Abstract
Background
Schistosomiasis is one of the neglected tropical diseases (NTDs) selected for worldwide elimination in the near future. Egypt has made strong progress against its two endemic species of Schistosoma mansoni and S. haematobium. The former is prevalent in the Nile Delta with the latter dominating in the Nile south of Cairo. Innovative efforts are needed to reach the goal as further reduction of the prevalence has stalled due to ongoing transmission. In this study we aimed to explore the difference between low and high prevalence villages with regard to knowledge attitude and practice about schistosomiasis, utilization of health services, infection and transmission indices.
Methods
A hybrid cross-sectional longitudinal study was conducted with three annual follow-ups conducted during 1994–1996. We used a representative systematic random sampling technique investigating 993 individuals from the high prevalence village and 614 from the low prevalence village. Data were analyzed using SPSS, comparing proportions with the Chi square test and means with the Student t test, and ANOVA.
Results
Compliance of faecal sampling and chemotherapy was above 70% in both villages over the whole study period. Selective praziquantel treatment resulted in a significant reduction of prevalence and intensity of infection in both villages, dropping from 35.8% prevalence to 20.6%, in the low-prevalence village, and from 69.5 to 45.9% in the high-prevalence one. Intensity of infection at the base line was 30 eggs per gram (EPG) of stool in the low-prevalence village versus 105 EPG in the high-prevalence village. However, after the second round, reinfection rebounded by 22% in the high-prevalence village, while a slight improvement of the infection indices was demonstrated in the low-prevalence one. The level of knowledge was modest in both villages: people knew about self-protection and treatment, but not much about the role of human excreta for schistosomiasis transmission. While all participants maintained that using the water from the canals was inevitable, inhabitants in the high-prevalence village showed significantly lower scores reflecting higher water contact compared to the low-prevalence one. Many of them (67%) did not utilize the health centre at all compared to 26% of the people in the low-prevalence village. Interestingly, private clinics were seen as the primary source of health care by both villages, but more frequently so in the high-prevalence village (used by 87.2% of the inhabitants) compared to the low-prevalence one (59.8%).
Conclusions
Even if chemotherapy works well as reflected by the observed downregulation of intensity of infection in both villages, reinfection continued due to difficulties to avoid water contact. Efforts must be made to make people understand the role of human excreta for transmission. There is also a need to make people better trust the medical services available.
Keywords: Schistosomiasis, Transmission, Praziquantel, Knowledge attitude and practice, Utilization of health services, Poverty, Egypt
Background
The World Health Organization (WHO)'s roadmap for the global control of the neglected tropical diseases (NTDs) [1] encourages endemic countries to shift control activities of schistosomiasis towards elimination. With more than 800 million people in the world at risk and a third of them actually infected [2, 3], the prevalence of this disease is still alarmingly high in spite of larger amounts of the anthelmintic drug praziquantel (PZQ) distributed in the endemic areas than ever before [4]. The global burden of disease (GBD) study in 2010 [5] estimated 3.3 million disease-adjusted life years (DALYs) for schistosomiasis, while later updates [6] show sharply lower DALY scores down to 1.496 million in 2016. However, the true impact of schistosomiasis is much higher because of limitation of parasitological techniques to reveal light infection [7]. Indeed, molecular diagnostics indicate that the number of infections in an endemic area is considerably higher than that shown by egg-detection [8, 9].
Since the early 1980s the strategic approach to control schistosomiasis has been based almost exclusively on chemotherapy, often provided by mass drug administration (MDA), which has contributed to the decline of the DALY metric [6, 10]. However, despite the political support to maintain PZQ donations, genuine concerns have been raised regarding drug coverage as well as long-term sustainability [11, 12]. Although the excellent modality of PZQ that effectively controls disease morbidity [13–16], its negligent effect on disease transmission encumbers reaching the target of disease elimination. Increasing the dose and/or the number of doses and/or shifting to regular MDA cycles has not achieved interruption of transmission [10, 17, 18].
In the regional strategy for 2014–2020, issued by the WHO Regional Office for Africa (AFRO), it emphasizes the need for improved capacity of health systems, resource mobilization and financial sustainability of national NTD programmes in addition to enhancing monitoring, evaluation, surveillance and research [19]. Control of the aquatic snail intermediate host where and when transmission occurs should take precedence, and that means definition of water contact including acceptable management of sewage disposal, health education and improved water sanitation and hygiene (WASH) [20]. Indeed, several recent studies highlight the fact that knowledge and attitude about schistosomiasis remain insufficient and poor in many endemic areas [21–24]. Some people may assume that previous treatment prevents reinfection, which affects negatively water contact activity and compliance to repeated chemotherapy campaign In Zanzibar, as many as 75% of the children thought that there would be no risk of reinfection after treatment with PZQ [21]. Another study in northern Côte d’Ivoire and southern Mauritania, revealed that some people believed that schistosomiasis is caused by exposure to goat or dog urine in the environment, while others thought that the disease is transmitted by environmental elements such as sunshine and dirty water [25].
Adherence to MDA using PZQ is critical to the success of control strategies; overall, poor compliance is attributed to traditional, religious beliefs, poor acceptability of the drug, fear of side-effects and, above all, inadequate health education [26–29]. In the Philippines, PZQ coverage was only 43%, i.e. far below the WHO target of 75% [30]. Uncertainties on whether schistosomiasis can be treated, fear of praziquantel adverse reactions, misconceptions about alternative forms of treatment were all associated with higher odds of non-compliance [31]. Similarly, in Zanzibar, treatment compliance was only 50–60% [32].
