Organ Procurement and Transplantation Network, 10616-10619 [E7-4267]
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10616
Federal Register / Vol. 72, No. 46 / Friday, March 9, 2007 / Rules and Regulations
Fairness Act of 1996, generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of the
Congress and to the Comptroller General
of the United States. EPA will submit a
report containing this rule and other
required information to the U.S. Senate,
the U.S. House of Representatives, and
the Comptroller General of the United
States prior to publication of the rule in
the Federal Register. A major rule
cannot take effect until 60 days after it
is published in the Federal Register.
This action is not a ‘‘major rule’’ as
defined by 5 U.S.C. 804(2).
Under section 307(b)(1) of the CAA,
petitions for judicial review of this
action must be filed in the United States
Court of Appeals for the appropriate
circuit by May 8, 2007. Filing a petition
for reconsideration by the Administrator
of this final rule does not affect the
finality of this rule for the purposes of
judicial review nor does it extend the
time within which a petition for judicial
review may be filed, and shall not
postpone the effectiveness of such rule
or action. This action may not be
challenged later in proceedings to
enforce its requirements. (See section
307(b)(2).)
permits, Reporting and recordkeeping
requirements.
Dated: February 27, 2007.
John B. Askew,
Regional Administrator, Region 7.
List of Subjects
Chapter I, Title 40 of the Code of
Federal Regulations is amended as
follows:
40 CFR Part 52
PART 52—[AMENDED]
Environmental protection, Air
pollution control, Carbon monoxide,
Incorporation by reference,
Intergovernmental relations, Lead,
Nitrogen dioxide, Ozone, Particulate
matter, Reporting and recordkeeping
requirements, Sulfur oxides, Volatile
organic compounds.
I
I
1. The authority citation for Part 52
continues to read as follows:
Authority: 42 U.S.C. 7401 et seq.
Subpart AA—Missouri
2. In § 52.1320(c) the table is amended
under Chapter 6 by revising the entry
for ‘‘10–6.110’’ to read as follows:
I
40 CFR Part 70
§ 52.1320
Administrative practice and
procedure, Air pollution control,
Intergovernmental relations, Operating
*
Identification of plan.
*
*
(c) * * *
*
*
EPA-APPROVED MISSOURI REGULATIONS
Missouri citation
State effective
date
Title
EPA approval date
Explanation
Missouri Department of Natural Resources
*
*
*
*
*
*
*
Chapter 6—Air Quality Standards, Definitions, Sampling and Reference Methods, and Air Pollution Control Regulations for the State of
Missouri
*
10–6.110 ...................
*
*
*
Submission of Emission Data, Emission Fees,
and Process Information.
*
*
*
12/30/06
*
*
*
3/9/07 [insert FR page
number where the
document begins].
*
PART 70—[AMENDED]
3. The authority citation for Part 70
continues to read as follows:
Emission Data, Emission Fees, and Process
Information’’ on December 11, 2006;
approval of sections (3)(D)1., (3)(D)2.E., and
(3)(D)2.F. effective May 8, 2007.
*
*
*
*
*
*
I
*
*
*
*
[FR Doc. E7–4176 Filed 3–8–07; 8:45 am]
Authority: 42 U.S.C. 7401, et seq.
BILLING CODE 6560–50–P
Appendix A—[Amended]
4. Appendix A to Part 70 is amended
by adding paragraph (u) under Missouri
to read as follows:
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15:24 Mar 08, 2007
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42 CFR Part 121
SUMMARY: This Final Rule sets forth the
Secretary’s decision to include
intestines within the definition of
organs covered by the regulations
governing the operations of the Organ
Procurement and Transplantation
(u) The Missouri Department of Natural
Resources submitted revisions to Missouri
rule 10 CSR 10–6.110, ‘‘Submission of
VerDate Aug<31>2005
Health Resources and Services
Administration
Health Resources and Services
Administration, HHS.
ACTION: Final rule.
