Schedule for Rating Disabilities: Infectious Diseases, Immune Disorders, and Nutritional Deficiencies, 1678-1690 [2019-00636]
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DEPARTMENT OF VETERANS
AFFAIRS
38 CFR Part 4
RIN 2900–AQ43
Schedule for Rating Disabilities:
Infectious Diseases, Immune
Disorders, and Nutritional Deficiencies
Department of Veterans Affairs.
Proposed rule.
AGENCY:
ACTION:
The Department of Veterans
Affairs (VA) proposes to amend the
section of the VA Schedule for Rating
Disabilities (VASRD or Rating Schedule)
that addresses infectious diseases and
immune disorders. The purpose of these
changes is to incorporate medical
advances since the last revision, update
medical terminology, and clarify
evaluation criteria. The proposed rule
considers comments from experts and
the public during a forum held from
January 31 to February 1, 2011, on
revising this section of the VASRD.
DATES: Comments must be received by
VA on or before April 8, 2019.
ADDRESSES: Written comments may be
submitted through www.regulations.gov;
by mail or hand-delivery to Director,
Regulation Policy and Management
(00REG), Department of Veterans
Affairs, 810 Vermont Ave. NW, Room
1063B, Washington, DC 20420; or by fax
to (202) 273–9026. (This is not a toll free
number.) Comments should indicate
that they are submitted in response to
‘‘RIN 2900–AQ43—Schedule for Rating
Disabilities: Infectious Diseases,
Immune Disorders, and Nutritional
Deficiencies.’’ Copies of comments
received will be available for public
inspection in the Office of Regulation
Policy and Management, Room 1063B,
between the hours of 8 a.m. and 4:30
p.m., Monday through Friday (except
holidays). Please call (202) 461–4902 for
an appointment. (This is not a toll free
number.) In addition, during the
comment period, comments may be
viewed online through the Federal
Docket Management System (FDMS) at
www.Regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Ioulia Vvedenskaya, M.D., M.B.A.,
Medical Officer, Part 4 VASRD
Regulations Staff (211C), Compensation
Service, Veterans Benefits
Administration, Department of Veterans
Affairs, 810 Vermont Avenue NW,
Washington, DC 20420, (202) 461–9700.
(This is not a toll-free telephone
number.)
SUPPLEMENTARY INFORMATION: As part of
its ongoing revision of the VASRD, VA
proposes changes to 38 CFR 4.88a,
SUMMARY:
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which pertains to chronic fatigue
syndrome (CFS), and 38 CFR 4.88b,
which pertains to the schedule of
ratings for infectious diseases and
immune disorders (we note that the
proposed changes for § 4.88b exclude
the schedule of ratings for nutritional
deficiencies—diagnostic codes (DC)
6313, 6314, and 6315). VA last updated
the schedule of ratings in § 4.88b on July
31, 1996 (see 61 FR 39875) and updated
§ 4.88a on July 19, 1995 (see 60 FR
37012).
VA proposes to: (1) Update the
medical terminology and definition of
certain infectious diseases and immune
disorders; (2) add medical conditions
not currently in the Rating Schedule; (3)
refine evaluation criteria based on
medical advances that have occurred
since the last revision; and (4)
incorporate current understanding of
functional changes associated with or
resulting from disease
(pathophysiology).
A panel of independent experts
convened by the Institute of Medicine
(IOM) in February 2015 proposed an
updated set of diagnostic criteria for
infectious disease and immune
disorders. This updated revision also
included changing the name of CFS to
‘‘Systemic Exertion Intolerance Disease
(SEID)/Chronic fatigue Syndrome
(CFS).’’
VA has clear authority to make this
regulatory change because of its broad
authority to ‘‘prescribe all rules and
regulations which are necessary or
appropriate to carry out the laws
administered by [VA] and are consistent
with those laws.’’ 38 U.S.C. 501(a); see
also 38 U.S.C. 1155 (VA’s authority to
adopt and apply schedule for rating
disabilities).
§ 4.88a Chronic Fatigue Syndrome
Currently, § 4.88a specifies older
diagnostic criteria for the diagnosis of
CFS and uses outdated terminology to
refer to this complex disease. VA
proposes to update the nomenclature for
this disease, which is also known as
systemic exertion intolerance disease
(SEID) or myalgic encephalomyelitis
(ME), by changing the diagnostic code
name to ‘‘Systemic Exertion Intolerance
Disease (SEID)/Chronic Fatigue
Syndrome (CFS).’’ This new name
captures a central characteristic of the
disease that reflects negative effects of
any exertion (physical, cognitive, or
emotional) on patients’ many organ
systems. IOM (Institute of Medicine),
Beyond Myalgic Encephalomyelitis/
Chronic Fatigue Syndrome: Redefining
an Illness (2015), https://www.national
academies.org/hmd/∼/media/Files/
Report%20Files/2015/
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MECFS/MECFScliniciansguide.pdf (last
accessed August 30, 2018).
VA is also proposing to revise the
current diagnostic criteria for SEID/CFS
to adhere to evidence-based criteria
which were adopted by the Centers for
Disease Control and Prevention (CDC).
IOM Report on ME/CFS (2015) (updated
July 3, 2017), https://www.cdc.gov/mecfs/symptoms-diagnosis/diagnosis.html
(last accessed July 17, 2018). According
to the 2015 IOM Report, up to 2.5
million Americans suffer from this
disease which is characterized by
profound fatigue, cognitive dysfunction,
sleep abnormalities, pain, autoimmune
manifestations, and a variety of other
symptoms that are made worse by
exertion of any sort. New diagnostic
criteria will take into consideration
whether this severe chronic fatigue
significantly interferes with daily
activities and work, if the affected
individual concurrently has four or
more of the eight symptoms as outlined
in CDC evidence-based criteria and
whether these symptoms first appeared
before the fatigue, have persisted or
recurred during six or more consecutive
months of illness, and were due to
ongoing exertion or other medical
conditions associated with fatigue.
The CDC mandates a thorough
medical history, physical examination,
mental status examination, and
laboratory tests to identify underlying or
contributing conditions that require
treatment. CDC recognizes and
identifies several conditions that do not
exclude a diagnosis of SEID/CFS.
Currently, § 4.88b lists 19 DCs
encompassing infectious diseases and
immune disorders. VA proposes to
revise these codes to reflect current
terminology, advances in medical
knowledge, recommendations from the
2015 IOM Report on ME/CFS and a
2007 IOM Report on evaluating veterans
for disability benefits, IOM, A 21st
Century System For Evaluating Veterans
for Disability Benefits (2007), https://
www.nap.edu/read/11885/chapter/1
(last accessed July 17, 2018).
Schedule of Ratings—Infectious
Diseases, Immune Disorders, and
Nutritional Deficiencies
Proposed General Rating Formula for
§ 4.88b
Currently, each infectious disease
listed under § 4.88b has its own
prescribed rating criteria. In most cases,
each specific infectious disease warrants
a 100 percent evaluation during an
active period of the disease. Thereafter,
any residual functional impairment
from the infectious disease determines
the level of disability. These evaluation
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principles are generally consistent with
the clinical presentation of infectious
diseases.
VA proposes one General Rating
Formula for § 4.88b. This approach is
based on the association between
clinical resolution or stabilization of an
infectious disease and elimination or
complete suppression of the causative
infectious agent. Regardless of whether
resolution occurs spontaneously or
because of treatment, long-term
disability in such situations results from
residual functional impairment of the
body systems affected by the infectious
disease, rather than the infection itself.
Sheila Davey, World Health
Organization, World Health
Organization Report on Infectious
Diseases: Removing Obstacles to
Healthy Development (1999).
Therefore, VA’s proposal to use a
General Rating Formula does not
substantively change the current
evaluation criteria so much as their
organization. This rulemaking proposes
to restructure rating criteria by creating
one General Rating Formula applicable
to multiple infectious diseases,
regardless of etiology. A General Rating
Formula for infectious diseases would
ensure consistency in rating these
conditions and be similar to the use of
a General Rating Formula in other
sections of the VASRD, such as in
§§ 4.97, 4.116, 4.130, and others. This
formula would be a familiar concept for
Veterans Benefits Administration (VBA)
employees and minimize the risk for
error by providing one criterion
applicable to multiple diagnostic codes.
Although each specific infectious
disease has a different etiology and
natural history, once the active disease
phase is over, disability would be rated
on residuals. VA would assign a 100
percent disability rating during the
variable length of each specific disease’s
active phase. For most infectious
diseases manifesting acutely, the length
of the active disease phase (i.e., the time
between disease onset and resolution or
stabilization) is at most usually six to
eight weeks. VA proposes to assign a
100 percent evaluation during the active
disease phase. VA recognizes that some
infectious diseases, such as
tuberculosis, may have a longer than
average active disease phase. Therefore,
VA proposes that the General Rating
Formula apply only in those cases
where specific rating criteria are not
otherwise provided. Diagnostic codes in
§ 4.88b that would not follow the
General Rating Formula would be 6301,
6302, 6310, 6311, 6312, 6313, 6314,
6315, 6325, 6326, 6351, and 6354.
After the disease becomes inactive,
VA proposes to assign a 0 percent
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evaluation. However, even though
advancements in antimicrobial therapy
have significantly lessened the
occurrence of residuals of infectious
diseases, they continue to occur.
Therefore, VA generally proposes to
append each diagnostic code with a
note describing the most common
residuals associated with a given
infection. See below for additional
details. As a list of every residual would
be impractical, these notes would
clearly indicate that they are not
exhaustive. Where ascertainable
residuals exist, VA proposes to assign
evaluations for those residuals under
the appropriate body system(s).
Certain infectious conditions are
prone to relapse and require laboratory
evaluation for confirmation. L. Joseph
Wheat et al., Clinical Practice
Guidelines for the Management of
Patients with Histoplasmosis: 2007
Update by the Infectious Diseases
Society of America, 45 Clinical
Infectious Diseases 807, 807–25 (2007).
Oftentimes, non-specific constitutional
symptoms (weakness, tiredness,
insomnia, weight loss, etc.) occur
following the active phase of an
infectious disease. However, such
symptoms may be due to other causes
than the infection. Therefore, to ensure
VA assigns the most appropriate
evaluations for relapsing infections, VA
proposes to include a note in the rule
requiring that relapses be confirmed by
pathogen-specific testing using
appropriate microbiologic, serologic,
biochemical (e.g., nucleic acid
detection)histopathologic methods.
Finally, although VA proposes using
a General Rating Formula for most
infectious diseases, VA notes that each
infectious disease has a different longterm impact. For those that have longer
active phases and/or are commonly
associated with relapse and residuals,
VA proposes to require VA examination
once the disease is no longer active so
that a medical professional can evaluate
the individual’s condition. In these
cases, VA also proposes to apply the
provisions of § 3.105(e) that require VA
to send beneficiaries notice of any
proposed reduction in evaluation and
provide an opportunity to respond
before it becomes effective.
Proposed Changes to Existing
Diagnostic Codes
As discussed above, VA proposes to
apply a General Rating Formula for
infectious diseases unless otherwise
noted. Additionally, VA proposes to
provide notes identifying common
residuals associated with particular
diseases and instructions to rating
personnel regarding the level of medical
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review necessary following cessation of
treatment and infection. These specific
proposed changes are discussed below.
Diagnostic Code 6300
Currently, DC 6300 is titled ‘‘Cholera,
Asiatic’’ referring only to infection with
toxigenic strains of Vibrio cholerae; it
does not reflect infections due to other
species within the genus Vibrio. Noncholera Vibrio species cause diarrheal
diseases, as well as wound infections
and septicemia. To reflect the total array
of diseases caused by Vibrio species, VA
proposes to rename this DC ‘‘Vibriosis
(cholera, non-cholera), to encompass
conditions caused by V. cholerae and by
non-cholera Vibrio organisms.
Cholera due to V. cholerae and
gastroenteritis due to other Vibrio
species are associated with severe
diarrhea of relatively short duration. Hoi
Ho et al., Vibrio Infections,
Medscape.com (July 24, 2018), https://
emedicine.medscape.com/article/
232038-overview. Including the
incubation period, cholera usually lasts
7 to 10 days and results in total
remission, or, in 5 to 10 percent of
cases, death if left untreated. Therefore,
the proposed General Rating Formula
would be appropriate for both cholera
and non-cholera gastroenteritis due to
other Vibrio species, and VA would
remove the existing provision for a
separate three-month convalescence
period as it would no longer be
necessary.
VA proposes to use a note to provide
information about common residual
disability of cholera and non-cholera
Vibrio infection, including renal failure,
skin, and musculoskeletal conditions,
such as necrotizing fasciitis. VA
proposes no changes to the evaluation
criterion for this DC except eliminating
the three-month convalescence and
adding a note to address rating of
residual disability.
Diagnostic Code 6301
VA evaluates DC 6301, visceral
leishmaniasis, at 100 percent for six
months following cessation of
treatment, after which a VA
examination helps determine residual
disability. VA proposes only minor
changes to this rating criteria, but
proposes to change the note regarding
rating residual disability. VA would
generally identify those residuals
commonly associated with postinfection or post-treatment residuals
that may warrant evaluation. Currently,
DC 6301 lists lymphadenopathy as one
such residual disability. However,
lymphadenopathy follows numerous
diseases and is a frequent physical
finding which, even when permanent, is
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otherwise without symptoms or
disability that would warrant
evaluation. Robert Ferrer,
Lymphadenopathy: Differential
Diagnosis and Evaluation, 58 a.m. Fam.
Physician 1313, 1313–20 (Oct. 15,
1998). In many cases, it may constitute
a normal physical finding. Vikramjit S.
Kanwar, Lymphadenopathy,
Medscape.com (Feb. 1, 2018), https://
emedicine.medscape.com/article/
956340-overview.
As lymphadenopathy is often
associated with other diseases and,
regardless of origin, commonly presents
without symptoms or disability
warranting evaluation, VA proposes to
remove it from the note in DC 6301. VA
notes that the list of possible residuals
in proposed DC 6301 would not be
exhaustive. Thus, if a veteran presents
with lymphadenopathy as a residual of
visceral leishmaniasis that results in
chronic, functional impairment, VA
would consider an evaluation under the
appropriate system.
In addition to the above revision, VA
proposes to amend the existing Note 1
to inform that the residual effects of
infection include bone marrow diseases.
Parasites—Leishmaniasis, CDC (Jan. 10,
2013), https://www.cdc.gov/parasites/
leishmaniasis/. This note
would also refer to the residuals listed
in 38 CFR 3.317(d), ‘‘Long-term health
effects potentially associated with
infectious diseases.’’
Finally, VA proposes to add a new
Note 2 to address the use of culture,
histopathology, and other diagnostic
testing to confirm relapses. Clinicians
rely on such diagnostic testing, which
has increased steadily in accuracy and
availability, to determine whether
symptoms are due to leishmaniasis or
some other disease. Shyam Sundar & M.
Rai, ‘‘Laboratory Diagnosis of Visceral
Leishmaniasis,’’ 9 Clinical and
Diagnostic Laboratory Immunology 951,
951–58 (2002). VA also proposes to
retitle the existing note as Note 1 to
account for the addition of this second
note.
Diagnostic Code 6302
VA would not change the rating
criteria for leprosy (Hansen’s disease),
but proposes to amend the current Note
under DC 6302 by adding amputations
as a residual in the proposed Note. The
neurologic impairment in leprosy
involves sensory and motor deficits/loss
in the extremities that may lead to autoamputation. Preenon Bagchi et al.,
Bacterio-Informatics: Identifying the
Cause of Hansen’s Disease and
Establish [sic] a Remedy for the Same,
2 Int’l J. of Bioinformatics Res. and
Applications 15, 15–19 (2010).
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Diagnostic Code 6304
VA proposes to evaluate DC 6304,
malaria, using the General Rating
Formula because it is an acute,
debilitating disease with predictable
clinical presentation.
VA proposes to amend an existing
note and to add one new notes. Note 1
would explicitly state that VA requires
diagnostic confirmation for both the
initial diagnosis and any relapse. To
reflect advances in malarial testing, VA
also proposes to refer to other specific
diagnostic tests such as antigen
detection, immunologic
(immunochromatographic) tests, and
molecular testing, such as polymerase
chain reaction tests. Malaria Diagnosis
(United States), CDC (Nov. 19, 2015),
https://www.cdc.gov/malaria/diagnosis_
treatment/diagnosis.html.
Note 2 would recognize potential
nervous system residuals because severe
forms of malaria affect the brain as an
encephalopathy. Pralay Sarkar et al.,
‘‘Critical care aspects of malaria,’’ 25 J.
of Intensive Care Med. 93, 93–103
(2010). In addition, this note would also
refer to the residuals listed in § 3.317(d).
Diagnostic Code 6305
VA proposes to amend the title of this
DC, currently ‘‘Lymphatic filariasis,’’ to
include the term elephantiasis, which is
another name commonly associated
with the chronic form of this condition.