Egypt has probably had the longest run of MDA with PZQ on the African continent, and it was claimed that that prevalence of Schistosoma mansoni in the Nile Delta has been reduced from 14.8% in 1993 to 2.7% in 2002 with a further decline to 1.5% in 2006 [33, 34]. However, this must have been an overestimation as the results represented pooled data and were carried out by stool examination using Kato-Katz standardized technique [35], which is known to miss light infections [9, 36]. Nevertheless, the Egyptian Ministry of Health and population (MoHP) upgraded the treatment strategy far beyond the WHO’s guidelines [14] aiming for interruption of transmission. However, transmission continued at an appreciable level in some foci [37, 38]. The MoHP is now planning to remap schistosomiasis in Egypt using a more sensitive diagnostic technique with the aim of identifying all areas of transmission where the elimination strategy should be applied. In 2018, a recent remapping survey using detection of the circulating cathodic antigen (CCA) from S. mansoni [39] was applied in the Nile Delta. This considerably more sensitive diagnostic tool detected S. mansoni infection in 31 districts out of 35 districts in the Nile Delta with prevalence ranging between 10 and 40% [40].
The role of primary health care is fundamental in sustaining a successful control strategy. Knowledge of the way people live in endemic communities and how they value and utilize the services provided by the primary health care facilities is crucial. At the 54th World Health Assembly (WHA54.19) in 2001, the planned minimum target for the year 2010 of PZQ coverage was given as 75% of all school-age children at risk, but the 65th Assembly meeting in 2012 (WHA65.21) noted that upon reaching that year, only 12.2% of people at risk benefitted from preventive chemotherapy [1]. Since then, however, the situation has improved and data for 2017 show that 44.9% of people requiring treatment for schistosomiasis globally were reached, while the proportion of school-aged children in this category amounted to 68% [41].
Few knowledge, attitude and practices (KAP) studies have been carried out in Egypt, and no studies looked at the peripheral health services. The main aim of the present study is to create community-based KAP portrays comparing a highly prevalent village to a low-prevalence community in the same region. In addition, we compared the healthcare service in the two villages and investigated the schistosomiasis transmission using multiple indicators not only limited to human infection, but also including malacological indices such as shedding and sentinel mice [42].
Material and methods
Study site and population
The data of the present study is part of the microlevel approach of Schistosomiasis Research Project (SRP) which was funded by the government of the USA and the MoHP aiming to improve control strategy of schistosomiasis [43]. Part of this project focused on the epidemiology of schistosomiasis using hybrid of cross-sectional prospective study designs, and included governorates in the Nile Delta, Nile Valley and new reclaimed areas [44].
Due to the the current, sometimes insecure situation, there was an unplanned, relatively long gap between the time of conducting the study and its finalization. However, this should not have caused any change of the level of transmission [40], the quality of peripheral healthcare services or the population education profile in the study area inrural Egypt.
This study was conducted in Kfer El-Sheikh Governorate, in the Northern part of the Nile Delta, Egypt (Fig. 1). Based on previous surveys in this region [45], two villages were selected: El-Rouse for high schistosomiasis prevalence and Ebiana for low.
El-Rouse is situated 1 km from the Rosetta branch of the River Nile and is a relatively new village built on reclaimed land. The village has only two schools; preparatory and mid-level. For water, the inhabitants depend on public taps in addition to canal water, but they lack a proper sanitary sewage disposal system. Most of the inhabitants are farmers producing mainly rice and vegetables. Ebiana is situated 20 km from El-Rouse and no more than 0.5 km from the Rosetta branch. This village is older and larger than El-Rouse and has a higher socioeconomic standard as well as an overall higher educational level. It has preparatory, mid- and high-level schools. There is a primitive sewage disposal system and most of the houses have access to clean water inside, however not always in adequate amounts, so some people depend partly on public tap water for domestic purposes. Farming is the main occupation also in this village and rice is the main crop. Each village has a peripheral health centre. From the health point of view, Ebiana is slightly better off than El-Rouse as it is just 1 km distant from Metobus City where there are multiple health care facilities including a governmental hospital and many private clinics.
Study design
During the period from 1994 through 1996, We conducted a cross-sectional longitudinal study including individuals ≥ 6 years old. A stratified random sample, comprising 25% of houses in El-Rouse and 10% houses in Ebiana, was selected. In Ebiana, the sample included 993 individuals in 123 houses; in El Rouse, the sample included 614 individuals in 66 houses.
The sample size calculation was mentioned in the first report [43], published in 1998, showing that the sample size was selected by multistage stratified random sample, was calculated to detect a prevalence of Schistosoma sp. as low as 5% with an 80% precision and 90% confidence level. In Ebiana, the sample was 10% of the whole population and in Elrouse was 25%.The field examination included three main arms: KAP, parasitology and malacology.
KAP study
The KAP questionnaire was designed by two specialists in health education and behavioural science, and the validity of the contents was confirmed by a panel of experts (Supp 1). Before the study, the questionnaire was piloted in the field to ensure face validity, while necessary modifications were implemented as necessary. Individuals ≥ 12 years old were interviewed by well-trained data collectors. Knowledge questions inquired about the disease, mode of transmission and preventive measures. This section included 13 questions with eight questions scored from 0 to 2 and 5 questions from 0 to 3. The maximum score was 31 with the total score levelled as: satisfactory (≥ 75% of the total), not quite satisfactory (74–50% of the total) and poor (< 50% of the total).
The attitude scale measured three domains including; perceived danger of canal water included seven items, perceived disease severity included three items, and perceived benefits of treatment included five items. In total, the scale comprised 15 items measured on a three point-Likert scale, i.e. agree; not certain; and don’t agree. The score ranged from 15 to 45, with higher scores indicating good attitudes. Water contact included six items scored from 1 to 3 (usually; sometimes; and never), The total score ranged from 6 to 18, where lower scores indicated more water contact. Experience of the study participants with regard to health services was investigated using questions that assessed the utilization of health services provided by the health center: four multiple option questions were designed to inquire about rating of the village health center as a source of care, place of latest stool analysis and treatment, and the principal source of health care. In addition, opinion of participants about the quality health services was investigated using 14 multiple options questions inquiring about physician’s performance, general proficiency of the health center, result of stool analysis, availability and cost of treatment, waiting and travel times.
Parasitological study
The standard Kato-Katz methodology [35] was used for stool examination. Stool samples were collected annually at the end of transmission season and at the same time from the houses. Diagnosis of S. mansoni infection was based on examination of two consecutives stool samples from each person utilizing two slides containing 41.7 mg from each sample [46]. Egg counts from the four slides of the two consecutive samples were averaged and the egg per gram of stool (EPG) was computed. The outcome was used to calculate the geometric mean EPG of stool (GMEC). All EPG values were transformed into log10 + 1 to allow for zero counts, and the GMEC was computed as the anti-log10 of the mean of the log10 egg counts. This approach was used because intensity of infection does not follow the Poisson distribution, which makes the GMEC preferable compared to the arithmetic mean. PZQ-selective chemotherapy 40 mg/kg was offered by the team each year. The prevalence of infection was determined at the base line with follow-up prevalence, incidence and reinfection rates determined annually comparing two consecutive years. Incidence was computed as the percentage of positives among those who had tested negative in the previous year whilst reinfection was determined for those who tested positive despite being treated on the previous year [47].
Malacological study
This part of the study focused on Biomphalaria alexandrina, the intermediate host of S. mansoni. Mapping of canals and drains in the two villages were performed to locate the transmission foci, i.e. hotspots, based on the density of infected snails and water contact activities. Only one snail survey per year was conducted in each village during the transmission season (May–December) at selected stations along a total length of 16.8 km of water courses in each village. Snails were collected with scoops using three dips from each station. At the central lab, the snails were identified with respect to species and examined for Schistosome Cercariae using the shedding technique [48]. In addition, sentinel mice experiments was conducted where a group of 10 white albino mice weighing 17–25 g were kept in water contact at the selected stations using floating cages with immersed bottoms for two hours between 10 AM and 2 PM. The mice were perfused eight weeks after exposure to determine the risk of infection at each station.
Statitical analysis
Data were analyzed using SPSS, version 21.0 (IBM, New York, NY, USA). Qualitative variables were described in percentages, while quantitative variables were described in means ± SD. Intensity of infection was expressed as GMEC. We used Pearson’s Chi square test to compare between proportions, and the independent student t-test or ANOVA as appropriate to test for difference between quantitative variables. All tests were two-sided, and P < 0.05 was considered statistically significant.
Results
The prevalence of S. mansoni was 35.8% at the baseline in Ebiana and nearly double that (69.5%) in El-Rouse. Additionally, the intensity of infection in El-Rouse was almost triple that found in Ebiana. Compliance was above 70% in both villages over the whole study period (Table 1).
Table 1.
Variable | Low prevalence village (Ebiana) |
High prevalence village (El-Rouse) |
---|---|---|
Households examined | 123 | 66 |
Population size examined | 993 | 614 |
Parasitological data at baseline (Round I) | ||
Compliance of stool samples% | 85.9 | 81.1 |
Prevalence% | 35.8 | 69.5 |
GMEC/EPG of infected people | 30.1 | 104.7 |
Parasitological data of First annual Follow-up (Round II) | ||
Compliance of stool samples% | 73 | 70 |
Prevalence% | 20.6 | 45.9 |
GMEC/ EPG of infected people | 20 | 41.7 |
Incidence% | 10.5 | 21.4 |
Reinfection% | 35.1 | 58 |
Parasitological data of second annual Follow-up (Round III) | ||
Compliance of stool samples% | 70 | 72 |
Prevalence% | 15.3 | 48.8 |
GMEC/ EPG of infected people | 20.9 | 41.7 |
Incidence% | 9.2 | 28.5 |
Reinfection% | 32.9 | 70.6 |
GMEC Geometric mean egg count, EPG Egg per gram of stool
Annual application of PZQ treatment for cases testing positive resulted in a significant reduction of prevalence and intensity of infection in both villages after the first intervention. However, while the prevalence fell faster in Ebiana than in El-Rouse, and continued to decrease there over the whole study period, the prevalence in the latter actually rebounded after the second round (Table 1). The force of transmission, as measured by incidence and reinfection, demonstrated a slight improvement in Ebiana, whilst reinfection increased from 58 to 70.6% and incidence shoot-up up from 21.4 to 28.4% in El-Rouse (Table 1). However, the intensity of infection remained very similar in both villages in the follow-up years after falling compared to the baseline, particularly in El-Rouse.
