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Epidemiology and Infection logoLink to Epidemiology and Infection
. 2017 Aug 23;145(13):2735–2744. doi: 10.1017/S0950268817001844

A cross-sectional study of acute diarrhea in Pudong, Shanghai, China: prevalence, risk factors, and healthcare-seeking practices

J-X YU 1,2,, W-P ZHU 3,, C-C YE 3,4,, C-Y XUE 3,4, S-J LAI 2, H-L ZHANG 2, Z-K ZHANG 2,5, Q-B GENG 2,6, W-Z YANG 2, Q SUN 3, Z-J LI 2,*
PMCID: PMC9148769  PMID: 28830575

SUMMARY

Diarrhea is a common cause of morbidity and mortality and the incidence of diarrhea in the world has changed little over the past four decades. To assess the prevalence of and healthcare practices for diarrhea, a cross-sectional study was conducted in Pudong, Shanghai, China. In October 2014, a total of 5324 community residents were interviewed. Respondents were asked if they had experienced diarrhea (defined as ⩾3 passages of watery, loose, bloody, or mucoid stools within a 24-h period) in the previous month prior to the interview. The monthly prevalence of diarrhea was 4·1% (95% CI: 3·3–4·8), corresponding to an incidence rate of 0·54 episodes per person-year. The proportion of individuals with diarrhea who sought healthcare was 21·2% (95% CI: 13·4–29·0). Diarrhea continues to impose a considerable burden on the community and healthcare system in Pudong. Young age and travel were identified as predictors of increased diarrhea occurrence.

Key words: Diarrhea, epidemiology, healthcare-seeking behavior, prevalence, risk factors

INTRODUCTION

Diarrhea is a common cause of morbidity and mortality worldwide, with an estimated loss of ~89·5 million disability-adjusted life years and 1·45 million deaths in 2010 [1, 2], which represents a major obstacle to the achievement of the United Nation's Fourth Millennium Development Goals [3]. China is one of the 15 high-burden countries for diarrhea in the world [4], and a recent national survey estimated that China's incidence rate for acute gastrointestinal illness (diarrhea and vomiting) was 0·56 episodes per person-year in 2010 [5]. However, in Pudong New Area, the largest district of Shanghai city, considerable data gaps exist regarding the risk factors and the burden of diarrhea on both the population and the healthcare system. From a public health perspective, these represent important data for planning, implementing and evaluating disease control programs, e.g., the development of recommendations for vaccines and the formulation of food and water hygiene regulations. To this end, a cross-sectional study of diarrhea was conducted in the community of Pudong in October 2014. At the end of year 2014, Pudong had a population of 5·4 million and about 90% of the population were living in urban areas; the average gross domestic product per capita was 97 370 yuan (~US$ 14 000), about twice that of the national average (47 203 yuan) [6].

The purpose of the present study was to measure the prevalence of diarrhea, explore its determinants, and determine the proportion of people who seek healthcare for diarrhea in the community of Pudong.

METHODS

Study design and sampling procedure

A complex sampling method was used to recruit survey respondents. Each referral area of the 46 community health centers in Pudong randomly selected one community, and all residents living in the selected community during the year prior to the survey were eligible for the interview. Trained community health workers traveled to the selected communities to conduct face-to-face surveys at several locations (residential areas, kindergartens and children's vaccination clinics) through Monday to Sunday during day time (from 9 A.M. to 5 P.M.) in our study period. Study subjects were recruited at these locations using a convenience (accidental) sampling method, in which community residents close at hand were interviewed. Because of the different methodologies used, the interviews were conducted separately for 2 age strata, e.g., children <5 years of age and people ⩾5 years of age (older children, adolescents and adults) (Fig. 1).

Fig. 1.

Fig. 1.

Schematic diagram of sampling frame for diarrhea survey in Pudong, Shanghai, China, 2014.

