Document yr9vmLzL06zXkO0dpeeMvq1O3
FILE NAME: Koppers/Beazer East (KBE)
DATE: 1960 July
DOC#: KBE128 DOCUMENT DESCRIPTION: Conference Proceedings- 13th International Congress on Occupational Health
Proceedings
THIRTEENTH INTERNATIONAL
CONGRESS ON OCCUPATIONAL HEALTH
The following corporations, governmental agencies, labor unions, professional societies, and individuals contributed to the financial support of the Congress:
AFL/CIO The Alcoa Foundation AMF Foundation Addressograph-Multigraph Corporation Allegheny Ludlum Steel Corporation Allis-Chalmers Manufacturing Company America Fore Loyalty Group American Brake Shoe Company American Can Company American Cast Iron Pipe Company American Cyanamid Company American Industrial Hygiene Association
(Northern California Section) American Medical Association American Metal Climax Foundation, Inc. American Mutual Insurance Alliance American President Lines Ltd. American Telephone and Telegraph Company American Viscose Corporation Armco Steel Corporation Armour and Company Atlantic Refining Company
]. T. Baker Chemical Company Bausch and Lomb Optical Company Baxter Laboratories, Inc. Bayuk Cigars, Inc. Bethlehem Steel Company Boeing Airplane Company Bristol-Myers Company Budd Company Burlington Industries, Inc. Burroughs Wellcome and Company
California Texas Oil Corporation Campbell Soup Company The Carrier Foundation, Inc. Carson, Pirie, Scott and Company Caterpillar Tractor Company Celanese Corporation of America Champion Paper and Fibre Company Chance Vought Aircraft, Inc. Chase Manhattan Bank The Chemstrand Corporation Chesapeake Corporation of Virginia Chrysler Corporation Cities Service Company Clevite Corporation
Colgate-Palm olive Com pany
Columbian Carbon Company Consolidated Edison Company
of New York, Inc. Continental Can Company, Inc. Continental Oil Company Corn Products Refining Company Corning Glass Works Crouse-Hinds Company Crown Zellerbach Foundation Cummins Engine Company Curtis Publishing Company
Deere and Company Detroit Edison Company Dodge Manufacturing Corporation Douglas Aircraft Company Dow Chemical Company E. I. Dupont de Nemours and Company Dupont, Mr. Irenee
East Ohio Gas Company Eastman Kodak Company Electric Storage Battery Company Endicott Johnson Corporation Equitable Life Assurance Society of U.S. Esso Standard Esso Research and Engineering Ethyl Corporation
Fairchild Camera and Instrument Company Fawcett-Dearing Printing Company Federal-Mogul-Bower Bearings, Inc. Federal Paper Board Company, Inc. Federated Department Stores, Inc. Firestone Tire and Rubber Company Food &Drug Research Laboratories, Inc. Ford Motor Company
The Garret Corporation General American Transportation Company General Aniline and Film Corporation General Dynamics Corporation General Electric Company General Foods Corporation General Mills, Inc. General Motors Corporation General Tire and Rubber Company Globe-Union, Incorporated
G oldm an, Sachs and Com pany
The B. F. Goodrich Company The Goodyear Tire and Rubber Company Gulf Oil Corporation Gulf Research and Development Company
Harnischfeger Corporation Hazleton Laboratories, Inc. Helm, Mr. Harold D. H. Hercules Powder Company, Inc. Heyden Newport Chemical Corporation Hine, C. H,, M.D. Hinman, Mr. John H. The Hoover Company Hoffman-La Roche, Incorporated Hope Natural Gas Company Geo. A. Hormel and Company Hughes Aircraft Company Humble Oil and Refining Company
Industrial Medical Association Inland Steel Company International Business Machines Corporation International Harvester Company International Minerals and Chemicals
Corporation International Resistance Company International Telephone and Telegraph
Corporation Iranian Oil Consortium
Johns-Manville Corporation Johnson and Johnson S. C. Johnson & Son, Inc. Jones & Laughlin Steel Corporation
Miles Laboratories, Inc. Mine Safety Appliances Company Monsanto Chemical Company
National Biscuit Company National Dairy Products Corporation National Institutes of Health, Public Health
Service, Department of Health, Education and Welfare National Lead Company New Orleans Public Service, Inc. Newport News Shipbuilding & Drydock Co. New York Life Insurance Company New York State Natural Gas Corporation New York State Society of Industrial Medicine The New York Times The News, New York North American Aviation, Inc. Norton Company
Ohio Oil Company Olin Mathieson Chemical Corporation Otis Elevator Company Owens-Corning Owens-Illinois Glass Company
Pan-American World Airways, Inc. Paramount Pictures Corporation Pennsylvania Railroad The Peoples Natural Gas Company Pepsi Cola Company Pittsburgh Steel Company Procter and Gamble Company Provident Life & Accident Insurance Co.
Kaiser Industries Corporation Kennecott Copper Corporation Kimberly-Clark Corporation Koppers Company, Incorporated
LaSalle Steel Company Legge, R. T., M.D. LeTourneau-Westinghouse Company Lever Bros. Company Liberty Mutual Insurance Company Life Extension Examiners Eli Lilly and Company Thomas J. Lipton, Incorporated
The Magnavox Company The Mead Corporation Medical Society of the State of New York Meigs, J. W., M.D. Metropolitan Life Insurance Company
Radio Corporation of America Raytheon Company Republic Steel Corporation Revlon Foundation, Incorporated Reynolds Metals Company R. J. Reynolds Tobacco Company Richfield Oil Corporation John A. Roeblings & Sons Corporation
Joseph E. Seagram 8c Sons, Inc. Shell Oil Company Simplex Wire and Cable Company Sinclair Refining Company A. O. Smith Corporation Socony Mobil Oil Company Sonoco Products Company Sperry Gyroscope Company Standard Oil Company (California)
Standard O il Com pany (Indiana)
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iUUO
Standard Oil Company (New Jersey) and affiliates
Standard Oil Company (Ohio) Standard Railway Equipment Company
Foundation Standard-Vacuum Oil Company Stauffer Corporation Studebaker Packard Corporation Sugar Beet Products Company Sun Oil Company Sunstrand Corporation Swift and Company Sylvania Electric Products, Inc.
Tampax, Incorporated Tennessee Corporation Texas Company Texas Instruments, Inc. Tidewater Oil Company The Michael Todd Estate Trans World Airways The Travelers
Union Carbide Corporation Union Oil Company of California United Artists Corporation United States Atomic Energy Commission United States Rubber Company United States Steel Corporation United Steel Workers of America Universal Oil Products Company Upjohn Company
VAW--International Executive Board
Washington Steel Corporation Weirton Steel Company Western Electric Company, Inc. Westinghouse Electric Corporation Wilson, Mr. Charles E. Wilson &Toomer Fertilizer Company Wiremold Company Woodard Research Corporation Wm. Wrigley, Jr. Company
Union Bag-Camp Paper Company
Zenith Radio Corporation
THIRTEENTH
CO NG RESS ON
Ju ly 25-29, i9 6 0
Copyright 1961 by the U. S. Executive Committee of the Thirteenth International Congress on Occupational Health
ALL RIGHTS RESERVED
Library of Congress Catalog Caul Number: 58-32683
Public Health GIFT
DESIGNED BY HARVEY SATENSTE1N MANUFACTURED IN THE UNITED STATES OF AMERICA BY
BOOK CRAFTSMEN ASSOCIATES, INC., NEW YORK
/f t 965
A I Z<o5T /<? (e V f ^ u b ! ` C' irletv / H ts L i brCLrtj
EXECUTIVE COMMITTEE
Chairman
. L. W ade, M.D.
Vice-Chairmen
L. Greenburg, M.D.
S. E. Miller, M.D.
Secretary-General
R. E. Eckardt, M.D.
Treasurer
H. E. T ebrock, M.D.
Executive Secretary
J. W. Muckell
E. R. Aston, D.D.S.
C. U. D ernehl, M.D.
T . Ely, M.D.
B. S. Fox
J. Lauer, M.D.
H. L. Magnuson, M.D.
H. B. N achtigall, M.D.
N . N elson, Ph.D.
M. N . N ewquist, M.D.
L. T . Robertson, M.D.
I. R. T abershaw, M.D.
S. P. W agner, R.N.
940
10
REPORTS OF ORGANIZING COMMITTEES
In addition, many others visited points of interest to them either before or after the Congress. When the debris had been cleared away and the hubbub had subsided by Saturday,
July 30, the paid registrations figures for the Congress were as shown in the following tabulation.
NUMBER OF REGISTRANTS -- BY COUNTRIES
Country
Total
Afghanistan ....................................... 1 Algeria .............................................. 1 Argentina ......................................... 19 Australia ........................................... 3 Austria ............................................... 8 Bahrein ............................................. 1 Belgium ............................................. 2 Bolivia .............................................. 1 Brazil ................................................ 5 British Guiana ................................. 2 Canada ............................................... 54 C h ile .................................................. 4 Colombia ........................................... 9 Cuba .................................................. 5 Czechoslovakia ................................. 1 Denmark ........................................... 4 Finland ............................................. 62 France ............................................... 39 Germany ........................................... 36 Greece .............................................. 1 I n d i a .................................................. 5 Indonesia ........................................... 1 Iran .................................................. 2 Ireland ............................................... 1 Israel ................................................. 2 Italy .................................................. 21
Country
Total
Japan ................................................ 20 Luxembourg .................................... 3 Mexico .............................................. 6 Morocco ............................................ 1 Netherlands ...................................... 16 Netherlands-Antilles ....................... 2 Northern Rhodesia ......................... 1 Norway ............................................ 13 Pakistan ............................................ 1 Peru .................................................. 4 Philippines ...................................... 5 Portugal ............................................ 5 Romania .......................................... 1 Spain ................................................ 5 Sweden .............................................. 29 Switzerland ...................................... 6 Thailand .......................................... 1 Trinidad .......................................... 2 Union of South A frica................... 9 United Kingdom ............................. 94 United States ................................... 1040 Uruguay .......................................... 2 U.S.S.R................................................ 1
Venezuela ........................................ 7
Yugoslavia ........................................ 4 Total ......................................... 1568
One hundred and ten people paid and registered but were unable, for one reason or another, to attend. Thus the total actually present, exclusive of wives or guests, was 1458.
It is the impression of the Organizing Committee that the Congress was an overwhelming success. Certainly the number and quality of the scientific papers delivered was outstanding. Dr. Irving Tabershaw and his whole Program Committee deserve a special note of thanks for the hard work entailed in bringing such an excellent program to the Congress. It is the hope of the Organizing Committee that all those who attended, especially those from foreign lands, not only learned much from their attendance at the Congress but found our land and our
people friendly an d hospitable. W e hope th at new friendships w ere m ade, new understand
ings reached, and that the memories of the Thirteenth International Congress on Occupa tional Health will linger long. Speaking for all members of the Organizing Committee, it was a pleasure and privilege for us to plan the Congress and welcome all who attended.
KIVILUOTO
311
ml of the buffer described in Appendix 1, and continue as in Appendix 1. Normally for blood specimens the final washing must be performed four times, instead of thrice as for urine specimens.
APPENDIX 3-- COPROPORPHYRIN
ESTIMATION
To 5 ml freshly voided urine in a stoppered test tube add 0.2 ml 3 per cent hydrogen peroxide solu tion, 1 ml glacial acetic acid and 3 ml ether. Shake gently, release pressure, and place in a lightproof box overnight. Observe the red fluorescence under ultra violet light, and grade the specimen 0 - --(--|--f- by degree of fluorescence.
APPENDIX 4-- HEMOGLOBIN
DETERMINATION
Take 0.05 ml blood, and make up to 9 mis volume with 0 4 per cent ammonium hydroxide. Measure absorption on a colorimeter, using a standard filter (EEL 404), and convert the reading to hemoglobin
percentage to the nearest even number from a pre pared calibration graph.
APPENDIX 5-- PUNCTATE BASOPHIL
COUNTS
Make a thin blood smear on a slide of 0 8-1 0 mm thickness, fix for about one minute in methyl alcohol, allow to dry and stain for 30 seconds in Sellars stain (1 g methylene blue, 6 g sodium bicarbonate in 100 ml deionized water). Wash in tap water until the slide is a sea green color.
Using a dark ground condenser and an Ehrlich eyepiece set to a 6-mm square, count the punctate cells in ten consecutive fields. (Although in counting, the punctate cells are classified as large, medium, small, very fine, or polychrome, according to the size of the intra cellular structure, this differentiation is for further reference on an individual case, and normally only the total count is given.) Close the eyepiece to a 2-mm square, and count the R.B.C. in this square. Repeat both counts five times on different parts of the slide, to give a punctate count of 50 large fields and an R.B.C. count of five small ones. Calculate punctate per 1000 R.B.C.
NONOCCUPATIONAL ASBESTOSIS
R aim o K iy ilu o to Roentgen Department of the Central Hospital of Northern Karelia
Introduction
Pleural reaction is very often observed in asbestosis. In the advanced cases of this pneumoconiosis pleural fibrosis has been almost always found, and a clear correlation between pleural changes and the severity of the pulmonary fibrosis has been observed by several investigators. Observations on the occurrence of pleural calcification in asbestosis have also been made. Reports of pleural calcification as a roentgenologic sign or complication of asbestosis have especially been made by the German authors (1). In addition to advanced cases of asbestosis, special cases have been presented in which pleural calcification has been the chief finding (2). Except in asbestosis, pleural calcification has also been observed among workers exposed to talc and mica (3,4) or to various dusts including a short exposure to asbestos (5).
The diagnosis of pneumoconiosis is primarily based on occupational exposure to dust. Only very few re ports of pneumoconioses without occupational exposure may be found in the literature (6,7,8). In Northern Karelia, Finland, during few past years interest has been attracted by the high incidence of cases of pleural calcification showing a rather curious and characteristic roentgenologic picture, very similar to that observed in pneumoconioses. The cases have been mainly found among the residents of a certain area, and in these cases no previous history of adequate pulmonary or pleural disease could be elicited. The occupations of the patients showed no uniformity, and the main part of the patients had no clinical symptoms of pneu moconiosis. A study of the areal distribution of cases revealed that they were grouped round two anthophyllite-asbestos mines. Asbestos constituted the common external factor sought. Even from a solely roent-
genologic point of view, asbestos dust inhalation had been considered the most probable etiology.
Pleural calcification resulting from hemothorax, tuberculosis, or empyema usually occurs unilaterally and is situated on the visceral pleura. In most cases marked pleural thickening and displacement of the intrathoracic organs is observed. The calcification re sulting from dust inhalation usually occurs bilaterally and is most often situated on the parietal pleura. In advanced cases calcium deposits are found in the lateral parts of the chest, basally and mediastinally. The calcium deposits take various forms--large con fluent plaques, bizarre figures, or roundish spots.