The trend of prevalence and incidence according to the participants’ ages shows that the prevalence peaked at the school-age level in both villages. Although no infection was detected among children younger than five years in Ebiana, ominously, more than quarter of the children of the same age were infected in El-Rouse. Incidence and reinfection data reveal that children below five were negative at the first annual follow-up in Ebiana, while more than one third of those of the same age category were re-infected, and one fifth were newly infected, in El-Rouse. Following PZQ chemotherapy, the first annual follow-up revealed an initial improvement followed by either stationary results, as shown in Ebiana, or deterioration, as shown in El-Rouse. This trend was similar among all age groups (Fig. 2).
The malacological and sentinel mice data are shown in Table 2. The number of transmission foci in El-Rouse exceeded that of Ebiana, i.e. in eight out of 14 stations, B. alexandrina snails tested positive for cercarial shedding in the former village compared to four out of 10 stations in the latter. Five of the eight infected test sites were drains in El-Rouse versus only one out of the four in Ebiana. The distribution of infected mice coincided with the foci harbouring infected snails. Furthermore, a longer canal area was infected in El-Rouse compared to Ebiana, where the transmission sites were closer to each other.
Table 2.
Ebiana Village (low prevalence) | ||
---|---|---|
Site No. & type | Frequency & (%) of infected snails | Frequency & % of infected mice |
1-Ca | 5.0 (2.9) | 0.0 (0) |
2-C | 4.0 (5.5) | 6.0 (20.6) |
3-C | 0.0 (0.0) | 0.0 (0.0) |
4-C | 0.0 (0.0) | 0.0 (0.0) |
5-Db | 2.0 (1.4) | 6.0 (53.8) |
6-D | 0.0 (0.0) | 0.0 (0.0) |
7-C | 0.0 (0.0) | 0.0 (0.0) |
8-C | 0.0 (0.0) | 0.0 (0.0) |
9-C | 2.0 (4.7) | 2.0 (10.0) |
10-C | 0.0 (0.0) | 0.0 (0.0) |
El-Rouse Village (high prevalence) | ||
1-C | 1.0 (6.0) | 4.0 (6.8) |
2-D | 0.0 (0.0) | 0.0 (0.0) |
3-D | 1.0 (0.15) | 0.0 (0.0) |
4-C | 0.0 (0.0) | 0.0 (0.0) |
5-C | 0.0 (0.0) | 1.0 (2.0) |
6-C | 0.0 (0.0) | 3.0 (12.0) |
7-C | 0.0 (0.0) | 1.0 (3.6) |
8-C | 3.0 (6.3) | 5.0 (26.4) |
9-C | 2.0 (1.7) | 5.0 (10.0) |
10-D | 2.0 (0.99) | 0.0 (0.0) |
11-D | 4.0 (0.12) | 2.0 (7.8) |
12-C | 0.0 (0.0) | 2.0 (12.3) |
13-C | 2.0 (0.32) | 1.0 (1.7) |
14-D | 1.0 (0.5) | 1.0 (3.4) |
aC: Canals
bD: drains
Results demonstrate different levels of general knowledge on schistosomiasis between the two villages. While both villages showed modest levels of knowledge (Ebiana: 16.17 ± 7.75 and El-Rouse: 12.83 ± 7.69) out of the maximum score of 31, the participants from Ebiana answered almost all questions referring to knowledge assessment more satisfactorily. Focusing on knowledge related to the individual, ways of self-protection and treatment were the most frequently correctly answered questions. Nevertheless, the role of human excreta and mode of transmission were the least correctly understood by all villagers (Table 3).
Table 3.
Knowledge Question | Knowledge level (Percentage) | |||||
---|---|---|---|---|---|---|
Poor | Unsatisfactory | Satisfactory | ||||
Ebiana | Elrouse | Ebiana | Elrouse | Ebiana | Elrouse | |
What is bilharziasis? | 27.7 | 46.0 | 15.6 | 9.6 | 56.7 | 44.4 |
Which organs are severely affected? | 8.6 | 13.0 | 21.0 | 26.6 | 60.4 | 60.4 |
How do people get infected? | 5.3 | 3.5 | 41.6 | 23.9 | 53.1 | 72.6 |
How does bilharzia infect via canal water? | 17.4 | 10.6 | 48.2 | 63.0 | 34.4 | 26.4 |
Which sources pollute the canal water? | 36.6 | 29.0 | 3.5 | 8.8 | 59.6 | 61.2 |
How does human excreta reach the canal? | 64.0 | 79.5 | 20.5 | 14.4 | 15.5 | 6.1 |
What, and where are snail habitat? | 40.5 | 55.1 | 1.8 | 0.2 | 57.7 | 44.7 |
What is the role of snails in the life cycle? | 58.9 | 68.9 | 2.8 | 2.6 | 38.3 | 28.5 |
How can one identify bilharziasis? | 21.8 | 33.8 | 31.3 | 28.5 | 47.0 | 37.7 |
What are the types of available treatment | 0.3 | 1.9 | 0.5 | 0.0 | 99.0 | 98.1 |
How can one be sure of cure after being treated? | 21.9 | 38.6 | 11.6 | 23.7 | 66.5 | 37.9 |
How can you protect water stream from Bilharzia? | 33.6 | 41.4 | 9.9 | 9.1 | 56.5 | 49.5 |
How can you protect yourself From Bilharzia? | 7.2 | 14.4 | 3.1 | 7.2 | 89.6 | 78.4 |
Overall Knowledge | 43.8 | 59.2 | 35.5 | 30.4 | 20.7 | 10.4 |
The total maximum score equaled 31: satisfactory (≥ 75%), Unsatisfactory (74–50%) and poor (< 50%)
The total knowledge score did not only significantly differ between the two villages, but varied also significantly according to age, gender, educational background and occupation. Poor knowledge was more prevalent among older age, females, lower educational levels, farmers and non-working groups (Table 4).