Lymphatic Filariasis Fact Sheet No. 102,
World Health Organization (May 11,
2018), https://www.who.int/mediacentre/
factsheets/fs102/en/.
The new General Rating Formula
would provide 100 percent evaluation
for the acute phase of active infection
for lymphatic filariasis. The proposed
General Rating Formula would be
appropriate for use in this acute
infection. However, no actual changes
in the evaluation criteria would result
from this organizational change
intended to help rating personnel easily
apply the VASRD.
VA proposes to add information to
more adequately address the range of
potential residuals, which include
lymphedema (permanent swelling) and
lymphatic obstruction. Parasites—
Lymphatic Filariasis, CDC (June 14,
2013), https://www.cdc.gov/parasites/
lymphaticfilariasis/disease.html. VA
proposes a new Note to instruct rating
personnel to evaluate under the
appropriate body system residuals such
as epididymitis, lymphangitis,
lymphatic obstruction, or lymphedema
affecting extremities, genitals, and/or
breasts.
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Diagnostic Code 6306
Bartonellosis, currently evaluated
under DC 6306, generally resolves
within two months with appropriate
treatment. Kassem A. Hammoud et al.,
Bartonellosis, Medscape.com (Oct. 17,
2012), https://emedicine.medscape.com/
article/213169-overview. Therefore, VA
proposes to rate active bartonellosis
under the General Rating Formula at
100 percent, and VA would remove the
existing provision for a separate threemonth convalescence period as it would
no longer be necessary.
VA also proposes to update the
residual disability to include
endocarditis, which occurs when the
bloodstream may carry this bacterium to
the heart valves. John L. Brusch et al.,
Infective Endocarditis—
Pathophysiology, Medscape.com (Dec.
17, 2013), https://
emedicine.medscape.com/article/
216650-overview#a0104.
Diagnostic Code 6307
VA proposes to evaluate DC 6307,
plague, which is an acute, debilitating
disease of short duration, using the
General Rating Formula.
Use of modern antibiotics renders
residual disability from the infection
itself extremely rare. Therefore, VA
proposes to delete the existing note
regarding specific residuals and replace
it with a note stating that VA would rate
any residual disability under the
appropriate body system. Again,
lymphadenopathy is a frequent physical
finding following numerous diseases,
often permanent and without disabling
symptoms. Robert Ferrer,
Lymphadenopathy: Differential
Diagnosis and Evaluation, 58 Am.Fam.
Physician at 1313–20. VA proposes
removing lymphadenopathy as a
residual because it may be a normal
physical finding. Vikramjit S. Kanwar,
Lymphasdenopathy, Medscape.com
(July 10, 2015), https://
emedicine.medscape.com/article/
956340-overview); Plague, CDC (Nov.
28, 2012), https://www.cdc.gov/plague/.
VA proposes a new Note adding iritis
and uveitis as residual disabilities and
retaining the remainder of the existing
information without substantive change.
VA does not propose any changes to
the evaluation criteria for this DC.
Diagnostic Code 6309
VA proposes to evaluate DC 6309,
rheumatic fever, which is an acute,
febrile disease typically lasting less than
a month, using the General Rating
Formula. The existing note regarding
residuals would remain substantively
unchanged.
Diagnostic Code 6310
VA does not propose substantive
change to the criteria under diagnostic
code 6310 for syphilis and other
treponemal infections. However, for
consistency with the remainder of this
section, VA proposes to replace the term
‘‘complications’’ with the term ‘‘residual
disability,’’ which VA would rate under
the appropriate body system.
Additionally, VA proposes to remove
specific references to the names
associated with each DC identified in
this note because future revisions of the
rating schedule would retitle several of
them.
Diagnostic Code 6311
Currently, DC 6311, miliary
tuberculosis, provides a 100 percent
evaluation during active infection.
Under § 4.88c, the 100 percent is
continued for one year following the
date of inactivity. Active infection may
last for months to years, and, if
undiagnosed or untreated, may result in
death. The standard treatment for drugsusceptible miliary tuberculosis is six to
nine months with a combination of antituberculosis drugs. If the meninges are
involved, treatment will last for 9 to12
months, but may occasionally require
longer a treatment duration. Nahid, P.,
et al., ‘‘Executive Summary: Official
American Thoracic Society/Centers for
Disease Control and Prevention/
Infectious Diseases Society of America
Clinical Practice Guidelines: Treatment
Diagnostic Code 6308
of Drug-Susceptible Tuberculosis,’’ 63
Clinical Infectious Diseases 853, 853–
VA proposes to evaluate DC 6308,
867 (Oct. 2016), https://
relapsing fever, which is an acute,
www.nidcd.nih.gov/health/balance/
debilitating disease of short duration,
pages/meniere.aspx (last visited January
using the General Rating Formula.
Modern treatment helps most patients 22, 2019). Relapses are common when
medication is not taken for the full time
recover from this disease within a few
prescribed and/or not taken in the
days, with little incidence of splenic
damage. Long-term sequelae of relapsing appropriate combination. Generally,
fever are rare, but include iritis, uveitis, most relapses occur within the first 12
months of treatment completion.
cranial nerve, and other neuropathies.
Tick-borne Relapsing Fever (TBRF), CDC Tuberculosis (TB) Guidelines. CDC (May
4, 2016), https://www.cdc.gov/tb/
(Jan. 8, 2016), https://www.cdc.gov/
publications/guidelines/treatment.htm.
relapsing-fever/clinicians/. Therefore,
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To ensure that individuals are entitled
to any resumption or continuation of the
100 percent evaluation after the initial
active disease, VA proposes to add a
Note requiring confirmation of relapse
by culture, histopathology, or other
diagnostic laboratory testing.
VA also proposes Note 2 addressing
residuals which may be found under
§ 4.88c. Infection residuals include, but
are not limited to, chronic diagnosed
disabilities affecting such body systems
as the skin and respiratory, central
nervous, musculoskeletal, ocular,
gastrointestinal, and genitourinary
systems. VA would rate them under the
appropriate body system. J.J. van der
Harst & G.J. Luijckx, Treatment of
Central Nervous System Tuberculosis
Infections and Neurological
Complications of Tuberculosis
Treatment, 17 Current Pharmaceutical
Design 2940, 2940–47 (2011).
Diagnostic Code 6316
VA proposes to evaluate DC 6316,
brucellosis, an acute, debilitating
disease of short duration usually lasting
several weeks or less, using the General
Rating Formula. Brucellosis is easily
treated with antibiotics, but, if
untreated, brucellosis may become
chronic and leave significant residuals.
VA proposes no changes to the
evaluation criteria.
As the correct diagnosis is essential in
determining if symptoms are due to
brucellosis or some other disease entity,
VA proposes to add a new Note 1
directing that culture, serologic testing,
or both must confirm both the initial
diagnosis and any relapse of active
infection. Wafa Al-Nassir, Brucellosis,
Medscape.com (June 16, 2017), https://
emedicine.medscape.com/article/
213430-overview.
VA proposes to amend the existing
note as Note 2 and expand the list of
residuals in light of advances in
medicine and early treatment. Note 2
would reflect the residuals most
commonly associated with this
infection, including meningitis, and
liver, spleen, or musculoskeletal
conditions. Brucellosis, CDC (Sept. 13,
2017) https://www.cdc.gov/brucellosis/
index.html. As this condition is a
presumptive disease related to Gulf War
service, this note would also refer to the
many specific residuals of brucellosis
listed in § 3.317(d).
Diagnostic Code 6317
Currently, DC 6317 represents scrub
typhus, an acute debilitating rickettsial
disease lasting for several weeks or less.
If untreated, a high mortality rate
results. Antibiotic treatment rapidly
eradicates the disease and significantly
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reduces the chances of complications.
Therefore, VA proposes to evaluate DC
6317 using the General Rating Formula.
VA proposes to rename this DC to
encompass all forms of rickettsial and
similar erlichial and Anaplasma
infections. These infections are not
specific to the veteran population as
they afflict travelers and field scientists
as well. Renaming this DC would mean
rating personnel need not further clarify
the type of typhus infecting a veteran.
VA is not proposing any changes to
the evaluation criteria except to use the
General Rating Formula. VA would also
remove the existing provision for a
separate three-month convalescence
period as it would no longer be
necessary.
VA proposes to update the existing
note to include such residuals
frequently associated with DC 6317 as
involvement of bone marrow and the
central nervous system, in addition to
the current list of spleen damage or skin
conditions.
Rickettsial, ehrlichial, and Anaplasma
infections cause similar nonspecific
influenza-like illness in humans,
including but not limited to, scrub
typhus, Rocky Mountain spotted fever,
African tick-borne fever, ehrlichiosis,
and anaplasmosis. Therefore, VA also
proposes to add a second note to list
other rickettsial infections, including
infections by Ehrlichia and Anaplasma
species (members of the order
Rickettsiales) to account for its
occurrence in the U.S. veteran
population. Johan S. Bakken & J.
Stephen Dumler, Ehrlichiosis and
Anaplasmosis, Medscape.com (2004),
https://www.medscape.com/viewarticle/
490468_4.
Diagnostic Code 6318
Currently, DC 6318 represents
melioidosis, an acute debilitating
bacterial disease lasting several weeks
or less, which, if left untreated, may
result in mortality. VA proposes no
changes to the evaluation criteria,
except use of the General Rating
Formula.
As accuracy is essential in diagnosing
melioidosis, VA proposes to add Note 1
directing that culture or other specific
diagnostic laboratory tests must confirm
both the initial diagnosis and any
relapse or chronic activity of infection.
VA would retain the existing
information regarding common
residuals and the instruction to rate
residuals under the appropriate body
system under Note 2.
Diagnostic Code 6319
VA currently assigns a 100 percent
evaluation for DC 6319, Lyme disease,
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when it is active. Lyme disease is an
acute illness, usually lasting several
weeks or less. Therefore, VA proposes to
rate Lyme disease under the General
Rating Formula, without changes to the
actual evaluation criteria. VA also
proposes to amend the existing note
associated with this DC to account for
residuals such as Bell’s palsy,
radiculopathy, ocular, and cognitive
dysfunction, in addition to arthritis.
Diagnostic Code 6320
Currently, DC 6320 represents
‘‘Parasitic diseases otherwise not
specified.’’ VA proposes no changes to
the evaluation criteria except to use the
General Rating Formula. VA also
proposes to amend the existing note
associated with this DC with general
instructions to rate any residuals of this
infection under the appropriate body
system.
Diagnostic Code 6351
VA proposes a number of changes to
DC 6351, which pertains to human
immunodeficiency virus (HIV) related
illness. Currently, VA provides a 100
percent evaluation for ‘‘AIDS with
recurrent opportunistic infections or
with secondary diseases affecting
multiple body systems; HIV-related
illness with debility and progressive
weight loss, without remission, or few
or brief remissions.’’ VA proposes to
remove the statement about remission
because the CDC considers AIDS a
chronic condition, and the diagnosis
continues once a person is properly
diagnosed, regardless of improvements
in that person’s condition.
When VA last revised the evaluation
criteria, the medical community
considered oral hairy leukoplakia (OHL)
a distinctive clinical marker of HIV
infection. Since then, measurement of
the peripheral CD4 cell count and HIV
viral load have become the standard
method for evaluating a patient’s stage
of HIV infection. Sowmya Nanjappa,
Anti-retroviral Therapy in TreatmentNaı¨ve Patients, Medscape.com (June 3,
2016), https://
emedicine.medscape.com/article/
2041458-overview. In addition, OHL by
itself rarely, if ever, requires specific
treatment in patients receiving antiretroviral therapy. James Cade, Hairy
Leukoplakia Treatment and
Management, Medscape.com (December
19, 2018), https://
emedicine.medscape.com/article/
279269-overview. VA proposes to
remove reference to OHL in the criteria
for a 30 percent evaluation.
Similarly, VA proposes to modify the
reference of oral candidiasis to
esophageal and lower respiratory tract
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candidiasis for the criteria for a 30
percent evaluation. In the past, oral
candidiasis was strongly associated with
HIV infection. However, the increased
use of antiretroviral medications has
greatly reduced the incidence of this
condition in HIV-positive individuals.
C. Frezzini et al., Current Trends of HIV
Disease of the Mouth, 34 J. of Oral
Pathology & Med. 513, 513–31 (2005).
For clarification, VA proposes to
replace the phrase ‘‘definite medical
symptoms’’ in the criteria for a 10
percent evaluation with ‘‘HIV-related
constitutional symptoms.’’ VA would
not change the remainder of the criteria
for a 10 percent evaluation. The criteria
for a 0 percent evaluation would not
change.
Existing Note 1 would continue to
provide that ‘‘medications prescribed as
part of a research protocol at an
accredited medical institution’’ are to be
considered ‘‘approved medication’’
within the context of the evaluation
criteria. VA proposes to add a reference
to treatment regimens as part of a
research protocol at an accredited
medical institution because some
research protocols use not only new
medications but also new regimens for
already FDA approved medications.
Existing Note 2 would continue to
provide for separate evaluation of
various manifestations of HIV infection
under the appropriate diagnostic codes.
VA proposes to retain the instruction to
evaluate on the basis of psychiatric or
central nervous system manifestations,
opportunistic infections, and
neoplasms, rather than based on this
diagnostic code, if a higher overall
evaluation results. However, VA
proposes to substitute the term
‘‘diagnosed psychiatric condition’’ for
the phrase ‘‘psychiatric manifestations.’’
VA recognizes that a veteran may
exhibit psychiatric symptoms, such as
depression, which do not rise to the
level of a diagnosed disability. Such
symptoms are more appropriately rated
under DC 6351 as 10 percent disabling,
provided there is evidence of activity
limitations. Note 2, however, would
refer to diagnosed, disabling acquired
psychiatric illness.
VA also proposes the addition of a
new Note 3 to assist rating personnel in
applying these revised evaluation
criteria. Note 3 would include a list of
current opportunistic infections, which
includes the following conditions:
Candidiasis of the bronchi, trachea,
esophagus, or lungs; invasive cervical
cancer; coccidioidomycosis;
cryptococcosis; cryptosporidiosis;
cytomegalovirus (particularly CMV
retinitis); HIV-related encephalopathy;
herpes simplex-chronic ulcers of greater
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than one month’s duration, or
bronchitis, pneumonia, or esophagitis;
histoplasmosis; isosporiasis (chronic
intestinal); Kaposi’s sarcoma;
lymphoma; Mycobacterium avium
complex; tuberculosis; Pneumocystis
jirovecii (carinii) pneumonia;
pneumonia, recurrent; progressive
multifocal leukoencephalopathy;
Salmonella septicemia, recurrent;
toxoplasmosis of the brain; and wasting
syndrome due to HIV. AIDS and
Opportunistic Infections, CDC (July 23,
2018), https://www.cdc.gov/hiv/basics/
livingwithhiv/
opportunisticinfections.html.
Diagnostic Code 6354
VA is proposing no change to the
rating criteria for this DC other than to
update the name from chronic fatigue
syndrome (CFS) to systemic exertion
intolerance disease/chronic fatigue
syndrome (CFS). VA would, however,
clarify the note to indicate that
incapacitation requires that a licensed
physician must prescribe both bed rest
and treatment, which would be
consistent with current VA practice.
Proposed New Diagnostic Codes
As discussed above, in addition to
updating existing DCs, VA proposes to
add medical conditions not currently
listed in the Rating Schedule:
Proposed New Diagnostic Code 6312
VA proposes to add a new DC 6312
for ‘‘Nontuberculosis mycobacterial
infection’’ (NTM). NTM lung infection
occurs when a person inhales the
organism from the environment. Most
people do not become ill but some
susceptible individuals require
prolonged treatment of one to two years.
Without treatment, many people, but
not all, will develop a progressive lung
infection characterized by cough,
fatigue, and often weight loss. However,
death directly related to NTM lung
disease is relatively rare in
immunocompetent individuals.
Systemic infection, which is the most
severe form, is most often seen in
individuals with other underlying
conditions, especially those that inhibit
immune function. Arry Dieudonne,
Atypical Mycobacterium Infection,
Medscape.com (Feb. 7, 2018), https://
emedicine.medscape.com/article/
972708-overview.
Similar to other infectious diseases
found in the Rating Schedule, VA
proposes to assign a 100 percent
evaluation during active infection, after
which a mandatory VA evaluation
would be conducted to determine the
appropriate evaluation based on
residuals, if any. Therefore, VA
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proposes a Note 1 to this effect and
instructs that any change in evaluation
based upon that or any subsequent
examination shall be subject to the
provisions of § 3.105(e). Furthermore,
the note would instruct rating personnel
to rate on residuals if there is no relapse.
Establishing the correct diagnosis is
essential in determining if symptoms
are due to NTM or some other disease
entity. Diagnostic testing has become
more accurate and readily available over
the years. Therefore, VA proposes a
Note 2, requiring diagnostic
confirmation for subsequent relapses.