The Roentgenologic and Clinical Picture of
Cases Observed in Northern Karelia
In the advanced cases calcium deposits are found bilaterally in the central parts of the diaphragm; on chest walls, especially anterolaterally but also dorsally, and on the mediastinal surfaces. In the incipient cases the calcium deposit takes place either on the antero lateral chest wall, more often on the left, or in the central parts of the diaphragm, apparently more often on the right. Pericardial calcification is sometimes present.
The calcium deposits are located on the parietal pleura. In a series of 150 cases no interlobar calcium deposits were observed. The parietal location has been demonstrated by diagnostic pneumothorax examina tions, and it has also been noted in some autopsied and surgical cases. Using a tangential roentgen beam, the parietal location of solitary plaques may be observed, these plaques having their bases toward the inner chest wall or toward the diaphragm. In advanced cases the lack of soft tissue mass between the calcium deposit
f'v ^ "I Uati
312
MEDICAL PRACTICES
and inner chest wall due to the parietal location is pulmonary fibrosis among residents around the two
apparent, and diagnostical pneumothorax examination asbestos mines.
is seldom needed.
Some investigators have pointed out the difficulty of
The majority of cases of pleural calcification de attributing the calcification to inhalation damage in
scribed above have been clinically symptomless. In a view of its parietal location, few, if any, changes being
series of 150 cases the ordinary chest roentgen examina observed in the lung or the visceral pleura (2, 5). It
tion by P-A and lateral projections revealed pulmonary seems possible that the asbestos fibers move with the
fibrosis, corresponding to the anteprimary or primary lung and visceral pleura in relation to the parietal
stage of pulmonary asbestosis in only about 14 per pleura, thus causing capillary hemorrhages on this
cent. Even the main part of these cases had no sub only, as previously presented by the author. The
jective respiratory symptoms.
hemorrhage coagulates and organizes, forming a col
The series mentioned above has been selected solely lagenous plaque which slowly calcifies. This theory
according to the roentgen diagnosis without reference could explain the course of the process resulting from
to other factors. The concentration of the cases around inhalation of small quantities of fibrous mineral dust. two asbestos mines in Kuusjrvi and its neighboring The clinical significance of the pleural calcification
communes has as yet been the only way to confirm the seems to be slight, the majority of cases showing no roentgen diagnosis. The majority of 25 cases living clinical respiratory symptoms. Further investigations
outside this area had previously lived there. According on this point are needed. to these facts, any other etiology would be very dif From roentgenologic point of view, this endemic
ficult to credit In very few cases a previous occupa tional exposure to asbestos dust has been observed,
which lends slight support to the roentgen diagnosis. The diagnosis has as yet not been confirmed by other methods. In the sputum of 20 cases no asbestos bodies were found, and asbestos fiber in one case. Small
amount of anthophyllite asbestos was found in the lung of an autopsied case and in the lung of a cow
pleural calcification is of some significance. The roent gen diagnosis is in typical cases easy but in some cases difficult. Early pleural changes on the anterolateral chest wall may simulate infiltrations, and large calcified plaques may cause difficulty in interpretation of pul monary changes by hiding infiltrations. The high kilovoltage technique can hereby be especially recom mended. In chest roentgen examinations of workers of
from the vicinity of the asbestos mine. Discussion
asbestos mines in Northern Karelia and of Outokumpu
Copper mines located in the same area attention must
be paid to the fact that even extensive bilateral
3
pleural calcification does not have to be a sign of
The total number of cases of pleural calcification severe pulmonary changes resulting from occupational around the two asbestos mines amounts to over 800, dust exposure.
as previously reported by the author. This number of cases was found in a mass survey of about 10,000 adult
REFERENCES
inhabitants and may include cases with previous occu pational exposure to asbestos dust. In the history of
the main part of cases examined at the Central Hos pital of Northern Karelia the lack of occupational ex
posure has, however, been apparent. Some of the patients have not had any idea how the dust inhalation
could have happened; the same cases have presumed that the dust rising on the roads might be responsible In Northern Karelia the roads (highways) do not have pavement. Without minralogie examinations it is, of course, impossible to decide whether these calcifications are resulting from inhalation of anthophyllite-asbestos
1. Jacob, G., and Bohlig, H.: Die rntgenologischen Komplikationen der Lungenasbestose. Fortschr. Rntgenstr.j 83:515, 1955.
2. Muller, H.: Uber schwere Formen der Asbestose. Die Staublungenerkrankungen, Band 3, Wissen schaft!. Forschungsberichte 66. Dietrich Steinkopff Verlag, Darmstadt, 1958.
3. Siegal, W.; Smith, A. R.; and Greenburg, L.: Study of talc miners and millers. Indust. Bull., 22:434, 1943.
4. Smith, A. R.: Pleural calcification resulting from exposure to certain dusts. Am. J. Roentgenol, 57:375, 1952.
dust originating from the asbestos mines or from sur face deposits of other fibrous dusts, such as tremoliteasbestos, which is a very common mineral in Northern Karelia. The first alternative seems to be more prob able.
In occupational pneumoconiosis some authors have called attention to the absence of pulmonary fibrosis besides the prominent appearance of the pleural calci fication (2,5); on the other hand, a clear correlation has been observed between the severity of pulmonary fibrosis and pleural calcification (9). In ncnoccupational
5. Fehre, W.: ber doppelseitige Pleuraverkalkungen infolge beruflicher Staubeinwirkungen. Fortschr. Rntgenstr., 55:16, 1956.
6. Eisenbud, M.; Wanta, R. C.; Dustan, C.; Stead man, L. T.; Harris, W. B.; and Wolf, B. S.: Nonoccupational berylliosis. Am. J. Indust. Hyg., 57:282, 1949.
7. Goyal, R. K.: Pneumoconiosis in the non-industrial population of Rajasthan. J. Indian Med. Ass., 30:19, 1958.
8. Kiviluoto, R.: Pleural calcification as a roent genologic sign of non-occupational endemic antho-
I asbestosis it is apparent that extensive calcification may
occur without any roentgenologically detectable pul
phyllite-asbestosis. Acta radiol., suppl. 194, 1960. 9. Bohlig, H.; Jacob, G.; and Muller, H.: Die Asbes
i(if
monary fibrosis. It seems possible that even very small
tose der Lungen. Georg Thieme Verlag, Stuttgart,
amounts of asbestos fibers may cause pleural calcifica
1960.
tions.
10. Vorwald, A. J.; Durkan, T. M.; and Pratt, P. C: Experimental studies of asbestosis. Arch. Indust.
Anthophyllite is more stiff than serpentine asbestos.
Hyg., 5:1, 1951.
X
In animal tests brittle mineral fibers have not caused 11. Noro, L.: On the histology of asbestosis. Acta
pulmonary fibrosis (10), but fibrosis has been observed
Pathol, et microbiol. Scand., 23:53, 1946.
i
in workers exposed to anthophyllite-asbestos dust (11, 12. Wegelius, C.: Changes in the lungs in 126 cases of
%
12). Further studies are needed to reveal the part
asbestosis observed in Finland. Acta radiol., 25:139,
possibly played by asbestos as an tiologie factor in
1947.
3
326
MEDICAL PRACTICES
A REVIEW OF RECENT DEVELOPMENTS IN OCCUPATIONAL PULMONARY DISEASES OTHER THAN SILICOSIS
L eo N o r o , M .D. Finland
At the Twelfth Internationa! Congress on Occupa tional Health held in Helsinki three years ago, the French Professor Marchand presented a review of the subject mentioned in the title, a large and comprehen sive bibliography being attached to his presentation. The Organizing Committee has at this time asked me to present a review of the same subject from the last several years. It must at once be said that the compil ing of such a bibliographic review has not been an easy task. More than ever before, research work has been focused on occupational pulmonary diseases. The problem has been discussed at national and interna tional meetings, the last time being only two months ago in Milan. From the literature which has been at my disposal, I have found almost 316 articles from the recent years dealing with this subject, and yet I cannot have had access to all the articles from this field pub lished in the world. I shall follow, with some excep
tions, Marchand's classification. There is reason to state at the onset that the con
stant industrializing is causing the air we breathe to become more and more polluted. Great masses of people, even the peoples of the so called less-developed countries, are changing their breathing air through their movement from agricultural to industrial centers. I am here thinking specifically about the huge indus trialization process right now taking place in India and China. But man's breathing organs, and especially
his lungs, do not come in contact with hazardous in fluences only in the working environment. The most common pollutant of our breathing air--tobacco smoke --is rapidly triumphing all over the world with the rising standard of living, in spite of the efforts we doctors take to warn mankind of its danger. The auto mobile industry is producing cars in a rapid tempo to pollute the air of the traffic roads. With the growing population centers, and their increased use of fuel for power and heating, more pollutants enter the air. Bacterias, viruses, sponges, and other small organisms have not disappeared either. Thus, the environment of man, with reference to lungs, is changing continuously. While the great enemy of the lungs, tuberculosis, is gradually disappearing, new diseases are arising, giving new importance to the air impurities. Chronic bron chitis, asthma, emphysema, and lung cancer are already much more important diseases than tuberculosis in countries with highly developed industry and a high
living standard, Man himself and the changing of his reaction to the
environment also require attention. Allergies are one problem, for example. The danger of allergens affect ing organisms through the respiratory and digestive organs and the skin is continuously increasing; new medicines, foods, cosmetics, etc., are common allergens. Allergic reactions are important when we consider the
breathing organs and their obvious connection with the air impurities. Many of the chronic occupational diseases of the lungs occur only after a long exposure time. We are gradually, however, observing the signs of these diseases among those occupational groups which have been exposed for some length of time.
Our knowledge of many factors influencing the lungs is already fairly complete: I am thinking only of asbestosis; those many chemicals causing acute lung injuries, such as chlor or nitrous fumes; and the diseases caused by bacteria, sponges, or viruses Often our knowledge is still very restricted, and the interpre tations in many individual cases are difficult to make, this is true of allergic diseases and chronic bronchitis, lung cancer, emphysema, and fibrosis on the whole, and especially of the role of nonprofessional and pro fessional environments in their occurrence. Yet we have, with special appreciation to Great Britain's ex cellent vital statistics, important evidence at our dis posal of the relationship between occupation and certain pulmonary diseases, such as chronic bronchitis.
After this general survey, now let us study the details. Since silicosis will be discussed in another connection, I shall begin with asbestosis.
A sbestosis
The major part of our present knowledge concerning asbestosis is contained in the excellent German book that appeared some months ago, Die Asbestose der Lungen by Bohlig-Jacob-Muller This book contains, in addition to 700 of their own cases, references to practically the entire world literature in this field (some 650 references). There is nothing basically new about the pathogenesis, clinic, prognosis, and preven tion of this disease. Further information is, however, obtained about the frequency of clinical symptoms as well as roentgenologic and bronchographic observations from the authors' careful examination on their material of 700 cases. The relationship between asbestosis and lung cancer is still statistically indetermined. In spite of this, "asbestos cancer" exists, and the authors give their own specification to it.
Does asbestos dust have similar nonoccupational affect as, for example, beryllium? This is a problem that has been exposed through the observations of 126 nonoccupational pleural calcification cases (so-called neighborhood cases) that had been found in the popu lation living around two open asbestos quarries, pub lished by the Finnish Dr. Kiviluoto. According to this study, the details of which the author will present him self at this Congress, more than 800 pleural calcifica tion cases were found in the minute x-ray investigation of farmers, workmen, and their wives, who never had any occupational exposure. Calcification was usually located in parietal pleura, as it is also most often in occupational asbestosis. In most instances it occurrecf bilaterally on the inner chest wall. Basal and medi astinal calcification was also often observed, a pul monary fibrosis being found only on a few cases. The calcification was noticed to appear slowly. These roentgenologically noticeable changes gave insignificant clin
ical symptoms. These observations make it evident that measures must be taken to prevent the air pollu tion of the environments surrounding the factories and asbestos quarries. The results of Dr. Kiviluoto's work are motivation for similar investigations in other coun tries to certify these observations.
NORO
327
Other fibrotic lung diseases and "benign pneumo coniosis" caused by silicates, mixed or non-silica dusts (Glass wool, seriate, sillimanite, talc, anthracol, carborundum, cement, Fuller's earth, china and ball clays, graphite, gypsum, kaolin, limestone, marble, mica, Thomas (basic) slag, etc.)
I shall pass this group with a brief mention of talcosis and graphite lung, which are still objects of continuous research. With great enough exposure, un doubtedly, the dusts of this group have their alfect in the occurrence of fibrosis. However, it is evident that with improved hygiene these types of pulmonary changes will become more and more rare.
Pneum opathies due to toxic chemicals and metals
G ases, F umes and V apors (Cl, NOz, S 0 2, borans, desmodur, hydrocarbons, oils, kerosene, etc.)
Metals (Aluminium, antimon, barium, beryllium, cadmium, chrom, cobalt, fluor, gold, iron, manganese, nickel, osmium, platinum, selenium, sulfur, tungsten, titanium, vanadium, wolfram, zirconium, etc.)
The amount of toxic chemicals and metals influenc ing the lungs is continuously growing. Vanadium, chrom, and beryllium have been subjects of research, especially in Sweden and in our host country, the U S.A. The importance of vanadium is especially in creasing. It is necessary, however, to bear in mind that with the expanding use of oil heating, the crude oil coming from various parts of the world contains vanadium in very different amounts. The role of the acic sulfur compounds in the ashes is also to be remembered. For a detailed study of beryllium, I would refer you to the proceedings of the conference held at the M.I.T. in 1958 (AM.A. Arch. Indust. Health); a comprehensive list of references on beryl lium is contained in a publication on these proceed ings. We in Europe, to my knowledge, do not have the big problems with beryllium which seem to exist in the U S.A.
It is impossible, in this short presentation, to name all the new chemicals with irritant effect on the lungs. We industrial physicians have special difficulties at tempting to evaluate the aftereffects of acute irritants to the lungs (nitrous fumes, Cl, S02, etc.), especially with reference to etiologic differential diagnostics in chronic bronchitis and emphysema.
Pneumopathies due to organic dusts, allergens and pneumomycoses (Actinomycosis, aspergillosis, cocci dioidomycosis, cork (suberosis), cotton (byssinosis), drugs, dyes, feathers, flour, grain, gum acacia, hair, hay (farmer's lung), histoplasmosis, jute, leather (cannabosis), linen, moniliasis, nocardiosis, sporotrichosis, sugar cane (bagassosis),- tobacco (tabaccosis), tropical
woods, etc.) The agricultural population has received increased
attention during the last few years in the investigation of the relationship between work and health. "Farmer's lung" and other pulmonary diseases found in agricul ture have proved surprisingly common upon closer investigations. Unfortunately, so far there have not been powers to investigate these conditions in the countries where the agricultural population works under the worst hygienic conditions. We have not enough knowl edge about the pulmonary diseases of the workers in the old Asian rice mills, for example.
