Вы находитесь на странице: 1из 5

Infection

Brief Report

Occupational Risk for Hepatitis A and Hepatitis E among Health Care Professionals?
M. Nbling, F. Hofmann, F.-W. Tiller

Abstract
Background: Since transmission routes of hepatitis E virus (HEV) and hepatitis A virus (HAV) are believed to be similar, comparable risk factors and a correlation between the two seroprevalence rates may be assumed. Materials and Methods: Anti-HAV and anti-HEV serology was assessed in 511 German subjects from nursing, pediatric nursing and administration groups, none of whom had been vaccinated against HAV. At the same time a standardized questionnaire on occupational and individual parameters was completed. Results: Overall seroprevalence for anti-HEV was 3.9%, for anti-HAV 28%. Multivariate analysis revealed that anti-HEV seroprevalence was significantly higher in persons working in emergency admission or in surgery, while persons working in childrens psychiatry were more likely to be anti-HAV positive. Comparing the two serological results, no contingency difference was found (2 = 0.42 (df = 1), p > 0.05). Conclusion: Specific departments of health care show higher prevalence of anti-HAV or anti-HEV. In the case of HEV further studies in the exposed working field are needed. Since no connection between the two serological results was found, transmission mechanisms might be (partly) different.

Key Words
Hepatitis E Hepatitis A Occupational risk Health care workers
Infection 2002; 30: 9497 DOI 10.1007/s15010-002-2023-3

can reach rates of up to 40% in endemic areas. In Central Europe it is estimated to be around 14% among the normal population; a study in Munich detected 4% in a relatively small sample [4].Transmission of HEV occurs mostly by the fecal-oral pathway via contaminated drinking water [5]. Parenteral infections or contact transmissions in health care professionals have also been observed [6].The latter are of special interest for occupational medicine in the field of health care workers. In general, epidemiological knowledge about seroprevalence, occupational and individual risk factors for hepatitis E is very limited and a lot of questions remain open [7]. Hepatitis A virus (HAV) was first isolated in 1973. Transmission of HAV is mostly fecal-oral. Seroprevalence is closely related to general socio-hygienic living standards and to age [8-10]. In Europe the seroprevalence has decreased rapidly during the last decades.Values of < 10% are currently observed in the younger generation. Tourists and other travelers to endemic regions [1114], food handlers [1517], sewage and (probably) sewage workers [1820], and some other smaller groups are considered as risk groups. Health care workers and personnel of day care centers are also at higher risk for infections with HAV [21, 22]. Since transmission routes and geographic spread of the two viruses are believed to be similar, it may be supposed that anti-HAV positive persons are more likely to be antiHEV reactive and vice versa. The main objective of this study was to identify (and quantify) factors associated with significantly higher antiHAV and anti-HEV seroprevalence (risk factors). The other objective was to check whether the risk groups for HAV infection were the same as the risk groups for HEV

Introduction
Hepatitis E is an acute, self-limiting disease caused by hepatitis E virus (HEV) and is endemic in a number of developing countries in Asia, Africa, the Middle East and Central America. HEV was first identified by immune electron microscopy in feces of patients with enterically transmitted non-A, non-B hepatitis [1, 2]. Case fatality is usually low (0.53%) [3], but is especially high among pregnant women (1530%, reason unknown). Seroprevalence of anti-HEV
M. Nbling (corresponding author), F. Hofmann Dept. of Applied Physiology, Occupational Medicine and Infectiology, University of Wuppertal, FB14 Safety Engineering, Gaustr. 20, D - 42097 Wuppertal, Germany; Phone: (+49/761) 82526, Fax: -83432, e-mail: ffas.freiburg@t-online.de F.-W. Tiller Medical Immunological Laboratories Munich, Bayerstr. 53, D-80336 Munich, Germany Received: February 15, 2001 Revision accepted: December 4, 2001

94

Infection 30 2002 No. 2 URBAN & VOGEL

M. Nbling et al. Hepatitis A and Hepatitis E Seroprevalence

Table 1 Contents of questionnaire.

Variable Age (years) Age dummy (years)

Categories for analysis

lence risk ratios) by far and were therefore not used as an approximation of the RR [23]. Instead, the b-coefficients and their standard errors are given. Following the suggestions of Hosmer and Lemeshow [24], the likelihood ratio test (LR) was used instead of the Wald statistic when performing logistic regression analysis.

Sociodemographic factors 1950 (in groups of 2 years) 1940, 4150 (born close to World War II) Sex Female, male No. of children 0 to 5 No. of brothers and sisters 0 to 14 Profession Years of occupation Occupational history Work related factors Administration, nurse, pediatric nurse < 5, 59, 1014, > 14 Area(s) and duration of occupation(s) in months

Results and Discussion


As can be seen from table 2, thanks to the age-standardized enrolment, mean and SD for age were very similar in the three professional groups. The overall seroprevalence of anti-HEV was 3.9% (20/511) and 28% (143/511) for anti-HAV (which included 102 positive and 41 borderline results). In the following results borderliners for anti-HAV are presented in a single group with the positives, since analysis revealed a close similarity between the positive and the borderline group.

Travel factors Travel during last 10 years 12 geographic world zones: travelling (yes/no)and length of stay in months

Risk factors
None of the sociodemographic factors such as age, sex, number of children or number of brothers and sisters, was significantly related to anti-HEV seroprevalence in a multivariate model. The same was shown for the general occupational parameters, profession and overall years of occupation. From the more detailed parameters concerning travelling and occupational history, two travel zones (Latin/South America and Far East/South East Asia) and two specific occupational areas, emergency admission and surgery, were significantly associated with higher seroprevalence (Table 3). In the multivariate model for anti-HAV positivity, the most important factor was a dummy buildup of age. This separated the persons born and growing up under the poor hygienic conditions prevailing in the first years after World War II (with a very high prevalence) from the subjects born later, during the German economic boom (showing a low anti-HAV prevalence). Further factors related to a higher probability of positive serological results were the parameters a) family size: number of brothers and sisters and number of children, underlining the possibility of secondary transmission and b) travel to the La-Plata states (Argentina and Uruguay). Of the occupational factors, the working time in childrens psychiatry was positively related to the anti-HAV seroprevalence (Table 4).

Table 2 Sample and mean of age by profession.

No. Administration Nurses Pediatric nurses Total 173 178 160 511

Mean (years) 33.5 32.8 33.5 33.3

SD 9.23 9.17 9.21 9.20

ANOVA: F = 0.28 (df = 2), eta = 0.03, p > 0.05 (0.76)

infection, determined from a contingency table of the two sets of serological results.

Materials and Methods


The study was performed as a cross-sectional study in three hospitals in southwestern Germany. Enrolment was standardized by age (range: 1950 years) and profession (control group working in administration, nurses and pediatric nurses). Serological results for anti-HAV and anti-HEV (IgG-ELISA) titers were combined with data collected by means of a standardized questionnaire on basic sociodemography, individual work history and travel behavior (Table 1). Both serological results and a questionnaire were available for 511 Germans (all born in Germany and not vaccinated against HAV).

Correlation of Anti-HEV and Anti-HAV


Since HAV and HEV are mostly transmitted in a similar way (fecal-oral), a correlation between anti-HEV- and antiHAV test results may be presumed. According to this hypothesis, persons with positive anti-HAV results would be more likely to test positive for anti-HEV and vice versa. However, as the results in the contingency table show (Table 5), our data do not substantiate this hypothesis. Serological results of anti-HAV and anti-HEV testing are not related to one another, they are statistically independent. The rate of anti-HEV positivity was 3.8% among the positives for HAV and, almost equally, 4.2% for the HAV negatives.

Statistics
Statistical analysis was carried out by means of crosstabs with Pearsons 2 statistic, analysis of variance and logistic regression analysis. Since the study type is cross-sectional and the outcome is not rare (at least in the case of anti-HAV), odds ratios (calculable as: OR = eb) would overestimate the relative risks (RR, as preva-

Infection 30 2002 No. 2 URBAN & VOGEL

95

M. Nbling et al. Hepatitis A and Hepatitis E Seroprevalence

Table 3 Predictors and estimation model for anti-HEV.

