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. 2014 Jul 3;143(3):452–460. doi: 10.1017/S0950268814001563

Prevalence of strongyloidiasis in Latin America: a systematic review of the literature

D BUONFRATE 1, M A MENA 2, A ANGHEBEN 1,*, A REQUENA-MENDEZ 3, J MUÑOZ 3, F GOBBI 1, M ALBONICO 1, E GOTUZZO 2, Z BISOFFI 1; the COHEMI Project Study Group
PMCID: PMC9507070  PMID: 24990510

SUMMARY

Strongyloides stercoralis is rarely recognized as a major public health issue, probably because its burden is largely underestimated. We reviewed the literature (both PubMed and ‘grey’ literature) about the prevalence of strongyloidiasis in Latin America, an area of presumable high endemicity. There were finally 88 papers involved in the analysis, covering the period between 1981 and 2011. Studies were heterogeneous in several aspects, such as the populations screened and the diagnostic methods used. Most of the studies relied on direct coproparasitological examination, which has low sensitivity for the detection of S. stercoralis larvae. The following countries presented areas of high prevalence (>20%): Argentina, Ecuador, Venezuela, Peru and Brazil. Globally, for most of the included countries it was not possible to define reliable data because of paucity and/or inadequacy of studies. S. stercoralis requires specific diagnostic methods for its detection; therefore, surveys should be specifically designed in order to avoid underestimation of the infection.

Key words: Latin America, prevalence, review, Strongyloides stercoralis

INTRODUCTION

Worldwide prevalence of strongyloidiasis has long been estimated to be between 30 and 100 million people [1]; however, in a recent Viewpoint paper [2], we suggest that this is an underestimation (there are probably at least 370 million infected people). In fact, previous data were mostly based on surveys conducted with diagnostic methods with suboptimal sensitivity for the detection of Strongyloides stercoralis. For instance, direct faecal smear examination, which is widely used for studies in the field, has very low sensitivity. Concentration techniques (such as the Baermann method) and agar plate culture give better performances, but are cumbersome and seldom used in population-based surveys. Serology is more sensitive than faecal-based methods, but so far only a few prevalence surveys have utilized it [2, 3].

In spite of the potential fatal outcome of strongyloidiasis when larvae disseminate all over the body in immunocompromised subjects [4], this parasite is rarely recognized as a major public health issue, precisely because its burden is underestimated for the reasons explained above. The distribution of the disease was poorly known in Latin America (LA) countries: only a few severe (and fatal) cases have been reported [4] and they are considered the tip of the iceberg of an unrecognized and often subclinical chronic disease. In the framework of a project [5] to assess and improve the health status of migrants from LA, we performed this review with the aim of collecting available information about the prevalence of strongyloidiasis in LA countries, where the disease is expected to be highly endemic.

METHODS

Searching

An electronic search in PubMed was done using the following key words, grouped into three main concepts: disease (strongyl*, anguillulose, helminth*, geohelminth*, geo-helminth*, nematod*), epidemiology (preval*, incidenc*, epidemiol*, surve*, rate*, frequenc*), countries of interest (Argentina OR Brazil OR Chile OR Colombia OR Costa Rica OR Cuba OR Dominican Republic OR Ecuador OR El Salvador OR Guatemala OR Guyana OR Honduras OR Mexico OR Nicaragua OR Panama OR Paraguay OR Peru OR Puerto Rico OR Uruguay OR Venezuela). Studies collected were published from 1 January 1981 to 1 January 2011, covering three decades. Search was limited to ‘humans’ and to the following languages: English, Spanish, Italian, French. The search was done on 16 May 2011. Reference lists of all the articles identified were also examined, and relevant cited references were similarly reviewed. A ‘grey’ literature search was also conducted, through consultation of libraries of Universidad Peruana Cayetano Heredia and Universidad Nacional Mayor de San Marcos (Lima, Peru).

Selection

Surveys, reports, reviews, epidemiological studies on prevalence of intestinal parasites or specifically strongyloidiasis were collected. The prevalence of S. stercoralis was extracted regardless to the type of population (children, immunosuppressed patients, etc.) and diagnostic method used (serology, stool examination, etc.). Moreover, other kind of data (not properly defined as prevalence, e.g. rates, frequencies) were taken into account.

Data abstraction

We identified possibly appropriate papers through titles and abstracts. We then read the whole papers to evaluate their appropriateness for inclusion in the review.

RESULTS

Flow of included papers

The electronic search in PubMed allowed identification of 1071 papers that were evaluated for possible inclusion. The ‘grey’ literature search provided a further nine studies. After scanning of the abstracts, a total of 223 papers were detected that may relate to our review. Based on the full text of these papers, 135 were rejected since they reported prevalence of other helminthic infections (95 papers) or since they did not report prevalence data (40 papers). Therefore, the total number of papers included was 88. The flow of included papers is shown in Figure 1.

Fig. 1.

Fig. 1.

PRISMA flow chart.