A minimum number of 45 completed interviews from children <5 years old and 70 completed interviews from older children, adolescents and adults were required for each selected community based on the total sample size of the study. For children <5 years old, a target sample of 2000 was required. This number was calculated based on an assumed monthly prevalence of 12% for children aged <5 years [5, 7], with a precision level of 2%, a confidence level of 95% and a design effect of two. For people ⩾5 years of age, a target sample of 3000 was required based on an assumed monthly prevalence of 4% [5], with a 1% precision level, a 95% confidence level and a design effect of two.

Data collection

Standardized questionnaires were used to collect data from the study subjects, which were adapted from previous works of World Health Organization and were modified to suit local context [7]. Diarrhea was defined as ⩾3 passages of watery, loose, mucoid, or bloody stools within a 24-h period [8]. A 7-day symptom-free interval was used to define a new episode of diarrhea. Surrogate interviews were conducted for the child subjects by interviewing the children's parents or guardians, while subjects ⩾14 years of age were interviewed directly. The questionnaires included three sets of questions: (i) socio-demographic characteristics, including age, sex, occupation (of parents or guardians for children), ethnic group, educational attainment (of parents or guardians for children), average monthly household income, out-of-province travel history in the previous month (defined as going to other parts of China or the rest of the world, of parents or guardians for children), and rotavirus vaccination history for children <5 years of age; (ii) characteristics of self-reported diarrhea, including episodes of diarrhea experienced in the previous month, signs/symptoms, and illness duration; and (iii) hospital utilization behavior (defined as consulting a doctor in private clinic or visiting a community health center or hospital) and attitudes of the respondents. For subjects who had experienced more than two episodes of diarrhea, the illness characteristics and healthcare-seeking behavior of the respondents were described and reported for only the most recent episode. Written and informed consent was obtained from all the participants or from the parents/guardian of children before the interviews.

To validate our results, all the interviews were conducted in Mandarin. A pilot study and training courses for the interviewers were conducted before the study began. An inspector was assigned to each site during the study period to review the finished questionnaires for completeness and logical errors and to eliminate duplicate surveys. Ineligible questionnaires were returned to the interviewers for verification or re-investigation. The collected data were entered into EpiData, version 3.1 (EpiData Association, Odense M, Denmark).

Statistical analysis

All the analyses were conducted in R, version 2.15.3 (R Foundation for Statistical Computing, Vienna, Austria), by using the ‘survey’ package to adjust for the complex sampling procedures [9, 10]. The prevalence of diarrhea was calculated as the number of subjects who reported experiencing diarrhea in previous month divided by the total number of subjects interviewed. All analyses were weighted to account for non-response of the studied subjects, according to the age, sex and site distribution of the Pudong population. The estimated incidence rate of diarrhea was calculated using the formulae and method employed by Thomas et al. [11] To compare demographic and epidemiological characteristics, Chi-square tests or Fisher exact tests were used for the categorical variables, and Wilcoxon rank-sum or Kruskal–Wallis tests were used for the continuous variables, as appropriate. Multivariable logistic regression models were used to investigate the predictors of diarrhea occurrence.

RESULTS

Characteristics of the study respondents

Between October 2nd and November 3rd 2014, we conducted 5324 interviews in 46 communities in Pudong. Of these, 2198 interviews were for child subjects aged <5 years, and 3126 interviews were with subjects ⩾5 years of age. The respondents for the child subjects were the children's parents or guardians (grandparents), and some variables, e.g., education level and travel history, were collected for the respondents rather than for the children. The education level of the respondents for the child subjects was significantly lower (87·0% of these respondents finished primary school or were illiterate) than the educational level of the other respondents (10·7%, P < 0·001). Out-of-province travel history in the previous month prior to the interview was reported by 20·2% of the study respondents. Thirty-two percent of the respondents for the child subjects reported that their children had received the rotavirus vaccination (Table 1).

Table 1.

