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Thromboprophylaxis patterns and determinants in critically ill patients: a multicenter audit.
[heparin-induced thrombocytopenia]
Heparin
is
safe
and
prevents
venous
thromboembolism
in
critical
illness
.
We
aimed
to
determine
the
guideline
concordance
for
thromboprophylaxis
in
critically
ill
patients
and
its
predictors
,
and
to
analyze
factors
associated
with
the
use
of
low
molecular
weight
heparin
(
LMWH
)
,
as
it
may
be
associated
with
a
lower
risk
of
pulmonary
embolism
and
heparin-induced
thrombocytopenia
without
increasing
the
bleeding
risk
.
We
performed
a
retrospective
audit
in
28
North
American
intensive
care
units
(
ICUs
)
,
including
all
consecutive
medical-surgical
patients
admitted
in
November
2011
.
We
documented
ICU
thromboprophylaxis
and
reasons
for
omission
.
Guideline
concordance
was
determined
by
adding
days
in
which
patients
without
contraindications
received
thromboprophylaxis
to
days
in
which
patients
with
contraindications
did
not
receive
it
,
divided
by
the
total
number
of
patient-
days
.
We
used
multilevel
logistic
regression
including
time-varying
,
center
and
patient-level
covariates
to
determine
the
predictors
of
guideline
concordance
and
use
of
LMWH
.
We
enrolled
1
,
935
patients
(
62
.
3
 
±
 
16
.
7
years
,
Acute
Physiology
and
Chronic
Health
Evaluation
[
APACHE
]
II
score
19
.
1
 
±
 
8
.
3
)
.
Patients
received
thromboprophylaxis
with
unfractionated
heparin
(
UFH
)
(
54
.
0
%
)
or
LMWH
(
27
.
6
%
)
.
Guideline
concordance
occurred
for
95
.
5
%
patient-
days
and
was
more
likely
in
patients
who
were
sicker
(
odds
ratio
(
OR
)
1
.
49
,
95
%
confidence
interval
(
CI
)
1
.
17
,
1
.
75
per
10
-
point
increase
in
APACHE
II
)
,
heavier
(
OR
1
.
32
,
95
%
CI
1
.
05
,
1
.
65
per
10
-
m
/
kg
2
increase
in
body
mass
index
)
,
had
cancer
(
OR
3
.
22
,
95
%
CI
1
.
81
,
5
.
72
)
,
previous
venous
thromboembolism
(
OR
3
.
94
,
95
%
CI
1
.
46
,
10
.
66
)
,
and
received
mechanical
ventilation
(
OR
1
.
83
,
95
%
CI
1
.
32
,
2
.
52
)
.
Reasons
for
not
receiving
thromboprophylaxis
were
high
risk
of
bleeding
(
44
.
5
%
)
,
current
bleeding
(
16
.
3
%
)
,
no
reason
(
12
.
9
%
)
,
recent
or
upcoming
invasive
procedure
(
10
.
2
%
)
,
nighttime
admission
or
discharge
(
9
.
7
%
)
,
and
life-support
limitation
(
6
.
9
%
)
.
LMWH
was
less
often
administered
to
sicker
patients
(
OR
0
.
65
,
95
%
CI
0
.
48
,
0
.
89
per
10
-
point
increase
in
APACHE
II
)
,
surgical
patients
(
OR
0
.
41
,
95
%
CI
0
.
24
,
0
.
72
)
,
those
receiving
vasoactive
drugs
(
OR
0
.
47
,
95
%
CI
0
.
35
,
0
.
64
)
or
renal
replacement
therapy
(
OR
0
.
10
,
95
%
CI
0
.
05
,
0
.
23
)
.
Guideline
concordance
for
thromboprophylaxis
was
high
,
but
LMWH
was
less
commonly
used
,
especially
in
patients
who
were
sicker
,
had
surgery
,
or
received
vasopressors
or
renal
replacement
therapy
,
representing
a
potential
quality
improvement
target
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated