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1.
Rev Paul Pediatr ; 41: e2022049, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37255107

RESUMEN

OBJECTIVE: This study aimed to describe the characteristics of mothers and children assisted in a follow-up clinic for congenital syphilis and identify the factors associated with the confirmation of the diagnosis. METHODS: This is a prospective study conducted from 2016 to 2019 in Montes Claros, Northern Minas Gerais, Brazil. Specific forms addressing maternal sociodemographic, behavioral, and lifestyle habit characteristics, as well as characteristics related to access to healthcare, were used. Hierarchical Poisson regression analysis was performed to define the factors associated with diagnostic confirmation, including the calculation of the prevalence ratios (PR) and respective 95% confidence intervals (95%CI). RESULTS: A total of 200 binomials (mother-child) who attended at least one appointment as part of the follow-up after discharge from the maternity hospital were eligible for the study. The mothers were mostly young (79.0%), with a low educational level (43.0%), and black (89.5%). Nearly half of the mothers reported not having a steady sexual partner (42.5%). About a quarter attended less than six prenatal appointments (27.5%). Nearly half did not treat the disease adequately during pregnancy (24.5%). The diagnosis of congenital syphilis was confirmed for 116 children. The following factors were associated with the diagnostic confirmation after multiple analyses: low maternal educational level (PR 1.30; 95%CI 1.05-1.60), maternal risky sexual behavior (PR 1.34; 95%CI 1.07-1.66), inadequate treatment of the mother (PR 3.16; 95%CI 2.42-4.47), and lack of treatment of the partner (PR 1.44; 95%CI 1,18-1.81). CONCLUSIONS: Syphilis remains a major challenge. The results highlight the social inequities associated with congenital syphilis and the lack of proper management of pregnant women and their partners.


Asunto(s)
Complicaciones Infecciosas del Embarazo , Sífilis Congénita , Embarazo , Femenino , Humanos , Sífilis Congénita/diagnóstico , Sífilis Congénita/epidemiología , Complicaciones Infecciosas del Embarazo/diagnóstico , Complicaciones Infecciosas del Embarazo/epidemiología , Estudios de Seguimiento , Estudios Prospectivos , Instituciones de Atención Ambulatoria , Brasil/epidemiología
2.
Rev. Paul. Pediatr. (Ed. Port., Online) ; 41: e2022049, 2023. tab, graf
Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1441051

RESUMEN

Abstract Objective: This study aimed to describe the characteristics of mothers and children assisted in a follow-up clinic for congenital syphilis and identify the factors associated with the confirmation of the diagnosis. Methods: This is a prospective study conducted from 2016 to 2019 in Montes Claros, Northern Minas Gerais, Brazil. Specific forms addressing maternal sociodemographic, behavioral, and lifestyle habit characteristics, as well as characteristics related to access to healthcare, were used. Hierarchical Poisson regression analysis was performed to define the factors associated with diagnostic confirmation, including the calculation of the prevalence ratios (PR) and respective 95% confidence intervals (95%CI). Results: A total of 200 binomials (mother-child) who attended at least one appointment as part of the follow-up after discharge from the maternity hospital were eligible for the study. The mothers were mostly young (79.0%), with a low educational level (43.0%), and black (89.5%). Nearly half of the mothers reported not having a steady sexual partner (42.5%). About a quarter attended less than six prenatal appointments (27.5%). Nearly half did not treat the disease adequately during pregnancy (24.5%). The diagnosis of congenital syphilis was confirmed for 116 children. The following factors were associated with the diagnostic confirmation after multiple analyses: low maternal educational level (PR 1.30; 95%CI 1.05-1.60), maternal risky sexual behavior (PR 1.34; 95%CI 1.07-1.66), inadequate treatment of the mother (PR 3.16; 95%CI 2.42-4.47), and lack of treatment of the partner (PR 1.44; 95%CI 1,18-1.81). Conclusions: Syphilis remains a major challenge. The results highlight the social inequities associated with congenital syphilis and the lack of proper management of pregnant women and their partners.


