Document 7MDaJeVqMrarnpKZaQ7YYdezB
INTER-LABORATORY COMPARISONS OF THE COUNTING OF ASBESTOS FIBRES SAMPLED ON
MEMBRANE FILTERS
S. T. Beckett and M. D. Attfield Institute of Occupational Medicine, Edinburgh
Abstract--Two series of exchanges of slide-mounted asbestos samples have been conducted between British laboratories, to determine the degree of agreement between different labora tories counting the same slides, the effectiveness of written compared with personal instruction, and the reasons for disagreements. It was found that disagreements between laboratories that were isolated or new to fibre counting were large, but were reduced by direct personal consultation. The main causes of these differences were uncertainties in the counting of irregular fibres and fibre masses, misalignment of the microscope phase rings, and failure to scan the full depth of focus in which fibres were present. Results of an exchange between several experienced laboratories showed that counting over the whole field of view of the microscope consistently returned substantially lower count densities than when only the central graticule area was evaluated. All disagreements were more serious for UICC asbestos samples than for samples collected from factory air. It is concluded that there is a need for closer definition and standardisation of counting procedures.
INTRODUCTION"
The most widely-used method of measuring airborne'asbestos fibre is to sample on a membrane filter and then to count the fibres by phase contrast microscopy. This method was developed by the Asbestosis Research Council (ARC) (Holmes, 1965) and forms the basis of the BOHS Hygiene Standards for Chrysotile Asbestos Dust
(BOHS Committee on Hygiene Standards, 1968). The counting procedure is described in an ARC publication (ARC, 1971) and in the BOHS standard.
When the Institute of Occupational Medicine began research on the asbestos hazard for the ARC, the staff had considerable experience of counting coalmine dusts but none of counting asbestos fibres. This previous experience had shown the
difficulties of ensuring closely comparable results between counters in different laboratories and the need for frequent interchange.of check, samples (Holdsworth et al, 1954). Two exchanges of asbestos samples mounted on slides were therefore planned.
The aim of the first exercise was to examine the variability of asbestos counts
between inexperienced laboratories starting to count asbestos on the basis of the
published descriptions. It was hoped that the information gained^ would indicate
any need for further clarification of the instructions, and also show what improvement
would follow personal tuition.
The second exchange was planned to examine the level of agreement between
experienced units regularly engaged in counting asbestos slides, and, if possible, the causes of any differences which occurred. All the laboratories involved had previously maintained regular contact.
The participating laboratories were widely dispersed throughout the country, and the slides were transmitted by post.
85
S0040061
86 S. T. Beckett and M. D. Armeld
TRIAL i: ASBESTOS FIBRE COUNTING BY INEXPERIENCED LABORATORIES
Procedure The laboratories involved were:
(a) Four laboratories (A,B,C,D) experienced in counting non-fibrous mineral dusts, but not asbestos: these were asked to count according to the instruc tions given in Technical Note 1 (ARC, 1971).
(b) A laboratory (E) experienced with asbestos, but with no regular contact with other counters.
(c) Two experienced laboratories (F, G) maintaining regular slide exchanges and comparisons, whose results were taken as the standards.
Eleven slides were used in the trial. All were routine samples from three of the participating laboratories prepared according to the method described by the ARC (1971). The sample densities ranged from 2xl03 to 112xl03 fibres/cm2; the materials were chrysotile (UICC standard reference samples (Timbrell and Rendall, 1971) and from an asbestos textile factory), amosite (from an asbestos cement factory), and crocidolite (from the removal of lagging). It was intended that all the slides would be counted by each participant, but this was not possible owing to breakages and the limited amount of time available at some of the laboratories; all the slides were evaluated by at least one of the `standard' laboratories. The counters could not identify individual slides; the exchange between laboratories was randomised. After the initial circulation of slides, some of the participants from the new laboratories met .at one centre and counted slides in collaboration with a more experienced counter. The reasons for any differences were examined and noted. Several slides were then recirculated in order to determine any changes in counting level.
