Journal of Clinical Medicine,
Journal Year:
2024,
Volume and Issue:
13(15), P. 4289 - 4289
Published: July 23, 2024
Objective:
This
study
assessed
the
patterns
and
clinical
significance
of
potential
drug–drug
interactions
(pDDIs)
in
patients
with
diseases
cardiovascular
system.
Methods:
Electronic
health
records
(EHRs),
established
2018–2023,
were
selected
using
probability
serial
nested
sampling
method
(n
=
1030).
Patients
aged
27
to
95
years
(65.0%
men).
Primary
diagnosis
COVID-19
was
present
17
EHRs
(1.7%).
Medscape
Drug
Interaction
Checker
used
characterize
pDDIs.
The
Mann–Whitney
U
test
chi-square
for
statistical
analysis.
Results:
numbers
per
record
ranged
from
1
23
T-List
20
P-List.
In
T-List,
567
drug
combinations
resulted
3781
P-List,
584
5185
Polypharmacy
detected
39.0%
versus
65.9%
P-List
(p-value
<
0.05).
rates
serious
monitor-closely
pDDIs
due
‘aspirin
+
captopril’
significantly
higher
than
enalapril’
lisinopril’
lower
compared
corresponding
Serious
administration
aspirin
fosinopril,
perindopril,
ramipril
less
frequently
Conclusions:
Obtained
data
may
suggest
better
patient
adherence
combinations,
which
are
potentially
superior
ramipril.
An
abundance
high-order
real-world
practice
warrants
development
a
decision
support
system
aimed
at
reducing
pharmacotherapy-associated
risks
while
integrating
pharmacokinetic,
pharmacodynamic,
pharmacogenetic
information.
The
current
standard
method
for
the
analysis
of
potential
drug–drug
interactions
(pDDIs)
is
time‐consuming
and
includes
use
multiple
clinical
decision
support
systems
(CDSSs)
interpretation
by
healthcare
professionals.
With
emergence
large
language
models
developed
with
artificial
intelligence,
an
interesting
alternative
arose.
This
retrospective
study
included
30
patients
polypharmacy,
who
underwent
a
pDDI
between
October
2022
August
2023,
compared
performance
Chat
GPT
established
CDSSs
(MediQ®,
Lexicomp®,
Micromedex®)
in
pDDIs.
A
multidisciplinary
team
interpreted
obtained
results
decided
upon
relevance
assigned
severity
grades
using
three
categories:
(i)
contraindicated,
(ii)
severe,
(iii)
moderate.
expert
review
identified
total
280
clinically
relevant
pDDIs
(3
contraindications,
13
264
moderate)
CDSSs,
80
(2
5
73
GPT.
almost
entirely
neglected
risk
to
QTc
prolongation
(85
vs.
8),
which
could
also
not
be
sufficiently
improved
specific
prompt.
To
assess
consistency
provided
GPT,
we
repeated
each
query
found
inconsistent
90%
cases.
In
contrast,
acceptable
comprehensible
recommendations
questions
on
side
effects.
identification
cannot
recommended
currently,
because
were
detected,
there
obvious
errors
inconsistent.
However,
if
these
limitations
are
addressed
accordingly,
it
promising
platform
future.
Indian Journal of Physiology and Pharmacology,
Journal Year:
2025,
Volume and Issue:
0, P. 1 - 6
Published: Jan. 13, 2025
Objectives:
Drug
interaction
programmes
are
considered
imperative
tools
utilised
by
healthcare
professionals
to
screen
potential
risks
that
may
occur
from
drug
combinations.
However,
the
outcomes
of
analysing
drug–drug
interactions
(DDIs)
differ
across
each
programme.
It
is
crucial
for
clinician
be
aware
varying
results
database
and
their
limitations
before
utilising
them.
This
study
aimed
compare
in
geriatric
patients
at
an
outpatient
clinic
a
tertiary
care
hospital.
Materials
Methods:
A
retrospective
was
performed
hospital
Thailand.
collected
all
prescriptions
during
November
2021
2022.
The
programs
using
Micromedex,
Medscape
Lexicomp
were
used
detect
assess
severity
DDIs.
