Advances in Clinical and Experimental Medicine,
Год журнала:
2024,
Номер
34(11), С. 0 - 0
Опубликована: Ноя. 18, 2024
Acute-on-chronic
liver
failure
(ACLF)
is
characterized
by
rapid
onset,
development
and
a
high
short-term
mortality
rate.
Systemic
inflammation
exerts
an
effect
on
the
disease
progression
of
ACLF.
United European Gastroenterology Journal,
Год журнала:
2024,
Номер
12(2), С. 194 - 202
Опубликована: Фев. 20, 2024
Abstract
It
is
essential
to
identify
the
subgroup
of
patients
who
experience
poorer
outcomes
in
order
adapt
clinical
management
effectively.
In
context
liver
disease,
earlier
identification
occurs,
greater
range
therapeutic
options
that
can
be
offered
patients.
past,
with
acute
decompensation
(AD)
chronic
disease
were
treated
as
a
homogeneous
group,
emphasis
on
identifying
those
at
highest
risk
death.
last
15
years,
differentiation
has
emerged
between
acute‐on‐chronic
failure
syndrome
(ACLF)
and
AD,
primarily
due
indications
latter
linked
less
favorable
short‐term
prognosis.
Nevertheless,
definition
ACLF
varies
among
different
knowledge
societies,
making
it
challenging
assess
its
true
impact
compared
AD.
Therefore,
purpose
this
review
provide
detailed
analysis
emphasizing
critical
importance
field
advanced
disease.
We
will
discuss
differences
Eastern
Western
approaches,
particularly
relation
occurrence
onset.
Common
characteristics,
such
dynamic
nature
course,
highlighted.
Finally,
we
focus
two
key
implications
arising
from
these
considerations:
prevention
before
onset
strategies
once
develops,
including
transplantation
withdrawal
care.
Frontiers in Medicine,
Год журнала:
2025,
Номер
11
Опубликована: Янв. 6, 2025
To
develop
a
nomogram
model
based
on
the
albumin-bilirubin
(ALBI)
score
for
predicting
90-day
prognosis
of
patients
with
acute-on-chronic
liver
failure
(ACLF)
and
to
evaluate
its
predictive
efficacy.
Clinical
data
290
ACLF
at
Third
People's
Hospital
Nantong
City,
collected
from
December
2020
2023,
were
analyzed.
The
divided
into
training
set
(n
=
200)
validation
90),
August
2022
as
cut-off
date.
Patients
in
categorized
an
improvement
group
133)
mortality
67)
their
outcomes.
power
baseline
parameters
was
assessed
using
univariate
multivariate
logistic
regression
construct
model.
Model
performance
receiver
operating
characteristic
(ROC)
curves,
calibration
decision
curve
analysis
(DCA)
Hosmer-Lemeshow
test.
Creatinine
(CR)
[odds
ratio
(OR)
1.013,
95%
confidence
interval
(CI):
1.004-1.022],
ALBI
(OR
10.831,
CI:
4.009-33.247),
Gender
1.931,
0.973-3.870)
ascites
3.032,
1.249-8.178)
identified
independent
prognostic
factors.
formula
derived
index
(PI)
-0.591
+
0.658
×
1.109
0.012
CR
2.382
ALBI.
area
under
(AUC)
0.804
(95%
0.741-0.866),
specificity
85.0%
sensitivity
65.7%
0.425.
AUC
0.811
0.697-0.926).
test
indicated
good
fit
p-value
0.287
0.423
set.
Calibration
curves
demonstrated
accuracy
model,
DCA
results
suggested
that
clinically
useful
when
threshold
below
0.6.
incorporating
CR,
can
predict
patients,
potentially
helping
optimize
treatment
strategies
improve
patient
Liver International,
Год журнала:
2025,
Номер
45(2)
Опубликована: Янв. 28, 2025
Acute
liver
failure
(ALF)
and
acute-on-chronic
(ACLF)
represent
critical
junctures
in
the
spectrum
of
diseases,
characterized
by
rapid
deterioration
function
often
multi-organ
dysfunction.
