Tungiasis in the Sanumás Amerindians in the Amazon Rainforest, Brazil: Prevalence, Intensity and Morbidity.

BACKGROUND: Tungiasis is a disease associated with extreme poverty. We aimed to evaluate the prevalence of tungiasis in six different settlements of the Sanumás indigenous community in a remote area in the Auaris region, Yanomami territory, Brazil. METHODS: We conducted an observational study to detect clinical and epidemiological factors associated with tungiasis using a cross-sectional strategy and multivariate logistic regression. Soil analysis was performed by visual and microscopic methods. RESULTS: We examined 555 persons, 45 of whom had active tungiasis; 18 cases were classified as mild, 16 as moderate and 11 as severe. The disease was significantly more prevalent in children than in adults (odds ratio (OR) 15.77; 95% confidence interval (CI) = 5.34-67.91; p < 0.001). Soil infestation was significantly related to the occurrence of human tungiasis (OR = 12.29; 95% CI = 3.75-45.88). The sex and GPS location of the houses were not related to the occurrence of tungiasis. CONCLUSIONS: We conclude that tungiasis is an important problem in the Sanumás community, especially for children. We suggest that interruption of the off-host transmission cycle, together with regular treatment [human and animal interventions], must be prioritized to achieve control of tungiasis in indigenous populations.

Perfil Epidemiológico de Gatos com Esporotricose no Município de São Paulo (SP), 2011 a 2022 / Epidemiological Profile of Cats with Sporotrichosis in the City of São Paulo (SP), 2011 to 2022

Objetivo: este estudo se propôs a caracterizar o perfil epidemiológico da esporotricose felina no município de São Paulo (SP) no período de 2011 a 2022. Métodos: estudo descritivo dos casos de esporotricose felina registrados entre 2011 e 2022. Foram utilizados dados secundários, provenientes dos bancos de dados da vigilância do município. Resultados: o perfil predominante dos animais é composto por machos, 71,4% (n=2.644), com idade inferior a 4 anos 70,1% (n=1.137) e com livre acesso à rua 51,0% (n=1.348). Foram registrados 811 óbitos, entre os quais foi informado o sexo para 381, sendo estes 77,4% (n=295) machos e 22,6% (n=86) fêmeas. Conclusão: diante dos achados deste estudo, compreende-se que a situação epidemiológica da doença requer ações conjuntas das vigilâncias epidemiológica e ambiental para serem desenvolvidas medidas de prevenção e controle embasadas em uma perspectiva de saúde única.

Objective: this study aimed to characterize the epidemiological profile of feline sporotrichosis in the city of São Paulo (SP) from 2011 to 2022. Methods: this is a descriptive study of feline sporotrichosis cases reported between 2011 and 2022. The data were obtained from a secondary database of the São Paulo Health Surveillance System. Results: the predominant profile of the animals is composed of males 71.4% (n=2,644), under the age of four years old 70.1% (n=1,137), and with free access to streets 51.0% (n=1,348). Furthermore, of the 811 deaths registered, 381 had the gender identified, 77.4% (n=295) were males, and 22.6% (n=86) were females. Conclusion: given the findings of this study, it is understood that the epidemiological situation of the disease requires joint actions by epidemiological and environmental surveillance in order to develop prevention and control measures based on one health perspective.

Congenital anomalies from the health surveillance perspective: compilation of a list based on ICD-10. / Anomalias congênitas na perspectiva da vigilância em saúde: compilação de uma lista com base na CID-10.

OBJECTIVE: To propose a list of congenital anomalies having corresponding codes in the International Statistical Classification of Diseases and Related Health Problems, 10thRevision (ICD-10), with the aim of applying it in health surveillance. METHODS: In December 2019, the following data sources were searched: ICD-10; ICD-11; anomalies monitored by three surveillance programs; and a database of rare diseases (Orphanet). Anomalies were retrieved from these data sources, processed to check for correspondence with ICD-10 and reviewed manually to compile the list. RESULTS: 898 codes were identified, of which 619 (68.9%) were contained in ICD-10 Chapter XVII. Of the 279 codes contained in other chapters, 19 were exclusive to the ICD-11 search, 72 to the surveillance programs, 79 to Orphanet and 36 to the search for terms in ICD-10. CONCLUSION: The codes contained in ICD-10 Chapter XVII do not capture the totality of congenital anomalies, indicating the need to adopt an expanded list.

