For the reporting radiologist
ECG reporting that fits between the other lists.
Open a study and the measurement, the findings and the severity are there, with the evidence for each. Read it, disagree with it if you disagree, sign it — and move on to the next modality.
What changes
What this means for radiologists, specifically.
Measured before you look
Severity decides what you open first
Disagreement that is visible
Reports that leave cleanly
What it removes
The arrangement this replaces.
ECGs are the interruption in a day built around images
A signing queue is not a reading session
Double reading is hard to demonstrate
Permissions held
What this role can do, read from the access-control table.
Reporting ECGs is an interpreting-clinician job in this system, so a radiologist is given the same clinical role a cardiologist holds: run the analysis, review, override and sign.
Cardiologist
16 permissions held- See patient demographics
- Name, hospital number and encounter details, for patients in this facility.
- See the study list and its metadata
- Which recordings exist, when they were taken, and what state each is in.
- View the waveform
- The stored samples themselves, rendered on calibrated ECG paper.
- Read interpretations
- Measurements, findings and severity for a study, including anything a clinician has written.
- Run the analysis engine
- Produce a new automated interpretation from the stored samples.
- Record a clinical review
- State agreement or disagreement with the automated interpretation, with a note.
- Override a finding
- Replace an automated finding with a clinician’s own, which is recorded as an override for ever.
- Sign an interpretation
- Attach a named, digest-bound signature to the exact interpretation it covers.
- Re-run the analysis
- Analyse a study again, for example after a newer algorithm version is approved.
- Generate a narrative report
- Produce the written summary, which describes validated findings and may not introduce new ones.
- Transmit a signed study
- Release a signed interpretation to another system over FHIR or HL7.
- See critical alerts
- The worklist of findings that need a person, and its acknowledgement state.
- Acknowledge an alert
- State that a person has seen it, so it is never left unattended.
- Close an alert
- Record how it was resolved, with a closure note.
- Read operational analytics
- Throughput, turnaround and worklist measures. Not a diagnostic accuracy figure.
- Read the governance register
- Which algorithm versions exist and under what intended use.
Screens this role opens
Navigation is filtered by permission rather than by role name, so a screen this role cannot open is rendered as a label explaining which permission it would need — rather than as a link that fails when it is clicked.
Separation of duties
What this role cannot do, and why that protects them.
You cannot interpret a study the quality gate withheld; you can record a manual read, which is stored as a human conclusion rather than an automated one.
You cannot transmit an unsigned study. Transmission is the moment a clinical document leaves under a professional’s name, and the signature is what makes it one.
You cannot change the engine’s rules. Thresholds you own are your escalation policy; the measurement logic is versioned separately and governed by an administrative role.
Read together with the full pipeline
The limits above are enforced by the same rules that govern the pipeline described in how it works, and the regulatory position — including what this build does not establish — is stated on safety & limits.
Other audiences
This is one seat in the room.
More ECGs read, by the same team.
Read CardiologistsSpend your hour on the ECGs that need you.
Read DoctorsAn answer attached to the trace, at the point of care.
Read NursesYou will know when something needs a person.
Read ECG TechniciansRecord it once, properly, with the judgement written down.
Read Pathology & diagnosticsAn ECG report before the patient leaves the building.
Read Audit & qualityInterrogate the record without being able to alter it.
ReadRegulatory position
What this is not
This is a demonstration-grade clinical system. It is not a medical device, it holds no regulatory clearance anywhere, and it has not been validated against a clinical dataset.
It does not diagnose and it does not replace clinical assessment. Every interpretation is decision support for a qualified professional, who reviews, overrides and signs it — and the record shows which professional.
No sensitivity, specificity, agreement or accuracy figure appears on this site, because none has been established for this build. Any such figure would be invented. Read the full position.
See it on your own recordings.
Send a request, and a person reviews it. If it is approved you get a link that creates your own organisation, with the first 2 analysed studies included and no card details — and you are its administrator from the moment you set your password.