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possible
ACS before and after the introduction
of a
lower di
nted with possible
ACS before and after the introduction
of a
lower diagnostic threshold (from 0.20
ng/ml
to 0.05 ng/ml) for myocard
ction of a
lower diagnostic threshold (from 0.20
ng/ml
to 0.05 ng/ml) for myocardial
infarction (MI)
using a high-sensitivity troponin
assay with
a low coefficient of variabili
al infarction (MI)
using a high-sensitivity troponin
assay with
a low coefficient of variability
(<10%).1 The
>1,000 patients who presented with
possible
ACS before and after the introduction
of a
lower diagnostic threshold (from 0.20
ng/ml
to 0.05 ng/ml) for myocardial
infarction (MI)
using a high-sensitivity troponin
assay with
a low coefficient of variability
(<10%).1 The
>1,000 patients who presented with
possible
ACS before and after the introduction
of a
lower diagnostic threshold (from 0.20
ng/ml
to 0.05 ng/ml) for myocardial
infarction (MI)
using a high-sensitivity troponin
assay with
a low coefficient of variability
(<10%).1
>1,000 patients who presented with
possible
ACS before and after the introduction
of a
lower diagnostic threshold (from 0.20
ng/ml
to 0.05 ng/ml) for myocardial
infarction (MI)
using a high-sensitivity troponin
assay with
a low coefficient of variability
(<10%).1 The
>1,000 patients who presented with
possible
ACS before and after the introduction
of a
lower diagnostic threshold (from 0.20
ng/ml
to 0.05 ng/ml) for myocardial
infarction (MI)
using a high-sensitivity troponin
assay with
a low coefficient of variability
(<10%).1 The
>1,000 patients who presented with
possible
ACS before and after the introduction
of a
lower diagnostic threshold (from 0.20
ng/ml
to 0.05 ng/ml) for myocardial
infarction (MI)