IQR/Median Ratio as a Quality Control Metric for FibroScan Reliability
The IQR/median ratio serves as a critical quality control parameter to identify unreliable FibroScan measurements, with values ≥0.30 (or ≥30%) indicating poor measurement quality that can lead to falsely elevated or inaccurate liver stiffness values, particularly overestimation of fibrosis severity. 1, 2
Understanding the IQR/Median Quality Metric
The interquartile range (IQR) divided by the median liver stiffness measurement (IQR/M) quantifies the variability between individual measurements during a FibroScan examination 2:
- IQR/M <0.30 (or <30%) indicates consistent, reliable measurements 3, 1
- IQR/M ≥0.30 (or ≥30%) signals excessive variability and unreliable results 3, 1
How IQR/Median Identifies Falsely Low (and High) Values
Mechanism of Detection
The IQR/median ratio functions as a precision indicator rather than specifically detecting "falsely low" values 2. More accurately, it identifies unreliable measurements in either direction:
- High IQR/median ratios (≥0.21-0.30) are associated with significant discordances between FibroScan and actual histological fibrosis stage 2
- Studies show that IQR/M ≥0.21 is specifically associated with overestimation of liver fibrosis, not underestimation 2
- When IQR/M ≥0.21, discordances of at least two fibrosis stages occurred in 15.1% of cases versus only 7.4% when IQR/M <0.21 2
Impact on Diagnostic Accuracy
The diagnostic performance of FibroScan deteriorates significantly with elevated IQR/median ratios 2:
- For cirrhosis (F4) detection: AUROC drops from 0.95 (95% CI 0.92-0.99) when IQR/M <0.21 to 0.86 (95% CI 0.77-0.94) when IQR/M ≥0.21 2
- For advanced fibrosis (≥F3): AUROC decreases from 0.89 (95% CI 0.83-0.95) to 0.80 (95% CI 0.72-0.88) with higher IQR/median ratios 2
Three Essential Validity Criteria for FibroScan
A valid liver stiffness evaluation (LSE) requires ALL three criteria to be met simultaneously 3, 1:
- ≥10 successful measurements obtained 3, 1
- Success rate ≥60% 3, 1
- IQR/median ratio <0.30 (or <30%) 3, 1
Clinical Consequences of Invalid Measurements
When these validity criteria are not met, diagnostic accuracy suffers substantially 1:
- Correlation with biopsy: Valid LSE showed rs=0.577 versus invalid LSE rs=0.259 (p=0.022) 1
- AUROC for significant fibrosis: 0.83 for valid LSE versus 0.66 for invalid LSE (p=0.048) 1
- Negative predictive value at 8 kPa cutoff:
Clinical Algorithm for Interpreting FibroScan Results
Step 1: Verify Measurement Validity
Before interpreting any FibroScan value, confirm all three validity criteria are met 3, 1:
- Check that ≥10 measurements were obtained 3, 1
- Verify success rate is ≥60% 3, 1
- Confirm IQR/median <0.30 3, 1
Step 2: Action Based on Validity Status
If ANY validity criterion fails 3, 1:
- Do not use the FibroScan result for clinical decision-making 1
- Repeat the examination, potentially with an experienced operator 1
- Consider alternative non-invasive tests (APRI, FIB-4, ELF) 3, 4
- Consider referral for MR elastography if available 3
- In high-risk patients, consider hepatology referral for further evaluation 3
If all validity criteria are met 5:
- Proceed with standard interpretation using established cutoffs:
Common Pitfalls and Technical Considerations
Factors Affecting IQR/Median Ratio
Several technical and patient factors can elevate the IQR/median ratio 3, 1:
- Operator inexperience: Validity rates improve significantly with the first 10-50 examinations performed 1
- Severe obesity: Limits ultrasound penetration and measurement consistency 3
- Narrow intercostal spaces: Reduces acoustic window quality 3
- Ascites: Interferes with measurement reliability 3
- Patient movement or inadequate breath-holding 1
Important Clarification on "Falsely Low" Values
The IQR/median ratio does not specifically identify "falsely low" FibroScan values 2. Research demonstrates that elevated IQR/median ratios are actually associated with overestimation rather than underestimation of fibrosis 2. The ratio serves as a general quality indicator for measurement precision, flagging results that may be inaccurate in either direction, though the predominant error pattern is overestimation 2.
When Non-Invasive Tests Are Discordant
If FibroScan results conflict with serological markers (APRI, FIB-4) 3: