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Article

Soil-Transmitted Helminth Infections among Antenatal Women in Primary Care Settings in Southern India: Prevalence, Associated Factors and Effect of Anti-Helminthic Treatment

by
Revathi Ulaganeethi
1,
Ganesh Kumar Saya
1,*,
Nonika Rajkumari
2,
Swetha S. Kumar
1,
Kalaiselvan Ganapathy
3 and
Gowri Dorairajan
4
1
Department of Preventive and Social Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry 605006, India
2
Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry 605006, India
3
Department of Preventive and Social Medicine, Sri Manakula Vinayagar Medical College and Hospital, Puducherry 605602, India
4
Department of Obstetrics and Gynecology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry 605006, India
*
Author to whom correspondence should be addressed.
Trop. Med. Infect. Dis. 2023, 8(1), 48; https://doi.org/10.3390/tropicalmed8010048
Submission received: 22 November 2022 / Revised: 19 December 2022 / Accepted: 28 December 2022 / Published: 7 January 2023

Abstract

:
Community-based studies from India on prevalence of soil-transmitted helminth (STH) infections have reported estimates as high as 50% in children. However, prevalence estimates during pregnancy in India are lacking. We aimed to describe the burden, associated factors of STH and cure rate after deworming in primary care settings. Pregnant women were recruited from four urban and five rural centers in Puducherry, South India, from December 2019 to April 2022. One stool sample was collected from each participant before deworming and one repeat sample was collected from STH positive woman after three weeks of deworming. The samples were processed with saline; iodine wet mount, and microscopic concentration techniques. Cure rate (CR) was assessed using Kato–Katz thick smear. Of 650 women included, 49 (7.5%, 95% CI 5.6–9.8) had one of the STH infections; the prevalence of Ascaris lumbricoides, hookworm and Strongyloides was 5.4%, 1.8% and 0.3%, respectively. The prevalence of any STH was higher among ages 26–30 years (9.1%), working women (8.3%), multigravida (8.3%), urban setting (8.3%), those who did not wash their hands before food (9%) and anemic women (8.9%), compared to their counterparts, but not statistically significant. The CR for hookworm was 100% and Ascaris lumbricoides was 88.6%. To conclude, the prevalence of STH was low among pregnant women compared to school aged children. Continued deworming activities along with improved sanitation could further reduce the burden.

1. Introduction

Protozoans and soil-transmitted helminths are the two main groups that cause intestinal parasitic infections (IPI) in humans and are a major public health concern in low-and middle income-countries (LMICs) [1]. Soil-transmitted helminths (STH) comprise Ascaris lumbricoides, Necator americanus, Ancylostoma duodenale, and Trichuris trichura. Globally more than 3.5 billion people were affected by one of the parasites, out of which 450 million were experiencing symptoms [2]. Annually, an estimated 44 million pregnancies are affected by soil transmitted helminths [3]. In India, the prevalence ranges from 12.5% to 66%, with a varying prevalence for individual parasites [4] and these infections are common where the sanitation and hygiene is poor [5].
As per World Health Organization, preschool children, school going children, adolescent and reproductive age group women are at greater risk of STH infection. Undernutrition (macronutrient and micronutrient) and repeated infections, including parasitic infections, lead to adverse consequences that can continue from one generation to the next [6]. Intestinal helminth infections adversely affect the food intake and digestion thereby causing iron depletion and anemia [7]. Additionally, hookworm infections in pregnancy results in chronic blood loss from the intestine and aggravates the development of iron-deficiency anemia. Increased physiological demands of iron during pregnancy combined with malnutrition and hookworm infection leads to severe iron deficiency anemia. This results in increased maternal mortality, inadequate weight gain, intra-uterine growth retardation, and a low birth weight [8,9,10].
In India, the prevalence of STH among children was reported as high as 50% in a systematic review published in 2017 [11]. A community-based study conducted during 2017–2018 in southern part of India reported an age-adjusted prevalence of 21% across all age groups [12]. In a tribal population in southern part of India, the prevalence was estimated to be 39% [13]. Hospital based studies in pregnant women in India have prevalence ranging from 8.3% to 12.4% [14,15]. To eliminate the morbidity of STH in preschool and school children by 2030, breaking the chain of transmission is essential. This could be attained by improving sanitation and hygiene practices with preventive strategies. Hence, WHO implemented biannual deworming with 400 mg of albendazole to all high-risk groups including pregnant women [16]. In India, all pregnant women receive deworming medication after the first trimester. Physiological and hormonal changes during pregnancy may alter the response to deworming. Development of resistance to albendazole may be a challenge in control efforts of STH infection. Hence it is essential to monitor the effect of deworming medication on controlling the parasitic infections.
The prevalence of intestinal parasitic infection and its associated factors were well studied in children, but not many studies have been done on pregnant women. Considering the importance and consequences of STH in pregnancy, routine community-based epidemiological studies are of prime importance in this high-risk group to know the baseline prevalence of infection. Hence, we undertook the study to estimate the prevalence of STH infections and its associated factors in pregnant women of Puducherry, India. We also reported cure rate (CR) and egg count reduction rate (ERR) after deworming medication.