VA proposes to include Note 3, which
would identify common residuals to
assist rating personnel in assigning
evaluations following cessation of the
100 percent evaluation. Residuals of
infection identified in Note 3 would
include skin conditions and conditions
of the respiratory, central nervous,
musculoskeletal, ocular,
gastrointestinal, and genitourinary
systems.
Proposed New Diagnostic Code 6325
VA proposes to add new DC 6325
which applies to hyperinfection
syndrome or disseminated
strongyloidiasis. Because
strongyloidiasis is not an acute, selflimited disease, VA would not use the
General Rating Formula. Similar to
other severe infectious diseases, VA
proposes to assign a 100 percent
evaluation during active disease
followed by a mandatory VA evaluation
to determine the appropriate evaluation
based on any residuals. Systemic
infection, which is the most severe form
of strongyloidiasis, with a mortality rate
approaching 90 percent, is most often
seen in individuals with other
underlying conditions, especially those
with compromised immune function.
Parasites—Strongyloides, Resources for
Health Professionals, CDC (Jan. 6, 2012),
https://www.cdc.gov/parasites/
strongyloides/. VA is not proposing to
list the most common residuals because
their number is so vast.
Proposed New Diagnostic Code 6326
VA proposes a new diagnostic code
for schistosomiasis, the second most
common parasitic disease in the world.
Parasites—Schistosomiasis, CDC (Apr.
30, 2018), https://www.cdc.gov/parasites/
schistosomiasis/. While the parasite is
not found in the United States, it is
sufficiently prevalent in tropical regions
that VA may presume service
connection if records indicate service in
such regions. See 38 CFR 3.309(b). VA
is proposing to add a distinct DC for
schistosomiasis because it otherwise
lacks a means to accurately track such
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claims and can evaluate them only by
analogy.
Most people who contract
schistosomiasis are asymptomatic and
have subclinical disease during both
acute and chronic stages of infection.
Persons with acute infection (also
known as Katayama syndrome) may
present with mild symptoms such as
rash, fever, headache, myalgia, and
respiratory symptoms that are not
disabling.
Chronic disease results from host
immune responses to schistosome eggs:
S. mansoni and S. japonicum. These
eggs most commonly lodge in the blood
vessels of the liver or intestine with
chronic inflammation leading to bowel
wall ulceration, hyperplasia, and
polyposis and, with heavy infections, to
liver fibrosis and portal hypertension.
S. haematobium eggs tend to lodge in
the urinary tract and the female genital
tract. Female genital schistosomiasis can
affect the cervix, fallopian tubes, and
vagina.
Central nervous system lesions, such
as in the spinal cord or brain and
inflammatory reactions, may cause the
formation of granulomas that act as
space-occupying lesions.
VA proposes to evaluate DC 6326 by
assigning a 0 percent evaluation for
acute and asymptomatic chronic
infections. Additionally, VA proposes to
note common residuals of infection,
such as liver and genitourinary tract
conditions. VA would rate residual
disability in the appropriate system.
Proposed New Diagnostic Code 6329
VA proposes new DC 6329 to
encompass hemorrhagic fevers,
including dengue, yellow fever, and
others. While these fevers are
uncommon in the United States, they
are prevalent in tropical regions and,
therefore, associated with military
deployments. David C. Pigott, CBRNE—
Viral Hemorrhagic Fevers,
Medscape.com (Mar. 16, 2017), https://
emedicine.medscape.com/article/
830594-overview. VA may presume
service connection for hemorrhagic
fever if records indicate service in
certain regions. See 38 CFR 3.309(b). VA
is proposing to add a distinct DC for
hemorrhagic fever because it otherwise
lacks a means to accurately track such
claims and can evaluate them only by
analogy.
VA proposes to apply the General
Rating Formula and assign a 100 percent
evaluation for active disease because
hemorrhagic fever is associated with a
debilitating, acute, febrile illness that
often lasts for several weeks at most. VA
also proposes to include a note listing
common residual disabilities of central
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nervous system, liver, or kidney
conditions.
chronic fatigue syndrome, and vascular
infections.
Proposed New Diagnostic Code 6330
Proposed New Diagnostic Code 6333
VA proposes a new diagnostic code to
encompass infections caused by
nontyphoidal Salmonella. In 2010, VA
issued a regulation establishing that
nontyphoidal salmonellosis is subject to
presumptive service connection for
certain veterans. See 75 FR 59968 and
38 CFR 3.317. To track claims decisions
regarding this infection and to more
consistently rate it, VA proposes a
diagnostic code specifically for
nontyphoidal salmonellosis.
VA proposes to assign a 100 percent
evaluation during active infection
according to the General Rating
Formula. Thereafter, VA would rate the
condition based on residuals, including
those listed in § 3.317(d), such as
reactive arthritis.
VA proposes new DC 6330 for
infections caused by Campylobacter
jejuni. In 2010, VA issued a regulation
establishing that Campylobacter jejuni
is subject to presumptive service
connection for certain veterans because
it is (1) prevalent in Southwest Asia, (2)
has been diagnosed among U.S. troops
serving in the Persian Gulf/Southwest
Asia Theater of operations, and (3) is
known to cause long-term adverse
health effects. See 75 FR 59968 and 38
CFR 3.317. To monitor claims for this
infection, VA proposes a diagnostic
code specifically for Campylobacter
jejuni.
VA proposes to rate Campylobacter
jejuni infection under the General
Rating Formula, meaning that it would
receive a 100 percent evaluation during
active infection. The symptoms of
Campylobacter jejuni infection consist
of diarrhea, cramping, abdominal pain,
and fever within two to five days after
exposure to the bacteria. The diarrhea
may be bloody and can be accompanied
by nausea and vomiting. The illness
typically lasts about one week.
Campylobacter (Campylobacteriosis),
CDC (Aug. 30, 2017), https://
www.cdc.gov/campylobacter/
index.html.
Thereafter, VA would rate the
condition based on residuals listed in
§ 3.317(d), ‘‘Long-Term Health Effects
Potentially Associated With Infectious
Diseases,’’ such as Guillain-Barre
syndrome, reactive arthritis, and uveitis.
Proposed New Diagnostic Code 6331
VA proposes a new diagnostic code to
encompass infections caused by
Coxiella burnetii. In 2010, VA issued a
regulation establishing that infection
due to Coxiella burnetii (Q fever) is
subject to presumptive service
connection for certain veterans because
it is (1) prevalent in Southwest Asia, (2)
has been diagnosed among U.S. troops
serving in the Persian Gulf/Southwest
Asia theater of operations, and (3) is
known to cause long-term adverse
health effects. See 75 FR 59968 and 38
CFR 3.317. To track claims for this
infection, VA proposes a diagnostic
code specifically for Coxiella burnetii
infection (Q fever).
VA proposes assigning a 100 percent
evaluation during active infection
according to the General Rating
Formula. Thereafter, VA would rate the
condition based on residuals listed in
§ 3.317(d), such as chronic hepatitis,
endocarditis, osteomyelitis, post Q-fever
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Proposed New Diagnostic Code 6334
VA proposes a new diagnostic code to
encompass infections caused by
Shigella, which would be rated under
the General Rating Formula. In 2010,
VA issued a regulation presuming
service connection for Shigella infection
in certain veterans. See 75 FR 59968 and
38 CFR 3.317. To allow for better
tracking of decisions on claims for this
infection and to more consistently rate
it, VA proposes a diagnostic code
specifically for Shigella infection.
VA would rate the condition based on
residuals, including those listed in
§ 3.317(d), such as hemolytic-uremic
syndrome, and reactive arthritis.
Proposed New Diagnostic Code 6335
VA proposes a new diagnostic code to
encompass infections caused by West
Nile virus. In 2010, VA issued a
regulation presuming service
connection for West Nile virus in
certain veterans. See 75 FR 59968. To
better track claims decisions regarding
this infection, VA proposes a separate
diagnostic code for West Nile virus,
which would be rated under the General
Rating Formula.
VA would rate the condition based on
residuals, including those listed in
§ 3.317(d), such as variable physical,
functional, or cognitive disability.
Executive Orders 12866, 13563, and
13771
Executive Orders 12866 and 13563
direct agencies to assess the costs and
benefits of available regulatory
alternatives and, when regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
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effects, and other advantages;
distributive impacts; and equity).
Executive Order 13563 (Improving
Regulation and Regulatory Review)
emphasizes the importance of
quantifying both costs and benefits,
reducing costs, harmonizing rules, and
promoting flexibility. Executive Order
12866 (Regulatory Planning and
Review) defines a ‘‘significant
regulatory action,’’ which requires
review by the Office of Management and
Budget (OMB), as ‘‘any regulatory action
that is likely to result in a rule that may:
(1) Have an annual effect on the
economy of $100 million or more or
adversely affect in a material way the
economy, a sector of the economy,
productivity, competition, jobs, the
environment, public health or safety, or
State, local, or tribal governments or
communities; (2) Create a serious
inconsistency or otherwise interfere
with an action taken or planned by
another agency; (3) Materially alter the
budgetary impact of entitlements,
grants, user fees, or loan programs or the
rights and obligations of recipients
thereof; or (4) Raise novel legal or policy
issues arising out of legal mandates, the
President’s priorities, or the principles
set forth in this Executive Order.’’
The economic, interagency,
budgetary, legal, and policy
implications of this regulatory action
have been examined, and it has been
determined not to be a significant
regulatory action under E.O. 12866.
VA’s impact analysis can be found as a
supporting document at https://
www.regulations.gov, usually within 48
hours after the rulemaking document is
published. Additionally, a copy of this
rulemaking and its impact analysis are
available on VA’s website at https://
www.va.gov/orpm/, by following the
link for ‘‘VA Regulations Published
From FY 2004 Through Fiscal Year to
Date.’’
This rule is not an E.O. 13771
regulatory action because this rule is not
significant under E.O. 12866.
Regulatory Flexibility Act
The Secretary hereby certifies that
this proposed rule would not have a
significant economic impact on a
substantial number of small entities as
they are defined in the Regulatory
Flexibility Act, 5 U.S.C. 601–612. This
proposed rule would not affect any
small entities. Only certain VA
beneficiaries could be directly affected.
Therefore, pursuant to 5 U.S.C. 605(b),
this rulemaking is exempt from the
initial and final regulatory flexibility
analysis requirements of sections 603
and 604.
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Unfunded Mandates
The Unfunded Mandates Reform Act
of 1995 requires, at 2 U.S.C. 1532, that
agencies prepare an assessment of
anticipated costs and benefits before
issuing any rule that may result in the
expenditure by State, local, and tribal
governments, in the aggregate, or by the
private sector, of $100 million or more
(adjusted annually for inflation) in any
given year. This proposed rule would
have no such effect on State, local, and
tribal governments, or on the private
sector.
Paperwork Reduction Act
This final rule contains no provisions
constituting a collection of information
under the Paperwork Reduction Act of
1995 (44 U.S.C. 3501–3521).
Catalog of Federal Domestic Assistance
Numbers and Titles
The Catalog of Federal Domestic
Assistance program numbers and titles
for this rule are 64.102, Compensation
for Service-Connected Deaths for
Veterans’ Dependents; 64.105, Pension
to Veterans, Surviving Spouses, and
Children; 64.109, Veterans
Compensation for Service-Connected
Disability; and 64.110, Veterans
Dependency and Indemnity
Compensation for Service-Connected
Death.
List of Subjects in 38 CFR Part 4
Disability benefits, Pensions,
Veterans.
Signing Authority
The Secretary of Veterans Affairs
approved this document and authorized
the undersigned to sign and submit the
document to the Office of the Federal
Register for publication electronically as
an official document of the Department
of Veterans Affairs. Robert L. Wilkie,
Secretary, Department of Veterans
Affairs, approved this document on
January 29, 2019, for publication.
Dated: January 29, 2019.
Jeffrey M. Martin,
Assistant Director, Office of Regulation Policy
& Management, Office of the Secretary,
Department of Veterans Affairs.
For the reasons stated in the
preamble, the Department of Veterans
Affairs proposes to amend 38 CFR part
4 as set forth below:
PART 4—SCHEDULE FOR RATING
DISABILITIES
Subpart B—Disability Ratings
1. The authority citation for part 4
continues to read as follows:
■
Authority: 38 U.S.C. 1155, unless
otherwise noted.
■
2. Revise § 4.88a to read as follows:
§ 4.88a Systemic exertion intolerance
disease/chronic fatigue syndrome (CFS).
(a) For VA purposes, the diagnosis of
Systemic Exertion Intolerance Disease/
Chronic Fatigue Syndrome (CFS) must
meet the following conditions:
(1) A severe chronic fatigue that
significantly interferes with daily
activities and work.
(2) The individual concerned
concurrently has four or more of the
following eight symptoms:
(i) Post-exertion malaise lasting more
than 24 hours
(ii) Unrefreshing sleep
(iii) Significant impairment of shortterm memory or concentration
(iv) Muscle pain
(v) Pain in the joints without swelling
or redness
(vi) Headaches of a new type, pattern,
or severity
(vii) Tender lymph nodes in the neck
or armpit
(viii) Sore throat that is frequent or
recurring
(3) These symptoms:
(i) Cannot have first appeared before
the fatigue
(ii) Have persisted or recurred during
six or more consecutive months of
illness, and
(iii) Are not due to ongoing exertion
or other medical conditions associated
with fatigue, as ruled out by a physician
who administered relevant diagnostic
tests.
(b) Several past or current medical
conditions exclude the diagnosis of
systemic exertion intolerance disease/
CFS to include:
(1) Any active condition that may
explain the presence of chronic fatigue,
such as untreated hypothyroidism, sleep
1685
apnea, narcolepsy, and iatrogenic
conditions such as side effects of
medication.
(2) Some illnesses, including some
types of cancers and chronic cases of
hepatitis B or C virus infection, which
could explain the presence of chronic
fatigue, and which have not clearly and
completely resolved.
(3) Any past or current diagnosis of:
major depressive disorder with
psychotic or melancholic features,
bipolar affective disorders, anorexia
nervosa, bulimia nervosa, or any
subtype of schizophrenia, delusional
disorders, or dementias.
(4) Alcohol or other substance abuse,
occurring within two years of the onset
of chronic fatigue and any time
afterwards.
(5) Severe obesity, defined as having
a body mass index equal to or greater
than 45. [Body mass index = weight in
kilograms ÷ (height in meters)2].
(6) Examination or testing detects any
abnormality that strongly suggests an
exclusionary condition that needs to be
treated or resolved before attempting
further diagnosis. Once fully treated,
diagnose accordingly if the individual
still meets criteria for Systemic Exertion
Intolerance Disease (SEID)/Chronic
Fatigue Syndrome (CFS).
■ 3. Amend § 4.88b by:
■ a. Revising the entries for diagnostic
codes 6300 through 6302 and 6304
through 6311;
■ b. Adding in numerical order an entry
for diagnostic code 6312;
■ c. Revising the entries for diagnostic
codes 6316 through 6320;
■ d. Adding in numerical order entires
for diagnostic codes 6325, 6326, 6329
through 6331, and 6333 through 6335;
and
■ e. Revising the entries for diagnostic
codes 6351 and 6354.
The revisions and additions read as
follows:
§ 4.88b Schedule of ratings-infectious
diseases, immune disorders, and nutritional
deficiencies.
Rating
General Rating Formula for Infectious Diseases:
For active disease ............................................................................................................................................................................
After active disease has resolved, rate at 0 percent for infection. Rate any residual disability of infection within the appropriate
body system.
6300 Vibriosis (Cholera, Non-cholera):
Evaluate under the General Rating Formula.
Note: Rate residuals of cholera and non-cholera Vibrio infections, such as renal failure, skin, and musculoskeletal conditions,
within the appropriate body system.
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Rating
6301 Visceral leishmaniasis:
As active disease .............................................................................................................................................................................
Note 1: Continue a 100 percent evaluation beyond the cessation of treatment for active disease. Six months after discontinuance of such treatment, determine the appropriate disability rating by mandatory VA examination. Any change in evaluation
based upon that or any subsequent examination shall be subject to the provisions of § 3.105(e) of this chapter. Thereafter,
rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, liver damage, bone marrow disease, and those residuals listed in § 3.317(d) of this chapter.
Note 2: Confirm the recurrence of active infection by culture, histopathology, or other diagnostic laboratory testing.
6302 Leprosy (Hansen’s disease):
As active disease .............................................................................................................................................................................
Note: Continue a 100 percent evaluation beyond the cessation of treatment for active disease. Six months after discontinuance of such treatment, determine the appropriate disability rating by mandatory VA examination. Any change in evaluation
based upon that or any subsequent examination shall be subject to the provisions of § 3.105(e) of this chapter. Thereafter,
rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, skin lesions,
peripheral neuropathy, or amputations.
6304 Malaria:
Evaluate under the General Rating Formula.
