Surveillance systems for neglected tropical diseases: global lessons from China’s evolving schistosomiasis reporting systems, 1949–2014
© Liang et al.; licensee BioMed Central Ltd. 2014
Received: 13 June 2014
Accepted: 7 November 2014
Published: 25 November 2014
Though it has been a focus of the country’s public health surveillance systems since the 1950s, schistosomiasis represents an ongoing public health challenge in China. Parallel, schistosomiasis-specific surveillance systems have been essential to China’s decades-long campaign to reduce the prevalence of the disease, and have contributed to the successful elimination in five of China’s twelve historically endemic provinces, and to the achievement of morbidity and transmission control in the other seven. More recently, an ambitious goal of achieving nation-wide transmission interruption by 2020 has been proposed. This paper details how schistosomiasis surveillance systems have been structured and restructured within China’s evolving public health system, and how parallel surveillance activities have provided an information system that has been integral to the characterization of, response to, and control of the disease. With the ongoing threat of re-emergence of schistosomiasis in areas previously considered to have achieved transmission control, a critical examination of China’s current surveillance capabilities is needed to direct future investments in health information systems and to enable improved coordination between systems in support of ongoing control. Lessons drawn from China’s experience are applied to the current global movement to reduce the burden of helminthiases, where surveillance capacity based on improved diagnostics is urgently needed.
Criteria for assigning county-level schistosomiasis transmission status
Human infection prevalence <5%
Bovine infection prevalence <5%
<10 acute cases over 2 week period in a village
Human infection prevalence <1%
Bovine infection prevalence <1%
No acute cases
No infected snails (O. hupensis) for two consecutive years
No human cases for five consecutive years
No bovine cases for five consecutive years
No snails (O. hupensis) for two consecutive years
No new infection in humans or bovines for five years after reaching transmission interruption
Summary of key characteristics of current schistosomiasis surveillance systems in China
1950s (1989 for schistosomiasis)
Individuals in hospitals
Nine sentinel villages
All villages in endemic counties
1% of villages in endemic provinces
Real-time, within 24 hours of patient diagnosis
All villages sampled over ~3 years, reporting occurs at completion of each village’s survey
Periodic every 6-9 years: 1989, 1995, 2004
Aid understanding of disease patterns; provide evidence for policy-making
Longitudinally and objectively monitor how the schistosome-endemic situation changes over time
Evaluate control measures
Clarify the endemic status of schistosomiasis as established by the previous national survey
Individual cases (demographics, patient residence, diagnosis, treatment and hospital)
Snail habitat, human infection prevalence and intensity, bovine infection prevalence
Snail habitat, human infection prevalence
Human infection prevalence and intensity, bovine infection prevalence, snail habitat
Clinical and laboratory
IHA screen then Kato-Katz and miracidium hatch
IHA screen then Kato-Katz
ELISA screen then Kato-Katz
2004: Replaced paper-based monthly or yearly reporting with internet-based real-time reporting system
2011: Added Miracidium Hatch Test to diagnostic procedure
2011: Replaced yearly reporting with internet-based parasitic disease reporting that occurs after completion of each village survey
2004: Inclusion criteria expanded to include areas with prevalence >0.5% from previous criterion of >1%
Inexpensive, Algorithms can be created to automatically detect outbreaks of emerging or reemerging disease
Provides longitudinal measures of disease prevalence and intensity
Provides greatest coverage since it samples all endemic villages in the province
Provides a nationwide estimate of schistosomiasis prevalence
Underreporting of chronic cases; potential underreporting of acute cases due to political pressure; potential information bias associated with variable clinical and diagnostic capacities of reporting sites; non-response bias associated with reporter fatigue
Sampling occurs at limited sites (20 in 1989, 80 in 2005); longitudinal follow-up over decades can yield non-response bias resulting from participation and reporter fatigue; potential selection bias associated with the choice of villages to sample longitudinally
Variable clinical and diagnostic capabilities can lead to information bias; potential selection bias associated with choice of survey sites, since those in charge of surveillance are also in charge of control efforts; potential reporting bias as funding can be tied to disease control success; potential non-response bias resulting from participation fatigue and temporary rural-to-urban migration
Occurs rarely and survey methods change, making it difficult to assess temporal patterns; only includes 1% of endemic villages in each province
Schistosomiasis, like many neglected tropical diseases and other human helminthiases in particular, presents several surveillance challenges. First, the disease is typically concentrated in low-income, rural areas where health infrastructure is limited. Second, the clinical presentation of the disease is rarely acute, and like many chronic diseases, long-term infections can evade clinical detection and eventually lead to severe health sequelae later in life. Thus reliance on passive hospital or clinic-based reporting can grossly underestimate the number of infections. China’s long history conducting schistosomiasis surveillance through multiple systems presents a unique opportunity to examine how their complementary structures, designs and sampling approaches—and their evolution over time—have provided essential epidemiological information to support the control of a neglected tropical disease.
The goal of this paper is to detail how China's schistosomiasis surveillance systems have been structured and restructured as part of China’s evolving public health system, yielding a combined information system that has been integral to the country's progress in reducing the burden of the disease. We discuss the diagnostic approaches underlying these systems, as well as additional tools necessary for cost-effective schistosomiasis surveillance in endemic settings that are approaching transmission control and elimination but face the threat of re-emergence. Finally, we discuss ways in which China’s experience with schistosomiasis surveillance can offer insights to other countries as they develop and strengthen their own infectious disease surveillance systems.
Diagnostic methods for detecting schistosomiasis infections in humans and animals
China’s schistosomiasis surveillance programs target three key hosts: humans, bovines and snails. Assays to detect schistosomiasis infections in human hosts are used to provide a direct measure of disease burden in the population, whereas surveys of bovines and snails (spatial distribution and infections) provide a means to evaluate the transmission potential of a given setting, and the particular role played by non-human reservoirs.
Detection of human infections
Detection of schistosomiasis infections in humans in China is typically accomplished by immunologic or coprologic assays. Immunologic assays commonly used in China include Schistosoma japonicum-specific immunoglobulin G standardized enzyme-linked immunosorbent assay (ELISA) and the indirect hemagglutination assay (IHA). Diagnostic immunological test kits have historically been subsidized by the national government, which has contributed to their widespread use. From a practical standpoint, immunologic methods are desirable as they require only a blood sample from a finger or ear-stick. Immunoassays generally have high sensitivity, but low specificity, due in part to the inability of the assay to distinguish between past and current infections. The immunological tests are generally used as a first-step screening method in large population surveys: those who test positive by immunoassay are then tested with a coprologic exam.
China relies on the Kato-Katz technique as the primary coprologic schistosomiasis diagnostic, following guidance of the World Health Organization. The method involves the microscopic examination of a stool sample smeared across three slides using a light microscope. Slides are examined by trained laboratory technicians who count Schistosoma eggs in standardized 41.7 mg smears and calculate eggs per gram (EPG) of the original sample, providing a widely accepted proxy measure of infection intensity. The assay lacks sensitivity in low infection-intensity regions[13, 14].
Another common coprologic assay is the miracidium hatch test, which detects the presence of viable schistosome eggs in stool by inducing miracidia to hatch in an aqueous solution. Typically performed in county-level anti-schistosomiasis stations, 30 g stool samples are strained through a 200 μm nylon mesh to concentrate schistosome eggs and remove small particles. The enmeshed material is then suspended in an aqueous solution, and placed in a lit, temperature-controlled environment where the sample is examined at two, five and eight hours for the presence of miracidia using low magnification.
Detection of bovine infections
Detection of S. japonicum in the bovine population serves as a complement to human surveillance, as bovines are a key non-human reservoir of S. japonicum in China. Thus detection of infections in bovines offers a means of monitoring the role of non-human hosts in introducing or sustaining transmission, particularly in agricultural settings where bovines are abundant. To test bovines for infection, a variant of the miracidium hatch test is used with modified observation times. Because the high water content of bovine stool can promote rapid hatching, the suspended sample is typically examined at shorter time intervals (one, two, and four hours) after preparation relative to the human exam.
