Deriving an actionable patient phenome from healthcare data
Lead Research Organisation:
University of Edinburgh
Abstract
Translating routinely collected health data into knowledge is a requirement of a "learning health system". Since joining the Biomedical Research Centre at the South London and Maudsley Hospital, Kings College London, my research has been focused on developing 'CogStack and SemEHR'. This is an integrated health informatics platform which aims to to unlock unstructured health records and assist in clinical decision making and research. The system does much to surface the deep data within the NHS, for example through providing a patient-centric search on semantically annotated clinical notes to support studies such as the recruitment of patients for Genomics England's 100,000 Genomes project [1,2] and predicting adverse drug reactions [3].
However, there is considerable further potential for the generation of knowledge and action, for example through the application of machine learning to the data from this platform. For instance, the data returned through these systems needs to be integrated, verified and cleaned with biomedical knowledge, enriched with an accurate clinical context (to enhance the current sentence-level language context) and aligned with the patient timeline to derive a comprehensive patient phenome. Clinical knowledge needs to be formalised from clinical ontologies and integrated with relevant open data, which will drive automated inferences to lift lower-level features (e.g. numeric blood pressure readings) up to higher-level clinical variables (e.g. hypertension) for supporting decision making.
A pilot study of the comprehensive phenome model, SemEHR's medical profiles [2], evaluated on publicly accessible data from the Medical Information Mart for Intensive Care (MIMIC), has proven that better contextual information can lead to much better accuracy in making clinical conclusions - e.g. using patient medical history for subtyping atrial fibrillation where we demonstrated that such phenome data is within the top 10 key features in identifying clinically-sensible patient clusters. For 'action' generation in clinical settings, we have demonstrated the feasibility of alerts through a number of simple examples using CogStack. For example, at Kings College Hospital, we have detected abnormal pathology results for 25 patients being prescribed methotrexate for rheumatoid arthritis, preventing potentially fatal renal failure.
The proposed research will devise a semantic electronic health record toolkit that is able to derive a consistent and comprehensive patient phenome from unstructured and structured electronic health records and provide semantic computation upon it to support decision making for tailored care, trial recruitment and research.
References:
1. Wu H, et al. SemEHR: surfacing semantic data from clinical notes in electronic health records for tailored care, trial recruitment, and clinical research. Lancet. 2017;390: S97.
2. Wu H, et al. A General-purpose Semantic Search System to Surface Semantic Data from Clinical Notes for Tailored Care, Trial Recruitment and Clinical Research. Journal of the American Medical Informatics Association. 2017; doi: https://doi.org/10.1101/235622.
3. Bean DM, Wu H, et al. Knowledge graph prediction of unknown adverse drug reactions and validation in electronic health records. Sci Rep. 2017;7: 16416.
However, there is considerable further potential for the generation of knowledge and action, for example through the application of machine learning to the data from this platform. For instance, the data returned through these systems needs to be integrated, verified and cleaned with biomedical knowledge, enriched with an accurate clinical context (to enhance the current sentence-level language context) and aligned with the patient timeline to derive a comprehensive patient phenome. Clinical knowledge needs to be formalised from clinical ontologies and integrated with relevant open data, which will drive automated inferences to lift lower-level features (e.g. numeric blood pressure readings) up to higher-level clinical variables (e.g. hypertension) for supporting decision making.
A pilot study of the comprehensive phenome model, SemEHR's medical profiles [2], evaluated on publicly accessible data from the Medical Information Mart for Intensive Care (MIMIC), has proven that better contextual information can lead to much better accuracy in making clinical conclusions - e.g. using patient medical history for subtyping atrial fibrillation where we demonstrated that such phenome data is within the top 10 key features in identifying clinically-sensible patient clusters. For 'action' generation in clinical settings, we have demonstrated the feasibility of alerts through a number of simple examples using CogStack. For example, at Kings College Hospital, we have detected abnormal pathology results for 25 patients being prescribed methotrexate for rheumatoid arthritis, preventing potentially fatal renal failure.
The proposed research will devise a semantic electronic health record toolkit that is able to derive a consistent and comprehensive patient phenome from unstructured and structured electronic health records and provide semantic computation upon it to support decision making for tailored care, trial recruitment and research.
References:
1. Wu H, et al. SemEHR: surfacing semantic data from clinical notes in electronic health records for tailored care, trial recruitment, and clinical research. Lancet. 2017;390: S97.
2. Wu H, et al. A General-purpose Semantic Search System to Surface Semantic Data from Clinical Notes for Tailored Care, Trial Recruitment and Clinical Research. Journal of the American Medical Informatics Association. 2017; doi: https://doi.org/10.1101/235622.
3. Bean DM, Wu H, et al. Knowledge graph prediction of unknown adverse drug reactions and validation in electronic health records. Sci Rep. 2017;7: 16416.
Technical Summary
For objective 1, at the data layer, my research will focus on a semantic phenome model that is able to detect/correct erroneous and inconsistent phenotypes, associate accurate contextual and temporal information with each phenotype mention and also support rule based reasoning to complete missing data. For objective 2, I will be devising and applying artificial intelligence models to derive unknown clinical knowledge from large scale, longitudinal and interlinked phenome data. potential use cases include predicting outcomes of septic shock treatments within intensive care units; predicting unknown adverse drug reactions in depression patients with comorbidities; subtyping atrial fibrillation to deliver tailored care. For objective 3, my research will provide actionable suggestions in clinical settings with applications of clinical trial recruitment and automated alerting for ensuring patient safety. Key challenges to be tackled here include how to make action suggestions explainable and reliable.
This project aims to deliver enabling technologies for The University of Edinburgh's HDR UK focus including deriving and applying health-related phenotypes at scale; computational tools for genetic and environmental risk prediction and causal inference. It will develop national leadership, partnerships, and interdisciplinary skills and capacity through the development of semantic computation infrastructure on top of deep and accurate patient phenome data, which if successful, can be disseminated to a wide range of healthcare service providers nationally/internationally and achieve high impact in research and patient care.
This project aims to deliver enabling technologies for The University of Edinburgh's HDR UK focus including deriving and applying health-related phenotypes at scale; computational tools for genetic and environmental risk prediction and causal inference. It will develop national leadership, partnerships, and interdisciplinary skills and capacity through the development of semantic computation infrastructure on top of deep and accurate patient phenome data, which if successful, can be disseminated to a wide range of healthcare service providers nationally/internationally and achieve high impact in research and patient care.
People |
ORCID iD |
Honghan Wu (Principal Investigator / Fellow) |
Publications