Note 1: The diagnosis of malaria, both initially and during relapse, depends on the identification of the malarial parasites in
blood smears or other specific diagnostic laboratory tests such as antigen detection, immunologic
(immunochromatographic) tests, and molecular testing such as polymerase chain reaction tests.
Note 2: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, liver
or splenic damage, central nervous system conditions, and those residuals listed in § 3.317(d) of this chapter.
6305 Lymphatic filariasis, to include elephantiasis:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to,
epididymitis, lymphangitis, lymphatic obstruction, or lymphedema affecting extremities, genitals, and/or breasts.
6306 Bartonellosis:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, endocarditis or skin lesions.
6307 Plague:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection.
6308 Relapsing Fever:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, liver or
spleen damage, iritis, uveitis, or central nervous system involvement.
6309 Rheumatic fever:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, heart
damage.
6310 Syphilis, and other treponemal infections:
Note : Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, diseases of the nervous system, vascular system, eyes, or ears (see DC 7004, DC 8013, DC 8014, DC 8015, and DC 9301).
6311 Tuberculosis, miliary:
As active disease .............................................................................................................................................................................
Inactive disease: See §§ 4.88c and 4.89.
Note 1: Confirm the recurrence of active infection by culture, histopathology, or other diagnostic laboratory testing.
Note 2: Rate under the appropriate body system any residual disability of infection which includes, but is not limited to, skin
conditions and conditions of the respiratory, central nervous, musculoskeletal, ocular, gastrointestinal, and genitourinary
systems and those residuals listed in § 4.88c of this chapter.
6312 Nontuberculosis mycobacterial infection:
As active disease .............................................................................................................................................................................
Note 1: Continue the rating of 100 percent for the duration of treatment for active disease followed by a mandatory VA exam.
If there is no relapse, rate on residuals. Any change in evaluation based upon that or any subsequent examination shall be
subject to the provisions of § 3.105(e) of this chapter.
Note 2: Confirm the recurrence of active infection by culture, histopathology, or other diagnostic laboratory testing.
Note 3: Rate under the appropriate body system any residual disability of infection which includes, but is not limited to, skin
conditions and conditions of the respiratory, central nervous, musculoskeletal, ocular, gastrointestinal, and genitourinary
systems and those residuals listed in § 4.88c of this chapter.
*
*
*
*
*
*
6316 Brucellosis:
Evaluate under the General Rating Formula.
Note 1: Culture, serologic testing, or both must confirm the initial diagnosis and recurrence of active infection.
Note 2: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, meningitis, liver, spleen and musculoskeletal conditions, and those residuals listed in § 3.317(d) of this chapter.
6317 Rickettsial, erlichial, and Anaplasma infections:
Evaluate under the General Rating Formula.
Note 1: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, bone
marrow, spleen, central nervous system, and skin conditions.
Note 2: This diagnostic code includes, but is not limited to, scrub typhus, Rickettsial pox, African tick-borne fever, Rocky
Mountain spotted fever, ehrlichiosis, or anaplasmosis.
6318 Melioidosis:
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Evaluate under the General Rating Formula.
Note 1: Confirm by culture or other specific diagnostic laboratory tests the initial diagnosis and any relapse or chronic activity
of infection.
Note 2: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, arthritis, lung lesions, or meningitis.
6319 Lyme disease:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, arthritis,
Bell’s palsy, radiculopathy, ocular, or cognitive dysfunction.
6320 Parasitic diseases otherwise not specified:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection.
*
*
*
*
*
*
6325 Hyperinfection syndrome or disseminated strongyloidiasis:
As active disease .............................................................................................................................................................................
Note: Continue the rating of 100 percent through active disease followed by a mandatory VA exam. If there is no relapse, rate
on residual disability. Any change in evaluation based upon that or any subsequent examination shall be subject to the provisions of § 3.105(e) of this chapter.
6326 Schistosomiasis:
As acute or asymptomatic chronic disease .....................................................................................................................................
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, conditions of the liver, intestinal system, female genital tract, genitourinary tract, or central nervous system.
6329 Hemorrhagic fevers, including dengue, yellow fever, and others:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, conditions of the central nervous system, liver, or kidney.
6330 Campylobacter jejuni infection:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, GuillainBarre syndrome, reactive arthritis, or uveitis as specified in § 3.317(d) of this chapter.
6331 Coxiella burnetii infection (Q fever):
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, chronic
hepatitis, endocarditis, osteomyelitis, post Q-fever chronic fatigue syndrome, or vascular infections as specified in § 3.317(d)
of this chapter.
6333 Nontyphoid Salmonella infections:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, reactive
arthritis as specified in § 3.317(d) of this chapter.
6334 Shigella infections:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, hemolytic-uremic syndrome or reactive arthritis as specified in § 3.317(d) of this chapter.
6335 West Nile virus infection:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any residual disability of infection, which includes, but is not limited to, variable
physical, functional, or cognitive disabilities as specified in § 3.317(d) of this chapter.
*
*
*
*
*
*
*
6351 HIV-related illness:
AIDS with recurrent opportunistic infections (see Note 3) or with secondary diseases afflicting multiple body systems; HIV-related illness with debility and progressive weight loss .................................................................................................................
Refractory constitutional symptoms, diarrhea, and pathological weight loss; or minimum rating following development of AIDSrelated opportunistic infection or neoplasm ..................................................................................................................................
Recurrent constitutional symptoms, intermittent diarrhea, and use of approved medication(s); or minimum rating with T4 cell
count less than 200 ......................................................................................................................................................................
Following development of HIV-related constitutional symptoms; T4 cell count between 200 and 500, and use of approved
medication(s); or with evidence of depression or memory loss with employment limitations .....................................................
Asymptomatic, following initial diagnosis of HIV infection, with or without lymphadenopathy or decreased T4 cell count ............
Note 1: In addition to standard therapies and regimens, the term ‘‘approved medication(s)’’ includes treatment regimens and
medications prescribed as part of a research protocol at an accredited medical institution.
Note 2: Diagnosed psychiatric illness, central nervous system manifestations, opportunistic infections, and neoplasms may be
rated separately under the appropriate diagnostic codes if a higher overall evaluation results, provided the disability symptoms do not overlap with evaluations otherwise assignable above.
Note 3: The following list of opportunistic infections are considered AIDS-defining conditions, that is, a diagnosis of AIDS follows if a person has HIV and one more of these infections, regardless of the CD4 count—candidiasis of the bronchi, trachea, esophagus, or lungs; invasive cervical cancer; coccidioidomycosis; cryptococcosis; cryptosporidiosis; cytomegalovirus
(particularly CMV retinitis); HIV-related encephalopathy; herpes simplex-chronic ulcers for greater than one month, or bronchitis, pneumonia, or esophagitis; histoplasmosis; isosporiasis (chronic intestinal); Kaposi’s sarcoma; lymphoma;
Mycobacterium avium complex; tuberculosis; Pneumocystis jirovecii (carinii) pneumonia; pneumonia, recurrent; progressive
multifocal leukoencephalopathy; Salmonella septicemia, recurrent; toxoplasmosis of the brain; and wasting syndrome due to
HIV.
6354 Systemic exertional intolerance disease/chronic fatigue syndrome (CFS):
*
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Debilitating fatigue, cognitive impairments (such as inability to concentrate, forgetfulness, or confusion), or a combination of
other signs and symptoms:
Which are nearly constant and so severe as to restrict routine daily activities almost completely and which may occasionally preclude self-care ............................................................................................................................................................
Which are nearly constant and restrict routine daily activities to less than 50 percent of the pre-illness level; or which wax
and wane, resulting in periods of incapacitation totaling at least six weeks per year ..........................................................
Which are nearly constant and restrict routine daily activities from 50 to 75 percent of the pre-illness level; or which wax
and wane, resulting in periods of incapacitation totaling at least four but less than six weeks per year ............................
Which are nearly constant and restrict routine daily activities by less than 25 percent of the pre-illness level; or which wax
and wane, resulting in periods of incapacitation totaling at least two but less than four weeks per year ...........................
Which wax and wane but result in periods of incapacitation totaling at least one but less than two weeks per year; or
symptoms controlled by continuous medication ....................................................................................................................
Note: For the purpose of evaluating this disability, incapacitation exists only when a licensed physician prescribes bed
rest and treatment.
4. In appendix A to part 4 by:
a. Revising the entries for diagnostic
codes 6300–6302, 6304–6311;
■ b. Adding in numerical order an entry
for diagnostic code 6312;
■
■
c. Revising the entries for diagnostic
codes 6316–6320;
■ d. Adding in numerical order entries
for diagnostic codes 6325, 6326, 6329
through 6331, and 6333 through 6335;
and
■
100
60
40
20
10
e. Revising the entries for diagnostic
codes 6351 and 6354.
The revisions and additions read as
follows:
■
APPENDIX A TO PART 4—TABLE OF AMENDMENTS AND EFFECTIVE DATES SINCE 1946
Sec.
Diagnostic
code No.
*
4.88a ..............
*
........................
4.88b ..............
........................
6310
6311
6312
*
*
*
*
*
March 11, 1969; re-designated § 4.88b November 29, 1994; § 4.88a added to read ‘‘Chronic fatigue syndrome’’; criterion November 29, 1994; title, criterion [insert effective date of final rule].
Added March 11, 1969; re-designated § 4.88c November 29, 1994; § 4.88a re-designated to § 4.88b November 29, 1994; General Rating Formula for Infectious Diseases added [insert effective date of final rule].
Criterion August 30, 1996; title, criterion, and note [insert effective date of final rule].
Criterion, note [insert effective date of final rule].
Criterion September 22, 1978; criterion August 30, 1996; criterion, note [insert effective date of final rule].
Evaluation August 30, 1996; criterion, note [insert effective date of final rule].
Criterion March 1, 1989; evaluation August 30, 1996; title, criterion, note [insert effective date of final rule].
Evaluation August 30, 1996; criterion, note [insert effective date of final rule].
Criterion May 13, 2018; criterion, note [insert effective date of final rule].
Criterion August 30, 1996; criterion, note [insert effective date of final rule].
Added March 1, 1963; criterion March 1, 1989; criterion August 30, 1996; criterion, note [insert effective date
of final rule].
Criterion, note [insert effective date of final rule].
Criterion, note [insert effective date of final rule].
Added [insert effective date of final rule].
*
*
6316
6317
6318
6319
6320
6325
6326
6329
6330
6331
6333
6334
6335
*
*
*
*
*
Evaluation March 1, 1989; evaluation August 30, 1996; criterion, note [insert effective date of final rule].
Criterion August 30, 1996; title, criterion, note [insert effective date of final rule].
Added March 1, 1989; criterion August 30, 1996; criterion, note [insert effective date of final rule].
Added August 30, 1996; criterion, note [insert effective date of final rule].
Added August 30, 1996; criterion, note [insert effective date of final rule].
Added [insert effective date of final rule].
Added [insert effective date of final rule].
Added [insert effective date of final rule].
Added [insert effective date of final rule].
Added [insert effective date of final rule].
Added [insert effective date of final rule].
Added [insert effective date of final rule].
Added [insert effective date of final rule].
*
*
6351
*
*
*
*
*
Added March 1, 1989; evaluation March 24, 1992; criterion August 30, 1996; criterion, note [insert effective
date of final rule].
Added November 29, 1994; criterion August 30, 1996; title, criterion, note [insert effective date of final rule].
6300
6301
6302
6304
6305
6306
6307
6308
6309
6354
*
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5. Amend appendix B to part 4 by:
a. Revising the entries for diagnostic
codes 6300 and 6305;
■ b. Adding in numerical order an entry
for diagnostic code 6312;
■
■
c. Revising the entry for diagnostic
code 6317; and,
■ d. Adding in numerical order entries
for diagnostic codes 6325, 6326, 6329
through 6331, and 6333 through 6335.
■
The revisions and additions read as
follows:
APPENDIX B TO PART 4—NUMERICAL INDEX OF DISABILITIES
Diagnostic
code No.
*
*
*
*
*
*
*
INFECTIOUS DISEASES, IMMUNE DISORDERS AND NUTRITIONAL DEFICIENCIES
*
*
*
6300 ..........................................................................................
*
*
Vibriosis (Cholera, Non-cholera).
*
*
*
*
*
6305 ..........................................................................................
*
*
Lymphatic filariasis, to include elephantiasis.
*
*
*
*
*
6312 ..........................................................................................
*
*
Nontuberculosis mycobacterial infection.
*
*
*
*
*
6317 ..........................................................................................
*
*
Rickettsial, erlichial, and Anaplasma infections.
*
*
6325
6326
6329
6330
6331
6333
6334
6335
*
*
*
..........................................................................................
..........................................................................................
..........................................................................................
..........................................................................................
..........................................................................................
..........................................................................................
..........................................................................................
..........................................................................................
*
*
*
6351 ..........................................................................................
6356 ..........................................................................................
6. Amend appendix C to part 4 by:
a. Adding in alphabetical order an
entry for ‘‘Campylobacter jejuni
infection’’;
■ b. Removing the entry for ‘‘Cholera,
Asiatic’’;
■ c. Adding in alphabetical order entries
for ‘‘Coxiella burnetii infection (Q
Fever)’’, ‘‘Hemorrhagic fevers, including
■
■
*
*
*
Hyperinfection syndrome or disseminated strongyloidiasis.
Schistosomiasis.
Hemorrhagic fevers, including dengue, yellow fever, and others.
Campylobacter jejuni infection.
Coxiella burnetii infection (Q Fever).
Nontyphoid salmonella infections.
Shigella infections.
West Nile virus infection.
*
*
*
*
*
HIV-related infection.
Systemic exertional intolerance disease/chronic fatigue syndrome (CFS).
dengue, yellow fever, and others’’, and
‘‘Hyperinfection syndrome or
disseminated strongyloidiasis’’;
■ d. Revise the entry for ‘‘Lymphatic
filariasis’’;
■ e. Adding in alphabetical order entries
for ‘‘Nontuberculosis mycobacterial
infection’’, ‘‘Nontyphoid salmonella
infection’’, ‘‘Rickettsial, erlichial, and
Anaplasma infections’’, Shigella
infections, and ‘‘Schistosomiasis’’;
■ f. Removing the entry for ‘‘Typhus,
scrub’’; and
■ g. Adding in alphabetical order entries
for ‘‘Vibriosis (Cholera, Non-cholera)’’
and ‘‘West Nile virus infection’’
The additions and revisions read as
follows:
APPENDIX C TO PART 4—ALPHABETICAL INDEX OF DISABILITIES
Diagnostic
code No.
*
*
*
*
*
*
Campylobacter jejuni infection .............................................................................................................................................................
*
*
*
*
*
*
*
Coxiella burnetii infection (Q Fever) ....................................................................................................................................................
*
*
*
*
*
*
*
Hemorrhagic fevers, including dengue, yellow fever, and others) ......................................................................................................
*
*
*
*
*
*
*
Hyperinfection syndrome or disseminated strongyloidiasis .................................................................................................................
*
*
*
*
*
*
*
Lymphatic filariasis, to include elephantiasis ......................................................................................................................................
*
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6329
6325
6305
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APPENDIX C TO PART 4—ALPHABETICAL INDEX OF DISABILITIES—Continued
Diagnostic
code No.
*
*
*
*
*
*
Nontyphoid salmonella infection ..........................................................................................................................................................
*
*
*
*
*
*
*
Nontuberculosis mycobacterial infection .............................................................................................................................................
*
*
*
*
*
*
*
Rickettsial, erlichial, and Anaplasma Infections ..................................................................................................................................
*
*
*
*
*
*
*
Schistosomiasis ...................................................................................................................................................................................
*
*
*
*
*
*
*
Shigella infections ................................................................................................................................................................................
*
*
*
*
*
*
*
Vibriosis (Cholera, Non-cholera) .........................................................................................................................................................
*
*
*
*
*
*
*
West Nile virus infection ......................................................................................................................................................................
*
*
*
*
[FR Doc. 2019–00636 Filed 2–4–19; 8:45 am]
BILLING CODE 8320–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 49 and 52
[EPA–R10–OAR–2017–0347; FRL–9988–88–
Region 10]
Indian Country: Air Quality Planning
and Management; Federal
Implementation Plan for the Kalispel
Indian Community of the Kalispel
Reservation, Washington;
Redesignation to a PSD Class I Area
Environmental Protection
Agency (EPA).
ACTION: Notice of proposed rulemaking;
reopening of comment period.
The Environmental Protection
Agency (EPA) is reopening the public
comment period for the proposed rule
‘‘Indian Country: Air Quality Planning
and Management; Federal
Implementation Plan for the Kalispel
Indian Community of the Kalispel
Reservation, Washington; Redesignation
to a PSD Class I Area’’ published on
October 31, 2018. In the October 31,
2018, publication, the EPA proposed to
approve the Kalispel Indian Community
of the Kalispel Reservation’s request to
redesignate certain lands within its
reservation to a Class I area under the
Prevention of Significant Deterioration
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program and revise the Federal
Implementation Plan for the Kalispel
Reservation and State Implementation
Plan for the State of Washington
accordingly. A commenter requested
additional time to review the proposal
and prepare comments. In response to
this request, the EPA is reopening the
comment period.