Study characteristics

We found data about the following countries: Argentina (10 papers), Bolivia (2), Brazil (31), Chile (5), Colombia (3), Costa Rica (3), Ecuador (7), Guatemala (1), Guyana (1), Honduras (3), Mexico (2), Nicaragua (1), Peru (12), Puerto Rico (2), Venezuela (5). Most of the studies were cross-sectional, while ten were retrospective and 12 prospective. Most of the studies were not specifically designed to detect S. stercoralis but rather to investigate the burden of parasites in general. This is why the diagnostic method used was usually stool examination, frequently without any of the techniques which can enhance the detection of S. stercoralis larvae (such as the Baermann method). In just a couple of surveys the authors relied on serology only [6, 7]; in three studies both serology and stool examination were used [810], while in one study conducted in Peru, serology (ELISA), stool examination and agar culture were all used [11].

Strongyloidiasis in the different LA countries

Of the 88 studies selected, 31 were conducted in Brazil [6, 8, 1240]. Studies were characterized by large heterogeneity in several aspects, such as population studied and diagnostic methods used. In Brazil, the lowest proportion of infected individuals was found by Menezes et al. [23], who conducted a study in children from municipal day centres in the city of Belo Horizonte from April to November 2006. They found 24·6% children positive for at least one intestinal parasite, but in the 472 stool samples analysed, only one (0·2%) resulted positive for S. stercoralis. The diagnostic method used was coproparasitological examination with merthiolate-iodine-formaline concentration. On the other hand, a retrospective study that used faecal examination by the sedimentation method [35] showed the highest percentage (43/198 patients, 21·7% of the examined population) of S. stercoralis in alcoholic patients (compared to two control groups). It is of note that one study was not conducted in humans, but it analysed the degree of soil contamination in a couple of indigenous territories in the state of Paraná, Southern Brazil: 111 soil samples were collected in the courtyard of schools and households, and S. stercoralis larvae were found in 0·9% and 1·5% of samples, respectively [28]. However, the relationship between soil contamination and intensity of infection in the human population was not analysed. A couple of studies analysed prevalence after treatment: Dorea et al. [32] performed stool examination in primary school children at 4 and 6 months after treatment with thiabendazole (with 4·1% prevalence at time 0) and found 50% prevalence reduction. Heukelback et al. [15] evaluated prevalence before and after 1 and 9 months from mass treatment with ivermectin (two doses given 10 days apart), finding a reduction from 11% to 0·6% and 0·7%, respectively. A survey conducted in a rural community in the Peruvian Amazon [11] demonstrated S. stercoralis larvae in 8·7% of stool samples (combining results from direct smear, Baermann method and simple sedimentation), while the ELISA was positive in 72% of the analysed sera. Given the high negative predictive value of serology (98% according to this study), the authors concluded that despite possible false-positive results (past infections, cross-reactivity) the ELISA was a highly appropriate screening tool. Two other studies conducted in different areas of the Peruvian Amazon found a high percentage of infection in the included subjects (19·5%) [41, 42] by coproparasitological examination [42]. One of those studies concerned subjects who presented symptoms compatible with S. stercoralis infection [42]. The proportion of infected subjects was lower (0·8–5%) in two studies conducted in children in different areas of the Peruvian Amazon [43, 44]. Surveys conducted in other areas of Peru [4550] reported a range of infected people between 0·3% (a study conducted in the small village of Chacas at 3300–3500 m above sea level [45]) and 16% found by Rodriguez & Calderon [48] in children living in a suburb of Tarapoto (which is the largest city in the Department of San Martin, on the edge of the Amazon basin). A study conducted in Lima in HIV-positive patients, found 6% infected people [49]. Of note, a report from the Peruvian Ministry of Health collected a series of transversal studies conducted in different areas of the country between 1981 and 2001; the average prevalence found was 6·6% [51].

The highest rates of strongyloidiasis were found in some areas of Argentina, using only faecal-based methods for diagnosis: a couple of studies performed in the province of Salta [52, 53] found 24% and 50·5% of infected subjects, respectively, and another two studies in the province of Misiones [54, 55] found percentages between 22·2% and 28·6%. In other parts of Argentina [5661] the figures resulted in a range of 0·2–9·6%, with the lowest rate found in a rural area located at 96 km from Buenos Aires [58].

Large variability in the proportion of S. stercoralis-infected subjects was outlined by surveys conducted in Ecuador [9, 6267] ranging from 0·7% to 24%. Different characteristics of the territories in which the studies were performed might have accounted for part of the disparity; for instance, Peplow [62] found globally 7% of infected people in the Ecuadorian regions analysed, but when we looked at subgroups, we found rates of 8%, 1% and 7% in the Ecuadorian Amazon, the Andean region and on the coast, respectively. A paper by Moncayo et al. [63] was particularly interesting: they made a comparison of levels of infection by S. stercoralis and other parasites between communities that had received ivermectin mass treatment and communities who were not treated, in Esmeraldas province. Stool samples were examined using a modified Kato-Katz technique and formol-ethyl acetate concentration. They found 35 (1·2%) positive children out of 2878 in the latter group, vs. three (0·1%) positive children out of 2528 in those who had received ivermectin. The authors stated that numbers were too small to estimate the impact of ivermectin treatment on strongyloidiasis, while a statistically significant reduction was observed in the ivermectin group when all helminths were considered.

