DOI: https://doi.org/10.21203/rs.3.rs-60139/v1
Background: Toxoplasmosis is caused by infection with the protozoan Toxoplasma gondii (T. gondii), an obligate intracellular parasite. The infections produced a wide range of clinical syndromes in humans, land and sea mammals, and various bird species. Toxoplasmosis is especially important among Immune-compromised patients and pregnant women. Infection of mothers during pregnancy by Toxoplasma gondii may have serious consequences for fetus ranging from miscarriage, central nervous system involvement, retinochoroditis, or at birth subclinical infection.
Objective: To determine Toxoplasmosis sero-prevalence, awareness and risk behavior among pregnant women following antenatal care in Asella Teaching and Referral Hospital, Asella, Ethiopia.
Methods: An institutional based quantitative cross sectional study design was conducted on sample size of 384 from December 1, 2018 to June 30, 2019. Structured, a pre-tested questionnaire was used to collect the demographic and risk factor related data. Serum sample, collected was tested for Toxoplasma Immunoglobulin G (IgG) and Toxoplasma Immunoglobulin M (IgM) antibodies using anti- IgG and IgM antibodies by Toxoplasma immune-chromatographic test (ICT) IgG-IgM test. A bivariable and multivariable logistic regression model was applied to show association between the dependent and independent variables considering P < 0.05 and the 95% confidence interval.
Result: The overall sero prevalence of T. gondii in the study area was 81.8 %. Three hundred and fourteen (81.8 %) of the pregnant women were IgG seropositive, fifty women (13 %) were IgM seropositive. fifty women were positive for both IgG and IgM. None of the pregnant women were positive exclusively for IgG and IgM ani-bodies. eating raw meat (COR=3.480, 95%CI: 1.450-8.352; P= 0.005, AOR=3.798, 95%CI: 1.249-11.550, P=0.19), using unpasteurized milk(COR=3.860, 95%CI: 2.118-7.037; P= 0.000, AOR=3.907, 95%CI:1.744-8.751, P=0.001), having three or more children(COR=2.194, 95%CI: 1.065-4.518; P= 0.033) and Consumption of raw egg(COR=2.042, 95%CI: 1.049-3.974; P= 0.036)
Conclusion: The sero-prevalence of T. gondii antibodies was high among the pregnant women. Those who consumed raw meat and egg, unpasteurized milk and those who have three or more children were at higher risk of T. gondii infection. Hence, blood screening for Toxoplasmosis, health education and awareness creation among pregnant women should be done during antenatal follow up.
Toxoplasmosis is caused by the Toxoplasma gondii (T. gondii), an obligate, intracellular protozoan, a widespread zoonotic parasite which can infect all warm-blooded animals (1), and is one of the most common zoonosis in the world (2). Because of the current high rates of infection among the human population (estimated as 30–50%) it is considered a global health hazard (3). In Ethiopia the highest prevalence (95.1%) was reported from Butajira from patients found in 15–49 age groups (4), 94% prevalence among HIV/AIDS patients from Tikur Anbessa Specialized Hospital (5), and 85.4% among pregnant women in Addis Ababa (6). Toxoplasmosis is characterized by a wide range of clinical syndromes. The majority of infections is typically asymptomatic or causes a mild self-limiting ‘flu’ like illness. Infection at primary gestation can be transmitted to the fetus and causes congenital toxoplasmosis and finally resulted in miscarriages, in utero death, retardation growth in neonate, ophthalmic and neurological diseases (7–10).
The estimated global burden of congenital toxoplasmosis was 19,000 new cases each year resulting in the loss of approximately 1.2 million Disability-Adjusted Life Years (DALYs) (11).
Cats and other felines are the definitive hosts of T. gondii and thus the only source of environmentally resistant oocysts in nature. From the major routes of infections for humans some of them are: close contact with cats or cat excreta ingestion of oocysts, eating of foods or soil contaminated with oocysts and drinking of contaminated water with oocysts; ingestions of tissue cysts due handling/consumption raw or undercooked meat of infected animals hosts, transplantation of infected organs, blood transfusion and congenital infection. Drinking of unpasteurized milk from infected animals and eating of raw egg can also transmit this parasite (9, 12–13).