*
*
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
AGENCY:
Missouri
*
*
Organ Procurement and
Transplantation Network
Appendix A to Part 70—Approval
Status of State and Local Operating
Permits Programs
*
*
RIN 0906AA62
I
*
*
Section (3)(D), Emissions Fees, has not
been approved as
part of the SIP.
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Federal Register / Vol. 72, No. 46 / Friday, March 9, 2007 / Rules and Regulations
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Network. The Secretary under the
authority granted by section 301 of the
National Organ Transplant Act, as
amended, further effects a
corresponding change to the definition
of human organs covered in the statute
with this Final Rule.
DATES: This Final Rule is effective
March 9, 2007.
FOR FURTHER INFORMATION CONTACT: Jim
Burdick, M.D., Director, Division of
Transplantation, Healthcare Systems
Bureau, Health Resources and Services
Administration (HRSA), 5600 Fishers
Lane, Room 12C–06, Rockville,
Maryland 20857.
SUPPLEMENTARY INFORMATION:
Adding Intestines to the Definition of
Organs Covered by the Rules Governing
the Operation of the Organ
Procurement and Transplantation
Network (OPTN)
Based upon a review of intestinal
transplants, the Secretary believes that
intestines should now be included
within the definition of organs covered
by the rules governing the operation of
the OPTN (42 CFR part 121) (hereinafter
the final rule). This Final Rule sets forth
the history of intestinal transplants, the
factors that have persuaded the
Department of the advisability of
including intestines within the ambit of
the regulations governing the operation
of the OPTN, and the anticipated
consequences of this Rule.
The first successful intestinal
transplant was performed in 1989.
Intestinal transplantation may be
considered for patients with irreversible
intestinal failure due to surgery, trauma,
or acquired or congenital disease who
cannot be managed through the
intravenous delivery of nutrients, also
referred to as total parenteral nutrition
(TPN). Although intestinal transplants
have been performed for years,
considerable morbidity and mortality
have limited widespread clinical use.
Complications are frequent and include
acute and chronic rejection,
lymphoproliferative disease, and serious
infections such as cytomegalovirus
disease. For patients who received
intestinal transplants in the United
States from January 2000 through June
2002, one-year graft and patient survival
rates were 67 percent and 81 percent
respectively for adults, and 58 percent
and 65 percent respectively for pediatric
recipients. Despite the shortcomings,
the number of candidates for intestinal
transplants and the number of intestinal
transplants performed annually is
increasing.
The OPTN first adopted voluntary
intestinal organ allocation policies and
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15:24 Mar 08, 2007
Jkt 211001
began to maintain a list of patients
waiting for intestinal transplants in
1993. On December 31, 1993, only 43
candidates were listed on the intestinal
transplant waiting list, compared to 169
candidates on this list on October 24,
2003. The number of intestinal
transplants performed annually has
more than tripled from 34 transplants in
1993 to 109 transplants in 2002.
However, the volume of transplants per
transplant center is relatively small. Ten
transplant centers performed one or
more intestinal transplants in 2002; only
five of these centers performed ten or
more transplants. Overall median
waiting time was 319 days for patients
added to the intestinal transplant
waiting list in 2001.
According to the OPTN, intestinal
organ allocation may include the
esophagus, stomach, small and/or large
intestine, or any portion of the
gastrointestinal tract as determined by
the medical needs of individual patients
(OPTN Policy 3.11). OPTN voluntary
policies are available at https://
www.optn.org/policiesandbylaws/
policies.asp. In addition to allocation for
isolated intestinal transplants, the
OPTN addresses allocation of the liverintestine combination and multiple
organs.
The nature of the regulatory
framework governing the operation of
the OPTN underlies the importance of
including intestines within the
definition of organs covered by the
regulations. Under the final rule, the
OPTN must submit proposed policies
for review and approval by the Secretary
according to the requirements of 42 CFR
121.4. Upon consideration of public
comments on proposed policies that are
considered significant, the Secretary
will determine whether to make such
proposed policies enforceable in
accordance with 42 CFR 121.10. Any
transplant hospital that fails to comply
with any allocation policy approved as
enforceable by the Secretary under this
process will be subject to the
enforcement sanctions delineated in 42
CFR 121.10, including termination from
the Medicare and Medicaid programs.