The effect mechanism of most organic dusts is still unclear, and we are also in a difficult field, where bacteriology and allergology will be of much help in
several cases. What factors effect in different conditions --acute, subacute, chronic; proteins, alcaloids, irritating mechanic factors, toxic, allergic, bacteria, the silica included--are questions that are still waiting to be answered. In addition, for example, the experience with byssinosis is still contradictory in different coun tries. The interesting research results of Dr. Schilling of England make one think that this disease has not yet disappeared as has been contemporary thought in my own country.
Infectious and parasitai pneumopathies (Amebiasis, anchylostomosis, anthrax, bilharziosis, brucellosis, hydatitosis, leptospirosis, ornithosis, tuberculosis, tularaemia, etc.)
With the diseases of this group there are continuous difficulties in etiologic diagnostics: when is the infec tion to be considered due to work and when not? The question is very important, for example, with tuber culosis. Of course, the relationship between tuberculosis and pneumoconioses is under constant study.
Lung cancer due to occupation (Arsen, asbestos, chromates, isopropyl alcohol manufacturing, nickel, radioactive substances, etc.)
The Secretary General of our Congress, Dr. Eckardt, handles the role of working conditions in the occur rence of cancer in his book Industrial Carcinogenesis most variedly and with good criticism. Yet it is to be suspected that in industry many other substances aise have a cancerogenetic effect. Our knowledge in this field, however, is still very limited, and although ex perimental cancer research has gone far, we still lack in practice necessary facts. It is hoped that the wellendowed cancer organizations and research institutes will more than before concern themselves with the occupational aspects in the etiology of cancer.
The results from the investigation by U.S. Publn Health Service concerning the hazards of radiations to miners are expected with great interest. Whether the cases of Schneeberg and Joachimstal will get successors in the very widespread uranium mining is a question that will presently be answered.
Pneumopathies caused by radiation
The influence of radiation as the cause of cancer has already been referred to above. Our knowledge about the other effects of radiation on the lungs are very small. In connection with therapy, large doses (10002000 r.) have been found to cause changes in the lungs in the form of pneumonitis and fibrosis. From East Germany there comes the report of a chronic pneu monia case of a chemist, which led to death; the cause of death being considered the breathing of radioactive dust over a period of 20 years.
Conclusion
To our present knowledge, we already have a foun dation for the technical prevention of these diseases We are as yet in a weaker position as to their medical prevention: we know too little about why one person gets them and one does not. This question requires much research.
We have already reached far in the roentgenologic diagnostics of the pulmonary diseases, and there we are making constant progress. We are also aware, however, of the difficulties therein as to several of the disease groups referred to above. Together with the roent genologic examination we must develop other clinical
328
MEDICAL PRACTICES
examination methods especially the physiologic lung
function diagnostics. In its most advanced form, we ha\e to apply it not only in laboratories but, above
all, in the field examinations to the examination of population groups exposed to different exposures.
Above all, we need also in this field keen interna tional collaboration to solve our common problems and to exchange information so that each of us in his own country could apply in practice the knowledge we already possess to the betterment of our working population.
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32- Friebei, H., and Luchtrath, H.: Gesundheitssch den durch neuartige Lacke und Schaumstoffe. Dtsch. med. Wschr., 57.980, 1956.
33. Friebei, H., and Stein, A.: Zur Genese des durch einfache Chemikalien hervorgerufenen Asthmas. Versuche mit p-Phenylendiamin. Arch. Gewerbe path., 76;620, 1959.
34. Friberg, L.: Edathamil calcium-disodium in cad mium poisoning. A.M.A. Arch. Indust. Health, 75:18, 1956.
35. Friberg, L.: Deposition and distribution of cad mium in man in chronic poisoning. A.M.A. Arch. Indust. Health, 16:27, 1957.
36. Friberg, L.: Chronic cadmium poisoning. A.M.A. Arch. Indust. Health, 29:401, 1959.
37. Gage, J. C.; The toxicity of epochlorhydrin vapour. Brit. J. Indust. Med., 76:11, 1959.
38. Galy, P.; Roche, L.; Bouvier, J.; and Perrin, L. F.: Pneumonie chronique interstitielle diffuse it evolution mortelle chez un metalliseur au zinc. Arch. mal. prof., 75:301, 1957.
39 Glmme, J , and Lundgren, K..-D.: Health hazards from chlorine dioxide. A.M.A. Arch. Indust. Health, 76:169, 1957.
40. Glmme, J., and Swensson, A.: Tierexperimentelle Untersuchungen ber den Staub in der Arbeitsatmosphare von Ferrosiliziumwerken. Staub lungenerkrankungen, Band 3. Herausg. Jtten 8c Klosterkotter, 1957.
4L Glmme, J., and Swensson, A.: Cases of siderosis, alumiosis and pneumoconiosis in the tungsten carbide tool industry. Proc. XU Int. Congr. Occup. Health, Helsinki, 5:166, 1957.
42 Gombos, B.: Pulmonary nodulation by inhaling barium dust. Pracovni Lekarstvi, P:399, 1959.
43. Gray, E. LeB : Oxides of nitrogen: their occur rence, toxicity, hazard. A.M.A. Arch. Indust. Health, 79:479, 1959.
44. Haglind, O.: Lung changes in electric welders. Proc. X ll lnt. Congr. Occup. Health, Helsinki, 5:169, 1957.
45. Hama, G. M.: Symptoms in Workers Exposed to Iso cy an ates. A.M A. Arch. Indust. Health, 76:232, 1957.
46. H a m lin , L . E .: Siderosis. J. Occup. Med., 7:79, 1959.
47. Hamlin, L. E.: Siderosis: additional observations over a period of eight years on sixty-nine foundry cleaning room employees. J. Occup. Med., 7:79, 1959.
48. Hardy, H. L , and Stoeckle, J. D.: Beryllium di sease. J. Chron. Disease, 9:152, 1959.
49. Hasegava, K. (and Teisinger, J., discussion): Diag nosis of chronic sulphur dioxide intoxication. Proc. X ll lnt. Congr. Occup. Health, Helsinki, 5:271, 1957.
50. Husten, K.: Hartmetall-Fibrose der lunge. Arch. Gewerbepath., 76:721, 1959.
51. Iannacone, A., and Mazella di Bosco, M.: Intossi cazione acuta da anhidride maleica in lavoratori del porto. Lav. umano (Napoli), 5:404, 1956.
52. Johnstone, R. T.: Toluene-2-4-Diisocyanate. clin ical features. Indust. Med., 26:33, 1957.
53. Karpov, B. D.: Angaben zur toxikologischen Charakteristik von Methylchlorakrylat. Gig. i San. 22:144:74, 1957.
54. Kasparov, A. A.: Probleme der Arbeitshygiene bei der Herstellung von Vulkanisationsakzeleratoren (Tiuram, Kaptaks). Gig. truda, 7:24, 1957.
55. Klavis, G.: Ammoniakvergiftungen und ihre Fo lgen unter Bercksichtigung neuer Kasuistik. Arch. T o x ic o l77:155, 1958.
56. Klavis, G.; Khler, H.; and Bister, F.: Die Ursache der Thomasschlackenpneumonie unter besonderer Bercksichtigung der vanadio- und manganhaltigen Schlackenbestandteile. Arch. Ge werbepath., 15:355, 607, 1956-1957.
57. Kleinfeld, M., and Giel, Ch. P.: Clinical manifes tations of ozone poisoning: report of a new source of exposure. Am. J. Med. Sc., 257:638, 1956.
332
MEDICAL PRACTICES
38. Koelsch, F.: Gesundheitsschden durch Metall karbide und Hartmetalle. Zbl. Arb. m e d 9:33, 1939; J. prophyl. Med. Soz.-hyg5:1, 1959.
59 Kunkel, A. M ; Murtha, E F.; Dikemus, H ; Stabile, D. E.; Saunders, J. P.; and Wills, J. H.: Some pharmacological effects of diborane A M .A . Arch Indust. Health, 75:346, 1956
60. Kutschera, W : Ein eigenartiger Fall einer Vergi ftung durch Dissousgas. Mitt, osterr. San verw., 57-228, 1956.
61 Lachnit, V . Zur Therapie der Reizgasvergiftung. Zbl Arb. m e d 8:117, 1958.
62. Leicher, F.: Zur Differentialdiagnose zwischen Aluininiumlunge und Morbus Boeck. Fortschr. Rontgenstr, 84.571, 1956.
63. Levinskas, G. J ; Pollis, A.; and Novick, W, J., J r : Distribution and excretion of poranes. A M.A. Arch. Indust. Healthf 14.346, 1956.
64 Lewis, C. E : The biological effects of vanadium. A M A Arch. Indust. Health, 19:497, 1959.
65 Lindgren, S A., and Swensson, A : Yrkesmedicinska synpunkter pa framstllnmg och bearbetnmg av plaster. Sv. Lakartidningen, 55.2227, 1938.
66. Lingen, Mane-Louise, and Sundell, C C : Lungforandringar lakttagna efter inandning av oljehaltig luft Nordisk Medicin, 5#. 1974, 1957.
67. Lowe, H. J , and Freeman, G : Boron hydride (borane) intoxication in man. A.M A. Arch. In dust, Health, 76:523, 1957.
68. Machabeli, M E.; Gdzeldze, E. G.; and Mgeladze, T. G.: Clinical picture and work capacity in manganokoniosis. Gig. Truda, 4:48, 1960.
69. Mann, B. T., and Lecutier, E. R.: Arc welder's lung. Brit. Med. J., 2:921, 1957.
70. Marks, J., and Nagelschmidt, G.: Study of the toxicity of dust with use of the in vitro dehydro genase technique. A M A. Arch. Indust. Health, 20:383, 1959.
71. Massmann, W.: Experimentelle Untersuchungen ber die biologische Wirkung von Vanadinver bindungen. Arch. T o x i c o l 76:182, 1956.
72- Massmann, W.: Tierexperimenteile Untersuchun gen ber die toxikologische Wirkung von Rauch en, die bei Schweissen mit kalkbasischen Ele ktroden entstehen. Arch. Gewerbepath., 74:291, 1956.
73. Massmann, W.. Untersuchungen ber die biologische Wirkung des Polyaerylnitrils. Z. exper. Med., 727:407, 1956.
74. Massmann, W., and Pilgrim, K.: Das Verhalten des Lungengewebes nach intratrachealer Injektion von Mangan-IV-Oxyd und Chrom-III-Oxyd. Arch. Gewerbepath., 75:203, 1956.
73. McLaughlin, A. I. G-. Iron and other radio opaque dusts. In the Symposium on Industrial Pulmonary Diseases, ed. by King and Fletcher. London, 1960, p. 146.
76. Meiklejohn, A., and Posner, E.: The effect of the use of calcined alumina in china biscuit placing on the health of the workman. Brit. J. Indust. Med., 74:229, 1957.
77. Melnikova, E. A : Angaben zur Bestimmung des zulssigen Kadmium- und Vanadiumgehaltes der Luft in Industrieraumen. Gig. i san., 27:25, 1957.
78. Mozentseva, N. V.: Hygienic characteristic of in dustrial aerosols of wolfram. Gig. t San., 22(4):25, 1957.
79. Minden, H.; Bruckner, Ch.; and Simon, J.: Bei trag zur Cadmiumvergiftung. Arch. Gewerbepath. Gewerbehyg., 77:531, 1959.
80. Mitchell, J.: Pulmonary fibrosis in an aluminium worker. B nt. J. Indust. Safety, 76:123, 1959.
81. Mittler, S.; King, M.; and Burkhardt, B.: Toxicity of ozone. A M A. Arch. Indust. Health, 75:191, 1957.
82. Mogilevskaya, O. Ya.: An experimental study of the effect of rare metals ore dust on the respira tory organs. Gig. t san., 25:30, 1960.
83. Moschinski, G.; Jurisch, A., and Reinl, W.: Die Lungenveranderungen bei S in te rh a rtm e ta llArbeitern. Arch, Gewerbepath, 76:697, 1959.
84. Molitor, L ; Mosinger, M.; Barthel, J.; Heyart, H ; and Perinet, G : Recherches sur les poussires de laminoir et leur capacit pathogne. Les sidroses pulmonaires. Luxembourg, 1957 (127 pages).
85. Moschinski, G : Jurisch, A.; and Reinl, W.* Die Lungenveranderungen bei Sinterhartmetallarbeitern. Arch. Gewerbepath, 76:697, 1958.
86 Nakaniski, S., and Namiki, S : Symptoms in woikers exposed to isocyanates. Rdkagaku, 54.980, 1958
87. Nebelung, W : Akute Vergiftung mit Dimethylsulfat. Aich. Gewerbepath., 75:581, 1957
88. Oyanguren, H.; Haddad, R.; and Maass, PL* Stannosis Benign pneumoconiosis owing to in halation of tin dust and fume. I. environmental and experimental studies. Indust. Med., 27ATI, 1958
89 Penlver, R : Diagnosis and treatment of man ganese intoxication. Report of a case. A.M.A. Aich. Indust. Health, 76:64, 1957.
90 Portela-Gomes, F : La reaction de l'alvole pul monaire quelques produits industriels. Proc. XII Int. Congr. Occup. Health, Helsinki, 5.311, 1957.
91. von Post-Lingen, Marie-Louise: Lungskador efter inhalation av olja eller oljehaltig luft. Nordisk Median, 59.290, 1958.
92. Poteryaeva, G. E : The toxic properties on anti mony pentachloride. Gig. Truda, 2:22, 1958.
93. QuilUgan, J J.; Boche, R. D.; Falk, L. H.; and Klotin, P : The toxicity of ozone for young chicks. A.M.A. Arch. Indust. Health, 7;16, 1958.
94. Oettel, H.: Gesundheitsgefahrdung durch Kunst stoffe? Arch, exper. Path. Pharmak., 252:77, 1958.
95. Reinl, W.: Ueber die Erkrankungen durch Tho masschlacke, Vanadinschlacke und Vanadinver bindungen und ihre Ursachen. Staub, 7^:143, 177, 1958.
96 Robertson, A. J.: Pneumoconiosis due to tin oxide. In the Symposium on Industrial Pul monary Diseases, ed. by King and Fletcher. Lon don, I960, p. 168.
97. Rogers, W. N.: Chronic beryllium poisoning treated with corticotrophin. Lancet, 275:267, 1957.
98. Rohrs, L. C.: Metal-fume fever from inhaling zinc oxide. A M A . Arch. Indust. Health, 16:42, 1957.
99. Roschtschin, I. V.: Das Vanadium als industrielles Gift. J. Hyg. Eptd. Microbiol. Immunol. (Prague), 2:492, 1958.
100. Roschina, T. A.: An experimental investigation of the action of the chromomagnesite and magnesitochromite refractories dust on the body. Hig. Truda, 5:28, 1959.
101. Rosmanith, J.; Volf, J.; and Knpfelmacher, E: Respiratory disease in workers producing sul phuric acid. Pracovni Ukarstvi, 9.411, 1957.