Quantification of intermediate host densities and infections
Assessments of the density and infection status of the intermediate snail host Oncomelania hupensis have long played an important role in China’s surveillance for schistosomiasis. Snail density surveys consist of collecting and counting snails from historical or newly identified snail habitat. Specimens are drawn from a consistent kuang-sized (0.11 m2) sampling frame at random or equal interval points along streams, irrigation canals, fields, and lakes in endemic and some formerly endemic areas. The infection status of sampled specimens is determined by microscopic examination for the presence of cercariae. This method is limited in that it is only capable of detecting patent infections, and even in regions where human infection prevalence is high, the prevalence of S. japonicum infections in snails is very low (<<1%;), and thus screening of a large number of snail hosts is needed. In areas where human infection prevalence is low, infected snails are rare and a poor indicator of the presence of human infections.
Future diagnostic needs
As schistosomiasis infection prevalence declines in China, more sensitive diagnostic methods are needed. Recent diagnostic innovations include methods that detect S. japonicum DNA in human and bovine stool or serum, as well as in snails[17–19], but these assays have not yet been widely adopted. Such approaches offer potentially greater sensitivity than existing methods, particularly in areas where infection intensities are low, which is a key technological need for schistosomiasis elimination. Issues of cost, standardization, laboratory infrastructure and technical training remain to be addressed for this new class of molecular diagnostic techniques.
History of institutional support for schistosomiasis surveillance in China
In 1956, a massive nationwide schistosomiasis control campaign was launched, which bore the slogan "Schistosomiasis has to be eliminated" and was subsequently memorialized by Chairman Mao Zedong’s poem "Farewell to the God of Plague" in which he mourned the advance of the disease and championed its subsequent retreat[21, 22]. Medical school graduates were required to spend time in rural areas, both to provide care directly as village doctors, as well as to train local residents to serve as paramedics, or so-called barefoot doctors[23, 24]. At the same time, China established administrative and professional health organizations at varying levels of government to carry out both surveillance and control tasks aimed at eliminating specific diseases. These included an Office of Endemic Disease (OED) in each province, which designed and managed surveillance and control programs, as well as units targeting specific infections. For schistosomiasis, county-level anti-schistosomiasis stations were established under the supervision of OEDs and were responsible for carrying out surveys on humans and the snail intermediate host, control activities and health education. These stations established the necessary infrastructure and recording procedures for documenting infection and treatment statuses, disease progression of patients, and distribution and abundance of the intermediate host of the pathogen, and hence played a central role in the first standardized schistosomiasis surveillance activities.
In the late 1970s, reforms to China’s health systems led to the dismantling of the cooperative health system in place of a market-based system, and by 1985, barefoot doctors either became village doctors who worked on a fee-for-service basis, or they shifted to other professions. This substantial change in government policy led to a dramatic decline in primary health care coverage in rural areas. The restructuring of the public health system also involved the establishment of Epidemic Prevention Stations (EPS) at provincial, prefecture and county administrative levels, with a vertical structure for disease reporting and for the provision of technical guidance. Provincial, prefecture, and county EPS were financed by the health bureau at the same administrative level, resulting in little administrative control of higher-level EPS over lower-level institutions (although technical guidance did flow from higher- to lower-level units). Prefecture and county EPS primarily reported to their local health bureau instead of provincial EPS or the Ministry of Health. This structure would change dramatically with the most recent major overhaul of China’s heath systems at the turn of the 21st century[26, 27].
China’s evolving schistosomiasis surveillance systems
Surveillance was spotty and inconsistent in the years following the founding of People’s Republic of China, and not until 1989 did robust schistosomiasis surveillance programs emerge. A massive, national survey in 1989 confirmed endemic counties and assessed schistosomiasis prevalence status in 12 provinces based on human infections and an assessment of intermediate host habitat. Starting in 1992, additional schistosomiasis surveillance systems came online, including annual, locally administered surveys in endemic villages, as well as intensive national surveys to estimate the prevalence of schistosomiasis across provinces and in several high priority areas. In 2003, the SARS epidemic exposed key weaknesses in China’s ability to detect and manage infectious disease epidemics. In response, the Chinese government invested heavily in an enhanced National Infectious Disease Reporting system (NIDRS), which launched in 2004. The overhauled NIDRS was fully internet-based, and the number of reportable diseases was increased to reflect the country’s need for key surveillance data to support infectious disease prevention and control programs. At the same time, China’s entire public health system was being streamlined as described above, leading to the formation of China CDC.
Infectious diseases covered by mandatory NIDRS reporting
# of diseases
SARS§, HIV/AIDS, Viral hepatitis (A, B, C, E, other), Poliomyelitis§, Human avian influenza§, Measles, Epidemic hemorrhagic fever, Rabies, Epidemic Japanese encephalitis B, Dengue fever, Anthrax§, Tuberculosis, Dysentery (viral or amebic), Epidemic cerebrospinal meningitis, Typhoid and Paratyphoid, Pertussis, Diphtheria, Tetanus neonatorum, Scarlet fever, Brucellosis, Gonorrhea, Syphilis, Leptospirosis, Schistosomiasis, Malaria, H1N1 swine flu
Influenza, Mumps, Rubella, Acute hemorrhagic conjunctivitis, Leprosy, Typhus, Leishmaniasis, Echinococcosis, Filariasis, Infectious Diarrhea other than cholera, dysentery or typhoid and paratyphoid, Foot-and-mouth disease
In the following sections, we describe the purpose, sampling approach, and diagnostics used in each of the four schistosomiasis surveillance systems—routine surveys, national surveys, sentinel surveys and NIDRS—and we describe how each surveillance system was impacted by changes in China’s health systems following the SARS epidemic in 2004.
Routine schistosomiasis surveys involve periodic infection screening in every endemic village in the seven endemic provinces. Staff at county-level anti-schistosomiasis stations have historically conducted these screenings in collaboration with local village governments and hospitals. Routine surveys generate data used by the Ministry of Health to evaluate control measures, and provide information used by provincial-level schistosomiasis control steering committees to determine which counties have satisfied the official criteria for transmission control (Table 1). The primary outcomes and other characteristics of routine surveys are summarized in Table 2.
Changes since 2004
With the substantial increase in central government support for schistosomiasis control since 2004, local anti-schistosomiasis stations began receiving funding directly from the central government to carry out and improve routine surveys, and to implement interventions based on survey findings. Because anti-schistosomiasis stations are responsible for both surveillance and control, and the funding they receive from the national government is in part correlated to control success, reporting bias may be present in routine surveillance data. The national and provincial health bureaus set annual goals (e.g., prevalence reduction targets) for anti-schistosomiasis stations, which were folded into annual control performance reviews for the stations. To improve reliability of these surveys, a real-time, internet-based reporting system was established in 2011 to file, store and manage routine survey data, and quality control checks are routinely performed on these electronic records to detect and reduce reporting biases.
Routine surveys in a given endemic county are typically conducted over the course of two, three or more years depending on the level of endemicity in—and the control status of—the county. For counties that have achieved transmission control (Table 1), all villages are surveyed over a three-year period (i.e., one-third of villages in the county are surveyed each year). In counties that have achieved transmission interruption, all villages are surveyed over four- or five-year periods, and in counties that have yet to achieve transmission control, all villages are surveyed over two years. Villages are randomly selected and grouped into two (for counties not yet achieving transmission control), three (for counties achieving transmission control), or four or five (for counties achieving transmission interruption) subgroups. Each year, one subgroup of villages is surveyed, and this is repeated annually until all subgroups are surveyed. At that point, villages are randomly grouped into new subgroups, and the multi-year survey process is repeated. In villages that are part of the sentinel schistosomiasis surveillance system (see below), routine surveys are not conducted and the necessary information is shared from the sentinel system.