The Secretary is legally obliged, as
part of his responsibilities in
administering the Medicare and
Medicaid programs, to require hospitals
that transplant organs to comply with
the rules and requirements of the OPTN
as a condition of their participation in
Medicare and Medicaid under 42 U.S.C.
1320b–8(a)(1)(B). Because intestines
currently are not included within the
regulation’s definition of organs, the
Secretary cannot make any intestinal
allocation policy enforceable. The
inclusion of intestines as covered organs
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10617
under this Final Rule will allow the
Secretary to take appropriate
enforcement actions against a transplant
hospital that fails to comply with any
OPTN intestinal allocation policy if
such a policy is approved by the
Secretary. This enforcement authority is
particularly significant given that many
recipients of transplanted intestines
receive such organs together with other
organs covered under the regulations. It
is necessary to ensure that intestinal
organ allocation, whether pertaining to
isolated intestinal transplants or
combined/multi-organ transplants, is
consistent with the goal of an equitable
national system for organ allocation.
Enforcing the allocation for organs
currently covered under the regulations,
such as livers, would be difficult when
intestines are transplanted together with
other such organs if an intestinal
allocation is not subject to the
Secretary’s enforcement authority.
As the field of intestinal
transplantation evolves, it will become
more critical that intestinal organ
allocation keeps pace with advances in
the field; that policy development
include performance indicators to assess
whether the goals of an equitable
transplant system are being achieved;
that the Secretary has the authority to
make those policies enforceable; and
that patients and physicians have timely
access to accurate data that will assist
them in making decisions regarding
intestinal transplantation. Upon
consideration of the foregoing factors,
and in order to achieve the most
equitable and medically effective use of
donated organs, the Secretary has
determined that intestines should
explicitly be added to the definition of
organs covered by the OPTN regulations
at 42 CFR Part 121.
Public Participation
The public was invited to respond to
the Notice of Proposed Rulemaking
(NPRM) which was published in the
Federal Register on November 23, 2005
(70 FR 70765–70768). The NPRM
provided for a 60-day comment period.
We received a total of three comments
from the public. All three comments
were in support of adding intestines to
the definition of organs covered by the
rules governing the OPTN and
encouraged coordination with the
Centers for Medicare and Medicaid
Services. Consequently, this Final Rule
is the same as the proposed rule
published on November 23, 2005.
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Federal Register / Vol. 72, No. 46 / Friday, March 9, 2007 / Rules and Regulations
Soliciting Public Comment as to
Whether Any Other Organs Should Be
Covered by the Rules Governing the
Operation of the OPTN
The Secretary invited public comment
as to the advisability of including any
other organ within the ambit of this
final rule. The comments we received
did not request the inclusion of any
other organ under the OPTN
regulations.
Including Intestines Within the
Definition of Human Organs Covered by
Section 301 of NOTA
The Secretary further invited public
comment on including intestines within
the definition of human organs covered
by section 301, as amended, of the
National Organ Transplant Act (NOTA)
(hereinafter section 301), which
prohibits the purchase or sale of human
organs for human transplantation.
Originally as enacted section 301 of
NOTA (Pub. L. 98–507) defined the term
‘‘human organ’’ as ‘‘the human kidney,
liver, heart, lung, pancreas, bone
marrow, cornea, eye, bone, and skin and
any other human organ specified by the
Secretary of Health and Human Services
by regulation.’’ NOTA, Public Law 98–
507, Title III, section 301, 98 Stat. 2346–
2347 (1984). This section was
subsequently amended by Congress to
include fetal organs, as well as subparts
of the specified organs, by Public Law
100–607, section 407.
As set forth by statute, Congress
authorized the Secretary to add
additional organs to the definition of
‘‘human organ’’ covered by section 301
through rulemaking in order to include
the transplantation of additional human
organs. Through this Final Rule, the
Secretary adds intestines to the list of
human organs covered by section 301.
