Clinical Psychology Review,
Journal Year:
2021,
Volume and Issue:
91, P. 102111 - 102111
Published: Dec. 11, 2021
Treatments
for
depression
have
improved,
and
their
availability
has
markedly
increased
since
the
1980s.
Mysteriously
general
population
prevalence
of
not
decreased.
This
"treatment-prevalence
paradox"
(TPP)
raises
fundamental
questions
about
diagnosis
treatment
depression.
We
propose
evaluate
seven
explanations
TPP.
First,
two
assume
that
improved
more
widely
available
treatments
reduced
prevalence,
but
reduction
been
offset
by
an
increase
in:
1)
misdiagnosing
distress
as
depression,
yielding
"false
positive"
diagnoses;
or
2)
actual
in
incidence.
Second,
remaining
five
decreased,
suggest
that:
3)
are
less
efficacious
4)
enduring
than
literature
suggests;
5)
trial
efficacy
doesn't
generalize
to
real-world
settings;
6)
population-level
impact
differs
chronic-recurrent
versus
non-recurrent
cases;
7)
some
iatrogenic
consequences.
Any
these
could
undermine
on
thereby
helping
explain
Our
analysis
reveals
there
is
little
evidence
incidence
a
result
error
fact
(Explanations
1
2),
strong
(a)
published
overestimates
short-
long-term
efficacy,
(b)
considerably
effective
deployed
"real
world"
settings,
(c)
substantially
cases
relative
cases.
Collectively,
a-c
likely
account
most
Lastly,
research
exists
effects
current
(Explanation
7),
further
exploration
critical.
BMC Psychiatry,
Journal Year:
2017,
Volume and Issue:
17(1)
Published: Feb. 8, 2017
The
evidence
on
selective
serotonin
reuptake
inhibitors
(SSRIs)
for
major
depressive
disorder
is
unclear.
Our
objective
was
to
conduct
a
systematic
review
assessing
the
effects
of
SSRIs
versus
placebo,
‘active’
or
no
intervention
in
adult
participants
with
disorder.
We
searched
eligible
randomised
clinical
trials
Cochrane
Library’s
CENTRAL,
PubMed,
EMBASE,
PsycLIT,
PsycINFO,
Science
Citation
Index
Expanded,
trial
registers
Europe
and
USA,
websites
pharmaceutical
companies,
U.S.
Food
Drug
Administration
(FDA),
European
Medicines
Agency
until
January
2016.
All
data
were
extracted
by
at
least
two
independent
investigators.
used
methodology,
Trial
Sequential
Analysis,
calculation
Bayes
factor.
An
eight-step
procedure
followed
assess
if
thresholds
statistical
significance
crossed.
Primary
outcomes
reduction
symptoms,
remission,
adverse
events.
Secondary
suicides,
suicide
attempts,
ideation,
quality
life.
A
total
131
placebo-controlled
enrolling
27,422
included.
None
placebo
as
control
intervention.
had
high
risk
bias.
significantly
reduced
Hamilton
Depression
Rating
Scale
(HDRS)
end
treatment
(mean
difference
−1.94
HDRS
points;
95%
CI
−2.50
−1.37;
P
<
0.00001;
49
trials;
Analysis-adjusted
−2.70
−1.18);
factor
below
predefined
threshold
(2.01*10−23).
effect
estimate,
however,
our
3
points.
decreased
remission
(RR
0.88;
0.84
0.91;
34
Analysis
adjusted
0.83
0.92);
(1426.81)
did
not
confirm
effect).
increased
risks
serious
events
(OR
1.37;
1.08
1.75;
=
0.009;
44
1.03
1.89).
This
corresponds
31/1000
SSRI
will
experience
event
compared
22/1000
participants.
also
number
non-serious
There
almost
suicidal
behaviour,
life,
long-term
effects.
might
have
statistically
significant
but
all
bias
seems
questionable.
increase
both
potential
small
beneficial
seem
be
outweighed
harmful
PROSPERO
CRD42013004420.
Alcohol and Alcoholism,
Journal Year:
2013,
Volume and Issue:
48(5), P. 570 - 578
Published: July 19, 2013
Aims:
The
aim
of
the
study
was
to
investigate
efficacy
and
safety
as-needed
use
nalmefene
18
mg
versus
placebo
in
reducing
alcohol
consumption
patients
who
did
not
reduce
their
after
an
initial
assessment,
i.e.
pooled
subgroup
with
at
least
a
high
drinking
risk
level
(men:
>60
g/day;
women:
>40
g/day)
both
screening
randomization
from
two
randomized
controlled
6-month
studies
ESENSE
1
(NCT00811720)
2
(NCT00812461).
Methods:
Nalmefene
were
taken
on
basis.
All
also
received
motivational
adherence-enhancing
intervention
(BRENDA).
co-primary
outcomes
number
heavy
days
(HDDs)
mean
total
(g/day)
Month
6
measured
using
Timeline
Follow-back
method.
Additionally,
data
clinical
improvement,
liver
function
collected
throughout
study.
Results:
population
consisted
667
patients:
n
=
332;
335.
There
superior
effect
compared
HDDs
[treatment
difference:
−3.2
(95%
CI:
−4.8;
−1.6);
P
<
0.0001]
−14.3
g/day
(−20.8;
−7.8);
6.
Improvements
status
parameters
greater
group
group.
Adverse
events
adverse
leading
dropout
more
common
than
placebo.
