Title: GIS using in Epidemiology and Risk Assessment
1GIS using in Epidemiology and Risk Assessment
2Content
- GIS and Epidemiology
- GIS and Risk Assessment
- Examples
3John Snow (1813-1858)
- GP based in Soho section of London
- Insight into communication of cholera by water
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17Health Risk Assessment- Modified from Health
Risk Assessment, Dr. Bill Hartley
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
18Basic Concepts and Definitions
- Risk Assessment
- The scientific estimation (qualitative or
quantitative) of hazard which is obtained by
combining the results of an exposure assessment
with the results of the toxicity assessment for
the subject chemical.
Modified from Health Risk Assessment, Dr. Bill
Hartley
19Basic Concepts and Definitions
- Risk Management
- The judgment and analysis that combine the
scientific results of a risk assessment with
economic, political, legal and social factors to
produce a decision about environmental action.
20Basic Concepts and Definitions
- Risk Communication
- Communication of risk assessment/management
information to the public, reporters, and
state/local officials.
21What is Risk?
- the likelihood of injury, disease, or death
- What is Environmental Risk?
- The likelihood of injury, disease, or death
resulting from human exposure to a potential
environmental hazard
22Comparative Risks of Death
23Comparative Risks Pesticides
24Risk
- Subjective
- Not a risk-free world
- Uncertainty complexity
- Probabilistic
- Benchmarks
- Product of probability consequence
25Risk Assessment
dose-response assessment
hazard identification
risk characterization
exposure assessment
26Risk Management and Risk Assessment Working
Together
dose-response assessment
regulatory decision
hazard identification
risk characterization
control options
exposure assessment
non-risk analyses
27Non-risk Analyses
economics
regulatory decision
risk characterization
politics
control options
statutory legal considerations
non-risk analyses
social factors
28Risk Management and Risk Assessment working
together
Risk Management
dose-response assessment
hazard identification
regulatory decision
risk characterization
exposure assessment
control options
non-risk analyses
29The Components of Risk Assessment
- Hazard Identification
- Dose-Response Evaluation
- Human Exposure Evaluation
- Risk Characterization
30Component 1 Hazard Identification
?
Effect
31Human Evidence
- Sufficient
- Limited
- Inadequate
- No Data
- No evidence
32Advantages Uncertainties of Animal Data
Dolly
33Weigh All the Evidence
Human Evidence
34Hazard Identification
- Review analyze toxicity data
- Weigh the evidence that a substance causes
various toxic effects - Evaluate whether toxic effects in one setting
will occur in other settings
35Component 2 Dose-Response Assessment
?
Dose
Response
36Dose-Response
- Dancing with proper limitations is a salutary
exercise, but when violent and long continued in
a crowded room it is extremely pernicious, and
has hurried many young people to the grave. - A.
Murray, M.D. 1826
37Sources of Toxicity Data
- Human Studies
- Case reports
- Epidemiological studies
- retrospective
- prospective
- case-control
- Animal Studies
- General toxicity studies
- acute sub-chronic
- sub-acute chronic
- Specialized toxicity studies
- teratology
- genotoxicity
- developmental
- male/female reproductive
- cancer
- endocrine disruption
38Animal Data
Approximate Oral LD50 in rats for a group of
well-known chemicals Chemical
LD50(mg/kg) Sucrose (table sugar) 29,700 Ethyl
alcohol 14,000 Sodium chloride 3,000
(table salt) Vitamin A 2,000 Aspirin
1,000 Chloroform 800 Copper Sulfate
300 Caffeine 192 Phenobarbital
162 DDT 113 Nicotine 53
39Dose-Response Evaluation
Cancer
Organ Damage
No effect
40Dose-Response Evaluation
Threshold-Systemic Toxicity (Non-cancer)
responding
MFO Slim
Fatty Change
Decreased Dye Clearance
Mortality
Dose (mg/kg)
mixed function oxidase
41Dose-Response Evaluation
Non-threshold--Cancer
Performed to estimate the incidence of the
adverse effect as a function of the magnitude of
human exposure to a substance
42Dose-Response Curve
Non-Threshold--Cancer
43Dose-Response Curve
Non-Threshold--Cancer
Observable range
Response
Range of inference
0
Dose
44Dose-Response Evaluation
- All substances are poisons there is none which
is not a poison. The right dose differentiates a
poison and a remedy. Paracelsus
(1495-1541)
45Dose-Two types of measurement
- Type I
- Measurement of the amount of the substance in the
medium (air, diet, etc.) in which it is present
or administered. - NOT DOSE
- Type II
- Measurement of the amount absorbed by the
subject, whether human or animal. - DOSE
46Dose
- Example
- Chemical HC-BAD is present in drinking water at a
concentration of 10mg/L (Type I measurement) - What is the dose (DAILY) for an adult (Type II)?