The Secretary adds a new section to 42
CFR Part 121 to effectuate this change.
The comments we received supported
adding intestines to the definition of
organs covered under section 301 of
NOTA and encouraged coordination
with the Centers for Medicare and
Medicaid Services regarding
implementation of the respective but
related authorities regarding organ
procurement and transplantation.
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Economic and Regulatory Impact
Executive Order 12866 directs
agencies to assess all costs and benefits
of available regulatory alternatives and,
when rulemaking is necessary, to select
regulatory approaches that provide the
greatest net benefits (including potential
economic, environmental, public health,
safety, distributive and equity effects).
In addition, under the Regulatory
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Flexibility Act, if a rule has a significant
economic effect on a substantial number
of small entities the Secretary must
specifically consider the economic
effect of a rule on small entities and
analyze regulatory options that could
lessen the impact of the rule.
Executive Order 12866 requires that
all regulations reflect consideration of
alternatives, of costs, of benefits, of
incentives, of equity, and of available
information. Regulations must meet
certain standards, such as avoiding an
unnecessary burden. Regulations which
are ‘‘significant’’ because of cost,
adverse effects on the economy,
inconsistency with other agency actions,
effects on the budget, or novel legal or
policy issues, require special analysis.
The Secretary has determined that no
resources are required to implement the
requirements in this Final Rule.
Therefore, in accordance with the
Regulatory Flexibility Act of 1980
(RFA), and the Small Business
Regulatory Enforcement Act of 1996,
which amended the RFA, the Secretary
certifies that this rule will not have a
significant impact on a substantial
number of small entities. Since
independent and hospital-based organ
procurement organizations (OPOs) are
not considered small rural hospitals
because OPOs generally service large
geographical areas, a regulatory
flexibility analysis under the RFA and a
rural impact analysis under section
1102(b) of the Act are not required.
The Secretary has also determined
that this Final Rule does not meet the
criteria for a major rule as defined by
Executive Order 12866, as amended by
Executive Order 13258, and would have
no major effect on the economy or
Federal expenditures. We have
determined that the Final Rule is not a
‘‘major rule’’ within the meaning of the
statute providing for Congressional
Review of Agency Rulemaking, 5 U.S.C.
801. Similarly, it will not have effects
on State, local, and tribal governments
and on the private sector such as to
require consultation under the
Unfunded Mandates Reform Act of
1995.
Nor on the basis of family well-being
will the provisions of this Final Rule
affect the following family elements:
Family safety, family stability, marital
commitment; parental rights in the
education, nurture and supervision of
their children; family functioning,
disposable income or poverty; or the
behavior and personal responsibility of
youth, as determined under section
654(c) of the Treasury and General
Government Appropriations Act of
1999.
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As stated above, this Final Rule will
modify the regulations governing the
OPTN and section 301 of NOTA based
on legal authority.
Impact of the New Rule
This Final Rule will have the effect of
including human intestines within the
ambit of the regulations governing the
operation of the OPTN, and will include
transplanted human intestines within
the changes made at section 301 of
NOTA. The changes made in this Rule
will authorize the Secretary to take
enforcement actions against entities
violating OPTN policies pertaining to
the transplantation of intestines once
such policies are approved as
enforceable by the Secretary. In
addition, individuals violating section
301 of NOTA with respect to intestinal
transplants will be subject to criminal
penalties.
Paperwork Reduction Act of 1995
The amendments proposed in this
Rule will not impose any additional
data collection requirements beyond
those already imposed under the current
regulations, which have been approved
by the Office of Management and
Budget (OMB No. 0915–0157). The
currently approved data collection
includes worksheets and burden for
intestinal transplants.
List of Subjects in 42 CFR Part 121
Health care, Hospitals, Organ
transplantation, Reporting and
recordkeeping requirements.
Dated: March 9, 2007.
Elizabeth M. Duke,
Administrator, Health Resources and Services
Administration.