The comment period for the
proposed rule published October 31,
2018 (83 FR 54691), is reopened, and
written comments must be received on
or before February 20, 2019.
DATES:
Submit your comments,
identified by Docket ID No. EPA–R10–
OAR–2017–0347 at https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Once submitted, comments cannot be
edited or removed from Regulations.gov.
The EPA may publish any comment
received to its public docket. Do not
submit electronically any information
you consider to be Confidential
Business Information (CBI) or other
information, the disclosure of which is
restricted by statute. Multimedia
submissions (audio, video, etc.) must be
accompanied by a written comment.
The written comment is considered the
official comment and should include
discussion of all points you wish to
make. The EPA will generally not
consider comments or comment
contents located outside of the primary
submission (i.e., on the web, cloud, or
other file sharing system). For
ADDRESSES:
AGENCY:
SUMMARY:
*
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*
6333
6312
6317
6326
6334
6300
6335
*
additional submission methods, the full
EPA public comment policy,
information about CBI or multimedia
submissions, and general guidance on
making effective comments, please visit
https://www.epa.gov/dockets/
commenting-epa-dockets.
FOR FURTHER INFORMATION CONTACT:
Sandra Brozusky at (206) 553–5317, or
brozusky.sandra@epa.gov.
On
October 31, 2018, the EPA published a
proposed rulemaking to approve the
Kalispel Indian Community of the
Kalispel Reservation’s request to
redesignate certain lands within its
reservation to a Class I area under the
Prevention of Significant Deterioration
program and revise the Federal
Implementation Plan for the Kalispel
Reservation (40 CFR part 49, subpart M)
and State Implementation Plan for the
State of Washington (40 CFR part 52,
subpart WW) accordingly. (83 FR
54691). A commenter requested
additional time to review the proposal
and prepare comments. In response to
this request, the EPA is reopening the
comment period.
SUPPLEMENTARY INFORMATION:
Dated: December 20, 2018.
Michelle L. Pirzadeh,
Acting Regional Administrator, Region 10.
[FR Doc. 2019–00935 Filed 2–4–19; 8:45 am]
BILLING CODE 6560–50–P
E:\FR\FM\05FEP1.SGM
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Agencies
[Federal Register Volume 84, Number 24 (Tuesday, February 5, 2019)]
[Proposed Rules]
[Pages 1678-1690]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-00636]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF VETERANS AFFAIRS
38 CFR Part 4
RIN 2900-AQ43
Schedule for Rating Disabilities: Infectious Diseases, Immune
Disorders, and Nutritional Deficiencies
AGENCY: Department of Veterans Affairs.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: The Department of Veterans Affairs (VA) proposes to amend the
section of the VA Schedule for Rating Disabilities (VASRD or Rating
Schedule) that addresses infectious diseases and immune disorders. The
purpose of these changes is to incorporate medical advances since the
last revision, update medical terminology, and clarify evaluation
criteria. The proposed rule considers comments from experts and the
public during a forum held from January 31 to February 1, 2011, on
revising this section of the VASRD.
DATES: Comments must be received by VA on or before April 8, 2019.
ADDRESSES: Written comments may be submitted through
www.regulations.gov; by mail or hand-delivery to Director, Regulation
Policy and Management (00REG), Department of Veterans Affairs, 810
Vermont Ave. NW, Room 1063B, Washington, DC 20420; or by fax to (202)
273-9026. (This is not a toll free number.) Comments should indicate
that they are submitted in response to ``RIN 2900-AQ43--Schedule for
Rating Disabilities: Infectious Diseases, Immune Disorders, and
Nutritional Deficiencies.'' Copies of comments received will be
available for public inspection in the Office of Regulation Policy and
Management, Room 1063B, between the hours of 8 a.m. and 4:30 p.m.,
Monday through Friday (except holidays). Please call (202) 461-4902 for
an appointment. (This is not a toll free number.) In addition, during
the comment period, comments may be viewed online through the Federal
Docket Management System (FDMS) at www.Regulations.gov.
FOR FURTHER INFORMATION CONTACT: Ioulia Vvedenskaya, M.D., M.B.A.,
Medical Officer, Part 4 VASRD Regulations Staff (211C), Compensation
Service, Veterans Benefits Administration, Department of Veterans
Affairs, 810 Vermont Avenue NW, Washington, DC 20420, (202) 461-9700.
(This is not a toll-free telephone number.)
SUPPLEMENTARY INFORMATION: As part of its ongoing revision of the
VASRD, VA proposes changes to 38 CFR 4.88a, which pertains to chronic
fatigue syndrome (CFS), and 38 CFR 4.88b, which pertains to the
schedule of ratings for infectious diseases and immune disorders (we
note that the proposed changes for Sec. 4.88b exclude the schedule of
ratings for nutritional deficiencies--diagnostic codes (DC) 6313, 6314,
and 6315). VA last updated the schedule of ratings in Sec. 4.88b on
July 31, 1996 (see 61 FR 39875) and updated Sec. 4.88a on July 19,
1995 (see 60 FR 37012).
VA proposes to: (1) Update the medical terminology and definition
of certain infectious diseases and immune disorders; (2) add medical
conditions not currently in the Rating Schedule; (3) refine evaluation
criteria based on medical advances that have occurred since the last
revision; and (4) incorporate current understanding of functional
changes associated with or resulting from disease (pathophysiology).
A panel of independent experts convened by the Institute of
Medicine (IOM) in February 2015 proposed an updated set of diagnostic
criteria for infectious disease and immune disorders. This updated
revision also included changing the name of CFS to ``Systemic Exertion
Intolerance Disease (SEID)/Chronic fatigue Syndrome (CFS).''
VA has clear authority to make this regulatory change because of
its broad authority to ``prescribe all rules and regulations which are
necessary or appropriate to carry out the laws administered by [VA] and
are consistent with those laws.'' 38 U.S.C. 501(a); see also 38 U.S.C.
1155 (VA's authority to adopt and apply schedule for rating
disabilities).
Sec. 4.88a Chronic Fatigue Syndrome
Currently, Sec. 4.88a specifies older diagnostic criteria for the
diagnosis of CFS and uses outdated terminology to refer to this complex
disease. VA proposes to update the nomenclature for this disease, which
is also known as systemic exertion intolerance disease (SEID) or
myalgic encephalomyelitis (ME), by changing the diagnostic code name to
``Systemic Exertion Intolerance Disease (SEID)/Chronic Fatigue Syndrome
(CFS).'' This new name captures a central characteristic of the disease
that reflects negative effects of any exertion (physical, cognitive, or
emotional) on patients' many organ systems. IOM (Institute of
Medicine), Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome:
Redefining an Illness (2015), https://www.nationalacademies.org/hmd/~/
media/Files/Report%20Files/2015/
[[Page 1679]]
MECFS/MECFScliniciansguide.pdf (last accessed August 30, 2018).
VA is also proposing to revise the current diagnostic criteria for
SEID/CFS to adhere to evidence-based criteria which were adopted by the
Centers for Disease Control and Prevention (CDC). IOM Report on ME/CFS
(2015) (updated July 3, 2017), https://www.cdc.gov/me-cfs/symptoms-diagnosis/diagnosis.html (last accessed July 17, 2018). According to
the 2015 IOM Report, up to 2.5 million Americans suffer from this
disease which is characterized by profound fatigue, cognitive
dysfunction, sleep abnormalities, pain, autoimmune manifestations, and
a variety of other symptoms that are made worse by exertion of any
sort. New diagnostic criteria will take into consideration whether this
severe chronic fatigue significantly interferes with daily activities
and work, if the affected individual concurrently has four or more of
the eight symptoms as outlined in CDC evidence-based criteria and
whether these symptoms first appeared before the fatigue, have
persisted or recurred during six or more consecutive months of illness,
and were due to ongoing exertion or other medical conditions associated
with fatigue.
The CDC mandates a thorough medical history, physical examination,
mental status examination, and laboratory tests to identify underlying
or contributing conditions that require treatment. CDC recognizes and
identifies several conditions that do not exclude a diagnosis of SEID/
CFS. Currently, Sec. 4.88b lists 19 DCs encompassing infectious
diseases and immune disorders. VA proposes to revise these codes to
reflect current terminology, advances in medical knowledge,
recommendations from the 2015 IOM Report on ME/CFS and a 2007 IOM
Report on evaluating veterans for disability benefits, IOM, A 21st
Century System For Evaluating Veterans for Disability Benefits (2007),
https://www.nap.edu/read/11885/chapter/1 (last accessed July 17, 2018).
Schedule of Ratings--Infectious Diseases, Immune Disorders, and
Nutritional Deficiencies
Proposed General Rating Formula for Sec. 4.88b
Currently, each infectious disease listed under Sec. 4.88b has its
own prescribed rating criteria. In most cases, each specific infectious
disease warrants a 100 percent evaluation during an active period of
the disease. Thereafter, any residual functional impairment from the
infectious disease determines the level of disability. These evaluation
principles are generally consistent with the clinical presentation of
infectious diseases.
VA proposes one General Rating Formula for Sec. 4.88b. This
approach is based on the association between clinical resolution or
stabilization of an infectious disease and elimination or complete
suppression of the causative infectious agent. Regardless of whether
resolution occurs spontaneously or because of treatment, long-term
disability in such situations results from residual functional
impairment of the body systems affected by the infectious disease,
rather than the infection itself. Sheila Davey, World Health
Organization, World Health Organization Report on Infectious Diseases:
Removing Obstacles to Healthy Development (1999).
Therefore, VA's proposal to use a General Rating Formula does not
substantively change the current evaluation criteria so much as their
organization. This rulemaking proposes to restructure rating criteria
by creating one General Rating Formula applicable to multiple
infectious diseases, regardless of etiology. A General Rating Formula
for infectious diseases would ensure consistency in rating these
conditions and be similar to the use of a General Rating Formula in
other sections of the VASRD, such as in Sec. Sec. 4.97, 4.116, 4.130,
and others. This formula would be a familiar concept for Veterans
Benefits Administration (VBA) employees and minimize the risk for error
by providing one criterion applicable to multiple diagnostic codes.
Although each specific infectious disease has a different etiology and
natural history, once the active disease phase is over, disability
would be rated on residuals. VA would assign a 100 percent disability
rating during the variable length of each specific disease's active
phase. For most infectious diseases manifesting acutely, the length of
the active disease phase (i.e., the time between disease onset and
resolution or stabilization) is at most usually six to eight weeks. VA
proposes to assign a 100 percent evaluation during the active disease
phase. VA recognizes that some infectious diseases, such as
tuberculosis, may have a longer than average active disease phase.
Therefore, VA proposes that the General Rating Formula apply only in
those cases where specific rating criteria are not otherwise provided.
Diagnostic codes in Sec. 4.88b that would not follow the General
Rating Formula would be 6301, 6302, 6310, 6311, 6312, 6313, 6314, 6315,
6325, 6326, 6351, and 6354.
After the disease becomes inactive, VA proposes to assign a 0
percent evaluation. However, even though advancements in antimicrobial
therapy have significantly lessened the occurrence of residuals of
infectious diseases, they continue to occur. Therefore, VA generally
proposes to append each diagnostic code with a note describing the most
common residuals associated with a given infection. See below for
additional details. As a list of every residual would be impractical,
these notes would clearly indicate that they are not exhaustive. Where
ascertainable residuals exist, VA proposes to assign evaluations for
those residuals under the appropriate body system(s).
Certain infectious conditions are prone to relapse and require
laboratory evaluation for confirmation. L. Joseph Wheat et al.,
Clinical Practice Guidelines for the Management of Patients with
Histoplasmosis: 2007 Update by the Infectious Diseases Society of
America, 45 Clinical Infectious Diseases 807, 807-25 (2007).
Oftentimes, non-specific constitutional symptoms (weakness, tiredness,
insomnia, weight loss, etc.) occur following the active phase of an
infectious disease. However, such symptoms may be due to other causes
than the infection. Therefore, to ensure VA assigns the most
appropriate evaluations for relapsing infections, VA proposes to
include a note in the rule requiring that relapses be confirmed by
pathogen-specific testing using appropriate microbiologic, serologic,
biochemical (e.g., nucleic acid detection)histopathologic methods.
Finally, although VA proposes using a General Rating Formula for
most infectious diseases, VA notes that each infectious disease has a
different long-term impact. For those that have longer active phases
and/or are commonly associated with relapse and residuals, VA proposes
to require VA examination once the disease is no longer active so that
a medical professional can evaluate the individual's condition. In
these cases, VA also proposes to apply the provisions of Sec. 3.105(e)
that require VA to send beneficiaries notice of any proposed reduction
in evaluation and provide an opportunity to respond before it becomes
effective.
Proposed Changes to Existing Diagnostic Codes
As discussed above, VA proposes to apply a General Rating Formula
for infectious diseases unless otherwise noted. Additionally, VA
proposes to provide notes identifying common residuals associated with
particular diseases and instructions to rating personnel regarding the
level of medical
[[Page 1680]]
review necessary following cessation of treatment and infection. These
specific proposed changes are discussed below.
Diagnostic Code 6300
Currently, DC 6300 is titled ``Cholera, Asiatic'' referring only to
infection with toxigenic strains of Vibrio cholerae; it does not
reflect infections due to other species within the genus Vibrio. Non-
cholera Vibrio species cause diarrheal diseases, as well as wound
infections and septicemia. To reflect the total array of diseases
caused by Vibrio species, VA proposes to rename this DC ``Vibriosis
(cholera, non-cholera), to encompass conditions caused by V. cholerae
and by non-cholera Vibrio organisms.
Cholera due to V. cholerae and gastroenteritis due to other Vibrio
species are associated with severe diarrhea of relatively short
duration. Hoi Ho et al., Vibrio Infections, Medscape.com (July 24,
2018), https://emedicine.medscape.com/article/232038-overview. Including
the incubation period, cholera usually lasts 7 to 10 days and results
in total remission, or, in 5 to 10 percent of cases, death if left
untreated. Therefore, the proposed General Rating Formula would be
appropriate for both cholera and non-cholera gastroenteritis due to
other Vibrio species, and VA would remove the existing provision for a
separate three-month convalescence period as it would no longer be
necessary.
VA proposes to use a note to provide information about common
residual disability of cholera and non-cholera Vibrio infection,
including renal failure, skin, and musculoskeletal conditions, such as
necrotizing fasciitis. VA proposes no changes to the evaluation
criterion for this DC except eliminating the three-month convalescence
and adding a note to address rating of residual disability.
Diagnostic Code 6301
VA evaluates DC 6301, visceral leishmaniasis, at 100 percent for
six months following cessation of treatment, after which a VA
examination helps determine residual disability. VA proposes only minor
changes to this rating criteria, but proposes to change the note
regarding rating residual disability. VA would generally identify those
residuals commonly associated with post-infection or post-treatment
residuals that may warrant evaluation. Currently, DC 6301 lists
lymphadenopathy as one such residual disability. However,
lymphadenopathy follows numerous diseases and is a frequent physical
finding which, even when permanent, is otherwise without symptoms or
disability that would warrant evaluation. Robert Ferrer,
Lymphadenopathy: Differential Diagnosis and Evaluation, 58 a.m. Fam.
Physician 1313, 1313-20 (Oct. 15, 1998). In many cases, it may
constitute a normal physical finding. Vikramjit S. Kanwar,
Lymphadenopathy, Medscape.com (Feb. 1, 2018), https://emedicine.medscape.com/article/956340-overview.
As lymphadenopathy is often associated with other diseases and,
regardless of origin, commonly presents without symptoms or disability
warranting evaluation, VA proposes to remove it from the note in DC
6301. VA notes that the list of possible residuals in proposed DC 6301
would not be exhaustive. Thus, if a veteran presents with
lymphadenopathy as a residual of visceral leishmaniasis that results in
chronic, functional impairment, VA would consider an evaluation under
the appropriate system.
In addition to the above revision, VA proposes to amend the
existing Note 1 to inform that the residual effects of infection
include bone marrow diseases. Parasites--Leishmaniasis, CDC (Jan. 10,
2013), https://www.cdc.gov/parasites/leishmaniasis/. This
note would also refer to the residuals listed in 38 CFR 3.317(d),
``Long-term health effects potentially associated with infectious
diseases.''
Finally, VA proposes to add a new Note 2 to address the use of
culture, histopathology, and other diagnostic testing to confirm
relapses. Clinicians rely on such diagnostic testing, which has
increased steadily in accuracy and availability, to determine whether
symptoms are due to leishmaniasis or some other disease. Shyam Sundar &
M. Rai, ``Laboratory Diagnosis of Visceral Leishmaniasis,'' 9 Clinical
and Diagnostic Laboratory Immunology 951, 951-58 (2002). VA also
proposes to retitle the existing note as Note 1 to account for the
addition of this second note.
