Higher congenital transmission rate of Trypanosoma cruzi associated with family history of congenital transmission

Abstract INTRODUCTION: Congenital transmission (CT) of Trypanosoma cruzi has led to globalization of Chagas disease and its growing relevance as a public health problem. Although the occurrence of CT has been associated with several factors, its mechanisms are still unknown. This study aimed to analyze the geographical and familiar variables of mothers and their association with CT of Chagas disease in a population living in non-endemic areas of Argentina for the last decades. METHODS: We developed a retrospective cohort study in a sample of 2120 mother-child pairs who attended three reference centers in the cities of Buenos Aires, Santa Fe, and Salta between 2002 and 2015. RESULTS: The highest CT rates were observed in children born to Argentinean mothers (10.7%) and in children born to mothers from Buenos Aires (11.7%). Considering the areas of origin of the mothers, those from areas of null-low risk for vector-borne infection had higher CT rates than those from areas of medium-high risk (11.1% vs 8.2%). We also observed a significant intra-familiar "cluster effect," with CT rates of 35.9% in children with an infected sibling, compared to 8.2% in children without infected siblings (RR=4.4 95% CI 2.3-8.4). CONCLUSIONS: The associations observed suggest a higher CT rate in children born to mothers who acquired the infection congenitally, with familiar antecedents, and from areas without the presence of vectors. These observations are considered new epidemiological evidence about Chagas disease in a contemporary urban population, which may contribute to the study of CT and may also be an interesting finding for healthcare professionals.

Chagas congénito en atención primaria de la salud en la Provincia de Santa Fe / Congenital Chagas disease in primary health care in Santa Fe province

Actualmente, la transmisión transplacentaria es la vía más frecuente de infección por Trypanosoma cruzi. El diagnóstico y tratamiento temprano de hijos infectados evita el riesgo de desarrollar miocardiopatía y las niñas dejan de ser potenciales fuentes de transmisión congénita. En este estudio se evaluó el seguimiento de hijos de mujeres infectadas por T. cruzi en Centros de Salud de la provincia de Santa Fe. Se estudiaron 19 madres y sus 51 hijos. 45% (23/51) de los hijos no habían sido estudiados previamente, y de éstos 21/23 resultaron negativos mientras que dos niñas de 3 y 7 años estaban infectadas. Los 28 niños restantes ya habían sido estudiados en los Centros de Salud, siendo positivas dos gemelas de 22 meses y una niña de 9 años; los otros 25/28 hijos no estaban infectados. Un 47% (9/19) de las madres tenían como único antecedente la serología materna positiva, y de las 4 mujeres que transmitieron la infección, tres pertenecían a este grupo. La edad promedio de diagnóstico fue: 20±6 años en las madres y 7,4±6,7 años en los hijos. Se requieren estrategias sanitarias que favorezcan el estudio para la infección por T. cruzi en mujeres antes del embarazo y el seguimiento de todos los hijos para no perder la oportunidad de tratamiento

Transplacental transmission is currently the most frequent route of infection by Trypanosoma cruzi. Early diagnosis and treatment of infected children avoids the risk of developing cardiomyopathy, and girls are no longer potential sources of congenital transmission. This study evaluated the follow-up of children of women infected with T. cruzi in Primary Care Centres of the province of Santa Fe. Nineteen mothers and their 51 children were studied. Among the 51 children, 23 had no previous diagnosis (45%). Of these, 21 were negative while 2 girls, ages 3 and 7, were infected. The remaining 28 children already had a diagnosis at the Health Centres, with 2 twins of 22 months and a 9-year-old girl who were positive; the other 25 children were not infected. Among the 19 mothers, 9 (47%) had the positive maternal serology as the only antecedent. Of the 4 women who transmitted the infection, 3 belonged to this group. The average age of diagnosis was: 20 ± 6 years in mothers and 7.4 ± 6.7 years in children. Health strategies are required to promote the detection of infected women before pregnancy and the monitoring of all children so as not to miss the opportunity for treatment

