INTRODUCTION
Infections by the soil-transmitted helminths (STH), including Ascaris lumbricoides, Trichuris trichiura, Ancylostoma duodenale/Necator americanus (hookworms), and Strongyloides stercoralis, disproportionately affect children around the world.1 Because of their transmission associated with poor sanitary conditions and inadequate hygiene practices, higher burden of disease is seen in children from developing countries from sub-Saharan Africa, Southeast Asia, and Latin America.1 Approximately 267 million preschool-age children (PSAC) and 568 million school-age children (SAC) worldwide are at risk of STH infection as well as impaired child growth and cognitive development from A. lumbricoides, T. trichiura, and hookworm infections,2 and death due to severe S. stercoralis infection.3 Thus, their control is a global health priority.
Water, sanitation, and hygiene (WASH) interventions alongside repeated chemotherapy at regular intervals are tenets for the control of STH.4,5 Despite the progress made, there are still 49% PSAC and 31% SAC in endemic countries not receiving preventive chemotherapy.6 Similarly, 2.3 billion people do not have adequate sanitation service, 892 million practice open defecation, and 884 million lack clean drinking water.7 Higher scale of deworming programs in endemic countries and global outreach of WASH programs are necessary.
The Amazon Basin in Peru is at special risk of STH infection because of its weather condition (favoring geohelminth survival) and the health inequalities present in the region. In Peru, although health interventions have rapidly increased in poor areas of the Andes, the Amazon has experienced less and slower health progress.8 Moreover, some antihelminth programs already implemented in the region have reported low chemotherapy drug coverage.9 Further research in Amazonian communities are needed to comprehensively identify barriers for the control of STH. The aim of this study was to determine the prevalence of STH infection in children in a rural community in the Amazon jungle, as well as to identify demographic, sanitation, and clinical factors associated with these parasitic infections.
METHODS
Study design.
We conducted a cross-sectional study to determine the point prevalence of A. lumbricoides, T. trichiura, hookworm, and S. stercoralis infections in children aged 2–14 years from Padre Cocha, an Amazonian community in Peru, through December 2nd–13th, 2015. This study included multiple stool-based diagnostic techniques to increase parasite detection, including direct smear examination, Kato–Katz technique (K-K), spontaneous sedimentation in tube technique (SSTT), modified Baermann technique (MBT), and agar plate culture (APC). Information about children’s demographics, past medical history, hygiene practices, and household sanitation conditions was obtained. Also, we explored the burden of STH in mothers of the participating children and examined the association between maternal characteristics and children’s STH infection status.
Study population.
The community of Padre Cocha is part of the district of Punchana, province of Maynas, in the region of Loreto, Peru, and it is located in the bay of the Nanay River (one of the main tributaries of the Amazon River) (Figure 1). It is only accessible by river and located 20 minutes away from the closest urban area, Iquitos city. Its population comprises 850 inhabitants, distributed in 195 households.10 In 2012, approximately 31% of the habitants were considered poor and 11% lived in extreme poverty. The main economic activities include fishing, farming, and craft-making. The great majority of inhabitants speak Spanish as their mother language.
Since 2012, a school-based deworming program was initiated in the region of Loreto. The program consisted on the administration of 500 mg of mebendazole on a quarterly basis to children aged 3–17 years, aiming to reduce the burden of A. lumbricoides, T. trichiura, and hookworm infections (known as common STH).9 The deworming program had been implemented for almost 4 years by the time of this study. Drugs were provided both in the nursing school to children aged 3–5 years, as well as in the elementary, middle, and high schools for children aged 6–17 years.11
Data and stool collection.
Authorization and support from the community leaders were obtained. Households with eligible children were identified: children aged 2–14 years and residing in Padre Cocha for at least 1 year. After obtaining informed consent from parents, children were approached at the local school or in their households and only those who assented to participate were included. Mothers who were willing to participate provided informed consent as well. A questionnaire was administered to collect information on sociodemographic characteristics, relevant medical history, hygiene practices, and household sanitation for both children and mothers. Weight and height of children were measured using calibrated instruments.
Two labeled plastic containers without preservatives were given to each participant to collect the stools. Mothers were instructed about appropriate stool sample collection techniques. Each stool sample was obtained at least 24 hours apart and was immediately transported to the local health center. The research team collected the stool samples every 6–12 hours at the local health center and rapidly transported them for analysis in Iquitos city.
Parasitological analyses.