Resumo Objetivo: Descrever as características de mães e crianças atendidas em um ambulatório de acompanhamento de sífilis congênita e identificar os fatores associados à confirmação do diagnóstico. Métodos: Trata-se de um estudo prospectivo realizado de 2016 a 2019, em Montes Claros, norte de Minas Gerais. Foram utilizados formulários específicos que abordavam características sociodemográficas, comportamentais e de hábitos de vida das mães, bem como características relacionadas ao acesso aos cuidados de saúde. Foi realizada análise de regressão de Poisson hierárquica para s definição dos fatores associados à confirmação diagnóstica, com cálculo das razões de prevalência (RP) e respectivos intervalos de confiança de 95% (IC95%). Resultados: Duzentos binômios (mãe-filho) que compareceram a pelo menos uma consulta como parte do acompanhamento após a alta da maternidade foram elegíveis para o estudo. As mães eram, em sua maioria, jovens (79,0%), com baixa escolaridade (43,0%) e negras (89,5%). Quase metade das mães relatou não ter parceiro sexual fixo (42,5%). Cerca de um quarto compareceu a menos de seis consultas de pré-natal (27,5%). Quase metade não tratou a doença adequadamente durante a gravidez (24,5%). O diagnóstico de sífilis congênita foi confirmado em 116 crianças. Os seguintes fatores foram associados à confirmação diagnóstica após análise múltipla: baixa escolaridade materna (RP 1,30; IC95% 1,05-1,60), comportamento de risco materno (RP 1,34; IC95% 1,07-1,66), tratamento inadequado da mãe (RP 3,16; IC95% 2,42-4,47) e falta de tratamento do companheiro (RP 1,44; IC95% 1,18-1,81). Conclusões: A sífilis continua sendo um grande desafio. Os resultados revelam as iniquidades sociais associadas à sífilis congênita e a falta de manejo adequado das gestantes e seus parceiros.

3.
Rev. Bras. Saúde Mater. Infant. (Online) ; 23: e20220225, 2023. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1431257

RESUMEN

Abstract Objectives: to characterize the profile of pregnant women and newborns accompanied at a reference center for infectious-parasitic diseases, after the exposure of T. gondii, establishing comparisons with a previous study, in the same location, ten years ago. Methods: this is a retrospective cohort study, with a follow-up of four years (2016 to 2019), using the previous study carried out from 2002 to 2010 as a comparative for the variables assessed. Mothers who presented tests suggestive of seroconversion for the disease during prenatal care and their respective concepts, followed up over a year, were included. The chi-square test was used, assuming a significance level of 5% for the comparison of the groups in the two periods. Results: during the period from 2016 to 2019, 79 binomials were studied, whereas 58 binomials were accompanied in the previous period. Comparing both periods, the findings showed lower proportions of adolescents (p<0.001), with low schooling (p<0.001), with low serological testing (p<0.001) and with late or postnatal diagnosis (p<0.001). As to the children, the findings showed fewer changes in fundoscopy (p<0.001), strabismus (p=0.002), hepatomegaly (p=0.026) and any sequelae (p<0.001). Conclusion: a positive advance was observed regarding the care provided for the mother-child binomial affected by T. gondii, with a reduction in negative outcomes for the child. However, there are still challenges concerning the diagnosis and proper management of the disease.


Resumo Objetivos: caracterizar o perfil de gestantes e neonatos acompanhadas em um centro de referência em doenças infecto-parasitárias, após exposição ao Toxoplasma gondii, estabelecendo comparações em relação a estudo prévio, no mesmo local, há dez anos. Métodos: trata-se de estudo de coorte retrospectivo, com seguimento de quatro anos (2016 a 2019), servindo o estudo prévio realizado de 2002 a 2010 como comparativo para as variáveis estudadas. Foram incluídas mães que apresentaram durante o pré-natal exames sugestivos soroconversão para a doença e seus respectivos conceptos, acompanhados ao longo de um ano. Utilizou-se o teste qui-quadrado, assumindo-se nível de significância de 5% para a comparação dos grupos nos dois períodos. Resultados: durante o período de 2016 a 2019, foram estudados 79 binômios, enquanto no período anterior foram acompanhados 58 binômios. Comparando-se os dois períodos, em relação às mães, registraram-se menores proporções de adolescentes (p<0,001), de baixa escolaridade (p<0,001), baixa realização de testes sorológicos (p<0,001) e com diagnóstico tardio ou pós-natal (p<0,001). Em relação às crianças, verificaram-se menores proporções de alterações de fundoscopia (p<0,001), estrabismo (p=0,002), hepatomegalia (p=0,026) e qualquer sequela (p<0,001). Conclusão: observou-se um avanço em relação aos cuidados para o binômio mãe-filho acometido pelo T. gondii, com redução de desfechos negativos sobre a criança. Todavia, ainda existem desafios para o diagnóstico e adequado manejo da doença.