Characteristics of surveyed respondents in Pudong, Shanghai, China, 2014, stratified by age group

Variables Age groups No. total (%)
No. children aged <5 years (%) No. persons aged ⩾5 years (%)
Gender
Male 1098 (50·0) 1555 (49·8) 2653 (49·9)
Female 1099 (50·0) 1569 (50·2) 2668 (50·1)
Educational attainment1
Primary school or illiterate 1892 (87·0) 335 (10·7) 2227 (42·1)
High school 80 (3·7) 1136 (36·4) 1216 (23·0)
College level and above 203 (9·4) 1647 (52·8) 1850 (34·9)
Average monthly household income, (Chinese yuan)2
<3000 379 (17·3) 744 (23·9) 1123 (21·2)
3000–9999 1030 (47·1) 1602 (51·5) 2632 (49·7)
10 000–19 999 264 (12·1) 271 (8·7) 535 (10·1)
⩾20 000 91 (4·2) 73 (2·3) 164 (3·1)
Don't know 424 (19·4) 418 (13·4) 842 (15·9)
Travel history1
Yes 446 (20·5) 611 (19·9) 1057 (20·2)
No 1731 (79·5) 2455 (80·1) 4186 (79·8)
Rotavirus vaccination
Yes 686 (32·0)
No 1460 (68·0)
1

For children aged <5 years, the numbers in this column represent data for the children's parents or guardians.

2

1 US dollar ≈6·9 Chinese yuan; An n-dash denotes that data were not available.

Prevalence of diarrhea and healthcare-seeking behavior among individuals with diarrhea

In total, 231 of the study respondents (4·3%) reported experiencing at least one newly occurring episode of diarrhea in the previous month prior to the interview. The reported median illness duration of diarrhea was 2 days (range: 1–30 days), with children aged <5 years significantly longer than that of subjects aged ⩾5 years (3 vs. 2 days, P < 0·001). The most frequently reported symptoms other than diarrhea was abdominal pain (n = 68, 28·1%), followed by fever (n = 29, 12·6%), fatigue (n = 24, 10·4%), vomiting (n = 21, 9·1%), restlessness (n = 21, 9·1%), respiratory symptoms (n = 13, 5·6%), and dehydration (n = 4, 1·7%).

The estimated monthly prevalence of diarrhea was 4·1% (95% CI: 3·3–4·8) in Pudong, which represented an incidence rate of 0·54 (95% CI 0·45–0·62) episodes of diarrhea per person-year. The estimated monthly prevalence of diarrhea varied among the age groups (Fig. 2): children <1 years old had the highest proportion (11·1%, 95% CI: 7·7–14·6), while adults aged 45–64 years had the lowest (2·5%, 95% CI: 1·2–3·8). The prevalence of diarrhea was higher among respondents who reported out-of-province travel history in the previous month than among those who had no travel history during that period (4·9% vs. 3·8%, P < 0·001) (Table 2).

Fig. 2.

Fig. 2.

Estimated monthly prevalence of diarrhea in Pudong, Shanghai, China, 2014, by age and sex.

Table 2.

Prevalence of diarrhea and healthcare-seeking practices of respondents with diarrhea in Pudong, Shanghai, China, 2014

Variable Respondents who reported diarrhea (n = 231) Respondents with diarrhea who sought healthcare (n = 77)
No. Weighted monthly prevalence (%) (95% CI) P-value No. Weighted proportion (%) (95% CI) P-value
Sex 0·201 1
Male, n = 2653 125 4·6 (3·5–5·7) 42 21·0 (10·4–31·7)
Female, n = 2668 106 3·5 (2·5–4·5) 35 21·4 (10·0–32·9)
Age in years <0·001 <0·001
<1, n = 393 42 11·1 (7·7–14·6) 18 41·6 (25·6–57·5)
1, n = 458 31 6·4 (3·8–9·0) 14 46·1 (26·7–65·4)
2–4, n = 1346 37 2·7 (1·8–3·6) 21 57·6 (40·4–74·9)
5–24, n = 667 29 4·2 (2·5–5·8) 4 12·0 (0·1–23·9)
25–44, n = 1370 59 4·6 (3·3–5·9) 7 7·7 (1·4–14·0)
45–64, n = 818 18 2·5 (1·2–3·8) 8 44·6 (28·1–80·0)
⩾65, n = 272 15 5·4 (2·5–8·3) 5 45·0 (15·7–61·0)
Educational attainment1 0·371 <0·001
Primary school or illiterate, n = 2227 93 2·8 (1·6–4·1) 46 40·9 (19·8–62·0)
High school, n = 1216 47 4·1 (2·7–5·4) 11 32·3 (15·3–49·2)
College level and above, n = 1850 90 4·4 (3·3–5·5) 19 11·1 (4·2–18·1)
Average monthly household income, (Chinese yuan)2 0·075 0·277
<3000, n = 1123 49 4·1 (2·5–5·8) 21 41·0 (19·5–62·6)
3000–9999, n = 2632 111 4·0 (2·9–5·0) 31 15·4 (7·0–23·8)
10 000–19 999, n = 535 35 5·8 (2·8–8·9) 13 16·6 (0·9–32·3)
⩾20 000, n = 164 8 6·0 (0–11·9) 4 6·9 (0–17·1)
Don't know, n = 842 28 2·9 (1·3–4·4) 8 16·6 (0–35·3)
Travel history1 <0·001 0·091
Yes, n = 1057 70 4·9 (3·3–6·5) 17 7·2 (0·9–13·4)
No, n = 4186 156 3·8 (3·0–4·7) 57 25·3 (15·2–35·4)
Rotavirus vaccination3 0·113 0·382
Yes, n = 686 27 3·5 (2·1–5·0) 11 41·1 (21·1–61·1)
No, n = 1460 82 5·8 (4·4–7·1) 42 50·8 (39·0–62·7)
1

