PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Tlenek diazotu. Dokumentacja proponowanych wartości dopuszczalnych wielkości narażenia zawodowego

Autorzy
Treść / Zawartość
Identyfikatory
Warianty tytułu
EN
Nitrous oxide
Języki publikacji
PL
Abstrakty
PL
Tlenek diazotu jest gazem stosowanym głównie do znieczulenia ogólnego w medycynie, stomatologii i weterynarii. Narażenie na ten związek zostało dobrze scharakteryzowane w szpitalnych salach zabiegowych i w gabinetach stomatologicznych. Najczęściej stężenia tego związku w powietrzu pomieszczeń zabiegowych wahają się w zakresie wartości 11 ÷ 7990 mg/m3. Duże stężenia tlenku diazotu stwierdzono w pomieszczeniach niewentylowanych oraz w przypadku nieszczelności aparatury anestezjologicznej. Usunięcie tylko tych przyczyn zmniejszało stężenia ksenobiotyku w powietrzu 3 ÷ 15-krotnie. Po obserwacji personelu medycznego i wynikach badań epidemiologicznych wykazano neurotoksyczne, embriotoksyczne, fetotoksyczne i teratogenne działanie tlenku diazotu. Na podstawie wyników badań przeprowadzonych na zwierzętach laboratoryjnych stwierdzono zaburzenia metabolizmu neuroprzekaźników, zahamowanie biosyntezy metioniny oraz działanie immunosupresyjne w zakresie odporności humoralnej. Nie wykazano mutagennego i kancerogennego działania tego związku. Za podstawę wartości najwyższego dopuszczalnego stężenia (NDS) tlenku diazotu przyjęto jego neurotoksyczne działanie u ludzi. Wychodząc z wartości NOAEL wynoszącej 180 mg/m3 i jednego współczynnika niepewności równego 2, obliczono wartość NDS wynoszącą 90 mg/m3. Zaproponowano wartość normatywną równą 90 mg/m3 łącznie z oznaczeniem literami „Ft”. Nie znaleziono merytorycznych podstaw do obliczenia wartości najwyższe go dopuszczalnego stężenia chwilowego (NDSCh) i wartości dopuszczalnego stężenia biologicznego (DSB) dla tlenku diazotu.
EN
Nitrous oxide (N2O) is a gas mainly used in medicine, dentistry, and veterinary medicine as an anaesthetic. Medical staff is a subpopulation exposed to this chemical. Nitrous oxide exerts neurotoxic, embriotoxic, fetotoxic, and teratogenic effects on human and animal organisms. This compound is an inhibitor of methionine synthase. The MAC (TWA) value of 90 mg/m3 was calculated on the basis of the LOAEL value (180 mg/m3) for neurotoxic effect in humans. The MAC (STEL) value has not been established. Moreover Ft (fetotoxicity) notation is recommended.
Słowa kluczowe
Rocznik
Tom
Strony
135--152
Opis fizyczny
Bibliogr. 66 poz., tab.
Twórcy
autor
  • Collegium Medicum Uniwersytetu Jagiellońskiego 30-688 Kraków ul. Medyczna 9
Bibliografia
  • 1. Abdul-Kareem H.S., Sharma R.P., Drown B.D. (1991) Effects of repeated intermittent exposures to nitrous oxide on central neurotransmitters and hepatic methionine synthetase activity in CD-1 mice. Toxicol. Ind. Health 7, 97-108.
  • 2. ACGIH, American Conference of Governmental Industrial Hygienists (2001) Nitrous oxide. CD-ROM 1-6.
  • 3. ACGIH, American Conference of Governmental Industrial Hygienists (2003) Guide to occupational exposure values. ACGIH 100.
  • 4. Alborg G., Jr Axelsson G., Bodin L. (1996) Shift work, nitrous oxide exposure and subfertility among Swedish midwives. Int. J. Epidemiol. 25, 783-790.
