BMJ Open,
Journal Year:
2016,
Volume and Issue:
6(3), P. e009781 - e009781
Published: March 1, 2016
Polypharmacy
and
multimorbidity
are
common
in
long-term
care
facilities
(LTCFs).
Reducing
polypharmacy
may
reduce
adverse
events
maintain
quality
of
life.
Deprescribing
refers
to
reducing
medications
after
consideration
therapeutic
goals,
benefits
risks,
medical
ethics.
The
objective
was
use
nominal
group
technique
(NGT)
generate
then
rank
factors
that
general
practitioners
(GPs),
nurses,
pharmacists
residents
or
their
representatives
perceive
most
important
when
deciding
whether
not
deprescribe
medications.Qualitative
research
using
NGT.Participants
were
invited
if
they
worked
with,
resided
LTCFs
across
metropolitan
regional
South
Australia.11
residents/representatives,
19
GPs,
12
nurses
14
participated
six
separate
groups.Individual
groups
residents/representatives
convened.
Using
NGT
each
ranked
perceived
be
deprescribe.
Then,
NGT,
the
prioritised
from
individual
discussed
by
a
multidisciplinary
comprised
resident
representatives,
pharmacists.No
two
had
same
priorities.
GPs
'evidence
for
deprescribing'
'communication
with
family/resident'
as
factors.
Nurses
'GP
receptivity
'nurses
ability
advocate
residents'
important.
Pharmacists
'clinical
appropriateness
therapy'
'identifying
goals
care'
Residents
'wellbeing
resident'
'continuity
nursing
staff'
'adequacy
medication
history'
important.While
different
factors,
contrasting
emerged.
Future
deprescribing
interventions
need
consider
similarities
differences
within
range
health
professionals.
JAMA Internal Medicine,
Journal Year:
2015,
Volume and Issue:
175(5), P. 827 - 827
Published: March 23, 2015
Inappropriate
polypharmacy,
especially
in
older
people,
imposes
a
substantial
burden
of
adverse
drug
events,
ill
health,
disability,
hospitalization,
and
even
death.
The
single
most
important
predictor
inappropriate
prescribing
risk
events
patients
is
the
number
prescribed
drugs.
Deprescribing
process
tapering
or
stopping
drugs,
aimed
at
minimizing
polypharmacy
improving
patient
outcomes.
Evidence
efficacy
for
deprescribing
emerging
from
randomized
trials
observational
studies.
A
protocol
proposed
comprising
5
steps:
(1)
ascertain
all
drugs
currently
taking
reasons
each
one;
(2)
consider
overall
drug-induced
harm
individual
determining
required
intensity
intervention;
(3)
assess
regard
to
its
current
future
benefit
potential
compared
with
potential;
(4)
prioritize
discontinuation
that
have
lowest
benefit-harm
ratio
likelihood
withdrawal
reactions
disease
rebound
syndromes;
(5)
implement
regimen
monitor
closely
improvement
outcomes
onset
effects.
Whereas
prescriber
barriers
exist,
resources
strategies
are
available
facilitate
deliberate
yet
judicious
deserve
wider
application.
British Journal of Clinical Pharmacology,
Journal Year:
2015,
Volume and Issue:
80(6), P. 1254 - 1268
Published: Aug. 7, 2015
The
aim
of
this
study
was
to
identify
what
definitions
have
been
published
for
the
term
'deprescribing',
and
determine
whether
a
unifying
definition
could
be
reached.
A
secondary
uncover
patterns
between
which
explain
any
variation.Systematic
literature
searches
were
performed
(earliest
records
February
2014)
in
MEDLINE,
Embase,
CINAHL,
Informit,
Scopus
Google
Scholar.
terms
deprescrib*
or
de-prescrib*
employed
as
keyword
search
all
fields.
Conventional
content
analysis
word
frequencies
used
characteristics
definitions.
Network
conducted
visualize
characteristic
distribution
across
authors
articles.Following
removal
duplicates,
231
articles
retrieved,
37
included
definition.
Eight
identified:
use
stop/withdraw/cease/discontinue
(35
articles),
aspect
prescribing
e.g.
long
therapy/inappropriate
medications
(n
=
18),
'process'
'structured'
13),
withdrawal
is
planned/supervised/judicious
11),
involving
multiple
steps
7),
includes
dose
reduction/substitution
desired
goals/outcomes
described
5)
involves
tapering
4).
did
not
reveal
responsible
variations
previously
definitions.These
findings
show
that
there
lack
consensus
on
deprescribing.