Whitfield E
(2021)
Axes of Prognosis: Identifying Subtypes of COVID-19 Outcomes.
in AMIA ... Annual Symposium proceedings. AMIA Symposium

Kuang X
(2020)
MRI-SegFlow: a novel unsupervised deep learning pipeline enabling accurate vertebral segmentation of MRI images.
in Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Dong H
(2021)
Rare Disease Identification from Clinical Notes with Ontologies and Weak Supervision.
in Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Davidson EM
(2021)
The reporting quality of natural language processing studies: systematic review of studies of radiology reports.
in BMC medical imaging

Casey A
(2021)
A systematic review of natural language processing applied to radiology reports.
in BMC medical informatics and decision making

Rannikmäe K
(2021)
Developing automated methods for disease subtyping in UK Biobank: an exemplar study on stroke.
in BMC medical informatics and decision making

Carr E
(2021)
Evaluation and improvement of the National Early Warning Score (NEWS2) for COVID-19: a multi-hospital study.
in BMC medicine

Wood A
(2021)
Linked electronic health records for research on a nationwide cohort of more than 54 million people in England: data resource.
in BMJ (Clinical research ed.)

Zhang H
(2021)
Benchmarking network-based gene prioritization methods for cerebral small vessel disease.
in Briefings in bioinformatics

