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HIGH PREVALENCE OF Strongyloides stercoralis INFECTION AMONG THE ELDERLY IN BRAZIL

Alta prevalência da infecção por Strongyloides stercoralis em idosos do Brasil

Abstracts

SUMMARY

Little is known about the frequency of intestinal parasites in the elderly due to a lack of attention given to the occurrence of these infections among older adults. This study compares the frequency of Strongyloides stercoralis and other enteroparasites between elderly living in nursing homes (n = 100) and those noninstitutionalized (n = 100) from Uberlândia, state of Minas Gerais, southeastern Brazil, associated with data of epidemiological and socio-demographic conditions. Through coproparasitological examination of both groups, enteroparasites were detected in 15 of 200 individuals examined (7.5%; CI: 5.1- 9.9). S. stercoralis was the most frequent parasite 10/200 (5%; CI: 4.2-5.8), being significantly higher in males and in individuals with autonomy for daily living activities. There were no statistical differences in the prevalence of parasites between the two groups compared. In conclusion, S. stercoralis infection was highly prevalent in elderly patients and it does not depend on whether the individual was institutionalized or not.

Strongyloides stercoralis; Elderly; Intestinal parasites; Brazil


RESUMO

Pouco é conhecido sobre a freqüência de parasitas intestinais em idosos devido à falta de atenção dada à ocorrência destas infecções nesta faixa etária. Este estudo compara a freqüência de Strongyloides stercoralis e outros parasitos intestinais entre idosos residindo em lares para idosos (n = 100) e aqueles não institucionalizados (n = 100) de Uberlândia, Minas Gerais, região sudeste do Brasil, associados com dados epidemiológicos e condições sócio-demográficas. Ambos os grupos foram submetidos a exames coproparasitológicos. Parasitos foram detectados em 15 dos 200 indivíduos examinados (7,5%; CI: 5,1 - 9,9). S. stercoralis foi o parasito mais freqüente 10/200 (5%; CI: 4,2 - 5,8), sendo significantemente maior em homens e indivíduos com autonomia das atividades diárias. Não houve diferença estatística entre a prevalência de parasitos quando os dois grupos foram comparados. Concluiu-se que a infecção por S. stercoralis foi altamente prevalente em idosos independente se institucionalizados ou não.


INTRODUCTION

The aging of the human population constitutes a great challenge for the modern society77. Bookman A, Kimbrel D. Families and elder care in the twenty-first century. Future Child. 2011;21:117-40. 1111. Cronin J, Livhits M, Mercado C, Chen F, Foster N, Chandler C, et al. Quality improvement pilot program for vulnerable elderly surgical patients. Am Surg. 2011;77:1305-8. 1313. Dong X, Simon MA, Mosqueda L, Evans DA. The prevalence of elder self-neglect in a community-dwelling population: hoarding, hygiene, and environmental hazards. J Aging Health. 2012;24:507-24. 1717. Elwér S, Aléx L, Hammarström A. Gender (in)equality among employees in elder care: implications for health. Int J Equity Health. 2012;11:1-10.. It became necessary to accomplish epidemiological studies to know the profile of the elderly population, and also the needs and demands for social and health services that guarantee good health and improvement of their life quality99. Chaimowicz F. A saúde dos idosos brasileiros às vésperas do século XXI: problemas, projeções e alternativas. Rev Saude Publica. 1997;31:184-200. 1414. Dong X, Simon MA, Evans D. Elder self-neglect and hospitalization: findings from the Chicago health and aging project. J Am Geriatr Soc. 2012;60:202-9. 4343. van Maanen HM. Being old does not always mean being sick: perspectives on conditions of health as perceived by British and American elderly 1987. J Adv Nurs. 2006;53:54-61..

Age-related malnutrition, morphological and physiological alterations and immunity dysfunction can enhance susceptibility for cancer, chronic degenerative and autoimmune diseases, increasing illness and death rates in elderly people8,15,18.34.