For children aged <5 years, the numbers in this column represent data for the children's parents or guardians.

2

1 US dollar ≈6·9 Chinese yuan.

3

History of rotavirus vaccination was collected only for children aged less than 5 years (n = 2146).

Seventy-seven of the respondents who had diarrhea reported seeking healthcare during their last episode of diarrhea. The proportion of respondents with diarrhea who sought healthcare was estimated to be 21·2% (95% CI: 13·4–29·0) in Pudong. The healthcare-seeking proportion varied among the age groups: children aged 2–4 years had the highest proportion (57·6%, 95% CI: 40·4–74·9), whereas people 25–44 years of age had the lowest (7·7%, 95% CI: 1·4–14·0) (Table 2).

Predictors of diarrhea occurrence

The factors affecting the occurrence of diarrhea are displayed in Table 3. Young age and travel history were significant predictors of frequent diarrhea occurrence in children less than 5 years old after adjusting for sex, average household income, education level of the children's parents/guardians and vaccination status. Rotavirus vaccination status exhibited no significant association with the occurrence of diarrhea among young children (adjusted odds ratio [aOR]: 0·8, 95% CI: 0·5–1·3). Among older children, adolescents and adults, travel history was a significant predictor of the frequent occurrence of diarrhea after adjusting for sex, age, average household income and educational attainment of the study subjects.

Table 3.

Multivariable logistic regression analysis of factors affecting the occurrence of diarrhea in Pudong, Shanghai, China, 2014, by age strata

Variable Children aged <5 years (n = 2198)
Adjusted odds ratio
(95% CI)
P value Variable Persons aged ⩾5 years (n = 3126)
Adjusted odds ratio
(95% CI)
P value
Gender Gender
Male 1·1(0·7–1·6) 0·912 Male 1·3(0·9–1·9) 0·137
Female Reference Female Reference
Age in years Age in years
<1 4·5(2·6–7·8) <0·001 5–24 Reference
1 2·6(1·5–4·6) <0·001 25–44 0·8(0·5–1·3) 0·386
2–4 Reference 45–64 0·4(0·2–0·8) 0·007
65+ 1·4(0·7–2·8) 0·340
Educational attainment1 Educational attainment
Primary school or illiterate Reference Primary school or illiterate Reference
High school 2·1(0·8–5·6) 0·245 High school 2·2(1·0–5·1) 0·062
College level and above 2·2(1·2–4·1) 0·017 College level and above 2·2(0·9–5·1) 0·072
Monthly average household income, (Chinese yuan)2 Monthly average household income, (Chinese yuan) b
<3000 Reference <3000 Reference
3000–9999 0·8(0·4–1·5) 0·288 3000–9999 0·9(0·5–1·6) 0·808
10,000–19,999 1·0(0·5–2·1) 0·745 10,000–19,999 1·4(0·7–2·9) 0·262
>20,000 0·7(0·2–2·8) 0·284 >20,000 1·4(0·4–4·9) 0·456
Don't know 0·6(0·3–1·3) 0·100 Don't know 0·6(0·3–1·3) 0·586
Travel history1 Travel history
Yes 2·0(1·2–3·3) <0·001 Yes 1·6(1·03–2·4) 0·036
No Reference No Reference
Rotavirus vaccine
Yes 0·8(0·5–1·3) 0·817
No Reference
1