This
article
proposes
following
definition:
'Deprescribing
process
an
inappropriate
medication,
supervised
by
health
care
professional
with
goal
managing
polypharmacy
improving
outcomes'.
has
yet
externally
validated
further
work
required
develop
internationally
accepted
appropriate
British Journal of Clinical Pharmacology,
Journal Year:
2016,
Volume and Issue:
82(3), P. 583 - 623
Published: April 15, 2016
Deprescribing
is
a
suggested
intervention
to
reverse
the
potential
iatrogenic
harms
of
inappropriate
polypharmacy.
The
review
aimed
determine
whether
or
not
deprescribing
safe,
effective
and
feasible
modify
mortality
health
outcomes
in
older
adults.
JAMA,
Journal Year:
2018,
Volume and Issue:
320(18), P. 1889 - 1889
Published: Nov. 13, 2018
Importance
High
rates
of
inappropriate
prescribing
persist
among
older
adults
in
many
outpatient
settings,
increasing
the
risk
adverse
drug
events
and
drug-related
hospitalizations.
Objective
To
compare
effectiveness
a
consumer-targeted,
pharmacist-led
educational
intervention
vs
usual
care
on
discontinuation
medication
community-dwelling
adults.
Design,
Setting,
Participants
A
cluster
randomized
trial
(D-PRESCRIBE
[Developing
Pharmacist-Led
Research
to
Educate
Sensitize
Community
Residents
Inappropriate
Prescriptions
Burden
Elderly])
that
recruited
community
pharmacies
Quebec,
Canada,
from
February
2014
September
2017,
with
follow-up
until
2018,
randomly
allocated
them
or
control
groups.
Patients
included
were
aged
65
years
who
prescribed
1
4
Beers
Criteria
medications
(sedative-hypnotics,
first-generation
antihistamines,
glyburide,
nonsteroidal
anti-inflammatory
drugs),
69
pharmacies.
screened
enrolled
before
randomization.
Interventions
Pharmacists
group
encouraged
send
patients
an
deprescribing
brochure
parallel
sending
their
physicians
evidence-based
pharmaceutical
opinion
recommend
deprescribing.
The
pharmacists
provided
care.
Randomization
occurred
at
pharmacy
level,
34
(248
patients)
35
(241
patients).
Patients,
physicians,
pharmacists,
evaluators
blinded
outcome
assessment.
Main
Outcomes
Measures
Discontinuation
prescriptions
for
6
months,
ascertained
by
renewal
profiles.
Results
Among
489
(mean
age,
75
years;
66%
women),
437
(89%)
completed
(219
[88%]
218
[91%]
group).
At
106
248
(43%)
no
longer
filled
compared
29
241
(12%)
(risk
difference,
31%
[95%
CI,
23%
38%]).
In
group,
63
146
sedative-hypnotic
users
(43.2%)
14
155
(9.0%),
respectively
34%
25%
43%]);
19
62
glyburide
(30.6%)
8
58
(13.8%),
17%
2%
31%]);
33
(57.6%)
5
23
(21.7%),
35%
10%
55%])
(Pfor
interaction
=
.09).
Analysis
antihistamine
class
was
not
possible
because
small
sample
size
(n
12).
No
requiring
hospitalization
reported,
although
77
(38%)
attempted
taper
sedative-hypnotics
reported
withdrawal
symptoms.
Conclusions
Relevance
resulted
greater
after
months.
generalizability
these
findings
other
settings
requires
further
research.
PLoS ONE,
Journal Year:
2016,
Volume and Issue:
11(3), P. e0149984 - e0149984
Published: March 4, 2016
Objectives
Deprescribing
has
been
proposed
as
a
way
to
reduce
polypharmacy
in
frail
older
people.
We
aimed
the
number
of
medicines
consumed
by
people
living
residential
aged
care
facilities
(RACF).
Secondary
objectives
were
explore
effect
deprescribing
on
survival,
falls,
fractures,
hospital
admissions,
cognitive,
physical,
and
bowel
function,
quality
life,
sleep.
Methods
Ninety-five
over
65
years
four
RACF
rural
mid-west
Western
Australia
randomised
an
open
study.
The
intervention
group
(n
=
47)
received
intervention,
planned
cessation
non-beneficial
medicines.
control
48)
usual
care.
Participants
monitored
for
twelve
months
from
randomisation.