In a given village, routine surveillance involves intermediate host surveys in the spring followed by surveys of the human population in the fall, at the end of the transmission season. The target human sample is >90% of residents between the ages of 6 and 65 years old. Sampling of cattle and other alternative mammalian hosts are also included in routine survey efforts, but these are the responsibility of the local animal husbandry department and the degree of coordination between the veterinary and public health efforts is highly variable. All residents are requested to present themselves at a designated location for screening on the day of the survey. Villager participation in these surveys has been inconsistent. Residents may not feel ill and therefore may see no need to be tested for schistosomiasis. In endemic areas, surveys have been completed every year or every other year for >50 years, leading to participation fatigue. To overcome this challenge, health workers have conducted health education campaigns that emphasize the impacts of undetected, chronic infections, and the importance of routine schistosomiasis examinations. When residents are missed by a routine survey screening, public health workers will seek them out in their homes and request their participation.
Sampling and screening protocols for routine surveys are standardized by the Ministry of Health to improve consistency between counties and provinces, though variations have been noted. In Sichuan Province, for example, different diagnostics have been used between counties, some carrying out serologic exams only, some serologic followed by stool exams and some stool exams only. Thus, there are limitations when directly comparing routine survey data between counties.
Relationship to routine surveillance systems for other parasites and diseases
In China, routine surveys are unique to schistosomiasis, providing spatial and temporal data on infection patterns that are generally unavailable for other parasitic diseases. The surveys are very resource-intensive, and thus they have not been adopted, for instance, for soil-transmitted helminths (STHs). A sentinel STH system exists and resembles routine schistosomiasis surveys with less exhaustive sampling. The standardized training of county-level staff that carry out routine survey screenings—and the infrastructure developed to support them—have provided ongoing quantitative data on the distribution of cases at fine spatial scales. These data are unique to schistosomiasis, and have provided essential information to schistosomiasis reduction programs throughout China.
In 1989, China carried out the first national schistosomiasis survey with the purpose of estimating the prevalence of the disease in each endemic province. The resulting information served as an important baseline dataset for the World Bank loan for schistosomiasis control (see Introduction), and the 1989 data were subsequently compared with the 1995 national survey in an economic valuation of the loan-financed programs. National surveys are large, periodic cross-sectional studies that generate estimates of prevalence among humans and domestic animals across endemic settings. They are carried out every 6–9 years in China, and their primary outcomes and other characteristics are summarized in Table 2.
Changes since 2004
The most recent national schistosomiasis survey in 2004 included considerable technical improvements over previous surveys, such as an additional sampling stratum targeting low intensity infection areas; use of ultrasonography to screen a small number of subjects tested for schistosome-induced fibrosis; use of a subset of surveyed villages to assess the sensitivity of the Kato-Katz test as performed by Chinese technicians; and sampling to estimate snail density and snail infection prevalence in one county within each province. Importantly, the 2004 national survey included all formerly endemic areas that had achieved infection control and transmission control (see Table 1), whereas previous surveys focused on formerly endemic areas that had achieved infection control only. These and other changes to the national survey sampling design in 2004 provided important information as China oriented its control programs towards national elimination, but also generated survey results that were not directly comparable to the 1989 or 1995 surveys.
Because national surveys use standardized sampling methodologies, the results are comparable between provinces. What is more, the Ministry of Health uses the national surveys’ representative population sampling strategy to estimate prevalence across each endemic province while decreasing the required size of the sample. However, the sampled population, chosen in part based on historical prevalence, may not be representative.
Relationship to national surveys for other parasitic diseases
The Chinese government has historically carried out national surveys for other human parasitic diseases. Between 1988 and 1992, and again between 2001 and 2004, national surveys tested for 56 different parasites, including protozoa and helminths[28, 39], using a random sampling scheme and a set of diagnostics similar to the national schistosomiasis surveys. However, sampling for these national surveys was not informed by routine surveillance data. Thus, in the absence of recent prevalence data, socioeconomic factors—including variables such as sanitation access, income and literacy—were used to stratify the population for sampling.
Ad hoc provincial surveys following national survey protocols
As an example of how new surveillance capacity can follow on existing efforts, some provinces carry out provincial schistosomiasis sampling surveys borrowing sampling methodology from the 1989 and 1995 national surveys, but with the purpose of including a larger population within the province to boost sensitivity. Provincial OEDs design provincial survey sampling protocols, including human, bovine and intermediate host surveys, and surveys are carried out by anti-schistosomiasis stations in each county with the support of the EPS. Endemic villages from each county are sampled randomly within three categories based on infection prevalence and infection intensity determined from prior routine surveys, as follows. One third of endemic villages are randomly selected from each of three categories of infection prevalence based on results from routine surveys: less than five percent prevalence; between 5 and 15 percent; and >15 percent. In settings with low variability in infection prevalence between villages, sampling is based on infection intensities, with one third of villages sampled each from light, medium and heavy infection categories, again based on the results of recent routine surveys. In Sichuan’s provincial survey in 2001, for instance, 1,188 villages were sampled, involving >1,810,000 people ranging from age 5 to 65. The survey took six months to complete, from April to October, and all cattle were screened in each sampled village. For comparison, for the national surveys in Sichuan, >52,000 people from 39 villages, and >51,000 people from 40 villages, were surveyed respectively in 1989 and 1995. The more intensive sampling regimen of the provincial survey provided more detailed spatial coverage than the national survey.
National sentinel surveillance
The sentinel schistosomiasis surveillance system was initiated in 1989 with 20 sites in the seven endemic provinces, selected to represent different eco-epidemiological zones of transmission. The purpose of the sentinel system is to monitor longitudinal prevalence and infection intensity. Sentinel surveys consist of human and bovine infection screening—along with snail surveys—with the purpose of capturing temporal changes in prevalence and intensity of infection. For example, in Sichuan Province there are four counties enrolled in sentinel surveillance—Xichang, Dangling, Guanghan and Pujiang—where snail sampling takes place two times a year, in late spring and in fall, and human and animal surveys are conducted in the fall. Within each county, one village is selected each year where at least 90% of village residents over the age of six are sampled.
Changes since 2004
The sentinel system expanded in 2005 to include 80 sites across China, reflecting the Chinese government’s increased commitment and funding to schistosomiasis surveillance and control. In Sichuan Province, the number of sentinel sites increased from four to nine, and of these, six are in hilly regions, one is from a plateau region, and two are from mountainous areas. Hilly areas are represented with the most sentinel sites because infections in Sichuan are most common in these regions. The nine Sichuan sites have remained constant since 2005, and there is a commitment to continue longitudinal tracking of schistosomiasis infections in these sites regardless of their transmission trajectories in order to take maximum advantage of a consistent longitudinal dataset.
Diagnostic protocols for the sentinel system have changed to accommodate the changing transmission profiles of sentinel sites, particularly challenges in detecting low-intensity infections. As of 2011, for instance, sentinel sites in Sichuan Province test all those classified as positive using a serologic assay with both Kato-Katz and a miracidium hatch test. These multiple rounds of diagnoses, and a history of intensive surveillance generally in these historically endemic regions, have led to community-wide surveillance fatigue in some sentinel sites. Costs of implementing the ongoing sentinel surveillance are likely to increase as it becomes more challenging to achieve high levels of community participation, necessitating more intensive follow-up with residents and more sensitive diagnostic methods.
The number of sentinel sites sustained by the system is based on the level of funding provided by the central government, and provinces with higher prevalence and infection intensity are allotted more resources (and thus sites). To select sites, national and provincial level OEDs consider two factors: variation in infection intensity (sites are selected from communities with heavy, medium and light infections based on infection intensity measurements from prior routine surveillance); and eco-epidemiological zone (e.g., plateau, lake, hilly or mountainous regions). Sentinel system screening has been conducted by Kato-Katz since 1989, and the IHA test was added in 2000, with patients found positive by IHA confirmed with the Kato-Katz exam. If acute or advanced cases are found, epidemiological investigations are conducted to collect more detailed information about each case.