For children aged <5 years, the numbers in this column represent data for the children’s parents or guardians.

2

1 US dollar ≈6·9 Chinese yuan.

Note: Estimates in bold are significant at P < 0·05.

DISCUSSION

This is the first population-based study of diarrhea conducted in Pudong. Over a period of 4 weeks in October 2014, 5324 community-based surveys were conducted to help determine the prevalence of diarrhea and the healthcare-seeking behavior of individuals who experienced diarrhea. We found that ≈4 in 100 persons reported having diarrhea in the previous month prior to the interview and that ≈1 in five individuals with diarrhea reported seeking healthcare during their most recent episode of diarrhea. The estimated incidence rate of diarrhea in Pudong was 0·54 episodes per person-year, which is very close to the 2010 national estimate of 0·56 episodes per person-year [5]. These findings confirm that the rate of diarrhea has not changed substantially over the past couple of years and that the burden of diarrhea experienced by the community and healthcare facilities is substantial in Pudong.

The pooled incidence of diarrhea in the world has changed little over the past four decades (from 2·2 episodes/child-year in 1980 to 2·9 episodes/child-year in 2010) [1215]. In our study, the overall monthly prevalence of diarrhea was 4·1% (95% CI: 3·3–4·8), which is similar to the 2010 national estimates for acute gastrointestinal illness (4·2%, 95% CI: 4·0–4·4) [5]. Based on this evidence, we believe that the prevalence of diarrhea in Pudong has not changed significantly during the past couple of years. However, we noticed that the estimated monthly prevalence of diarrhea was lower in our studied population than estimates reported for some other countries, e.g., Northern Ireland and the Republic of Ireland (4·5%) [16], England (6·5%) [17], and the USA (5·1%) [18]. These results should be interpreted with caution, however. The case definitions, study periods and study designs used in these studies were very different; thus, their results are not directly comparable to those of the present study. For example, Majowicz et al. noted that a different diarrhea case definition would have an impact of approximately 1·5–2·1 times on the observed incidence of diarrhea [19], and Cantwell et al. observed that studies with a short recall period had a higher incidence rate than those with a longer period [20]. Additionally, the study period also influences the estimated incidence of diarrhea in cross-sectional studies, as the occurrence of diarrhea exhibits substantial seasonal variations, with a peak during the winter months for most countries according to previous studies [5, 21, 22]. The differences between the estimates in our study and others may simply reflect the different approaches the researchers adopted to study the occurrence of diarrhea. More reliable estimates of incidence rates are needed in the future, especially rates obtained from prospectively conducted active-surveillance studies.

Young children represent the population group that is most vulnerable to diarrhea. The 2010 Global Burden of Disease Study estimated that half of the deaths caused by diarrhea (0·7 million deaths) were among young children [1, 4]. The estimated monthly prevalence of diarrhea was highest among children aged 0–11 months in our study (11%) and was slightly increased among people aged 25–44 years (4·6%). This age distribution pattern of diarrhea occurrence has also been observed in some other studies [4, 15] and can be explained by the high susceptibility of infants to infectious agents during the early ages of their life and by increased exposure to infectious agents among people aged 25–44 years as their social life becomes more active and diverse. Although other studies have reported that the lowest prevalence of diarrhea occurs among people aged ⩾65 years [18, 23, 24], this pattern was not observed in our study. As the sample size of study subjects who were ⩾65 years of age was slightly smaller (n = 272), our results relating to the elderly may be less representative than the results for other age groups. The occurrence of diarrhea reported by some other studies was higher among females than among males [5, 11, 23]. However, we did not observe a similar association in our study, which may be because most of the females in our survey were career women and only 10% of the females were housewives; thus, their risk of exposure to kitchen practices was not higher than that of men in Pudong. The association of education level with diarrhea in our study was also inconsistent with the findings of previous studies, which reported a high prevalence of diarrhea associated with low education levels [5]. We believe that this difference may be caused by our study's reliance on grandparents as interview surrogates to assess the child subjects. As most of the children's parents were at work during the day, the children in our study were cared for by their grandparents. Elderly people generally have low educational attainment, and people exhibit a larger recall bias as they age. Our results suggest that when conducting retrospective surveys involving young children, the children's mothers would be a better interview source to help minimize recall biases.