Stool samples were evaluated in Iquitos city immediately on reception. Senior laboratory professionals from the Institute of Tropical Medicine Alexander von Humboldt-Universidad Peruana Cayetano Heredia, analyzed the samples. The first part of the analysis consisted in a macroscopic analysis for stool consistency, presence of blood, mucus, or adult helminth parasites. During the microscopic analysis, five stool-based parasitological techniques were conducted, including direct smear examination, SSTT, K-K, MBT, and APC. Spontaneous sedimentation in tube technique and K-K were performed mainly for the detection of A. lumbricoides, T. trichiura, and hookworm infection,12 whereas MBT and APC were used for the detection of S. stercoralis.13 We considered a positive stool sample if the parasite was detected by any of these diagnostic methods. Parasitological techniques were performed following the guidelines for intestinal parasites diagnosis from the National Institute of Health of Peru.14
Sample size calculation and statistical analysis.
From a total of 850 inhabitants in Padre Cocha, approximately 32% of them are younger than 15 years.10,15 Based on previous epidemiological reports, the expected frequency of any STH was 50%, as of December 2015.9 Thus, the estimated sample considering a 5% margin of error was 136, as per Epi Info 3.5.4 (CDC, Atlanta, GA). The point prevalence of STH infection was defined as the prevalence of one or more STH in the stool samples; individual prevalence rates were also calculated for each parasite. Children aged 2–5 years were considered as PSAC and those aged between 6 and 14 years were considered as SAC. Data were entered in a Microsoft Excel spreadsheet and posteriorly evaluated using STATA v14 (StataCorp, College Station, TX). Categorical data were evaluated by χ2 test or Fisher’s exact test with a significance level of 0.05. Bivariate analyses with odds ratio calculation were conducted to assess the association between STH infection and the characteristics of interest considering a 95% CI. Missing data were reported when values missing were > 5%.
Ethics statement.
This study was approved by the Institutional Review Boards of Universidad Peruana Cayetano Heredia (IRB #65959) and Hospital Cayetano Heredia (IRB #126-015). Parents provided written informed consent for participating children. Children who participated provided their assent. Mothers who were also willing to participate provided written informed consent as well.
RESULTS
Stool samples from 124 children were collected. The mean age was 7 ± 3.4 years, and 53.2% were male. In terms of age classification, 30.7% were PSAC, whereas 69.3% were SAC. Regarding anthropometric characteristics, 60.8% had stunting based on the WHO criteria. During the last year, 79% of the children took antiparasitic medicines, 23% reported at least three episodes of diarrhea, and 14.6% were significantly absent from school (≥ 4 missed days). About hygiene practices, 84% reported inconsistent handwashing, 66.7% walked barefoot, 28.2% were nail biters, and 20.1% used the river for bathing or recreational activities. Children included in the study belonged to 78 households characterized by the lack of running water (55.6%) and of pavemented floor (40.8%); 97.4% had latrines for defecation.
The point prevalence of STH infection among children was 25.8%. Ascaris lumbricoides was the most frequent parasite (16.1%), followed by S. stercoralis (10.5%); the prevalence of hookworm and T. trichiura infections was the same (1.6%) (Table 1). The point prevalence of STH tended to be higher among PSAC than among SAC (36.8% versus 20.9%; P = 0.06). When considered only the most common STH (A. lumbricoides, T. trichiura, and hookworm), the prevalence was significantly higher in PSAC than in SAC (31.6% versus 12.8%; P = 0.01). During the assessment of factors associated with STH infection, walking barefoot was a risk factor for the infection with STH (OR = 3.28; 95% CI = [1.11–12.07]; P = 0.02). Further details are seen in Table 2.
Prevalence of soil-transmitted helminth infection in 124 children in Padre Cocha
No | % | |
---|---|---|
Ascaris lumbricoides | 20 | 16.1 |
Strongyloides stercoralis | 13 | 10.5 |
Necator americanus/Ancylostoma duodenale | 2 | 1.6 |
Trichuris trichiura | 2 | 1.6 |
Any STH | 32 | 25.8 |
STH = soil-transmitted helminth.