Diagnostic Code 6302
VA would not change the rating criteria for leprosy (Hansen's
disease), but proposes to amend the current Note under DC 6302 by
adding amputations as a residual in the proposed Note. The neurologic
impairment in leprosy involves sensory and motor deficits/loss in the
extremities that may lead to auto-amputation. Preenon Bagchi et al.,
Bacterio-Informatics: Identifying the Cause of Hansen's Disease and
Establish [sic] a Remedy for the Same, 2 Int'l J. of Bioinformatics
Res. and Applications 15, 15-19 (2010).
Diagnostic Code 6304
VA proposes to evaluate DC 6304, malaria, using the General Rating
Formula because it is an acute, debilitating disease with predictable
clinical presentation.
VA proposes to amend an existing note and to add one new notes.
Note 1 would explicitly state that VA requires diagnostic confirmation
for both the initial diagnosis and any relapse. To reflect advances in
malarial testing, VA also proposes to refer to other specific
diagnostic tests such as antigen detection, immunologic
(immunochromatographic) tests, and molecular testing, such as
polymerase chain reaction tests. Malaria Diagnosis (United States), CDC
(Nov. 19, 2015), https://www.cdc.gov/malaria/diagnosis_treatment/diagnosis.html.
Note 2 would recognize potential nervous system residuals because
severe forms of malaria affect the brain as an encephalopathy. Pralay
Sarkar et al., ``Critical care aspects of malaria,'' 25 J. of Intensive
Care Med. 93, 93-103 (2010). In addition, this note would also refer to
the residuals listed in Sec. 3.317(d).
Diagnostic Code 6305
VA proposes to amend the title of this DC, currently ``Lymphatic
filariasis,'' to include the term elephantiasis, which is another name
commonly associated with the chronic form of this condition. Lymphatic
Filariasis Fact Sheet No. 102, World Health Organization (May 11,
2018), https://www.who.int/mediacentre/factsheets/fs102/en/.
The new General Rating Formula would provide 100 percent evaluation
for the acute phase of active infection for lymphatic filariasis. The
proposed General Rating Formula would be appropriate for use in this
acute infection. However, no actual changes in the evaluation criteria
would result from this organizational change intended to help rating
personnel easily apply the VASRD.
VA proposes to add information to more adequately address the range
of potential residuals, which include lymphedema (permanent swelling)
and lymphatic obstruction. Parasites--Lymphatic Filariasis, CDC (June
14, 2013), https://www.cdc.gov/parasites/lymphaticfilariasis/disease.html. VA proposes a new Note to instruct rating personnel to
evaluate under the appropriate body system residuals such as
epididymitis, lymphangitis, lymphatic obstruction, or lymphedema
affecting extremities, genitals, and/or breasts.
[[Page 1681]]
Diagnostic Code 6306
Bartonellosis, currently evaluated under DC 6306, generally
resolves within two months with appropriate treatment. Kassem A.
Hammoud et al., Bartonellosis, Medscape.com (Oct. 17, 2012), https://emedicine.medscape.com/article/213169-overview. Therefore, VA proposes
to rate active bartonellosis under the General Rating Formula at 100
percent, and VA would remove the existing provision for a separate
three-month convalescence period as it would no longer be necessary.
VA also proposes to update the residual disability to include
endocarditis, which occurs when the bloodstream may carry this
bacterium to the heart valves. John L. Brusch et al., Infective
Endocarditis--Pathophysiology, Medscape.com (Dec. 17, 2013), https://emedicine.medscape.com/article/216650-overview#a0104.
Diagnostic Code 6307
VA proposes to evaluate DC 6307, plague, which is an acute,
debilitating disease of short duration, using the General Rating
Formula.
Use of modern antibiotics renders residual disability from the
infection itself extremely rare. Therefore, VA proposes to delete the
existing note regarding specific residuals and replace it with a note
stating that VA would rate any residual disability under the
appropriate body system. Again, lymphadenopathy is a frequent physical
finding following numerous diseases, often permanent and without
disabling symptoms. Robert Ferrer, Lymphadenopathy: Differential
Diagnosis and Evaluation, 58 Am.Fam. Physician at 1313-20. VA proposes
removing lymphadenopathy as a residual because it may be a normal
physical finding. Vikramjit S. Kanwar, Lymphasdenopathy, Medscape.com
(July 10, 2015), https://emedicine.medscape.com/article/956340-overview); Plague, CDC (Nov. 28, 2012), https://www.cdc.gov/plague/.
Diagnostic Code 6308
VA proposes to evaluate DC 6308, relapsing fever, which is an
acute, debilitating disease of short duration, using the General Rating
Formula.
Modern treatment helps most patients recover from this disease
within a few days, with little incidence of splenic damage. Long-term
sequelae of relapsing fever are rare, but include iritis, uveitis,
cranial nerve, and other neuropathies. Tick-borne Relapsing Fever
(TBRF), CDC (Jan. 8, 2016), https://www.cdc.gov/relapsing-fever/clinicians/. Therefore, VA proposes a new Note adding iritis and
uveitis as residual disabilities and retaining the remainder of the
existing information without substantive change.
VA does not propose any changes to the evaluation criteria for this
DC.
Diagnostic Code 6309
VA proposes to evaluate DC 6309, rheumatic fever, which is an
acute, febrile disease typically lasting less than a month, using the
General Rating Formula. The existing note regarding residuals would
remain substantively unchanged.
Diagnostic Code 6310
VA does not propose substantive change to the criteria under
diagnostic code 6310 for syphilis and other treponemal infections.
However, for consistency with the remainder of this section, VA
proposes to replace the term ``complications'' with the term ``residual
disability,'' which VA would rate under the appropriate body system.
Additionally, VA proposes to remove specific references to the
names associated with each DC identified in this note because future
revisions of the rating schedule would retitle several of them.
Diagnostic Code 6311
Currently, DC 6311, miliary tuberculosis, provides a 100 percent
evaluation during active infection. Under Sec. 4.88c, the 100 percent
is continued for one year following the date of inactivity. Active
infection may last for months to years, and, if undiagnosed or
untreated, may result in death. The standard treatment for drug-
susceptible miliary tuberculosis is six to nine months with a
combination of anti-tuberculosis drugs. If the meninges are involved,
treatment will last for 9 to12 months, but may occasionally require
longer a treatment duration. Nahid, P., et al., ``Executive Summary:
Official American Thoracic Society/Centers for Disease Control and
Prevention/Infectious Diseases Society of America Clinical Practice
Guidelines: Treatment of Drug-Susceptible Tuberculosis,'' 63 Clinical
Infectious Diseases 853, 853-867 (Oct. 2016), https://www.nidcd.nih.gov/health/balance/pages/meniere.aspx (last visited
January 22, 2019). Relapses are common when medication is not taken for
the full time prescribed and/or not taken in the appropriate
combination. Generally, most relapses occur within the first 12 months
of treatment completion. Tuberculosis (TB) Guidelines. CDC (May 4,
2016), https://www.cdc.gov/tb/publications/guidelines/treatment.htm.
To ensure that individuals are entitled to any resumption or
continuation of the 100 percent evaluation after the initial active
disease, VA proposes to add a Note requiring confirmation of relapse by
culture, histopathology, or other diagnostic laboratory testing.
VA also proposes Note 2 addressing residuals which may be found
under Sec. 4.88c. Infection residuals include, but are not limited to,
chronic diagnosed disabilities affecting such body systems as the skin
and respiratory, central nervous, musculoskeletal, ocular,
gastrointestinal, and genitourinary systems. VA would rate them under
the appropriate body system. J.J. van der Harst & G.J. Luijckx,
Treatment of Central Nervous System Tuberculosis Infections and
Neurological Complications of Tuberculosis Treatment, 17 Current
Pharmaceutical Design 2940, 2940-47 (2011).
Diagnostic Code 6316
VA proposes to evaluate DC 6316, brucellosis, an acute,
debilitating disease of short duration usually lasting several weeks or
less, using the General Rating Formula. Brucellosis is easily treated
with antibiotics, but, if untreated, brucellosis may become chronic and
leave significant residuals. VA proposes no changes to the evaluation
criteria.
As the correct diagnosis is essential in determining if symptoms
are due to brucellosis or some other disease entity, VA proposes to add
a new Note 1 directing that culture, serologic testing, or both must
confirm both the initial diagnosis and any relapse of active infection.
Wafa Al-Nassir, Brucellosis, Medscape.com (June 16, 2017), https://emedicine.medscape.com/article/213430-overview.
VA proposes to amend the existing note as Note 2 and expand the
list of residuals in light of advances in medicine and early treatment.
Note 2 would reflect the residuals most commonly associated with this
infection, including meningitis, and liver, spleen, or musculoskeletal
conditions. Brucellosis, CDC (Sept. 13, 2017) https://www.cdc.gov/brucellosis/. As this condition is a presumptive disease
related to Gulf War service, this note would also refer to the many
specific residuals of brucellosis listed in Sec. 3.317(d).
Diagnostic Code 6317
Currently, DC 6317 represents scrub typhus, an acute debilitating
rickettsial disease lasting for several weeks or less. If untreated, a
high mortality rate results. Antibiotic treatment rapidly eradicates
the disease and significantly
[[Page 1682]]
reduces the chances of complications. Therefore, VA proposes to
evaluate DC 6317 using the General Rating Formula. VA proposes to
rename this DC to encompass all forms of rickettsial and similar
erlichial and Anaplasma infections. These infections are not specific
to the veteran population as they afflict travelers and field
scientists as well. Renaming this DC would mean rating personnel need
not further clarify the type of typhus infecting a veteran.
VA is not proposing any changes to the evaluation criteria except
to use the General Rating Formula. VA would also remove the existing
provision for a separate three-month convalescence period as it would
no longer be necessary.
VA proposes to update the existing note to include such residuals
frequently associated with DC 6317 as involvement of bone marrow and
the central nervous system, in addition to the current list of spleen
damage or skin conditions.
Rickettsial, ehrlichial, and Anaplasma infections cause similar
nonspecific influenza-like illness in humans, including but not limited
to, scrub typhus, Rocky Mountain spotted fever, African tick-borne
fever, ehrlichiosis, and anaplasmosis. Therefore, VA also proposes to
add a second note to list other rickettsial infections, including
infections by Ehrlichia and Anaplasma species (members of the order
Rickettsiales) to account for its occurrence in the U.S. veteran
population. Johan S. Bakken & J. Stephen Dumler, Ehrlichiosis and
Anaplasmosis, Medscape.com (2004), https://www.medscape.com/viewarticle/490468_4.
Diagnostic Code 6318
Currently, DC 6318 represents melioidosis, an acute debilitating
bacterial disease lasting several weeks or less, which, if left
untreated, may result in mortality. VA proposes no changes to the
evaluation criteria, except use of the General Rating Formula.
As accuracy is essential in diagnosing melioidosis, VA proposes to
add Note 1 directing that culture or other specific diagnostic
laboratory tests must confirm both the initial diagnosis and any
relapse or chronic activity of infection.
VA would retain the existing information regarding common residuals
and the instruction to rate residuals under the appropriate body system
under Note 2.
Diagnostic Code 6319
VA currently assigns a 100 percent evaluation for DC 6319, Lyme
disease, when it is active. Lyme disease is an acute illness, usually
lasting several weeks or less. Therefore, VA proposes to rate Lyme
disease under the General Rating Formula, without changes to the actual
evaluation criteria. VA also proposes to amend the existing note
associated with this DC to account for residuals such as Bell's palsy,
radiculopathy, ocular, and cognitive dysfunction, in addition to
arthritis.
Diagnostic Code 6320
Currently, DC 6320 represents ``Parasitic diseases otherwise not
specified.'' VA proposes no changes to the evaluation criteria except
to use the General Rating Formula. VA also proposes to amend the
existing note associated with this DC with general instructions to rate
any residuals of this infection under the appropriate body system.
Diagnostic Code 6351
VA proposes a number of changes to DC 6351, which pertains to human
immunodeficiency virus (HIV) related illness. Currently, VA provides a
100 percent evaluation for ``AIDS with recurrent opportunistic
infections or with secondary diseases affecting multiple body systems;
HIV-related illness with debility and progressive weight loss, without
remission, or few or brief remissions.'' VA proposes to remove the
statement about remission because the CDC considers AIDS a chronic
condition, and the diagnosis continues once a person is properly
diagnosed, regardless of improvements in that person's condition.
When VA last revised the evaluation criteria, the medical community
considered oral hairy leukoplakia (OHL) a distinctive clinical marker
of HIV infection. Since then, measurement of the peripheral CD4 cell
count and HIV viral load have become the standard method for evaluating
a patient's stage of HIV infection. Sowmya Nanjappa, Anti-retroviral
Therapy in Treatment-Na[iuml]ve Patients, Medscape.com (June 3, 2016),
https://emedicine.medscape.com/article/2041458-overview. In addition,
OHL by itself rarely, if ever, requires specific treatment in patients
receiving anti-retroviral therapy. James Cade, Hairy Leukoplakia
Treatment and Management, Medscape.com (December 19, 2018), https://emedicine.medscape.com/article/279269-overview. VA proposes to remove
reference to OHL in the criteria for a 30 percent evaluation.
Similarly, VA proposes to modify the reference of oral candidiasis
to esophageal and lower respiratory tract candidiasis for the criteria
for a 30 percent evaluation. In the past, oral candidiasis was strongly
associated with HIV infection. However, the increased use of
antiretroviral medications has greatly reduced the incidence of this
condition in HIV-positive individuals. C. Frezzini et al., Current
Trends of HIV Disease of the Mouth, 34 J. of Oral Pathology & Med. 513,
513-31 (2005).
For clarification, VA proposes to replace the phrase ``definite
medical symptoms'' in the criteria for a 10 percent evaluation with
``HIV-related constitutional symptoms.'' VA would not change the
remainder of the criteria for a 10 percent evaluation. The criteria for
a 0 percent evaluation would not change.
Existing Note 1 would continue to provide that ``medications
prescribed as part of a research protocol at an accredited medical
institution'' are to be considered ``approved medication'' within the
context of the evaluation criteria. VA proposes to add a reference to
treatment regimens as part of a research protocol at an accredited
medical institution because some research protocols use not only new
medications but also new regimens for already FDA approved medications.
Existing Note 2 would continue to provide for separate evaluation
of various manifestations of HIV infection under the appropriate
diagnostic codes. VA proposes to retain the instruction to evaluate on
the basis of psychiatric or central nervous system manifestations,
opportunistic infections, and neoplasms, rather than based on this
diagnostic code, if a higher overall evaluation results. However, VA
proposes to substitute the term ``diagnosed psychiatric condition'' for
the phrase ``psychiatric manifestations.'' VA recognizes that a veteran
may exhibit psychiatric symptoms, such as depression, which do not rise
to the level of a diagnosed disability. Such symptoms are more
appropriately rated under DC 6351 as 10 percent disabling, provided
there is evidence of activity limitations. Note 2, however, would refer
to diagnosed, disabling acquired psychiatric illness.
VA also proposes the addition of a new Note 3 to assist rating
personnel in applying these revised evaluation criteria. Note 3 would
include a list of current opportunistic infections, which includes the
following conditions: Candidiasis of the bronchi, trachea, esophagus,
or lungs; invasive cervical cancer; coccidioidomycosis; cryptococcosis;
cryptosporidiosis; cytomegalovirus (particularly CMV retinitis); HIV-
related encephalopathy; herpes simplex-chronic ulcers of greater
[[Page 1683]]
than one month's duration, or bronchitis, pneumonia, or esophagitis;
histoplasmosis; isosporiasis (chronic intestinal); Kaposi's sarcoma;
lymphoma; Mycobacterium avium complex; tuberculosis; Pneumocystis
jirovecii (carinii) pneumonia; pneumonia, recurrent; progressive
multifocal leukoencephalopathy; Salmonella septicemia, recurrent;
toxoplasmosis of the brain; and wasting syndrome due to HIV. AIDS and
Opportunistic Infections, CDC (July 23, 2018), https://www.cdc.gov/hiv/basics/livingwithhiv/opportunisticinfections.html.
Diagnostic Code 6354
VA is proposing no change to the rating criteria for this DC other
than to update the name from chronic fatigue syndrome (CFS) to systemic
exertion intolerance disease/chronic fatigue syndrome (CFS). VA would,
however, clarify the note to indicate that incapacitation requires that
a licensed physician must prescribe both bed rest and treatment, which
would be consistent with current VA practice.