The overall design of the sentinel system was developed and approved by a national steering committee, yielding a system that is consistent among all surveillance sites, and making the data comparable between sites in all seven endemic provinces. It is sometimes necessary to move sites when implementing an intensive longitudinal surveillance system. For instance, after >10 years at one site in Sichuan, the population exhibited fatigue from yearly surveys and a new site was substituted to increase community participation. In one instance, as infection intensity and prevalence decreased dramatically across Sichuan Province, a very low prevalence sentinel site was replaced with a high prevalence site. Substituting sites interrupts the sentinel surveillance time-series, and data at new sites provide few insights into temporal trends until the series is allowed to accumulate over a number of years.
National infectious disease reporting system
The National infectious disease reporting system (NIDRS) was established in the 1950s, but it was not until 1989, with the passing of China’s Law on Preventing and Treating Infectious Diseases, that the reporting of selected infectious diseases was mandated by law. The NIDRS has historically involved a vertical reporting structure where hospitals reported the aggregated number of cases monthly by post to the county health department, who in turn report aggregate cases to the prefecture, then to the province, and finally to the central government. The information is used by Chinese public health officials to understand national patterns of infectious disease transmission, and to develop appropriate prevention and control programs.
Changes since 2004
Following the SARS outbreak, China’s Law on Preventing and Treating Infectious Diseases was revised, and the NIDRS was transformed into an internet-based, real-time system. The new system involves the routing of individual cases (rather than strictly aggregated data) up the hierarchy of public health institutions. The system provides for timely reporting of schistosomiasis cases to public health officials, allowing for rapid identification of, and response to, suspected re-emergence of the disease. The reporting of individual cases also enhances the spatial and temporal resolution of disease reporting, allowing for assessment of, for example, seasonal trends and persistent hot-spots of transmission.
Cases of schistosomiasis diagnosed in clinics or hospitals are reported directly to the NIDRS. Reporting includes both acute and chronic cases, however acute schistosomiasis contributes a disproportionate number of reported schistosomiasis cases. Acute schistosomiasis is a severe allergic reaction to the migrating schistosomule in the blood stream following infection and typically occurs only in naïve populations such as children or military personnel deployed to a new region. The rapid onset of severe symptoms typical of acute schistosomiasis is more likely to prompt health-seeking behavior, therefore resulting in more frequent capture by NIDRS. Because the symptoms of chronic S. japonicum infection are non-specific and often sub-clinical, chronic infections are poorly captured by clinic-based surveillance. Thus NIDRS schistosomiasis surveillance is considered key for identifying areas of disease emergence (or re-emergence), but not for assessing infection prevalence. What is more, diagnosis of a reported case is coded in the NIDRS as using either a clinical or a laboratory diagnostic, without further differentiation such as between stool and serologic exams. The primary outcomes and other characteristics of the NIDRS system are listed in Table 2.
Schistosomiasis diagnostic and clinical capabilities, and therefore reporting capacity, differ considerably across China, and the transition to the internet-based NIDRS revealed several limitations of surveillance capacity in China. The availability of computing resources and internet coverage required to connect directly to NIDRS varied within and between provinces, limiting the generation and transmission of electronic case reports. Hospitals that lack sufficient information technology resources were required to send paper forms to the county CDC for entry into the online system, introducing a reporting delay. A national initiative was launched to equip such hospitals with computer workstations and network coverage, resulting in the delivery of >4,000 computers to hospitals and clinics in Sichuan Province in 2005, for example. Other challenges were revealed relating to disparities in clinical resources. For instance, a disproportionate number of the cases of schistosomiasis present in NIDRS have been reported by county-level hospitals, in part because diagnostic capabilities are poorer at township-level hospitals, and diagnostic capabilities for parasitic diseases are sometimes entirely absent at private clinics and village healthcare centers.
Relationship to reporting systems for other diseases
At present, the NIDRS covers 39 infectious diseases in three classes based on their public health importance (Table 3;). The Class A list includes two diseases, cholera and plague, that are required to be reported within two hours of diagnosis. Pulmonary anthrax, SARS, poliomyelitis, and human infection with highly pathogenic avian influenza are in Class B, and are also required to be reported within two hours. Other Class B and Class C diseases must be reported within 24 hours of diagnosis. Class C diseases include newly identified diseases or diseases with emerging public health importance, including foot and mouth disease. Schistosomiasis was listed as a Class B nationally reportable infectious disease in 2004, in part to rapidly capture reports of acute cases that may signal an outbreak of infection.
Future directions in surveillance
Ideally, surveillance systems provide data that support evidence-based policy decisions and contribute to effective and efficient disease control[48, 49]. Additionally, effective surveillance systems must respond to advances in technology and changes in programmatic goals. While multiple, complementary systems can provide rich spatial and temporal information on the distribution of cases, resource constraints necessitate surveillance systems that minimize redundancies, particularly in low- and middle-income countries.
Key factors in the evolution of China’s schistosomiasis surveillance over the past six decades include the World Bank loan (and the rise in cases following its termination in 2001); changes in the epidemiology of schistosomiasis; changes in available technologies for diagnosis and treatment; and major public health events such as the 2003 SARS epidemic. The SARS epidemic in particular revealed weaknesses in China’s public health system with respect to the detection of, and prompt response to, disease outbreaks. Following the epidemic, the country’s infectious disease surveillance infrastructure underwent a massive overhaul, which included construction of new infectious disease facilities and laboratories that were crucial to improving the quality of surveillance data, as well as facilitation of improved data sharing and of more efficient coordination between public health agencies. The overhaul also included a complete redesign of the real-time infectious disease reporting system, as well as the Ministry of Health's listing of schistosomiasis among diseases such as HIV/AIDS, tuberculosis and hepatitis B as a high priority for control. This classification raised the profile of the disease among public health officials, increased the commitment of health care workers and government agencies to schistosomiasis elimination, and stimulated heightened surveillance and control efforts[43, 52].
Throughout these major transitions, China has made remarkable progress towards controlling schistosomiasis. The country’s evolving, parallel surveillance systems have each played a distinct role in characterizing the dynamic state of schistosomiasis transmission across diverse regions of the country. Thus far, the systems and the information they provide have been used independently; numerous reports, based on routine surveys, sentinel surveys and national surveys have been published and used to develop control strategies and monitor progress towards achieving elimination. More recently, there has been an effort to expand the use of these data beyond endemic disease control. Routine surveillance data, for instance, has been used to provide evidence of re-emerging schistosomiasis in Sichuan Province in areas that had previously achieved local control. Surveillance data from multiple systems can be fruitfully combined, as evidenced by integration of national and NIDRS surveillance data from all provinces to estimate the incidence, prevalence and disease burden of schistosomiasis, as well as malaria, hookworm and other water, sanitation, and hygiene-associated infections. The analysis revealed large regional disparities in the burden of these infections, particularly among children, who experience the greatest risk of water, sanitation and hygiene-attributable disease in China. In a separate study, combined national and NIDRS data were used to estimate the future burden of these infections under climate change. While this work demonstrates the value of China’s parallel surveillance systems, understanding of how data from these systems can be effectively combined, to characterize and inform the many dimensions of disease transmission and control, remains limited.