Maternal risk factors for the transmission of congenital chagas disease

The present article looks at the association between the epidemiological history of women infected with Trypanosoma cruzi and the risk of vertical transmission. Eighty-three chronically infected mothers and their 237 children were studied, using a cohort design. All patients reside in Santa Fe city, Argentina. Twenty-five women transmitted the infection to 38 children. The potential risk factors evaluated in the mothers were exposure to vector transmission, blood transfusion history, maternal seropositivity, parasitemia and age at birth of the child. 72% (18/25) of the mothers who transmitted the infection to their children, had little or no contact with the vector, while only 28% (7/25) of the mothers presented a history of medium or high risk of vector infection. The differences were significant (p < 0.05). Forty-one percent of the women who presented maternal history as the probable route of infection, transmitted the parasite to more than one child (1.86 ± 0.33; CI95% = 1.03-2.68). In addition, the most frequent history, among the women who transmitted the disease to their children, was the absence of exposure to vector transmission and transfusion with unknown maternal serology. The route of infection was probably transplacental. These observations suggest that there are family genetic characteristics involved in vertical transmission. The parasite was found in 71% of the mothers who transmitted the infection to their children and were able to perform xenodiagnoses. After controlling for the other variables, the logistic regression analysis showed that xenodiagnosis (+) is a risk factor for congenital transmission; the relative risk was 12.2 (95% confidence interval: 2.9 - 50.1). No differences were found when analyzing the mother's age and transfusion history. The highest risk of congenital transmission was associated with detectable parasitemia and less maternal exposure to the vector.

Infección chagásica en niños de cuatro distritos de riesgo de la provincia de Santa Fe / Chagas' infection in children of four districts at risk in Santa Fe province / Infecgáo chagasica em changas de quatro distritos de risco da provincia de Santa Fe

El objetivo del presente estudio fue investigar infección chagásica en niños de 1 a 15 años que residen en zona de riesgo vectorial o con antecedentes migratorios en la provincia de Santa Fe, estimar la/s vía/s más probable/s de infección y comparar la prevalencia con trabajos anteriores. Se realizó un estudio seroepidemiológico en escuelas de los Distritos Garabato, Fortín Olmos y Gato Colorado y la escuela de la comunidad Com Caia del Departamento La Capital. A los seropositivos se les realizó una encuesta para determinar las probables vías de infección. Se comparó la prevalencia actual con la del último control de cada distrito. No se hallaron seropositivos en Com Caia (prevalencia 0%, 0/130). La prevalencia en Garabato fue 1,0% (6/604), Fortín Olmos 1,9% (13/688), Gato Colorado 3,0% (12/399). Disminuyó respecto de los últimos estudios: Garabato 11,2% (año 2000), Fortín Olmos 14,6% (2004), Gato Colorado 6,3% (2006). La vía de infección que se sospecha más frecuente es la congènita, seguida por la vectorial. Se concluye que, a pesar de la disminución de la prevalencia, se deben continuar las acciones de control, principalmente por vías vectorial y congènita.

The aim of the present study was to diagnose Chagas infection in children 1 to 15 years of age living in a risk area or with migrant background in Santa Fe province, to estimate the most probable way of infection and to compare the prevalence with previous works. A seroepidemiological study was conducted in schools in the districts Garabato, Fortin Olmos and Gato Colorado and the community Com Caia in La Capital Department. An inquiry was conducted in positive patients to determine the most probable way of infection. The current prevalence was compared with the last control in each district. No seropositive were found in Com Caia (prevalence 0%, 0/130). In Garabato the prevalence was 1.0% (6/604), Fortin Olmos 1.9% (13/688), Gato Colorado 3.0% (12/399). It decreased in comparison with the latest study: Garabato 11.2% (2000), Fortin Olmos 14.6% (2004), Gato Colorado 6.3% (2006). The most suspected way of infection was congenital, followed by vector one. We conclude that, although the prevalence decreased, it must be continued mainly vector and congenital controls actions.

