Proposed Collection; Comment Request; Investigating the Causes of Post Donation Information (PDI): Errors in the Donor Screening Process, 8080-8081 [2010-3449]
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8080
Federal Register / Vol. 75, No. 35 / Tuesday, February 23, 2010 / Notices
Dated: Feb. 17, 2010.
Mara L. Vanderslice,
Special Assistant.
[FR Doc. 2010–3559 Filed 2–22–10; 8:45 am]
BILLING CODE 4154–07–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; Investigating the Causes of
Post Donation Information (PDI):
Errors in the Donor Screening Process
mstockstill on DSKH9S0YB1PROD with NOTICES
SUMMARY: In compliance with the
requirement of Section 3506(c) (2) (A) of
the Paperwork Reduction Act of 1995,
for opportunity for public comment on
proposed data collection projects, the
National Heart, Lung, and Blood
Institute (NHLBI), the National
Institutes of Health (NIH), will publish
periodic summaries of proposed
projects to the Office of Management
and Budget (OMB) for review and
approval.
Proposed Collection: Title:
Investigating the causes of post donation
information (PDI): Errors in the donor
screening process. Type of Information
Collection Request: NEW. Need and Use
of Information Collection: Blood centers
are required to use a health history
screening questionnaire to obtain
eligibility information for the protection
of the donor and recipient prior to blood
donation. However, the health history
process is known to be error-prone and
the reasons for those errors are largely
unknown and untested. Donors often
fail to report a risk that would have
resulted in deferral. This deferral risk
may be disclosed at a subsequent
donation and is classified as Post
Donation Information (PDI). While this
deferral risk may be at the next donation
event, many examples of PDI are not
disclosed nor discovered until several
intervening donation events have
occurred. The reasons why donors fail
to disclose a deferrable history at the
time of one donation but subsequently
disclose this information at a later time
are unidentified. This protocol is
designed to ascertain why PDI error
events occur. It will be the first study of
any kind to address the issue of PDI
errors in any systematic fashion. By
conducting interviews with donors
involved in PDI errors, we will gain
important qualitative knowledge about
this problem. Information gathered from
these interviews will not only elucidate
the issue of PDI but will provide insight
into donor understanding of the
screening process and their feelings
about the process and blood donation in
general.
The main objectives of the study are:
1. To explore reasons behind errors in
the donor screening process when
donors initially fail to disclose an
accurate and complete health history.
2. To explore PDI donors’ knowledge,
attitudes, behaviors and beliefs (KABB)
about the health history questionnaire
and their experience with the screening
process and the center.
3. To compare KABB in PDI donors to
deferred (but not PDI) donors and
accepted donors.
The study sample will consist of three
donor groups:
1. Donors with a PDI: all identified
donors of interest with an FDA
reportable donor suitability error
classified as PDI at the REDS–II centers
2. Deferred donors: appropriately
deferred (but not PDI deferred donors) at
the REDS–II centers
3. Accepted Donors: appropriately
accepted for donation at the REDS–II
centers
Telephone interviews will be
conducted with consented donors to
collect information regarding their
knowledge, attitudes, behaviors and
beliefs about the donor health history
process. Even though the interviews
with the donors will be individual, we
would like to form groups of similar PDI
and deferred donors for analysis
purposes.
The five groups of interest include
PDI occurrences or deferrals that are due
to
• Travel (malaria, vCJD)
• Medical (history of diseases including
jaundice/hepatitis, surgery and
medications needed to treat disease
including Tegison, Proscar and
Accutane)
• Blood/Disease Exposure (tattoo,
piercings, accidental needle stick)
• High Risk Behavior—Sexual (MSM,
sex with IV drug-user or test-positive
individual)
• High Risk Behavior—Non-Sexual (IV
drug use, non-sexual exposure to
Hepatitis C or Hepatitis B.
All interviews will be digitallyrecorded and the recordings uploaded
onto computers as dss files; these files
will be transcribed and then coupled to
the interviewer notes to form an analytic
package for the data analysts. Once the
interview is conducted successfully,
each study donor will be mailed a check
of $25 as an incentive for participating
in the study.
The cognitive testing of the interview
guide will be conducted at the
Hoxworth Blood Center and at the
Coordinating Center. For this purpose,
the blood center staff will identify 2 PDI
and 2 deferred donors from the five
broad categories of interest. They will
also contact 2 accepted donors for study
consent and interview. These donors
will be approached and consented by
following the same procedures that will
be used for the actual study.
