Nervenheilkunde,
Journal Year:
2024,
Volume and Issue:
43(07/08), P. 434 - 437
Published: July 1, 2024
ZUSAMMENFASSUNG
Die
letzten
Jahre
waren
geprägt
von
der
Etablierung
neuer,
innovativer
Diagnose-
und
Therapieverfahren
im
Bereich
Epileptologie.
Es
sind
beispielsweise
Systeme
zur
Ultra-Langzeit-EEG-Registrierung
verfügbar.
Frühtherapie
einer
refraktären
Epilepsie
wird
zunehmend
durch
die
Entwicklung
neuer
Therapiemethoden
verbessert.
Neurostimulationsverfahren
werden
weiterentwickelt
neue
Technologien
wurden
eingeführt.
Vielversprechend
auch
synergistischen
Effekte
Neurostimulation
in
Kombination
mit
bestimmten
Wirkmechanismen
anfallsunterdrückender
Medikamente
Rahmen
Neuromodulation.
Dieser
Überblick
beleuchtet
all
diese
Entwicklungen
anderthalb
Jahre.
CNS Drugs,
Journal Year:
2024,
Volume and Issue:
38(9), P. 733 - 742
Published: Aug. 3, 2024
Cenobamate
(CNB)
is
a
new
antiseizure
medication
(ASM)
to
treat
drug-resistant,
focal-onset
seizures.
Data
on
its
use
in
early
therapy
lines
are
not
yet
available,
and
clinicians
frequently
consider
CNB
be
later
ASM
drug
choice.
We
investigated
the
efficacy
safety
of
as
an
adjunctive
treatment
The
study
population
were
patients
with
seizures
who
initiated
after
they
did
respond
two
or
three
lifetime
ASMs,
including
all
prior
concomitant
ASMs.
These
matched
(1:2)
by
sex,
age,
seizure
frequency
controls
any
other
than
CNB.
All
participants
participated
Mainz
Epilepsy
Registry.
evaluated
retention
rate
12
months
each
control
group.
In
addition,
freedom
response
(reduction
≥
50%
from
baseline)
estimated.
included
231
aged
44.4
±
15.8
years.
Of
these,
33.3%
(n
=
77)
CNB,
19.0%
44)
valproate
(VPA),
17.3%
40)
lacosamide
(LCS),
16.4%
38)
levetiracetam
(LEV),
13.9%
32)
topiramate
(TPM).
highest
since
beginning
was
observed
(92.0%),
compared
LCS
(80.0%),
LEV
(73.3%),
VPA
(68.2%),
TPM
(62.5%)
(p
<
0.05).
Seizure
also
best
(19.5%
71.4%,
respectively)
ASMs
(8.3%
52.5%,
respectively;
p
No
significant
differences
adverse
events
between
observed.
Our
provides
evidence
that
effective
good
profile
This
data
should
support
medical
decision
making
management
refractory
epilepsy.
NCT05267405.
Epilepsia,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 4, 2025
Acute
ischemic
stroke
(AIS)
is
a
leading
hospitalization
cause
and
significantly
contributes
to
seizures
among
older
adults.
We
examined
outpatient
epilepsy-specific
medication
(ESM)
initiation
patterns
after
AIS
discharge
in
adults
65
years
older,
trends
over
time
(by
stratifying
the
analysis
from
2013
2021),
racial/ethnic
differences.
analyzed
nationwide
administrative
claims
data
for
20%
sample
of
US
Medicare
beneficiaries
(enrolled
Traditional
Parts
A,
B,
D
at
least
12
months
before
admission)
aged
≥65
hospitalized
between
2021.
estimated
cumulative
incidence
ESM
within
90
days
discharge,
with
mortality
as
competing
risk
censoring
person
if
individuals
experienced
an
inpatient
readmission.
described
drug
type
stratified
our
by
race,
ethnicity,
geographic
region,
hospital
year
discharge.
Of
128
174
community-dwelling
2435
(1.9%,
95%
confidence
interval
[CI]
=
1.8%-2.0%)
initiated
90-day
follow-up
period
levetiracetam
was
most
common
across
all
(81%).
Mean
age
79
(range
65-110),
56%
were
female,
81%
non-Hispanic
White,
10%
Black/African
American,
5%
Hispanic,
3%
Asian.