O objetivo deste estudo foi investigar a infecgáo chagásica em criangas de 1 a 15 anos que moram em zona de risco vetorial ou com antecedentes de migragáo na provincia de Santa Fe, estimar a/as via/s mais provável/veis de infecgáo e comparar prevalencia com trabalhos anteriores. Foi realizado um estudo soroepidemiológico em escolas nos distritos Garabato, Fortin Olmos e Gato Colorado e na escola da comunidade Com Caia no departamento La Capital. Os soropositivos foram entrevistados para determinar as prováveis vias da infecgáo. A prevalencia atual foi comparada com a do último controle em cada distrito. Náo foram encontrados soropositivos em Com Caia (prevalencia 0%, 0/130). A prevalencia em Garabato foi 1,0% (6/604), Fortin Olmos 1,9% (13/688), Gato Colorado 3,0% (12/399). Diminuiu a respeito dos últimos estudos: Garabato 11,2% (ano 2000), Fortin Olmos 14,6% (2004), Gato Colorado 6,3% (2006). A via de infecgáo que se suspeita como sendo a mais frequente é a congenita, seguida pela vetorial. Concluise que, apesar da diminuigáo da prevalencia, devem continuar sendo realizadas agoes de controle, principalmente por vias vetorial e congenita.

Evaluation of the ELISA-F29 test as an early marker of therapeutic efficacy in adults with chronic Chagas disease / Avaliação do tratamento tripanossomicida em coorte de adultos chagásicos crônicos através de técnicas sorológicas convencionais e ELISA-F29

This work compared the time at which negative seroconversion was detected by conventional serology (CS) and by the ELISA-F29 test on a cohort of chronic chagasic patients treated with nifurtimox or benznidazole. A retrospective study was performed using preserved serum from 66 asymptomatic chagasic adults under clinical supervision, and bi-annual serological examinations over a mean follow-up of 23 years. Twenty nine patients received trypanocide treatment and 37 remained untreated. The ELISA-F29 test used a recombinant antigen which was obtained by expressing the Trypanosoma cruzi flagellar calcium-binding protein gene in Escherichia coli. Among the untreated patients, 36 maintained CS titers. One patient showed a doubtful serology in some check-ups. ELISA-F29 showed constant reactivity in 35 out of 37 patients and was negative for the patient with fluctuating CS. The treated patients were divided into three groups according to the CS titers: in 13 they became negative; in 12 they decreased and in four they remained unchanged. ELISA-F29 was negative for the first two groups. The time at which negativization was detected was significantly lower for the ELISA-F29 test than for CS, 14.5 ± 5.7 and 22 ± 4.9 years respectively. Negative seroconversion was observed in treated patients only. The results obtained confirm that the ELISA-F29 test is useful as an early indicator of negative seroconversion in treated chronic patients.

Este trabalho comparou os tempos de soroconversão negativos obtidos pela sorologia convencional (CS) e teste ELISA-F29 em uma coorte de pacientes chagásicos crônicos tratados com nifurtimox ou benznidazol. Um estudo retrospectivo foi realizado com soro preservado de 66 adultos chagásicos assintomáticos com acompanhamento clínico e sorológico semestral ao longo de um seguimento médio de 23 anos. 29 pacientes receberam tratamento tripanossomicida e 37 outras permaneceram sem tratamento. O teste ELISA-F29 usou um antígeno recombinante obtido por expressão do gene de uma proteína flagelar de Trypanosoma cruzi de ligação de cálcio em Escherichia coli. Entre os pacientes não tratados, 36 mantiveram os títulos da CS. Um paciente apresentou sorologia duvidosa em alguns controles. ELISA-F29 apresentou reatividade constante em 35/37 e foi negativo no paciente com CS flutuante. Os pacientes tratados foram agrupados de acordo com os títulos da CS, em três grupos: 13 tornaram-se negativos, 12 diminuíram e quatro permaneceram inalterados. ELISA-F29 foi negativo nos dois primeiros grupos. O tempo de negativização foi significativamente menor para o teste ELISA-F29 do que para CS (14,5 ± 5,7 e 22 ± 4,9 anos, respectivamente). A soroconversão negativa foi observada somente nos pacientes tratados. Os resultados obtidos confirmam que o teste ELISA-F29 é útil como um indicador precoce de soronegativação em pacientes crônicos tratados.

