Hostname: page-component-7c8c6479df-7qhmt Total loading time: 0 Render date: 2024-03-29T11:28:34.987Z Has data issue: false hasContentIssue false

Epidemic characteristics and spatio-temporal patterns of scrub typhus during 2006–2013 in Tai'an, Northern China

Published online by Cambridge University Press:  29 December 2014

L. ZHENG
Affiliation:
Department of Epidemiology and Health Statistics, School of Public Health, Shandong University, Jinan, China
H.-L. YANG
Affiliation:
Tai'an Center for Disease Control and Prevention, Tai'an, China
Z.-W. BI
Affiliation:
Institute for Bacterial Infectious Disease Control and Prevention, Shandong Center for Disease Control and Prevention, Jinan, China
Z.-Q. KOU
Affiliation:
Institute for Bacterial Infectious Disease Control and Prevention, Shandong Center for Disease Control and Prevention, Jinan, China
L.-Y. ZHANG
Affiliation:
Department of Epidemiology and Health Statistics, School of Public Health, Shandong University, Jinan, China
A.-H. ZHANG
Affiliation:
Tai'an Center for Disease Control and Prevention, Tai'an, China
L. YANG
Affiliation:
Department of Epidemiology and Health Statistics, School of Public Health, Shandong University, Jinan, China
Z.-T. ZHAO*
Affiliation:
Department of Epidemiology and Health Statistics, School of Public Health, Shandong University, Jinan, China
*
*Author for correspondence: Professor Z.-T. Zhao, Department of Epidemiology and Health Statistics, School of Public Health, Shandong University, 44 Wenhuaxi Road, Jinan 250012, China. (Email: ztzhao@sdu.edu.cn)
Rights & Permissions [Opens in a new window]

Summary

Tai'an, a famous cultural tourist district, is a new endemic foci of scrub typhus in northern China. Frequent reports of travel-acquired cases and absence of effective vaccine indicated a significant health problem of scrub typhus in Tai'an. Thus, descriptive epidemiological methods and spatial-temporal scan statistics were used to describe the epidemic characteristics and detect the significant clusters of the high incidence of scrub typhus at the town level in Tai'an. Results of descriptive epidemiological analysis showed a total of 490 cases were reported in Tai'an with the annual average incidence ranging from 0·48 to 2·27/100 000 during 2006–2013. Females, the elderly and farmers are the high-risk groups. Monthly changes of scrub typhus cases indicated an obvious epidemic period in autumn. Spatial-temporal distribution analysis, showed significant clusters of high incidence mainly located in eastern and northern Tai'an. Our study suggests that more effective, targeted measures for local residents should be implemented in the eastern and northern areas of Tai'an in autumn. Meanwhile, it may prove beneficial for health policy makers to advise travellers to take preventive measures in order to minimize the risk of infection of scrub typhus in Tai'an.

Type
Original Papers
Copyright
Copyright © Cambridge University Press 2014 

INTRODUCTION

Scrub typhus is an acute infectious disease caused by Orientia tsutsugamushi (Ot), which is transmitted to humans by infected larval trombiculid mites (chiggers). It is characterized by high fever, eschar or skin ulcer, enlarged lymph glands and rashes [Reference Liu1, Reference Zhang2]. Some patients may suffer with severe complications, including pneumonia, encephalitis, multi-organ failure or even death [Reference Sirisanthana, Puthanakit and Sirisanthana3Reference Lee6]. Scrub typhus is widely prevalent in the ‘tsutsugamushi triangle’, north to northern Japan and eastern Russia, south to northern Australia and west to Pakistan and Afghanistan. It has been estimated that about 1 billion people are at risk for scrub typhus, and almost 1 million scrub typhus cases occur annually [Reference Watt and Parola7].

