DOI: https://doi.org/10.21203/rs.2.9532/v1
Between 1990 and 2010, the global prevalence of anemia declined by nearly 20% from 40% to 33% [1]. Yet, anemia remains a major concern with moderate or severe public health significance in more than 80% of the world countries [2]. In 2010 anemia affected more than two billion people globally and contributed to 9% of total years of life lived with disability [1]. Children under five years of age, pregnant women and women of reproductive age bear the highest burden [1,2]. Anemia prevalence exceeds 50% in many regions of the sub-Saharan Africa [1]. According to the 2005 estimate, anemia has severe public health significance in Ethiopia [2]. In 2016, the national prevalence among pregnant women was 29% and the figure did not declined over the previous decade [3,4].
Anemia has multifaceted and frequently coexisting etiologies. Iron deficiency is regarded as the primary cause contributing to nearly 50% of the global burden of anemia [1,2]. Parasitic infections including malaria, hookworms and shistosomiasis may explain nearly a quarter of anemia [1]. Further hemoglobinopathies, acute or chronic infections and other nutritional deficiencies have ethological significances [1,2]. During pregnancy, hemodilution – disproportionate increase in plasma volume as compared with red cell mass – is a key cause of prenatal hemoglobin decline. Contextual factors including poverty and limited access to health care are also important root causes [1].
Maternal anemia leads to multiple and serious consequences. There is unequivocal evidence that anemia in pregnancy increases the risks of maternal mortality and low birthweight (LBW) [5]. A systematic review confirmed that 1 g/dl increase in mean hemoglobin level in late pregnancy is associated with nearly 30% reduction in the odds of maternal mortality [6]. Further prenatal iron supplementation during pregnancy is associated 20% reduction in the risk of LBW [7]. Anemia in pregnancy may also increase risks of premature birth and perinatal mortality [8].
According to the World Health Organization (WHO), about one-fourth of the world population is infected with intestinal parasites primarily Ascaris lumbricoides, Trichuris trichiura and hookworms [9]. Intestinal parasites may cause or aggravate anemia via multiple and interactive mechanisms [10,11]. Hook worms and schistosomiasis lead to chronic intestinal blood loss. Many intestinal parasites reduce appetite and compromise nutrient intake. Further helminthiasis-inducted intestinal inflammation may limit absorption of nutrients. Intestinal parasites may promote indigenous nutrient loss by inducing intestinal mucosa damage, impairing digestion and causing diarrhea [10,11].
The association between intestinal parasitosis and anemia among children is well established and systematic reviews suggested deworming after a confirmed infection results in a significant hemoglobin rise in children [5,11]. However, the significance of parasitic infection to anemia in pregnancy has not been thoroughly explored and the existing evidence is equivocal. Observational studies conducted in Western Ethiopia [13], Nigeria [14], Venezuela [15] and Philippines [16] reported positive associations. Conversely, a study conducted in Papua New Guinea found no significant relationship [17]. Further, according to a systematic review, a single dose of antihelminthic in the second trimester of pregnancy showed no effect on the hemoglobin status of pregnant women [5].
In this cross-sectional study we aimed to determine the prevalence of intestinal parasitic infection and its relationship with anemia among pregnant women in Wondo Genet district, Southern Ethiopia.
This facility-based cross-sectional study was conducted in June and July 2018 among pregnant women booked for antenatal care (ANC) in five public health centers of Wondo Genet district, Southern Ethiopia.
Wondo Genet is situated in Sidama zone, Southern Ethiopia and has an estimated population size of 163,000. Administratively it is classified into 13 rural and 2 urban villages. The altitude of the district ranges from 1,761 to 2,695 meters above sea level (ASL) and the area is characterized by two distinct agro-ecological zones. Midlands, land mass ranging between 1,750 to 2,300 m ASL, contribute for 62% of the population; whereas, highlands (above 2,300 m ASL), contribute for the remaining 38% the population. The average rainfall is 1,120 mm per annum and according to the season, temperatures vary from 7 to 26 0C. The main rainy season is between July and early October. About 85% of the population livelihood depends on subsistent farming. The district has 5 health centers and 16 functional health posts.