Proposed New Diagnostic Codes
As discussed above, in addition to updating existing DCs, VA
proposes to add medical conditions not currently listed in the Rating
Schedule:
Proposed New Diagnostic Code 6312
VA proposes to add a new DC 6312 for ``Nontuberculosis
mycobacterial infection'' (NTM). NTM lung infection occurs when a
person inhales the organism from the environment. Most people do not
become ill but some susceptible individuals require prolonged treatment
of one to two years. Without treatment, many people, but not all, will
develop a progressive lung infection characterized by cough, fatigue,
and often weight loss. However, death directly related to NTM lung
disease is relatively rare in immunocompetent individuals.
Systemic infection, which is the most severe form, is most often
seen in individuals with other underlying conditions, especially those
that inhibit immune function. Arry Dieudonne, Atypical Mycobacterium
Infection, Medscape.com (Feb. 7, 2018), https://emedicine.medscape.com/article/972708-overview.
Similar to other infectious diseases found in the Rating Schedule,
VA proposes to assign a 100 percent evaluation during active infection,
after which a mandatory VA evaluation would be conducted to determine
the appropriate evaluation based on residuals, if any. Therefore, VA
proposes a Note 1 to this effect and instructs that any change in
evaluation based upon that or any subsequent examination shall be
subject to the provisions of Sec. 3.105(e). Furthermore, the note
would instruct rating personnel to rate on residuals if there is no
relapse.
Establishing the correct diagnosis is essential in determining if
symptoms are due to NTM or some other disease entity. Diagnostic
testing has become more accurate and readily available over the years.
Therefore, VA proposes a Note 2, requiring diagnostic confirmation for
subsequent relapses.
VA proposes to include Note 3, which would identify common
residuals to assist rating personnel in assigning evaluations following
cessation of the 100 percent evaluation. Residuals of infection
identified in Note 3 would include skin conditions and conditions of
the respiratory, central nervous, musculoskeletal, ocular,
gastrointestinal, and genitourinary systems.
Proposed New Diagnostic Code 6325
VA proposes to add new DC 6325 which applies to hyperinfection
syndrome or disseminated strongyloidiasis. Because strongyloidiasis is
not an acute, self-limited disease, VA would not use the General Rating
Formula. Similar to other severe infectious diseases, VA proposes to
assign a 100 percent evaluation during active disease followed by a
mandatory VA evaluation to determine the appropriate evaluation based
on any residuals. Systemic infection, which is the most severe form of
strongyloidiasis, with a mortality rate approaching 90 percent, is most
often seen in individuals with other underlying conditions, especially
those with compromised immune function. Parasites--Strongyloides,
Resources for Health Professionals, CDC (Jan. 6, 2012), https://www.cdc.gov/parasites/strongyloides/. VA is not proposing to list the
most common residuals because their number is so vast.
Proposed New Diagnostic Code 6326
VA proposes a new diagnostic code for schistosomiasis, the second
most common parasitic disease in the world. Parasites--Schistosomiasis,
CDC (Apr. 30, 2018), https://www.cdc.gov/parasites/schistosomiasis/.
While the parasite is not found in the United States, it is
sufficiently prevalent in tropical regions that VA may presume service
connection if records indicate service in such regions. See 38 CFR
3.309(b). VA is proposing to add a distinct DC for schistosomiasis
because it otherwise lacks a means to accurately track such claims and
can evaluate them only by analogy.
Most people who contract schistosomiasis are asymptomatic and have
subclinical disease during both acute and chronic stages of infection.
Persons with acute infection (also known as Katayama syndrome) may
present with mild symptoms such as rash, fever, headache, myalgia, and
respiratory symptoms that are not disabling.
Chronic disease results from host immune responses to schistosome
eggs: S. mansoni and S. japonicum. These eggs most commonly lodge in
the blood vessels of the liver or intestine with chronic inflammation
leading to bowel wall ulceration, hyperplasia, and polyposis and, with
heavy infections, to liver fibrosis and portal hypertension.
S. haematobium eggs tend to lodge in the urinary tract and the
female genital tract. Female genital schistosomiasis can affect the
cervix, fallopian tubes, and vagina.
Central nervous system lesions, such as in the spinal cord or brain
and inflammatory reactions, may cause the formation of granulomas that
act as space-occupying lesions.
VA proposes to evaluate DC 6326 by assigning a 0 percent evaluation
for acute and asymptomatic chronic infections. Additionally, VA
proposes to note common residuals of infection, such as liver and
genitourinary tract conditions. VA would rate residual disability in
the appropriate system.
Proposed New Diagnostic Code 6329
VA proposes new DC 6329 to encompass hemorrhagic fevers, including
dengue, yellow fever, and others. While these fevers are uncommon in
the United States, they are prevalent in tropical regions and,
therefore, associated with military deployments. David C. Pigott,
CBRNE--Viral Hemorrhagic Fevers, Medscape.com (Mar. 16, 2017), https://emedicine.medscape.com/article/830594-overview. VA may presume service
connection for hemorrhagic fever if records indicate service in certain
regions. See 38 CFR 3.309(b). VA is proposing to add a distinct DC for
hemorrhagic fever because it otherwise lacks a means to accurately
track such claims and can evaluate them only by analogy.
VA proposes to apply the General Rating Formula and assign a 100
percent evaluation for active disease because hemorrhagic fever is
associated with a debilitating, acute, febrile illness that often lasts
for several weeks at most. VA also proposes to include a note listing
common residual disabilities of central
[[Page 1684]]
nervous system, liver, or kidney conditions.
Proposed New Diagnostic Code 6330
VA proposes new DC 6330 for infections caused by Campylobacter
jejuni. In 2010, VA issued a regulation establishing that Campylobacter
jejuni is subject to presumptive service connection for certain
veterans because it is (1) prevalent in Southwest Asia, (2) has been
diagnosed among U.S. troops serving in the Persian Gulf/Southwest Asia
Theater of operations, and (3) is known to cause long-term adverse
health effects. See 75 FR 59968 and 38 CFR 3.317. To monitor claims for
this infection, VA proposes a diagnostic code specifically for
Campylobacter jejuni.
VA proposes to rate Campylobacter jejuni infection under the
General Rating Formula, meaning that it would receive a 100 percent
evaluation during active infection. The symptoms of Campylobacter
jejuni infection consist of diarrhea, cramping, abdominal pain, and
fever within two to five days after exposure to the bacteria. The
diarrhea may be bloody and can be accompanied by nausea and vomiting.
The illness typically lasts about one week. Campylobacter
(Campylobacteriosis), CDC (Aug. 30, 2017), https://www.cdc.gov/campylobacter/.
Thereafter, VA would rate the condition based on residuals listed
in Sec. 3.317(d), ``Long-Term Health Effects Potentially Associated
With Infectious Diseases,'' such as Guillain-Barre syndrome, reactive
arthritis, and uveitis.
Proposed New Diagnostic Code 6331
VA proposes a new diagnostic code to encompass infections caused by
Coxiella burnetii. In 2010, VA issued a regulation establishing that
infection due to Coxiella burnetii (Q fever) is subject to presumptive
service connection for certain veterans because it is (1) prevalent in
Southwest Asia, (2) has been diagnosed among U.S. troops serving in the
Persian Gulf/Southwest Asia theater of operations, and (3) is known to
cause long-term adverse health effects. See 75 FR 59968 and 38 CFR
3.317. To track claims for this infection, VA proposes a diagnostic
code specifically for Coxiella burnetii infection (Q fever).
VA proposes assigning a 100 percent evaluation during active
infection according to the General Rating Formula. Thereafter, VA would
rate the condition based on residuals listed in Sec. 3.317(d), such as
chronic hepatitis, endocarditis, osteomyelitis, post Q-fever chronic
fatigue syndrome, and vascular infections.
Proposed New Diagnostic Code 6333
VA proposes a new diagnostic code to encompass infections caused by
nontyphoidal Salmonella. In 2010, VA issued a regulation establishing
that nontyphoidal salmonellosis is subject to presumptive service
connection for certain veterans. See 75 FR 59968 and 38 CFR 3.317. To
track claims decisions regarding this infection and to more
consistently rate it, VA proposes a diagnostic code specifically for
nontyphoidal salmonellosis.
VA proposes to assign a 100 percent evaluation during active
infection according to the General Rating Formula. Thereafter, VA would
rate the condition based on residuals, including those listed in Sec.
3.317(d), such as reactive arthritis.
Proposed New Diagnostic Code 6334
VA proposes a new diagnostic code to encompass infections caused by
Shigella, which would be rated under the General Rating Formula. In
2010, VA issued a regulation presuming service connection for Shigella
infection in certain veterans. See 75 FR 59968 and 38 CFR 3.317. To
allow for better tracking of decisions on claims for this infection and
to more consistently rate it, VA proposes a diagnostic code
specifically for Shigella infection.
VA would rate the condition based on residuals, including those
listed in Sec. 3.317(d), such as hemolytic-uremic syndrome, and
reactive arthritis.
Proposed New Diagnostic Code 6335
VA proposes a new diagnostic code to encompass infections caused by
West Nile virus. In 2010, VA issued a regulation presuming service
connection for West Nile virus in certain veterans. See 75 FR 59968. To
better track claims decisions regarding this infection, VA proposes a
separate diagnostic code for West Nile virus, which would be rated
under the General Rating Formula.
VA would rate the condition based on residuals, including those
listed in Sec. 3.317(d), such as variable physical, functional, or
cognitive disability.
Executive Orders 12866, 13563, and 13771
Executive Orders 12866 and 13563 direct agencies to assess the
costs and benefits of available regulatory alternatives and, when
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety effects, and other advantages; distributive impacts;
and equity). Executive Order 13563 (Improving Regulation and Regulatory
Review) emphasizes the importance of quantifying both costs and
benefits, reducing costs, harmonizing rules, and promoting flexibility.
Executive Order 12866 (Regulatory Planning and Review) defines a
``significant regulatory action,'' which requires review by the Office
of Management and Budget (OMB), as ``any regulatory action that is
likely to result in a rule that may: (1) Have an annual effect on the
economy of $100 million or more or adversely affect in a material way
the economy, a sector of the economy, productivity, competition, jobs,
the environment, public health or safety, or State, local, or tribal
governments or communities; (2) Create a serious inconsistency or
otherwise interfere with an action taken or planned by another agency;
(3) Materially alter the budgetary impact of entitlements, grants, user
fees, or loan programs or the rights and obligations of recipients
thereof; or (4) Raise novel legal or policy issues arising out of legal
mandates, the President's priorities, or the principles set forth in
this Executive Order.''
The economic, interagency, budgetary, legal, and policy
implications of this regulatory action have been examined, and it has
been determined not to be a significant regulatory action under E.O.
12866. VA's impact analysis can be found as a supporting document at
https://www.regulations.gov, usually within 48 hours after the
rulemaking document is published. Additionally, a copy of this
rulemaking and its impact analysis are available on VA's website at
https://www.va.gov/orpm/, by following the link for ``VA Regulations
Published From FY 2004 Through Fiscal Year to Date.''
This rule is not an E.O. 13771 regulatory action because this rule
is not significant under E.O. 12866.
Regulatory Flexibility Act
The Secretary hereby certifies that this proposed rule would not
have a significant economic impact on a substantial number of small
entities as they are defined in the Regulatory Flexibility Act, 5
U.S.C. 601-612. This proposed rule would not affect any small entities.
Only certain VA beneficiaries could be directly affected. Therefore,
pursuant to 5 U.S.C. 605(b), this rulemaking is exempt from the initial
and final regulatory flexibility analysis requirements of sections 603
and 604.
[[Page 1685]]
Unfunded Mandates
The Unfunded Mandates Reform Act of 1995 requires, at 2 U.S.C.
1532, that agencies prepare an assessment of anticipated costs and
benefits before issuing any rule that may result in the expenditure by
State, local, and tribal governments, in the aggregate, or by the
private sector, of $100 million or more (adjusted annually for
inflation) in any given year. This proposed rule would have no such
effect on State, local, and tribal governments, or on the private
sector.
Paperwork Reduction Act
This final rule contains no provisions constituting a collection of
information under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-
3521).
Catalog of Federal Domestic Assistance Numbers and Titles
The Catalog of Federal Domestic Assistance program numbers and
titles for this rule are 64.102, Compensation for Service-Connected
Deaths for Veterans' Dependents; 64.105, Pension to Veterans, Surviving
Spouses, and Children; 64.109, Veterans Compensation for Service-
Connected Disability; and 64.110, Veterans Dependency and Indemnity
Compensation for Service-Connected Death.
List of Subjects in 38 CFR Part 4
Disability benefits, Pensions, Veterans.
Signing Authority
The Secretary of Veterans Affairs approved this document and
authorized the undersigned to sign and submit the document to the
Office of the Federal Register for publication electronically as an
official document of the Department of Veterans Affairs. Robert L.
Wilkie, Secretary, Department of Veterans Affairs, approved this
document on January 29, 2019, for publication.
Dated: January 29, 2019.
Jeffrey M. Martin,
Assistant Director, Office of Regulation Policy & Management, Office of
the Secretary, Department of Veterans Affairs.
For the reasons stated in the preamble, the Department of Veterans
Affairs proposes to amend 38 CFR part 4 as set forth below:
PART 4--SCHEDULE FOR RATING DISABILITIES
Subpart B--Disability Ratings
0
1. The authority citation for part 4 continues to read as follows:
Authority: 38 U.S.C. 1155, unless otherwise noted.
0
2. Revise Sec. 4.88a to read as follows:
Sec. 4.88a Systemic exertion intolerance disease/chronic fatigue
syndrome (CFS).
(a) For VA purposes, the diagnosis of Systemic Exertion Intolerance
Disease/Chronic Fatigue Syndrome (CFS) must meet the following
conditions:
(1) A severe chronic fatigue that significantly interferes with
daily activities and work.
(2) The individual concerned concurrently has four or more of the
following eight symptoms:
(i) Post-exertion malaise lasting more than 24 hours
(ii) Unrefreshing sleep
(iii) Significant impairment of short-term memory or concentration
(iv) Muscle pain
(v) Pain in the joints without swelling or redness
(vi) Headaches of a new type, pattern, or severity
(vii) Tender lymph nodes in the neck or armpit
(viii) Sore throat that is frequent or recurring
(3) These symptoms:
(i) Cannot have first appeared before the fatigue
(ii) Have persisted or recurred during six or more consecutive
months of illness, and
(iii) Are not due to ongoing exertion or other medical conditions
associated with fatigue, as ruled out by a physician who administered
relevant diagnostic tests.
(b) Several past or current medical conditions exclude the
diagnosis of systemic exertion intolerance disease/CFS to include:
(1) Any active condition that may explain the presence of chronic
fatigue, such as untreated hypothyroidism, sleep apnea, narcolepsy, and
iatrogenic conditions such as side effects of medication.
(2) Some illnesses, including some types of cancers and chronic
cases of hepatitis B or C virus infection, which could explain the
presence of chronic fatigue, and which have not clearly and completely
resolved.
(3) Any past or current diagnosis of: major depressive disorder
with psychotic or melancholic features, bipolar affective disorders,
anorexia nervosa, bulimia nervosa, or any subtype of schizophrenia,
delusional disorders, or dementias.
(4) Alcohol or other substance abuse, occurring within two years of
the onset of chronic fatigue and any time afterwards.
(5) Severe obesity, defined as having a body mass index equal to or
greater than 45. [Body mass index = weight in kilograms / (height in
meters)\2\].
(6) Examination or testing detects any abnormality that strongly
suggests an exclusionary condition that needs to be treated or resolved
before attempting further diagnosis. Once fully treated, diagnose
accordingly if the individual still meets criteria for Systemic
Exertion Intolerance Disease (SEID)/Chronic Fatigue Syndrome (CFS).
0
3. Amend Sec. 4.88b by:
0
a. Revising the entries for diagnostic codes 6300 through 6302 and 6304
through 6311;
0
b. Adding in numerical order an entry for diagnostic code 6312;
0
c. Revising the entries for diagnostic codes 6316 through 6320;
0
d. Adding in numerical order entires for diagnostic codes 6325, 6326,
6329 through 6331, and 6333 through 6335; and
0
e. Revising the entries for diagnostic codes 6351 and 6354.
The revisions and additions read as follows:
Sec. 4.88b Schedule of ratings-infectious diseases, immune
disorders, and nutritional deficiencies.
------------------------------------------------------------------------
Rating
------------------------------------------------------------------------
General Rating Formula for Infectious Diseases:
For active disease..................................... 100
After active disease has resolved, rate at 0 percent
for infection. Rate any residual disability of
infection within the appropriate body system.
6300 Vibriosis (Cholera, Non-cholera):
Evaluate under the General Rating Formula.
Note: Rate residuals of cholera and non-cholera Vibrio
infections, such as renal failure, skin, and
musculoskeletal conditions, within the appropriate
body system.