  • 5. American Society of Anesthesiologists (1974) Occupational disease among operating room personnel: a national study. Report of an ad hoc committee on the effect of trace anesthetics on the health of operating room personnel. Anesthesiology 41, 321-340.
  • 6. Baden J.M., Fujinaga M. (1991) Effects of nitrous oxide on day 9 rat embryos grown in culture. Br. J. Anaesth. 66, 500-503.
  • 7. Baden J.M. i in. (1986) Carcinogen bioassay of nitrous oxide in mice. Anaesthesiology 64, 747-750.
  • 8. Baden J.M., Monk S.J. (1981) Mutagenicity and toxicity studies with high pressure nitrous oxide. Toxicol. Lett. 7, 259-262. Balster R.L. (1998) Neural basis of inhalant abuse. Drug. Alcohol. Depend. 51, 207-214.
  • 9. Beard R.R. (1982) W: Patty’s Industrial hygiene and toxicology. 3rd Rev. ed., vol. 2C, Toxicology. New York, John Wiley & Sons, 4096-4097.
  • 10. Bodin L., Axelsson G., Ahlborg G. Jr (1999) The association of shift work and nitrous oxide exposure in pregnancy with birth weight and gestational age. Epidemiology 10, 429-436.
  • 11. Borm P.J.A. i in. (1990) Monitoring of nitrous oxide in operating rooms. Identification of sources and estimation of occupational exposure. J. Occup. Med. 32, 1112-1116.
  • 12. Bruce D.L., Bach M.J. (1976) Effects of trace anaesthetic gases on behavioural perfomance of volunteers. Br. J. Anaesth. 48, 871-876.
  • 13. Bruce D.L. i in. (1968) Causes of death among anesthesiologists. A 20-year survey. Anesthesiology 29, 565-569.
  • 14. Bruce D.L. i in. (1974) A prospective survey of anesthesiologist mortality, 1967-1971. Anesthesiology 41, 71-74.
  • 15. Chang W.P. i in. (1996) Increased micronucleus formation in nurses with occupational nitrous oxide exposure in operating theaters. Environ. Mol. Mutag. 27, 93-97.
  • 16. Cleaton-Jones P. i in. (1977) Effect of intermittent exposure to a low concentration of nitrous oxide on haemopoiesis in rats. Br. J. Anaesth. 49, 223-226.
  • 17. Coate W.B., Ulland B.M., Lewis T.R. (1979) Chronic exposure to low concentrations of halothane-nitrous oxide: lack of carcinogenic effect in the rat. Anesthesiology 50, 306-309.
  • 18. Cohen E.N., Bellville J.W., Brown B.J.Jr. (1971) Anesthesia, pregnancy, and miscarriage. A study of operating room nurses and anesthetists. Anesthesiology 35, 343-347.
  • 19. Cohen E.N., Brown B.W., Bruce D.L. (1974) Occupational disease among operating room personnel: a national study. Anesthesiology 41, 321-340.
  • 20. Cohen E.N., Brown B.W., Wu M.L. (1980) Occupational disease in dentistry and chronic exposure to trace anesthetic gases. J. Am. Dent. Assoc. 101, 21-31 (cyt. za ACGIH 2001).
  • 21. Corbett T.H., Cornell R.G., Endres J.L. (1974) Birth defects among children of nurse anesthetists. Anesthesiology 41, 341-344.
  • 22. Corbett T.H. i in. (1973) Incidence of cancer among Michigen nurse-anesthetists. Anesthesiology 38, 260-263.
  • 23. DFG, Deutsche Forschungsgemeinschaft (2003) List of MAK and BAT Values 2003. Wiley – VCH 88.
  • 24. Eells J.T. i in. (1981) Methanol poisoning and formate oxidation in nitrous oxide-treated rats. J. Pharmacol. Exp. Ther. 217, 57-61.