Sample size determination and sampling approach
Sample size adequate for estimating prevalence of anemia and intestinal parasitosis was determined independently using single population proportion formula. The specifications made in the computation were: 95% confidence level, 5% margin of error, 32.8% expected prevalence of anemia [19], 29.5% expected prevalence of intestinal parasitosis [20] and 10% compensation for possible non-response. Ultimately sample size of 352 was judged to be sufficient.
Similarly, the adequacy of the sample size for determining the association between intestinal parasitosis and anemia status was evaluated using double population proportion formula using Epi InfoTM 7 statistical package with the inputs of: 95% confidence level, 80% power, 1:3 ratio between subjects with and without intestinal parasitosis and odds ratio (OR) of 2.4 [21].
Study participants were selected from the five health centers using stratified sampling approach (i.e. considering each health facility as stratum). During the survey 1,739 women were booked for ANC and were eligible for the study. Initially, the total sample size was allocated to the facilities proportional to their ANC clients flow rate. Ultimately the individual women were selected using systematic random sampling technique with sampling interval of five.
Data were collected using pretested, structured and interviewer administered questionnaire by seven trained nurses and public health officers. Socio-demographic related questions were directly extracted from the standard Demographic and Health Survey (DHS) questionnaire [3]. Gestational age was determined based on women’s recall of last normal menstrual period. Knowledge of the mothers on anemia was assessed using a set of questions developed by the investigators. Dietary diversity of the women was assessed using the Women’s Dietary Diversity Score (WDDS) questionnaire of the Food and Agriculture Organization of the United Nations (FAO). The respondents were asked whether they ate from nine standard food groups in the previous day of the survey without setting minimum intake restrictions. Ultimately dietary diversity score (DDS) was computed out of maximum score of nine and categorized into low (<4), medium (4-5) or high (>5) [22]. Mid-upper arm circumference (MUAC) and height was measured following standard procedures.
Stool samples were collected from the women using clean screw-top containers on the day of the interview. Stool samples collected as part of the routine ANC are used for the study. The same day, stool microscopy was made at the respective health centers by five Bachelor’s degree holder laboratory technicians. Direct microscopy with Formalin-ether concentration technique was employed to identify the parasites [23]. In order to reduce inter-observer variation, stool samples were independently examined by two technicians.
Hemoglobin concentration was determined from a random finger-tip capillary blood using HemoCue 301. Hemoglobin measurements were adjusted for altitude according to the recommendation of the WHO [24] and, classified as normal (>11.0 g/dl) or mild (10.0-10.9 g/dl), moderate (7.0-9.9g/dl) and severe (<7.0g.dl) anemia.
This manuscript is organized according to the STrengthening the Reporting of OBservational studies in Epidemiology (STROBE) guideline and the STROBE checklist is provided as a supporting file (Supporting File 1)
Collected data were checked for completeness and consistency and entered into SPSS version 20 statistical package for analysis. Data were described using frequency distributions, tables and measures of central tendency and dispersion. The association between specific type of intestinal parasites and anemia was presented using chi-square or fisher exact test. Further, the relationship between intestinal parasitosis and anemia was determined using bivariable and multivariable binary logistic regression analyses and the outputs are presented using crude (COR) and adjusted (AOR) odds ratio. Independent variables having p-value of 0.2 or less in the bivariable models were considered as potential confounders, and hence adjusted in the multivariable model. The thirteen variables that were adjusted in the multivariable model were age, educational status, place of residence, monthly income, family size, birth interval, parity, history of deworming in the last 6 months, iron supplementation during the pregnancy, feeding pattern during pregnancy (as usual or more than usual), receiving nutritional counseling during pregnancy, MUAC and toilet ownership. In the multivariable model multicollinearity among independent variables was assessed using variance inflation factor (VIF) and found to be within acceptable limits (VIF< 10). The model goodness-of-fit was evaluated using the Hosmer-Lemeshow statistic.
Ethical clearance was obtained from Institutional Review Board of College of Medicine and Health Science, Hawassa University. Data were collected after taking informed verbal consent from each of the study participants. As all the study subjects were 18 years or above, consent was directly taken from them. Verbal consent, rather than written consent, was preferred because most of the study subjects did not have formal education. The same was approved by the institutional review board. Pregnant mothers found to have anemia and/or intestinal parasites were linked with clinicians at the health centers and received treatment.