The
overall
1.4%
(95%
CI
1.3%-1.4%);
it
1.8%
1.6%-2.1%)
1.9%
1.6%-2.3%)
1.2%
1.2%-1.3%)
White
beneficiaries.
also
varied
Census
division,
1.0%
.8-1.3;
West
North
Central)
1.5%
1.3%-1.8%;
East
South
Central).
observed
increase
time,
1.0%-1.5%)
1.7%
1.5%-1.9%)
1.6%
1.4%-1.8%)
65-70-year
group
decreased
groups.
American
Hispanic
had
higher
post-AIS
than
Whites.
Journal of Orthopaedic Surgery and Research,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: Feb. 3, 2024
Abstract
Background
Although
prior
observational
studies
indicate
an
association
between
cardiovascular
diseases
(CVDs)
and
frozen
shoulder
(FS),
the
potential
causal
relationship
them
remains
uncertain.
This
study
aims
to
explore
genetic
CVDs
FS
using
Mendelian
randomization
(MR).
Methods
Genetic
variations
closely
associated
with
were
obtained
from
FinnGen
Consortium.
Summary
data
for
CVD,
including
atrial
fibrillation
(AF),
coronary
artery
disease
(CAD),
heart
failure
(HF),
myocardial
infarction
(MI),
stroke,
ischemic
stroke
(IS),
sourced
several
large-scale
genome-wide
(GWAS).
MR
analysis
was
performed
inverse
variance
weighting
(IVW),
Egger,
weighted
median
methods.
IVW,
as
primary
method,
complemented
by
other
sensitivity
analyses,
utilized
validate
robustness
of
results.
Further
reverse
conducted
presence
relationships.
Results
In
forward
analysis,
genetically
determined
risk
IS
positively
(OR
[95%
CI]
=
1.58
(1.23–2.03),
P
<
0.01;
OR
1.46
(1.16–1.85),
0.01,
respectively).
There
no
strong
evidence
effect
predicted
on
risk.
Sensitivity
analyses
confirmed
relationships
observed
various
CVDs.
Conclusion
The
suggests
that
increases
developing
FS.
However,
further
basic
clinical
research
is
needed
substantiate
our
findings.
Epilepsia,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 22, 2025
Abstract
Acute
symptomatic
seizures,
occurring
shortly
after
a
central
nervous
system
insult,
constitute
nearly
half
of
all
seizure
cases.
However,
there
is
conspicuous
absence
clear,
comprehensive,
and
cohesive
guidelines
for
the
management
these
seizures
with
antiseizure
medications,
especially
their
duration
use.
This
lack
consensus
on
optimal
therapy
leads
to
prolonged
treatments
that
may
carry
adverse
consequences.
The
primary
objective
this
narrative
review
present
existing
evidence‐based
literature
acute
within
context
underlying
pathologies
trigger
them.
We
explore
risk
developing
epilepsy
each
specific
etiology
identify
factors
influence
risk.
Finally,
facilitate
decision‐making
regarding
treatment
duration,
we
categorize
based
temporal
characteristics
hyperexcitability
as
acute,
subacute,
prolonged.
Such
rubric
offer
clarity
in
an
area
where
are
lacking.
Neurology,
Journal Year:
2025,
Volume and Issue:
104(3)
Published: Jan. 14, 2025
The
most
effective
antiseizure
medications
(ASMs)
for
poststroke
seizures
(PSSs)
remain
unclear.
We
aimed
to
determine
outcomes
associated
with
ASMs
in
people
PSS.
systematically
searched
electronic
databases
studies
on
patients
PSS
ASMs.
Our
were
seizure
recurrence,
adverse
events,
drug
discontinuation
rate,
and
mortality.
assessed
the
risk
of
bias
using
Cochrane
Risk
Bias
tool
randomized
controlled
trials
Of
In
Non-randomized
Studies
Interventions
tools.
Using
levetiracetam
as
reference
treatment,
we
conducted
a
frequentist
network
meta-analysis
determined
certainty
evidence
Grading
Recommendations
Assessment,
Development,
Evaluation
methodology.
search
yielded
15
(3
randomized,
12
nonrandomized,
N
=
18,676
(121
early
18,547
late
seizures),
60%
male,
mean
age
69
years)
comparing
13
Three
had
moderate
high
bias.
Seizure
recurrence
was
24.8%.
Compared
levetiracetam,
very
low-certainty
suggested
that
phenytoin
higher
recurrences
(odds
ratio
[OR]
7.3,
95%
CI
3.7-14.5)
more
events
(OR
5.2,
1.2-22.9).
