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2005 Syndromic Surveillance 1
Estimating the Expected Warning Time of Outbreak-Detection AlgorithmsYanna Shen, Weng-Keen Wong,
Gregory F. Cooper
RODS Laboratory, Center of Biomedical Informatics, University of Pittsburgh
2005 Syndromic Surveillance 2
Overview
Objective Background Methods Experimental Results Conclusions Future Work
2005 Syndromic Surveillance 3
Objective
A new measure for evaluating alerting algorithms, which is called Expected Warning Time (EWT).
It is a generalization of the standard AMOC curve.
2005 Syndromic Surveillance 4
Why Useful?
Can compare expected clinician detection time to expected computer-based algorithm detection time
Can provide a promising new approach for optimizing and comparing outbreak detection algorithms
2005 Syndromic Surveillance 5
Background
Maximum meaningful detection timeMaximum meaningful WT
Time
Warning Time Computer Detection Time
False Alerts (in red)
Incubation
Time
Release occurs
Computers raise alert
Clinicians detect outbreak
Last outbreak case appears
… … …hit
hithit
hit
2005 Syndromic Surveillance 6
Model
A simple model of clinician outbreak detection Assumes that
People with disease D are diagnosed independently of each other.
The probability of a person with disease D being diagnosed is constant (p).
2005 Syndromic Surveillance 7
Equation
Definitions: p – probability that a person with D is diagnosed as
having D upon presentation with that disease time(i) – maps patient case i to the time at which that
patient presented with D to clinicians M – total # of patient cases with D t – time at which the alerting score first exceeds a
given threshold
M
i
iM pptitimeptMtimetEWT1
11,0max1,0max
2005 Syndromic Surveillance 8
Equation
0
tMtime Mp1 11 ippx x+
WT if clinicians
never detect the outbreak
Probability that clinicians
will never detect the outbreak
WT if clinicians first
detect the outbreak on the ith case
Probability that clinicians will
detect the outbreak on the
ith case
0
titime
M
i 1
M
i
iM pptitimeptMtimetEWT1
11,0max1,0max
2005 Syndromic Surveillance 9
Experiment Setup
Apply PANDA to simulated cases of inhalational anthrax
For various value of p, derive EWT for PANDA
2005 Syndromic Surveillance 10
PANDA
An outbreak detection system Uses causal Bayesian networks to model spatio-
temporal patterns of a non-contagious disease in a population (Cooper, 2004)
Contains a model to detect inhalational anthrax
2005 Syndromic Surveillance 11
BARD
BARD simulator produces the simulated cases of anthrax.
It models the effects of an outdoor airborne anthrax release using the Gaussian plume model of atmospheric dispersion and a model of inhalational anthrax (Hogan, 2004).
2005 Syndromic Surveillance 12
Performance of Clinicians
p P(CD)ECDT (hours)
0.001 0.992 167.9
0.005 0.999 104.1
0.01 0.9999 88.6
0.05 0.99999 64.5
1 1 0
p – Clinician detection proficiency
P(CD) – Probability that clinicians will detect the outbreak at all
ECDT – Expected clinician detection time given that clinicians detect the outbreak
2005 Syndromic Surveillance 13
0
20
40
60
80
100
120
140
160
180
0 100 200 300 400 500 600 700
False Alerts Per Month
Exp
ecte
d W
arn
ing
Tim
e (H
ou
rs)
p = 0.001
p = 0.005
p = 0.01
p = 0.05
p = 1
Experimental Results
p increases, EWT decreases p = 1, EWT = 0
?
2005 Syndromic Surveillance 14
Experimental Results
Clinician-detection-
proficiency (p)
Expected Warning Time
(EWT)
0.001 76 hours
0.005 13 hours
0.01 5 hours
0.05 34 minutes
1 0
False alert rate = 1 per month
If and false alert rate = 1 per month, then EWT minutes.
05.0p 34
0
10
20
30
40
50
60
70
80
90
100
1 3 5 7 9 11
False Alerts Per Month
Exp
ecte
d W
arn
ing
Tim
e (H
ou
rs)
p = 0.001
p = 0.005
p = 0.01
p = 0.05
p = 1
2005 Syndromic Surveillance 15
Conclusions
The Expected Warning Time (EWT) is a useful concept for evaluating outbreak-detection algorithms.
We illustrated the general idea of EWT using a simple model of clinician detection and simulated cases of inhalational anthrax.
Our example analysis suggests that PANDA is most helpful when clinicians’ detection proficiency < 5%.
2005 Syndromic Surveillance 16
Future Work
Extend the model: Instead of a constant (p), use the function p(t),
where t is time Develop and apply more disease-specific models
of clinician detection (please see the poster by Christina Adamou)
2005 Syndromic Surveillance 17
Acknowledgements
This research was supported by grants from the National Science Foundation (IIS-0325581), the Department of Homeland Security (F30602-01-2-0550), and the Pennsylvania Department of Health (ME-01-737).
We thank members of the Bayesian Biosurveillance Project for helpful comments.