Evidence map›Paper›PMID 36776454›Full record

ArticleLancet regional health. Americas2022

Validation of SmartVA using conventional autopsy: A study of adult deaths in Brazil.

John D Hart, Paulo Afonso de André, Carmen Diva Saldiva de André, Tim Adair, Lucia Pereira Barroso, Sandra Valongueiro, Ana Luiza Bierrenbach, Patrícia Ismael de Carvalho, Maria Bernadete de Cerqueira Antunes, Conceição Maria de Oliveira and 14 more

Abstract read
In one paragraph

Article in Lancet regional health. Americas, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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

24 authors.

John D HartMelbourne School of Population and Global Health, The University of Melbourne, Carlton, Victoria, Australia.
Paulo Afonso de AndréUniversity of São Paulo, School of Medicine, São Paulo, São Paulo, Brazil.
Carmen Diva Saldiva de AndréUniversity of São Paulo, Institute of Mathematics and Statistics, São Paulo, São Paulo, Brazil.
Tim AdairMelbourne School of Population and Global Health, The University of Melbourne, Carlton, Victoria, Australia.
Lucia Pereira BarrosoUniversity of São Paulo, Institute of Mathematics and Statistics, São Paulo, São Paulo, Brazil.
Sandra ValongueiroFederal University of Pernambuco, Recife, Pernambuco, Brazil.
Ana Luiza BierrenbachSírio-Libanês Hospital, São Paulo, São Paulo, Brazil.
Patrícia Ismael de CarvalhoExecutive Secretary of Health Surveillance of the State of Pernambuco, Brazil.
Maria Bernadete de Cerqueira AntunesUniversity of Pernambuco, Recife, Pernambuco, Brazil.
Conceição Maria de OliveiraExecutive Secretary of the Municipal Health Surveillance of Recife, Pernambuco, Brazil.
Luiz Alberto Amador PereiraUniversity of São Paulo, School of Medicine, São Paulo, São Paulo, Brazil.
Cátia Martinez MintoSão Paulo Health State Secretary, São Paulo, São Paulo, Brazil.
Tânia Maria da Silva BezerraSecretary of State for Health, Recife, Pernambuco, Brazil.
Sérgio Parente CostaHealth Surveillance, Municipal Department of Health, Olinda, Pernambuco, Brazil.
Bárbara Araújo de AzevedoSecretary of State for Health, Recife, Pernambuco, Brazil.
José Ricardo Alves de LimaRecife Autopsy Service, Recife, Brazil.
Denise Souza de Meira MotaRecife Autopsy Service, Recife, Brazil.
Ana Maria de Oliveira RamosFederal University of Rio Grande do Norte, Health Sciences Center, Natal, Rio Grande do Norte, Brazil.
Maria de Fátima Marinho de SouzaVital Strategies, São Paulo, São Paulo, Brazil.
Luiz Fernando Ferraz da SilvaUniversity of São Paulo, School of Medicine, São Paulo, São Paulo, Brazil.
Elisabeth Barboza FrançaFederal University of Minas Gerais, School of Medicine, Belo Horizonte, Minas Gerais, Brazil.
Deirdre McLaughlinMelbourne School of Population and Global Health, The University of Melbourne, Carlton, Victoria, Australia.
Ian D RileyMelbourne School of Population and Global Health, The University of Melbourne, Carlton, Victoria, Australia.
Paulo Hilário Nascimento SaldivaUniversity of São Paulo, School of Medicine, São Paulo, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Accurate cause of death data are essential to guide health policy. However, mortality surveillance is limited in many low-income countries. In such settings, verbal autopsy (VA) is increasingly used to provide population-level cause of death data. VAs are now widely interpreted using the automated algorithms SmartVA and InterVA. Here we use conventional autopsy as the gold standard to validate SmartVA methodology. Methods: This study included adult deaths from natural causes in São Paulo and Recife for which conventional autopsy was indicated. VA was conducted with a relative of the deceased using an amended version of the SmartVA instrument to suit the local context. Causes of death from VA were produced using the SmartVA-Analyze program. Physician coded verbal autopsy (PCVA), conducted on the same questionnaires, and Global Burden of Disease Study data were used as additional comparators. Cause of death data were grouped into 10 broad causes for the validation due to the real-world utility of VA lying in identifying broad population cause of death patterns. Findings: The study included 2,060 deaths in São Paulo and 1,079 in Recife. The cause specific mortality fractions (CSMFs) estimated using SmartVA were broadly similar to conventional autopsy for: cardiovascular diseases (46.8% vs 54.0%, respectively), cancers (10.6% vs 11.4%), infections (7.0% vs 10.4%) and chronic respiratory disease (4.1% vs 3.7%), causes accounting for 76.1% of the autopsy dataset. The SmartVA CSMF estimates were lower than autopsy for "Other NCDs" (7.8% vs 14.6%) and higher for diabetes (13.0% vs 6.6%). CSMF accuracy of SmartVA compared to autopsy was 84.5%. CSMF accuracy for PCVA was 93.0%. Interpretation: The results suggest that SmartVA can, with reasonable accuracy, predict the broad cause of death groups important to assess a population's epidemiological transition. VA remains a useful tool for understanding causes of death where medical certification is not possible.

Indexed as

AutopsyBrazilCause of deathValidationVerbal autopsyVital statistics

Identifiers

PMID36776454
PMCPMC9904092

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LicenceCC BY-NC-ND
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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.