International collaboration networks for the surveillance of congenital anomalies: a narrative review. / Redes internacionais de colaboração para a vigilância das anomalias congênitas: uma revisão narrativa.

Objective to identify international congenital anomaly surveillance collaboration networks, to list the programs that compose them and to compare their main characteristics. Methods this was a narrative literature review by means of a MEDLINE database search (via PubMed) and searches involving websites, reports and official documents. Results six international congenital anomaly surveillance collaboration networks were identified (ECLAMC, ICBDSR, EUROCAT, BINOCAR, SEAR-NBBD and ReLAMC), comprised of 98 programs present in 58 different countries on all continents, except Africa; the main characteristics regarding type of surveillance, coverage and location were discussed in a comparative manner. Conclusion international collaborative networks are important players for congenital anomaly surveillance, contributing to the understanding of the global epidemiological scenario of these conditions, in addition to acting both to strengthen individual existing programs and also to create surveillance initiatives in unassisted regions.

Redes internacionais de colaboração para a vigilância das anomalias congênitas: uma revisão narrativa / Redes de colaboración internacional para la vigilancia de anomalías congénitas: una revisión narrativa / International collaboration networks for the surveillance of congenital anomalies: a narrative review

Objetivo: identificar as redes de colaboração internacional para vigilância das anomalias congênitas, elencar os programas que as compõem e comparar suas principais características. Métodos: revisão narrativa de literatura, mediante busca na base MEDLINE (via PubMed), em endereços on-line, relatórios e documentos oficiais. Resultados: foram identificadas seis redes de colaboração internacional para a vigilância de anomalias congênitas (ECLAMC, ICBDSR, EUROCAT, BINOCAR, SEAR-NBBD e ReLAMC), compostas por 98 programas presentes em 58 diferentes países de todos os continentes, exceto a África; as principais características quanto ao tipo de vigilância, cobertura e localização foram discutidas de modo comparativo. Conclusão: as redes colaborativas internacionais constituem importantes atores para a vigilância das anomalias congênitas, contribuindo com o entendimento do cenário epidemiológico global desses agravos, além de atuar tanto para o fortalecimento de programas individuais já existentes quanto para a criação de iniciativas de vigilância em regiões desassistidas.

Objetivo analizar la prevalencia de enfermedades respiratorias y diarrea en trabajadores de cooperativas de materiales reciclables en São Paulo, Brasil, y factores asociados. Métodos: estudio transversal en tres cooperativas, con datos recopilados por entrevistas estructuradas y medición de la concentración fungica ambiental; se usó la regresión de Poisson para estimar las razones de prevalencia (RP). Resultados: 156 personas fueron entrevistadas; la mayor prevalencia de asma, enfermedad pulmonar obstructiva crónica (EPOC) y diarrea se produjo en cooperativas con la mayor concentración fúngica total; se observó una mayor prevalencia ajustada de asma en la cooperativa A (RP=8,44 - IC95% 1,09;65,37) y diarrea en C (RP=2,09 - IC95% 1,11;3,94), en comparación con la cooperativa B; la mayor prevalencia de EPOC se observó en los fumadores y ex fumadores (RP=8,66 - IC95% 2,84;26,35). Conclusión: se deben adoptar medidas de control fúngica como prevención de enfermedades en cooperativas de materiales reciclables.

Objective: to identify international congenital anomaly surveillance collaboration networks, to list the programs that compose them and to compare their main characteristics. Methods: this was a narrative literature review by means of a MEDLINE database search (via PubMed) and searches involving websites, reports and official documents. Results: six international congenital anomaly surveillance collaboration networks were identified (ECLAMC, ICBDSR, EUROCAT, BINOCAR, SEAR-NBBD and ReLAMC), comprised of 98 programs present in 58 different countries on all continents, except Africa; the main characteristics regarding type of surveillance, coverage and location were discussed in a comparative manner. Conclusion: international collaborative networks are important players for congenital anomaly surveillance, contributing to the understanding of the global epidemiological scenario of these conditions, in addition to acting both to strengthen individual existing programs and also to create surveillance initiatives in unassisted regions.