Table 4.
Variable | Ebiana N = 639 |
El-Rouse N = 377 |
---|---|---|
Mean ± SD | Mean ± SD | |
Age group | ||
12–19 | 16.37 ± 7.09 | 12.99 ± 7.69 |
20–29 | 18.65 ± 7.23 | 15.12 ± 7.63 |
30–39 | 16.14 ± 7.95 | 12.31 ± 7.39 |
40–49 | 15.07 ± 7.74 | 11.30 ± 7.27 |
50+ | 12.77 ± 7.00 | 9.63 ± 7.15 |
Statistics: F & (P value) | 9.80 (< 0.001) | 6.19 (< 0.001) |
Gender | ||
Male | 17.3 ± 7.75 | 16.06 ± 7.47 |
Female | 15.15 ± 7.62 | 10.12 ± 6.79 |
Statistics: t & (P value) | 12.59 (< 0.001) | 64.77 (< 0.001) |
Education | ||
Illiterate/read & write | 13.33 ± 6.89 | 10.96 ± 6.82 |
Primary | 15.66 ± 7.70 | 18.41 ± 7.01 |
Preparatory | 21.21 ± 6.49 | 22.10 ± 4.94 |
Secondary | 21.74 ± 5.4 | 21.44 ± 5.06 |
University | 25.56 ± 4.29 | 26.33 ± 3.22 |
Statistics: F & (P value) | 57.94 (< 0.001) | 31.69 (< 0.001) |
Occupation | ||
House wife | 13.36 ± 7.06 | 9.5 ± 6.42 |
Fishermen | 15.00 ± 0.0 | 15.18 ± 6.91 |
Farmers | 15.59 ± 6.19 | 13.66 ± 6.95 |
Not working | 15.83 ± 7.69 | 10.12 ± 7.09 |
Drivers | 16.22 ± 7.10 | 15.92 ± 8.71 |
Students | 18.8 ± 7.68 | 20.11 ± 6.43 |
Professionals | 23.12 ± 6.19 | 22.60 ± 4.22 |
Others | 15.36 ± 7.75 | 15.10 ± 7.14 |
Statistics: F & (P value) | 13.70 (< 0.001) | 16.27 (< 0.001) |
Total knowledge score (mean ± SD) | 16.17 ± 7.75 | 12.83 ± 7.69 |
Statistics: studentsttest, (P-value) | 8.73 (< 0.001) |
SD Standard deviation
The mean attitude scores regarding prevention and control of schistosomiasis as perceived by Ebiana and E-Rouse inhabitants is displayed in Table 5. Despite the favourable attitude reported by both villagers across all domains, the participants maintained that they could not avoid using canals even if public water taps and indoor water are available. Many reasons were reported, such as no water in the tap water for days on end, poor quality of tap water when available, crowding around public taps in addition to exposure to canal water as a natural occupational part of various activities. Ebiana’s inhabitants perceived the danger of water contact more profoundly than those in El-Rouse while the inhabitants of the latter village perceived the benefit and importance of treatment more positively than those living in Ebiana.
Table 5.
Attitude Scale | Ebiana N = 639 |
El-Rouse N = 377 |
t value |
---|---|---|---|
Perceived danger of using canals’ water | |||
Despite the presence of public tap water, people still use canals | 2.73 | 1.88 | 16.26* |
Despite having clean water indoors, people still use canals | 2.28 | 2.26 | 11.26* |
People claim that they are used to handle canal’s water, and they had never been infected | 2.55 | 2.57 | 0.39 |
Belief that just washing cloths and utensils in canals, doesn’t cause bilharziasis | 2.84 | 2.92 | 2.80* |
Belief that irrigating land bare-footed doesn’t cause bilharziasis | 2.83 | 2.95 | 4.55* |
Belief that swimming in canals once/twice doesn’t cause bilharziasis | 2.87 | 2.95 | 3.23* |
Belief that just washing hands, legs or ablution in canals doesn’t cause bilharziasis | 2.27 | 2.85 | 3.43* |
Subtotal score (out of 21) | 19.33 | 18.39 | 5.51 |
Perceived severity of bilharziasis | |||
Belief that bilharziasis is not a serious infection with potentially grave symptoms | 2.99 | 2.98 | 0.99 |
Belief that bilharziasis should not make you seriously worried | 2.84 | 2.92 | 2.48* |
Belief that bilharziasis does not seriously affect person’s work capacity | 2.95 | 2.96 | 0.52 |
Subtotal score (out of 9) | 8.78 | 8.86 | 1.87 |
Perceived benefits of treatment and avoiding canals’ water | |||
Belief that you would never be infected if you had never used canal water | 2.03 | 2.59 | 9.22 |
Belief that avoiding urination and defecation in streams will prevent bilharziasis | 2.81 | 2.88 | 1.95 |
Belief that medicine from the Health center can cure bilharziasis | 3.00 | 2.96 | 3.49* |
Belief that that repeated urine and stool examination is important | 2.97 | 2.99 | 1.54 |
Belief that there is no need for treatment because you are going to be infected again | 2.97 | 2.99 | 1.54 |
Subtotal score (out of 15) | 13.79 | 14.41 | 7.97* |
Overall mean total score ± SD(out of 45) | 41.89 ± 3.43 | 41.60 ± 2.83 | 1.1 |
*P < 0.005
SD Standard deviation
As for water contact practices, Ebiana’s inhabitants showed significantly higher scores reflecting less water contact compared to El-Rouse villagers. However, people seemed to use the canals for many different domestic and occupational purposes, i.e. to survive, farm, fish and wash (Table 6).