Despite
advances
medical
care,
they
remain
significant
challenges
clinical
practice,
necessitating
a
deeper
understanding
their
pathophysiology
development
effective
therapeutic
strategies.
This
special
issue
intents
to
address
these
topics
15
selected
reviews.
The
first
two
reviews
are
ALF
pathogenesis
therapy
focus.1,
2
is
rare
but
life-threatening
condition
sudden
loss
individuals
with
no
pre-existing
disease.
It
associated
high
mortality
rate,
typically
ranging
from
50%
80%.
aetiology
can
be
diverse,
including
viral
hepatitis,
drug-induced
injury,
autoimmune
hepatitis
acute
ischaemic
injury
among
others
(Figure
1).
Regardless
underlying
cause,
hallmark
massive
hepatocyte
death,
leading
impaired
synthetic
metabolic
functions
liver.
presentation
vary
widely,
common
features
include
jaundice,
coagulopathy,
hepatic
encephalopathy,
often,
deterioration.
management
involves
intensive
supportive
measures
maintain
hemodynamic
stability,
correct
coagulopathy
manage
complications
such
as
cerebral
oedema
encephalopathy.1
Liver
transplantation
remains
only
definitive
treatment
option
for
many
patients
ALF,
offering
possibility
long-term
survival.
However,
availability
donor
organs
timing
crucial
factors
that
significantly
impact
outcomes.
In
recent
years,
there
has
been
growing
interest
artificial
support
systems
bridge
or
promote
regeneration
ALF.
These
aim
remove
toxins,
imbalances
provide
temporary
while
awaiting
recovery
transplantation.
Various
modalities,
extracorporeal
devices
bioartificial
systems,
have
investigated,
efficacy
subject
debate.2
ACLF,
on
other
hand,
represents
distinct
syndrome
chronic
disease,
most
commonly
cirrhosis.
Hernaez
colleagues
summarized
comprehensive
review
definition,
diagnosis
epidemiology
ACLF.3
ACLF
develops
setting
decompensation
may
also
develop
stage
decompensation,
so-called
non-acute
decompensation.4
For
precipitating
event,
bacterial
infection,
alcoholic
gastrointestinal
bleeding,
triggers
systemic
inflammatory
response
exacerbates
injury.
But
necessary
interventions
2)
induce
precipitate
Praktiknjo
et
al.5
dysregulated
immune
leads
widespread
tissue
damage
organ
dysfunction,
extra-hepatic
failures,
driving
extreme
short-term
30%
50%.6
Alcoholic
specific
trigger
still
unaddressed
condition.7
Similarly
hepatitis,7
complex
multifactorial,
involving
interactions
between
system,
gut
microbiota
inflammation.
progress
made,
we
expect
technological
(omics)
digital
(artificial
intelligence)
improve
understanding,
potentially
design
approaches.8
Especially
using
large
cohorts
omics
data
sets
will
facilitate
construction
algorithms
predict
prognosis
ACLF.
Existing
future
reviewed
Valainathan
al.9
Current
focuses
treating
factors,
providing
care
and,
some
cases,
considering
life-saving
intervention.10
role
inflammation
dysregulation
demonstrated
over
last
this
exploration
novel
targets,
interleukin-22
Hwang
al.11
Strategies
aimed
at
modulating
response,
corticosteroids,
immunomodulatory
agents
anti-inflammatory
cytokines,
shown
promise
preclinical
studies
early-phase
trials.12
approaches
multimodal,
indeed,
one
shape
strategy
based
molecular
mechanism
supporting
clear
rationale
3),
nicely
Morrison
al.13
addition
pharmacological
interventions,
increasing
use
potential
support,
toxins
mediators,
regeneration.