Results:
participants
recruited
electronic
medical
records
enrolment
total
10,877
individuals.
majority
these
male,
with
average
age
74.3
(standard
deviation
6.8)
years.
prevalence
major
DDIs
Lexicomp,
Micromedex
28.1%,
57.9%
18.2%,
respectively.
Only
1700
(15.6%)
observed
consistent
three
programmes.
strength
agreement
amongst
Kappa
statistics
0.15,
0.35
0.61
(
P
<0.01)
major,
moderate
minor
+
no
groups,
Conclusion:
degree
among
three-drug
programmes,
Medscape,
minimal.
To
maintain
uniformity
information
sources,
it
essential
apply
measures
standardisation
documentation.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: April 2, 2024
Background:
Toxicity
or
treatment
failure
related
to
drug-drug
interactions
(DDIs)
are
known
significantly
affect
morbidity
and
hospitalization
rates.
Despite
the
availability
of
numerous
databases
for
DDIs
identification
management,
their
information
often
differs.
Oral
anticoagulants
deemed
at
risk
a
leading
cause
adverse
drug
events,
most
which
being
preventable.
Although
many
include
involving
anticoagulants,
none
specialized
in
them.
Aim
method:
This
study
aims
compare
content
four
direct
oral
two
vitamin
K
antagonists
three
major
DDI
used
Switzerland:
Lexi-Interact,
Pharmavista,
MediQ.
It
evaluates
consistency
terms
differences
severity
rating
systems,
mechanism
interaction,
extraction
documentation
processes
transparency.
Results:
revealed
2’496
six
with
discrepant
classifications.
Only
13.2%
were
common
all
databases.
Overall
concordance
classification
(high,
moderate,
low
risk)
was
slight
(Fleiss’
kappa
=
0.131),
while
high-risk
demonstrated
fair
agreement
0.398).
The
nature
more
consistent
across
Qualitative
assessments
highlighted
process
transparency,
similarities
references.
Discussion:
highlights
discrepancies
between
commonly
inconsistency
how
terminology
is
standardised
incorporated
when
classifying
these
DDIs.
also
need
creation
specialised
tools
anticoagulant-related
interactions.
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
16(1), P. 3 - 3
Published: Dec. 19, 2023
Patients
with
multiple
sclerosis
(MS)
often
take
drugs
at
the
same
time
to
modify
course
of
disease,
alleviate
neurological
symptoms
and
manage
co-existing
conditions.
A
major
consequence
for
a
patient
taking
different
medications
is
higher
risk
treatment
failure
side
effects.
This
because
drug
may
alter
pharmacokinetic
and/or
pharmacodynamic
properties
another
drug,
which
referred
as
drug-drug
interaction
(DDI).
We
aimed
predict
interactions
that
are
used
by
patients
MS
based
on
deep
neural
network
(DNN)
using
structural
information
input.
further
identify
potential
drug-food
(DFIs),
can
affect
efficacy
safety
well.
DeepDDI,
multi-label
classification
model
specific
DDI
types,
changes
in
pharmacological
effects
adverse
events
when
two
or
more
taken
together.
The
original
~34
million
trainable
parameters
was
updated
>1
DDIs
recorded
DrugBank
database.
Structure
data
food
components
were
obtained
from
FooDB
medication
plans
(n
=
627)
then
searched
pairwise
between
compounds.
DeepDDI
achieved
accuracies
92.2%
92.1%
validation
testing
sets,
respectively.
312
small
molecule
prescription
over-the-counter
medications.
In
plans,
we
identified
3748
13,365
DeepDDI.
At
least
one
found
most
509
81.2%
DNN
model).
predictions
revealed
many
would
be
increased
bleeding
bradycardic
complications
due
if
they
start
disease-modifying
therapy
cladribine
242
38.6%)
fingolimod
279
44.5%),
also
numerous
Bruton’s
tyrosine
kinase
inhibitors
clinical
development
MS,
such
evobrutinib
434
DDIs).
Food
sources
related
DFIs
corn
5456
DFIs)
cow’s
milk
4243
DFIs).
demonstrate
learning
techniques
exploit
chemical
structure
similarity
accurately
MS.
Our
study
specifies
pairs
potentially
interact,
suggests
mechanisms
causing
effects,
informs
about
whether
interacting
replaced
alternative
avoid
critical
provides
dietary
recommendations
who
certain
drugs.