Predictor Occupation in surgery unit (yes no) Occupation in emergency unit (months) Travel to Latin/South America (excluding Argentina/Uruguay) (months) Travel to Far East/South East Asia (excluding Japan) (months) Constant

b 1.6141 0.0202 0.0335 0.0492 3.6802

SE (b) 0.6231 0.0078 0.0207 0.0238 0.2914

Sig (LR) < 0.05 (0.022) < 0.05 (0.011) < 0.01(0.0098) < 0.10 (0.072)

df 1 1 1 1

Model build and fit by logistic regression analysis. Sig(LR): likelihood ratio test; borders: p(in) < 0.05, p(out) > 0.10; model parameters: n = 511; -2LL = 147; GOF = 526; Hosmer/Lemeshow C = 3.2, df = 2, p > 0.20; model 2 = 21.7, df = 4, p < 0.001; cases correctly classified (cutoff = 0.5): 96.3%

Table 4 Predictors and estimation model for anti-HAV.

A general risk for the whole working sector of health care professionals for HAV and/or HEV infections was not found (in Germany). However, employment in certain departments or units of nursing and pediatric nursing was associated with higher anti-HEV or higher anti-HAV prevalence rates.This was also true of travel to endemic regions and some sociodemographic factors. In the case of anti-HEV, further studies, especially in the exposed working fields (e. g. endoscopy), are necessary to control these findings and to provide more detailed results. Concerning a correlation presumed between anti-HEV and anti-HAV on the basis of the similar transmission route, no such connection could be demonstrated. Whether or not transmission mechanisms other than the fecal-oral route are responsible for these findings is unclear.

Predictor Occupation in childrens psychiatry (months)

b 0.0280

SE (b) 0.0155

Sig (LR) < 0.05 (0.0473)

df 1
1.

References

Balayan, MS, Andjaparidze, AG, Savinskaya SS, Ketiladze ES, Braginsky DM, Savinov AP, Poleschuk VF: Evidence for a virus non-A, Travel to the La-Plata states 0.3057 0.1604 < 0.10 (0.05) 1 non-B hepatitis transmitted via fecal-oral (Argentina/Uruguay) (months) route. Intervirology 1983; 20: 2331. No. of children 0.2231 0.1032 < 0.05 (0.031) 1 2. Kane MA, Bradley DW, Shrestna, SM, Maynard JE, Cood EH, Mishra PP, Joshi No. of brothers and sisters 0.1150 0.0614 < 0.10 (0.061) 1 DD: Epidemic non-A, non-B hepatitis in Nepal: recovery of a possible etiologic Age (dummy: <= 40, > 40 years) 1.4271 0.2345 < 0.001 (< 0.0005) 1 agent and transmission studies in marConstant 1.9024 0.2053 mosets. JAMA 1984; 252: 31403145. 3. Mast EE, Alter MJ: Epidemiology of viral Model build and fit by logistic regression analysis. Sig(LR): likelihood ratio test; borders: hepatitis: an overview. Semin Virol 1993; p(in) < 0.05, p(out) > 0.10; model parameters: n = 508 (3 missing values for number of 4: 273283. children/number of brothers and sisters), 2LL = 529; GOF = 500; Hosmer/Lemeshow 4. Langer B, Frsner GG, Dathe O, Zachoval C = 9.9, df = 7, p > 0.15; model 2 = 71.0, df = 5, p < 0.001; cases correctly classified R, Rabe C: HEV-Infektion: ein differential(cutoff = 0.5): 73.6% diagnostisches Problem in Deutschland? In: Maass G, Stck B (eds): Virushepatitis A bis E, Diagnose, Therapie, Prophylaxe. Kilian, Marburg 1994, pp 245248. 5. Bradley DW: Hepatitis E: epidemiology, aetiology and molecular Table 5 biology. Rev Med Virol 1992; 2: 1928. Serological results concernig HEV and HAV. 6. Robson SC, Adams S, Brink N, Woodruff B, Bradley D: Hospital outbreak of hepatitis E. Lancet 1992; 339: 14241425. Hepatitis E Not reactive Reactive Total 7. Krawczynski K, Mast EE, Purdy MA: Hepatitis E: an overview. In: Hepatitis A n (%) n (%) n (%) Rizzetto M, Purcell RH, Gerin JL, Verme G (eds) Viral hepatitis and liver disease. Edizioni Minerva Medica, Torino 1997, pp 305312. Negative 354 (96.2) 14 (3.8) 368 (100) 8. Gust, ID: Epidemiological patterns of hepatitis A in different Positive/borderline 137 (95.8) 6 (4.2) 143 (100) parts of the world. Vaccine 1992;10 (suppl 1): 5658. Total 491 (96.1) 20 (3.9) 511 (100) 9. Mausezahl D, Cheng F, Zhang SQ, Tanner M: Hepatitis A in a Chinese urban population: the spectrum of social and behavioural 2 = 0.42 (df = 1), Phi = 0.01, p = n.s. (0.838) risk. Int J Epidemiol 1996; 25: 12711279.