While
early
promising
results,
larger
randomized
controlled
trials
needed
establish
ACLF.14,
conclusion,
morbidity
mortality.
need
further
research
better
understand
conditions
more
targeted
therapies
holds
improving
outcomes
validate
safety
practice.
Jonel
Trebicka
was
supported
German
Research
Foundation
(DFG)
project
ID
403224013—SFB
1382
(A09),
Federal
Ministry
Education
(BMBF)
DEEP-HCC
Hessian
Higher
Education,
Arts
(HMWK)
ENABLE
ACLF-I
cluster
projects.
MICROB-PREDICT
(project
825694),
DECISION
847949),
GALAXY
668031),
LIVERHOPE
731875)
IHMCSA
964590)
projects
received
funding
European
Union's
Horizon
2020
innovation
program.
manuscript
reflects
authors'
views,
Commission
not
responsible
any
made
information
it
contains.
funders
had
influence
study
design,
collection
analysis,
decision
publish
preparation
manuscript.
speaking
and/or
consulting
fees
Versantis,
Gore,
Boehringer-Ingelheim,
Falk,
Grifols,
Genfit
CSL
Behring.
article
does
contain
primary
patient
nor
did
involve
human
animal
subjects.
As
such,
ethical
approval
required
production
article.
data,
materials
sources.
authors
writing
assistance
disclose.
editorial
present
new
synthesis
existing
findings.
Therefore,
sets,
code
submission.
All
included
publicly
available
literature
references
cited
within
text.
Journal of Viral Hepatitis,
Год журнала:
2025,
Номер
32(3)
Опубликована: Фев. 20, 2025
Acute-on-chronic
liver
failure
(ACLF)
is
a
severe
clinical
condition
with
high
short-term
mortality,
in
part
due
to
the
dysfunctional
immune
response.
Identifying
mechanism
under
ACLF
critical
understand
its
pathogenesis
and
develop
novel
targeted
therapeutics.
Among
cells,
how
are
B
cells
involved
remains
largely
unknown.
We
performed
scRNA-seq
on
peripheral
blood
mononuclear
from
patients
healthy
controls.
Integrated
analysis
was
identify
role
of
ACLF.
Subsequently,
different
subsets
were
validated
through
flow
cytometry
based
their
highlighted
markers.
Six
B-cell
subgroups,
including
naive
B2
nonclass-switched
memory
class-switched
autoimmune-related
plasma
identified.
The
proportions
significantly
expand
ACLF,
compared
control.
Function
enrichment
revealed
activation
inflammatory
response
cells.
Further
confirmed
elevated
circulating
Our
study
uncovered
altered
landscape
after
proportion
dynamics
functional
perturbation
indicate
potential
as
intervention
targets
future
therapy.
Artificial Organs,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 25, 2025
ABSTRACT
Background
Acute‐on‐chronic
liver
failure
(ACLF)
is
associated
with
high
short‐term
mortality
of
up
to
40%.
Albumin
dialysis
a
therapeutic
option
that
can
be
used
bridge
patients
ACLF
transplantation
or
recovery.
Methods
This
retrospective
cohort
study
was
conducted
determine
the
effectiveness
and
adverse
effects
open
albumin
(OPAL)
by
comparing
biochemical
clinical
variables
model
for
end‐stage
disease
(MELD)‐matched
who
received
one
three
treatments:
OPAL
plus
standard
medical
treatment
(SMT;
22
patients),
Prometheus
fractionated
plasma
separation
adsorption
(FPSA)
SMT
(41
hemodialysis
(24
patients)
at
University
Hospital
Essen.
Results
significantly
reduced
function
tests
such
as
bilirubin
(
p
=
0.0001)
creatinine
levels
0.049).
Therefore,
therapy
MELD
score
0.001)
Chronic
Liver
Failure
Consortium
(CLIF‐C)
0.0005)
score.
In
both
extracorporeal
support
groups,
decrease
in
stronger
than
achieved
(OPAL
vs.