Characteristics of the respondents
A total of 349 pregnant women following ANC took part in the study making the response rate 99.1%. The participants were selected from five health centers located at altitude ranging from 1,761 to 2,690 meters ASL. Nearly three-fourths (72.2%) of the study participants were drawn from the midland kebeles. The majority of the women (72.2%) were rural dwellers.
The mean (± SD) age of the women was 25.7(± 4.7) years and the vast majority (87.1%) were within the age bracket of 20 to 35 years. The majority of women worked as housewives (80.2%), were from the Sidama ethnic group (72.8%), were predominantly Protestant (85.4%) and nearly 1 in 3 (29.2%) were illiterate. The median monthly income was 2,500 Ethiopian birr (equivalence of 90 USD) and ranged from 600 to 5,995 birr. The average (± SD) household size was 4.8 (±1.8) (Table 1).
During the study the mean gestational age of the women was 26.6 (±5.5) weeks. Near to two-thirds (63.3%) were in their third trimester and the remaining (36.7%) were in the second trimester. The median parity was 2 and ranged from 0-8. About 18.6% and 11.7% of the study participants were nulliparas and grand multiparas, respectively. Among those who had at least two births before, 45.0% had short (less than 2 years) birth interval.
Three fourth (78.5%) of the respondents use piped water as their usual source of drinking water; while remaining 14.6% and 6.9% use protected and unprotected well/spring, respectively. Majority (81.4%) of the women reported that they somehow treat water before consumption. The approaches used for treating water include: adding disinfectants (74.3%), strain through cloth (16.9%), use of water filter (6.7%) and boiling (2.1%). About three-fourths (71.3%) owned a toilet facility.
Knowledge of pregnant women on anemia
Out of the 349 respondents, 76.8% reported they had ever heard of anemia before. Among those who were aware of anemia, 83.9%, 96.3% and 48.1% knew anemia during pregnancy can be caused by bleeding, under-nutrition and infections, respectively. Out of total respondents, 72.8% were aware of at least one possible consequence of anemia in pregnancy. The most frequently mentioned consequences were: perinatal mortality (92.5%), maternal mortality (82.3%), low birthweight (66.1%) and neonatal morbidity and mortality (55.5%). Three-fourths of the respondents (74.5%) knew anemia is a preventable condition. The most commonly cited preventive measures were: eating diversified diet (97.7%), taking iron and folic acid tablets during pregnancy (94.6%), birth spacing (88.46%), preventing infection including intestinal parasites (47.7%) and specifically taking deworming medications (43.0%).
Dietary diversity and nutritional status of pregnant women
The overall quality of diet of the pregnant women was also assessed based on the diet consumed in the preceding day. Cereals (99.1%), vitamin A rich fruits and vegetables (88.3%), roots and tubers (86.2%) and foods made of oil, fat or butter (83.1%) were consumed by the vast majority of the subjects. Legumes (69.6%) and milk or milk products (55.3%) were also taken by more than half of them. Food groups that were less frequently consumed were: other fruits (37.0%), other vegetables (23.5%), eggs (18.1%), flesh foods (12.6%) and fish (0.0%).
The mean (± SD) DDS was 4.0 (± 1.6). Only 19.5% consumed from 6 or more groups indicative of high dietary diversity. Conversely, 38.4% had medium (4-5 food groups) and 42.1% had low DDS (less than 4 food groups).
The mean MUAC of the respondents’ was 22.8 (±1.9) cm. About one-fifth (20.6%) of the pregnant women had MUAC less than 21cm suggestive of acute malnutrition. Smaller proportions (1.1%) of the pregnant women had short stature (height less than 145 cm).
Fifty five percent of the pregnant women took deworming medication at least once in the preceding 6 months of the survey. Similarly, 45.3% reported that they took iron supplement during the current pregnancy.
Prevalence of intestine parasitosis and anemia
The overall prevalence of intestinal parasite infection was 38.7% (95% CI: 33.6-43.8%). One-tenth (9.7%) were infected with polyparasites. A. lumbricoides was the most common infection (24.9%) followed by hookworms (11.2%), G. lamblia (5.4%), E. histolytica (3.4%), T. trichiura (2.9%) and S. mansoni (2.3%).
