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Latent rheumatic heart disease: outcomes 2 years after echocardiographic detection.
[acute rheumatic fever]
Screening
with
portable
echocardiography
has
uncovered
a
large
burden
of
latent
rheumatic
heart
disease
(
RHD
)
among
asymptomatic
children
in
endemic
regions
,
the
significance
of
which
remains
unclear
.
This
study
aimed
to
determine
the
2
-
year
outcomes
for
children
with
latent
RHD
diagnosed
by
echocardiographic
screening
.
Children
identified
with
latent
RHD
enrolled
in
a
biannual
follow-up
program
.
Risk
factors
for
disease
persistence
and
progression
were
examined
.
Of
62
children
,
51
(
82
%
)
with
latent
RHD
had
a
median
follow-up
period
of
25
months
.
Of
these
51
children
,
17
(
33
.
3
%
)
reported
an
interval
sore
throat
or
symptoms
consistent
with
acute
rheumatic
fever
(
ARF
)
.
Of
43
children
initially
classified
as
having
borderline
RHD
,
21
(
49
%
)
remained
stable
,
18
(
42
%
)
improved
(
to
no
RHD
)
and
4
(
10
%
)
worsened
to
definite
RHD
.
Of
the
8
children
initially
classified
as
having
definite
RHD
,
6
(
75
%
)
remained
stable
,
and
2
(
25
%
)
improved
to
borderline
RHD
.
Two
children
had
confirmed
episodes
of
recurrent
ARF
,
one
of
which
represented
the
sole
case
of
clinical
worsening
.
The
risk
factors
for
disease
persistence
or
progression
included
younger
age
(
p
=
0
.
05
)
,
higher
antistreptolysin
O
titers
at
diagnosis
(
p
=
0
.
05
)
,
and
more
morphologic
valve
abnormalities
(
p
=
0
.
01
)
.
After
2
years
,
most
of
the
children
had
a
benign
course
,
with
91
%
remaining
stable
or
showing
improvement
.
Education
may
improve
recognition
of
streptococcal
sore
throat
.
Longer-term
follow-up
evaluation
,
however
,
is
warranted
to
confirm
disease
progression
and
risk
factor
profile
.
This
could
help
tailor
screening
protocols
for
those
at
highest
risk
.
Diseases
Validation
Diseases presenting
"fever"
symptom
22q11.2 deletion syndrome
acute rheumatic fever
alexander disease
allergic bronchopulmonary aspergillosis
canavan disease
carcinoma of the gallbladder
child syndrome
congenital toxoplasmosis
cushing syndrome
cystinuria
dracunculiasis
erdheim-chester disease
esophageal adenocarcinoma
esophageal carcinoma
familial mediterranean fever
focal myositis
hodgkin lymphoma, classical
lamellar ichthyosis
legionellosis
locked-in syndrome
malignant atrophic papulosis
neonatal adrenoleukodystrophy
neuralgic amyotrophy
oculocutaneous albinism
papillon-lefèvre syndrome
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
typhoid
waldenström macroglobulinemia
wolf-hirschhorn syndrome
This symptom has already been validated