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PLOS Neglected Tropical Diseases logoLink to PLOS Neglected Tropical Diseases
. 2014 Oct 16;8(10):e3248. doi: 10.1371/journal.pntd.0003248

Prevalence and Intensity of Soil-Transmitted Helminthiasis, Prevalence of Malaria and Nutritional Status of School Going Children in Honduras

Rosa Elena Mejia Torres 1,*, Dora Nelly Franco Garcia 2, Gustavo Adolfo Fontecha Sandoval 3, Adriana Hernandez Santana 4, Prabhjot Singh 5, Sandra Tamara Mancero Bucheli 5, Martha Saboya 6, Mirian Yolanda Paz 2
Editor: Nilanthi de Silva7
PMCID: PMC4199552  PMID: 25330010

Abstract

Background

Many small studies have been done in Honduras estimating soil-transmitted helminthiasis (STH) prevalence but a country-wide study was last done in 2005. The country has the highest burden of malaria among all Central American countries. The present study was done to estimate country-wide STH prevalence and intensity, malaria prevalence and nutritional status in school going children.

Methods and Findings

A cross-sectional study was conducted following PAHO/WHO guidelines to select a sample of school going children of 3rd to 5th grades, representative of ecological regions in the country. A survey questionnaire was filled; anthropometric measurements, stool sample for STH and blood sample for malaria were taken. Kato-Katz method was used for STH prevalence and intensity and rapid diagnostic tests, microscopy, and polymerase chain reaction (PCR) were used for malaria parasite detection. A total of 2554 students were studied of which 43.5% had one or more STH. Trichuriasis was the most prevalent (34%) followed by ascariasis (22.3%) and hookworm (0.9%). Ecological regions II (59.7%) and VI (55.6%) in the north had the highest STH prevalence rates while IV had the lowest (10.6%). Prevalence of one or more high intensity STH was low (1.6%). Plasmodium vivax was detected by PCR in only 5 students (0.2%), all of which belonged to the same municipality; no P. falciparum infection was detected. The majority of children (83%) had normal body mass index for their respective age but a significant proportion were overweight (10.42%) and obese (4.35%).

Conclusions

Biannual deworming campaigns would be necessary in ecological regions II and VI, where STH prevalence is >50%. High prevalence of obesity in school going children is a worrying trend and portends of future increase in obesity related diseases. Malaria prevalence, both symptomatic and asymptomatic, was low and provides evidence for Honduras to embark on elimination of the disease.

Author Summary

Soil-transmitted helminthiasis (STH) are one of the most important neglected infectious diseases (NID). These not only have the potential to affect the growth and development of children, but can have irreversible consequences that carry into adulthood. However its prevalence has not been estimated since many years in Honduras. Although Honduras is the country with the highest burden of malaria in Central America, efforts to reduce the number of cases due to Plasmodium falciparum have lead the country towards an initiative for elimination. Using common platforms to do mapping of NID allows countries to reduce costs, build local capacities and strengthen monitoring and evaluation systems to track progress towards control and elimination goals. Honduras, one of the poorest countries in Central America, took advantage of an initiative to establish the prevalence of STH in school age children to assess the prevalence of malaria as a step in compiling evidence to support a future process of elimination of the disease. This innovative manner to put together epidemiological information for several NID might be replicated in other countries in the Americas to produce baseline and follow-up data to support decision making for processes to reach the goals established for these diseases.

Introduction

Four nematode species are the most widely distributed and the most common in the world: Ascaris lumbricoides, Trichuris trichiura, and hookworms including Ancylostoma duodenale and Necator americanus [1][3]. Infestation with either one or more of these nematodes is referred to as soil-transmitted helminthiasis (STH). The Pan American Health Organization/World Health Organization (PAHO/WHO) estimates that globally almost 2 billion people are infected by schistosomiasis and STH and about 890 million children require treatment for STH [4], [5], while in the Latin American region it estimates that in 201346 million children are at risk of STH in 24 countries [6]. These estimates have been calculated based on the percentage of people without access to improved sanitation facilities, differentiated by rural and urban areas, due to the fact that STH prevalence and intensity of infection in LAC are not well mapped. The estimated disability adjusted life years (DALYs) represents a total loss of 3.8 million years due to STH globally [7]. The World Health Assembly in 2001 adopted a resolution which considers these parasites a serious public health problem [4], and in 2012 it further urged to expand interventions against these diseases [8].

As STH in children can affect their growth and development and can even lead to problems in adulthood, a multi-pronged strategy to control and prevent them involving various sections of the government and society has been advocated. Different control strategies for STH have been implemented in Latin American countries. Ecuador established a Program for Elimination of Intestinal Parasites (PEPIN) in 1994 and the Ministry of Health formed an alliance with the private organizations and volunteers involved in the deworming campaigns [9], [10]. In Honduras, deworming forms a part of the “Escuelas Saludables” or Healthy Schools Program which was started in 1998 and is carried out by the Ministry of Social Development. This program provides free lunch to children in public schools and carries out two deworming cycles annually in coordination with the World Food Program, among other activities, with an objective of providing an environment for adequate biological, social and emotional development of children [10]. On the other hand, data for prevalence of STH is lacking. The last country-wide prevalence study for STH was done in 2005 but was not published. The national surveillance system is not adequate for estimation of prevalence or for monitoring temporal trends of STH. Smith et al reported a prevalence of 45% for ascariasis and 38% for trichuriasis in four rural communities of the province of Francisco Morazan in Honduras in 1998 [11]. In 2005 a study to determine the intensity of STH, found that 47% of cases with severe ascariasis occurred in the province of Copan, and severe hookworm infection was found only in Copan and Colon [10]. Prevalence studies done from 2002–2006 showed an overall STH prevalence range from 12.2–97% at the province level for Honduras [12]. An unpublished study, conducted by W. Sosa, in Macuelizo valley of Santa Barbara in 2006 reported prevalence rates of 24% for ascariasis, 61% for trichuriasis and 5% for hookworm infections. More recently, a cross-sectional study among 320 school-children from Olancho reported an overall STH prevalence of 72.5% [13]. A systematic review of literature regarding the impact and prevalence of STH in Honduras during the last eight decades revealed an overall prevalence higher than 50% in more than 40% of municipalities [14].