Antenatal screening for T. gondii infection is based detection of anti-toxoplasma specific IgM and IgG is the backbone in controlling the risk of inherited toxoplasmosis. Maternal-fetal intervention can be achieved through drugs such as spiramycine which prevent congenital tox- oplasmosis by more than 60% (14).
Exposure rates to toxoplasmosis vary greatly to the topographical locality, socioeconomic prominence, traditional and spiritual opinions of a population (15). Therefore, there is a need to determine the prevalence in different settings. Confirmation of zoonotic infection among cats and livestock animals of Ethiopia shows the presence of the parasite and hence the potential for human infection (16–18). Current trends in foods and lifestyle with fast foods substituting traditional cooking and popularity of cohort animals, (especially cats, as they require minimal care) and the plenty of stray cats, could increase the probability of experience to toxoplasmosis.
Prevention of congenital toxoplasmosis depends mainly on avoidance of risk factors during pregnancy. But, uncertainty about how most women acquire infection results in advice to avoid numerous risk factors which makes compliance difficult. Therefore, alertness is required with regard to toxoplasmosis and identification of significant associations between known risk factors and seropositivity to T. gondii among susceptible groups. This will be surely helpful in adopting appropriate prevention and control methods as accommodated for each group. In addition since, only few sero-prevalence among females and neonates have been studied and there is no antenatal screening program for pregnant women for toxoplamosis in Ethiopia and also there is no studies have investigated the sero-prevalence, awareness of toxoplasmosis and related preventive behavior patterns among pregnant women in Aris zone, it necessities to have evidence concerning T. gondii in Arsi zone.
Therefore, the aim of this study is to determine Toxoplasmosis sero-prevalence, awareness and risk behavior among pregnant women following antenatal care in Asella Teaching and Referral Hospital, Asella, Ethiopia.
Study area and period
A institutional based cross-sectional study design was done at Asella Teaching and Referral) Hospitals from December 01, 2018 to February 30, 2019. Asella Teaching and Referral Hospital found in Assela town, Arsi Zone, at 175 kilometers to the east of Addis Ababa, the capital city of Ethiopia.
Study design and period
An institutional based quantitative cross-sectional study design was conducted from December 01, 2018 up to February 30, 2019 to determine the sero-prevalence of toxoplasmosis, awareness and its associated risk factors in Asella Teaching and Referral Hospital,
Source population
All pregnant women in Asella referral and teaching Hospital catchment area.
Study population
All pregnant women following antenatal care in Asella referral and teaching Hospital.
Eligibility Criteria
Inclusion criteria: A pregnant woman who was come to selected Hospitals for the first time for antenatal care during sample collection period for current pregnancy.
Exclusion criteria: Mothers who can’t respond because of serious illness and who was come more than once during sample collection period to selected Hospital for antenatal service.
Sample Size Determination
The sample size was calculated to estimate the prevalence of toxoplasma antibodies in this population. For the calculation, prevalence was assumed to be 50% because there is no previous research done on this parasite among pregnant women in Arsi zone by considering a confidence interval of 95% and the acceptable difference to be 5%, the minimum required sample size was 384. The sample was collected by recruiting all consenting pregnant woman at their first visit to the antenatal clinic of Asella Teaching and Referral Hospital.
Sample size =(Z α/2)2 p (1-p)
d2
Where:
P: An estimate of the prevalence rate for the population (P= 50%)
d: absolute precision(d= 5%=0.05)
Zα/2: The standard normal variable at 95% confidence level when α =5 %.( Z α/2 = 1.96)
So, n = Z α/2)2 p (1-p) = 2(1.96)2x 0.5(1-0.5) = 384
d2 (0.05)2
Sampling Techniques
All pregnant women who were come to Asella Teaching and Referral Hospital for the 1st time for antenatal care and willing to participate in the study were included until required sample size was achieved.
