DOI: https://doi.org/10.21203/rs.3.rs-154048/v1
Background
Schistosomiasis remains a major public health concern in sub-Saharan Africa. Although schistosomiasis is well documented in school-aged children in Burkina Faso, prevalence data among preschool-aged children (PSAC) are limited and outdated, and its risk factors in this group remain poorly documented. The main objective of this study was to assess the prevalence and risk factors associated with Schistosoma (S.) mansoni infection among PSAC from Panamasso village, western Burkina Faso.
Methodology
A cross-sectional study was carried out among 228 children under 6 years old from Panamasso village. Sociodemographic and water contact data were collected using a structured questionnaire. Kato-Katz and formol-ether concentration techniques were used to detect S. mansoni eggs in stool samples. Urine samples were subjected to a point-of-care circulating cathodic antigen (POC-CCA) cassette test and a centrifugation method to check for both S. mansoni and S. haematobium infection, respectively. Potential risk factors for S. mansoni infection were explored using multivariable logistic regression.
Results
The mean age of children was 40.2 ± 15.0 months. The prevalence of S. mansoni infection as determined by Kato-Katz, formol-ether concentration, and POC-CCA was 42.1%, 39.5% and 80.7%, respectively. Based on the combined results of the three methods, the overall prevalence of S. mansoni infection was 81.1%. No case of S. haematobium infection was found. The geometric mean intensity of S. mansoni infection was 107.2 eggs per gram of faeces with 54.2%, 33.3%, and 12.5% of the children having light, moderate, and heavy infections, respectively. Girls (AOR = 2.9, 95% CI: 1.3-6.1), a household located within 500 m from the pond (AOR = 3.0, 95% CI: 1.0-8.6), or between 500 and 1000 m from the pond (AOR = 3.0, 95% CI: 1.2-7.2), and child’s history of going to the pond (AOR = 5.0, 95% CI: 1.7-14.3) were the variables significantly associated with S. mansoni infection.
Conclusion
S. mansoni was the sole species infecting a high proportion of PSAC in the study area. A mass drug administration program with praziquantel is therefore urgently required for those below 6 year-old. Other control strategies should include increased community-awareness and provision of safe water.
Schistosomiasis is a major public health concern in sub-Saharan Africa (SSA) with around a third of the annual 192 million cases of schistosomiasis caused by S. mansoni, the causative agent of intestinal schistosomiasis (1). About 4.4 million people infected with S. mansoni suffer from bloody diarrhea, while 8.5 million people have hepatomegaly associated with periportal fibrosis, portal hypertension and hematemesis (2,3). In addition, it is estimated that each year 130,000 deaths occur due to complications of the disease (4,5). In school-aged children (SAC) (i.e. 6-15 years), chronic infections with S. mansoni cause anemia, growth retardation and cognitive impairment (5). The main morbidities due to S. mansoni infection in preschool-aged children (PSAC) i.e. under 6 years, are anemia, hepatosplenomegaly, and hepatic fibrosis with a higher risk in PSAC of age group 37-60 months (6).
PSAC have been considered as a low risk group for S. mansoni infection (7,8), and are therefore so far excluded from various schistosomiasis control programs in Africa, resulting in a health inequity in affected people (9). Although several studies have reported prevalences of S. mansoni infection ranging from 0.9 to 86% in PSAC (6,10–19), the risk factors associated with this parasite infection remain poorly studied (11,12,14,16,20).
In Burkina Faso, S. mansoni infection was endemic in the western and southern areas of the country with a focal distribution before the implementation of the national schistosomiasis control program (NSCP) in 2004 (21). The program mainly focused on mass drug administration (MDA) with praziquantel in SAC with a coverage rate over 90% (22). In 2010, the prevalence of S. mansoni infection among SAC ranged from 3.3 to 39.1% with the highest prevalence (39.1%) recorded in Panamasso village (23). In this village, the prevalence in SAC was 26.2% after many years of MDA with praziquantel in 2013(24).
The abundant literature on schistosomiasis-infections among SAC in Burkina Faso contrast with scarce and outdated data in the PSAC-group (25). In addition, risk factors associated with S. mansoni infection are so far unknown. This study sought to fill this knowledge gap with the goal of including these children into MDA program with praziquantel.
