Journal of the American Heart Association,
Journal Year:
2024,
Volume and Issue:
13(22)
Published: Nov. 11, 2024
Systemic
inflammatory
response
syndrome
(SIRS)
following
cardiovascular
interventions
is
associated
with
adverse
events
during
hospitalization
and
follow-up.
Mitral
transcatheter
edge-to-edge
repair
increasingly
utilized
for
treatment
of
mitral
regurgitation
(MR).
We
investigated
whether
SIRS
may
occur
be
clinical
outcomes.
New England Journal of Medicine,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 31, 2024
BackgroundCurrent
treatment
recommendations
for
patients
with
heart
failure
and
secondary
mitral
regurgitation
include
transcatheter
edge-to-edge
repair
mitral-valve
surgery.
Data
from
randomized
trials
comparing
these
therapies
are
lacking
in
this
patient
population.MethodsIn
noninferiority
trial
conducted
Germany,
who
continued
to
have
symptoms
despite
guideline-directed
medical
therapy
were
randomly
assigned,
a
1:1
ratio,
undergo
either
(intervention
group)
or
surgical
replacement
(surgery
group).
The
primary
efficacy
end
point
was
composite
of
death,
hospitalization
failure,
reintervention,
implantation
an
assist
device,
stroke
within
1
year
after
the
procedure.
safety
major
adverse
events
30
days
procedure.ResultsA
total
210
underwent
randomization.
mean
(±SD)
age
70.5±7.9
years,
39.9%
women,
left
ventricular
ejection
fraction
43.0±11.7%.
Within
year,
at
least
one
components
occurred
16
96
available
data
(16.7%)
intervention
group
20
89
(22.5%)
surgery
(estimated
difference,
−6
percentage
points;
95%
confidence
interval
[CI],
−17
6;
P<0.001
noninferiority).
A
end-point
event
15
101
(14.9%)
51
93
(54.8%)
−40
CI,
−51
−27;
P<0.001).ConclusionsAmong
regurgitation,
noninferior
respect
rehospitalization
stroke,
device
ventricle
year.
(Funded
by
Abbott
Vascular;
MATTERHORN
ClinicalTrials.gov
number,
NCT02371512.)
КАРДИОЛОГИЯ УЗБЕКИСТАНА,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 1, 2025
Treating
anterior
and
bileaflet
mitral
valve
disease
in
patients
with
primary
or
degenerative
regurgitation
(DMR)
is
considered
more
challenging
than
posterior
leaflet
repair.
The
aim
of
this
analysis
was
to
evaluate
the
impact
anterior,
posterior,
on
outcomes
following
transcatheter
edge-to-edge
repair
(M-TEER)
EXPANDed
studies.
a
pooled,
patient-level
subjects
undergoing
M-TEER
MitraClip
G3
G4
system
as
part
contemporary
EXPAND
Subjects
DMR
were
categorized
according
echocardiography
core
laboratory-assessed
prolapse
flail
location
into
(prolapse
at
P1,
P2,
and/or
P3),
A1,
A2,
A3)
any
combination
A3
P3).
Key
assessed
included
procedural
outcomes,
30-day
major
adverse
events,
1-year
(MR)
severity.
Of
2,205
EXPANDed,
556
had
location.
Three
hundred
eighty-nine
106
61
disease.
All
groups
experienced
low
device
procedure
times
high
success
rates
(defined
discharge
MR
≤
2+).
Thirty-day
events
across
all
(posterior,
4.4%
[17
388];
3.8%
[4
105];
bileaflet,
6.6%
61];
P
=
0.65).
Through
1
year,
showed
significant
reduction
severity
from
baseline
(MR
1+
82%
[179
219];
93%
[53
57];
97%
[28
29]).
Results
studies
demonstrate
that
treated
improvements
regardless
flail.
Trends in Cardiovascular Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 1, 2025
Mitral
valve
transcatheter
edge-to-edge
repair
(M-TEER)
has
emerged
as
a
transformative
therapy
for
mitral
regurgitation
(MR),
addressing
the
unmet
needs
of
patients
unsuitable
surgery.
Landmark
trials
such
EVEREST
II,
COAPT,
and
MITRA-FR
have
established
safety
efficacy
M-TEER,
in
both
with
primary
(PMR)
secondary
MR
(SMR).
Recent
trials,
including
RESHAPE-HF2
MATTERHORN,
expanded
our
understanding
refueled
discussions
regarding
patient
selection
appropriate
treatment
indications
SMR.
These
also
contributed
to
discussion
SMR
phenotypes
most
M-TEER.
This
review
summarizes
evidence
from
pivotal
discusses
selection,
device
advancements,
potential
future
directions,
outlines
ongoing
that
may
shape
clinical
practice.
КАРДИОЛОГИЯ УЗБЕКИСТАНА,
Journal Year:
2024,
Volume and Issue:
17(7), P. 890 - 903
Published: April 1, 2024
Mitral
transcatheter
edge-to-edge
repair
(M-TEER)
is
a
guideline-recommended
treatment
option
for
patients
with
severe
symptomatic
mitral
regurgitation
(MR).
Outcomes
the
PASCAL
system
in
post-market
setting
have
not
been
established.
The
authors
report
30-day
and
1-year
outcomes
from
MiCLASP
(Transcatheter
Repair
of
Regurgitation
Edwards
Transcatheter
Valve
System)
European
clinical
follow-up
study.
Patients
symptomatic,
clinically
significant
MR
were
prospectively
enrolled.
primary
safety
endpoint
was
events
committee-adjudicated
composite
major
adverse
event
rate
effectiveness
echocardiographic
core
laboratory-assessed
severity
at
discharge
compared
baseline.