Association between soil-transmitted helminth infection and past medical history, hygiene practices, and household sanitation characteristics in children in Padre Cocha
Characteristic | STH infection (n = 32) No (%) | No STH infection (n = 92) No (%) | OR | 95% CI | P-value |
---|---|---|---|---|---|
≥ 3 episodes of diarrhea in the last year | 8/32 (25) | 23/91 (25.3) | 0.99 | 0.34–2.68 | 0.98 |
Chronic malnutrition | 19/31 (61.3) | 54/89 (60.7) | 1.03 | 0.41–2.63 | 0.95 |
≥ 4 days school absenteeism in the last year | 5/31 (16.1) | 13/91 (14.3) | 1.15 | 0.29–3.88 | 0.78 |
Walking barefoot | 26/31 (83.9) | 56/92 (60.9) | 3.28 | 1.11–12.07 | 0.02 |
Irregular handwashing | 24/32 (75) | 80/92 (87) | 0.45 | 0.15–1.44 | 0.11 |
Use of river | 12/31 (38.7) | 31/92 (33.7) | 1.24 | 0.48–3.11 | 0.61 |
Nail biting | 7/32 (21.9) | 28/92 (30.4) | 0.64 | 0.21–1.76 | 0.35 |
Soil floor | 15/32 (46.9) | 36/91 (39.6) | 1.35 | 0.55–3.28 | 0.47 |
Open defecation | 0/32 (0) | 1/90 (1.1) | – | – | – |
No running water | 16/31 (51.6) | 51/88 (58) | 0.77 | 0.31–1.92 | 0.54 |
STH = soil-transmitted helminth.
Stool samples from 51 mothers were also collected, representing the caregivers of 69.4% of the pediatric population that participated in this study. The mean age was 35.4 ± 9.2 years. The point prevalence of STH infection in this subgroup was 19.6%: 9.8% were infected by A. lumbricoides, 5.9% by S. stercoralis, and 3.9% by hookworms; none were infected by T. trichiura. Twenty-five percent were single mothers and 59.2% had low education level (incomplete high-school education or below). There was no significant statistical difference between single marital status, low educational level, or young age (≤ 25 years) of the mother and STH infection in children (Table 3). However, children who were infected by STH were more likely to have a mother who was also infected by one of these organisms when compared with non-STH–infected children (36.4% versus 14.1%, P = 0.02).
Association between characteristics of the mothers and soil-transmitted helminth infection in children in Padre Cocha
Characteristic | STH infection in children (n = 22), No (%) | No STH infection in children (n = 64), No (%) | P-value |
---|---|---|---|
Single marital status | 5/22 (22.7) | 16/64 (25) | 0.83 |
Young age | 4/22 (18.2) | 4/63 (6.4) | 0.12 |
Low educational status | 17/22 (77.3) | 36/62 (58.1) | 0.11 |
STH infection | 8/22 (36.4) | 9/64 (14.1) | 0.02 |
STH = soil-transmitted helminth.
DISCUSSION
A high overall prevalence of STH infection (26%) was found among children from an Amazonian rural community who were part of a school-based deworming program. Most of the burden was related to A. lumbricoides infection (16.5%) despite its known susceptibility to mebendazole.16 Also, a relatively high prevalence of S. Stercoralis (10.5%) was noticed, which is concordant to that reported in a local study.17 By contrast, infections by T. trichiura and hookworm were rare in this study when compared with other studies conducted in the Peruvian rainforest.9,12,18,19
The prevalence of the common STH (A. lumbricoides, T. trichiura, and hookworm) was significantly higher among PSAC than among SAC (31.6% versus 12.8%, P = 0.01). This finding is important as recent evidence has shown robust positive health effects of deworming in PSAC, reflected in decreased stunting and anemia rates.20 In Padre Cocha, PSAC and SAC attended separate schools and were approached by the deworming program staff under different procedures. This may have resulted in different practices, medication supply, or program surveillance between PSAC and SAC.21
Strongyloides stercoralis infection was common in children of this community. Strongyloidiasis can cause diarrhea and abdominal pain in the pediatric population and has also been associated with stunting in children with severe infection.22,23 Mebendazole, the drug administered as part of the deworming program in this community, is not effective against S. stercoralis.16 On the other side, thiabendazole and ivermectin have shown to be effective within strongyloidiasis control programs elsewhere.24–26 Appropriate strategies including therapy with thiabendazole or ivermectin could potentially contribute to reduce the extent of infection among children. Unfortunately, and to the best of our knowledge, there are presently no national policies that promote the eradication of S. stercoralis in children or adults in Peru.