Data Collection Procedures
Socio demographic and clinical features
After clear training was given for five midwifes, five medical laboratory technologists and five facilitators from who were selected from Asella teaching and referral hospitals data collection was started. To collect Socio demographic and clinical features a pretested questionnaire was administered by Midwifes and trained research assistants’ information from pregnant women at selected hospitals antenatal care unit was gathered. The questions was produced information on four major areas: (a) socio-demographic information of the participants such as age, ethnicity, level of education, employment status, marital status, area of residence; (b) details of prior adverse birth outcomes, from multigravida i.e. miscarriages, still births, children with delayed milestones; (c) disease-related risk factors such as cat ownership, personal hygiene (frequency of hand washing), kitchen hygiene (frequency of washing utensils, cutting board and knife after preparation of meat), consumption of raw meat, cooking of meat, frequency of consuming unwashed raw vegetables and fruits, frequency of having non-homemade meals and exposure to soil; and finally, (d) the awareness of toxoplasmosis and sources of information. After implementation the questionnaire, each subject will be educated on significance and prophylactic actions against toxoplasmosis using an information sheet.
Laboratory tests
Two milliliters of blood was collected aseptically from each participant into sterile containers and centrifuged in the collected Hospitals and serum was separated by trained laboratory technologist at Arsi University Asella Teaching and Referral Hospital laboratory department. At Arsi University Asella Teaching and Referral Hospital laboratory department, the serum was tested on the day of receipt for T. gondii-specific antibodies using a commercial kit (On Site Toxo IgG/IgM Rapid Test-Dip Strip® CTK Biotech. Inc.USA) according to the manufacturer’s instructions by two senior laboratory technologists. The participants were made aware of the results of the serological investigations and its interpretation.
Data Analysis procedures
Data generated from questionnaire survey and laboratory investigations was recorded and coded using Microsoft Excel spreadsheet (Microsoft Corporation) and was analyzed using STATA version 13.0 for Windows (Stata Corp. College Station, TX, USA) by researchers. The sero-prevalence was calculated as the number of seropositive samples divided by the total number of samples tested. To identify predictors of seropositivity, first the association of the potential risk factors (age, gestational age, educational status, contact with cats’ feces, presence of domestic cat, way of life of domestic cats, etc) was analyzed by univariable logistic regression. Then all non- collinear variables with P-value ≤ 0.25 in univariable logistic regression analysis was included in the final multivariable logistic regression model to construct the likely model (P < 0 .05). The model will be reduced by backwards elimination of non-significant variables (P > 0.05) based on likelihood ratio test to define the model that would best fit the data.
Dissemination of Research finding
The research findings will be presented to the Arsi University and other stake holders, shared to Arsi Zonal Health Bureau, Regional Health Bureau, Federal Minister of Health (FMOH) and organizations/partners working on human health in the country. Finally effort will be made to publish the findings on peer reviewed scientific journal.
Significance and beneficiary of the study
The finding will be significant both for researcher, communities and government in adding information regarding Toxoplasmosis sero-prevalence, awareness, and risk behavior among pregnant women following antenatal care in Arsi zone, Ethiopia. Nationally it develops the understanding of relationship between having cat, eating raw meat and vegetables, blood transfusion, organ transplantation, drinking contaminated water, eating soil and so on with congenital toxoplasmosis.
Expected Outcome
A wide range of data based on which rigorous generalizations and recommendations can be made based on the data was obtained from the diversity score survey and laboratory analysis of sample.
Quality assurance
Strict measures were taken throughout the analytic process. Five percent of the Questionnaire was pre-tested among pregnant women attending at Asella Referal and teaching Hospital (Asella town), and Questionnaire was revised accordingly. Data collectors were trained for 3 days on how to con duct the interview and the sampling process. Completed questionnaires were reviewed immediately to ensure accuracy and legibility. Quality control samples were tested parallel with the research samples and standard operating procedures were followed during the laboratory investigation.
Socio-demographic characteristics
This study included a total of 384 pregnant women with a response rate of 100%. Majority (65%) of them were urban dwellers and the mean age (± SD) of the study subjects were 26.2 (± 6.55) years. The majority (51%) of the study participants were found within the age group of 15-24.9 years. Almost all (98.2%) of the study participants were not have any information about Toxoplasmosis and its mode of transmission (Table-1).