2. Materials and Methods

2.1. Study Design and Setting

A community-based cross sectional study was conducted among pregnant women attending antenatal clinics in different primary health centers (PHCs) of Puducherry district during December 2019 to April 2022. Puducherry is a Union Territory in the southern part of India with a population of approximately 13 lakhs with 69% residing in urban areas and 31% in rural areas [17] Literacy rate was 91% and 80% in men and women respectively. Approximately 17% of the population was involved in agriculture related work. Approximately 75% of the employment was in services and industries (working as skilled and semi-skilled laborer’s) [18]. The estimated per capita income was around 210 thousand Indian rupees (~2546 US$) in the financial year 2021 [19]. Almost all households (99.9%) had access to improved drinking water source like piped water, protected dug well, tube well, bore well and community RO plant [20]. Majority of the houses were pucca houses (walls and roof made of permanent materials like concrete/galvanized sheets with cemented floor).
Puducherry district has 27 primary health centers. Out of these, five urban and four rural were chosen by simple random sampling (Figure 1). In general, all pregnant women registered their pregnancy in PHCs in the first trimester. On registration, pregnant women received iron-folic acid and calcium tablets and tetanus toxoid injection. Deworming was given (a single dose of albendazole 400 mg) to all pregnant women during their second trimester of pregnancy without screening for a parasitic intestinal infection. All the supplements and deworming medications were provided free of cost. During the antenatal visits, hemoglobin was measured at the PHCs using a digital hemoglobinometer (Hbcheck, Biosense technologies Pvt.Ltd, Thane, Maharashtra, India).

2.2. Study Population

All pregnant women who were registered for antenatal care at selected PHCs (five urban and four rural) were considered as the source population. The women who visited the same during our sample collection period were considered our study population.

2.3. Inclusion and Exclusion Criteria

The pregnant women in any trimester of pregnancy before taking albendazole and willing to provide stool samples were included in the current study. Women who refused to provide stool samples were excluded.

2.4. Sample Size Estimation

Considering the prevalence of intestinal parasitic infection among pregnant women as 12.4% [15], absolute precision of 3, and design effect of 1.4, the calculated sample size was 649 for 95% confidence level. Open Epi version 3.01 was used for sample size calculation.

2.5. Methods

After obtaining the written informed consent, information regarding the women’s age, education, occupation, monthly household income, residence, gravida status, number of living children and behavioral characteristics were collected with the help of a questionnaire. Data on hemoglobin levels were extracted from individual case record of mothers and laboratory records maintained at PHCs. All the consecutive eligible pregnant women were enrolled in the study.
A labeled screw-capped plastic container was given to the pregnant women for the stool sample collection, and they were instructed to collect stool sample without urine contamination. Stool samples were transported to the laboratory within four hours of collection. The samples were screened with saline, iodine wet mount, and 10% formol- ether sedimentation microscopic methods for the presence of helminths and other parasites. Additionally, Kato-Katz egg counting method was done for STH positive samples. We informed the results to all the women. Those women who were STH positive were referred to the medical officer of the PHC for management. Additionally, the line list of STH positive women was shared with the medical officers of PHC to ensure administration of deworming tablets (a single dose of Albendazole 400 mg) as treatment. After three weeks, a repeat sample was collected from STH positive women who received deworming medication. The repeat sample was screened with Kato-Katz to calculate the cure rate (CR) and egg reduction rate (ERR). The number of eggs were multiplied by 24 to derive the number of eggs per gram of feces [21]. The slides were examined under 10× and 40× magnifications. The cure rate was calculated by dividing the number of women who became STH negative after treatment by the total number of STH positive women. Fecal egg count reduction was defined as 1-(mean fecal egg count in the post-treatment/mean egg count in the pre-treatment)*100 [22]. The women infected with Strongyloides had been excluded for the calculation of CR and ERR Since albendazole was not the drug of choice for strongyloides. Flow Chart 1 described the methods in short.