Perspectiva interdisciplinaria para el abordaje de una enfermedad infecciosa: chagas o tripanosomiasis americana / Interdisciplinary perspective to approach an infectious disease: american trypanosomiasis or chagas disease

La enfermedad de Chagas, producida por elTrypanosomacruziy transmitida por un insecto triatomino, es de grancomplejidad. En el control de esta endemia no puedeconsiderarse la enfermedad como un hecho individualy sólo biológico. Entre sus múltiples componentes debeconsiderarse la relación de los sujetos con el hábitat, losmodos de producción, las condiciones culturales, lasrelaciones sociales y las formas organizativas.Como profesionales del campo de la salud intentamosnuevos enfoques que integran diferentes miradas disciplinaresy modos de intervención distintos, donde “el otro” recuperesu ser sujeto y no esté convocado a desempeñar un merorol de paciente. Posiciones que implican favorecer procesosparticipativos, escuchar a los propios protagonistas (mujerescon Chagas, equipos de salud, referentes comunitarios)recuperar sus peculiares visiones, poner en palabras lo nodicho sobre esta enfermedad silenciosa y silenciada, y develarlo que el Chagas esconde. Constituye una herramientaimportante a la hora de pensar propuestas de trabajo.

Chagas disease, caused by Trypanosoma cruzi and transmitted by a triatomine insectis extremely complicated. When controlling this endemic disease, the disease cannot beconsidered as an individual and merely biological fact. Among its many components therelationship of individuals to the habitat, production modes, cultural conditions, socialrelationships and organizational forms must be considered.As health professionals we present new approaches that integrate different disciplinesand modes of intervention, where “the other” recovers his/her individual being and isnot merely called upon to play a role as a patient. Positions that encourage participativeprocesses involving listening to the protagonists themselves (women with Chagas, healthteams, community references), recovering their unique visions, communicating what isnot said about this silent and hushed up disease, and revealing what Chagas hides areimportant tools when thinking about work proposals.

Utilidad de la técnica de aglutinación directa en el diagnóstico de la infección chagásica / Usefulness of the direct agglutination test for the diagnosis of chagasic infection

La técnica de aglutinación directa para diagnóstico de infección chagásica es sencilla y económica. Tiene buena sensibilidad y especificidad cuando es utilizada junto con otras técnicas serológicas y/o parasitológicas. Ha sido reemplazada por otras reacciones de mayor rapidez en los resultadosy más fácil lectura (ELISA, hemaglutinación indirecta). Actualmente es difícil conseguir equipos comerciales. Se presentan en el siguiente trabajo una serie de casos que muestran la utilidad de la aglutinación directa para determinar precozmente infección aguda y/o congénita y para diferenciarinfecciones agudas de crónicas.

The direct agglutination technique for chagasic infection diagnosis is easy to perform and inexpensive. It has good sensitivity and specificity when used in conjunction with other serological and/or parasitological techniques. It has been replaced with other reactions with faster results and easiness to read (i.e. immunoenzymatic assay (ELISA) and indirect hemagglutination). Currently it is difficult to obtaincommercial kits. In the present paper we present a series of cases that show the usefulness of the direct agglutination test to early determine acute and/or congenital infection and to differentiate acute from chronic infections.

Confirman la utilidad de la quimioterapia específica en la enfermedad de Chagas crónica / Confirmation of the usefulness of chemotherapy in the treatment of chronic Chagas disease

La evaluación del tratamiento tripanocida en adultos con enfermedad de Chagas crónica requiere estudios de seguimiento muy prolongados. Ciento doce adultos con infección crónica por T. cruzi, asintomáticos, residentes en la Ciudad de Santa Fe fueron evaluados durante 23 años en promedio mediante estudios parasitológicos, serológicos y clínicos. De ellos, 55 fueron tratados (27 con nifurtimox y 28 con benznidazol) y 57 permanecieron sin tratar. Se demostró la eficacia del tratamiento específico en el 45.5% de los pacientes tratados, por su negativización parasitológica y serológica convencional persistente, acompañada de un efecto preventivo en la evolución del daño miocárdico. En este grupo tratado, otro 23.6% de los infectados presentaron serología dudosa o seroconversión negativa completa en el último control. Estos probablemente se incorporen en los próximos años al grupo de pacientes curados. En los infectados que no recibieron tratamiento específico se observó que la serología convencional permaneció siempre positiva y que las alteraciones electrocardiográficas compatibles con miocardiopatía chagásica crónica fueron 5 veces mayores que la que presentó el grupo de pacientes tratados.