SMT,
0.002;
0.0001;
0.90).
comparison
group,
survival
rates
after
14
30
days
were
higher
group
0.0008
0.03)
tended
better
although
statistical
significance
not
reached
0.06
0.11).
Conclusions
Our
analysis
revealed
an
efficient
method
yielding
reduction
improving
scoring
patients.
well
relevant
amelioration
SMT.
However,
it
should
considered
from
older
experienced
progressive
risks
compared
groups.
Thus,
when
interpreting
results,
several
limitations
including
small
sample
size
heterogeneity
groups
due
lack
randomization
taken
into
account.
Diagnostics,
Год журнала:
2025,
Номер
15(6), С. 751 - 751
Опубликована: Март 17, 2025
Acute-on-chronic
liver
failure
(ACLF)
is
a
clinical
syndrome
characterized
by
organ
and
high
short-term
mortality.
Since
its
first
definition
in
2013,
many
international
organizations
have
defined
this
and,
till
now,
there
has
been
no
agreement
regarding
definitions
diagnostic
criteria.
Although
the
precise
mechanism
of
ACLF
unknown,
precipitant
factors
systemic
inflammation
response
play
major
role.
Specific
management
high-mortality
still
under
development,
but
general
consensus
diagnosis
needed.
ABSTRACT
In
this
review,
we
discuss
the
pathophysiology
and
management
of
acute
kidney
injury
(AKI)
in
setting
acute‐on‐chronic
liver
failure
(ACLF).
ACLF
is
characterised
by
occurrence
hepatic
and/or
extrahepatic
organ
failure,
induced
immune
dysregulation
systemic
inflammation
patients
with
chronic
disease.
Kidney
involvement
common,
AKI
occurring
30%
to
>
95%
patients,
depending
on
definition
used.
Since
there
a
lack
biopsy
data
these
underlying
pathophysiological
basis
remains
incompletely
understood,
believed
be
primary
driver
injury.
The
has
been
largely
extrapolated
from
studies
decompensated
cirrhosis,
little
specifically
setting.
However,
available
evidence
suggests
that
structural
more
common
than
CLD,
therefore,
less
likely
respond
volume
repletion
vasopressors.
Treatment
options
remain
limited
for
those
who
are
non‐responsive
intravenous
fluids
Liver
transplantation
(LT),
or
without
transplantation,
definitive
treatment
patients.
At
present,
extracorporeal
therapies
such
as
therapeutic
plasma
exchange
replacement
play
supportive
role
bridge
LT;
however,
optimal
timing
dosing
unclear.
While
theoretically,
have
potential
reverse
halt
progression
damage
ACLF,
currently.
JHEP Reports,
Год журнала:
2024,
Номер
6(12), С. 101233 - 101233
Опубликована: Окт. 10, 2024
Decompensated
cirrhosis
has
long
been
considered
an
irreversible
end
stage
of
liver
disease,
characterized
by
further
decompensating
events
until
death
or
transplantation.
However,
the
observed
clinical
improvements
after
effective
antiviral
treatments
for
HBV
and
HCV
sustained
alcohol
abstinence
have
changed
this
paradigm,
leading
to
concept
"cirrhosis
recompensation".
Recompensation
recently
defined
BAVENO
VII
patients
with
(i)
cure
primary
disease
etiology;
(ii)
disappearance
signs
decompensation
(ascites,
encephalopathy
portal
hypertensive
bleeding)
off
therapy;
(iii)
stable
improvement
function
tests
(bilirubin,
INR
albumin).
Achieving
these
recompensation
criteria
is
linked
a
significant
survival
benefit.
next
etiological
therapies,
no
interventions/treatments
that
facilitate
are
available,
molecular
mechanisms
underlying
remain
incompletely
understood,
early
predictors
lacking.
Moreover,
current
based
on
expert
opinion
may
be
refined
in
future.Herein
we
review
available
evidence
recompensation,
provide
guidance
management
recompensated
discuss
future
challenges
related
recompensation.