Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Clinical complications in pregnant women with sickle cell disease: prospective study of factors predicting maternal death or near miss.
[alpha-thalassemia]
To
evaluate
complications
in
pregnant
women
with
sickle
cell
disease
,
especially
those
leading
to
maternal
death
or
near
miss
(
severe
obstetric
complications
)
.
A
prospective
cohort
of
104
pregnant
women
registered
in
the
Blood
Center
of
Belo
Horizonte
(
Hemominas
Foundation
)
was
followed
up
at
high
-risk
prenatal
units
.
They
belonged
to
Group
I
(
51
hemoglobin
SS
and
three
hemoglobin
S
/
β
(
0
)
-
thalassemia
)
or
Group
II
(
49
hemoglobin
SC
and
one
hemoglobin
S
/
β
(
+
)
-
thalassemia
)
.
Both
groups
had
similar
median
ages
.
Predictive
factors
for
'
near
miss
'
or
maternal
death
with
p
-value
≤
0
.
25
in
the
univariate
analysis
were
included
in
a
multivariate
logistic
model
(
significance
set
for
p
-value
≤
0
.
05
)
.
Group
I
had
more
frequent
episodes
of
vaso-occlusive
crises
,
more
transfusions
in
the
antepartum
and
postpartum
,
and
higher
percentage
of
preterm
deliveries
than
Group
II
.
Infections
and
painful
crises
during
the
postpartum
period
were
similar
in
both
the
groups
.
The
mortality
rate
was
4
.
8
%
:
three
deaths
in
Group
I
and
two
in
Group
II
.
One
-
third
of
the
women
in
both
the
groups
experienced
near
miss
.
The
most
frequent
event
was
pneumonia
/
acute
chest
syndrome
.
Alpha-thalassemia
co
-inheritance
and
β-
gene
haplotypes
were
not
associated
with
near
miss
or
maternal
death
.
In
multivariate
analysis
predictors
of
near
miss
or
death
were
parity
above
one
and
baseline
red
blood
cell
macrocytosis
.
In
Group
I
,
baseline
hypoxemia
(
saturation
<
94
%
)
was
also
predictive
of
near
miss
or
death
.
One
-
third
of
pregnant
women
had
near
miss
and
4
.
8
%
died
.
Both
hemoglobin
SS
and
SC
pregnant
women
shared
the
same
risk
of
death
or
of
severe
complications
,
especially
pulmonary
events
.
Diseases
Validation
Diseases presenting
"pneumonia"
symptom
22q11.2 deletion syndrome
acute rheumatic fever
allergic bronchopulmonary aspergillosis
alpha-thalassemia
classical phenylketonuria
cohen syndrome
congenital diaphragmatic hernia
heparin-induced thrombocytopenia
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
lamellar ichthyosis
legionellosis
liposarcoma
lymphangioleiomyomatosis
monosomy 21
oculocutaneous albinism
omenn syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
scrub typhus
severe combined immunodeficiency
triple a syndrome
waldenström macroglobulinemia
wiskott-aldrich syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
This symptom has already been validated