Ankara Universitesi Eczacilik Fakultesi Dergisi,
Journal Year:
2024,
Volume and Issue:
48(3), P. 22 - 22
Published: Aug. 5, 2024
Objective:
The
study
aims
to
compare
the
ability
of
free
artificial
intelligence
(AI)
chatbots
detect
drug
interactions
with
freely
available
interaction
tools,
using
clopidogrel
as
an
example.
Material
and
Method:
Lexicomp
database
was
used
a
reference
determine
clopidogrel.
ChatGPT-3.5
AI
Bing
were
selected
chatbots.
Medscape
Drug
Interaction
Checker,
DrugBank
Checker
Epocrates
Check
tools.
Accuracy
score
comprehensiveness
calculated
for
each
tool
kappa
coefficient
assess
inter-source
agreement
severity.
Result
Discussion:
results
most
similar
those
obtained
from
chatbot.
chatbot
performed
best,
69
correct
accuracy
307.
has
highest
overall
387
points
comprehensiveness.
In
addition,
found
(0.201,
fair
agreement).
However,
some
by
need
be
improved
they
are
incorrect/inadequate.
Therefore,
information
tools
should
not
clinical
applications
healthcare
professionals
patients
change
their
treatment
without
consulting
doctor.
Journal of Clinical Medicine,
Journal Year:
2023,
Volume and Issue:
12(15), P. 5061 - 5061
Published: Aug. 1, 2023
The
study
aimed
to
assess
clinical
pharmacology
patterns
of
prescribed
and
taken
medications
in
older
cardiovascular
patients
using
electronic
health
records
(EHRs)
(n
=
704)
(2019–2022).
Medscape
Drug
Interaction
Checker
was
used
identify
pairwise
drug–drug
interactions
(DDIs).
Prevalence
rates
DDIs
were
73.5%
68.5%
among
drugs,
respectively.
However,
the
total
number
significantly
higher
(p
<
0.05).
Serious
comprised
16%
7%
all
medications,
respectively
Median
numbers
between
vs.
Me
2,
IQR
0–7
3,
per
record,
polypharmacy
compared
with
that
drugs
Women
taking
more
had
prevalence
No
sex-related
differences
observed
list
medications.
ICD
code
U07.1
(COVID-19,
virus
identified)
associated
highest
median
DDI
record.
Further
research
is
warranted
improve
EHR
structure,
implement
patient
engagement
reporting
adverse
drug
reactions,
provide
genetic
profiling
avoid
potentially
serious
DDIs.
Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
16(3), P. 339 - 339
Published: Feb. 28, 2024
Drug–drug
interactions
(DDIs)
can
either
enhance
or
diminish
the
positive
negative
effects
of
associated
drugs.
Multiple
drug
combinations
create
difficulties
in
identifying
clinically
relevant
interactions;
this
is
why
electronic
interaction
checkers
frequently
report
DDI
results
inconsistently.
Our
paper
aims
to
analyze
cardiovascular
diseases
by
selecting
drugs
from
pharmacotherapeutic
subcategories
interest
according
Level
2
Anatomical
Therapeutic
Chemical
(ATC)
classification
system.
We
checked
DDIs
between
9316
pairs
and
25,893
other
then
evaluated
overall
agreement
on
severity
two
checkers.
Thus,
we
obtained
a
fair
for
category,
as
well
(i.e.,
non-cardiovascular)
categories,
reflected
Fleiss’
kappa
coefficients
κ=0.3363
κ=0.3572,
respectively.
The
categorical
analysis
ATC-defined
reveals
that
indicate
levels
varying
poor
(κ<0)
perfect
(κ=1).
main
drawback
assessment
it
includes
same
subcategory,
situation
therapeutic
duplication
seldom
encountered
clinical
practice.
conclusion
more
insightful
than
approach,
allows
thorough
investigation
disparities
databases
better
exposes
factors
influence
different
responses
Using
avoids
potential
inaccuracies
caused
particularizing
an
statistical
heterogeneous
dataset.
Die
Ergebnisse
der
Studie
und
die
Diversität
Datenbanken
ist
groß.
Für
12
wurde
ein
Punktesystem
mit
elf
Items
entworfen,
um
Qualität
einzelnen
zu
objektivieren.
Keine
Datenbank
konnte
alle
Bewertungskriterien
erfüllen.