The data from the semi-structured
interviews will be analyzed in two
ways. The close-ended responses will be
analyzed quantitatively. This will likely
take the form of 3-way cross-tabulations
of frequency distributions in responses
to key questions. The open-ended
responses will be analyzed as
qualitative data. All analytic steps and
assumptions that led up to the
conclusions, including competing
interpretations of the data, will be fully
discussed in the final report.
Frequency of Response: Once.
Affected Public: Individuals. Type of
Respondents: Adult blood donors. The
annual reporting burden is a follows:
Estimated Number of Respondents: 408;
Estimated Number of Responses per
Respondent: 1; Average Burden of
Hours per Response: 0.08 for the initial
phone call and 0.5 for responding to the
actual interview; and Estimated Total
Annual Burden Hours Requested: 83.64.
The annualized cost to respondents is
estimated at: $1505.52 (based on $18
per hour). There are no Capital Costs to
report. There are no Operating or
Maintenance Costs to report.
Table 1: Estimate of Requested Burden
Hours and Dollar Value of Burden
Hours
TABLE A.12–1 ESTIMATES OF HOUR BURDEN
Number of respondents
Type of respondents
Donors initially contacted .............................................................
PDI Donors ..................................................................................
Deferred Donors ..........................................................................
VerDate Nov<24>2008
16:25 Feb 22, 2010
Jkt 220001
PO 00000
Frm 00050
408
* 60
* 30
Fmt 4703
Sfmt 4703
Estimated number of responses
per respondent
Average burden
hours per response
1
1
1
E:\FR\FM\23FEN1.SGM
.08
0.5
0.5
23FEN1
Estimated total
annual burden
hours requested
32.6
30
15
8081
Federal Register / Vol. 75, No. 35 / Tuesday, February 23, 2010 / Notices
TABLE A.12–1 ESTIMATES OF HOUR BURDEN—Continued
Number of respondents
Type of respondents
Estimated number of responses
per respondent
Average burden
hours per response
0.5
Accepted Donors .........................................................................
* 12
1
Total ......................................................................................
408
............................
..............................
Estimated total
annual burden
hours requested
6
83.64
* These respondents are a subgroup of total 408 donors who will be initially contacted to participate in the study.
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies should
address one or more of the following
points: (1) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the function of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) Minimize the burden
of the collection of information on those
who are to respond, including the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
For Further Information Contact: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact Dr. George Nemo,
Project Officer, NHLBI, Two Rockledge
Center, Room 9144, 6701 Rockledge
Drive, Bethesda, MD 20892–7950, or
call 301–435–0075, or E-mail your
request to nemog@nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
Dated: February 16, 2010.
George Nemo,
NHLBI Project Officer, NHLBI, National
Institutes of Health.
[FR Doc. 2010–3449 Filed 2–22–10; 8:45 am]
BILLING CODE 4140–01–P
mstockstill on DSKH9S0YB1PROD with NOTICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0585]
Patrick J. Lais: Debarment Order
AGENCY:
Food and Drug Administration,
HHS.
VerDate Nov<24>2008
16:25 Feb 22, 2010
Jkt 220001
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is issuing an
order under the Federal Food, Drug, and
Cosmetic Act (the act) permanently
debarring Patrick J. Lais from providing
services in any capacity to a person that
has an approved or pending drug
product application. We base this order
on a finding that Mr. Lais was convicted
of a felony under Federal law for
conduct relating to the regulation of a
drug product under the act. Mr. Lais has
notified FDA that he acquiesces to
debarment, and therefore has waived his
opportunity for a hearing concerning
this action.
DATES: This order is effective February
23, 2010.
ADDRESSES: Submit applications for
special termination of debarment to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
FOR FURTHER INFORMATION CONTACT:
Kenny Shade, Office of Regulatory
Affairs (HFC–230), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 240–632–6844.
SUPPLEMENTARY INFORMATION:
I. Background
On April 25, 2005, Mr. Patrick J. Lais,
formerly president of York
Pharmaceutical, pleaded guilty to
introducing and delivering, and causing
to be introduced and delivered into
interstate commerce, a drug that was
adulterated within the meaning of 21
U.S.C. 351(a)(2)(B) of the act, a felony
under Federal law in violation of 21
U.S.C. 331(a) and 333(a)(2). Judgment
was entered against him for this felony
on August 15, 2005. The basis for this
conviction was as follows:
Beginning in 1997 and lasting until
September 2001, Mr. Lais was the
president of York Pharmaceutical
(York). Mr. Lais had responsibility for
and authority over drug manufacturing
at York. York manufactured generic
over-the-counter drugs during the
period January 1999 through July 2001.
