[Federal Register Volume 66, Number 167 (Tuesday, August 28, 2001)]
[Notices]
[Pages 45314-45315]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-21687]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Agency for Healthcare Research and Quality


Agency Information Collection Activities: Proposed Collection; 
Comment Request

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 the Office of 
Management and Budget (OMB) to allow a proposed information collection 
project: ``Primary Care Network Survey (PRINS)''. In accordance with 
the Paperwork Reduction Act as amended (see in particular 44 U.S.C. 
3506(c)(2)(A)), AHRQ invites the public to comment on this proposed 
information collection request to allow AHRQ to conduct research in 
primary care settings.
    This proposed information collection was previously published in 
the Federal Register on June 19, 2001 and allowed 60 days for public 
comment. No public comments were received. The purpose of this notice 
is to allow an additional 30 days for public comment.

DATES: Comments on this notice must be received by September 27, 2001.

ADDRESSES: Written comments should be submitted to: Allison Eydt, Human 
Resources and Housing Branch, Office of Information and Regulatory 
Affairs, OMB, New Executive Office Building, Room 10235, Washington, DC 
20503.
    Comments submitted in response to this notice will be summarized 
and included in the request for OMB approval of the proposed 
information collection. All comments will become a matter of public 
record.

FOR FURTHER INFORMATION CONTACT: Cynthia D. McMichael, AHRQ, Reports 
Clearance Officer, (301) 594-3132.

SUPPLEMENTARY INFORMATION:

Primary Care Network Survey (PRINS)

    As directed in its reauthorization legislation, AHRQ supports 
activities designated to improve the capacity of practice-based 
research networks (PBRNs) to conduct research in primary care settings. 
A PBRN is a group of ambulatory practices devoted principally to the 
primary care of patients, affiliated with each other in order to 
investigate questions related to community-based practice. AHRQ has 
recently established cooperative agreements with 19 PBRNs who have 
specifically been asked to conduct

[[Page 45315]]

network-defining surveys using a modified version of the 1999-2000 
version of the National Ambulatory Medical Care Survey (NAMCS) 
instrument. We will be dropping a couple of items included in the NAMCS 
instrument.

Method of Collection

    PRINS will provide a range of baseline data on the clinicians 
enrolled in each network, the services provided, and characteristics of 
patients receiving those services. Data to be collected include the 
patients' demographic characteristics and reason(s) for visit, and the 
providers' diagnosis(es) and diagnostic services, medications and 
disposition.
    These data may be used by the PBRN to define the network's capacity 
to study specific clinical conditions seen in primary care, establish a 
denominator for epidemoiological or surveillance studies, and stimulate 
further research on the use, organization and delivery of primary care. 
All identifiable data that is collected will be protected in accordance 
with the AHRQ confidentiality statute, 42 USC 299c-3(c).
    The estimated annual hour burden is as follows:

----------------------------------------------------------------------------------------------------------------
                                                 Number of
                                                respondents    Number of forms/   Avg. burden/       Response
                                                (clinicians)       respondent    form  (in hrs)  burden (hrs)  =
                                                         (1)              (2)              (3)     (1)*(2)*(3)*
                                                                                                 (for rows 1 and
                                                                                                             2)
----------------------------------------------------------------------------------------------------------------
Intake Form.................................           1,000                1              .25              250
Patient Form................................           1,000               30              .03              900
                                             -------------------------------------------------------------------
    Total...................................           1,000               31             .037            1.150
----------------------------------------------------------------------------------------------------------------

    To calculate the burden hours, the number of respondents for PRINS 
is based on a sample of 1,000 clinicians who have agreed to advance to 
participate. Each clinician fills out an intake form (which requires 
about 15 minutes).
    The same 1,000 then record (on separate forms) information about 30 
consecutive patients seen in his/her practice (requiring less than 2 
minutes per form to complete). The total cost to the volunteer 
respondents is estimated to be $150,000 or $150 each.

Request for Comments

    Comments are invited on: (a) The necessity of the proposed 
collections; (b) the accuracy of the Agency's estimate of burden 
(including hours and cost) of the proposed collection 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 request for OMB approval of the proposed 
information collection. All comments will become a matter of public 
record.
    Copies of these proposed collection plans and instruments can be 
obtained from the AHRQ Reports Clearance Officer (see above).

    Dated: August 21, 2001.
John M. Eisenberg,
Director.
[FR Doc. 01-21687 Filed 8-27-01; 8:45 am]
BILLING CODE 4160-90-M