We found five studies conducted in Chile [7, 10, 6870]. One of which was a survey from 1970 to 1980 in five different geographical areas on the general population [69]. Of the 9489 stool samples, only one (0·01%) was positive at direct examination for S. stercoralis. Low infection levels were also demonstrated in a study conducted in children living in a semi-rural county of Santiago province [10] using serology: only one out of 206 children had a positive ELISA test. On the other hand, a couple of studies were conducted in psychiatric institutions [68, 70], where 7–11·6% of patients were found positive. The fourth study was the only one to rely on serology (ELISA) for diagnosis [7]; the authors compared the prevalence in three subgroups: psychiatric patients, health workers and blood donors. Again, percentages of S. stercoralis infection were significant only in the psychiatric patients (12%), while strongyloidiasis was almost absent in healthy controls (no infection in health workers, 0·25% in blood donors). The five studies conducted in Venezuela were performed in children (two studies) [71, 72], pregnant women [73], and the general population from different villages [74, 75]. The range found in children and pregnant women was 2·2–7%. Levels of infection in the general population were found to be higher, particularly in the study by Figuera et al. [75], where the frequency of strongyloidiasis was investigated by faecal-based methods (13% direct smear, 16% enrichment technique, 24% culture). Moreover, the three studies in Colombia were conducted in heterogeneous populations (general population [76], children [77], immunocompromised patients [78]) and the range was 1·5–3·6%. Two studies conducted in Honduras in HIV patients both found a percentage of infected people around 7·5% [79, 80], while in children living in rural communities and marginal barrios it was 2·6% [81]. All these studies relied on stool examination only.

Range of infection based on the three studies conducted in Costa Rica was between 2% and 5·7%: the lowest figure (2%) was found in a study conducted in the elderly population [82], while the other two studies were conducted in particular subgroups of subjects: patients and health workers from a psychiatric institution [83] (2·5%) and alcoholic patients [84] (5·7%).

We found fewer than three studies each for Bolivia [85, 86], Guatemala [87], Guyana [88], Mexico [89, 90], Nicaragua [91], and Puerto Rico [92, 93]. In all of these studies the percentage of infected subjects was very low, exceeding 2% in only one study in Puerto Rico [92].

Figure 2 shows the detected levels of prevalence of infection with S. stercoralis in different LA countries, based on data obtained from school-based and population-based surveys. Each country is coloured after the highest level of prevalence found (which is not necessarily representative of the whole country). Supplementary Table S1 reports in detail the number of patients screened and the percentage of patients found positive. Data are reported only for countries with at least four studies conducted in the general population and/or school children.

Fig. 2.

Fig. 2.

Prevalence of strongyloidiasis in Latin America according to population-based and school-based surveys. Colours are representative of the highest level of prevalence found in the country.

DISCUSSION

Globally, we believe that for most countries it is not possible to define a reliable estimation of prevalence because of scarceness and/or inadequacy of studies. In fact, S. stercoralis requires specific diagnostic methods, therefore surveys to assess its burden should be specifically designed. As mentioned in the Introduction, direct stool examination without any concentration techniques, or the Kato-Katz method (which is the most widely used method for helminth faecal surveys), are likely to miss most Strongyloides infections, as was recently shown by a paper published after the timeframe considered for our review. The authors clearly demonstrated that a survey conducted with inadequate methods provides unreliable figures: in a population living in the Amazon basin of Peru, they detected 0% positive for Strongyloides with the Kato-Katz method, while they found 22% of positive samples by agar plate culture. In the same study, the authors showed that alternative techniques, less cumbersome than culture, can also be used, such as the spontaneous sedimentation in tube technique (SSTT), which can be applied also for all other helminths. Interestingly, these researchers found the same prevalence with both techniques (Kato-Katz and SSTT) for hookworm as well as for Ascaris lumbricoides and Trichuris trichiura, while for S. stercoralis the prevalence increased from 0% with the Kato-Katz method, to 16% with the alternative method [94].

Serology will be a useful tool, once it is validated and made widely available, especially if blood can be simply collected with a finger prick on filter paper. Different serological techniques are available, and all are more sensitive than faecal-based methods, and also virtually 100% specific above a given cut-off [95]. Alternatively, when resources are limited and ELISA or an alternative serological test can not be used, suitable copro-microscopic methods for S. stercoralis should be adopted, such as those mentioned above and in the Introduction. However, it should be borne in mind that the sensitivity of such tests is not perfect, especially when performed on a single faecal specimen, and therefore they are likely to underestimate the real prevalence. There is a need to define a standard protocol to assess the burden of strongyloidiasis, both in terms of diagnostic method and of adequate sampling and statistical analysis. Such recommendations were made for soil-transmitted helminths by the World Health Organization, and mapping guidelines are being elaborated. An attempt to globally map S. stercoralis prevalence has just been published [96], confirming our recent view [2] that the global prevalence is probably much higher than previously estimated and that this parasite should be given greater attention by policy makers. We encourage policy makers to include S. stercoralis in the soil-transmitted helminths package, as a first step to move forward to the control of strongyloidiasis through an integrated strategic approach.

