Better answers, shakier reasoning in small medical AI
Small medical AI models trained to copy a larger model's reasoning get more answers right, but the steps they write out along the way contain more mistakes.
One short story for each paper we publish. No jargon, written for anyone curious about health and AI.
Small medical AI models trained to copy a larger model's reasoning get more answers right, but the steps they write out along the way contain more mistakes.
Our invited commentary argues for catching at-risk babies early enough to prevent injury, by combining several kinds of data.
Combining a language model with an ontology-based ranking tool improves rare-disease diagnosis while keeping the evidence trail.
A diagnostic tool needs to know when to commit to its top guess and when to pass the case to a person, and for rare diseases that is hard to get right.
A fancier memory for AI seemed to beat a simple one, but most of the gain came from how the information was laid out, not from how the memory works.
We built a hand-annotated collection of discharge summaries so that language models can learn to find geriatric syndromes in them.
We describe how a huge set of Scottish head scans was prepared, linked to health records and made available for AI research.
OLIVE is a UK study plan to learn what predicts, and what follows, lung cancer in people who have never smoked, using routine health records and language technology.
A theory for choosing how clever the decision-maker in front of an AI model needs to be, based on how much data you have to set it up.
BioMedArena is an open toolkit that makes it easy to build biomedical AI research agents and compare them fairly on the same footing.
We tested a machine learning model for predicting type 2 diabetes on 3,081 people with prediabetes, and checked whether it could guide who benefits most from treatment.
LoV3D reads a patient’s brain MRI scans over time, measures regions step by step, and only then gives a diagnosis, which cuts down on made-up conclusions.
We reviewed how language technology has been used to find geriatric syndromes in the free text of health records, and what is still hard.
RareArena is a large test built from real case reports, designed to show how well AI language models can spot rare diseases.
Studies of AI language models in radiology are often reported in ways that make them hard to repeat or compare, so an international panel built a checklist.
A three-stage method that detects, locates and corrects mistakes in radiology reports, using medical knowledge to help language models do it.
Of 62.5 million people in England, 1.7% had one of 406 rare diseases, and they had more recorded COVID-19 infection (32.8% vs 29.0%).
A review of 262 trials in ten rare diseases shows digital tools increasingly used for remote monitoring, treatment and long-term care.
A perspective from many authors arguing that multimodal AI should be designed around real-world deployment constraints from the start, and reaching beyond images and text.
HARE is a way to score generated histopathology reports by checking the key findings and how they relate, which matches pathologists better than standard metrics.
K-Tokeniser builds medical concepts such as drugs and diseases into the way a language model reads text, so it needs less training data.
Turning a radiologist's eye movements into a short video helped general-purpose vision-language models write better chest X-ray reports and diagnoses, in one case beating specialist medical models.
A hand-labelled collection of discharge summaries from older patients, covering 14 adverse events such as falls and delirium, shows where language models still struggle.
Giving a multimodal model the places radiologists look and the regions they mark improves the reports it writes, without retraining it.
BioHopR tests whether AI models can chain several facts together to answer biomedical questions with more than one correct answer.
Larger language models wrote more complete synthetic health records, but also showed stronger gender and racial bias.
Generative latent replay plus attention-based regularisation reduced catastrophic forgetting in a histology image task without storing past examples.
A transformer-based model estimated what would have happened under different blood pressure treatments, using data from over 300,000 patients.
Interviews with 16 radiologists show that checking AI tools in practice is mostly manual, slow and unsupported by clear guidelines.
IHC-LLMiner uses a language model to find and extract tumour staining profiles from PubMed abstracts, faster and more accurately than GPT-4o on this task.
Eight rare diseases carried a clearly higher risk of dying from COVID-19, even after vaccination, in a study covering 331 rare diseases and 58 million people.
A deep learning model that reads both the structured and the free-text parts of regional health records to predict who with type 2 diabetes will develop depression or anxiety.
