PadChest: A large chest x-ray image dataset with multi-label annotated reports

We present a labeled large-scale, high resolution chest x-ray dataset for the automated exploration of medical images along with their associated reports. This dataset includes more than 160,000 images obtained from 67,000 patients that were interpreted and reported by radiologists at Hospital San Juan Hospital (Spain) from 2009 to 2017, covering six different position views and additional information on image acquisition and patient demography. The reports were labeled with 174 different radiographic findings, 19 differential diagnoses and 104 anatomic locations organized as a hierarchical taxonomy and mapped onto standard Unified Medical Language System (UMLS) terminology. Of these reports, 27% were manually annotated by trained physicians and the remaining set was labeled using a supervised method based on a recurrent neural network with attention mechanisms. The labels generated were then validated in an independent test set achieving a 0.93 Micro-F1 score. To the best of our knowledge, this is one of the largest public chest x-ray database suitable for training supervised models concerning radiographs, and the first to contain radiographic reports in Spanish. The PadChest dataset can be downloaded from http://bimcv.cipf.es/bimcv-projects/padchest/

Answering clinical questions with knowledge-based and statistical techniques

The combination of recent developments in question-answering research and the availability of unparalleled resources developed specifically for automatic semantic processing of text in the medical domain provides a unique opportunity to explore complex question answering in the domain of clinical medicine. This article presents a system designed to satisfy the information needs of physicians practicing evidence-based medicine. We have developed a series of knowledge extractors, which employ a combination of knowledge-based and statistical techniques, for automatically identifying clinically relevant aspects of MEDLINE abstracts. These extracted elements serve as the input to an algorithm that scores the relevance of citations with respect to structured representations of information needs, in accordance with the principles of evidencebased medicine. Starting with an initial list of citations retrieved by PubMed, our system can bring relevant abstracts into higher ranking positions, and from these abstracts generate responses that directly answer physicians ’ questions. We describe three separate evaluations: one focused on the accuracy of the knowledge extractors, one conceptualized as a document reranking task, and finally, an evaluation of answers by two physicians. Experiments on a collection of real-world clinical questions show that our approach significantly outperforms the already competitive PubMed baseline. 1

Three Essays on Enhancing Clinical Trial Subject Recruitment Using Natural Language Processing and Text Mining

Patient recruitment and enrollment are critical factors for a successful clinical trial; however, recruitment tends to be the most common problem in most clinical trials. The success of a clinical trial depends on efficiently recruiting suitable patients to conduct the trial. Every clinical trial research has a protocol, which describes what will be done in the study and how it will be conducted. Also, the protocol ensures the safety of the trial subjects and the integrity of the data collected. The eligibility criteria section of clinical trial protocols is important because it specifies the necessary conditions that participants have to satisfy. Since clinical trial eligibility criteria are usually written in free text form, they are not computer interpretable. To automate the analysis of the eligibility criteria, it is therefore necessary to transform those criteria into a computer-interpretable format. Unstructured format of eligibility criteria additionally create search efficiency issues. Thus, searching and selecting appropriate clinical trials for a patient from relatively large number of available trials is a complex task. A few attempts have been made to automate the matching process between patients and clinical trials. However, those attempts have not fully integrated the entire matching process and have not exploited the state-of-the-art Natural Language Processing (NLP) techniques that may improve the matching performance. Given the importance of patient recruitment in clinical trial research, the objective of this research is to automate the matching process using NLP and text mining techniques and, thereby, improve the efficiency and effectiveness of the recruitment process. This dissertation research, which comprises three essays, investigates the issues of clinical trial subject recruitment using state-of-the-art NLP and text mining techniques. Essay 1: Building a Domain-Specific Lexicon for Clinical Trial Subject Eligibility Analysis Essay 2: Clustering Clinical Trials Using Semantic-Based Feature Expansion Essay 3: An Automatic Matching Process of Clinical Trial Subject Recruitment In essay1, I develop a domain-specific lexicon for n-gram Named Entity Recognition (NER) in the breast cancer domain. The domain-specific dictionary is used for selection and reduction of n-gram features in clustering in eassy2. The domain-specific dictionary was evaluated by comparing it with Systematized Nomenclature of Medicine--Clinical Terms (SNOMED CT). The results showed that it add significant number of new terms which is very useful in effective natural language processing In essay 2, I explore the clustering of similar clinical trials using the domain-specific lexicon and term expansion using synonym from the Unified Medical Language System (UMLS). I generate word n-gram features and modify the features with the domain-specific dictionary matching process. In order to resolve semantic ambiguity, a semantic-based feature expansion technique using UMLS is applied. A hierarchical agglomerative clustering algorithm is used to generate clinical trial clusters. The focus is on summarization of clinical trial information in order to enhance trial search efficiency. Finally, in essay 3, I investigate an automatic matching process of clinical trial clusters and patient medical records. The patient records collected from a prior study were used to test our approach. The patient records were pre-processed by tokenization and lemmatization. The pre-processed patient information were then further enhanced by matching with breast cancer custom dictionary described in essay 1 and semantic feature expansion using UMLS Metathesaurus. Finally, I matched the patient record with clinical trial clusters to select the best matched cluster(s) and then with trials within the clusters. The matching results were evaluated by internal expert as well as external medical expert