In China, scrub typhus was known to occur mainly in southern regions before 1985. It has emerged and expanded rapidly in northern China since an outbreak in Shandong Province in 1986 [Reference Zhang, Wang and Zhao8, Reference Zhang, Bi and Zhao9]. Tai'an, a new epidemic foci of scrub typhus, has gradually become one of the most seriously affected area for the disease in northern China since an outbreak in 2000 [Reference Wang10, Reference Ding11]. A recent study identified the genetic diversity of Ot in Tai'an district [Reference Zhang12] where the infection rate of Ot in rodents (the major host of chiggers) was 5·88% [Reference Yang13]. These factors might affect the severity and incidence of scrub typhus in Tai'an. Moreover, as a famous tourist attraction, Tai'an receives millions of visitors every year, this large number of tourists may increase the probability of scrub typhus infection. Moreover, with frequent reports of travel-acquired cases and absence of effective vaccine [Reference Watt and Parola7, Reference Nachega14Reference Chattopadhyay and Richards16], a better understanding of the spatial-temporal distribution patterns of scrub typhus in order to identify high-risk areas is imperative.

Thus, we explored the epidemic characteristics and spatial-temporal patterns of scrub typhus in Tai'an during 2006–2013 to detect high-risk groups and clustering areas, in order to provide information for the local health department to implement targeted surveillance and a control policy; moreover, this study will have important implications for the design of preventive measures for travellers.

MATERIAL AND METHODS

Study area

Tai'an is located in the central part of Shandong province (latitude 35° 38′ to 36° 28′ N, longitude 116° 02′ to 117° 59′ E) (Fig. 1). It includes 86 towns belonging to six counties with a population of about 5·53 million and has a temperate, semi-humid monsoonal climate. Tai'an has a variety of landscape types including mountains, hills, plains and lakes.

Fig. 1. Location of the study area, Tai'an district, Shandong Province, China.

Data source

Surveillance data on reported scrub typhus cases from 2006 to 2013, including information about sex, age, residential address, occupation and onset date of symptoms were obtained from the Shandong Disease Reporting Information System (SDRIS). The diagnostic criteria for scrub typhus were based on epidemiological exposure history, clinical manifestations, and laboratory tests such as the Weil–Felix test. Confirmed cases were clinical cases with a positive result by indirect immunofluorescence antibody assay (IFA) or nested polymerase chain reaction (PCR) test targeting the 56-kDa type-specific antigen gene of Ot [Reference Zhang2, Reference Peng.17].

METHODS

Demographic distribution analysis

The demographic distribution characteristics including age, sex and occupation distribution of scrub typhus cases from 2006 to 2013 in Tai'an were analysed according to surveillance data using χ 2 test and Kruskal–Wallis H signed-rank test with SPSS v. 16.0 (SPSS Inc., USA), P < 0·05 was considered statistically significant.

Spatial autocorrelation analysis

To investigate global spatial autocorrelation of scrub typhus incidence at the town level, we used the spatial autocorrelation statistic (Moran's I) of GeoDa0.9.5-i, a freely available spatial statistics software package (https://geodacenter.asu.edu/). Monte Carlo randomization was employed to assess the significance of Moran's I and the number of permutation tests was set to 999. Z score (⩾1·96) indicated that scrub typhus incidence was not distributed randomly and cases were likely to cluster at the town level.

Spatial and spatial-temporal cluster analysis

We explored spatial and spatial-temporal distribution of scrub typhus based on the town-level polygon map of Tai'an at a scale of 1:100 000, on which all scrub typhus cases were geocoded to latitude and longitude coordinates and matched to the point layers. Demographic information of each town was obtained from the Tai'an Statistical Yearbook and ArcGIS 9.3 software (ESRI Inc., USA) was used for making quantitative thematic maps.

SaTScan v. 9.1.1 (http://www.satscan.org/) was applied to identify spatial and spatial-temopal potential clusters of scrub typhus. According to the town-level scrub typhus cases, demographic data and geographical data, a retrospective spatial cluster analysis for higher incidence based on Possion model was used [Reference Kulldorff18]. The spatial scan statistic is defined by a circular (or elliptic) window which is in turn centred on each geographical area throughout the study area. The space–time scan statistic imposes a cylindrical window with a circular (or elliptic) geographical base and with height corresponding to time. Clusters were scanned by the variable-sized circular (or elliptic) or cylindrical moving window. The circular window was choosen for the analysis in our study. Monte Carlo simulation was used to test the null hypothesis assumed that the relative risk (RR) of scrub typhus was the same within the window compared to outside [Reference Fang19]. Meanwhile, SaTScan reported the most likely clusters comprised the one with the maximum likelihood, and secondary clusters in the same way as for the most likely cluster [20]. In this study, we set 50% of the total population at risk as the maximum spatial cluster size and 50% of the total population at risk as the maximum temporal cluster size to find possible sub-clusters. We set 999 as the number of Monte Carlo replications, and P < 0·05 was considered statistically significant for clusters.