Asunto(s)
Humanos , Femenino , Embarazo , Recién Nacido , Lactante , Atención Prenatal , Toxoplasmosis Congénita/epidemiología , Transmisión Vertical de Enfermedad Infecciosa , Brasil/epidemiología , Estudios Retrospectivos , Estudios de Cohortes , Encuestas Epidemiológicas
4.
Rev. Bras. Saúde Mater. Infant. (Online) ; 22(3): 463-470, July-Sept. 2022. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1406673

RESUMEN

Abstract Objectives: to elaborate and analyze the psychometric properties of a questionnaire to assess among pregnant women's knowledge about toxoplasmosis. Methods: methodological study elaborating an instrument conducted in the north of Minas Gerais in 2019. The steps followed were: 1. Elaboration of the questionnaire items based on medical literature available in indexed databases. 2. Content validation. 3. Apparent validation. 4. Construct validation with hypothesis testing after the application of the questionnaire and comparison of the mean scores using the Mann-Whitney U test. 5. Reliability analysis with internal consistency analysis and test-retest. Results: the final instrument consisted of 26 items. Content validation reached 90% agreement among experts. The hypothesis test found a significant diference among the scores of the groups evaluated (p<0.001). Cronbach's alpha found a value of 0.84 and the test-retest showed an intra-class correlation index of 0.78 (p<0.001). Conclusions: the instrument elaborated proved to be valid and reliable and could be used to assess among pregnant women's knowledge about toxoplasmosis and, therefore, guiding to the educational and preventive measures.


Resumo Objetivos: elaborar e analisar as propriedades psicométricasde um questionáriopara avaliação do conhecimento sobre toxoplasmose entre gestantes. Métodos: estudo metodológico de elaboração de instrumento, realizado no norte de Minas Gerais, em 2019. O estudo seguiu os seguintes passos: 1. Elaboração dos itens a do questionário, com base na literatura médica disponível em bases indexadas. 2. Validação de conteúdo. 3. Validação aparente. 4. Validação de constructo, com teste de hipóteses, após aplicação do questionário e comparação de médias dos escores por meio do teste U de Mann-Whitney. 5. Análise de confabilidade, com análise da consistência interna e teste-reteste. Resultados: o instrumento final foi composto por 26 itens. Na validação de conteúdo alcançou 90% de concordância entre os experts. O teste de hipótese registrou diferença significativa entre os escores dos grupos avaliados (p<0,001). O alfa de Cronbach apresentou valor de 0,84 e o teste-reteste apresentou índice de correlação intra-classe de 0,78 (p<0,001). Conclusão: o instrumento elaborado apresentou-se válido e confável e poderá ser utilizado para avaliação de conhecimento sobre toxoplasmose entre gestantes, norteando medidas educativas e preventivas.


Asunto(s)
Humanos , Femenino , Embarazo , Psicometría , Toxoplasmosis/prevención & control , Educación en Salud , Encuestas y Cuestionarios , Mujeres Embarazadas/educación , Brasil , Estudio de Validación
5.
Rev Bras Enferm ; 73(3): e20190491, 2020.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-32321146

RESUMEN

OBJECTIVES: assess the implementation of actions to prevent vertical transmission of HIV. METHODS: a retrospective cohort study conducted in two maternity hospitals in the city of Montes Claros, State of Minas Gerais. All women admitted for childbirth diagnosed with HIV and their respective newborns were included from 2014 to 2017. Data were collected from medical records and analyzed descriptively. RESULTS: population consisted of 46 pairs of mothers and newborns. Management was considered inadequate in 30 cases of parturient/postpartum women (65.2%) and 14 cases of newborns (30.4%). The main reasons for inadequate maternal management were lack of pharmacological inhibition of lactation (53.3%) and counseling/consent for HIV testing (43.3%). For newborns, late onsetoffirst dose ofZidovudine (50.0%) and no prescriptionofNevirapine (28.6%). CONCLUSIONS: important prevention opportunities were missed, pointing to the need for improved care.


Asunto(s)
Infecciones por VIH/transmisión , Transmisión Vertical de Enfermedad Infecciosa/prevención & control , Calidad de la Atención de Salud/normas , Adulto , Brasil/epidemiología , Estudios de Cohortes , Femenino , Infecciones por VIH/epidemiología , Infecciones por VIH/prevención & control , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos
6.
Rev. bras. enferm ; 73(3): e20190491, 2020. tab
Artículo en Inglés | LILACS, BDENF - Enfermería | ID: biblio-1101489

RESUMEN

ABSTRACT Objectives: assess the implementation of actions to prevent vertical transmission of HIV. Methods: a retrospective cohort study conducted in two maternity hospitals in the city of Montes Claros, State of Minas Gerais. All women admitted for childbirth diagnosed with HIV and their respective newborns were included from 2014 to 2017. Data were collected from medical records and analyzed descriptively. Results: population consisted of 46 pairs of mothers and newborns. Management was considered inadequate in 30 cases of parturient/postpartum women (65.2%) and 14 cases of newborns (30.4%). The main reasons for inadequate maternal management were lack of pharmacological inhibition of lactation (53.3%) and counseling/consent for HIV testing (43.3%). For newborns, late onsetoffirst dose ofZidovudine (50.0%) and no prescriptionofNevirapine (28.6%). Conclusions: important prevention opportunities were missed, pointing to the need for improved care.