Despite these studies and control efforts of various entities, risk factors for STH continue to be prevalent, information about STH prevalence is not available and impact of interventions not assessed. The impact of deworming component of Healthy Schools Program has never been evaluated. The Ministry of Health of Honduras carried out this study with the objective to determine the prevalence and intensity of STH in school going children, their nutritional status, and identifying local socio-demographic, cultural and environmental factors related to STH.

In Central America, Honduras is the country with the highest burden of malaria and the highest number of cases due to Plasmodium falciparum infection [15]. Prevention and control efforts by the national malaria program have had a big impact as evidenced by the decrease in cases, from 35,125 in 2000 to 9,628 in the year 2010. Furthermore, many municipalities have not reported a single locally acquired case of malaria over the past five years or more, laying grounds for a call towards elimination of malaria in Honduras. This study took advantage of an effort to establish baseline prevalence of STH in school children and included an assessment of the prevalence of malaria, both symptomatic and asymptomatic, among children as a step in identifying criteria for the efforts towards elimination of the disease in Honduras.

Materials and Methods

Ethical considerations

The study protocol was submitted to and approved by the Institutional Review Board of the Cardio-thoracic Hospital, Tegucigalpa. Written and informed consent of parents or teacher for all students assenting to participate in the study was taken 3 days prior to the survey. Either a parent or a teacher was present while the survey was being conducted and samples taken.

Study setting and population

A cross-sectional study was conducted with a randomly selected sample following PAHO/WHO guidelines [16]. Fifty students of third grade and between 9 and 10 years of age per school were to be included. In schools where third grade students were less than 50 in number, fourth and fifth grade students were included; the guidelines were thus adapted to the country setting. A sample size of 2554 school going children of the third, fourth and fifth grade of 50 schools in 44 of the 298 municipalities in the country was calculated to be adequate, with a sample of at least 50 students from each school. Representation of all 18 provinces and at least 300 students from each of the six ecological regions of the country was ensured (Figure 1). Students studying in the selected schools, assenting to participate in the study and with a written and informed consent of their parents or teachers were included, while those who could not submit a stool sample on the day of the study were excluded. Children below the age of 7 and older than 14 years at the time of study were excluded.

Figure 1. Ecological regions and municipalities selected for study, Honduras.

Figure 1

Honduras is divided into six ecological regions. Schools from forty four different municipalities representing all the six ecological regions were selected and surveyed.

The study was conducted under the leadership of the Sub-Secretariat of Population Risks of the Ministry of Health of Honduras and was carried out between March and December of 2011. A pilot test was done to validate the survey instruments in two schools of Francisco Morazan province, prior to their implementation. Six teams of investigators were formed and trained in the survey methodology and instruments. These teams simultaneously visited different areas of the country over a period of six weeks, each team visiting on an average 8 schools.

Field and laboratory procedures

An individual survey questionnaire was administered to each participating student to collect demographic information (age and gender) and risk-factors (hand washing, use of slippers, and availability of drinking water and toilets at home) and history of previous deworming treatment received. Information about treatment history and water treatment method used at home was asked to the parents when present, else the child was asked. Another questionnaire for information about schools (number of students by sex, highest grade and number of teachers), their conditions (availability of water, toilets and their condition and accessibility to health center) was filled for each one visited. Principals of the school provided the answers and conditions were physically verified by the survey team. Condition of toilet was assessed to be good, regular or bad based on a subjective evaluation by the survey team.

Weight of each child was measured using electronic weighing machines after removing shoes and heavy clothes. Height was measured after removing shoe and headgears, and making the child stand alongside a wall. A container for collecting stool samples was provided to the children a day before the survey and the method of collecting the sample was explained. Stool samples were collected at home by the majority of children, and for the rest samples at school were taken; one sample per child was taken. Blood sample from finger prick was taken for evaluation of hemoglobin levels and another sample was taken on filter paper to conduct nucleic acid assays for malaria. A malaria rapid diagnostic test (Bioline, Standard Diagnostic) was done and a blood slide taken for those reporting fever on the day of the survey. At the end of the study each student received one chewable tablet of 400 mg of albendazole as deworming treatment.

The stool samples were analyzed within two hours of receipt or saved in ice where time exceeded two hours. Samples were examined in the local health center or the school using the Kato-Katz methodology for determining the prevalence and intensity of STH. Intensity of STH was analyzed as eggs per gram of stool by trained microbiologists and laboratory technicians, and was classified according to WHO guidelines (Table 1) [16]. Blood samples were analyzed for anemia using a hemoglobinometer; values below 12 mg/dl and 7 mg/dl of hemoglobin were classified as anemia and severe anemia, respectively based on guidelines followed by the Ministry of Health. Microscopic slide examination and RDTs were used for malaria diagnosis for children reporting fever, while a polymerase chain reaction (PCR) examination was carried out for all children. Detection of parasite's DNA in blood samples on filter paper was performed according to Singh et al and after a Chelex-based DNA extraction method [17], [18]. WHO Reference 2007 standard for 5 to 19 years old was used for classification of children based on body mass index (BMI) as severely thin (<−3 standard deviations), thin (<−2SD), overweight (>+1SD) and obese (>+2SD) [19], [20]. Height for age and weight for age for children less than ten years old was calculated using the WHO reference.

Table 1. Classification criteria for intensity of STH.