  • 25. Eger E.I. i in. (1978) A test of the carcinogenicity of enflurane, isoflurane, halothane, methoxyflurane, and nitrous oxide in mice. Anesth. Analg. 57, 678-694.
  • 26. Ericson A., Källén B. (1979) Survey of infants born in 1973 or 1975 to Swedish women working in operating rooms during their pregnancies. Anesth. Analg. 58, 302-305.
  • 27. Frankhuizen J.L. i in. (1978) Failure to replicate negative effects of trace anaesthetics on mental performance. Br. J. Anaesth. 50, 229-234.
  • 28. Fröhlich D. i in. (1998) Nitrous oxide impairs the neutrophil oxidative response. Anesthesiology 88, 1281-1290.
  • 29. Fujinaga M., Baden J.M. (1994) Methionine prevents nitrous oxide-induced teratogenicity in rat embryos grown in culture. Anesthesiology 81, 184-189.
  • 30. Fujinaga M., Baden J.M., Mazze R.I. (1989) Susceptible period of nitrous oxide teratogenicity in Sprague-Dawley rats. Teratology 40, 439-444.
  • 31. Gardner R.J. (1989) Inhalation anaesthetics-exposure and control: a statistical comparison of personal exposures in operating theatres with and without anaesthjetic gas scavenging. Ann. Occup. Hyg. 33, 159-173.
  • 32. Hardin B.D. i in. (1981) Testing of selected workplace chemicals for teratogenic potential. Scand. J. Work Environ. Health 7, 66-75.
  • 33. Healy C.E., Drown D.B., Sharma R.P. (1990) Short term toxicity of nitrous oxide on the immune, hemopoietic, and endocrine systems in CD-1 mice. Toxicol. Ind. Health 6, 57-70.
  • 34. Henderson K.A., Matthews J.P. (2000) Staff exposure to anaesthetic gases in theatre and non theatre areas. Europ. J. Anaesth. 17, 149-151.
  • 35. Hillman K.M. i in. (1981) Nitrous oxide concentrations in the dental surgery. Atmospheric and blood concentrations of personnel. Anaesthesia 36, 257-262.
  • 36. Holson R.R. i in. (1995) Behavioral teratology and dominant lethal evaluation of nitrous oxide exposure in rats. Neurotoxicol. Teratol. 17, 583-592.
  • 37. Kanmura Y. i in. (1999) Causes of nitrous oxide contamination in operating rooms. Anesthesiology 90, 693-696.
  • 38. Kano Y. i in. (1981) Effect of nitrous oxide on human bone marrow cells and its synergistic effect with methionine and methotrexate on functional folate deficiency. Cancer Res. 41, 4698-4701.
  • 39. Knill-Jones R.P. i in. (1972) Anaesthetic practice and pregnancy: a controlled survey of women anaesthetists in the United Kingdom. Lancet 1, 1326-1328.
  • 40. Knill-Jones R.P., Newman B.J., Spence A.A. (1975) Anaesthetic practice and pregnancy: controlled survey of male anaesthetists in the United Kingdom. Lancet 2, 807-809.
  • 41. Koblin D.D. i in. (1981) Inactivation of methionine synthetase by nitrous oxide in mice. Anaesthesiology 54, 318-324.
  • 42. Kondo H. i in. (1981) Nitrous oxide has multiple deleterious effects on cobalamin metabolism and causes decreases in activities of both mammalian cobalamin-dependent enzymes in rats. J. Clin. Invest. 67, 1270-1283.
  • 43. Kundomal Y.R., Baden J.M. (1984) Anesthetic mutagenicity in Drosophila. Environ. Mut. 6, 417 (Abs. Cb-38).
  • 44. Lane G.A. i in. (1980) Anesthetics as teratogens: nitrous oxide is fetotoxic, xenon is not. Science 210, 899-901.
  • 45. Layzer R.B. (1978) Myeloneuropathy after prolonged exposure to nitrous oxide. Lancet 2, 1227-1230.