The overlapping nature of these systems, both spatially and temporally, provides a unique opportunity to explore how a country can maximize the value of multiple, distinctive information sources to inform public health campaigns and investments. This in an area where future research is needed both in China and elsewhere. Furthermore, as many provinces move towards schistosomiasis elimination and case detection becomes ever more challenging and expensive, it will be even more important to determine how the data, sampling approaches, and detection methods these systems provide can be used to optimize the performance of surveillance efforts. Successful schistosomiasis elimination will require the ability to efficiently and accurately identify the few remaining infected individuals and non-human reservoirs among large uninfected populations. This will be complicated by decreased diagnostic sensitivity owing to reduced infection intensity, testing fatigue among residents as a result of long-standing repeated examinations, and ever-increasing health care costs associated with diagnosis. To be successful, China’s surveillance system must be prepared to modify sampling methods, reporting approaches and diagnostics in response to new scientific and technological advances and changing schistosomiasis infection patterns. Recent attempts to establish diagnostic standards through the systematic evaluation of an array of immunological assays and new mobile reporting methods, discussed below, are a promising step in this direction. Further, as China's national disease burden continues its shift from infectious diseases to chronic, non-communicable diseases (NCDs), additional strain will be placed on surveillance personnel and institutions currently devoted to infectious disease, and opportunities for integrating the surveillance and care of NCDs and infectious diseases will be needed[56, 57]. Care must be taken to ensure that the resources are adequate and to avoid surveillance fatigue among healthcare workers and those in sentinel villages.
For China, research and innovations needed to succeed in continuing control and elimination of schistosomiasis include the development of diagnostic tools with higher sensitivity for the detection of human infections, and new ways of assessing human susceptibility to infection. In addition, effective ways to deploy recently developed tools for detecting the infectious stage of schistosomes (cercariae) in the natural environment[30, 58, 59] will be needed. Likewise, mobile disease reporting technologies (e.g. use of mobile phones or positioning systems with wireless capability for spatially explicit reporting of cases or vectors) show considerable promise and have been recently applied for surveillance of other neglected tropical diseases. These technologies have been used in field surveys of schistosomiasis endemic areas, to file reports of acute cases and infected snails into a centralized surveillance database, and to coordinate responses to disease outbreaks after the 2008 earthquake in Sichuan province[16, 61]. Yet effective integration of mobile technologies into large-scale surveillance procedures is still relatively new, and will need further evaluation. At the same time, new approaches will be needed to estimate the cost-effectiveness of the combination of existing surveillance systems in achieving specific surveillance endpoints, such as a characterization of spatial and temporal variability in cases. While considerable effort has been devoted to evaluating surveillance systems from a functional standpoint[62–66] —assessing timeliness, record accuracy[68, 69] and enhancing operational efficiency[70–72] —few analytical tools exist for quantitatively assessing how changes to design translate into improved (or inferior) estimates of the underlying rates of disease taking into account system sensitivity, coverage, bias and other factors. Development of such tools in China would provide a useful precedent as schistosomiasis surveillance is increasingly brought online in other countries.
Globally, there is a major movement underway to reduce the burden of helminthiases. The priorities for the global control and elimination of schistosomiasis, along with STHs, were articulated by the WHO in 2013. The surveillance needs of these global efforts are immense. Nearly 240 million people, most of whom live in sub-Saharan Africa, are estimated to require preventive chemotherapy for schistosomiasis alone as of 2009, yet coverage is reaching only 8% of those in need[74, 75]. While many factors contribute to this deficit, the lack of surveillance capabilities in nearly all schistosomiasis-endemic countries is a major obstacle to efficiently expanding coverage. Accurate, timely, country-level data are generally unavailable, and targeting drug delivery for schistosomiasis control in these settings is predominantly based on risk maps generated using ad-hoc epidemiological data (e.g., research data, historical drug delivery data, etc.), rather than surveillance. China’s history with surveillance of schistosomiasis can serve as a guide for countries, in sub-Saharan Africa and elsewhere, that require low-cost, simple surveillance and diagnostic technologies.
Given the current efforts to roll-out preventative chemotherapy, there will be a need to identify areas where disease burden is declining and mass-treatment efforts can be transitioned to targeted treatment and monitoring, as well as areas where disease burden is not declining, where more broad control efforts are needed. Throughout Africa, where over 90% of schistosomiasis cases occur, the capacity to conduct population-based surveys is limited, and current control recommendations do not include surveillance activities. There is some movement towards developing the infrastructure for parallel active surveillance systems—sentinel systems to track progress of control strategies coupled with regular provincial surveys—in highly endemic areas. China’s sentinel systems offer a model for deploying targeted surveillance resources and monitoring control progress over time. Similar to China’s provincial surveys, which borrow from standardized national survey protocols, province-level schistosomiasis mapping of all endemic districts has recently begun in a few countries (e.g. Ethiopia), and is rapidly scaling up for other neglected tropical diseases such as trachoma, with the benefit of funds provided by the UK Department for International Development and The Bill & Melinda Gates Foundation. These efforts are moving incrementally towards the electronic collection and reporting of epidemiological data, and may benefit from lessons learned during China’s 2011 adoption of a simple, internet-based system to file, store and manage routine survey data. Crucially, this system provides a model for electronic data collection even in the absence of a sophisticated NIDRS capacity. As many low-resource countries aspire for control and even elimination of schistosomiasis, understanding the synergy of parallel systems will prove cost-effective both by reducing unnecessary redundancy in data collection and in maximizing programming dollars. The systems described in China have distinct utility, but how these systems may be translated to other areas of schistosomiasis endemicity is not yet known and must be explored. Looking forward, targeted surveillance capacity is needed to understand and respond to the transmission consequences of rapid environmental, social, and technological changes, such as the construction of dams and changes in agricultural practices, that can result in an upsurge in schistosomiasis cases[54, 77, 80–82]. China’s sentinel system offers a model for deploying targeted surveillance capacity in regions undergoing such changes.
Optimal surveillance of schistosomiasis and other neglected tropical diseases must evolve with changing programmatic needs and technical advances. Currently, real-time electronic surveillance is limited by lack of broadband internet infrastructure in many rural schistosomiasis-endemic areas. However, mobile disease reporting technologies offer new opportunities in areas where traditional means of communication are limited, and may become increasingly relevant as attention turns to elimination. In the context of elimination, new diagnostic tools are urgently needed that offer rapid, sensitive, low-cost alternatives to current methods. China is currently dealing with this issue, and as other settings move towards achieving elimination, the traditional diagnostics that are currently relied upon by many surveillance systems will need to be replaced. Recently developed methods offer improved opportunities for point-of-care surveillance (e.g.,), and future investments will be needed to ensure advances like these are pursued and, ultimately, incorporated into surveillance practice.