Infección chagásica en estudiantes universitarios de Santa Fe (Argentina) / Chagas' infection in universitary students of Santa Fe (Argentina)

La tripanosomiasis americana se transmite por picadura de triatominos hematófagos (principalmente), o por vía connatal o transfusional. Generalmente es asintomática en fase aguda y en fase crónica puede evolucionar a trastornos cardíacos (más comunes) o digestivos. El tratamiento etiológico es más efectivo en casos agudos y en menores de 15 años con infección crónica. Nuestro objetivo fue determinar: a) si existen infectados jóvenes que perdieron su oportunidad de tratamiento por superar la edad cuando fueron diagnosticados y b) probable vía de infección. Se estudiaron 14374 ingresantes a universidades de Santa Fe entre marzo de 2004 y julio de 2008. Se realizó serología para Chagas y encuesta sobre datos relacionados con las posibles vías de transmisión. Se identificaron 20 infectados chagásicos, 80% menores de 25 años. En 4 la transmisión probablemente fue congénita, 3 transfusionaly 3 vectorial. En 10 no se pudo determinar. Concluimos que, de haberse realizado análisis para Chagas al ingreso escolar, estos jóvenes infectados chagásicos podrían haber recibido el tratamiento tripanocida en el momento oportuno. En ellos es importante tener en cuenta todas las vías de transmisión.

Evaluación de ELISA F29 como marcador de eficacia del tratamiento etiológico en la enfermedad de Chagas / Assessment of ELISA F29 as a marker of etiological treatment efficacy for Chagas disease

A transversal study was performed on sera from chronic chagas ic patients treated with nifurtimox (Nx) or benznidazole (Bz), in order to evaluate the Trypanosoma cruzi flagellar calcium-binding protein (F29) as a marker for therapeutic effectiveness. An ELISA was used with these F29 recombinant antigen, and its relation to conventional serology (CS) and parasitological and clinical evolution was analysed. Sera from 118 patients with retrospective, serological, parasitological and clinical information was available, were analyzed. Patients were grouped into: A) 30 treated patients whose CS became negative after treatment; B) 34 treated patients whose CS remained positive; C) 54 untreated patients. A double-blind trial was conducted simultaneously in all serum samples, by means ofCS (indirect hemagglutination, direct agglutination and indirect immunofluorescence) and ELISA F29. The ELISA F29 test was non reactive in: 100 percent of group A, 82.4 percent of group B and 13 percent> of group C. The infected patients who presented electrocardiographic alterations compatible with chronic chagasic myocardiopathy (n = 11) were reactive for ELISA F29. All patients whose parasitological studies (xenodiagnosis and/or strout method) were positive presented a high reactivity to the ELISA F29 test. The correlation between ELISA F29 and CS was statistically significant (p < 005) in the treated group whose CS was non reactive (group A) and the untreated group (group C). As opposed to this, in the group of treated patients whose CS remained positive (group B), the ELISA F29 test was reactive only in a 17.6 percent>. These results suggest that the fast and user-friendly ELISA F29 test could be useful to monitor changes after trypanocidal treatment.