Approved: November 27, 2006.
Michael O. Leavitt,
Secretary.
Accordingly, 42 CFR part 121 is
amended as set forth below:
I
PART 121—ORGAN PROCUREMENT
AND TRANSPLANTATION NETWORK
1. The authority citation for part 121
is revised to read as follows:
I
Authority: Sections 215, 371–376 of the
Public Health Service Act (42 U.S.C. 216,
273–274d); sections 1102, 1106, 1138 and
1871 of the Social Security Act (42 U.S.C.
1302, 1306, 1320b–8 and 1395hh); and
section 301 of the National Organ Transplant
Act, as amended (42 U.S.C. 274e).
2. Amend § 121.1 as follows:
a. Amend paragraph (a) by removing
the phrase ‘‘this part apply’’ and adding
in its place the phrase ‘‘this part, with
the exception of § 121.13, apply.’’
I
I
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09MRR1
Federal Register / Vol. 72, No. 46 / Friday, March 9, 2007 / Rules and Regulations
§ 121.2
b. Redesignate paragraph (b) as
paragraph (c).
I c. Add a new paragraph (b).
The revision reads as follows:
I
§ 121.1
Applicability.
*
*
*
*
*
(b) The provisions of § 121.13 apply to
the prohibition set forth in section 301
of the National Organ Transplant Act, as
amended.
*
*
*
*
*
[Amended]
I 3. Amend the definition of ‘‘organ’’ in
§ 121.2 by removing the word ‘‘or’’ and
by adding the phrase ‘‘, or intestine
(including the esophagus, stomach,
small and/or large intestine, or any
portion of the gastrointestinal tract)’’
after the term ‘‘pancreas.’’
4. Add a new § 121.13 to read as
follows:
I
§ 121.13 Definition of Human Organ Under
section 301 of the National Organ
Transplant Act, as amended.
‘‘Human organ,’’ as covered by section
301 of the National Organ Transplant
Act, as amended, means the human
(including fetal) kidney, liver, heart,
lung, pancreas, bone marrow, cornea,
eye, bone, skin, and intestine, including
the esophagus, stomach, small and/or
large intestine, or any portion of the
gastrointestinal tract.
[FR Doc. E7–4267 Filed 3–8–07; 8:45 am]
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BILLING CODE 4160–15–P
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Agencies
[Federal Register Volume 72, Number 46 (Friday, March 9, 2007)]
[Rules and Regulations]
[Pages 10616-10619]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-4267]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
42 CFR Part 121
RIN 0906AA62
Organ Procurement and Transplantation Network
AGENCY: Health Resources and Services Administration, HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This Final Rule sets forth the Secretary's decision to include
intestines within the definition of organs covered by the regulations
governing the operations of the Organ Procurement and Transplantation
[[Page 10617]]
Network. The Secretary under the authority granted by section 301 of
the National Organ Transplant Act, as amended, further effects a
corresponding change to the definition of human organs covered in the
statute with this Final Rule.
DATES: This Final Rule is effective March 9, 2007.
FOR FURTHER INFORMATION CONTACT: Jim Burdick, M.D., Director, Division
of Transplantation, Healthcare Systems Bureau, Health Resources and
Services Administration (HRSA), 5600 Fishers Lane, Room 12C-06,
Rockville, Maryland 20857.
SUPPLEMENTARY INFORMATION:
Adding Intestines to the Definition of Organs Covered by the Rules
Governing the Operation of the Organ Procurement and Transplantation
Network (OPTN)
Based upon a review of intestinal transplants, the Secretary
believes that intestines should now be included within the definition
of organs covered by the rules governing the operation of the OPTN (42
CFR part 121) (hereinafter the final rule). This Final Rule sets forth
the history of intestinal transplants, the factors that have persuaded
the Department of the advisability of including intestines within the
ambit of the regulations governing the operation of the OPTN, and the
anticipated consequences of this Rule.
The first successful intestinal transplant was performed in 1989.