Results The results are summarised in Table 1. It can be seen that the counts by the
inexperienced laboratories before contact were considerably lower than the standard, being about half the standard for the `factory' samples and one quarter for UICC chrysotile. The agreement with the standard counters greatly improved after personal tuition (see Table 1).. Occasionally the new observers, after tuition, tended to over compensate and get exceedingly high counts. It is also clear that the consistency between the counters was worse for the UICC chrysotile than for the other types of asbestos, presumably-because, of its smaller fibre diameter and irregular shape. ' '
It was found that the counts obtained by the experienced laboratory which had previously remained without contact with outside establishments (E, in Table I) were as far from the standard values as the counts by the novices.
Problems encountered by the new readers
Three main difficulties encountered by the new readers were; (i) the problem of
deciding what to count as one fibre ; (ii) the need to scan through a considerable
depth of focus; and (iii) the use of a phase contrast microscope.
.
The problem of defining a fibre which is to be counted arises because of the
presence of abnormal and split fibres, fibres attached to other particles, and fibre
conglomerates.
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Unlike normal mineral dust deposited directly on a glass slide, asbestos deposited on a filter does not all lie in one plane (especially in the case of larger pore size filters). In order to view all the fibres, therefore, scanning must be done over a range of focal planes of the microscope. A failure to do this usually leads to undercounting by the inexperienced, although chrysotile fibres can twist in and out of a focal plane and be counted more than once. In one case, in this exchange, it was found that only one fifth of the fibres were counted because only one focal plane had been scanned.
A further difficulty was connected with the use of a phase contrast microscope. Some of the participants in the present exchange were unsure how to line up the phase rings within their microscope. Correct alignment, however, is critical in ob taining good agreement. In one establishment not involved in this exchange, counts were reduced by 50 per cent by misalignment of the rings.
There were also differences in visual acuity and thoroughness of searching for fibres near the limit of visibility; microscopists accustomed to counting easily-seen particles above a defined size limit (as customary for many mineral dusts) may not identify faint unresolved images of thin fibres as particles that should be counted.
In this exchange the participants were asked to record whether the counts were made over the whole field of view of the microscope or only in the area of the graticule grid (see next section). No analysis could be made of the significance of this factor, however, as its effect was masked by the large variations in readings arising from the inexperience of the counters.
TRIAL 2: SLIDE. EXCHANGE BETWEEN EXPERIENCED LABORATORIES
Methods The second trial was divided into two parts: one involving laboratories experi
enced in counting chrysotile asbestos and the other laboratories used to counting amosite. Five laboratories participated in this exercise; four took part in the exchange of chrysotile slides (F, G, H and K) and three in the amosite exchange (G, J and K.). Two laboratories continuously engaged in counting both types of asbestos were included in both exchanges (G and K.). Laboratories F and G took part in the exchange described in the first section of this paper. The following description applies to both the chrysotile and amosite exchanges.
Each of the participants was asked to supply one or more sets of three slides. Each set was to consist of a light, a medium and a dense slide (< 1 fibre/grid, 1-5 fibres/grid, >5 fibres/grid,-when using a normal graticule grid area of c. 104 pm1, i.e. ~l/10>of the full field area).* Before the slides were despatched to the Institute they were counted by the originating laboratory. At the Institute the slides were re-labelled to conceal their identity and then sent to the different participants. All slides were factory samples except those supplied by laboratory G which were UICC chrysotile.
Each set of three slides was counted by one other laboratory and then returned to the originator where a final count was made. The distribution of the slides was organised by the Institute and was unknown to the rest of the participants. The exchange plan followed an incomplete block design. This ensured that every possible
-
Not ail graticules used in the trial were of this size. Laboratory H used a graticule St t of the full field, and laboratory K used several different sizes.
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Inter-laboratory comparisons of the counting of asbestos fibres
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! pair of laboratories read one set of slides in common so that all could be directly , compared. > The chosen design had a number of advantages over a procedure which required > every laboratory to count every slide. Firstly it reduced the risk of disenchantment
with the trial which might ensue if the number of slides to be counted was large, thus ; encouraging careful reading of the slides: (some laboratories were involved in both
exchanges and suffered a correspondingly increased reading load). Secondly, the transport and handling of slides was minimised, reducing the chance of slide breakage i or deterioration. Finally, the duration of the trial could be kept short ensuring that the possibility of a change in reading standards was small.
