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Agency for Healthcare Research and Quality, HHS.
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 implementation of the U.S. Preventive Services Task Force recommendation for prophylactic aspirin use among adults at risk for cardiovascular disease.” 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.
Comments on this notice must be received by January 20, 2009.
Written comments should be submitted to: Doris Lefkowitz, Reports Clearance Officer, AHRQ, by e-mail at firstname.lastname@example.org.
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 Info
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports Clearance Officer, (301) 427-1477, or by e-mail at email@example.com.End Further Info End Preamble Start Supplemental Information
“Improving implementation of the U.S. Preventive Services Task Force recommendation for prophylactic aspirin use among adults at risk for cardiovascular disease.”
This proposed information collection aims to identify, test and disseminate methods to improve patient-physician communication about aspirin prophylaxis in health care systems. This project falls under AHRQ's Accelerating Change and Transformation in Organizations and Networks (ACTION) program and will be conducted for AHRQ by Abt Associates in collaboration with Geisinger Health Systems. ACTION promotes innovation in health care delivery by accelerating the development, implementation, diffusion, and uptake of demand-driven and evidence-based products, tools, strategies and findings. ACTION develops and diffuses scientific evidence about what does and does not work to improve health care delivery systems. The program emphasizes projects—that are broadly responsive to user needs and operational interests and which are expected to be generalizable across a number of settings.
In this project, a randomized controlled trial with two intervention arms and one control arm will be conducted to evaluate two interventions designed to improve physician-patient communication and decision-making regarding the use of prophylactic aspirin use among adults at risk for cardiovascular disease. Each of the three study arms will take place in one of three similar clinics.
The first intervention uses a paper “pre-visit summary” handout describing the benefits and possible harms of daily low-dose aspirin use to prevent heart attack in men and stroke in women. The handout is given to patients in the waiting room of non-emergency outpatient clinics. The content of the handout, including baseline cardiovascular event risk and the magnitude of potential benefits and harms of aspirin use, is generated specifically for each patient using data in his or her electronic health record. The purpose of the handout is to increase the patients' knowledge of their own cardiovascular risk and increase awareness of prophylactic aspirin regimens as a-treatment option. The study will assess whether the handout is effective in stimulating subsequent discussion with physicians about cardiovascular risk and aspirin.
The second intervention also uses the pre-visit summary handout, but adds a computer-based clinical decision support tool. During the patient's visit with the physician, the electronic health record software used by the physician will alert the physician of the patient's elevated cardiovascular risk and prompt the physician to discuss prophylactic aspirin use with the patient. If the physician chooses to do so, he or she can use a computer-based tool as a decision aid during the discussion with the patient. The tool displays the patient's risk of cardiovascular event (heart attack or stroke) and the potential risk-reducing effect of daily aspirin use. The tool also shows the likelihood of potential harms of aspirin use (e.g., gastrointestinal bleeding). The tool is interactive and allows the patient and doctor to explore the expected effects of behavior change related to modifiable cardiovascular risk factors (e.g., smoking cessation) as well as prophylactic aspirin use.
The proposed data collection supports the ACTION program mission by promoting health care quality improvement. The overall aim of the study is to explore the effectiveness of innovative health care delivery methods in improving patient health behaviors (i.e., using aspirin prophylaxis). The study has been constructed to produce results that will be helpful in a broad range of clinic settings including those utilizing electronic health records and those that rely on paper-based record systems. The proposed data collection will assess the study's main outcome: initiating a discussion about prophylactic aspirin use between at-risk patients and their physicians in order to facilitate a shared decision-making process, and is therefore a necessary and integral element of the overall research study and of the ACTION program mission.
This project is being conducted pursuant to AHRQ's statutory authority to conduct and support research on health care and on systems for the delivery of such care, including activities with respect to the quality, effectiveness, efficiency, appropriateness and value of health care Start Printed Page 70652services 42 U.S.C. 299a(a)(1). The parties involved in the study will comply with the Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule, 45 CFR parts 160 and 164, and the study will be required to obtain approval of the institutional review boards of Geisinger Health Systems and Abt Associates.
Method of Collection
Data for this study will be collected directly from study participants (patients, doctors, and clinic staff) and indirectly from patients' electronic health records and observation of the intervention in clinic waiting rooms. The first phase of the direct data collection will occur after a patient gives his or her informed consent to participate in the study and written authorization for the use of his or her protected health information for this study. Patients will complete a 5-minute pre-visit questionnaire. Fourteen days after a patient's visit, he or she will be contacted to complete a one-time, 25-minute telephone follow-up questionnaire to assess aspirin use, knowledge, and the relevant patient/physician encounter. Data will be collected from participating physicians through 30-minute semi-structured interviews. Similarly, a 10-minute semi-structured interview of participating clinic staff will also be administered to gather information about the feasibility and perceived effectiveness of the intervention.
Estimated Annual Respondent Burden
Exhibit 1 presents an estimate of the annual reporting time burden on respondents participating in the data collection process. Time estimates are based on experience with similar instruments used with comparable respondents. A total of 1,000 patients are expected to participate in the study, distributed into approximately equal groups across the three arms of the study. The pre-visit questionnaire will be completed by 1,000 respondents and will take about 5 minutes. The telephone follow-up questionnaire will be completed by 1,000 respondents and will take about 25 minutes. Qualitative interviews will be conducted with 10 physicians and 8 staff members from each of the two intervention clinics; the physician interview will require about 30 minutes while the staff interview will last about 10 minutes. The total estimated burden hours for the respondents' time to participate in this data collection is 513 hours.
Exhibit 2 shows the estimated cost burden based on the respondents' time to participate in this project and their hourly wage. The estimated cost burden is $10,388.
|Form name||Number of respondents||Number of responses per respondent||Hours per response||Total burden hours|
|Telephone Follow-up Questionnaire||1,000||1||25/60||417|
|Qualitative Interviews: Physicians||2||10||30/60||10|
|Qualitative Interviews: Clinic Staff||2||8||10/60||3|
|Form name||Number of respondents||Total burden hours||Average hourly wage rate*||Total cost burden|
|Telephone Follow-up Questionnaire||1,000||417||19.29||8,044|
|Qualitative Interviews: Physicians||2||10||66.11||661|
|Qualitative Interviews: Clinic Staff||2||3||27.44||82|
|*National Compensation Survey: Occupational wages in the United States, June 2006, U.S. Department of Labor, Bureau of Labor Statistics.|
Estimated Annual Costs to the Federal Government
The total cost to the government of this two-year project is expected to be $300,000. Exhibit 3 details the costs associated with this project, which include $74,206 for project development, $42,760 for data collection activities, $29,510 for data processing and analysis, $31,165 for the publication of results, $27,136 for project management and $95,222 for overhead.
|Cost component||Total cost||Annualized cost|
|Data Collection Activities||42,760||21,380|
|Data Processing and Analysis||29,510||14,755|
|Publication of Results||31,165||15,583|
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 is necessary for the proper performance of AHRQ health care research, quality improvement and 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 Signature
Dated: November 6, 2008.
Carolyn M. Clancy,
[FR Doc. E8-27523 Filed 11-20-08; 8:45 am]
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