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MOLD
RISK MANAGEMENT CRITERIA
December
5, 2002
������������ADVANCED
CHEMICAL SAFETY uses the procedures and criteria described
in the following to develop an opinion concerning mold and fungi
in a building. Given the lack of agreement on interpreting the
highly variable viable and non-viable mold data, these interpretation
criteria are general and are subject to local conditions at a
site, professional judgement, and a subjective assessment of the
overall quality of indoor air.
������������Initially
a walk through evaluation is made to attempt to identify potential
sources of fungal amplification. Fungi need a source of moisture,
a source of carbon, and proper temperature. Because fungi grow
well at room temperature, control is achieved through adequate
filtration and control of moisture. Areas which have poor filtration
and a source of moisture are likely to be sources for fungal amplification.
������������A
walk through investigation will look for possible sources for
fungal amplification. These include: visible filamentous fungal
growth, water damage, poor housekeeping, poor ventilation, and
inadequate filtration. A "Mold Potential Survey" is completed
to help insure a comprehensive investigation.
������������Samples
may be taken. ACSafety routinely obtains viable samples in suspected
locations. The samples are collected with an RCS Centrifugal sampler
and allowed to grow in a certified microbiology laboratory. Viable
molds are counted and reported in terms of viable spores per cubic
meter of air. The three major species are usually identified.
Conclusions are based on the relative concentration of viable
spores when comparing indoor air to outdoor air, and the relative
abundance of specific species. The following table is a guide
to the interpretation of the relative concentration data.
|
Indoor/Outdoor Concentration
Ratio |
Interpretation Guide
|
|
≤ 2 |
Low viable spores
indoors - no reason for concern |
|
>2 - ≤ 4 |
Medium viable spores
indoors - Control water sources and improve ventilation
|
|
>4 - 8 |
Moderate - Corrective
action should be taken |
|
>8 |
Heavy - Corrective
action should be taken |
������������Bulk
samples may be taken from the suspect material. These may be swab
samples, bulk dilution samples, or plate samples taken on sterile
commercial plates. For bulk samples, the following numbers are
rough rules of thumb.
|
Viable Spores/gram |
Interpretation Guide
|
|
<10,000
|
Low viable spores
indoors - no reason for concern |
|
10,000 - 100,000 |
Medium viable spores
indoors - Control water sources and improve ventilation
|
|
100,000 - 1,000,000
|
Moderate - Corrective
action should be taken |
|
>1,000,000 |
Heavy - Corrective
action should be taken |
The
species of organisms present in a sample have a bearing on whether
or not an area is considered a problem.
Attempts to link bulk sources
such as visible mold on a wall to airborne concentrations of fungal
organisms are often problematic. The levels of fungal organisms
vary by several orders of magnitude during the course of a day
due to activity levels in an area and other factors such as fluctuations
in temperature or humidity which cause the release of spores.
The spores may no longer be viable and though allergenic and possibly
toxigenic it will not grow on any media. Rapidly growing fungi
may crowd out slower growing fungi. The wrong media may be used
for viable sampling.
There are at present no
strict numerical guidelines which are appropriate for assessing
whether the contamination in an area is acceptable or not. Further
investigation of contamination sources is warranted in the following
circumstances.
1. Total indoor counts are
substantially greater than outdoor fungal counts (compare indoor
and outdoor ratios). This comparison is not valid when the outdoor
sample was taken during or immediately after precipitation. It
probably is not valid during some winter months where outdoor
fungal counts are usually below that indoors.
2. Comparison of indoor
and outdoor levels of fungal organisms show one of the following:
A. Organisms are present
in the indoor sample and not in the outdoor sample.
B. The predominant organism found in the indoor sample is
different than the predominant organism in the outdoor sample.
C. A unique species of an organism is found in the indoor
sample. The organism may be present in a mixed outdoor sample.
It may be absent from samples taken in other areas of the
building.
3. If the criteria in #2
are met and the organism is capable of producing a carcinogen
(e.g., aflatoxin produced by Aspergillus flavus). The spores may
be toxic by inhalation (e.g., satratoxin H in the case of Stachybotrys
atra). The production of the toxin is very dependent on the source
of nutrition for the organism.
4. In some cases, (especially
at non-residential locations, to comply with the American's With
Disabilities Act), efforts will be suggested to further reduce
levels even though they are not identified as a problem in section
1, 2 and 3. This would be the case where an individual has been
diagnosed by a physician to be allergic to a specific fungal organism.
Efforts may then be made to further reduce exposure through increase
filtration of the air. There are often problems linking an environmental
exposure to an allergy test. The antigenic material produced by
a fungus of a particular genus will vary according to species
or a strain within the species and vary with the source of nutrition
for the organism. Other factors also influence the antigenicity
of the fungal spore. Thus, establishing a direct link between
environmental exposure and the results of an allergy test is often
problematic. Removal of the person from the area is often the
most successful approach.
5. An opportunistic fungal
pathogen is found in an area which houses individuals who are
immune compromised.
6. Aggressive sampling and
sampling of suspected sources of fungal organisms is often warranted.
The amount of fungi present in an air sample is highly variable.
Changes in airflow, humidity, light level and temperature can
all trigger a spore release. A single air sample will often underestimate
the fungal contamination in the air.
In applying the principles
some additional considerations are:
A. If the numbers are
high (air or bulk).
B. Fungi indoors are different from outdoors or other controls.
C. The fungi are allergenic or toxic.
D. The area is likely to be disturbed.
E. There is or was a source of water or high relative humidity.
F. There is or was a source of water or high relative humidity.
G. People are occupying this area or have contact with air
from this location.
H. There are immune compromised individuals or individuals
with elevated sensitivity to molds.
Note: If A through G are
not true, then there probably is not a fungal related problem.
Common species that may
raise the level of concern:
Absidia
sp.
Alternaria sp.
Aspergillus flavus, A. fumigatus and Aspergillus sp.
Cladosporium sp.
Fusarium sp.
Penicillium sp.
Rhizpus sp.
Stachybotrys sp.