STH infection* Severity of Infection (eggs per gram)
Mild Moderate Severe
Ascaris lumbricoides 1–4,999 5,000–49,999 ≥50,000
Trichuris trichiura 1–999 1,000–9,999 ≥10,000
Hookworms 1–1,999 2,000–3,999 ≥4,000

* STH: Soil transmitted helminthiasis.

Statistical analyses

Double data entry was done in Epi-info and Epi-Info, SAS and Arc-GIS were used for analysis and creating tables, graphs and maps. Anthropometric data was analyzed using Anthro-plus [21]. Univariate and multi-variate analyses of prevalence and intensity of STH was done with the socio-demographic indicators of age, sex, ecological region, risk-behaviors such as hand-washing and use of slippers, previous history of deworming treatment, drinking water and use of toilets. School level prevalence was analyzed with information on participation of the school in the Healthy Schools Program, drinking water facilities, condition of toilets and distance from the nearest health center. Prevalence of symptomatic (fever at the time of study) and asymptomatic malaria was estimated.

Results

A little more than half of the 2554 students enrolled in the study were females and most of the students were between 8 to 11 years old (Table 2). PAHO/WHO advises to select students of third grade and between 9 and 10 year olds; however the pilot study had found many students of 7 years in 3rd grade. Children up till 14 years in higher grades had to be selected to complete the sample of at least 50 per school.

Table 2. Children surveyed and infected according to demographic characteristics.

Category Children surveyed Children infected P-value*
Ascariasis Trichuriasis Hookworms All STH
N (%) % % % % (95% CI)
Age 0.001
7 24 (0.9%) 25.0% 37.5% 0.0% 50.0 (30.0, 70.0)
8 393 (15.4%) 17.6% 30.3% 1.5% 36.6 (31.9, 41.4)
9 978 (38.3%) 18.7% 32.7% 0.4% 41.1 (38.0, 44.2)
10 635 (24.9%) 22.8% 32.1% 0.6% 42.5 (38.7, 46.4)
11 405 (15.9%) 27.4% 39.3% 1.2% 51.1 (46.2, 56.0)
12 96 (3.8%) 46.9% 52.1% 1.0% 64.6 (55.0, 74.2)
13 18 (0.7%) 44.4% 33.3% 11.1% 66.7 (44.9, 88.4)
14 5 (0.2%) 40.0% 20.0% 0.0% 40.0 (0.0, 82.9)
Sex 0.011
Males 1223 (47.9%) 23.0% 35.8% 0.7% 46.1 (43.3, 48.9)
Females 1331 (52.1%) 21.6% 32.3% 1.1% 41.1 (38.5, 43.7)
Ecological Region 0.001
I 713 (27.9%) 24.0% 42.5% 0.4% 49.2 (45.6, 52.9)
II 347 (13.6%) 28.5% 47.6% 2.3% 55.6 (50.4, 60.8)
III 405 (15.9%) 22.5% 33.3% 0.2% 43.2 (38.4, 48.0)
IV 360 (14.1%) 4.2% 6.9% 0.0% 10.6 (7.4, 13.7)
V 431 (16.9%) 31.8% 17.4% 2.1% 40.8 (36.2, 45.5)
VI 298 (11.7%) 18.8% 55.4% 0.3% 59.7 (54.2, 65.3)
Total 2554 569 (22.3%) 868 (34%) 22 (0.9%) 43.5 (41.6, 45.4)

*Association of demographic indicator with all children infected with STH.

STH: Soil transmitted helminthiasis; CI: Confidence Interval.

Soil transmitted helminthiasis prevalence

Of the children studied, 43.5% had one or more STH. Trichuriasis was the most prevalent infection and affected 34% of children, ascariasis 22.3% and only 22 children had hookworm infection. Hymenolepsis nana (n = 22), Strongyloides stercoralis (n = 9) and Enterobius vermicularis (n = 2) were also found. Ecological region VI formed of the Bay Islands and a major tourist spot, had the highest STH prevalence (59.73%) and region II in the north of the country also had more than half the children infected (Figure 2). All other regions had more than 40% STH prevalence rates except region IV in the south of the country. Males had higher prevalence of ascariasis, trichuriasis and any STH and had 23% (1.23; 95% CI 1.05–1.44) higher odds of having STH than females. More than one STH was present in 14.6% of children (Table 3). Prevalence of one or more heavy STH was low and most children had only moderate or light STH.

Figure 2. Prevalence of any STH by ecological regions, Honduras.

Figure 2

Total prevalence of having any soil transmitted helminthiasis (STH) including ascariasis, trichuriasis or hookworm by six ecological regions of the country is shown in this map. Region II & VI had the highest prevalence while Region IV had the lowest.

Table 3. Children infected by severity of infection.

Type of STH infection Severity of Infection
Severe Moderate Mild
Ascariasis 24 (0.9%) 233 (9.1%) 312 (12.2%)
Trichuriasis 20 (0.8%) 163 (6.4%) 685 (26.8%)
Hookworms 0 2 (0.1%) 20 (0.8%)
All STH 40 (1.6%) 308 (12.1%) 738 (28.9%)

STH: Soil transmitted helminthiasis.

Anemia and nutritional status

Anemia was detected in 19.2% of children but only five children (0.2%) had severe anemia (Table 4). Using WHO reference for BMI, 2.3% children were thin or severely thin (<−2SD), but 10.4% were overweight and another 4.4% were obese. A similar pattern was seen in children up to 10 years of age, where over 12% had more than +1 SD weight-for-age and 84% were normal. Stunting (<−2SD height-for-age) was found in 11% of the children and 82% were normal. Childhood obesity was highest in region VI where almost 25% of the children were either obese or overweight followed by almost 19% in region IV. Regions II, III & VI had slightly higher proportion of children who were thin or severely thin than the national average. Two of these regions, II & VI, also had the highest prevalence of anemia. No relation was observed between thinness and prevalence of any STH (Chi-square: 3.101, p-value: 0.68).

Table 4. Malaria, anemia and nutritional status in children surveyed.