딥 뉴럴 네트워크를 활용한 의학 개념 및 환자 표현 학습과 의료 문제에의 응용

학위논문(박사) -- 서울대학교대학원 : 공과대학 전기·정보공학부, 2022. 8. 정교민.본 학위 논문은 전국민 의료 보험데이터인 표본코호트DB를 활용하여 딥 뉴럴 네트워크 기반의 의학 개념 및 환자 표현 학습 방법과 의료 문제 해결 방법을 제안한다. 먼저 순차적인 환자 의료 기록과 개인 프로파일 정보를 기반으로 환자 표현을 학습하고 향후 질병 진단 가능성을 예측하는 재귀신경망 모델을 제안하였다. 우리는 다양한 성격의 환자 정보를 효율적으로 혼합하는 구조를 도입하여 큰 성능 향상을 얻었다. 또한 환자의 의료 기록을 이루는 의료 코드들을 분산 표현으로 나타내 추가 성능 개선을 이루었다. 이를 통해 의료 코드의 분산 표현이 중요한 시간적 정보를 담고 있음을 확인하였고, 이어지는 연구에서는 이러한 시간적 정보가 강화될 수 있도록 그래프 구조를 도입하였다. 우리는 의료 코드의 분산 표현 간의 유사도와 통계적 정보를 가지고 그래프를 구축하였고 그래프 뉴럴 네트워크를 활용, 시간/통계적 정보가 강화된 의료 코드의 표현 벡터를 얻었다. 획득한 의료 코드 벡터를 통해 시판 약물의 잠재적인 부작용 신호를 탐지하는 모델을 제안한 결과, 기존의 부작용 데이터베이스에 존재하지 않는 사례까지도 예측할 수 있음을 보였다. 마지막으로 분량에 비해 주요 정보가 희소하다는 의료 기록의 한계를 극복하기 위해 지식그래프를 활용하여 사전 의학 지식을 보강하였다. 이때 환자의 의료 기록을 구성하는 지식그래프의 부분만을 추출하여 개인화된 지식그래프를 만들고 그래프 뉴럴 네트워크를 통해 그래프의 표현 벡터를 획득하였다. 최종적으로 순차적인 의료 기록을 함축한 환자 표현과 더불어 개인화된 의학 지식을 함축한 표현을 함께 사용하여 향후 질병 및 진단 예측 문제에 활용하였다.This dissertation proposes a deep neural network-based medical concept and patient representation learning methods using medical claims data to solve two healthcare tasks, i.e., clinical outcome prediction and post-marketing adverse drug reaction (ADR) signal detection. First, we propose SAF-RNN, a Recurrent Neural Network (RNN)-based model that learns a deep patient representation based on the clinical sequences and patient characteristics. Our proposed model fuses different types of patient records using feature-based gating and self-attention. We demonstrate that high-level associations between two heterogeneous records are effectively extracted by our model, thus achieving state-of-the-art performances for predicting the risk probability of cardiovascular disease. Secondly, based on the observation that the distributed medical code embeddings represent temporal proximity between the medical codes, we introduce a graph structure to enhance the code embeddings with such temporal information. We construct a graph using the distributed code embeddings and the statistical information from the claims data. We then propose the Graph Neural Network(GNN)-based representation learning for post-marketing ADR detection. Our model shows competitive performances and provides valid ADR candidates. Finally, rather than using patient records alone, we utilize a knowledge graph to augment the patient representation