RESULTS

Descriptive analysis of scrub typhus in Tai'an

A total of 490 cases were reported in Tai'an from 2006 to 2013 with the annual average incidence ranging from 0·48/100 000 in 2007 to 2·27/100 000 in 2012. Of these, 198 cases (40·4%) were males and 292 cases (59·6%) were females. The annualized average incidence of females was significantly higher than that of males (χ 2 = 20·41, P < 0·001) and distribution of cases by sex changed significantly (χ 2 = 16·16, P = 0·024) during 2006–2013. We found there was no significant change in distribution of cases by age group (<10, 10–19, 20–29, 30–39, 40–49, 50–59, 60–69, ⩾70 years) during the 8-year study period (H = 10·47, P = 0·164), and patients aged >50 years accounted for 59·0% of cases. Regarding occupation, 83·9% of scrub typhus patients were farmers. Workers (5·1%), preschoolers (3·7%) and pupils (2·7%) were also present (Table 1). The monthly changes of scrub typhus cases showed an obvious epidemic period from October to November, with a peak in October (Fig. 2).

Fig. 2. Monthly distribution of scrub typhus cases in Tai'an, 2006–2013.

Table 1. Demographic characteristics of scrub typhus cases in Tai'an, 2006–2013

Spatial autocorrelation of scrub typhus in Tai'an

Moran's scatter plot and the significance assessment by permutation test of spatial autocorrelation for annualized average incidence of scrub typhus in Tai'an is presented in Figure 3. The value of global Moran's I statistic (0·4776) is shown in Figure 3a , and the number of permutations (999) and Z scores (7·4137) are shown in Figure 3b . Spatial autocorrelation analysis for annual incidence of scrub typhus in Tai'an from 2006 to 2013 showed that Moran's I statistic was significant from 2008 to 2013 at a significance level of 0·05, while it was not significant in 2006 and 2007 (Table 2).

Fig. 3. Global spatial autocorrelation analysis for annual average incidence of scrub typhus in Tai'an from 2006 to 2013. (a) Moran's scatter plot for annualized average incidence of scrub typhus. (b) Histogram for significance assessment of Moran's I.

Table 2. Spatial autocorrelation analysis for annualized incidence of scrub typhus in Tai'an, 2006–2013

Purely spatial analysis

Scrub typhus cases in Tai'an during 2006–2013 showed non-random distribution in space. The significant clusters of high incidence per year are listed in Table 3 and illustrated graphically in Figure 4. It was apparent that the locations of these clusters changed little by year. The most likely clusters were in the northern (2006) and eastern (2008–2013) regions of Tai'an, the size of the clusters expanded in 2008, 2011 and 2013. Secondary clusters were detected in eastern (2006) and northern (2012, 2013) Tai'an.

Fig. 4. Spatial clusters with significant higher incidence in Tai'an, 2006–2013.

Table 3. SaTScan statistics for spatial cluster with significant higher incidence in Tai'an, 2006–2013

Spatial-temporal analysis

Table 4 and Figure 5 show statistically significant spatial-temporal clusters for high incidence of scrub typhus in Tai'an from 2006 to 2013 detected by the space–time scan statistic based on a Poisson model. It is noticeable that scrub typhus was not distributed randomly in space–time. One most likely statistically significant cluster was identified in the eastern region of Tai'an from September 2009 to November 2012 (RR = 20·67, P < 0·001), with 166 observed cases compared to 11·83 expected cases. One statistically significant secondary cluster was located in the area encompassing 42 towns around Mount Tai, with 35 observed cases compared to 2·52 expected cases in October 2012 (RR = 14·85, P < 0·001). It can be seen that scrub typhus endemic areas have expanded from the initial eastern parts of Tai'an in 2009 to the northern parts by 2012.

Fig. 5. Spatial-temporal clusters for high incidence of scrub typhus in Tai'an, 2006–2013. RR, Relative risk.