York distributed in interstate
commerce human drug products that
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
were adulterated within the meaning of
21 U.S.C. 351(a)(2)(B) of the act, in that
York manufactured and distributed,
among other things, subpotent burn
spray, aspirin that had failed dissolution
testing, and antacid products
contaminated with bacteria.
Mr. Lais knew that York’s
manufacturing facility lacked basic
validation processes and controls and
that York’s drug products were
adulterated within the meaning of the
act. Mr. Lais also knew that York: (1)
Did not use procedures that ensured
that its drugs had the identity, strength,
quality, and purity characteristics that
they were represented to possess; (2) did
not test raw materials before using them;
(3) did not perform appropriate
laboratory determinations of
conformance with final specifications
for each of its drug products; (4)
shipped drug product known not to
meet established quality control criteria;
(5) frequently failed to assess the
stability characteristics of the drugs it
produced; (6) did not maintain the
buildings used in the manufacture,
processing, packing, and holding of its
drug products in a clean and sanitary
condition; and (7) did not clean,
maintain, and sanitize its manufacturing
equipment and utensils in such a way
as to prevent contamination of final
drug products.
In January 2000, York manufactured
and compressed a drug product
identified as ‘‘Uncoated Aspirin.’’ This
drug failed its final dissolution testing.
Neither Mr. Lais nor the employees
under his authority and control
determined the cause of the dissolution
failure. Rather, York coated the failed
aspirin and renumbered the lot. Part of
this lot then was packaged as ‘‘Coated
Aspirin.’’ On or about February 21,
2000, Mr. Lais caused the shipment of
625 cases of adulterated drug products,
identified as ‘‘Coated Aspirin,’’ to
customers in Kansas City, MO. In May
2000, this ‘‘Coated Aspirin’’ failed 3–
month stability testing. Mr. Lais and the
employees under his authority and
control did not determine the cause of
the failure and did not inform York’s
customers that the aspirin was
adulterated.
E:\FR\FM\23FEN1.SGM
23FEN1
Agencies
[Federal Register Volume 75, Number 35 (Tuesday, February 23, 2010)]
[Notices]
[Pages 8080-8081]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-3449]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment Request; Investigating the Causes of
Post Donation Information (PDI): Errors in the Donor Screening Process
SUMMARY: In compliance with the requirement of Section 3506(c) (2) (A)
of the Paperwork Reduction Act of 1995, for opportunity for public
comment on proposed data collection projects, the National Heart, Lung,
and Blood Institute (NHLBI), the National Institutes of Health (NIH),
will publish periodic summaries of proposed projects to the Office of
Management and Budget (OMB) for review and approval.
Proposed Collection: Title: Investigating the causes of post
donation information (PDI): Errors in the donor screening process. Type
of Information Collection Request: NEW. Need and Use of Information
Collection: Blood centers are required to use a health history
screening questionnaire to obtain eligibility information for the
protection of the donor and recipient prior to blood donation. However,
the health history process is known to be error-prone and the reasons
for those errors are largely unknown and untested. Donors often fail to
report a risk that would have resulted in deferral. This deferral risk
may be disclosed at a subsequent donation and is classified as Post
Donation Information (PDI). While this deferral risk may be at the next
donation event, many examples of PDI are not disclosed nor discovered
until several intervening donation events have occurred. The reasons
why donors fail to disclose a deferrable history at the time of one
donation but subsequently disclose this information at a later time are
unidentified. This protocol is designed to ascertain why PDI error
events occur. It will be the first study of any kind to address the
issue of PDI errors in any systematic fashion. By conducting interviews
with donors involved in PDI errors, we will gain important qualitative
knowledge about this problem. Information gathered from these
interviews will not only elucidate the issue of PDI but will provide
insight into donor understanding of the screening process and their
feelings about the process and blood donation in general.
The main objectives of the study are:
1. To explore reasons behind errors in the donor screening process
when donors initially fail to disclose an accurate and complete health
history.
2. To explore PDI donors' knowledge, attitudes, behaviors and
beliefs (KABB) about the health history questionnaire and their
experience with the screening process and the center.
3. To compare KABB in PDI donors to deferred (but not PDI) donors
and accepted donors.