The participants were asked to follow their usual counting procedure and no j constraints were imposed on the methods they could use. In this way it was hoped that the results would be typical of routine counting standards. Forms were supplied . on which the laboratories were asked to give details of their microscopes (manu
facturer, model, optical system, illumination and magnification) and counting methods (whether by counting selected grids, scanning continuously or intermittently across the filter or by some other method). Other forms were provided on which to record the counts obtained for each slide. Information was also asked about the time taken to count the slide and whether the slide was counted using the full field of view of the eyepiece or the area delineated by the grid of the eyepiece graticule.* It was ; hoped that the influence of these various factors on the counts could be investigated.
Results The counts by each laboratory are shown in Tables 2 (a) and (b) for chrysotile
and amosite respectively. Firstly, the initial and repeat counts were examined to ascertain whether the slides deteriorated over the period of the trial. Factors such as differences between apparatus and counting technique which might influence the counting levels were next investigated. Observations were then made on the inter counter differences bearing in mind divergencies in technique and apparatus. Finally the data were analysed using a statistical model which included the important factors. As the counting trial between inexperienced laboratories has shown a greater vari ability for UICC chrysotile than for factory chrysotile, the analysis for the chrysotile exchange was carried out both including and excluding the UICC samples.
Slide deterioration and repeatability-of counts Table 3 shows the mean, minimum and maximum ratio of final to initial counts
for each of the originating laboratories. There appears to be no obvious overall systematic difference. A r-test of the differences in the logarithms of the counts showed that there was no evidence of such an effect. The chrysotile results were found to be more variable than those of amosite (standard deviations of the (natural) log differences were 0-47 (0-26 excluding UICC samples) and 0-14 respectively). From these figures it can be inferred that, if there is no true systematic change and all variability is of random origin, ratios between 0-6 and 1-6 (0-77 and 1-33 excluding
*Henceforth `grid method' will refer to the technique of counting using the slide area delineated by the grid of the eyepiece graticule and `full field ' will be used when the full field of view of the eye-piece is referred to.
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Table 2 (b). Results of slide exchange between experienced laboratories: reported results ' FOR AMOSITE ASBESTOS
Slide identification
Originating
laboratory
Density
Reported counts for each laboratory (101 fibres/cm1)
G JK
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Dense '
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Light J Medium
Dense
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Light K Medium
Dense
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3-78/ 6-29/
7-99/
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9-6 g
2-36 g 101 g 9-56
2-05 g 10-8 g 84-4/j
Key : 1. Initial count. 2. Count by recipient laboratory. 3. Repeat count by the originating laboratory. g Grid method of counting./Full field method, n.a. No count available.
Table 3.
Mean, minimum and maximum ratios of repeat to initial counts for each
laboratorv and each exchange
F
Chrysotile exchange
Mean*Minimum. Maximum
n
Amosite exchange
Mean Minimum Maximum
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39
UICC), and 0-9 and J -2 would be.expected for repeat counts 68 times out of 100 for chrysotile and amositc respectively. As there was no evidence that the final and initial counts varied systematically all results are employed in the following analysis. The greater variability for UICC chrysotile will again be noted.
The effects of counting techniques and different apparatus Inspection of the data in Tables 2 (a) and 2 (b) shows that when slides were
counted by both grid and full-field methods the grid counts were invariably the greater. This suggests- that the counting technique should be taken into account when inter-laboratory reading levels are examined.
The time taken to count a slide was another factor of interest that could be studied although there were many missing values. The average time taken to count the chrysotile slides was 40 min (range 70-20 min) compared with 30 min (range 47-15 min) for the amosite; the longer counting time for the chrysotile did not appear to reduce the variability of the results mentioned earlier. No association could be found between the time taken and the count reported.
^0040067
92 S. T. Beckett and M. D. Attfield
The effects of other factors concerned with counting methods and microscopes could not be examined because they were peculiar to the different establishments and could not be separated from the reader effect.
Comparison of laboratory counting standards The counts made of the various laboratory pairs on the same slides are expressed
as ratios in Tables 4 (a) and (b). Where both initial and repeat counts are available
from the same laboratory, the geometric mean is used as that laboratory's count of '
the slide. The ratios in corresponding boxes to either side of the main diagonals of
the Tables are reciprocals of one another derived from the same data, and are not independent. It will be noted that the ratios are not always mutually consistent, for example, the mean (all slides) ratio F : G (1 -23) is not equal to the product of F : H
(0-54) and H : G (0-55). This is due to differences in counting methods and to
random errors. The `Expected' values, derived from statistical analysis of the data as
described later, are consistent. It can be seen from Tables 4 (a) and (b) that the ratios of grid counts to field
counts (gif) are generally greater, and the fig ratios lower, than the ratios of counts made by similar methods (g/g and ///), in agreement with previous observations on the effects of counting method. There is some evidence that, for chrysotile, the
difference between the ratios is greater for the light slides than for the medium and
dense ones, but the data are insufficient for definite conclusions to be drawn. The further analyses to be described are based on all slides irrespective of density.'