RESUMEN Objetivos: evaluar la implementación de acciones para prevenir la transmisión vertical del VIH. Métodos: estudio de cohorte retrospectivo realizado en dos hospitales de maternidad em la ciudad de Montes Claros, estado de Minas Gerais. Todas las mujeres ingresadas para el parto diagnosticadas con VIH y sus respectivos reciénnacidos se incluyeron entre 2014 y 2017. Los datos se recopilaron de los registros médicos y se analizaron descriptivamente. Resultados: la población consistió en 46 pares de madres y reciénnacidos. El manejo se consideró inadecuado en 30 casos de mujeres parturientas/posparto (65,2%) y 14 casos de reciénnacidos(30,4%). Las razones principales para el manejo materno inadecuado fueron: falta de inhibición farmacológica de lalactancia (53.3%) y asesoramiento/consentimiento para la prueba del VIH (43,3%). Para los reciénnacidos, inicio tardío de la primera dosis de zidovudina (50.0%) y sin prescripción de nevirapina (28,6%). Conclusiones: se perdieron importantes oportunidades de prevención, lo que indica la necesidad de una mejor atención.


RESUMO Objetivos: avaliar a implementação das ações de prevenção da transmissão vertical do HIV. Métodos: estudo de coorte retrospectivo, realizado em duas maternidades de Montes Claros, Minas Gerais. Foram incluídas todas as mulheres admitidas para o parto com diagnóstico de HIV e seus respectivos recém-nascidos, nos anos de 2014 a 2017. Os dados foram coletados de prontuários e analisados de forma descritiva. Resultados: a população foi composta por 46 pares de mães e recém-nascidos. O manejo foi considerado inadequado em 30 casos de parturientes/puérperas (65,2 %) e em 14 casos de recém-nascidos (30,4%). Os principais motivos para a inadequação do manejo materno foram: ausência da inibição farmacológica da lactação (53,3%) e do aconselhamento/consentimento na realização do exame anti-HIV (43,3%). Para os recém-nascidos, início tardio da primeira dose daZidovudina (50,0%) e não prescrição da Nevirapina (28,6%). Conclusões: oportunidades importantes de prevenção foram perdidas, apontando para a necessidade de melhoria da assistência.


Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Calidad de la Atención de Salud/normas , Infecciones por VIH/transmisión , Transmisión Vertical de Enfermedad Infecciosa/prevención & control , Brasil/epidemiología , Infecciones por VIH/prevención & control , Infecciones por VIH/epidemiología , Estudios Retrospectivos , Estudios de Cohortes
7.
Rev Soc Bras Med Trop ; 52: e20180228, 2019 Apr 11.
Artículo en Inglés | MEDLINE | ID: mdl-30994797

RESUMEN

The objective of this study was to report a case of congenital toxoplasmosis that illustrates the difficulties in diagnosing this disease. The case highlights the lack of prophylactic guidelines and shortcomings in the gestational screening process. It demonstrates the peculiarities of the non-specific clinical picture of the infection acquired during pregnancy and identifies the challenges of ophthalmological and high-sensitivity exams in newborns that are crucial for an early diagnosis. These factors contribute to a delay in early treatment of both the mother and the newborn. The lack of skill and expertise of clinical physicians to manage the disease is also addressed.


Asunto(s)
Toxoplasmosis Congénita/diagnóstico , Femenino , Humanos , Lactante , Enfermedades Desatendidas , Toxoplasmosis Congénita/tratamiento farmacológico
8.
Rev. Soc. Bras. Med. Trop ; 52: e20180228, 2019. graf
Artículo en Inglés | LILACS | ID: biblio-1003130

RESUMEN

Abstract The objective of this study was to report a case of congenital toxoplasmosis that illustrates the difficulties in diagnosing this disease. The case highlights the lack of prophylactic guidelines and shortcomings in the gestational screening process. It demonstrates the peculiarities of the non-specific clinical picture of the infection acquired during pregnancy and identifies the challenges of ophthalmological and high-sensitivity exams in newborns that are crucial for an early diagnosis. These factors contribute to a delay in early treatment of both the mother and the newborn. The lack of skill and expertise of clinical physicians to manage the disease is also addressed.