The authors thank Margaret Bale, Meredith Stocks and Gwendolyn Parker for their input on early drafts of this manuscript. The authors acknowledge Philip Collender, whose input considerably strengthened the work. This work was supported in part by the National Institute for Allergy and Infectious Disease (grant no. K01AI091864), by the Chemical, Bioengineering, Environmental, and Transport Systems Division of the National Science Foundation under grant no. 1249250, by the Division of Earth Sciences of the National Science Foundation under grant no. 1360330, by the Emory Global Health Institute Faculty Distinction Fund, and by the Chinese Ministry of Health Key Project (grant no. 2009BAI78B00-06). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
- Schistosomiasis. [http://www.who.int/mediacentre/factsheets/fs115/en/index.html]
- Utzinger J, Zhou XN, Chen MG, Bergquist R: Conquering schistosomiasis in China: the long march. Acta Trop. 2005, 96 (2–3): 69-96.PubMedGoogle Scholar
- Zhou XN, Bergquist R, Leonardo L, Yang GJ, Yang K, Sudomo M, Olveda R: Schistosomiasis japonica control and research needs. Adv Parasitol. 2010, 72: 145-178.View ArticlePubMedGoogle Scholar
- Li S, Zheng H, Gao Q, Zhang L-J, Zhu R, Xu J, Guo J, Xiao N, Zhou XN: Endemic status of schistosomiasis in People’s Republic of China in 2012. Chinese Journal of Schistosomiasis Control. 2013, 25 (6): 557-563.PubMedGoogle Scholar
- Spear RC, Seto EY, Carlton EJ, Liang S, Remais JV, Zhong B, Qiu D: The challenge of effective surveillance in moving from low transmission to elimination of schistosomiasis in China. Int J Parasitol. 2011, 41 (12): 1243-1247. 10.1016/j.ijpara.2011.08.002PubMed CentralView ArticlePubMedGoogle Scholar
- Wang LD, Guo JG, Wu XH, Chen HG, Wang TP, Zhu SP, Zhang ZH, Steinmann P, Yang GJ, Wang SP, Wu ZD, Wang LY, Hao Y, Bergquist R, Utzinger J, Zhou XN: China's new strategy to block Schistosoma japonicum transmission: experiences and impact beyond schistosomiasis. Trop Med Int Health. 2009, 14 (12): 1475-1483. 10.1111/j.1365-3156.2009.02403.xView ArticlePubMedGoogle Scholar
- Liang S, Yang C, Zhong B, Qiu D: Re-emerging schistosomiasis in hilly and mountainous areas of Sichuan, China. Bull World Health Organ. 2006, 84 (2): 139-144. 10.2471/BLT.05.025031PubMed CentralView ArticlePubMedGoogle Scholar
- Xianyi C, Liying W, Jiming C, Xiaonong Z, Jiang Z, Jiagang G, Xiaohua W, Engels D, Minggang C: Schistosomiasis control in China: the impact of a 10-year World Bank Loan Project (1992–2001). Bull World Health Organ. 2005, 83 (1): 43-48.PubMed CentralPubMedGoogle Scholar
- Zhao GM, Zhao Q, Jiang QW, Chen XY, Wang LY, Yuan HC: Surveillance for schistosomiasis japonica in China from 2000 to 2003. Acta Trop. 2005, 96 (2–3): 288-295.View ArticlePubMedGoogle Scholar
- Zhou XN, Xu J, Chen HG, Wang TP, Huang XB, Lin DD, Wang QZ, Tang L, Guo JG, Wu XH, Feng T, Chen JX, Guo J, Chen SH, Li H, Wu ZD, Peeling RW: Tools to support policy decisions related to treatment strategies and surveillance of Schistosomiasis japonica towards elimination. PLoS Negl Trop Dis. 2011, 5 (12): e1408. 10.1371/journal.pntd.0001408PubMed CentralView ArticlePubMedGoogle Scholar
- WHO: Preventive chemotherapy in human helminthiasis. Coordinated use of anthelminthic drugs in control interventions: a manual for health professionals and program managers. Geneva: World Health Organization; 2006.Google Scholar
- Anderson RM, May RM: Infectious Diseases of Humans: Dynamics and Control. Oxford, New York: Oxford University Press; 1991.Google Scholar
- Lin DD, Liu JX, Liu YM, Hu F, Zhang YY, Xu JM, Li JY, Ji MJ, Bergquist R, Wu GL, Wu HW: Routine Kato-Katz technique underestimates the prevalence of Schistosoma japonicum: a case study in an endemic area of the People's Republic of China. Parasitol Int. 2008, 57 (3): 281-286. 10.1016/j.parint.2008.04.005View ArticlePubMedGoogle Scholar
- Carlton EJ, Bates MN, Zhong B, Seto EY, Spear RC: Evaluation of mammalian and intermediate host surveillance methods for detecting schistosomiasis reemergence in southwest China. PLoS Negl Trop Dis. 2011, 5 (3): e987. 10.1371/journal.pntd.0000987PubMed CentralView ArticlePubMedGoogle Scholar
- Department of Disease Control MoH: Handbook of Prevention and Cure of Schistosomiasis. 3rd edition. Shanghai: Press of Science and Technology, Shanghai; 2000.Google Scholar
- Spear RC, Seto E, Liang S, Birkner M, Hubbard A, Qiu D, Yang C, Zhong B, Xu F, Gu X, Davis GM: Factors influencing the transmission of Schistosoma japonicum in the mountains of Sichuan Province of China. Am J Trop Med Hyg. 2004, 70 (1): 48-56.PubMedGoogle Scholar
- Fung MS, Xiao N, Wang S, Carlton EJ: Field evaluation of a PCR test for Schistosoma japonicum egg detection in low-prevalence regions of China. AmJTrop Med Hyg. 2012, 87 (6): 1053-1058. 10.4269/ajtmh.2012.12-0177. 10.4269/ajtmh.2012.12-0177View ArticleGoogle Scholar
- Kumagai T, Furushima-Shimogawara R, Ohmae H, Wang TP, Lu S, Chen R, Wen L, Ohta N: Detection of early and single infections of Schistosoma japonicum in the intermediate host snail, Oncomelania hupensis, by PCR and loop-mediated isothermal amplification (LAMP) assay. AmJTrop Med Hyg. 2010, 83 (3): 542-548. 10.4269/ajtmh.2010.10-0016. 10.4269/ajtmh.2010.10-0016View ArticleGoogle Scholar
- Xia CM, Rong R, Lu ZX, Shi CJ, Xu J, Zhang HQ, Gong W, Luo W: Schistosoma japonicum: a PCR assay for the early detection and evaluation of treatment in a rabbit model. Exp Parasitol. 2009, 121 (2): 175-179. 10.1016/j.exppara.2008.10.017View ArticlePubMedGoogle Scholar
- WHO: Elimination of schistosomiasis from low-transmission areas: report of a WHO informal consultation. Geneva: World Health Organization; 2009.Google Scholar
- Berry-Caban C: Return of the God of plague: schistosomiasis in China. J Rural Trop Health. 2007, 6: 45-53.Google Scholar
- Gross M: Chasing Snails: Anti-Schistosomiasis Campaigns in the People’s Republic of China. San Diego: University of California; 2010.Google Scholar
- Hesketh T, Wei XZ: Health in China. From Mao to market reform. BMJ. 1997, 314 (7093): 1543-1545. 10.1136/bmj.314.7093.1543PubMed CentralView ArticlePubMedGoogle Scholar
- Shi L: Health care in China: a rural–urban comparison after the socioeconomic reforms. Bull World Health Organ. 1993, 71 (6): 723-736.PubMed CentralPubMedGoogle Scholar
- Zhang D, Unschuld PU: China's barefoot doctor: past, present, and future. Lancet. 2008, 372 (9653): 1865-1867. 10.1016/S0140-6736(08)61355-0View ArticlePubMedGoogle Scholar
- Liu Y: China's public health-care system: facing the challenges. Bull World Health Organ. 2004, 82 (7): 532-538.PubMed CentralPubMedGoogle Scholar
- Zhou XN, Chen JX, Chen MG, Bergquist R: The national institute of parasitic diseases, Chinese center for disease control and prevention: a new administrative structure for schistosomiasis control. Acta Trop. 2005, 96 (2–3): 296-302.View ArticlePubMedGoogle Scholar
