Evidence map›Paper›PMID 30496801›Full record

ArticleHuman pathology2019

Contribution of the clinical information to the accuracy of the minimally invasive and the complete diagnostic autopsy.

Fabiola Fernandes, Paola Castillo, Quique Bassat, Llorenç Quintó, Juan Carlos Hurtado, Miguel J Martínez, Lucilia Lovane, Dercio Jordao, Rosa Bene, Tacilta Nhampossa and 22 more

Abstract read
In one paragraph

Article in Human pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
–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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Minimally invasive autopsy - endoscopic approach to post-mortem diagnostics.Wideochirurgia i inne techniki maloinwazyjne = Videosurgery and other miniinvasive techniques · 2024
    Review
  6. Article
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  8. 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

32 authors.

Fabiola FernandesDepartment of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.
Paola CastilloISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Pathology, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
Quique BassatISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique; ICREA, Catalan Institution for Research and Advanced Studies, Pg. Lluís Companys 23, 08010 Barcelona, Spain; Pediatric Infectious Diseases Unit, Pediatrics Department, Hospital Sant Joan de Déu, Universitat de Barcelona, 8950 Barcelona, Spain; Universidad Europea de Madrid, 28670 Madrid, Spain.
Llorenç QuintóISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
Juan Carlos HurtadoISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Microbiology, Hospital Clinic of Barcelona, Universitat de Barcelona, 08036 Barcelona, Spain.
Miguel J MartínezISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Microbiology, Hospital Clinic of Barcelona, Universitat de Barcelona, 08036 Barcelona, Spain.
Lucilia LovaneDepartment of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique.
Dercio JordaoDepartment of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique.
Rosa BeneDepartment of Medicine, Maputo Central Hospital, 1100 Maputo, Mozambique.
Tacilta NhampossaCentro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
Paula Santos RitchieDepartment of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
Sónia BandeiraDepartment of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
Calvino SamboDepartment of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
Valeria ChicambaDepartment of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
Sibone MocumbiDepartment of Gynecology and Obstetrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
Zara JazeDepartment of Gynecology and Obstetrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
Flora MabotaDepartment of Gynecology and Obstetrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
Mamudo R IsmailDepartment of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.
Cesaltina LorenzoniDepartment of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.
Ariadna SanzISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
Natalia RakislovaISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Pathology, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
Lorena MarimonISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
Anelsio CossaCentro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
Inacio MandomandoCentro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
Jordi VilaISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Microbiology, Hospital Clinic of Barcelona, Universitat de Barcelona, 08036 Barcelona, Spain.
Maria MaixenchsISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
Khátia MunguambeCentro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
Eusebio MaceteCentro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
Pedro AlonsoISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
Clara MenéndezISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique; Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), 28029 Madrid, Spain.
Jaume OrdiISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Pathology, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain. Electronic address: jordi@clinic.ub.es.
Carla CarrilhoDepartment of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although autopsy diagnosis includes routinely, a thorough evaluation of all available pathological results and also of any available clinical data, the contribution of this clinical information to the diagnostic yield of the autopsy has not been analyzed. We aimed to determine to which degree the use of clinical data improves the diagnostic accuracy of the complete diagnostic autopsy (CDA) and the minimally invasive autopsy (MIA), a simplified pathological postmortem procedure designed for low-income sites. A total of 264 coupled MIA and CDA procedures (112 adults, 57 maternal deaths, 54 children, and 41 neonates) were performed at the Maputo Hospital, Mozambique. We compared the diagnoses obtained by the MIA blind to clinical data (MIAb), the MIA adding the clinical information (MIAc), and the CDA blind to clinical information (CDAb), with the results of the gold standard, the CDA with clinical data, by comparing the International Classification of Diseases, Tenth Revision codes and the main diagnostic classes obtained with each evaluation strategy (MIAb, MIAc, CDAb, CDAc). The clinical data increased diagnostic coincidence to the MIAb with the gold standard in 30 (11%) of 264 cases and modified the CDAb diagnosis in 20 (8%) of 264 cases. The increase in concordance between MIAb and MIAc with the gold standard was significant in neonatal deaths (κ increasing from 0.404 to 0.618, P = .0271), adult deaths (κ increasing from 0.732 to 0.813, P = .0221), and maternal deaths (κ increasing from 0.485 to 0.836, 0.;P < .0001). In conclusion, the use of clinical information increases the precision of MIA and CDA and may strengthen the performance of the MIA in resource-limited settings.

Indexed as

DeathAdolescentAdultAgedAutopsyChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleMiddle AgedYoung AdultCause of death determinationComplete diagnostic autopsyInternational Classification of Diseases, Tenth RevisionMinimally invasive autopsyResource-limited settings

Identifiers

PMID30496801
PMCPMC6478426

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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.