Ecological Region Children surveyed Confirmed malaria* Anemia Obese Overweight Thinness or severe thinness
N N N (%) N (%) N (%) N (%)
I 713 0 93 (13.0%) 22 (3.1%) 68 (9.5%) 13 (1.8%)
II 347 0 148 (42.7%) 19 (5.5%) 36 (10.4%) 14 (4%)
III 405 5 47 (11.6%) 11 (2.7%) 36 (8.9%) 12 (3%)
IV 360 0 59 (16.4%) 22 (6.1%) 46 (12.8%) 6 (1.7%)
V 431 0 62 (14.4%) 10 (2.3%) 32 (7.4%) 5 (1.2%)
VI 298 0 81 (27.2%) 28 (9.4%) 48 (16.1%) 8 (2.7%)
Total 2554 5 490 (19.2%) 112 (4.4%) 266 (10.4%) 58 (2.3%)

*Using polymerase chain reaction.

Obese (>+2 Standard deviations), Overweight (>+1 SD & ≤+2SD), Thin (<−2 SD and ≥−3SD) and Severe thinness (<−3 SD) according to WHO standards.

STH risk factors

Of those responding, 95% of children washed their hands and had half the odds of having STH than those who didn't wash hands regularly (Table 5). Private tap water was the source of drinking water for more than half of the children while purified water was the second most common source. Water from wells and public taps were other frequent sources of drinking water while rain water and rain water harvesting were rare sources. Compared to those who used private tap water, children where the household used well water had significantly higher STH prevalence rates, meanwhile those using purified water had significantly lower rates. Slightly more than half of the houses of children used some form of purification method for drinking water. Chlorine tablets and boiling water were the most common methods for water purification. Children residing in houses which used boiling or other forms (except boiling and chlorine tablets) of water purification had significantly lesser odds of having STH than those where no water purification method was used, but use of chlorine tablets was not associated with any significant decline in odds of having any STH.

Table 5. Children surveyed and infected according to risk factors.

Category Sub-category Children surveyed Children infected Odds ratio§
N % Ascariasis % Trichuriasis % Hookworm % All STH % (95% CI)
Hand-washing 2518 98.6%
No 121 4.7% 24.0% 57.0% 1.7% 60.3 (51.6, 69.0) *
Yes 2394 93.7% 22.2% 32.8% 0.8% 42.6 (40.6, 44.6) 0.488
Sometimes 3 0.1% 0.0% 0.0% 0.0% 0.0%
Sanitary service in house 2529 99.0%
No 114 4.5% 33.3% 46.5% 1.8% 57.0 (47.9, 66.1) *
Yes 2415 94.6% 21.4% 33.6% 0.8% 42.7 (40.8, 44.7) 0.563
Use of toilets 2341 91.7%
Never 7 0.3% 42.9% 42.9% 0.0% 57.1 (20.5, 93.8)
Sometimes 304 11.9% 24.7% 43.4% 0.0% 50.3 (44.7, 55.9) *
Always 2030 79.5% 21.1% 32.4% 1.0% 42.1 (39.9, 44.2) 0.717
Source of Drinking Water 2548 99.8%
Private tap water 1431 56% 24.6% 34.2% 1.1% 44.9 (42.3, 47.4) *
Well water 197 7.7% 44.7% 51.3% 1.0% 62.9 (56.2, 69.7) 2.088
Public tap water 156 6.1% 17.3% 21.8% 0.6% 35.9 (28.4, 43.4) 0.688
Harvested rain water 22 0.9% 27.3% 36.4% 0.0% 45.5 (24.6, 66.3) 1.024
Rain water 44 1.7% 34.1% 54.5% 0.0% 61.4 (47.0, 75.8) 1.952
Purified 808 31.6% 13.1% 31.6% 1.0% 37.3 (33.9, 40.6) 0.730
Other 13 0.5% 30.8% 38.5% 0.0% 46.2 (19.1, 73.3) 1.053
Type of Treatment of Drinking water 2098 82.1%
None 1027 40.2% 25.1% 37.8% 0.4% 48.2 (45.1, 51.3) *
Chlorine tablets 411 16.1% 29.0% 38.9% 1.0% 49.4 (44.6, 54.2) 1.049
Boiling 356 13.9% 21.1% 23.6% 1.7% 38.8 (33.7, 43.8) 0.680
Other 297 11.6% 16.5% 35.4% 1.7% 39.7 (34.2, 45.3) 0.708
Don't know 7 0.3% 14.3% 57.1% 0.0% 57.1 (20.5, 93.8) 1.433

*Reference group.

§

Association with all STH infections.

Significant at p-value = 0.05.

Almost all (99%) children used slippers, and a majority of these always used slippers. Open slippers were more commonly used than closed slippers (Table 6). Slippers were used while going to school by almost 90% of the children, but almost or less than one-third of these used slippers at home, for playing outside or while going to church. Although history of deworming treatment was not significantly related to STH rates, children who had recently received deworming treatment (<3 months) had half the odds of having STH than those who had not received any treatment.

Table 6. Children surveyed and infected according to risk factors.