Low-certainty
carbamazepine
1.8,
1.5-2.2)
1.9,
1.4-2.8)
rates.
Moderate
high-certainty
valproic
acid
4.7,
3.6-6.3)
8.3,
5.7-11.9)
mortality
Considering
all
treatments
GRADE
approach
treatment
ranking,
eslicarbazepine,
lacosamide,
fewest
recurrences.
Low
lamotrigine
discontinuations,
whereas
exhibited
low
rates
moderate-certainty
evidence.
found
may
be
safe
tolerable
Despite
ASM
use,
rate
remains
population.
Owing
confounding
risks,
these
findings
should
interpreted
cautiously.
PROSPERO:
CRD42022363844.
Epilepsia,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 11, 2025
Abstract
Objective
The
aim
of
this
study
was
to
compare
the
risk
seizure,
recurrent
stroke,
fall
or
fracture,
and
mortality
in
individuals
prescribed
different
antiseizure
medications
(ASMs)
following
an
ischemic
stroke.
Methods
We
identified
all
patients
admitted
a
Victorian
public
private
hospital
with
principal
diagnosis
incident
stroke
between
2013
2017
dispensed
ASM
within
12
months
discharge.
Cox
proportional
hazards
regression
used
estimate
cause‐specific
rehospitalization
emergency
department
visits
(seizure,
stroke)
all‐cause
over
2‐year
period.
Inverse
probability
treatment
weighting
applied
each
model
adjust
for
baseline
covariates.
Results
Of
19
601
hospitalized
897
initiated
months.
More
than
three
quarters
were
on
non‐enzyme‐inducing
(78.0%).
Levetiracetam
(41.9%),
valproate
(28.4%),
carbamazepine
(11.4%)
commonly
initial
ASMs.
Non‐enzyme‐inducing
ASMs
demonstrated
similar
seizure
(hazard
ratio
[HR]
=
.93,
95%
confidence
interval
[CI]
.63–1.37),
fracture
(HR
1.47,
CI
.92–2.34),
.83;
.52–1.33),
.96;
.69–1.32)
compared
enzyme‐inducing
However,
when
grouped
as
separate
class,
1.67,
1.04–2.71)
showed
higher
Significance
At
population
level,
types
no
significant
differences
hospitalization
presentation
2
years
presentation,
suggesting
short‐term
health
outcomes
real‐world
setting.
Future
research
should
investigate
decision‐making
around
choice
survivors
examine
impact
long‐term
exposure
outcomes.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 20, 2025
The
lack
of
specific
guidelines
for
seizure
treatment
after
acute
ischemic
stroke
(AIS),
makes
the
choice
an
appropriate
anti-seizure
medication
a
challenge
providers
because
each
drug
may
have
different
adverse
effects
and
outcomes.
In
this
retrospective
matched
cohort
study,
we
analyzed
20%
sample
U.S.
Medicare
beneficiaries
aged
65
over
hospitalized
first
(AIS)
between
2009-2021
who
were
discharged
home.
We
included
individuals
enrolled
in
hospital,
medical
prescription
insurance
12
months
prior
to
hospitalization
not
taking
epilepsy-specific
(ESM)
hospitalization.
on
days
from
discharge
ESM
initiation.
Individuals
initiated
ESMs
other
than
Levetiracetam,
i.e.
Lamotrigine,
Carbamazepine,
Oxcarbazepine
within
30
(N
=
229)
Levetiracetam
initiators
=687).
investigated
time
seizure-like
events,
emergency
department
(ED)
visits,
re-hospitalizations
with
follow-up
180
initiation
using
semi-competing
risk
framework.
estimated
average
effect
among
treated
those
received
ESMs.
916
had
median
age
74
(IQR
69,
82)
was
57%
female
71%
Non-Hispanic
White.
Using
framework,
37%
lower
hazard
events
compared
receiving
LEV,
given
that
death
occurred,
ratio
0.63
(95%
CI:
0.43,
0.91).
Among
ED
visits
hospitalizations,
did
significantly
initiating
Levetiracetam;
ratios
1.00
0.80,
1.25)
0.98
0.75,
1.28),
respectively.
home,
outpatient
setting
associated
higher
However,
no
significant
differences
observed
incidence
or
suggesting
comparable
safety
profiles
these
broader
clinical