102. Rosmanith, J., and Knopfeimacher, E : A case of BaSQ, pneumoconiosis. Prac. lk., 9:140, 1957.
103. Roush, G., Jr.: The toxicology of the boranes. J. Oaup. Med., 7:46, 1959.
104. Rowe, V. K., et al.: Toxicity of propylene oxide determined on experimental animals. A M A . Arch. Indust. Health, 75:228, 1956.
/>-,
i f '*<r.i. %uf inftiV j
NORO
333
105. Ruiz, R. F., and Iribarren, R. R.: Neumopatas Pneumopathies due to organic dusts, allergens por querosn. The Medical Bulletin (Standard and pneum om ycoses
Oil Co., N.J.), 20:35, i960. 106. Rumyantsev, G. T.: On the question of barytosis.
Gig. i San., 23(4):17, 1958.
107. Sarai, S., and Ueno, K.: Electron microscopic views of dust produced in electric steel melting. Proc. X II Int. Congr. Occup. Health, Helsinki, 5:325, 1957.
108. Schepers, G. W. H.; Durkan, T. M.; Delahant, A. B.; Redlin, A. J.; Schmidt, J. G.; Creedon, F. T.; Jacobson, J. W.; and Bailey, D. A.: The biological action of fiberglas-plastic dust. AM.A. Arch. Indust. Health, 18:34, 1958.
109. Schneider, H.: Ueber Siderose. Zbl. Arb. med., 7.142, 1957.
1. Bringhurst, L. S.; Byrne, R. N., and GershonCohen, J.: Respiratory disease of mushroom workers, farmer's lung. J.A.M.A., 777:15, 1959.
2. Bugyi, B,, and Molnar, L.: Lungenschden durch Reisstrohstaub. Beitr. Silikoseforsch., 57:37, 1958.
3. Bugyi, B.: On Conionmycoses. Prac. lekarstvi, 70:200, 1958.
4. Chinachoti, N., and Tangchai, P.: Pulmonary alveolar microlithiasis associated with the inhala tion of snuff in Thailand. Dis. Chest, 52:687, 1957.
5. DaSilva Horta, J., and De Carvalho Cancella, L.: ' Experimentelle Korkstaubkoniose (Experimen telle Suberose). Arch. Gewerbepath., 75:319, 1957.
110. Schechter, W. H.: How toxic are high energy 6. Dnner, L.: Pneumokoniosen durch Staub von
fuels? Nat. Safety News, 77:28, 1958.
Getreide und Saaten. In Staublungenerkrankun
111. Schler, P., ft al.: Stannosis. II. clinical study.
gen, Band 3, ed. by Jotten and Klosterktter.
Indust. Med., 27:432, 1958.
Darmstadt, 1958, p. 541.
112. Schuler, P., et al.: Manganese poisoning. Environ
7. Dickie, H, A., and Rankin, J.: Farmers lung an acute granulomatous interstitial pneumonitis
mental and medical study at a Chilean mine Indust. Med., 26:367, 1937.
occurring m agricultural workers. J.A.M.A., 167:
1069, 1958.
113. Serenko, A. S.; Stanislavsky, Y. M.; Khazan, G. L., et al.: Sanitary conditions of work and peculiari
8 Frank, R. C.: Farmer's lung--a form of pneumo coniosis due to organic dusts A.J. Roentgenol.,
ties of pneumoconiosis in workers at the Iron ore
79.189, 1958.
Agiomerating plants. Gig. Truda, 2.17, 1958.
9. Frost, T,, and Georg. J.: Taerskerlunge. Ugeskr.
114. Soriano, M : Asthme experimental par l'acroline.
Laeg, 775:1383, 1956.
Sem. hop., 54:3213, 1958.
10. Groetschel, H , and Trense, E.: Tod eines Druck
115. Sim, V M., and Paule, R. E.: Effect of possible
ers an Asthma bronciale nach Umgang mit
0
smog irritants on human subjects. JAM .A., 765:1908, 1957.
Nasszerstaubemitteln. Arch. Gewerbepath., 16: 375, 1958.
116. Sjberg, S. G.: Vanadium dust, chronic bronchitis 11. Gupta, A. S.; Ferris, B. G.; and Rao, M. N.:
and possible risk of emphysema, Acta med.
Oxygen consumption of male Indian jute workers.
Scand., 754:381, 1956.
A M A. Arch. Indust. Health, 20:96, 1959.
117. Sjberg, S. G., and Rgnr, K. G : Besvar fran 12 Klunker, W.: Zur Frage der tiologie und Path
luftvagar m.m. hos sotare i oljeeldningsanlggnin-
ogenese des sogenannten Bacher- und Mullerasth-
gar. Nordisk Median, 58:1973, 1957.
mas. Schweiz, med. Wschr., 87:714, 1957.
118. Smith, J. S., and Kench, J E.: Observations on urinary cadmium and protein excretion in men exposed to cadmium oxide dust and fume. Bril. ]. Indust. M ed, 74:240, 1957.
119. Smith, J. C.; Kench, J. E.; and Smith, J. P : Chemical and historical post-mortem studies on a workman exposed for many years to cadmium oxide fume. Brit. ]. Indust. Med., 74:246, 1957.
120. Tebrock, H. E., and Machle, W.: Advances in the management of chronic berylliosis. Proc. X ll Int. Congr. Occup. Health, Helsinki, 5:167, 1957.
121. Thomas, D. L. G , and Stiebris, K.: VanadiumVergiftung in der Industrie. Med. J. Australia, 45:607, 1956.
122. Thomas, M. D., Hendricks, R. H.; Gunn, F. D.; and Critchlow, J : Prolonged exposure of guinea pigs to sulfuric acid aerosol. A M A . Arch. Indust. Health, 17:70, 1958.
123. Timokhin, D. I : Problems of industrial hygiene in employment of magnesium-torium-cobak catalyzer, Hig. Truda, 2.42, 1938.
124. Tur, J : Liderosis pulmonum. Med. Pracy., 70:33, 1959.
125. Vallee, B. L.: Zinc and its biological significance A.MM. Arch. Indust. Health, 16 147, 1957.
126. Vorobjeva, R. S : The question of the toxicity of cadmium oxide J. Hyg. Epidemiol. Microbiol. Immunol. (Prague), 2 244, 1958.
127 Zapp, J. A.: Hazards of isocyanates in polyure thane foam plastic production. A M.A. Arch. Indust. Health, 75:324, 1957.
13. Kyung, V. A : Dust of the kukkersite shale as an etiological factor of occupational pneumoconiosis. Gig. Truda, 5:44, 1959
14. Lowry, T., and Schuman, L. M.: "Silo-filler's disease"--a svndrome caused by nitrogen dioxide. J A M A , 762:153, 1956.
15. Murray, R ; Dingwall-Fordyce, I.; and Lane, R. E.* An outbreak of weaver's cough associated with tamarind seed powder. Brit. J. Indust. Med., 74 105, 1957.
16. Pestalozzi, C.: Febrile Gruppenerkrankungen in einer Modellschreinerei durch Inhalation von mit Schimmelpilzen kontaminiertem Befeuchter wasser (Befeuchterfieber). Schweiz. Med. Wschr, 89:710, 1959.
17 Poliak, K; Guthert, H , and Schanzenbach, H.: Experimentelle Untersuchungen zur Frage der Getreidestaublunge. Arch. Gewerbepath. Gewerbehyg, 77:519, 1959
18. Roach, S. A , and Schilling, R S. F.: A clinical and environmental study of byssinosis in the Lancashire cotton industry. Biit. J. Indust. Med., 17-1, 1960.
19. Schilling, R. $. F.: The epidemiology of byssinosis. In the Symposium on Industrial Pulmonary Diseases, ed. by King and Fletcher. London, 1960. p. 185.
20. Schilling, R. S. F The epidemiology of byssino sis--adventure and misadventure. J. Occup. M ed, 7*33, 1959.
21 Stott, H.: Pulmonary disease amongst sisal work ers. Bnt. J. Indust. Med., 75:23, 1958.
334
MEDICAL PRACTICES
22. Smetanin, N. I.; The maximal permissible con centration of the loess dust in the air of cotton spinning plants. Gig. Truda, 2:53, 1959.
23. Tiller, J. R.: An investigation of byssinosis in a rayon mill. Trans. Ass. Indust. Med. Off., 7:157, 1958.
24. Totten, R. S.; Reid, D. H, S.; Davis, H. D.; and Moran, T. J.: Farmer's lung, report of two cases in which lung biopsies were performed. Amer. J. Med., 25:803, 1958.
25 Tuffnell, P. G., and Dingwall-Fordyce, I.: An investigation into the acute respiratory reaction to the inhalation of tamarind seed preparations. Brit. J. Indust. Med., 14:250, 1957.
26. Wassermann, M.; Bugeag-Mihail, G.; and Iosubas, S : Recherches experimentales concernant "la maladie des fileurs et des tisseurs de chauvre". Proc. X II Int. Cojigr. Occup. Health, Helsinki, 3 374, 1957.
27. Wegmann, T.; Galietti, P.; and Amrein, H. P.: Baumwollstaublunge. Schweiz. Med. Wschr., 88.437, 1958.
28 Zanmni, D (and Wassermann, M., Discussion) : \ propos de la " Fivre des cereales" des travdlleurs des silos. Proc. X II Int. Congr. Occup. Health, Helsinki, 7:386, 1957.
Infectious and parasital pneumopathies
1. Drankin, D. I., and Gerasimova, M. M.: Brucello sis and occupation. Gig. Truda, 2:8, 1958.
2. Gross, P.; Westrick, M. L.; McNerney, J. M.; and Pittsburgh, M. P. H.: Experimental Tubrculopneumoconiosis. A.M.A. Arch. Indust. Health, 19:320, 1959.
3 Harris, H. J.: Treatment of Brucellosis. J.AM.A., 177:709, 1960.
4. Junak, G.: Leptospireninfektionen bei Kanalar beitern. Arch. G ew erbepath15:565, 1957.
5. Kthe, J.: Die Leptospirose als Berufskrankheit. Arch. G ew erbepath17:316, 1959.
6. King, E. J.: Recent Research in Infective Pneu moconiosis. Proc. X II Int. Congr. Occup. Health, Helsinki, 7:283, 1957.
7. King, E. J.; Yoganathan, M.; Harrison, C. V.; and Mitchison, D. A.: Experimental infective Pneumoconiosis. A.M.A. Arch. Indust. Health, 16:380, 1957.
8. Ramsay, J. H., and Pines, A.: Results of treat ment of pneumoconiosis complicated by tuber culosis. Brit. Med. J 2.345, 1959.
9. Schppert, R.: Lungentuberkulose als Beruf skrankheit bei Metzgern und bei in Landwirt schaft beschftigten Personen. Z. drztl. Fortbild., 22:417, 1958.
10. Spink, W. W.: Current status of therapy of brucellosis in human beings. J.A.M.A.y 172:697, 1960.
11. Terzin, A. L.: Psittacosis--ornathosis--mam malian pneumonitis (POMP) viruses in man, mammals and birds. /. Hyg. Epid. Microbiol. Immunol. (Prague), 2:129, 1958.
Lung cancer due to occupation and radiation
1. Causation of Cancer. British Med. Bull. 14(2), 1958.
2. Ask-Upmark, E.: Bronchial carcinoma in printing workers. Dis. Chest, 27:4, 1955.
3. Azhbel, S. I.: On cancer diagnosis in patients suf fering from toxic pneumoscleroses. Hig. Truda, 7:11, 1959.
4. Barborik, N. et al.: Carcinoma of the lungs in electrolytic chromium plating. Prac. Lkarstvi, 10:413, 1958.
5. Baetjer, A. M.; Damron, C.; and Budacz, V.: The distribution and retention of chromium in men and animals. A.M.A. Arch. Indust. Health, 20:136, 1959.
6. Baetjer, A. M.; Lowney, J. F.; Steffee, M.D.; and Budacz, B. A.: Effect of chromium on incidence of lung tumors in mice and rats. A.M.A. Arch. Indust. Med., 20:124, 1959.
7. Bidstrup, P. L.: Occupational causes of lung cancer. Trans. Ass. Indust. Med. Off., 9:2, 1959.
8. Bohlig, H., and Jacob, C.: Die Hufigkeit des Lungenkrebses bei deutschen Asbestarbeitern. Proc. X II Int. Congr. Occup. Health, Helsinki, 7:308, 1957.
9. Braun, W.: Krebs an Haut und inneren Organen, hervorgerufen durch Arsen. Dtsch. Med. Wschr, <97:870, 1958.
10. Browning, Ethel: Harmful effects of ionising ra diations. Elsevier Monographs: Industrial Toxic Agents. Amsterdam, 1959.
11. Cember, H.: Bronchogenic carcinoma from radio active particulates. Second United Nations Con ference on the Peaceful Uses of Atomic Energy. Geneva, 1958. Paper A/Conf. 15/P/900.
12. Chiurco, G. A.* Lavoro e tumori. Archivo di Medicina Mutualistica, 4:Voi. 14, 1959 (372 pages). Vide also: Proc. XII Int. Congr. Occup. Health, Helsinki, 147, (Fr.), 139, (Engl.), 1957.
13. Davies, D. F.: A review of the evidence on the relationship between smoking and lung cancer. J. Chron. Dis., 77:579, 1960.
14. Doll, R.: Occupational lung cancer. In the Sym posium on Industrial Pulmonary Diseases, ed. by King and Fletcher. London, 1960, p. 208.
15. Dol, R.: Occupational lung canter: a review. Brit. J. Indust. Med., 75:181, 1959.
16. Dvizkov, P. P.: Occupational cancer. Gig. Truda, 4(3): 3, 1960.
17. Eckardt, R. E.: Industrial Carcinogens. New York and London, 1959.
18. Ellinger, F.: Medical Radiation Biology. Springfield, Ilk, 1957, p. 224 ff.
19. Espinos-Prez, D.; Cancer pulmonar y neumoconiosis. Med. y seg. trabajo, 5:5, 1957.
20. Finkel, Miriam P.: Internal emitters and tumor induction. Proc. Int. Conf. Peaceful Uses of Atomic Energy, Geneva, 1955, Vol. 11. New York, 1956, p. 160.
21. Gallego, J. D.: Pulmonary lesions in pneumo pathies due to dust. Proc. X II Int. Congr. Occup. Health, Helsinki, 7:378, 1957.
22. Goldblatt, M. W.: Occupational Carcinogenesis. Brit. Med. Bull., 74:136, 1958.
23. Grosse, H.: Mischstaubinduration der Hiluslymphknoten und Lungenkrebs. Frankf. Z. Path., 67:220, 1956.
24. Haddow, A. (ed.): Causation of cancer. Brit. Med. Bull., 74(2), 1958.
25. Harris, W. B.; Breslin, A. J.; Glauberman, B.; and Weinstein, M. S.: Environmental hazards associated with the milling of uranium ore. A.M.A. Arch. Indust. Health, 20:365, 1959.