Anomalias congênitas na perspectiva da vigilância em saúde: compilação de uma lista com base na CID-10 / Anomalías congénitas desde la perspectiva de la vigilancia de la salud: compilación de una lista basada en la CIE-10 / Congenital anomalies from the health surveillance perspective: compilation of a list based on ICD-10

Objetivo: Propor uma lista de anomalias congênitas com códigos correspondentes na Classificação Estatística Internacional de Doenças e Problemas Relacionados à Saúde - 10ᵃ Revisão (CID-10), visando a aplicação no âmbito da vigilância em saúde. Métodos: Em dezembro de 2019, realizou-se busca nas seguintes fontes de dados: CID-10; CID-11; anomalias monitoradas por três modelos de vigilância; base de informações sobre doenças raras (Orphanet). Realizou-se extração das anomalias a partir dessas fontes, processamento para correspondência com base na CID-10 e compilação mediante revisão manual. Resultados: Foram identificados 898 códigos, dos quais 619 (68,9%) constavam no capítulo XVII da CID-10. Dos 279 códigos de outros capítulos, 19 foram exclusivos da busca na CID-11, 72 dos modelos de vigilância, 79 da Orphanet e 36 da busca de termos na CID-10. Conclusão: Os códigos que constam do capítulo XVII da CID-10 não captam a totalidade das anomalias congênitas, indicando a necessidade de adoção de uma lista ampliada.

Objetivo: Proponer una lista de anomalías congénitas con códigos correspondientes en la décima revisión de la Clasificación Internacional de Enfermedades (CIE), con el objetivo de su aplicación en el ámbito de la vigilancia de la salud. Métodos: En diciembre de 2019, se buscaron las siguientes fuentes: CIE-10; CIE-11; anomalías monitoreadas por tres modelos de vigilancia; y base de informaciones sobre enfermedades raras (Orphanet). Las anomalías se extrajeron de estas fuentes de datos, se procesó en base a la CIE-10 y se compiló con una revisión manual. Resultados: Se identificaron 898 códigos, de los cuales 619 (68,9%) estaban en el Capítulo XVII de la CIE-10. De los 279 códigos en otros capítulos, 19 fueron exclusivos de la búsqueda en la CIE-11, 72 de los modelos de vigilancia, 79 de Orphanet y 36 de la búsqueda de términos en la CIE-10. Conclusión: Los códigos contenidos en el capítulo XVII de la CIE-10 no capturan la totalidad de las anomalías congénitas, lo que indica la necesidad de adoptar una lista ampliada.

Objective: To propose a list of congenital anomalies having corresponding codes in the International Statistical Classification of Diseases and Related Health Problems, 10thRevision (ICD-10), with the aim of applying it in health surveillance. Methods: In December 2019, the following data sources were searched: ICD-10; ICD-11; anomalies monitored by three surveillance programs; and a database of rare diseases (Orphanet). Anomalies were retrieved from these data sources, processed to check for correspondence with ICD-10 and reviewed manually to compile the list. Results: 898 codes were identified, of which 619 (68.9%) were contained in ICD-10 Chapter XVII. Of the 279 codes contained in other chapters, 19 were exclusive to the ICD-11 search, 72 to the surveillance programs, 79 to Orphanet and 36 to the search for terms in ICD-10. Conclusion: The codes contained in ICD-10 Chapter XVII do not capture the totality of congenital anomalies, indicating the need to adopt an expanded list.

Human leptospirosis in Porto Alegre, Rio Grande do Sul, Brazil, 2007-2013: characterization of confirmed cases and spatial distribution. / Leptospirose humana em Porto Alegre, Rio Grande do Sul, de 2007 a 2013: caracterização dos casos confirmados e distribuição espacial.

