-660 Filed 2-14-08; 8:45 am]
BILLING CODE 4160-90-M
Document Information
- Published:
- 02/15/2008
- Department:
- Agency for Healthcare Research and Quality
- Entry Type:
- Notice
- Action:
- Notice.
- Document Number:
- 08-660
- Dates:
- Comments on this notice must be received by April 15, 2008.
- Pages:
- 8874-8875 (2 pages)
- PDF File:
- 08-660.pdf
- Supporting Documents:
- » Meetings: National Advisory Council for Healthcare Research and Quality
- » Agency Information Collection Activities; Proposals, Submissions, and Approvals
- » Agency Information Collection Activities; Proposals, Submissions, and Approvals
- » Agency Information Collection Activities; Proposals, Submissions, and Approvals
- » Agency Information Collection Activities; Proposals, Submissions, and Approvals
- » Common Formats for Patient Safety Data Collection
- » Meetings: Agency for Healthcare Research and Quality and Patient-Centered Outcomes Research Institute Learning Health Systems Mentored Career Development Program
- » Agency Information Collection Activities; Proposals, Submissions, and Approvals
- » Patient Safety Organizations: Voluntary Relinquishment from NCH Healthcare System
- » Meetings: National Advisory Council for Healthcare Research and Quality