Asunto(s)
Humanos , Femenino , Lactante , Toxoplasmosis Congénita/diagnóstico , Toxoplasmosis Congénita/tratamiento farmacológico , Enfermedades Desatendidas
9.
Rev Inst Med Trop Sao Paulo ; 56(3): 267-70, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24879007

RESUMEN

Dengue is currently a major public-health problem. Dengue virus (DENV) is classified into four distinct serotypes, DENV 1-4. After 28 years of absence, DENV-4 was again detected in Brazil in 2010 in Roraima State, and one year later, the virus was identified in the northern Brazilian states of Amazonas and Pará, followed by Rio de Janeiro and São Paulo. In Minas Gerais, the first confirmed case of DENV-4 occurred in the municipality of Frutal in 2011 and has now been isolated from a growing number of patients. Although DENV-2 is associated with the highest risk of severe forms of the disease and death due to the infection, DENV-4 has also been associated with severe forms of the disease and an increasing risk of hemorrhagic manifestations. Herein, the first fatal case of confirmed DENV-4 in Brazil is reported. The patient was an 11-year-old girl from the municipality of Montes Claros in northern Minas Gerais State, Brazil. She had idiopathic thrombocytopenic purpura as a comorbid condition and presented with a fulminant course of infection, leading to death due to hemorrhagic complications. Diagnosis was confirmed by detection of Dengue-specific antibodies using IgM capture enzyme-linked immunosorbent assay and semi-nested RT-PCR. Primary care physicians and other health-care providers should bear in mind that DENV-4 can also result in severe forms of the disease and lead to hemorrhagic complications and death, mainly when dengue infection is associated with coexisting conditions.


Asunto(s)
Virus del Dengue/aislamiento & purificación , Dengue/virología , Púrpura Trombocitopénica/complicaciones , Anticuerpos Antivirales/sangre , Niño , Dengue/complicaciones , Virus del Dengue/genética , Virus del Dengue/inmunología , Ensayo de Inmunoadsorción Enzimática , Resultado Fatal , Femenino , Humanos , Inmunoglobulina M/sangre , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
10.
Rev. Inst. Med. Trop. Säo Paulo ; 56(3): 267-270, May-Jun/2014. tab, graf
Artículo en Inglés | LILACS | ID: lil-710403

RESUMEN

Dengue is currently a major public-health problem. Dengue virus (DENV) is classified into four distinct serotypes, DENV 1-4. After 28 years of absence, DENV-4 was again detected in Brazil in 2010 in Roraima State, and one year later, the virus was identified in the northern Brazilian states of Amazonas and Pará, followed by Rio de Janeiro and São Paulo. In Minas Gerais, the first confirmed case of DENV-4 occurred in the municipality of Frutal in 2011 and has now been isolated from a growing number of patients. Although DENV-2 is associated with the highest risk of severe forms of the disease and death due to the infection, DENV-4 has also been associated with severe forms of the disease and an increasing risk of hemorrhagic manifestations. Herein, the first fatal case of confirmed DENV-4 in Brazil is reported. The patient was an 11-year-old girl from the municipality of Montes Claros in northern Minas Gerais State, Brazil. She had idiopathic thrombocytopenic purpura as a comorbid condition and presented with a fulminant course of infection, leading to death due to hemorrhagic complications. Diagnosis was confirmed by detection of Dengue-specific antibodies using IgM capture enzyme-linked immunosorbent assay and semi-nested RT-PCR. Primary care physicians and other health-care providers should bear in mind that DENV-4 can also result in severe forms of the disease and lead to hemorrhagic complications and death, mainly when dengue infection is associated with coexisting conditions.


Dengue é atualmente um importante problema de saúde pública. O vírus da dengue (DENV) é classificado em quatro sorotipos distintos, DENV 1-4. Após 28 anos de ausência, o DENV-4 foi detectado novamente no Brasil em 2010 no Estado de Roraima, e um ano depois, o vírus foi identificado em outros estados do norte do país, Amazonas e Pará, seguido pelos estados do Rio de Janeiro e São Paulo. Em Minas Gerais, o primeiro caso confirmado de DENV-4 ocorreu no município de Frutal em 2011 e, desde então, o sorotipo foi isolado em um número crescente de pacientes. Apesar do DENV-2 estar associado a um maior risco de formas graves e morte, o DENV-4 também tem sido associado a casos graves e a risco aumentado de manifestações hemorrágicas. Neste relato, descrevemos o primeiro caso fatal confirmado por DENV-4 no Brasil. A paciente era uma menina de 11 anos do município de Montes Claros, no norte de Minas Gerais, Brasil. Apresentava púrpura trombocitopênica idiopática e evoluiu de forma fulminante durante a infecção por dengue, com óbito associado a complicações hemorrágicas. O diagnóstico foi confirmado pela detecção de anticorpos IgM específicos para dengue, por método imunoenzimático, e por semi-nested RT-PCR. Médicos e outros profissionais de saúde devem estar cientes que infecções por DENV-4 também podem resultar em formas graves da doença com complicações hemorrágicas e óbito, principalmente em pacientes com comorbidades.