The proportion of individuals with diarrhea who reported seeking healthcare was 21% in our study. This number is much lower than the 2010 national estimate (56%) [5], but it is very similar to estimates reported by studies conducted in some other developed countries, e.g., the USA (19·5%) [18], Australia, Canada, and Ireland (19–20%) [23]. Healthcare-seeking practices were disproportionately affected in our study by the age of the respondents and were highest among children aged <5 years (42–58%). Higher levels of healthcare-seeking practices may represent a high level of severity and/or a high disease burden on healthcare facilities. Given the high rate of diarrhea occurrence and high level of healthcare practices among young children <5 years of age, control and prevention programs for diarrheal illness should be better targeted to this vulnerable group. In Pudong and in China, a common practice for controlling diarrhea, especially diarrhea caused by fatal cholera, is to conduct laboratory-based surveillance of diarrhea at gastrointestinal clinics. Pediatric departments/clinics are not covered by this practice, however. Since cholera cases have rarely been reported in China in recent years [25], we strongly suggest modifying national surveillance programs to include the pediatric population in future studies.

Young age [5, 11, 23] and travel [5, 26, 27] have been reported as risk factors for diarrhea in some previous studies. In our multivariable analysis, these factors were also significant predictors of diarrhea occurrence. Out-of-province travel in the previous month prior to the interviews was reported by 20·2% of the respondents. This implies that each month, one in every five people in Pudong are involved in intra-provincial travel. Traveler's diarrhea should be more comprehensively addressed in the future, especially for those who travel internationally.

Interestingly, approximately 32·0% of the study respondents reported a rotavirus vaccination history for their children. This proportion was close to the value (25%) reported by a previous study in 2012–2013 [28]. However, we did not find an association between rotavirus vaccination and the occurrence of diarrhea, although the monthly prevalence of diarrhea was lower among children with a history of rotavirus vaccination than among those with no reported vaccination history (3·5% vs. 5·8%, P = 0·113). We presume that some important factors that were not measured in our study (e.g., the predominance of etiological agents during the study period) could have confounded the results. Rotavirus vaccines have been demonstrated to be efficacious in preventing rotavirus gastroenteritis and in decreasing severe disease onset (hospitalizations) in previous studies [29, 30]. However, there is no evidence that the rotavirus vaccine can reduce the overall rate of diarrhea. Other etiologic agents, e.g., norovirus, non-typhoidal Salmonella, Shigella spp., and Campylobacter spp., could also cause diarrhea. To help identify public health priorities for diarrheal illness control and prevention in Pudong, the prevalence of specific pathogens in diarrhea patients should be assessed through laboratory-based surveillance in the future.

