Evidence map›Paper›PMID 41961529›Full record

ArticleJMIR medical informatics2026

Code-Based Versus AutoML Methods for Pill Recognition in Clinical Settings: Comparative Performance Study.

Amir Reza Ashraf, Richárd Rádli, Zsolt Vörösházi, András Fittler

Abstract readComparative Study
In one paragraph

Article in JMIR medical informatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Amir Reza AshrafDepartment of Pharmaceutics, Faculty of Pharmacy, University of Pécs, Rókus utca 4, Pécs, H-7624, Hungary, +36 72503650 ext 28841.ORCID 0000-0003-0339-5653
Richárd RádliImage Processing Research Laboratory, University of Pannonia, Veszprém, Hungary.ORCID 0009-0009-3160-1275
Zsolt VörösháziImage Processing Research Laboratory, University of Pannonia, Veszprém, Hungary.ORCID 0009-0004-3032-8784
András FittlerDepartment of Pharmaceutics, Faculty of Pharmacy, University of Pécs, Rókus utca 4, Pécs, H-7624, Hungary, +36 72503650 ext 28841.ORCID 0000-0002-8243-6179

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Visual identification and verification of medications during dispensing and administration are prone to human error, particularly in high-pressure and high-volume clinical settings. Misidentification can lead to medication errors, posing risks to patient safety and placing a burden on health care systems. Recent advances in computer vision and object detection offer promising solutions for automated solid oral dosage form (pill) recognition. However, comprehensive studies comparing code-based and no-code (automated machine learning [AutoML]) approaches for pill recognition are lacking. Objective: This study aimed to evaluate and compare the performance, cost, usability, and deployment feasibility of pill recognition models developed with Ultralytics YOLO11 and 3 cloud-based AutoML platforms (Amazon Rekognition Custom Labels, Google Vertex artificial intelligence [AI] AutoML Vision, and Microsoft Azure Custom Vision) using multiple datasets, including real-world clinical images. Methods: Five training subsets of increasing size (1230, 3450, 7380, 14,400, and 26,880 images) from 30 commonly dispensed medications were used to train models on YOLO11 and 3 AutoML platforms. Models were evaluated on 6 datasets from different environments: clinical images from 3 hospitals, a verification dataset, a laboratory dataset, and an exhaustive testing set. Performance metrics, including accuracy, precision, recall, and mean average precision, were calculated. We evaluated the impact of training data size on performance and benchmarked training time, platform costs, and limitations. Results: No single platform dominated across all test environments. On the verification dataset (optimal conditions), accuracy ranged from 80.83% (YOLO11) to 91.60% (Google Vertex AI) when trained with the full training dataset. YOLO11 showed consistent performance improvement with increasing training data (accuracy: 63.06%-80.83%) and achieved near-perfect precision and mean average precision scores (0.95-1.00). Google Vertex AI reached above 90% accuracy on 3 training subsets but showed unpredictable declines. Amazon Rekognition maintained near-perfect precision (0.92-1.00) but had the highest false negative rates (up to 0.74), missing many pills. Custom Vision demonstrated steady performance improvements (77.08%-85.62% accuracy) but lagged behind other AutoML platforms, probably due to its older YOLOv2-based architecture. On clinical datasets, accuracy fluctuated (20.62%-90%) depending on the dataset and platform. Training costs and time varied: YOLO11 (open-source), Microsoft Azure (US $9.50-US $28.60, allowed user-predefined training duration), Google Vertex AI (US $69.30 with consistent 2.5-3-hour training times), and Amazon Rekognition (US $5.43-US $43.89 with size-dependent training time scaling, reaching nearly 40 hours on the full 26,880-image dataset). Conclusions: Each platform offers distinct advantages and trade-offs: YOLO11 provides the highest flexibility and lowest platform costs but requires technical expertise, while AutoML platforms can offer high performance at a higher cost but with limited user control, introducing unpredictability. The performance variations demonstrate that successful clinical deployment requires careful platform selection based on specific performance requirements, budget constraints, and available technical resources, followed by rigorous validation using real-world, representative data to ensure patient safety in clinical workflows.

Indexed as

Machine LearningDetection AlgorithmsHumansautomated machine learningAutoMLclinical decision supportclinical pharmacycomputer visiondeep learningmedication errorsmedication safetyobject detectionpill recognitionYOLO11You Only Look Once

Identifiers

PMID41961529
PMCPMC13068000

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.