ABSTRACT
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.
Subject(s)
Humans , Female , Pregnancy , Child , Risk Factors , Chagas Disease/transmission , Trypanosoma cruzi , Infectious Disease Transmission, Vertical , Maternal-Fetal ExchangeABSTRACT
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.
Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Chagas Disease/blood , Chagas Disease/epidemiology , Trypanosoma cruzi , Argentina , Chagas Disease , Rural PopulationABSTRACT
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.
Subject(s)
Adolescent , Adult , Female , Humans , Male , Middle Aged , Young Adult , Chagas Disease/drug therapy , Enzyme-Linked Immunosorbent Assay/methods , Nifurtimox/therapeutic use , Nitroimidazoles/therapeutic use , Trypanocidal Agents/therapeutic use , Trypanosoma cruzi/immunology , Antibodies, Protozoan/blood , Antigens, Protozoan/immunology , Case-Control Studies , Chronic Disease , Cohort Studies , Chagas Disease/parasitology , Retrospective Studies , Time Factors , Treatment OutcomeABSTRACT
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.
Subject(s)
Humans , Male , Female , Chagas Disease/epidemiology , Chagas Disease/prevention & control , Health Services Research , Community Participation/statistics & numerical data , Community Participation/trendsABSTRACT
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.
Subject(s)
Chagas Disease/diagnosis , Trypanosoma cruzi , Enzyme-Linked Immunosorbent AssayABSTRACT
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.
Subject(s)
Humans , Male , Adult , Female , Therapeutic Uses , Chagas Disease/drug therapy , Chagas Disease/therapy , Drug Therapy , Trypanosoma cruziABSTRACT
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.