# Machine learning-based prediction of intensive care unit admission in COVID-19 patients presenting with mild respiratory failure

**Authors:** Bahadır Ceylan, Şule Ceylan, Oktay Olmuşçelik, Banu Karaalioğlu, Melih Akan, Meyha Şahin, Mebrule Muğlu, Selda Aydın, Ezgi Yılmaz, Rıdvan Dumlu, Kamil Mert, Abdullah Kansu, Mustafa Düger, Ufuk Süleyman, Esra Demir, İhsan Boyacı, Ali Mert

PMC · DOI: 10.3389/fmed.2026.1724947 · Frontiers in Medicine · 2026-02-16

## TL;DR

This study uses machine learning to predict which mild COVID-19 patients will need ICU admission and identifies key factors like age and lab results.

## Contribution

A novel machine learning approach for predicting ICU admission in mild COVID-19 patients with reliable performance and key predictor identification.

## Key findings

- ML models like multilayer perceptron and XGBoost achieved high accuracy (0.79) in predicting ICU admission.
- Low lymphocyte count, high age, and other clinical factors were the strongest predictors of ICU admission.

## Abstract

Previous studies applying machine learning to predict severe respiratory failure in COVID-19 patients have shown inconsistent results due to variations in study populations and predictor variables. This study aimed to predict intensive care unit admission and identify key predictive factors.

This retrospective cohort study included patients with COVID-19 who presented with mild respiratory failure, most of whom received oxygen via a mask or nasal cannula. Eight machine learning algorithms—XGBoost, support vector machines, neural networks, k-nearest neighbors, random forest, decision trees, logistic regression, and naïve Bayes—were applied to predict intensive care unit admission.

A total of 392 patients (63.5% male, mean age, 55.0 ± 15.3 years) were included in the study. During follow-up, 80 patients (20.4%) required intensive care unit admission. Among them, 320 (81.6%) received steroid therapy, 301 (76.8%) underwent pulse steroid therapy, and 76 (19%) had been vaccinated. The multilayer perceptron, XGBoost, and radial basis function support vector machine models achieved the best overall performance based on ROC-AUC and accuracy values (ROC-AUC: 0.75, 0.70, and 0.71; accuracy: 0.79, 0.79, and 0.79, respectively). The strongest predictors of intensive care unit admission were low lymphocyte count on the first day, as well as high age, ferritin, body mass index, Charlson Comorbidity Index, and computed tomography score.

Machine learning algorithms can reliably predict intensive care unit admission in COVID-19 patients with mild respiratory failure. These models identified key clinical and laboratory factors that may facilitate early risk stratification and guide treatment planning.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** BSG (basigin (Ok blood group)) [NCBI Gene 682] {aka 5F7, CD147, EMMPRIN, EMPRIN, HAb18G, OK}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ITIH2 (inter-alpha-trypsin inhibitor heavy chain 2) [NCBI Gene 3698] {aka H2P, ITI-HC2, SHAP}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}
- **Diseases:** renal failure (MESH:D051437), multiple myeloma (MESH:D009101), idiopathic pulmonary fibrosis (MESH:D054990), dyspnea (MESH:D004417), infection (MESH:D007239), chronic renal failure (MESH:D007676), ischemic heart disease (MESH:D017202), COVID (MESH:D000086382), diabetes mellitus (MESH:D003920), Lymphopenia (MESH:D008231), end-organ damage (MESH:C564816), Cancer (MESH:D009369), diabetic retinopathy (MESH:D003930), pulmonary edema (MESH:D011654), cerebrovascular disease (MESH:D002561), liver cirrhosis (MESH:D008103), asthma (MESH:D001249), CCI (MESH:C566784), Charlson Comorbidity (MESH:D004194), rheumatoid arthritis (MESH:D001172), metastasis (MESH:D009362), hypertension (MESH:D006973), death (MESH:D003643), bronchiectasis (MESH:D001987), leukemia (MESH:D007938), Parkinson's disease (MESH:D010300), neutrophilia (MESH:C563010), fever (MESH:D005334), pulmonary embolism (MESH:D011655), neuropathy (MESH:D009422), myasthenia gravis (MESH:D009157), hypoxia (MESH:D000860), respiratory (MESH:D012131), bacterial infection (MESH:D001424), CT (MESH:C000719218), lymphoma (MESH:D008223), heart failure (MESH:D006333), nephropathy (MESH:D007674), aplastic anemia (MESH:D000741), chronic obstructive pulmonary disease (MESH:D029424), dementia (MESH:D003704), hypercoagulability (MESH:D019851)
- **Chemicals:** dexamethasone (MESH:D003907), D (MESH:D003903), oxygen (MESH:D010100), creatinine (MESH:D003404), methylprednisolone (MESH:D008775), steroid (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606], Meleagris gallopavo (common turkey, species) [taxon 9103], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12951780/full.md

## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC12951780/full.md

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Source: https://tomesphere.com/paper/PMC12951780