According to the World Health Organization, protozoal and helminthic intestinal infections are believed to affect 3.5 billion people worldwide, causing illness in 450 million3535. Schuster H, Chiodini PL. Parasitic infections of the intestine. Curr Opin Infect Dis. 2001;14:587-91.. Helminth infections are highly prevalent in tropical and subtropical areas, where the low socioeconomic level and the precarious hygienic-sanitary conditions are favorable for the transmission and maintenance of these pathogens4545. Ziegelbauer K, Speich B, Mäusezahl D, Bos R, Keiser J, Utzinger J. Effect of sanitation on soil-transmitted helminth infection: systematic review and meta-analysis. PLoS Med. 2012;9(1):e1001162.. Among the parasitic nematodes, Strongyloides stercoralis is the most aggressive parasite, since it may cause hyperinfection and dissemination of strongyloidiasis through auto-infection2020. Gotuzzo E, Terashima A, Alvarez H, Tello R, Infante R, Watts DM, et al. Strongyloides stercoralis hyperinfection associated with human T cell lymphotropic virus type-1 infection in Peru. Am J Trop Med Hyg. 1999;60:146-9. 2323. Marcos LA, Terashima A, Canales M, Gotuzzo E. Update on strongyloidiasis in the immunocompromised host. Curr Infect Dis Rep. 2011;13:35-46. 2727. Paula FM, Costa-Cruz JM. Epidemiological aspects of strongyloidiasis in Brazil. Parasitology. 2011;138:1331-40. Thus, chronic intestinal parasitism in elderly patients may result in a serious health problem2727. Paula FM, Costa-Cruz JM. Epidemiological aspects of strongyloidiasis in Brazil. Parasitology. 2011;138:1331-40 2929. Pirisi M, Salvador E, Bisoffi Z, Gobbo M, Smirne C, Gigli C, et al. Unsuspected strongyloidiasis in hospitalised elderly patients with and without eosinophilia. Clin Microbiol Infect. 2006;12:787-92. 3232. Rodrigues MA, Fróes RC, Anefalos A, Kobayasi S. Invasive enteritis by Strongyloides stercoralis presenting as acute abdominal distress under corticosteroid therapy. Rev Hosp Clin Fac Med Sao Paulo. 2001;56:103-6..

According to the prevalence, the infection by Strongyloides is classified as: sporadic (< 1%), endemic (1-5%) and hyperendemic (> 5%)2828. Pires ML, Dreyer G. The importance of Strongyloides stercoralis revisited. Rev Hosp Clin Fac Med Sao Paulo. 1993;48:175-82. and its heterogeneous worldwide distribution makes the strongyloidiasis an important current subject. For instance, in healthcare of the Valencian community (Spain), in a total of 493 cases of strongyloidiasis diagnosed, 94% were found in patients in the 51-91 years age group22. Alcaraz CO, Adell RI, Sánchez PS, Blasco MJ, Sánchez OA, Auñón AS, et al. Characteristics and geographical profile of strongyloidiasis in healthcare area 11 of the Valencian community (Spain). J Infect. 2004;49:152-8.. Little is known about the frequency of intestinal parasites in the elderly in Brazil or in the rest of the world due to a lack of studies on the occurrence of some neglected infections among older individuals.

Thus, the aim of this study was to compare the frequency of S. stercoralis and other enteroparasites among older adults living in nursing homes and non-institutionalized older individuals, associated with data of epidemiological and socio-demographic conditions.

MATERIALS AND METHODS

This study was approved by the Research Ethics Committee of the Federal University of Uberlândia and was evaluated from August 2002 to August 2003.

Group 1 consisted of 100 (42 men and 58 women) asymptomatic older people (≥ 60 years old), picked randomly from among the 139 individuals living in nursing homes, from four philanthropic institutions in Uberlândia, state of Minas Gerais, southeastern region of Brazil.

Group 2 consisted of 100 (41 men and 59 women) randomly selected asymptomatic non-institutionalized elderly (≥ 60 years old) from the Centro Educacional de Assistência Integrada (CEAI) that renders service in health, education, culture, leisure and social welfare fields. A questionnaire was used to evaluate the epidemiological and sociodemographic data of the elderly people.

