Evidence and trials
Antevion Observatory
PlannedAntevion Observatory is designed to produce, with academic partners, outcome data for each written recommendation: whether it was done, never done or stated as not needed, linked to outcomes inside the hospital or the cancer registry.
Planned products are plans, not current operations. Each will be subject to its own regulatory review before any pilot.
The gap
What it addresses
Follow-up intervals need outcome data.
The core is designed to record, for each written follow-up recommendation, whether it was done, never done or stated as not needed. Linked to outcomes, with academic partners and ethics approval, that record will become evidence about the intervals themselves.
Intervals remain a clinical choice. Antevion will record and link; it will never choose, randomise or suggest an interval.
Workflow
How it is designed to work
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The protocol
It will be set with an academic partner and ethics approval, building on the leakage audits.
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The cohort
Each written recommendation, done, never done or stated as not needed, will be linked to outcomes inside the hospital or the cancer registry, and Antevion will never hold the linkage key.
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The trial platform
The same record is designed to support academic trials of follow-up intervals, in which trial units and clinicians will choose, and Antevion will never choose, randomise or suggest an interval.
Example
One written recommendation, linked to an outcome
Quoted sentence
Nódulo da suprarrenal; sugere-se reavaliação imagiológica.
Quoted from the signed report, as written. Translation: “Adrenal nodule; imaging reassessment is suggested.”
What is recorded
Follow-up
- Done
- Never done
- Stated as not needed
Confirmed by a person
- Outcome linkage
- Inside the hospital or the cancer registry
- Linkage key
- Never held by Antevion
- Interval
- Chosen by clinicians
Guardrails
Its guardrails
It will be built within these limits.
- With academic partners and ethics approval.
- Outcome linkage will happen inside the hospital or the registry; Antevion will never hold the linkage key.
- Antevion will never choose, randomise or suggest an interval.
- One hospital's data will never be used for another.
- A separate regulatory review before any pilot.
Designed for
Academic partners and trial units, research funders and health authorities, and the bodies that write follow-up guidance.
Same core
Every Antevion product is designed on the same core: it quotes what a clinician wrote, gives it an owner and proves whether it happened. It never generates an interval or a verdict; a person decides.
See the product familyTalk to us about follow-up evidence
Antevion Observatory is planned with academic partners, on the same core as imaging follow-up. Tell us which follow-up question your group would study.