ACKNOWLEDGEMENTS

This work was supported by the EC within the 7th Framework Programme under the COHEMI project (grant agreement no. FP7-GA-261495).

Appendix. COHEMI Project Study Group

Maurizio Bonati, Francesca Severino, Valeria Confalonieri, Chiara Pandolfini, Zeno Bisoffi, Dora Buonfrate, Andrea Angheben, Marco Albonico, Alessandro Bartoloni, Marianne Strohmeyer, Lorenzo Zammarchi, Jose Muñoz, Robert Pool, Ana Requeña, Maria Roura, Anita Hardon, Christopher Pell, Peter Chiodini, Juan Moreira, Roberto Sempértegui, Mariella Anselmi, Eduardo Gotuzzo, Maria Alejandra Mena, Hector H. Garcia, Javier Bustos, Saul Santiva, Faustino Torrico, Daniel Lozano, Guido Chumiray Rojas, Teresa Hinojosa Cabrera, Javier Ochoa Morón, Ignacio Abapori Cuellar, Jaime Amorós Suarez, Gianni Tognoni, Alessandra Nicoletti, Elisa Bruno.

Supplementary material

For supplementary material accompanying this paper visit http://dx.doi.org/10.1017/S0950268814001563.

S0950268814001563sup001.doc (92KB, doc)