It is clear from Tables 4 (a) and (b) that laboratory K. counts higher than the
others, for in every case the mean (all slides) ratio of its count to that of other laboratories is greater than 1. The other results also show considerable variations and inconsistencies, much of which may be attributed to the use of different counting methods. By taking the counts where both laboratories used the same method,
unbiased estimates are obtained. The geometric means of these gig and /// ratios
are given in Tables 4 (a) and (b). In the chrysotile exchange K. and F appear to have
been counting the highest while H returned the lowest counts. In the amosite trial
the results were much closer and there was little to choose between the three readers.
Although these ratios indicate how the establishments compare, they still suffer from , inconsistency.' It has not yet been determined whether the differences between ~
laboratories are random in origin or are due to true divergence in counting standards:
To analyse the data further, the following model was fitted to the data from each ,
exchanged
1- '
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St Is the `true' count for slide /,
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and EtJ accounts for the remainder of the variability which is assumed to be random
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Tabi.f. 4 (b). Ratios of counts: amosite
Laboratories forming the numerator of the ratio GJK
Light Medium G Dense Geom. mean. All slides
Geom. mean, gig and flf only Expected
i ll (flf) 1-37 (g/f) 0-63 (fig) 1-72 (g/f)
0-92 (fig) 0-94 (gig) 0-87 1-31 1-11 0-94 119 0-94
Laboratories forming the denominator of the ratio
Light 1 Medium
Dense Geom. mean. All slides Geom. mean, gig and///only
. Expected
0-90 (flf) 1-58 (gif) 109 (gif)
1-16 0-90 0-84
1-25 (g/f) 1-27 (g/f) 1-14 (gif)
1-22
--
0-79
. Light Medium
K Dense Geom. mean. All slides
Geom. mean, gig and flf only Expected
0-73 (f/g) 0-80 (fig)
0-58 (f/g) 0-79 (fig)
1-06 (g/g) 0-88 (fig)
0-77 0-82
106
------ -
106 1-26
and unassignable to any definable cause. By taking logarithms the model becomes:
cu^s^rj+t+eij
(2)
where the coefficients are the logarithms of the corresponding coefficients of equation
(1) . If the e,j are assumed to be Gaussian distributed with zero mean and unknown
standard deviation a, and are independent of slide density, the coefficients in equation
(2) can be estimated by least squares methods and their statistical significance
investigated. Logarithms and geometric means were used in the preliminary analysis
to ensure the data were treated uniformly with this model. In practice, the ratio, T, of
grid to full field counts may not be the same for each counter. The design of the
trial did not allow the estimation of separate TJt however, since to do this would have
involved asking the establishments to count the same slide by different methods.
Applying such a constraint might have resulted in the values not being typical of
routine counting.
'' ' '
'
Analysis of the chrysotile data using this model revealed that the grid method
appeared to give counts about three times greater than full field values, i.e. T = 3--0
(2-9 excluding UICC chrysotile). The probability that this finding-is due to chance is-
small (P<0-1 per cent). The ratio for the amosite data was smaller, 1-57, but again
was found to be unlikely to be due to chance (P<0-1 per cent).
Estimates of the Rj are listed in Tables 5 (a) and (b) for the chrysotile and amosite
results respectively. These are the expected long-term ratios of the different reader'sr
counts to the average level if all use the same method, i.e. all grid or ail full-field.
The probability that the differences found arose by chance is less than 5 per cent.
The Rj may be used to obtain ratios of the counts of individual laboratory pairs;
these are the `expected' values listed in Tables 4 (a) and (b).
