What is the fractional area change of the right ventricle in echocardiography?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 18, 2026 • View editorial policy

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.

Right Ventricular Fractional Area Change in Echocardiography

RV fractional area change (RV-FAC) is calculated as: [(RV end-diastolic area - RV end-systolic area) / RV end-diastolic area] × 100, and normal values are >35%, with values <35% indicating RV systolic dysfunction. 1

Definition and Calculation

RV-FAC represents the proportion of RV area change during right ventricular systole. The measurement requires:

  • Optimal imaging view: RV-focused apical four-chamber view 2
  • Measurement technique: Planimetry of RV end-diastolic area (RVEDA) and RV end-systolic area (RVESA) 1
  • Important technical point: Include trabeculae within the RV cavity when tracing, and ensure the entire right ventricle (apex and free wall) is contained in the imaging sector during both systole and diastole 2

Normal Values and Thresholds

The key cutoff values are:

  • Normal: RV-FAC >35% 2
  • Abnormal/RV dysfunction: RV-FAC <35% 2
  • Mean normal value: 49 ± 7% 2

Context-Specific Thresholds

For arrhythmogenic cardiomyopathy diagnosis, different criteria apply 3:

  • Major criterion: RV-FAC ≤33% (with regional wall motion abnormalities)
  • Minor criterion: RV-FAC >33% to ≤40% (with regional wall motion abnormalities)

For advanced heart failure, RV-FAC <27% was independently associated with death or need for heart transplantation 4, and RV-FAC <35% indicates dysfunction 4.

Clinical Utility and Prognostic Value

RV-FAC provides important prognostic information across multiple conditions:

  • In heart failure with reduced ejection fraction (HFrEF): RV-FAC <35% was present in 33% of patients and associated with increased mortality 5
  • In heart failure with preserved ejection fraction (HFpEF): RV-FAC <35% occurred in 28-33% of patients and predicted worse outcomes 5
  • Prognostic accuracy: RV-FAC is more accurate than tricuspid annular S' velocity in predicting cardiac death, though TAPSE shows similar accuracy 6
  • Combined assessment: Using both RV-FAC and TAPSE together provides incremental prognostic value beyond either parameter alone 6

Technical Considerations and Limitations

Measurement Reliability

  • Reproducibility: RV-FAC demonstrates acceptable reproducibility with intraclass correlation coefficients ranging from 0.69-0.97 depending on the study population 7, 8
  • Feasibility: Successfully obtained in approximately 99% of patients 7

Important Caveats

RV-FAC has significant limitations for serial assessment:

  • While correlated with cardiac MRI-derived RV ejection fraction (r² = 0.567), RV-FAC showed poor sensitivity (33-56%) for detecting deterioration in RV function during follow-up in pulmonary hypertension patients 9
  • Load dependency: RV-FAC is sensitive to both preload and afterload, making interpretation challenging when RV function is borderline 4
  • Post-surgical changes: After cardiac surgery, RV-FAC may decrease less than longitudinal parameters like TAPSE, indicating non-uniform changes in RV function measures 10

Optimal Assessment Strategy

For comprehensive RV evaluation, combine RV-FAC with:

  • Qualitative visual assessment of RV function 11
  • TAPSE (tricuspid annular plane systolic excursion) 6
  • RV free wall longitudinal strain when available 3

The combination of FAC <35% plus qualitative RV dysfunction assessment correlates best with severe RV dysfunction on cardiac MRI 11, making this integrated approach superior to relying on any single parameter.

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.