- Zhou XN, Guo JG, Wu XH, Jiang QW, Zheng J, Dang H, Wang XH, Xu J, Zhu HQ, Wu GL, Li YS, Xu XJ, Chen HG, Wang TP, Zhu YC, Qiu DC, Dong XQ, Zhao GM, Zhang SJ, Zhao NQ, Xia G, Wang LY, Zhang SQ, Lin DD, Chen MG, Hao Y: Epidemiology of schistosomiasis in the People's Republic of China, 2004. Emerg Infect Dis. 2007, 13 (10): 1470-1476. 10.3201/eid1310.061423PubMed CentralView ArticlePubMedGoogle Scholar
- Chen M, Feng Z: Schistosomiasis control in China. Parasitol Int. 1999, 48 (1): 11-19. 10.1016/S1383-5769(99)00004-5View ArticleGoogle Scholar
- Driscoll AJ, Kyle JL, Remais J: Development of a novel PCR assay capable of detecting a single Schistosoma japonicum cercaria recovered from Oncomelania hupensis. Parasitology. 2005, 131 (Pt 4): 497-500.View ArticlePubMedGoogle Scholar
- Wang L, Wang Y, Jin S, Wu Z, Chin DP, Koplan JP, Wilson ME: Emergence and control of infectious diseases in China. Lancet. 2008, 372 (9649): 1598-1605. 10.1016/S0140-6736(08)61365-3View ArticlePubMedGoogle Scholar
- Kaufman JA: China's heath care system and avian influenza preparedness. J Infect Dis. 2008, 197 (Suppl 1): S7-S13.View ArticlePubMedGoogle Scholar
- McManus DP, Gray DJ, Ross AG, Williams GM, He HB, Li YS: Schistosomiasis research in the dongting lake region and its impact on local and national treatment and control in China. PLoS Negl Trop Dis. 2011, 5 (8): e1053. 10.1371/journal.pntd.0001053PubMed CentralView ArticlePubMedGoogle Scholar
- Ministry of Health State Council on the Forward Development Ministry of Finance, Ministry of Agriculture Ministry of Water Resource, Bureau of Forestation: National Guidelines for Mid- and Long-Term Plan for Prevention and Control of Schistosomiasis (2004–2015). Beijing: State Council on the Forward Development; 2004.Google Scholar
- ChinaCDC: China Information System for Diseases Control and Prevention. Shanghai: Institute of Parasitic Disease Control, China CDC; 2013.Google Scholar
- Qing-Wu J, Li-Ying W, Jia-Gang G, Ming-Gang C, Xiao-Nong Z, Engels D: Morbidity control of schistosomiasis in China. Acta Trop. 2002, 82 (2): 115-125. 10.1016/S0001-706X(02)00006-2View ArticlePubMedGoogle Scholar
- Li YS, Zhao ZY, Ellis M, McManus DP: Applications and outcomes of periodic epidemiological surveys for schistosomiasis and related economic evaluation in the People's Republic of China. Acta Trop. 2005, 96 (2–3): 266-275.View ArticlePubMedGoogle Scholar
- Li T, He S, Zhao H, Zhao G, Zhu XQ: Major trends in human parasitic diseases in China. Trends Parasitol. 2010, 26 (5): 264-270. 10.1016/j.pt.2010.02.007View ArticlePubMedGoogle Scholar
- Yu SH, Xu LQ, Jiang ZX, Xu SH, Han JJ, Zhu YG, Chang J, Lin JX, Xu FN: Nationwide survey of human parasite in China. Southeast Asian J Trop Med Public Health. 1994, 25 (1): 4-10.PubMedGoogle Scholar
- Xu LQ, Yu SH, Jiang ZX, Yang JL, Lai LQ, Zhang XJ, Zheng CQ: Soil-transmitted helminthiases: nationwide survey in China. Bull World Health Organ. 1995, 73 (4): 507-513.PubMed CentralPubMedGoogle Scholar
- Yang GH, Stroup DF, Thacker SB: National public health surveillance in China: implications for public health in China and the United States. Biomed Environ Sci. 1997, 10 (1): 1-13.PubMedGoogle Scholar
- Ross AG, Vickers D, Olds GR, Shah SM, McManus DP: Katayama syndrome. Lancet Infect Dis. 2007, 7 (3): 218-224. 10.1016/S1473-3099(07)70053-1View ArticlePubMedGoogle Scholar
- Li SZ, Luz A, Wang XH, Xu LL, Wang Q, Qian YJ, Wu XH, Guo JG, Xia G, Wang LY, Zhou XN: Schistosomiasis in China: acute infections during 2005–2008. Chin Med J (Engl). 2009, 122 (9): 1009-1014.Google Scholar
- Xiong W, Lv J, Li L: A survey of core and support activities of communicable disease surveillance systems at operating-level CDCs in China. BMC Public Health. 2010, 10: 704. 10.1186/1471-2458-10-704PubMed CentralView ArticlePubMedGoogle Scholar
- Yang WZ, Li ZJ, Lai SJ, Jin LM, Zhang HL, Ye CC, Zhao D, Sun Q, Lu W, Ma JQ, Wang JF, Lan YJ: [Preliminary application on China Infectious Diseases Automated-alert and Response System (CIDARS), between 2008 and 2010]. Zhonghua Liu Xing Bing Xue Za Zhi. 2011, 32 (5): 431-435.PubMedGoogle Scholar
- Liu Y: The Anatomy of China's Public Health System. China's Capacity to Manage Infectious Diseases: Global Implications. Edited by: Lu X, Freeman CWI. Center for Strategic & International Studies; 2009, 33-47.Google Scholar
- National People’s Congress: Prevention and Treatment of Infectious Diseases Law. Beijing: Standing Committee of the National People’s Congress; 2004.Google Scholar
- WHO: Monitoring the Building Blocks of Health Systems: A Handbook of Indicators and Their Measurement Strategies. Geneva: World Health Organization; 2010.Google Scholar
- Lee LM, Teutsch SM, Thacker SB, St. Louis ME: Principles & Practice of Public Health Surveillance. 3rd edition. Oxford: Oxford University Press; 2010.View ArticleGoogle Scholar
- China CDC, Ministry of Health: Protocol of National Schistosomiasis Surveillance. Beijing: Office of Endemic Disease Control, Ministry of Health; Institute of Parasitic Disease Control, China Center for Disease Control and Prevention; 2006.Google Scholar
- Feng Z, Li W, Varma JK: Gaps remain in China's ability to detect emerging infectious diseases despite advances since the onset of SARS and avian flu. Health Aff (Millwood). 2011, 30 (1): 127-135. 10.1377/hlthaff.2010.0606View ArticleGoogle Scholar
- Rollinson D, Knopp S, Levitz S, Stothard JR, Tchuem Tchuente LA, Garba A, Mohammed KA, Schur N, Person B, Colley DG, Utzinger J: Time to set the agenda for schistosomiasis elimination. Acta Trop. 2013, 128 (2): 423-440. 10.1016/j.actatropica.2012.04.013View ArticlePubMedGoogle Scholar
- Carlton EJ, Liang S, McDowell JZ, Li H, Luo W, Remais JV: Regional disparities in the burden of disease attributable to unsafe water and poor sanitation in China. Bull World Health Organ. 2012, 90 (8): 578-587. 10.2471/BLT.11.098343PubMed CentralView ArticlePubMedGoogle Scholar
- Hodges M, Belle J, Carlton E, Liang S, Li H, Luo W, Freeman M, Liu Y, Gao Y, Hess J, Remais JV: Delays reducing infectious diseases attributable to unsafe water and sanitation in China under climate change. Nat Clim Chang. 2014, published online doi:10.1038/NCLIMATE2428.Google Scholar
- Xu J, Peeling RW, Chen JX, Wu XH, Wu ZD, Wang SP, Feng T, Chen SH, Li H, Guo JG, Zhou XN: Evaluation of immunoassays for the diagnosis of Schistosoma japonicum infection using archived sera. PLoS Negl Trop Dis. 2011, 5 (1): e949. 10.1371/journal.pntd.0000949PubMed CentralView ArticlePubMedGoogle Scholar
- Remais JV, Zeng G, Li G, Tian L, Engelgau MM: Convergence of non-communicable and infectious diseases in low- and middle-income countries. Int J Epidemiol. 2013, 42 (1): 221-227. 10.1093/ije/dys135PubMed CentralView ArticlePubMedGoogle Scholar