A great proportion of participants lacked optimal sanitation conditions and adequate hygiene practices. Although several risk factors were assessed, walking barefoot was the only characteristic that was significantly associated with a higher STH burden. The lack of power of this study may have limited the elucidation of further factors associated with parasite infection as inconsistent hygiene practices, lack of clean water, or pavemented floor have been described as important factors that may increase the rate of STH infection.4,27 Interventions that promote hygiene education have been found to be effective in reducing helminth infection in other local Amazonian communities.19 Padre Cocha urges similar education initiatives as well as sustained public efforts for improving access to clean water and pavement floor as key mechanisms to tackle these infectious diseases.
More than half of the pediatric population studied had stunting, proportion substantially higher than the 17.3% national estimate.8 Although stunting was not associated with STH infection in this study, also probably because of underpower, several studies have reported the effect of moderate-to-high STH infection rates on child nutritional status.28 Moreover, low nutritional status also influences the impact of STH infections.28 As has also been found by neighbor countries,29 rural Amazon communities may be at special risk of children stunting. Thus, nutrition status of children in Padre Cocha requires public health attention.
In this study, children who were infected by STH were more likely to have a mother who was also infected by one of these organisms when compared with non-STH–infected children. Helminth infection in mothers has been reported as a risk factor for infection in children and could potentially contribute to the high prevalence of STH infection in this population because they likely share the same source of the infection.30 As mothers are not part of the MDA local program, infected mothers could be playing a role in the perpetuation of STH infection within the household. Following the present WHO recommendation of also administering antiparasitic drugs to women of childbearing age,5 mass administration in mothers may help to control STH infection in this community. Similarly, although not assessed in this study, other household members could also be infected; thus, it may also be appropriate to study the impact of expanding the deworming program not only to mothers but also to the entire community, as a meta-analysis has shown better morbidity outcomes of community-wide programs than selective approaches.31 This could contribute to elucidate the best effective strategy in this community.
The study had several limitations. First, accurate information about previous participation in the deworming program was not available, which impeded to assess the relationship between recent antihelminthic drug administration and STH infection. Second, the lack of multiple stool samples per participant could have reduced the detection rate of parasites; however, we used multiple parasitological techniques per sample to increase the rate.12,13 Also, for the specific case of S. stercoralis, the use of serology-based tests could have increased its detection because of their reported higher sensitivity; however, concerns about specificity as well as the challenge of implementing such tests under limited laboratory conditions of on-field research studies remain.32 Fourth, our results are underpowered because of the relatively small sample size. This also prevented further multivariate analysis of meaningful risk factors. Fifth, we only obtained stool samples from around 70% of the mothers. In addition, mothers from infected children could have been more motivated to participate than mothers from uninfected children, representing a potential selection bias. Despite these limitations, our study may represent the context of other similar rural communities in the Peruvian rainforest and our results should be discussed to promote alternative approaches to the control of STH.
In conclusion, STH infection was highly prevalent in children in Padre Cocha despite routine deworming. Among helminth infections, A. lumbricoides and S. stercoralis were the most frequent. Preschool-age children and children who walk barefoot may be at an increased risk of STH burden. Future studies may address the relationship between maternal and children infection. Improvement of sanitary and hygiene conditions is also necessary in this community.
Acknowledgments:
We are grateful to the participants of this study, the local community and health authorities for their kind support. Our sincere gratitude to Carmen Quijano and Matilde Quijano from the Laboratory of Parasitology of the Tropical Medicine Institute “Alexander von Humboldt” for their collaboration with specimen analysis. We thank the American Society of Tropical Medicine and Hygiene for letting us present the preliminary results of this study in the ASTMH Annual Meeting in 2016 through a travel award granted to the first author; we received important feedback which was included in this manuscript. Partial funding was provided by the Harvard Medical School Master of Medical Sciences in Global Health Delivery program and the Hospital Cayetano Heredia 2015 Research Grant.
REFERENCES
- 1.↑
Jourdan PM, Lamberton PHL, Fenwick A, Addiss DG, 2018. Soil-transmitted helminth infections. Lancet 391: 252–265.
- 2.↑
World Health Organization, 2018. Fact Sheets: Soil-Transmitted Helminth Infections. Geneva, Switzerland: WHO. Available at: http://www.who.int/en/news-room/fact-sheets/detail/soil-transmitted-helminth-infections. Accessed August 29, 2018.
- 3.↑
Nutman TB, 2017. Human infection with Strongyloides stercoralis and other related Strongyloides species. Parasitology 144: 263–273.