Clinical,
echocardiographic,
functional,
quality-of-life
assessed
1
year.
A
total
544
enrolled
(59%
functional
MR,
30%
degenerative
MR).
6.8%.
reduction
baseline
to
sustained
year
98%
achieving
≤2+
82.6%
≤1+
(all
P
<
0.001
vs
baseline).
One-year
Kaplan-Meier
estimate
survival
87.3%,
freedom
heart
failure
hospitalization
84.3%.
Significant
improvements
observed
year,
including
71.6%
NYHA
class
I/II,
14.4-point
increase
Kansas
City
Cardiomyopathy
Questionnaire
score,
24.2-m
improvement
6-minute
walk
distance
this
large
cohort
study
demonstrate
continued
M-TEER
setting.
Results
high
hospitalization,
reduction,
symptoms,
capacity,
quality
life.
European Journal of Heart Failure,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 8, 2025
Abstract
Aims
Secondary
mitral
regurgitation
(SMR)
and
tricuspid
(TR)
are
the
most
common
valvular
heart
diseases
in
patients
with
failure
(HF).
Transcatheter
edge‐to‐edge
repair
(TEER)
devices
designed
for
treating
MR
TR
have
been
successfully
tested
randomized
controlled
trials,
but
methodological
issues
often
challenged
their
interpretation.
This
manuscript
aimed
to
provide
an
overview
of
TEER
registries
on
SMR
HF,
highlighting
key
features,
describing
clinical
characteristics
outcomes
receiving
these
devices,
exploring
available
data
limitations.
Methods
results
PubMed,
Web
Science,
EMBASE
were
searched
reporting
or
TR.
Registries
excluded
if
single‐centre
<100
patients.
Twenty‐six
(46%
prospective,
12%
ongoing),
including
a
total
cohort
18
925
patients,
retrieved
SMR,
six
(50%
retrospective,
33%
ongoing)
reported
use
1412
Limited
geographical
representativity
outside
North
America
Europe,
high
number
missing
values,
inconsistency
main
existing
evidence
Conclusion
represent
source
setting
where
it
is
difficult
conduct
trials.
However,
limitations
design,
patient
characterization,
restrain
use.
A
novel
conceptual
framework
future
prospective
registries,
as
proposed
this
document,
might
inform
current
practice,
address
relevant
questions
trial
design.
Aktuelle Kardiologie,
Journal Year:
2025,
Volume and Issue:
14(01), P. 40 - 46
Published: Feb. 1, 2025
Zusammenfassung
Die
Therapie
der
Mitralklappeninsuffizienz
(MI)
mittels
transvenöser
Mitralklappenprothesen
(TMVR)
bietet
eine
vielversprechende
minimalinvasive
Option
für
Hochrisikopatienten,
die
keine
Operation
erhalten
können.
komplexe
Anatomie
Mitralklappe
und
ihre
Nähe
zum
linksventrikulären
Ausflusstrakt
(LVOT)
stellen
jedoch
technische
Herausforderungen
dar.
Verkalkungen
des
Mitralklappenanulus
erschweren
zudem
Behandlung.
TMVR-Systeme
zeigen
Ergebnisse,
wobei
innovative
Verankerungsmechanismen
Risiken,
wie
LVOT-Obstruktion,
minimieren.
Dennoch
bleibt
Patientenauswahl
problematisch,
da
viele
Patienten
aufgrund
anatomischer
Einschränkungen
TMVR
ungeeignet
sind.
Zukünftige
Entwicklungen
in
Prothesentechnologie
Zugangsverfahren
könnten
diese
Therapieoption
weiter
verbessern.
Langfristige
Daten
technologische
Fortschritte
sind
notwendig,
um
als
Standardbehandlung
zu
etablieren
von
MI
revolutionieren.
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(4), P. 1075 - 1075
Published: Feb. 8, 2025
Background/Objectives:
Over
the
past
two
decades,
MitraClip™
therapy
has
proven
to
be
an
effective
and
safe
treatment
for
severe
mitral
regurgitation
(MR),
with
more
than
200,000
patients
treated
globally
through
continuous
advancements
in
device
design
implantation
techniques.
This
retrospective,
observational,
single-center
study
aimed
assess
safety
efficacy
of
latest
generation
MitraClip
compared
earlier
models
Real-World
Florence
Registry.
The
primary
endpoint
was
a
comparison
terms
rate
successful
procedures,
time
deployment
duration
hospital
stay.
secondary
regarded
long-term
all-cause
mortality
hospitalization
heart
failure.
Methods:
Patients
at
our
center
from
January
2016
June
2022
were
included.
They
divided
into
groups:
those
receiving
early-generation
devices
(G1–G3)
last-generation
(G4).
All
underwent
comprehensive
preoperative
echocardiographic
assessment,
re-evaluation
before
discharge
after
12
months.
A
follow-up
focusing
on
failure
conducted.
Results:
Of
131
patients,
81
received
device.
mean
age
79.4
years.
Both
groups
exhibited
high
burden
comorbidities
(overall
n
=
2.85).
Procedural
success
(97%)
across
groups,
significantly
better
MR
reduction
(Grade
≤
1)
G4
group
(47%
vs.
70%,
p
0.009).
shorter
system
(72
135
min,
<
0.001),
there
trend
towards
stays
(6.1
7.9
days,
0.08).
Kaplan–Meier
analysis
demonstrated
5-year
survival
rates
(p
0.019),
no
significant
difference
rehospitalization
0.186).
Conclusions:
real
world
is
effective,
achieving
immediate
durable
procedural
success,
accompanied
by
improved
NYHA
functional
class.
Moreover,
observed,
along
comparable
recurrent
HF
hospitalization,
reflecting
comorbidity
this
frail
population.