Both groups were submitted to an individual stool examination of three fecal samples. Fecal samples were collected in plastic vials without preservatives with intervals of one to four days, and processed by three coprological methods: the Baermann33. Baermann G. Eine Einfache Methode zur Auffindung von Ankylostomun (Nematoden) Larven in Erdproben Mededeel. mith. H. Geneesk. Batavia: Lab. Weltreveden Feestbundel; 1917. p. 41-7., HOFFMANN et al. 2121. Hoffmann WA, Pons JA, Janer JL. The sedimentation concentration method in schistosomiasis mansoni. Puerto Rico J Public Health Trop Med. 1934;9:283-91. and RITCHIE3030. Ritchie LS. An ether sedimentation technique for routine stool examinations. Bull U S Army Med Dep. 1948;8:326. and by the Safranin/Methylene Blue staining technique44. Baxby D, Blundell N, Hart CA. The development and performance of a simple, sensitive method for detection Cryptosporidium oocysts in faeces. J Hyg. (Lond.) 1984;93:317-23.. Six hundred samples were collected. There being four slides for each sample and for each method. A total of 9,600 slides were analyzed under light microscope (Olympus, CH-2, Japan) at ×100, ×400 and ×1000 by two investigators. Positive cases for parasites were referred to the nearest health unit in order to receive specific treatment.

Statistical analysis was performed with a relative test of the difference between two proportions (Z) using Statistics for Windows - Release 4.5 statistical software (Statsoft Inc. 1993) to determine the association between Groups 1 and 2. A 95% confidence interval (CI) was stipulated. Results were considered significant when p < 0.05.

RESULTS

Table 1 characterizes both groups according to epidemiological and socio-demographic aspects. In Group 1 the ages ranged from 60 to 98 years old and in Group 2 from 60 to 96 years old. In both groups, women were predominant (58% in Group 1 and 59% in Group 2).

Table 1
Distribution of epidemiological and socio-demographic parameters in institutionalized (Group 1) and non-institutionalized (Group 2) elderly from Uberlândia, Brazil

Parasites were detected in 15 of 200 elderly individuals examined (7.5% CI: 5.1-9.9). Fecal consistence of all the samples collected was not diarrheic. The age group distribution of enteroparasite infected elderly respectively for Groups 1 and 2 was 60-69 y [3/28 (9.3%) and 0/35]; 70-79 y [0/32 and 5/47 (10.6%)] and ≥ 80 y [5/40 (12.5%) and 2/18 (11.1%)]. A possible tendency for progressive increase of the parasitism was observed among the age groups, though a statistically significant difference was not seen.

Table 2 presents the frequency of the parasites in both groups; S. stercoralis was the most frequent parasite 10/200 (5% CI 4.2-5.8). All infected subjects presented asymptomatic strongyloidiasis. The proportion of infected men in relation to women was 4:1 in both groups. A case of co-infection was observed in Group 1. From the 10 S. stercoralis positive cases eight (80%) were male subjects with autonomy for activities of daily living (ADL) (p < 0.05). Three of the ten infected elderly (30%) had a past history of alcoholism, two (20%) being from subjects of Group 1, one of them shedding filariform larvae (L3) in the feces, as well as the individual of Group 2.

Table 2
Frequency of enteroparasites in institutionalized of Group 1(n = 100) and non-institutionalized Group 2 (n = 100) elderly from Uberlândia, Southeastern Brazil

DISCUSSION

The frequency (7.5%) of enteroparasites found in this study reveals clinical and epidemiological importance. The control of enteroparasite infection is still a challenge in developing countries due to susceptibility of the host, favorable conditions of the environment, low socioeconomic level and precarious hygienic sanitary conditions1616. Egido JM, De Diego JA, Penin P. The prevalence of enteropathy due to strongyloidiasis in Puerto Maldonado (Peruvian Amazon). Braz J Infect Dis. 2001;5:119-23. 4545. Ziegelbauer K, Speich B, Mäusezahl D, Bos R, Keiser J, Utzinger J. Effect of sanitation on soil-transmitted helminth infection: systematic review and meta-analysis. PLoS Med. 2012;9(1):e1001162.. SIRIVICHAYAKUL et al. 3939. Sirivichayakul C, Pojjaroen-anant C, Wisetsing P, Siripanth C, Chanthavanich P, Pengsaa K. Prevalence of intestinal parasitic infection among Thai people with mental handicaps. Southeast Asian J Trop Med Public Health. 2003;34:259-63. have found that the prevalence of infection is much higher in institutionalized mentally handicapped than in non-institutionalized people, since collective living conditions are risk factors for high prevalence of parasitism at the institutions. However, the parasite prevalence detected in the present study cannot be compared to the other studies due to the lack of studies among institutionalized individuals.

