Cited by 380Salmonella and Campylobacter epidemiologyFood Safety and HygieneListeria monocytogenes in Food Safety

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Disease burden of foodborne pathogens in the Netherlands, 2009

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Havelaar, Arie H., Haagsma, Juanita A., Mangen, Marie-Josée J., Kemmeren, Jeanet M., Verhoef, Linda P.B., Vijgen, Sylvia M.C., Wilson, Margaret, Friesema, Ingrid H.M., Kortbeek, Laetitia M., van Duynhoven, Yvonne T.H.P., van Pelt, Wilfrid·2012·International Journal of Food Microbiology

DOI 10.1016/j.ijfoodmicro.2012.03.029

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Abstract

To inform risk management decisions on control, prevention and surveillance of foodborne disease, the disease burden of foodborne pathogens is estimated using Disability Adjusted Life Years as a summary metric of public health. Fourteen pathogens that can be transmitted by food are included in the study (four infectious bacteria, three toxin-producing bacteria, four viruses and three protozoa). Data represent the burden in the Netherlands in 2009. The incidence of community-acquired non-consulting cases, patients consulting their general practitioner, those admitted to hospital, as well as the incidence of sequelae and fatal cases is estimated using surveillance data, cohort studies and published data. Disease burden includes estimates of duration and disability weights for non-fatal cases and loss of statistical life expectancy for fatal cases. Results at pathogen level are combined with data from an expert survey to assess the fraction of cases attributable to food, and the main food groups contributing to transmission. Among 1.8 million cases of disease (approx. 10,600 per 100,000) and 233 deaths (1.4 per 100,000) by these fourteen pathogens, approximately one-third (680,000 cases; 4100 per 100,000) and 78 deaths (0.5 per 100,000) are attributable to foodborne transmission. The total burden is 13,500 DALY (82 DALY per 100,000). On a population level, Toxoplasma gondii, thermophilic Campylobacter spp., rotaviruses, noroviruses and Salmonella spp. cause the highest disease burden. The burden per case is highest for perinatal listeriosis and congenital toxoplasmosis. Approximately 45% of the total burden is attributed to food. T. gondii and Campylobacter spp. appear to be key targets for additional intervention efforts, with a focus on food and environmental pathways. The ranking of foodborne pathogens based on burden is very different compared to when only incidence is considered. The burden of acute disease is a relatively small part of the total burden. In the Netherlands, the burden of foodborne pathogens is similar to the burden of upper respiratory and urinary tract infections.

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Foodborne illness acquired in the United States—Major pathogens
Scallan, E., Hoekstra, R. M., Angulo, F. J., Tauxe, R. V., Widdowson, M.-A., Roy, S. L., Jones, J. L., & Griffin, P. M. (2011) · Emerging Infectious Diseases · doi:10.3201/eid1701.p11101 · Cited by 7,657
Untitled work
(1996) · Cited by 6,884
Encyclopedia of food sciences and nutrition
Caballero, B. H., Trugo, L. C., & Finglas, P. M. (2003) · Academic eBooks · Cited by 1,639
Quantifying the burden of disease: the technical basis for disability-adjusted life years.
Murray, C. J. (1994) · PubMed · Cited by 1,556
Foodborne Illness Acquired in the United States—Unspecified Agents
Scallan, E., Griffin, P. M., Angulo, F. J., Tauxe, R. V., & Hoekstra, R. M. (2010) · Emerging infectious diseases · doi:10.3201/eid1701.p21101 · Cited by 1,048
Study of infectious intestinal disease in England: rates in the community, presenting to general practice, and reported to national surveillance
Wheeler, J. G., Sethi, D., Cowden, J. M., Wall, P. G., Rodrigues, L. C., Tompkins, D. S., Hudson, M. J., & Roderick, P. J. (1999) · BMJ · doi:10.1136/bmj.318.7190.1046 · Cited by 794
Summary Measures of Population Health: Concepts, Ethics, Measurement and Applications
Murray, C. J. L., Salomon, J. A., Mathers, C. D., & López, A. D. (2002) · Cited by 655
Understanding DALYs
Murray, C., & Acharya, A. K. (1997) · Journal of Health Economics · doi:10.1016/s0167-6296(97)00004-0 · Cited by 634
Sensor, a Population-based Cohort Study on Gastroenteritis in the Netherlands: Incidence and Etiology
de Wit, M. A. S., Koopmans, M. P. G., Kortbeek, L. M., Wannet, W. J. B., Vinjé, J., van Leusden, F., Bartelds, A. I. M., & van Duynhoven, Y. T. H. P. (2001) · American Journal of Epidemiology · doi:10.1093/aje/154.7.666 · Cited by 583
Self-citation
Longitudinal study of infectious intestinal disease in the UK (IID2 study): incidence in the community and presenting to general practice
Tam, C. C., Rodrigues, L. C., Viviani, L., Dodds, J. P., Evans, M. R., Hunter, P. R., Gray, J. J., Letley, L. H., Rait, G., Tompkins, D. S., et al. (2011) · Gut · doi:10.1136/gut.2011.238386 · Cited by 565

