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. 2011 Aug 4:9:29.
doi: 10.1186/1478-7954-9-29.

Random forests for verbal autopsy analysis: multisite validation study using clinical diagnostic gold standards

Affiliations

Random forests for verbal autopsy analysis: multisite validation study using clinical diagnostic gold standards

Abraham D Flaxman et al. Popul Health Metr. .

Abstract

Background: Computer-coded verbal autopsy (CCVA) is a promising alternative to the standard approach of physician-certified verbal autopsy (PCVA), because of its high speed, low cost, and reliability. This study introduces a new CCVA technique and validates its performance using defined clinical diagnostic criteria as a gold standard for a multisite sample of 12,542 verbal autopsies (VAs).

Methods: The Random Forest (RF) Method from machine learning (ML) was adapted to predict cause of death by training random forests to distinguish between each pair of causes, and then combining the results through a novel ranking technique. We assessed quality of the new method at the individual level using chance-corrected concordance and at the population level using cause-specific mortality fraction (CSMF) accuracy as well as linear regression. We also compared the quality of RF to PCVA for all of these metrics. We performed this analysis separately for adult, child, and neonatal VAs. We also assessed the variation in performance with and without household recall of health care experience (HCE).

Results: For all metrics, for all settings, RF was as good as or better than PCVA, with the exception of a nonsignificantly lower CSMF accuracy for neonates with HCE information. With HCE, the chance-corrected concordance of RF was 3.4 percentage points higher for adults, 3.2 percentage points higher for children, and 1.6 percentage points higher for neonates. The CSMF accuracy was 0.097 higher for adults, 0.097 higher for children, and 0.007 lower for neonates. Without HCE, the chance-corrected concordance of RF was 8.1 percentage points higher than PCVA for adults, 10.2 percentage points higher for children, and 5.9 percentage points higher for neonates. The CSMF accuracy was higher for RF by 0.102 for adults, 0.131 for children, and 0.025 for neonates.

Conclusions: We found that our RF Method outperformed the PCVA method in terms of chance-corrected concordance and CSMF accuracy for adult and child VA with and without HCE and for neonatal VA without HCE. It is also preferable to PCVA in terms of time and cost. Therefore, we recommend it as the technique of choice for analyzing past and current verbal autopsies.

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Figures

Figure 1
Figure 1
Expert algorithm and RF decision trees. A right branch from a node represents "yes" and a left branch represents "no." a) Decision tree representation of expert algorithm to identify malaria deaths in child VAs (one-versus-all approach); b) Two random decision trees generated by RF to distinguish AIDS deaths from maternal sepsis deaths (one-versus-one approach).
Figure 2
Figure 2
Schematic representation of RF.
Figure 3
Figure 3
Schematic representation of "ranking" technique for cause prediction from random forest scores.
Figure 4
Figure 4
Partial-cause assignment increases partial chance-corrected concordance for adult, child, and neonate VAs with and without HCE. Slope of increase is higher between one and two cause assignments.
Figure 5
Figure 5
Median chance-corrected concordance (%) for RF across 500 splits, by cause, for adult VA, with and without HCE.
Figure 6
Figure 6
Median chance-corrected concordance (%) for RF across 500 splits, by cause, for child VA, with and without HCE.
Figure 7
Figure 7
Median chance-corrected concordance (%) for RF across 500 splits, by cause, for neonatal VA, with and without HCE.
Figure 8
Figure 8
Scatter of median chance-corrected concordance of RF versus PCVA, for adult module.
Figure 9
Figure 9
Scatter of median chance-corrected concordance of RF versus PCVA, for child module.
Figure 10
Figure 10
Estimated versus true CSMFs for 500 Dirichlet splits, showing that for selected causes of adult mortality (AIDS, colorectal cancer, maternal, and IHD), the performance of RF varies. For AIDS and IHD, RF tends to overestimate the cause fraction when the true CSMF is small and underestimate otherwise. For colorectal cancer, RF mostly assigns the same CSMF regardless of true CSMF, and for maternal causes, RF is more accurate.

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