96

Infection 30 2002 No. 2 URBAN & VOGEL

M. Nbling et al. Hepatitis A and Hepatitis E Seroprevalence

10. Papaevangelou, G: Epidemiology of hepatitis A in Mediterranean countries. Vaccine 1992; 10 (suppl 1): 6366. 11. Steffen R: Risk of hepatitis A in travellers. Vaccine 1992; 10 (suppl 1): 6972. 12. Smalligan RD, Lange WR, Frame JD, Yarbough PO, Frankenfield DL, Hyams KC: The risk of viral hepatitis A, B, C, and E among North American missionaries. Am J Trop Med Hyg 1995; 53: 233236. 13. Nordenfelt E: Hepatitis A in Swedish travellers. Vaccine 1992; 10 (suppl 1): 7374. 14. Bienzle U, Bock HL, Meister W, Clemens R, Kruppenbacher JP: Anti-HAV seroprevalence in German travellers and hepatitis A vaccination in immune subjects. Lancet 1993; 341: 1028. 15. Weltman AC, Bennett NM, Ackman DA, Misage JH, Campana JJ, Fine LS, Doninger AS, Balzano GJ, Birkhead GS: An outbreak of hepatitis A associated with a bakery, New York, 1994: the 1968 West Branch, Michigan outbreak repeated. Epidemiol Infect 1996; 117: 333341. 16. Koester D, Hofmann F, Berthold H: Hepatitis A immunity of food handling staff. Eur J Clin Microbiol Infect Dis 1990; 9: 304305. 17. Dienstag JL, Routenberg JA, Purcell RH, Hooper RR, Harrison WO: Foodhandler-associated outbreak of hepatitis type A: an immune electron microscopic study. Ann Intern Med 1975; 83: 647650.

18.

19.

20.

21.

22. 23. 24.

Heng BH, Goh KT, Doraisingham S, Quek GH: Prevalence of hepatitis A virus infection among sewage workers in Singapore. Epidemiol Infect 1994; 113: 121128. Skinhj P, Hollinger FB, Hovind-Hougen K, Lous P: Infectious liver diseases in three groups of Copenhagen workers: correlations of hepatitis A infection to sewage exposure. Arch Environ Health 1980; 36: 139143. Nuebling M, Hofmann, F: Task profile and risk of occupational hepatitis A infection in sewerage workers. Int Arch Occup Environ Health 2001; 74: 589593. Van Damme P, Thoelen S, Van der Auwera JC, Bar R, Meheus A: Viral hepatitis among health care workers - epidemiology and prevention. In: Hagberg M, Hofmann F, Stoessel U, Westlander G (eds): Occupational health for health care workers. Ecomed, Landsberg/Lech 1993, 133137. Hofmann F, Wehrle G, Berthold H, Koester, D: Hepatitis A as an occupational hazard. Vaccine 1992; 10 (suppl 1): 8284. Axelson O: Some recent developments in occupational epidemiology. Scand J Work Environ Health 1994; 20: 918. Hosmer DW Jr, Lemeshow S: Applied logistic regression. J. Wiley & Sons, New York, Chichester, Brisbane, Toronto, Singapore 1989.

Infection 30 2002 No. 2 URBAN & VOGEL

97

Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.

Вам также может понравиться