2.6. Quality Assurance

The collected stool samples reached the laboratory within four of collection. Hence, the motility of the trophozoites was appreciated. All of the samples were read by a single investigator, and all the positive samples and 10% of the negative slides were cross-checked by the laboratory supervisor to confirm the results.

2.7. Statistical Analysis

The collected data was entered in the EpiData manager and analyzed using Stata version 14.0 [23]. The presence of STH was reported as proportions with 95% confidence intervals (CI). Age was converted into age categories and hemoglobin values were categorized into normal (≥11 gm/dL), mild (9–10.9 gm/dL), moderate (7–8.9 gm/dL) and severe (<7 gm/dL) anemia and reported as percentages. Association of socio-demographic, behavioral and obstetric factors with STH infection was assessed using Chi squared test and crude prevalence ratios with 95% CI were reported. A log binomial regression analysis was done to find the independent association of risk factors with STH infection A p-value of less than 0.05 was considered statistically significant. CR and ERR was calculated and expressed as percentages.

3. Results

3.1. Socio-Demographic and Obstetric Characteristics of Pregnant Women

Out of 650 pregnant women included, nearly half of them, 317 (48.8%), were aged less than 25 years and 372 (58%) had completed bachelor’s or master’s degrees. Approximately half of the women (N = 323, 49.7%) were from rural areas. Of all the women, 205 (31.5%) were working.
Of all the participants, 385 (59.2%) were primigravida. In total, 283 (43.8%) had mild anemia, and 51 (7.9%) had anemia of moderate grade and 2 (0.3%) had severe anemia. In total, 49 (7.5%) women reported taking deworming medication within one year before pregnancy. Table 1 describes the socio-demographic and obstetric characteristics of the pregnant women included in the study.

3.2. Behavioral Characteristics of Pregnant Women

A total of 598 (92%) and 539 (82.9%) women respectively reported washing their hands after using the toilet and before eating food, with soap and water. More than half, 411 (63.2%), reported walking barefoot outdoors sometimes or always, and 35 (5.4%) practiced open defecation. The majority of them, 571 (87.9%) were drinking tap water, and three fourths reported boiling of water before drinking (Table 2).

3.3. Prevalence of STH Infections

Of 650 women, 49 (7.5%, 95% CI 5.6–9.8) were harboring any of the STH infection. The prevalence of Ascaris lumbricoides was the highest (5.4%, 35/650), followed by hookworm (1.9%, 12/650), and Strongyloides was seen in 2 (0.3%). Other parasite found were: Taenia (4/650) and Entamoeba histolytica (2/650) (Figure 2). The prevalence of any parasitic infection was 10.2%, (66/650, 95% CI: 7.9–12.7). One woman had a co-infection of Ascaris lumbricoides with hookworm species.

3.4. Factors Associated with STH Infections in Pregnancy

Prevalence of STH infections was 1.4 times higher in ages 26–30 years (9.1% vs. 6.3%) and 1.3 times higher in those more than 30 years (7.9% vs. 6.3%), when compared to 17–25 years. Nearly 1.4 times higher prevalence was observed in women residing in urban areas than rural (8.9% vs. 6.2%) The burden of STH was slightly higher in women who did not wash their hands before meals (9%), drank tap water (7.7%) and did not deworm in the previous year of pregnancy (7.7%) compared to women who washed their hands before food (7.2%), took purified water (6.3%) and who had dewormed in the previous year (6.1%). Though, these associations were not found to be statistically significant (Table 3). The prevalence of STH was higher in anemic women when compared to non-anemic women (5.8% in normal, 8.5% in mild, 9.8% in moderate and 50% in severe anemic) and an increasing trend was observed between the grading of anemia and STH prevalence (Chi squared for trend p value: 0.08).

3.5. Efficacy of Anti-Helminthic Treatment

Out of 47 women identified with STH infection other than Strongyloides, 43 had provided repeat stool samples after three weeks of deworming. The overall mean (SD) egg count in the pre and post treatment was 72.1 (35.2) and 3.3 (11.2) eggs per gram of stool. The overall cure rate was 90.7% (39/43, 95% CI 77.9–97.4). The mean (SD) egg count for Ascaris lumbricoides in the pre and post treatment was 72.1 (37.0) and 4.7 (13.0). For hookworm, it was 72 (30.7) in the pre-treatment and 0 count in the post treatment. The cure rate was 88.6% for Ascaris lumbricoides and 100% for hookworm. The egg reduction rate for Ascaris was 93.6%.