with prior medical knowledge. Using SAF-RNN and GNN, the deep patient representation is learned from the clinical sequences and the personalized medical knowledge. It is then used to predict clinical outcomes, i.e., next diagnosis prediction and CVD risk prediction, resulting in state-of-the-art performances.1 Introduction 1 2 Background 8 2.1 Medical Concept Embedding 8 2.2 Encoding Sequential Information in Clinical Records 11 3 Deep Patient Representation with Heterogeneous Information 14 3.1 Related Work 16 3.2 Problem Statement 19 3.3 Method 20 3.3.1 RNN-based Disease Prediction Model 20 3.3.2 Self-Attentive Fusion (SAF) Encoder 23 3.4 Dataset and Experimental Setup 24 3.4.1 Dataset 24 3.4.2 Experimental Design 26 ii 3.4.3 Implementation Details 27 3.5 Experimental Results 28 3.5.1 Evaluation of CVD Prediction 28 3.5.2 Sensitivity Analysis 28 3.5.3 Ablation Studies 31 3.6 Further Investigation 32 3.6.1 Case Study: Patient-Centered Analysis 32 3.6.2 Data-Driven CVD Risk Factors 32 3.7 Conclusion 33 4 Graph-Enhanced Medical Concept Embedding 40 4.1 Related Work 42 4.2 Problem Statement 43 4.3 Method 44 4.3.1 Code Embedding Learning with Skip-gram Model 44 4.3.2 Drug-disease Graph Construction 45 4.3.3 A GNN-based Method for Learning Graph Structure 47 4.4 Dataset and Experimental Setup 49 4.4.1 Dataset 49 4.4.2 Experimental Design 50 4.4.3 Implementation Details 52 4.5 Experimental Results 53 4.5.1 Evaluation of ADR Detection 53 4.5.2 Newly-Described ADR Candidates 54 4.6 Conclusion 55 5 Knowledge-Augmented Deep Patient Representation 57 5.1 Related Work 60 5.1.1 Incorporating Prior Medical Knowledge for Clinical Outcome Prediction 60 5.1.2 Inductive KGC based on Subgraph Learning 61 5.2 Method 61 5.2.1 Extracting Personalized KG 61 5.2.2 KA-SAF: Knowledge-Augmented Self-Attentive Fusion Encoder 64 5.2.3 KGC as a Pre-training Task 68 5.2.4 Subgraph Infomax: SGI 69 5.3 Dataset and Experimental Setup 72 5.3.1 Clinical Outcome Prediction 72 5.3.2 Next Diagnosis Prediction 72 5.4 Experimental Results 73 5.4.1 Cardiovascular Disease Prediction 73 5.4.2 Next Diagnosis Prediction 73 5.4.3 KGC on SemMed KG 73 5.5 Conclusion 74 6 Conclusion 77 Abstract (In Korean) 90 Acknowlegement 92박

Measuring diversity in medical reports based on categorized attributes and international classification systems

