sábado, 19 de marzo de 2016

Nontyphoidal Salmonella Infection, Guangdong Province, China, 20121 - Volume 22, Number 4—April 2016 - Emerging Infectious Disease journal - CDC

Nontyphoidal Salmonella Infection, Guangdong Province, China, 20121 - Volume 22, Number 4—April 2016 - Emerging Infectious Disease journal - CDC





Volume 22, Number 4—April 2016

Dispatch

Nontyphoidal Salmonella Infection, Guangdong Province, China, 20121

Xi Huang2, Qiong Huang2, Zhongjun Dun, Wei Huang, Shuyu Wu, Junhua Liang, Xiaoling Deng, and Yonghui ZhangComments to Author 
Author affiliations: Guangdong Provincial Center for Disease Control and Prevention, Guangzhou, China (X. Huang, Q. Huang, J. Liang, X. Deng, Y. Zhang)Guangdong Provincial Institute of Public Health, Guangzhou (Z. Dun)Liwan District Center for Disease Control and Prevention, Guangzhou (W. Huang)Centers for Disease Control and Prevention, Atlanta, Georgia, USA (S. Wu)

Abstract

We used active and passive surveillance to estimate nontyphoidal Salmonella (NTS) infection during 2012 in Guangdong Province, China. Under passive surveillance, for every reported NTS infection, an estimated 414.8 cases occurred annually. Under active surveillance, an estimated 35.8 cases occurred. Active surveillance provides remarkable advantages in incidence estimate.
Gastrointestinal illness or diarrhea caused by foodborne pathogens, such as nontyphoidal Salmonella (NTS), is a global public health concern (1). Many countries (e.g., the United States, England and Wales, Australia, Canada, Jordan, and Japan) have estimated the incidence of gastrointestinal illness caused by specific pathogens (28). However, in China, information is limited about the incidence of specific foodborne pathogens.
In 2003, China initiated a national, internet-based disease reporting system called the National Notifiable Disease Reporting System (NNDRS). This system legally requires routine reporting from all medical institutions and public health units of a list of infectious diseases. In this system, diarrheal pathogens other than Vibiro cholerae and Shigella dysenteriae, such as Salmonella spp., Escherichia coli, and Listeria spp., are reported as “other infectious diarrhea”; information about etiology is provided as an additional comment (9). Because NNDRS is passive, few reports include laboratory confirmation. According to previous data from passive surveillance, <1,000 NTS cases were reported in Guangdong Province annually since 2009, representing only a small proportion of actual infections.
In 2009, Guangdong Provincial Center for Disease Control and Prevention (Guangdong CDC) established laboratory-based active surveillance for NTS infection. In 2012, this system covered more than half of the Guangdong Province prefectures, capturing 61.5% of the population served by 27 sentinel hospitals (21 general hospitals and 6 specialized hospitals, including pediatric and gynecologic). In the surveillance system, patients with >3 loose stools in a 24-hour period plus fever, vomiting, or abdominal pain who visited the sentinel hospitals were enrolled as cases, and fecal samples were collected. The sentinel hospitals were required to forward Salmonellaisolates to Guangdong CDC, along with epidemiologic data, for analysis. Culture-confirmed cases were then reported to NNDRS with pathogen information. Based on the pyramid model of burden of illness, we used data from active and passive surveillance to estimate NTS infection and to clarify the advantages and disadvantages of each system (2,7,10).

