Evidence map›Paper›PMID 39032935›Full record

ArticleBMJ paediatrics open2024

Clinicopathological discrepancies in the diagnoses of childhood causes of death in the CHAMPS network: An analysis of antemortem diagnostic inaccuracies.

Haleluya Leulseged, Christine Bethencourt, Kitiezo Aggrey Igunza, Victor Akelo, Dickens Onyango, Richard Omore, Ikechukwu U Ogbuanu, Soter Ameh, Andrew Moseray, Dickens Kowuor and 35 more

Abstract readMulticenter Study
In one paragraph

Article in BMJ paediatrics open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

45 authors.

Haleluya Leulseged *College of Health and Medical Sciences, Haramaya University, Harar, Ethiopia.
Christine Bethencourt *Children's Hospital of Philadelphia Pediatrics Residency Program, Philadelphia, Pennsylvania, USA.
Kitiezo Aggrey IgunzaCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Victor AkeloLiverpool School of Tropical Medicine, Liverpool, UK.
Dickens OnyangoKisumu County Department of Health, Kisumu, Kenya.
Richard OmoreCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Ikechukwu U OgbuanuCrown Agents, Freetown, Sierra Leone.
Soter AmehCrown Agents, Freetown, Sierra Leone.
Andrew MoserayCrown Agents, Freetown, Sierra Leone.
Dickens KowuorCrown Agents, Freetown, Sierra Leone.
Ima-Abasi BasseyCrown Agents, Freetown, Sierra Leone.
Shams El ArifeenInternational Centre for Diarrhoeal Disease Research Bangladesh, Dhaka, Bangladesh.
Emily S GurleyInternational Centre for Diarrhoeal Disease Research Bangladesh, Dhaka, Bangladesh.
Mohammad Zahid HossainInternational Centre for Diarrhoeal Disease Research Bangladesh, Dhaka, Bangladesh.
Afruna RahmanInternational Centre for Diarrhoeal Disease Research Bangladesh, Dhaka, Bangladesh.
Muntasir AlamInternational Centre for Diarrhoeal Disease Research Bangladesh, Dhaka, Bangladesh.
Nega AssefaCollege of Health and Medical Sciences, Haramaya University, Harar, Ethiopia.
Lola MadridLondon School of Hygiene & Tropical Medicine, London, UK.ORCID http://orcid.org/0000-0003-4034-6033
Addisu AlemuCollege of Health and Medical Sciences, Haramaya University, Harar, Ethiopia.
Yasir Y AbdullahiCollege of Health and Medical Sciences, Haramaya University, Harar, Ethiopia.
Karen L KotloffDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Samba O SowCentre pour le Développement des Vaccins-Mali, Bamako, Mali.
Milagritos D TapiaDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Nana KouroumaCentre pour le Développement des Vaccins-Mali, Bamako, Mali.
Seydou SissokoCentre pour le Développement des Vaccins-Mali, Bamako, Mali.
Quique BassatCentro de Investigação em Saúde de Manhiça [CISM], Maputo, Mozambique.ORCID http://orcid.org/0000-0003-0875-7596
Rosauro VaroISGlobal - Hospital Clínic, Universitat de Barcelona, Barcelona, Spain.
Inacio MandomandoCentro de Investigação em Saúde de Manhiça [CISM], Maputo, Mozambique.ORCID http://orcid.org/0000-0002-1078-2187
Carla CarrilhoDepartment of Pathology, Maputo Central Hospital, Maputo, Mozambique.
Natalia RakislovaISGlobal - Hospital Clínic, Universitat de Barcelona, Barcelona, Spain.
Fabiola FernandesDepartment of Pathology, Maputo Central Hospital, Maputo, Mozambique.
Shabir MadhiSouth African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Ziyaad DangorSouth African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Sana MahtabSouth African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Martin HaleDepartment of Anatomical Pathology, University of the Witwatersrand Johannesburg, Johannesburg, South Africa.
Vicky BaillieSouth African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Jeanie du ToitSouth African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Zachary J MadewellCenter for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.ORCID http://orcid.org/0000-0002-5667-9660
Dianna M BlauCenter for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Roosecelis B MartinesInfectious Diseases Pathology Branch, NCEZID, DHCPP, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Portia C MutevedziGlobal Health Institute, Emory University, Atlanta, Georgia, USA.
Robert F BreimanHubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Cynthia G Whitney *Global Health Institute, Emory University, Atlanta, Georgia, USA.
Chris A Rees *Pediatric Emergency Medicine, Emory University School of Medicine, Atlanta, Georgia, USA chrisrees2@gmail.com.ORCID http://orcid.org/0009-0005-7268-4346
Child Health and Mortality Prevention Surveillance (CHAMPS) network

Funding

Advancing Approaches to Identify Young Children at Risk for Post-Discharge MortalityK23HL173694 · NHLBI · EMORY UNIVERSITY · PI Christopher A. Rees · 2024 to 2026
$585k
NHLBI NIH HHS K23 HL173694
6 · The paper itself

Abstract

introductionDetermining aetiology of severe illness can be difficult, especially in settings with limited diagnostic resources, yet critical for providing life-saving care. Our objective was to describe the accuracy of antemortem clinical diagnoses in young children in high-mortality settings, compared with results of specific postmortem diagnoses obtained from Child Health and Mortality Prevention Surveillance (CHAMPS).

methodsWe analysed data collected during 2016-2022 from seven sites in Africa and South Asia. We compared antemortem clinical diagnoses from clinical records to a reference standard of postmortem diagnoses determined by expert panels at each site who reviewed the results of histopathological and microbiological testing of tissue, blood, and cerebrospinal fluid. We calculated test characteristics and 95% CIs of antemortem clinical diagnostic accuracy for the 10 most common causes of death. We classified diagnostic discrepancies as major and minor, per Goldman criteria later modified by Battle.

resultsCHAMPS enrolled 1454 deceased young children aged 1-59 months during the study period; 881 had available clinical records and were analysed. The median age at death was 11 months (IQR 4-21 months) and 47.3% (n=417) were female. We identified a clinicopathological discrepancy in 39.5% (n=348) of deaths; 82.3% of diagnostic errors were major. The sensitivity of clinician antemortem diagnosis ranged from 26% (95% CI 14.6% to 40.3%) for non-infectious respiratory diseases (eg, aspiration pneumonia, interstitial lung disease, etc) to 82.2% (95% CI 72.7% to 89.5%) for diarrhoeal diseases. Antemortem clinical diagnostic specificity ranged from 75.2% (95% CI 72.1% to 78.2%) for diarrhoeal diseases to 99.0% (95% CI 98.1% to 99.6%) for HIV.

conclusionsAntemortem clinical diagnostic errors were common for young children who died in areas with high childhood mortality rates. To further reduce childhood mortality in resource-limited settings, there is an urgent need to improve antemortem diagnostic capability through advances in the availability of diagnostic testing and clinical skills.

Indexed as

Cause of DeathDiagnostic ErrorsAfricaAutopsyChild MortalityChild, PreschoolFemaleHumansInfantInfant, NewbornMaleChild HealthMortality

Identifiers

PMID39032935
PMCPMC11409330

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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.