<p>Abstract</p> <p>Background</p> <p>Narrative medical reports do not use standardized terminology and often bring insufficient information for statistical processing and medical decision making. Objectives of the paper are to propose a method for measuring diversity in medical reports written in any language, to compare diversities in narrative and structured medical reports and to map attributes and terms to selected classification systems.</p> <p>Methods</p> <p>A new method based on a general concept of f-diversity is proposed for measuring diversity of medical reports in any language. The method is based on categorized attributes recorded in narrative or structured medical reports and on international classification systems. Values of categories are expressed by terms. Using SNOMED CT and ICD 10 we are mapping attributes and terms to predefined codes. We use f-diversities of Gini-Simpson and Number of Categories types to compare diversities of narrative and structured medical reports. The comparison is based on attributes selected from the Minimal Data Model for Cardiology (MDMC).</p> <p>Results</p> <p>We compared diversities of 110 Czech narrative medical reports and 1119 Czech structured medical reports. Selected categorized attributes of MDMC had mostly different numbers of categories and used different terms in narrative and structured reports. We found more than 60% of MDMC attributes in SNOMED CT. We showed that attributes in narrative medical reports had greater diversity than the same attributes in structured medical reports. Further, we replaced each value of category (term) used for attributes in narrative medical reports by the closest term and the category used in MDMC for structured medical reports. We found that relative Gini-Simpson diversities in structured medical reports were significantly smaller than those in narrative medical reports except the "Allergy" attribute.</p> <p>Conclusions</p> <p>Terminology in narrative medical reports is not standardized. Therefore it is nearly impossible to map values of attributes (terms) to codes of known classification systems. A high diversity in narrative medical reports terminology leads to more difficult computer processing than in structured medical reports and some information may be lost during this process. Setting a standardized terminology would help healthcare providers to have complete and easily accessible information about patients that would result in better healthcare.</p

Clinical Natural Language Processing in languages other than English: opportunities and challenges

Background: Natural language processing applied to clinical text or aimed at a clinical outcome has been thriving in recent years. This paper offers the first broad overview of clinical Natural Language Processing (NLP) for languages other than English. Recent studies are summarized to offer insights and outline opportunities in this area. Main Body We envision three groups of intended readers: (1) NLP researchers leveraging experience gained in other languages, (2) NLP researchers faced with establishing clinical text processing in a language other than English, and (3) clinical informatics researchers and practitioners looking for resources in their languages in order to apply NLP techniques and tools to clinical practice and/or investigation. We review work in clinical NLP in languages other than English. We classify these studies into three groups: (i) studies describing the development of new NLP systems or components de novo, (ii) studies describing the adaptation of NLP architectures developed for English to another language, and (iii) studies focusing on a particular clinical application. Conclusion: We show the advantages and drawbacks of each method, and highlight the appropriate application context. Finally, we identify major challenges and opportunities that will affect the impact of NLP on clinical practice and public health studies in a context that encompasses English as well as other languages

Adverse Drug Event Detection, Causality Inference, Patient Communication and Translational Research

Adverse drug events (ADEs) are injuries resulting from a medical intervention related to a drug. ADEs are responsible for nearly 20% of all the adverse events that occur in hospitalized patients. ADEs have been shown to increase the cost of health care and the length of stays in hospital. Therefore, detecting and preventing ADEs for pharmacovigilance is an important task that can improve the quality of health care and reduce the cost in a hospital setting. In this dissertation, we focus on the development of ADEtector, a system that identifies ADEs and medication information from electronic medical records and the FDA Adverse Event Reporting System reports. The ADEtector system employs novel natural language processing approaches for ADE detection and provides a user interface to display ADE information. The ADEtector employs machine learning techniques to automatically processes the narrative text and identify the adverse event (AE) and medication entities that appear in that narrative text. The system will analyze the entities recognized to infer the causal relation that exists between AEs and medications by automating the elements of Naranjo score using knowledge and rule based approaches. The Naranjo Adverse Drug Reaction Probability Scale is a validated tool for finding the causality of a drug induced adverse event or ADE. The scale calculates the likelihood of an adverse event related to drugs based on a list of weighted questions. The ADEtector also presents the user with evidence for ADEs by extracting figures that contain ADE related information from biomedical literature. A brief summary is generated for each of the figures that are extracted to help users better comprehend the figure. This will further enhance the user experience in understanding the ADE information better. The ADEtector also helps patients better understand the narrative text by recognizing complex medical jargon and abbreviations that appear in the text and providing definitions and explanations for them from external knowledge resources. This system could help clinicians and researchers in discovering novel ADEs and drug relations and also hypothesize new research questions within the ADE domain

Enhancing the interactivity of a clinical decision support system by using knowledge engineering and natural language processing