- 4.↑
World Health Organization, 2015. Water, Sanitation and Hygiene for Accelerating and Sustaining Progress on Neglected Tropical Diseases. A Global Strategy 2015–2020. Geneva, Switzerland: WHO. Available at: https://www.who.int/water_sanitation_health/publications/wash-and-ntd-strategy/en. Accessed September 12, 2018.
- 5.↑
World Health Organization, 2017. Guideline: Preventive Chemotherapy to Control Soil-Transmitted Helminth Infections in at-Risk Population Groups. Geneva, Switzerland: WHO. Available at: https://www.who.int/nutrition/publications/guidelines/deworming/en. Accessed September 12, 2018.
- 6.↑
Uniting to Combat Neglected Tropical Diseases, 2017. Reaching a Billion: Ending Neglected Tropical Diseases: A Gateway to Universal Health Coverage. Fifth Progress Report on the London Declaration on NTDs. Available at: https://unitingtocombatntds.org/reports/5th-report. Accessed September 15, 2018.
- 7.↑
World Health Organization and the United Nations Children’s Fund, 2017. Progress on Drinking Water, Sanitation and Hygiene: 2017 Update and SDG Baselines. Available at: https://www.who.int/mediacentre/news/releases/2017/launch-version-report-jmp-water-sanitation-hygiene.pdf. Accessed September 15, 2018.
- 8.↑
Huicho L, Segura ER, Huayanay-Espinoza CA, de Guzman JN, Restrepo-Méndez MC, Tam Y, Barros AJ, Victora CG, the Peruvian Countdown Country Case Study Working Group, 2016. Child health and nutrition in Peru within an antipoverty political agenda: a countdown to 2015 country case study. Lancet Glob Health 4: 414–426.
- 9.↑
Rodriguez Ferruci H, Razuri H, Casapia M, Rahme E, Silva H, Ault S, Blouin B, Mofid LS, Montresor A, Gyorkos TW, 2016. Governance, organization, accountability and sustainability of a region-wide school-based deworming program in Loreto, Peru. Acta Trop 59: 219–226.
- 10.↑
Instituto Nacional de Estadística e Informática, 2018. Directorio Nacional de Centros Poblados. Censos Nacionales 2017: XII de Población, VII de Vivienda y III de Comunidades Indígenas. Lima, Peru: Instituto Nacional de Estadística e Informática. Available at: https://www.inei.gob.pe/media/MenuRecursivo/publicaciones_digitales/Est/Lib1541/index.htm.
- 11.↑
United Nations Development Program, 2012. Perú: Consulta Nacional Sobre Agenda de Desarrollo Post 2015 Resumen de Relatoría: Taller con Poblaciones en Especial Situación de Vulnerabilidad Líderes de Organizaciones Sociales de Base de la comunidad de Padre Cocha, Loreto. Lima, Peru: Oficina de la Coordinadora Residente del Sistema de las Naciones Unidas. Available at: http://onu.org.pe/wp-content/uploads/2013/06/2-Post-2015-Informe-Taller-ONUMUJERES-Mujeres-Altoandinas-Puno-1-feb-13.pdf. Accessed October 3, 2018.
- 12.↑
Machicado JD, Marcos LA, Tello R, Canales M, Terashima A, Gotuzzo E, 2012. Diagnosis of soil-transmitted helminthiasis in an Amazonic community of Peru using multiple diagnostic techniques. Trans R Soc Trop Med Hyg 106: 333–339.
- 13.↑
Campo Polanco L, Gutiérrez LA, Cardona Arias J, 2014. Diagnosis of Strongyloides stercoralis infection: meta-analysis on evaluation of conventional parasitological methods (1980–2013). Rev Esp Salud Publica 88: 581–600.
- 14.↑
Instituto Nacional de Salud del Perú, 2003. Manual de Procedimientos de Laboratorio para el Diagnóstico de los Parásitos Intestinales del Hombre. Series de Normas Técnicas #37. Lima, Peru: Ministerio de Salud. Available at: http://bvs.minsa.gob.pe/local/INS/165_NT37.pdf. Accessed October 5, 2018.
- 15.↑
Instituto Nacional de Estadística e Informática, 2018. Resultados Definitivos de los Censos Nacionales 2017. Loreto. Resultados definitivos. Lima, Peru: Instituto Nacional de Estadística e Informática. Available at: https://www.inei.gob.pe/media/MenuRecursivo/publicaciones_digitales/Est/Lib1561/. Accessed October 5, 2018.
