Rare Diseases Symptoms Automatic Extraction
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Clinical characteristics of acute kidney injury in patients with scrub typhus--RIFLE criteria validation.
[scrub typhus]
There
are
limited
data
available
on
the
validity
of
the
RIFLE
classification
for
AKI
in
patients
with
scrub
typhus
.
We
investigated
the
incidence
and
clinical
characteristics
of
scrub
typhus
associated
AKI
using
the
RIFLE
criteria
.
From
2010
to
2012
,
238
patients
were
diagnosed
with
scrub
typhus
.
Of
these
,
we
included
223
patients
who
were
followed
up
until
renal
recovery
or
for
at
least
three
months
.
We
evaluated
the
incidence
,
clinical
characteristics
,
and
severity
of
AKI
based
on
the
RIFLE
classification
.
Of
the
223
patients
,
47
(
21
%
)
had
scrub
typhus
-associated
AKI
.
The
incidence
of
AKI
was
21
.
1
%
;
of
which
,
10
.
7
%
,
9
.
4
%
and
1
%
were
classified
as
Risk
,
Injury
and
Failure
,
respectively
.
In
comparison
with
patients
in
the
non-
AKI
group
,
the
patients
in
the
AKI
group
were
older
(
70
Â
±
Â
9
vs
61
Â
±
Â
14
year
,
P
Â
=
Â
0
.
01
)
and
had
one
or
more
comorbidities
such
as
hypertension
,
diabetes
,
and
chronic
kidney
disease
(
77
%
vs
22
%
,
p
Â
=
Â
0
.
01
)
.
In
the
AKI
group
,
forty-
four
patients
had
AKI
prior
to
admission
,
and
three
patients
experienced
AKI
during
their
hospitalization
.
By
multivariate
logistic
regression
analysis
,
age
and
comorbidity
were
significant
predictors
of
AKI
.
All
patients
recovered
baseline
renal
function
without
renal
replacement
therapy
following
antibiotics
therapy
and
supportive
care
.
The
incidence
of
AKI
in
patient
with
scrub
typhus
is
21
%
.
Age
and
co
-morbidity
are
significant
predictors
of
AKI
in
scrub
typhus
.
In
cases
of
scrub
typhus
-associated
AKI
,
anti-rickettsia
agent
and
supportive
care
are
very
important
.
Diseases
Validation
Diseases presenting
"hypertension"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
aniridia
aromatase deficiency
cadasil
child syndrome
cohen syndrome
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cushing syndrome
cystinuria
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
fabry disease
familial hypocalciuric hypercalcemia
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
holt-oram syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
kallmann syndrome
kindler syndrome
lamellar ichthyosis
lymphangioleiomyomatosis
pendred syndrome
primary effusion lymphoma
scrub typhus
severe combined immunodeficiency
sneddon syndrome
typhoid
von hippel-lindau disease
well-differentiated liposarcoma
werner syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
This symptom has already been validated