Asunto(s)
Niño , Femenino , Humanos , Virus del Dengue/aislamiento & purificación , Dengue/virología , Púrpura Trombocitopénica/complicaciones , Anticuerpos Antivirales/sangre , Virus del Dengue/genética , Virus del Dengue/inmunología , Dengue/complicaciones , Ensayo de Inmunoadsorción Enzimática , Resultado Fatal , Inmunoglobulina M/sangre , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
11.
Rev Soc Bras Med Trop ; 45(1): 55-9, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22370829

RESUMEN

INTRODUCTION: To describe the clinical and epidemiological profile of pregnant women and children treated at a reference outpatient clinic for congenital toxoplasmosis. METHODS: Pregnant women potentially exposed to Toxoplasma gondii were observed. Diagnoses were made using serologic tests compatible with acute toxoplasmosis. Children presenting with: Toxoplasma-specific antibodies (IgM or IgA or ascending IgG titers higher than maternal titers in the first 3 months of life) coupled with toxoplasmosis symptoms; intracranial calcifications (by transfontanelar ultrasound or cephalic segment tomography); or retinochoroiditis (by fundoscopy examination) in the first 8 months of life were also included in the study. RESULTS: Fifty-eight mother-child pairs were observed (mean age of the mothers was 22.1 years). Most patients lived in urban areas (86.2%) and had attended less than 8 years of school (51.7%). Diagnosis was made after birth in 19 (32.8%) children. Thirty-four (58.6%) women received some type of treatment during pregnancy. Most (72.4%) of the children did not present with clinical alterations at birth. The main findings were ophthalmological: 20 (34.5%) children with retinochoroiditis, 17 (29.3%) with strabismus, and 7 (12.1%) with nystagmus. Of the children with retinochoroiditis, 9 presented with subnormal vision. Ten (32.3%) out of 31 children presented with intracranial calcifications by cephalic segment congenital toxoplasmosis, and 9 (42.9%) children presented with delayed psychomotor development. CONCLUSIONS: Our results highlight a critical situation. Protocols for follow-up of pregnant women and their children must be created to improve medical care and minimize sequelae.


Asunto(s)
Anticuerpos Antiprotozoarios/sangre , Isotipos de Inmunoglobulinas/sangre , Complicaciones Parasitarias del Embarazo/diagnóstico , Toxoplasmosis/diagnóstico , Enfermedad Aguda , Antiprotozoarios/uso terapéutico , Escolaridad , Ensayo de Inmunoadsorción Enzimática , Femenino , Humanos , Lactante , Recién Nacido , Embarazo , Complicaciones Parasitarias del Embarazo/tratamiento farmacológico , Toxoplasmosis/tratamiento farmacológico , Toxoplasmosis Congénita/complicaciones , Toxoplasmosis Congénita/diagnóstico , Toxoplasmosis Congénita/tratamiento farmacológico
12.
Rev. Soc. Bras. Med. Trop ; 45(1): 55-59, Jan.-Feb. 2012. tab
Artículo en Inglés | LILACS | ID: lil-614909

RESUMEN

INTRODUCTION: To describe the clinical and epidemiological profile of pregnant women and children treated at a reference outpatient clinic for congenital toxoplasmosis. METHODS: Pregnant women potentially exposed to Toxoplasma gondii were observed. Diagnoses were made using serologic tests compatible with acute toxoplasmosis. Children presenting with: Toxoplasma-specific antibodies (IgM or IgA or ascending IgG titers higher than maternal titers in the first 3 months of life) coupled with toxoplasmosis symptoms; intracranial calcifications (by transfontanelar ultrasound or cephalic segment tomography); or retinochoroiditis (by fundoscopy examination) in the first 8 months of life were also included in the study. RESULTS: Fifty-eight mother-child pairs were observed (mean age of the mothers was 22.1 years). Most patients lived in urban areas (86.2 percent) and had attended less than 8 years of school (51.7 percent). Diagnosis was made after birth in 19 (32.8 percent) children. Thirty-four (58.6 percent) women received some type of treatment during pregnancy. Most (72.4 percent) of the children did not present with clinical alterations at birth. The main findings were ophthalmological: 20 (34.5 percent) children with retinochoroiditis, 17 (29.3 percent) with strabismus, and 7 (12.1 percent) with nystagmus. Of the children with retinochoroiditis, 9 presented with subnormal vision. Ten (32.3 percent) out of 31 children presented with intracranial calcifications by cephalic segment congenital toxoplasmosis, and 9 (42.9 percent) children presented with delayed psychomotor development. CONCLUSIONS: Our results highlight a critical situation. Protocols for follow-up of pregnant women and their children must be created to improve medical care and minimize sequelae.