The Study

The estimation requires multiple steps. First, a person must have symptoms severe enough for medical care (multiplier 1). Second, the physician must collect patients’ specimens (multiplier 2) and forward them for testing by bacterial culture (multiplier 3). Third, the sample test result must be positive (multiplier 4), and the confirmed case must be reported (multiplier 5) (2,7,8).
To obtain multiplier 1, we conducted a 12-month population-based household survey during March 1, 2012–February 28, 2013 (approved by the Ethics Committee of Guangdong CDC). Respondents were randomly selected from 4 districts in western, eastern, and central Guangdong Province. The case definition was the same as that for active surveillance. We used a standard questionnaire to collect information about diarrhea in the previous 4 weeks. The incidence rate of diarrhea was 0.1081 (95% CI 0.1004–0.1158) episodes/person-year; 38.6% of the household survey respondents with diarrhea sought medical care. Multipliers 2 and 3 were based on data from sentinel hospitals and comprised the overall number of diarrhea cases, samples collected, and samples submitted for culture during the year. A total of 75,583 (45.3%) samples of 166,729 registered diarrhea cases in the sentinel hospitals were collected, of which 22,577 (29.9%) were tested. Laboratories of sentinel hospitals cultured samples for Salmonella in accordance with standard protocol provided by the national reference laboratory by using MacConkey agar as plating medium. According to a proficiency testing program, the Salmonellaisolation sensitivity rate of these laboratories was 87.5% (multiplier 4). The numbers of Salmonella isolates identified and reported to NNDRS as NTS infectious diarrhea by all sentinel hospitals yielded the proportion of cases reported (648/1,061, 61.1%) (multiplier 5). We estimated the number of infections using the above 5 multipliers. Thus, active surveillance for each reported NTS infection identified 35.8 cases. We also analyzed multipliers of specialized hospitals (Table 1).
In the population survey–based passive surveillance system, multiplier 1 was the same as for active surveillance. According to a comparison with samples from the submission proportion in a survey of physician-diagnosed diarrhea in Guangdong Province during 2009 (Mann-Whitney test, p = 0.246) (11), and a comparison between medical institutions that charged and did not charge for testing (Kolmogorov-Smirnov test, p = 0.837), the proportion of samples submitted and tested from active surveillance were also used as estimates of passive surveillance. The average test sensitivity of sentinel laboratories before active surveillance began was used as an estimate of all medical institutions (i.e., the sensitivity of passive surveillance [48.2%]). Using numbers ofSalmonella isolates in Guangdong Province from laboratory data, and number of reported NTS cases by all medical institutions, we determined the proportion of reported NTS was 9.6% (991/10,360). Thus, for each reported NTS case under passive surveillance, 414.8 cases actually occurred. Multipliers of 5 age groups also were presented (Table 1).
To generate a more robust estimate, we conducted uncertainty and sensitivity analyses (online Technical Appendix,http://wwwnc.cdc.gov/EID/article/22/4/15-1372-Techapp1.pdf[PDF - 257 KB - 3 pages]) on passive surveillance data using Monte Carlo simulation (@Risk 6.0; Palisade, Ithaca, NY, USA) (12). We used β distribution to describe the uncertainty of proportions and negative binominal distribution to estimate the number of cases. The sensitivity analysis helped determine factors that provide higher uncertainty in the estimate.
Thumbnail of Rank correlations for the total number of nontyphoidal Salmonella cases in the population (tornado diagram), Guangdong Province, China, 2012.
Figure. Rank correlations for the total number of nontyphoidal Salmonella cases in the population (tornado diagram), Guangdong Province, China, 2012.
The uncertainty analysis model predicted a 411.9 (95% CI 308.4–592.7) overall multiplier and estimated that 408,499 (95% CI 302,899–591,901) Salmonella cases occurred per year when the overall multiplier was applied to the 991 reported NTS cases, resulting in 391.6 (95% CI 290.3–567.4) cases/100,000 persons in 2012. Incidence for 5 age groups was also estimated (Table 2). The rank correlation of various factors in the model showed that patients seeking medical care provided the highest uncertainty in the overall estimate (influence rate 96%) (Figure).

Conclusions

Our estimated NTS incidence was lower than the incidence in China as determined from a literature review (626.5 cases/100,000 persons) (13) but close to that in the United States (352.1 cases/100,000 persons) (3). However, incidences for persons <5 years of age and 5–24 years of age in our study were higher than those for persons in China and the United States, highlighting that Salmonella represents a major health problem in Guangdong Province, especially among younger persons. Our estimated active surveillance rate (35.8) of NTS infections per reported case is similar to estimates in the United States (38.6 and 39) (2,10) but different from those for England (3.2), Jordan (278), and Japan (63) (7,8,14). Such differences might be due to differences in methods used and to actual differences in Salmonella infections.
With fewer missing cases and less underestimation, active surveillance has lower overall multipliers than passive surveillance, indicating smaller surveillance artifacts and more accurate incidence estimate and presents remarkable advantages over passive surveillance. The estimate for active surveillance also showed that if we seek to reduce uncertainty in the overall estimate, we should first focus on encouraging patients to seek medical care.
Our study provides policymakers in China with a reference for the importance of Salmonella incidence and calls for balanced surveillance on both foodborne infections and foods and enlarging active surveillance scales. More surveillance guidelines need to be developed to help physicians identify timing of sampling, tests, and performance. Laws requiring reporting of foodborne diseases and pathogens need to be enacted to increase quantity and quality of reporting. The result suggests that to increase care seeking and sample submission, government health insurance schemes should be further developed to cover diagnostic tests and treatments of diseases of public health significance.
Ms. Xi Huang is a master of medicine and works as a public health physician at the Guangdong CDC, Guangdong, China. Her research interests include foodborne disease surveillance, outbreak detection, and epidemiologic investigation.