In spite of the fact that there were differences between the two groups regarding the socio-demographic parameters, these did not influence the results, due to the fact that the prevalence of enteroparasites was similar in both groups. In the population studied a slight increase frequency among women can be explained by a higher female life expectancy than that of men. The marital status, bachelors or widowers, associated with the lack of financial resources and loss of autonomy for ADL, may play an important role in the institutionalization process3131. Robles L, Rizo Curiel G, Camarena Garcia LM, Cervantes Coles L, Gomez Medrano M, Siordia Gonzalez M. Redes y apoyo social en ancianos enfermos de escasos recursos en Gualadajara, México. Cad Saude Publica. 2000;16:557-60.. In Brazil, the idea that the care of the elderly is the responsibility of the family still flourishes. However, social policies are needed to aid and support those elderly without financial resources in order to avoid institutionalization99. Chaimowicz F. A saúde dos idosos brasileiros às vésperas do século XXI: problemas, projeções e alternativas. Rev Saude Publica. 1997;31:184-200. 1212. de Queiroz ZP, Lemos N de F, Ramos LR. Fatores potencialmente associados à negligência doméstica entre idosos atendidos em programa de assistência domiciliar. Cien Saude Colet. 2010;15:2815-24..

In the present study, S. stercoralis was the most frequent enteroparasite among the infected individuals, 80% of them being men, all having presented asymptomatic strongyloidiasis. These findings were in accordance with other studies22. Alcaraz CO, Adell RI, Sánchez PS, Blasco MJ, Sánchez OA, Auñón AS, et al. Characteristics and geographical profile of strongyloidiasis in healthcare area 11 of the Valencian community (Spain). J Infect. 2004;49:152-8. 1616. Egido JM, De Diego JA, Penin P. The prevalence of enteropathy due to strongyloidiasis in Puerto Maldonado (Peruvian Amazon). Braz J Infect Dis. 2001;5:119-23. 3333. Rodriguez Calabuig D, Oltra Alcaraz C, Igual Adell R, Parra Godoy F, Martinez Sanchez J, Angle Rodenas C, et al. Treinta casos de estrongiloidiasis en un centro de atención primaria. Aten Primaria. 1998;21:271-4.. The asymptomatic infection which occurs in most of the patients chronically infected may persist for several decades2626. Oliveira LCM, Ribeiro CT, Mendes DM, Oliveira TC, Costa-Cruz JM. Frequency of Strongyloides stercoralis infection in alcoholics. Mem Inst Oswaldo Cruz. 2002;97:119-21. 3737. Segovia Hernández M, Martinez Toldos C. Clinical significance of Strongyloides stercoralis in our environment. Rev Clin Esp. 2001;201:57-8.. However, in some cases the infection may be followed by symptoms such as diarrhea, abdominal pain, nausea, malabsorption, weight loss and anemia11. Adedayo O, Grell G, Bellot P. Hyperinfective strongyloidiasis in the medical ward: review of 27 cases in 5 years. South Med J. 2002;95:711-6. 2323. Marcos LA, Terashima A, Canales M, Gotuzzo E. Update on strongyloidiasis in the immunocompromised host. Curr Infect Dis Rep. 2011;13:35-46.. Some reports have described a significant association between human T cell lymphotropic virus type-1 (HTLV-1) and S. stercoralis hyperinfection2020. Gotuzzo E, Terashima A, Alvarez H, Tello R, Infante R, Watts DM, et al. Strongyloides stercoralis hyperinfection associated with human T cell lymphotropic virus type-1 infection in Peru. Am J Trop Med Hyg. 1999;60:146-9. 4040. Terashima A, Gotuzzo E, Alvarez H, Infante R, Tello R, Watts D, et al. Strongyloides stercoralis: formas clínicas severas asociadas a infección por HTLV-1. Rev Gastroenterol Peru. 1999;19:35-40. 4141. Terashima A, Alvarez H, Tello R, Infante R, Freedman DO, Gotuzzo E. Treatment failure in intestinal strongyloidiasis: an indicator of HTLV-I infection. Int J Infect Dis. 2002;6:28-30.. Case reports of hyperinfection syndrome or disseminated infection in immunocompromised elderly showed high mortality indexes associated with the use of immunosuppressive therapy as well as protein-caloric malnutrition and the aging process3232. Rodrigues MA, Fróes RC, Anefalos A, Kobayasi S. Invasive enteritis by Strongyloides stercoralis presenting as acute abdominal distress under corticosteroid therapy. Rev Hosp Clin Fac Med Sao Paulo. 2001;56:103-6. 4242. Upadhyay D, Corbridge T, Jain M, Shah R. Pulmonary hyperinfection syndrome with Strongyloides stercoralis. Am J Med. 2001;111:167-9.. Chronic alcoholism is another factor referred to as a predisposition to strongyloidiasis, and the frequency of infection by S. stercoralis in alcoholic patient varies from 33.3% to 44%11. Adedayo O, Grell G, Bellot P. Hyperinfective strongyloidiasis in the medical ward: review of 27 cases in 5 years. South Med J. 2002;95:711-6. 4242. Upadhyay D, Corbridge T, Jain M, Shah R. Pulmonary hyperinfection syndrome with Strongyloides stercoralis. Am J Med. 2001;111:167-9.. In this study, among the individuals that had a past history of alcoholism, two were shedding (L3) larvae in feces, suggesting cases of hyperinfection. The findings suggest that strongyloidiasis remains a serious public health problem in older individuals. As demonstrated by three fecal samples, the prevalence of strongyloidiasis is probably underestimated in literature because the diagnosis is difficult and false negative results become frequent due to a scarcity or absence of worms at the moment of the examination in asymptomatic patients, because it is imperative that multiple stool samples be examined in order to make a correct diagnosis3838. Siddiqui AA, Berk SL. Diagnosis of Strongyloides stercoralis infection. Clin Infect Dis. 2001;33:1040-7..

