Evidence map›Paper›PMID 42848618›Full record

ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2026

Sentinel surveillance of acute febrile illness in a Brazilian Amazon region: laboratory findings and epidemiological implications.

Erick Matheus Garcia Barbosa, Antonio Charlys da Costa, Noely Evangelista Ferreira, Heuder Gustavo Oliveira Paião, Wilton Santos Freire, Anderson Vicente de Paula, Layla Honorato, Vanessa Dos Santos Morais, Márlisson Octávio da Silva Rego, Edcelha Soares D'Athaide Ribeiro and 6 more

Abstract read
In one paragraph

Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Erick Matheus Garcia BarbosaUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0009-0004-0908-7170
Antonio Charlys da CostaUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-5516-5177
Noely Evangelista FerreiraUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0009-0000-8987-4465
Heuder Gustavo Oliveira PaiãoUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-4358-1146
Wilton Santos FreireUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0009-0001-2580-3817
Anderson Vicente de PaulaUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-7919-3516
Layla HonoratoUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-7084-3095
Vanessa Dos Santos MoraisUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3813-3154
Márlisson Octávio da Silva RegoSuperintendência de Vigilância em Saúde do Amapá, Laboratório de Saúde Pública do Amapá, Macapá, Amapá, Brazil.ORCID http://orcid.org/0000-0002-0098-9889
Edcelha Soares D'Athaide RibeiroSuperintendência de Vigilância em Saúde do Amapá, Laboratório de Saúde Pública do Amapá, Macapá, Amapá, Brazil.ORCID http://orcid.org/0000-0003-2875-8158
Diuliana Dos Santos MendesSuperintendência de Vigilância em Saúde do Amapá, Laboratório de Saúde Pública do Amapá, Macapá, Amapá, Brazil.ORCID http://orcid.org/0009-0008-2181-9142
Júlia Pantoja MarquesSuperintendência de Vigilância em Saúde do Amapá, Laboratório de Saúde Pública do Amapá, Macapá, Amapá, Brazil.ORCID http://orcid.org/0009-0007-1387-6043
Geovani de Oliveira RibeiroMinistério da Saúde, Secretaria de Vigilância em Saúde e Ambiente, Coordenação-Geral de Laboratórios de Saúde Pública, Brasília, DF, Brazil.ORCID http://orcid.org/0000-0002-8832-7803
Steven Sol WitkinUniversidade de São Paulo, Faculdade de Medicina, Instituto de Medicina Tropical de São Paulo, Laboratório de Investigação Médica (LIM-52), São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3502-3929
Tania Regina Tozetto-MendozaUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-5659-1052
Maria Cassia Mendes-CorreaUniversidade de São Paulo, Faculdade de Medicina, Departamento de Infectologia e Medicina Tropical, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-5655-8108

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Amapa State, Brazil, in the Amazon region and bordering French Guiana, is a strategic sentinel location for infectious disease surveillance. Ecological pressures such as deforestation, artisanal gold mining, and high human mobility contribute to complex transmission dynamics of arboviruses, bacterial infections, and other pathogens. This study aims to characterize the etiologies of acute febrile illness (AFI) reported in Amapa State in 2018-2020, focusing on arbovirus circulation, bacterial contributions, and emerging pathogens. A retrospective analysis was carried out with 727 AFI cases. Laboratory diagnoses were established using molecular and serological assays, with systematic testing for different pathogens. Definitive diagnoses were obtained in 185 individuals (25.4%), yielding 209 positive results and including 23 cases of co-infection. Dengue virus was the predominant etiological agent (n=109, 52%), followed by leptospirosis (n=20, 9.5%), chikungunya virus (n=16, 7.6%), parvovirus B19 (n=16, 7.6%), measles (n=15, 7.1%), zika virus (n=10, 4.8%), mayaro virus (n=1,0.5%), and other bacterial infections (n=5, 2.4%). Isolated cases of hepatitis A and B, malaria, SARS-CoV-2, enterovirus, and acute Chagas disease were also identified. No hepatitis E virus or oropouche cases were detected. Dengue virus was the leading cause of AFI. Leptospirosis, chikungunya virus, and parvovirus B19 were other prevalent and often underrecognized contributors. The detection of additional viruses highlights Amapa State as a potential zone of "silent expansion" for emerging arboviruses. Co-detection of multiple pathogens underscores diagnostic complexity in regions with overlapping transmission. Strengthening surveillance, expanding laboratory capacity, and prioritizing differential diagnostics are essential to capture epidemiological dynamics and guide public health interventions.

Indexed as

Arbovirus InfectionsBacterial InfectionsFeverSentinel SurveillanceAcute DiseaseAdolescentAdultBrazilChildChild, PreschoolFemaleHumansInfantMaleMiddle AgedRetrospective Studies

Identifiers

PMID42848618
PMCPMC13641766

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.