J84.114
BillableAcute interstitial pneumonitis
HCC Category Mapping
V28HCC 280 — Chronic Obstructive Pulmonary Disease
0.334V24HCC 112 — Fibrosis of Lung and Other Chronic Lung Disorders
0.268ESRDHCC 112 — Fibrosis of Lung and Other Chronic Lung Disorders
0.000RxHCCHCC 227 — Sarcoidosis, Pulmonary Alveolar Disorders
0.000What This Code Means
A sudden inflammation of the lung tissue between the air sacs, often caused by an immune reaction or infection that develops rapidly.
Coding Tips
- •Verify the acute onset and distinguish from chronic interstitial pneumonitis (J84.111)
- •Document the underlying cause if identifiable, as this may affect coding specificity
Clinical Significance
Acute interstitial pneumonitis (Hamman-Rich syndrome) is a rare, rapidly progressive form of interstitial lung disease that often requires intensive care unit admission and mechanical ventilation. This fulminant condition has high mortality and represents extreme resource utilization. Capturing this diagnosis is important for reflecting the acute severity and complexity of care required.
Documentation Requirements
- ✓Documentation of acute onset (days to weeks) of respiratory failure without identifiable cause
- ✓High-resolution computed tomography showing diffuse bilateral ground-glass opacities and consolidation
- ✓Lung biopsy showing diffuse alveolar damage pattern if performed
- ✓Exclusion of other causes of acute respiratory distress syndrome including infection, drug reaction, and connective tissue disease
- ✓Documentation of severity including ventilator requirements, oxygen needs, and ICU status
Excludes 1 — Do NOT code together
- pneumocystis pneumonia (B59)
Commonly Confused Codes
J80 — Acute respiratory distress syndrome (ARDS) is a clinical syndrome with a known trigger, while acute interstitial pneumonitis is idiopathic ARDSJ84.111 — Idiopathic interstitial pneumonia NOS is used for chronic presentations, not the acute fulminant formJ18.9 — Pneumonia unspecified describes infectious pneumonia, not the non-infectious acute interstitial pneumonitisJ84.112 — IPF is a chronic progressive disease, unlike the acute onset of Hamman-Rich syndrome