Sero-prevalence and Risk factors for Toxoplasmosis
In this study, the serum sample was collected from a total of 384 pregnant women for the serological test, out of these, 314 (81.8%) were found to be positive for anti-bodies specific to T. gondii. Furthermore, 264(68.8%) were found to be positive only for IgG; the rest 50(13 %) were positive both for IgM and IgG (Table-2). Out of the 50 women with recent infection, 10 were in the first trimester, 22 were in the second trimester and only 18 mothers were in the third trimester of pregnancy (Table-3).
According to the bivariate and multivariate logistic regression analysis, 21 variables including: age, educational level, trimester of pregnancy, source of drinking water, presence of rat at home , contact with cat’s feces , consumption of raw:egg, milk, meat, undercooked meat ,undercooked embedded meat, and fruit and vegetable/ fruit and vegetables without adequate hygiene ,Gestational age, blood donated or organ transplanted before, contact with soil without glove, abortion history, number of prenatal care appointments, number of pregnancies information about toxoplasmosis were included. From these risk factors for Toxoplasmosis eating raw meat (OR=3.480, 95%CI: 1.450-8.352; p-value= 0.005, AOR=3.798, 95%CI: 1.249-11.550,p-value=0.19), using unpasteurized milk(OR=3.860, 95%CI: 2.118-7.037; p-value= 0.000, AOR=3.907, 95%CI:1.744-8.751,p-value=0.001), having three or more children(OR=2.194, 95%CI: 1.065-4.518; p-value= 0.033) and Consumption of raw egg(OR=2.042, 95%CI: 1.049-3.974; p-value= 0.036) were showed significant association with anti-Toxoplasma antibody sero- positivity of the pregnant women (Table -1).
Previously there wasn’t known any information about the sero-prevalence of T. gondii in Arsi zone and this is the first report of T. gondii infection in Asella, Ethiopia. The sero- prevalence of T.gondii among pregnant women in the study area was found to be 81.8 %( Table-2). This finding is greater than the findings from Arba minch, Ethiopia 79.3% (19), Brazil 68.6% (20), Ghana 51 .2% (21), Tanz ania 30.9% (22), Sri L anka 29.9 % (23), China 16.8 % (24),and Mexico 10.8 % (25). The present discovery is also higher than the sero- prevalence of T. gondii in the lower altitude and higher humidly cities of Kenya: Kisumu (52%) and Mombasa (57%) (26). But silt lower than Bench Maji Ethiopia 85.3% (27) and Addis Ababa 85.4% (28).
Amongst the sero-positive females, the majority of them were found to have a chronic or past infection. However, fifty women (50/314, 16 %) or 13% of the 384 women was found to have a recent infection(Table-2) which is higher than the studies conducted in Arba Minch Hospital 9(3.9%) and Mizan Aman General Hospital 7(3.0%) in Ethiopia (19, 27 ). Bearing in mind the asymptomatic nature of the disease and the opportunity of congenital spread, the serologic finding of this study should not be overlooked. This is because the health -care facilities in the study area lack specific tests for T. gondii and diagnosis isn’t completely made which may result in misdiagnosis or delayed diagnosis.
In this study, there were 21 different risk factors have been also evaluated for the sero- prevalence of T. gondii but only : eating raw meat, drinking unpasteurized milk, eating raw egg and having three or more children (Table-1) were showed significant association. This finding is consistent with the studies conducted in Tanzania (22), Mali (29) and have of south of Iran (30).
In these findings, contact with garden soil, owing to a domestic cat or presence of rat at home, and consumption of raw vegetables, inadequate washing of fruits and vegetables, educational status, contact with cat’s feces and soil without gloves weren’t showed significantly associated with T. gondii infection (Table-1) which contradicted other studies conducted in Ethiopia (19, 27, 30), China (32) and Brazil (33).This difference might be due to the differences in socioeconomic status, personal hygiene practices, feeding habits, differences in testing methods, variation immune staus of the study participants and sample size of each study.
Cats and dogs are thought to be the important amplifiers of infection of T. gondii (34). In the Ethiopian context, it is common to see domestic cats live and sleep to get her with human beings. Cats can directly contaminate humans, other animals, and their surrounding through their feces (35). Similarly, after contact with cat’s feces, dogs can contribute to the spread of the organism through mechanical contamination of garden soil, vegetables, and human beings. Therefore, human beings can possibly acquire the infection or ingest the oocyst of the parasite through their dirtied hands after direct contact with cats or dogs, garden soil, and surfaces or ingesting of contaminated vegetables. Oocysts of T. gondii are hard free living phases of the parasite, and consequently are a major contributor to infections associated with the above-mentioned risk factors (34). Since they on the other hand, cats or dogs may acquire the infection from other warm blooded animals through carnivore contamination, and in sequence infect human beings (36).