Table 6.
Water contact practicesc | Ebiana | El-Rouse | t value | ||
---|---|---|---|---|---|
No. | Mean ± SD | No. | Mean ± SD | ||
Farming | 814 | 2.59 ± 0.75 | 485 | 2.31 ± 0.86 | 5.89d |
Ablution/hand washing | 814 | 2.63 ± 0.69 | 485 | 2.41 ± 0.78 | 5.29d |
Swimming | 814 | 2.81 ± 0.50 | 485 | 2.55 ± 0.75 | 7.41d |
Washing clothsa | 424 | 2.80 ± 0.47 | 255 | 1.60 ± 0.85 | 23.69d |
Washing animalsb | 390 | 2.55 ± 0.64 | 230 | 2.32 ± 0.77 | 4.01d |
Bringing water from canals | 814 | 2.76 ± 0.54 | 485 | 1.70 ± 0.78 | 28.06d |
Fishing | 814 | 2.82 ± 0.44 | 485 | 2.78 ± 0.52 | 1.48 |
aAsked to females only
bAsked to males only
cLower scores indicate more water contact
dP < 0.005 SD: Standard deviation
Findings related to source of health care indicated clearly that the role of the health centre differed substantially between the two villages. In Ebiana, the village health centre was found to be the primary or secondary source of care more frequently (34.6 and 37.9%, respectively), while the corresponding figures were 7.6 and 23.5%, respectively, in El-Rouse. As many as 66.9% of the inhabitants in El-Rouse, compared to 26.3% in Ebiana, said that they never used the health centre. Private clinics were found to be the primary source of health care by the greater proportion at both villages, but more frequently at El-Rouse (87.2%) than at Ebiana (59.8%). Concerning analysis and treatment for schistosomiasis, it appears that the current project was the site of the last analysis and treatment for the greater proportion at Ebiana (78.5 and 54.8%, respectively) as well as El-Rouse (76.9 and 64.4% respectively) (Table 7).
Table 7.
Ebiana N = 818 |
El-Rouse N = 486 |
|
---|---|---|
Rating of health center as a source of health care | ||
Primary source | 283 (34.6) | 37 (7.6) |
Secondary source | 310 (37.9) | 114 (23.5) |
Not a source | 215 (26.3) | 325 (66.9) |
Never sought health care | 10 (1.2) | 10 (2.1) |
Primary source of health care | ||
Private clinic | 489 (59.8) | 424 (87.2) |
Health center | 283 (34.6) | 37 (7.6) |
MOPH hospitals | 24 (2.9) | 13 (2.7) |
Health insurance unit | 11(1.4) | 1 (0.2) |
Other sources | 11(1.3) | 11(2.3) |
Place of last stool analysis | N = 804 | N = 463 |
Project | 631(78.5) | 356 (76.9) |
Health center | 110(13.7) | 42(9.1) |
Private physician | 17(2.1) | 44(9.5) |
MOPH hospital | 19(2.4) | 8(1.7) |
Private laboratory | 15(1.9) | 4(0.9) |
School | 6(0.7) | 1(0.2) |
Other governmental facility | 6(0.7) | 8(1.7) |
Source of last treatment | N = 516 | N = 388 |
Project | 283 (54.8) | 250 (64.4) |
Health center | 119 (23.0) | 34 (8.8) |
Private physician | 9 (1.8) | 22 (5.7) |
MOPH hospital | 35 (6.8) | 27 (7.0) |
Pharmacy | 66 (12.8) | 48 (12.3) |
School | 0(0.0) | 1 (0.3) |
Other governmental facility | 4 (0.8) | 6 (1.5) |
Findings related to the opinion of respondents towards several aspects of the services available at the village health centres indicate a more favourable score at the lower-prevalence village Ebiana, which has a greater utilization of the health centre than El-Rouse. The difference was particularly marked in relation to opinion with respect to the physicians. Thus, 72.6–85% at Ebiana thought that the physicians there examine the patients professionally and treat them well in general as well as spend enough time with the patients, explains conditions and medications and are generally competent, while the corresponding figures ranged between 30.8 to 41.6% in El-Rouse (Table 8).
Table 8.