The mean hemoglobin concentration was 12.3 (±1.9) g/dl and ranged from 7.1 to 18.2 g/dl. It was found that 31.5% (95% CI: 26.6-36.4%) pregnant women were anemic. The prevalence of mild and moderate anemia were 21.5% and 10.0%, respectively. None of the women had severe anemia.
Association between intestinal parasitosis and anemia
The prevalence of anemia among pregnant women infected with intestinal parasite (55.6%) was significantly higher than the prevalence among women who were not infected (16.4%) (p<0.001). Nearly all of the mothers infected with hookworm (92.3%) were anemic. Further the prevalence of anemia was alarmingly high among mothers diagnosed with other parasites: G lamblia (78.9%), S mansoni (75.0%), E histolytica (50.0%), T trichiura (50.0%) and A lumbricoides 40.2%. Statistically significant association was observed between anemia and hookworm, G. lamblia, S. mansoni and A. lumbricoides infections (p<0.05) (Table 2).
The bivariable logistic regression analysis suggested women who were infected with intestinal parasites had 6 times increased odds of anemia (COR = 6.39, 95% CI: 3.89-10.50) as compared to their counterparts. In the multivariable model in which 13 potential confounders were adjusted, the odds of anemia were also six times increased (AOR=6.14, 2.04-18.45) among individuals infected with intestinal parasites (Table 3). The outputs of the full regression model is now provided as a supporting file (Supporting File 2).
The study suggested that more than one-third (38.7%) of pregnant women in Wondo Genert have intestinal parasitic infections and co-infection with polyparasites was common. Further, 31.5% have low hemoglobin level indicative of anemia. After adjusting for potential confounders, we observed a strong positive association between intestinal parasitic infection and anemia.
The prevalence of anemia reported in this study is within the 20 to 40% range indicative of moderate public health significance of anemia in a population [2]. Multiple community- or facility-based surveys in Ethiopia concluded the same [3,25-28]. The recent DHS found 24% of women of reproductive age and 29% of pregnant women in Ethiopia anemic [3]. Facility-based surveys in Butajira general hospital, Southern Ethiopia (27.6%) [25]; Bisdimo district hospital, Southeast Ethiopia (27.9%) [26]; Nekemte Referral hospital, Western Ethiopia (29%) [27]; and Arba Minch town health institutions, Southern Ethiopia (32.8%) [28], also reported comparable prevalence figures.
In this study the overall magnitude of the intestinal parasitic infection was 39%, with the highest prevalence for A. lumbricoides (25%) and hookworms (11%). Other studies in Ethiopia reported assorted magnitudes and patterns, suggesting the existence of substantial variation in the epidemiology of intestinal parasites in the country [13, 20, 28-30]. A study in Mecha district, Northwest Ethiopia reported an exceptionally high prevalence (70%) and identified A. lumbricoides (33%), S. mansoni (17%) and Hookworms (14%) as the predominant infections [29]. A study among pregnant women following ANC in a referral hospital in Northwest Ethiopia reported a comparable figure to our finding (32%) yet the major infections were protozoan: G. lamblia (13%) and E. histolytica (8%) [30]. A similar study conducted in a district hospital in Hossana town, reported 30% total prevalence and A. lumbricoides was the commonest infection affecting 10% of the women [20]. A study in West Gojam zone estimated 37% aggregate prevalence and, hookworm was most frequently encountered parasite (19%) [31]. A study in Western Ethiopia based on data from multiple health centers found 25% prevalence of parasitosis with the predominance of Hookworms (15%) followed by A. lumbricoides (7%) [13].
After controlling for potential confounders including multiple socioeconomic status indicators, we observed a statistically significant and strong association (AOR=6.14) between intestinal parasitosis and anemia. In Ethiopia, a couple of studies conducted in Eastern Wollega (AOR=1.8) and Gilgil Gibe Dam area (AOR=1.8) reported significant but weaker associations [13,32]. The differences observed in the strength of association can possibly be due to variation in intensity of parasitic infections or other contextual factors not studied in the study. As described earlier, the observed association could be explained by several biological mechanisms. Intestinal parasites may impair iron status by sucking blood from intestinal wall or by facilitating chronic blood loss, reducing appetite and nutrient intake, competing for micronutrients important for hematopoiesis and causing diarrhea/dysentery [10,11].