4. Discussion

The present study estimated the prevalence of STH infections among pregnant women and the effect of anti-helminthic treatment in primary care setting. The prevalence of STH was 7.5% and Acaris lumbricoides was predominant. Our study findings are similar to the prevalence estimates of 8.3% among pregnant women from a study conducted in the states of Rajasthan and Maharashtra from India [14]. Another hospital-based study from southern part of India reported the prevalence of 12.4%, which was slightly higher than the current study [15]. Another study done in Benin, Africa reported a prevalence of 13% and 9% in the first and second antenatal visits [24]. Two more studies in children had been published from the same setting reporting the prevalence of 34.6% in 2010 [4] and 6.4% in 2021 [25]. There was a major difference in the prevalence of helminth infection in our setting between 2010 and 2021. The difference might be due to the reason that in 2015, the Government of India launched a fixed day National Deworming day, wherein all children aged 1–19 years undergo deworming (single dose of Tab/Syrup) Albendazole 400 mg) to combat the infection [26]. In addition, Swachh Bharat Abhiyaan was also launched in 2014 to tackle the challenges related to water, sanitation, and hygiene [27]. These, with increased awareness, might reduce the existence of parasites in the study setting.
Other studies reported the burden of 51.5% in Ethiopia [28], 21.2% among refugees in Thailand [29], 38% in Gabon [30] and this was higher compared to the present study. Possible reasons for the high rate could be the differences in the method of diagnosis and poor living, environmental conditions and lack of awareness regarding the parasitic infections.
The present study revealed that the prevalence was slightly higher in women practicing barefoot walking outdoors, and were more likely to be infected with STH. These observations were in line with the findings of a review [31] and a study conducted in Ethiopia [28]. Barefoot foot walking outdoors increases the probability of carrying contaminated soil to home, which could be the reason for higher STH infection. In addition to this, hookworm larva could directly penetrate the skin and cause infection. The current study observed a higher STH burden in women with anemia. Similar findings were observed in a study among pregnant women in southern India [15] and Myanmar [29]. In our study, the prevalence was slightly higher in urban settings than in rural. This was contradictory to the other studies [14,32]. Puducherry, being a union territory, had no marked difference in the living conditions, education level, and health access between rural and urban areas. In addition, barefoot walking, overcrowding and usage of public toilets especially in urban slums might be the reasons of higher prevalence in urban pockets. Overall, there has been an improvement in adapting good practices over last few decades and it is possible that the above factors may not play a major role in the STH transmission. Furthermore, false reporting of behavioral practices cannot be ruled out.
In our study, we achieved a cure rate of 88.6% for ascaris with albendazole and 100% for hook worm. A Cochrane review reported the cure rate of 93% for ascaris [33]. Another review among pregnant women found CR of 90% for both ascaris and hookworm [34]. A review done in children showed that the CR after 400 mg of albendazole for hookworm was 53.3% [35]. A study among Rwandan children showed an overall cure rate of 88.6% and an ERR of 75.4% by wet mount microscopy, and in our study the CR was 90.7% [22].The cure rates depend on the individual parasitic load and the presence of parasites in the environment, which could cause reinfection. In addition, the cure rate depends on the number of doses, quality of the drug, and dosage [36,37].
To our knowledge, this was the first community-based study on STH involving pregnant women, recruited from five rural and four urban primary care settings in southern part of India. A single observer screened all the samples for STH infection; hence inter-observer bias was avoided. The study also reported the effect of use of 400 mg of albendazole for treating STH during pregnancy in primary care setting. We had collected one stool sample from each participant, and the results relied on only microscopic techniques; thus, there is a possibility of under estimation of prevalence because of lower sensitivity. Additionally, previous studies have shown misclassification of artefacts as Ascaris, thus human errors in diagnosis of Ascaris eggs cannot be ruled out. Eggs of the two species of hookworm cannot be differentiated with microscopic techniques. Further molecular studies are advisable to confirm the diagnosis and species differentiation.