Der
insgesamt
schlechte
Punktedurchschnitt
Indikator
für
Mängel
aktuell
verfügbaren
Datenbanken.
Außerdem
konnten
wir
einen
Qualitätsunterschied
zwischen
kostenpflichtigen
kostenfreien
beweisen
mussten
im
Zuge
dieser
Frage
stellen,
ob
kostenfreie
überhaupt
nützlich
sind.
Zwischen
den
fallen
Qualitätsunterschiede
weniger
gravierend
aus,
wenngleich
Stärken
Schwächen
sich
deutlich
unterscheiden.
häufigsten
Wechselwirkungen
wurden
in
allen
großem
Abstand
rein
psychiatrischen
Interaktionspaaren
erfasst.
Dieses
zeigt,
wie
wechselwirkungsreich
Psychopharmaka
sind
dass
psychiatrische
Patienten
besonders
vulnerabel
Nutzung
digitaler
Hilfsmittel
scheint
bei
Betrachtung
hohen
Anzahl
ausgegebener
Warnmeldungen
unabdingbar
sein,
dennoch
existiert
große
Uneinheitlichkeit
Bewertung
Interaktionen.
Vorstellung,
zwei
Kliniker
zweier
unterschiedlicher
völlig
unterschiedlichen
Empfehlungen
kommen,
fällt
nicht
schwer.
Gleichzeitig
könnte
Kooperation
von
Heilberuflern,
unterschiedliche
verwenden,
Chance
auf
zusätzlichen
Informationsgewinn
Austausch
erhöhen,
was
Umkehrschluss
einer
erhöhten
Arzneimitteltherapiesicherheit
resultiert.
In
Studien
positive
Effekt
interdisziplinärer
Zusammenarbeit
bereits
bewiesen
werden.
Zusammenfassend
umfangreiche
Differenzen
untersuchten
aufgezeigt
Um
Anforderungen
des
klinischen
Alltags
genügen,
müssen
digitale
Unterstützungssysteme
weiterentwickelt
„ideale
Datenbank“
gibt
es
bisher
–
das
lässt
durch
unser
beweisen.
Alltag
Patientensicherheit
gewährleisten
ausreichend.
Gewährung
sollte
oberstes
Ziel
sein
dieses
erreichen,
bedarf
vieler
Komponenten.
Neben
vor
allem
Weiterentwicklung
auch
zwischenmenschliche
weiter
gefördert
Interdisziplinäre
Sinne
pharmazeutischer
Dienstleistungen
zur
Medikationsanalyse
könnten
zusätzliches
Instrument
Vermeidung
arzneimittelbezogener
Probleme
Zukünftig
werden
unsere
am
meisten
optimaler
weiterentwickelter
Technologien,
sowie
wachsendem
zwischenmenschlichem
profitieren.
Healthcare,
Journal Year:
2024,
Volume and Issue:
12(13), P. 1275 - 1275
Published: June 26, 2024
Institutionalized
older
adults
often
face
complex
medication
regimens,
increasing
their
risk
of
adverse
drug
events
due
to
polypharmacy,
overprescribing,
interactions,
or
the
use
Potentially
Inappropriate
Medications
(PIM).
However,
data
on
and
associated
risks
in
this
population
remain
scarce.
This
pilot
study
aimed
characterize
sociodemographic,
clinical
pharmacotherapeutic
profiles,
PIM
among
institutionalized
elders
residing
Residential
Structures
for
Elderly
People
(ERPI)
Faro
municipality,
located
Portuguese
region
Algarve.
We
conducted
a
cross-sectional
non-randomized
sample
96
participants
(mean
age:
86.6
±
7.86
years)
where
trained
researchers
reviewed
profiles
identified
potentially
inappropriate
medications
using
EU(7)-PIM
list.
Over
90%
exhibited
polypharmacy
(≥5
medications),
with
an
average
9.1
4.15
per
person.
About
92%
had
potential
including
major
moderate
interactions.
More
than
86%
used
at
least
one
medication,
most
commonly
central
nervous
system
drugs.
demonstrates
that
may
be
high
medication-related
problems.
Implementing
comprehensive
review
programs
promoting
adapted
prescribing
practices
are
crucial
optimize
improve
well-being
vulnerable
population.