- Exposure Assumptions Body weight 70kg (150
lbs) - Water consumption 2L water/day
by convention
or .29mg/kg ? day
47Component 3 Exposure Assessment
Agent
People
48Exposure Issues Assumptions
- Extent frequency of human exposure
- how much?
- how often?
- how certain?
- Number of people exposed
- Degree of absorption by various routes of
exposure - Use of average or typical individual
- Use of high risk groups
49Routes of Exposure
- Ingestion (Drinking, Food)
- Skin Absorption (Water, Soil)
- Inhalation
- Total Dose is equal to the sum of the doses from
the above routes ( pathways)
50Estimation of exposure levels
- Direct
- Measure the actual concentration of chemical in
the air, water or food used by an individual. - Measure the actual amount of air, water or food
used by the individual. - Calculate the actual dose to the individual.
51Estimation of exposure levels
- Reconstructive
- Measure the level of the chemical, its
metabolites, or some other chemical-specific
change (biomarker) in the body. - Based on toxicokinectic models, calculate the
dose to the individual from the level of the
biomarker.
52Estimation of exposure levels
- Predictive
- Measure or calculate the concentration of
chemical in environmental media around the
source. - Estimate human contact with the media.
- Estimate the resulting dose to the average person.
53Component 4 Risk Characterization
Hazard Identification
Risk Characterization
Dose-Response
Exposure
54Risk Assessment Issues
Hazard Animal data Identification
Epidemiological Studies
Weight of Evidence Dose-Response
Extrapolation from high to low Assessment
dose Extrapolation from
animals to humans Exposure
Assessment Modeling vs. monitoring vs.
biological monitoring Risk Characterization
Qualitative or quantitative
55Quantitative Analysis of Cancer Risk
- In Air (mg/kg-day)-1 -gt ? (mg/m3)-1
- -gt Unit from (kg-day/mg) to (m3/mg)
- Exposure Assumption (adult only)
- Respiratory rate 20 m3/day
- Body weight 70 kg
- Absorption rate 100
56Quantitative Analysis of Cancer Risk
- In Drinking water (mg/kg-day)-1 -gt ? (ug/L)-1
- -gt Unit from (kg-day/mg) to (L/ug)
- Exposure Assumption (adult only)
- Drinking water 2 L/day
- Body weight 70 kg
- Absorption rate 100
57Risk Analysis (Systematic and Cancer)
- Step 1. Dose Calculation
- Child and Adult
- Step 2. Margin of Exposure (MOE) (Threshold
model NOAEL/LOAEL with UFs and MF) - Children and Adults
- Step 3. Cancer risk (No child cancer model yet,
Non-threshold model currently) - Cancer Potency Factor (q1) dose (adult only)
- Cancer Risk (no unit) (mg/kg-day)-1
(mg/kg-day) - Unit Risk Concentration
- Cancer Risk (no unit) (mg/m3)-1 (mg/m3) (air)
- or (ug/L)-1 (ug/L) (drinking water)
- (General speaking, acceptable cancer risk 10-4
10-6) - Step 4. Size of population (estimate how many
excess cancer cases will be caused by exposure to
chemical in drinking water and/or air
(life-time)) - Step 5. Fact Sheet for public (systematic and
cancer)
58Key Variables in Exposure Assessment
Visitors/Trespassers
Current and Future Residents
Workers
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Sensitive Groups
59Key Variables in Exposure Assessment
- Location
- On-site
- Off-site
Outside
Inside
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
60Key Variables in Exposure Assessment
Food
Air
Soil/sediments
House dust
Surface Ground Water
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61Key Variables in Exposure Assessment
- Duration
- acute
- sub-chronic
- chronic
- lifetime
- Exposure Route
- oral
- inhalation
- dermal
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
62Estimation of Exposure Levels
- Direct
- Measure the actual concentration of chemical in
the air, water or food used by an individual. - Measure the actual amount of air, water or food
used by the individual. - Calculate the actual dose to the individual.