There are some limitations to our study. First, our respondents were recruited using a convenience sampling method. This approach was employed because the response rate for the household survey was very low in our pilot study, which could have potentially affected the validity of the study. To increase the response rate, we adopted a different approach that involved interviewing community residents who were readily available at different locations, such as children's vaccination clinics, kindergartens and residential areas, where most of the population in the community gathered. This approach may introduce bias because community residents who never leave their homes or who never visit these locations during day time could not be interviewed, and children who are more likely to seek healthcare at children's vaccination clinics would be oversampled even though the overall coverage rate of the clinics for children eligible for immunization was estimated at 99% in 2014 [31]. To help increase the representativeness of the study data, the surveys of children and adults were conducted separately and population weights were applied to adjust for the complex sampling procedures in the study. Second, our study was conducted in October in autumn. Since diarrheal diseases tend to peak during winter months in most countries, the calculated prevalence of diarrhea in our study might be underestimated. Third, recall bias was an important issue in our study; for example, ‘telescoping bias’ may have led to an overestimation of the frequency of diarrhea in our study. Fourth, we did not collect data on the proportion of diarrheal patients who submitted a stool sample for pathogen testing in the study, which would potentially hamper the allocation of resources to public health laboratories that conducted surveillance for diarrhea at Pudong. Finally, the travel history and educational attainment of child subjects <5 years of age were not collected; instead, we collected data for the individuals who responded on behalf of those children (parents/guardians). Whether the child subjects had travelled with their parents/guardians was not recorded in our study. However, our results confirm that the travel history of parents/guardians also has an effect on the occurrence of diarrhea among young children. Avoiding close contacts with young children or practicing better hygiene following recent travel could help prevent diarrhea in children.

CONCLUSIONS

In summary, the population in Pudong remains at frequent risk for diarrhea, and diarrhea continues to impose a considerable burden on the community and the healthcare system. Young children are the most vulnerable group, and diarrhea control and prevention programs, e.g., laboratory-based surveillance, should be modified to include this high-risk group.

ACKNOWLEDGEMENTS

We wish to thank the community health workers working in the 46 community health centers of Pudong for their enthusiasm and diligence in carrying out the interviews and the community respondents for their cooperation. This work was supported by the Ministry of Science and Technology of the People's Republic of China funded program, the National Key Science and Technology Project on Infectious Disease Surveillance Technique Platform of China [2012ZX10004201], and by the key discipline construction of health system project in Pudong New Area [No.PWzx2014-14].

ETHICAL STANDARDS

The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008. Ethical approval was obtained from Shanghai Pudong New Area Center for Disease Control and Prevention Review Board. Written and informed consent was obtained from all the participants or from the parents/guardians of child subjects before the interviews. The participants’ information was anonymized and de-identified prior to analysis.

DECLARATION OF INTEREST

None.