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REFERENCES

  • 1.Genta RM. Global prevalence of strongyloidiasis: critical review with epidemiologic insights into the prevention of disseminated disease. Reviews of Infectious Diseases 1989; 11: 755–767. [DOI] [PubMed] [Google Scholar]
  • 2.Bisoffi Z, et al. Strongyloides stercoralis: a plea for action. PLoS Neglected Tropical Diseases 2013; 7: e2214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Requena-Mendez A, et al. The laboratory diagnosis and follow up of strongyloidiasis: a systematic review. PLoS Neglected Tropical Diseases 2013; 7: e2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Buonfrate D, et al. Severe strongyloidiasis: a systematic review of case reports. BMC Infectious Diseases 2013; 13: 78. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.COHEMI (www.cohemi-project.eu).
  • 6.Costa-Cruz JM, Machado ER, Campos DM. Seroepidemiological study of human strongyloidiasis with blood samples collected on filter paper, in Abadia Dos Dourados (Minas Gerais, Brazil). Revista do Instituto de Medicina Tropical de São Paulo 1998; 40: 329–331. [DOI] [PubMed] [Google Scholar]
  • 7.Mercado R, et al. Seroepidemiological aspects of human Strongyloides stercoralis infections in Chile. Revista do Instituto de Medicina Tropical de São Paulo 2007; 49: 247–249. [DOI] [PubMed] [Google Scholar]
  • 8.Rossi CL, et al. Strongyloidiasis in Campinas city region (Brazil). Parasitological and serological data. Tropical and Geographical Medicine 1993; 45: 189–190. [PubMed] [Google Scholar]
  • 9.Moreira J, et al. Strongyloidiasis in primary-school children of Borbon, Equador – evaluation of prevalence and diagnostic tests validity by ‘latent class analysis'. Giornale Italiano di Medicina Tropicale 2006; 11: 51–55. [Google Scholar]
  • 10.Mercado R, et al. Intestinal protozoa and helminth infections in pre-school and elementary school-children from Colina county, Santiago, Chile, 2003. Parasitología Latinoamericana 2003; 58: 173–176. [Google Scholar]
  • 11.Yori PP, et al. Seroepidemiology of strongyloidiasis in the Peruvian Amazon. American Journal of Tropical Medicine and Hygiene 2006; 74: 97–102. [PMC free article] [PubMed] [Google Scholar]
  • 12.Santos RV, et al. Intestinal parasitism in the Xavante Indians, central Brazil. Revista do Instituto de Medicina Tropical de São Paulo 1995; 37: 145–148. [DOI] [PubMed] [Google Scholar]
  • 13.Kobayashi J, et al. Prevalence of intestinal parasitic infection in five farms in Holambra, Sao Paulo, Brazil. Revista do Instituto de Medicina Tropical de São Paulo 1995; 37: 13–18. [DOI] [PubMed] [Google Scholar]
  • 14.Guerrant RL, et al. Prospective study of diarrheal illnesses in northeastern Brazil: patterns of disease, nutritional impact, etiologies, and risk factors. Journal of Infectious Diseases 1983; 148: 987–997. [DOI] [PubMed] [Google Scholar]
  • 15.Heukelbach J, et al. Selective mass treatment with ivermectin to control intestinal helminthiases and parasitic skin diseases in a severely affected population. Bulletin of the World Health Organization 2004; 82: 563–571. [PMC free article] [PubMed] [Google Scholar]
  • 16.Perez E, et al. Intestinal parasite infections and schistosomiasis in a poor urban area, in townships of the sugar cane belt and in villages of the semi-arid area of North-East Brazil. Cahiers d'études et de Recherches Francophones/Santé 2000; 10: 127–129. [PubMed] [Google Scholar]
  • 17.Feitosa G, et al. High prevalence of giardiasis and strongyloidiasis among HIV infected patients in Bahia, Brazil. Brazilian Journal of Infectious Diseases 2001; 5: 339–344. [DOI] [PubMed] [Google Scholar]
  • 18.Oliveira MC, Silva CV, Costa-Cruz JM. Intestinal parasites and commensals among individuals from a landless camping in the rural area of Uberlandia, Minas Gerais, Brazil. Revista do Instituto de Medicina Tropical de São Paulo 2003; 45: 173–176. [DOI] [PubMed] [Google Scholar]
  • 19.Morrone FB, et al. Study of enteroparasites infection frequency and chemotherapeutic agents used in pediatric patients in a community living in Porto Alegre, RS, Brazil. Revista do Instituto de Medicina Tropical de São Paulo 2004; 46: 77–80. [DOI] [PubMed] [Google Scholar]
  • 20.Nascimento SA, Moitinho MLR. Blastocystis hominis and other intestinal parasites in a community of Pitanga City, Paranà State, Brazil. Revista do Instituto de Medicina Tropical de São Paulo 2005; 47: 213–217. [DOI] [PubMed] [Google Scholar]
  • 21.De Sousa EA, et al. Prevalence and spatial distribution of intestinal parasitic infections in a rural Amazonian settlement, Acre State, Brazil. Cad Saùde Pùblica, Rio de Janeiro 2007; 23: 427–434. [DOI] [PubMed] [Google Scholar]
  • 22.De Carvalho TB, De Carvalho LR, Mascarini LM. Occurrence of enteroparasites in day care centers in Botucatu (Sao Paulo State, Brazil) with emphasis on Cryptosporidium sp., Giardia duodenalis and Enterobius vermicularis. Revista do Instituto de Medicina Tropical de São Paulo 2006; 48: 269–273. [DOI] [PubMed] [Google Scholar]
  • 23.Menezes AL, et al. Prevalence of intestinal parasites in children from public daycare centers in the city of Belo Horizonte, Minas Gerais, Brazil. Revista do Instituto de Medicina Tropical de São Paulo 2008; 50: 57–59. [DOI] [PubMed] [Google Scholar]