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
63Estimation of Exposure Levels
- Reconstructive
- Measure the level of the chemical, its
metabolites, or some other chemical-specific
change (biomarker) in the body. - Based on Toxicokinetic models, calculate the dose
to the individual from the level of the biomarker.
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
64Estimation of Exposure Levels
- Predictive
- Measure or calculate the concentration of
chemical in environmental media around the
source. - Estimate human contact with the media.
- Estimate the resulting dose to the average person.
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
65Identify Major Uncertainty Factors in Risk
Estimates
- Assumptions variables that contribute most to
uncertainty in risk estimates - Site specific factors monitoring data quality,
likelihood of exposure scenarios occurring,
chemicals not included in risk estimates, key
assumptions for contaminant transport fate
models - Toxicity values weight of evidence, adjustment
factors, dose additivity/extrapolation, less than
lifetime cancer risk estimates
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
66Evaluate Uncertainty Factors
- Identify data gaps default values
- Provide distributions for parameter values, where
possible - Statistical treatment of uncertainty possible in
very few situations - A qualitative evaluation of uncertainty factors
is typical - Describe impacts (bias) on risk estimates
(direction order of magnitude) - Qualify risk estimates for risk management
decisions
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ENHS 762 Health Risk Assessment, Dr. Bill Hartley
67GIS and Risk AssessmentA Fruitful Combination
- Results from evaluations of human health risks
associated with environmental contamination are
traditionally presented non-spatially. - Because of the expense associated with sampling
and analysis, samples of environmental
contaminants are often taken from relatively few
spatial locations, such as test wells. - Moreover, in many cases, the environmental
gradient of contamination is known to be
anisotropic due to directional forces like
groundwater flow or wind. - In an effort to avoid presenting misleading
information, non-spatial tabular reporting of
single values, such as increased incidence of
human cancer, has become the widely-accepted
convention for communication of human health risk
results.
68GIS and Risk AssessmentA Fruitful Combination
- Ultimately, interpolation of contaminant data
which are rare in space and time is necessary for
full evaluation of human risks. - We present an alternative spatial format for the
communication of contamination and risk an array
of maps which we call a 'Map Spreadsheet.' The
Map Spreadsheet is analogous to a data
spreadsheet, except that each cell is a spatially
co-registered interpolated map of contaminant
concentration. - Columns and rows in the Map Spreadsheet could
represent alternative ingestion pathways,
chemical classes and/or species of contaminants,
or years through time. - The viewer of a Map Spreadsheet obtains a
perspective of the combined risk from exposure to
multiple contaminants, as well as an idea of the
heterogeneity of contamination across space.
69The Spatial Nature of Risk
- Environmental risk professionals typically report
risk as single values or tables of values. Often,
separate numbers are calculated and reported for
different pathways, each of which are considered
independently. - Yet it is clear that risk assessments have an
important spatial component. Risk evaluations are
generated by reference to specific environmental
data collected from specific locations. - We argue that the presentation of risk benefits
greatly from a spatial approach, and that the
marriage of GIS and risk analysis is a sensible
one. Although difficulties and problems certainly
exist in the spatial analysis of risk, we suggest
that it is a better - and more conservative -
strategy to openly present these details and
assumptions spatially rather than allowing them
to remain implicit. Risk professionals will not
mislead by presenting maps - they mislead by not
presenting maps.