The study sample will consist of three donor groups:
1. Donors with a PDI: all identified donors of interest with an FDA
reportable donor suitability error classified as PDI at the REDS-II
centers
2. Deferred donors: appropriately deferred (but not PDI deferred
donors) at the REDS-II centers
3. Accepted Donors: appropriately accepted for donation at the
REDS-II centers
Telephone interviews will be conducted with consented donors to
collect information regarding their knowledge, attitudes, behaviors and
beliefs about the donor health history process. Even though the
interviews with the donors will be individual, we would like to form
groups of similar PDI and deferred donors for analysis purposes.
The five groups of interest include PDI occurrences or deferrals
that are due to
Travel (malaria, vCJD)
Medical (history of diseases including jaundice/hepatitis,
surgery and medications needed to treat disease including Tegison,
Proscar and Accutane)
Blood/Disease Exposure (tattoo, piercings, accidental needle
stick)
High Risk Behavior--Sexual (MSM, sex with IV drug-user or
test-positive individual)
High Risk Behavior--Non-Sexual (IV drug use, non-sexual
exposure to Hepatitis C or Hepatitis B.
All interviews will be digitally-recorded and the recordings
uploaded onto computers as dss files; these files will be transcribed
and then coupled to the interviewer notes to form an analytic package
for the data analysts. Once the interview is conducted successfully,
each study donor will be mailed a check of $25 as an incentive for
participating in the study.
The cognitive testing of the interview guide will be conducted at
the Hoxworth Blood Center and at the Coordinating Center. For this
purpose, the blood center staff will identify 2 PDI and 2 deferred
donors from the five broad categories of interest. They will also
contact 2 accepted donors for study consent and interview. These donors
will be approached and consented by following the same procedures that
will be used for the actual study.
The data from the semi-structured interviews will be analyzed in
two ways. The close-ended responses will be analyzed quantitatively.
This will likely take the form of 3-way cross-tabulations of frequency
distributions in responses to key questions. The open-ended responses
will be analyzed as qualitative data. All analytic steps and
assumptions that led up to the conclusions, including competing
interpretations of the data, will be fully discussed in the final
report.
Frequency of Response: Once. Affected Public: Individuals. Type of
Respondents: Adult blood donors. The annual reporting burden is a
follows: Estimated Number of Respondents: 408; Estimated Number of
Responses per Respondent: 1; Average Burden of Hours per Response: 0.08
for the initial phone call and 0.5 for responding to the actual
interview; and Estimated Total Annual Burden Hours Requested: 83.64.
The annualized cost to respondents is estimated at: $1505.52 (based on
$18 per hour). There are no Capital Costs to report. There are no
Operating or Maintenance Costs to report.
Table 1: Estimate of Requested Burden Hours and Dollar Value of Burden
Hours
Table A.12-1 Estimates of Hour Burden
----------------------------------------------------------------------------------------------------------------
Estimated number Average burden Estimated total
Type of respondents Number of of responses per hours per annual burden
respondents respondent response hours requested
----------------------------------------------------------------------------------------------------------------
Donors initially contacted............ 408 1 .08 32.6
PDI Donors............................ * 60 1 0.5 30
Deferred Donors....................... * 30 1 0.5 15
[[Page 8081]]
Accepted Donors....................... * 12 1 0.5 6
-------------------------------------------------------------------------
Total............................. 408 ................ ................. 83.64
----------------------------------------------------------------------------------------------------------------
* These respondents are a subgroup of total 408 donors who will be initially contacted to participate in the
study.
Request for Comments: Written comments and/or suggestions from the
public and affected agencies should address one or more of the
following points: (1) Evaluate whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) Evaluate the accuracy of the agency's estimate of the
burden of the proposed collection of information, including the
validity of the methodology and assumptions used; (3) Enhance the
quality, utility, and clarity of the information to be collected; and
(4) Minimize the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
For Further Information Contact: To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact Dr. George Nemo, Project Officer, NHLBI, Two
Rockledge Center, Room 9144, 6701 Rockledge Drive, Bethesda, MD 20892-
7950, or call 301-435-0075, or E-mail your request to nemog@nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 60 days
of the date of this publication.
Dated: February 16, 2010.
George Nemo,
NHLBI Project Officer, NHLBI, National Institutes of Health.
[FR Doc. 2010-3449 Filed 2-22-10; 8:45 am]
BILLING CODE 4140-01-P