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Cost Analysis of Patients Referred for Inherited Heart Rhythm Disorder Evaluation
Mikyla L Janzen1, Christopher Cheung1, Shubhayan Sanatani2
1Heart Rhythm Services, Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Insights
Multidisciplinary clinics effectively diagnose inherited heart rhythm disorders (IHRDs). Primary referrals are costlier than family screening, but both yield high diagnostic rates for these rare conditions.
Area of Science:
- Cardiology
- Genetics
- Clinical Medicine
Background:
- Inherited heart rhythm disorders (IHRDs) are rare, complex conditions.
- These arrhythmogenic disorders can cause sudden unexpected death in healthy individuals.
- Multidisciplinary programs are crucial for diagnosing IHRDs in patients and families.
Purpose of the Study:
- To characterize patients evaluated in a specialized adult and pediatric IHRD clinic.
- To calculate the total costs associated with IHRD evaluation and diagnosis.
- To compare costs and diagnostic yields between primary referrals and family members undergoing cascade screening.
Main Methods:
- Evaluation of 618 patients in a specialized IHRD clinic (April 2013-February 2015).
- Patients categorized as primary referrals or family members for cascade screening.
- Calculation of per-patient costs and total costs per diagnosis.
Main Results:
- A total of 618 patients were evaluated; 77% received a diagnosis.
- Primary referrals required more tests and incurred higher evaluation costs ($3096 vs $983).
- The total cost per diagnosis was significantly higher for primary referrals ($4021) than family members ($1277).
Conclusions:
- Clinical evaluation in specialized IHRD clinics yields a high diagnostic rate.
- Costs are comparable to other complex multidisciplinary disorder clinics.
- Evaluation costs are higher for primary referrals than for family members in cascade screening.
Background:
Inherited heart rhythm disorders (IHRDs) are complex and uncommon arrhythmogenic conditions that can lead to sudden unexpected death in seemingly healthy individuals. Multidisciplinary programs can assist in the diagnostic testing of potentially affected individuals and their family members.
Methods:
Patients evaluated in a specialized adult and pediatric IHRD clinic between April 2013 and February 2015 were characterized. The total costs per evaluation and diagnosis were calculated. Patients were divided according to referral indication (primary referral or family member).
Results:
A total of 618 patients were evaluated (age 36 ± 21 years; 52% male), of which 274 (44%) were primary referrals and 344 (56%) were family members referred for cascade screening. Overall, 47% had at least 1 follow-up visit. Patients had a median of 3 tests; primary referrals required more tests (4 vs 2; P < 0.01). The median cost per patient was $1340 CAD. Evaluation of the primary referrals was costlier than family members ($3096 vs $983; P < 0.01). A definite or probable diagnosis was determined in 464 patients (77%), with no difference according to patient type (P = 0.18). The total cost per diagnosis was $4021 in primary referrals compared with $1277 in family members (P < 0.01).
Conclusions:
Clinical evaluation of patients with suspected IHRD results in a high diagnostic yield and costs aligned with other complex disorders involving multidisciplinary clinics. Evaluation costs are expectedly higher in primary referrals compared with targeted family screening.
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