This study was showed as the difference in educational status of the study participants have no effect on the sero-prevalence, because only 1.8% was heard about Toxoplasmosis even though they were in different educational level and 98.2% doesn’t have any information (table-1).This agrees with the study done in Hawassa and Yirgalem Hospitals southern, Ethiopia which indicated as 99.6% of the study participants was no information about Toxoplasmosis (37). But in reality it is extremely important to increase awareness on the transmission of toxoplasmosis at all level.
Even though it weren’t showed significant association with Toxoplasmosis in this study, contact with: cat’s feces, contaminated soil and water, raw or under cocked fruits and vegetables, gestational age, information about toxoplasmosis, abortion history and presence of rat and domestic cat’s it is important to prevent these risk factors as it is evidence by different researches as these were some of the risk factors for Toxoplasmosis (9, 27, 32, 38-42). But some of current findings agree with research done in northwest Ethiopia which showed as there are no any significant risk factors associated with sero-positivity in relation socio-demographic characters, gestational age, gravidity, consumption of raw vegetable, and blood transfusion (28, 43).
The sero-prevalence of T. gondii antibodies was high among the pregnant women. Those who consumed raw: meat, milk and egg were at higher risk of T. gondii infection. Hence, blood screening for Toxoplasmosis, health education and awareness creation among women of reproductive age group in general and pregnant women in particular should be done during antenatal follow up. It is also alarming to add Toxoplasmosis screening during antenatal follow up. Moreover, there is need to control urban stray cat population to reduce the risk of zoonotic transmission of the parasite and further epidemiological studies to ascertain additional risk factors, economic and health impact of toxoplasmosis are called for.
FMOH Federal Minister of Health |
||||
ICT Chromatographic test |
||||
IgG Immunoglobulin G |
||||
IgM |
Immunoglobulin M |
|||
PI Principal Investigator |
||||
RPD Research and publication director |
Ethics approval and consent to participate
The study was approved by the Ethical Review Committee of the Arsi University Collage of Health Sciences by Ref.No. 2-16/09/151/11 by date of 12 November 2018 with budget code COHS/R/0033/2018/19. Informed written consent was obtained from the participating pregnant women at the first booking visit. The participants were informed that enrolment to the study was purely voluntary and non-participation was not in any way influence the services provided by the antenatal clinic.
Consent for publication
Not applicable
Availability of data and materials
The data sets used and /or analyzed during the current study are available from the corresponding author or on reasonable request.
Conflict of interest
The authors declare that there is no conflict of interests.
Funding
The source of this research is Arsi University. The fund is used to buy reagents, kits, data collection and diagnosis only.
Authors’ contributions
SA provided conceptual framework for the project, data collection, guidance for interpretation of the data, perform data analysis, participated in the Parasitological work, performance of statically analysis and guidance for data interpretation. I also read and approved the final manuscript.
Acknowledgements
I would like to acknowledge Arsi University for fund allocation, Asella referral and teaching hospital laboratory department for parasitological diagnosis and the study participants for their willingness to participate.
Authors’ information
1Arsi University Collage of Health Sciences Medical Laboratory sciences department, E-mail: [email protected], P.O.Box 396
Table-1: Sero-prevalence of Toxoplasma gondii antibody and the associated risk factors in pregnant women (n = 384), Asella, Ethiopia 2019.