Yuan Y
(2022)
Development and Validation of a Prognostic Risk Score System for COVID-19 Inpatients: A Multi-Center Retrospective Study in China.
in Engineering (Beijing, China)
Description | Findings from international COVID-19 collaborations informed SAGE during the pandemic |
Geographic Reach | National |
Policy Influence Type | Implementation circular/rapid advice/letter to e.g. Ministry of Health |
Impact | We developed a novel artificial intelligence method (ensemble learning) to synergise seven multinational prediction models to realise a robust and high-performing prediction model. This is the first work to use ensemble learning for risk prediction of COVID-19 and the validation cohorts are one of the most diverse international COVID-19 datasets (4 cohorts with mortality rates: 2.4-45%). The ensemble model consistently outperformed any single models in all aspects validated and can be used in clinical practice to inform the COVID-19 triage, treatments and resource allocations. |
URL | https://www.hdruk.ac.uk/wp-content/uploads/2020/09/200915-Health-Data-Research-UK-COVID-19-fortnight... |
Description | Invited talk at 1st International Symposium on Evidence-based Artificial Intelligence and Medicine (ISEAIM) |
Geographic Reach | Multiple continents/international |
Policy Influence Type | Influenced training of practitioners or researchers |
Impact | My talk was titled "Derive insights from health data using knowledge graph technologies". I started with a brief introduction about what is a knowledge graph. Then, I used real-world examples to introduce how knowledge graph technologies could help clinical natural language processing. I finalised the talk with a bit of my own thinking in challenges and future directions of knowledge graphs for health care. |
Description | Artificial Intelligence and Multimorbidity: Clustering in Individuals, Space and Clinical Context (AIM-CISC) |
Amount | £3,919,510 (GBP) |
Funding ID | NIHR202639 |
Organisation | National Institute for Health Research |
Sector | Public |
Country | United Kingdom |
Start | 07/2021 |
End | 08/2024 |
Description | ISCF HDRUK DIH Sprint Exemplar: Graph-Based Data Federation for Healthcare Data Science |
Amount | £260,057 (GBP) |
Funding ID | MC_PC_18029 |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 03/2019 |
End | 11/2019 |
Description | Improving the quality and value of care for people with poor prognosis cancers - a national, mixed methods study across Scotland |
Amount | £399,224 (GBP) |
Organisation | Health Foundation |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 03/2020 |
End | 08/2023 |
Description | Iris.AI - The AI Chemist |
Amount | £39,000 (GBP) |
Organisation | Research Council of Norway |
Sector | Public |
Country | Norway |
Start | 07/2021 |
End | 01/2022 |
Description | The Advanced Care Research Centre Programme |
Amount | £20,000,000 (GBP) |
Organisation | Legal and General Group |
Sector | Private |
Country | United Kingdom |
Start | 03/2020 |
End | 04/2026 |
Description | Towards an AI-driven Health Informatics Platform for supporting clinical decision making in Scotland - a pilot study in NHS Lothian |
Amount | £29,200 (GBP) |
Organisation | Wellcome Trust |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 01/2020 |
End | 02/2021 |
Description | UCL-NMU-SEU International Collaboration On Artificial Intelligence In Medicine: Tackling Challenges Of Low Generalisability And Health Inequality |
Amount | £29,400 (GBP) |
Organisation | British Council |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 02/2022 |
End | 02/2024 |
Description | Using rare disease phenotype models to identify people at risk of COVID-19 adverse outcomes |
Amount | £38,065 (GBP) |
Organisation | National Institute for Health Research |
Sector | Public |
Country | United Kingdom |
Start | 01/2023 |
End | 03/2023 |
Description | Use natural language processing for surfacing stroke phenotypes from Scottish radiology reports: a comparison of different methodologies |
Organisation | University of Edinburgh |
Department | School of Informatics Edinburgh |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | Investigate NLP model adaptation by reusing models trained on EHRs of London NHS trusts in Scottish radiology reports. |
Collaborator Contribution | Collaborators from Centre for Clinical Brain Sciences, University of Edinburgh provide ESS Stroke study data and Tayside radiology reports. They also manually labelled the data. Collaborators from Informatics Department provide computational resources for accessing data. They also provided their results on the same task by using rule based NLP and a neural network method. |
Impact | Named Entity Recognition for Electronic Health Records: A Comparison of Rule-based and Machine Learning Approaches. Philip John Gorinski, Honghan Wu, Claire Grover, Richard Tobin, Conn Talbot, Heather Whalley, Cathie Sudlow, William Whiteley, Beatrice Alex. Accepted by HealTAC 2019. This is a multi-disciplinary study involves neurology and computing science. |