Primary
outcome
was
change
mean
unique
regular
All
outcomes
assessed
at
baseline,
six,
months.
Results
Study
participants
had
age
84.3±6.9
52%
female.
Intervention
9.6±5.0
9.5±3.6
baseline.
Of
348
targeted
(7.4±3.8
per
person,
78%
medicines),
207
(4.4±3.4
59%
medicines)
successfully
discontinued.
12
-1.9±4.1
+0.1±3.5
(estimated
difference
2.0±0.9,
95%CI
0.08,
3.8,
p
0.04).
Twelve
19
died
within
randomisation
(26%
versus
40%
mortality,
0.16,
HR
0.60,
0.30
1.22)
There
no
significant
differences
between
groups
other
secondary
outcomes.
main
limitations
this
study
design
small
participant
numbers.
Conclusions
reduced
with
adverse
effects
survival
or
clinical
Trial
Registration
Australian
New
Zealand
Clinical
Trials
Registry
ACTRN12611000370909
Journal of Clinical Pharmacy and Therapeutics,
Journal Year:
2016,
Volume and Issue:
41(2), P. 158 - 169
Published: March 17, 2016
What
is
known
and
objective
STOPP/START
are
explicit
screening
tools
that
identify
potentially
inappropriate
prescribing
in
older
adults.
Our
was
to
update
our
2013
systematic
review
showed
limited
evidence
of
impact,
using
new
from
randomized
controlled
trials
(RCTs)
assessing
clinical,
humanistic
economic
outcomes
Methods
We
performed
a
search
PubMed,
EMBASE,
CINAHL,
Web
Science
grey
literature
for
RCTs
published
English
since
the
previous
through
June
2014.
The
Cochrane
Risk
Bias
Tool
used.
meta-analysis
on
effect
STOPP
medication
(PIM)
rates
narrative
synthesis
other
outcomes.
Results
discussion
Four
(n
=
1925
adults)
four
countries
were
included,
reporting
both
acute
2)
long-term
care
patients.
Studies
differed
implementation.
Two
studies
judged
have
low
risk,
two
moderate-to-high
risk
bias
key
domains.
Meta-analysis
found
criteria
reduced
PIM
all
studies,
but
study
heterogeneity
(I2
86·7%)
prevented
calculation
meaningful
statistical
summary.
use
reduces
falls,
delirium
episodes,
hospital
length-of-stay,
visits
(primary
emergency)
costs,
no
improvements
quality
life
or
mortality.
conclusion
may
be
effective
improving
quality,
Additional
research
investigating
these
needed,
especially
frail
elderly
community-living
patients
receiving
primary
care.
PLoS ONE,
Journal Year:
2016,
Volume and Issue:
11(4), P. e0151066 - e0151066
Published: April 19, 2016
Aims
Deprescribing
is
the
process
of
reducing
or
discontinuing
medicines
that
are
unnecessary
deemed
to
be
harmful.
We
aimed
investigate
general
practitioner
(GP)
perceived
challenges
deprescribing
in
residential
care
and
possible
enablers
support
GPs
implement
deprescribing.
Methods
A
qualitative
study
was
undertaken
using
semi-structured,
face-to-face
interviews
from
two
cities
New
Zealand
a
purpose-developed
pilot-tested
interview
schedule.
Interviews
were
recorded
with
permission
transcribed
verbatim.
Transcripts
read
re-read
themes
identified
iterative
building
coding
list
until
all
data
accounted
for.
continued
saturation
ideas
occurred.
Analysis
carried
out
assistance
Theoretical
Domains
Framework
(TDF)
constant
comparison
techniques.
Several
identified.
Challenges
determined
based
on
participants'
answers.
Results
Ten
agreed
participate.
Four
define
issues
around
prescribing
for
older
people,
GPs'
perspectives.
Theme
1,
'recognition
problem',
discusses
difficulties
involved
people.
2
outlines
behaviour
change
factors
relevant
problem.
drawn
these
summarised
3
under
three
major
headings;
'prescribing
factors',
'social
influences'
'policy
processes'.
enablers,
opinions
professional
experience
GPs,
retrieved
4.
Conclusion
The
laced
many
GPs.
uncertainty
research
evidence
people
social
such
as
specialists'
nurses'
influences
among
encompassed
awareness
knowledge,
improvement
communication
between
multiple
prescribers,
adequate
reimbursement
pharmacists
being
multidisciplinary
team.