Hookworm infections have heterogeneous global distribution and high prevalence in the developing countries in tropical and subtropical areas66. Bethony J, Chen J, Lin S, Xiao S, Zhan B, Li S, et al. Emerging patterns of hookworm infection: influence of aging on the intensity of Necator infection in Hainan Province, People's Republic of China. Clin Infect Dis. 2002;35:1336-44. 1010. Changhua L, Xiaorong Z, Dongchuan Q, Shuhua X, Hotez PJ, Defu Z, et al. Epidemiology of human hookworm infections among adult villagers in Hejiang and Santai Counties, Sichuan Province, China. Acta Trop. 1999;73:243-9. 4545. Ziegelbauer K, Speich B, Mäusezahl D, Bos R, Keiser J, Utzinger J. Effect of sanitation on soil-transmitted helminth infection: systematic review and meta-analysis. PLoS Med. 2012;9(1):e1001162.. CHANGHUA et al. 1010. Changhua L, Xiaorong Z, Dongchuan Q, Shuhua X, Hotez PJ, Defu Z, et al. Epidemiology of human hookworm infections among adult villagers in Hejiang and Santai Counties, Sichuan Province, China. Acta Trop. 1999;73:243-9. observed that the prevalence of hookworm infection increased with age. The frequency of hookworm infection (2%) found in this study was lower than that reported by different researchers in epidemiological studies carried out in provinces of China. The high prevalence of hookworm infections in elderly Chinese patients has been attributed to the constant soil polluted with human feces that is used for fertilizing vegetables66. Bethony J, Chen J, Lin S, Xiao S, Zhan B, Li S, et al. Emerging patterns of hookworm infection: influence of aging on the intensity of Necator infection in Hainan Province, People's Republic of China. Clin Infect Dis. 2002;35:1336-44. 1010. Changhua L, Xiaorong Z, Dongchuan Q, Shuhua X, Hotez PJ, Defu Z, et al. Epidemiology of human hookworm infections among adult villagers in Hejiang and Santai Counties, Sichuan Province, China. Acta Trop. 1999;73:243-9., which does not occur in Brazil.

The highly significant association between hookworm and S. stercoralis (OR > 6), and the series of self-reported morbidity markers associated with these two helminth species are particularly noteworthy. The S. stercoralis age-prevalence curve showed an almost parallel shape to the hookworm age-prevalence curve, reaching an infection rate of approximately 20% in older adults55. Becker SL, Sieto B, Silué KD, Adjossan L, Koné S, Hatz C, et al. Diagnosis, clinical features, and self-reported morbidity of Strongyloides stercoralis and hookworm infection in a co-endemic setting. PLoS Negl Trop Dis. 2011;5(8):e1292.. In the present study, infection by S. stercoralis and hookworm in institutionalized elderly was also detected; however, the probable source of infection was not due to institutionalization. They had no contact with the ground in any of the four institutions neither did they have contact with the external environment of the institutions; therefore it is possible that the elderly were infected prior to institutionalization.

