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Screening procedures are standardized methods used to identify individuals in a population who may have a disease or condition, often before symptoms appear. They aim to reduce morbidity and mortality by enabling early diagnosis and treatment. Screening programs may be population-based or targeted to higher-risk groups and rely on validated tests with known sensitivity and specificity.

A typical screening process includes defining eligibility criteria, obtaining informed consent, collecting relevant risk information, performing

Common screening modalities include imaging, laboratory tests, or simple clinical measures. Examples in health care include

Key considerations involve balancing sensitivity and specificity to minimize false positives and negatives, addressing overdiagnosis, and

the
screening
test,
and
communicating
results.
Positive
or
equivocal
results
usually
trigger
follow-up
diagnostic
evaluation
and
treatment
planning.
Data
management,
quality
control,
and
privacy
protections
are
integral.
cancer
screening
programs
(such
as
mammography
or
colon
cancer
screening),
as
well
as
screening
for
cardiovascular
risk,
infectious
diseases,
and
metabolic
abnormalities.
The
choice
of
tests
reflects
evidence
on
benefits,
harms,
and
cost-effectiveness,
and
guidelines
emphasize
informed
participation
and
equity
of
access.
ensuring
appropriate
follow-up.
Ethical
and
regulatory
aspects
cover
voluntary
participation,
informed
consent,
data
privacy,
and
safeguarding
vulnerable
populations.
Limitations
should
be
acknowledged:
screening
cannot
diagnose
disease;
abnormal
results
require
confirmatory
testing;
not
all
screenings
reduce
mortality,
and
some
may
lead
to
unnecessary
interventions.
Continuous
evaluation
and
program
adjustment
are
essential
to
maintain
effectiveness
and
safety.