Intestinal transplantation may be considered for patients with
irreversible intestinal failure due to surgery, trauma, or acquired or
congenital disease who cannot be managed through the intravenous
delivery of nutrients, also referred to as total parenteral nutrition
(TPN). Although intestinal transplants have been performed for years,
considerable morbidity and mortality have limited widespread clinical
use. Complications are frequent and include acute and chronic
rejection, lymphoproliferative disease, and serious infections such as
cytomegalovirus disease. For patients who received intestinal
transplants in the United States from January 2000 through June 2002,
one-year graft and patient survival rates were 67 percent and 81
percent respectively for adults, and 58 percent and 65 percent
respectively for pediatric recipients. Despite the shortcomings, the
number of candidates for intestinal transplants and the number of
intestinal transplants performed annually is increasing.
The OPTN first adopted voluntary intestinal organ allocation
policies and began to maintain a list of patients waiting for
intestinal transplants in 1993. On December 31, 1993, only 43
candidates were listed on the intestinal transplant waiting list,
compared to 169 candidates on this list on October 24, 2003. The number
of intestinal transplants performed annually has more than tripled from
34 transplants in 1993 to 109 transplants in 2002. However, the volume
of transplants per transplant center is relatively small. Ten
transplant centers performed one or more intestinal transplants in
2002; only five of these centers performed ten or more transplants.
Overall median waiting time was 319 days for patients added to the
intestinal transplant waiting list in 2001.
According to the OPTN, intestinal organ allocation may include the
esophagus, stomach, small and/or large intestine, or any portion of the
gastrointestinal tract as determined by the medical needs of individual
patients (OPTN Policy 3.11). OPTN voluntary policies are available at
https://www.optn.org/policiesandbylaws/policies.asp. In addition to
allocation for isolated intestinal transplants, the OPTN addresses
allocation of the liver-intestine combination and multiple organs.
The nature of the regulatory framework governing the operation of
the OPTN underlies the importance of including intestines within the
definition of organs covered by the regulations. Under the final rule,
the OPTN must submit proposed policies for review and approval by the
Secretary according to the requirements of 42 CFR 121.4. Upon
consideration of public comments on proposed policies that are
considered significant, the Secretary will determine whether to make
such proposed policies enforceable in accordance with 42 CFR 121.10.
Any transplant hospital that fails to comply with any allocation policy
approved as enforceable by the Secretary under this process will be
subject to the enforcement sanctions delineated in 42 CFR 121.10,
including termination from the Medicare and Medicaid programs.
The Secretary is legally obliged, as part of his responsibilities
in administering the Medicare and Medicaid programs, to require
hospitals that transplant organs to comply with the rules and
requirements of the OPTN as a condition of their participation in
Medicare and Medicaid under 42 U.S.C. 1320b-8(a)(1)(B). Because
intestines currently are not included within the regulation's
definition of organs, the Secretary cannot make any intestinal
allocation policy enforceable. The inclusion of intestines as covered
organs under this Final Rule will allow the Secretary to take
appropriate enforcement actions against a transplant hospital that
fails to comply with any OPTN intestinal allocation policy if such a
policy is approved by the Secretary. This enforcement authority is
particularly significant given that many recipients of transplanted
intestines receive such organs together with other organs covered under
the regulations. It is necessary to ensure that intestinal organ
allocation, whether pertaining to isolated intestinal transplants or
combined/multi-organ transplants, is consistent with the goal of an
equitable national system for organ allocation. Enforcing the
allocation for organs currently covered under the regulations, such as
livers, would be difficult when intestines are transplanted together
with other such organs if an intestinal allocation is not subject to
the Secretary's enforcement authority.
As the field of intestinal transplantation evolves, it will become
more critical that intestinal organ allocation keeps pace with advances
in the field; that policy development include performance indicators to
assess whether the goals of an equitable transplant system are being
achieved; that the Secretary has the authority to make those policies
enforceable; and that patients and physicians have timely access to
accurate data that will assist them in making decisions regarding
intestinal transplantation. Upon consideration of the foregoing
factors, and in order to achieve the most equitable and medically
effective use of donated organs, the Secretary has determined that
intestines should explicitly be added to the definition of organs
covered by the OPTN regulations at 42 CFR Part 121.