REFERENCES

  • 1.Lozano R, et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. The Lancet 2012; 380(9859): 2095–2128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Murray CJ, et al. Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010. The Lancet 2012; 380(9859): 2197–2223. [DOI] [PubMed] [Google Scholar]
  • 3.World Health Organization. The United Nations Fourth Millennium Development Goals (http://www.who.int/topics/millennium_development_goals/child_mortality/en/). Accessed 28 March 2017.
  • 4.Walker CL, et al. Global burden of childhood pneumonia and diarrhoea. The Lancet 2013; 381(9875): 1405–1416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Chen Y, et al. Burden of self-reported acute gastrointestinal illness in China: a population-based survey. BMC Public Health 2013; 13: 456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Chen S, Zhang J. Shanghai Pudong New Area Statistical Yearbook. China Statistics Press, Beijing, China. 2015, p. 321. [Google Scholar]
  • 7.Bresee J, Biritwum RB. Generic protocols for (i) hospital-based surveillance to estimate the burden of rotavirus gastroenteritis in children and (ii) a community-based survey on utilization of health care services for gastroenteritis in children. In: Document WHO/V&B/0215. Geneva: World Health Organization, 2002, pp. 45–67.
  • 8.Yu J, et al. Etiology of diarrhea among children under the age five in China: results from a five-year surveillance. Journal of Infection 2015; 71(1): 19–27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.R Core Team. A Language and Environment for Statistical Computing. Vienna, Austria: R Foundation for Statistical Computing, 2013. [Google Scholar]
  • 10.Lumley T. Complex Surveys: A Guide to Analysis using R. John Wiley & Sons, Hoboken, New Jersey. 2011. [Google Scholar]
  • 11.Thomas MK, et al. Population distribution and burden of acute gastrointestinal illness in British Columbia, Canada. BMC Public Health 2006; 6: 307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Snyder JD, Merson MH. The magnitude of the global problem of acute diarrhoeal disease: a review of active surveillance data. Bulletin of the World Health Organization 1982; 60(4): 605. [PMC free article] [PubMed] [Google Scholar]
  • 13.Bern C, et al. The magnitude of the global problem of diarrhoeal disease: a ten-year update. Bulletin of the World Health Organization 1992; 70(6): 705–714. [PMC free article] [PubMed] [Google Scholar]
  • 14.Kosek M, Bern C, Guerrant RL. The global burden of diarrhoeal disease, as estimated from studies published between 1992 and 2000. Bulletin of the World Health Organization 2003; 81(3): 197–204. [PMC free article] [PubMed] [Google Scholar]
  • 15.Fischer Walker CL, et al. Diarrhea incidence in low- and middle-income countries in 1990 and 2010: a systematic review. BMC Public Health 2012; 12: 220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Scallan E, et al. Acute gastroenteritis in northern Ireland and the Republic of Ireland: a telephone survey. Communicable Disease and Public Health/PHLS 2004; 7(1): 61–67. [PubMed] [Google Scholar]
  • 17.Wheeler JG, et al. Study 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. BMJ 1999; 318(7190): 1046–1050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Jones TF, et al. A population-based estimate of the substantial burden of diarrhoeal disease in the United States; FoodNet, 1996–2003. Epidemiology and Infection 2007; 135(2): 293–301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Majowicz S, et al. A common, symptom-based case definition for gastroenteritis. Epidemiology and Infection 2008; 136(7): 886–894. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Cantwell LB, et al. The effect of different recall periods on estimates of acute gastroenteritis in the United States, FoodNet Population Survey 2006–2007. Foodborne Pathogens and Disease 2010; 7(10): 1225–1228. [DOI] [PubMed] [Google Scholar]
  • 21.de Wit MA, et al. Sensor, a population-based cohort study on gastroenteritis in the Netherlands: incidence and etiology. American Journal of Epidemiology 2001; 154(7): 666–674. [DOI] [PubMed] [Google Scholar]
  • 22.Roy SL, Scallan E, Beach MJ. The rate of acute gastrointestinal illness in developed countries. Journal of Water and Health 2006; 4(Suppl. 2): 31–69. [DOI] [PubMed] [Google Scholar]
  • 23.Scallan E, et al. Prevalence of diarrhoea in the community in Australia, Canada, Ireland, and the United States. International Journal of Epidemiology 2005; 34(2): 454–460. [DOI] [PubMed] [Google Scholar]
  • 24.Tam CC, et al. The second study of infectious intestinal disease (IID2): increased rates of recurrent diarrhoea in individuals aged 65 years and above. BMC Public Health 2013; 13(1): 1–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Yang G, et al. Rapid health transition in China, 1990–2010: findings from the Global Burden of Disease Study 2010. The Lancet 2013; 381(9882): 1987–2015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Vrbova L, et al. A descriptive study of reportable gastrointestinal illnesses in Ontario, Canada, from 2007 to 2009. BMC Public Health 2012; 12: 970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Kuusi M, et al. Incidence of gastroenteritis in Norway – a population-based survey. Epidemiology and Infection 2003; 131(1): 591–597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Yi F, et al. Study on the prevalence and determinants of viral diarrhea among children aged under five years in Pudong New Area. Chinese Journal of Disease Control & Prevention 2014; 18(1): 44–47 (in Chinese). [Google Scholar]
  • 29.Vesikari T, et al. Safety and efficacy of a pentavalent human-bovine (WC3) reassortant rotavirus vaccine. New England Journal of Medicine 2006; 354(1): 23–33. [DOI] [PubMed] [Google Scholar]
  • 30.Ruiz-Palacios GM, et al. Safety and efficacy of an attenuated vaccine against severe rotavirus gastroenteritis. New England Journal of Medicine 2006; 354(1): 11–22. [DOI] [PubMed] [Google Scholar]
  • 31.Shanghai Municipal Commission of Health and Family Planning. The coverage rate of children immunization in shanghai (http://www.wsjsw.gov.cn/wsj/n429/n432/n1488/n1490/u1ai141465.html). Accessed 30 June 2017 (in Chinese).

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