Study design, area and population
A community based cross-sectional study was carried out in PSAC living in Panamasso, from February to March 2020. Panamasso is a village located in Dafra District at 30 kms from Bobo-Dioulasso, the second largest city of Burkina Faso, at 11°23'0'' North and 4°12'0'' West. This locality is located on the edge of one of the tributaries of the Mouhoun River. It is an area with high humidity from May to October and sheltering a pond, thus providing an environment suitable for growing of intermediate snail hosts of S. mansoni i.e. Biomphalaria pfeifferi (21). Panamasso had 600 households with 4,403 inhabitants in 2019. The pond is the main source of water for domestic activities (drinking, cooking, washing, bathing, and recreation) despite well-functioning water supplies. This village is the only sentinel site of the NSCP to record in 2013 and in 2016 high prevalence of S. mansoni infection in SAC with respective values of 39.1% and 26.2 % (23,24). PSAC who were under the age of six years old were the source population. PSAC who had been living in Panamasso for at least 6 months before the study began, whose parents/guardians provided written informed consent, and who had no history of having been treated with praziquantel and anti-helminthic drug in the past 6 months were included. Children who did not provide any stool sample during the survey were not included.
Sample size and sampling technique
Sample size was calculed upon a S. mansoni infection prevalence of 26.2 % previoulsy reported in SAC from Panamasso (24), a relative precision of 8 %, for alpha = 0.05, and using design effect of two. It was estimated to 230 participants accounting for 10% of parent’s refusal. A multiple-stage sampling procedure was used to randomly select 300 households from a list of the total households of the study village, then all eligible PSAC were included up to the sample size was reached.
Field data collection
A community information meeting was organized by the research team before the beginning of study. Then, an individual structured questionnaire was administered to the PSAC’s parents or guardians after having obtained their informed consent. Thereafter, sociodemographic data of the PSAC and their parents’ sociodemographic data and level of knowledge about schistosomiasis, and water contact data were collected. Water contact was assessed by inquiring on child’s history of going to the pond, child’s habit of swimming in the pond, frequency swimming habit of child in the pond per week (i.e. the reported number of days in the week that the child had been to the pond), and period of swimming in the pond.
Sample collection and laboratory procedures
Single stool and urine samples were collected in separate clean containers from each PSAC and processed at the Laboratory of Parasitology of Centre MURAZ.
Kato-Katz technique
One Kato-Katz thick smear was prepared from each stool sample using a template holding
41.7 mg of stool sample (26). The slides were left for 24 hours to clear for easy visualization of S. mansoni eggs before being examined. Infection intensity of S. mansoni was estimated by multiplying the total number of eggs counted by 24, which was given as the eggs per gram (epg) of faeces and classified as light, moderate and heavy per the threshold set by the World health organization (27). Two independent lab technicians examined each slide and any resulting discrepancies were resolved by the senior parasitologist. As a quality control check, 20% of all positive and negative slides were randomly chosen and re-read by the senior parasitologist in order to confirm positive or negative results.
Formol ether concentration technique (FEC)
After having diluted a small amount of stool (about 2 g) in 7 mL of 10% salt formalin solution (mixture of 100 mL of pure formalin, 900 mL of distilled water and 8.5 g of sodium), the mixture was sieved in a centrifuge tube to remove large debris and 3 mL of ether was added thereto. The mixture was stirred vigorously for 30 seconds and centrifuged at 2,000 rpm for 2 minutes. Then, the supernatant was discarded and the pellet was plated, using a pipette, between slide and coverslip with lugol and read on 10x and 40x objectives (28).
Qualitative examination for S. mansoni circulating cathodic Antigens(CCA)
All urine samples were tested for S. mansoni CCA using a commercially available point-of-care (POC-CCA) cassette test (Batch numbers 191031120, ICT INTERNATIONAL, Noordhoek, South Africa) performed at room temperature according to the manufacturer’s instructions on the day of the sample collection. Briefly, two drops of urine were added to the well of the testing cassette and allowed to absorb. The test results were read visually 20 minutes later. In cases when the control bands did not develop, the test was considered as invalid. Invalid tests were repeated using the same urine sample. Valid tests were scored as negative or positive. Trace (weak band) was also considered as positive (29). All the tests were read independently by two lab technicians, and in case of discordant results, the senior parasitologist examined it until an agreement was reached.
Urine centrifugation method
Briefly, 10 mL urine were centrifuged at 5,000 rpm for 5 minutes. Then, the supernatant was discarded and the pellet was plated, using a pipette, between slide and coverslip with lugol and read on 10x and 40x objectives. This method was used to check for S. haematobium infection.