OBJECTIVE: to characterize confirmed human leptospirosis cases resident in Porto Alegre, Rio Grande do Sul, Brazil, between 2007 and 2013, and their spatial distribution. METHODS: this was a descriptive study of cases registered on the Notifiable Diseases Information System; we investigated neighborhoods and areas in the catchment area of Health Units (US) with highest case occurrence, using spatial analysis as per the Kernel technique. RESULTS: 228 cases were confirmed in the period, with cumulative incidence of 2.3 cases/100,000 inhabitants; the majority were adult males (81.6%), economically active (82.5%) and had low schooling (45.8%); the main occupations were recyclable waste collector (15.8%) and builder/builder's mate (15.2%); six priority US were identified for leptospirosis control and prevention actions. CONCLUSION: the epidemiological profile and spatial distribution of cases suggest that there continue to be environmental risk factors favoring human leptospirosis occurrence in these areas.

Leptospirose humana em Porto Alegre, Rio Grande do Sul, de 2007 a 2013: caracterização dos casos confirmados e distribuição espacial / Leptospirosis humana en Porto Alegre, Rio Grande do Sul, Brasil, de 2007 a 2013: caracterización de los casos confirmados y distribución espacial / Human leptospirosis in Porto Alegre, Rio Grande do Sul, Brazil, 2007-2013: characterization of confirmed cases and spatial distribution

Resumo Objetivo: caracterizar os casos confirmados de leptospirose humana residentes em Porto Alegre, Rio Grande do Sul, Brasil, entre 2007 e 2013, e sua distribuição espacial. Métodos: estudo descritivo dos casos registrados no Sistema de Informação de Agravos de Notificação (Sinan); foram investigados bairros e territórios de abrangência das unidades de saúde (US) com maior ocorrência de casos, utilizando-se análise espacial por meio da técnica de Kernel. Resultados: 228 casos foram confirmados no período, com incidência acumulada de 2,3 casos/100 mil habitantes; a maioria era de homens adultos (81,6%), economicamente ativos (82,5%), com baixa escolaridade (45,8%); as principais ocupações foram catador de material reciclável (15,8%) e pedreiro/servente de obras (15,2%); foram identificadas seis US prioritárias para ações de controle e prevenção da leptospirose. Conclusão: o perfil epidemiológico dos casos e sua distribuição espacial sugerem a manutenção dos fatores de risco ambientais favoráveis à ocorrência da doença nessas áreas.

Resumen Objetivo: caracterizar casos confirmados de Leptospirosis humana residentes en Porto Alegre, Rio Grande do Sul, Brasil, entre 2007 y 2013, y su distribución espacial. Métodos: estudio descriptivo de los casos registrados en el Sistema de Información de Agravamientos de Notificación; se investigaron barrios y territorios abarcados por las Unidades de Salud (US) con mayor incidencia de casos, utilizando el análisis espacial por medio de la técnica de Kernel. Resultados: fueron confirmados 228 casos en el período, con incidencia acumulada de 2,3 casos/100.000 habitantes; la mayoría hombres adultos (81,6%), económicamente activos (82,5%), baja escolaridad (45,8%); las principales ocupaciones fueron recicladores (15,8%) y albañiles / peones de obra (15,2%); se identificaron seis US como prioritarias para acciones en el control y prevención de la leptospirosis. Conclusión: el perfil epidemiológico de los casos y su distribución espacial indica el mantenimiento de los factores de riesgo ambiental que favorecen la aparición de la enfermedad en esas áreas.

Abstract Objective: to characterize confirmed human leptospirosis cases resident in Porto Alegre, Rio Grande do Sul, Brazil, between 2007 and 2013, and their spatial distribution. Methods: this was a descriptive study of cases registered on the Notifiable Diseases Information System; we investigated neighborhoods and areas in the catchment area of Health Units (US) with highest case occurrence, using spatial analysis as per the Kernel technique. Results: 228 cases were confirmed in the period, with cumulative incidence of 2.3 cases/100,000 inhabitants; the majority were adult males (81.6%), economically active (82.5%) and had low schooling (45.8%); the main occupations were recyclable waste collector (15.8%) and builder/builder's mate (15.2%); six priority US were identified for leptospirosis control and prevention actions. Conclusion: the epidemiological profile and spatial distribution of cases suggest that there continue to be environmental risk factors favoring human leptospirosis occurrence in these areas.