Evidence map›Paper›PMID 38356547›Full record

ArticleHeliyon2024

Concordance and generalization of an AI algorithm with real-world clinical data in the pre-omicron and omicron era.

Gulsen Yilmaz, Sevilay Sezer, Aliye Bastug, Vivek Singh, Raj Gopalan, Omer Aydos, Busra Yuce Ozturk, Derya Gokcinar, Ali Kamen, Jamie Gramz and 2 more

Abstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

12 authors.

Gulsen YilmazDepartment of Medical Biochemistry, Ankara Yıldırım Beyazıt University, Ankara, Turkey.
Sevilay SezerDepartment of Medical Biochemistry, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Turkey.
Aliye BastugDepartment of Infectious Disease and Clinical Microbiology, Health Science University of Turkey, Gulhane Medical School, Ankara City Hospital, Ankara, Turkey.
Vivek SinghSiemens Healthineers, Digital Technology and Innovation, Princeton, NJ, USA.
Raj GopalanSiemens Healthineers, Diagnostics, Tarrytown, NY, USA.
Omer AydosDepartment of Infectious Disease and Clinical Microbiology, Ankara Bilkent City Hospital, Ankara, Turkey.
Busra Yuce OzturkDepartment of Infectious Disease and Clinical Microbiology, Ankara Bilkent City Hospital, Ankara, Turkey.
Derya GokcinarDepartment of Anesthesiology and Reanimation, Health Science University Turkey, Ankara Bilkent City Hospital, Ankara, Turkey.
Ali KamenSiemens Healthineers, Digital Technology and Innovation, Princeton, NJ, USA.
Jamie GramzSiemens Healthineers, Diagnostics, Tarrytown, NY, USA.
Hurrem BodurDepartment of Infectious Disease and Clinical Microbiology, Health Science University of Turkey, Gulhane Medical School, Ankara City Hospital, Ankara, Turkey.
Filiz AkbiyikAnkara Bilkent City Hospital Laboratory, Medical Director, Siemens Healthineers, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All viruses, including SARS-CoV-2, the virus responsible for COVID-19, continue to evolve, which can lead to new variants. The objective of this study is to assess the agreement between real-world clinical data and an algorithm that utilizes laboratory markers and age to predict the progression of disease severity in COVID-19 patients during the pre-Omicron and Omicron variant periods. The study evaluated the performance of a deep learning (DL) algorithm in predicting disease severity scores for COVID-19 patients using data from the USA, Spain, and Turkey (Ankara City Hospital (ACH) data set). The algorithm was developed and validated using pre-Omicron era data and was tested on both pre-Omicron and Omicron-era data. The predictions were compared to the actual clinical outcomes using a multidisciplinary approach. The concordance index values for all datasets ranged from 0.71 to 0.81. In the ACH cohort, a negative predictive value (NPV) of 0.78 or higher was observed for severe patients in both the pre-Omicron and Omicron eras, which is consistent with the algorithm's performance in the development cohort.

Indexed as

AlgorithmsClinical laboratory testsCOVID-19Disease severityPredictive value of tests

Identifiers

PMID38356547
PMCPMC10864957

What OpenQuestion holds

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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.