Table 4. SaTScan statistics for space–time clusters with significant higher incidence in Tai'an, 2006–2013

DISCUSSION

In this study, we describ the epidemic characteristics of scrub typhus cases reported in Tai'an district, northern China from 2006 to 2013. Our study found that the annualized average incidence of females was significantly higher than that of males in Tai'an (χ 2 = 20·41, P < 0·01), which means that women were more susceptible to scrub typhus than men in this area. Farmers and the elderly (people aged >50 years) are high-risk groups, which is consistent with previous studies [Reference Bang, Lee and Lee21, Reference Kim, Kim and Lee22]. It is possible that the changing demographics of rural areas means that most younger males move to the cities for work leaving the elderly age group to engage in agriculture activities.

SaTScan was used to test whether a disease is randomly distributed, to detect the statistically significant clusters over space or space–time, to find risk factors, and to detect or predict disease outbreaks [20]. This method is being widely used in many diseases, including haemorrhagic fever with renal syndrome [Reference Wu23, Reference Wu24], tuberculosis [Reference Onozuka and Hagihara25], cancer [Reference Amin and Burns26] and scrub typhus [Reference Wei27, Reference Zhang28], etc.

Our study found scrub typhus incidence had a positive spatial autocorrelation at the town level in Tai'an from 2008 to 2013. Cases detected by scan statistic analysis were non-randomly distributed and clustered in space and space–time. Purely spatial analysis found that the significant clusters (including most likely and secondary clusters) were located mainly in the eastern and northern regions of Tai'an, the location of clusters for high incidence changed little by year, while the size of clusters expanded in 2008, 2011 and 2013. Hills and mountains make up the main landform of eastern and northern Tai'an. The bushes and grassland vegetation of these areas provide an advantageous habitat for rodents, as well as for chigger mites [Reference Kuo29Reference Traub and Wisseman31]. Meanwhile, the growth of the rural population and increasing outdoor activities during harvest time may also contribute to the incidence of scrub typhus in these areas. Moreover, Xintai and Daiyue are both adjacent to Laiwu, the hyperendemic district of scrub typhus in Shandong Province, which may contribute to significant clusters of high incidence of scrub typhus. Thus, policy makers should give more attention to these regions.

Spatial-temporal analysis detected one most likely cluster for a high occurrence of scrub typhus in eastern Tai'an from September 2009 to November 2012, and one secondary cluster at the area around Mount Tai, including 42 towns belong to three regions (Taishan, Daiyue, Feicheng) in October 2012. The seasonal characteristic pattern of scrub typhus shown by our study may be associated with the following factors. First, Leptotrombidium scutellare, the dominant transmission vector of scrub typhus in Shandong Province, was present from September to November with a peak in November [Reference Liu32]. Second, Apodemus agrarius was the main reservoir host in the field and its density fluctuation was consistent with the seasonal distribution of scrub typhus cases [Reference Yang33]. Third, the infection rate of Ot in rodents in Tai'an was high (5·88%) [Reference Yang13]. Fourth, poor living conditions in rural areas and increasing outdoor activities during harvest time enhanced the risk for local people to come into contact with the transmission vector [Reference Lyu34]. The above factors may contribute to the high infection rate of scrub typhus during autumn.

Scrub typhus is a travel-associated disease and more than 20 travel-acquired cases have been reported since 1988 throughout the world [Reference Jensenius, Fournier and Raoult15], which indicates a significant health problem for popular tourist attractions. Tai'an is a famous tourist district which attracts millions of visitors; however, it is also a new epidemic foci of scrub typhus, which may increase the risk of tourists becoming infected. Thus, our study, which detected high-risk areas and time periods, will assist tourists in understanding the epidemic status of scrub typhus in Tai'an and help in taking preventive measures, such as choosing a non-epidemic season to visit, avoiding jungle areas with an abundance of chiggers, and wearing protective clothing, etc.

Our study had some limitations. First, cluster detection was based on the circular or cylindrical scan window, while the actual shapes of clusters were not all like that. Second, many factors related to incidence of scrub typhus were not considered, and future research should take environmental and socioeconomic factors into account.

In conclusion, our study described the epidemic characteristics, and identified spatio-temporal high-risk clusters of scrub typhus in Tai'an during 2006–2013. Our findings may help health authorities to implement efficient, targeted scrub typhus control measures for local residents, as well as for travellers.

ACKNOWLEDGEMENTS

The work was supported by a grant from the National Natural Science Foundation of China (No. 81 273 133).

