ORCAA Cardiac
Capabilities Brief · v1.0

Continuous ECG, clinically routed.

A continuous ECG analysis platform — detecting arrhythmias, quantifying burden, and routing clinically meaningful findings into a structured two-tier escalation workflow.

Detection classes
8
Clinical templates
3
Escalation tiers
Orange · Red
Status
Pre-pilot
01 — Capabilities

Detection

Eight independent analytical streams running continuously on raw ECG and PPG-derived signals.

AF

Atrial fibrillation

Binary presence, episode probability, rolling 24-hour AF burden percentage.

PAUSE

Asystole / pause

Maximum RR pause duration measured to millisecond precision.

AVB

AV-block flagging

Presence and severity indication with clinical-review prompting.

ECTOPY

PVC / PAC quantification

Per-minute counts with banded thresholds for escalation.

HRV

Heart-rate variability

SDNN & RMSSD — gold-standard HRV metrics from RR-interval series.

SQI

Signal quality grading

Waveform fidelity, motion artifact, and lead-contact assessment.

LOG

Episode log

Timestamped events with physiologic snapshots, classed by clinical action.

REPORT

Per-recording report

Summary metrics, arrhythmia burden chart, HRV radar visualisation.

02 — Evidence

Escalation thresholds

Two-tier band model. Orange — clinical attention warranted. Red — urgent action. Values derived from published guidelines, configurable per template.

ParameterOrangeRedClinical rationale
Pause / asystole duration≥ 2.5 s≥ 4.0 s≥3s often symptomatic; ≥4s pacing consideration (ESC 2021)
Ectopic frequency (PVC/PAC)≥ 10 /min≥ 30 /minFrequent ectopy linked to cardiomyopathy risk (Baman 2010)
AF burden (24h rolling)≥ 5%≥ 20%Aligned with CHA₂DS₂-VASc stratification guidance
Heart rate (sustained)> 110 or < 50> 130 or < 40Standard cardiac-ward escalation thresholds
03 — Deployment-ready

Clinical templates

Three configurations ship with the system. Sites deploy with a template and tune from there.

TEMPLATE 01

Cardiac Standard

General cardiac-ward monitoring. Default thresholds across all parameters; balanced escalation. Suitable for stable post-cardiac patients and general cardiac wards.

TEMPLATE 02

Post-Ablation

AF recurrence surveillance after catheter ablation. Lower AF-burden trigger thresholds; tighter ectopic monitoring during the 3-month blanking period.

TEMPLATE 03

Heart Failure

Tachy / desat / hypotension emphasis. Lower tachycardia thresholds, integrated SpO₂ desaturation. Suitable for HF-decompensation surveillance.

04 — Deployment status

Production state & blockers

Live

Production

  • Production UI live at frontend-orcaa-cardiac-production.up.railway.app
  • Rules engine well-tested with comprehensive unit coverage
  • Three clinical templates configured and deployment-ready
  • Episode logging, HRV computation, per-recording reports working end-to-end
Pre-pilot blockers

In flight

1. AU server migration

APP 8 requires AU-region processing. Migration from Railway US to Fly.io Sydney is documented and executing.

2. Interface & escalation tuning

UI flow and escalation routing refinement, scoped and progressing alongside the migration.

Honest framing

"Production UI live, rules engine well-tested, evidence-grounded thresholds, ready for prospective pilot validation."

Prospective benchmark numbers (sensitivity, specificity, AUC) are not yet established — that evidence runs through the first clinical pilot.

05 — Integration & trajectory

Devices & roadmap

Device-agnostic ingestion. Two pathways active, more under evaluation.

Device integration

Polar H10
REFERENCE

Standard BLE heart-rate service. Production-ready gateway for bench testing and rapid prototyping.

PCardio (2M Engineering)
INTEGRATING

Wearable with raw ECG and bioimpedance respiration. SpO₂/temperature variant pending evaluation.

FDA/CE-marked wearables
EVALUATING

Generic device-source field accepts any ingestion partner under evaluation.

Roadmap

  1. Now
    Complete AU server migration; finalise escalation/interface tuning; prepare for first clinical pilot.
  2. Q1
    First prospective pilot in cardiac-ward / cardiac-rehab; establish baseline against adjudicated outcomes.
  3. Q2
    Integration with FDA/CE-marked wearable partner for ambulatory post-discharge cardiac surveillance.
  4. Q3+
    Refinement from real-world data; additional templates (post-MI, atrial-flutter cohorts, etc.).