The lower lines of Tables 5 (a) and (b) give the expected long term ratios of the
laboratory counts to the average if the laboratories use the counting methods that
50010070
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Inter-laboratory comparisons of the counting of asbestos fibres
95
Table 5. Expected lono-term ratios of laboratory's counts to the average level
Counting method () Chrysotile Same method throughout (Rj)
As in trial (light slides)
F 1-35 (1-321
0-78 (0-78) (/)
Laboratory
GH 099 (H6) 067 (0-68)
All (/) or all (g) 0-57 (0-68) 1-16 (1-16)
(/) (g)
K M2 (0-95)
1-95 (1-62) (g)
(b) Amosite Same method throughout (Rj) As in trial (light slides) As in trial (dense slides)
G 0-96
0-83 (/) 1-12 (g)
J 114 All (/) or all (g) 0-98
(f) 0-85
(/)
K 0-91
1-23 (g) 106 (g)
Bracketed figures are calculated neglecting UICC samples
they employed in the trial. It can be seen that the variations between laboratories are greater than expected if all use the same counting method.
DISCUSSION AND CONCLUSION
In the trial between inexperienced laboratories, novice counters using only the
published instructions obtained results which were of the order of half those of the
standard laboratories for industrial samples and a quarter for UICC chrysotile
asbestos. Following personal instruction, however, good agreement was obtained
between all laboratories for industrial slides, and a greatly improved agreement
(67 per cent) for UICC chrysotile.
This exchange showed that written instructions should emphasise the importance
of scanning a full range of focal planes and the regular checking of phase ring align
ment, and give guidance on the classification of problem fibres. F,xchanges of sample
slides and personal tuition clearly improves the consistency of counters, experienced
as well as inexperienced.
'
In the second exchange the counting of fibres only within the grid area of the
eyepiece graticule compared to using the full field of view was found to be of major
importance, giving differences of 3x for chrysotile (2-9x excluding UICC) and,
l-5x for amosite. This is possibly due to the greater resolution of the microscope in
the central (grid) area compared with the periphery of the field. Perhaps an additional
factor.is that the smaller area can be studied more thoroughly and the positions of the
fibres more easily remembered.
The difference between grid and full field counting found in the present trial may
possibly have been accentuated by the wide range of slide densities deliberately
introduced into the trial. It is unlikely to be the same in other situations with different
samples and microscope optical systems.
Direct experimental verification of the effect for amosite was obtained by asking
laboratory J to recount by the grid method three slides which they had previously counted `full field'. The count was increased 1 -5 x, in agreement with the value of T found in the trial. Further work is desirable, especially with chrysotile.
50010071
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96 S. T. Beckett and M. D. Attfield .
The results of the trial indicate that the four experienced laboratories, using their normal (different) counting methods have somewhat different counting levels, the lowest and highest ratios to the mean being 0-57 and l -95 (CT-68 and I -62 excluding UICC) for chrysotile, and 0-83 and 1 -23 for amosite, respectively. It is estimated that if all laboratories adopted the same counting method the spread of the ratios would be from 0 67 to 1 *35 (0-68 to 1*32 excluding UICC) for chrysotile, and 0-91 to 1 -14 for amosite. This is approximately half the present spread for both chrysotile and amosite (two-thirds for chrysotile excluding UICC).
When two separate evaluations of the same" slides were made by the same laboratories, the standard deviation of the (natural) log differences was 0-47 (0-26) for chrysotile and 0-14 for amosite. From this it can be inferred that, if there is no true systematic change and all variability is of random origin, ratios between 0-6 and 1 -6 (0-75 and 1 -3), and 0-9 and 1 -2 would be expected for repeat counts 68 times out of 100 for chrysotile and amosite respectively. The inclusion of UICC samples greatly increased the variability of the chrysotile evaluations and. reduced, the inter-laboratory agreement for low density slides. For high density slides, however, the agreement was practically unchanged as was the grid factor, T.
The problems indicated by this relatively small-scale trial are being investigated further by the Institute and the member Companies of the Asbestosis Research Council. The results will be published shortly. It is anticipated that the ARC will revise its Technical Note 1 to include improved procedures suggested by this work.
Acknowledgements--This work was done as part ofa research programme'supported by the Asbestosis Research Council. The authors are grateful to the member Companies of the ARC, the Industrial Hygiene Laboratory of HM Factory Inspectorate and others who took part in the trial, and to Mr W. H. Walton for suggesting the exercise and for his help and advice in carrying it out.
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