DECLARATION OF INTEREST

None.

References

REFERENCES

1. Liu, YX, et al. Clinical characteristics of the autumn-winter type scrub typhus cases in south of Shandong province, northern China. BMC Infectious Diseases 2009; 9: 82.CrossRefGoogle ScholarPubMed
2. Zhang, M, et al. Scrub typhus: surveillance, clinical profile and diagnostic issues in Shandong, China. American Journal of Tropical Medicine and Hygiene 2012; 87: 10991104.CrossRefGoogle ScholarPubMed
3. Sirisanthana, V, Puthanakit, T, Sirisanthana, T. Epidemiologic, clinical and laboratory features of scrub typhus in thirty Thai children. Pediatric Infectious Disease Journal 2003; 22: 341345.CrossRefGoogle ScholarPubMed
4. Cracco, C, et al. Multiple organ failure complicating probable scrub typhus. Clinical Infectious Diseases 2000; 31: 191192.CrossRefGoogle ScholarPubMed
5. Kim, DM, et al. Scrub typhus meningitis or meningoencephalitis. American Journal of Tropical Medicine and Hygiene 2013; 89: 12061211.CrossRefGoogle ScholarPubMed
6. Lee, CS, et al. Risk factors leading to fatal outcome in scrub typhus patients. American Journal of Tropical Medicine and Hygiene 2009; 81: 484488.CrossRefGoogle ScholarPubMed
7. Watt, G, Parola, P. Scrub typhus and tropical rickettsioses. Current Opinion in Infectious Diseases 2003; 16: 429436.CrossRefGoogle ScholarPubMed
8. Zhang, M, Wang, XJ, Zhao, ZT. Current epidemic status and issues on prevention and control of scrub typhus [in Chinese]. Zhonghua liu xing bing xue za zhi 2011; 32: 419423.Google ScholarPubMed
9. Zhang, L, Bi, Z, Zhao, Z. Recent advances in molecular epidemiology of Orientia tsutsugamushi in China [in Chinese]. Zhonghua liu xing bing xue za zhi 2014; 35: 8892.Google ScholarPubMed
10. Wang, ZW, et al. Investigation of the first outbreak of scrub typhus in Feicheng. Disease Surveillance 2001; 8: 307308.Google Scholar
11. Ding, L, et al. Analysis of epidemic features of scrub typhus between year 2006 and 2010 in Shandong province, China [in Chinese]. Chinese Journal of Preventive Medicine 2012; 46: 338342.Google ScholarPubMed
12. Zhang, M, et al. Genetic variants of Orientia tsutsugamushi in domestic rodents, Northern China. Emerging Infectious Diseases 2013; 19: 11351137.CrossRefGoogle ScholarPubMed
13. Yang, LP, et al. Comparative analysis of nucleotide sequences of Orientia tsutsugamushi in different epidemic areas of scrub typhus in Shandong, China. American Journal of Tropical Medicine and Hygiene 2008; 78: 968972.CrossRefGoogle ScholarPubMed
14. Nachega, JB, et al. Travel-acquired scrub typhus: emphasis on the differential diagnosis, treatment, and prevention strategies. Journal of Travel Medicine 2007; 14: 352355.CrossRefGoogle ScholarPubMed
15. Jensenius, M, Fournier, PE, Raoult, D. Rickettsioses and the international traveler. Clinical Infectious Diseases 2004; 39: 14931499.Google ScholarPubMed
16. Chattopadhyay, S, Richards, AL. Scrub typhus vaccines: past history and recent developments. Human Vaccines 2007; 3: 7380.CrossRefGoogle ScholarPubMed
17. Peng., WW. Infectious Diseases, 6th edn. Beijing: People's Medical Publishing House, 2004, pp. 118121.Google Scholar
18. Kulldorff, M, et al. A space-time permutation scan statistic for disease outbreak detection. PLoS Medicine 2005; 2: e59.CrossRefGoogle ScholarPubMed
19. Fang, L, et al. Spatial analysis of hemorrhagic fever with renal syndrome in China. BMC Infectious Diseases 2006; 6: 77.CrossRefGoogle ScholarPubMed
20. SaTScan. User's Guide for version 9.1.1. (2011). (http://www.satscan.org/).Google Scholar
21. Bang, HA, Lee, MJ, Lee, WC. Comparative research on epidemiological aspects of tsutsugamushi disease (scrub typhus) between Korea and Japan. Japanese Journal of Infectious Diseases 2008; 61: 148150.CrossRefGoogle ScholarPubMed