This finding may imply that, on top of the routine prenatal iron supplementation, preventive or therapeutic deworming integrated with ANC may help to reduce the burden of maternal anemia. From public health perspectives this would give more sense in consideration of the fact that merely half of the pregnant women in our study received deworming medications in the preceding 6 months. According to the national guideline of Ethiopia, pregnant women should be routinely dewormed in the second or third trimester of pregnancy. Yet, a national survey indicated that in 2016 only 6% of the pregnant women received deworming medication [3].
The strength of the study is the fact that it enrolled relatively large number of pregnant women (n=349) from multiple health facilities and presented prevalence figures for various intestinal parasites. Further, we attempted to measure and account for multiple confounders that can independently explain the association between the variables of interest. Yet, the following shortcomings should be taken into considerations while interpreting our findings. Like many other observational studies, we adjusted for potential confounders using regression model. Yet, residual confounding or confounding from unmeasured confounding (e.g. malaria, HIV, other co-morbidities) cannot be excluded. As nearly half of the study subjects received deworming treatment in the preceding 6 months of the survey, the study is likely to underestimate the underlying magnitude of the problem. Due to the cross-sectional nature of the study we could not be able to capture the seasonal variations in the prevalence of intestinal parasitosis. Previous studies have witnessed that prevalence of many intestinal parasites in human population is subjected to inter-seasonal fluctuation [33,34]. Further, as the study was limited to pregnant women attending ANC, the findings may not be directly extrapolated to pregnant women devoid of prenatal care. In addition, we did not measure intensity of parasitic infection and accordingly we did not manage to explore the does-effect relationship between intestinal parasitosis and anemia. It is also important to note that the study was only limited to intestinal parasitosis and did not look into the effect of malaria – an important hemoparasite in the locality.
The study indicated that 39% of the pregnant women in Shebedio district have intestinal parasitic infections and 32% were anemic. The most common types of intestinal parasites were A. lumbricoides and hookworm. Co-infection with multiple parasites was commonly encountered. Further, a strong association was observed between intestinal parasitosis and anemia. Strengthening the existing water, sanitation and hygiene programs and routine deworming of pregnant mothers may help to reduce the burden of anemia.
AOR Adjusted Odds Ratio
ANC Antenatal Care
ASL Above Sea Level
COR Crude Odds Ratio
CI Confidence Intervals
DHS Demographic and Health Survey
FAO Food and Agriculture Organization
LBW Low Birthweight
MUAC Mid-upper arm circumference
OR Odds Ratio
SD Standard Deviation
WDDS Women’s Dietary Diversity Score
WHO World Health Organization
VIF Variance Inflation Factor
Ethics approval and consent to participate
Ethical clearance was obtained from the Institutional Review Board of Hawassa University, College of Medicine and Health Sciences. Prior to data collection, verbal informed consent was obtained from the respondents. Verbal consent, rather than written consent, was preferred because most of the study subjects did not have formal education. The same was approved by the institutional review board.
Consent for publication
Not applicable
Availability of data and material
The datasets analyzed during the current study are not publicly available due institutional regulation but are available from the corresponding author on reasonable request.
Competing interests
The authors declare no competing interest.
Funding
The financial support for this study came from Hawassa University and Wonedo Genet Town Health Unit, Ethiopia. Both of the funding bodies did not involve in the collection, analysis, and interpretation of data and in writing of the manuscript.
Authors' contributions
AB conceived and designed the study; collected analyzed and interpreted the data; and drafted the manuscript. SG participated in the designing of the study and supervised of the fieldwork and the data analysis. Both the authors critically reviewed the manuscript for intellectual content and approved the final manuscript.
Acknowledgements
We are grateful to the Hawassa University and Wondo Genet District Health Unit for funding the study. We also like to sincerely acknowledge the managers of the health centers, study participants and the data collectors.