Ethical considerations
This study was approved by the institutional ethical committee from Centre MURAZ (ref 2019-66/MS/SG/INSP/DG/CEI). Following an explanation of the purpose, the benefits and the possible risks of the study, written consent was obtained from PSAC’ parents/guardians. Children who were positive for S. mansoni were treated free of charge with praziquantel. All the information obtained from the PSAC and their parents was treated as private and confidential and the records were stored in a locked cabinet.
Data analysis
Data were double entered using Microsoft Excel 2013, then cleaned and analyzed with Stata 12 software (Stata Corp., College Station, Texas, USA).
S. mansoni infection was defined as any positive test result irrespective of the laboratory methods used. Pearson's chi-square test or Fisher's exact test was used to compare proportions between groups. Geometric means of intensity infection (GMI) and their 95% confidence intervals (95% CI) were estimated. Log-transformed means eggs count were compared between groups using parametric tests (Student or ANOVA) or nonparametric tests (Wilcoxon or Kruskal-Wallis), where appropriate. The Bonferroni test was used when the ANOVA test was statistically significant.
Potential risk factors for S. mansoni infection were screened through univariable logistic regressions when P-value < 0.2. Multivariable logistic regression model was built using a stepwise backward method by including in the model all independent variables of the univariable analysis with a P-value < 0.2. The results were presented with odds ratios (OR) and their 95% CI. Statistical significance was set for a P-value < 0.05.
Sociodemographic characteristics of study population
A total of 228 out of 230 PSAC were included into this study. Indeed, one of the two excluded PSAC was unable to provide a stool sample while the other one was 72 months old. Out of these PSAC, 110 (48.3%) were males. Their mean age was 40.2 ± 15.0 months. The majority of PSAC’ parents were illiterate (87.7%), had no knowledge about ways of transmission of S. mansoni infection (96.5%) and did not know ways of prevention of S. mansoni infection (98.3%) (Table 1).
Prevalence of S. mansoni and S. haematobium infection
Based on the Kato-Katz technique, 42.1% (96/228) PSAC were found to be infected with S. mansoni whereas 90 out of 228 (39.5%) were found to be infected by FEC technique. Prevalence of S. mansoni infection based on POC-CCA test was 80.7% (180/223) (Table 2). The youngest child found to be infected with S. mansoni based on each of the three methods was 15 months old.
The overall prevalence of S. mansoni infection based on the combined results of the three methods was 81.1% (185/228). The overall prevalence of S. mansoni infection in girls (87.3%) was significantly higher compared to that of boys (74.6%, P = 0.014). The overall prevalence of S. mansoni infection was higher in age group 36-47 months than that of children in other age groups. However, the difference was not statistically significant (P = 0.767).
No case of S. haematobium was found.
Intensity of S. mansoni infection
The overall GMI for the study participants was 107.2 epg (95% CI: 84.0-136.8). The GMI did not differ between girls (129.2 epg (95% CI: 90.94-183.6)) and boys (85.2 epg (95% CI: 61.1-118.8)) (P = 0.092). The GMI increased with age and, PSAC in the age group 60-71 months had significantly the highest GMI (F = 2.73, P = 0.034) (Table 3). Using Bonferroni’s test, the MGI differed significantly between children in age group 60-71 months and children in age group 12-23 months (P = 0.02).
Among the 96 children with S. mansoni infection based on the Kato-Katz technique, 54.2%, 33.3% and 12.5% had light, moderate and heavy infections, respectively. In addition, the prevalence of heavy infection was significantly higher in children in age group 60-71 months than those of children in other age groups (P = 0.007) (Figure 1). In contrast, the prevalence of light infection was significantly higher in children in age group 12-23 months than those found in the other age groups (P = 0.007).
Factors associated with S. mansoni infection
In univariable logistic regression analysis, girls, low distance of home from the pond, child’s history of going to the pond, child’s swimming habit in the pond, frequency swimming habit of child in the pond per week, and period of swimming in the pond were significantly associated with S. mansoni infection (Table 4). In multivariable logistic regression (Table 4), Girls (AOR = 2.9, 95% CI: 1.3-6.1), a household located within 500 m from the pond (AOR = 3.0, 95% CI: 1.0-8.6), or between 500 and 1000 m from the pond (AOR = 3.0, 95% CI: 1.2-7.2), and child’s history of going to the pond (AOR = 5.0, 95% CI: 1.7-14.3) remained the variables significantly associated with S. mansoni infection.
To the best of our knowledge, this is the first study in Burkina Faso that has attempted to well assess the prevalence and intensity of schistosomiasis among PSAC, and to address the issue of risk factors.