Show all 54 references

Research works printed but not linked: 4

European Food Safety Authority; European Centre for Disease Prevention and Control, 2011, Trends and sources of zoonoses and zoonotic agents in the European Union in 2009, The EFSA Journal, 9, 2090
Friesema, 2011, Intensieve surveillance van Shiga toxine producerende Escherichia coli in Nederland, 2009, Infectieziekten Bulletin, 22, 22
Kortbeek, 2009, 104, 370
Van de Laar, 2000, Vaccineren tegen hepatitis A: een verkenning van kosten, Infectieziekten Bulletin, 11, 262

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Self-citation
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Salvat, G., Guyot, M., & Protino, J. (2016) · Journal of Applied Microbiology · doi:10.1111/jam.13313 · Cited by 5
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Self-citation
Tracing Back the Source of an Outbreak of Salmonella Typhimurium; National Outbreak Linked to the Consumption of Raw and Undercooked Beef Products, the Netherlands, October to December 2015
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Self-citation
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Coluccini, M. L. (2020) · Revista de la Facultad de Ciencias Médicas de Córdoba · doi:10.31053/1853.0605.v77.n1.24070 · Cited by 3

Authors: Havelaar, A. H., Haagsma, J. A., Mangen, M.-J. J., Kemmeren, J. M., Verhoef, L. P. B., Vijgen, S. M. C., Wilson, M., Friesema, I. H. M., Kortbeek, L. M., van Duynhoven, Y. T. H. P., & van Pelt, W.
Affiliations: Utrecht University (NL)
Erasmus MC (NL)
University Medical Center Utrecht (NL)
National Institute for Public Health and the Environment (NL)
Corresponding author: Havelaar, Arie H.
ORCID: Havelaar, Arie H.
Haagsma, Juanita A.
Mangen, Marie-Josée J.
Kemmeren, Jeanet M.
Friesema, Ingrid H.M.
Kortbeek, Laetitia M.
Venue: International Journal of Food Microbiology
Publisher: Elsevier BV
Published: 2012-06
Volume: 156
Issue: 3
Pages: 231-238
ISSN: 0168-1605 (ISSN-L)
DOI: 10.1016/j.ijfoodmicro.2012.03.029
OpenAlex: W2040888966
Cited by: 380
References: 54
Citations by year: 2026: 10 · 2025: 11 · 2024: 16 · 2023: 11 · 2022: 23 · 2021: 18 · 2020: 34 · 2019: 24 · 2018: 31 · 2017: 30 · 2016: 39 · 2015: 30 · 2014: 50 · 2013: 42 · 2012: 10
FWCI: 64.79
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: International Journal of Food Microbiology (publishedVersion)
PubMed (publishedVersion)
EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
Utrecht University Repository (Utrecht University) (submittedVersion)
Rivm Repository (Netherlands National Institute for Public Health and the Environment) (submittedVersion)
Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
Topics: Life Sciences › Agricultural and Biological Sciences › Food Science › Salmonella and Campylobacter epidemiology
Life Sciences › Agricultural and Biological Sciences › Food Science › Food Safety and Hygiene
Life Sciences › Agricultural and Biological Sciences › Food Science › Listeria monocytogenes in Food Safety
Keywords: foodborne pathogens, disease burden, disability-adjusted life years, foodborne transmission, Toxoplasma gondii, Campylobacter, Salmonella, norovirus, rotavirus, listeriosis, congenital toxoplasmosis, attributable fraction, foodborne illness prevention, Netherlands
MeSH terms: Adolescent, Adult, Aged, Bacterial Infections, Cause of Death, Child, Child, Preschool, Foodborne Diseases, Persons with Disabilities, Humans, Infant, Listeriosis, Male, Middle Aged, Netherlands, Population Surveillance, Public Health, Salmonella, Salmonella Infections, Cohort Studies, Incidence, Cost of Illness, Risk Assessment, Quality-Adjusted Life Years, Norovirus

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Disease burden of foodborne pathogens in the Netherlands, 2009

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