Understanding IQR/Median of 12.4%
An IQR (Interquartile Range) to median ratio of 12.4% indicates relatively low variability in the data, suggesting consistent measurements across the middle 50% of observations, which generally reflects stable disease characteristics or treatment responses with minimal outliers.
Statistical Interpretation
The IQR/median ratio is a measure of relative variability:
- Low ratio (<20%): Indicates tight clustering of data around the median, suggesting homogeneous patient populations or consistent disease behavior 1
- A 12.4% ratio specifically: Demonstrates that the spread between the 25th and 75th percentiles is only 12.4% of the median value, indicating minimal dispersion 1
Clinical Implications for Disease Risk
Risk Stratification Context
When this ratio appears in clinical studies:
- Homogeneous risk profile: A low IQR/median ratio suggests patients within a study cohort have similar baseline characteristics and disease severity, making treatment effect estimates more reliable 1
- Predictable disease progression: In chronic kidney disease studies, for example, consistent GFR decline rates (low variability) allow more accurate prognostic counseling 1, 2
- Reduced confounding: Less variability in key parameters means fewer unmeasured confounders affecting outcomes 1
Fragility of Evidence Consideration
Critical caveat: Studies with low variability may have fragile statistical significance 1:
- The median Fragility Index across cardiovascular trials was 8.0 (IQR 3.0-15.0), meaning only 8 event changes could reverse statistical significance 1
- 27.5% of trials had a Fragility Index ≤3, indicating extremely fragile results despite appearing statistically significant 1
- When IQR is narrow relative to median, small absolute changes in outcomes can dramatically alter conclusions 1
Management Implications
Treatment Decision Framework
For conditions with low IQR/median ratios in outcome measures:
Expect consistent treatment responses: Patients are likely to respond similarly to interventions, making guideline recommendations more universally applicable 1
Monitor for deviation from expected patterns: Any individual patient showing outcomes outside the narrow IQR range warrants investigation for non-adherence, drug interactions, or alternative diagnoses 1
Use population-based targets confidently: When variability is low (12.4%), population median values serve as reasonable individual patient targets 1, 2
Specific Clinical Scenarios
In chronic kidney disease management (where IQR/median ratios are commonly reported):
- GFR decline rates with median 1.03 mL/min/1.73m²/year and narrow IQR indicate predictable progression, allowing accurate timing of nephrology referral and renal replacement therapy planning 1
- Initiate SGLT2 inhibitors at eGFR ≥20 mL/min/1.73m² when albuminuria is present, as consistent benefit is demonstrated across patients with minimal variability 3
In oncology trials (particularly HER2-positive metastatic breast cancer):
- Median overall survival of 57 months with narrow IQR supports aggressive first-line dual HER2 blockade for virtually all eligible patients 1, 4
- Do not delay trastuzumab plus pertuzumab initiation, as consistent survival benefits (low variability) mean nearly all patients derive meaningful benefit 4
Common Pitfalls to Avoid
Misinterpretation Risks
Assuming low variability equals strong evidence: A narrow IQR does not guarantee robust findings—always check the Fragility Index, which was ≤3 in 27.5% of cardiovascular trials despite appearing statistically significant 1
Ignoring loss to follow-up: In 42.5% of trials, the Fragility Index was lower than the number of patients lost to follow-up, meaning missing data alone could reverse conclusions 1
Overgeneralizing from homogeneous populations: Low IQR/median ratios may reflect restrictive inclusion criteria rather than true biological consistency—verify the study population matches your patient 1
Practical Application Errors
Do not assume individual patient outcomes will match population medians exactly, even with low variability:
- In aspiration pneumonia risk assessment, despite consistent median PAS scores, individual factors (impaired laryngeal sensation, performance status) dramatically alter risk (OR 5.01 and 1.85 respectively) 1
- Always assess individual risk modifiers beyond population statistics, particularly comorbidities and functional status 1
Recognize when narrow IQR reflects measurement limitations rather than true consistency:
- Clinician-documented response assessments showed median 77.5% evaluability but variable timing, potentially creating artificially narrow IQR through selective reporting 5
Actionable Clinical Algorithm
When encountering IQR/median = 12.4% in clinical literature:
Verify the Fragility Index if available—if ≤3, treat conclusions cautiously despite statistical significance 1
Confirm your patient matches the study population—narrow IQR may reflect homogeneous enrollment rather than universal applicability 1
Apply population-based recommendations confidently for patients matching inclusion criteria, as low variability indicates consistent treatment effects 1, 3, 4
Investigate aggressively if individual patient outcomes deviate from the narrow expected range, as this suggests important modifying factors 1