The prevalence of S. mansoni infection based on the Kato-Katz technique in this study (42.1%) was moderate and lower than those reported in Niger (43.8%) (19), in Tanzania (44, 4%) (11) and in Uganda (74.9%) (6). However, it was higher than those found in Burkina Faso (36.3%) (25) as well as in other countries in SSA ranging from 0.9 to 39.3% (12–18). The differences in prevalence among these studies could be attributed to the types of water bodies, water contact practices, study design, time of survey, and environmental and socio-economic factors (14,16,18,30). In addition, the actual prevalence of S. mansoni infection in our study could be considerably higher if the Kato-Katz technique had been performed from several stool samples provided by the same study participant (6,18).
The overall prevalence of S. mansoni infection observed in this study was similar to that reported in Tanzania (82.1%) (11) but lower than that reported in Uganda (89.4%) (31). Altogether, these findings suggest that the use of only one technique including Kato-Katz technique in PSAC may result into underestimation of the prevalence of S. mansoni infection. Indeed, POC-CCA test was up to 2-fold accurate than Kato-Katz in this study and this corroborates findings of previous studies done in other areas of moderate prevalence (18,32). Therefore, we recommend usage of POC-CCA test alongside Kato-Katz to accurately estimate the true prevalence of schistosomiasis in PSAC (13).
The overall GM in the present study was of moderate intensity and was lower than those reported elsewhere ranged from 111 to 5721 epg (6,11,20,31). This difference could be due to frequency of water contacts and density of infected intermediate snail hosts in the water bodies, especially during the hot hours of the day (30). The higher GMI observed in older PSAC corroborates findings of previous studies (11,20,30). Older PSAC are known to have frequent water contacts (33) (11,14) and to spend more time in the infested water compared to their young ones (20), thus increasing the exposure time for S. mansoni infection. The build-up of schistosome loads with age due the long life-span of S. mansoni worms (approximately 10 years) could be another explanation of this higher GMI in the oldest age group (34). In addition, the high proportion of light infection has been previously reported (6,11,14,18,20,31) and could be due to a shorter time of exposure to infection and thus reduced worm burden and less egg excretion in PSAC (20). It could be also attributed to positive impact of prior MDA with praziquantel in SAC on schistosomiasis morbidity in the study area as reported elsewhere (19). Nevertheless, heavy S. mansoni infection was observed even in younger PSAC (i.e. those in age group 12-23 months) with a prevalence of 6.3%. Our findings corroborate those of Ruganuza et al. in Tanzania (11) and are of serious concern as the heavier the infection, the more severe the morbidity (6). Therefore, we recommend that all PSAC be included in the target population for MDA with praziquantel to prevent chronic and severe disease (6).
The association between the female sex of PSAC and the prevalence of S. mansoni infection could be attributed to the fact that in Panamasso, girls were more likely to go with their mothers to the pond for domestic activities compared to the boys. However, other authors have found no association between sex and the prevalence of S. mansoni infection (11,14,20). This may be an indication that boys and girls are equally exposed to infection through water contacts (30). In addition, PSAC who accompanied their parents to the pond were about 5 times more likely to be infected with S. mansoni than those who stayed at home. This corroborates findings of other studies conducted elsewhere (16,20,35). However, in Côte d'Ivoire, Coulibaly et al. found that children who stayed at home were twice more likely to be positive for S. mansoni (36). Altogether, these results indicate that PSAC are at higher risk for S. mansoni infection and are a potential reservoir for schistosome parasites which should benefit from MDA with praziquantel to reach the disease elimination goal (37,38). This study showed that PSAC living at low distance from the pond are at threefold increased odds of having S. mansoni infection. This is consistent with findings reported in Tanzania (12). In fact, in Panamasso, the pond is the main source of water for domestic activities for most of the villagers especially for those living at low distance from the pond despite well-functioning water supplies. This ensures the continual contamination of the pond with S. mansoni eggs due to poor hygiene and sanitation practices at the pond. Moreover, the majority of mothers had no knowledge about ways of transmission and ways of prevention of S. mansoni infection. Therefore, implementation of schistosomiasis control measures involving the whole community in this village is needed. These measures should focus on developing participatory health education programs with community members not only to effect continuous behavioral change in parents who expose their young children to S. mansoni infection but also to understand the disease ways of transmission. Also, involving communities in repairing their drinking water source could help reduce their contact with pond water and disease transmission (30).
