Pacemaker & ICD Interrogation Report Decoder

Paste the text of a pacemaker, ICD, CRT or loop-recorder interrogation or remote-monitoring report. You get the device and lead table, battery status, programming, every arrhythmia and therapy episode on a dated timeline, the alerts, the findings that matter in a cardiac, sudden-death or syncope case, and the records to request next. Nothing is added that is not in the report: unknowns stay blank and anything the decoder infers is labelled "Inferred".

Report text (copy from the PDF or EMR; up to 30,000 characters)

0 / 30,000

Remove patient identifiers before pasting if your matter requires it. Text is sent to the decoder once and is not stored with the result. Twelve runs per hour without an account.

Decoded report

Device

Leads

Programming

Pacing & burden

Episode timeline (sorted by date; undated episodes last)

Alerts

Clinical flags for the case

How to use the result

Check every quoted value against the original report page before it goes into a chronology or an expert's file. The "quote found in text" marks show that the supporting sentence exists in what you pasted, not that the decoder read it correctly.
Line the episode timeline up against the clinical chronology. An episode time that falls before a clinic note, a discharge, or a call to the office is where the case usually lives. Device clocks can drift and may be set to a different time zone; ask who confirmed the device clock.
Treat lead and battery flags as questions, not conclusions. A high impedance or a battery at elective replacement is a prompt to request the trend across prior interrogations.
Anything marked "Inferred" was not stated in the report. Decide whether an expert needs to confirm it.
Compare the programmed settings against earlier reports to find undocumented programming changes.

What to request next

Standard requests in a device case

Every prior in-clinic interrogation and the full remote-transmission log for the life of the device, in native vendor format (not only the summary PDF).
Alert and notification records with the timestamp each alert was generated, received, viewed and acknowledged, and by whom.
Programming change history (parameter print-outs before and after each change) and the orders or notes that authorised each change.
Stored electrograms (EGMs) and marker channels for every episode listed above, including non-sustained and noise episodes.
Device clock settings and any time-zone or clock-correction entries.
Manufacturer technical-services notes, any product advisories or recalls applying to the device and lead models named in the report, and the explant or returned-product analysis if the device was removed.
The clinic's device-follow-up protocol and the remote-monitoring enrolment and consent paperwork.

Need the whole cardiac record read, not just the device report?

MedLegal AI reads the full chart, pins every finding to the Bates page, and builds the chronology with the device episodes already placed on it. Free account to start.

Not legal or medical advice. Verify against the record.