INTRODUÇÃO: Descrever o perfil clínico e epidemiológico de gestantes e crianças atendidas em um centro de referência para toxoplasmose congênita. MÉTODOS: Gestantes potencialmente expostas ao Toxoplasma gondii foram estudadas. Os diagnósticos foram feitos através de testes sorológicos compatíveis com toxoplasmose aguda. Crianças que apresentaram anticorpos específicos (IgM e IgA ou títulos ascendentes de IgG, superiores aos títulos maternos nos primeiros três meses de vida), juntamente com os sintomas da toxoplasmose, calcificações intracranianas (ultrassom transfontanela ou tomografia do segmento cefálico), ou retinocoroidite (fundoscopia) nos primeiros oito meses de vida, também foram estudadas. RESULTADOS: Foram estudados 58 pares mãe-filho (a média de idade das mães foi de 22,1 anos). A maioria (86,2 por cento) das mães residia em áreas urbanas e tinham até 8 anos de escolaridade (51,7 por cento). O diagnóstico foi feito após o nascimento para 19 (32,8 por cento) crianças; 34 (58,6 por cento) mulheres receberam algum tipo de tratamento durante a gravidez. A maioria (72,4 por cento) das crianças não apresentou alterações clínicas ao nascimento. Os principais achados foram oftalmológicos: 20 (34,5 por cento) crianças com retinocoroidite, 17 (29,3 por cento) com estrabismo e 7 (12,1 por cento) com nistagmo. Das crianças com retinocoroidite, 9 apresentaram visão subnormal. Calcificações intracranianas estiveram presentes em 10 (32,3 por cento) das 31 crianças que realizaram toxoplasmose congênita de segmento cefálico e 9 (42,9 por cento) crianças apresentaram atraso do desenvolvimento psicomotor. CONCLUSÕES: Os resultados mostram uma situação crítica. Protocolos para acompanhamento de gestantes e seus filhos devem ser criados para melhorar o atendimento médico e minimizar sequelas.


Asunto(s)
Femenino , Humanos , Lactante , Recién Nacido , Embarazo , Anticuerpos Antiprotozoarios/sangre , Isotipos de Inmunoglobulinas/sangre , Complicaciones Parasitarias del Embarazo/diagnóstico , Toxoplasmosis/diagnóstico , Enfermedad Aguda , Antiprotozoarios/uso terapéutico , Escolaridad , Ensayo de Inmunoadsorción Enzimática , Complicaciones Parasitarias del Embarazo/tratamiento farmacológico , Toxoplasmosis Congénita/complicaciones , Toxoplasmosis Congénita/diagnóstico , Toxoplasmosis Congénita/tratamiento farmacológico , Toxoplasmosis/tratamiento farmacológico
13.
Arq Bras Oftalmol ; 74(4): 255-7, 2011.
Artículo en Portugués | MEDLINE | ID: mdl-22068851

RESUMEN

PURPOSE: This study aimed to know the most common ocular findings in children with congenital toxoplasmosis. METHODS: This is a retrospective study carried out from a historical cohort, with a quantitative approach. We evaluated children referred to a pediatric infectious disease service and included only those with confirmed diagnosis of congenital toxoplasmosis. The ophthalmologic evaluation included regular fundus examination under pupil dilation. RESULTS: Of 58 children presumably exposed to risk of the disease during the pregnancy, 20 had ocular lesions during the first year of life (34 eyes). Of these, 12 were asymptomatic at birth. Strabismus was noted in 14 children (70%). In one child there was ptosis, and another had decrease in the palpebral fissure (microphthalmia). Retinochoroiditis was the most common complication, present in all 20 children. Seven children (35%) showed unilateral changes and 13 children showed bilateral changes (65%), with emphasis on the location in the posterior pole and macula. CONCLUSION: Retinochoroiditis and strabismus were outstanding as important sequelae of congenital toxoplasmosis.


Asunto(s)
Blefaroptosis/etiología , Coriorretinitis/etiología , Microftalmía/etiología , Estrabismo/etiología , Toxoplasmosis Ocular/congénito , Toxoplasmosis Ocular/complicaciones , Niño , Estudios de Cohortes , Femenino , Humanos , Masculino , Investigación Cualitativa , Estudios Retrospectivos
14.
Arq. bras. oftalmol ; 74(4): 255-257, jul.-ago. 2011. tab
Artículo en Portugués | LILACS | ID: lil-604173