Table 1: Socio-demographic and economic characteristics among pregnant women attending antenatal care in health centers of Wondo Genet district, Southern Ethiopia, 2018.
|
Variables (n =349) |
Frequency |
Percent |
|
Age (years) |
|
|
|
18-20 |
36 |
10.3 |
|
20-35 |
304 |
87.1 |
|
>35 |
9 |
2.6 |
|
Ethnic group |
|
|
|
Sidama |
254 |
72.8 |
|
Oromo |
54 |
15.5 |
|
Amhara |
19 |
5.4 |
|
Others |
22 |
6.3 |
|
Religion |
|
|
|
Protestant |
298 |
85.4 |
|
Muslim |
33 |
9.5 |
|
Orthodox |
18 |
5.2 |
|
Place of residence |
|
|
|
Rural |
252 |
72.2 |
|
Urban |
97 |
27.8 |
|
Educational status (n=347) |
|
|
|
Illiterate |
102 |
29.2 |
|
Informal education |
35 |
10.0 |
|
Primary level |
147 |
42.7 |
|
Secondary level or above |
63 |
18.1 |
|
Education level of the husbands |
|
|
|
Illiterate |
72 |
20.6 |
|
Informal education |
51 |
14.6 |
|
Primary level |
115 |
33.0 |
|
Secondary level and above |
111 |
31.8 |
|
Occupation of the respondent |
|
|
|
Housewife |
280 |
80.2 |
|
Merchant |
39 |
11.2 |
|
Government employee |
25 |
7.2 |
|
Daily laborer |
5 |
1.4 |
|
Occupation (husband) |
|
|
|
Farmer |
176 |
50.4 |
|
Merchant |
105 |
30.1 |
|
Government employee |
48 |
13.8 |
|
Daily laborer |
20 |
5.7 |
|
Monthly income of the household (ETB) |
|
|
|
<2480 Eth birr |
166 |
47.6 |
|
>=2480 Eth birr |
183 |
52.4 |
|
Household size |
|
|
|
1-4 member |
178 |
51.0 |
|
>= 5 member |
171 |
49.0 |
Table 2: Association between specific types of intestinal parasitosis and anemia among pregnant women from Wondo Genet district, Southern Ethiopia, 2018.
|
Type of helminth infection |
Anemia |
Prevalence of anemia (%) |
Statistical test (p-value)× |
|
|
Yes |
No |
|||
|
Any helminth infection |
|
|||
|
Yes |
75 |
60 |
55.6 |
< 0.001* |
|
No |
35 |
179 |
16.4 |
|
|
Hookworm |
|
|||
|
Yes |
36 |
3 |
92.3 |
< 0.001* |
|
No |
74 |
236 |
23.9 |
|
|
Giardia lamblia |
|
|||
|
Yes |
15 |
4 |
78.9 |
< 0.001* |
|
No |
95 |
235 |
28.8 |
|
|
Schistosoma mansoni |
|
|||
|
Yes |
6 |
2 |
75.0 |
0.007* |
|
No |
104 |
237 |
30.5 |
|
|
Ascaris lumbricoides |
|
|||
|
Yes |
35 |
52 |
40.2 |
0.043* |
|
No |
75 |
187 |
28.6 |
|
|
Entamoeba histolytica |
|
|||
|
Yes |
6 |
6 |
50.0 |
0.205 |
|
No |
104 |
233 |
30.9 |
|
|
Trichuris trichiura |
|
|||
|
Yes |
5 |
5 |
50.0 |
0.298 |
|
No |
105 |
234 |
31.0 |
|
|
× Chi-square test for the first 5 variables and fisher exact test for the last 2 variables * Statistically significant difference at p-value of 0.05. |
||||
Table 3: Association between intestinal parasitosis and anemia among pregnant women from Wondo Genet district, Southern Ethiopia, 2018.
|
Intestinal parasitosis (n =349) |
Anemia |
COR |
AOR× |
|
|
Yes |
No |
|||
|
Yes |
75 |
60 |
6.39 (3.89-10.50)* |
6.14(2.04-18.45)* |
|
No |
35 |
179 |
1 |
1 |
|
×Adjusted for age, educational status, place of residence, family size, monthly income, birth interval, parity, history of deworming in the last 6 months, iron supplementation during the pregnancy, feeding pattern during pregnancy (as usual or more than usual), receiving nutritional counseling during pregnancy, MUAC and toilet ownership. |
||||