  • 24.Albuquerque Aguiar JI, et al. Intestinal protozoa and helminths among Terena Indians in the State of Mato Grosso do Sul: high prevalence of Blastocystis hominis. Revista da Sociedade Brasileira de Medicina Tropical 2007; 40: 631–634. [DOI] [PubMed] [Google Scholar]
  • 25.Minè JC, da Rosa JA. Frequency of Blastocystis hominis and other intestinal parasites in stool samples examined at the Parasitology Laboratory of the School of Pharmaceutical Sciences at the Sao Paulo State University, Araraquara. Revista da Sociedade Brasileira de Medicina Tropical 2008; 41: 565–569. [DOI] [PubMed] [Google Scholar]
  • 26.Rodriguez Machado E, Silva Santos D, Costa-Cruz JM. Enteroparasites and commensals among children in four peripheral districts of Uberlandia, State of Minas Gerais. Revista da Sociedade Brasileira de Medicina Tropical 2008; 41: 581–585. [DOI] [PubMed] [Google Scholar]
  • 27.Toledo MJO, et al. Evaluation of enteroparasite control activities in a Kaingàng community of Southern Brazil. Revista de Saude Publica 2009; 43: 1–9. [DOI] [PubMed] [Google Scholar]
  • 28.Moura FT, et al. Enteroparasite contamination in peridomiciliar soils of two indigenous territories, State of Paranà, southern Brazil. Revista Panamericana de Salud Publica 2010; 27: 414–422. [DOI] [PubMed] [Google Scholar]
  • 29.Cimerman S, Cimerman B, Salomao Lewi D. Prevalence of intestinal parasitic infections in patients with acquired immunodeficiency syndrome in Brazil. International Journal of Infectious Diseases 1999; 3: 203–206. [DOI] [PubMed] [Google Scholar]
  • 30.Goncalves JF, et al. Parasitological and serological studies on amoebiasis and other intestinal parasitic infections in the rural sector around recife, Northeast Brazil. Revista do Instituto de Medicina Tropical de São Paulo 1990; 32: 428–435. [DOI] [PubMed] [Google Scholar]
  • 31.Kobayashi J, et al. Studies on prevalence of Strongyloides infection in Holambra and Maceiò, Brazil, by the agar plate faecal culture methos. Revista do Instituto de Medicina Tropical de São Paulo 1996; 38: 279–284. [DOI] [PubMed] [Google Scholar]
  • 32.Dorea RCC, et al. Control of parasitic infections among school children in the periurban area of Batuvatu, Sao Paulo, Brazil. Revista da Sociedade Brasileira de Medicina Tropical 1996; 29: 425–430. [DOI] [PubMed] [Google Scholar]
  • 33.Rodriguez Machado E, Costa-Cruz JM. Strongyloides stercoralis and other enteroparasites in children at Uberlandia City, State of Minas Gerais, Brasil. Memorias do Instituto Oswaldo Cruz 1998; 93: 161–164. [DOI] [PubMed] [Google Scholar]
  • 34.Tietz Marquez SM, Bandeira C, Quadros RM. Prevalence of enteroparasites in inhabitants of Concordia, Santa Catarina, Brazil. Parasitología Latinoamericana 2005; 60: 78–81. [Google Scholar]
  • 35.Zago-Gomes MP, et al. Prevalence of intestinal nematodes in alcoholic patients. Revista da Sociedade Brasileira de Medicina Tropical 2002; 35: 571–574. [DOI] [PubMed] [Google Scholar]
  • 36.Santos SA, Merlini LS. Prevalence of enteroparasitosis in the population of Maria Helena, Paraná State. Ciencia & Saùde Coletiva 2010; 15: 899–905. [DOI] [PubMed] [Google Scholar]
  • 37.Miranda RA, Xavier FB, Menezes RC. Intestinal parasitism in a Parakanã indigenous community in southwestern Pará State, Brazil. Cadernos de Saùde Pùblica, Rio de Janeiro 1998; 14: 507–511. [DOI] [PubMed] [Google Scholar]
  • 38.Hurtado-Guerrero AF, Alencar FH, Hurtado-Guerrero JC. Occurrence of enteroparasites in the elderly population of Nova Olinda do Norte, Amazonas, Brazil. Acta Amazonica 2005; 35: 487–490. [Google Scholar]
  • 39.Graeff-Teixeira C, et al. Prospective study of strongyloidosis in patients with hematologic malignancies. Revista da Sociedade Brasileira de Medicina Tropical 1997; 30: 355–357. [DOI] [PubMed] [Google Scholar]
  • 40.Dias RMDS, et al. Presence of Strongyloides stercoralis in patients with acquired immunodeficiency syndrome (AIDS). Revista do Instituto de Medicina Tropical de São Paulo 1992; 34: 15–17. [PubMed] [Google Scholar]
  • 41.Cutti E, Eloy A. Strongyloidiasis in Santa Clotilde (Rio NApo): use of modified Baermann technique with cup for faeces and sputum. Thesis. Faculdad de Medicina Alberto Hurtado, 1992. [Google Scholar]
  • 42.Egido JM, De Diego JA, Penin P. The prevalence of enteropathy due to strongyloidiasis in Puerto Maldonado (Peruvian Amazonia). Brazilian Journal of Infectious Diseases 2001; 5: 119–123. [DOI] [PubMed] [Google Scholar]
  • 43.Nicanor Ibañez H, et al. Prevalence of entero-parasites in school-age children of native communities of Alto Maranon, Amazon, Peru. Revista Peruana de Medicina Experimental y Salud Publica 2004; 21: 126–133. [Google Scholar]
  • 44.Bourée P, et al. Epidemiologic survey of intestinal parasitoses in Peruvian Amazonia. Bulletin de la Société de Pathologie Exotique Filiales 1984; 77: 690–698. [PubMed] [Google Scholar]
  • 45.Crotti D, et al. Preliminary survey of human intestinal parasitosis in a Peruvian Andean zone. Le Infezioni in Medicina 2007; 3: 181–186. [PubMed] [Google Scholar]
  • 46.Marcos L, et al. Intestinal parasitoses in rural and urban populations in Sandia, Department of Puno, Perù. Parasitología latinoamericana 2003; 58: 35–40. [Google Scholar]