The frequency (1%) of Giardia lamblia was found lower than that observed by other authors, being all asymptomatic individuals1919. Giacometti A, Cirione O, Fortuna M, Drenaggi D, Veccia S, D'Errico MM, et al. La giardiasi: una parassitosi di continua attualità. Indagine tra una selezionata popolazione adulta. Infez Med. 2000;8:82-6. 2222. Laishram S, Kang G, Ajjampur SS. Giardiasis: a review on assemblage distribution and epidemiology in India. Indian J Gastroenterol. 2012;31:3-12.. Nevertheless, G. lamblia may cause acute diarrhea, besides other symptoms such as, abdominal pain, nausea, vomiting, malabsorption, fever, appetite and weight loss2222. Laishram S, Kang G, Ajjampur SS. Giardiasis: a review on assemblage distribution and epidemiology in India. Indian J Gastroenterol. 2012;31:3-12..

Balantidium coli is the only known pathogenic ciliated protozoa that can produce disease in humans. The infection may be subclinical in humans, as it is mostly in pigs, or may develop as a fulminant infection with bloody and mucus-containing diarrhea; this can lead to perforation of the colon. Occasionally, the parasite is able to invade organs and cause ulcerations in the mucosa and submucosa membranes, thrombosis in the affected vessels and even pulmonary colonization3636. Schuster FL, Ramirez-Avila L. Current world status of Balantidium coli. Clin Microbiol Rev. 2008,21:626-38. 4444. Vasilakopoulou A, Dimarongona K, Samakovli A, Papadimitris K, Avlami A. Balantidium coli pneumonia in an immunocompromised patient. Scand J Infect Dis. 2003;35:144-6.. In the present study, a case of asymptomatic balantidiasis was detected; possibly a chronic infection, since the infected individual was an 87 year old woman, who had been living in the institution for more than two years.

Balantidiasis is a zoonotic disease and is acquired by humans via the fecal-oral route from the normal host, the pig, where it is asymptomatic. Water is the vehicle for most cases of balantidiasis. Human-to-human transmission may also occur. The major factors leading to human balantidiasis include (i) close contact between pigs and humans, (ii) a lack of appropriate waste disposal in swine and human excrement contaminate drinking water sources (e.g., wells and streams) and food, and (iii) subtropical and/or tropical climatic conditions (e.g., warmth and humidity) favoring survival of cysts. In institutional populations (mental hospitals, prisons, and orphanages), where pigs are an unlikely source of infection, outbreaks are the result of asymptomatic carriers and the difficulties involved in maintaining hygienic control3636. Schuster FL, Ramirez-Avila L. Current world status of Balantidium coli. Clin Microbiol Rev. 2008,21:626-38.. In our study, the only elderly that presented B. coli in the feces were institutionalized and probably acquired the protozoan prior to the admission to the institution considering that the local hygienic conditions were strictly controlled and the elderly had no contact with the external environment.

Studies have suggested that elderly individuals have an increased risk for occurrence of severe cryptosporidiosis. Cryptosporidium is a cause of acute infectious diarrhea in elderly, the disease being characterized by a shorter incubation period, probably due to a greater inherent host susceptibility to parasite infection2424. Naumova EN, Egorov AI, Morris RD, Griffiths JK. The elderly and waterborne Cryptosporidium infection: gastroenteritis hospitalizations before and during the 1993 Milwaukee outbreak. Emerg Infect Dis. 2003;9:418-25. 2525. Neill MA, Rice SK, Ahmad NV, Flanigan TP. Cryptosporidiosis: an unrecognized cause of diarrhea in elderly hospitalized patients. Clin Infect Dis. 1996;22:168-70.. This fact was not observed in this study and no case of cryptosporidiosis was detected in the elderly by using Safranin/Methylene-Blue staining technique44. Baxby D, Blundell N, Hart CA. The development and performance of a simple, sensitive method for detection Cryptosporidium oocysts in faeces. J Hyg. (Lond.) 1984;93:317-23..

In conclusion, S. stercoralis infection was highly prevalent in the studied population and it does not depend on whether the individual was institutionalized or not. Therefore, early diagnosis through specific methods is relevant in asymptomatic elderly in order to prevent the risk of hyperinfection or disseminated infection, thus avoiding high mortality rates.

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Publication Dates

  • Publication in this collection
    Sep-Oct 2013

History

  • Received
    16 Mar 2012
  • Accepted
    20 Feb 2013
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