Category Sub-category Children surveyed Children infected Odds ratio§
N% Ascariasis % Trichuriasis % Hookworm % All STH % (95% CI)
Use of slippers 2546 99.7% -
No 24 0.9% 41.7% 29.2% 4.2% 50.0 (30.0, 70.0)
Yes 2522 99.1% 22% 33.9% 0.8% 43.5 (41.5, 45.4)
Frequency of use of slippers Always 1220 48.4% 35.1% 53.9% 1.6% 39.1 (36.4, 41.8) -
Sometimes 1122 44.5% 6.7% 11.8% 0.0% 46.1 (43.2, 49.0)
Type of slippers 2364 92.6% -
Open 1312 55.5% 22.4% 40.6% 0.8% 47.8 (45.1, 50.5)
Both 286 12.1% 19.6% 31.1% 0.7% 39.5 (33.8, 45.2)
Closed 766 32.4% 22.6% 27.9% 0.9% 40.7 (37.3, 44.2)
Place of using slippers 2522 98.7% -
Home 866 34.3% 23.1% 25.4% 0.8% 37.8 (34.5, 41.0)
School 2243 88.9% 22.6% 35.3% 0.8% 44.8 (42.7, 46.9)
Church 974 38.6% 23.6% 28.7% 0.6% 40.2 (37.2, 43.3)
Playing outside 773 30.7% 23.8% 26.1% 0.8% 39.2 (35.8, 42.6)
Others 254 10.1% 30.7% 21.7% 0.4% 40.9 (34.9, 47.0)
History of deworming 2537 99.3%
No 326 12.8% 25.8% 35.9% 0.6% 47.2 (41.8, 52.7) *
Yes 2211 87.2% 21.7% 33.8% 0.9% 43.0 (40.9, 45.0) 0.841
Time since deworming treatment Never 326 12.8% 25.8% 35.9% 0.6% 47.2 (47.2, 47.2) *
>3 months 1748 68.9% 23.9% 36.5% 1.0% 45.9 (43.6, 48.3) 0.949
<3 months 452 17.8% 13.1% 23.5% 0.4% 31.6 (27.3, 35.9) 0.517

*Reference group.

§

Association with all STH infections.

Significant at p-value = 0.05.

- Association not investigated.

School characteristics

Sixty eight per cent of the schools in the study were part of the Healthy Schools Program and 82% of all schools were within 3 kilometers of a health center (Table 7). On an average the teacher-student ratio was 1∶25 in the schools studied. All except one school had toilets, and most of these toilets were either in good or acceptable conditions. Three schools didn't have a water source and another four didn't have a potable water source. In only 56% of the schools was the water source close-by. When relating STH prevalence rates to school characteristics, it was found that children from schools included in Healthy Schools Program had 24% higher odds of having STH. Better condition of school toilets was directly related to lower odds of STH prevalence rates, as also the availability of drinking water in the school and the relative closeness of the water source to the school. Schools with better health infrastructure close-by also had lower prevalence of STH in children.

Table 7. School characteristics and STH prevalence rates.

School characteristics Sub-category Number of schools STH Prevalence- children infected Odds ratio§
N N %
Total Schools 50
Number of students 385.8 (252.5)
Male 193.5 (128)
Female 192.3 (125.1)
Number of teachers 15.1 (9.4)
School included in Healthy School Program
No 16 323 39.88% *
Yes 34 788 45.18% 1.24
Water source available
No 3 81 55.48% *
Yes 47 1030 42.77% 0.6
Type of water available
Non-potable 7 158 47.73% *
Potable 40 872 41.98% 0.79
Water source close to school
No 22 662 45.19% *
Yes 28 449 41.23% 0.85
Type of toilet
None 1 34 68.00% *
Latrine (only) 14 129 36.24% 0.27
Sanitary Service (only) 28 773 43.82% 0.37
Both 7 175 45.57% 0.39
Condition of toilets
Good 28 566 39.97% *
Regular 14 325 45.84% 1.27
Bad 7 186 49.08% 1.45
No toilets 1 34 68.00% 3.19
Distance of closest health center from school (km) 1.649 (2.574)
Type of Health Center
Hospital 4 140 72.54% *
Health Center with a Doctor 36 726 39.07% 0.24
Health Center with a Nurse 7 181 50.00% 0.38
Other 3 64 45.39% 0.31

Mean (Standard deviation) for continuous variables.

*Reference group.

§

Association with all soil transmitted helminthiais (STH).

Significant at p-value = 0.05.

Malaria prevalence

Twelve of all the students surveyed had fever at the time of the study, but all of these were negative for malaria by RDTs and by microscopy. Only 5 of the 2554 student blood samples analyzed by PCR amplification demonstrated presence of malaria parasite and all of these were P. vivax (Table 3). No P. falciparum infection was found in any sample. All these five students were asymptomatic at the time of the study and belonged to the municipality of Wampusirpi, which is known to be historically endemic for malaria, in Gracias a Dios province in the eastern part of ecological region III. No infections due to either P. vivax or P. falciparum were found using PCR as the diagnostic method in any other region of the country.

Discussion

Prevalence rates for all STH, ascariasis and trichuriasis found in this study are similar to other previous studies but not so for hookworm infections. A study done by PAHO/WHO based on data published between 2000 and 2010 showed that 83.3% of data points found for STH prevalence for Honduras correspond to prevalence above 20% [22]. A prevalence study in Olancho province in region III in 2011 showed an overall prevalence of 72.5% for all STH, 30% for ascariasis, 67% for trichuriasis and 16% for hookworms [13].

A hospital based study of both inpatients and outpatients found hookworm prevalence rates of 0.7% and 1.5% respectively, similar to ours [23]. A study done in Atlantida (primarily Region II) and Choluteca (Region IV) in 2002 found a hookworm prevalence rate of 30–40% and 3–10% respectively in children less than 10 years of age and 40–60% and 8–10% in 10–19 year olds respectively [24]. Detection of hookworm eggs requires immediate study of stool samples which was not possible in our study owing to inadequate infrastructure in remote locations [25]. Stool samples from students had to be transported to a facility where electricity was available and in some cases could only be studied at the end of the day. This could have led to an underestimation of hookworm infection prevalence in our study.

Under the Healthy Schools Program, the Ministry of Education of Honduras in partnership with World Food Program has been deworming school age children (SAC) in schools. In 2010 it reported that 1,305,302 of an estimated 1,832,476 SAC were treated with preventive chemotherapy with a coverage of over 70% of SAC at risk which decreased to 61% in 2011 [26], [27]. However, the information regarding performance indicators such as program, geographical and national deworming coverage is not accurate. Our results show that children studying in schools included in the Healthy Schools Program had significantly higher odds of having STH. This is worrying and contrary to what is expected considering six monthly deworming campaigns in many of these schools over many years.