  • 46. Lew E.A. (1979) Mortality expirience among anesthesiologists, 1954-1976. Anesthesiology 51, 195-199.
  • 47. Lucchini R. i in. (1997) Neurobehavioral functions in operating theatre personnel: a multicenter study. Med. Lav. 88, 396-405.
  • 48. Mankowitz E., Brock-Utne J.G., Downing J.W. (1981) Nitrous oxide elimination by the newborn. Anaesthesia 36, 1014-1016.
  • 49. Marié R. M. i in. (2000) Nitrous oxide anesthesia – associated myelopathy. Arch. Neurol. 57, 380-382.
  • 50. Mazze R.I. i in. (1983) Germ cell studies in mice after prolonged exposure to nitrous oxide. Toxicol. Appl. Pharmacol. 67, 370-375.
  • 51. McGregor D.G., Senjem D.H., Mazze R.I. (1999) Trace nitrous oxide levels in the postanesthesia care unit. Anesth. Analg. 89, 472-475.
  • 52. Nunn J.F. i in. (1982) Serum methionine and hepatic enzyme activity in anaesthetists exposed to nitrous oxide. Br. J. Anaesth. 54, 593-597.
  • 53. O’Sullivan H. i in. (1981) Human bone marrow biochemical function and megaloblastic hematopoiesis after nitrous oxide anesthesia. Anesthesiology 55, 645-649.
  • 54. Pharoah P.O.D., Alberman E., Doyle P. (1977) Outcome of pregnancy among women in anaesthetic practice. Lancet 1, 34-36.
  • 55. Rice S.A., Mazze R.T., Baden J.M. (1985) Effects of subchronic intermittent exposure to nitrous oxide in Swiss-Webster mice. J. Environ. Pathol. Toxicol. Oncol. 6, 271-282.
  • 56. Rowland A.S. i in. (1995) Nitrous oxide and spontaneous abortion in female dental assistants. Am. J. Epidemiol. 141, 531-538.
  • 57. Schuyt H.C., Verberk M.M. (1996) Measurement and reduction of nitrous oxide in operating rooms. JOEM 38, 1036-1040.
  • 58. Sessler D.I., Badgwell J.M. (1998) Exposure of postoperative nurses to exhaled anesthetic gases. Anesth. Analg. 87, 1083-1088.
  • 59. Sharer N.M. i in. (1983) Effects of chronic exposure to nitrous oxide on methionine synthase activity. Br. J. Anaesth. 55, 693-701.
  • 60. Sitarek K. i in. (2000) Concentrations of anaesthetic gases in hospital operating theatres. Int. J. Occup. Environ. Health 13, 61-66.
  • 61. Smith G., Shirley A.W. (1977) Failure to demonstrate effects of trace concentrations of trace concentrations of nitrous oxide and halothane on psychomotor performance. Br. J. Anaesth. 49, 65-70.
  • 62. The Merck index (2001) An encyclopedia of chemicals, drugs, and biologicals. 13th ed. Merck & CO. INC. Whitehouse Station NJ, 1191.
  • 63. Tran N. i in. (1994) Evaluation of waste anesthetic gases, monitoring strategies, and correlations between nitrous oxide levels and health symptoms. Am. Ind. Hyg. Assoc. J. 55, 36-41.
  • 64. Trevisan A., Gori G.P. (1990) Biological monitoring of nitrous oxide exposure in surgical areas. Am. J. Ind. Med. 17, 357-362.
  • 65. Warren D.J., Christensen B., Slørdal L. (1993) Effect of nitrous oxide on haematopoiesis in vitro: biochemical and functional features. Pharmacol. Toxicol. 72, 69-72.
  • 66. White A.E., Takehisa S., Eiger E.I. (1979) Sister chromatid exchanges induced by inhaled anesthetics. Anesthesiology 50, 426-430.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-ac44a77d-e107-4d68-9f28-23ec511f30e0
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.