Cardiovascular Care

Hereditary heart disease is common, underdiagnosed, and highly actionable.

Intersect on FHIR™ connects cardiovascular genomics, remote patient monitoring, and integrated telehealth into a single care pathway — bringing the genetic counselor, the cardiologist, and the patient together across any distance.

1 in 250
Americans with familial hypercholesterolemia — 90% undiagnosed
700K
Cardiovascular deaths annually — disproportionate in underserved communities
50%
Of sudden cardiac deaths have no prior symptoms — hereditary risk is the hidden factor

Three conditions. Millions of undiagnosed patients.

Inherited cardiovascular conditions are among the most common hereditary diseases — and among the most undertreated. Each is highly actionable when identified. Each disproportionately affects patients who never reach a genetic counselor.

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Familial Hypercholesterolemia

1 in 250
Most common inherited cardiovascular condition

FH causes severely elevated LDL cholesterol from birth, leading to premature coronary artery disease and heart attack — often before age 50. Standard lipid panels alone miss the hereditary component. Cascade testing of first-degree relatives is the most cost-effective cardiovascular intervention available.

LDLR APOB PCSK9 LDLRAP1
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Hypertrophic Cardiomyopathy

1 in 500
Leading cause of sudden death in young athletes

HCM is the most common inherited heart muscle disease — and the leading cause of sudden cardiac death in people under 35. Most patients are asymptomatic until a life-threatening arrhythmia occurs. Genetic diagnosis enables proactive monitoring, activity modification, and device therapy consideration before a catastrophic event.

MYH7 MYBPC3 TNNT2 TNNI3

Inherited Arrhythmia Syndromes

1 in 2,000
Long QT alone — many more undiagnosed

Long QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia cause sudden cardiac death in structurally normal hearts — frequently in children and young adults. Many patients are identified only after a family member dies suddenly. Genetic diagnosis changes everything about how these patients are managed.

KCNQ1 KCNH2 SCN5A RYR2

From genetic finding to ongoing care — in one platform.

Intersect on FHIR™ supports the complete cardiovascular genetics care pathway — from initial risk identification through ongoing remote monitoring — without requiring the patient to travel to an academic center for every touchpoint.

01

Risk Identification

Family history, lipid panel results, or clinical presentation triggers genetic testing referral from the primary care provider.

CPOE · Referral
02

Genetic Testing & Counseling

Genetic counselor conducts a telehealth visit. Test is ordered within the platform. Results return as structured FHIR DiagnosticReport resources.

Telehealth · Genomics
03

Specialist Review

Cardiologist reviews genetic findings alongside the full longitudinal record — medications, ECGs, imaging, family history — in a single view.

Genomic Panel · CDS
04

Treatment & Monitoring Plan

Pharmacogenomics-informed medication selection. RPM device enrolled. Care plan documented and visible to every provider in the network.

RPM · Pharmacogenomics
05

Ongoing Remote Care

Continuous vital monitoring with automated alerts. Virtual follow-up visits. Patient receives summaries and medication reminders via mobile app.

RPM · Mobile · Alerts
The critical difference: In this model, the community PCP in a rural town can identify a patient with FH, refer to a genetic counselor via telehealth, have the cardiologist review results at the academic center, and monitor that patient at home — all within the same platform, with every provider seeing the same complete record. No fax. No duplicate data entry. No lost results.

Two dedicated cardiovascular panels — built and live.

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Cardiovascular Genetics Panel

Inherited conditions affecting heart structure, lipid metabolism, and cardiovascular risk — the most clinically actionable hereditary cardiovascular diseases.

Conditions Covered
  • Familial Hypercholesterolemia (FH) — LDLR, APOB, PCSK9
  • Hypertrophic Cardiomyopathy (HCM) — sarcomere gene variants
  • Dilated Cardiomyopathy (DCM) — TTN, LMNA, SCN5A and others
  • Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
  • Marfan Syndrome and related aortopathies — FBN1, TGFBR1/2
Clinical Integration
  • Lipid panel correlation for FH Dutch Criteria scoring
  • Statin pharmacogenomics cross-reference (SLCO1B1)
  • Cascade testing family member identification support
  • Imaging and ECG context visible alongside genetic findings

Cardiac Arrhythmia Panel

Inherited electrical disorders causing sudden cardiac death in structurally normal hearts — often in young, otherwise healthy individuals.

Conditions Covered
  • Long QT Syndrome (LQTS) Types 1–3 — KCNQ1, KCNH2, SCN5A
  • Brugada Syndrome — SCN5A loss-of-function variants
  • Catecholaminergic Polymorphic VT (CPVT) — RYR2, CASQ2
  • Short QT Syndrome — KCNH2, KCNQ1 gain-of-function
  • Progressive Cardiac Conduction Disease
Clinical Integration
  • QTc-prolonging drug interaction alerts in CPOE workflow
  • Sports participation and activity guidance context
  • ICD / device therapy consideration support
  • Family screening cascade workflow support

The right drug. The right dose. The first time.