Total n (%) |
P-Value |
COR 95%(CI) |
P-Value |
AOR 95%(CI) |
|||
|
Negative n (%) |
Positive n(%) |
|||||
Age group (in Years) |
|||||||
15-24.9 |
196(51%) |
35(50%) |
161(51.2%) |
.943 |
1 |
.736 |
1 |
26-24.9 |
174(45.3%) |
32(45.7%) |
142(45.2%) |
.738 |
1.255(.332-4.734) |
.658 |
0.551(.039-7.704) |
35+ |
14(3.6%) |
3(4.3%) |
11(3.5%) |
.779 |
1.210(.319-4.590) |
.553 |
0.457(.034-6.076) |
Educational Status |
|||||||
illiterate |
29(7.6%) |
5(7.1%) |
24(7.6%) |
.723 |
1 |
.470 |
1 |
incomplete elementary school |
120(31.3%) |
26(37.1%) |
94(29.9%) |
.900 |
.928(.290-2.974) |
.614 |
0.694(.168-2.866) |
complete elementary school |
4612%) |
4(5.7%) |
42(13.4%) |
.602 |
1.232(.562-2.701) |
.274 |
1.67(.667-4.182) |
incomplete high school |
30(7.8%) |
6(8.6%) |
24(7.6%) |
.167 |
.424(.126-1.432) |
.319 |
0.496(.125-1.970) |
complete high school |
73(19%) |
13(18.6%) |
60(19.1%) |
.849 |
1.114(.368-3.373) |
.565 |
1.476(.392-5.558) |
incomplete higher education |
26(6.8%) |
5(7.1%) |
21(6.7%) |
.938 |
.965(.397-2.344) |
.329 |
1.668(.598-4.656) |
complete higher education |
60(15.6%) |
11(15.7%) |
49(15.6%) |
.922 |
1.061(.328-3.432) |
.673 |
1.348(.337-5.390) |
Trimesters |
|||||||
first(<14weeks) |
77(20.1%) |
8(11.4%) |
69(22%) |
.068 |
1 |
.124 |
1 |
second<14-28 weeks) |
150(39.1%) |
26(37.1%) |
124(39.5%) |
.024 |
0.39(.171-.886) |
.062 |
.410(.161-1.047) |
third(>28 weeks) |
157(40.9%) |
36(51.4%) |
157(40.9%) |
.223 |
0.705(.401-1.238) |
.879 |
1.055(.531-2.093) |
Information about Toxoplasmosis |
|||||||
Yes |
7(1.8%) |
1(1.4%) |
6(1.9%) |
1 |
1 |
||
No |
377(98.2%) |
69(98.6%) |
308(98.1%) |
.786 |
.744(.088-6.279) |
.789 |
.713(.059-8.546) |
Number of children |
|||||||
< or = one |
150(39.1%) |
31(44.3%) |
119(37.9%) |
.075 |
1 |
.063 |
1 |
two |
115(29.9%) |
13(18.6%) |
102(32.5%) |
.814 |
1.073(.596-1.931) |
.764 |
.891(.420-1.891) |
three and above |
74(19.3%) |
16(22.9%) |
58(18.5%) |
.033 |
2.194(1.065-4.518)* |
.034 |
.389(.163-.931)* |
History of abortion |
|||||||
Yes |
119(31%) |
100(31.8%) |
19(27.1%) |
.442 |
.797(.447-1.421) |
.240 |
.669(.342-1.308) |
No |
265(69%) |
214(68.2%) |
51(72.9%) |
1 |
1 |
||
History of contact with cat's feces |
|||||||
Yes |
375(97.7%) |
67(95.7%) |
308(98.1%) |
.248 |
.435(.106-1.784 |
.078 |
.203(.342-1.308) |
No |
9(2.3%) |
3(4.3%) |
6(1.9%) |
1 |
1 |
||
Consumption of fruit and vegetables without adequate hygiene |
|||||||
Yes |
302(78.6%) |
59(84.3%) |
243(77.4%) |
.206 |
1.567(.781-3.143) |
.953 |
.971(.361-2.609) |
No |
82(21.4%) |
11(15.7%) |
71(22.6%) |
1 |
1 |
||
Consumption of raw fruit and vegetable |
|||||||
Yes |
359(93.5%) |
65(92.9%) |
294(93.6%) |
.813 |
0.884(.320-2.443) |
.089 |
.285(.067-1.209) |
No |
25(6.5%) |
5(7.1%) |
20(6.4%) |
1 |
1 |
||
Consumption of raw meat |
|||||||
Yes |
301(78.4%) |
64(91.4%) |
237(75.5%) |