Conclusion:
As-needed
efficacious
randomization,
this
larger
population.
World Psychiatry,
Journal Year:
2022,
Volume and Issue:
21(1), P. 133 - 145
Published: Jan. 11, 2022
Mental
disorders
represent
a
worldwide
public
health
concern.
Psychotherapies
and
pharmacotherapies
are
recommended
as
first
line
treatments.
However,
evidence
has
emerged
that
their
efficacy
may
be
overestimated,
due
to
variety
of
shortcomings
in
clinical
trials
(e.g.,
publication
bias,
weak
control
conditions
such
waiting
list).
We
performed
an
umbrella
review
recent
meta-analyses
randomized
controlled
(RCTs)
psychotherapies
for
the
main
mental
adults.
selected
formally
assessed
risk
bias
or
quality
studies,
excluded
comparators,
used
effect
sizes
target
symptoms
primary
outcome.
searched
PubMed
PsycINFO
individual
records
Cochrane
Library
published
between
January
2014
March
2021
comparing
with
placebo
treatment-as-usual
(TAU),
vs.
head-to-head,
combination
psychotherapy
pharmacotherapy
either
monotherapy.
One
hundred
two
meta-analyses,
encompassing
3,782
RCTs
650,514
patients,
were
included,
covering
depressive
disorders,
anxiety
post-traumatic
stress
disorder,
obsessive-compulsive
somatoform
eating
attention-deficit/hyperactivity
substance
use
insomnia,
schizophrenia
spectrum
bipolar
disorder.
Across
treatments,
majority
small.
A
random
meta-analytic
evaluation
reported
by
largest
per
disorder
yielded
standardized
mean
difference
(SMD)
0.34
(95%
CI:
0.26-0.42)
0.36
0.32-0.41)
compared
TAU.
The
SMD
head-to-head
comparisons
was
0.11
-0.05
0.26).
combined
treatment
monotherapy
0.31
0.19-0.44).
Risk
often
high.
After
more
than
half
century
research,
thousands
millions
invested
funds,
limited,
suggesting
ceiling
research
presently
conducted.
paradigm
shift
seems
required
achieve
further
progress.
JAMA Psychiatry,
Journal Year:
2014,
Volume and Issue:
71(6), P. 706 - 706
Published: April 30, 2014
Importance
There
is
debate
about
the
effectiveness
of
psychiatric
treatments
and
whether
pharmacotherapy
or
psychotherapy
should
be
primarily
used.
Objectives
To
perform
a
systematic
overview
on
efficacy
pharmacotherapies
psychotherapies
for
major
disorders
to
compare
quality
trials.
Evidence
Review
We
searched
MEDLINE,
EMBASE,
PsycINFO,
Cochrane
Library
(April
2012,
with
no
time
language
limit)
reviews
vs
placebo,
psychotherapy,
their
combination
either
modality
alone.
Two
reviewers
independently
selected
meta-analyses
extracted
effect
sizes.
assessed
individual
trials
included
in
risk
bias
tool.
Findings
The
search
yielded
45
233
results.
61
21
disorders,
which
contained
852
137
126
participants.
mean
size
was
medium
(mean,
0.50;
95%
CI,
0.41-0.59).
Effect
sizes
placebo
tended
higher
than
those
medication,
but
direct
comparisons,
albeit
usually
based
few
trials,
did
not
reveal
consistent
differences.
Individual
were
more
likely
have
large
sample
sizes,
blinding,
control
groups,
intention-to-treat
analyses.
In
contrast,
had
lower
dropout
rates
provided
follow-up
data.
studies,
wait-list
designs
showed
larger
effects
comparisons
placebo.
Conclusions
Relevance
Many
are
effective,
there
lot
room
improvement.
Because
multiple
differences
methods
used
indirect
compared
treatment
problematic.
Well-designed
scarce,
need
public
funding.
patients
often
benefit
from
both
forms
therapy,
research
also
focus
how
modalities
can
best
combined
maximize
synergy
rather
use
one
over
other.
New England Journal of Medicine,
Journal Year:
2020,
Volume and Issue:
383(11), P. 1050 - 1056
Published: Sept. 9, 2020
Amphetamines
and
methylphenidate
and,
less
often,
nonstimulants
(atomoxetine,
clonidine,
guanfacine)
are
used
to
treat
ADHD.
Inattentiveness
restlessness
improved
more
than
quality-of-life
measures
in
short-term
trials.
The Journal of Nervous and Mental Disease,
Journal Year:
2015,
Volume and Issue:
203(5), P. 310 - 318
Published: April 28, 2015
Early
intervention
for
potentially
serious
disorder
is
a
fundamental
feature
of
healthcare
across
the
spectrum
physical
illness.
It
has
been
major
factor
in
reductions
morbidity
and
mortality
that
have
achieved
some
non-communicable
diseases,
notably
cancer
cardiovascular
disease.
Over
past
two
decades,
an
international
collaborative
effort
mounted
to
build
evidence
capacity
early
psychotic
disorders,
schizophrenia,
where
so
long
deep
pessimism
had
reigned.
The
origins
rapid
development
psychosis
are
described
from
personal
Australian
perspective.
This
uniquely
evidence-informed,
evidence-building
cost-effective
reform
provides
blueprint
launch
pad
radically
change
wider
landscape
mental
health
care
dissolve
many
barriers
constrained
progress
long.