  • 47.Carpio IN, et al. Presence of Strongyloides stercoralis in an enteroparasites study in school students of 'La Candelaria', district of Chancay, province of Huaral, department of Lima. Acta Médica Peruana 2007; 24: 177–180. [Google Scholar]
  • 48.Rodriguez J, Calderon J. Intestinal parasitoses in pre-school children of Tarapoto. Revista de Gastroenterología del Perú 1991; 11: 153–160. [PubMed] [Google Scholar]
  • 49.Garcia C, et al. Intestinal parasitosis in HIV/AIDS patients. Revista de Gastroenterología del Perú 2006; 26: 21–24. [PubMed] [Google Scholar]
  • 50.Huaroto Sedda M, Osorio Naupari M, Ayala Espinoza L. Study of Strongyloides stercoralis in the duodenal juice obtained by the examination of a string capsule or the Enterotest. Revista de Gastroenterología del Perú 1990; 10: 107–110. [PubMed] [Google Scholar]
  • 51.Ministerio de Salud. Oficina General de Epidemiología. Intestinal helminths in Perù: analysis of prevalence (1981–2001), 2003; Peru, Lima. [Google Scholar]
  • 52.Menghi CI, et al. Survey of intestinal parasites among an aborigenal community in Salta. Medicina (Buenos Aires) 2007; 67: 705–708. [PubMed] [Google Scholar]
  • 53.Taranto NJ, et al. Clinical status and parasitic infection in a Wichì Aboriginal community in Salta, Argentina. Transactions of the Royal Society of Tropical Medicine and Hygiene 2003; 97: 554–558. [DOI] [PubMed] [Google Scholar]
  • 54.Zonta ML, Oyhenart EE, Navone GT. Nutritional status, body composition, and intestinal parasitism among the Mbya-Guarani communities of Misiones, Argentina. American Journal of Human Biology 2010; 22: 193–200. [DOI] [PubMed] [Google Scholar]
  • 55.Navone GT, et al. Intestinal parasitosis in Mbyà-Guaranì populations from Misiones Province, Argentina: epidemiological and nutritional aspects. Cadernos de Saùde Pùblica, Rio de Janeiro 2006; 22: 1089–1110. [DOI] [PubMed] [Google Scholar]
  • 56.Milano AM, et al. Children enteroparasitosis in north east Argentine urban area. Medicina (Buenos Aires) 2007; 67: 238–242. [PubMed] [Google Scholar]
  • 57.Borda CE, et al. Intestinal parasitism in San Caytano, Corrientes, Argentina. Bulletin of the Pan American Health Organization 1996; 30: 227–233. [PubMed] [Google Scholar]
  • 58.Basualdo JA, et al. Intestinal parasitoses and enviromental factors in a rural population of Argentina, 2002–2003. Revista do Instituto de Medicina Tropical de São Paulo 2007; 49: 251–255. [DOI] [PubMed] [Google Scholar]
  • 59.Gamboa MI, et al. Associations between geo-helminths and socio-environmental conditions among different human populations in Argentina. Revista Panamericana de Salud Publica 2009; 26: 1–8. [DOI] [PubMed] [Google Scholar]
  • 60.Lura MCE, Beltramino DM, De Carrera EF. Prevalence of intestinal helminths in students of the city of Santa Fe. Medicina (Buenos Aires) 2002; 62: 29–36. [PubMed] [Google Scholar]
  • 61.Pezzani BC, et al. Intestinal parasite infections in a periurban community from the Province of Buenos Aires, Argentina. Boletín Chileno de Parasitología 1996; 51: 42–45. [PubMed] [Google Scholar]
  • 62.Peplow D. Intestinal parasites among the populations of various regions of Ecuador: statistical study. Boletín de la Oficina Sanitaria Panamericana 1982; 93: 233–239. [PubMed] [Google Scholar]
  • 63.Moncayo AL, et al. Impact of long-term treatment with ivermectin on the prevalence and intensity of soil-transmitted helminth infections. PLoS Neglected Tropical Diseases 2008; 2: e293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Andrade C, et al. Prevalence and intensity of soil-transmitted helminthiasis in the city of Portoviejo (Ecuador). Memorias do Instituto Oswaldo Cruz 2001; 96: 1075–1079. [DOI] [PubMed] [Google Scholar]
  • 65.Jacobsen KH, et al. Prevalence of intestinal parasites in young Quichua children in the Highlands of rural Ecuador. Journal of Health Population and Nutrition 2007; 25: 399–405. [PMC free article] [PubMed] [Google Scholar]
  • 66.Cooper PJ, et al. Relationship between bacille Calmette-Guérin vaccination, Mantoux test positivity, and geohelminth infection. Transactions of the Royal Society of Tropical Medicine and Hygiene 2003; 97: 473–476. [DOI] [PubMed] [Google Scholar]
  • 67.Cooper PJ, Guevara A, Guderian RH. Intestinal helminthiases in Ecuador: the relationship between prevalence, genetic, and socioeconomic factors. Revista de Sociedade Brasileira de Medicina Tropical 1993; 26: 175–180. [DOI] [PubMed] [Google Scholar]
  • 68.Garibaldi R, et al. Intestinal parasites and ectoparasites in the V region, Chile: study in the Psychiatric Hospital of Putaendo. Boletín Chileno de Parasitología 1990; 45: 83–85. [PubMed] [Google Scholar]
  • 69.Schenone H, et al. Epidemiological aspects of protozoan and intestinal helminthic human infections in Chile (1970–1980). Boletín Chileno de Parasitología 1981; 36: 44–48. [PubMed] [Google Scholar]
  • 70.Cornejo J, et al. Epidemiological survey of protozoans and intestinal helminths in 490 chronic patients of the Psychiatric Hospital of Putaendo, V region, Chile, 1985. Boletín Chileno de Parasitología 1985; 40: 91–93. [PubMed] [Google Scholar]
  • 71.Diaz AI, et al. Prevalence of intestinal parasites in children in Yukpa Ethnia in Toromo, Zulia State, Venezuela. Revista Médica de Chile 2006; 134: 72–78. [DOI] [PubMed] [Google Scholar]
