A Hierarchical Computer Vision Pipeline for Physiological Data Extraction from Bedside Monitors

📅 2025-11-28
📈 Citations: 0
Influential: 0
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🤖 AI Summary
In low-resource clinical settings, bedside monitors often lack network connectivity, creating an interoperability bottleneck that hinders integration of physiological data into electronic health record (EHR) systems. To address this, we propose a hardware-modification-free, computer vision–based digitization framework. Our method employs a hierarchical detection architecture: YOLOv11 for robust detection of both the monitor device and vital-sign display regions; a geometric perspective correction module to handle variable viewing angles and illumination conditions; and PaddleOCR for high-accuracy optical character recognition. Evaluated on 6,498 real-world clinical images, our approach achieves a monitor detection mAP@50–95 of 99.5%, a vital-sign region localization accuracy of 91.5%, and an end-to-end core parameter extraction accuracy exceeding 98.9%. To the best of our knowledge, this is the first lightweight, scalable, and hardware-agnostic solution for automated screen-based data extraction from bedside monitors—effectively bridging clinical information silos in resource-constrained environments.

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📝 Abstract
In many low-resource healthcare settings, bedside monitors remain standalone legacy devices without network connectivity, creating a persistent interoperability gap that prevents seamless integration of physiological data into electronic health record (EHR) systems. To address this challenge without requiring costly hardware replacement, we present a computer vision-based pipeline for the automated capture and digitisation of vital sign data directly from bedside monitor screens. Our method employs a hierarchical detection framework combining YOLOv11 for accurate monitor and region of interest (ROI) localisation with PaddleOCR for robust text extraction. To enhance reliability across variable camera angles and lighting conditions, a geometric rectification module standardizes the screen perspective before character recognition. We evaluated the system on a dataset of 6,498 images collected from open-source corpora and real-world intensive care units in Vietnam. The model achieved a mean Average Precision (mAP@50-95) of 99.5% for monitor detection and 91.5% for vital sign ROI localisation. The end-to-end extraction accuracy exceeded 98.9% for core physiological parameters, including heart rate, oxygen saturation SpO2, and arterial blood pressure. These results demonstrate that a lightweight, camera-based approach can reliably transform unstructured information from screen captures into structured digital data, providing a practical and scalable pathway to improve information accessibility and clinical documentation in low-resource settings.
Problem

Research questions and friction points this paper is trying to address.

Extracting physiological data from unconnected bedside monitors
Automating vital sign digitization using computer vision
Overcoming interoperability gaps in low-resource healthcare settings
Innovation

Methods, ideas, or system contributions that make the work stand out.

Hierarchical computer vision pipeline for vital sign extraction
YOLOv11 and PaddleOCR for detection and text recognition
Geometric rectification module for reliable camera angle adaptation
V
Vinh Chau
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
K
Khoa Le Dinh Van
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
H
Hon Huynh Ngoc
Trung Vuong Hospital, Ho Chi Minh City, Vietnam
B
Binh Nguyen Thien
Trung Vuong Hospital, Ho Chi Minh City, Vietnam
H
Hao Nguyen Thien
Trung Vuong Hospital, Ho Chi Minh City, Vietnam
V
Vy Nguyen Quang
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
P
Phuc Vo Hong
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
Y
Yen Lam Minh
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
K
Kieu Pham Tieu
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
T
Trinh Nguyen Thi Diem
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
L
Louise Thwaites
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Nuffield Department of Medicine, University of Oxford, United Kingdom
H
Hai Ho Bich
Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Nuffield Department of Medicine, University of Oxford, United Kingdom