26. Hueper, W. C.: Experimental studies in metal cancerigenesis. X. cancerigenic effects of chromite ore roast deposited in muscle tissue and pleural cavity of rats. A.M.A. Arch. Indust. Health, 18:284, 1958.
27. Irmscher, G.: Ueber einen Todesfall an chro nischer Pneumonie nach Inhalation von alphaund betastrahlenaktivem "Industriestaub" vor rund 20 Jahren. Das Deutsche Gesundheitswesen, 52:1732, 1958.
NORWOOD
335
28. James, W. R. L.: Primary lung cancer in South Wales coal-workers with pneumoconiosis. Brit. J. Indust. Med., J2;87, 1955.
29. Kcnnaway, E., and Lindsey, A. J.: Some possible exogenous factors in the causation of lung cancer. Brit. Med. Bull., 14:124, 1958.
30. Koelsch, F.: Der Arsenkrebs. Zbl. Arbeitsmed., S: 129, 161, 1958.
31. McLaughlin, A. I. G.: Iron as a Carcinogen. In the Symposium on Industrial Pulmonary Diseases, ed. by King and Fletcher. London, 1960, p. 162.
32. Puccini, C.: Le problema della cancro-silicosi. Med. Lavoro, 51:18, 1960.
3**. Rinck, H.: Der Chromatkrebs der Lunge als Berufserkrankung. Medizinische, 342, 1956.
34. Sepke, G.: Zum Schneeberger Lungenkrebs. Zbl. Arb. Med., 7:114, 1957.
35. Smith, R. A.: Lung Cancer in Coal-Miners. Brit. J. Indust. Med., 10:318, 1959.
36. Sunderman, F. W.; Donnelly, A. J.: West, Bob: and Kincaid, J. F.: Nickel poisoning. A M A . Arch. Indust. Health, 20;$6, 1959.
37. Sunderman, F. W.; Kincaid, J. F.; Donnelly, A. J.; and West, Bob: Nickel poisoning. A.M.A. Arch. Indust. Health, 76:480, 1957.
TREATMENT OF PLUTONIUM DEPOSITION IN HUMANS WITH DTPA -- EFFECTIVENESS OF LONG-TERM ADMINISTRATION AND ORAL ADMINISTRATION*
W . D a c c e t t N o r w o o d , M .D .
Manager, Health Operation, Hanford Atomic Products Operation, operated by General Electric Company for the Atomic Energy Commission Richland, Washington
The recommended maximum permissible amount of soluble plutonium (Pu 239) in the human body is 0.04 microcurie -- 0.6 /g (1). Rigid control methods are necessary to limit body deposition to this extent. For instance, allowable concentrations in air are lower by a factor of millions than the comparable allowable concentrations of many of our most toxic chemicals. There will be increasing potential for exposure to such isotopes with the expanding use of such materials in industry, defence, and medicine. Hence it becomes most important to have the safest, best, and most con venient method possible for treating the individual who has accidentally acquired a deposition of Pu 239 which exceeds the maximum permissible limit.
Treatment, here, of five employees who had har bored small quantities of Pu 239 for some years indi cated that intravenously administered diethylenetriaminepentaacetic acid (DTPA) was much the most effective agent discovered to date for increasing the urinary elimination of Pu 239 (2).
The present study was made to improve knowledge of the effectiveness of DTPA in eliminating Pu 239 via the urine when treatment is extended over a pe riod of many months. It was also directed toward determining the effectiveness of DTPA in increasing elimination of Pu 239 via the urine and feces when administered orally.
Long-Term Administration of DTPA
An employee who had accidentally received a depo sition of about .4 microcurie of Pu 239 some 30 months previously was treated with DTPA intraven ously. Initially the daily urinary output of Pu 239 was about 665 disintegrations per minute per 24-hour specimen of urine (Table I). It was considered advis able to cautiously continue treatment over an extended period unless evidence of kidney irritation or other untoward effect appeared during the treatment. This
*The DTPA for this study was kindly supplied by Dr. Murray Weiner, Geigy Pharmaceuticals, P.O. Box 430, Yonkers, New York. R. H. Wilson was most helpful in coordinating sample collection and assisting in the inletpretation of results. G. D. Brown and staff performed the btoassays of the many samples.
would serve the dual purpose of eliminating a fair amount of Pu 239 and indicating whether or not there
was .a change in effectiveness of this agent when used over an extended period.
T able I
EFFECTIVENESS OF INTRAVENOUSLY ADMINISTERED DTPA IN INCREASING URINARY EXCRETION OF PU 239 WHEN
GIVEN FOR MANY MONTHS
Week of
T reatm ent
Dose--DTPA in Grams
Per Week
Average Daily
Urinary Excretion of
Pu 239 Expressed as Disintegrations
Per Minute
Effectiveness
Expressed as % of Initial Effectiveness
1
2
665
100
2
1.6
610
92
N o treatm ent for
period of 5 weeks
12
11-12
1.6
481
72
13-14
2
49 5
74
N o treatm ent for
period of 5 weeks
15
26
2
496
74
27
2
456
66
33
2
246
37
46
2
190
29
50
2
125
19
Average daily elimination of Pu 239 for periods
preceding and following the above treatment was ,, 12 disintegrations per minute in 24 hours.
Except for minor changes as shown in Table 1, the employee was given 1 g of DTPA Intravenously, in the Manufacturing Area Medical Center, on Monday and 1 g on Thursday of each week for three successive weeks. Such periods of treatment were alternated with periods of three weeks of no treatment. This was con-
610
SOCIAL AND LEGAL ASPECTS
element above the loss of wages the longer he was off
work. This case illustrates how an individual deliberately
perpetrates his disability on a subjective basis in order to increase the size of his monetary settlement.
Casf No. 3 -- A 37-year-old tTainman was injured while standing too close to a slowly moving train when his arm was struck by a grab iron, causing him to spin around and strike his head against the side of a Car He received a 5-cm vertical laceration across the
middle of his forehead. The man was stunned but re mained on his feet The laceration was repaired at the plant dispensary. X-rays of the skull were negative. There were no other injuries except for a slight con tusion of the right upper arm Neurologic examina tion was entirely negative and remained so thereafter. No tieatment was indicated other than analgesic medi cation for pain The patient did not work his next turn and was seen again the following day. The previ ous night he had a mild headache but was now asymptomatic. Examination was again negative The patient was seen again four days after the accident. The sutures were removed, and adhesive bridges were applied. His only complaint was occasional frontal headache which was relieved by aspirin. He had not returned to work' and when questioned as to why, he gave some vague complaints of soreness in his right arm and upper back Examination was again negative for objective findings. It seemed to the physician that the man believed he could and should be working but for some reason had not done so. He was formally approved for work and was so advised. The patient returned to work six days after the accident and worked for several hours but then reported off because of headache. He was seen again the following day, complaining of headache, dizziness, and soreness of the upper back and right arm. The laceration was healing well. Examination results were negative once again. He apparently did not intend to work; he was treated symptomatically and seen again one week later, at which time his condition was unchanged. Fol lowing this visit he was not seen again for another two weeks. It was then 24 days since the injury. The
patient had taken his vacation in the interim, for which he had received vacation pay. He offered no complaints, and the examination was again negative. The man finally returned to work 30 days after this injury and remained at work thereafter. He instituted litigation against the company, because he demanded compensation about seven times his actual loss of earnings, and the company refused to grant the claim.
Each time this patient was seen during the 30-day period it seemed that he really believed he could work and that he actually wanted to. He was phys ically able and was not considered as having posttraumatic neurosis. Why then did he not work? There appeared to be several reasons. While the patient was being treated in the dispensary shortly after the acci dent, a company representative remarked that it would be good if he did not miss work, since his work group had gone for an unusual length of time without a lost-time accident. This was interpreted by the pa tient and his fellow workers as company interest in avoiding lost time rather than the employe's welfare. Resentment was incited and led to deliberate lost time. The patient was also encouraged to miss work because he had a head injury which required suturing Another factor which played a part was encourage ment by certain parties to deliberately perpetrate un necessary lost time for the purpose of establishing a claim against the company for income greater than his regular earnings
This case illustrates how management action, work group standards for lost time, and litigation practices in work groups interfere with the medical manage ment of the injured employe and create unnecessary disability leading to excessive monetary gain.
Summary
In summary, I have outlined certain socio-economic factors that have a negative influence on the disabled employee. The discussion has dealt with why and how such factors interfere with the individual's recovery from an occupational injury, with the thought that a dearer understanding must precede any effort to do anything about them.
BASIC PRINCIPLES FOR PRECAUTIONARY LABELING
Edward J. H ogan
Vice-Chairman, Labels and Precautionary Information Committee, Manufacturing Chemists9 Association, Inc; ;
Packaging Coordinator, Allied Chemical Corporation, New York, N. Y.
It is an honor and a privilege to speak to you, as a representative of the Manufacturing Chemists' Association, regarding one if its activities. The Man
ufacturing Chemists' Association is an incorporated national trade organization composed of more than
180 companies engaged in the manufacture and sale of chemicals. These companies account for more
than 90 per cent of the chemical production capacity of the United States.
From its founding in 1872, the MCA has been concerned with the many problems accompanying the growth of the chemical industry. Prominent among these has been t h e p r o m o t i o n o f s a f e t y , a n d t h e Asso ciation is proud of its contributions to the record of chemical manufacturers in this regard, which is among the best in all industry. This achievement is the
more notable in view of the inherent hazards in many of the industry's processes and products.
The Association's interest in safety goes far beyond that of its members' employees to include those transporting, handling, and using its products. The objectives are promoted in a number of ways, but I shall discuss at this time only that phase concerned with the labeling of chemicals to instruct those hand ling or using them how to do so safely.
In the early days of the industry both the chemicals distributed and the trades using them were limited in number and each had been long established. Cus to m e rs were so accustomed to the use of the existing compounds that specific instructions seemed unnec essary, and such warning labels as were used on industrial chemicals were limited to the stronger
HOGAN
611
acids and alkalies, and extreme poisons. There were, of course, the 1927 Federal Caustic Poison Act and
a number of state poison and pharmacy acts, but these were chiefly directed to the labeling of house hold packages. In most cases they were pointed toward the hazard of ingestion and relied solely on the word "POISON'' to warn the user.
The expansion of the industry and the broadened use of its products brought recognition of the need for more comprehensive labeling. One of the early steps in this direction came in 1934 and covered the uniform precautionary labeling of six products or product groups under a series of voluntary agree ments between the manufacturers of these products and the Surgeon General of the United States. These agreements served a very useful purpose until they were discontinued by the United States Public Health Service in 1952 because specific labels for these pro ducts which had, in the meantime, been developed under the Manufacturing Chemists' Association's program were considered more appropriate.
As chemical products, especially in the organic group, mulitiplied and grew more complex, the need for further steps became evident. This was emphasized by a survey conducted by the Association in 1936 which resulted in distribution to its member executives of a printed book titled "A Confidential Report on Adequate Labeling--Its Importance to the Chemical Manufacturer." This report persuaded many com panies to embark upon their own warning label programs or to expand those already begun.
World War II greatly accelerated the growth of our industry. Not only did established companies ex pand their production of well-known chemicals, but they developed innumerable new ones. Many cor porations from other segments of industry, as well as completely new concerns, began chemical manu facture. And--most important of all, from the point of view of precautionary labeling--thousands of in dividual companies, large and small, and millions of workers began to operate processes using chemicals entirely foreign to any of their previous experiences. The need for a comprehensive program of education in the safe handling of chemicals was obvious. Early in 1944 MCA considered the problem at a meeting of its member executives. It was decided that the best method to reach the man in the shop using chemical products was by means of instruction labels, and the formation of a "Labels and Precautionary Information Committee" was accordingly authorized.
The LAPI Committee, as it has since been popularly called, met for the first time on May 17, 1944. To insure a broad view of the problem, the members selected included those with chemical, medical, legal, research, administrative, and sales backgrounds. Since that date, this has been a continuing and active committee. The work of LAPI is well known to industry and administrators of health and safety pro grams through its publication "Warning Labels--A Guide For the Preparation of Warning Labels for Hazardous Chemicals." This manual, frequently re ferred to as the ``LAPI Manual," is now in the review
stage, with a Fifth Revision scheduled for publica tion this year.
It might be assumed that, having agreed upon the
need for precautionary labeling, the writing of labels
would be simple. All one need do, you would say,
is to mark a hazardous product POISON and add the
do's and don'ts. Unfortunately, the problem is more involved than that.
What are the meanings of the terms used? Chemi cals may be harmful in a variety of ways. A product which may threaten your life solely by ingestion should not be labeled the same as one that may kill by absorption through the skin. Of course, there is also the matter ok degree. How shall we distinguish between the vapor or gas which asphyxiates and one which causes cyanosis? What really is a "poison"? There is the difficulty of language. Statements must be brief but accurate. They must be expressed in terms that ordinary workmen understand. Not only must the statements help avoid accidents, but if such occur, first aid should not be delayed while someone hunts an interpreter. In the case of trade-named chemicals or proprietary compounds, what is our responsibility to the doctor who may be asked to treat persons injured by them?
As a result of these and many similar questions, the following principles were adopted. These principles are set forth in detail in and comprise Part I of the LAPI Manual.
1. Each chemical product presents a distinct prob lem and must be treated individually in the light of its own characteristics. Conclusions regarding the hazards of a product cannot safely be drawn either from the properties of the materials from which it is formed or by analogies based upon chemical struc ture. Mixtures of two or more chemicals may have properties that vary in kind or degree from those of the individual components; any warning label for mixtures should be based on the properties of the finished product. Impurities may contribute hazardous properties and should not be overlooked.
2. All statements on warning labels should be brief, accurate, and expressed in simple, easily under stood terms.
3. Precautionary labeling should be used only when and to the extent necessary. The language should be practical, not based upon the inherent properties of a product alone, but directed toward the avoidance of hazards resulting from such use, handling, and storage as may reasonably be anticipated. The use of warning labels for relatively harmless products or the use of unnecessary words will develop a disregard for labels and defeat their purpose as surely as will failure to give adequate notice of hazards.
4. On labels of different products uniformity in lan guage to indicate the same hazards and same degrees of hazard is most desirable in order to gain greater understanding through standardization.
5. The following subject matter should be con sidered for inclusion on a warning label: (a) name of product; (b) signal word designating degree of hazard--DANGER!, WARNING!, or CAUTION! (c) Affirmative statement of hazards; (d) precautionary measures covering actions to be followed Or avoided; (e) Instructions in case of contact or exposure where advisable. (NOTE: under some laws antidotes are re quired when the word "POISON" is used.) Instruc
tions for the handling and storage of containers should also be considered for inclusion on the label. This is information relating to characteristics of the con tainer as well as those o its contents.*
6. The inclusion of the word "POISON" and the skull and crossbones on a label should be limited to those cases where the product is a poison according
612
SOCIAL AND LEGAL ASPECTS
to a definite toxicity standard or where such use is prescribed by law. When used, this legend should be in addition to the other label warnings and should not take the place ol the words DANGER!, WARN ING!, and CAUTION!, which are designed to show the relative degree of hazard.f
7, A nondescriptive code designation or trade name should not be used as the only identification of a hazardous chemical. If the complete name is not shown, the label should clearly state the type of chemical--e.g, "Corrosive Acid", "Lead Compound".