70Maps with Icons
- This series of maps shows the spatial
relationships bewteen chemical concentrations in
a series of test wells and a manufacturing
facility, a series of buried pipelines, and a
group of holding ponds. Concentration data are
presented spatially for 1,1-dichloroethene,
trichloroethene, and vinyl chloride in this
K-1420 industrial area. Although we chose to plot
each contaminant on separate maps, the icons
could have been combined on a single map, and
differentiated by the shape of the icons used. - Only slightly more sophisticated is the plotting
not of simple contaminant concentrations, but of
risk due to the contamination at that
concentration. In this map of total human health
risk due to vinyl chloride contamination, human
risk values calculated for the water ingestion
pathway are mapped directly. Mapped units are in
terms of likelihood of excess'' human cancers.
71Map and Chart Hybrids
- The combination of charts with maps allows for
the inclusion of additional information regarding
contaminants. The simple maps above presented a
static snapshot of contamination no information
was included about the way that contaminant
concentrations changed through time (figure
left). - All maps to this point have shown total
contamination or risk. By plotting size-dependent
pie diagrams at sampled locations, we can
communicate not only the total but the proportion
of total contamination or risk contributed by
each of several contaminants. This map of the
X-10 area shows proportional human health risk by
all pathways posed by test well concentrations.
The size of each pie reflects total relative
human health risk in terms of increased incidence
of human cancer, while the color and proportion
of each pie slice indicate each contaminants'
contributions. The locations of each data point
are maintained, so that the spatial distribution
of the test wells and their proximity to
prominent features is obvious. (figure right)
72GIS and Risk AssessmentA Fruitful Combination (
CONCLUSIONS )
- It is clearly not sufficient to report risk
non-spatially. Risk is an inherently spatial
phenomenon. A risk map should be considered the
ultimate product of any risk investigation, and
should be the first resource sought for any risk
decision or evaluation. GIS techniques can be
central to these important and critical processes
of risk identification, quantification, and
evaluation.
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105Case Study I An investigation of the association
between traffic exposure and thediagnosis of
asthma in children
- Gordian ME, Haneuse S, Wakefield J.
- J Expo Sci Environ Epidemiol. 2006
Jan16(1)49-55. - ??????? ??
- ??????
106Introduction
- Several studies have indicated that children who
live near traffic have greater symptoms and
increased hospitalizations for asthma (Edwards et
al., 1994, Brauer et al., 2002). - The severity of asthma symptoms is also
associated with ambient benzene concentrations
(Thompson et al., 2001 Delfino et al., 2003).
107Objective
- This paper reports the results of a study that
investigated the association between a
traffic-density related measure of exposure and
the prevalence of diagnosed asthma among school
children5 to 7 years of age in Anchorage, Alaska
(an area with high ambient benzene
concentrations), adjusting for gender, parental
asthma, a smoker in the home, and family income.
108Exposure Assessment
- Traffic counts on roadways were obtained from the
Alaska Department of Transportation and the city
Planning Office. - We used the GIS to map the coordinates of the
nearest cross streets to each childs home. - We calculated a traffic exposure variable by
drawing a 100-m buffer zone around each
intersection of interest.
109Materials Methods
- All the road segments that fell within the 100-m
buffer were multiplied by the traffic count of
that road at that point and then summed to create
a measure of traffic exposure. - A total of 1106 surveys were received. The
overall return rate by school for surveys was
75, with a range of 5492 across schools.
110Statistical Analysis
- We used logistic regression to model the lifetime
probability of being diagnosed with asthma, as a
function of the traffic count in vehicle-meters
(vm), and additional confounder and precision
variables that were known to be associated with
diagnosis of asthma.