We do acknowledge some limitations in this study. First, the results of this study cannot be generalized to other settings. Second, it was not possible to assess the temporal relationship between some of the risk factors and the study outcomes due to the cross-sectional nature of the study. Third, the diarrheic consistency of the stool samples from study participants rendered the preparation of Kato-Katz slides difficult, resulting hence in underestimation of the prevalence of S. mansoni infection (18).
The present study has shown that S. mansoni infection is highly prevalent among PSAC from Panamasso village. The overall GM is of moderate intensity with high proportion of light infection. Nevertheless, heavy infection was observed in very young children i.e. those aged 12 to 23 months. Female sex of PSAC, living at low distance from the pond, and child’s history of going to the pond were significantly associated with prevalence of S. mansoni infection. The study also revealed that PSAC’ mothers of Panamasso village had no knowledge about ways of transmission and ways of prevention of S. mansoni infection. These findings stress the need to include all PSAC regardless of their age in the MDA program with praziquantel. However, studies to assess the efficacy and safety of praziquantel in this group of children are warranted. In addition, our findings also call for a need to develop health education programs on schistosomiasis with community members to effect continuous change in the population’s behavior and to strengthen provision of safe water.
AOR: adjusted odd ratio; CI: confident interval; COR: crude odd ratio; epg: eggs per gram of faeces; FEC: formol ether concentration; GMI: geometric mean of intensity infection; MDA: mass drug administration; OR: odd ratio; POC-CCA: point-of-care circulating cathodic antigen; PSAC: preschool-aged children; SAC: school-aged children; SSA: sub-Saharan Africa.
Authors’ contributions
MC and IB conceived and designed the study. MC conducted the field study. JKWB and SK performed field data collection under MC’s supervision. ADD, SG, and SK performed the lab analysis under MC’s supervision. MC analyzed the data and drafted the manuscript. IB, ADD, MCT, SG, JKWB, SK, and AHD critically revised the manuscript. All authors read and approved the final manuscript.
Acknowledgements
We are very grateful to the study participants and mothers of PSAC from Panamasso village. We wish also to thank the Panamasso health centre staff.
Competing interests
The authors declare that they have no competing interests.
Availability of data and materials
Data supporting the conclusions of this article are included within the article.
Consent for publication
This part is not applicable because the manuscript contains no individual person’s data in any form (including individual details, images or videos).
Ethics approval and consent to participate
This study was approved by the institutional ethical committee from Centre MURAZ (ref 2019-66/MS/SG/INSP/DG/CEI). Written informed consent was obtained from all study participants.
Funding
Part of this work was supported by fund from a World Bank African Centres of Excellence grant (ACE02‑WACCBIP) as part of regional partnership between Centre MURAZ and University of Ghana. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Table 1 Sociodemographic data of study participants
Variables |
Category |
Frequency |
(%) |
Sex |
Boys |
110 |
48.3 |
Girls |
118 |
51.7 |
|
Age (in months) |
12-23 |
44 |
19.3 |
24-35 |
35 |
15.4 |
|
36-47 |