8. Warning statements should be grouped together in a prominent location on the label and should be printed in easily legible type which is in contrast by typography, layout, or color with other printed mat ter on the label. The label should be affixed firmly to and in a conspicuous place on the container.
In accordance with the principles just stated the usual warning label includes: (a) a "signal" word-- "DANGER!", "WARNING", or "CAUTION"--to give a general indication of the severity of hazard; (b) a statement of hazard or hazards--such as "Vapor Extremely Hazardous", "Causes Burns," or "Rapidly Absorbed Through Skin"; (c) precautionary measures --such as "Do not breathe vapor," "Keep away from heat and open flame," or "Avoid contact with skin and eyes"; and (d), where appropriate, instructions in case of accident, as "In case of contact immediately flush skin or eyes for 15 minutes; for eyes get medical
attention."
Using these or sim ilar statem ents, a typical label
may read: ANILINE
DANGER! HAZARDOUS LIQUID AND VAPOR RAPIDLY ABSORBED THROUGH
SKIN
Do not get in eyes, on skin, on clothing. Avoid breathing vapor. Use only with adequate ventilation. In case of contact, immediately remove all contaminated clothing, including shoes, and flush skin or eyes with plenty of water for at least 15 minutes; get medical attention. Wash clothing before re-use.
POISON
*Author's Note: The Manufacturing Chemists*Associa tion has available at its office, 1825 Connecticut Avenue, N.W., Washington 9, D.C., at nominal cost, a series of individual Chemical Safety Data Sheets on the properties and essential information for safe hand ling and use of 79 chemicals, Manuals on Standards and Recommended Practices on the use and handling of spectfic containers, and an outline of recommended general precautions for handling and storage of certain classes of containers in the MCA LAPl Manual. These data will serve as excellent guides in the devel opment of applicable phrases for container handling and storage statements.
[Author's Note: The word "POISON" has been used indiscriminately in the past, and its meaning has been ill defined. For labeling purposes the MCA Manual recognizes poisonings by three modes of entry--viz., ingestion, inhalation, and absorption through skin-- but limits use of the word to those cases where the toxicity has been demonstrated, either by human ex perience or laboratory animals tests, to exceed certain defined limits.
Parts II and III of the LAPI Manual contain several hundred illustrative labels such as the one shown.
Those in Part II are for industrial chemicals. Ex amples included are generally for those products most important commercially, and, as a whole, they take in a broad range of hazards. The labels in Part III cover the majority of pesticides sold in large volume. This section was added following the passage of the Federal Insecticide, Fungicide, and Rodenricide Act in 1947. The latter requires adequate warning labels for this important group of chemicals, and the MCA labels have the informal approval of the United States De partment of Agriculture and are consistent with its Interpretation 18, Revision 1.
How successful is the LAPI Program? As may be expected, the LAPI principles have the broad support of MCA members, who, as stated earlier, represent 90 per cent of the U S production of industrial chemicals. In lact, chemical manufacturers, both in and out of the Association, fully supported these principles. The very fact that such a program exists and is supported exerts a persuasive force upon the manufacturer who might otherwise neglect proper labeling The latter knows that, should he be called to court because of claimed injury by one of his inadequately labeled products, the opposing counsel would surely cue the warning statement used on similar competitive products.
Within months after the organization of the LAPI Committee in 1944, Us chairman was asked to serve
as advisor to the State of California, which sub sequently became the first of several states to regulate the precautionary labeling of hazardous chemicals. Besides California, the ensuing years have seen sim ilar regulations or laws adopted by Connecticut, Oregon, Hawaii, Illinois, Texas, New Jersey, New York State and New York City. AH have been based upon the MCA principles.
Reference has already been made to the Federal Insecticide, Fungicide, and Rodenricide Act, and to the fact that LAPI labels comply with the regula tions issued pursuant to it.
At meetings of the International Labor Organization, held in Geneva, Switzerland, the MCA's precaution ary labeling system was endorsed and much of its content adopted for ultimate use by ILO on a world
wide basis.
A committee of the International Association of Governmental Labor Officials, which consists of U-S. and Canadian state, provincial, and federal admin istrators, has developed a "Suggested Draft for Uni
form Rules and Regulations relating to the Labeling for Use, Handling, and Storage of Containers Hold ing Substances Harmful to the Safety and Health of Employees." This draft adheres to LAPI principles and was the foundation for the current regulations in New Jersey and New York State and City.
In this highly regulated era--when all of us, and industry particularly, are subjected to many restrictive laws and regulations--it is to the credit of the chem
ical industry that its adequate labeling practices began as a voluntary program and that the labeling legis lation of recent years has been in support of the industry's principles rather than controverting them.
Further evidence of the LAPI Committee's in fluence is the fact that definitions for "POISON" sub
stantially identical with that of its manual were written into the regulations under the Federal In
secticide Act and have also been substituted in the
KLEIN
613
Interstate Commerce Commission Regulations for the former definition of "Class B. Poisons." Again, LAPI
has been instrumental in obtaining the acceptance of the word "flammable" by ICC and other public
agencies as less likely to be misunderstood than "inflammable." Its reputation has extended so far that in 1953 the Association of British Chemical Manufacturers, which is MCA's British counterpart,
sent representatives to this country solely to study the LAPI program and subsequently adopted one p a r alleling it.
This program is receiving additional impetus from other trade associations, which have been most gener ous in their cooperation. As already indicated, the LAPI objective is principally aimed at industrial chemicals. While the principles are generally accept able to all groups, their application may vary in detail for different segments. A committee of the Chemical Specialties Manufacturers Association has prepared a model law for the labeling of household products. Directions for use are usually an important addition to small household packages and may convey information for proper use which supplements the precautionary statements. Similarly, the American Pe troleum Institute recently published a manual of pre cautionary labels for petroleum products as distinct from petrochemicals. Both associations support LAPI
principles.
The common aim of all these groups is the adequate and uniform labeling of the hazardous substances which they produce. Uniformity is essential for the free flow of commerce and important in educating
people to understand the significance of label warn ings. The public must be led to recognize that chemi cal products may, on occasion, be hazardous and re quire care in handling, just as experience teaches us that care in handling is necessary with edged tools and with electrical and mechanical devices. Unlike the latter, which seldom carry warning labels, chemicals will always require some precautionary labeling, because their properties can seldom be deter mined by visual inspection.
In conclusion, I should like to emphasize that any precautionary labeling program based upon the prin ciples set forth by the Manufacturing Chemist's Asso ciation could not be considered experimental. The concept on which such a program was based has been time-proven and accepted in similar programs inter nationally. With such a program you have not only taken out insurance on the future of your products, but you have provided a necessary adjunct in the fundamental obligation to warn of the health hazards involved in the use of either new or established
products.
I thank you!
THE CARDIAC CASE IN WORKMEN'S COMPENSATION
I r v in K l e in , M JX Medical Director, Workmen's Compensation Board, State of New York
It is my great pleasure to be able to address this thirteenth International Congress on Occupational
Health, It is significant that common problems know no national boundaries, and together we have sought remedies in different countries of the world for over 30 years. It is apparent that this is the only sound method by which we can solve these problems. It is of additional significance that we are thus able to set a good example of the way in which other matters may be disposed of.
This afternoon we are to consider the cardiac case in workmen's compensation. To merely dismiss it with the wave of the hand is unworthy of the talent and intention of this organization. A search into the causes and results in this area is necessary and important. There is a continuing and growing
interest in the cardiovascular episodes during and in the course of employment. Recently great attention has been paid to the increasing number of these cases which have come before the workmen's compen sation boards for evaluation and adjudication. In New York State for the years 1947 to 1957 the figures have risen from 167 compensated cases to 545. For the first six months of i960 up to 150 cases were closed without award for many reasons (failure to prosecute, withdrawal of claim, and failure to make out a proper case after trial). The most frequent involvement has been the coronary arteries resulting in postocclusive angina, failure, pulse irregularities, and infarction.
It is not necessary at this time to review the var ious skills involved in the diagnostic procedures, nor is it necessary to review the need for proper history and record keeping. We can safely assume that the
trained physician is fully aware of the need for these. There remains, therefore, only the consideration of the relationship of the pathologic process to the work load and the proper rehabilitation of the pa tient. It is suggested that the exact mechanics involved in the closure of a coronary vessel and the resultant myocardial infarction are not fully understood It must be further conceded that the sclerotic process begins fairly early in adult life and this, undoubtedly, plays a large part in the occurrence in industry.
It has been the philosophy that the working man is hired for his abilities along with all of his dis abilities, whether manifest or hidden. It is therefore incumbent upon the physician to be the first to rec ognize this in industry. Others should be cognizant of this as well. It appears to me that no defenses can be set up on the thought that in a given case with
any degree of sclerosis the clinical end result would have occurred in any event. We must recognize that this type of reasoning leads nowheres, since general izations have little value in this area. It is best to be prepared to take an attitude which appears rea sonable to ordinary analysis and be ready to review each case on its own merits. Recognition that we do not have a full explanation at this time should not preclude us from drawing a conclusion.
It is important to keep in mind that the legal process is the dominant factor when the cardiac case in industry is discussed. Too often the physician becomes involved in a case to a point beyond his medical sphere. At that point he attains the status of an advocate in the proceedings for which he is not trained, for which he is obviously ill prepared and
988
MAXIMUM ALLOWABLE CONCENTRATIONS
daily work without intervals (which are not considered ethylene cases because they have great desaturations by
in stating MAC either) performing physical work lungs and have entirely different ways of metabolizing
which requires average minute lung volume of 12:1 trichlorethylene.
(or 10:1; lower volume could be considered only for The dose required by Swedish authors, 50 mg of
entirely sedentary work). From this calculation it trichloracetic acid in urine, corresponds theoretically
ir
was evident that a workman absorbs 3.4 g (or 2.8 g) only to the Soviet MAC--that is, 9 ppm about 50
of trichlorethylene in eight hours, modifies it into From our previous experiments, where we consid
850 mg (700 mg) of trichloracetic add and into 1897 ered only trichloracetic acid in smaller percentage,
mg (1412 mg) of trichlorethanol.
10 per cent was found that in lower concentrations
It is difficult to say how great is the pharmacologic of trichlorethylene in air (up to about 400 fig per
effect of daily administration of 3 g of trichlorethylene, liter--that is, 75 ppm) the ratio of trichloracetic
due to the fact that it does not occur in such doses acid in mg to trichlorethylene in fig in 1 I of air is
in medical practice. In the past years 1 ml was admin about 1:2. This ratio was decreasing with the increas
istered per case in cases of angina pectoris or ing concentration of trichlorethylene. Several obser
neuralgia n.trigemini, four times a day maximum. vations from practice bear witness to this fact. From
Beforehand, however, we can suppose a hypnotic effect our recent experiments results that the ratio is the 3
especially if we lake into consideration that the inter oretically 1.1 (Souiek-Vlachovi, Bartoniiek). I think
s
mediary product in the metabolism of trichlorethylene that it is not possible to give more accurate directions
is chloralhydrate The ascertained daily dose of tri for practice, due to the great difficulties occurring in
chlorethylene corresponds, according to the American practical work and thus we can conclude that this
#
MAC, to 4 3 g of choralhydrate It is well known that ratio lies within the mentioned values I I or 12.
I
the current hypnotic dose is 1-2 g, and it is also On the basis of literature data that a great part
known that chronic intoxication with chloral is not of working people have health disturbances after
%
very rare and is similar to chronic intoxication with a long-time work at 50 mg or 100 mg of trichloracetic
trichlorethylene
acid in urine per liter we see that it would corre
It is also possible to see to the effect of trichlor- spond with 100 toJ 200 f i g of trichlorethylene in air
ethanol, which is the principal metabolite of trichlor This concentration in air corresponds with 100*200 fig
ethylene and, in our opinion, it is primarily responsible of trichlorethanol in urine
for the symptoms of intoxication. Owing to the fact For the purpose of solving the question of MAC
that pharmacologic literature does not often mention values in the most important industrial poisons there
this substance, we can compare it with tribromethanol. ought to be available a great number of carefully
Narcosis is attained by this substance after a dose of made observations in practice. It is also necessary to
S.5-5.6 g in a man weighing 70 kg. In our case there investigate, in laboratory experiments, the absorption,
forms 19 g of trichlorethanol daily
metabolism, and elimination of these substances. For
I think that these considerations result in the fact medical thinking it is acceptable to consider the
that the American MAC is rather too high. If it was actually absorbed dose. Experiments with animals
created from experiments with animals, it is necessary are suitable only for the orientation of newly intro
to declare that animals are not suitable in trichlor duced chemical substances.
SCIENTIFIC BASIS FOR THE ESTABLISHMENT OF TOLERABLE LIMITS ADOPTED IN THE UNITED STATES FOR THE PRINCIPAL INDUSTRIAL TOXINS
Ch a r l e s R . W il l ia m s , P h .D.
Assistant Vice President, Liberty Mutual Insurance Company, Boston, Massachusetts
In the United States, hygienic standards (tolerable limits) for inhalation are developed for the purpose of providing guides to be used for controlling expo sures to toxic materials in industry. These guides are dependent on the basic philosophy that for most such materials there are levels of exposure which can be tolerated without adverse effect. The principal excep tions to this philosophy are those which are applied to carcinogenic and sensitizing materials. So little is known of the processes of carcinogenicity and sensitiza tion that the tendency is to consider that levels of known carcinogenic and sensitizing materials should be kept as dose to zero as possible. The problem, then, is to develop information which can provide a valid basis for establishing levels of toxic materials which can be tolerated in the industrial environment.
TERMINOLOGY
In order to avoid confusion it must be pointed out
that there are differences in terminology with refer
ence to acceptable values for exposures to potential toxic materials. Thus we find such terms as "Maxi mum Allowable Concentration," which certainly has the broadest usage; "Maximal Acceptable Concentra tion/* which has been utilized by the American Standards Association Z37 Committee (1); and "Threshold Limit Values," which is used by the American Conference of Governmental Industrial Hygienists (2). All of these terms have the same basic implication--namely, that these values are allowable or acceptable or that there is a limit which denotes a
fine line between toxic and nontoxic. As a matter of fact, the users of these terms rarely accept the implied connotations. The problem is one of semantics. In 1949 the Committee on Chemical Agents at the 9th Annual Congress on Occupational Health (United States) recommended that the term "Hygienic Guide" was much more descriptive of the actual utilization of the numbers. In September, 1955, the American Industrial Hygiene Association began publishing its
WILLIAMS
989
"Hygienic Guide Series'* using the term "Recom
excess of the acceptable concentration prob
mended Maximum Atmospheric Concentration (8 hours)." In 1956 Smyth (3) proposed the use of "Hygienic Standards for Daily Inhalation.** For some time the writer (4) has been urging the general accept ance of the concept of "Hygienic Standard** or "Hygienic Guide/* since these terms express much more accurately the actual purpose of the application of such criteria in the occupational health field.
ably would produce injury. When the level has been established on the basis of a func tional change or discomfort, it is logical to assume that exposure to concentrations not greatly exceeding the acceptable concentration would not produce materially injurious effects.
