Evidence map›Paper›PMID 31328221›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

Case Fatality Ratio Estimates for the 2013-2016 West African Ebola Epidemic: Application of Boosted Regression Trees for Imputation.

Alpha Forna, Pierre Nouvellet, Ilaria Dorigatti, Christl A Donnelly

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 2 syntheses or guidelines 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

4 authors.

Alpha FornaMedical Research Council Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Brighton, Brighton, United Kingdom, and Imperial College London, London, United Kingdom.
Pierre NouvelletMedical Research Council Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Brighton, Brighton, United Kingdom, and Imperial College London, London, United Kingdom.
Ilaria DorigattiMedical Research Council Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Brighton, Brighton, United Kingdom, and Imperial College London, London, United Kingdom.
Christl A DonnellyMedical Research Council Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Brighton, Brighton, United Kingdom, and Imperial College London, London, United Kingdom.

Funding

Medical Research Council MR/R015600/1
6 · The paper itself

Abstract

backgroundThe 2013-2016 West African Ebola epidemic has been the largest to date with >11 000 deaths in the affected countries. The data collected have provided more insight into the case fatality ratio (CFR) and how it varies with age and other characteristics. However, the accuracy and precision of the naive CFR remain limited because 44% of survival outcomes were unreported.

methodsUsing a boosted regression tree model, we imputed survival outcomes (ie, survival or death) when unreported, corrected for model imperfection to estimate the CFR without imputation, with imputation, and adjusted with imputation. The method allowed us to further identify and explore relevant clinical and demographic predictors of the CFR.

resultsThe out-of-sample performance (95% confidence interval [CI]) of our model was good: sensitivity, 69.7% (52.5-75.6%); specificity, 69.8% (54.1-75.6%); percentage correctly classified, 69.9% (53.7-75.5%); and area under the receiver operating characteristic curve, 76.0% (56.8-82.1%). The adjusted CFR estimates (95% CI) for the 2013-2016 West African epidemic were 82.8% (45.6-85.6%) overall and 89.1% (40.8-91.6%), 65.6% (61.3-69.6%), and 79.2% (45.4-84.1%) for Sierra Leone, Guinea, and Liberia, respectively. We found that district, hospitalisation status, age, case classification, and quarter (date of case reporting aggregated at three-month intervals) explained 93.6% of the variance in the naive CFR.

conclusionsThe adjusted CFR estimates improved the naive CFR estimates obtained without imputation and were more representative. Used in conjunction with other resources, adjusted estimates will inform public health contingency planning for future Ebola epidemics, and help better allocate resources and evaluate the effectiveness of future inventions.

Indexed as

EpidemicsHemorrhagic Fever, EbolaGuineaHumansLiberiaSierra Leoneimputationinfectious disease epidemiologymachine learningsurvivalviral hemorrhagic disease

Identifiers

PMID31328221
PMCPMC7286386

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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.