However, it is well documented that both host-specific and environmental factors may affect the risk of acquiring or harboring heavy-intensity helminth infections [28]. Specific occupations, household clustering, and behaviors influence the prevalence and intensity of helminth infections. STH and other helminthiases depend on environments contaminated with egg-carrying feces for transmission. Consequently, they are intimately associated with poverty, poor sanitation and lack of clean water. Due to these aforementioned factors, careful analysis of the finding of high prevalence in schools implementing the Healthy Schools Program in our study is required.

The most striking epidemiological features of human helminth infections are aggregated distributions in human communities, predisposition of individuals to heavy (or light) infection, rapid reinfection following chemotherapy, and age-intensity profiles that are typically high in children and older adults (with the exception of hookworm). The latter was also seen in our study as the odds of being infected with any STH increased by 22% (1.22; 95% CI: 1.13–1.30) for every one year increase in age of children. The rate of reinfection is specific to certain species of helminths and depends on the life expectancy of that species (short-lived helminths reinfect more rapidly), on the intensity of transmission within a given community, and on the treatment efficacy and coverage [28]. School-age children typically have the highest intensity of worm infection of any age group, and chronic infection negatively affects all aspects of children's health, nutrition, cognitive development, learning, and educational access and achievement [29]. However, the benefits of a school-based control program should also be extended to other high-risk groups (i.e. preschool children and pregnant women) and to the community at large to tackle STH prevalence [16]. A more comprehensive and coordinated approach is required in Honduras with the integration of deworming to other public health platforms to target other populations groups at risk of soil transmitted helminthic infection, as well as to integrate actions for hygiene education, water and sanitation to accelerate efforts towards STH control goals. Although the soil transmitted helminthic infections are neglected diseases that occur predominantly in rural areas, the social and environmental conditions in many unplanned slums and squatter settlements of developing countries are ideal for the persistence of A. lumbricoides.

If the results of our study were taken as a baseline by the Ministry of Health of Honduras in order to implement a plan to increase deworming for STH in the country, provinces and municipalities in ecological regions II and VI in the north would require targeted drug administration for STH twice a year, while regions I, III and V would require it once according to WHO guidelines [16]. Although STH prevalence in region III in the east was less than 50%, two municipalities of Gracias a Dios province had more than 90% surveyed children infected. Although the data is not representative for the province, given the low access to safe drinking water, basic sanitation and remote location, a twice-annual targeted drug administration in the province can be considered. Region IV in the south had less than 20% prevalence of any STH yet the Ministry of Health could decide to maintain the targeted drug administration at least once a year as municipalities in that region also have low rates of access to safe water and basic sanitation.

In the study done by PAHO/WHO for the period 2000–2010, 27.9% of data points found for Honduras showed heavy intensity of infection and 46.2% moderate intensity [22]. Our study found low prevalence of severe intensity infections that concurs with finding of low prevalence of anemia in the children studied. However, 12.1% of the infections were moderate. Moderate to heavy intensity infections have been documented to have significant implications for children's physical and cognitive development, as well as for severe or even fatal complications among children below 15 years of age, especially school age children [2], [30], [31]. Massive and sustained deworming has an important impact on the reduction of intensity of infection and this has a remarkably positive impact on the well-being of children [1].

Established risk factors such as hand washing, water and sewage services were significantly associated with STH prevalence rates. Most children had good hand washing habits and used toilets for their daily needs. However, water purification is done in few households and it is a continuing challenge in several parts of the country where formal public water distribution systems are still not available or are of low quality. Although almost all children replied that they used slippers and especially so while going to school, only a few used them at home or while playing outdoors. Health education interventions need to focus on promotion of use of slippers in children not only when going to school but throughout the day and in all places. Improving access to clean drinking water and good condition of toilets in schools are vital as they were directly related to lower STH prevalence. The reduction in infection prevalence will be slower if interventions rely only on deworming, as it depends on the effect of other social determinants such as access to safe water, basic sanitation, nutrition, use of footwear and housing improvement (e.g., eliminating dirt floors, adding ventilation, lighting), amongst others [1].

In 2005, Riviera found that 13.5% of school going children were overweight and 6.4% were obese in Tegucigalpa, the national capital (Region IV) [32]. In a recently concluded national demographic health survey (DHS) in 2011–12, 5.1% of children born since January 2006 were reported to be either obese or overweight [33]. The global school-based student health survey conducted in 13–15 year old students in 2012 in Honduras found 2.9%, 5.6% and 17.8% to be underweight, obese and overweight respectively [34]. Our study has found similar results in school going children. The trend of onset of obesity very early in childhood is worrying and portends of an adult population with much higher rates of obesity and associated morbidities in the near future in the country. Health and nutritional education along with physical activity programs are of utmost importance given the epidemic state of obesity in the country. On the other hand anemia in DHS was 29% in 6–59 month year olds, much higher than that in our study; however the same study also concluded that less than 1% had severe anemia similar to our results. These results reveal the precarious situation the country is in, where both under-nutrition and over-nutrition prevalence is high in children presenting significant challenges in tailoring nutritional interventions.

The very low prevalence of malaria, both symptomatic and asymptomatic, concurs with the low or no transmission of the disease in most parts of the country. All five cases of asymptomatic malaria were from the same municipality, which has historically been hyper-endemic for the disease [35]. Children sick with malaria (symptomatic) may not have attended the school on the day of the study and this could have led to an underestimation. In a malaria transmission area, asymptomatic malaria prevalence is considerable owing to immunity [36]. This study demonstrates very low prevalence rate of asymptomatic malaria carriers in children all over the country estimated using a very sensitive technique (PCR), including areas of highest malaria transmission in the country like Wampusirpi municipality (10%; 95% CI: 1.68, 18.32) in the eastern part of ecological region III. However, Honduras reports the highest number of malaria cases in Central America and the maximum number of cases are in adults. Achieving the recently declared malaria elimination goal by the council of health ministers of these countries would require surveys including residents of all ages in present or historic malaria endemic communities to find asymptomatic cases [37].