5. Conclusions

The prevalence of STH infections was less among pregnant women in our setting compared to other regions. Mass deworming programs with improvement in water, sanitation and hygiene (WASH) measures help to interrupt the transmission and reinfection in the community, thereby reducing the burden further. Periodic assessment of prevalence of STH in pregnancy is recommended and this will help in deciding the deworming strategies in the national programs.

Author Contributions

R.U., G.K.S., N.R. and G.D. conceptualized and designed the study. R.U. collected and processed the samples. N.R. guided and supervised the process of lab work. R.U. analyzed the data and wrote the initial draft of the manuscript. S.S.K. assisted in sample collection, processing and formal analysis. G.K.S., N.R., G.D. and K.G. critically reviewed the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the intra mural grant from the tertiary institute located in Puducherry (Jawaharlal Institute of Postgraduate Medical Education and Research).

Institutional Review Board Statement

The study proposal was approved by the scientific advisory committee and Institute ethics committee of a tertiary care hospital in Puducherry (JIP/IEC/2019/137). Written informed consent was obtained from the participants.

Informed Consent Statement

Written informed consent was obtained from each participant before enrolling into the study. The consent includes participation, provision of initial sample and provision of repeat sample.

Data Availability Statement

The dataset used for this study are available with the corresponding author on a reasonable request.

Acknowledgments

We thank all the study participants who gave a sample for analysis and all the health workers from the primary health centers for their support.

Conflicts of Interest

The authors declare no conflict of interest with respect to research, authorship or publication of this article.

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Figure 1. Map showing the location of the Primary health centers included in the study in Puducherry district, South India during December 2019–April 2022. Map was created using QGIS (Free open source software) and map data was obtained from Open Street Map.
Figure 1. Map showing the location of the Primary health centers included in the study in Puducherry district, South India during December 2019–April 2022. Map was created using QGIS (Free open source software) and map data was obtained from Open Street Map.
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Chart 1. Flow diagram of study methodology.
Chart 1. Flow diagram of study methodology.
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Figure 2. Prevalence of parasites among ante-natal women in primary care settings from Puducherry (N = 650).
Figure 2. Prevalence of parasites among ante-natal women in primary care settings from Puducherry (N = 650).
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Table 1. Socio-demographic and obstetric characteristics of the pregnant women in primary care settings in Puducherry (N = 650).
Table 1. Socio-demographic and obstetric characteristics of the pregnant women in primary care settings in Puducherry (N = 650).
ParameterNumberPercentage
Age categories (Years)
Up to 2531748.8
26–3023235.7
>3010115.5
Occupation
Home maker44568.5
Working20531.5
Education
No/Up to primary172.7
Secondary to higher secondary25239.3
Bachelor/Master’s37258.0
Gravida
Primi gravida38559.2
Multi gravida26540.8
No of living children
None40261.9
One22334.3
Two or three253.8
Residence
Rural32349.7
Urban32750.3
Period of gestation
first28243.4
second34753.4
third213.2
Hemoglobin status (g/dl)
Normal (≥11 gm/dl)31048.0
Mild (9–10.9 gm/dl)28343.8
Moderate (7–8.9 gm/dl)517.9
Severe (<7 gm/dl)20.3
Table 2. Behavioral characteristics of the pregnant women in primary care settings in Puducherry (N = 650).
Table 2. Behavioral characteristics of the pregnant women in primary care settings in Puducherry (N = 650).
ParameterNumberPercentage
Handwashing after toilet use
No/sometimes528.0
Always59892.0
Handwashing before food
No/sometimes11117.1
Always53982.9
Walking barefoot in outdoors
No23936.8
sometime/always41163.2
Open defecation
No61594.6
Yes355.4
Drinking water
Tap57187.9
Purified7912.2
Nature of water
Boiled15023.1
Un boiled50076.9
Pet/Farm animal
No39360.5
Yes25739.5
Table 3. Factors associated with STH infections among pregnant women recruited in primary care settings in Puducherry, South India. (N = 650).
Table 3. Factors associated with STH infections among pregnant women recruited in primary care settings in Puducherry, South India. (N = 650).
ParameterTotalWomen with STH (n = 49)Unadjusted PRAdjusted PRp Value
Age categories (Years)
17–2531720 (6.3)11
26–3023221 (9.1)1.4 (0.8–2.6)1.3 (0.7–2.4)0.4
>301018 (7.9)1.3 (0.6–2.8)1.1 (0.5–2.5)0.87
Education
Up to primary school170
Secondary/Higher secondary25220 (7.9)1.1 (0.7–1.8)
Bachelor/Master’s degree37228 (7.5)1
Occupation
Working20517 (8.3)1.2 (0.7–2.0)
Not working44532 (7.2)1
Gravida
Primi38527 (7.0)1
Multi24322 (8.3)1.2 (0.7–2.0)
Number of living children
None40227 (6.7)11
One22318 (8.1)1.2 (0.7–2.3)1.2 (0.7–2.1)0.59
Two or three254 (16.0)2.4 (0.9–6.3)1.3 (0.4–4.7)0.7
Period of gestation
First trimester28222 (7.8)1.2 (0.7–2.1)1.3 (0.7–2.3)0.42
Second trimester34723 (6.6)11
Third trimester214 (9.1)2.9 (1.1–7.6)3.1 (0.4–4.7)0.02
Residence
Rural32320 (6.2)11
Urban32729 (8.9)1.4 (0.8–2.5)1.5 (0.9–2.7)0.14
Walking barefoot in outdoors
Always/sometime41134 (8.3)1.3 (0.8–2.4)
No23915 (6.3)1
Handwashing before meals with soap
No/some times11110 (9.0)1.2 (0.6–2.4)
Always53939 (7.2)1
Drinking water
Tap57144 (7.7)1.2 (0.5–3.0)
Purified795 (6.3)1
Nature of water
Boiled15011 (7.3)1
Not boiled50038 (7.6)1.03 (0.54–2.0)
Handwashing after toilet use
No/some times522 (3.9)0.5 (0.1–1.96)
Always59847 (7.9)1
Raw/unwashed vegetable
Sometimes29520 (6.8)1
Never35529 (8.2)1.2 (0.7–2.1)
Pet/Farm animals
No39333 (8.4)1.3 (0.8–2.4)
Yes25716 (6.2)1
Hemoglobin (g/dl) *
Normal (≥11)31018 (5.8)11
Mild anemia (9–10.9)28324 (8.5)1.5 (0.8–2.6)1.7 (1.0–3.2)0.07
Moderate anemia (7–8.9)515 (9.8)1.7 (0.7–4.3)2.0 (0.8–5.2)0.16
Severe anemia (<7)21 (50.0)8.6 (2.0–37.0)8.1 (1.3–50.5)0.03
H/o deworming in the previous year
Yes493 (6.1)1
No60146 (7.7)1.3 (0.4–3.9)
Open defecation
No61547 (7.6)0.7 (0.2–3.0)
Yes352 (5.7)1
* Hemoglobin values were missing for four participants, PR-Prevalence ratio. p value: adjusted for others.
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MDPI and ACS Style