Hence it is important to understand the cri teria upon which any such maximal accept
able concentration has been established.
Though the purpose of the acceptable con
ORGANIZATIONS
centration is to minimize health hazards, its immediate use is for guidance in establishing
In the United States the establishment of hygienic guides is carried on by groups of competent indi viduals operating within existing organizations and utilizing available technical information. The Amer ican Standards Association, a private organization representing American industry, has been sponsoring development of standards in the occupational health
engineering procedures to prevent objection able concentrations of toxic or noxious ma
terials from being present in the air of work places. Comparison of the results ot air
analyses with those concentrations indicates acceptable conditions or otherwise the need, extent, and urgency of control measures.
Sampling and analysis should be carried out
field since 1941, chiefly through its Z37 Committee. These ``American Standards" include the scope and purpose as well as general physical-chemical and toxic properties, "Maximal Acceptable Concentration,"
and sampling and analytical methods and references Since their start 19 such standards have been pub lished, and the Committee is continuing to be ex tremely active in the field. The basis on which this
by competent personnel using an acceptable method which will provide a reliable measure
of exposure.
Air analyses in conjunction with acceptable concentrations of such atmospheric contam inants as are encountered in industrial opera tions serve as a measure of exposure--not as a means of diagnosis of occupational disease.
Diagnoses should be based on a consideration
Committee operates is set forth in the introductory statement provided with all of their standards, as follows:
of all factors including results of clinical and physical examination as well as of air analyses, means of assessing amounts of materials in the body, and a knowledge of toxicologic
"The Meaning of Maximal Acceptable Concentration" (1 )
effects of the materials in question. In the application of the standards, it
should be kept in mind that:
It is generally recognized that there are
(1) The acceptable concentrations serve as
levels of concentration of atmospheric con
standards of good practice.
taminants to which a person may be exposed
(2} They serve as engineering guides. De
without known ill effects or discomfort. In
sign and operation should aim at main
view of the impracticability of maintaining
taining all concentrations below the
uncontaminated air in most industrial envir
acceptable maximum.
onments, it is necessary to establish accept
(3) They should be applied and interpreted
able concentrations of atmospheric contam
by competent individuals with a full
inants encountered in industrial operations.
understanding of the basis and limita
These concentrations in themselves do not
tions of the information from which the
represent a scale of relative toxicity; they
standard has been developed.
represent the concentrations of contaminants
(4) It is advised that these standards are
i
below which ill effects are unlikely to be
considered to be guides toward good
1
experienced by any but hypersusceptible indi
industrial hygiene and are not intended
t
viduals.
as legal requirements.
3 ?
These concentrations are usually based upon data obtained by one or more of the
(5) The levels are applicable only to ex posure to a single substance. In the
following procedures:
case of exposure to mixtures, the effect
(1) Laboratory tests on animals
may be increased or decreased, and con
(2) Laboratory tests using human subjects
trols should be based on the specific
(3) Environmental and medical investiga
situation.
tions in plants A common feature of these procedures is
that the experimental exposure shall cor respond to the normal work pattern. This should be taken into consideration also in the application of maximal acceptable concentra
tion values. Three criteria have governed the establish
ment of these concentrations: (1) Organic or other tissue changes
(2) Functional reactions which have no discernible untoward effects on health but cause impairments, such as in-co
The American Conference of Governmental Indus trial Hygienists began its work in the standards field in 1947. They publish annually a list of the materials, with values, which they call "threshold limits/' The values which are given represent the concensus of a committee of qualified experts in the occupational health field. They are reviewed and brought up to
date each year The most recent published list dated 1959 (2) contains values for 169 gases and vapors; 71 toxic dusts, fumes, and mists; 11 mineral dusts; and a list of 21 so-called tentative values. The basic
ordinations and increased proneness to
philosophy of this group is set fo rth in paragraphs
accidents
(3) Discomfort or adverse sensory effects
preceding its listing of values:
In those cases in which the concentrations have been established on the basis of organic changes, it is logical to assume that repeated
exposure to concentrations significantly in
"Threshold Limit Values for 1959" (2)
Threshold limits should be used as guides in the control of health hazards and should
990
MAXIMUM ALLOWABLE CONCENTRATIONS
not be regarded as fine lines between safe and dangerous concentrations. They represent conditions under which it is believed that nearly all workers may be repeatedly exposed, day after day, without adverse effect. The values listed refer to time weighted average concentrations for a normal work-day. The amount by which these figures may be ex ceeded for short periods without injury to health depends upon a number of factors such as the nature of the contaminant, whether very high concentrations even for short periods produce acute poisoning, whether the effects are cumulative, the fre quency with which high concentrations occur, and the duration of such periods. All must be taken into consideration in arriving at a decision as to whether a hazardous situation exists. Special consideration should be given to the application of these values in the evaluation of the health hazards which may be associated with exposure to combinations of two or more substances.
Threshold limits are based on the best avail able information from industrial experience, fom experimental studies, and, when pos sible, from a combination of the two. These values are based on various criteria of toxic effects or on marked discomfort; thus, they should not be used as a common denominator of toxicity, nor should they be considered as the sole criterion in proving or disproving diagnosis of suspected occupational diseases.
These limits are intended for use in the field of industrial hygiene and should be employed by persons trained in this field. They are not intended for use, or for modi fication for use, in the evaluation or control of community air pollution or air-pollution nuisances.
These values are reviewed annually by the Committee on Threshold Limits for changes, revisions, or additions as further information becomes available. The Committee welcomes the suggestion of substances to be added to the list and also comments, references, or reports of experience with these materials.
In addition to these two groups, the American
Industrial Hygiene Association has, since 1955, been
publishing the Hygienic Guide Series. To date guides
have been published for 97 substances. In many
respects this series is similar to the recommendations
of Smyth in his report to the A.I.H.A. in April 1956.
Information is provided for each material relative to
the recommended maximum atmospheric concentra
tions; severity of the hazards (both health and fire);
the short-exposure tolerance; atmospheric concentra
tions immediately hazardous to life; physical and
chemical properties. In addition, under the heading
of "Industrial Hygiene Practice'* brief statements are given as to recognition, evaluation of exposures and
recommended control procedures. Also, under the
heading "Specific Procedures," brief descriptions are
given of first aid, prophylactic measures, and special
medical procedures. Finally, a list of references is
given. It is also significant that in each case, under
the heading of "Recommended Maximum Atmospheric
Concentration," a statement is made as to the basis
of the recommendation. This approach represents by
far the most desirable way of dealing with the problem of establishing hygienic standards. Mere lists
of numbers leave much to be desired. It is extremely
important that all available information relative to
the establishment of the standard be included with it.
BASES FOR THE ESTABLISHMENT OF HYGIENIC GUIDES
The establishment of numbers for "tolerable limits" in the United States is based primarily on two kinds of information; animal experiments and human ex perience. The scientific research which produces the basic data is carried on by private industry, univer sities, research laboratories, and governmental agencies. The results of such investigations are published in many United States technical and scientific journals
In some cases, particularly new chemicals, the tech nique of applying analogy with other well-known chemically similar materials has sometimes been used until valid data have been accumulated
The committees or organizations referred to above utilize all available published and unpublished data in arriving at their judgments as to the kinds of levels which will provide a basis for safeguarding employee health.
Animal Experiments
The technique of evaluating toxicologic and physiologic responses in animals as a means of pre dicting possible effects of toxic materials, physical agents, or other environmental conditions on man has long been a routine tool in the occupational health field. In'* spite of this, however, there has been little attempt made to provide a standardized approach to investigative techniques in industrial toxicology. In many respects this is fortunate, for in dealing with the effects of a toxic material on a biologic system considerable flexibility is required in applying estab lished criteria. Usually early tests will indicate the course of further study. The magnitude of acute lethal doses and the effects on different organs will indicate the severity of the acute hazard and the importance of various routes of absorption. Corollary information relative to species variability, sex, age, and possible synergistic effects can be obtained at this time. All of this information will then provide a basis for future, more extensive long-term studies
In the case of new substances, the first step which is generally adopted by toxicologists or industrial laboratories in the determination of toxicity is the utilization of screening tests on experimental animals These are usually followed by detailed studies of acute effects resulting from single injection, ingestion, or inhalation experiments. In addition, irritating effects on skin and eyes are evaluated.
In 1956 a complete compilation of acute toxicides for an extensive series of materials was published under the auspices of the Aero Medical Laboratory (5). The purpose of this volume was to bring together available data on "acute toxicity of various substances for several species of commonly used laboratory animals as determined by oral or parenteral admin istration, or inhalation, of fatal doses." In the intro duction to this volume the various significant con ditions influencing the acute toxicity for any given compound were discussed. These include the dose, the rate of absorption, route of administration, site of injection, and other influences, including disease, environment, temperature, habit and tolerance, etc In addition, it was pointed out that the toxicity of chemicals will vary with species of animals and some times even with different strains of the same species. Within the same strain the toxicity may differ with age, weight, sex, and general condition of the animals.
i
WILLIAMS
991
Because of all these variables it is virtually impossible to be certain that all experiments are conducted in precisely the same way. In fact, only rarely does one find detailed discussion of all such factors involved in an experiment.
Following accumulation of data on acute effects, long-time chronic effects are then studied through
inhalation, feeding, injection, and skin-absorption ex periments. The nature of these is determined by the results of earlier screening tests. At a conference on The Toxicological Basis of Threshold Limit Values in 1959 (6) V. K. Rowe and his coworkers presented an extensive summary of the kinds of observations
which had been made over a period of more than 20 years by several industrial groups. This discussion summarized and tabulated observations on mortality, food intake, body weight, organ weights, gross pathol
ogy, micropathology, hematology, blood urea nitrogen, clinical urine analyses, central nervous system, and cholinesterase.
Tables I-IV summarizing the frequency with which particular effects were observed under various circum stances give an indication of the significance of sev eral biologic and biochemical determinations. The significance of growth studies and cholinesterase in Tables I and II and the significance of the liver and kidney in all of these studies are well demonstrated in Tables III and IV. The authors (6) point out that
there is increasing pressure for more and more precise kinds of measurements in the biochemical and toxi cologic fields as a means of establishing valid threshold
limits. They point out, however, that while this is an excellent objective and one toward which all should strive, it is essential that one make the most practical use of available manpower and funds to obtain the most meaningful information. The criteria which are set forth in this paper are those which are most widely used and certainly accepted by all workers in the field. The best hope for increasing our fund of knowledge derived from animal experiments must come from the development of new techniques and new criteria. In summary, the authors of this paper state:
In spite of the fact that there are many new criteria being developed and tested today, the data presented herein emphasize the high value of certain of the older criteria. It would seem only prudent to make use of those studies which experience has shown to be most productive. This does not mean that only those criteria showing a high degree of efficiency in the series of investigations re ported herein should be used, but certainly it suggests that they should be basic to any toxicological study designed to determine a threshold limit for repeated exposure.
One other set of criteria which is attracting more and more attention are those physiologic studies which can be made on animals as well as on humans. In the symposium mentioned above, Dr. John A. Zapp, Jr. (7) discussed the importance of utilizing physiologic observations such as systolic and diastolic
T able I
FREQUENCY WITH WHICH A PARTICULAR EFFECT WAS OBSERVED AT THE LOWEST DOSAGE LEVEL AT WHICH ANY EFFECT WAS OBSERVED (6)
Criteria of effect
Oral
a
Data from 1952-1959
Vapor
%
a
%
Data from last 22-25 years
All routes
a
%
Growth Hematology Clinical urines CNS Cholinesterase
64 (172)
37
16 (38)
42
152 (410)
37
1 (79)
1.3
1 (21)
5
5 (170)
2.9
1 (7)
14
0 (7)
0
2 (43)
4.6
4 (109)
3.7
1 (32)
3.1
5 (141)
3.5
8 (10)
80
8 (10)
80
Number of positive findings (number of observations)
T a ble II
FREQUENCY WITH WHICH A PARTICULAR EFFECT WAS THE SOLE EFFECT AT THE LOWEST DOSAGE LEVEL AT WHICH ANY EFFECT WAS OBSERVED (6)
Criteria of effect
Oral
a
Data from 1952-1959
Vapor
%
a
%
Data from last 22-25 years
All routes
&
%
Growth
Hematology Clinical urine CNS Cholinesterase
25 (172)
15
0 (79)
0
0 (7)
0
4 (109)
3.7
4 (10)
40
2 (38) 1 (21)
0 (7) 1 (32)
5
44 (410)
11
5
1 (170)
0.6
0
0 (43)
0
3.1
5 (141)
3.5
4 (10)
40
`Num ber of positive findings (num ber of observations)
WILLIAMS
993
terms of the significance of such information in application to humans.
Human Experience
While animal data provide some basis for judgment about the possible levels of toxic materials which may be used safely in industry, they cannot be extrapolated to humans with complete confidence. The ultimate criteria must come from human experience The validity of such criteria is based on the amount of experience in terms of both numbers of exposed people and time of exposure, on the methods of
evaluation of the effects of the toxic material on people, and on the completeness of the evaluation of exposure levels in the environment and correlation
of these levels with human exposure Data with reference to human effects are obtained from both
controlled experiments and industrial environment exposures.
In the case of irritants, for example, such factors as odor detection, sensory response, and levels of exposure which are irritating to eyes, skin, and upper respiratory tract have been studied quantitatively in
humans under controlled conditions In general, such
studies, combined with experience gained with actual plant use, provide an adequate basis for establishing or confirming hygienic standards for such substances.
It is much more difficult to provide a sound basis of human experience for substances which require rela
tively long periods of time before producing evidence of injury. Whereas the acute effects can be evaluated relatively rapidly and by simple procedures, long-time detailed studies of controlled groups of industrial
workers are required to provide adequate evidence in the case of those substances which may produce
chronic injury. The kinds of information which are available from
industrial experience with various chemicals fall into three basic categories. One of these is limited t<? com plaints associated generally with the sensory response or with more severe forms of acute irritation reactions
affecting skin, eyes, or upper respiratory tract The second kind of data result from clinical examination
of exposed workmen. The third is the result of human toxicologic or physiologic studies. To be of value in
establishing hygienic standards such medical informa
tion must be correlated with adequate data relating
to the concentrations to which workers have been exposed.