Ebiana N = 643 |
El-Rouse N = 377 |
|
---|---|---|
General handling of the patient by the physician | ||
Good | 551 (85.7) | 143 (37.9) |
Average | 48 (7.5) | 35 (9.3) |
Bad | 28 (4.4) | 167 (44.3) |
Don’t know | 16 (2.5) | 32 (8.5) |
Subjected to physical examination | ||
Yes | 475 (73.9) | 133 (35.3) |
Sometimes | 51 (7.9) | 48 (12.7) |
No | 89 (13.8) | 140 (37.1) |
Don’t know | 28 (4.4) | 56 (14.9) |
Time spent with patient by the physician | ||
Enough | 467 (72.6) | 116 (30.8) |
Sometimes enough | 15 (2.3) | 33 (8.8) |
Not enough | 109 (17.0) | 160 (42.4) |
Don’t know | 52 (8.1) | 68 (18.0) |
Patients given chance to explain condition and symptoms | ||
Yes | 543 (84.4) | 139 (36.9) |
Sometimes | 20 (3.1) | 43 (11.4) |
No | 50 (7.8) | 126 (33.4) |
Don’t know | 30 (4.7) | 69 (18.3) |
Condition and medications prescribed explained by the physician | ||
Yes | 530 (82.4) | 129 (34.2) |
Sometimes | 26 (4.0) | 41 (10.9) |
No | 60 (9.3) | 137 (36.3) |
Don’t know | 27 (4.2) | 70 (18.6) |
General proficiency of the health center | ||
Competent | 518 (80.6) | 157 (41.6) |
Average | 92 (14.3) | 162 (43.0) |
Don’t know | 33 (5.1) | 58 (15.4) |
Treatment in general | ||
Good | 508 (79.0) | 143 (37.9) |
Average | 53 (8.2) | 35 (9.3) |
makes me not want to seek treatment at health center | 61 (9.5) | 167 (44.3) |
Don’t know | 21 (3.3) | 32 (8.5) |
Results of analysis | ||
Mostly right | 403 (63.5) | 189 (50.3) |
Mostly wrong | 94 (14.8) | 85 (22.5) |
Sometimes wrong | 13 (2.1) | 3 (0.8) |
wrong if extra fees not paid | 31 (4.9) | 13 (3.4) |
Don’t know | 93(14.7) | 87 (23.0) |
Bilharzia tablets available | ||
Yes | 382 (60.2) | 158 (41.9) |
Sometimes | 124 (19.6) | 85 (23.7) |
No | 48 (7.6) | 37 (10.3) |
Don’t know | 80 (12.6) | 86 (24.0) |
Cost of diagnosis and treatment of Bilharziasis | ||
Reasonable | 568 (89.6) | 278 (73.7) |
A lot | 13 (2.1) | 34 (8.9) |
Don’t know | 53 (8.4) | 65 (17.3) |
Accessibility (among users of centers only) | N = 439 | N = 116 |
Travel time to the health center | ||
1–5 min | 231 (52.6) | 17 (14.7) |
6–10 min | 125 (28.5) | 21 (18.1) |
11–15 min | 62 (14.1) | 44 (37.9) |
16+ minutes | 21 (4.8) | 34 (29.3) |
Opinion about travel time to the health center | ||
Reasonable | 433 (98.6) | 92 (79.3) |
Too much | 6 (1.4) | 24 (20.7) |
Waiting time before seeing the physician at latest visit | ||
1–15 min | 332 (75.6) | 39 (33.6) |
16–30 min | 56 (12.7) | 22 (19.0) |
31–60 min | 31 (7.1) | 19 (16.4) |
61+ minutes | 11 (2.5) | 28 (24.1) |
Doctor did not arrive | 9 (2.1) | 8 (6.9) |
Opinion about waiting time at latest visit | ||
Reasonable | 433 (98.6) | 91 (78.4) |
Too much | 6 (1.4) | 25 (21.6) |
The health centres at both villages were felt to be reasonably accessible to their users, but the centre at Ebiana more so than in the neighbouring village. The travelling time was only 1–5 min for 52.6% of the users at Ebiana compared to 14.7% at El-Rouse, and it was rated reasonable by 98.6 and 79.3%, respectively. Waiting time in the centre to see a physician during the latest visit was rated as reasonable by 98.6% compared to 78.4% at Ebiana and El-Rouse, respectively. Waiting time did not exceed 15 min for 75% of the users at Ebiana versus 33.6% at El-Rouse, while it exceeded 1 hour at Ebiana for 2.5% compared to 24.1% at El-Rouse.
Discussion
Primary care healthcare centres maintain the NTD control strategies in the field on a day-to-day basis dispensing health education, diagnosis and treatment under the supervision of the MoHP. In order to visualize how this role functions in the periphery with regard to schistosomiasis, this is the first Egyptian study investigating the influence of knowledge and practises on the infection status over a 3-year period in two villages in Egypt’s Nile Delta, one of the remaining areas in the country endemic for S. mansoni. Despite the generally favourable attitude towards the health centres and their work reported by villagers across all domains, the participants felt that they could not completely avoid canal water contact. Although most villagers participating in the study had an understanding of the type of infections lurking in the canal water, they downplayed the risk. Local knowledge how schistosomiasis is transmitted and prevented and view of the healthcare services available are crucial to achieve the target of effective control. In accordance with our results, previous studies highlight the insufficient knowledge about schistosomiasis in the endemic areas [21, 22, 25]. Although people responding to the questions in the questionnaire had a good general understanding of the disease, most of them still lacked knowledge of specifics, such as the parasite’s life cycle and the high risk even of the slightest water contact. This leads to a false feeling of safety indicating that education needs to be strengthened. In addition, tap water provision must be improved encouraging people to abstain from other forms of water contact. This was underlined by the more favourable scores obtained at the low-prevalence village and its greater utilization of the health centre and more positive attitude towards the physicians there. Access and waiting time, which were more favourable at the low-prevalence village, might also play a role.