  • 72.Miller SA, et al. Intestinal parasitic infection and associated symptoms in children attending day care centres in Trujillo, Venezuela. Tropical Medicine and International Health 2003; 8: 342–347. [DOI] [PubMed] [Google Scholar]
  • 73.Rodriguez-Morales AJ, et al. Intestinal parasitic infections among pregnant women in Venezuela. Infectious Diseases in Obstetrics and Gynecology 2006; 23125: 1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Chacin-Bonilla L, Sanchez-Chavez Y. Intestinal parasitic infections, with a special emphasis on cryptosporidiosis, in amerindians from Western Venezuela. American Journal of Tropical Medicine and Hygiene 2000; 62: 347–352. [DOI] [PubMed] [Google Scholar]
  • 75.Figuera L, Ramirez E, Merchàn E. Strongyloides stercoralis: prevalence and diagnosis evaluation using four coproparasitologic methods. Revista de la Sociedad Venezolana de Microbiología 2002; 22. [Google Scholar]
  • 76.Agudelo-Lopez S, et al. Prevalence of intestinal parasitism and associated factors in a village on the Colombian Atlantic Coast. Revista de Salud Publica 2008; 10: 633–642. [DOI] [PubMed] [Google Scholar]
  • 77.Alvarado BE, Vasquez LR. Social determinants, feeding practices and nutritional consequences of intestinal parasitism in young children. Biomedica 2006; 26: 82–94. [PubMed] [Google Scholar]
  • 78.Botero JH, et al. A preliminary study of the prevalence of intestinal parasites in immunocompromised patients with and without gastrointestinal manifestations. Revista do Instituto de Medicina Tropical de São Paulo 2003; 45: 197–200. [DOI] [PubMed] [Google Scholar]
  • 79.Lindo JF, et al. Intestinal parasitic infections in human immunodeficiency virus (HIV)-positive and HIV-negative individuals in San Pedro Sula, Honduras. American Journal of Tropical Medicine and Hygiene 1998; 58: 431–435. [DOI] [PubMed] [Google Scholar]
  • 80.Kaminsky RG, et al. Intestinal parasitic infections and eosinophilia in a human immunodeficiency virus positive population in Honduras. Memórias do Instituto Oswaldo Cruz 2004; 99: 773–778. [DOI] [PubMed] [Google Scholar]
  • 81.Kaminsky RG. Parasitism and diarrhoea in children from two rural communities and marginal barrio in Honduras. Transactions of the Royal Society of Tropical Medicine and Hygiene 1991; 85: 70–73. [DOI] [PubMed] [Google Scholar]
  • 82.Sanchez A, Mora J, Hemandez F. Prevalence of intestinal parasites in older adults, Hospital Raùl Blanco Cervantes. Revista Costarricense de Ciencias Medicas 1999; 20: 3–4. [Google Scholar]
  • 83.Bouza-Mora L, et al. Strongyloides stercoralis in psychiatric patients. Revista Costarricense de Ciencias Medicas 2004; 25: 3–4. [Google Scholar]
  • 84.Avedano L, et al. Strongyloides stercoralis in alcoholic patients. Parasitologìa al Dìa 1999; 23: 3–4. [Google Scholar]
  • 85.Cancrini G, et al. Parasitological observations on three Bolivian localities including rural communities, cities and institutions. Annals of Tropical Medicine and Parasitology 1989; 83: 591–594. [DOI] [PubMed] [Google Scholar]
  • 86.Muñoz Ortiz V, et al. Blastocistosis and other intestinal parasitosis in elderly residents from San Ramón home, La Paz, Bolivia. Biofarbo 2008; 16: 9–15. [Google Scholar]
  • 87.Aguilar FJ. Soil-transmitted human helminthiasis in Guatemala. Boletín Chileno de Parasitología 1981; 36: 6–9. [PubMed] [Google Scholar]
  • 88.Lindo JF, et al. Intestinal parasites among young children in the interior of Guyana. West Indian Medical Journal 2002; 51: 25–27. [PubMed] [Google Scholar]
  • 89.Guarner J, et al. Frequency of intestinal parasites in adult cancer patients in Mexico. Archives of Medical Research 1997; 28: 219–222. [PubMed] [Google Scholar]
  • 90.Faulkner CT, et al. Prevalence of endoparasitic infection in children and its relation with cholera prevention efforts in Mexico. Revista Panamericana de Salud Publica 2003; 14: 31–41. [DOI] [PubMed] [Google Scholar]
  • 91.Tellez A, et al. Prevalence of intestinal parasites in the human population of Leon, Nicaragua. Acta Tropica 1997; 66: 119–125. [DOI] [PubMed] [Google Scholar]
  • 92.Hillyer GV, de Galanes MS, Lawrence S. Prevalence of intestinal parasites in a rural community in North-Central Puerto Rico. Boletín de la Asociación Médica de Puerto Rico 1990; 82: 111–114. [PubMed] [Google Scholar]
  • 93.Rivera-Marrero CA. Prevalence and intensity of helminth infections in South-West Puerto Rico. Journal of Parasitology 1986; 72: 787–788. [PubMed] [Google Scholar]
  • 94.Machicado JD, et al. Diagnosis of soil-transmitted helminthiasis in an Amazonic community of Peru using multiple diagnostic techniques. Transactions of the Royal Society of Tropical Medicine and Hygiene 2012; 106: 333–339. [DOI] [PubMed] [Google Scholar]
  • 95.Bisoffi Z, et al. Diagnostic accuracy of five serologic tests for Strongyloides stercoralis infection. PLoS Neglected Tropical Diseases 2014; 8: e2640. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Shär F, et al. Strongyloides stercoralis: global distribution and risk factors. PLoS Neglected Tropical Diseases 2013; 7: e2288. [DOI] [PMC free article] [PubMed] [Google Scholar]

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