It is necessary to formulate an operational plan of action for control of STH in Honduras with the aim to integrate efforts to implement not only deworming activities but interventions to increase access to hygiene education, safe water and basic sanitation. The results of this study can be used as baseline and for monitoring the progress towards control goals of STH. The Ministry of Health of Honduras launched its national plan of action for prevention, control and elimination of nine neglected infectious diseases including STH for 2012–2017, and it is working on subnational operational plans to implement actions in priority provinces. This plan is steered by a national committee integrated by delegates of public health programs, the Ministry of Education, Non-Governmental Organizations, international organizations, donors and partners that meet monthly for monitoring the progress on the implementation of actions. Due to this national effort, deworming activities are moving forward in an integrated way since 2013, reaching pre-school age children and school age children.

As part of the monitoring of the progress towards control of STH and surveillance for malaria in the scenario of its possible elimination in Honduras, some joint activities of surveillance could be implemented in an integrated manner, for instance, through sentinel surveillance of some indicators. WHO recommends monitoring parasitological indicators for STH just before a drug administration round. Monitoring at this point will provide reliable information on reinfection occurring since the previous treatment, allowing the impact of previous treatment cycle(s) to be assessed. These data are normally collected in sentinel sites (sentinel schools) where a sample of schoolchildren should be selected in each of the ecological zones of the country [16]. Using the same platform, samples for malaria could be taken to monitor the rate of asymptomatic malaria carriers in children as part of surveillance for elimination. This is a great opportunity to improve coordination and intersectoral actions with the aims to reach STH control goals and malaria elimination.

Supporting Information

Checklist S1

STROBE checklist.

(DOC)

Acknowledgments

The authors would like to thank health personnel and teachers of the provinces and municipalities surveyed, who actively participated in the study. Dr. Maria Paz Ade provided support in drafting of the protocol. Dr. Franklin Hernandez, Dr. Carlos Ponce, Dr. Fabiola Prado & Monica Heinheman helped in collection and analysis of data and in drafting of the first report. Laura Catala reviewed initial draft of the article and provided valuable comments. The authors would like to acknowledge the technical and logistical support provided by consultants of the Ministry of Health of Honduras, Pan American Health Organization/World Health Organization, Technical round table for neglected diseases, World Food Program, Health Schools Initiative, Ministry of Education of Honduras and National Parasitological Laboratory.

Data Availability

The authors confirm that all data underlying the findings are fully available without restriction. Data is available upon request from the Ministry of Health. There doesn't exist a public repository of such data in Honduras so the data can't be deposited.

Funding Statement

This study was funded by the Ministry of Health of Honduras and the AMI project of United States Agency for International Development. The funders had no role in the study design, data collection and analysis, preparation of the manuscript or decision to publish this article.