Mental illness is a serious health problem and it affects many people. Increasingly,Clinical Decision Support Systems (CDSS) are being used for diagnosis and it is important to improve the reliability and performance of these systems. Missing a potential clue or a wrong diagnosis can have a detrimental effect on the patient's quality of life and could lead to a fatal outcome. The context of this research is the Galatean Risk and Safety Tool (GRiST), a mental-health-risk assessment system. Previous research has shown that success of a CDSS depends on its ease of use, reliability and interactivity. This research addresses these concerns for the GRiST by deploying data mining techniques. Clinical narratives and numerical data have both been analysed for this purpose.Clinical narratives have been processed by natural language processing (NLP)technology to extract knowledge from them. SNOMED-CT was used as a reference ontology and the performance of the different extraction algorithms have been compared. A new Ensemble Concept Mining (ECM) method has been proposed, which may eliminate the need for domain specific phrase annotation requirements. Word embedding has been used to filter phrases semantically and to build a semantic representation of each of the GRiST ontology nodes.The Chi-square and FP-growth methods have been used to find relationships between GRiST ontology nodes. Interesting patterns have been found that could be used to provide real-time feedback to clinicians. Information gain has been used efficaciously to explain the differences between the clinicians and the consensus risk. A new risk management strategy has been explored by analysing repeat assessments. A few novel methods have been proposed to perform automatic background analysis of the patient data and improve the interactivity and reliability of GRiST and similar systems

Contributions to information extraction for spanish written biomedical text

285 p.Healthcare practice and clinical research produce vast amounts of digitised, unstructured data in multiple languages that are currently underexploited, despite their potential applications in improving healthcare experiences, supporting trainee education, or enabling biomedical research, for example. To automatically transform those contents into relevant, structured information, advanced Natural Language Processing (NLP) mechanisms are required. In NLP, this task is known as Information Extraction. Our work takes place within this growing field of clinical NLP for the Spanish language, as we tackle three distinct problems. First, we compare several supervised machine learning approaches to the problem of sensitive data detection and classification. Specifically, we study the different approaches and their transferability in two corpora, one synthetic and the other authentic. Second, we present and evaluate UMLSmapper, a knowledge-intensive system for biomedical term identification based on the UMLS Metathesaurus. This system recognises and codifies terms without relying on annotated data nor external Named Entity Recognition tools. Although technically naive, it performs on par with more evolved systems, and does not exhibit a considerable deviation from other approaches that rely on oracle terms. Finally, we present and exploit a new corpus of real health records manually annotated with negation and uncertainty information: NUBes. This corpus is the basis for two sets of experiments, one on cue andscope detection, and the other on assertion classification. Throughout the thesis, we apply and compare techniques of varying levels of sophistication and novelty, which reflects the rapid advancement of the field

COMPLEX QUESTION ANSWERING BASED ON A SEMANTIC DOMAIN MODEL OF CLINICAL MEDICINE

Much research in recent years has focused on question answering. Due to significant advances in answering simple fact-seeking questions, research is moving towards resolving complex questions. An approach adopted by many researchers is to decompose a complex question into a series of fact-seeking questions and reuse techniques developed for answering simple questions. This thesis presents an alternative novel approach to domain-specific complex question answering based on consistently applying a semantic domain model to question and document understanding as well as to answer extraction and generation. This study uses a semantic domain model of clinical medicine to encode (a) a clinician's information need expressed as a question on the one hand and (b) the meaning of scientific publications on the other to yield a common representation. It is hypothesized that this approach will work well for (1) finding documents that contain answers to clinical questions and (2) extracting these answers from the documents. The domain of clinical question answering was selected primarily because of its unparalleled resources that permit providing a proof by construction for this hypothesis. In addition, a working prototype of a clinical question answering system will support research in informed clinical decision making. The proposed methodology is based on the semantic domain model developed within the paradigm of Evidence Based Medicine. Three basic components of this model - the clinical task, a framework for capturing a synopsis of a clinical scenario that generated the question, and strength of evidence presented in an answer - are identified and discussed in detail. Algorithms and methods were developed that combine knowledge-based and statistical techniques to extract the basic components of the domain model from abstracts of biomedical articles. These algorithms serve as a foundation for the prototype end-to-end clinical question answering system that was built and evaluated to test the hypotheses. Evaluation of the system on test collections developed in the course of this work and based on real life clinical questions demonstrates feasibility of complex question answering and high accuracy information retrieval using a semantic domain model