65 |
28.5 |
|
48-59 |
58 |
25.4 |
|
60-71 |
26 |
11.4 |
|
Mothers’ educational status |
No formal schooling |
200 |
87.7 |
Formal schooling |
28 |
12.3 |
|
Mothers’ knowledge about ways of transmission |
No |
220 |
96.5 |
Yes |
8 |
3.5 |
|
Mothers’ knowledge about ways of prevention |
No |
224 |
98.3 |
Yes |
4 |
1.7 |
Table 2 Prevalence of S. mansoni infection per used laboratory method
Techniques |
Frequency |
No infected |
Prevalence (%) |
Kato-Katz |
228 |
96 |
42.1 |
FEC |
228 |
90 |
39.5 |
POC-CCA |
223* |
180 |
80.7 |
Combined three methods |
228 |
185 |
81.1 |
*5 PSAC did not provide any urine sample
Table 3 Relationship between the GMI and the sociodemographic and water contact data
Variables |
No infected |
GMI |
95% CI |
P value |
Sex |
0.092s |
|||
Boys |
43 |
85.2 |
61.1-118.8 |
|
Girls |
53 |
129.2 |
90.9-183.6 |
|
Age (in months) |
|
|
|
0.034a |
12-23 |
16 |
63.9 |
37.5-108.9 |
|
24-35 |
14 |
85.8 |
51.2-143.6 |
|
36-47 |
34 |
116.0 |
69.9-192.5 |
|
48-59 |
23 |
104.1 |
66.9-162.0 |
|
60-71 |
9 |
305.7 |
172.4-542.2 |
|
Child’s shoe wearing habit |
|
0.356s |
||
No at all |
8 |
161.5 |
57.6-452.7 |
|
Always |
88 |
103.3 |
80.1-133.2 |
|
Distance of home from the pond |
|
0.996k |
||
< 500 m |
22 |
118.3 |
58.0-241.5 |
|
500-1000 m |
64 |
105.7 |
80.7-138.4 |
|
> 1000 m |
10 |
94.8 |
45.6-197.1 |
|
Go to the pond |
|
0.866s |
||
No |
3 |
124.6 |
61.9-250.9 |
|
Yes |
93 |
106.7 |
83.0-137.2 |
|
Child’s swimming habit in the pond |
|
0.701w |
||
No |
13 |
87.7 |
56.8-135.3 |
|
Yes |
83 |
110.7 |
84.0-145.8 |
|
Child’s swimming frequency per week |
|
0.590a |
||
Never |
13 |
87.7 |
56.8-135.3 |
|
Moderate |
16 |
139.1 |
69.0-280.3 |
|
High |
67 |
104.8 |
77.2-142.3 |
|
Child’s swimming period in a day |
|
0.920k |
||
Never |
13 |
87.7 |
56.8-135.3 |
|
7 a.m.-10 a.m. |
31 |
118.6 |
69.2-203.4 |
|
11 a.m.-2 p.m. |
27 |
114.7 |
77.6-169.3 |
|
3 p.m.-6 p.m. |
25 |
97.8 |
57.4-166.6 |
aANOVA test; Kruskal-Wallis test ; sStudent’s test; wWilcoxon test
Table 4 Factors associated with prevalence of S. mansoni infection
Variables |
S. mansoni infection |
COR (95% CI) |
AOR (95% CI) |
P value |
Sex |
|
|
|
|
Boys |
74.6 (82/110) |
1 |
|
|
Girls |
87.3 (103/118) |
2.3 (1.2-4.7) |
2.9 (1.3-6.1) |
0.007 |
Age (in months) |
||||
12-23 |
77.3 (34/44) |
1 |
||
24-35 |
80.0 (28/35) |
1.2 (0.4-3.5) |
|
|
36-47 |
86.2 (56/65) |
1.8 (0.7-5.0) |
|
|
48-59 |
81.0 (47/58) |
1.3 (0.5-3.3) |
|
|
60-71 |
76.9 (20/26) |
1.0 (0.3-3.1) |
|
|
Child’s shoe wearing habit |
|
|||
Always |
80.0 (16/20) |
1 |
|
|
No at all |
81.3 (169/208) |
1.1 (0.3-3.4) |
||
Distance of home from the pond |
||||
> 1000 m |
61.2 (30/49) |
1 |
|
|
500-1000 m |
86.9 (113/130) |
4.2 (2.0-9.1) |
3.0 (1.2-7.2) |
0.014 |
< 500 m |
85.7 (42/49) |
3.8 (1.4-10.2) |
3.0 (1.0-8.6) |
0.047 |
Go to the pond |
||||
No |
42.9 (9/21) |
1 |
|
|
Yes |
85.0 (176/207) |
7.6 (2.9-19.5) |
5.0 (1.7-14.3) |
0.003 |
Child’s swimming habit in the pond |
||||
No |
64.3 (27/42) |
1 |
|
|
Yes |
85.0 (158/186) |
3.1 (1.5-6.6) |
|
|
Child’s swimming frequency per week |
|
|||
Never |
64.3 (27/42) |
1 |
|
|
Moderate |
85.3 (29/34) |
3.2 (1.0-10.1) |
|
|
High |
84.9 (129/152) |
3.1 (1.4-6.7) |
|
|
Child’s swimming period in a day |
|
|||
Never |
64.3 (27/42) |
1 |
|
|
7 a.m.-10 a.m. |
87.0 (67/77) |
3.7 (1.5-9.3) |
|
|
11 a.m.-2 p.m. |
81.5 (44/54) |
2.4 (1.0-6.2) |
|
|
3 p.m.-6 p.m. |
85.5 (47/55) |
3.3 (1.2-8.7) |
|
|
Mothers’ educational status |
|
|
||
Formal schooling |
75.0 (21/28) |
1 |
|
|
No formal schooling |
82.0 (164/200) |
1.5 (0.6-3.8) |
|
|