Cardiovascular medicine is among the most pharmacogenomically complex specialties. Statins, beta-blockers, antiarrhythmics, and anticoagulants all have significant gene-drug interactions. Intersect surfaces these at the point of prescribing — not after the adverse event.

Drug Class Key Gene Clinical Action
Statins
SLCO1B1
Myopathy risk — dose adjustment or alternative
Warfarin
CYP2C9 / VKORC1
Dosing algorithm adjustment for INR stability
Clopidogrel
CYP2C19
Poor metabolizer — consider prasugrel/ticagrelor
Beta-blockers
CYP2D6
Ultrarapid metabolizer — dose escalation may be needed
Antiarrhythmics
SCN5A / KCNH2
QTc-prolonging risk — contraindicated in LQTS
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Alerts at the Point of Prescribing

When a provider orders a QTc-prolonging drug for a patient with a known LQTS variant, Intersect generates a clinical decision support alert before the order is placed — not after the patient experiences a dangerous arrhythmia.

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Genomics Informs Prescribing

The pharmacogenomics panel result lives in the FHIR record and is visible to every prescriber. A hospitalist covering overnight who orders a new medication sees the same genomic context as the cardiologist who ordered the original genetic test.

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Statin Therapy & FH

For FH patients requiring high-intensity statin therapy, SLCO1B1 status informs myopathy risk stratification — enabling personalized statin selection and dosing before the patient experiences muscle toxicity.

Continuous monitoring for high-risk cardiac patients.

For patients with identified hereditary cardiovascular risk, remote monitoring is not a convenience — it is a clinical necessity. Intersect on FHIR™ closes the gap between the genetic diagnosis and the ongoing surveillance that makes it actionable.

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Continuous Vital Monitoring

Wearable device data flows into the FHIR patient record as Observation resources — with automated alerts triggered by configurable thresholds tailored to each patient's condition and risk profile.

  • Heart rate and rhythm monitoring for arrhythmia detection
  • Blood pressure trending for hypertensive FH patients
  • Activity and exertion monitoring for HCM patients
  • Configurable alert thresholds per condition and provider preference
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Provider Dashboard Alerts

Out-of-range readings, trending deterioration, and missed readings surface directly on the provider dashboard — prioritized by severity so the care team focuses on the patients who need attention most.

  • Patients Needing Attention card with real-time triage
  • Trending deterioration detection before acute events
  • Missed reading notifications for adherence monitoring
  • Alert history integrated into the patient encounter record
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Virtual Follow-Up

Telehealth visits built into the same platform as RPM and genomics — so the follow-up visit happens in the context of the complete record, not a separate application with incomplete information.

  • Genetic counseling visits via telehealth — no travel required
  • Cardiologist review of RPM trends during virtual visit
  • AI-assisted SOAP note generation reducing documentation burden
  • Visit summary delivered to patient mobile app post-encounter
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Patient Mobile App

Patients with hereditary cardiovascular conditions need to understand their diagnosis and stay engaged with their care. The Intersect mobile app puts the right information in their hands.

  • Medication reminders with pharmacogenomics context
  • Visit summaries and genetic counseling notes
  • Self-scheduling for follow-up appointments
  • Direct messaging with the care team

Hereditary risk doesn't discriminate. Access to diagnosis does.

Familial hypercholesterolemia, inherited arrhythmias, and hypertrophic cardiomyopathy affect all populations with equal frequency. But genetic testing, genetic counseling, and specialist cardiology care are concentrated in academic medical centers — far from the rural and underserved communities that bear a disproportionate burden of cardiovascular mortality.

700K
Cardiovascular deaths per year in the U.S. — the leading cause of death, with hereditary factors in a significant proportion
90%
Of FH patients estimated to be undiagnosed — concentrated in populations without access to genetic counseling
46M+
Rural Americans with limited access to specialist cardiology and genetic counseling services
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The Hub-and-Spoke Solution

An academic medical center with a cardiovascular genetics program can extend its reach to every community hospital and FQHC in its service area — through a shared Intersect platform where the specialist reviews results and conducts telehealth visits without the patient traveling.

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Empowering the Community PCP

A rural primary care provider who suspects FH in a patient can order a genetic test, refer to a genetic counselor via telehealth, and have the cardiologist's recommendations visible in the same record — all without leaving the Intersect platform.

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Directly Relevant to AHA Priorities

The American Heart Association has identified hereditary cardiovascular risk in underserved populations as a strategic priority. Intersect on FHIR™ is purpose-built to address this gap — connecting genomics, remote monitoring, and telehealth in a model designed for reach.

Help us bring cardiovascular genomics to every patient.

We are seeking a cardiovascular genetics program at a large integrated health system to serve as our first clinical validation partner — co-developing the care model and shaping how genomic data flows across the network. If this is your organization, let's talk.

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Hereditary heart disease is diagnosable. Let's diagnose it.

See how Intersect on FHIR™ connects cardiovascular genomics, remote monitoring, and telehealth into a single care pathway.

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