MEHMET ONUR ONAL

Dr. MEHMET ONUR ONAL

orcid

Research Focus & Metrics

Academic Career Length

1Year (2026-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 July 2026 in Scientific Reports
Verified
Journal Article
Open access
PDF file
YBYeliz Başar
Yeliz Başar
Mustafa Ege SekerMustafa Ege Seker
Mustafa Ege Seker
GKGalina Ivanova Kirova-Nedyalkova
Galina Ivanova Kirova-Nedyalkova
EMElina Plamenova Milkovska
Elina Plamenova Milkovska
BMBoyan Emilov Manov
Boyan Emilov Manov
GDGamze Durhan
Gamze Durhan
This retrospective bi-national multicenter diagnostic accuracy study evaluated the locked default-threshold performance of a commercial chest radiograph AI system for selected thoracic findings using a CT-anchored, radiographic-detectability reference framework. Consecutive eligible adult patients who underwent frontal chest radiography and chest CT at four tertiary-care centers in Turkey and Bulgaria between June and December 2024 were included. Reference labels were assigned using temporally paired CT, with adjudication of whether CT-confirmed abnormalities had a corresponding radiographic manifestation on the paired chest radiograph. For potentially dynamic findings, the allowable CT–CXR interval was restricted to ≤ 2 days. The AI system was evaluated at the manufacturer’s default threshold of 0.50. Diagnostic performance was summarized using prevalence, sensitivity, specificity, positive predictive value, negative predictive value, and false-positive burden with 95% confidence intervals. The study included 940 patients with paired CXR-CT examinations. Reference-positive prevalence ranged from 2.2% for pneumothorax to 21.0% for pleural effusion. Sensitivity was highest for fracture (91%) and pneumothorax (90%) and lowest for atelectasis (64%); specificity ranged from 82% for consolidation/opacity to 98% for fracture and pneumothorax. PPV ranged from 43% to 63%, indicating a non-trivial false-positive burden at the evaluated operating point. Because continuous probability scores, human-reader comparison, and workflow outcomes were unavailable, these findings should be interpreted as default-threshold technical validation and support further evaluation of the system as radiologist-supervised decision support with local performance monitoring, rather than standalone diagnosis.

17 February 2026 in Diagnostics
Verified
Journal Article
Open access
PDF file
MOMujgan Orman
Mujgan Orman
DADeniz Can Aliş
Deniz Can Aliş
MOMEHMET ONUR ONAL
MEHMET ONUR ONAL
Mustafa Ege SekerMustafa Ege Seker
Mustafa Ege Seker
AAAhmet Akyol
Ahmet Akyol
EKErcan Karaarslan
Ercan Karaarslan
Background/Objectives: Whether PCCT-derived virtual non-iodine (VNI) images can replace true non-contrast (TNC) for coronary artery calcium scoring (CACS) remains uncertain, particularly for small, low-density plaques. We aimed to evaluate agreement between VNI and TNC for CACS at the patient and lesion levels and to quantify risk-category reclassification. Methods: In this retrospective single-center sample (May 2024–May 2025), 211 patients without prior coronary intervention and with nonzero CAC on TNC underwent PCCT. VNI (55 keV, QIR 1; 60 keV, QIR 4; PureCalcium) and TNC were reconstructed with matched section thickness/increment and kernel. Agatston and total calcified volume were recorded. Paired comparisons used Wilcoxon tests; reclassification across CAC categories (0, 1–99, 100–399, ≥400) and lesion-level false negatives (FNs) were assessed with TNC as the reference. Results: Low-keV VNIs (55–60 keV) underestimated CAC versus TNC. The median Agatston score decreased from 35.9 (IQR, 10.3–121.2) on TNC to 23.6 at 55 keV (p = 0.0006) and 22.2 at 60 keV (p = 0.0003); the total volume declined from 37.8 mm3 to 20.2 mm3 (p = 0.001) and 18.3 mm3 (p < 0.0001), respectively. More than half of patients were reassigned to a lower CAC category; despite no patient being CAC = 0 on TNC, 46.9% (55 keV) and 47.4% (60 keV) were labeled CAC = 0 on VNI. Because this study deliberately included only patients with nonzero CAC on the TNC reference, these CAC = 0 rates on VNI represent misclassification within a CAC-positive sample and should not be interpreted as population-level prevalence. At the lesion level, 95% of patients had ≥1 FN plaques (430 FN plaques total), typically small (median 8 mm3) and of low density (median Agatston 6). Conclusions: In this single-center sample with relatively low-burden calcification, low-keV VNI (55–60 keV) significantly underestimates CAC and down-classifies patients, with frequent “false-zero” assignments (defined as CAC_VNI = 0 despite CAC_TNC > 0) driven predominantly by small, low-density plaques.