[[Page 1686]]
6301 Visceral leishmaniasis:
As active disease...................................... 100
Note 1: Continue a 100 percent evaluation beyond the
cessation of treatment for active disease. Six months
after discontinuance of such treatment, determine the
appropriate disability rating by mandatory VA
examination. Any change in evaluation based upon that
or any subsequent examination shall be subject to the
provisions of Sec. 3.105(e) of this chapter.
Thereafter, rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, liver damage, bone marrow disease,
and those residuals listed in Sec. 3.317(d) of this
chapter.
Note 2: Confirm the recurrence of active infection by
culture, histopathology, or other diagnostic
laboratory testing.
6302 Leprosy (Hansen's disease):
As active disease...................................... 100
Note: Continue a 100 percent evaluation beyond the
cessation of treatment for active disease. Six months
after discontinuance of such treatment, determine the
appropriate disability rating by mandatory VA
examination. Any change in evaluation based upon that
or any subsequent examination shall be subject to the
provisions of Sec. 3.105(e) of this chapter.
Thereafter, rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, skin lesions, peripheral
neuropathy, or amputations.
6304 Malaria:
Evaluate under the General Rating Formula.
Note 1: The diagnosis of malaria, both initially and
during relapse, depends on the identification of the
malarial parasites in blood smears or other specific
diagnostic laboratory tests such as antigen detection,
immunologic (immunochromatographic) tests, and
molecular testing such as polymerase chain reaction
tests.
Note 2: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, liver or splenic damage, central
nervous system conditions, and those residuals listed
in Sec. 3.317(d) of this chapter.
6305 Lymphatic filariasis, to include elephantiasis:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, epididymitis, lymphangitis,
lymphatic obstruction, or lymphedema affecting
extremities, genitals, and/or breasts.
6306 Bartonellosis:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, endocarditis or skin lesions.
6307 Plague:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection.
6308 Relapsing Fever:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, liver or spleen damage, iritis,
uveitis, or central nervous system involvement.
6309 Rheumatic fever:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, heart damage.
6310 Syphilis, and other treponemal infections:
Note : Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, diseases of the nervous system,
vascular system, eyes, or ears (see DC 7004, DC 8013,
DC 8014, DC 8015, and DC 9301).
6311 Tuberculosis, miliary:
As active disease...................................... 100
Inactive disease: See Sec. Sec. 4.88c and 4.89.
Note 1: Confirm the recurrence of active infection by
culture, histopathology, or other diagnostic
laboratory testing.
Note 2: Rate under the appropriate body system any
residual disability of infection which includes, but
is not limited to, skin conditions and conditions of
the respiratory, central nervous, musculoskeletal,
ocular, gastrointestinal, and genitourinary systems
and those residuals listed in Sec. 4.88c of this
chapter.
6312 Nontuberculosis mycobacterial infection:
As active disease...................................... 100
Note 1: Continue the rating of 100 percent for the
duration of treatment for active disease followed by a
mandatory VA exam. If there is no relapse, rate on
residuals. Any change in evaluation based upon that or
any subsequent examination shall be subject to the
provisions of Sec. 3.105(e) of this chapter.
Note 2: Confirm the recurrence of active infection by
culture, histopathology, or other diagnostic
laboratory testing.
Note 3: Rate under the appropriate body system any
residual disability of infection which includes, but
is not limited to, skin conditions and conditions of
the respiratory, central nervous, musculoskeletal,
ocular, gastrointestinal, and genitourinary systems
and those residuals listed in Sec. 4.88c of this
chapter.
* * * * * * *
6316 Brucellosis:
Evaluate under the General Rating Formula.
Note 1: Culture, serologic testing, or both must
confirm the initial diagnosis and recurrence of active
infection.
Note 2: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, meningitis, liver, spleen and
musculoskeletal conditions, and those residuals listed
in Sec. 3.317(d) of this chapter.
6317 Rickettsial, erlichial, and Anaplasma infections:
Evaluate under the General Rating Formula.
Note 1: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, bone marrow, spleen, central
nervous system, and skin conditions.
Note 2: This diagnostic code includes, but is not
limited to, scrub typhus, Rickettsial pox, African
tick-borne fever, Rocky Mountain spotted fever,
ehrlichiosis, or anaplasmosis.
6318 Melioidosis:
[[Page 1687]]
Evaluate under the General Rating Formula.
Note 1: Confirm by culture or other specific diagnostic
laboratory tests the initial diagnosis and any relapse
or chronic activity of infection.
Note 2: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, arthritis, lung lesions, or
meningitis.
6319 Lyme disease:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, arthritis, Bell's palsy,
radiculopathy, ocular, or cognitive dysfunction.
6320 Parasitic diseases otherwise not specified:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection.
* * * * * * *
6325 Hyperinfection syndrome or disseminated
strongyloidiasis:
As active disease...................................... 100
Note: Continue the rating of 100 percent through active
disease followed by a mandatory VA exam. If there is
no relapse, rate on residual disability. Any change in
evaluation based upon that or any subsequent
examination shall be subject to the provisions of Sec.
3.105(e) of this chapter.
6326 Schistosomiasis:
As acute or asymptomatic chronic disease............... 0
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, conditions of the liver, intestinal
system, female genital tract, genitourinary tract, or
central nervous system.
6329 Hemorrhagic fevers, including dengue, yellow fever,
and others:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, conditions of the central nervous
system, liver, or kidney.
6330 Campylobacter jejuni infection:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, Guillain-Barre syndrome, reactive
arthritis, or uveitis as specified in Sec. 3.317(d)
of this chapter.
6331 Coxiella burnetii infection (Q fever):
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, chronic hepatitis, endocarditis,
osteomyelitis, post Q-fever chronic fatigue syndrome,
or vascular infections as specified in Sec. 3.317(d)
of this chapter.
6333 Nontyphoid Salmonella infections:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, reactive arthritis as specified in
Sec. 3.317(d) of this chapter.
6334 Shigella infections:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, hemolytic-uremic syndrome or
reactive arthritis as specified in Sec. 3.317(d) of
this chapter.
6335 West Nile virus infection:
Evaluate under the General Rating Formula.
Note: Rate under the appropriate body system any
residual disability of infection, which includes, but
is not limited to, variable physical, functional, or
cognitive disabilities as specified in Sec. 3.317(d)
of this chapter.
* * * * * * *
6351 HIV-related illness:
AIDS with recurrent opportunistic infections (see Note 100
3) or with secondary diseases afflicting multiple body
systems; HIV-related illness with debility and
progressive weight loss...............................
Refractory constitutional symptoms, diarrhea, and 60
pathological weight loss; or minimum rating following
development of AIDS-related opportunistic infection or
neoplasm..............................................
Recurrent constitutional symptoms, intermittent 30
diarrhea, and use of approved medication(s); or
minimum rating with T4 cell count less than 200.......
Following development of HIV-related constitutional 10
symptoms; T4 cell count between 200 and 500, and use
of approved medication(s); or with evidence of
depression or memory loss with employment limitations.
Asymptomatic, following initial diagnosis of HIV 0
infection, with or without lymphadenopathy or
decreased T4 cell count...............................
Note 1: In addition to standard therapies and regimens,
the term ``approved medication(s)'' includes treatment
regimens and medications prescribed as part of a
research protocol at an accredited medical
institution.
Note 2: Diagnosed psychiatric illness, central nervous
system manifestations, opportunistic infections, and
neoplasms may be rated separately under the
appropriate diagnostic codes if a higher overall
evaluation results, provided the disability symptoms
do not overlap with evaluations otherwise assignable
above.
Note 3: The following list of opportunistic infections
are considered AIDS-defining conditions, that is, a
diagnosis of AIDS follows if a person has HIV and one
more of these infections, regardless of the CD4 count--
candidiasis of the bronchi, trachea, esophagus, or
lungs; invasive cervical cancer; coccidioidomycosis;
cryptococcosis; cryptosporidiosis; cytomegalovirus
(particularly CMV retinitis); HIV-related
encephalopathy; herpes simplex-chronic ulcers for
greater than one month, or bronchitis, pneumonia, or
esophagitis; histoplasmosis; isosporiasis (chronic
intestinal); Kaposi's sarcoma; lymphoma; Mycobacterium
avium complex; tuberculosis; Pneumocystis jirovecii
(carinii) pneumonia; pneumonia, recurrent; progressive
multifocal leukoencephalopathy; Salmonella septicemia,
recurrent; toxoplasmosis of the brain; and wasting
syndrome due to HIV.
6354 Systemic exertional intolerance disease/chronic
fatigue syndrome (CFS):
[[Page 1688]]
Debilitating fatigue, cognitive impairments (such as
inability to concentrate, forgetfulness, or
confusion), or a combination of other signs and
symptoms:
Which are nearly constant and so severe as to 100
restrict routine daily activities almost
completely and which may occasionally preclude
self-care.........................................
Which are nearly constant and restrict routine 60
daily activities to less than 50 percent of the
pre-illness level; or which wax and wane,
resulting in periods of incapacitation totaling at
least six weeks per year..........................
Which are nearly constant and restrict routine 40
daily activities from 50 to 75 percent of the pre-
illness level; or which wax and wane, resulting in
periods of incapacitation totaling at least four
but less than six weeks per year..................
Which are nearly constant and restrict routine 20
daily activities by less than 25 percent of the
pre-illness level; or which wax and wane,
resulting in periods of incapacitation totaling at
least two but less than four weeks per year.......
Which wax and wane but result in periods of 10
incapacitation totaling at least one but less than
two weeks per year; or symptoms controlled by
continuous medication.............................
Note: For the purpose of evaluating this
disability, incapacitation exists only when a
licensed physician prescribes bed rest and
treatment.
------------------------------------------------------------------------
0
4. In appendix A to part 4 by:
0
a. Revising the entries for diagnostic codes 6300-6302, 6304-6311;
0
b. Adding in numerical order an entry for diagnostic code 6312;
0
c. Revising the entries for diagnostic codes 6316-6320;
0
d. Adding in numerical order entries for diagnostic codes 6325, 6326,
6329 through 6331, and 6333 through 6335; and
0
e. Revising the entries for diagnostic codes 6351 and 6354.
The revisions and additions read as follows:
Appendix A to Part 4--Table of Amendments and Effective Dates Since 1946
------------------------------------------------------------------------
Diagnostic
Sec. code No.
------------------------------------------------------------------------
* * * * * * *
4.88a..................... .............. March 11, 1969; re-
designated Sec. 4.88b
November 29, 1994; Sec.
4.88a added to read
``Chronic fatigue
syndrome''; criterion
November 29, 1994; title,
criterion [insert effective
date of final rule].
4.88b..................... .............. Added March 11, 1969; re-
designated Sec. 4.88c
November 29, 1994; Sec.
4.88a re-designated to Sec.
4.88b November 29, 1994;
General Rating Formula for
Infectious Diseases added
[insert effective date of
final rule].
6300 Criterion August 30, 1996;
title, criterion, and note
[insert effective date of
final rule].
6301 Criterion, note [insert
effective date of final
rule].
6302 Criterion September 22,
1978; criterion August 30,
1996; criterion, note
[insert effective date of
final rule].
6304 Evaluation August 30, 1996;
criterion, note [insert
effective date of final
rule].
6305 Criterion March 1, 1989;
evaluation August 30, 1996;
title, criterion, note
[insert effective date of
final rule].
6306 Evaluation August 30, 1996;
criterion, note [insert
effective date of final
rule].
6307 Criterion May 13, 2018;
criterion, note [insert
effective date of final
rule].
6308 Criterion August 30, 1996;
criterion, note [insert
effective date of final
rule].
6309 Added March 1, 1963;
criterion March 1, 1989;
criterion August 30, 1996;
criterion, note [insert
effective date of final
rule].
6310 Criterion, note [insert
effective date of final
rule].
6311 Criterion, note [insert
effective date of final
rule].
6312 Added [insert effective date
of final rule].
* * * * * * *
6316 Evaluation March 1, 1989;
evaluation August 30, 1996;
criterion, note [insert
effective date of final
rule].
6317 Criterion August 30, 1996;
title, criterion, note
[insert effective date of
final rule].
6318 Added March 1, 1989;
criterion August 30, 1996;
criterion, note [insert
effective date of final
rule].
6319 Added August 30, 1996;
criterion, note [insert
effective date of final
rule].
6320 Added August 30, 1996;
criterion, note [insert
effective date of final
rule].
6325 Added [insert effective date
of final rule].
6326 Added [insert effective date
of final rule].
6329 Added [insert effective date
of final rule].
6330 Added [insert effective date
of final rule].
6331 Added [insert effective date
of final rule].
6333 Added [insert effective date
of final rule].
6334 Added [insert effective date
of final rule].
6335 Added [insert effective date
of final rule].
* * * * * * *
6351 Added March 1, 1989;
evaluation March 24, 1992;
criterion August 30, 1996;
criterion, note [insert
effective date of final
rule].
6354 Added November 29, 1994;
criterion August 30, 1996;
title, criterion, note
[insert effective date of
final rule].
* * * * * * *
------------------------------------------------------------------------
[[Page 1689]]
0
5. Amend appendix B to part 4 by:
0
a. Revising the entries for diagnostic codes 6300 and 6305;
0
b. Adding in numerical order an entry for diagnostic code 6312;
0
c. Revising the entry for diagnostic code 6317; and,
0
d. Adding in numerical order entries for diagnostic codes 6325, 6326,
6329 through 6331, and 6333 through 6335.
The revisions and additions read as follows:
Appendix B to Part 4--Numerical Index of Disabilities
------------------------------------------------------------------------
Diagnostic code No.
------------------------------------------------------------------------
* * * * * * *
------------------------------------------------------------------------
INFECTIOUS DISEASES, IMMUNE DISORDERS AND NUTRITIONAL DEFICIENCIES
------------------------------------------------------------------------
* * * * * * *
6300.......................... Vibriosis (Cholera, Non-cholera).
* * * * * * *
6305.......................... Lymphatic filariasis, to include
elephantiasis.
* * * * * * *
6312.......................... Nontuberculosis mycobacterial infection.
* * * * * * *
6317.......................... Rickettsial, erlichial, and Anaplasma
infections.
* * * * * * *
6325.......................... Hyperinfection syndrome or disseminated
strongyloidiasis.
6326.......................... Schistosomiasis.
6329.......................... Hemorrhagic fevers, including dengue,
yellow fever, and others.
6330.......................... Campylobacter jejuni infection.
6331.......................... Coxiella burnetii infection (Q Fever).
6333.......................... Nontyphoid salmonella infections.
6334.......................... Shigella infections.
6335.......................... West Nile virus infection.
* * * * * * *
6351.......................... HIV-related infection.
6356.......................... Systemic exertional intolerance disease/
chronic fatigue syndrome (CFS).
------------------------------------------------------------------------
0
6. Amend appendix C to part 4 by:
0
a. Adding in alphabetical order an entry for ``Campylobacter jejuni
infection'';
0
b. Removing the entry for ``Cholera, Asiatic'';
0
c. Adding in alphabetical order entries for ``Coxiella burnetii
infection (Q Fever)'', ``Hemorrhagic fevers, including dengue, yellow
fever, and others'', and ``Hyperinfection syndrome or disseminated
strongyloidiasis'';
0
d. Revise the entry for ``Lymphatic filariasis'';
0
e. Adding in alphabetical order entries for ``Nontuberculosis
mycobacterial infection'', ``Nontyphoid salmonella infection'',
``Rickettsial, erlichial, and Anaplasma infections'', Shigella
infections, and ``Schistosomiasis'';
0
f. Removing the entry for ``Typhus, scrub''; and
0
g. Adding in alphabetical order entries for ``Vibriosis (Cholera, Non-
cholera)'' and ``West Nile virus infection''
The additions and revisions read as follows:
Appendix C to Part 4--Alphabetical Index of Disabilities
------------------------------------------------------------------------
Diagnostic
code No.
------------------------------------------------------------------------
* * * * * * *
Campylobacter jejuni infection.......................... 6330
* * * * * * *
Coxiella burnetii infection (Q Fever)................... 6331
* * * * * * *
Hemorrhagic fevers, including dengue, yellow fever, and 6329
others)................................................
* * * * * * *
Hyperinfection syndrome or disseminated strongyloidiasis 6325
* * * * * * *
Lymphatic filariasis, to include elephantiasis.......... 6305
[[Page 1690]]
* * * * * * *
Nontyphoid salmonella infection......................... 6333
* * * * * * *
Nontuberculosis mycobacterial infection................. 6312
* * * * * * *
Rickettsial, erlichial, and Anaplasma Infections........ 6317
* * * * * * *
Schistosomiasis......................................... 6326
* * * * * * *
Shigella infections..................................... 6334
* * * * * * *
Vibriosis (Cholera, Non-cholera)........................ 6300
* * * * * * *
West Nile virus infection............................... 6335
* * * * * * *
------------------------------------------------------------------------
[FR Doc. 2019-00636 Filed 2-4-19; 8:45 am]
BILLING CODE 8320-01-P