Evidence map›Paper›PMID 28369287›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2017

Toward Improving Early Diagnosis of Congenital Chagas Disease in an Endemic Setting.

Louisa A Messenger, Robert H Gilman, Manuela Verastegui, Gerson Galdos-Cardenas, Gerardo Sanchez, Edward Valencia, Leny Sanchez, Edith Malaga, Victoria R Rendell, Malasa Jois and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 4 pooled it
5.5field-weighted citation impact, top 3% of its field
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

48 citing papers in PubMed, 4 syntheses or guidelines pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Risk factors for vertical transmission of Chagas disease: A systematic review and meta-analysis.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Pooled it
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  18. Laboratory diagnosis ofFrontiers in parasitology · 2023
    Review
  19. Extracellular vesicles ofFrontiers in immunology · 2023
    Article
  20. Clinical use of molecular methods forFrontiers in parasitology · 2023
    Article
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

18 authors at 7 institutions in 3 countries.

Louisa A MessengerDepartment of Disease Control, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, United Kingdom.
Robert H GilmanDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Manuela VerasteguiLaboratorio de Investigación en Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
Gerson Galdos-CardenasDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Gerardo SanchezLaboratorio de Investigación en Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
Edward ValenciaLaboratorio de Investigación en Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
Leny SanchezLaboratorio de Investigación en Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
Edith MalagaLaboratorio de Investigación en Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
Victoria R RendellDepartment of Surgery, Duke University, Durham, North Carolina.
Malasa JoisDivision of Internal Medicine, Brown University, Providence, Rhode Island.
Vishal ShahDepartment of Medicine, New York University, New York.
Nicole SantosDepartment of Epidemiology and Biostatistics, School of Medicine, University of California, San Francisco.
Maria Del Carmen AbastoflorHospital Universitario Japones, Santa Cruz.
Carlos LaFuenteHospital Universitario Japones, Santa Cruz.
Rony ColanziHospital Universitario Japones, Santa Cruz.
Ricardo BozoHospital Municipal Camiri, Plurinational State of Bolivia.
Caryn BernDepartment of Epidemiology and Biostatistics, School of Medicine, University of California, San Francisco.
Working Group on Chagas Disease in Bolivia and Peru
Universidad Peruana Cayetano Heredia · PEJohns Hopkins University · USUniversity of California, San Francisco · USBrown University · USDuke University · USLondon School of Hygiene & Tropical Medicine · GBNew York University · US

Funding

Early Detection of Congenital Chagas DiseaseR01AI087776 · NIAID · JOHNS HOPKINS UNIVERSITY · PI GILMAN, ROBERT H · 2010 to 2014
$2.9M
Medical Research Council MR/K007467/1NIAID NIH HHS R01 AI087776
6 · The paper itself

Abstract

backgroundCongenital Trypanosoma cruzi transmission is now estimated to account for 22% of new infections, representing a significant public health problem across Latin America and internationally. Treatment during infancy is highly efficacious and well tolerated, but current assays for early detection fail to detect >50% of infected neonates, and 9-month follow-up is low.

methodsWomen who presented for delivery at 2 urban hospitals in Santa Cruz Department, Bolivia, were screened by rapid test. Specimens from infants of infected women were tested by microscopy (micromethod), quantitative PCR (qPCR), and immunoglobulin (Ig)M trypomastigote excreted-secreted antigen (TESA)-blots at birth and 1 month and by IgG serology at 6 and 9 months.

resultsAmong 487 infants of 476 seropositive women, congenital T. cruzi infection was detected in 38 infants of 35 mothers (7.8%). In cord blood, qPCR, TESA-blot, and micromethod sensitivities/specificities were 68.6%/99.1%, 58.3%/99.1%, and 16.7%/100%, respectively. When birth and 1-month results were combined, cumulative sensitivities reached 84.2%, 73.7%, and 34.2%, respectively. Low birthweight and/or respiratory distress were reported in 11 (29%) infected infants. Infants with clinical signs had higher parasite loads and were significantly more likely to be detected by micromethod.

conclusionsThe proportion of T. cruzi-infected infants with clinical signs has fallen since the 1990s, but symptomatic congenital Chagas disease still represents a significant, albeit challenging to detect, public health problem. Molecular methods could facilitate earlier diagnosis and circumvent loss to follow-up but remain logistically and economically prohibitive for routine screening in resource-limited settings.

Indexed as

Early DiagnosisEndemic DiseasesAdultAntibodies, ProtozoanAntigens, ProtozoanChagas DiseaseEnzyme-Linked Immunosorbent AssayFemaleHumansImmunoglobulin GImmunoglobulin MInfantInfant, Low Birth WeightInfant, NewbornInfectious Disease Transmission, VerticalMaleAntibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GImmunoglobulin MBoliviaChagas diseasecongenitaldiagnosticsTrypanosoma cruzi

Identifiers

PMID28369287
PMCPMC5848221
OpenAlexW2598624334

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.