RESUMEN

OBJETIVO: Conhecer as lesões oculares mais frequentes encontradas em crianças expostas à toxoplasmose congênita. MÉTODOS: Trata-se de um estudo retrospectivo, a partir de uma coorte histórica, de abordagem quantitativa. Foram avaliadas crianças encaminhadas de um serviço de infectologia pediátrica e inseridas apenas aquelas com diagnóstico confirmado de toxoplasmose congênita. A avaliação oftalmológica incluiu o mapeamento de retina sequencial, sob dilatação pupilar. RESULTADOS: Das 58 crianças presumivelmente expostas ao risco de doença durante a gestação, 20 apresentaram lesões oftalmológicas ao longo do primeiro ano de vida (34 olhos). Destas, 12 estavam assintomáticas ao nascimento. Estrabismo foi registrado em 14 crianças (70 por cento). Em uma criança observou-se ptose palpebral e em outra diminuição da fenda palpebral (microftalmia). Retinocoroidite foi a complicação mais frequente, presente em todas as 20 crianças. Sete crianças apresentaram alterações unilaterais (35 por cento) e 13 crianças apresentaram alterações bilaterais (65 por cento), prevalecendo a localização no polo posterior e mácula. CONCLUSÃO: Retinocoroidite e estrabismo destacaram-se como importantes sequelas da toxoplasmose congênita.


PURPOSE: This study aimed to know the most common ocular findings in children with congenital toxoplasmosis. METHODS: This is a retrospective study carried out from a historical cohort, with a quantitative approach. We evaluated children referred to a pediatric infectious disease service and included only those with confirmed diagnosis of congenital toxoplasmosis. The ophthalmologic evaluation included regular fundus examination under pupil dilation. RESULTS: Of 58 children presumably exposed to risk of the disease during the pregnancy, 20 had ocular lesions during the first year of life (34 eyes). Of these, 12 were asymptomatic at birth. Strabismus was noted in 14 children (70 percent). In one child there was ptosis, and another had decrease in the palpebral fissure (microphthalmia). Retinochoroiditis was the most common complication, present in all 20 children. Seven children (35 percent) showed unilateral changes and 13 children showed bilateral changes (65 percent), with emphasis on the location in the posterior pole and macula. CONCLUSION: Retinochoroiditis and strabismus were outstanding as important sequelae of congenital toxoplasmosis.


Asunto(s)
Niño , Femenino , Humanos , Masculino , Blefaroptosis/etiología , Coriorretinitis/etiología , Microftalmía/etiología , Estrabismo/etiología , Toxoplasmosis Ocular/complicaciones , Toxoplasmosis Ocular/congénito , Estudios de Cohortes , Investigación Cualitativa , Estudios Retrospectivos
15.
Rev. bras. saúde matern. infant ; 7(3): 289-295, jul.-set. 2007. tab
Artículo en Portugués | LILACS | ID: lil-464732

RESUMEN

OBJETIVOS: avaliar a qualidade das informações nas declarações de óbitos infantis e a confiabilidade da causa básica do óbito em menores de um ano de idade. MÉTODOS: Foram investigadas todas as declarações de óbitos de menores de um ano ocorridos de 2002 a 2005, cujas mães informavam residência em Montes Claros, Minas Gerais, na ocasião do óbito. Para verificar a confiabilidade da causa básica do óbito, foram selecionadas as declarações de óbitos infantis registrados em 2004 e uma certidão de óbito nova foi preenchida (DO Nova) para comparação com a original (DO Original) com base nos registros hospitalares. O teste de kappa foi usado para comparar o nível de concordância. RESULTADOS: verificou-se elevada proporção de dados faltosos nas declarações de óbitos infantis. Observou-se que a confiabilidade da causa básica do óbito somente foi considerada excelente para o grupo das malformações congênitas (kappa=0,83). Havia concordância moderada para o grupo mais comum, de causas relacionadas com a prematuridade (kappa=0,57). A concordância foi baixa para o grupo das causas infecciosas (kappa=0,24). CONCLUSÕES: Constatou-se a necessidade de melhoria da qualidade do preenchimento da declaração do óbito infantil.


OBJECTIVES: to assess the quality of the information in infants'death certificates and reliability of the reported underlying death cause in children under one year old. METHODS: information was obtained from all death certificates of children under one year old between 2002 and 2005 whose mothers declared their addresses as being Monte Claros, Minas Gerais when death occurred. To verify report reliability of the underlying death cause, children's death certificates issued in 2004 and a new death certificate was filled (New Death Certificate) to be compared with the ori-ginal (Original Death Certificate) based on hospital records. The kappa test was used for concordance level comparison. RESULTS: there was a high rate of missing data in infants'death certificates. Reliability of the underlying death cause was considered excellent only for the congenital malformation group (kappa=0.83). A moderate concordance was noted for the more common prematurity related causes (kappa=0.57). The lowest concordance related to the infection death cause group (kappa=0.24). CONCLUSIONS: the need for quality improvement in the information contained in children's death certificates was verified.


Asunto(s)
Humanos , Recién Nacido , Certificado de Defunción , Mortalidad Infantil , Causa Básica de Muerte , Brasil , Epidemiología Descriptiva
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