22. Kim, S, Kim, JS, Lee, H. Epidemiological characteristics of scrub typhus in Korea, 2009. Osong Public Health and Research Perspectives 2010; 1: 5560.CrossRefGoogle ScholarPubMed
23. Wu, W, et al. Clusters of spatial, temporal, and space-time distribution of hemorrhagic fever with renal syndrome in Liaoning Province, Northeastern China. BMC Infectious Diseases 2011; 11: 229.CrossRefGoogle ScholarPubMed
24. Wu, W, et al. GIS-based spatial, temporal, and space-time analysis of haemorrhagic fever with renal syndrome. Epidemiology and Infection 2009; 137: 17661775.CrossRefGoogle ScholarPubMed
25. Onozuka, D, Hagihara, A. Geographic prediction of tuberculosis clusters in Fukuoka, Japan, using the space-time scan statistic. BMC Infectious Diseases 2007; 7: 26.CrossRefGoogle ScholarPubMed
26. Amin, R, Burns, JJ. Clusters of adolescent and young adult thyroid cancer in Florida counties. BioMed Research International 2014; 2014: 832573.CrossRefGoogle Scholar
27. Wei, Y, et al. Rapid increase of scrub typhus: an epidemiology and spatial-temporal cluster analysis in Guangzhou City, Southern China, 2006–2012. PLoS ONE 2014; 9: e101976.Google ScholarPubMed
28. Zhang, WY, et al. Scrub typhus in mainland China, 2006–2012: the need for targeted public health interventions. PLoS Neglected Tropical Diseases 2013; 7: e2493.CrossRefGoogle ScholarPubMed
29. Kuo, CC, et al. Spatial analysis of scrub typhus infection and its association with environmental and socioeconomic factors in Taiwan. Acta Tropica 2011; 120: 5258.CrossRefGoogle ScholarPubMed
30. Tsai, PJ, Yeh, HC. Scrub typhus islands in the Taiwan area and the association between scrub typhus disease and forest land use and farmer population density: geographically weighted regression. BMC Infectious Diseases 2013; 13: 191.CrossRefGoogle ScholarPubMed
31. Traub, R, Wisseman, CL Jr. The ecology of chigger-borne rickettsiosis (scrub typhus). Journal of Medical Entomology 1974; 11: 237303.CrossRefGoogle ScholarPubMed
32. Liu, YX, et al. Investigation on the vectors of scrub typhus in the foci of Shandong Province [in Chinese]. Modern Preventive Medicine 2004; 676: 678684.Google Scholar
33. Yang, LP, et al. Investigation on rodents' natural infection of Oientia tsutsugamushi in Tai'an area of Shandong, China [in Chinese]. Chinese Journal of Public Health 2008; 7: 877878.Google Scholar
34. Lyu, Y, et al. A case-control study of risk factors associated with scrub typhus infection in Beijing, China. PLoS ONE 2013; 8: e63668.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. Location of the study area, Tai'an district, Shandong Province, China.

Figure 1

Fig. 2. Monthly distribution of scrub typhus cases in Tai'an, 2006–2013.

Figure 2

Table 1. Demographic characteristics of scrub typhus cases in Tai'an, 2006–2013

Figure 3

Fig. 3. Global spatial autocorrelation analysis for annual average incidence of scrub typhus in Tai'an from 2006 to 2013. (a) Moran's scatter plot for annualized average incidence of scrub typhus. (b) Histogram for significance assessment of Moran's I.

Figure 4

Table 2. Spatial autocorrelation analysis for annualized incidence of scrub typhus in Tai'an, 2006–2013

Figure 5

Fig. 4. Spatial clusters with significant higher incidence in Tai'an, 2006–2013.

Figure 6

Table 3. SaTScan statistics for spatial cluster with significant higher incidence in Tai'an, 2006–2013

Figure 7

Fig. 5. Spatial-temporal clusters for high incidence of scrub typhus in Tai'an, 2006–2013. RR, Relative risk.

Figure 8

Table 4. SaTScan statistics for space–time clusters with significant higher incidence in Tai'an, 2006–2013