Vitrubo

Every upload, read together. Not file by file.

One report over the whole record — labs, questionnaires and manual entries, read against the person's conditions, medications and history, regenerated with every new result.

The report — a dozen deviations read as a few connected stories

Lab results arrive as flat lists of values against reference ranges. The meaning lives between the values. The Health Report is built to find it.

How markers relate, what the medication list changes, what a borderline result means next to two other borderline results.

How the report reads a record.

01

Weight of evidence

Labs, questionnaires and manual entries are read as one picture — against the person’s conditions, medications and history, not in isolation.

02

A few connected stories, sorted by urgency

Nine flags become a few connected stories: needs attention, worth watching, returned to normal, worth re-testing.

03

A new version on every event

Upload a test and the report regenerates — a reason to come back with every result. Previous versions stay as history.

04

Plain language, next steps

What stands out, why it’s grouped that way, and what to discuss with a doctor.

Four states, in order of attention.

Needs attention

the story to bring to a doctor first

Worth watching

not urgent, kept in view

Returned to normal

back in range as of the latest event

Worth re-testing

measured too long ago to rely on

The report's triage summary

Every biomarker, explained.

01

Value, trend, plain words

The current value against its range, the trend across draws, and what it means — the guidance it rests on one click away.

02

One scale across labs

Different labs report different reference ranges and units. Vitrubo normalises them, so draws from different labs read as one trend, not three charts.

03

Connections on the card

Each card links the markers that explain it — found in the record, or named as missing so the next draw can close the gap.

A biomarker card with its value, trend and the guidance behind it

No marker is read alone.

01

Grouped by what explains what

For every flagged result, the markers that explain it are pulled from the record and grouped: found, or named as missing. Pairings come from medical guidance, not model intuition.

02

Checked for freshness

A supporting value can be too old to lean on. Every connection carries its relevance window: in window, with a caveat, or past it.

03

Tests to consider

Markers not on file that would sharpen the picture — and values worth re-testing — raised with the reason attached.

Connections — the markers that explain a flagged result

Across years and labs, on one line.

Different labs, different units — one clean trend. Values are normalized to one standard (17,000+ LOINC codes), so history reads as a single line, not a folder of formats.

A biomarker's history across labs, on one line

A new version on every event.

Every upload regenerates the report; previous versions stay as history. For a partner product, that is a reason for users to come back with every result.

Same analysis, two readings.

The patient reading of an observation

Patient view

Plain language. What it means and what to do next.

The doctor reading of the same observation

Doctor view

Clinical terminology. Full reasoning behind each observation.

Same interpretation underneath, shown at two depths — a View as: Patient / Doctor switcher sits inside every report.

See the doctor view

No diagnosis. A clear next step instead.

The report does not diagnose and does not select treatment. It shows what stands out, why, and what to discuss with a clinician — the reasoning is visible and auditable, and the conclusion stays with the human.

Let's look at a demo profile.

Emily Carter · 34 · five visits over nine months. A dozen scattered deviations, read as one coherent story — side findings not over-attributed, stale results flagged as out of date. Inside, a View as: Patient / Doctor switcher shows both depths.

Emily Carter's report — five visits over nine months

Questions we get first.

Lab panels — blood, urine, allergy — arrive as values; hospital records, prescriptions and notes are parsed as context for every interpretation.

Every statement links to the clinical guideline it rests on; source chips open the actual publication.

The report regenerates as a new version; previous versions stay as history.