La proteína flagelar F29 es una proteína ligadora de calcio del Trypanosoma cruzi. En el presente trabajo se realizó un estudio transversal en sueros de pacientes con infección crónica por T. cruzi tratados con nifurtimox (Nx) o benznidazol (Bz) y no tratados, para evaluar el antígeno F29 como marcador de eficacia terapéutica. Se utilizó un ensayo inmuno-enzimático con la proteína recombinante F29 (ELISA F29) y se analizó su relación con la serología convencional (SC) y la evolución parasitológica y clínica en esos pacientes. Se estudiaron 118 sueros de pacientes que formaban parte de una cohorte, de los cuales se disponía de información retrospectiva, serológica, parasitológica y clínica. Los pacientes se dividieron en 3 grupos: A) 30 tratados negativizaron SC post-tratamiento; B) 34 tratados permanecieron con SC reactiva; C) 54 no tratados. Las muestras de suero se procesaron a doble ciego en forma simultánea mediante serología convencional (hemoaglutinación indirecta, aglutinación directa e inmunofluorescencia indirecta) y ELISA F29. El test ELISA F29 resultó no reactivo en: 100 por ciento del grupo A, 82,4 por ciento del grupo B y 13 por ciento del grupo C. Los infectados con alteraciones electrocardiográficas compatibles con miocardiopatía chagásica crónica (n = 11) fueron reactivos al ELISA F29. Los pacientes en quienes los estudios parasitológicos (xenodiagnóstico y/o strout) fueron (+) presentaron elevada reactividad al ELISA F29. La correlación entre ELISA F29 y SC en los pacientes tratados con SC no reactiva (grupo A) y no tratados (grupo C), fue significativa (p < 0,05). En cambio, en pacientes tratados que mantuvieron la SC reactiva (grupo B) el test de ELISA F29 fue reactivo sólo en 17,6 por ciento. Estos resultados sugieren que el test ELISA F29, rápido y sencillo, podría ser útil para monitorear cambios post-tratamiento tripanocida.

Trypanocide treatment among adults with chronic Chagas disease living in Santa Fe city (Argentina), over a mean follow-up of 21 years: parasitological, serological and clinical evolution

The efficacy of treatment with nifurtimox and/or benznidazole among adults with chronic Chagas disease with no previous electrocardiographic disturbances was evaluated over a mean follow-up of 21 years, by means of conventional serology, xenodiagnosis, clinical examination, electrocardiograms and chest X-ray. One hundred and eleven patients, between 17 and 46 years old, were studied: 54 underwent treatment (nifurtimox 27, benznidazole 27) and 57 remained untreated (control group). Xenodiagnosis was performed on 65 percent of them: 36/38 of the treated and 9/34 of the untreated patients had previous positive xenodiagnosis. Post-treatment, 133 xenodiagnoses were performed on 41 patients, all resulting negative. In the control group, 29 xenodiagnoses were performed on 14 patients; 2 resulted positive. Sera stored during the follow-up were simultaneously analyzed through conventional serology tests (IHA; DA-2ME; IIF). The serological evolution in the treated group was: a) 37 percent underwent negative seroconversion (nifurtimox 11, benznidazole 9); b) 27.8 percent decreased titers (nifurtimox 9, benznidazole 6), 9 showed inconclusive final serology (nifurtimox 7, benznidazole 2); c) 35.2 percent remained positive with constant titers (nifurtimox 7; benznidazole 12). The control group conserved the initial antibody levels during the follow-up. In the clinical evolution, 2/54 (3.7 percent) of the treated and 9/57 (15.8 percent) of the untreated patients showed electrocardiographic disturbances attributable to Chagas myocardiopathy, with a statistically relevant difference (p<0.05). Treatment caused deparasitation in at least 37 percent of the chronically infected adults and a protective effect on their clinical evolution.

Avaliamos a eficácia do nifurtimox e/ou benznidazol, durante 21 anos em média, em adultos chagásicos crônicos sem alterações eletrocardiográficas iniciais, mediante sorologia convencional, xenodiagnóstico, exames clínicos, eletrocardiográficos e radiografia do tórax. Estudamos 111 pacientes (17 a 46 anos): 54 foram tratados (27 com nifurtimox e 27 com benznidazol) e 57 formaram o grupo controle. Foram submetidos ao xenodiagnóstico 65 por cento dos pacientes estudados: 36/38 tratados e 9/34 do grupo controle com xenodiagnóstico positivo prévio. Após tratamento, foram realizados 133 xenodiagnósticos em 41 pacientes, sendo todos negativos. Foram realizados 29 xenodiagnósticos em 14 pacientes do grupo controle, 2 foram positivos. A sorologia convencional foi realizada em soros estocados durante o seguimento. Evolução sorológica. Grupo tratado: a) 37 por cento negativaram (nifurtimox 11, benznidazol 9); b) 27,8 por cento diminuíram a titulação (nifurtimox 9, benznidazol 6), 9 deles apresentaram sorologia final discordante (nifurtimox 7, benznidazol 2; c) 35,2 por cento permaneceram positivos com titulação constante (nifurtimox 7, benznidazol 12). Grupo controle: conservou os níveis iniciais de anticorpos durante o seguimento. Evolução clínica: 2/54 (3,7 por cento) pacientes tratados e 9/57 não tratados apresentaram alterações eletrocardiográficas atribuíveis a miocardiopatia chagásica. Diferenças estatisticamente significantes (p<0,05). O tratamento produziu efeito de combate ao parasita em pelo menos 37 por cento dos infetados crônicos adultos e efeito protetor na evolução clínica.