CliniCoCo, a human-AI coding system, cut coding time by 40% and let professional coders reach an F1 score above 0.93.
Combining dictionary-based language processing with large language models identified rare diseases better than either alone, and found patients missing from structured records.
Eye-fixation prompts improved a multimodal model for chest X-ray diagnosis, and fine-tuning with only 658 reports beat a model trained on 17,000.
In a study of 451,291 people, those with several long-term conditions were far more likely to die within 30 days, and the link was stronger in people under 65.
Continued pretraining on chemistry text made a small language model far better at describing molecules, even though it never saw molecule notation in that stage.
A three-stage method that detects, locates and corrects errors in radiology reports using internal and external knowledge retrieval.
Our entry to the MEDIQA-CORR 2024 shared task used step-by-step prompts to detect and correct medical errors, and placed in the top three for two of the three tasks.
MedExQA is a medical question benchmark with several reference explanations per answer, plus a small open model, MedPhi-2.
RadBARTsum retrains a language model with medical-entity masking so it learns radiology knowledge, which improves summaries of radiology reports.
A survey that breaks automated medical coding models into four building blocks so the field can be understood and compared.
Overlaying a radiologist’s eye-gaze heatmap on the X-ray improved the accuracy of vision-language models across several chest X-ray tasks.
Between 2004 and 2021 in Scotland, antidepressant prescribing in people with type 2 diabetes rose from 20.0 to 33.3 per 100 person-years.
A scoping review of 36 studies found promise for predicting fetal hypoxia from cardiotocography, but weak benchmarks and small, repeated datasets.
A systematic review of deep learning studies that predict outcomes using sequences of diagnosis codes, and how well they generalise and explain themselves.
We built a benchmark of medical images with question-answer sets to test how often AI models hallucinate, and which prompting strategies help.
We tested multimodal language models on spotting errors in chest X-ray reports by checking them against the radiograph.
For building a biomedical ontology, we compared in-context learning, fine-tuning and supervised learning on more than 1.8 million facts.
We pre-trained a model on good-quality hospital records and fine-tuned it on primary care data, which predicted post-discharge depression and anxiety much better than baselines.
TBLAT borrows ideas from BLAST, the tool for searching DNA sequences, to match misspelt and abbreviated clinical terms to the right concepts.
FLAP links free-text addresses to the UK's official property database with 99.2% adjusted accuracy and is released as open-source software.
Comparing four off-the-shelf tools on brain radiology reports showed that performance varies widely, so tools need checking and adapting before clinical use.
RMCA U-net is a neural network that outlines hard exudates in retinal photos more accurately than standard networks.
Our entry to a BioNLP shared task compared generative language models on summarising radiology reports and used a two-stage fine-tuning approach.
By combining language technology with a disease ontology, we identified rare disease mentions in health records with over 90% accuracy, with no human annotation of the training data.
A systematic review of explainable AI for predicting comorbidity from health records, and what it offers clinicians.
A systematic review found little and mixed evidence on how these medicines relate to diabetes outcomes, so general diabetes guidance should apply for now.
An ontology-guided, self-supervised method for spotting adverse childhood experiences in social media posts, producing a public resource for further research.
Eleven intensive care consultants labelled the same patients differently, and the usual way of settling disagreements, a majority vote, gave worse AI models.
We mapped the UK landscape of clinical natural language processing by starting from the funded projects, and set out who is involved, what they build, and what holds the field back.
A perspective on why coding clinical records is hard to automate, covering seven challenges and why knowledge-based methods should be combined with deep learning.
A systematic review found promising AI performance, but only one of the reviewed models had been externally validated and reporting quality was low.
A five-year cardiovascular risk model built from routine Nanjing hospital data held up in a Scottish population (C-statistic 0.716 externally).
Spine-GFlow segments vertebrae, discs and the spinal canal in lumbar MRI without any manual annotation, matching a fully supervised model (Dice 0.914 vs 0.916).
