AI-Driven Dose Optimization for Digital Radiography Imaging Systems | Blazingprojects Postgraduate Thesis
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AI-Driven Dose Optimization for Digital Radiography Imaging Systems

 

Table Of Contents


Chapter ONE

INTRODUCTION

  • 1.
  • 1.1Introduction
  • 2.
  • 1.2Background of the Study
  • 3.
  • 1.3Statement of the Problem
  • 4.
  • 1.4Aim and Objectives of the Study
  • 5.
  • 1.5Research Questions
  • 6.
  • 1.6Research Hypotheses
  • 7.
  • 1.7Significance of the Study
  • 8.
  • 1.8Scope and Delimitation of the Study
  • 9.
  • 1.9Limitations of the Study
  • 10.
  • 1.10Organisation of the Study
  • 11.
  • 1.11Operational Definition of Terms

Chapter TWO

LITERATURE REVIEW

  • 1.
  • 2.1Conceptual Review: AI-Driven Dose Optimization in Digital Radiography
  • 2.
  • 2.2Digital Radiography Dose Metrics and Image Quality Trade-offs
  • 3.
  • 2.3Deep Learning for Dose Prediction in Radiography
  • 4.
  • 2.4Reinforcement Learning for Adaptive Exposure Control
  • 5.
  • 2.5Transfer Learning in Medical Imaging Dose Management
  • 6.
  • 2.6Data Privacy and Security in AI-Driven Radiography Systems
  • 7.
  • 2.7Regulatory and Safety Standards Guiding Dose Optimization
  • 8.
  • 2.8Imaging Protocols and Workflow Integration
  • 9.
  • 2.9Hardware and Sensor Technologies Supporting AI Dose Tools
  • 10.
  • 2.10Explainability and Trust in Medical AI Dose Systems
  • 11.
  • 2.11Human–AI Collaboration in Radiography
  • 12.
  • 2.12Gaps in the Literature and Proposed Conceptual Model
  • 13.
  • 2.13Conceptual Model or Summary of the Review

Chapter THREE

RESEARCH METHODOLOGY

  • 1.
  • 3.1Research Design: AI-Driven Dose Optimization Framework Evaluation
  • 2.
  • 3.2Philosophical Paradigm: Pragmatism and Mixed Methods Rationale
  • 3.
  • 3.3Population of the Study: Radiography Departments and Systems
  • 4.
  • 3.4Sample Size and Sampling Technique: Stratified and Purposive Sampling
  • 5.
  • 3.5Sources and Instruments of Data Collection: System Logs, Protocol Records, and Surveys
  • 6.
  • 3.6Validity and Reliability of Instruments: Pilot Testing and Triangulation
  • 7.
  • 3.7Data Processing and Pre-processing Procedures
  • 8.
  • 3.8Model Specification: AI Dose-Optimization Algorithms and Evaluation Metrics
  • 9.
  • 3.9Data Analysis Methods: Statistical and AI Performance Analyses
  • 10.
  • 3.10Ethical Considerations: Patient Privacy and Data Governance

Chapter FOUR

DATA PRESENTATION AND ANALYSIS

  • ANALYSIS AND DISCUSSION OF FINDINGS
  • 1.
  • 4.1Data Presentation: Baseline Dose and Image Quality Profiles
  • 2.
  • 4.2Descriptive Analysis of Protocol Variability
  • 3.
  • 4.3Hypotheses Testing: AI Dose Optimization Performance
  • 4.
  • 4.4Results of Image Quality vs. Dose Trade-off Analyses
  • 5.
  • 4.5Algorithmic Fairness and Robustness Findings
  • 6.
  • 4.6Usability and Workflow Impact Findings
  • 7.
  • 4.7Comparative Discussion with Traditional Protocols
  • 8.
  • 4.8Interpretation of Results in the Context of Reviewed Literature

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • CONCLUSION AND RECOMMENDATIONS
  • 1.
  • 5.1Summary of Findings
  • 2.
  • 5.2Conclusion
  • 3.
  • 5.3Contributions to Knowledge
  • 4.
  • 5.4Practical Recommendations for Radiography Practice
  • 5.
  • 5.5Recommendations for Future Research