In his paper "Improved Communication. Hygienic Standards for Daily Inhalation" Smyth (3) reviewed
238 values from the 1956 American Conference of Government'*] Industrial Hygienists list, together with
his interpretation of these values. He has also eval uated the nature of the supporting data--animal and
human. An analysis of the four kinds of sources of human data indicates the role of such experience in
establishing hygienic standards in the United States. Of a total of 238 values which were analyzed human
data were utilized in 108*, distributed as follows:
Clinical Examination of Workmen Was
Correlated With Their Exposure
34
Industrial Complaints or Observations
Less Quantitative Than Clinical Observations 33
Human Sensory Data
42
Human Toxicologic or Physiologic Data
10
* 0 / the 119 values distributed in the above tabulation
there were 11 duplicates wherein the same material appeared under two or more headings; thus there were actually 108 separate substances analyzed.
In such an extensive list as this there are many materials which are so little used that there is negligible industrial experience available to assist our standards people. For such materials reliance is placed primarily on animal experiments and the use of analogy as guides in setting limits
Fox the more common industrial chemicals many years of experience in using them has presided the necessary background to verify existing standards Such experience is generally of a negative nature. Where it is supported by clinical or physiological data correlated with levels of exposure, as in the case of the ten-year study of butyl alcohol by Sternei and his colleagues (10), the information is most significant.
Such medica) programs are designed to evaluate the general physical condition of employees and to include specific physiologic tests which may be expected to provide early evidence ot injury Studies of this type are by far the most valuable for establishing valid hygienic standards
SUMMARY AND CONCLUSIONS
In summary, it can be stated that hygienic standards for inhalation in the occupational health field in the United States are based on the application of the best known biochemical, toxicologic, physiologic, and pathologic techniques to animals and to human experience. Investigations are carried on by private industry, universities, research laboratories, and gov ernmental agencies. The analysis of such data and interpretation in terms of hygienic standards is done by standards groups composed of competent scientists representing every facet of the occupational health field The validity of these standards is demonstrated by the low occupational disease attack rate in the United States. Verified cases of such injury are the result of exposures far above the established limits.
Many approaches are being made to the problem of establishing hygienic standards in the occupational health field It became obvious some time ago that research people in various parts of the world were in some cases utilizing varying techniques As a result, values for some substances differ by as much as an order of magnitude In an attempt to get some uni fication in the basic approach to the problem and to provide a mechanism to permit a much broader exchange of information and data among occupational health workers, the Permanent International Com mission on Industrial Medicine set up a Subcommittee to study this problem. This Subcommittee held a symposium on Maximum Allowable Concentrations of Toxic Substances in Industry in Prague, Czechoslo vakia, on April 14-17, 1959 The Transactions of the Symposium, which appeared in four sections, deal with general areas of agreement among the delegates. This statement of principles is an important first step in establishing international cooperation in this im portant field On the basis of this work it is hoped not only that we can look forward to the development of a series of internationally acceptable hygienic standard values but that agreement can be obtained with regard to general principles and to methods and procedures which will be utilized in the establishment of such standards. The present Symposium, which is the second under the auspices of the Subcommittee will, I hope, crystallize even further the thinking of those in the occupational health field concerned with establishing sound standards to be used in assuring safe industrial environments.
998
Eckardt, Robert E., 7-10, 64-65 Eckhardt, W., 850-857 Elkins, Hervey B., 981-983 Erhardt, J, Th. G., 850-857 Estadella-Botha, S., 663-668 '
Fabre, Ren, 686-692 Felton, J. S., 413-426 Ference, Anne M., 12-14 Ferran, G. H,, 486-503 Fiandaca, S., 353-359 Finulli, M., 770-772 Fischer, R., 872-876 Fisher, R. E. W., 250-256 Folsom, Marion B., 72-82 Formnek, J., 714-721, 872-876 Fornells-Martinez, E., 663-668 Forssman, Sven, 68-72, 257-258 Fortuin, G. J,, 258-259 Fournier, Et., 694-698 Frad, G., 259-260 Frantik, E., 714-721 Frantikov, D., 872-876 Fri berg, Lars, 201-203, 977-980 Friedland, I. G., 692-694
Gabor, Sylvia, 465-466 Gasque, Mac Roy, 260-263 Gaultier, M., 694-698 Georgescu, A. M., 343-345 Ghosh, P. K., 426-427 Gillquist, B., 257-258 Glorig, Aram, 699-700 Goldman, Rose, 314-316 Goldstein, Bernard, 263-266 Goldstein, David H., 266-270 Gorospe, Alfredo A., 636-639 Gradina, C., 700-702 Grant, Ellsworth S., 118-120 Greene, Katrine R. C., 314-316 Grimaldi, John V., 607-608 Grimlund, K., 703-707 Gross, Paul, 707-712 Gucciardi, G., 259-260 Guymer, R. F., 270-275 Guyotjeannin, Ch., 694-698 Gwozdz, B., 795-798
Hamilton, Gilbert L., 656-661 Hargreaves, M argaret S., 275-278 Harris, E. S., 281-283 Harris, William B., 466-472 Hatch, T. F., 839-845 Hayes, Wayland J., Jr., 120-122 Hertig, B. A., 839-845 Hinchcliffe, R., 712-714 Hine, C. H,, 281-283
INDEX OF AUTHORS
Hinkle, Lawrence E., Jr., 283-288 Hipps, John G., 608-610 Hogan, Edward J., 610-613 Holden, F. R., 281-283 Holm, A., 257-258 Holmquist, Carl-Eric, 122-126 Holstein, Ernst, 278-281 Holtz, John, 783-785 Horiuchi, Kazuya, 288-289 Horvath, M., 714-721, 872-876 Hueper, W. C., 473-486 Hughes, James P., 879-882 Hyatt, E. C., 486-503
Inoue, Toshi, 289-290 International Labour Office, 721-724 International Symposium on Maximum Allowable
Concentrations of Toxic Substances in Industry, 33-39 Iorga, M., 341-343
Jensen, C. R,, 486-503 Juin, Grard, 942-947 Jullien, Georges, 724-726
Kammer, A. G,, 427-428 Kantor, M., 753-755 Kazantzis, G., 290-298 Keatinge, Gerald F., 298-301 Keenan, Robert G., 503-506, 783-785 Kehoe, Robert A., 126-129, 433-436 Kesy, Irena, 726-730 Killens, Richard, 783-785 King, E., 301-311 Kingston, James R., 911-917 Kitagawa, Tetsuzo, 506-512 Kiviluoto, Raimo, 311-312 Klein, Irvin, 613-615 Klutas, Edna May, 428-431 Kopp, John, 783-785 Kruger, Daniel H., 615-621 Krger, P. D., 971-973 Kubota, Juko, 313-314
LaBelle, Charles W,, 730-735 Lachnit, V., 947-950 Laham, Souheil, 686-692, 735-738 Lammers, B., 876-878 Landry, A. S., 512-519 Lavergne, Rafael, 214-217 Lehmann, Gunther, 878-879 Leoca-Radu, Mina, 349-351 Letavet, A. A., 431-433, 891-892, 983-987 Liber, Amour Fiscus, 738-740 Lieben, Jan, 316-319 Lienhard, Wendell F., 879-882 Lillis, R., 679-681
INDEX OF AUTHORS
999
Linch, A. L., 580-585 Limi, A. R., 882-887 Liniecki, J., 800-801 Littler, T. S., 712-714 Lubin, Isador, 621-622 Lund, O.-E., 740-741 Lundervold, Arne, 887-891 Lutier, J., 401-402 Lutz, E arl F., 184-186
McCallum, R. ., 741-745 McClintock, R. S., 879-882 McKerrow, C. B,, 745-749 McNerney, Jam es M., 707-712 Magnuson, Harold J., 129-131 Malysheva, A. E., 891-892 Manheimer, Robert H., 314-316 Matthews, James, 131-134 Matuoka, Syukiti, 893-902 Maxiield, Mary E., 857-862 Meiklejohn, A., 134-138 Meila, I., 677-678 Metzner, Franz N-, 316-319 Michon, R., 902-904 Mihaila, I., 904-908 Mikaelian, Michel, 320-322 Mikisha, A., 714-721 Milijic, Bosko, 950-951 Miller, S. E,, 937-939 Miox, M., 908-911 Minard, David, 911-917 Miskolczy, Wilhelm, 322-324 Mitchell, R. N., 486-50C Mose, Gh,, 676-678 Molfino, F., 952 Monaco, Alfred, 749-753 Morris, George E., 324 Morrow, C. S., 753-755 Moscovici, B., 341-343 Moss, N. Henry, 182-184 Motley, A rthur W., 623-624 Mountain, John T., 783-785 Moyer, Burton J., 519-522 Muica, N., 679-681 M urray, Robert, 139-145
Nadudvary, George, 465-466, 755-757 Naie, Thomas W., 625-628 Namba, Tatsuji, 757-758 Nestorescu, B., 679-681 Newnham, C. T., 324-325 Niebroj, I., 795-798 Nixon, Jam es, 699-700 Noro, Leo, 326-335 Norviit, Lembit, 952-957 Norwood, W. Daggett, 335-338 Nystrom, A., 257-258, 653-656
Olloqui, Fernando Flores, 628-631 Oyanguren, Hernan, 227-230
Pafnote, Maria, 845-847 Paggi, Edoardo, 758-767 Pancheri, Giovanni, 145-146, 767-768 Parker, H. G., 147-150 Patrascu, M., 465-466 Payne, William W., 473-486 Pendergrass, Eugene P., 768-769 Pendergrass, Henry P., 768-769 Perales y Herrero, Narciso, 631-632 Pernis, B., 770-772, 817-818 Pesce, Giuseppe, 958-959 Petrescu, Leonid, 661-663 Pettinati, L., 348-349 Petrovic, Lj., 338-341, 368-371 Phillips, A. M., 553-556 Pietschmann, H., 947-950 Pilt, L., 341-343, 679-681 Piotrowski, J., 780-782 Piscator, M., 201-203 Plumb, Carl S., 260-263 Plummer, Norman, 283-288 Poleti, D., 338-341, 368-371 Potter, A. Lloyd, 150-155 Powles, William E., 351-353 Pradel, J., 522-531 Preda, N., 343-345 Princi, Frank, 433-436 Puertas, Benito Nogales, 633-634
Quer-Brossa, 3., 663-668 Quigley, J. A., 65
Radcliffe, J. C., 65-66 Rdulescu, I. G, 343-345, 679-681 Rae, Stewart, 772-776 Rainsford, S. G., 345-348 Rasetti, L., 348-349, 359-361 Raucher, Karl, 349-351 Reeve, A. Louise, 634-635 Renker, K., 917-921 Riedesel, M. L,, 839-845 Riegrt, A. L., 819-825 Rgner, K. G., 257-258 Risquez-Iribarren, Rafael, 155-158 Rogan, John, 772-776 Ross, W. Donald, 351-353 Rossi, Mario, 960-961 Rossier, P. H., 776-780 Rotta, C., 353-359 Rubino, G. F., 359-361 Rye, W. A., 361-364
Sakai, Yoshimichi, 158-162 Salmowa, J. 780-782 Sands, Frederick W., 531-532 Santillan, Jose S., 636-639 Sarfeh, R., 436-438 Saruta, Namio, 532-535
1000
INDEX O F AUTHORS
Savicevic, M., 338-341
Sawyer, William A., 438-441
Scansetti, G., 348-349
Scheel, Lester D., 783-785
'
Schepers, G. W. H., 786-795
Schermerhorn, W., 850-858
Schiller, Hans, 961-962
Schindl, Karl, 364-365
Schmidt, Heinz-Gnther, 365-367
Schmidt, Marjorie D., 367-368
Schmidtke, H., 921-923
Schulte, H. F., 486-503
Schunck, Karl-Hans, 377-378
Schwartz, Louis, 639-642
Seles, L., 237-238
Serati, A., 963-965
Sherrill, S. S., 281-283
Shipman, Thomas L., 642-645
Shoib, M. O., 85, 162-166
Sick Absence Statistics Committee of
nent Committee and International
on Occupational Health, 40-55
Silverman, Leslie, 441-448
Simpson, H. Marjorie, 448-452
Simu, George, 755-757
Smith, Paul E., Jr., 857-862
Sodergren, David, 122-126
Sox, Ellis D., 281-283
Spett, K., 795-798
Spiers, F. W., 535-540
Spioch, F. M., 795-798
Stankovic, M., 338-341, 368-371
Staskiel, L. J., 753-755
Steele, Earl C., 371-373
Steele, Margaret L., 66-68
Steiner, S. D., 373-377
Stokinger, Herbert E., 540-544
Stopps, Gordon J., 857-862
Stowell, Thomas E. A., 186-191
Strange, John P., 544-551
Sumner, Philip, 314-316
Symanski, H.-J., 798-800
Szpakowa, T., 800-801
Szymczykiewicz, K-, 801-805
the Perma Association
Udel, Melvin M., 397-401 Ursoniu, C., 676-678
Vacher, J., 401-402 Valentin, H., 810-817 Van der Velden, W., 850-857 Van Liew, Hugh D., 911-917 Van Valzah, H. J., 678-679 Vigan, C., 965-971 Vigliami, Enrico C,, 87, 452-457, Viles, Frederick J., Jr., 556-563 Villarroel, Sergio, 227-230 Viola, P. Luigi, 818
Voelz, George L., 564-569 Vosburgh, B. L., 931-933
770-772,
817-818
Wade, Leo, 7, 61, 88 Wald, Neil, 569-572 Walker, Mildred I., 167-169 Walsh, Richard F., 645-648 Warnock, Dorothy M., 402-404 Wassermann, M., 572-580 Weaver, Neill K,, 381-387 Wechselberger, F., 191-194 Wells, R. Lomax, 170 Westrick, Marian L., 707-712 Wetherhold, J. M., 580-585 Wheatley, B. M., 585-587 Whipple, G. Hoyt, 171-178 Whitney, L. Holland, 283-288 Wiecek, E., 801-805 Wieland, H., 740-741 Williams, Charles R., 988-994 Williams, Katherine, 587-590 Williams, May M., 194-197 Williams, N., 819-825 Willman, Helvi, 404-405 Winter, Kurt, 405-410 Worth, G., 826-827 Wyndham, C., 924-931
Tabershaw, Irving R., 11-12 Taylor, Edmund W., Jr., 182-184 Teisinger, J., 987-988 Teso, G. A., 359-361 Thaxter, M. D., 147-150 Thom, W. F. J. M,, 379-381 Thoma, George E., 569-572 Thompson, A. R., 301-311 Thorpe, John J., 381-387 Tompkins, Paul C., 551-553 Tripsa, Rodica, 806-810 Troisi, Fortunato Maria, 387-397 Truhaut, Ren, 33-34, 39, 209-214, Tucker, F. E., 553-556
686-692
Yingling, Doris B., 457-459 Yoder, John D., 590-592 Yoshimi, S., 827-828 Yount, Hubert W., 649-650
Zahorski, Witold, 828-832 Zanetti, Ennio, 767-768 Zannini, D., 971 Zielinski, John F., 592-600 Zorn, O., 971-973