Linking eight national NHS datasets, we defined ten COVID-19 stages and mapped how patients moved between them in the first two waves.
A generic framework quantifies inequality in data and AI models as the area between two curves, and found significant inequalities in real intensive care data and models.
Models built from a widely used liver disease dataset had a higher false-negative rate for women, which would mean more missed diagnoses.
In 283 Genomics England participants, rare disease was linked to higher COVID-19 death, especially neurological and neurodevelopmental conditions, though numbers were small.
In nearly 14,000 people with severe mental illness, over 60% had several physical conditions, and each type of comorbidity was linked to higher disability.
Of 164 studies, few shared data or code or tested their work externally, so we called for reporting standards specific to clinical NLP.
How knowledge graph technologies help computers read free-text health records, told through real examples from an invited talk.
Much of what hospitals record is free text. Here is why it is worth reading for research and patient care.
A quick, jargon-light introduction to knowledge graphs and why they matter for health data science.
A two-part model learns what the first 24 hours of a patient looks like before a bad outcome and predicts mortality and ICU admission with PR-AUCs around 0.9.
Two clustering methods using axes of prognosis revealed distinct subgroups of poor outcome, especially among respiratory patients, and predicted membership on admission.
Combining language processing with clinical rules on brain scan reports identified bleeding strokes in UK Biobank with high accuracy, improving on coded data alone.
A systematic review of 164 studies shows rapid growth in NLP for radiology reports, but little sharing of data or code and little evidence of real clinical use.
HLAN highlights the words and sentences behind each code an AI assigns to a discharge summary, and a label-embedding trick made most coding models more accurate.
We benchmarked seven network-based gene-ranking methods for cerebral small vessel disease and found one clearly best overall, with an important limit on discovering truly new genes.
An ensemble that picks the most competent models for each patient beat every individual model across four cohorts in the UK and China.
The NEWS2 score was a weak predictor of severe COVID-19, but adding age and a few routine blood tests improved it across hospitals in the UK, Norway and China.
Hospital activity for cardiovascular disease fell by 60 to 100% during the pandemic, and we estimated tens of thousands of excess deaths in England, direct and indirect.
A simple model using age, sex and routine blood tests worked well in Wuhan but less well in London, where patients were far sicker, showing why external validation matters.
A framework that spots rare, meaningful interactions between patient measurements in intensive care and uses them to predict outcomes such as sepsis, while explaining why.
Grouping ICU patients by their pattern of organ dysfunction improved sepsis prediction across three machine-learning models, especially in specificity.
A knowledge-driven framework turns a clinical definition of a phenotype into queries that run automatically on different data sources, tested on five Scottish health datasets.
Two thirds of 9,775 people with schizophrenia-spectrum disorders had several physical conditions, and some combinations roughly doubled the risk of death.
An open-source language-processing pipeline calculated stroke and bleeding risk scores from 10,030 discharge summaries and showed rising anticoagulant use over seven years.
A phenotype-embedding approach shows where an existing model will work on new records and where it won't, saving around 80% of the effort of blind adaptation.
On Scottish stroke imaging reports, a hand-crafted system was the most accurate, but machine learning was a feasible alternative when no one has time to write rules.
CogStack, an open-source system deployed at King's College Hospital, has processed over 300 million lines of clinical data and is the only open-source, easily deployable option built for the UK.
SemEHR is an open-source tool that finds what clinical notes say about patients, cutting recruitment-criteria checking from days to minutes.
A knowledge-graph method predicted unknown adverse drug reactions (AUC 0.92 on known ones), and high-confidence predictions were checked against real hospital records.
NapEasy automatically highlights the sentences a curator needs in Parkinson's and Alzheimer's papers; in about 65% of cases the highlights were enough without reading the full text.
ADEPt, a rule-based pipeline built with clinicians and pharmacists, found 19 side effects of antipsychotics and antidepressants in free-text records, with an average F-measure of 0.83.
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