Public Participation
The public was invited to respond to the Notice of Proposed
Rulemaking (NPRM) which was published in the Federal Register on
November 23, 2005 (70 FR 70765-70768). The NPRM provided for a 60-day
comment period. We received a total of three comments from the public.
All three comments were in support of adding intestines to the
definition of organs covered by the rules governing the OPTN and
encouraged coordination with the Centers for Medicare and Medicaid
Services. Consequently, this Final Rule is the same as the proposed
rule published on November 23, 2005.
[[Page 10618]]
Soliciting Public Comment as to Whether Any Other Organs Should Be
Covered by the Rules Governing the Operation of the OPTN
The Secretary invited public comment as to the advisability of
including any other organ within the ambit of this final rule. The
comments we received did not request the inclusion of any other organ
under the OPTN regulations.
Including Intestines Within the Definition of Human Organs Covered by
Section 301 of NOTA
The Secretary further invited public comment on including
intestines within the definition of human organs covered by section
301, as amended, of the National Organ Transplant Act (NOTA)
(hereinafter section 301), which prohibits the purchase or sale of
human organs for human transplantation.
Originally as enacted section 301 of NOTA (Pub. L. 98-507) defined
the term ``human organ'' as ``the human kidney, liver, heart, lung,
pancreas, bone marrow, cornea, eye, bone, and skin and any other human
organ specified by the Secretary of Health and Human Services by
regulation.'' NOTA, Public Law 98-507, Title III, section 301, 98 Stat.
2346-2347 (1984). This section was subsequently amended by Congress to
include fetal organs, as well as subparts of the specified organs, by
Public Law 100-607, section 407.
As set forth by statute, Congress authorized the Secretary to add
additional organs to the definition of ``human organ'' covered by
section 301 through rulemaking in order to include the transplantation
of additional human organs. Through this Final Rule, the Secretary adds
intestines to the list of human organs covered by section 301. The
Secretary adds a new section to 42 CFR Part 121 to effectuate this
change.
The comments we received supported adding intestines to the
definition of organs covered under section 301 of NOTA and encouraged
coordination with the Centers for Medicare and Medicaid Services
regarding implementation of the respective but related authorities
regarding organ procurement and transplantation.
Economic and Regulatory Impact
Executive Order 12866 directs agencies to assess all costs and
benefits of available regulatory alternatives and, when rulemaking is
necessary, to select regulatory approaches that provide the greatest
net benefits (including potential economic, environmental, public
health, safety, distributive and equity effects). In addition, under
the Regulatory Flexibility Act, if a rule has a significant economic
effect on a substantial number of small entities the Secretary must
specifically consider the economic effect of a rule on small entities
and analyze regulatory options that could lessen the impact of the
rule.
Executive Order 12866 requires that all regulations reflect
consideration of alternatives, of costs, of benefits, of incentives, of
equity, and of available information. Regulations must meet certain
standards, such as avoiding an unnecessary burden. Regulations which
are ``significant'' because of cost, adverse effects on the economy,
inconsistency with other agency actions, effects on the budget, or
novel legal or policy issues, require special analysis.
The Secretary has determined that no resources are required to
implement the requirements in this Final Rule. Therefore, in accordance
with the Regulatory Flexibility Act of 1980 (RFA), and the Small
Business Regulatory Enforcement Act of 1996, which amended the RFA, the
Secretary certifies that this rule will not have a significant impact
on a substantial number of small entities. Since independent and
hospital-based organ procurement organizations (OPOs) are not
considered small rural hospitals because OPOs generally service large
geographical areas, a regulatory flexibility analysis under the RFA and
a rural impact analysis under section 1102(b) of the Act are not
required.