Ulaganeethi, R.; Saya, G.K.; Rajkumari, N.; Kumar, S.S.; Ganapathy, K.; Dorairajan, G. Soil-Transmitted Helminth Infections among Antenatal Women in Primary Care Settings in Southern India: Prevalence, Associated Factors and Effect of Anti-Helminthic Treatment. Trop. Med. Infect. Dis. 2023, 8, 48. https://doi.org/10.3390/tropicalmed8010048

AMA Style

Ulaganeethi R, Saya GK, Rajkumari N, Kumar SS, Ganapathy K, Dorairajan G. Soil-Transmitted Helminth Infections among Antenatal Women in Primary Care Settings in Southern India: Prevalence, Associated Factors and Effect of Anti-Helminthic Treatment. Tropical Medicine and Infectious Disease. 2023; 8(1):48. https://doi.org/10.3390/tropicalmed8010048

Chicago/Turabian Style

Ulaganeethi, Revathi, Ganesh Kumar Saya, Nonika Rajkumari, Swetha S. Kumar, Kalaiselvan Ganapathy, and Gowri Dorairajan. 2023. "Soil-Transmitted Helminth Infections among Antenatal Women in Primary Care Settings in Southern India: Prevalence, Associated Factors and Effect of Anti-Helminthic Treatment" Tropical Medicine and Infectious Disease 8, no. 1: 48. https://doi.org/10.3390/tropicalmed8010048

APA Style

Ulaganeethi, R., Saya, G. K., Rajkumari, N., Kumar, S. S., Ganapathy, K., & Dorairajan, G. (2023). Soil-Transmitted Helminth Infections among Antenatal Women in Primary Care Settings in Southern India: Prevalence, Associated Factors and Effect of Anti-Helminthic Treatment. Tropical Medicine and Infectious Disease, 8(1), 48. https://doi.org/10.3390/tropicalmed8010048

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