Evidence map›Paper›PMID 35507111›Full record

ArticleMedical & biological engineering & computing2022

Efficient analysis of COVID-19 clinical data using machine learning models.

Sarwan Ali, Yijing Zhou, Murray Patterson

Abstract read
In one paragraph

Article in Medical & biological engineering & computing, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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

  1. 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

3 authors.

Sarwan AliGeorgia State University, Atlanta, GA, USA. sali85@student.gsu.edu.ORCID http://orcid.org/0000-0001-8121-2168
Yijing ZhouGeorgia State University, Atlanta, GA, USA.
Murray PattersonGeorgia State University, Atlanta, GA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Because of the rapid spread of COVID-19 to almost every part of the globe, huge volumes of data and case studies have been made available, providing researchers with a unique opportunity to find trends and make discoveries like never before by leveraging such big data. This data is of many different varieties and can be of different levels of veracity, e.g., precise, imprecise, uncertain, and missing, making it challenging to extract meaningful information from such data. Yet, efficient analyses of this continuously growing and evolving COVID-19 data is crucial to inform - often in real-time - the relevant measures needed for controlling, mitigating, and ultimately avoiding viral spread. Applying machine learning-based algorithms to this big data is a natural approach to take to this aim since they can quickly scale to such data and extract the relevant information in the presence of variety and different levels of veracity. This is important for COVID-19 and potential future pandemics in general. In this paper, we design a straightforward encoding of clinical data (on categorical attributes) into a fixed-length feature vector representation and then propose a model that first performs efficient feature selection from such representation. We apply this approach to two clinical datasets of the COVID-19 patients and then apply different machine learning algorithms downstream for classification purposes. We show that with the efficient feature selection algorithm, we can achieve a prediction accuracy of more than 90% in most cases. We also computed the importance of different attributes in the dataset using information gain. This can help the policymakers focus on only certain attributes to study this disease rather than focusing on multiple random factors that may not be very informative to patient outcomes.

Indexed as

COVID-19AlgorithmsHumansMachine LearningPandemicsClassificationClinical dataCoronavirusCOVID-19Feature selection

Identifiers

PMID35507111
PMCPMC9066140

What OpenQuestion holds

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Registered trials

None linked

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.