The Secretary has also determined that this Final Rule does not
meet the criteria for a major rule as defined by Executive Order 12866,
as amended by Executive Order 13258, and would have no major effect on
the economy or Federal expenditures. We have determined that the Final
Rule is not a ``major rule'' within the meaning of the statute
providing for Congressional Review of Agency Rulemaking, 5 U.S.C. 801.
Similarly, it will not have effects on State, local, and tribal
governments and on the private sector such as to require consultation
under the Unfunded Mandates Reform Act of 1995.
Nor on the basis of family well-being will the provisions of this
Final Rule affect the following family elements: Family safety, family
stability, marital commitment; parental rights in the education,
nurture and supervision of their children; family functioning,
disposable income or poverty; or the behavior and personal
responsibility of youth, as determined under section 654(c) of the
Treasury and General Government Appropriations Act of 1999.
As stated above, this Final Rule will modify the regulations
governing the OPTN and section 301 of NOTA based on legal authority.
Impact of the New Rule
This Final Rule will have the effect of including human intestines
within the ambit of the regulations governing the operation of the
OPTN, and will include transplanted human intestines within the changes
made at section 301 of NOTA. The changes made in this Rule will
authorize the Secretary to take enforcement actions against entities
violating OPTN policies pertaining to the transplantation of intestines
once such policies are approved as enforceable by the Secretary. In
addition, individuals violating section 301 of NOTA with respect to
intestinal transplants will be subject to criminal penalties.
Paperwork Reduction Act of 1995
The amendments proposed in this Rule will not impose any additional
data collection requirements beyond those already imposed under the
current regulations, which have been approved by the Office of
Management and Budget (OMB No. 0915-0157). The currently approved data
collection includes worksheets and burden for intestinal transplants.
List of Subjects in 42 CFR Part 121
Health care, Hospitals, Organ transplantation, Reporting and
recordkeeping requirements.
Dated: March 9, 2007.
Elizabeth M. Duke,
Administrator, Health Resources and Services Administration.
Approved: November 27, 2006.
Michael O. Leavitt,
Secretary.
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Accordingly, 42 CFR part 121 is amended as set forth below:
PART 121--ORGAN PROCUREMENT AND TRANSPLANTATION NETWORK
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1. The authority citation for part 121 is revised to read as follows:
Authority: Sections 215, 371-376 of the Public Health Service
Act (42 U.S.C. 216, 273-274d); sections 1102, 1106, 1138 and 1871 of
the Social Security Act (42 U.S.C. 1302, 1306, 1320b-8 and 1395hh);
and section 301 of the National Organ Transplant Act, as amended (42
U.S.C. 274e).
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2. Amend Sec. 121.1 as follows:
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a. Amend paragraph (a) by removing the phrase ``this part apply'' and
adding in its place the phrase ``this part, with the exception of Sec.
121.13, apply.''
[[Page 10619]]
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b. Redesignate paragraph (b) as paragraph (c).
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c. Add a new paragraph (b).
The revision reads as follows:
Sec. 121.1 Applicability.
* * * * *
(b) The provisions of Sec. 121.13 apply to the prohibition set
forth in section 301 of the National Organ Transplant Act, as amended.
* * * * *
Sec. 121.2 [Amended]
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3. Amend the definition of ``organ'' in Sec. 121.2 by removing the
word ``or'' and by adding the phrase ``, or intestine (including the
esophagus, stomach, small and/or large intestine, or any portion of the
gastrointestinal tract)'' after the term ``pancreas.''
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4. Add a new Sec. 121.13 to read as follows:
Sec. 121.13 Definition of Human Organ Under section 301 of the
National Organ Transplant Act, as amended.
``Human organ,'' as covered by section 301 of the National Organ
Transplant Act, as amended, means the human (including fetal) kidney,
liver, heart, lung, pancreas, bone marrow, cornea, eye, bone, skin, and
intestine, including the esophagus, stomach, small and/or large
intestine, or any portion of the gastrointestinal tract.
[FR Doc. E7-4267 Filed 3-8-07; 8:45 am]
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