Estudo longitudinal e quimioterapia específica em crianças, com doença de Chagas crônica, residentes em área de baixa endemicidade da República Argentina / Longitudinal study and specific chemotherapy in children with chronic Chagas' disease, residing in a low endemicity area of Argentina

Apresenta-se a avaliação clinicoepidemiológica de 95 crianças chagásicas crônicas em idades entre 1 e 14 anos moradoras de Santa Fé, Argentina, não tratadas e tratadas com nifurtimox ou benznidazol, com acompanhamento de até 24 anos. Todas tinham vários antecedentes de risco para transmissão do Trypanosoma cruzi: vetorial, congênito e/ou transfusão sangüínea. O diagnóstico da infecção foi feito através de sorologia convencional. O exame clínico foi complementado por eletrocardiograma, radiografias de tórax e, análise de sangue e urina para avaliação das funções hepáticas. No pós-tratamento, utilizaram-se técnicas idênticas às do diagnóstico, sendo que 33 crianças tiveram, também, avaliação parasitológica. Dentre 24 crianças não tratadas, 14 foram controlados por 8 a 24 anos e mantiveram sorologia positiva e o estado clínico inicial. Das 71 crianças tratadas, 49 tiveram acompanhamento de 4 a 24 anos: 14 mantiveram anticorpos anti-Trypanosoma cruzi; 6 resultados discordantes e 29 negativaram a sorologia. Destas, 9 apresentaram oscilações sorológicas, antes da negativação definitiva. A mediana do tempo de negativação pós-tratamento foi, respectivamente, de 3,5 e 8 anos para crianças de 1 a 6 e 7 a 14 anos. A percentagem de soronegativos diminuiu com a idade em que se medicou, desde 75 por cento em <4 anos até 43 por cento em > 9 anos. A intolerância ao tratamento foi de 3,8 por cento. Nenhuma criança modificou seu estado clínico nesta observação.

Chagas congénito en la ciudad de Santa Fé. Diagnóstico y tratamiento / Congenital Chagas disease in the city of Santa Fé. Diagnosis and treatment

We studied 6123 pregnant women and their 341 newborn (NB), from Santa Fe city, by the following serological tests for chagasic infection: Direct Agglutination with and without 2-mercaptoethanol, Indirect Hemagglutination and Indirect Immunofluorescence test, and by identification of parasites by Fresh drops, Strout and/or by Xenodiagnosis. The prevalence of seropositivity found in pregnant women was of 14.62 with a 73 of migratory history. The parasitological studies yielded 9/341 incidence of transplacentary infection. Clinical examinations were made in the infected newborn (NB). They were treated with Benznidazol or Nifurtimox, and post-treatment evolution was evaluated. We registered connatal infection in twin-brothers. Brothers/sisters (siblings) of infected NB were also studied. Some of them were seropositive and the others seronegative. Results here obtained show that this way of transmission is important, and should be considered even in low endemicity areas. The parasitological assays proved to be decisive for the NB infection diagnosis (Table 1). The serological assays enabled us to follow the non-infected NB up to their negativization. A 6 month follow-up is recommended. It is impossible to define only one clinical outline because both symptomatic and asymptomatic infected NB may be found with gestational age at term and pre-term and when born with a weight above or below 2000 g. We obtained parasitological and serological negativization in all cases. The chagasic pregnant woman does not necessarily transmit the infection to all her descendents. Only 2.64 are infected. It is possible to systematize the diagnosis without extra resources beyond the usual ones.