Lack of knowledge is the ultimate outcome of poverty and the attenuated role of the healthcare services. They both perpetuate the risk of reinfection and negatively affect treatment seeking. This clearly applies to sub-Saharan Africa, having the highest prevalence of schistosomiasis coupled with the lowest income per-capita [49], and to the situation in Yemen [38]. This is in contrast to developed countries which succeeded in eliminating this infection; for example, Japan [50] and modern-day China [51], which has made a remarkable progress towards elimination. Also, in the Middle East and North Africa (MENA) region, the economic transition in Saudi Arabia played an immense role in diseases elimination [38].
The malacological study, based both on cercarial shedding and sentinel mice showed the whereabouts of the hotspots and the level of transmission experienced in the two villages. The number of foci in the high-prevalence village exceeded that of the low-prevalence one, and many more places tested positive for cercarial shedding in the low-prevalence village compared the high-prevalence one, which was also reflected by the distribution of mice infection. In El-Rouse, most of the infected snail stations were drains, an observation clearly reflecting that this village lacks sewerage system and human excreta are just poured into drains — the same as in communities where poverty is rampant. Therefore, despite PZQ treatment for two successive rounds, infection indices shoot-up in the second round after the initial downregulation achieved in the first round. In contrast, the downward trend in infection indices in Ebiana continued till the end of the study. Therefore, despite the complex interrelation between the burden of schistosomiasis as one of the neglected tropical diseases and poverty, the disease could be eliminated simply by improved sanitation [49]. It is worth mentioning that both Ebiana and El-Rouse share the same geographic situation — being located at the end of the stream of the Rosetta branch of the Nile River, they both have the same farming practices where rice is the predominant crop, yet the two villages differ with respect to sewerage system and water supply as well as appreciation of health services.
Limitations of the study
Diagnosis of schistosomiasis was based on parasitological techniques using two consecutive samples instead of the ideal three consecutive samples. Thus, the infection indices are likely to be underestimated. Because rural communities in the Nile Delta share similar characteristics thus, we believe that our findings are generalizable to the entire rural population. However, further studies are required to update the available knowledge.
Conclusions
Application of PZQ chemotherapy resulted in a significant reduction of prevalence and intensity of infection in both villages but rebounded after the second round in the high-prevalence village. Nevertheless, transmission continues at an appreciable level in both villages. KAP data revealed an overall modest level of knowledge in both villages, but population knowledge was poor with regard to disease transmission, and the role of human excreta in contaminating water bodies. The high-prevalence village showed more water contact activities compared to the low-prevalence village. People in the high-prevalence village were considerably more negative about the health services offered than in the low prevalence village.
Supplementary information
Acknowledgments
The authors wish to thank the coordinators of Schistosomiasis Research Project – Professor Alan Fenwick, Dr. Taha Alkhoby, and Dr. Nabil Gala for facilitating all the logistics to conduct this study, their endless help and scientific support contributed evidently to achieve our goals.
Abbreviations
- AFRO
WHO Regional Office for Africa
- CCA
Circulating cathodic antigen
- DALYs
Disease-adjusted life years
- EPG
Egg Per Gram
- GBD
Global burden of disease
- GMEC
Geometric Mean Egg per gram
- KAP
Knowledge, attitude and practices
- MDA
Mass drug administration
- MENA
Middle East and North Africa
- MoHP
Ministry of Health and Population
- NTDs
Neglected tropical diseases
- OR
Odds Ratio
- POC-CCA
Point of care test based on the schistosome cathodic circulating antigen
- PZQ
Praziquantel
- SRP
Schistosomiasis Research Project
- USA
United States of America
- USAID
United State of America International Development
- WASH
Water Sanitation and Hygiene
- WHA
World Health Assembly
- WHO
World Health Organization
Authors’ contributions
Elmorshedy H and Barakat R conceived the research idea and supervised the conduction of the research. Eissa S supervised the field work. Guirguis WW was responsible about health services evaluation. Abdel-Gawwad ES supervised the KAP study, Fayed A participated in the data analysis, Bergquist R prepared the final draft. All authors reviewed and approved the final manuscript.
Authors information
Affiliations.
College of Medicine, Princess Nourah Bint Abdulrahman University, Riyadh Saudi Arabia.
High Institute of Public Health, Alexandria University, Alexandria, Egypt.
Professor Rashida Barakat (1941–2013) was a member of the WHO Expert Advisory Panel on Schistosomiasis from 2001 until 2013.
Professor Ensaf Said Abdel-Gawwad (1960–2017) was a former Professor of Health Education and Behavioral Sciences, High Institute of Public Health, Egypt and King Saud University, Saudi Arabia.
Funding
The Schistosomiasis Research Project (SRP) was conducted under the USAID and MoHP in Egypt. This study was funded by Deanship of Scientific Research at Princess Nourah Bint Abdulrahman University via fast-track research funding program, Riyadh, Saudi Arabia.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The research was approved by research ethical committee at High Institute of Public Health at Alexandria University and The Schistosomiasis Research Project. All participants submitted written informed consents and younger participants submitted their assents prior to participation in the study.
Consent for publication
Not applicable
Competing interests
The authors declare that they have no competing interests.
Footnotes
Ensaf Abdel-Gawwad and Rashida Barakat are deceased.
Supplementary information
Supplementary information accompanies this paper at 10.1186/s40249-020-00648-9.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.