.005 |
3.480(1.450-8.352)* |
.019 |
3.798(1.249-11.550)* |
No |
83(21.6%) |
6(8.6%) |
77(24.5%) |
1 |
1 |
||
Consumption of undercooked raw meat |
|||||||
Yes |
361(94.0%) |
67(95.7%) |
294(93.6%) |
.509 |
1.519(.439-5.261) |
.812 |
1.227(.227-6.623) |
No |
23(6%) |
3(4.3%) |
20(6.4%) |
1 |
|||
Consumption of unpasteurized milk |
|||||||
Yes |
200(52.1%) |
54(77.1%) |
146(46.5%) |
.000 |
3.860(2.118-7.037)* |
.001 |
3.907(1.744-8.751)* |
No |
184(47.9%) |
16(22.9%) |
168(53.5%) |
1 |
1 |
||
Consumption of raw egg |
|||||||
Yes |
52(13.5%) |
15(21.4%) |
37(11.8%) |
.036 |
2.042(1.049-3.974)* |
.122 |
1.921(.840-4.391) |
No |
332(86.5%) |
55(78.6%) |
277(88.2%) |
1 |
1 |
||
Blood donated or organ transplanted before |
|||||||
Yes |
18(4.7%) |
5(7.1%) |
13(4.1%) |
.288 |
1.781(0.614-5.170) |
1.114(.318-3.904) |
|
No |
366(95.3%) |
65(62.9%) |
301(95.9%) |
||||
Type of water for drinking |
|||||||
public supply filtered |
271(70.6%) |
60(85.7%) |
211(67.2%) |
.060 |
1 |
.289 |
1 |
public supply unfiltered |
85(22.1%) |
7(10%) |
78(24.8%) |
.523 |
1.991(.240-16.498) |
.902 |
0.865(086-8.686) |
well water filtered |
14(3.6%) |
1(1.4%) |
13(4.1%) |
.683 |
0.628(.067-5.862) |
.345 |
0.313(0.028-3.493) |
well water unfiltered |
6(1.6%) |
1(1.4%) |
5(1.6%) |
.678 |
0.538(.029-9.985) |
.553 |
0.393(0.018-8.571) |
Bottled mineral water |
8(2.1%) |
1(1.4%) |
7(2.2%) |
.826 |
1.400(0.07-28.120) |
.854 |
.738(0.029-18.873) |
presence of rat at home |
|||||||
Yes |
276(71.9%) |
51(72.9%) |
225(71.7%) |
.840 |
1.062(.594-1.899) |
.856 |
.937(.463-1.895) |
No |
108(28.1%) |
19(27.1%) |
89(28.3%) |
1 |
1 |
*= statistically significant at p, 0.05, COR: Crude Odds Ratio, AOR: Adjusted Odds Ratio, CI: Confidence Interval
Table-2: IgG sero-prevalence status of study Participant * IgM sero-prevalence status of study Participant Cross tabulation (n=384), Asella, Ethiopia 2019.
|
|||||
|
IgM sero-prevalence status of study Participant |
Total |
|||
positive |
negative |
||||
IgG sero-prevalence status of study Participant |
positive |
Count |
50 |
264 |
314 |
% of Total |
13.0% |
68.8% |
81.8% |
||
negative |
Count |
0 |
70 |
70 |
|
% of Total |
0.0% |
18.2% |
18.2% |
||
Total |
Count |
50 |
334 |
384 |
|
% of Total |
13.0% |
87.0% |
100.0% |
Table - 3: Respondent's Gestational age * IgM sero-prevalence status of study Participant (n=384), Asella, Ethiopia 2019.
Crosstab |
|||||
|
IgM sero-prevalence status of study Participant |
Total |
|||
positive |
negative |
||||
Respondent's Gestational age |
first trimester |
Count |
10 |
67 |
77 |
% of Total |
2.6% |
17.4% |
20.1% |
||
second trimester |
Count |
22 |
128 |
150 |
|
% of Total |
5.7% |
33.3% |
39.1% |
||
third trimester |
Count |
18 |
139 |
157 |
|
% of Total |
4.7% |
36.2% |
40.9% |
||
Total |
Count |
50 |
334 |
384 |
|
% of Total |
13.0% |
87.0% |
100.0% |