- Gong P, Liang S, Carlton EJ, Jiang Q, Wu J, Wang L, Remais JV: Urbanisation and health in China. Lancet. 2012, 379 (9818): 843-852. 10.1016/S0140-6736(11)61878-3PubMed CentralView ArticlePubMedGoogle Scholar
- Worrell C, Xiao N, Vidal JE, Chen L, Zhong B, Remais J: Field detection of Schistosoma japonicum cercariae in environmental water samples by quantitative PCR. Appl Environ Microbiol. 2011, 77 (6): 2192-2195. 10.1128/AEM.01561-10PubMed CentralView ArticlePubMedGoogle Scholar
- Hung YW, Remais J: Quantitative detection of Schistosoma japonicum cercariae in water by real-time PCR. PLoS Negl Trop Dis. 2008, 2 (11): e337. 10.1371/journal.pntd.0000337PubMed CentralView ArticlePubMedGoogle Scholar
- International Trachoma Initiative. [http://trachoma.org/over-half-million-people-checked-trachoma-global-mapping-project]
- Yang C, Yang J, Luo X, Gong P: Use of mobile phones in an emergency reporting system for infectious disease surveillance after the Sichuan earthquake in China. Bull World Health Organ. 2009, 87 (8): 619-623. 10.2471/BLT.08.060905PubMed CentralView ArticlePubMedGoogle Scholar
- Buehler JW, Hopkins RS, Overhage JM, Sosin DM, Tong V: Framework for evaluating public health surveillance systems for early detection of outbreaks: recommendations from the CDC Working Group. MMWR Recomm Rep. 2004, 53 (RR-5): 1-11.PubMedGoogle Scholar
- WHO: Protocol for the Evaluation of Epidemiological Surveillance Systems. Geneva: WHO; 1997.Google Scholar
- Hendrikx P, Gay E, Chazel M, Moutou F, Danan C, Richomme C, Boue F, Souillard R, Gauchard F, Dufour B: OASIS: an assessment tool of epidemiological surveillance systems in animal health and food safety. Epidemiol Infect. 2011, 139 (10): 1486-1496. 10.1017/S0950268811000161View ArticlePubMedGoogle Scholar
- German RR, Lee LM, Horan JM, Milstein RL, Pertowski CA, Waller MN: Updated guidelines for evaluating public health surveillance systems: recommendations from the Guidelines Working Group. MMWR Recomm Rep. 2001, 50 (RR-13): 1-35. quiz CE31-37.PubMedGoogle Scholar
- Groseclose SL, German RR, Nsubuga P: Evaluating Public Health Surveillance. Principles and Practice of Public Health Surveillance. Edited by: Lee LM, Teutsch SM, Thacker SB, St. Louis ME. Oxford: Oxford University Press; 2010.Google Scholar
- Jajosky RA, Groseclose SL: Evaluation of reporting timeliness of public health surveillance systems for infectious diseases. BMC Public Health. 2004, 4: 29. 10.1186/1471-2458-4-29PubMed CentralView ArticlePubMedGoogle Scholar
- Mate KS, Bennett B, Mphatswe W, Barker P, Rollins N: Challenges for routine health system data management in a large public programme to prevent mother-to-child HIV transmission in South Africa. PLoS ONE. 2009, 4 (5): e5483. 10.1371/journal.pone.0005483PubMed CentralView ArticlePubMedGoogle Scholar
- Thiru K, Hassey A, Sullivan F: Systematic review of scope and quality of electronic patient record data in primary care. BMJ. 2003, 326 (7398): 1070. 10.1136/bmj.326.7398.1070PubMed CentralView ArticlePubMedGoogle Scholar
- Baker MG, Easther S, Wilson N: A surveillance sector review applied to infectious diseases at a country level. BMC Public Health. 2010, 10: 332. 10.1186/1471-2458-10-332PubMed CentralView ArticlePubMedGoogle Scholar
- Yoo HS, Park O, Park HK, Lee EG, Jeong EK, Lee JK, Cho SI: Timeliness of national notifiable diseases surveillance system in Korea: a cross-sectional study. BMC Public Health. 2009, 9: 93. 10.1186/1471-2458-9-93PubMed CentralView ArticlePubMedGoogle Scholar
- Reijn E, Swaan CM, Kretzschmar ME, van Steenbergen JE: Analysis of timeliness of infectious disease reporting in the Netherlands. BMC Public Health. 2011, 11: 409. 10.1186/1471-2458-11-409PubMed CentralView ArticlePubMedGoogle Scholar
- WHO: Sustaining the Drive to Overcome the Global Impact of Neglected Tropical Diseases: Second WHO Report on Neglected Diseases. Geneva: World Health Organization; 2013.Google Scholar
- WHO: Accelerating Work to Overcome the Global Impact of Neglected Tropical Disease: A Roadmap for Implementation. Geneva: World Health Organization; 2012.Google Scholar
- Hotez PJ, Engels D, Fenwick A, Savioli L: Africa is desperate for praziquantel. Lancet. 2010, 376 (9740): 496-498. 10.1016/S0140-6736(10)60879-3View ArticlePubMedGoogle Scholar
- Brooker S: Spatial epidemiology of human schistosomiasis in Africa: risk models, transmission dynamics and control. Trans R Soc Trop Med Hyg. 2007, 101 (1): 1-8. 10.1016/j.trstmh.2006.08.004PubMed CentralView ArticlePubMedGoogle Scholar
- Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J: Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect Dis. 2006, 6 (7): 411-425. 10.1016/S1473-3099(06)70521-7View ArticlePubMedGoogle Scholar
- Kolaczinski JH, Kabatereine NB, Onapa AW, Ndyomugyenyi R, Kakembo AS, Brooker S: Neglected tropical diseases in Uganda: the prospect and challenge of integrated control. Trends Parasitol. 2007, 23 (10): 485-493. 10.1016/j.pt.2007.08.007PubMed CentralView ArticlePubMedGoogle Scholar
- Smith JL, Haddad D, Polack S, Harding-Esch EM, Hooper PJ, Mabey DC, Solomon AW, Brooker S: Mapping the global distribution of trachoma: why an updated atlas is needed. PLoS Negl Trop Dis. 2011, 5 (6): e973. 10.1371/journal.pntd.0000973PubMed CentralView ArticlePubMedGoogle Scholar
- Jobin W: Dams and Disease: Ecological Design and Health Impacts of Large Dams, Canals, and Irrigation Systems. London: Routledge; 1999.View ArticleGoogle Scholar
- Keiser J, De Castro MC, Maltese MF, Bos R, Tanner M, Singer BH, Utzinger J: Effect of irrigation and large dams on the burden of malaria on a global and regional scale. Am J Trop Med Hyg. 2005, 72 (4): 392-406.PubMedGoogle Scholar
- Matthys B, Tschannen AB, Tian-Bi NT, Comoe H, Diabate S, Traore M, Vounatsou P, Raso G, Gosoniu L, Tanner M, Cissé G, N’Goran EK, Utzinger J: Risk factors for Schistosoma mansoni and hookworm in urban farming communities in western Cote d'Ivoire. Trop Med Int Health. 2007, 12 (6): 709-723. 10.1111/j.1365-3156.2007.01841.xView ArticlePubMedGoogle Scholar
- Dang H, Xu J, Li SZ, Cao ZG, Huang YX, Wu CG, Tu ZW, Zhou XN: Monitoring the transmission of Schistosoma japonicum in potential risk regions of China, 2008–2012. Int J Environ Res Public Health. 2014, 11 (2): 2278-2287. 10.3390/ijerph110202278PubMed CentralView ArticlePubMedGoogle Scholar
- Bergquist R, Johansen MV, Utzinger J: Diagnostic dilemmas in helminthology: what tools to use and when?. Trends Parasitol. 2009, 25 (4): 151-156. 10.1016/j.pt.2009.01.004View ArticlePubMedGoogle Scholar
- Shane HL, Verani JR, Abudho B, Montgomery SP, Blackstock AJ, Mwinzi PN, Butler SE, Karanja DM, Secor WE: Evaluation of urine CCA assays for detection of Schistosoma mansoni infection in Western Kenya. PLoS Negl Trop Dis. 2011, 5 (1): e951. 10.1371/journal.pntd.0000951PubMed CentralView ArticlePubMedGoogle Scholar
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