111Conclusion
- We have evidence of a weak association between
asthma prevalence in children 57 years of age
exposed to traffic in an area where the primary
air pollutants are VOCs and coarse fraction
particulate matter(2.5µm lt PM lt 10µm). - Children without genetic predisposition to asthma
appear to be most at risk. - More epidemiological studies are needed regarding
the effects of traffic pollutants, especially
VOCs.
112Case Study II Cancer Risk Near a Polluted River
in Finland
- Verkasalo PK, Kokki E, Pukkala E, Vartiainen T,
Kiviranta H, Penttinen A, Pekkanen J. - Environ Health Perspect. 2004112(9)1026-31.
- ??????? ??
- ??????
113PCDD/Fs
- The surface sediment levels of PCDD/Fs are
between 0.5 and 350 ng/g in dry weight as toxic
equivalents and thus are among the highest
sediment levels observed worldwide. - The most toxic congener, 2,3,7,8-tetrachlorodibenz
o-p-dioxin (2,3,7,8-TCDD), has also been
classified by the International Agency for
Research on Cancer (IARC) as carcinogenic to
humans in 1997. - Overall, the strongest epidemiologic evidence for
the carcinogenicity of 2,3,7,8-TCDD is for all
cancers combined rather than for any specific
site.
114- In this study we investigated cancer risk in
people living near the River Kymijoki (lt 20.0
km). - We assumed that PCDD/Fs are mobilized from the
river surface sediments and reach nearby
residents via the food chain (e.g., by
consumption of locally caught fish). - We hypothesized that cancer risk increases with
decreasing distance to the river. Furthermore, we
hypothesized that farmers show a higher risk than
most other people.
115Materials and Methods Small-Area Statistics on
Health System
- The SMASH system has previously been used to
investigate cancer risk near geographically
defined exposure sources in Finland. - Data include population counts by age, sex,
socioeconomic status (SES), and location
coordinate of residence for 1980 and all cancer
cases from 1981 to 2000. - The original data sets were linked using personal
identification numbers unique to every resident
in Finland. The data were available in 500 m
500 m grid squares and were further aggregated
according to our hypothesis on geographic
reference to the river.
116Small-Area Statistics on Health System
- A total of 27 cancers were selected to be
studied. They were classified traditionally
according to the ICD-7(WHO1995). - Basal cell carcinomas (BCCs) of the skin were not
included in the total numbers because there are
large variations in the BCC rates by hospital
catchment area, suggesting that many cases may
remain undetected.
117Exposure Assessment
- The study population was defined as all people
(farmers in particular) living within 20.0 km
from the River Kymijoki (i.e., in a 500 m 500 m
grid square at least partially located within
20.0 km from the river shoreline) on 31 December
1980. - The study area was divided into nine subareas
according to increasing distance to the river
downstream from the factory producing Ky-5 (lt 1.0
km 1.04.9 km 5.019.9 km), and according to
increasing distance to the sea (lt 20.0 km
20.039.9 km 40.059.9 km) (Figure 1).
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119Statistical Analyses
- We estimated reference incidence rates separately
for total Finnish population and Finnish farmers,
dividing the number of new cases of cancer by the
population at risk in 1980, by sex, age, time
period, and SES (in analyses of all people but
not farmers). - For the study area, we calculated expected
numbers of cancers as the number of subjects
multiplied by reference incidence rate for that
cancer by sex, age, time period, SES, distance to
sea, and distance to river.
120Statistical Analyses
- For distance to river comparisons, we used
Poisson regression main-effect models for the
observed numbers of cases in 3 3 contingency
tables, where the classification is based on
distance to river (three categories) and distance
to sea (three categories).
121Conclusions
- This study cannot exclude the possibility that
residence near the River Kymijoki may have
contributed to a subtle increase in the risk of
total cancer, especially among farmers. - This study can provide only first approximations
of risks and tell only a little about causality.
122Case Study III ??GIS???????
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