References

  • 1. Crompton DW, Nesheim MC (2002) Nutritional impact of intestinal helminthiasis during the human life cycle. Annu Rev Nutr 22: 35–59. [DOI] [PubMed] [Google Scholar]
  • 2. Hall A, Hewitt G, Tuffrey V, de Silva N (2008) A review and meta-analysis of the impact of intestinal worms on child growth and nutrition. Matern Child Nutr 4 Suppl 1: 118–236. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Nokes C, Grantham-McGregor SM, Sawyer AW, Cooper ES, Bundy DA (1992) Parasitic helminth infection and cognitive function in school children. Proc Biol Sci 247: 77–81. [DOI] [PubMed] [Google Scholar]
  • 4.World Health Organization (2001) WAH54.19: Schistosomiasis and soil-transmitted helminth infections. 54th World Health Assembly Geneva.
  • 5. World Health Organization (2012) Soil-transmitted helminthiases: number of children treated in 2010. Weekly epidemiological record 23: 225–232. [PubMed] [Google Scholar]
  • 6. Hotez PJ, Bottazzi ME, Franco-Paredes C, Ault SK, Periago MR (2008) The neglected tropical diseases of Latin America and the Caribbean: a review of disease burden and distribution and a roadmap for control and elimination. PLoS Negl Trop Dis 2: e300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Mathers CD, Ezzati M, Lopez AD (2007) Measuring the burden of neglected tropical diseases: the global burden of disease framework. PLoS Negl Trop Dis 1: e114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.World Health Organization. Resolution WHA66.12. Neglected Tropical Diseases; 2012; Geneva. World Health Organization.
  • 9.World Health Organization. Report of the third global meeting of the partners for parasite control: Deworming for Health and Development; 2004; Geneva. pp. 64.
  • 10.Pan American Health Organization. Final Report: Workshop for control of geohelminths in the Central American countries, Mexico and Dominican Republic; July, 2007; Copan, Honduras.
  • 11. Smith H, Dekaminsky R, Niwas S, Soto R, Jolly P (2001) Prevalence and intensity of infections of Ascaris lumbricoides and Trichuris trichiura and associated socio-demographic variables in four rural Honduran communities. Mem Inst Oswaldo Cruz 96: 303–314. [DOI] [PubMed] [Google Scholar]
  • 12. Schneider MC, Aguilera XP, Barbosa da Silva Junior J, Ault SK, Najera P, et al. (2011) Elimination of neglected diseases in latin america and the Caribbean: a mapping of selected diseases. PLoS Negl Trop Dis 5: e964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Sanchez AL, Gabrie JA, Usuanlele MT, Rueda MM, Canales M, et al. (2013) Soil-transmitted helminth infections and nutritional status in school-age children from rural communities in Honduras. PLoS Negl Trop Dis 7: e2378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Sanchez AL, Gabrie JA, Rueda MM, Mejia RE, Bottazzi ME, et al. (2014) A scoping review and prevalence analysis of soil-transmitted helminth infections in honduras. PLoS Negl Trop Dis 8: e2653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.National Malaria Program (2012) National Strategic Plan for Malaria, 2012–2015. Tegucigalpa, Hondruas: Ministry of Health of Honduras. [Google Scholar]
  • 16.World Health Organization (2011) Helminth control in school-age children: A guide for managers of control programmes. Geneva: World Health Organization. 75 p. [Google Scholar]
  • 17. Singh B, Bobogare A, Cox-Singh J, Snounou G, Abdullah MS, et al. (1999) A genus- and species-specific nested polymerase chain reaction malaria detection assay for epidemiologic studies. Am J Trop Med Hyg 60: 687–692. [DOI] [PubMed] [Google Scholar]
  • 18. de Lamballerie X, Zandotti C, Vignoli C, Bollet C, de Micco P (1992) A one-step microbial DNA extraction method using “Chelex 100” suitable for gene amplification. Res Microbiol 143: 785–790. [DOI] [PubMed] [Google Scholar]
  • 19. de Onis M, Onyango AW, Borghi E, Siyam A, Nishida C, et al. (2007) Development of a WHO growth reference for school-aged children and adolescents. Bull World Health Organ 85: 660–667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. de Onis M, Lobstein T (2010) Defining obesity risk status in the general childhood population: which cut-offs should we use? Int J Pediatr Obes 5: 458–460. [DOI] [PubMed] [Google Scholar]
  • 21.World Health Organization (2009) WHO AnthroPlus for personal computers Manual: Software for assessing growth of the world's children and adolescents. 1.0.4 ed. Geneva.
  • 22. Saboya MI, Catala L, Nicholls RS, Ault SK (2013) Update on the mapping of prevalence and intensity of infection for soil-transmitted helminth infections in Latin America and the Caribbean: a call for action. PLoS Negl Trop Dis 7: e2419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Kaminsky RG (2012) Aspectos Epidemiológicos y Conceptuales de Parasitosis Intestinales en el Hospital Regional de Tela, Honduras. REV MED HONDUR 80. [Google Scholar]
  • 24.Zuniga C, Hawdon J, sentz J, Cosenza H, Hotez P, et al.. (2003) Epidemiology of human hookworm infection in northern and southern regions of Honduras. Tegucigalpa, MDC: The Ministry of Health of Honduras, Teguciglapa, Honduras. 20 p. [Google Scholar]
  • 25. Gabrie JA, Rueda MM, Canales M, Sánchez A (2012) Utilidad del Método KATO-KATZ para Diagnóstico de Uncinariasis: Experiencia en una Zona Rural de Honduras, 2011. REV MED HONDUR 80. [Google Scholar]
  • 26.Pan American Health Organization (2011) Workshop on integrating deworming intervention into preschool child packages in the Americas. Report of the meeting held in Washington, D.C., USA. Washignton, D.C.: Pan American Health Organization,. [Google Scholar]
  • 27.World Health Organization (2013) Soil-transmitted helminthiasis. Geneva: World Health Organization. [Google Scholar]
  • 28.Hotez PJ, Bundy DA, Beegle K, Brooker S, Drake L, et al. (2006) Helminth infections: soil-transmitted helminth infections and schistosomiasis. In: Jamison DT, Breman JG, Measham AR, et al., editors. Disease Control Priorities in Developing Countries. 2nd edition. Washington (DC): World Bank; 2006. Chapter 24. Available from: http://www.ncbi.nlm.nih.gov/books/NBK11748/ [Google Scholar]
  • 29.World Bank (2003) School Deworming. Washignton, D.C.: World Bank. [Google Scholar]
  • 30. Dickson R, Awasthi S, Williamson P, Demellweek C, Garner P (2000) Effects of treatment for intestinal helminth infection on growth and cognitive performance in children: systematic review of randomised trials. BMJ 320: 1697–1701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Bundy DA, Chan MS, Savioli L (1995) Hookworm infection in pregnancy. Trans R Soc Trop Med Hyg 89: 521–522. [DOI] [PubMed] [Google Scholar]
  • 32. Rivera MF (2005) Obesidad en condiciones de pobreza. Estudio epidemiológico en escolares de escuelas públicas de Tegucigalpa, Honduras, 2000. Rev Med Hondur 73: 10–14. [Google Scholar]
  • 33.Secretaría de Salud de Honduras, Instituto Nacional de Estadística (INE), ICF International (2013) Encuesta Nacional de Salud y Demografía 2011–2012. Tegucigalpa, Honduras: SS, INE e ICF International. [Google Scholar]
  • 34.World Health Organization (2014) Global School-based Student Health Survey: Honduras 2012 Fact Sheet. 2 p.
  • 35.Banegas EI, Mejia RE, Singh P, Burgos E, Aguilar J, et al.. (2012) An integral intervention for malaria control in the municipality of Wampusirpi, Gracias a Dios. Research without borders 6th Biennial NeTropica Meeting Copan, Honduras.
  • 36. Lindblade KA, Steinhardt L, Samuels A, Kachur SP, Slutsker L (2013) The silent threat: asymptomatic parasitemia and malaria transmission. Expert review of anti-infective therapy 11: 623–639. [DOI] [PubMed] [Google Scholar]
  • 37.Consejo de Ministros de Salud de Centroamérica y República Dominicana (COMISCA) (2013) Declaración- Hacia la eliminación de la malaria en Mesoamérica y la Isla de la Española en el 2020. San José, Costa Rica: XXXXVIII Reunión Ordinaria del COMISCA. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Checklist S1

STROBE checklist.

(DOC)

Data Availability Statement

The authors confirm that all data underlying the findings are fully available without restriction. Data is available upon request from the Ministry of Health. There doesn't exist a public repository of such data in Honduras so the data can't be deposited.


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