Evidence map›Paper›PMID 36668951›Full record

ArticleTropical medicine and infectious disease2023

Evaluation of Two Different Strategies for Schistosomiasis Screening in High-Risk Groups in a Non-Endemic Setting.

Luisa Roade, Elena Sulleiro, Cristina Bocanegra, Fernando Salvador, Begoña Treviño, Francesc Zarzuela, Lidia Goterris, Nuria Serre-Delcor, Inés Oliveira-Souto, Maria Luisa Aznar and 5 more

Open access · goldAbstract read
In one paragraph

Article in Tropical medicine and infectious disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Observational
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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

15 authors at 1 institution in 1 country.

Luisa RoadeInternal Medicine Department, University Hospital Vall d'Hebron, 08035 Barcelona, Spain.ORCID 0000-0002-8160-9613
Elena SulleiroMicrobiology Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-9783-6060
Cristina BocanegraTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Fernando SalvadorTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-0546-1354
Begoña TreviñoTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Francesc ZarzuelaMicrobiology Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Lidia GoterrisMicrobiology Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.ORCID 0000-0003-1471-4461
Nuria Serre-DelcorTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Inés Oliveira-SoutoTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Maria Luisa AznarTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.ORCID 0000-0001-9223-7790
Diana PouTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Adrián Sánchez-MontalvàTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-2194-5447
Pau Bosch-NicolauTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-7435-1829
Juan Espinosa-PereiroTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Israel MolinaTropical Medicine and International Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, University Hospital Vall d'Hebron, PROSICS Barcelona, 08035 Barcelona, Spain.
Vall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A consensus on the recommended screening algorithms for schistosomiasis in asymptomatic high-risk subjects in non-endemic areas is lacking. The objective of this study was to evaluate the real-life performance of direct microscopy and ELISA serology for schistosomiasis screening in a high-risk population in a non-endemic setting. A retrospective cohort study was conducted in two out-patient Tropical Medicine units in Barcelona (Spain) from 2014 to 2017. Asymptomatic adults arriving from the Sub-Saharan region were included. Schistosomiasis screening was conducted according to clinical practice following a different strategy in each setting: (A) feces and urine direct examination plus S. mansoni serology if non-explained eosinophilia was present and (B) S. mansoni serology plus uroparasitological examination as the second step in case of a positive serology. Demographic, clinical and laboratory features were collected. Schistosomiasis cases, clinical management and a 24 month follow-up were recorded for each group. Four-hundred forty individuals were included. The patients were mainly from West African countries. Fifty schistosomiasis cases were detected (11.5% group A vs. 4 % group B, p = 0.733). When both microscopic and serological techniques were performed, discordant results were recorded in 18.4% (16/88). Schistosomiasis cases were younger (p < 0.001) and presented eosinophilia and elevated IgE (p < 0.001) more frequently. Schistosomiasis is a frequent diagnosis among high-risk populations. Serology achieves a similar performance to direct diagnosis for the screening of schistosomiasis in a high-risk population.

Indexed as

diagnosisnon-endemicschistosomiasis

Identifiers

PMID36668951
PMCPMC9862038
OpenAlexW4313640228

What OpenQuestion holds

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LicenceCC BY
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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.