Evidence map›Paper›PMID 29669548›Full record

ArticleBMC medicine2018

Performance of InSilicoVA for assigning causes of death to verbal autopsies: multisite validation study using clinical diagnostic gold standards.

Abraham D Flaxman, Jonathan C Joseph, Christopher J L Murray, Ian Douglas Riley, Alan D Lopez

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in BMC medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

5 authors.

Abraham D FlaxmanInstitute for Health Metrics and Evaluation, University of Washington, Seattle, Washington, USA. abie@uw.edu.
Jonathan C JosephInstitute for Health Metrics and Evaluation, University of Washington, Seattle, Washington, USA.
Christopher J L MurrayInstitute for Health Metrics and Evaluation, University of Washington, Seattle, Washington, USA.
Ian Douglas RileySchool of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
Alan D LopezSchool of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.

Funding

National Health and Medical Research Council (AU) 00885National Health and Medical Research Council (AU) 631494
6 · The paper itself

Abstract

backgroundRecently, a new algorithm for automatic computer certification of verbal autopsy data named InSilicoVA was published. The authors presented their algorithm as a statistical method and assessed its performance using a single set of model predictors and one age group.

methodsWe perform a standard procedure for analyzing the predictive accuracy of verbal autopsy classification methods using the same data and the publicly available implementation of the algorithm released by the authors. We extend the original analysis to include children and neonates, instead of only adults, and test accuracy using different sets of predictors, including the set used in the original paper and a set that matches the released software.

resultsThe population-level performance (i.e., predictive accuracy) of the algorithm varied from 2.1 to 37.6% when trained on data preprocessed similarly as in the original study. When trained on data that matched the software default format, the performance ranged from -11.5 to 17.5%. When using the default training data provided, the performance ranged from -59.4 to -38.5%. Overall, the InSilicoVA predictive accuracy was found to be 11.6-8.2 percentage points lower than that of an alternative algorithm. Additionally, the sensitivity for InSilicoVA was consistently lower than that for an alternative diagnostic algorithm (Tariff 2.0), although the specificity was comparable.

conclusionsThe default format and training data provided by the software lead to results that are at best suboptimal, with poor cause-of-death predictive performance. This method is likely to generate erroneous cause of death predictions and, even if properly configured, is not as accurate as alternative automated diagnostic methods.

Indexed as

AlgorithmsCause of DeathAdultAutopsyChildComputer SimulationFemaleHumansInfantInfant, NewbornMaleCause-of-death diagnosisValidationVerbal autopsy

Identifiers

PMID29669548
PMCPMC5907465

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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.