- 16.↑
Keiser J, Utzinger J, 2010. The drugs we have and the drugs we need against major helminth infections. Adv Parasitol 73: 197–230.
- 17.↑
Yori PP et al. 2006. Seroepidemiology of strongyloidiasis in the Peruvian Amazon. Am J Trop Med Hyg 74: 97–102.
- 18.↑
Cabada MM, Lopez M, Arque E, Clinton White A, 2014. Prevalence of soil-transmitted helminths after mass albendazole administration in an indigenous community of the Manu jungle in Peru. Pathog Glob Health 108: 200–205.
- 19.↑
Gyorkos TW, Maheu-Giroux M, Blouin B, Casapia M, 2013. Impact of health education on soil-transmitted helminth infections in schoolchildren of the Peruvian Amazon: a cluster-randomized controlled trial. PLoS Negl Trop Dis 7: e2397.
- 20.↑
Lo NC, Snyder J, Addiss DG, Heft-Neal S, Andrews JR, Bendavid E, 2018. Deworming in pre-school age children: a global empirical analysis of health outcomes. PLoS Negl Trop Dis 12: e0006500.
- 21.↑
Musuva RM, Matey E, Masaku J, Odhiambo G, Mwende F, Thuita I, Kihara J, Njomo D, 2017. Lessons from implementing mass drug administration for soil transmitted helminths among pre-school aged children during school-based deworming program at the Kenyan coast. BMC Public Health 17: 575.
- 22.↑
Khieu V, Schar F, Marti H, Sayasone S, Duong S, Muth S, Odermatt P, 2013. Diagnosis, treatment and risk factors of Strongyloides stercoralis in schoolchildren in Cambodia. PLoS Negl Trop Dis 7: e2035.
- 23.↑
Forrer A, Khieu V, Schär F, Hattendorf J, Marti H, Neumayr A, Char MC, Hatz C, Muth S, Odermatt P, 2017. Strongyloides stercoralis is associated with significant morbidity in rural Cambodia, including stunting in children. PLoS Negl Trop Dis 11: e0005685.
- 24.↑
Forrer A, Khieu V, Schindler C, Schär F, Marti H, Char MC, Muth S, Odermatt P, 2016. Ivermectin treatment and sanitation effectively reduce Strongyloides stercoralis infection risk in rural communities in Cambodia. PLoS Negl Trop Dis 10: e0004909.
- 25.
Anselmi M et al. 2015. Mass administration of ivermectin for the elimination of onchocerciasis significantly reduced and maintained low the prevalence of Strongyloides stercoralis in Esmeraldas, Ecuador. PLoS Negl Trop Dis 9: e0004150.
- 26.↑
Echazú A et al. 2017. Albendazole and ivermectin for the control of soil-transmitted helminths in an area with high prevalence of Strongyloides stercoralis and hookworm in northwestern Argentina: a community-based pragmatic study. PLoS Negl Trop Dis 11: e0006003.
- 27.↑
Strunz EC, Addiss DG, Stocks ME, Ogden S, Utzinger J, Freeman MC, 2014. Water, sanitation, hygiene, and soil-transmitted helminth infection: a systematic review and meta-analysis. PLoS Med 11: e1001620.
- 28.↑
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: 118–236.
- 29.↑
Moncayo AL, Lovato R, Cooper PJ, 2018. Soil-transmitted helminth infections and nutritional status in Ecuador: findings from a national survey and implications for control strategies. BMJ Open 8: e021319.
- 30.↑
Mehta RS, Rodriguez A, Chico M, Guadalupe I, Broncano N, Sandoval C, Tupiza F, Mitre E, Cooper PJ, 2012. Maternal geohelminth infections are associated with an increased susceptibility to geohelminth infection in children: a case-control study. PLoS Negl Trop Dis 6: e1753.
- 31.↑
Clarke NE, Clements ACA, Doi SA, Wang D, Campbell SJ, Gray D, Nery SV, 2017. Differential effect of mass deworming and targeted deworming for soil-transmitted helminth control in children: a systematic review and meta-analysis. Lancet 389: 287–297.
- 32.↑
Mendes T, Minori K, Ueta M, Miguel DC, Allegrettu SM, 2017. Strongyloidiasis current status with emphasis in diagnosis and drug research. J Parasitol Res 2017: 5056314.