Start Year | 2018 |
Title | Ensemble Learning for COVID-19 Risk Prediction |
Description | - implemented 7 prognosis risk prediction models for COVID-19. Detailed info in this paper: DOI:10.1093/jamia/ocaa295 - introduced a competence quantification framework for assessing the competence/confidence of a model in predicting a given data entry (i.e. a digital representation of a covid patient) - ensembled 7 prediction models for prediction using fusion strategies based on their competences - evaluated single models and the ensembled mode on two large COVID-19 cohorts from Wuhan, China (N=2,384) and King's College Hospital (N=1,475) |
Type Of Technology | Software |
Year Produced | 2020 |
Open Source License? | Yes |
Impact | - Ensemble model works the best on all aspects evaluated (PPV/Sensitivity/Calibration/Discrimination) - Findings from this study informed SAGE during the COVID-19 pandemic |
URL | https://github.com/Honghan/EnsemblePrediction |
Title | Knowledge Graph based Phenotyping on Heterogenous Data Sources |
Description | Extracting patient phenotypes from routinely collected health data (such as Electronic Health Records) requires translating clinically-sound phenotype definitions into queries/computations executable on the underlying data sources by clinical researchers. This requires significant knowledge and skills to deal with heterogeneous and often imperfect data. Translations are time-consuming, error-prone and, most importantly, hard to share and reproduce across different settings. This software implements a knowledge driven phenotyping framework that decouples the specification of phenotype semantics from underlying data sources; can automatically populate and conduct phenotype computations on heterogeneous data spaces. |
Type Of Technology | Software |
Year Produced | 2019 |
Open Source License? | Yes |
Impact | This software is used to federate 5 health datasets across Scotland for asking important clinical questions. It helps the initiation of a national integrated laboratory dataset across Scotland. |
Title | nlp2phenome: using AI models to infer patient phenotypes from identified named entities (instances of biomedical concepts) |
Description | Using natural language processing(NLP) to identify mentions of biomedical concepts from free text medical records is just the first step. There is often a gap between NLP results and what the clinical study is after. For example, a radiology report does not contain the term - ischemic stroke. Instead, it reports the patient had blocked arteries and stroke. To infer the "unspoken" ischemic stroke, a mechanism is needed to do such inferences from NLP identifiable mentions of blocked arteries and stroke. nlp2phenome is designed for doing this extra step from NLP to patient phenome. |
Type Of Technology | Software |
Year Produced | 2018 |
Open Source License? | Yes |
Impact | nlp2phenome was developed for a stroke subtyping study using NLP on radiology reports in Edinburgh University. It is based on top of SemEHR results. It identified 2,922 mentions of 32 types of phenotypes from 266 radiology reports and achieved an average F1: 0.929; Precision: 0.925; Recall: 0.939. |
URL | https://github.com/CogStack/nlp2phenome |
Description | Towards an AI-driven Health Informatics Platform for supporting clinical decision making in Scotland - a pilot study in NHS Lothian |
Form Of Engagement Activity | A formal working group, expert panel or dialogue |
Part Of Official Scheme? | No |
Geographic Reach | Regional |
Primary Audience | Professional Practitioners |
Results and Impact | This is a pilot study with NHS Lothian (Edinburgh), which is supported by Wellcome Trust iTPA award. The long term objective is to enhance Electronic Health Records (EHRs) across NHS Lothian Health Board using artificial intelligence (AI) driven data science infrastructure to benefit patients and the health service provision. This project will serve as a pilot study for the larger Data Loch City Deal collaboration, which aims to use all of our health and social care data assets to drive research and innovation, improve patient care and reduce health inequalities for all patients. This particular pilot project will develop two exemplar use cases in NHS Lothian: (a) improving the management of hypoglycaemia; and (b) decision support in prescribing anticoagulants to patients with Atrial Fibrillation. These pilot studies will (1) initialise collaborations with NHS Lothian eHealth team; (2) understand the data landscape (data formats, storage, data schema, access control restrictions); (3) investigate integration approaches with TrakCare - the EHR information system. |
Year(s) Of Engagement Activity | 2019,2020 |