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Areas of interest

Where rigorous evidence meets machine learning.

Medevi is an academic research group building open tools for medicine. Our work sits where clinical science and machine learning meet, and it is organized around four areas.

Context

Six decades of AI in medicine.

Medicine has reasoned with computers since the 1950s and synthesized evidence systematically since the 1970s. Our work builds on both histories.

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Sources for the timeline Show
  1. 1959Ledley RS, Lusted LB. Science 1959;130(3366):9–21
  2. 1966Weizenbaum J. Commun ACM 1966;9(1):36–45
  3. 1972Cochrane AL. Effectiveness and Efficiency. Nuffield Provincial Hospitals Trust, 1972
  4. 1976Shortliffe EH. Computer-Based Medical Consultations: MYCIN. Elsevier, 1976
  5. 1976Glass GV. Educational Researcher 1976;5(10):3–8
  6. 1982Miller RA, Pople HE, Myers JD. N Engl J Med 1982;307(8):468–76
  7. 1992Evidence-Based Medicine Working Group. JAMA 1992;268(17):2420–5
  8. 1993Cochrane, founded 1993
  9. 1998US FDA premarket approval, ImageChecker (R2 Technology), 1998
  10. 2004GRADE Working Group. BMJ 2004;328:1490
  11. 2009Moher D et al. BMJ 2009;339:b2535
  12. 2012Krizhevsky A, Sutskever I, Hinton GE. NeurIPS 2012
  13. 2015Hinton G, Vinyals O, Dean J. arXiv:1503.02531, 2015
  14. 2016Gulshan V et al. JAMA 2016;316(22):2402–10
  15. 2017Vaswani A et al. NeurIPS 2017
  16. 2018Abràmoff MD et al. npj Digit Med 2018;1:39
  17. 2019Obermeyer Z et al. Science 2019;366(6464):447–53
  18. 2021Wong A et al. JAMA Intern Med 2021;181(8):1065–70
  19. 2021Hu EJ et al. arXiv:2106.09685, 2021
  20. 2022OpenAI, November 2022
  21. 2023Singhal K et al. Nature 2023;620:172–80
  22. 2024Collins GS et al. BMJ 2024;385:e078378

01 · Area of interest

Evidence synthesis

We are dedicated to accelerating the pace of rigorous evidence synthesis, and envision a future where clinicians always have the latest evidence at their fingertips for decision-making.

67 weeks
Mean time to complete and publish a systematic review registered in PROSPERO.
Borah R et al. BMJ Open 2017;7:e012545
23%
Of systematic reviews showed a signal that they needed updating within two years.
Shojania KG et al. Ann Intern Med 2007;147(4):224–33
Living meta-analysis · illustrative dataRisk ratio, fixed effect
Trial A2011Trial B2013Trial C2014Trial D2016Trial E2017Trial F2019Trial G2020Trial H2022Trial I2023Trial J2025Pooled3 trials0.250.512
RR 0.8195% CI 0.58–1.14

Drag the slider or press Play. Each new trial narrows the pooled estimate. A living review would update the moment a trial is published, not years later.

02 · Area of interest

Clinical decision support systems

Validated clinical decision scores and ML tools are increasingly used in medicine. We seek to facilitate their implementation in real-world systems.

A score is only as good as its implementation. When a widely used proprietary sepsis model was externally validated, it performed far worse than reported (Wong et al., 2021). We build open, versioned, cited implementations that any system can call and anyone can check.

Open risk-score calculators, coming soon →
  1. 01Derived and validatedPublished score with external validation
  2. 02Open specificationVersioned, cited, machine-readable
  3. 03InterfacesMCP tools and EMR integration
  4. 04Point of careSame result, wherever it is used
Age
70+1
Sex
Female+1
Congestive heart failure
No0
Hypertension
Yes+1
Stroke, TIA or thromboembolism
No0
Vascular disease
No0
Diabetes mellitus
Yes+1
CHA₂DS₂-VASc4/ 9 pointsElevated risk. Shown with its source, so the clinician can check it.

Draft schema, for illustration · not for clinical use

03 · Area of interest

Trustworthiness, bias and interpretability

We are interested in creating open models which clinicians can trust, understand, and use reliably, while being cognizant of potential biases inherent to our models.

  • Source-linkedEvery judgement points to the sentence that supports it.
  • MeasuredAgreement with expert reviewers, with confidence intervals.
  • AuditedPerformance reported by subgroup, and errors described.
  • OpenModels, prompts and benchmarks others can rerun.
Source-linked judgements · RoB 2Fictional trial report

Methods. Adults with community-acquired pneumonia were enrolled at six centres. Participants were randomized 1:1 using a computer-generated sequence, with allocation concealed in sequentially numbered, opaque, sealed envelopes. Owing to the nature of the intervention, participants and treating clinicians were aware of group assignment. The primary outcome, clinical cure at day 14, was assessed by investigators blinded to allocation. Results. Outcome data were available for 412 of 420 randomized participants (98%). The trial was registered after enrolment began, and the statistical analysis plan was not published.

Report by subgroupIllustrative AUROC
  • Overall0.84
  • Age ≥ 750.71
  • Female0.83
  • Male0.85
  • Rural sites0.74

A model can look strong overall and still underperform for some patients. We report results by subgroup, with intervals, before anyone relies on them.

04 · Area of interest

Model efficiency

Clinical data and tasks alike face redundancy. We aim to make clinical implementations of machine intelligence more parsimonious.

Fewer inputs to collect, smaller models to host, lower cost per task: parsimony is what lets a tool run inside a hospital's own infrastructure, not just in a lab.

$0.0034
per paper for single-shot RoB 2 assessment with the open gpt-oss-120b model.
Medevi research →
29–57 s
per paper for automated MERSQI and NOS-E appraisal, against 65–130 minutes for a human reviewer.
Medevi research →
Diminishing returns · illustrativeDiscrimination vs model inputs
0.50.60.70.80.9110203040Number of inputs
80%of full-model discrimination

Drag the slider. In many clinical prediction tasks, the first few inputs carry most of the signal; the rest add cost and burden for little gain.

Collaborate

We are a growing academic collective looking for skilled computational collaborators.