Acknowledgments

We thank professionals from prefectural and county level CDCs for the household survey and physicians at sentinel hospitals for data collection. We also thank Olga Henao, Dana Cole, and Shua Chai for suggestions on the study and Jianghui Zhu and Xiaoyu Song for statistical review.
The study was supported by the China–US Collaborative Program on Emerging and Re-emerging Infectious Diseases (subproject 6) (1U2GHH00018-01) and Guangdong Medical Research Foundation (sponsored projectA2013069).

References

  1. Majowicz SEMusto JScallan EAngulo FJKirk MO’Brien SJThe global burden of nontyphoidal Salmonella gastroenteritis. Clin Infect Dis.2010;50:8829 and. DOIPubMed
  2. Voetsch ACVan Glider TJAngulo FJFarley MMShallow SMarcus RFoodNet estimate of the burden of illness caused by nontyphoidal Salmonellainfections in the United States. Clin Infect Dis2004;38(Suppl 3):S12734 and. DOIPubMed
  3. Scallan EHoekstra RMAngulo FJTauxe RVWiddowson MARoy SLFoodborne illness acquired in the United States—major pathogens. Emerg Infect Dis2011;17:715 and. DOIPubMed
  4. Adak GKMeakins SMYip HLopman BAO’Brien SJDisease risks from foods, England and Wales, 1996–2000. Emerg Infect Dis2005;11:36572 .DOIPubMed
  5. Hall GKirk MDBecker NGregory JEUnicomb LMillard GEstimating foodborne gastroenteritis, Australia. Emerg Infect Dis2005;11:125764and. DOIPubMed
  6. Thomas MKMajowicz SESockett PNFazil APollari FDoré KEstimated numbers of community cases of illness due to Salmonella, Campylobacterand verotoxigenic Escherichia coli: pathogen-specific community rates. Can J Infect Dis Med Microbiol2006;17:22934 .PubMed
  7. Gargouri NWalke HBelbeisi AHadadin ASalah SEllis AEstimated burden of human Salmonella, Shigella, and Brucella infections in Jordan, 2003–2004. Foodborne Pathog Dis2009;6:4816 . DOIPubMed
  8. Kubota KIwasaki EInagaki SNokubo TSakurai YKomatsu MThe human health burden of foodborne infections caused by Campylobacter, Salmonella, and Vibrio parahaemolyticus in Miyagi Prefecture, Japan. Foodborne Pathog Dis2008;5:6418 and. DOIPubMed
  9. Varma JKWu SFeng ZDetecting and controlling foodborne infections in humans: lessons for China from the United States experience. Glob Public Health2012;7:76678 and. DOIPubMed
  10. Chalker RBBlaser MJA review of human salmonellosis: III. Magnitude of Salmonella infection in the United States. Rev Infect Dis1988;10:11124and. DOIPubMed
  11. Ke BRan LWu SDeng XKe CFeng ZSurvey of physician diagnostic and treatment practices for patients with acute diarrhea in Guangdong Province, China. Foodborne Pathog Dis2012;9:4753 and. DOIPubMed
  12. Powell MEbel ESchlosser WConsidering uncertainty in comparing the burden of illness due to foodborne microbial pathogens. Int J Food Microbiol2001;69:20915 and. DOIPubMed
  13. Mao XHu JLiu XEstimation on disease burden of foodborne nontyphoid salmonellosis in China using literature review method. Chinese Journal of Disease Control and Prevention. 2011;15:6225.
  14. Wheeler JGSethi DCowden JMWall PGRodrigues LCTompkins DSStudy of infectious intestinal disease in England: rates in the community, presenting to general practice, and reported to national surveillance. The Infectious Intestinal Disease Study Executive. BMJ1999;318:104650and. DOIPubMed

Figure

Tables

Technical Appendix

Suggested citation for this article: Huang X, Huang Q, Dun Z, Huang W, Wu S, Liang J, et al. Nontyphoidal Salmonella infection, Guangdong Province, China, 2012. Emerg Infect Dis. 2016 Apr [date cited]. http://dx.doi.org/10.3201/eid2204.151372
DOI: 10.3201/eid2204.151372


1Preliminary results from this study were presented at the 2015 International Conference on Emerging Infectious Diseases (board 189), August 24–26, 2015, Atlanta, Georgia, USA.
2These authors contributed equally to this article.

No hay comentarios:

Publicar un comentario