Thesis Abstract

This study addresses the challenge of balancing diagnostic image quality with patient safety in digital radiography through the development of an AI-driven dose optimization framework that dynamically adapts exposure parameters to individual patient characteristics and exam types. The aim is to minimize unnecessary radiation while preserving clinically acceptable image quality, thereby reducing stochastic and deterministic risks without compromising diagnostic efficacy. Specific objectives include (1) to quantify the relationship between patient demographics, body habitus, and optimal exposure indices across common radiographic projections; (2) to develop and validate a machine learning model that prescribes tube current, voltage, and exposure time to achieve target image quality metrics; (3) to compare dose and image quality outcomes between the AI-driven protocol and conventional fixed or protocol-based approaches; (4) to assess radiographer acceptance, workflow impact, and potential for integration with existing picture archiving and communication systems (PACS) and dose monitoring software; and (5) to evaluate generalizability across equipment brands and clinical settings. The study adopts a mixed-methods design, combining quantitative model development and validation with qualitative usability evaluation. The population comprises adult patients undergoing standard radiographic examinations (chest, abdomen, pelvis, and extremities) at three tertiary hospitals equipped with digital radiography systems. A stratified sample of 1,200 examinations will be collected, with 600 used to train the optimization model and 600 reserved for prospective validation. Instrumentation includes standardized imaging equipment capable of recording exposure indices (EIs, DAP, entrance surface dose), alongside anonymized patient demographic data and clinical indications. A radiographic image quality assessment protocol, based on a validated 5-point Lombard scale and objective metrics such as contrast-to-noise ratio (CNR) and signal-to-noise ratio (SNR), will be employed. The AI model will be developed using supervised learning algorithms (random forests, gradient boosting, and deep learning regression networks) and optimized through cross-validation and grid search. Feature sets will include patient BMI, age, sex, projection, technique factors, and prior image quality metrics. Model outputs will include recommended tube current, kVp, and exposure time tailored to each examination. Data analysis will proceed in two streams. The quantitative stream will involve regression analyses to quantify dose-quality trade-offs, receiver operating characteristic (ROC) analyses to determine diagnostic thresholds, and Bland–Altman plots to assess agreement between AI-suggested and clinician-chosen exposure parameters. Model performance will be evaluated using RMSE, mean absolute error (MAE), and area under the ROC curve for diagnostic adequacy. Sensitivity analyses will test robustness to missing data and equipment variability. The qualitative stream will use thematic analysis of semi-structured interviews with radiographers to evaluate usability, perceived workflow impact, and trust in AI recommendations, with coding grounded in the Technology Acceptance Model (TAM) and the Unified Theory of Acceptance and Use of Technology (UTAUT). The study is expected to show that AI-driven dose optimization maintains diagnostic image quality within clinically acceptable thresholds while achieving a statistically significant reduction in mean entrance skin dose and DAP by at least 15% across examined projections, compared to conventional protocols. Anticipated findings include strong correlations between patient habitus, projection, and optimal exposure settings, and improved consistency of image quality across operators. The research will contribute to knowledge by providing a validated, transportable decision-support model that integrates with PACS and dose-monitoring systems, thereby enabling real-time dose reduction without compromising diagnostic accuracy. Theoretical underpinnings will draw on the ALARA principle and the Technology Acceptance Model to frame dose optimization adoption. The study’s main conclusion is that AI-driven personalized exposure control is feasible and effective across diverse radiography settings, with measurable dose savings and maintained image quality. Recommendations include phased clinical deployment with ongoing performance auditing, integration of the model into radiography workflows, development of standardized calibration procedures across vendors, and continuous model retraining with new data to sustain performance gains. Further research should examine broader modality integration (e.g., mammography, fluoroscopy) and long-term patient outcomes related to reduced radiation exposure.

Thesis Overview

This research explores how artificial intelligence can automatically adjust radiation dose settings in digital radiography to achieve diagnostic image quality with the lowest reasonable exposure. The core idea is to replace or augment manual dose selection with intelligent systems that learn from patient characteristics, exam type, and prior image data to optimize safety and image clarity. Why it matters: Repeated or unnecessary high doses increase patient radiation exposure and cancer risk, while too low doses degrade image quality and can lead to misdiagnosis or repeat scans. An AI-driven solution has the potential to standardize dose levels across patients and sites, reduce variability among radiographers, and improve workflow efficiency without compromising diagnostic performance. Problem or knowledge gap: While dose optimization tools exist, they are often rule-based and inflexible, or they require extensive manual input. There is limited evidence on end-to-end AI systems that integrate image quality assessment, clinical workflow, and patient-specific factors to continuously adapt dose in real time. This study addresses the gap by developing and evaluating a data-driven framework that maps patient and exam features to optimal dose parameters. What the researcher will do (step by step): 1) Define target imaging tasks (e.g., chest and extremity radiographs) and establish acceptable diagnostic image quality criteria. 2) Collect a dataset from clinical partners including patient demographics, exam type, initial dose settings, acquired images, and radiologist quality assessments. 3) Develop an AI model (supervised learning) that predicts optimal dose parameters based on inputs such as body habitus, age, exam request, and preliminary image features. 4) Integrate a feedback loop where radiologist evaluations refine the model (active learning). 5) Validate the model with a held-out test set and compare against standard practice using metrics like dose per exam, image quality scores, and diagnostic accuracy. 6) Perform sensitivity analyses to understand robustness across scanner types and clinical sites. 7) Assess clinical workflow impact and feasibility through pilot testing in collaboration with radiology departments. 8) Conduct ethical and safety reviews, including patient privacy and data handling. Expected contribution: A validated AI-based dose optimization framework that can be deployed to improve patient safety by reducing unnecessary radiation while maintaining or enhancing diagnostic image quality, along with guidelines for integration into clinical workflows and recommendations for regulatory considerations. Anticipated outcome: Demonstrated reduction in average effective dose per exam with non-inferior or superior image quality and diagnostic confidence, enabling scalable implementation across radiology departments.

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